VAERS Reports FK 9894

VAERS 2680491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MN
Alter: 58,0
Geschlecht: M
Eingang: 08.09.2023
Impfdatum: 03.03.2023
Beginn: 07.09.2023
Tage bis Beginn: 188,0
Dosis: 4
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Patient expired 9/7/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: HTN, T2DM, CKD3, HFpEF, paroxysmal afib/flutter on rivaroxaban, COPD, super morbid obesity BMI 46, Obesity Hypoventilation Syndrome/Obstructive Sleep Apnea
Andere Medikamente: Unknown
Allergien: Shrimp
Vorherige Impfungen: -

VAERS 2677569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MN
Alter: 76,0
Geschlecht: M
Eingang: 29.08.2023
Impfdatum: 09.02.2023
Beginn: 26.08.2023
Tage bis Beginn: 198,0
Dosis: 4
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Patient expired 8/26/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Emphysema, pulmonary hypertension, lung cancer
Andere Medikamente: Unknown
Allergien: Pecans, almonds, walnuts, shellfish, hydrocodone, morphine
Vorherige Impfungen: -

VAERS 2650326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 28.06.2023
Impfdatum: 25.03.2022
Beginn: 28.03.2023
Tage bis Beginn: 368,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Deep vein thrombosis Hypercholesterolaemia Pulmonary embolism

Symptomtext

I26.99 ACUTE PULMONARY EMBOLISM 3/29/2023 HYPERCHOLESTEROLEMIA I82.409 ACUTE DVT, UNSPECIFIED VEIN 4/28/2023 HYPERCHOLESTEROLEMIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2644660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 04.04.2022
Beginn: 29.12.2022
Tage bis Beginn: 269,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Pulmonary embolism

Symptomtext

ACUTE PULMONARY EMBOLISM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2641077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MN
Alter: 79,0
Geschlecht: F
Eingang: 05.06.2023
Impfdatum: 28.04.2022
Beginn: 12.03.2023
Tage bis Beginn: 318,0
Dosis: N/A
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 Cough Dyspnoea Pain Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient with history of COPD, on 3.5 L O2 as needed. She was brought to the ED by EMS on 3/12/23 with cough, worsening shortness of breath, and body aches that have been present for several days. A COVID PCR test performed in the ED resulted positive. The patient was admitted 3/12/23 - 3/16/23 with discharge diagnoses including acute on chronic hypoxic respiratory failure. During admission, she was on increased supplemental O2 but was able to be weaned back to her baseline 3.5L O2. Of note, she has received the primary COVID vaccine series and two boosters.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2636862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 87,0
Geschlecht: F
Eingang: 25.05.2023
Impfdatum: 07.04.2022
Beginn: 28.09.2022
Tage bis Beginn: 174,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute myocardial infarction

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2631003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 26,0
Geschlecht: M
Eingang: 12.05.2023
Impfdatum: 10.03.2022
Beginn: 21.08.2022
Tage bis Beginn: 164,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Pulmonary embolism

Symptomtext

MULTIPLE SUBSEGMENTAL PULMONARY EMBOLI WITHOUT ACUTE COR PULMONALE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2624193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: GA
Alter: 77,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 28.04.2022
Beginn: 30.10.2022
Tage bis Beginn: 185,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Anticoagulant therapy Asthenia Cerebrovascular accident Colonoscopy abnormal Computerised tomogram head abnormal Deep vein thrombosis Endoscopy abnormal Gastrointestinal haemorrhage Haemoglobin decreased Magnetic resonance imaging head abnormal Peripheral swelling Ultrasound Doppler abnormal

Symptomtext

I went in for my left leg swelling, my doctor ordered an ultrasound on my leg. They found that I had a blood clot in my left leg, I was told I had DVT. I was put on blood thinners to help break up the blood clot. I was admitted into the hospital for an endoscopy and colonoscopy because my hemoglobin had dropped. They found my GI bleed and were able to fix it. They were going to put a in a filter for the blood clot but the at the time the doctor did not have the size needed. I went in for a second ultrasound. The second ultrasound showed that the blood clot was no longer there, it had dissolved from the blood thinners I was taking. I was discharged from the hospital went home and was experiencing weakness. My doctor ordered an MRI and CT scan of my brain. It was discovered that I had, had a pinpoint stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 7,0
Labordaten: 30OCT2022 Ultrasound - positive for DVT; 17NOV2022 Ultrasound - blood clot not visible; 00DEC2022 MRI - positive for pinpoint stroke; 00DEC2022 - CT scan - positive for a pinpoint stroke
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension
Andere Medikamente: N/A
Allergien: Lipitor
Vorherige Impfungen: -

VAERS 2619811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 19.04.2022
Beginn: 08.06.2022
Tage bis Beginn: 50,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute myocardial infarction Aortic valve stenosis Hypotension

Symptomtext

ACUTE ST ELEVATION MI, INFERIOR WALL 6/23/2022 AORTIC VALVE STENOSIS HYPOTENSION 6/23/2022 AORTIC VALVE STENOSIS ACUTE ST ELEVATION MI, INFERIOR WALL 6/23/2022 AORTIC VALVE STENOSIS HYPOTENSION 6/23/2022 AORTIC VALVE STENOSIS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2616034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 17.11.2022
Beginn: 11.04.2023
Tage bis Beginn: 145,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute myocardial infarction Brain natriuretic peptide increased COVID-19 Catheterisation cardiac abnormal Chest pain Coronary angioplasty Coronary arterial stent insertion Coronary artery disease Coronary artery occlusion Cough Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Hyperhidrosis Left ventricular dysfunction Left ventricular end-diastolic pressure increased Malaise Pain in extremity

Symptomtext

Heart Cath 4/11/2023, Dr 1. Coronary artery disease as follows: 100% distal right coronary artery culprit lesion, 70% mid LAD, 70-80% distal LAD, 50% mid circumflex artery, 50-60% mid 1st obtuse marginal branch. 2. Successful PTCA stent mid right coronary artery with a 3.55 x 18 mm drug-eluting stent, successful PTCA stent distal right coronary artery/PDA with a 3 mm x 38 mm drug-eluting stent. 3. Mild LV dysfunction with ejection fraction of 45-50% with severe inferior apical hypokinesis. 4. No significant mitral regurgitation. 5. No aortic stenosis. 6. Mildly elevated left ventricular end-diastolic pressure of 20 mmHg. Echo 4/11/2023 1. Left Ventricle: Left ventricle cavity appears normal. Wall thickness is normal. Systolic function is mildly decreased with an ejection fraction of 50 - 55%. Regional wall motion abnormalities present. Inferior wall hypokinesia There is no diastolic dysfunction. Hospital Course: Patient is a 71 year-old Male who presented via EMS due to complaints of crushing chest pain, Left arm pain, and diaphoresis that started at 4/11 at 800 when he was raking the leaves. EKG in field significant for STEMI in inferior posterior aspect. In the ED, Vitals : 97.2F, 56 HR, 18 RR, 121/76, 97% RA, Labs significant for Trope 2120-- >2823, BNP 389 and positive Covid-19 test. Patient admitted to cardiology team with emergent heart-cath. Heart cath performed by Dr showed complete RCA occlusion requiring 2x DES, notable 70% occlusion of mid LAD and 70-80% distal LAD, 50% mid circumflex and 0-60% obtuse marginal artery. Echocardiogram obtained showed EF of 50-55% with regional wall motion abnormalities, inferior wall hypokinesis with history of diastolic dysfunction. Patient was initiated on DAPT: ASA and Prasugrel, Lisinopril, and Metoprolol. Patients COVID symptoms remained stable with no significant symptomatology besides occasional cough. Pts hospital course not complicated and patient was discharged with instructions to follow-up with pcp, Cardiology while obtaining stress test and referral for cardiac rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: Positive COVID PCR 4/11/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2607016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

kritisch

Staat: -
Alter: 94,0
Geschlecht: M
Eingang: 30.03.2023
Impfdatum: 20.04.2022
Beginn: 14.02.2023
Tage bis Beginn: 300,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Atrial fibrillation Blood creatinine normal Blood thyroid stimulating hormone normal COVID-19 Chest X-ray abnormal Chronic kidney disease Citrobacter test positive Computerised tomogram head normal Condition aggravated Cough Culture urine positive Cystitis Delirium Dementia Dizziness Dyspnoea Echocardiogram normal

Symptomtext

Patient is a 95 y.o. female patient of DO with history of AAA, iliac aneurysm, OA, atrial fibrillation, hypothyroidism, HLD, and HTN who presented to a local Hospital with dyspnea, cough, and found to be in atrial fibrillation with RVR and have COVID. Discharge Diagnoses: Acute metabolic encephalopathy In setting of COVID, UTI, had intermittent episodes of delirium with hallucinations B12 <400, TSH normal, vit D mildly low CT head on admission without acute intracranial abnormalities B12 and vit D replacement initiated Seroquel scheduled nightly Mentation overall improved at time of discharge Acute cystitis Urine showed positive nitrate and moderate WBC Prescribed Keflex as outpatient, but did not pick up prescription prior to being admitted Urine culture 2/14 with >100K Citrobacter freundii Bactrim 5-day course completed on 2/22 Acute respiratory failure with hypoxia, resolved Respiratory failure secondary to COVID O2 sat 86% on room air on admission Mild leukocytosis on admission with mild lactic acidosis CXR with left basilar consolidation, possible small left pleural effusion Procalcitonin normal Urinary antigens negative Initially required NC O2, but now off oxygen Covid-19 Virus Infection Date of onset of symptoms: 2/10/2023 Symptoms present on admission: Dyspnea, cough Date of covid positive test: 2/13/2023 Vaccination status: vaccinated, boosted Imaging: as above with basilar consolidation Oxygen requirements on admission: 2L NC O2 Current oxygen requirements: room air Medical therapy: received decadron, discontinued when no longer requiring supplemental O2 Consultants following: None Special isolation end date: 2/21/23 Inflammatory markers not elevated Atrial fibrillation with RVR Has underlying atrial fibrillation, likely exacerbated by acute infection HR on admission in the 140s Echo (5/4/22): LVSF normal, EF 65%, no wall motion abnormality, no significant valvular disease Received IV metoprolol in ED, then started on diltiazem drip. Drip discontinued when rate improved. Increased Toprol-XL to 200 mg, rate now better controlled Conintued xarelto CKD3 Creatinine 0.86 at time of discharge Hypothyroidism Continued outpatient Synthroid Dizziness/vertigo Meclizine provided as needed Bilateral feet pain Normal exam Ibuprofen given as needed Pain improved prior to discharge Goals of care Previously living at home with son, but has become more difficult to manage due to dementia. Family requesting discharge to SNF for rehab, but expressing some concerns regarding long-term management. Discussed with daughter, who feels patient has been declining significantly. Patient currently DNR CCA. Palliative care consulted and assisted family with decision making.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2605050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 11.05.2022
Beginn: 22.02.2023
Tage bis Beginn: 287,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Angiogram pulmonary abnormal Asthenia COVID-19 COVID-19 pneumonia Cough Dysstasia Encephalopathy Fall Fatigue Haemoglobin normal Hallucination Hypoxia Iron deficiency anaemia Lung opacity Mantle cell lymphoma Metabolic encephalopathy Metastases to bone marrow

Symptomtext

Patient is a 69 y.o. male with a history of Non-Hodgkin Lymphoma, DVT (off anticoagulation), HTN, Anemia who presented to Hospital 2/22/2023 with several hours of weakness, fatigue, cough, fever, and mechanical fall from which he was unable to stand after due to weakness. In ED: SARS-CoV-2 positive. Admitted due to hypoxia with evidence of Covid-19 pneumonia. Symptoms improved with decadron/remdesivir and supportive care. Did require low flow O2 for discharge. 1. COVID-19 pneumonia : Patient with fever cough fatigue and generalized weakness since 2/22/23 (0 days prior to admission). SARS-CoV-2 positive on 2/22/23. Patient is vaccinated. CTPA 2/23/23: mild ground glass opacities bases, no PE. Dexamethasone 6mg PO x10 days (last dose 3/3/23). Started remdesivir IV x5 days (last dose 2/25/23 given planned discharge). Symptoms improved overall. 2. Acute hypoxic respiratory failure: Patient not on oxygen at home but requiring 2 L oxygen through nasal cannula. Likely secondary to COVID. Received steroid and remdesivir as above and supportive treatment. Required O2 for home-going (1L). Further weaning in outptient setting. 3. Mechanical Fall: No loss of consciousness, no head strike. PT/OT followed, patient and spouse declined HHC. 4. Mantle Cell Lymphoma: Followed by Dr. (Oncology), daignosed 3/2021, stage IV with marrow and splenic involvement on bendamustine and Rituximab. Last chemo ~10/2022, next dose rituxan due 2/24/23, will need to reschedule and follow up outpatient. 5. Chronic DVT: Diagnosed 3/2021. Venous duplex 5/2021 chronic left femoral to gastrocnemius venous thrombosis. Patient taken off Xarelto ~10/2022. 6. Chronic Iron Def Anemia: baseline Hgb ~10-12. Hgb of 12 (MCV 98) in ED. 7. Chronic Thrombocytopenia: baseline plt count ~100-200k. Plt of 106k in ED. Suspect due to lymphoma. Monitored. 8. Hypertension: by history, not on medications prior to admission. Monitored. 9. Osteoarthritis: Followed by Orthopedics s/p left knee steroid injection 1/17/23. Monitored. 10. Chronic Encephalopathy: Followed by Dr. (Neurology). Admitted to Facility 11/2022 for hallucinations and metabolic encephalopathy, negative workup, eventually resolved. Continued home Seroquel taper.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2586938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 11.05.2022
Beginn: 13.02.2023
Tage bis Beginn: 278,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure Angiogram pulmonary abnormal Bronchiolitis COVID-19 COVID-19 pneumonia Cough Dyspnoea Emphysema Legionella test Lung infiltration Pneumonia Pulmonary cavitation Sputum culture Streptococcus test negative

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 2/13/2023 Discharge Date: Feb 16, 2023 PRESENTING PROBLEM: Acute respiratory failure with hypoxia [J96.01] Community acquired pneumonia of right lung, unspecified part of lung [J18.9] COVID-19 [U07.1] HOSPITAL COURSE: 58 y.o. female with a pertinent past medical history of asthma, hx asplenia and nephrectomy 2/2 trauma, chronic pain, HTN, who presented with cough, SOB. Admitted for AHRF. CTA chest was negative for PE. Did show multifocal right pneumonia with small areas of cavitation. Pulmonology evaluated. Cavitations thought to be infiltrates superimposed on emphysema. Clinical presentation was consistent with COVID-19 pneumonia with respiratory bronchiolitis. Was recommended for outpatient follow-up and signed off. Patient's history was also not suggestive of cavitary pneumonia such as TB. She denied any history of incarceration or recent travel outside the country, or any hemoptysis. Patient was initially started on Unasyn and azithromycin for antibiotics. Also started on Decadron and remdesivir. DVT prophylaxis had been held in the setting of a possible bronchoscopy with pulmonology which patient eventually did not have. Infectious Disease followed. Strep and Legionella were negative. Sputum culture with no result. Blood cultures were not collected. Patient initially required 4 L nasal cannula, remained hemodynamically stable throughout her admission. She progressively improved and was weaned to room air. She was discharged on a course of Augmentin to complete 5 day course for CAP, as well as continued Decadron to continue total 10 day course. Case was discussed with ID who was in agreement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Urinary retention Incomplete bladder emptying Asplenia Moderate persistent asthma without complication Chronic low back pain Primary hypertension Attention deficit hyperactivity disorder (ADHD), predominantly inattentive type H/O partial nephrectomy Tobacco abuse Hx of sexual abuse Migraine without aura and without status migrainosus, not intractable Prediabetes DDD (degenerative disc disease), lumbar Sleep apnea, obstructive Postmenopausal bleeding Opioid withdrawal Degenerative lumbar spinal stenosis Severe major depression, single episode, without psychotic features Cigarette nicotine dependence with other nicotine-induced disorder COVID-19 virus infection Abnormal CT of the chest CAP (community acquired pneumonia)
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amphetamine-dextroamphetamine (ADDERALL XR) 30 MG 24 hr capsule budesonide (PULMICORT) 180 MCG/ACT inhaler buPROPion (WELLBUTRIN XL) 150 MG 24 hr tablet
Allergien: DemerolAnaphylaxis ClonidineSwelling
Vorherige Impfungen: -

VAERS 2580426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MN
Alter: 49,0
Geschlecht: F
Eingang: 13.02.2023
Impfdatum: 05.04.2022
Beginn: 12.02.2023
Tage bis Beginn: 313,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure

Symptomtext

hospitalized for acute respiratory failure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Hypokalemia, Nodules of lung, chemotherapy, PE, Radiation, recurrent breast cancer, tobaccu use
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MN
Alter: 90,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 06.08.2022
Beginn: 13.11.2022
Tage bis Beginn: 99,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 COVID-19 pneumonia Cerebrovascular accident Hyperglycaemia Hypophagia Hyporesponsive to stimuli Intensive care Metabolic encephalopathy SARS-CoV-2 test positive Septic shock

Symptomtext

Patient brought to the ED by EMS on 11/13 for weakness and decreased responsiveness. EMS reported the patient is suspected to not have eaten for the past 2 days. She tested positive for COVID by PCR in the ED. Ultimately patient was admitted 11/13/22 - 11/20/22 with acute metabolic encephalopathy secondary to septic shock requiring an ICU admission and pressure support. She was found to have a subacute CVA, severe hyperglycemia without DKA, and COVID pneumonia. Patient was on oxygen and started on dexamethasone, which was eventually stopped. Patient was discharged to home on 11/20. She has received the COVID primary vaccine series and one booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: OK
Alter: 42,0
Geschlecht: F
Eingang: 23.01.2023
Impfdatum: 27.05.2022
Beginn: 01.05.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Bedridden Cerebrovascular accident

Symptomtext

Daughter had what doctors described as a brain blowout. She had 9 strokes plus?. She is completely bed ridden.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 220,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2563488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MN
Alter: 80,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 13.05.2022
Beginn: 02.11.2022
Tage bis Beginn: 173,0
Dosis: 4
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Arteriogram coronary abnormal COVID-19 pneumonia Cardiac failure Cardiac failure acute Coronary artery bypass Coronary artery stenosis Death Dyspnoea Haemoptysis Oedema peripheral SARS-CoV-2 test positive

Symptomtext

Patient with history of diabetes, CKD stage III, and COPD. He was seen in the ED on 10/25 for shortness of breath and difficulty breathing over the past week. He additionally reported lower extremity edema. While in the ED, patient tested negative for COVID-19. He was admitted on 10/25 for acute on chronic HFrEF. On 10/28, patient underwent a coronary angiogram and was found to have 99% stenosis of the ostial LAD. On 11/1 patient had new onset of hemoptysis. COVID test was ordered on 11/2 and patient tested positive for COVID-19 by PCR. On 11/3 patient underwent CABG. On 11/5, patient had shortness of breath with increased oxygen requirements and coughing. IV dexamethasone was started for suspected Covid pneumonia. Ultimately, patient was transitioned to comfort measures, and passed away on 11/12/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2559708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 94,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 23.05.2022
Beginn: 13.12.2022
Tage bis Beginn: 204,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Angiogram pulmonary abnormal Bronchitis COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Respiratory disorder SARS-CoV-2 test positive

Symptomtext

Patient is a 95 y.o. female patient of MD with history of HTN, HLD, COPD presented to a local Hospital with SOB . Acute hypoxic respiratory failure COVID-19 virus infection Tested positive: 12/13/2022 Fully vaccinated Oxygen requirements at baseline: Room air Current oxygen requirement: The patient initially had worsening of her respiratory status and required increasing levels of supplemental oxygen. However this improved and the patient was weaned off of oxygen to room air. Treatment: Dexamethasone COPD with exacerbation Chest x-ray and CT angiogram consistent with acute bronchitis Patient is improved noting improvement in her respiratory status. Continue azithromycin and guaifenesin. Continue nebulizer treatments as needed. Essential hypertension Continue losartan Hyperlipidemia Continue statin

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2552686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 06.01.2023
Impfdatum: 28.04.2022
Beginn: 23.12.2022
Tage bis Beginn: 239,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Blood gases Blood pH decreased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Forced expiratory volume Fraction of inspired oxygen Lung infiltration PCO2 increased PO2 decreased Pneumonia Pneumonia viral Positive airway pressure therapy

Symptomtext

66 y.o. male patient with history of COPD and hypertension presented to hospital with acute respiratory failure with COVID-19 pneumonia Covid-19 Viral Pneumonia Date of onset of symptoms: 12/22/2022 Symptoms present on admission: shortness of breath Date of covid positive test: 12/23/2022 Vaccination status: vaccinated but did not get 2022 booster Imaging: CXR with left lower lobe infiltrate Oxygen requirements on admission: BiPAP Current oxygen requirements: NC Medical therapy: steroids (continue 2 more days), rocephin, and zithromax (completed); started remdesivir 12/26 (completed) Consultants following: Pulm Anticipated special isolation end date: 1/2/2023 Weaned down to 6L NC 12/29 -> weaned to 4 L NC prior to discharge, patient uses 3-6 L at home. He has a pulse ox at home and was instructed to keep O2 sat greater than 88%. He also has a CPAP machine that he uses at night. He will need to follow up with his PCP and pulmonology Acute on chronic hypoxic and hypercapnic respiratory failure Community acquired pneumonia Normally wears 3L O2 at home but occasionally bumps up O2 to 6L with activity, required BiPAP at 50% FiO2 on transfer VBG - pH 7.31, pCO2 77, pO2 58 CXR as above appears concerning for CAP in addition to COVID-19 PNA Azithromycin (completed 5 days) and Rocephin completed 7 days Wean oxygen as tolerated Continue pulmonary toilet, showed patient how to use incentive spirometer Pulmonology following COPD exacerbation Increasing dyspnea, cough, and sputum production w/ color change Gold stage IV with FEV1 0.65 25% Treating above underlying causes Duonebs and inhalers ordered Primary hypertension Continue lisinopril Restarting home amlodipine 12/29

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2550347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: KS
Alter: 77,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 22.04.2022
Beginn: 03.05.2022
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac arrest Death Feeling abnormal Malaise

Symptomtext

"sick" and not feeling right for the day and then died that night, labeled as cardiac arrest resulting in death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: cardiomyopathy arthritis
Andere Medikamente: -
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2526869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 07.04.2022
Beginn: 25.11.2022
Tage bis Beginn: 232,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure COVID-19 COVID-19 pneumonia Hypoxia Laboratory test SARS-CoV-2 test positive

Symptomtext

"Patient with history of 4 COVID vaccines who admitted with hypoxia and COVID detected PCR. Provider d/c note: ""Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) treated for COVID-19 pneumonia, oxygenation gradually improved Acute Respiratory Failure due to COVID-19 pneumonia -clinically stable on 3 liters , labs stable, increase activity,prone positioning, continue decadron, remdesivir day 4/5 - no known history of COPD or CHF - O2 saturation at 88% on RA, Initially needed 4 liter/nc, 96% with supplemental oxygen - dexamethasone, remdesivir, vitamin D3, remdesivir stopped on 11/29"""

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: COVID Detected PCR on 11/25/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular; Carotid Artery Stenosis s/p CEA; Hypertension; Small vessel disease (HCC) Bradycardia, sinus; Digestive; Diverticulosis of colon; Respiratory; OSA (obstructive sleep apnea); Acute respiratory failure due to COVID-19 (HCC); Other; Essential thrombocythemia History of multiple strokes; Alcohol use without signs of abuse; T12 compression fracture (HCC); Dysarthria; Debility; Status post bilateral L3-4 minimally invasive decompressions of stenosis on 5/17/17. Normocytic anemia; Noncompliance with CPAP treatment Hemiparesis affecting left side as late effect of cerebrovascular accident (CVA) (HCC) Acute pain of left knee; Encounter to discuss test results; Low blood magnesium level.
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2525407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 27.04.2022
Beginn: 05.12.2022
Tage bis Beginn: 222,0
Dosis: 4
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Acute respiratory failure Arthralgia Atelectasis COVID-19 Cardiac arrest Cardio-respiratory arrest Chest X-ray normal Chills Computerised tomogram thorax normal Cough Death Dyspnoea Dyspnoea exertional Emphysema Endotracheal intubation Haemoglobin decreased Heart rate increased

Symptomtext

Discharge Provider: Primary Care Physician at Discharge: MD Date of Death: 12/6/2022 COVID positive Date 11/29/2022 PRESENTING PROBLEM: Cardiac arrest (HCC) [I46.9] HOSPITAL COURSE: Pt is a 66 y.o. female who initially presented to hospital with worsening dyspnea and cough. She was found to be positive for COVID-19. She was treated with Redemsivir and steroids as well as treated with ceftriaxone and azithromycin. Then was transitioned to Levaquin when cultures were positive for Pseudomonas. Her oxygen needs were initially improving, however this morning patient had a PEA arrest. She also required multple transfusions (13). ROSC was achieved and she was transferred to heart center. On arrival patient was unstable and she went into PEA arrest twice. When back board was placed, it was noted she had a possible retroperitoneal bleed. Due to the acuity of her condition, family decided that she would be DNR/DNI and that they would pursue comfort care once their family would all be able to gather. Once family arrived a consensus decision was made amongst first degree relatives to pursue comfort care. These orders were initiated and patient was extubated. She passed away at 0048 on 12/6/22. Notes from Hospital before transferred to Heart Center Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 11/28/2022 Discharge Date: 12/5/2022 PRESENTING PROBLEM: Hypokalemia [E87.6] Acute on chronic respiratory failure with hypoxia (HCC) [J96.21] COVID-19 [U07.1] Pneumonia due to organism [J18.9] HOSPITAL COURSE: Pt is a 66 y.o. female with PMH of COPD, hypertension, chronic respiratory failure, hypertension, hyperlipidemia, OSA and morbid obesity who presented to hospital on 11/28/2022. The patient states that she has been having shortness of breath x 3 days. + coughing and subjective fevers. + chills. No nausea or diarrhea. No rhinorrhea or sore throat. Last vaccination for COVID 19 was 4/27/2022. Has been taking her home inhalers with no improvement in her breahting. She does not have significant shortness of breath during the interview but quickly gets short of breath even if she moves from the ER stretcher to the medsurg bed. 11/30/2022 She is feeling markedly better today. She is still requiring high-flow oxygen. She is coughing up some phlegm. She has not been febrile. She denies nausea, vomiting, diarrhea, weakness. We did discuss that leaving early would likely require her to return. 12/01/2022 Patient did well overnight, with reduced oxygen requirements. I initially reduced Solu-medrol to prednisone, but she sat up at bedside and desaturated. She was put back on Solu-Medrol. CT scan was performed due to the worsening and an essentially normal chest x-ray. 12/02/2022 Breathing better today after starting percussion and up in chair. Extensive thick sputum production. Oxygen demand improved. CT yesterday revealed: 1. Near complete consolidation of the bilateral lower lobes with associated volume loss, likely a combination of atelectasis and airspace disease. Additional nodular consolidation in the posterior right upper lobe is likely infectious or inflammatory. Given significant risk factors for lung cancer, a follow-up chest CT after appropriate therapy is recommended to ensure resolution. 2. Advanced emphysema. 3. No pulmonary embolism. 12/03/2022 Coughing up excessive sputum, but breathing markedly better. Sputum positive for a few Pseudomonas. Considering the severity of her illness, will switch ceftriaxone and doxycycline to Levaquin PO. 12/04/2022 She is having sinus tachycardia. She is having abdominal pain. She refused CT abdomen/pelvis. She is breathing well. Her oxygen demand is improving. Down to 4 liters. She has not been very motivated to get out of bed. She declined PT today as well. Likely will need SAR at discharge. 12/05/2022 Concern over continued sinus tachycardia and leukocytosis. Will decrease steroids and stop furosemide. Breathing is improving clinically. Patient's complaints are left shoulder pain and abdominal pain. She refused a CT abdomen/pelvis yesterday bc she does not feel well laying down. Also refused PT yesterday. This morning says she is in severe pain, but refuses "the donut" again. I asked if we sedated her, if she would be willing to have a CT scan and she said "absolutely not" I explained that for the second day her WBC is up and so is her heart rate, but she still refuses. When x-ray came to do KUB she said "I am not going in the donut!" Have had to treat her empirically for all options, Pantoprazole bolus 80 mg given and 40 mg IV BID. DC pepcid. Start metronidazole 500 mg IV TID. Make NPO. A few minutes after discussing with the patient and left the ICU, a code blue was called. She was found in PEA and CPR was started. She was qqickly intubated. She received 8-9 mgs of epinephrine, 3 ampules of bicarbonate, magnesium, calcium. Her hemoglobin returned< 7 and 3 units of emergency blood was given. She received IV fluids and started on bicarbonate dripp, norepinephrine, epinephrine, and vasopressin. She had ROSC after 20-25 minutes. She was breathing over the ventilator. CXR finally performed for ET placement. Aeromed contacted for transfer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: 11/28/2022 - 12/5/2022 (7 days) HOSPITAL Admission To Hospital notes: PRESENTING PROBLEM: Hypokalemia [E87.6] Acute on chronic respiratory failure with hypoxia (HCC) [J96.21] COVID-19 [U07.1] Pneumonia due to organism [J18.9] HOSPITAL COURSE: Pt is a 66 y.o. female with PMH of COPD, hypertension, chronic respiratory failure, hypertension, hyperlipidemia, OSA and morbid obesity who presented to hospital on 11/28/2022. The patient states that she has been having shortness of breath x 3 days. + coughing and subjective fevers. + chills. No nausea or diarrhea. No rhinorrhea or sore throat. Last vaccination for COVID 19 was 4/27/2022. Has been taking her home inhalers with no improvement in her breahting. She does not have significant shortness of breath during the interview but quickly gets short of breath even if she moves from the ER stretcher to the medsurg bed. 11/30/2022 She is feeling markedly better today. She is still requiring high-flow oxygen. She is coughing up some phlegm. She has not been febrile. She denies nausea, vomiting, diarrhea, weakness. We did discuss that leaving early would likely require her to return. 12/01/2022 Patient did well overnight, with reduced oxygen requirements. I initially reduced Solu-medrol to prednisone, but she sat up at bedside and desaturated. She was put back on Solu-Medrol. CT scan was performed due to the worsening and an essentially normal chest x-ray. 12/02/2022 Breathing better today after starting percussion and up in chair. Extensive thick sputum production. Oxygen demand improved. CT yesterday revealed: 1. Near complete consolidation of the bilateral lower lobes with associated volume loss, likely a combination of atelectasis and airspace disease. Additional nodular consolidation in the posterior right upper lobe is likely infectious or inflammatory. Given significant risk factors for lung cancer, a follow-up chest CT after appropriate therapy is recommended to ensure resolution. 2. Advanced emphysema. 3. No pulmonary embolism. 12/03/2022 Coughing up excessive sputum, but breathing markedly better. Sputum positive for a few Pseudomonas. Considering the severity of her illness, will switch ceftriaxone and doxycycline to Levaquin PO. 12/04/2022 She is having sinus tachycardia. She is having abdominal pain. She refused CT abdomen/pelvis. She is breathing well. Her oxygen demand is improving. Down to 4 liters. She has not been very motivated to get out of bed. She declined PT today as well. Likely will need SAR at discharge. 12/05/2022 Concern over continued sinus tachycardia and leukocytosis. Will decrease steroids and stop furosemide. Breathing is improving clinically. Patient's complaints are left shoulder pain and abdominal pain. She refused a CT abdomen/pelvis yesterday bc she does not feel well laying down. Also refused PT yesterday. This morning says she is in severe pain, but refuses "the donut" again. I asked if we sedated her, if she would be willing to have a CT scan and she said "absolutely not" I explained that for the second day her WBC is up and so is her heart rate, but she still refuses. When x-ray came to do KUB she said "I am not going in the donut!" Have had to treat her empirically for all options, Pantoprazole bolus 80 mg given and 40 mg IV BID. DC pepcid. Start metronidazole 500 mg IV TID. Make NPO. A few minutes after discussing with the patient and left the ICU, a code blue was called. She was found in PEA and CPR was started. She was qqickly intubated. She received 8-9 mgs of epinephrine, 3 ampules of bicarbonate, magnesium, calcium. Her hemoglobin returned< 7 and 3 units of emergency blood was given. She received IV fluids and started on bicarbonate dripp, norepinephrine, epinephrine, and vasopressin. She had ROSC after 20-25 minutes. She was breathing over the ventilator. CXR finally performed for ET placement. Aeromed contacted for transfer. Transfered to Heart Center
Vorgeschichte: OSA (obstructive sleep apnea) COPD (chronic obstructive pulmonary disease) (HCC) Chronic respiratory failure with hypoxia (HCC) Allergic rhinitis Acute on chronic respiratory failure (HCC) Essential hypertension Arrhythmia Cardiac arrest (HCC) Morbid obesity with BMI of 40.0-44.9, adult (HCC) GERD (gastroesophageal reflux disease) Leukocytosis Generalized abdominal pain AKI (acute kidney injury) (HCC) Hyperlipidemia Impaired glucose tolerance Hyponatremia Lactic acidosis Hyperglycemia Former heavy tobacco smoker Risk for coronary artery disease between 10% and 20% in next 10 years per Framingham score Shock (HCC) Elevated LFTs
Andere Medikamente: albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler atorvastatin (LIPITOR) 10 MG tablet famotidine (PEPCID) 20 MG tablet Fluticasone-Salmeterol (ADVAIR
Allergien: NKA
Vorherige Impfungen: -

VAERS 2520969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MN
Alter: 76,0
Geschlecht: M
Eingang: 01.12.2022
Impfdatum: 14.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 8,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 COVID-19 pneumonia Hypoglycaemia Oxygen saturation decreased Pneumonia aspiration Pneumonitis aspiration SARS-CoV-2 test positive Sepsis

Symptomtext

Patient brought to the ED via EMS on 10/22 for hypoglycemia. On EMS arrival, O2 sats were in the low 80's room air and he had a low sinus rhythm in the 40's. While in the ED, he had a COVID PCR test done which was positive. Patient was admitted to the hospital on 10/22 for hypoglycemia, sepsis, and acute hypoxic respiratory failure possibly secondary to COVID. Patient was placed on supplemental oxygen and intermittently required supplemental oxygen. Patient has received COVID vaccine and boosters. During his hospitalization, he was diagnosed with pneumonia, COVID vs aspiration pneumonitis/pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hx of diabetes type II
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2520967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 01.12.2022
Impfdatum: 25.04.2022
Beginn: 25.11.2022
Tage bis Beginn: 214,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Acute respiratory failure Angiogram pulmonary normal Blood glucose increased COVID-19 Chest discomfort Condition aggravated Cough Diarrhoea Dyspnoea Dyspnoea exertional Electrocardiogram Fatigue Full blood count normal Glycosylated haemoglobin increased Laboratory test Malaise Metabolic function test normal Nausea

Symptomtext

COVID+ 11/26/22. Vaccination status - moderna x2, Pfizer x1 BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider at Discharge: DO Admission Date: 11/25/2022 Discharge Date: 11/26/2022 Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 11/25/2022 Yes ? Statin started by Vascular Surgery with Rx to be taken over by patient's PCP 11/26/2022 Unknown ? OSA on CPAP 09/07/2022 Yes ? Stage 3b chronic kidney disease (HCC) 04/20/2021 Yes ? Hypertension associated with diabetes (HCC) 01/01/2021 Yes ? COPD (chronic obstructive pulmonary disease) with chronic bronchitis (HCC) 01/01/2021 Yes ? Class 3 severe obesity with serious comorbidity and body mass index (BMI) of 45.0 to 49.9 in adult, unspecified obesity type (HCC) 03/06/2020 Yes ? Depression 05/31/2018 Yes ? Dyslipidemia associated with type 2 diabetes mellitus (HCC) 04/13/2018 Yes ? Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) 04/09/2018 Yes ? Fibromyalgia Yes ? Peripheral neuropathy 05/22/2012 Yes ? Gastro-esophageal reflux disease without esophagitis 08/31/2009 Yes DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute respiratory failure with hypoxemia (HCC) [J96.01] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 57 y.o. female with an extensive past medical history of chronic obstructive pulmonary disease and asthma. Also hypertension, type 2 diabetes, fibromyalgia, chronic kidney disease, elevated body mass index. Former smoker, quit 3.5 years ago. She presents today to Health clinic with worsening shortness of breath and cough. She tested positive for COVID 6 days ago at home with symptoms starting 7 days prior. For the last four days she has taken Paxlovid. Reports worsening symptoms of cough, shortness of breath, and now chest pressure for the past two days. Reports last fever Tuesday. Reports nausea and diarrhea. In the ER, patient arrived hypoxic 88 on room air, tachycardic, and tachypnea. EKG revealed sinus rhythm at 109 beats per minute. CTA no acute cardiopulmonary process, no PE. Laboratory- CBC, CMP, troponin unremarkable. Glucose 234 and 224. Will need to monitor glucose trend closely and adjust insulin regimen appropriately. Patient will be admitted for supplemental oxygen, antiviral, and steroid treatment. Patient is agreeable to admission and treatment plan. During the hospital course, patient was weaned off of supplemental oxygen. Received one dose of remdesivir. Patient able to ambulate in room. Reports she is able to ambulate further and not as short of breath. During ambulation patient's SPO2 > 90%. RT50 completed with recommendations of no need for supplemental oxygen at this time. Discuss with patient in depth the importance of monitoring glucose at home, she does have a test libre. Reports she has a sliding scale insulin regimen from endocrine. Discuss that steroids will increase blood glucose. Patient is establish with endocrine, follow up 1/3/2023. Discuss with patient to call the office and update provider about hospitalization and steroid use, patient should follow up sooner than 1/3/2022. Follow up appointment with PCP on 1/12/2022. Patient is discharged with tessalon, 3 days of prednisone for a 5 day treatment, and 3 days of azithromycin for a 5 day treatment. Patient seen and examined- she is alert and oriented. She reports she is feeling better and believe she is stable to go home. Denies chest pain, fever, chills, abdominal pain, urinary symptoms. Reports fatigue and shortness of breath with activity. Discuss the findings of RT50. Discuss medication to take at home. Patient is discharged in stable condition- all labs and imaging reviewed. No concerns at this time. All questions were answered prior to discharge. * COVID-19 COVID positive at home 6 days ago, will retest with PCR -Reports 4 days of paxlovid -Acute respiratory failure with hypoxia -Remdesivir ordered 1 day -Decadron ordered, 2/5 -Monitor respiratory status -- > Continuous pulse ox ordered -COVID labs ordered OSA on CPAP Continue with CPAP Stage 3b chronic kidney disease (HCC) Monitor renal function with AM labs - Renally dose medications and avoid nephrotoxic agents Class 3 severe obesity with serious comorbidity and body mass index (BMI) of 45.0 to 49.9 in adult, unspecified obesity type (HCC) Continue to follow up outpatient Peripheral neuropathy Continue home regimen- Neurontin Gastro-esophageal reflux disease without esophagitis Prilosec-> formulary protonix Depression Continue Wellbutrin and Cymbalta Dyslipidemia associated with type 2 diabetes mellitus (HCC) Controlled, not on medications outpatient. Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) A1C 9.8 > 2 months ago, repeat A1C 10.9 Holding metformin and actos -On insulin at home -ISS and lantus ordered -Monitor blood glucose -Diabetic diet Hypertension associated with diabetes (HCC) Continue with lisinopril, hydrochlorothiazide Fibromyalgia Continue home regimen COPD (chronic obstructive pulmonary disease) with chronic bronchitis (HCC) Continue home regimen- albuterol and tiotopium bromide -Monitor respiratory status -In acute excerbation due to covid -Remdesivir and decadron ordered -DuoNebs ordered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: 4/5/22 OV with PCP ? DDD lumbar ? new Percocet 10-325 mg 0.5-1 nightly Chronic left shoulder pain/Numbness & tingling in left arm ? PT eval - MRI
Vorgeschichte: Arthritis COPD (chronic obstructive pulmonary disease) with chronic bronchitis (HCC) DDD (degenerative disc disease), lumbar Fibromyalgia Hypertension associated with diabetes (HCC) Psoriasis, unspecified Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) Dyslipidemia associated with type 2 diabetes mellitus (HCC) Family history of heart attack Leg cramps Screen for colon cancer Depression Dry eye Gastro-esophageal reflux disease without esophagitis Cigarette nicotine dependence in remission Peripheral neuropathy Polyarthralgia Vitamin D deficiency Vitreous syneresis Corn of foot Class 3 severe obesity with serious comorbidity and body mass index (BMI) of 45.0 to 49.9 in adult, unspecified obesity type (HCC) Polymyalgia rheumatica (HCC) Atherosclerosis of aorta (HCC) Long term (current) use of insulin (HCC) Family history of colonic polyps Stage 3b chronic kidney disease (HCC) Dyspnea on exertion Age-related nuclear cataract, bilateral Bilateral leg edema Chronic prescription opiate use Aftercare following surgery of the musculoskeletal system Carpal tunnel syndrome of left wrist OSA on CPAP
Andere Medikamente: Albuterol Sulfate 108 (90 Base) MCG/ACT 2 puffs Inhalation Every 6 hours PRN Allopurinol 300 mg Oral Every evening buPROPion HCl 150 mg Oral 2 times daily Carbidopa-Levodopa 25-100 MG 2 tablets Oral Nightly Celecoxib 200 MG TAKE (1) CAPSULE
Allergien: Chantix [Varenicline]Hives MetoclopramideNausea and Vomiting, Other, Myalgia Sulfa DrugsHives CodeineNausea/Vomiting/Diarrhea Requip [Ropinirole]Other
Vorherige Impfungen: -

VAERS 2505892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 88,0
Geschlecht: M
Eingang: 11.11.2022
Impfdatum: 18.04.2022
Beginn: 14.10.2022
Tage bis Beginn: 179,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Angiogram pulmonary abnormal Aortic stenosis Blood culture Blood osmolarity decreased Blood sodium decreased CHA2DS2-VASc-score COVID-19 COVID-19 pneumonia Chills Dyspnoea Echocardiogram abnormal Ejection fraction normal Fluid intake restriction Hyponatraemia Inappropriate antidiuretic hormone secretion Intensive care Interstitial lung disease

Symptomtext

Patient is a 89 y.o. male with a PMHx of paroxysmal atrial fibrillation (on Xarelto & propafenone), coronary artery disease s/p MI 2003 and 2009, hypertension, dyslipidemia, moderate obstructive sleep apnea, COPD, former tobacco use disorder, daily alcohol dependence was directly admitted to ICU for acute hypoxic respiratory failure secondary to COVID-19 infection, CAP, and bilateral pleural effusions. Complicated by hyponatremia, likely secondary to SIADH, which is resolving. Stable for transfer out of the ICU. Acute respiratory failure with hypoxia COVID-19 PNA Pleural effusion only; CHF ruled out Leukocytosis of 13K. PCT wnl. Date of symptom onset: 10/1/2022 Date of COVID positive test: 10/4/2022 this was scanned into media tab on 10/16/22 Traveled to PRIVATE 9/19/22-10/11/22. Vaccination status: vaccinated and boosted Symptoms present on admission: Fevers, chills, shortness of breath, productive cough with yellow sputum CTPA no PE, bilateral pleural effusion, patchy irregular interstitial and groundglass infiltrates bilaterally, biapical parenchymal scarring with calcifications. Oxygen requirements: RA < 6 L nasal cannula Medical therapy: Dexamethasone 6 mg daily, he is beyond time frame for remdesivir ID following. On Pepcid 20 mg BID, Vitamin C 500 mg TID, Vit D 5000U Daily, Loratadine 10 mg Daily, Zinc 50 mg BID. Received one dose of tocilizumab 10/16 Follow up Sputum cultures - unable to collect. 1/2 blood Cx Staph Epi - appears to be a contaminant 2 D echo with EF 55-65% with LV segmental wall motion grossly normal and no pulmonary hypertension Continue Scheduled and as needed albuterol On room air with oxygen sats above 92% Acute on chronic hyponatremia Sodium on admission 110 Multifactorial, likely SIADH versus poor solute. Sodium correction 6-8 mEq/day Serum osmolality was 260 and urine osmolality 546 with urine Na 34 Liver US with normal liver echotexture. Nephrology following - Likely SIADH versus poor solute intake. Sodium up at 128, now seems to be trending down Started on salt tabs 1 g twice daily and continue fluid restriction Today at 124 < < 128 Given a dose of tolvaptan 7.5 mg Continue to monitor sodium levels. Per nephrology if by tomorrow sodium > 130, can discharge on salt tabs with repeat BMP in 1 week On discharge Na is 130 Repeat BMP in 3 days Paroxysmal atrial bibrillation Continue home metoprolol, stop propafenone for now Has hx of ischemic heart disease, afib and HR have been well controlled with the metoprolol. Echo ordered. In NSR today with HR down in 50-60. Anticoagulation home Xarelto CHA2DS2-VASc Score 4. Follows with Dr., EP. Consider cardio consult for propafenone management - with CAD, stop rythmal and continue AC with Xarelto Coronary artery disease S/P PCI. No anginal symptoms at this time ECHO- EF 55-65% with mild aortic stenosis and no pulmonary hypertension Continue aspirin, beta-blocker, high intensity statin Essential hypertension Continue metoprolol succinate 50 mg Amlodipine added BP controlled Dyslipidemia Controlled on home Lipitor Moderate obstructive sleep apnea Sleep study March 2018 apnea-hypopnea index > 20 Compliant with home CPAP Alcohol use disorder Reports drinks 1 beer daily total of 7 beers a week No history of alcohol withdrawal symptoms Monitor for signs of withdrawal Code status Full code but does not want prolonged intubation or life support. Urinary retention Reports being on testosterone in past which was stopped multiple years ago Admits to hx of gynecomastia and follows with urologist. Encouraged up to bathroom. Check PVR. If > 500 consider straight cath. Per patient and family has been urinating well with less retention issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2500673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

kritisch

Staat: MN
Alter: 69,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 02.07.2022
Beginn: 05.11.2022
Tage bis Beginn: 126,0
Dosis: 3
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Patient expired 11/5/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Paraplegia,/incomplete quadriplegia, DVT, chronic systolic heart failure, diabetes mellitus, chronic Foley catheter for neurogenic bladder, diverting colostomy, chronic pressure ulcers
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2481698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 21.03.2022
Beginn: 08.10.2022
Tage bis Beginn: 201,0
Dosis: 3
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute myocardial infarction Acute respiratory failure Asthenia COVID-19 Death Echocardiogram normal Ejection fraction normal Electrocardiogram ST segment elevation Failure to thrive Feeding disorder Electrocardiogram abnormal Gastritis erosive Gastrointestinal haemorrhage Lethargy Myocarditis Oesophagitis Somnolence Troponin increased

Symptomtext

Admitted 10/8/2022 Deceased 10/13/2022 Discharge Provider: MD Primary Care Physician at Discharge: DO Admission Date: 10/8/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Somnolence STEMI (ST elevation myocardial infarction) (HCC) ST elevation myocardial infarction (STEMI), unspecified artery (HCC) COVID Failure to thrive HOSPITAL COURSE: 87 y.o. female with a history of CAD s/p CABG, recent GIB due to gastric erosions/esophagitis, HTN, HLD, carotid stenosis who presented with weakness and lethargy and found to have ST elevation, elevated troponins concerning for STEMI, in addition to COVID. Patient was not a candidate for catheterization per cardiology and unable to be put on heparin drip due to recent GIB. On admission, patient initially admitted as comfort care. Given further evaluation, the EKG more likely indicative of NSTEMI or myocarditis (less likely STEMI) based off prior EKG, discussion with patient's daughter to change patient from comfort care to DNR/DNI (on 10/9). Echo showed normal EF 66%. Patient also given one dose remdemisvir and decadron, given her COVID infection. Discussion with family on 10/10: The family came to the conclusion to move the patient to comfort care status given her overall well being, including her inability to eat, her body mass index, and her other medical comorbidities. Patient was then admitted to general inpatient hospice, and her symptoms were well controlled with scheduled sublingual morphine and ativan. Patient passed away comfortably on the morning of 10/13/22 with daughter at bedside

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CAD (coronary artery disease) Mild aortic insufficiency Mild mitral regurgitation Hypertension STEMI (ST elevation myocardial infarction) (HCC) GERD (gastroesophageal reflux disease) Esophageal stricture Pyloric stricture Protein-calorie malnutrition, unspecified severity (HCC) Failure to thrive in adult Chronic pain of both knees Dyslipidemia
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ALPRAZolam (XANAX) 0.25 MG tablet atorvastatin (LIPITOR) 40 MG tablet BABY ASPIRIN PO diltiazem (DILT-XR) 120 MG 24 hr capsule doxazosin (CARDURA) 4 MG t
Allergien: Levofloxacin Erythromycin Macrolides Norvasc [Amlodipine] Simvastatin Sulfa Drugs Tramadol
Vorherige Impfungen: -

VAERS 2478332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: WI
Alter: 88,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 11.05.2022
Beginn: 08.10.2022
Tage bis Beginn: 150,0
Dosis: 4
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Death on 10/08/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID-19 test on 09/23/2022
Aktuelle Erkrankungen: -
Vorgeschichte: COVID-19; OSC: Alzheimer's disease; HLD; PVD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 08.04.2022
Beginn: 27.07.2022
Tage bis Beginn: 110,0
Dosis: 4
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Blood test Cardiac stress test abnormal Catheterisation cardiac abnormal Chest pain Electrocardiogram abnormal Myocardial infarction Stent placement

Symptomtext

I had a heart attack on 8/1. On July 27th I had an abnormal stress test. I had a scheduled Cath to check on blockage but a few days before that procedure I was having chest pains and went to the ER where my DR is located. I was transported to the heart and lung center and the next day had a Cath and a stent. After that all my biomarkers went back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: Nuclear stress test - abnormal; ECG - borderline 7/18; bloodwork
Aktuelle Erkrankungen: No
Vorgeschichte: Type 1 insulin dependent diabetic; Asthma; High blood pressure; High cholesterol; Heart disease, heart attach in 2019 and 08/01/2022
Andere Medikamente: Midodrine; Metoprolol; Repatha; COQ10; Rosuvastatin; Aspirin low dose; Vitamin D; Multivitamin; Symbicort; Insulin Lispro; Iron; Loratadine; Cingular generic; Flonase
Allergien: Zolrolto
Vorherige Impfungen: -

VAERS 2466890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: OH
Alter: 85,0
Geschlecht: M
Eingang: 02.10.2022
Impfdatum: 01.04.2022
Beginn: 22.09.2022
Tage bis Beginn: 174,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure COVID-19 Cardiac failure Condition aggravated Dyspnoea Hypervolaemia Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

85 y.o. male history of HFpEF (EF of 50 %), paroxysmal A. fib, T2DM, BPH, hypertension, hyperlipidemia, CAD, SSS, and chronic respiratory failure secondary to ILD on 2 L cannula at home presents to the ED with worsening shortness of breath. The patient was found to be COVID-positive and was placed on BiPAP. Patient weaned off BiPAP back to his baseline oxygen 2 L nasal cannula. Pulmonology was following throughout this hospitalization. Patient was also treated with steroids due to COVID infection and decline in history of status. Per pulmonology patient to be tapered from 40 mg daily to 30 mg daily x7 days then continue with home 20 mg prednisone daily. Patient also completed a course of remdesivir during this hospitalization. While in the hospital patient endorsed that he needed some help at home. Social work was consulted and patient was approved to have home health upon discharge. Patient is stable and states that he is almost back to baseline. Patient is stable enough to be discharged home this evening. Acute on chronic respiratory failure-patient back to baseline O2 2 L nasal cannula COVID-19-completed remdesivir, continue steroid taper to home regimen of 20 mg daily Acute exacerbation of HFpEF-resolved Volume overload-patient seems to be back to euvolemic, continue home Lasix 40 mg daily Hypertension-continue home antihypertensive medication Paroxysmal A. Fib-continue home Eliquis Type 2 diabetes-continue Levemir 8 units nightly and metformin 100 mg twice daily BPH-continue home meds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2462045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

kritisch

Staat: MN
Alter: 54,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 14.04.2022
Beginn: 25.09.2022
Tage bis Beginn: 164,0
Dosis: 2
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Patient expired 9/25/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Cirrhosis, incomplete L3 paraplegia, chronic pain, severe malnutrition, chronic diarrhea, chronic sacral wounds, cervical cancer and hepatitis C
Andere Medikamente: Unknown
Allergien: Iodinated diagnostic agents, acetaminophen, blood-group specific substance Anti-Duffy a (Fya) antibody, naproxen
Vorherige Impfungen: -

VAERS 2461835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 13.06.2022
Beginn: 18.09.2022
Tage bis Beginn: 97,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure Asthenia COVID-19 Chest X-ray abnormal Computerised tomogram thorax abnormal Dizziness Dyspnoea Echocardiogram Electrolyte imbalance Fatigue Malaise Nausea Oxygen saturation decreased Pneumonia bacterial Pneumonitis Polyuria SARS-CoV-2 test positive Troponin

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 9/18/2022 Discharge Date: 9/26/2022 PRESENTING PROBLEM: Acute respiratory failure with hypoxia [J96.01] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 65 y.o. female with extensive medical conditions including type 2 DM, chronic pain and fibromyalgia on subutex, chronic nausea s/p esophageal surgery, rheumatoid arthritis, who presents today with feeling unwell, shortness of breath, nausea, vomiting, and fatigue for 10-12 days. Note that patient is independent at baseline; walk independently; not on oxygen; lives with husband. She was seen by PCP approx 4 days ago, was diagnosed with covid infection, but was not candidate for antiviral as she had symptoms for 6 days. She presented today due to worsening shortness of breath, weakness, nausea and vomiting; generally doesn't feel well. She has not been able to take her home medications due to nausea. Started taking macrobid on Wednesday for UTI. In ED, oxygen was 85% on room air, was 98% on 3L. BP 230/80 on arrival. Na 131. Cl 86. Cr 1.59 which was baseline. Covid positive again. Her imaging show acute pneumonitis from covid. She is on IV steroid and breathing treatment. She has chronic nausea from history of esophageal surgery. Still feel lightheaded and nausea today, so I kept her and continue with hydration. She can be discharge when her ox sat improved, and electrolytes improved, and tolerating some oral intake. During hospitalization she did not improve quickly. A CT scan was performed that revealed obvious bacterial pneumonia. She was started on ceftriaxone and doxycycline due to her multiple allergies. Even with this and steroids it occurred 2-3 days to wean off of oxygen. Her biggest problem was that she would desaturate with minimal activity. Her diuretics were restarted as well and she diuresed quite well. By the time she was discharged she was on room air 95% at rest and 92% with any activity. I did call her primary care physician personally and reviewed the fact that her last chest x-ray did show some decline in her pneumonia. I did explain she was being discharged with 7 days more of antibiotics, steroids. I also reviewed her results of her echocardiogram mentioned above. I also discussed that she had a borderline troponin that never really increased, but had a stress test October 2021 and had really no chest pain and was alreadypositive for COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: 5/31/2022 (1 hours) Hospitals Emergency DIAGNOSIS at time of disposition: 1. Gastroparesis 5/28/2022 - 5/30/2022 (2 days) HOSPITAL DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Essential hypertension [I10] Intractable vomiting with nausea, unspecified vomiting type [R11.2] Intractable nausea and vomiting [R11.2] 5/26/2022 - 5/27/2022 (16 hours) HOSPITAL DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Accelerated hypertension [I10] Intractable nausea and vomiting [R11.2] Intractable vomiting with nausea [R11.2]
Vorgeschichte: Type 2 diabetes mellitus without complications Primary fibromyalgia syndrome Chronic nausea Dyslipidemia Chronic neck pain Essential (primary) hypertension Type 2 diabetes mellitus with hypoglycemia without coma Chronic left-sided low back pain without sciatica Chronic pain of both shoulders Hiatal hernia Adrenal adenoma Drug-induced constipation Stage 4 chronic kidney disease Unspecified intestinal obstruction, unspecified as to partial versus complete obstruction Sacroiliitis, not elsewhere classified Carpal tunnel syndrome Major depressive disorder, single episode, unspecified Heart murmur Herpes labialis Hyperlipidemia, unspecified Kidney stone Lesion of liver Anxiety Sacroiliac joint pain Spinal stenosis in cervical region Thrombocytopenia, unspecified Hypoglycemia unawareness associated with type 2 diabetes mellitus Gastro-esophageal reflux disease with esophagitis Type 2 diabetes mellitus with diabetic polyneuropathy Callus of foot Hammer toes, bilateral Rheumatoid arthritis without rheumatoid factor, multiple sites Hematuria Localized edema Multifocal motor neuropathy Anemia due to stage 4 chronic kidney disease Disorder of adrenal gland, unspecified Rotator cuff tear arthropathy of right shoulder Gastro-esophageal reflux disease without esophagitis Acute kidney failure, unspecified Age-related osteoporosis without current pathological fracture Long term (current) use of insulin Opioid dependence, uncomplicated Rheumatoid polyneuropathy with rheumatoid arthritis of unspecified site Type 2 diabetes mellitus with diabetic peripheral angiopathy without gangrene Chronic kidney disease (CKD), stage III (moderate) Osteoarthritis of left shoulder Insomnia Restless leg syndrome Shoulder arthritis COVID-19 virus infection Acute respiratory failure with hypoxia Hypertensive urgency Acute pneumonitis Acute dehydration Acute cystitis without hematuria
Andere Medikamente: amitriptyline (ELAVIL) 50 MG tablet amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet Ascorbic Acid (VITAMIN C) 500 MG tablet buprenorphine (SUBUTEX) 2 MG SUBL Calcium Carbonate-Vitamin D (CALCIUM + D PO) cholecalciferol (VITAMIN D3
Allergien: Contrast Dye [Ivp Dye, Iodine Containing]Anaphylaxis, Swelling Flu Virus VaccineOther LinezolidNausea and Vomiting, Rash, Dizziness, Headache Pneumococcal VaccinesUnknown ClindamycinNausea and Vomiting, Dizziness, Headache Haldol [Haloperidol]Other MethadoneConfusion AdhesiveRash Lyrica [Pregabalin]Nausea and Vomiting, Rash, Dizziness, Headache MeloxicamItching, Nausea and Vomiting, Rash, Dizziness, Headache MethocarbamolNausea and Vomiting, Rash, Dizziness, Headache PenicillinsDiarrhea, Nausea and Vomiting, Nausea Only, Dizziness Zoloft [Selective Serotonin Reuptake Inhibitors]Nausea/Vomiting/Diarrhea
Vorherige Impfungen: -

VAERS 2460565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 16.05.2022
Beginn: 17.09.2022
Tage bis Beginn: 124,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure COVID-19 Chest X-ray abnormal Condition aggravated Cough Gastrooesophageal reflux disease Hypertension Hypoxia Interstitial lung disease Oropharyngeal pain Pyrexia Respiratory symptom Rhinorrhoea SARS-CoV-2 test positive Ultrasound kidney normal

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 9/17/2022 Discharge Date: Sep 21, 2022 PRESENTING PROBLEM: COVID-19 [U07.1] Acute respiratory failure due to COVID-19 [U07.1, J96.00] HOSPITAL COURSE: 89F with HTN, GERD, and breast cancer s/p resection on letrozole. She came to the ER for URI symptoms and fevers. 2 days ago, 9/15 she began to have upper respiratory symptoms including nonproductive cough, rhinorrhea and sore throat. She developed subjective fevers. She is vaccinated for COVID 19 and received 2 boosters, last on 5/16/22 In the ER she was hypoxic with ambulation down 89%. She was placed on 2lpm NC. COVID 19 +. CXR showed no consolidation but with accentuated interstitial markings. She declined remdesivir and was started on decadron plan to complete 10 days. Subsequently she has been weaned off oxygen. She was noted to have accelerated HTN. Renal US negative for RAS. She was continued on Cozaar, change hydrochlorothiazide to on amlodipine and started on Coreg 6.25 mg BID with good response. She was then discharged home stable

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: GERD (gastroesophageal reflux disease) Essential hypertension Breast cancer History of colon polyps Sleep disturbance Dyspnea Obesity Muscular deconditioning Diffusion capacity of lung (dl), decreased-moderate Encounter for long-term (current) use of steroids Osteoarthritis, multiple sites Chronic low back pain Right lumbar radiculopathy Mixed incontinence urge and stress (male)(female) Long term current use of systemic steroids Type 2 diabetes mellitus with stage 3b chronic kidney disease, without long-term current use of insulin Hypercholesterolemia Hypertriglyceridemia Osteoporosis, unspecified osteoporosis type, unspecified pathological fracture presence Eczema, unspecified type 08/2018: Stage IA (pT1cpN0Mx) (20 mm, 0/1) poorly diff'd ER 100%, PR 96%, Her2neu negative ILCa left breast 8:00 position, 7 CFN sp left total mastectomy, left ax SLNBx Dense breast Pulmonary calcification determined by X-ray History of cardiac murmur 08/09/18: Abnormal CXR : increased density right lower lung, recommend follow up x-ray 08/22/18: MyRisk: No deleterious mutation, no VUS Use of exemestane (Aromasin) Personal history of breast cancer Statin intolerance Personal history of DVT (deep vein thrombosis) CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min COVID-19 Hyponatremia Pneumonia due to COVID-19 virus
Andere Medikamente: Accu-Chek Aviva Plus Test Strips Accu-Chek Softclix Lancets acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 10 MG tablet Ascorbic Acid (VITAMIN C) 1000 MG tablet Biotin w/ Vitamins C & E (HAIR/SKIN/NAILS PO) BLACK ELDERBERRY PO c
Allergien: Cardizem [Diltiazem]Itching TramadolNausea and Vomiting
Vorherige Impfungen: -

VAERS 2433664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FK9894

kritisch

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 08.02.2021
Beginn: 22.08.2022
Tage bis Beginn: 560,0
Dosis: 4
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 pneumonia Chest tube insertion Death Dyspnoea Endotracheal intubation Haemodynamic instability Hypoxia Mechanical ventilation Oxygen saturation decreased Pneumothorax Respiratory distress SARS-CoV-2 antibody test SARS-CoV-2 antibody test positive

Symptomtext

68y.o. female with PMH pertinent for seronegative RA on chronic prednisone recent COVID PNA presented for worsening SOB. In the ER, patient was hypoxic requiring HFNC 100% FiO2/50 L and a nonrebreather maintaining SPO2 in the early 90s. Significant increase in work of breathing. Patient was intubated. On 8/28, the patient developed resp distress. Patient had a needle decompression and then chest tube placement for right sided tension pneumothorax. Patient was unable to be weaned off ventilator and on 9/5 had a drop in SpO2 with increased WOB. Patient required multiple pressors for hemodynamic instability. Patient transitioned to comfort care, and passed peacefully that evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 15,0
Labordaten: 8/23/22 SARS-CoV-2 IgG (Anti-Spike) -- positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FK9894

kritisch

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 12.03.2021
Beginn: 22.08.2022
Tage bis Beginn: 528,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Catheterisation cardiac abnormal Confusional state Hypoxia Lethargy Respiratory failure SARS-CoV-2 test positive Syncope Pulmonary embolism Thrombectomy

Symptomtext

62y.o. male who recently traveled and was diagnosed with COvid about 1 week ago, treated with zithromax/ amoxicillin then atovaquone and proguanil presents with acut syncope. EMS found him quite hypoxic put on NRB and brought to ER where massive PE found. He was taken urgently to cath lab for thrombectomy- 5-6 thrombectomies were performed in both left and right sides. After, Right heart pressures were much improved. Oxygen has been weaned to room air. Evaluation on Day of Discharge: Feeling great, denies any dyspnea chest pain or bleeding, no overnight events. No lower extremity edema, lungs clear to auscultation, patient is eager to go home as soon as possible. is very lethargic and confused. Attempts to follow directions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: 8/23/22 SARS-COV-2 (COVID-19) by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2426456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: WI
Alter: 83,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 05.05.2022
Beginn: 29.08.2022
Tage bis Beginn: 116,0
Dosis: 3
Route/Site: IM / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Death on 08/29/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID-19 test on 08/17/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Complications of COVID-19; OSC: COPD; DM2; dilated cardiomyopathy; a-fib; PVD; HNT; HLD; dementia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2414147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: WI
Alter: 91,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 27.04.2022
Beginn: 08.08.2022
Tage bis Beginn: 103,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Death on 8/8/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive Covid-19 test on 7/25/2022
Aktuelle Erkrankungen: -
Vorgeschichte: : Complications of COVID-19; hypertensive heart disease with heart failure; paroxysmal a-fib; CKD; HLD; anemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2388089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 21.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Blood pressure increased Blood test abnormal Chest X-ray Computerised tomogram thorax abnormal Cough Dyspnoea Feeling abnormal Heart rate increased Heart rate irregular Hyperhidrosis Injection site erythema Injection site pain Injection site swelling Injection site warmth Nausea Oropharyngeal pain Pneumonia

Symptomtext

04/21/2022 The area I got my shot was a little swollen, red and warm to the touch. I felt a little funny, not real sick, just a little nauseous. It hurt a little bit where I could not lay on that side. This lasted for a couple of days. It began to go down after a couple of days. I noticed I noticed I was having a little shortness of breath in the morning, then it would go away. It became more regular around the middle of May, I began getting a cough and my throat was getting sore. I took some allergy medicine. I noticed after coughing; I was having trouble inhaling. I went to the Emergency Room and told me to see my PCP. I went to my PCP and they did a CT scan of my lungs. I had pneumonia in both lungs. I was prescribed an antibiotic which I took for seven days. I still had shortness of breath and sweating, and I could feel my heart beating in my neck. I went back to the doctor. They did bloodwork and an x-ray of my lungs. My bloodwork did not look good and they wanted to check for blood clots. I went to the Emergency Room and they did another CT. They saw a Pulmonary Embolism and I was admitted. I was placed on a Heparin Drip. I was released after 3 days and prescribed a blood thinner for 9 months, they were unable to see where the clot came from. The Heparin did help. . I do, however, still have shortness of breath , sweat and my heart rate goes up. My Blood Pressure also goes up. It just is not as regular

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Bloodwork, abnormal , unsure results CT , Bilateral pneumonia CT, Pulmonary Embolism
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Zinc; Vitamin D; Vitamin Supplement for Women; Magnesium
Allergien: None
Vorherige Impfungen: -

VAERS 2370681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 15.07.2022
Impfdatum: 12.04.2022
Beginn: 30.06.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Asymptomatic COVID-19 Blood test Coronary arterial stent insertion Echocardiogram Electrocardiogram Myocardial infarction SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on June 30, 2022 while being seen for a heart attack. I was asymptomatic. I had to have two stents put in my main arteries and I was released from the hospital July 3, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: Tested post for COVID-19, blood work, EKG, Echocardiogram.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; Acid Reflux
Andere Medikamente: Rosuvastatin; amlodipine valsartan; omeprazole; multivitamin; aspirin
Allergien: Prednisone
Vorherige Impfungen: -

VAERS 2357762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 17.05.2022
Beginn: 23.06.2022
Tage bis Beginn: 37,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure Anticoagulant therapy Blood albumin Blood calcium abnormal Blood lactic acid C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray normal Choking Cough Exposure to SARS-CoV-2 Fatigue Fibrin D dimer General physical condition abnormal Hypoxia Laboratory test normal Nausea

Symptomtext

Admission Date: 6/23/2022 Discharge Date: 7/4/2022 PRESENTING PROBLEM: Acute respiratory failure with hypoxia (HCC) [J96.01] Pneumonia due to COVID-19 virus [U07.1, J12.82] COVID-19 [U07.1] Additional information for Item 18: HOSPITAL COURSE: Patient is a 85F with past medical history significant for PMR, vasculitis, giant cell arteritis, hx stroke, asthma who presented to the ER for hypoxia. She was exposed to COVID this weekend by home caretaker. The day prior to arrival, she started to develop an occasional cough along with occasional nausea and vomiting. She also reported fatigue and rhinorrhea. Earlier on day of admission, when her daughter went over to visit her, she noticed she was breathing faster and "didn't look right". Daughter had a pulse ox that she put on her and pt's SpO2 was at 80% on room air. Pt denied fever, chills, chest pain, lower extremity swelling, sore throat, abd pain. She has received the COVID vaccines. Upon presentation to the ER, she was non-toxic appearing and saturating at 88% on room air. PCR confirmed that she had covid. Lab work was relatively unremarkable. CXR was reassuring and did not show evidence of pneumonia or infiltrate. She ultimately required 4L O2 and was then saturating well. She was also given dexamethasone 6mg IV. She was admitted to medicine in stable condition. Overall, patient's respiratory status remained stable, with some mild respiratory distress, requiring up to 5L O2 via NC at rest. She was weaned down to room air by discharge with respiratory status improved. She continued home asthma meds: symbicort BID, duo neb BID (albuterol inhaler ordered while inpatient to limit COVID aerosolization), additional albuterol PRN. Started on mucinex BID, decadron 6mg daily x 10 days. Lovenox for VTE prevention. Patient/family declined remdesivir; Covid labs with lactic acid 1.9, d-dimer 690, CRP 23.7. Encouraged prone positioning, which patient was interested in and tolerated intermittently, along with frequent incentive spirometer use. Pt reported some coughing/choking with thin liquids on 6/24. Consulted Speech therapy and patient transitioned to nectar thick liquids (which she had been on in the past) with improvement. PT/OT were consulted and recommended discharge to SAR once out of COVID isolation. For patient's chronic illnesses, she takes home daily predsione for her history of Giant cell arteritis, PMR, and vasculitis. This was held while on dexamethasone and resumed once complete. She continued her home oral Vit D 1000 units daily with home Ca-Vit additional supplements held (Ca level corrected for albumin near upper limit normal on labs and Vit D high at 71). Continued home PPI for GERD, as was as statin/Plavix for her history of stroke (2009)/hyperlipidemia and Zoloft for depression. She continued home vesicare for overactive bladder. No acute issues related to these

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: N/a
Aktuelle Erkrankungen: None
Vorgeschichte: See Below Additional information for Item 12: PMR (polymyalgia rheumatica) (HCC), Acute respiratory failure with hypoxia (HCC), Chronic rhinitis, Head pain, H/O: stroke, Abnormality of gait, Temporal arteritis (HCC), GERD (gastroesophageal reflux disease), Obesity (BMI 30.0-34.9), Hyperlipidemia, Osteopenia, Small vessel disease (HCC), Sepsis (HCC), Pneumonia due to organism, Asthma exacerbation, Influenza A, Closed compression fracture of body of lumbar vertebra (HCC), Renal stones, AKI (acute kidney injury) (HCC), Hypoxia, Asthma, Weakness, Subconjunctival hemorrhage, Rheumatoid arthritis (HCC), Overactive bladder, Long term current use of systemic steroids, Macular degeneration, Idiopathic osteoarthritis, Fall from ground level.
Andere Medikamente: See Below Additional information for Item 9: acetaminophen (TYLENOL) 500 MG tablet, albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler, alendronate (FOSAMAX) 70 MG tablet, atorvastatin (LIPITOR) 20 MG tab
Allergien: Cymbalta, Cats
Vorherige Impfungen: -

VAERS 2357232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MT
Alter: 73,0
Geschlecht: M
Eingang: 04.07.2022
Impfdatum: 16.03.2022
Beginn: 04.07.2022
Tage bis Beginn: 110,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure Atelectasis COVID-19 COVID-19 pneumonia Influenza A virus test Influenza B virus test Pneumonia Respiratory syncytial virus test SARS-CoV-2 test positive

Symptomtext

Case was vaccinated and boosted x2, and was then hospitalized for Covid treatment. Hospitalized at: Local facility. * Acute respiratory failure (HCC) Assessment & Plan We had suspected this was due to CAP and/ or COVID19 PNA. Now looks more like COVID PNA alone. Treatment as elsewhere. Oxygen needs vacillate with activity and there may be a component of atelectasis as he had sats of 90% on RA in the afternoon on the 24 th and was 86-88% on RA at rest the am of discharge. Sats would improve to 92% after using IS ( does 3200 cc on IS)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: Ordered Test: FLUABV+SARS-CoV-2+RSV RNA Pnl Resp NAA+p (SARS CoV2-Flu-RSV PCR) Ordered Test Codes: 95941-1 (LN LOINC)/7778328789 (L LOCAL) Status: Final Accession Number: Unknown Specimen Source: Nasopharynx Specimen Site: Specimen Collection Date/Time: 2022-05-18 10:38:00.0 * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe (SARS CoV-2 PCR (COVID-19)) Coded Result: Positive (LOCAL) Numeric Result: Units: Text Result: Reference Range From: Negative Reference Range To: Performing Facility Details: Date/Time: 2022-05-18 13:51:24.0 Performing Facility: Community Med Center Facility ID: Unknown Interpretation: Abnormal Result Method: (Xpert Xpress SARS-Co) Status: Final Test Code: (LN LOINC)/7140701041 (L LOCAL) Result Code: (SCT/Positive (L LOCAL)
Aktuelle Erkrankungen: Cancer (HCC) squamous cell ? Depression ? Environmental allergies ? Gout
Vorgeschichte: Cancer (HCC) squamous cell ? Depression ? Environmental allergies ? Gout
Andere Medikamente: acyclovir (ZOVIRAX) 400 MG tablet Take 400 mg by mouth 2 times daily . allopurinol (ZYLOPRIM) 300 mg tablet Take 300 mg by mouth Daily. diazePAM (VALIUM) 2 mg tablet Take 2 mg by mouth every morning . fexofenadine (ALLEGRA ALLER
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2314133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 09.06.2022
Impfdatum: 08.05.2022
Beginn: 01.06.2022
Tage bis Beginn: 24,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Anticoagulant therapy Blood culture positive COVID-19 Condition aggravated Deep vein thrombosis Echocardiogram normal Enterococcus test positive Escherichia infection Flank pain Haemoglobin decreased Hydronephrosis Prostate cancer stage IV Pulmonary embolism Radical prostatectomy Sepsis Urinary tract infection

Symptomtext

BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 6/1/2022 Discharge Date: Jun 6, 2022 PRESENTING PROBLEM: Sepsis [A41.9] AKI (acute kidney injury) [N17.9] Sepsis with acute organ dysfunction without septic shock, due to unspecified organism, unspecified type [A41.9, R65.20] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 67 year old man who recently had radical prostatectomy with LN dissection for stage IV prostate cancer 6 weeks prior to admission. He had left PCN placed recently for hydronephrosis and right PCN placed for urinary diversion after bladder leak was discovered. Recently tx for E coli uti with ciproflocacin as well. He presented this time with severe sepsis with aki and left flank pain found to have left PCN tube malpositioned and incidentally covid +. He has hx of copd and has been on 3L oxygen since prior discharge during surgery admission. He was started on broad spectrum antibiotics and urology and IR were consulted. IR repositioned the left PCN and converted both tubes to nephroureteral tubes for better diversion. Urology had no further reccs. He also had recent DVT and PE so he was maintained on heparin gtt while home eliquis was held. He required 1 u prbcs for hgb < 7 but had no active bleeding. IR noted ascites and placed a drain into peritoneal fluid as well. He grew enterococcus on blood cultures and antibiotics changed to add vancomcin and ultimately de escalated to ampicillin with planned amoxicillin on discharge per ID. Echo was negative for vegetations. His aki resolved and home lasix was resumed. PT recommended home discharge which was arranged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: CAD (coronary artery disease) Benign essential HTN Mixed hyperlipidemia OSA (obstructive sleep apnea) Ischemic cardiomyopathy COPD (chronic obstructive pulmonary disease) CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min CTS (carpal tunnel syndrome) Derangement of posterior horn of medial meniscus of left knee ED (erectile dysfunction) Family history of colon cancer Foraminal stenosis of cervical region GERD (gastroesophageal reflux disease) Hemochromatosis carrier Hypothyroidism LVH (left ventricular hypertrophy) Prostate cancer MUSIC no PRO S/P CABG x 3 Type 2 diabetes mellitus without complication, without long-term current use of insulin Chronic systolic heart failure Hematuria, unspecified type History of hepatitis C Advanced care planning/counseling discussion Shock Pulmonary embolism AKI (acute kidney injury) Change in bowel habits Restless legs syndrome (RLS) Hospital discharge follow-up Nephrostomy tube failure with subsequent urine leak Sepsis
Andere Medikamente: potassium chloride SA (K-DUR, KLOR-CON M) 10 MEQ controlled release tablet acetaminophen (TYLENOL) 325 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base)
Allergien: None
Vorherige Impfungen: -

VAERS 2304977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: DC
Alter: 69,0
Geschlecht: M
Eingang: 01.06.2022
Impfdatum: 25.04.2022
Beginn: 16.05.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac arrest Death

Symptomtext

Participant admitted to hospital with cardiac arrest 5/16. Expired 5/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CKD Type 2 Diabetes
Andere Medikamente: Aspirin, Glipizide, Atorvastatin, Nifidipene, Labetalol, furosemide,
Allergien: Metformin
Vorherige Impfungen: -

VAERS 2298625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: -
Alter: 97,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 20.05.2022
Beginn: 26.05.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Resident passed away on 05/26/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2284744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: SD
Alter: 88,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 06.05.2022
Beginn: 10.05.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute kidney injury Acute myocardial infarction Alanine aminotransferase increased Ammonia increased Analgesic drug level therapeutic Aspartate aminotransferase increased Blood alcohol normal Blood bilirubin increased Condition aggravated Congestive hepatopathy Cytomegalovirus test Death Epstein-Barr virus test Failure to thrive Hepatic enzyme increased Hepatic vascular disorder Hepatitis B surface antigen negative Hepatitis C antibody negative

Symptomtext

failure to thrive, AKI, NSTEMI transaminitis - concern vaccine related by some specialists Severe acute liver injury: -Etiology likely related congestive hepatopathy and ischemic hepatitis in setting of congestive HF. urine tox screen -ve, acetaminophen level -ve, blood alcohol level -ve. HBSAG/HCV ab -ve. Autoimmune work up, Hep E IgM, EBV/CMV/HSV testing are pending. Doppler US of liver sowed patent hepatic vasculature. Right upper quadrant ultrasound reviewed with no evidence of chronic liver disease or biliary obstruction -Stopped NAC as acetamniophen is undetectable. Liver enzymes trending down -Monitor LFTs and INR daily Patient expired on day 5 of hospitalization

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 4,0
Labordaten: elevated INR t bili 2.9 AST 3089 on admit to 916 four days later ALT 2716 on admit to 1547 four days later ammonia 125 - 79
Aktuelle Erkrankungen: AKI
Vorgeschichte: CKD stage 4 afib dementia HF CAD with hx MI 2010
Andere Medikamente: of note - APAP and Pravastatin
Allergien: ACE inhibitors simvastatin - myalgias
Vorherige Impfungen: -

VAERS 2275695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MN
Alter: 78,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 29.03.2022
Beginn: 12.05.2022
Tage bis Beginn: 44,0
Dosis: 4
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 Condition aggravated Dyspnoea Death Respiratory failure

Symptomtext

update to previous report (e report # 841885)- updating with pt death 5/15/22 PRINCIPAL DIAGNOSIS Respiratory Failure With Hypoxia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2258517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: CA
Alter: 50,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 01.04.2022
Beginn: 02.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Spouse claims that the patient passed away two days after receiving Pfizer booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 2258517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

kritisch

Staat: CA
Alter: 50,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 01.04.2022
Beginn: 02.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Spouse claims that the patient passed away two days after receiving Pfizer booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 2257081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

kritisch

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 08.04.2022
Beginn: 10.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Atrioventricular block Blood test Catheterisation cardiac abnormal Chest X-ray Chest pain Electrocardiogram abnormal Fatigue Headache Herpes zoster Myocardial infarction Pain in jaw Skin lesion Stent placement

Symptomtext

The day after the vaccine, I had headaches and fatigue. The two days later, I noticed skin lesions. I called my PCP because I suspected shingles. He saw me but I didn't go on anything until the next day when it got worse. I started on Valtrex 5oomg (two tablets 3 times a day for ten days)for the shingles. My symptoms lasted about 4 to 5 days and then dried up after that. I have fully recovered from the shingles. Then on 4/24/2022, I had an episode of chest pain and jaw pain late at night. It passed within about ten minutes. On 4/25/2022 around 11, I had a similar episode and ended up in the emergency room. My EKG came back positive for a heart attack. I had a cardiac cast done that showed a blockage and they put a stint in. I am now on Metoprolol 25mg, Prasugrel 10mg, Atorvastatin 80mg, and Aspirin 81mg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 2,0
Labordaten: EKG 04/25/2022, Cardiac Catheterization 04/25/2022, blood work 04/25/2022, Chest XR 04/25/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Recovered from breast cancer in 2011
Andere Medikamente: None
Allergien: Compazine, IVP dye
Vorherige Impfungen: Shringrix dose 1 (2018) High fever, headaches and Rigors

VAERS 2710762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

schwer

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 07.11.2023
Impfdatum: 14.04.2022
Beginn: 03.11.2023
Tage bis Beginn: 568,0
Dosis: 4
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anion gap Atrial flutter Bacterial test positive Basophil count normal Basophil percentage Bilirubin urine Blood calcium decreased Blood chloride decreased Blood creatine Blood creatinine increased Blood glucose increased Blood potassium increased Blood sodium decreased Blood thyroid stimulating hormone Blood urea increased Brain natriuretic peptide increased Carbon dioxide normal Cardiac telemetry abnormal

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on November 03, 2023 18:05 EDT Verified By: MD on November 03, 2023 18:05 EDT Encounter Info: Hospital, Inpatient, 11/03/23 - * Final Report * Chief Complaint Rapid HR History of Present Illness/Subjective Patient is an 85 year old man w/ T2DM and a fib who presents to the ER w/ a rapid HR. The patient was found to be in rapid a flutter. He is a poor historian and can't tell me much about his past medical history or what meds he takes. Labs at the Facility were notable for a normal trop. WBC count was 10. Cr was 1.6 which is around his baseline. CT head and neck showed no acute findings or fractures. Synchronized cardioversion was attempted twice in the ER at 200J however patient failed this. His case was discussed w/ Cardiology on call who recommended starting an amiodarone infusion and admitting him to the ICU. Upon arrival his HR remains in the 110s to 120s. He has no complaints at this time. Telemetry shows a flutter. BP is normal. Review of Systems With the exception of that noted in the HPI all systems were reviewed and were negative. Physical Exam/Objective Vitals & Measurements most recent past 24 hours Constitutional: No acute distress, well-nourished Eyes: no scleral icterus ENMT: Moist oral mucosa Respiratory: Increased WOB Cardiovascular: Tachycardic, irregularly irregular rhythm Gastrointestinal: non-distended Musculoskeletal: intact ROM Integumentary: no rashes Neurologic: no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan Patient is an 85 year old man admitted w/ rapid a flutter. 1. Atrial flutter I48.92 -Failed cardioversion in the ER x 2 -Amio gtt for now -TTE -Cardiology consultation if refractory -Continue apixaban -Continue coreg -TSH -Telemetry 2. CAD (coronary artery disease) I25.10 -Continue home ASA and statin 3. Stage 3 chronic kidney disease N18.30 -Serum creatinine is at baseline -Renally dose medications -Avoid nephrotoxic agents -Monitor with daily CMP 4. Type 2 diabetes mellitus with hyperglycemia E11.65 -CDA in place -Carb controlled diet -Hypoglycemia protocol -Hold oral DM meds 5. Dyslipidemia E78.5 -Continue statin 6. Gout M10.9 -Continue allopurinol 7. Hypertension I10 -Continue home antihypertensive regimen 8. Diabetic neuropathy E11.40 -Continue gabapentin Due to a high probability of clinically significant, life threatening deterioration, the patient required my highest level of preparedness to intervene emergently and I personally spent 40 minutes of critical care time directly and personally managing the patient. This critical care time included obtaining a history, examining the patient, pulse oximetry, ordering and reviewing the studies, arranging urgent treatment with development of a management plan, evaluation of the patient?s response to treatment, frequent reassessment, and discussions with other clinicians. The critical care time was performed to assess and manage the high probability of imminent, life-threatening deterioration that could result in multi-organ failure. It was exclusive of separately billable procedures and treating other patients and teaching time. Please see the MDM section and the rest of this note for further information on patient assessment and treatment. Code Status Resuscitation Status - Ordered -- 11/03/23 17:58:00 EDT, Full Code Chronic Problem List AKI (acute kidney injury) CAD (coronary artery disease) Diabetes type 2, controlled Diabetic neuropathy Dyslipidemia GERD (gastroesophageal reflux disease) Gout Hypertension Primary osteoarthritis of both knees Stage 3 chronic kidney disease Procedure/Surgical History ?EGD and Colonoscopy with biopsy (08/11/2008) ?back ?shoulder-right Medications Home Medications (20) Active acetaminophen 325 mg oral tablet 650 mg = 2 Tablet, PRN, Orally, Q4H allopurinol 100 mg oral tablet 100 mg = 1 Tablet, Orally, TID apixaban 2.5 mg oral tablet 2.5 mg = 1 Tablet, Orally, BID aspirin 81 mg oral tablet, chewable 81 mg = 1 Tablet, Orally, QHS Cinnamon 1,000 mg, Orally, QAM Coreg 25 mg oral tablet 25 mg = 1 Tablet, Orally, BID ferrous sulfate 325 mg (65 mg elemental iron) oral tablet 325 mg = 1 Tablet, Orally, Daily finasteride 5 mg oral tablet 5 mg = 1 Tablet, Orally, Daily Fish Oil 1200 mg oral capsule 1,200 mg = 1 Capsule, Orally, QHS FLUoxetine 20 mg oral capsule 20 mg = 1 Capsule, Orally, QAM Garlic oral capsule 1,000 mg, Orally, QAM glimepiride 2 mg oral tablet 2 mg = 1 Tablet, Orally, Every Afternoon Lantus (insulin glargine) SoloStar Pen 100 units/mL subcutaneous solution See Instructions, Inject 40 units SubQ in the morning and 80 units at bedtime. Lutein 20 mg oral capsule 20 mg = 1 Capsule, Orally, QAM meloxicam 15 mg oral tablet NovoLOG (insulin aspart) FlexPen 100 units/mL subcutaneous solution omeprazole 20 mg oral delayed release tablet 20 mg = 1 Tablet, Orally, At Bedtime pravastatin 20 mg oral tablet 20 mg = 1 Tablet, Orally, At Bedtime sodium bicarbonate 325 mg oral tablet 1,300 mg = 4 Tablet, Orally, BID tamsulosin 0.4 mg oral capsule 0.4 mg = 1 Capsule, Orally, Daily Active Scheduled Inpatient Medications amiodarone infusion bolus dose, Infusion, 150 mg, Via Infusion Pump, ONCE, Start: 11/03/23 18:00:00 apixaban, Tablet, 2.5 mg, Orally, BID, Start: 11/03/23 21:00:00 insulin glargine (insulin glargine (Core Diabetes App)), Injection, 20 Units, Subcutaneous, BID, Start: 11/03/23 21:00:00 Amiodarone PREMIX + Dextrose 5% in Water PREMIX IV Continuous See Comments 15 mg/min Amiodarone PREMIX + Dextrose 5% in Water PREMIX IV Continuous See Comments Dextrose 10% in Water 500 mL IV Continuous Per Core Diabetes App - See Comments One-Time Medications Given 11/02/23 00:00:00 TO 11/03/23 18:01:35 None Reported PRN Medications (0600 - 0559) from 11/02 - 11/03 glucagon, 1 mg, IM, Unscheduled, 0 Dose(s) glucose, Per Core Diabetes App , IV Push, Unscheduled, 0 Dose(s) insulin lispro, Per Core Diabetes App , Subcutaneous, Unscheduled, 0 Dose(s) Allergies Neurontin Social History Alcohol Past Electronic Cigarette/Vaping E-Cigarette Use Never. Home/Environment Lives with Spouse. Substance Abuse Denies Tobacco Tobacco Use: Former smokeless tobacco user, quit more than 30 days ago. Family History Cancer....: Mother. Father: History is unknown Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 10.7 k/cumm High (11/03/23 09:56:00) RBC: 4.46 million/cumm (11/03/23 09:56:00) Hgb: 12.3 GM/dL Low (11/03/23 09:56:00) Hct: 37.8 % Low (11/03/23 09:56:00) MCV: 85 fL (11/03/23 09:56:00) MCH: 27.7 pg (11/03/23 09:56:00) MCHC: 32.7 GM/dL (11/03/23 09:56:00) RDW: 17.1 % High (11/03/23 09:56:00) Platelet: 170 k/cumm (11/03/23 09:56:00) MPV: 6.9 fL Low (11/03/23 09:56:00) Neutrophils %: 87 % (11/03/23 09:56:00) Lymphocytes %: 5 % (11/03/23 09:56:00) Monocytes %: 7 % (11/03/23 09:56:00) Eosinophils %: 0 % (11/03/23 09:56:00) Basophils %: 1 % (11/03/23 09:56:00) Absolute Neutrophil: 9.3 k/cumm High (11/03/23 09:56:00) Absolute Lymphocyte: 0.5 k/cumm Low (11/03/23 09:56:00) Absolute Monocyte: 0.8 k/cumm (11/03/23 09:56:00) Absolute Eosinophil: 0 k/cumm (11/03/23 09:56:00) Absolute Basophil: 0.1 k/cumm (11/03/23 09:56:00) Chemistry: Sodium SerPl QN: 135 mmol/L (11/03/23 09:56:00) Potassium SerPl QN: 5.4 mmol/L (11/03/23 09:56:00) Chloride SerPl QN: 96 mmol/L Low (11/03/23 09:56:00) Carbon Dioxide SerPl QN: 25 mmol/L (11/03/23 09:56:00) Anion Gap: 14 mmol/L High (11/03/23 09:56:00) BUN SerPl QN: 23 mg/dL High (11/03/23 09:56:00) Creatinine SerPl QN: 1.68 mg/dL High (11/03/23 09:56:00) Estimated GFR (CKD-EPI, no race): 40 mL/min/1.73m2 Low (11/03/23 09:56:00) Estimated CRCL (CG): 43 mL/min Low (11/03/23 09:56:00) Glucose SerPl QN: 344 mg/dL High (11/03/23 09:56:00) Calcium Total SerPl QN: 8.7 mg/dL (11/03/23 09:56:00) Troponin-I High Sensitivity: 16 ng/L (11/03/23 09:56:00) BNP Pl QN: 125 pg/mL High (11/03/23 09:56:00) Gluc-Strip, POC: 246 mg/dL High (11/03/23 15:42:00) Urine Studies: Color: Yellow (11/03/23 10:22:00) Clarity: Clear (11/03/23 10:22:00) Specific Gravity: >=1.030 (11/03/23 10:22:00) pH: 6.0 (11/03/23 10:22:00) Protein: >=300 Abnormal (11/03/23 10:22:00) Glucose: >=1000 Abnormal (11/03/23 10:22:00) Ketones: 15 Abnormal (11/03/23 10:22:00) Bilirubin: NEGATIVE (11/03/23 10:22:00) Hgb Ur: MODERATE. Abnormal (11/03/23 10:22:00) Nitrite: NEGATIVE (11/03/23 10:22:00) Urobilinogen: NormalUro (11/03/23 10:22:00) Leukocyte Esterase Ur: NEGATIVE (11/03/23 10:22:00) WBC: 11-20 Abnormal (11/03/23 10:22:00) RBC: 3-5 Abnormal (11/03/23 10:22:00) Bacteria: Moderate Abnormal (11/03/23 10:22:00) Squamous Epithelial: Few (11/03/23 10:22:00) Hyaline Casts: 0-2 (11/03/23 10:22:00) Granular Casts: 0-2 Abnormal (11/03/23 10:22:00) Diagnostics Radiology Results - Last 24 hours Across Visits 11/03/2023 10:43 - XR Chest PA or AP Portable IMPRESSION:1. Possible minimal congestion with no focal infiltrateThank you for consulting our team of subspecialty radiologists at Radiology. 11/03/2023 12:14 - CT Cervical Spine W/o IV Contrast IMPRESSION:1. No acute fracture or traumatic subluxation.2. Congenital spinal canal stenosis with superimposed degenerativechanges resulting in moderate to severe spinal canal stenosis atC5-C6 and C6-C7 levels. Multilevel moderate to severe neuralforaminal narrowing. Recommend MRI cervical spine without intravenouscontrast if clinical concern for spondylitic myelopathy.Thank you for consulting our team of subspecialty radiologists at Radiology. 11/03/2023 12:14 - CT Head W/o IV Contrast IMPRESSION:1. No acute intracranial findings, specifically no intracranialhemorrhage, hydrocephalus or herniation.2. Sequela of advanced chronic small vessel ischemic disease whichlimits evaluation for small foci of acute ischemia.Thank you for consulting our team of subspecialty radiologists at Radiology. Signature Line Electronically Signed on 11/03/23 18:05 EDT ________________________________________________________ MD

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Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2677913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: -
Alter: 33,0
Geschlecht: M
Eingang: 30.08.2023
Impfdatum: 30.03.2022
Beginn: 07.02.2023
Tage bis Beginn: 314,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Facial paralysis

Symptomtext

G51.0 RIGHT FACIAL PALSY 3/27/2023 (blank)

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Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2633556

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 18.05.2023
Impfdatum: 26.03.2022
Beginn: 28.12.2022
Tage bis Beginn: 277,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Anaemia Hypovolaemic shock

Symptomtext

HYPOVOLEMIC SHOCK 12/28/2022 ANEMIA

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Praegender Schweregrund: Hypovolaemic shock
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2574313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: PA
Alter: 22,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 05.05.2022
Beginn: 01.10.2022
Tage bis Beginn: 149,0
Dosis: 2
Route/Site: - / UN

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein

Blood test Colectomy Colitis ulcerative Colonoscopy abnormal Computerised tomogram Diarrhoea Gastrointestinal disorder Intensive care Large intestinal ulcer Migraine Peripheral swelling

Symptomtext

Migraines and swollen hands were first experienced in October 2022. By November she was experiencing severe gut and diarrhea; she went to her PCP, who did bloodwork and sent her home. She went back again and then went for more bloodwork. They gave several diagnoses that proved incorrect after two different ER visits. On January 6, she was in the ER for the third time and they transferred her to the hospital and was admitted; they did a colonospy on January 9th and diagnosed 3/4 of her colon was ulcerated. On january 13 she was transferred to a local hospital and they removed her colon. Dr said that ' the colon disintegrated in his hands like a wet paper towel." She was in ICU for 5 days and did not get released until February 1, 2023. The diagnoses was ulcerative colitis, one of the adverse events listed by Pfizer as an 'adverse event'. The doctor said she would have died if they did n ot remove the colon.

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Praegender Schweregrund: Intensive care
Hospital-Tage: 22,0
Labordaten: Bloodwork, CAT scan, mulitple CAT scans and emergency surgery
Aktuelle Erkrankungen: sensitive stomach
Vorgeschichte: None
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2560843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: WV
Alter: 61,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 04.05.2022
Beginn: 26.05.2022
Tage bis Beginn: 22,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Angiogram cerebral abnormal Computerised tomogram head abnormal Ischaemic stroke Magnetic resonance imaging head abnormal

Symptomtext

Ischemic stroke

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Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: -
Labordaten: CT scan 06/22 MRI 08/22 MRA 08/22
Aktuelle Erkrankungen: None
Vorgeschichte: Neuropathy
Andere Medikamente: Vitamin C
Allergien: None
Vorherige Impfungen: -

VAERS 2540632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 22.12.2022
Impfdatum: 23.02.2022
Beginn: 14.10.2022
Tage bis Beginn: 233,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Anxiety Back pain Blood glucose abnormal COVID-19 Cerebral palsy Chronic obstructive pulmonary disease Condition aggravated Coronary artery disease Cough Depression Dyspnoea Electroencephalogram normal HIV infection Influenza virus test positive Obesity Obstructive sleep apnoea syndrome Psychogenic seizure

Symptomtext

DATE OF ADMISSION: 10/14/2022 DATE OF DISCHARGE: 10/18/2022 DISCHARGE DIAGNOSIS: 1. Cough, shortness of breath due to COVID and chronic obstructive pulmonary disease exacerbation. 2. Pseudoseizures and history of seizure disorder. EEG was unremarkable. 3. Diabetes mellitus, insulin dependent with uncontrolled blood sugars due to steroids. 4. Acute kidney injury with history of chronic kidney disease, stage 3. 5. Morbid obesity, obstructive sleep apnea. Does not use CPAP. 6. History of deep venous thrombosis, pulmonary embolism, on Eliquis. 7. Cerebral palsy. 8. Chronic low back pain. 9. Human immunodeficiency virus, on medications. 10. Anxiety and depression. 11. Coronary artery disease with his history of cardiac cath and stenting.

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Praegender Schweregrund: Psychogenic seizure
Hospital-Tage: -
Labordaten: 10/14 Covid-19, Flu, RSV by NAA, Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2539121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 08.03.2021
Beginn: 07.10.2022
Tage bis Beginn: 578,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest pain Coronary artery bypass Coronary artery disease Electrocardiogram ST segment depression Electrocardiogram ST segment elevation Hypertension Intensive care Pain SARS-CoV-2 test positive Tachycardia

Symptomtext

67 year old female admitted to local Hospital with chest pain. The chest pain has been pesent for 2-3 weeks prior to admission. The patient was scheduled for a stress 10/7, overnight she had intermittent worsening chest pain . The chest pain was substernal, radiated to her left arm, and was described as an aching sensation. In the EC she was hypertensive (185/74) and tachycardic (110's). A Level I AMI was paged due to EKG concerning for ischemia, with ST elevation in aVR and diffuse ST depression. Due to patient's hemodynamic instability and critical left main disease, patient was scheduled for emergent CABG on 10/7/2022. The patient was taken to the operating room on 10/07/2022 and underwent the

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Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: 10/7 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2527311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: PA
Alter: 21,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 11.05.2022
Beginn: 23.06.2022
Tage bis Beginn: 43,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure measurement Computerised tomogram Contusion Fatigue Hypertensive crisis Magnetic resonance imaging Migraine Myocarditis Papilloedema Petechiae Retinal exudates Urine analysis

Symptomtext

she was in the hospital with the blood pressure of 252/190; myocarditis; optic nerve swelling; severe bruising; migraines; exhaustion; petechiae on her back; cotton wool spots on her eye; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 21-year-old female patient received BNT162b2 (BNT162B2), on 11May2022 as dose 2, single (Lot number: FK9894) at the age of 21 years for covid-19 immunisation. The patient's relevant medical history included: "Covid-19", start date: Sep2020 (unspecified if ongoing), notes: had covid in Sep2020 and then again this year Jan/Feb2022 and then was vaccinated in Apr.; "Covid-19", start date: 2022 (unspecified if ongoing), notes: had covid in Sep2020 and then again this year Jan/Feb2022 and then was vaccinated in Apr. The patient took concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot: FK9894), administration date: 20Apr2022, when the patient was 21-year-old, for COVID-19 immunization, reaction(s): "Hypertensive crisis", "bruising", "headaches", "visual changes", "slowing of optic nerve". The following information was reported: HYPERTENSIVE CRISIS (hospitalization, medically significant) with onset 23Jun2022, outcome "unknown", described as "she was in the hospital with the blood pressure of 252/190"; MYOCARDITIS (medically significant), outcome "unknown"; PAPILLOEDEMA (medically significant), outcome "unknown", described as "optic nerve swelling"; CONTUSION (non-serious), outcome "unknown", described as "severe bruising"; MIGRAINE (non-serious), outcome "unknown", described as "migraines"; FATIGUE (non-serious), outcome "unknown", described as "exhaustion"; PETECHIAE (non-serious), outcome "unknown", described as "petechiae on her back"; RETINAL EXUDATES (non-serious), outcome "unknown", described as "cotton wool spots on her eye". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: 252/190; 252, notes: (hospital name withheld and the hospital (withheld) ran multiple tests and they couldn't find any reason for her blood pressure to go from normal to 252; Computerised tomogram: Unknown results; Magnetic resonance imaging: Unknown results; Urine analysis: Unknown results. Therapeutic measures were taken as a result of hypertensive crisis. Clinical course: Patient received 2 doses of the Pfizer Covid vaccine. 1st dose on 20Apr2022, 2nd dose on 11May2022. On 23Jun2022 she went to the hospital in (hospital name withheld) and was admitted with a blood pressure of 252/190. She spent 5 days in ICU, and 3 days in a regular room. She had severe bruising on both legs and both arms, and petechiae on her back, migraines, and was severely exhausted. (hospital name withheld and the hospital (withheld) ran multiple tests and they couldn't find any reason for her blood pressure to go from normal to 252. They did a CAT scan, MRI's, and a 24 hour Urinalysis for her kidneys to check for adrenal gland tumors. Patient is a 21 year old athlete, that is now on 4 medications to control her blood pressure. States that they have been treating this as myocarditis. Caller believes all this was an adverse reaction to the vaccine. Has anyone else reported any of these effects after receiving this shot? Stated that it took the hospital 3 days of giving her daughter IV medications to get her blood pressure under control before she could go to oral medications.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201340703 same reporter/patient, different dose/AE;

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Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:252/190; Test Name: blood pressure; Result Unstructured Data: Test Result:252; Comments: (hospital name withheld and the hospital (withheld) ran multiple tests and they couldn't find any reason for her blood pressure to go from normal to 252; Test Name: CAT scan; Result Unstructured Data: Test Result:Unknown results; Test Name: MRI's; Result Unstructured Data: Test Result:Unknown results; Test Name: Urinalysis; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (had covid in Sep2020 and then again this year Jan/Feb2022 and then was vaccinated in Apr.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2522581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: CA
Alter: 26,0
Geschlecht: M
Eingang: 03.12.2022
Impfdatum: 13.04.2022
Beginn: 16.04.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal distension Amnesia Anxiety Arrhythmia Asthenia Blood test Bradycardia COVID-19 Cardiac imaging procedure normal Chest discomfort Chest pain Computerised tomogram Cough Diarrhoea haemorrhagic Dyspnoea Echocardiogram Electrocardiogram Electrocardiogram ambulatory normal

Symptomtext

Summary: Symptoms due to adverse event began as chest pain originally, then developed later into coughing, tight chest, increased chest pain severity while lying down, pounding heart, swelling of abdomen, arrhythmia and shortness of breath. All symptoms except chest pain, arrhythmia and pounding heart resolved but patient continues to have these symptoms at time of writing this report. Received the third shot (booster) of Pfizer on 4/13/2022. Went on a run 3 days later (4/16/2022) and began to experience severe and crippling chest pain. Stopped running but pain continued throughout the day. By next day 4/17/2022, went on another run and experienced same symptoms but worse in severity. Pain continued throughout the day and visited urgent care facility by the end of the day (4/17/2022). The pain persisted so patient self admitted to Hospital ER at 00:40 on 4/18/2022. ER staff administered anti-inflammatory medication which relieved pain temporarily. Patient was discharged without diagnosis other than nonspecific chest pain. Pain persisted consistently for 9 days until patient self admitted to the ER again for the same symptoms on 4/27/2022. The 4/27/2022 ER visit is where patient was diagnosed with pericarditis. Patient was released from the ER with a Naproxen prescription. Naproxen relieved pain but after 3 days, patient experienced severe internal bleeding in small intestine, large intestine and stomach. Vomited blood and had bloody diarrhea. Patient stopped the medication and was prescribed colchicine instead on 5/3/2022 by PCP. Patient was cleared by medical staff to travel. For one month, chest pain persisted continuously and peaked after brief moments of physical strain due to general travel along with coughing, tight chest, increased chest pain severity while lying down, pounding heart, swlling of abdomen, and shortness of breath. From now on, these will simply be referred to as "cardiovascular symptoms" since all or most symptoms continued up to the time of writing. On 6/5/2022 patient experienced abnormal chest pain (More than the regular pain experienced up to this point) along with severe leg pain. The patient contacted emergency services that performed and EKG and administered morphine for the pain. The patient was delivered to the hospital by emergency services where he underwent tests to determine cause of symptoms. This yielded a diagnosis of muscle cramping coupled with pericarditis that mimicked symptoms similar to a pulmonary embolism. The patient returned back from trip and two days after arrival, was self administered to the Hospital ER on 6/13/2022 due to an unknown, viral infection that was not COVID related. The cardiovascular symptoms peaked in severity during this visit, then decreased over the course of a week but still remained. The main symptoms, chest pain and arrhythmias continued for two more weeks until patient developed new symptoms: fever, nausea, severe coughing, congestion, severe chest pain and palpitations. Patient went to local, COVID testing facility and received a positive result. Patient then self admitted to the Medical Center on 6/28/2022 at the recommendation of cardiology nurse. Patient began taking Aspirin dosage of ~1600 mg per day. Patient spent 10 days in isolation and all symptoms except the pericarditis related ones resolved. Pericarditis symptoms continue to persist to the time of this report. Pain severity has decreased substantially, but arrhythmia and pounding heart continue with same prevalence. Patient was on a colchicine treatment of 0.125 mg, twice daily since 5/3/2022, but ran out of medication on 10/1/2022. A cardiologist re-prescribed a new prescription for the same dosage for 3 more months along with cardiac MRI study. Cardiac MRI study was conducted on 11/17/2022 along with a cardiologist review. Results of the study looked normal. Patient will continue the colchicine treatment but wane off the daily Aspirin by 325 mg per week. Cardiologist prescribed Metoprolol for patient to self administer when needed for continued arrhythmias.

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Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Facility: Hospital Symptoms: Chest pain Diagnosis: Chest pain Medical/Laboratory tests: EKG, X-ray, blood work Date: 4/18/2022 Facility: Hospital Symptoms: Chest pain Diagnosis: Chest pain, pericarditis Medical/Laboratory tests: EKG, X-ray, blood work Date: 4/27/2022 Facility: Hospital Symptoms: Chest pain, leg pain, arrhythmias, pounding heart, fatigue, dry coughs Diagnosis: Chest pain, pericarditis Medical/Laboratory tests: EKG, ultrasound, blood work Date: 6/5/2022 Facility: Hospital Symptoms: Weakness, memory loss,fever, nausea, full body pain with highest severity in chest Diagnosis: 1. Viral syndrome, 2. History of pericarditis, 3. Chest pain, 4. Hematochezia Medical/Laboratory tests: EKG, X-ray, blood work, CT scan, echocardiagram Date: 6/13/2022 Facility: facility Symptoms: Chest pain, arrhythmias, pounding heart, fatigue Diagnosis: None Medical/Laboratory tests: EKG Date: 6/23/2022 Facility: Medical Center Symptoms: COVID19 positive, arrhythmias, pericarditis Diagnosis: Reconfirmed symptoms Medical/Laboratory tests: EKG, Xray, blood work Date: 6/28/2022 Facility: Hospital Symptoms: Arrhythmias, panic attacks, memory loss, headaches, generalized GI pain, tachycardia, bradycardia, uncontrollable body temperature regulation Diagnosis: 1. Palpitations, 2. Adverse effect of homeopathic agent Medical/Laboratory tests: EKG, Xray, blood work, echocardiagram Date: 7/25/2022 Facility: Hospital Symptoms: Arrhythmias, anxiety Diagnosis: 1. Anxiety, 2. Palpitations Medical/Laboratory tests: EKG, holter monitor assigned Date: 8/1/2022 Facility: medical center Symptoms: Arrhythmias, chest pain, pounding heart Diagnosis: N/A Medical/Laboratory tests: Echocardiagram Date: 10/12/2022 Facility: Imaging facility Symptoms: Arrhythmias, chest pain, pounding heart Diagnosis: N/A Medical/Laboratory tests: Cardiac MRI study Date: 11/17/2022 All Holter Monitor Studies: Date: 8/16/2022 Result: Normal Date: 8/1/2022 Result: Normal Date: 7/25/2022 Result: Normal Date: 7/8/2022 Result: Normal Date: 10/12/2022 - 10/14/2022 Result: Normal
Aktuelle Erkrankungen: None
Vorgeschichte: Gastroesophageal reflux Irritable bowel syndrome with predominant constipation Nausea Rectal bleeding Reflux esophagitis Stress headaches
Andere Medikamente: Omeprazole 40 mg oral capsule (Once a day) Hyoscyamine 0.125 mg oral tablet (When needed)
Allergien: None
Vorherige Impfungen: -

VAERS 2195169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 03.12.2022
Impfdatum: 15.03.2022
Beginn: 01.03.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Bell's palsy Ear pain Facial paralysis Musculoskeletal stiffness Gait disturbance Muscle tightness Neck pain Pain Nerve injury Paralysis Vaccination site pain Pain in extremity

Symptomtext

whole body was like paralyzed and he couldn't even move; face got paralyzed/ paralyzed his face; Bell's Palsy; body was all stiff and neck; nerve issues/nerve damage; pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear; pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear; pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear; pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID: (Unknown). The reporter is the patient. A 51-year-old male patient received BNT162b2 (BNT162B2), on 15Mar2022 as dose 3 (booster), single (Lot number: FK9894) at the age of 51 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "blood pressure" (unspecified if ongoing); "Psoriasis" (unspecified if ongoing). The patient took concomitant medications which included unknown blood pressure medication and unknown medication for psoriasis. Patient has been taking medication for psoriasis for a few years, since right when COVID started, only takes a half a dose, (dose) was really strong. Vaccination history included: BNT162b2 (dose 1, Lot number: FA6780), administration date: 10Aug2021, when the patient was 50-year-old, for COVID-19 immunization, reaction(s): "vaccination failure", "COVID-19"; BNT162b2 (dose 2, Lot number: FC3183), administration date: 31Aug2021, when the patient was 50-year-old, for COVID-19 immunization, reaction(s): "vaccination failure", "COVID-19". The following information was reported: BELL'S PALSY (medically significant) with onset Mar2022, outcome "unknown"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset Mar2022, outcome "unknown", described as "body was all stiff and neck"; FACIAL PARALYSIS (medically significant) with onset Mar2022, outcome "unknown", described as "face got paralyzed/ paralyzed his face"; NERVE INJURY (non-serious) with onset Mar2022, outcome "not recovered", described as "nerve issues/nerve damage"; NECK PAIN (non-serious), ARTHRALGIA (non-serious), VACCINATION SITE PAIN (non-serious), EAR PAIN (non-serious) all with onset Mar2022, outcome "unknown" and all described as "pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear"; PARALYSIS (medically significant) with onset 15Mar2022, outcome "unknown", described as "whole body was like paralyzed and he couldn't even move". The events "whole body was like paralyzed and he couldn't even move", "face got paralyzed/ paralyzed his face", "bell's palsy", "body was all stiff and neck", "nerve issues/nerve damage" and "pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear" required physician office visit and emergency room visit. The clinical course was as follows: Patient reported that the COVID booster gave him Bell's palsy and he still had nerve damage. When he smiled, he noticed in eye brows and he started getting pain in back of his neck, down to his shoulder area where the shots were taken. Bell's palsy has gone back to 90 percent but not normal. Pain was not as severe as it was the first time; it has subsided but, pain was still there periodically. Pain was in back of neck, down to shoulder area, right around ear; it was the muscle or nerves, where the shots were done. He clarified this was all in the right side, right shoulder, right ear. Patient went to the emergency room (ER) and they explained that he should not have taken the booster and should have waited 3 months. When he went to the ER, he was there for a while and they gave him pain medication. He was not admitted to the hospital. It was like 2 weeks prior to taking COVID booster that he tested positive for COVID. Patient said it was most definitely the booster shot because, the day he took it, that night, his whole body was like paralyzed and he couldn't even move. It was Bell's palsy and he didn't move until 2 days later. His body was all stiff and neck. he couldn't move and everything else was stuck. It subsided a couple of days after that, 2 days later. Then, face started drooping and neck had the pain. He thought he was going to die, it was hurting so bad. The first doctor said it was caused by the booster. Then, for some reason, someone called back and said it was not enough known about the vaccine to say that the vaccine would have caused it. Everybody else said it was related to the booster. The doctors said they didn't have enough to say that this was the booster. Therapeutic measures were taken as a result of paralysis, facial paralysis, bell's palsy, musculoskeletal stiffness, nerve injury, neck pain, arthralgia, vaccination site pain, ear pain. Patient has had acupuncture that really helped a lot for the pain. He had to get his own physician because nobody was helping him. He couldn't stand the pain any longer. The doctor gave him some pills for nerves, to relax the nerves in the neck. They just made the pain even worse. It was so bad, they gave him a topical ointment for nerves, which seemed to work and has been using it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal; Psoriasis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2195169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 03.12.2022
Impfdatum: 15.03.2022
Beginn: 01.03.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Bell's palsy Ear pain Facial paralysis Musculoskeletal stiffness Gait disturbance Muscle tightness Neck pain Pain Nerve injury Paralysis Vaccination site pain Pain in extremity

Symptomtext

whole body was like paralyzed and he couldn't even move; face got paralyzed/ paralyzed his face; Bell's Palsy; body was all stiff and neck; nerve issues/nerve damage; pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear; pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear; pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear; pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID: (Unknown). The reporter is the patient. A 51-year-old male patient received BNT162b2 (BNT162B2), on 15Mar2022 as dose 3 (booster), single (Lot number: FK9894) at the age of 51 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "blood pressure" (unspecified if ongoing); "Psoriasis" (unspecified if ongoing). The patient took concomitant medications which included unknown blood pressure medication and unknown medication for psoriasis. Patient has been taking medication for psoriasis for a few years, since right when COVID started, only takes a half a dose, (dose) was really strong. Vaccination history included: BNT162b2 (dose 1, Lot number: FA6780), administration date: 10Aug2021, when the patient was 50-year-old, for COVID-19 immunization, reaction(s): "vaccination failure", "COVID-19"; BNT162b2 (dose 2, Lot number: FC3183), administration date: 31Aug2021, when the patient was 50-year-old, for COVID-19 immunization, reaction(s): "vaccination failure", "COVID-19". The following information was reported: BELL'S PALSY (medically significant) with onset Mar2022, outcome "unknown"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset Mar2022, outcome "unknown", described as "body was all stiff and neck"; FACIAL PARALYSIS (medically significant) with onset Mar2022, outcome "unknown", described as "face got paralyzed/ paralyzed his face"; NERVE INJURY (non-serious) with onset Mar2022, outcome "not recovered", described as "nerve issues/nerve damage"; NECK PAIN (non-serious), ARTHRALGIA (non-serious), VACCINATION SITE PAIN (non-serious), EAR PAIN (non-serious) all with onset Mar2022, outcome "unknown" and all described as "pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear"; PARALYSIS (medically significant) with onset 15Mar2022, outcome "unknown", described as "whole body was like paralyzed and he couldn't even move". The events "whole body was like paralyzed and he couldn't even move", "face got paralyzed/ paralyzed his face", "bell's palsy", "body was all stiff and neck", "nerve issues/nerve damage" and "pain in back of his neck, down to his shoulder area where the shots were taken/ all in the right side, right shoulder, right ear" required physician office visit and emergency room visit. The clinical course was as follows: Patient reported that the COVID booster gave him Bell's palsy and he still had nerve damage. When he smiled, he noticed in eye brows and he started getting pain in back of his neck, down to his shoulder area where the shots were taken. Bell's palsy has gone back to 90 percent but not normal. Pain was not as severe as it was the first time; it has subsided but, pain was still there periodically. Pain was in back of neck, down to shoulder area, right around ear; it was the muscle or nerves, where the shots were done. He clarified this was all in the right side, right shoulder, right ear. Patient went to the emergency room (ER) and they explained that he should not have taken the booster and should have waited 3 months. When he went to the ER, he was there for a while and they gave him pain medication. He was not admitted to the hospital. It was like 2 weeks prior to taking COVID booster that he tested positive for COVID. Patient said it was most definitely the booster shot because, the day he took it, that night, his whole body was like paralyzed and he couldn't even move. It was Bell's palsy and he didn't move until 2 days later. His body was all stiff and neck. he couldn't move and everything else was stuck. It subsided a couple of days after that, 2 days later. Then, face started drooping and neck had the pain. He thought he was going to die, it was hurting so bad. The first doctor said it was caused by the booster. Then, for some reason, someone called back and said it was not enough known about the vaccine to say that the vaccine would have caused it. Everybody else said it was related to the booster. The doctors said they didn't have enough to say that this was the booster. Therapeutic measures were taken as a result of paralysis, facial paralysis, bell's palsy, musculoskeletal stiffness, nerve injury, neck pain, arthralgia, vaccination site pain, ear pain. Patient has had acupuncture that really helped a lot for the pain. He had to get his own physician because nobody was helping him. He couldn't stand the pain any longer. The doctor gave him some pills for nerves, to relax the nerves in the neck. They just made the pain even worse. It was so bad, they gave him a topical ointment for nerves, which seemed to work and has been using it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal; Psoriasis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2514207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 22.11.2022
Impfdatum: 06.05.2022
Beginn: 04.10.2022
Tage bis Beginn: 151,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Cellulitis Debridement Gait disturbance Hypotension Intensive care Oedema peripheral SARS-CoV-2 test positive Sepsis

Symptomtext

Patient is a 53 y.o. male with a past medical history that includes NIDDM2, chronic lymphedema and LE wounds, HFpEF, HTN, CKD, and CAD. He presented on 10/4/2022 with generalized weakness, unsteady gait, and worsening BLE edema. Home health had found him to be hypotensive and he was brought to the ED and admitted to the ICU requiring pressors and broad spectrum antibiotics for sepsis related to LE cellulitis. He underwent wound debridement with podiatry. He was transitioned to oral antibiotics and transferred out of the ICU 10/15, but found to be COVID-19 positive 10/15 leading to delay in disposition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 28,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2484862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MD
Alter: 20,0
Geschlecht: M
Eingang: 20.10.2022
Impfdatum: 25.04.2022
Beginn: 20.05.2022
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: unbekannt Erholt: nein

Autoimmune haemolytic anaemia CTLA4 deficiency Chemotherapy Computerised tomogram abdomen abnormal Dyspnoea Dyspnoea exertional Fatigue Haemoglobin decreased Hepatomegaly Immunoglobulin therapy Intensive care Jaundice Laboratory test abnormal Liver function test abnormal Lymphadenopathy Ocular icterus Splenomegaly Transfusion

Symptomtext

Within 2-3 weeks of receiving the booster patient developed significant dyspnea with low level activities such a going up a flight of stairs. On approximately 5/20 he was noted to have yellowing of his eyes and continually worsening shortness of breath and fatigue. His dyspnea and jaundice progressed over the next few days On May 24th we went to the ER and was found to have Autoimmune Hemolytic Anemia with a Hemoglobin of 4.4, enlarged inguinal lymph node on L, as well as splenic and liver enlargement. He was transferred to hospital and was admitted to the ICU where he received a blood transfusion which required a full medical team to be present in the case of an allergic reaction. He stayed at hospital for approximately 1- 1 1/2 weeks where he received multiple blood transfusions, steroid infusions, and eventually was started on chemotherapy with Rituximab. He was discharged home with oral steroids and returned to hospital weekly for 4 weeks for Rituximab infusions. He then started a drug called Mycophenolate Mofetil. As of this week he continues with monthly IVIG infusions and had been transitioned to Abatacept to manage his newly acquired condition. He was found to have an underlying genetic condition called CTLA 4 protein deficiency. He has had no symptoms related to this in the past 20 years.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 8,0
Labordaten: 5/24/22: CT scan showed liver, spleen, and L inguinal lymph node enlargement. Labs showed HgB 4.4 (d/t AIHA) among other abnormal labs including liver function tests.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Approximately 2014 Age 12 Tdap/meningococcal: Severe edema of maxillary lymph nodes. Hospitalized

VAERS 2481782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: ME
Alter: 65,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 14.04.2022
Beginn: 21.09.2022
Tage bis Beginn: 160,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 COVID-19 pneumonia Haemoptysis Intensive care Laboratory test Pneumonia Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

10/11 Coughing up blood, ambulance to hospital. Currently in ICU. Covid pneumonia in both lungs Antibiotics Antiviral 100%oxygen via bipap machine try nasal when possible during day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: Positive home test 10/10 Many hospital tests
Aktuelle Erkrankungen: Birdshot chorioretinopathy
Vorgeschichte: Birdshot chorioretinopathy
Andere Medikamente: Latanoprost 0.005% Brimonidine 0.2% Prednisone 10 mg Mycophenolate 500mg 3tabs twice a day
Allergien: Penicillin Erythromycin
Vorherige Impfungen: -

VAERS 2473703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 06.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Loss of consciousness Nausea

Symptomtext

I had nausea and dizziness the following day after the vaccine. I passed out from it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Benadryl
Allergien: Amitriptyline; Ciprofloxacin; Cyclobenzaprine; Gabapentin; Hydrocodone; Methocarbamol; Nitrofurantoin; Nortriptyline; Pregabalin; Tricyclic Compounds
Vorherige Impfungen: -

VAERS 2470535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MI
Alter: -
Geschlecht: F
Eingang: 06.10.2022
Impfdatum: 22.08.2022
Beginn: 28.08.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 pneumonia Drug ineffective Haemodynamic instability Hypoxia Oxygen saturation decreased Pneumothorax Respiratory distress SARS-CoV-2 antibody test

Symptomtext

Haemodynamic instability; Respiratory distress; Hypoxia; Pneumothorax; COVID-19 pneumonia; COVID-19 pneumonia; This is a spontaneous report received from a non-contactable reporter(s) (Consumer). A 68-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Aug2022 as dose 4 (booster), single (Lot number: FK9894) for COVID-19 immunization; BNT162b2 (BNT162B2), on 08Feb2021 as dose 1, single (Lot number: EL9269), as dose 2, single (Lot number: EN6198) and as dose 3 (booster), single (Lot number: FH8028) for COVID-19 immunization. The patient's relevant medical history included: "Seronegative RA" (unspecified if ongoing). The patient's concomitant medications were not reported. The patient had positive SARS-CoV-2 IgG (Anti-Spike) on 23Aug2022. The patient had COVID-19 pneumonia in 2022 (positive SARS-COV-2 antibody test) presented for worsening shortness of breath (SOB). In the emergency room (ER), the patient was hypoxic requiring high flow nasal cannula (HFNC) 100% with Fi02/50 L and a nonrebreather maintaining SP02 in the early 90s. A significant increase in work of breathing was noted and patient was intubated. On 28Aug2022, the patient developed respiratory distress. Patient had a needle decompression and then chest tube placement for right sided tension pneumothorax. Patient was unable to be weaned off ventilator and on 05Sep2022 had a drop in Sp02 with increased WOB. The patient required multiple pressors for hemodynamic instability. She was then transitioned to comfort care and passed peacefully that evening of 06Sep2022. The reported cause of death: "COVID-19 pneumonia", "Haemodynamic instability", "Hypoxia", "Pneumothorax", "Respiratory distress". It was not reported if an autopsy was performed. No follow-up attempts are possible. No further information is expected.; Reported Cause(s) of Death: COVID-19 pneumonia; Haemodynamic instability; Hypoxia; Pneumothorax; Respiratory distress

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: Test Date: 2022; Test Name: SP02; Result Unstructured Data: Test Result:Decreased; Comments: in the early 90s; Test Date: 20220905; Test Name: SP02; Result Unstructured Data: Test Result:drop; Test Date: 2022; Test Name: SARS-COV-2 antibody test; Test Result: Positive ; Test Date: 20220823; Test Name: SARS-CoV-2 IgG (Anti-Spike); Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seronegative rheumatoid arthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MI
Alter: 25,0
Geschlecht: M
Eingang: 20.09.2022
Impfdatum: 24.03.2022
Beginn: 12.09.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Blood phosphorus decreased COVID-19 Condition aggravated Decreased appetite Diabetic ketoacidosis Intensive care Type 1 diabetes mellitus

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 9/12/2022 Discharge Date: Sep 14, 2022 PRESENTING PROBLEM: DKA, type 1, not at goal (HCC) Type 1 diabetes mellitus with ketoacidosis without coma (HCC) HOSPITAL COURSE: 25-year-old female with past medical history of type 1 diabetes who was admitted to the hospital with DKA. Was also found in the ER to have acute kidney injury. After admission to the intensive care unit DKA quickly resolved with gap closure and resolution of AKI. Was also found upon arrival to have COVID diagnosis. Main symptom from COVID illness was decreased appetite but was not having any shortness of breath or other respiratory symptoms. Was felt that DKA was exacerbated from missing dose of long-acting insulin and from COVID illness. Day of discharge, patient stated was not having abdominal pain, was tolerating diet with good appetite. Phosphate day of discharge was low at 1.8. Did give IV K-Phos. Did send with 3 days of K-Phos tablets 2 times a day. Diabetes team Dr. cleared for discharge and said that he is to continue with the same previous insulin regimen. Discharged stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Discharge Provider: MD Primary Care Provider at Discharge: None Physician, MD None Admission Date: 3/15/2022 Discharge Date: 3/17/2022 Active Hospital Problems Diagnosis Date Noted POA ? Diabetic ketoacidosis without coma associated with type 1 diabetes mellitus (HCC) 03/15/2022 Yes ? Lactic acidosis 03/15/2022 Yes ? AKI (acute kidney injury) (HCC) 03/15/2022 Yes ? DKA, type 1, not at goal (HCC) 11/05/2021 Yes ? Moderate protein-calorie malnutrition (HCC)
Vorgeschichte: DKA (diabetic ketoacidosis) (HCC) Type 1 diabetes mellitus with hyperglycemia (HCC) COVID-19 virus infection Hyperkalemia Elevated lipase
Andere Medikamente: Continuous Blood Gluc Sensor (FREESTYLE LIBRE 2 SENSOR SYSTM) MISC Contour Next Test Strips insulin glargine (LANTUS SOLOSTAR) 100 UNIT/ML pen-injector insulin lispro (HUMALOG KWIKPEN) 100 UNIT/ML pen-injector Insulin Pen Needle (BD ULTRA-F
Allergien: None
Vorherige Impfungen: -

VAERS 2433645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: ID
Alter: 24,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 21.03.2022
Beginn: 04.09.2022
Tage bis Beginn: 167,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Generalised tonic-clonic seizure Interchange of vaccine products Sleep disorder

Symptomtext

My first vaccine dose was Moderna and two weeks later I had a localized rash and giant lump on my arm. For my second dose I did Pfizer and had a grand mal seizure in my sleep at 4 am 6 months later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma and allergies
Andere Medikamente: Advair, Singulair, Allegra, Flonase
Allergien: Environmental allergies
Vorherige Impfungen: -

VAERS 2433451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 02.03.2021
Beginn: 18.08.2022
Tage bis Beginn: 534,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Anaemia Blood creatinine increased COVID-19 Chest X-ray normal Computerised tomogram abdomen normal Computerised tomogram head normal Computerised tomogram spine Cough Haemoglobin decreased Laboratory test abnormal Loss of consciousness Road traffic accident SARS-CoV-2 test positive Troponin normal Urine analysis normal

Symptomtext

72y.o. male with hx of prostate CA, DM-II, HTN, CAD (mild), PAD, recurrent syncope, current smoker presented to the ED after a MVC. Patient was driving at around 45 mph when he hit a fire hydrant and his car flipped over in the city. Pt states he lost consciousness prior to the crash. On arrival in ED BP 181/78, O2 100% on RA. Labs revealed Cr 1.49, mild anemia hgb 11.9, trop negative x1. UA negative. COVID-19 PCR positive in ED. CT hea/C-spine negative for acute process. CT C/A/P negative for acute process. CXR negative for acute process or infiltrates. He was cleared by trauma sx team for DC. However, he was admitted for further work up for recurrent syncopal episodes and cardiology is consulted.Patient states he had a similar episodes few months ago but he was not driving at, did not seek medical attention at that time. Patient denies any recent changes to his meds. Pt states he is vaccinated against COVID 19 x2 and boosted x2. He reports mild dry cough, but no shortness of breath, chest pain, or GI symptoms. Patient was not aware that he had COVID-19 infection a prior to the admission. States his mild dry cough started about couple days ago but he thought was related to allergies. All imaging studies including CT head/C-spine, CT C/A/P, CXR, pelvic XR all negative for acute process or fracture. Okay to discharge and schedule loop monitor implant outpatient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 10,0
Labordaten: 8/18 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2419468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: AR
Alter: 18,0
Geschlecht: F
Eingang: 24.08.2022
Impfdatum: 28.06.2022
Beginn: 11.07.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Electroencephalogram Juvenile myoclonic epilepsy Magnetic resonance imaging normal Seizure

Symptomtext

On July 11, 2022, she had a seizure for the first time ever and was transported by ambulance to local hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: EEG on July 11, 2022, at hospital reported juvenile myoclonic epilepsy. EEG on Aug 2, 2022, at hospital reported normal. MRI on Aug 3, 2022, at hospital reported normal.
Aktuelle Erkrankungen: Hashimoto, asthma, environmental allergies, Tourettes
Vorgeschichte: Hashimoto, asthma, environmental allergies, Tourettes
Andere Medikamente: Levothyroxine, Clonidine, Lexapro
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2368844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 20.08.2022
Impfdatum: 13.05.2022
Beginn: 03.07.2022
Tage bis Beginn: 51,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Areflexia Computerised tomogram normal Electromyogram normal Fatigue Guillain-Barre syndrome CSF protein increased Chills Chronic sinusitis Computerised tomogram abnormal Epididymitis Gait disturbance Hypoaesthesia Immunoglobulin therapy Loss of personal independence in daily activities Lumbar puncture abnormal Magnetic resonance imaging head normal Magnetic resonance imaging neck Magnetic resonance imaging spinal normal

Symptomtext

Diagnosed Guillain-Barree Syndrome (GBS). Patient experienced severe weakness and motor control of legs, Experienced numbness/tingling in feet to nipple line, fingertips to shoulders and in neck upwards to jaw. Initial presentation on or about July 3. Hospitalized on July 10th. No reflexes noted in knees, ankles or arms. Treatment - 5 Immunoglobulin infusions given 24 hours apart. Patient continues to have mild tingling in hands and feet with mild fatigue and weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 5,0
Labordaten: Lumbar puncture on July 10 - Positive for GBS CT Scan on July 10, - no abnormalities. MRI on Head, Neck - no abnormalities, MRI on Lumbar Region - no abnormalities, MRI on Thorax Region - no abnormalities, EMG Test - Negative for GBS.
Aktuelle Erkrankungen: Severe fever (103+) unknown cause, Only symptoms were aches, fever, fatigue and chills. Covid tests 1PCR, 2 in home tests were negative.
Vorgeschichte: Borderline High cholesterol,
Andere Medikamente: Rosuvastatin 20mg, CoQ10 200mg, Multivitamin, D3 1000IU.
Allergien: None known
Vorherige Impfungen: -

VAERS 2400344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: IN
Alter: 66,0
Geschlecht: M
Eingang: 03.08.2022
Impfdatum: 07.04.2022
Beginn: 12.04.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Diplopia IVth nerve paralysis Magnetic resonance imaging head normal

Symptomtext

WHITHIN 5 DAYS OF RECEIVING HIS FOURTH VACCINE, THE PATIENT DEVELOPED DOUBLE VISION. THIS WAS FOUND TO BE SECONDARY TO CRANIAL NERVE 4TH PALSY. MRI OF THE BRAIN WAS NORMAL AND THIS CLEARED AT ABOUT 5 WEEKS AFTER ONSET. NORMALYY IT TAKES 3 MONTHS FOR THESE TO CLEAR.

Weitere VAERSDATA-Felder

Praegender Schweregrund: IVth nerve paralysis
Hospital-Tage: -
Labordaten: MRI BRAIN AND ORBIT: NO EVIDENCE OF RECENT INTRACRANIAL ISCHEMIA OR HEMORRHAGE. UNREMARKABLE APPEARANCE OF THE ORBITS
Aktuelle Erkrankungen: HYPERTENSIVE HEART DISEASE WITH HEART FAILURE
Vorgeschichte: HYPERTENSIVE HEART DISEASE WITH HEART FAILURE
Andere Medikamente: valacyclovir (valacyclovir) tablet: 1 gram Klisyri (tirbanibulin) ointment in packet: 1% amoxicillin-pot clavulanate (amoxicillin-pot clavulanate) tablet: 875-125 mg atorvastatin (atorvastatin) tablet: 80 mg clopidogrel (clopidogrel) tablet
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 2379355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: SD
Alter: 70,0
Geschlecht: M
Eingang: 22.07.2022
Impfdatum: 21.04.2022
Beginn: 16.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Cold sweat Fatigue Pyrexia SARS-CoV-2 test positive Syncope

Symptomtext

I developed chills and severe fatigue on 7/15. Tested positive on 7/16. On 7/17 my skin became clammy and I developed a fever and I fainted. I went to the ER and was there for a few days. I received 3 days of an anti-viral infusion. I went home on 7/19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: AFIB; Heart failure
Andere Medikamente: Amiodarone; Potassium Chloride; Latanoprost; Famotidine;
Allergien: Heparin; Vancomycin
Vorherige Impfungen: -

VAERS 2357233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: TN
Alter: 26,0
Geschlecht: F
Eingang: 04.07.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Dizziness Electrocardiogram abnormal Haemoglobin normal Musculoskeletal disorder Presyncope Sinus tachycardia

Symptomtext

5 minutes after receiving Pfizer booster, patient was checking out at front desk when she felt "weak and dizzy". Felt legs crumple like she was going to pass out. She was observed for over 1 hour and given juice and water with improvement in her dizziness/ weakness. Felt better at the time of discharge. BP was 118/84. O2 100%. pulse initially 130s, but then low 90s at time of discharge. Thought to be pre-vasovagal syncope. Pt has hx of syncope during panic attacks. EKG was sinus tachycardia with no acute abnormality.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: EKG 5/2/2022 sinus tachycardia with pulse of 102 without acute abnormality. Hgb 12.0 5/2/2022
Aktuelle Erkrankungen: PCOS, anemia, IBS
Vorgeschichte: PCOS, anemia, IBS
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2331891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 24.03.2022
Beginn: 12.05.2022
Tage bis Beginn: 49,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Malaise Oropharyngeal pain Pulmonary oedema Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I did not have any symptoms with the vaccine. I tested positive for Covid 19 on 5/14/2022. I started feeling symptoms 5/12 with a sore throat and congestion. On the 14th I had a fever, ran 100 to 101 for a couple of days. I do not recall taking anything for symptoms prior to going to pharmacy clinic. They prescribed PAXLOVID, Z-PAK, prescription cough medication and inhaler (I had a fluid in my lungs). I was really sick for five days and slowly started to feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: Covid 19 test at home and at the clinic (nose swab) both positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamins
Allergien: Penicillin; sulfa
Vorherige Impfungen: -

VAERS 2324220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 20.06.2022
Impfdatum: 27.04.2021
Beginn: 17.06.2022
Tage bis Beginn: 416,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute kidney injury Asthenia Blood creatinine normal Blood glucose abnormal Blood glucose decreased COVID-19 Chronic kidney disease Cough Decreased appetite Diabetes mellitus Diarrhoea Hypertension Illness Malaise Osteoarthritis Pyrexia Renal impairment SARS-CoV-2 test positive

Symptomtext

She went shopping with an unvaccinated friend who also got sick around the same time as her, but otherwise has no clear exposure history. Since her illness started she reports labile blood sugars, generalized weakness, orthostasis and very poor appetite in addition to above symptoms. She's felt too unwell to take her medications for about two days last week but has otherwise taking her tacrolimus, mycophenolic acid, and prednisone 5mg daily as prescribed. She's on chronic suppressive cephalexin for recurrent UTIs. She actually called EMS last Saturday due to not feeling well and low blood sugar, but opted not to be brought in at that time. Admitted 06/18/2022 and currently hospitalized.MPRESSION AND PLAN: 1. Acute kidney injury on chronic kidney disease. Currently, the patient with renal function, which is worse than previous baseline with a creatinine of 2.3, her baseline is usually 1.8-1.9. The patient may have hyperabsorbed the Prograf and may have a high tacrolimus level, although she does not demonstrate symptoms of toxicity. We will check levels obviously. The patient may also have some soft hemodynamics, acute tubular necrosis. We have seen COVID related renal impairment many times. Once again, I think this is volume contraction in the setting of a complex drug regimen. We will hydrate and monitor. 2. COVID-19 infection. Main manifestations at this time would include cough, fever, and diarrhea. We will continue to monitor intake and output, hydrate as described. The patient has about 10 days out, so not really a candidate for Paxlovid or monoclonal antibody therapy. 3. Diabetes mellitus. Continues on a sliding scale insulin regimen. 4. Hypertension, well controlled on current medical regimen. 5. Distant seizure disorder, stable on current medical regimen. Other problems not as active.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Tested positive for COVID-19 on 06/17/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2320395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fk9894

schwer

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Chest pain Dyspnoea Palpitations Pericarditis

Symptomtext

Shortness of breath, palpitations, chest pain, chest discomfort. Pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2317232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: IL
Alter: 22,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 13.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Nausea Syncope Vomiting

Symptomtext

Patient felt nauseas, dizzy, and faint while waiting the 15 min after the vaccine administration. We brought her back into the consult room and had her lie down. She tried throwing up, but nothing happened. After laying down for few minutes, she felt much better. Her mom came to drive her home. She was completely fine when leaving, but I will follow up with patient later this afternoon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown
Andere Medikamente: unknown
Allergien: None
Vorherige Impfungen: -

VAERS 2296604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: IN
Alter: 76,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 20.05.2022
Beginn: 21.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Erythema Joint swelling Product administered at inappropriate site Skin warm Superficial vein thrombosis Ultrasound Doppler abnormal

Symptomtext

Patient claims vaccine was give too low in arm. Adverse event = redness and swelling of elbow and area around elbow of right arm. Warm to touch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Superficial vein thrombosis
Hospital-Tage: -
Labordaten: Patient went to PCP, then referred to hospital. Received an ultrasound test, which showed no DVT, but did show a superficial blood clot.
Aktuelle Erkrankungen: None reported
Vorgeschichte: Heart disease, cholesterol, hypothyroidism
Andere Medikamente: Ezetimibe, Metoprolol, Isosorbide, Spironolactone, Escitalopram, Plavix, Synthroid, Repatha
Allergien: None reported
Vorherige Impfungen: -

VAERS 2293181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: HI
Alter: 14,0
Geschlecht: M
Eingang: 24.05.2022
Impfdatum: 17.05.2022
Beginn: 18.05.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Influenza A virus test positive Myalgia Oropharyngeal pain SARS-CoV-2 test negative Streptococcus test positive Syncope

Symptomtext

HEADACHE, SYNCOPE, SORE THROAT, AND MUSCLE ACHES.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: INFLUENZA A TEST POSITIVE. STREPTOCOCCUS TYPE A TEST POSITIVE. COVID TEST NEGATIVE.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: HE WAS GIVEN IMMUNIZATIONS FOR INFLUENZA AND ALSO MEASLES, MUMPS, AND RUBELLA.
Allergien: None
Vorherige Impfungen: -

VAERS 2290251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: OR
Alter: 76,0
Geschlecht: M
Eingang: 22.05.2022
Impfdatum: 21.05.2022
Beginn: 22.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Atrioventricular block first degree Blood magnesium normal Blood potassium normal Bradycardia Cardiac telemetry Electrocardiogram ST segment elevation Electrocardiogram abnormal Syncope Troponin normal

Symptomtext

Admitted to hospital one day following vaccination with syncope due to symptomatic bradycardia (HR into 20s on telemetry during episodes)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 1,0
Labordaten: Troponin negative K 3.6, Mg 1.8 EKG with 1st degree AV block, trace ST elevations in I, II
Aktuelle Erkrankungen: None
Vorgeschichte: BPH Essential tremor Hyperlipidemia
Andere Medikamente: Atenolol 25 mg daily Atorvastatin 40 mg daily Unspecific CBD-containing gummy Acyclovir 400 mg BID
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2275542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: RI
Alter: 58,0
Geschlecht: M
Eingang: 13.05.2022
Impfdatum: 12.04.2022
Beginn: 05.05.2022
Tage bis Beginn: 23,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Catheterisation cardiac Chest pain Echocardiogram Electrocardiogram abnormal Pericarditis Troponin I increased

Symptomtext

Pericarditis requiring catheterization due to chest pain and abnormal EKG and 1 day hospitalization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 1,0
Labordaten: 5/5/2022 EKG. Cardiac cath. 5/6/2022: Troponin 1 peaked at 1473, echo of heart
Aktuelle Erkrankungen: None
Vorgeschichte: DM, obesity
Andere Medikamente: Metformin, multivitamin, iron, calcium, atorvastatin
Allergien: raspberry, lisinopril, naproxen, ciprofloxacin.
Vorherige Impfungen: -

VAERS 2273472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: NY
Alter: 47,0
Geschlecht: M
Eingang: 12.05.2022
Impfdatum: 12.05.2022
Beginn: 12.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Contusion Fall Haemorrhage Loss of consciousness Syncope Tooth fracture

Symptomtext

Patient fainted approximately 3 mins after receiving the booster dose of Pfizer, 0.3 ml. Patient fell from the chair and hit his head on the ground. Patient was unconscious for approximately 10-15 seconds, and was noted with a chipped tooth and contusion on the head, with slight bleeding. Patient was A&O x 3 upon regaining consciousness and vital signs remained WNL. EMS was called.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2269081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: SC
Alter: 55,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Bell's palsy Fatigue Influenza virus test negative Pain Peripheral swelling Pyrexia SARS-CoV-2 test negative Sneezing

Symptomtext

Bell?s Palsy left arm swelling(needing steroids). Then three days later I start to sneezing fever body aches pains fatigue. Tested negative for COVID-19 and Flu

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Negative tests date 05/09/2022
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Diovan 160-12.5mg Paxil 20mg
Allergien: None
Vorherige Impfungen: -

VAERS 2263139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: CO
Alter: 80,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 21.04.2022
Beginn: 24.04.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Angiopathy Arterial compression therapy Arterial disorder Arteriogram coronary abnormal Arteriosclerosis coronary artery Atrial fibrillation Back pain Blood loss assessment Bundle branch block right Cardiomegaly Cardioversion Catheterisation cardiac abnormal Chest X-ray abnormal Chest pain Computerised tomogram head normal Coronary artery disease Coronary ostial stenosis Electrocardiogram abnormal

Symptomtext

Patient is a 80 y.o. y.o. female presenting with vomiting. Fell one week ago with bruise on forehead. Fell twice on weekend without injury. 4 days ago had 2nd covid booster. Did not have vomiting side effect with prior shots. 2 days ago started vomiting continuously. Initially food then yellow bile. Has been unable to take meds for 2 days including diltiazem and eliquis. Husband had bronchitis a couple of weeks ago but no GI illness. Ate the same food as husband. She does take an H2 blocker for stomach acid. Has had 7 BMs in same time period but doesn't think they have been loose. At 1030pm had last vomit and BM episode. Felt burning chest pain after she vomited, radiated sharply to back, better now. Called 911 for fast heartrate. Had HR 150s-180s by paramedics. SBP 70s. Tried to cardiovert her twice without success. In ER finishing 2nd liter bolus with SBP 70s on diltiazem 2.5mg/hour infusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 2,0
Labordaten: XR CHEST SINGLE VIEW: Result Date: 4/28/2022 Impression: Mild cardiomegaly and mild vascular congestion. Report E-Signed By: MD at 4/28/2022 12:48 AM CT BRAIN WITHOUT CONTRAST: Result Date: 4/28/2022: IMPRESSION: 1. No acute intracranial hemorrhage or mass effect. Report E-Signed By: at 4/28/2022 12:34 AM I have personally interpreted the cxr without infiltrate, ct brain without SDH, and ekg with rapid afib RBBB. 40 minutes of critical care time spent at the bedside, personally reviewing studies, speaking with family, and speaking with ER physician. MD 4/28/2022 12:34 AM. CATH LAB: Post Procedure Diagnosis: Non-Obstructive CAD Procedure Performed: Left Heart Cath and Selective Coronary Angiography Findings: Left main: Left main coronary is a large vessel which bifurcates in the LAD and left circumflex. It is angiographically free of sign of disease. Left anterior descending artery: Left anterior descending artery is a large vessel which extends to the apex. The LAD is angiographically free of sign of disease. The first second branch is a large vessel which has a mild 20% ostial stenosis. The distal vessels are noted to be tortuous. Left circumflex: Left circumflex is a large, nondominant vessel. The left circumflex and OM branches are angiographically free of sign of disease. The distal vessels are noted to be tortuous. Right coronary: The right coronary is a large, dominant vessel. The proximal RCA is angiographically free of sign of disease. There is mildly calcified mild diffuse disease of the mid RCA which appears 20% at most severe. The distal RCA is angiographically free of significant disease. The large RPDA and large set of RPL branches are angiographically free of significant disease. The distal vessels are noted to be tortuous. LVEDP 14 mmHg. Percutaneous Interventions: None LVSF: (Left ventricular Systolic Function) Not Performed Wall Motion Abnormality: Not Performed Procedural Characteristics: There were no hemorrhagic complications. Estimated blood loss: <20 mls. No specimens obtained. Moderate sedation utilized for anesthesia. Arterial Management: Closure Device Type Radial artery compression device. Door to balloon in STEMI delayed secondary to: Not relevant to this patient. Patient Disposition: Intensive Care Unit. 4/29/2022 9:32 AM, MD
Aktuelle Erkrankungen: no/unknown
Vorgeschichte: Atrial fibrillation, abnormal echocardiogram, vasculopathy, coronary artery disease, mild, nonobstructive, recurrent deep vein thrombosis, pulmonary embolism, nonthrombocytopenic purpura, allergic rhinitis, vertigo, GERD, bowel and bladder incontinence, breast asymmetry, dysuria, arthritis, osteopenia, osteopenia, falls, asthma, chronic migraine without aura, acquired scoliosis, headache, thoracic spondylosis, chronic pain, degeneration of lumbosacral intervertebral disc, cervical dystonia, post concussion syndrome
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet, alendronate (FOSAMAX) 70 mg tablet, apixaban (ELIQUIS) 2.5 mg tablet, ascorbic acid 500 mg tablet, atorvaSTATin (LIPITOR) 10 mg tablet, cholecalciferol, vitamin D3, (VITAMIN D3) 1,000 unit tablet, e
Allergien: Demerol, penicillins, sulfa antibiotics
Vorherige Impfungen: -

VAERS 2260448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: PA
Alter: 26,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 28.04.2022
Beginn: 01.05.2022
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Epistaxis Thrombosis

Symptomtext

Patient reported that he was fine for several days after receiving the vaccine, but after the weekend he developed persistent nose bleeding, which he said has not stopped and is also producing chunky clots of blood. He did not report any other symptoms, and was advised to contact his doctor if the bleeding continues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2257509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: NJ
Alter: 21,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 25.04.2022
Beginn: 25.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anaphylactic reaction Hypotension Rash Tachycardia Throat tightness

Symptomtext

Anaphylaxis (rash on chest), sensation of throat closing, tachycardia and hypotension.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2254880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

schwer

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 27.04.2022
Beginn: 27.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dyspnoea Hyperhidrosis Hypoaesthesia Paraesthesia Presyncope

Symptomtext

Patient complained that around 130-145 she started having numbness and tingling in her arms, light headedness, sweats,SOB and felt like she was going to pass out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2242043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MI
Alter: 25,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anaphylactic reaction Blood pressure increased Cardiac monitoring Dyspnoea Immunisation reaction Periorbital swelling Pharyngeal erythema Pharyngeal swelling Rash SARS-CoV-2 test positive Swelling face Throat tightness Tremor Urticaria

Symptomtext

Patient experienced an anaphylactic reaction to the COVID-19 Pfizer vaccine. (difficulty breathing, swelling of face and throat, rash - within 4 hours; emergency treatment sought) Immediately after administering the COVID-19 booster dose - patient complained of some tightness is the throat and was shaking. Office Notes: "He was feeling some tightness in his throat when I arrived and was talking to him. He was not having any respiratory distress. We examined the heart lungs and he appeared to have a regular rate and rhythm along with normal breath sounds. No wheezing audible. I asked him if he had a history of anxiety which he stated he did. I also asked if he had any reaction to the 1st or 2nd COVID-19 vaccinations and he stated he did not. We discussed that this could just be an anxiety provoked reaction. I reassured the patient that everything looks good and sounds good Obviously we cannot examine the inside of his throat to look at his airway but I advised him to drink some water while he waited the 15 minutes he was also sent after receiving the COVID vaccination. I checked on the patient multiple times throughout the 15 minutes. Each time I spoke with him his symptoms were improving. We discussed that if he was having an anaphylactic reaction the water would not improve the symptoms and it would have worsened. I gave him reassurance that this is likely just related to anxiety and there is no indication for us to call EMS or inject steroids at this time. He was advised that if his symptoms were worsening he should call 911 for further evaluation. Patient in agreement the plan." Telemedicine appointment 2 hours after vaccine - "Wheezing, some dyspnea, throat feels tight after COVID 19 vaccination 2 hours ago. I have escalated patient to in person at the ER. His parents will drive him now." When to Emergency Department - 4.11.22 - DIAGNOSIS at time of disposition: 1. Anaphylaxis due to COVID-19 vaccine. HISTORY OF PRESENT ILLNESS: Patient is a 25-year-old male with the chief complaint of a possible allergic reaction. Patient explains that this morning he received his booster dose of the Pfizer COVID-19 vaccination. Patient describes that immediately after the shot he noticed chest tightness and sore throat, describing this as tight. He notified his PCP of his symptoms who told him they were likely related to anxiety and told him to take a dose of his anxiety medication when he returned home. Patient describes that upon returning home he noticed continued chest tightness along with wheezing. He also describes a rash to his neck, abdomen, and back. Patient notes that he took a dose of Benadryl and Ativan around 1130. He notes that he was not feeling particularly anxious prior to the vaccination. He received both doses of the Pfizer COVID-19 vaccination in March 2021 and April 2021 without similar reaction. He notes that he tested positive for COVID-19 February 2022. Denies fever. He reports that he does have peanut allergies and has an EpiPen at home. 1336: On exam he does have some bilateral expiratory wheezing, rash on his back neck and arms with some urticaria where he has scratched the rash. Oropharynx is clear, voice is normal and there is no oral swelling. Some erythema to the posterior pharynx noted I did order IV Solu-Medrol, IV Benadryl and Pepcid, fluids and albuterol for wheezing. I do not feel patient needs EpiPen at this time. 1338: Patient's rash was worsening, he started having swelling around his eyes. He continued to have wheezing. We decided to give him epinephrine and move him to a monitored room. Patient was placed on a cardiac monitor, administered epinephrine will continue to monitor his symptoms. 1620: Patient was reassessed around 3:30 p.m., his rash had resolved, he was having no sensation of throat swelling, wheezing had resolved and he fell back to baseline. Will continue to monitor the patient until around 4:30 p.m 1636: Patient reassessed again, no recurrent symptoms, no wheezing, pulse ox 99%, no facial swelling, no rash. I did offer to observe the patient for an hour or 2 longer but they were comfortable going home at this point in time with no recurrent symptoms. I will prescribe prednisone 40 mg for 2 more days, have him continue Benadryl every 6 hours and follow up with this with his doctor. He has an EpiPen at home that is not expired and he is educated about symptoms that require using it and calling 911. He is welcome to come back with any new or worsening symptoms. He is advised never to receive a COVID-19 vaccine again due to the severe allergy. + elevated BP - to be evaluated by PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Unspecified constipation Peanut allergy Simple Renal cyst Family hx of colon cancer GAD (generalized anxiety disorder) Recurrent major depressive disorder, in full remission (HCC) Panic disorder Hashimoto's disease Multiple food allergies Insomnia Mixed hyperlipidemia
Andere Medikamente: EPINEPHrine 0.3 MG/0.3ML auto-injector LORazepam (ATIVAN) 0.5 MG tablet Magnesium 300 MG CAPS MULTIPLE VITAMIN PO Omega-3 Fatty Acids (OMEGA 3 PO) Probiotic Product (PHILLIPS COLON HEALTH PO) traZODone (DESYREL) 150 MG tablet
Allergien: NutsHives Lortab [Codeine]Itching, Rash Peanuts [Peanuts]Swelling TetracyclineItching, Rash Vicodin [Hydrocodone-acetaminophen]Itching, Rash Wellbutrin [Bupropion]
Vorherige Impfungen: -

VAERS 2236306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 24.03.2022
Beginn: 14.04.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Bell's palsy

Symptomtext

Bells palsy about 3 weeks after vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2236185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: TX
Alter: 18,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 12.04.2022
Beginn: 14.04.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Electrocardiogram ST segment elevation Electrocardiogram T wave inversion Musculoskeletal pain Myocarditis Pain Sleep disorder

Symptomtext

Patient developed mild chest pain on 4/13. It worsened on 4/14 and woke him up from sleep that night. His mother administered tylenol and Tums with moderate relief. Chest pain radiates to the left scapula. Denies dyspnea, cough, headaches or dizziness. Denies fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG done 4/15/2022- showed inverted T wave in lead III which was a change from previous EKG. 1 mm ST elevations in II, V1-V3. Post-vaccine myocarditis suspected. Patient prescribed ibuprofen 600 mg TID and was referred to cardiology.
Aktuelle Erkrankungen: none
Vorgeschichte: Seasonal allergic rhinitis; Eczema; Overweight
Andere Medikamente: none
Allergien: seafood
Vorherige Impfungen: -

VAERS 2234199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 14.04.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest discomfort Chest pain Cold sweat Condition aggravated Depressed level of consciousness Dizziness Generalised tonic-clonic seizure Hyperhidrosis Paraesthesia Tremor

Symptomtext

Pt received her first dose of pfizer vaccine for covid. About 10 minutes post injection she began to get diaphoretic, clammy, lighthheaded, shaking. VSS were taken and blood pressure was 174/117 and pulse was 115. Pt started to complain of chest pain and tightness. Stating she felt tingly all over. In house MD was called to evaluate pt. At this time pt started to have what appeared to be a tonic clonic seizure. Pt's head and airway were secured and pt was lowered to the floor from the chair. After evaluation by the MD, 911 was called for assistance. After about 10 minutes pt slowly became more alert and awake. Pt was A&O x3 upon EMS arrival. Pts blood pressure returned to 134/82. Pt was put on the cart and transferred to hospital ER for further evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: none at Vaccine clinic
Aktuelle Erkrankungen: none
Vorgeschichte: allergic rhinitis due to allergan, irritable bowel syndrome, ventral hernia without obstruction or gangrene, hx of abdominal surgery, abdominal pain, endometriosis, dysmenorrhea, menorrhagia with regular cycle, alcohol abuse, adhd, hx of prescription drug abuse, panic disorder, anxiety, patellofemoral arthralgia of both knees, migraines, seizures
Andere Medikamente: famotidine, Ritalin, NECON 1/35, 28, Zoloft, imitrex, topamax
Allergien: lithium, lurasidone, morphine, Phenergan, toradol, Vicodin, Fentanyl, Zofran
Vorherige Impfungen: -

VAERS 2233781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK 9894

schwer

Staat: MN
Alter: 42,0
Geschlecht: F
Eingang: 14.04.2022
Impfdatum: 14.04.2022
Beginn: 14.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood test Syncope

Symptomtext

Patient was administered dose at 8:36 am of Covid vaccine. Patient went to lab to have blood drawn and had syncopal episode at 8:56 am. Patient recovered and was sent home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Vitamin D deficiency, anxiety, asthma, essential hypertension, prediabetes, insomnia
Andere Medikamente: Albuterol HFA (pro-air; ventolin; proventil) 90 mcg/actuation inhaler Albuterol-ipratropium (duoneb 2.5-0.5g) in 3 mL nebulization solution Citalopram (celexa) 20 mg tablet Levonorgestrel-ethinyl estrad, 0.15-30 mg-mcg, (kurvelo, 28,) 0.15-
Allergien: Sulfa-hives
Vorherige Impfungen: -

VAERS 2231263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: AK
Alter: 86,0
Geschlecht: M
Eingang: 13.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Face injury Fall Gait disturbance Syncope

Symptomtext

approx 15-20 minutes after vaccine and pt had left exam room-notified that pt. had "collapsed down the hallway" and that emergency had been called. reported he had used restroom- and was hurrying down the hall and had fallen face first after stumbliing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: chronic acquired lymphedema essential hypertension diastolic heart failure with preserved injection fraction malignant neoplasm of urinary bladder renal lesion limited mobility
Vorgeschichte: Afib hypertension lymphedema DM diastolic heart failure
Andere Medikamente: melatonin 3m, elequis 5mg, Potassium chloride, vitamin C, vitamin B12, folic acid, lasix 40mg, coreg 2mg, ibersartan 150mg, escitalopram 10mg, atorvastatin 40mg, vitamin D3,
Allergien: NKA
Vorherige Impfungen: -

VAERS 2225351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: GA
Alter: 16,0
Geschlecht: F
Eingang: 09.04.2022
Impfdatum: 09.04.2022
Beginn: 09.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Loss of consciousness Vomiting

Symptomtext

PT WAS LIGHT-HEADED WHILE SEATED, BLACKED OUT FOR A FEW SECONDS AND VOMITED 3 TIMES WITHIN 10 MINS. BP ~103/80 . EMT ARRIVE 20 MINUTES LATER AND PT WAS ALMOST RECOVERED BEFORE TAKEN AWAY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2225220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: AZ
Alter: 62,0
Geschlecht: F
Eingang: 09.04.2022
Impfdatum: 18.02.2022
Beginn: 27.02.2022
Tage bis Beginn: 9,0
Dosis: 4
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Bell's palsy

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 18Feb2022 11:15 (Lot number: FK9894) at the age of 62 years as dose 4 (booster), single for Covid-19 immunisation. Relevant medical history included: "Lupus" (unspecified if ongoing); "High Blood pressure" (unspecified if ongoing); "High Cholesterol" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Covid-19 vaccine (Dose=3, Manufacturer name unknown.), for Covid-19 immunization; Covid-19 vaccine (Primary immunization series completed, Manufacturer name unknown), for Covid-19 immunization. The following information was reported: BELL'S PALSY (medically significant) with onset 27Feb2022 17:00, outcome "recovering", described as "9 days after my #4 vaccine I got Bell's Palsy on the right side of my face. My mouth was opened more to the right side, my right eye didn't blink automatically, my right eye brow didn't move". The event "9 days after my 4 vaccine I got Bell's palsy on the right side of my face, my mouth was opened more to the right side, my right eye didn't blink automatically. my right eye brow didn't move", was evaluated at the emergency room visit. Therapeutic measures were taken as a result of Bell's palsy. The patient had no other vaccine in four weeks. The patient had no Covid prior vaccination not tested post vaccination. The patient was treated with Prednisone for 11 days. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol; Hypertension; Lupus erythematosus
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2216404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MI
Alter: 19,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Syncope

Symptomtext

The PATIENT FAINTED WITHIN 10 MINUTES OF RECEIVING THE DOSE. PATIENT WAS ALERT AND DRINKING WATER WITHIN 5 MINUTES OF THE INCIDENT. WAS EVALUATED BY EMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2201455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: IN
Alter: 28,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 27.03.2022
Beginn: 27.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Hyperhidrosis Immediate post-injection reaction Loss of consciousness Paraesthesia Syncope

Symptomtext

VASOVAGEL SYCOPE IMMEDIATELY AFTER INJECTION. PATIENT BLACKED OUT FOR A MOMENT THEN FELT DIZZY HANDS TINGLED. SWEATY. FELT BETTER UPON DRINKING WATER AND LAYING ACCOSS 2 CHAIRS. DID NOT FALL OR OTHERWISE INJURED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 2194712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 22.03.2022
Beginn: 22.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Feeling abnormal Incoherent Injection site haemorrhage Loss of consciousness Seizure like phenomena Staring Vomiting

Symptomtext

PATIENT SAW A SMALL AMOUNT OF BLOOD RUN DOWN HER ARM AFTER VACCINATION AND IMMEDIATELY SAID SHE DIDN'T FEEL GOOD. SHE THEN LOST CONCIOUSNESS AND SHOOK AS THOUGH HAVING A SEIZURE, WHICH LASTED A FEW SECONDS. THE LOSS OF CONSCIOUSNESS LASTED APPROXIMATELY ONE MINUTE. PATIENT SLOUCHED DOWN IN HER CHAIR BEFORE SITTING UP AND STARING INTO SPACE, NOT FULLY COHERENT. SHE THEN REGAINED CONCIOUSNESS AND SEEMED COHERENT. EMERGENCY SERVICES WERE CALLED AND HER VITAL SIGNS SEEMED NORMAL. PATIENT VOMITED ONCE AFTER EMERGENCY SERVICES ARRIVED. PATIENT WAS NOT TAKEN TO THE HOSPITAL AND WENT HOME WITH HER MOTHER. AT A 5 HOUR FOLLOW UP THE PATIENT DID NOT HAVE FURTHER EFFECTS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2189352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

schwer

Staat: PA
Alter: 12,0
Geschlecht: M
Eingang: 21.03.2022
Impfdatum: 20.03.2022
Beginn: 20.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Flushing Hyperhidrosis Injection site erythema Syncope Tremor Unresponsive to stimuli

Symptomtext

Site: Redness at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Shakiness-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2184015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: MA
Alter: 18,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 16.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Loss of consciousness

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: PATIENT WAS UNCONSIOUS FOR ABOUT 10 SECONDS, ONCE HE CAME TO HE WAS ALERT AND ORIENTED. EMT ARRIVED WITHIN 5 MINUTES. BP118/82 HEART RATE 62 PULSE 100

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

schwer

Staat: TX
Alter: 24,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 06.03.2022
Beginn: 06.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Chills Confusional state Dizziness Fatigue Flushing Hyperhidrosis Hypotension Injection site erythema Injection site pain Lethargy Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Systemic: Chills-Mild, Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Mild, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Mild, Systemic: Weakness-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2124632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

schwer

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 18.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Syncope

Symptomtext

Syncope reaction after vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: unknown
Andere Medikamente: Unknown
Allergien: none
Vorherige Impfungen: -

VAERS 2109942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 14.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Energy increased Seizure

Symptomtext

3 minutes after receiving the IM injection patient had seizure like reaction follow by a burst of energy. Symptoms resolved in less than 1 minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A.
Vorgeschichte: N/A.
Andere Medikamente: N/A.
Allergien: N/A.
Vorherige Impfungen: -

VAERS 2099366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: FL
Alter: 17,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 09.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Facial paralysis Fear Hypoaesthesia Movement disorder Pallor

Symptomtext

Patient presented within 15 minutes of getting the vaccine with left arm, hand and finger numbness. His mouth was also slightly drooping. He turned pale and was scared that he couldn't move his fingers and hand. 911 was called and while waiting, patient stated he was feeling better. EMS took to hospital to evaluate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2091904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

schwer

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 06.02.2022
Impfdatum: 04.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood glucose decreased Deafness Nausea Presyncope Vomiting

Symptomtext

About 5 min after administration of Vaccine, pt said that is feeling nausea and cannot hear. While running towards bathroom, she throw up. Father wanted us to call 911. Patient did not show any symptoms of anaphylaxis or breathing issues. Paramedics arrived and check the patient out shortly. By the time paramedics arrived, she was already feeling better. Per paramedics, pt experienced "Vagal Reaction". Upon further investigation, it appeared that patient had not eaten much from the night before and blood sugar was slightly on lower end. Patient was ok and walked out with her father.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: EKG, Blood Sugar, Blood Pressure performed by paramedics at the seen.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Unknown
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2726704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: FL
Alter: 71,0
Geschlecht: M
Eingang: 20.12.2023
Impfdatum: 19.03.2021
Beginn: 21.08.2023
Tage bis Beginn: 885,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute kidney injury Asthenia COVID-19 COVID-19 pneumonia Cardiac failure acute Diarrhoea Dizziness Dyspnoea Fall Lethargy Respiratory depression Respiratory failure SARS-CoV-2 test positive Tachypnoea

Symptomtext

Reported Symptoms: 10012727:DIARRHEA; 10013573:DIZZINESS; 10038436:RENAL FAILURE ACUTE; 10038678:RESPIRATORY DEPRESSION; 10043088:TACHYPNEA; 10084380:COVID-19 PNEUMONIA; Narrative: Patient received five doses of Pfizer COVID 19 vaccine (Mar/Apr/Oct 21/Mar/Oct 22). The patient presented to the ED on 21 August 2023 with shortness of breath, falling, diarrhea, and weakness. The patient tested positive for COVID 19 on 21 August 2023. The patient was admitted with acute covid 19 infection and acute heart failure. The patient was treated with supportive care and furosemide. The patient was discharged on 23 August 23, but the patient was readmitted on 25 August 2023 with increased lethargy and COVID pneumonia, acute renal injury, and respiratory failure. The patient was treated appropriately and discharged on 6 Sep 23 in stable condition. Reported per EUA. Other Relevant HX: Other: covid pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2707360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 79,0
Geschlecht: M
Eingang: 31.10.2023
Impfdatum: 26.10.2022
Beginn: 23.10.2023
Tage bis Beginn: 362,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pt presents in ED 10/23/23 for weakness and SOB. Pt is vaccinated against COVID with 5 previous shots. He tested positive for COVID on 10/23 and was admitted to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2673522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: FL
Alter: 92,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 08.10.2022
Beginn: 09.06.2023
Tage bis Beginn: 244,0
Dosis: 4
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia Dyspnoea exertional

Symptomtext

2/10/2021 010M20A 3/10/2021 048A21A 10/27/2021 FE3590 5/5/2022 FK9894 10/8/2022 GH9702 Pfizer BiValent 6/9/2023 - 6/13/2023 (4 days) Presents hospital progressively worsening generalized weakness for last 1 week and dyspnea on exertion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2654528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MA
Alter: 68,0
Geschlecht: F
Eingang: 11.07.2023
Impfdatum: 08.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Pneumonia SARS-CoV-1 test Vaccination site pain

Symptomtext

Went to outdoor wedding in Maine last September and got pneumonia from kids running around; Then had more, the 4th in Apr2022. A little fatigued and a little soreness at site; Then had more, the 4th in Apr2022. A little fatigued and a little soreness at site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient received BNT162b2 (BNT162B2), on 08Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 68 years for covid-19 immunisation. The patient's relevant medical history included: "Osteoporosis" (ongoing), notes: Osteoporosis, takes Prolia 60mg subcutaneous injection twice a year. diagnosed 7 years ago.; "Arthritis" (unspecified if ongoing); "Left branch bundle blockage" (unspecified if ongoing); "Post traumatic stress syndrome" (unspecified if ongoing); "Asthma" (unspecified if ongoing). Concomitant medication(s) included: XANAX taken for stress, anxiety, start date: 2004 (ongoing); ALBUTEROL HFA taken for asthma (ongoing). Vaccination history included: BNT162b2 (Dose 1, Lot No: ER2613), administration date: 19Mar2021, when the patient was 67-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, Lot No: EW0153), administration date: 09Apr2021, when the patient was 67-year-old, for COVID-19 immunization; BNT162b2 (Dose 3, Lot No: FH8020), administration date: 19Oct2021, when the patient was 67-year-old, for COVID-19 immunization. The following information was reported: FATIGUE (non-serious), VACCINATION SITE PAIN (non-serious) all with onset Apr2022, outcome "unknown" and all described as "Then had more, the 4th in Apr2022. A little fatigued and a little soreness at site"; PNEUMONIA (medically significant) with onset Sep2022, outcome "unknown", described as "Went to outdoor wedding last September and got pneumonia from kids running around". The patient underwent the following laboratory tests and procedures: SARS-CoV-1 test: Negative covid. Therapeutic measures were taken as a result of pneumonia. Clinical course details: The patient went to outdoor wedding last September and got pneumonia from kids running around. 6 other people at wedding got pneumonia in their 40's. Thought had Covid and went to hospital and did test. She was Negative covid but it was pneumonia and she was put on 2 types antibiotics and a steroid prednisone to help deal with it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Test Name: did test; Result Unstructured Data: Test Result:Negative covid
Aktuelle Erkrankungen: Osteoporosis (Osteoporosis takes Prolia 60mg subcutaneous injection twice a year. diagnosed 7 years ago.)
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Asthma; Left bundle branch block; Stress
Andere Medikamente: XANAX; ALBUTEROL HFA
Allergien: -
Vorherige Impfungen: -

VAERS 2652737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 90,0
Geschlecht: F
Eingang: 05.07.2023
Impfdatum: 14.05.2022
Beginn: 30.05.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anaemia Dyspnoea Fatigue Laboratory test Pyrexia

Symptomtext

I had a fever after receiving the vaccine for three days. Towards the end of May, I was feeling tired and out of breath. I went to the doctor and was diagnosed with anemia and my BNT was at 231. I did not receive any prescriptions to help with my symptoms. My BNT number has been fluctuating for several months. I have had to go to the emergency room for observation twice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis
Andere Medikamente: N/A
Allergien: Shrimp
Vorherige Impfungen: Pneumonia; in 2000; I had fever and my arm swelled.

VAERS 2643160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CO
Alter: 67,0
Geschlecht: F
Eingang: 09.06.2023
Impfdatum: 01.04.2022
Beginn: 06.07.2022
Tage bis Beginn: 96,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Biopsy Computerised tomogram Dislocation of vertebra Encephalitis viral Formication Headache Investigation Magnetic resonance imaging Noninfective encephalitis Paraesthesia SARS-CoV-2 test X-ray

Symptomtext

brain infection/inflammation was really debilitating; C1 and C2 were slightly out of alignment; nothing stopped the prickly, crawling feeling in her brain.; nothing stopped the prickly, crawling feeling in her brain.; This brain inflammation was since 06Jul2022; inflammation of her brain membranes.; She had a viral brain infection; From the back of her head, up her occipital and up front of her face it was as if she had shingles on the inside with nothing showing on the outside. It was that intense and beyond painful; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID. The reporter is the patient. A 67-year-old female patient received BNT162b2 (BNT162B2), on 01Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 67 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "Little high blood pressure", start date: 2015 (unspecified if ongoing), notes: Diagnosed 8 years ago, it's minor. Takes 5mg Benazepril every day.; "Migraine" (unspecified if ongoing), notes: Migraine Takes Sumatriptan; "Muscle spasms" (unspecified if ongoing), notes: She takes 50mg of Tramadol each day and Soma 350mg. A year ago, started on neurotoxin Botox.; "Severe Osteoporosis" (unspecified if ongoing). Concomitant medication(s) included: BENAZEPRIL taken for hypertension (ongoing); SUMATRIPTAN taken for migraine; TRAMADOL taken for muscle spasms; SOMA [CARISOPRODOL] taken for muscle spasms; BOTOX taken for muscle spasms, start date: 2023. Past drug history included: Forteo for osteoporosis, reaction(s): "didn't do anything", notes: She did go through an 18 month program with Forteo, an injectable drug injected into abdomen, which didn't do anything.; Boniva for Osteoporosis, reaction(s): "it's totally useless", notes: She just lets them fill it and she doesn't take it. Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: FD8448, Time: probably before noon; Anatomical Site of injection: usually in left arm, Route: injection), administration date: 20Aug2021, when the patient was 66-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: EL3302, Time: given before noon, Anatomical Site of injection: usually in the left arm; Route: injected), administration date: 05Mar2021, when the patient was 66-year-old, for COVID-19 immunization; BNT162b2 (DOSE 1, SINGLE; Lot number: EL3302, Anatomical Site of injection: Arm, Route: injection), administration date: 13Feb2021, when the patient was 66-year-old, for COVID-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 06Jul2022, outcome "recovering", described as "From the back of her head, up her occipital and up front of her face it was as if she had shingles on the inside with nothing showing on the outside. It was that intense and beyond painful"; ENCEPHALITIS VIRAL (medically significant) with onset 06Jul2022, outcome "recovering", described as "She had a viral brain infection"; NONINFECTIVE ENCEPHALITIS (medically significant) with onset 06Jul2022, outcome "recovering", described as "This brain inflammation was since 06Jul2022; inflammation of her brain membranes."; ASTHENIA (non-serious), outcome "unknown", described as "brain infection/inflammation was really debilitating"; DISLOCATION OF VERTEBRA (non-serious), outcome "unknown", described as "C1 and C2 were slightly out of alignment"; FORMICATION (non-serious), outcome "unknown", PARAESTHESIA (non-serious), outcome "not recovered" and all described as "nothing stopped the prickly, crawling feeling in her brain.". The patient underwent the following laboratory tests and procedures: Biopsy: (unspecified date) Unknown results, notes: They did biopsies and they were all benign, but did discover she had silicone in her lymph nodes from a breast implant. When that happened, who knows. She has really small breasts and was told to not go for more surgeries. Is scheduled to see for another ultrasound this month and another bone scan this month; Computerised tomogram: (unspecified date) Unknown results, notes: When she first started developing symptoms in her brain and skull, primary care immediately sent her in for a CAT scan or MRI. The scans definitely didn't show any type of masses or tumors or anything like that. Also had X-rays done to see if her cervical spine, C1 and C2 were out of alignment and possibly creating the symptoms. C1 and C2 were slightly out of alignment and the treatment she received did get her back in alignment; Investigation: (unspecified date) Unknown results, notes: They did biopsies and they were all benign, but did discover she had silicone in her lymph nodes from a breast implant. When that happened, who knows. She has really small breasts and was told to not go for more surgeries. Is scheduled to see for another ultrasound this month and another bone scan this month; Magnetic resonance imaging: (unspecified date) Unknown results, notes: They had done MRIs and there was no blockage, no masses. Went to neurologist who wanted to do a nerve block, but refused the nerve block because she wasn't in that type of pain; SARS-CoV-2 test: (19May2023) Negative, notes: First Test; (20May2023) Positive, notes: She took two more tests and at midnight on 20May2023, she was COVID-19 positive; X-ray: (unspecified date) Unknown results, notes: When she first started developing symptoms in her brain and skull, primary care immediately sent her in for a CAT scan or MRI. The scans definitely didn't show any type of masses or tumors or anything like that. Also had X-rays done to see if her cervical spine, C1 and C2 were out of alignment and possibly creating the symptoms. C1 and C2 were slightly out of alignment and the treatment she received did get her back in alignment. Therapeutic measures were taken as a result of noninfective encephalitis, encephalitis viral, headache, asthenia, dislocation of vertebra, formication. Clinical course: She takes 50mg of Tramadol each day and Soma 350mg because she gets severe muscle spasms. Muscle spasms have been so severe over a 27-year period that finally, a year ago, some pain management doctor started injecting her with neurotoxin Botox to help keep those under control. She also has severe osteoporosis, which is shocking but not shocking because women get it all the time. She did go through an 18-month program with Forteo, an injectable drug injected into abdomen, which didn't do anything. NDC/LOT/EXP are unknown, this was about 8 years ago and [Name withheld] may be retired now. Now she's just taking Boniva, it's totally useless. She just lets them fill it and she doesn't take it. Caller wanted to tell the good side effects regarding Paxlovid. She had a viral brain infection. Once she took Paxlovid, it started helping with other issues she was already experiencing due to the brain infection. Paxlovid was like divine intervention. Doctors didn't know what brought this one, but it's been happening since 06Jul2022. Clarified she went to the dentist, and afterwards, something happened. From the back of her head, up her occipital and up front of her face it was as if she had shingles on the inside with nothing showing on the outside. It was that intense and beyond painful. She's fully vaccinated and hadn't had COVID. Then ended up getting COVID around 21May2023 and her doctor called in Paxlovid. Within 36 hours of taking Paxlovid, for the first time in a year, she had 80% relief from her symptoms. The best way she could describe was she was going through was an inflammation of her brain membranes. Wanted to tell Pfizer that Paxlovid can help other conditions besides COVID. This to her was a breakthrough. She had written 4 pages of notes of her experience. All of her COVID-19 Vaccines were manufactured by Pfizer. She didn't have any side effects with the vaccines. She eats really healthy has no cholesterol. Has slightly elevated blood pressure, but overall, she is healthy. Caller does everything via [withheld], except for examine and blood work. COVID-19 symptoms started 19May2023. First test was negative. She took two more tests and at midnight on 20May2023, she was COVID-19 positive. [Withheld], immediately called in Paxlovid. Started Paxlovid on 20May2023 or 21May2023, but was pretty sure it was Sunday, 21May2023. There was 80 percent relief from brain infection/inflammation symptoms. The symptoms from the brain infection/inflammation was really debilitating. She wanted to die. The COVID-19 was nothing. This brain infection/inflammation was since 06Jul2022. They had done MRIs and there was no blockage, no masses. Went to neurologist who wanted to do a nerve block, but refused the nerve block because she wasn't in that type of pain. The neurologist fired her as a patient. Confirmed caller was not suicidal and caller declined the phone number. Caller clarified she was just left in debilitating state with no answers and spent money on expensive doctors. She doesn't want to be treated like she was a bat-shit crazy person because she was highly educated and on her own figured out she has a viral inflammation in her brain because it follows the SARS and she had chicken pox. Her symptoms followed so much down that autoimmune type of area. She was spending $30,000 out of pocket a year and she wanted answers. Confirmed she completed the Paxlovid treatment and discarded the packaging. Can't remember time of COVID-19 Vaccines but pretty sure they were administered before noon. Thought her COVID-19 was pretty mild, but she was vaccinated and boosted. Thinks because of her age. In her opinion, COVID-19 has not gone away. States they stay up to date on the shingles and flu vaccine. Got the fifth COVID-19 Vaccine just to be proactive and because her husband is 77 and she is 68. Because she didn't have COVID-19, she hadn't built up any immunity because she hadn't had it. She's never had a cold in her life. She takes Alendronate sodium (Boniva) tablets USP 70mg tablet once a week. It doesn't create new bones. It hardens bones so if a person has a fall. She is part of an experimental [program name withheld]. When she first started developing symptoms in her brain and skull, primary care immediately sent her in for a CAT scan or MRI. The scans definitely didn't show any type of masses or tumors or anything like that. Also had X-rays done to see if her cervical spine, C1 and C2 were out of alignment and possibly creating the symptoms. C1 and C2 were slightly out of alignment and the treatment she received did get her back in alignment. But nothing stopped the prickly, crawling feeling in her brain. She doesn't know how relevant this is, but when she went for breast exam last year, she did have 3 small masses. They did biopsies and they were all benign, but did discover she had silicone in her lymph nodes from a breast implant. When that happened, who knows. She has really small breasts and was told to not go for more surgeries. She was scheduled to see for another ultrasound this month and another bone scan this month. Whatever Paxlovid did to her, is like winning money, it's a miracle. She was suffering, she was curled up in bed thinking she was going to die of a brain injury. When she gets back to [Place name withheld], [Name withheld] is doing a study long term COVID-19 and will be meeting with her to make her aware of caller's response to the Paxlovid. Once she completed Paxlovid, doctor put her on another anti-viral, Valacyclovir 1 gram tablet 3 times a day. After taking that for 48 hours, last night the inflammation in her head/brain came back with a vengeance to where she was hysterical. She called her neighbor who had some Paxlovid she didn't take. Caller got one dose of the 3 tablets, and within 1 hour and 45 minutes, her brain inflammation was over 80% gone. Caller was pretty savvy, and she doesn't mind being a guinea pig, but was in a debilitating state with her doctor for a year. It wasn't cool to do what she did, but states she is not talking about fentanyl or a street drug. This information could help hundreds or thousands of people. Her doctor was by the book. Caller stated she will take matters into her own hands and is not going back into a critical state, she was 103lbs and she was exhausted. Aware this was discrepant from caller previously providing she is 105 lbs, but this was confirmed and documented as provided. She would get her neighbor's Paxlovid again. If the symptoms come back again, she will call her friend across the street and get another dose of her Paxlovid. Stated it's scary is that it's an unknown variable. On normal COVID, she takes Paxlovid twice a day. She was experimenting. After she took Paxlovid last night, she woke up without the severe symptoms in her head, she is going to see how long she goes today with her symptoms being kept at bay. Then if the symptoms in her head come back tomorrow or the next day, she will get Paxlovid and will take another dose. This was vitally important. A a lot of drugs created for one condition and then down the road are found out to be wonderful for 4-5 other conditions. Her doctor wouldn't call in a second prescription of Paxlovid because it's not FDA approved beyond COVID-19. She was not going to let herself go back to feeling like she's going to die.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300211892 same patient and drug; different dose and event;

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: biopsies; Result Unstructured Data: Test Result:Unknown results; Comments: They did biopsies and they were all benign, but did discover she had silicone in her lymph nodes from a breast implant. When that happened, who knows. She has really small breasts and was told to not go for more surgeries. Is scheduled to see for another ultrasound this month and another bone scan this month.; Test Name: CAT scan; Result Unstructured Data: Test Result:Unknown results; Comments: When she first started developing symptoms in her brain and skull, primary care immediately sent her in for a CAT scan or MRI. The scans definitely didn't show any type of masses or tumors or anything like that. Also had X-rays done to see if her cervical spine, C1 and C2 were out of alignment and possibly creating the symptoms. C1 and C2 were slightly out of alignment and the treatment she received did get her back in alignment.; Test Name: Investigation; Result Unstructured Data: Test Result:Unknown results; Comments: They did biopsies and they were all benign, but did discover she had silicone in her lymph nodes from a breast implant. When that happened, who knows. She has really small breasts and was told to not go for more surgeries. Is scheduled to see for another ultrasound this month and another bone scan this month.; Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Comments: They had done MRIs and there was no blockage, no masses. Went to neurologist who wanted to do a nerve block, but refused the nerve block because she wasn't in that type of pain.; Test Date: 20230519; Test Name: COVID-19 Test; Test Result: Negative ; Comments: First Test; Test Date: 20230520; Test Name: COVID-19 Test; Test Result: Positive ; Comments: She took two more tests and at midnight on 20May2023, she was COVID-19 positive; Test Name: X-ray; Result Unstructured Data: Test Result:Unknown results; Comments: When she first started developing symptoms in her brain and skull, primary care immediately sent her in for a CAT scan or MRI. The scans definitely didn't show any type of masses or tumors or anything like that. Also had X-rays done to see if her cervical spine, C1 and C2 were out of alignment and possibly creating the symptoms. C1 and C2 were slightly out of alignment and the treatment she received did get her back in alignment.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Diagnosed 8 years ago, it's minor. Takes 5mg Benazepril every day.); Migraine (Migraine Takes Sumatriptan); Muscle spasms (She takes 50mg of Tramadol each day and Soma 350mg. A year ago, started on neurotoxin Botox.); Osteoporosis
Andere Medikamente: BENAZEPRIL; SUMATRIPTAN; TRAMADOL; SOMA [CARISOPRODOL]; BOTOX
Allergien: -
Vorherige Impfungen: -

VAERS 2632959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 17.05.2023
Impfdatum: 06.05.2022
Beginn: 05.04.2023
Tage bis Beginn: 334,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

04/05/23 presents to ED for "shortness of breath". PMHx of "ESRD sp renal transplant (2018), HTN, T2DM"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 04/05/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2629210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: AK
Alter: 79,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 05.05.2022
Beginn: 27.03.2023
Tage bis Beginn: 326,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Mobility decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

On 03/27/2023, I began to notice a feeling of tiredness and not being able to do much. I knew that I had COVID-19, because my husband had already tested positive. I went to the doctor, where I tested for COVID-19. He prescribed Paxlovid right away. I might have developed a slight fever, but I'm not certain. I did have a cough, but I didn't blow my nose or anything until 10 days later, when I think I developed the flu.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 27MAR2023 -COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Viactive; Omeprazole; Vitamin D; Vitamin C; Vitamin B Complex; Probiotics; Enzymes; Levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 2629186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OR
Alter: 66,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 04.05.2022
Beginn: 26.07.2022
Tage bis Beginn: 83,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Brain fog COVID-19 Concussion Headache Migraine Mobility decreased Nasopharyngitis Panic attack Pyrexia SARS-CoV-2 test positive Sleep disorder Taste disorder Vertigo

Symptomtext

I started with a low grade fever and cold symptoms and then a throbbing headache in a previous concussion site and it just started pounding in that and I was prescribed Paxlovid and knocked all the could symptoms out within two days although the headache continued and progressively got worse and I have had migraines unable to get out of bed never before experienced and this continued for three months before seeing a neurologist then I had to wait three weeks before he injected me with Botox to relieve the pain prior t that I was prescribed Gabapentin it made the brain fog worse and I began to have severe panic attacks and with the first set of Botox injections it helped some and then another set three months, IT WS HORRIFIC AS i libe by myself I hasp withdrawal symptoms on top of the other stuff no appetize I could no longer sleep favorite foods tasted horrific every three months I get my Botox shots and they seem to headaches a other pains but then I've gotten vertigo since March and wafting to see a vestibular OT long wait to get anything to get it taken.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 07JUL2022 COVID-19 Test-Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; High Cholesterol; Pre Diabetec; Hypothyroid
Andere Medikamente: Levothyroxine; Liothyronine; Potassium Chloride; Metformin; Rosuvastatin; Losartan; Clonazepam; Zinc; D3; Fish oil
Allergien: Eggs; Almonds; Penicillin; Gabapentin
Vorherige Impfungen: -

VAERS 2623964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 21.09.2022
Beginn: 26.04.2023
Tage bis Beginn: 217,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Anticoagulant therapy Asthenia Atrial fibrillation Bladder mass Blood creatinine increased CHA2DS2-VASc-score COVID-19 Computerised tomogram head normal Condition aggravated Culture urine positive Escherichia test positive Fall Gout Heart rate increased Infection Renal ischaemia SARS-CoV-2 test positive Sepsis

Symptomtext

Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) This is a 86 yr old male with PMHx of CKD-3, gout, persistent Afib, HTN, HLD and BPH who presented for generalized weakness and falls. CT head was negative. UA showed evidence of infection and Ucx grew 2 strains of E coli so he was started on ceftriaxone. He had a CT urogram which showed 2 new bladder masses. Urology was consulted and said workup can be done outpt. He follows with Urology at other facility and he will decide if he wants to follow up with them or stay here for the workup. During his stay he developed a gout flare and was started on a steroid taper along with colchicine. His heart rate was elevated so Toprol dose was increased. PT/OT recommended SNF. Pt was stable on discharge. He will be discharged. Sepsis 2/2 UTI - elevated wbc and HR - sepsis resolved - Ucx growing E coli 2 strains - continue cefdinir 300mg BID for 3 more days New bladder masses Hx of bladder cancer - s/p TURBT - CT urogram showed 2 new bladder masses - follow up with Urology outpt for workup Elevated Cr on CKD-3 - baseline Cr 1.4 - likely due to poor perfusion in setting of infection - resolved Gout flare - evidence of polyarticular disease with tophi - continue prednisone 40mg for 3 days, then 30mg for 3 days then 20mg for 3 days - start colchicine 0.6mg every other day - start allopurinol 100mg daily on 5/6/23 - referral placed to Rheumatology Afib with RVR - CHADS-VASc- 3 - continue Eliquis 2.5mg BID - increased Toprol to 100mg daily, monitor HR and may need dose reduced HTN - continue HCTZ 12.5mg daily, lisinopril 10mg nighlty and Toprol HLD - continue atorvastatin 20mg daily BPH - s/p HoLEP Issues Requiring Follow Up: (Who, what, when, and how communicated?) Follow up with PCP and Urology. Referral placed to Rheumatology. Complete 3 more days of antibiotics. Complete steroid taper. Start colchicine and allopurinol. Toprol dose increased, monitor HR for dose adjustments.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: COVID positive PCR 4/13/2023
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2623945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 25.06.2021
Beginn: 29.04.2023
Tage bis Beginn: 673,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Atrial fibrillation COVID-19 Cardiac failure Cardiac failure congestive SARS-CoV-2 test positive Tachycardia

Symptomtext

Pt admitted on 4/23 with afib, tachycardia, and biventricular heart failure. On 4/29 he had a COVID test for SNF placement that was positive despite being asymptomatic.

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Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2620751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 21.04.2022
Beginn: 25.10.2022
Tage bis Beginn: 187,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Auditory disorder COVID-19 Diarrhoea Dyspnoea Headache Nausea Pyrexia SARS-CoV-2 test positive Thirst

Symptomtext

I contracted COVID-19 in October 2022. I had a headache, nausea, diarrhea, breathing problems, and a fever. I felt like I wanted to vomit. I always felt thirsty and was craving for something cold. I spoke to my doctor and I was prescribed Paxlovid. The symptoms lasted for about 4 days. I do currently have a hearing problem.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 25Oct2022 - COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Depression; COPD; Sleep Apnea; High Blood pressure; Kidney cancer; PTSD; Abnormal heart rhythm; Type 2 Diabetes
Andere Medikamente: Duloxetine; Multivitamin; Aspirin; Buspirone HCL; Metoprolol; Tartrate
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2615233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: VT
Alter: 76,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 11.04.2022
Beginn: 14.10.2022
Tage bis Beginn: 186,0
Dosis: 4
Route/Site: - / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dysphonia Dyspnoea Exposure to SARS-CoV-2 Foreign travel Malaise Renal impairment SARS-CoV-2 test positive Throat irritation

Symptomtext

I was traveling in another country and a number of the people on the tour contracted the COVID-19 virus they left early and an older woman contracted the virus later around the end of the tour. 14OCT2022 I was feeling ill and my throat was scratchy by the time I got home which was about ten at night or so, not that I was really ill but like a cold with no fever I never had a fever so I tested when I got home for COVID-19 and I was positive. I slept in the guest room so my elderly husband would not contract the virus. I knew I was positive but did not feel real awful. I called the on call line and I was prescribed PAXLOVID but my kidney functions were not normal so I was given half dose around Christmas time or around January. I started to feel short of breath and my voice would be very hoarse or throaty and people would notice it. Around the middle of March I had my annual physical and was put on a new inhaler and the voice thing is still going on.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Asthma
Andere Medikamente: Losartan; DIURIL; metformin; gabapentin; PROLIA; calcium; vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2613073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 07.04.2022
Beginn: 14.09.2022
Tage bis Beginn: 160,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Eyelid disorder Gait disturbance Magnetic resonance imaging Meniscus injury Meniscus operation Mobility decreased Tremor

Symptomtext

I had started to notice that I was having a shakiness in my finger and when I was walking there was an issue in my gait, and I was dragging my left leg. I also had an issue with my left arm where I was not able to hold it correctly. In January of 2023 I reached out to my health care provider, and we concluded these were tremors. She referred me to a neuroscientist, and he said that what I am experiencing is consistent with Parkinson's Disease. He did see that I was having a lack of blinking and that I am slow in my physical actions. He got me on a medication, got me an MRI on my head to see if there may be more signs with Parkinson's or if I have a stroke or something along those lines. We did find that I blew out my right meniscus which I had surgery today to repair as well.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: MRI; Blood Work- Unknown
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Flomax, Nasonex, Iron, Vitamin B12; Saw Palmetto
Allergien: N/A
Vorherige Impfungen: -

VAERS 2611486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OR
Alter: 67,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 28.04.2022
Beginn: 01.08.2022
Tage bis Beginn: 95,0
Dosis: 4
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Dysstasia Headache Influenza like illness Joint stiffness Mobility decreased Muscle tightness Myalgia Neck pain Pain Pain in extremity

Symptomtext

I notice a sore neck and my legs were tight in the calf area. I became unable to bend my knees. Sometimes my hips hurt and my muscles in my arms hurt. I have even noticed that my thumbs and toes hurt. This all began in or about August 2022. Now when I try to stand, it takes a moment to get started due to the pain. The pain causes headaches because of the tightness. The pain is like an ache as compared to flu-like body aches. I've done exercises to loosen but this does not help. I have seen a chiropractor, but we have not been able to find a solution. Two weeks ago, when I woke up, I felt very good and was able to kneel down. The next day my pain returned. I have an appointment at the end of April to see a general doctor.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2450080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 80,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 26.05.2022
Beginn: 31.05.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Pruritus Vaccination site haemorrhage Urticaria

Symptomtext

Through the previous 3 vaccines which I had breast cancer but the Doctor okayed with getting pfizer in that arm. The 4th dose I got intense itching and migrating all around my body with urticaria and have continued for the past year. I didn't know if it was vaccine related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sibo Arthritis
Vorgeschichte: Perpheril Neurology Chronic Headaches
Andere Medikamente: Yes. Tylenol headache medication (apap butalbital) Lorazapam
Allergien: Quinilones medication
Vorherige Impfungen: -

VAERS 2450080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 80,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 26.05.2022
Beginn: 31.05.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Pruritus Vaccination site haemorrhage Urticaria

Symptomtext

Through the previous 3 vaccines which I had breast cancer but the Doctor okayed with getting pfizer in that arm. The 4th dose I got intense itching and migrating all around my body with urticaria and have continued for the past year. I didn't know if it was vaccine related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sibo Arthritis
Vorgeschichte: Perpheril Neurology Chronic Headaches
Andere Medikamente: Yes. Tylenol headache medication (apap butalbital) Lorazapam
Allergien: Quinilones medication
Vorherige Impfungen: -

VAERS 2594760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: TN
Alter: 18,0
Geschlecht: F
Eingang: 10.03.2023
Impfdatum: 09.04.2022
Beginn: 10.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Arrhythmia COVID-19 Chest pain Computerised tomogram thorax Echocardiogram Electrocardiogram Electrocardiogram ambulatory Laboratory test Postural orthostatic tachycardia syndrome

Symptomtext

PATIENT HAD 2 COVID VACCINES IN 2021, CONTRACTED COVID-19 AND THEN TOOK A BOOSTER. 18 YEAR OLD WITH NO HEALTH CONDITIONS, NOW WITH CHRONIC ONGOING CHEST PAIN, ARRYTHMIAS, NEW DIAGNOSIS OF POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: EKG, ECHOCARDIOGRAM, HOLTOR MONITOR, CT CHEST, LABS DONE MANY TIMES. THERE ARE MULTIPLE RESULTS ON DIFFERENT DATES AND TIMES, MULTIPLE ER VISITS, CARDIOLOGY AND PRIMARY CARE OFFICE ALSO ORDERING TESTS.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Levora, Venlafaxine, Risperidone
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2588562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 92,0
Geschlecht: M
Eingang: 28.02.2023
Impfdatum: 22.04.2022
Beginn: 06.12.2022
Tage bis Beginn: 228,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Dyspnoea Fall SARS-CoV-2 test positive Wheelchair user

Symptomtext

Patient brought in by EMS to ED on 12/6/22 for weakness and shortness of breath. To note, patient fell transferring to wheelchair the morning of 12/6. COVID PCR test done in the ED was positive, and he notably tested positive for COVID the day before. Ultimately, patient admitted to the hospital 12/6/22 - 12/8/22 for COVID-19 and generalized weakness attributed to COVID-19 infection, among other problems. Patient has received the COVID primary vaccine series and two boosters.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2584756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CT
Alter: 50,0
Geschlecht: F
Eingang: 21.02.2023
Impfdatum: 19.02.2022
Beginn: 20.02.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angiogram Arthralgia Balance disorder Dizziness Erythema Feeling abnormal Migraine Muscle tightness Peripheral swelling

Symptomtext

I got it in my arm I started getting dizzy I have history of vertigo, so I thought that's what was going on. I sat down and the back of my neck started to feel tight, I had turned beat red and the staff asked if I wanted an ambulance and I felt weird not like myself at all. Then my husband made me walk to the car and took me home and my husband helped put ice all over my body (head, neck, and arms) then I started having a migraine and my joints hurt. I asked some of my nursing friends about TYLENOLs and was told not to and after some time I took some anyways. I also used BIOFREEZE and the pain went away after a few days. I also noticed some swelling in my legs that I still currently have. They got the size of grapefruit, and no doctor has been able to pinpoint why I lost my balance. I was given anti-vertigo and anti-nausea medication that I didn't take. I just elevated which did help some.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: MRA
Aktuelle Erkrankungen: N/A
Vorgeschichte: History of Aneurysm
Andere Medikamente: N/A
Allergien: Shellfish; penicillin; sulfa drugs
Vorherige Impfungen: Flu-2019 sore arms, rash, headaches, dizzy

VAERS 2577363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 92,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 05.05.2022
Beginn: 02.12.2022
Tage bis Beginn: 211,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 COVID-19 pneumonia Dementia Fatigue Gait inability Productive cough SARS-CoV-2 test positive

Symptomtext

Patient with history of dementia and brought to the ED on 12/2/22 by her family. Family reports for the past two days, patient has become increasingly weak to the point where she is no longer able to walk with her walker. Additionally reports new and worsening productive cough and fatigue. COVID PCR test performed in the ED resulted positive. Ultimately, patient admitted 12/2/22 - 12/4/22 for COVID-19 pneumonia, among other problems. She did not require supplemental O2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2577331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 83,0
Geschlecht: M
Eingang: 07.02.2023
Impfdatum: 23.11.2022
Beginn: 29.11.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Anaemia COVID-19 Chromaturia Confusional state Lethargy SARS-CoV-2 test positive Sepsis Tachycardia Urinary tract infection Urine analysis

Symptomtext

Patient history of asthma, COPD. Patient brought to the ED by EMS on 11/29 for lethargy and confusion. The day prior, patient's living facility staff collected a dark brown urine sample that was sent for evaluation. EMS reports patient had a temperature of 99.5 F, and noted patient was tachycardic and breathing rapidly. COVID PCR test completed in the ED also resulted positive. Patient admitted 11/29 - 12/9 for COVID-19 infection, sepsis, suspected UTI, anemia.

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Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2577207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 33,0
Geschlecht: M
Eingang: 07.02.2023
Impfdatum: 09.04.2022
Beginn: 09.01.2023
Tage bis Beginn: 275,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/09/23 presents to ED for "SOB". PMHx of "alcohol use disorder, ureteral stone, blind right eye"

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/09/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 95,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 16.05.2022
Beginn: 23.01.2023
Tage bis Beginn: 252,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Anxiety Asthenia Atrial fibrillation COVID-19 Condition aggravated Electrolyte depletion Electrolyte substitution therapy Fall Hyponatraemia Impaired self-care Lung infiltration Mental status changes Pleural effusion Pneumonia Pneumonia bacterial Procalcitonin normal Pulmonary imaging procedure abnormal Pulmonary mass

Symptomtext

Discharge Physician: MD Primary Care Physician: MD Date of Admission: 1/26/2023 Discharge Date: 1/31/2023 Room Number: 2023/2023-1 PRESENTING PROBLEM: Pleural effusion [J90] Generalized weakness [R53.1] Pulmonary nodules [R91.8] Community acquired bacterial pneumonia [J15.9] Atrial fibrillation with rapid ventricular response [I48.91] Fall, initial encounter [W19.XXXA] HOSPITAL COURSE: Patient is a 96-year-old man who presented to Hospital with altered mental status and weakness, including a fall in the bathroom. Patient was recently treated for bilateral pneumonia as an outpatient with two courses of antibiotics. He was also given Xanax for anxiety but unclear if he had taken any of this. In the emergency department images demonstrated new infiltrate, and his COVID test was noted to be positive. Due to the new infiltrative sites he was started on IV antibiotics. He was on room air. Images also demonstrated bilateral pleural effusions. He was admitted under the hospitalist service. Negative pro calcitonin and antibiotics stopped. He was not hypoxic and thus did not meet criteria for any specific treatment for COVID, but did clinically improve. He worked with Physical therapy and Occupational therapy and felt to benefit from subacute rehab. Discussions with his daughter and Case Management, she is unable to continue caring for him at this time and will require long-term placement. Case management and his daughter were able to secure long term care at facility. A hospital bed was requested and ordered. He clinically improved overall throughout his admission but continued to have some mild hyponatremia and a small pleural effusion on imaging the day of discharge. He had no hypoxia, fevers, increased WOB or other indication for thoracentesis. Recommended avoiding any further xanax at this time. Electrolytes were monitored and repleted PRN throughout the admission. Patient hemodynamically stable for discharge. Discussed plan of care discharge with patient and daughter including outpatient follow-up PCP within 7 days, as well as follow up labs and chest XR to assess hyponatremia and pleural effusion. Patient voiced understanding was agreeable with plan of care discharge.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Dysphagia Diabetes mellitus Hypertension Acquired varus deformity of knee, right Mixed hyperlipidemia Peripheral artery disease Diabetic nephropathy associated with type 2 diabetes mellitus Pleural effusion A-fib Generalized weakness and fall COVID-19 Pulmonary nodule Hyponatremia CHF (congestive heart failure) Moderate late onset Alzheimer's dementia Acute pain of left knee Falls Bilateral leg edema Leg skin lesion, right
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet ASPIRIN ADULT LOW STRENGTH 81 MG enteric coated tablet Calcium-Vitamin D (CALTRATE 600 PLUS-VIT D PO) docusate (STOOL SOFTENER) 100 MG capsule guaiFENesin (MUCINE
Allergien: Advair Diskus Celebrex [Celecoxib]GI Upset Motrin [Nsaids] Septra [Sulfamethoxazole W-trimethoprim] Vicodin [Hydrocodone-acetaminophen] Vioxx [Rofecoxib] Warfarin
Vorherige Impfungen: -

VAERS 2561352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 02.02.2021
Beginn: 18.12.2022
Tage bis Beginn: 684,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Dyspnoea Fatigue SARS-CoV-2 test positive

Symptomtext

12/18/22 presents to EC ED for "weakness, fatigue, shortness of breath". PMHx of "CAD CHF A. fib, recently diagnosed DVT, PE on Eliquis, abdominal aortic aneurysm, hypertension hyperlipidemia, COPD, NPH GERD"

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/18/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2561144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: PR
Alter: 52,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 13.04.2022
Beginn: 13.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Abdominal hernia Breast pain Dyspnoea Pain Periorbital swelling Sensitive skin Tachycardia Vulvovaginal discomfort

Symptomtext

Body ache, pain on breasts, puffy eyes, sensitive skin, vaginal irritation, tachycardia, shortness of breath. Patient also reported a resurgence in a stomach hernia.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes mellitus type 2, HBP. hypothyroidism
Andere Medikamente: -
Allergien: Aspirin
Vorherige Impfungen: -

VAERS 2559590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: AR
Alter: 60,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 15.12.2022
Beginn: 12.01.2023
Tage bis Beginn: 28,0
Dosis: 4
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest pain

Symptomtext

Patient was seen in the office of Dr. with c/o chest pain for 1 week. Placed on observation status for evaluation and treatment. Patient was diagnosed with Covid. Patient was evaluated by cardiology and released from there care. Patient chest pain was treated with pain medication and patient was discharged home 1/13/23.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: angina, GERD, Diabetes mellitus, hypertension, rheumatoid arthritis
Andere Medikamente: Potassium Chloride ER 20 mEq po BID Lantus 100units/ML- 70 units sq Novolog 100 units/ml-26 units sq Folic acid 1 mg po BID Metoprolol Succinate ER 200 mg po hs Pravastatin 80 mg po daily Methotrexate 15 mg po weekly Esomeprazole magnesium
Allergien: sulfa, ampicillin, iodine, codeine, hydrocodone, leflunomide, abatacept (with maltose)
Vorherige Impfungen: -

VAERS 2539325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NC
Alter: 62,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 21.06.2022
Beginn: 19.11.2022
Tage bis Beginn: 151,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Dyspnoea Headache Influenza virus test positive Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had runny nose that would not stop, I had trouble breathing, a cough deep in my chest, headache. I called made an appointment to see my doctor who did both a COVID-19 and influenza test, both came back positive. I was prescribed TAMIFLU, additional breathing treatments. I do feel better no but it took until 12/10/22 for me to finally feel like myself.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid-19 test positive; Influenza positive
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma; Depression
Andere Medikamente: ZOLOFT; SINGULAIR; vitamin D; ALLEGRA; CENTUM SILVER; ibuprofen; atenolol; albuterol; FLONASE
Allergien: Penicillin; tetracycline; BACTRIM; beef; dairy
Vorherige Impfungen: -

VAERS 2538988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 23.05.2022
Beginn: 13.12.2022
Tage bis Beginn: 204,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 COVID-19 pneumonia Chronic obstructive pulmonary disease Condition aggravated Diabetic neuropathy Hyperlipidaemia Hypertension Intramedullary rod insertion Osteoporosis Pulmonary fibrosis SARS-CoV-2 test positive Type 2 diabetes mellitus Urinary tract infection

Symptomtext

Discharge Provider: MD Primary Care Provider : DO Admission Date: 12/13/2022 Discharge Date: 12/17/2022 COVID positive Date 12/13/2022 CONDITION ON DISCHARGE: Stable and improved. Home Health Care Svc HOSPITAL COURSE: Admitted for COVID pneumonia, complicated by Pulmonary fibrosis and COPD. Had full course of remdesivir. History of long intubation and prolonged recovery from covid at the start of the pandemic. Also: recent intramedullary nail left femur (October), HTN, DM2 with neuropathy, HLD, Osteoporosis, Recurrent UTIs

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Pulmonary fibrosis Benign essential hypertension Chronic UTI (urinary tract infection) Tenosynovitis of hand COVID-19 virus infection Infected hardware in left leg, sequela Chronic ITP (idiopathic thrombocytopenia) Peripheral neuropathy Vaginal atrophy Diabetes mellitus Rosacea Osteoporosis Ganglion cyst Vertigo Intensive care (ICU) myopathy Closed displaced comminuted fracture of shaft of left femur with nonunion Closed fracture of distal end of femur with nonunion, unspecified fracture morphology, unspecified laterality, subsequent encounter Closed fracture of femur with nonunion, unspecified fracture morphology, unspecified laterality, unspecified portion of femur, s ubsequent encounter
Andere Medikamente: acetaminophen (TYLENOL) 500 MG capsule alendronate (FOSAMAX) 70 MG tablet ascorbic acid (VITAMIN C) 1000 MG tablet atorvastatin (LIPITOR) 10 MG tablet Blood Glucose Monitoring Suppl MISC budesonide (PULMICORT) 0.5 MG/2ML nebulizer solution
Allergien: Bydureon [Exenatide]Diarrhea Adhesive Birch Trees Cats Cocklebur Codeine Corn Pollen Doxycycline English Plantain Feathers Fusarium Fusarium Indomethacin Kochia Licorice Flavor [Flavoring Agent] Meadow Fescue Pollen Extract [Gramineae Pollens] Methadone Mushrooms Penicillins Propoxyphene Sheep-derived Products Teucrium White Ash Wormwood [Artemisia Absinthium] Hydrocodone-acetaminophen
Vorherige Impfungen: -

VAERS 2525196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 20.01.2021
Beginn: 24.10.2022
Tage bis Beginn: 642,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cough Dyspnoea Hypoxia Pneumonia aspiration Pyrexia SARS-CoV-2 test positive Sepsis

Symptomtext

Narrative: Patient received four doses COVID 19 vaccine in Jan/Feb/Apr/Oct 2021. The patient tested positive for COVID 19 on 24 Oct 2022. The patient presented to the ED with shortness of breath, cough, and fever. The patient was admitted with aspiration pneumonia, sepsis, and hypoxia. The patient was treated with antibiotics, oxygen, and steroids. The patient was discharged in stable condition on 4 Nov 2022. Reported per EUA.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NE
Alter: 73,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 25.05.2022
Beginn: 16.06.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia COVID-19 Chest X-ray normal Chest pain Computerised tomogram Cough Diarrhoea Oropharyngeal pain Productive cough Pruritus Rhinorrhoea

Symptomtext

After my vaccination my ankles were itchy and sore for 4-6 days after all 5 of my COVID-19 vaccinations. But when I had COVID-19 I had a running nose, slight sore throat, cough, and last two days I had diarrhea. I still have the cough and sometimes its dry and phlegmy. I tested positive for COVID-19 with a test that my daughter had. The middle of my chest had pain, so I went to the doctor to do an x-ray on my lungs, and it was clear. I also did a CAT scan today and I am also going to do a stress test.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: X-ray of lungs, Clear, 11/03/2022; CAT Scan, 11/28/2022, No results yet
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Diabetes
Andere Medikamente: Metformin; rosuvastatin; aspirin; levothyroxine; amlodipine; glimepiride; carvedilol; PREVAGEN; PRESERVISION; calcium; D3; zinc; vitamin C; magnesium; ZYRTEC
Allergien: Some blood pressure medications
Vorherige Impfungen: -

VAERS 2506503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 49,0
Geschlecht: F
Eingang: 12.11.2022
Impfdatum: 26.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angiotensin converting enzyme Anion gap Biopsy Blood calcium Blood chloride Blood creatinine Blood glucose Blood potassium Blood pressure measurement Blood sodium Blood urea Body fluid analysis Body height Body mass index Carbon dioxide Chest X-ray Computerised tomogram thorax Diagnostic aspiration

Symptomtext

Diffuse mediastinal and hilar adenopathy is again noted; Blood Pressure: 134/84; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old female patient received BNT162b2 (BNT162B2), on 26May2022 as dose 4 (booster), single (Lot number FK9894) at the age of 49 years intramuscular, in right arm for covid-19 immunisation. The patient's relevant medical history included "Anxiety" (ongoing), notes Onset date For years, Stop date Ongoing, "Depression" (ongoing), notes Onset date For years, Stop date Ongoing, "Positive ANA", start date 2019 (ongoing), notes Onset date 2019 , Stop date Ongoing, "Hypertension" (ongoing), notes Onset date For years , Stop date Ongoing, "Moderate pain" (unspecified if ongoing), "Migraine" (unspecified if ongoing), "wheezing" (unspecified if ongoing), "Shortness of breath" (unspecified if ongoing), "Cough" (unspecified if ongoing). Concomitant medication(s) included RIZATRIPTAN oral taken for migraine, ASPIRIN 81 oral, CYANOCOBALAMIN oral, IBUPROFEN oral taken for pain, BREO ELLIPTA, CALCIUM CARBONATE AND VITAMIN D3 oral, AMITRIPTYLINE oral, METOPROLOL SUCCINATE oral, SERTRALINE oral, ALPRAZOLAM taken for anxiety, ALBUTEROL SULFATE HFA taken for wheezing, dyspnoea, cough. Vaccination history included BNT162b2 (Dose 1st, Date/time, Date 22Dec2020, Site and route of injection , Anatomical site of injection Left Arm, Route of administration Intramuscular, Batch/lot number EJ1685), administration date 22Dec2020, when the patient was 47-year-old, for COVID-19 Immunization, reaction(s) "feel under the weather", BNT162b2 (Dose 2nd, Date/time, Date 12Jan2021, Site and route of injection, Anatomical site of injection Left arm, Route of administration Intramuscular, Batch/lot number EJ1686), administration date 12Jan2021, when the patient was 47-year-old, for COVID-19 Immunization, reaction(s) "feel under the weather", BNT162b2 (Dose 3rd , Date/time, Date 07Oct2021, Site and route of injection, Anatomical site of injection Arm Right, Route of administration Intramuscular, Batch/lot number EW0179), administration date 07Oct2022, when the patient was 48-year-old, for COVID-19 Immunization, reaction(s) "enlarged lymphnodes", "FEVl/FVC_POST 91.03%, Standard Range 70.81 - 90.40 %", "Cough", "long term breathing issues", "chronic cough", "I had to really fight to breath", "acid reflux", "allergies", "Somedays I can walk the stairs at work other days I can't", "mildly reduced vital capacity". The following information was reported HILAR LYMPHADENOPATHY (medically significant), outcome "unknown", described as "Diffuse mediastinal and hilar adenopathy is again noted", HYPERTENSION (medically significant), outcome "unknown", described as "Blood Pressure 134/84". The patient underwent the following laboratory tests and procedures Angiotensin converting enzyme (16-85) (unspecified date) 29 U/L, notes Component Angio Convert Enzyme Your value 29 U/LStandard range 16-85 U/L, Anion gap (9-18) unspecified date) 11mmol/L, notes Component Anion Gap Your value 11mmol/L Standard range 9-18 mmol/L, Biopsy (unspecified date) Non-cancerous but still no answer, Blood calcium (8.6-10.3) (unspecified date) 9.6 mg/dL, notes Component Calcium Your value 9.6 mg/dL Standard range 8.6- 10.3 mg/dL, Blood chloride (98-108) (unspecified date) 99mmol/L, notes Component Chloride Your value 99mmol/L Standard range 98-108mmol/L, Blood creatinine (0.60-1.10) (unspecified date) 0.92mg/dL, notes Component Creatinine Your value 0.92mg/dL Standard range 0.60-1.10 mg/dL, (unspecified date) 9 mg/dl, notes Component BUN/ Creatinine ratioYour value 9 Standard range 6-20, Blood glucose (70-99) (unspecified date) 87mg/dL, notes Component glucose (not fasting) Your value 87mg/dL Standard range 70-99 mg/dL, Blood potassium (3.5-5.3) (unspecified date) 4.1 mmol/L, notes Component Potassium Your value 4.1 mmol/L Standard range 3.5-5.3 mmol/L, Blood pressure measurement (27Sep2022) 126/74, notes Blood pressure 126/74, (03Oct2022) 134/84, notes Blood pressure 134/84, Blood sodium (135-145) (unspecified date) 139mmol/ L, notes Component Sodium Your value 139mmol/ L Standard range 135-145mmol/L, Blood urea (6-20) (unspecified date) 8mg/dL, notes Component BUN Your value 8mg/dL Standard range 6-20 mg/dL, (unspecified date) 9 mg/dl, notes Component BUN/ Creatinine ratio Your value 9 Standard range 6-20, Body fluid analysis (unspecified date) Bronchus, right lower lobe, notes Component Source, Body fluid Your value Bronchus, right lower lobe, Body height (27Sep2022) 159.99 cm, (03Oct2022) 159.99 cm, Body mass index (27Sep2022) 39.16, notes BMI 39.16, (03Oct2022) 39.05, notes BMI 39.05, Carbon dioxide (23-32) (unspecified date) 29mmol/L, notes Component CO2 Your value 29mmol/L Standard range 23-32 mmol/L, Chest X-ray (26Oct2021) Unknown results, notes Unremarkable, Computerised tomogram thorax (unspecified date) my lymph nodes in my chest had grown significantly, (unspecified date) I did not pass, (26Oct2021) Unknown results, (23Dec2021) Unknown results, notes EXAMINATION CT Chest with IV contrast EXAM DATE 23Dec2021 821 AM, Diagnostic aspiration (unspecified date) inconclusive, EGFR status assay (normal high range 60) (unspecified date) 76mL/min, notes Component eGFR Your value 76mL/min Standard range >60 mL/min, Eosinophil percentage (unspecified date) 4% %, notes Component Eosinophil %, Fluid Your value 4% Standard range %, FEV1/FVC ratio (70.81-90.40) (30Mar2022) 91.03 %, notes Flag H, (30Mar2022) 87.85 %, notes Component FEV1/FVC PRE Your value 87.85% Standard Range 70.81-90.40%, Forced expiratory volume (2.12-3.32) (30Mar2022) 2.24 L, notes Flag H, Forced expiratory volume (2.19-3.32) (30Mar2022) 2.27 L, Forced vital capacity (2.78-4.13) (30Mar2022) 2.47 L, notes Flag L, (30Mar2022) 2.59 L, notes Component FVC PRE Your value 2.59L Standard Range 2.78-4.13L Flag L, Gram stain (unspecified date) Many WBC's, notes Component Gram stain result Your Value Many WBC's, (unspecified date) No organism seen, notes Gram stain resultYour Value No organism seen, Imaging procedure (unspecified date) Unknown results, notes I have had multiple imaging and testing done, Body Fluid cell Count (unspecified date) 240199756, notes There is no component information for this result, (unspecified date) 1241820823, (unspecified date) Negative, notes Histoplasma Immunodiff Your value Negative Standard Range Negative, (unspecified date) Negative, notes Component Results Component Histoplasma Mycelial Your value Negative Standard Range Negative, (unspecified date) Negative, notes Component Histoplasma Yeast Your value Negative Standard Range Negative, RV PRE (0.92-2.47) (30Mar2022) 1.41 L, (unspecified date) Unknown results, notes I have had multiple imaging and testing done, Lymphocyte percentage (unspecified date) 9% %, notes Component Lymphocyte %, Fluid Your value 9% Standard range %, Mononuclear cell percentage (unspecified date) 71% %, notes Component Mononuclear %, Fluid Your value 71% Standard range %, Nucleated red cells (unspecified date) 254/uL, notes Component Nucleated cells, fluid Your value 254/uL Standard range /uL, Oxygen saturation (27Sep2022) 98%, notes Oxygen Saturation 98%, (03Oct2022) 98%, notes Oxygen Saturation 98%, Peak expiratory flow rate (4.99-8.30) (30Mar2022) 4.21 L/S, notes Flag L, (30Mar2022) 5.55 L/S, notes Your value 5.55 L/S Standard Range 4.99-8.30 L/S, Pulmonary function test (unspecified date) I did not pass, Red blood cell count (normal high range 1000) (unspecified date) <1000/ uL, notes Component RBC, Fluid Your value <1000/ uL Standard range /uL, SARS-CoV-2 test (unspecified date) Negative, notes Neg covid testing, (unspecified date) Negative, notes I tested multiple times for COVID all were negative, (unspecified date) Negative, Total lung capacity (3.83-5.98) (30Mar2022) 3.86 L, Weight (unspecified date) 220 lb, (unspecified date) 3552.1 oz, notes Weight 222 lb 0.1 oz, (27Sep2022) 221 lb, (03Oct2022) 3526.4 OZ, notes Weight 220 lb, 6.4 oz, White blood cell count (unspecified date) 16% %, notes Component Polymorphonuclear % fluid Your value 16% Standard range %.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: Angio Convert Enzyme; Result Unstructured Data: Test Result:29 U/L uL; Comments: Component Angio Convert Enzyme Your value: 29 U/L Standard range: 16-85 U/L; Test Name: Anion Gap; Result Unstructured Data: Test Result:11mmol/L mmol/L; Comments: Component: Anion Gap Your value: 11mmol/L Standard range: 9-18 mmol/L; Test Name: Biopsy; Result Unstructured Data: Test Result:Non-cancerous but still no answer; Test Name: Calcium; Result Unstructured Data: Test Result:9.6 mg/dL mg/dl; Comments: Component: Calcium Your value: 9.6 mg/dL Standard range: 8.6- 10.3 mg/dL; Test Name: Chloride; Result Unstructured Data: Test Result:99mmol/L mmol/L; Comments: Component: Chloride Your value: 99mmol/L Standard range: 98-108mmol/L; Test Name: Creatinine; Result Unstructured Data: Test Result:0.92mg/dL mg/dl; Comments: Component: Creatinine Your value: 0.92mg/dL Standard range: 0.60-1.10 mg/dL; Test Name: Creatinine; Test Result: 9 mg/dl; Comments: Component: BUN/ Creatinine ratio Your value: 9 Standard range: 6-20; Test Name: glucose; Result Unstructured Data: Test Result:87mg/dL mg/dl; Comments: Component: glucose (not fasting) Your value: 87mg/dL Standard range: 70-99 mg/dL; Test Name: Potassium; Result Unstructured Data: Test Result:4.1 mmol/L mmol/L; Comments: Component: Potassium Your value: 4.1 mmol/L Standard range: 3.5-5.3 mmol/L; Test Date: 20220927; Test Name: Blood pressure; Result Unstructured Data: Test Result:126/74; Comments: Blood pressure: 126/74; Test Date: 20221003; Test Name: Blood pressure; Result Unstructured Data: Test Result:134/84; Comments: Blood pressure: 134/84; Test Name: Sodium; Result Unstructured Data: Test Result:139mmol/ L mmol/L; Comments: Component: Sodium Your value: 139mmol/ L Standard range: 135-145mmol/L; Test Name: BUN; Result Unstructured Data: Test Result:8mg/dL mg/dl; Comments: Component: BUN Your value: 8mg/dL Standard range: 6-20 mg/dL; Test Name: BUN; Test Result: 9 mg/dl; Comments: Component: BUN/ Creatinine ratio Your value: 9 Standard range: 6-20; Test Name: Body fluid; Result Unstructured Data: Test Result:Bronchus, right lower lobe; Comments: Component: Source, Body fluid Your value: Bronchus, right lower lobe; Test Date: 20220927; Test Name: Height; Result Unstructured Data: Test Result:159.99 cm; Test Date: 20221003; Test Name: Height; Result Unstructured Data: Test Result:159.99 cm; Test Date: 20220927; Test Name: BMI; Result Unstructured Data: Test Result:39.16; Comments: BMI: 39.16; Test Date: 20221003; Test Name: BMI; Result Unstructured Data: Test Result:39.05; Comments: BMI: 39.05; Test Name: CO2; Result Unstructured Data: Test Result:29mmol/L mmol/L; Comments: Component: CO2 Your value: 29mmol/L Standard range: 23-32 mmol/L; Test Date: 20211026; Test Name: Chest Xray; Result Unstructured Data: Test Result:Unknown results; Comments: Unremarkable; Test Name: Chest CT; Result Unstructured Data: Test Result:my lymph nodes in my chest had grown significantly; Test Name: Chest CT; Result Unstructured Data: Test Result:I did not pass; Test Date: 20211026; Test Name: Chest CT; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211223; Test Name: Chest CT; Result Unstructured Data: Test Result:Unknown results; Comments: EXAMINATION: CT Chest with IV contrast EXAM DATE: 23Dec2021 8:21 AM; Test Name: fine needle aspiration; Test Result: Inconclusive ; Test Name: eGFR; Result Unstructured Data: Test Result:76mL/min ml/min; Comments: Component: eGFR Your value: 76mL/min Standard range: >60 mL/min; Test Name: Eosinophil; Result Unstructured Data: Test Result:4% %; Comments: Component: Eosinophil %, Fluid Your value: 4% Standard range: %; Test Date: 20220330; Test Name: FEV1/FVC Post; Test Result: 91.03 %; Comments: Flag: H; Test Date: 20220330; Test Name: FEV1/FVC Post; Test Result: 87.85 %; Comments: Component: FEV1/FVC PRE Your value: 87.85% Standard Range: 70.81-90.40%; Test Date: 20220330; Test Name: FEV 1 Post; Test Result: 2.24 l; Comments: Flag: H; Test Date: 20220330; Test Name: FEV 1 PRE; Test Result: 2.27 l; Test Date: 20220330; Test Name: FVC Post; Test Result: 2.47 l; Comments: Flag: L; Test Date: 20220330; Test Name: FVC Post; Test Result: 2.59 l; Comments: Component: FVC PRE Your value: 2.59L Standard Range: 2.78-4.13L Flag: L; Test Name: Gram stain; Result Unstructured Data: Test Result:Many WBC's; Comments: Component: Gram stain result: Your Value: Many WBC's; Test Name: Gram stain; Result Unstructured Data: Test Result:No organism seen; Comments: Gram stain result:Your Value: No organism seen; Test Name: Multiple imaging; Result Unstructured Data: Test Result:Unknown results; Comments: I have had multiple imaging and testing done; Test Name: Body Fluid cell Count; Result Unstructured Data: Test Result:240199756; Comments: There is no component information for this result; Test Name: Body Fluid cell Count; Result Unstructured Data: Test Result:1241820823; Test Name: Histoplasma Immunodiff; Test Result: Negative ; Comments: Histoplasma Immunodiff Your value: Negative Standard Range: Negative; Test Name: Histoplasma Mycelial; Test Result: Negative ; Comments: Component Results: Component: Histoplasma Mycelial Your value: Negative Standard Range: Negative; Test Name: Histoplasma Yeast; Test Result: Negative ; Comments: Component: Histoplasma Yeast Your value: Negative Standard Range: Negative; Test Date: 20220330; Test Name: RV PRE; Test Result: 1.41 l; Test Name: Testing; Result Unstructured Data: Test Result:Unknown results; Comments: I have had multiple imaging and testing done; Test Name: Lymphocyte; Result Unstructured Data: Test Result:9% %; Comments: Component: Lymphocyte %, Fluid Your value: 9% Standard range: %; Test Name: Mononuclear; Result Unstructured Data: Test Result:71% %; Comments: Component: Mononuclear %, Fluid Your value: 71% Standard range: %; Test Name: Nucleated cells; Result Unstructured Data: Test Result:254/uL uL; Comments: Component: Nucleated cells, fluid Your value: 254/uL Standard range: /uL; Test Date: 20220927; Test Name: Oxygen Saturation; Result Unstructured Data: Test Result:98%; Comments: Oxygen Saturation: 98%; Test Date: 20221003; Test Name: Oxygen Saturation; Result Unstructured Data: Test Result:98%; Comments: Oxygen Saturation: 98%; Test Date: 20220330; Test Name: PEF Post; Result Unstructured Data: Test Result:4.21 L/S L; Comments: Flag: L; Test Date: 20220330; Test Name: PEF Post; Result Unstructured Data: Test Result:5.55 L/S L; Comments: Your value: 5.55 L/S Standard Range: 4.99-8.30 L/S; Test Name: pulmonary function test; Result Unstructured Data: Test Result:I did not pass; Test Name: RBC; Result Unstructured Data: Test Result:<1000/ uL uL; Comments: Component: RBC, Fluid Your value: <1000/ uL Standard range: /uL; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Neg covid testing; Test Name: COVID-19 Test; Test Result: Negative ; Comments: I tested multiple times for COVID all were negative; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20220330; Test Name: TLC PRE; Test Result: 3.86 l; Test Name: Weight; Result Unstructured Data: Test Result:220 lb; Test Name: Weight; Result Unstructured Data: Test Result:3552.1 oz; Comments: Weight 222 lb 0.1 oz; Test Date: 20220927; Test Name: Weight; Result Unstructured Data: Test Result:221 lb; Test Date: 20221003; Test Name: Weight; Result Unstructured Data: Test Result:3526.4 OZ; Comments: Weight: 220 lb, 6.4 oz; Test Name: Polymorphonuclear; Result Unstructured Data: Test Result:16% %; Comments: Component: Polymorphonuclear % fluid Your value: 16% Standard range: %
Aktuelle Erkrankungen: Antinuclear antibody positive (Onset date: 2019 Stop date: Ongoing); Anxiety (Onset date: For years Stop date: Ongoing); Depression (Onset date: For years Stop date: Ongoing); Hypertension (Onset date: For years Stop date: Ongoing)
Vorgeschichte: Medical History/Concurrent Conditions: Cough; Migraine; Pain; Shortness of breath; Wheezing
Andere Medikamente: RIZATRIPTAN; ASPIRIN 81; CYANOCOBALAMIN; IBUPROFEN; BREO ELLIPTA; CALCIUM CARBONATE AND VITAMIN D3; AMITRIPTYLINE; METOPROLOL SUCCINATE; SERTRALINE; ALPRAZOLAM; ALBUTEROL SULFATE HFA
Allergien: -
Vorherige Impfungen: -

VAERS 2504571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OH
Alter: 87,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 04.04.2022
Beginn: 01.11.2022
Tage bis Beginn: 211,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Tested COVID-19 positive, resulted in hospital admission. Symptoms include chills, cough, and shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Nasal swab collected 11/02/2022 detected 2019 Novel Coronavirus RNA on 11/02/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes mellitus, cardiovascular disease, and hypertension.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2502776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CT
Alter: 56,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 11.04.2022
Beginn: 01.09.2022
Tage bis Beginn: 143,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood thyroid stimulating hormone Fatigue Feeling abnormal Hyperthyroidism Movement disorder Palpitations

Symptomtext

seems after receiving 3 Pfizer Covid Vaccines I have now been diagnosed as Hyperthroid- or Subclinical Hyperthyroid; she couldn't hardly lift her arm and felt like she came down with something for a week.; tired and feels more tired than normal; felt like she was coming down with something/felt weird; heart pound; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old female patient received BNT162b2 (BNT162B2), on 11Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 56 years for covid-19 immunisation. The patient's relevant medical history included: "hypothyroid" (unspecified if ongoing); "Hashimoto's disease" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE taken for hyperthyroidism. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Expiry date: Jul2021), administration date: 06May2021, when the patient was 55-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: FW0172), administration date: 27May2021, when the patient was 55-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: FG3527), administration date: 29Nov2021, when the patient was 55-year-old, for COVID-19 Immunization, reaction(s): "seems after receiving 3 Pfizer Covid Vaccines I have now been diagnosed as Hyperthroid- or Subclinical Hyperthyroid"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: FG3527), administration date: 29Nov2021, when the patient was 55-year-old, for COVID-19 immunisation, reaction(s): "My TSH is low", "TSI high". The following information was reported: FEELING ABNORMAL (non-serious) with onset 2022, outcome "unknown", described as "felt like she was coming down with something/felt weird"; PALPITATIONS (non-serious) with onset 2022, outcome "unknown", described as "heart pound "; MOVEMENT DISORDER (non-serious) with onset 2022, outcome "unknown", described as "she couldn't hardly lift her arm and felt like she came down with something for a week."; FATIGUE (non-serious) with onset 2022, outcome "unknown", described as "tired and feels more tired than normal"; HYPERTHYROIDISM (medically significant) with onset Sep2022, outcome "not recovered", described as "seems after receiving 3 Pfizer Covid Vaccines I have now been diagnosed as Hyperthroid- or Subclinical Hyperthyroid". Patient didn't feel much of anything for the previous 3 doses but her most recent dose she couldn't hardly lift her arm and felt like she came down with something for a week. She was on levothyroxine, a low dose, and stopped taking it between the first blood test Jun2022 with a low TSH and her most current bloodwork Sept2022. Had stopped her levothyroxine when her HCP had changed her to a different brand. The different brand made her heart pound and she felt weird. Decided not to take Levothyroxine anymore then TSH went down again Sep2022 after she stopped taking Levothyroxine. Diagnosed as hyperthyroid or subclinical hyperthyroid. Her HCP didn't say anything about it the first time her TSH went down. Determined she was hyperthyroid from her last blood test Sep2022 when her TSI was tested and it looked like she was hyperthyroid. Confirmed start date as Sep2022. Outcome: Didn't feel any symptoms at all, subclinical hyperthyroid doesn't have any obvious symptoms. Didn't feel anything until her latest Pfizer COVID-19 shot. Didn't feel right, her arm was hurting really bad. All the other vaccines she didn't feel anything. Latest Pfizer COVID-19 shot she had trouble lifting her arm and felt like she was coming down with something for an entire week. Had a hard time shaking it off like she was fighting off something that never came. Her first blood test showed her TSH had gone down in Jun2022 and then her TSH went lower on her Sep2022 blood test. She'd stopped taking her levothyroxine between those two blood tests. Levothyroxine is supposed to lower her TSH but she didn't take it in between June2022 and now. Stopped Levothyroxine: Her HCP had changed her to a different brand and it made her heart pound and feel weird. Felt fine on the one she had been taking all along. When her HCP discovered her TSH went down her HCP wanted to lower the lose. Was taking 25mcg and her HCP ordered another levothyroxine and only wanted her to take half the dose, only 12.5mcg. She picked up her prescription, took one pill, and her heart was racing. HCP wanted to lower her dose when the blood test results in Jun2022 said her TSH had gone down. The patient underwent the following laboratory tests and procedures: Blood thyroid stimulating hormone: (Jun2022) low; (Sep2022) low.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 202206; Test Name: TSH; Result Unstructured Data: Test Result:low; Test Date: 202209; Test Name: TSH; Result Unstructured Data: Test Result:low
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's disease; Hypothyroidism
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2501873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NY
Alter: 83,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 28.04.2022
Beginn: 20.07.2022
Tage bis Beginn: 83,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Pneumonia Respiratory failure SARS-CoV-2 test positive White blood cell count increased

Symptomtext

7/20/2022-Presnts to ED, Admit chronic hypoxic resp failure s/t to severe COPD with recent exacerbation and unresolved pna. Covid + test. Ordered Levaquin, decadron and bebtelovimab. On 3L NC, on baseline oxygen . WBC-27.3 Recent IP stay 7/10-7/14/2022 for PNA had been on ceftriaxone and azithromycin. Chest CT potential R lower lobe infiltrate. 7/22/2022. Improved, continue prednisone taper ad Levaquin. WBC-22.6. D/C home with home health services.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 DM, HTN, COPD, HLD, peptic ulcer disease with hemorrhage, GE junction carcinoma and sepsis
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2497661

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: IN
Alter: 66,0
Geschlecht: M
Eingang: 03.11.2022
Impfdatum: 10.06.2022
Beginn: 19.09.2022
Tage bis Beginn: 101,0
Dosis: 3
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal hernia Activated partial thromboplastin time prolonged Alanine aminotransferase normal Anion gap Aspartate aminotransferase normal Basophil count normal Basophil percentage Blood albumin normal Blood alkaline phosphatase increased Blood bilirubin normal Blood calcium normal Blood chloride decreased Blood creatinine normal Blood glucose normal Blood lactic acid Blood magnesium normal Blood potassium normal Blood sodium decreased

Symptomtext

Document Type: ED Physician Progress Note Document Subject: ED Progress Note Performed By: on September 19, 2022 17:31 EDT Verified By: DO on September 21, 2022 09:22 EDT Encounter Info: Hospital, Emergency, 09/19/22 - 09/19/22 * Final Report * Basic Information Time Seen: DO / 09/19/2022 16:39 Chief Complaint Dizziness (Complaint of), SOB (Complaint of) History of Present Illness A 67 year old male presents from public housing to the ED via private vehicle complaining of worsening dyspnea onset one week. Patient said last night his shortness of breath continued to worsen with associated fever, chills, diaphoresis, headache, and "ringing" in bilateral ears. He endorses nausea and mild dehydration. Denies diarrhea or any known sick contacts. Pt reports using an inhaler and Mucinex for symptom relief. Denies PMHx of CHF or A-fib but reports having pneumonia once. Pt smokes. Denies other drug use. Review of Systems Constitutional: +fever +chills, +dehydration, +diaphoresis Respiratory: +dyspnea Gastrointestinal: no diarrhea, , +nausea Neurologic: +headache Additional ROS info: Except as noted in the above Review of Systems and in the History of Present Illness, all other systems have been reviewed and are negative or noncontributory. Physical Exam/Objective Vitals & Measurements last 24 hours VITAL SIGNS Temp C: 36.4 DegC Heart Rate: 88 bpm Resp Rate: 18 br/min BP #1: 95 / 50 mmHg SpO2 (%): 94 % O2 Device: Room air Weight KG: 100.5 kg General: alert, no acute distress Skin: warm, dry Head: normocephalic, atraumatic Eye: PERRL, EOMI ENT: TMs normal, Tongue midline, uvula midline, oral mucosa mildly dry Neck: supple , no tenderness, trachea midline Cardiovascular: regular rate and rhythm, no murmur, normal peripheral perfusion Respiratory: lungs CTA, respirations non-labored, breath sounds equal Chest Wall: no tenderness, no deformity Back: Non tender, normal ROM, normal alignment Gastrointestinal: soft, non tender, non distended, normal bowel sounds, no rebound, no guarding, two large ventral hernias-not reducible Extremities: no deformity, no tenderness, no swelling, normal ROM, normal strength Neurological: CN II-XII intact, normal speech, normal motor, normal sensory, no focal neuro deficits Psych: cooperative, appropriate mood & affect Medical Decision Making ED RN notes reviewed. Prior charts reviewed. Labs: Reviewed Diagnostic imaging: Reviewed 09/19/22 18:07:40 Pt is pending another liter of fluids and repeat troponin. I have transitioned care of the patient to Dr., we have discussed the clinical presentation, work-up, and ED course thus far. Condition Stable Attestations I, scribing for Dr. on 09/19/22 17:14:33 Signed by, scribe 09/19/22 17:14:33 I, D.O, attest that the scribe's documentation has been prepared under my direction and personally reviewed by me in its entirety. I confirm that the note above accurately reflected all work, treatment, procedures, and medical decision making by me. Assessment/Plan 1. Dyspnea R06.00 2. Bronchitis J40 3. Dizziness R42 4. Dehydration E86.0 Follow Up No qualifying data available Chronic Problem List Incisional hernia Tobacco use Procedure/Surgical History ?Appendectomy (01/01/2015) Medications Home Medications (4) Active gabapentin , Orally Lipitor 40 mg, Orally, Daily metFORMIN , Orally Xarelto , Orally Medication Administration Given NS - ED Bolus, 1000 mL, IVPB Allergies NKA Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse Denies Tobacco Tobacco Use: 10 or more cigarettes (1/2 pack or more)/day in last 30 days. Family History Cardiovascular disease: Father. Lab Results Hemogram-Platelets-WBC Differential FS LATEST RESULTS WBC 09/19/22 16:47 9.3 RBC 09/19/22 16:47 4.23 Hgb 09/19/22 16:47 10.8 Low Hct 09/19/22 16:47 32.6 Low MCV 09/19/22 16:47 77 Low MCH 09/19/22 16:47 25.5 Low MCHC 09/19/22 16:47 33.1 RDW 09/19/22 16:47 16.8 High Platelet 09/19/22 16:47 268 MPV 09/19/22 16:47 8.2 Neutrophils % 09/19/22 16:47 75 Lymphocytes % 09/19/22 16:47 9 Monocytes % 09/19/22 16:47 15 Eosinophils % 09/19/22 16:47 0 Basophils % 09/19/22 16:47 1 Absolute Neutrophil 09/19/22 16:47 7.0 Absolute Lymphocyte 09/19/22 16:47 0.9 Low Absolute Monocyte 09/19/22 16:47 1.4 High Absolute Eosinophil 09/19/22 16:47 0.0 Absolute Basophil 09/19/22 16:47 0.1 Routine Coagulation Studies FS LATEST RESULTS PT 09/19/22 16:47 16.9 High INR 09/19/22 16:47 1.46 High aPTT 09/19/22 16:47 40.6 High Routine Chemistry Tests FS LATEST RESULTS Sodium SerPl QN 09/19/22 16:47 131 Low Potassium SerPl QN 09/19/22 16:47 4.1 Chloride SerPl QN 09/19/22 16:47 96 Low Carbon Dioxide SerPl QN 09/19/22 16:47 22 Anion Gap 09/19/22 16:47 13 High BUN SerPl QN 09/19/22 16:47 14 Creatinine SerPl QN 09/19/22 16:47 0.91 Estimated GFR (CKD-EPI) 09/19/22 16:47 87 Estimated GFR (CKD-EPI, no race) 09/19/22 16:47 >90 Estimated CRCL (CG) 09/19/22 16:47 105 Glucose SerPl QN 09/19/22 16:47 154 High Calcium Total SerPl QN 09/19/22 16:47 9.1 Alkaline Phos SerPl QN 09/19/22 16:47 253 High ALT SerPl QN 09/19/22 16:47 8 AST SerPl QN 09/19/22 16:47 10 Low Bilirubin Total SerPl QN 09/19/22 16:47 0.6 Total Protein SerPl QN 09/19/22 16:47 7.6 Albumin SerPl QN 09/19/22 16:47 3.6 Magnesium SerPl QN 09/19/22 16:47 1.8 Troponin-I High Sensitivity 09/19/22 16:47 7 BNP Pl QN 09/19/22 16:47 138 High Lactate Venous Pl QN 09/19/22 16:47 3.1 High Diagnostic Results XR Chest PA or AP Portable 09/19/22 17:39:38 IMPRESSION: Bibasilar interstitial and airspace opacities which may reflect atelectasis/scarring or bibasilar infiltrates. Thank you for consulting our team of subspecialty radiologists at Radiology. Healthcare providers wishing to discuss this case further can contact the Cardiothoracic Reading Room at. For after-hours or emergency department cases, please call. Electronically Signed by: Signed By: MD EKG Time: 9/19/2022 16:06 Rate: 85 bpm Rhythm: normal sinus rhythm Axis: normal ST-T segments: no changes T waves: normal Ectopy: none P waves and PR interval: within normal limits QT/QTc interval: within normal limits QRS interval: within normal limits Previous EKG: none available EP Interpretation Signature Line Electronically Signed on 09/19/22 18:08 EDT ________________________________________________________ Electronically Signed on 09/21/22 09:22 EDT ________________________________________________________ DO

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Document Type: XR Chest PA or AP Portable Document Subject: XR Chest PA or AP Portable Performed By: MD on September 19, 2022 17:27 EDT Verified By: MD on September 19, 2022 17:49 EDT Encounter Info: Hospital, Emergency, 09/19/22 - 09/19/22 * Final Report * Reason For Exam dyspnea Report PHYSICIANS RADIOLOGY REPORT EXAM: XR Chest PA or AP Portable DATE: 09/19/2022 17:27 hours INDICATION: dyspnea; dyspnea COMPARISON: Chest radiograph 9/5/2012; CT abdomen and pelvis 7/19/2021 TECHNIQUE: 1 view of the chest FINDINGS: Medical devices: None. Cardiomediastinal Contours: Normal cardiac and mediastinal contours. Lungs and Pleural Space: Negative for pneumothorax. Negative for moderate or large pleural effusion. Mild prominence of the central pulmonary vasculature. Streaky bibasilar airspace opacities. Question subtle superimposed bibasilar airspace disease Bones/Other: No acute, displaced rib fracture. No free air under the hemidiaphragms. IMPRESSION: Bibasilar interstitial and airspace opacities which may reflect atelectasis/scarring or bibasilar infiltrates. Thank you for consulting our team of subspecialty radiologists at Physicians Radiology. Healthcare providers wishing to discuss this case further can contact the Cardiothoracic Reading Room. For after-hours or emergency department cases, please. Electronically Signed by: Dictated on: 9/19/2022 5:39 PM Signature Line This examination and reported findings have been reviewed and confirmed by the undersigned. Read By: MD I authorize my name to be Electronically affixed by using my unique signature access code. Click VIEW IMAGE icon to Display Image This document has an image
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 29.04.2022
Beginn: 21.08.2022
Tage bis Beginn: 114,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test normal Muscular weakness Tremor

Symptomtext

I started to have tremors in my right forearm, and in my right leg, and I have also had muscle weakness on the right side. No medications have been prescribed, but my primary care recommended that I started taking a baby aspirin. I am having no other symptoms other than that. I have an appointment to have an MRI done of the brain on Thursday 11/3/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: 11OCT22 blood panel normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2494659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: PA
Alter: 82,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 18.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Alopecia Blood pressure measurement Condition aggravated

Symptomtext

has lost all her hair; lost all her hair was reported as worsened.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. An 82-year-old female patient received BNT162b2 (BNT162B2), on 18May2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 82 years for covid-19 immunisation. The patient's relevant medical history included: "cataract surgery", start date: Mar2022 (unspecified if ongoing), notes: cataract surgery had cataract surgery in Mar2022 and before that in Aug2021.; "cataract surgery", start date: Aug2021 (unspecified if ongoing), notes: cataract surgery had cataract surgery in Mar2022 and before that in Aug2021.; "High blood pressure" (unspecified if ongoing), notes: She has high blood pressure and stuff like that. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose: 1, SINGLE, Lot: EL9269, Expiry date: Unknown, Site: Unknown), administration date: 04Mar2021, when the patient was 81-year-old, for COVID-19 immunization; BNT162b2 (Dose: 2, SINGLE, Lot: EP7534, Expiry date: Unknown, Site: Unknown), administration date: 25Mar2021, when the patient was 81-year-old, for COVID-19 immunization; BNT162b2 (Dose: 3, SINGLE, Lot: FF2590, Expiry: Unknown, Site: Unknown), administration date: 12Oct2021, when the patient was 81-year-old, for COVID-19 immunization, reaction(s): "hair loss", "cataract surgery". The following information was reported: ALOPECIA (non-serious) with onset 2022, outcome "not recovered", described as "has lost all her hair"; CONDITION AGGRAVATED (non-serious) with onset 2022, outcome "not recovered", described as "lost all her hair was reported as worsened.". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Patient had high blood pressure and stuff like that, but nothing that is out of the ordinary for someone that is 82 years old. Started hair loss at the end of February early March. The beauticians said lots of women are losing their hair at various ages. Patient had lost all her hair, and if she has to live with it, she has to live with it. Patient scheduled to get next booster. She had a very thick head of hair. The beauticians mentioned something to her about the amount of women that lost their hair and the only thing that they could come up with was that all the women had been vaccinated. Her hair loss started in the spring 2022 like late Feb2022 or Mar2022. She was curious as to why this happened. It may have nothing to do with it, but this was strange. Her hair loss started in the spring 2022 like late Feb2022 or Mar2022. She is curious as to why this happened. It may have nothing to do with it, but this is strange. Other Conditions: No, Investigations: No. She has had 4 doses of the Covid-19 Vaccine. 2 primary doses and 2 booster doses. Her last dose before she lost her hair was on 12Oct2021. Her last dose she had in May2022 after she had already lost most of her hair. Booster dose due to high risk or frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 complications): Not applicable. Booster dose due to a weakened immune system: if the reason is a weakened immune system: Not applicable. Prior Vaccinations (within 4 weeks): none, but had cataract surgery in Mar2022 and before that in Aug2021.Family Medical History Relevant to Adverse Events (AEs): none. Relevant Tests: None. Specific Relevant Test: Not applicable.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201261871 same patient, different drug dose and different event.;US-PFIZER INC-202201268158 same patient, different drug dose and different event.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: Blood pressure measurement; Result Unstructured Data: Test Result:High
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (She has high blood pressure and stuff like that); Cataract operation (cataract surgery had cataract surgery in Mar2022 and before that in Aug2021.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2488635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 02.06.2022
Beginn: 16.10.2022
Tage bis Beginn: 136,0
Dosis: 4
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Anal incontinence Asthenia Blood magnesium normal COVID-19 Chest X-ray normal Cough Decreased appetite Dehydration Diarrhoea Electrocardiogram QT prolonged Electrolyte imbalance Hypertransaminasaemia Hypokalaemia Laboratory test abnormal Liver function test increased Mobility decreased SARS-CoV-2 test positive Urinary incontinence

Symptomtext

COVID + 10/16/22 - Vaccinated with pfizer x4 BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider at Discharge: Admission Date: 10/16/2022 Discharge Date: 10/19/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Dehydration [E86.0] Hypokalemia [E87.6] Generalized weakness [R53.1] Diarrhea, unspecified type [R19.7] COVID-19 virus detected [U07.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 77 y.o. female who presents to hospital with weakness. Patient reports developing cough approximately 4 days ago. She began to be increasingly weak at this time with poor appetite and diarrhea. She was unable to get off of her couch and was found in urine and stool at her home. She was brought to the emergency department for evaluation. She was afebrile, hemodynamically stable and not hypoxic. Lab evaluation revealed a hypokalemia with normal magnesium level. LFTs were elevated an EKG showed a significantly prolonged QT interval. She denied of any nausea vomiting in the emergency department. She was cleaned up by the nursing staff and bolused with IV fluids and given oral and IV potassium. COVID testing was found to be positive and chest x-ray was negative. Because of her weakness and severe electrolyte deficiency she was referred to the hospital for further evaluation and care. Patient was given fluids and potassium was replaced. The following day her electrolytes were stable but she remained very weak. She was evaluated by Physical and Occupational therapy and felt to be a candidate for subacute rehab. Patient was initially resistant to the idea of rehab however we did re-evaluate her for potential discharge home with home health therapy and she was unable to participate enough to make this option viable. Care management found a COVID bed for her at hospital and she was subsequently discharged there to undergo physical therapy in a subacute rehab environment. Her COVID symptoms never presented. Her mild transaminitis is resolving. We are going to discontinue her statin therapy at this point. She was seen on the day of discharge doing well and discharged to assured in subacute rehab facility in stable condition

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Praegender Schweregrund: Dehydration
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: HHC started for worsening management of Parkinsons disease 5/14/22
Vorgeschichte: Hyperlipidemia GERD (gastroesophageal reflux disease) DM (diabetes mellitus), type 2 (HCC) Left carotid stenosis Osteoarthritis of back Tubular adenoma Parkinson disease (HCC) Age-related osteoporosis without current pathological fracture Paroxysmal atrial fibrillation (HCC) Hypertension Chronic diastolic heart failure (HCC) Fatigue, unspecified type Frequent falls Anemia Orthostatic hypotension Compression fracture of T1 vertebra with routine healing, subsequent encounter Senile osteoporosis Anticoagulant long-term use Stage 3a chronic kidney disease (HCC) Personal history of transient ischemic attack (TIA), and cerebral infarction without residual deficits History of cervical fracture Abnormal LFTs
Andere Medikamente: Acetaminophen 1,000 mg Oral Every 6 hours PRN Amiodarone HCl 200 mg Oral Daily Apixaban 5 mg Oral 2 times daily Bisacodyl 5 MG 5- 15mg daily prn for BM. Max dose 15mg daily. Calcium Carbonate 1 tablet Oral Daily Carbidopa-Levodopa 25-100 MG
Allergien: DemerolNausea and Vomiting
Vorherige Impfungen: -

VAERS 2486332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fk9894

moderat

Staat: MA
Alter: 53,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 11.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Delirium Gait inability Gastric disorder Headache Insomnia Mobility decreased Pain Pyrexia Restless legs syndrome Restlessness Sleep disorder

Symptomtext

Got vaccine in the morning about 11:00 am By midnight it woke me up fever of 101 very unsettled felt like i had to keep moving then in the bathroom with stomach issues tried laying down could not sleep my legs would not stop moving pain from head to toe massive head ache in the back of skull fever went up to 104 Delirious could not walk 4 days in bed taken Tylenol

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Fish oil vitamin D
Allergien: -
Vorherige Impfungen: -

VAERS 2485621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 16.04.2021
Beginn: 31.08.2022
Tage bis Beginn: 502,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest pain Dizziness SARS-CoV-2 test positive

Symptomtext

08/31/22 presents to ED for "chest pain" "lightheadedness". PMHx of "heavy alcohol use, DVT, subdural hematoma, delirium tremens, Warnicke encephalopathy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 08/31/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2215896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NJ
Alter: 75,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 01.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Body temperature Chills Fatigue Illness Extra dose administered Headache Pyrexia Influenza Somnolence Tremor Vomiting

Symptomtext

fever/ fever went up to 103; terrible fatigue; horrendous chills; sick; weak; like a bad flu; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 75-year-old female patient received BNT162b2 (BNT162B2), on 01Apr2022 as dose 4 (booster), single (Lot number: F69894) at the age of 75 years for covid-19 immunisation. The patient's relevant medical history included: "Type II diabetes" (unspecified if ongoing), notes: Type II diabetes diagnosed 7 years ago. Concomitant medication(s) included: METFORMIN [METFORMIN HYDROCHLORIDE] taken for type 2 diabetes mellitus. Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot Number: 301308A), administration date: 27Sep2021, when the patient was 74-year-old, for Covid-19 Immunization, reaction(s): "little bit of fever but it only went up 1 degree"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot Number: 301308A), administration date: 27Sep2021, when the patient was 74-year-old, for Covid-19 immunization, reaction(s): "swelling in arm, soreness to that area", "swelling in arm"; BNT162b2 (DOSE 2, SINGLE; Lot Number: EN6208), administration date: 16Mar2021, when the patient was 74-year-old, for Covid-19 immunization, reaction(s): "swelling in arm, soreness to that area"; BNT162b2 (DOSE 2, SINGLE; Lot Number: EN6208), administration date: 16Mar2021, when the patient was 74-year-old, for Covid-19 Immunization, reaction(s): "swelling in arm"; BNT162b2 (DOSE 1, SINGLE; Lot Number: EN6201), administration date: 24Feb2021, when the patient was 74-year-old, for Covid-19 Immunization, reaction(s): "swelling in arm, soreness to that area"; BNT162b2 (DOSE 1, SINGLE; Lot Number: EN6201), administration date: 24Feb2021, when the patient was 74-year-old, for Covid-19 immunization, reaction(s): "swelling in arm". The following information was reported: PYREXIA (non-serious), outcome "unknown", described as "fever/ fever went up to 103"; FATIGUE (non-serious), outcome "unknown", described as "terrible fatigue"; CHILLS (non-serious), outcome "unknown", described as "horrendous chills"; ILLNESS (non-serious), outcome "unknown", described as "sick"; ASTHENIA (non-serious), outcome "unknown", described as "weak"; INFLUENZA (non-serious), outcome "unknown", described as "like a bad flu". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The reporter assessed the events as non-serious. It was reported as the patient had kind of side effect you get when you have the flu. The patient was sick for 4 days and on 5th day her fever broke. The did not administered other vaccine on same date of suspect vaccination and no other vaccine within 4 weeks prior to suspect vaccination. The patient had no family history and relevant tests or investigation. The patient was wanted to know if it is safe get the new booster; would it be the same booster. The patient also received flu shot last Thursday or Friday and her arm was a little swollen and red around the injection site and tender to the touch.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201236853 same patient and product, different doses;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: Body Temperature; Result Unstructured Data: Test Result:103; Comments: her fever went up to 103.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type II diabetes mellitus (Type II diabetes diagnosed 7 years ago)
Andere Medikamente: METFORMIN [METFORMIN HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2482130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 02.05.2022
Beginn: 06.10.2022
Tage bis Beginn: 157,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Blood alkaline phosphatase increased C-reactive protein abnormal COVID-19 Chest X-ray abnormal Cough Hypoxia Lung opacity Oxygen saturation decreased Pneumonia Prohormone brain natriuretic peptide increased SARS-CoV-2 test positive Troponin normal Urine analysis normal White blood cell count normal

Symptomtext

Discharge Provider: DO Primary Care Provider at Discharge: PA-C Admission Date: 10/6/2022 Discharge Date: 10/12/2022 PRESENTING PROBLEM: COVID-19 virus infection [U07.1] HOSPITAL COURSE BY PROBLEM: * COVID-19 virus infection Assessment & Plan Patient is a 80 y.o. male with past medical history significant for hepatocellular carcinoma and cirrhosis without ascites, insulin-dependent type 2 diabetes, coronary artery disease, Parkinson's disease, hypertension, hyperlipidemia, obstructive sleep apnea, depression presented with acute hypoxia. Patient was recently admitted to hospital from September 24th through the 28th for a diagnosis of pneumonia and was treated with levofloxacin and vancomycin for a 5 day course of IV antibiotics. Patient was discharged to a nursing facility. Patient tested positive for COVID at his nursing facility on 10/5/2022. Nursing staff there reported that patient's oxygenation saturations dropped to 70% on room air. EMS was called and patient was transported to the hospital. Patient received a nebulizer treatment and 500 mL of fluids per EMS. Patient was complaining of only cough and denied any other symptoms. Workup in the ER significant for low oxygen saturations (85% on room air). Patient was placed on 2 L via nasal cannula with improvement in oxygen saturations to around 95-97% on the 2 L. Labs significant for alk-phos of 428, pro-BNP of 437, normal troponin, normal white blood cell count. UA was unremarkable and showed no acute signs of infection. Chest x-ray does show his multifocal areas of opacification, but this is improved from his previous admission. Due to patient having a new diagnosis of COVID 19 virus infection and currently needing supplemental oxygen, he was admitted to the hospital for further evaluation. As patient requiring supplemental oxygen was started on dexamethasone. Three days of dexamethasone patient's saturations dexamethasone discontinued. But due to fluctuating oxygen requirements patient restarted on dexamethasone with plans for discharge to subacute on oral dexamethasone and supplemental oxygen. Currently on 1L only with improving symptoms. CRP downtrend is also reassuring, currently 7.3. he has been vaccinated, but once he is recovered should receive the Bivalent vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: 4/6/2022 (1 hours) Hospital Emergency Hemorrhagic Cystitis
Vorgeschichte: Elevated Prostate Specific Antigen (PSA) - TRUS/BX - neg 2008 Kidney stone - s/p Right ureteroscopy 2006 - stone analysis 100% Ca Ox monohydrate, S/P C-Litholapaxy, R dx Ureteroscopy 7-17-11. 100% Uric Acid BPH (benign prostatic hypertrophy) Hyperlipidemia associated with type 2 diabetes mellitus Hypertension associated with type 2 diabetes mellitus Parkinson's disease Hepatocellular carcinoma Type 2 diabetes mellitus with diabetic polyneuropathy, with long-term current use of insulin OSA on CPAP Class 1 obesity due to excess calories with serious comorbidity and body mass index (BMI) of 33.0 to 33.9 in adult Dizziness Cortical senile cataract of right eye Dermatochalasis of both upper eyelids Nuclear senile cataract of right eye Surgical aftercare, sense organs Coronary artery calcification Balance disorder Other chest pain Chest pain Grief Memory loss Goals of care, counseling/discussion Chronic nausea Skin irritation Confusion Coordination of complex care Major depressive disorder, single episode in full remission Cirrhosis of liver without ascites Medicare annual wellness visit, subsequent COVID-19 virus infection PAC (premature atrial contraction)
Andere Medikamente: ACETAMINOPHEN EXTRA STRENGTH 500 MG tablet Alcohol Swabs (PHARMACIST CHOICE ALCOHOL) PADS amLODIPine (NORVASC) 10 MG tablet ASPIRIN LOW DOSE 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet benzonatate (TESSALON) 100 MG capsu
Allergien: CephalexinHives, Rash
Vorherige Impfungen: -

VAERS 2480515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NY
Alter: 76,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 15.04.2022
Beginn: 27.09.2022
Tage bis Beginn: 165,0
Dosis: 4
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthma COVID-19 Chills Condition aggravated Nervousness SARS-CoV-2 test positive

Symptomtext

I had vaccination on 04/15/2022. On 09/27/2022, I was feeling very chilly and shaky. I took an at home COVID-19 and it was Positive. I contacted my PCM who prescribed Paxlovid. I still presently have asthma symptoms in my chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 09/27/2022 COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Multivitamins; Albuterol; Flovent
Allergien: Flowers; Cats; Dust
Vorherige Impfungen: -

VAERS 2467345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 01.06.2022
Beginn: 04.08.2022
Tage bis Beginn: 64,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest pain Cough Fatigue SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of chest pains. The next day I developed a cough. I took a COVID-19 test that was negative. The next day the cough was stronger. I then took another COVID-19 test that was positive as well as another test a few hours later. I contacted my doctor and was prescribed Paxlovid and OTC Mucinex. I took that for 5 days. My cough did reside eventually but I still had chest pains that were a mild onset. I was extremely tired and fatigued. My symptoms lasted a total of 8 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; Fioricet; Losartan
Allergien: N/A
Vorherige Impfungen: Shingles vaccine - 2021 - chills and malaise

VAERS 2464392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 91,0
Geschlecht: M
Eingang: 29.09.2022
Impfdatum: 14.04.2022
Beginn: 28.09.2022
Tage bis Beginn: 167,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Chills Cough Dyspnoea

Symptomtext

Hospitalized for chills, dry cough, dyspnea. Requiring O2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Prostate Cancer, RA, OSA, Thrombocytopenia, COVID (2020), Vertigo, Tremor, HTN
Andere Medikamente: -
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2450238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 16.03.2022
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Feeling abnormal Hypoacusis Inner ear disorder Palpitations Peripheral swelling Tinnitus Weight Weight increased

Symptomtext

heart palpitations/periodically heart palpitations; clouded ears; ringing in the ears; swollen feet; brain fog; weight gain; its hard for me to hear at times; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 39-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Mar2022 as dose 2, 0.3 ml single (Lot number: FK9894) at the age of 39 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: 33036BD, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 16Feb2022, when the patient was 39-year-old, for Covid-19 Immunization, reaction(s): "heart palpitations"; BNT162b2 (Dose Number: 1, Batch/Lot No: 33036BD, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 16Feb2022, when the patient was 39-year-old, for Covid-19 immunization, reaction(s): "clouded ears", "ringing in the ears", "swollen feet", "brain fog", "weight gain". The following information was reported: PALPITATIONS (non-serious), outcome "not recovered", described as "heart palpitations/periodically heart palpitations"; INNER EAR DISORDER (non-serious), outcome "not recovered", described as "clouded ears"; TINNITUS (non-serious), outcome "not recovered", described as "ringing in the ears"; PERIPHERAL SWELLING (non-serious), outcome "not recovered", described as "swollen feet"; FEELING ABNORMAL (non-serious), outcome "not recovered", described as "brain fog"; WEIGHT INCREASED (non-serious), outcome "not recovered", described as "weight gain"; HYPOACUSIS (non-serious), outcome "not recovered", described as "its hard for me to hear at times". The events "heart palpitations/periodically heart palpitations", "clouded ears", "ringing in the ears", "swollen feet", "brain fog", "weight gain" and "its hard for me to hear at times" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of palpitations, inner ear disorder, tinnitus, peripheral swelling, feeling abnormal, weight increased, hypoacusis. Clinical information: Patient reported that, I received the first dose on 16Feb2022 and second dose on 16Mar2022 but after both doses I experienced clouded ears, ringing in the ears, heart palpitations, swollen feet, brain fog and weight gain. Still til this day in Sep2022 experiencing clouded ears where its hard for me to hear at times and periodically heart palpitations, brain fog, and increase weight gain. Adverse events resulted in Doctor or other healthcare professional office/clinic visit. Patient did not have covid prior to vaccination. Patient did not have covid tested post vaccination. There were no known Allergies. Other medical history was none. No other vaccine was taken in four weeks. No other medications were taken in two weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Name: Weight; Result Unstructured Data: Test Result:Increase; Comments: increase weight gain
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2427529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: KY
Alter: 57,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 30.03.2022
Beginn: 26.07.2022
Tage bis Beginn: 118,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Angina pectoris Anticoagulant therapy Bradycardia COVID-19 Catheterisation cardiac Essential hypertension Tobacco abuse Troponin normal

Symptomtext

MD Physician Specialty: Cardiology Consults Signed Date of Service: 07/27/22 0722 Hide copied text Hover for details 1. Accelerating angina 2. Tobacco abuse 3. Essential hypertension- uncontrolled 4. Normal troponin 5. COVID Pe cv rrr no m/g/r Lung clear to a and p abd soft nontender Ext no c/c/e Plan -- Start heparin GTT. Smoking cessation encouraged. Continue asa, norvasc.. No b blocker due to bradycardia. Increase lisinopril. LHC in am Patient left AMA after heart cath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Essential hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2418273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CO
Alter: 44,0
Geschlecht: F
Eingang: 23.08.2022
Impfdatum: 12.07.2022
Beginn: 01.08.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Antinuclear antibody negative Blood folate normal Blood thyroid stimulating hormone Full blood count normal Glycosylated haemoglobin normal Hypoacusis Laboratory test normal Lipids normal Metabolic function test normal Paraesthesia Paraesthesia ear Serum ferritin normal Vitamin B12 normal Vitamin D

Symptomtext

About two weeks after vaccination I noticed left-sided paresthesias over a section of my scalp and ear (including decreased hearing), left lateral hand and arm, left lateral foot and leg. Three weeks later symptoms continue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 8/15/22 labs: Hemoglobin A1c, Vitamin D, TSH, Vitamin B12 and folate, ferritin, ANA, CBC, CMP, lipid panel all normal.
Aktuelle Erkrankungen: none
Vorgeschichte: Raynaud's syndrome Migraines
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2415924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: IN
Alter: 48,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 30.12.2020
Beginn: 01.05.2021
Tage bis Beginn: 122,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Asthenia Blood test Hypoaesthesia Impaired work ability Musculoskeletal stiffness No reaction on previous exposure to drug Nodule Pain Paraesthesia Rheumatoid factor negative Ultrasound scan X-ray

Symptomtext

After first dose on 12/30/2020 everything was fine. After 2nd dose of 1/20/2021, knot formed in right wrist in June of 2021. Patient started prednisone for the next full year until present. Numbness, tingling, stiffness persists in right arm, has lost strength in right arm. Persisted from June 2021 until present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: After knot formation: bloodwork, ultrasound, x-rays done summer of 2021. Bloodwork drawn every 3 months to diagnose if it is rheumatoid arthritis, so far negative.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Lorsartin, Buspar
Allergien: None
Vorherige Impfungen: -

VAERS 2409941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: AZ
Alter: 61,0
Geschlecht: F
Eingang: 12.08.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Axillary mass Chills Condition aggravated Headache Pyrexia

Symptomtext

I usually get a headache after vaccinations but it was worse this time. Half hour after vaccination I a had fever with chills and a few days later, and then I got a softball size lump under my left arm that was there 4 weeks. As I have MS, I see my Dr. regularly, so on my next visit (about 2 months later) it had gone away by then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: MS; Cognitive Decline; Hypothyroidism; Homocysteinemia; Fibromyalgia; Sudden Sensory Hearing Loss
Andere Medikamente: Gabapentin; COPAXONE; levothyroxine; cyanocobalamin; hydroxyzine; calcium; multivitamin; vitamin B12; triple omega 369.
Allergien: Morphine; TYSABRI; naproxen; IVP dye
Vorherige Impfungen: -

VAERS 2407226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OH
Alter: 56,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 03.05.2022
Beginn: 28.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Back pain Blood test Chest pain Electrocardiogram normal Feeling hot Nausea Pain Pyrexia Vomiting

Symptomtext

Starting on 07/28/2022, I started having a lot of body aches all over and chest pain. My back was throbbing at one point. I had some nausea and threw up once. I also had a fever which lasted for a full week. Thursday, Friday, and Saturday, the fever was over 100 degrees. On Thursday, it got up to 102. Sunday and Monday, it was between 99.5 and 100.5. I saw my PCP on Tuesday and my temperature was still elevated to 99 degrees and they said that they could feel the heat radiating off me. My temperature is normally around 97.7 degrees. My doctor did not prescribe anything or do a COVID-19 test. They advised that I treat with Advil and Tylenol and call back if things worsened. My fever finally broke on Thursday and got back down to 98 degrees.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG-08/03/2022-nothing of concern; Blood Panel-08/08/2022-waiting on results.
Aktuelle Erkrankungen: None.
Vorgeschichte: C.O.P.D; Bipolar Disorder.
Andere Medikamente: Melatonin; Calcium with Vitamin D3; Levothyroxine; Venlafaxine; Buspirone; Ropinirole; Iron; Lamotrigine; Trazadone; Omeprazole; Docusate; Anoro; Albuterol.
Allergien: None.
Vorherige Impfungen: -

VAERS 2405655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OH
Alter: 62,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 03.06.2022
Beginn: 01.06.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Immediate post-injection reaction Nodule Pain in extremity Paraesthesia

Symptomtext

Patient states that she has a knot in her arm that was not there prior to the booster and has not gone away. Complains of pain in her arm since time of injection and needing to use tylenol and pain cream to cope. Also states that soon after injection, she began having tingling going down into her hand and fingers, especially at night. Patient has not reported until today, stating she was hoping that this was a normal reaction and that it would subside.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none at this time- was advised to contact PCP for evaluation
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2400422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MO
Alter: 59,0
Geschlecht: M
Eingang: 03.08.2022
Impfdatum: 22.04.2022
Beginn: 07.06.2022
Tage bis Beginn: 46,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood test COVID-19 Cardiac function test normal Chest discomfort Chills Cough Dyspnoea Dyspnoea exertional Electrocardiogram Emotional distress Feeling cold Hyperhidrosis Loss of personal independence in daily activities Pyrexia SARS-CoV-2 test positive Swollen tongue Troponin X-ray

Symptomtext

I received my second Pfizer booster for COVID-19 on 4/22/2022. On 6/7/2022, I began occasionally having shortness of breath. I felt like I had run up two flights of stairs, though I hadn't exerted myself. This would only happen for a few seconds at a time; I would struggle to catch one or two breaths and then my breathing became normal again. At about 6 PM that evening, I began to feel like an elephant was sitting on my chest; it was very difficult to breathe. I then developed a strange, dry cough that kept increasing in frequency. I then started feeling like I was in a refrigerator. I had the chills, but I was also sweating. I checked my temperature, and it was over 100. The coughing and difficulty breathing really bothered me. I didn't lose my senses of taste or smell, though, and I also didn't lose my appetite. I called my sister, who is a nurse, to get her opinion. She told me that it sounded like I had COVID-19, and she told me that she would pick me up to take me to the ER. I then remembered that I had a home COVID-19 test, so I took it, and it yielded a negative result. Despite the negative result, she told me that she still thought that I had COVID-19, and she insisted on taking me to the ER. She then picked me up and took me to the ER. At the ER, I was PCR tested for COVID-19. The result was positive, and I was put in a room for isolation. I underwent blood tests, an X-ray, and an EKG. During the process, they checked my troponin levels. I was then moved from the isolation room to an ER suite. I was then given a saline IV line. I sat there with the IV line for 2 hours. A doctor and an advanced nurse practitioner then came to explain my test results. They told me that they would like to give me monoclonal antibodies. According to the test results, I was positive for COVID-19, but my heart function was normal, and my lungs were clear. When they suggested that I get the antibodies, I asked them if it would help me get over COVID-19. They then told me that it would reduce the severity of my symptoms and reduce the recovery time, so I agreed to get the monoclonal antibodies, which were administered intravenously. I sat in the suite for another 2 hours, so the staff could make sure I didn't have an adverse event after receiving the antibodies. After the 2 hours were up, I was then discharged. My sister then came to pick me up, and she took me home. During the following four days, my symptoms improved. My cough became less severe and frequent and my breathing was much improved, On 6/9/2022, my fever finally broke. This may or may not be related, but I will mention it just in case. On 6/5/2022, I noticed that there was a white bump on the tip of my tongue. I told my dentist on 6/11/2022 about the bump, and he prescribed me chlorhexidine mouthwash. I used the mouthwash 3 times a day whenever I would brush my teeth, and the bump finally went away about 6/30/2022. When I called my internist's office and spoke to his nurse practitioner, she told me that I should be fully recovered by 6/30/2022 or 7/1/2022. She also said that if any of the symptoms returned, I was to either call the doctor's office, or if the symptoms were severe, I was to go to the ER. Since then, I have recovered and I feel like my normal self. I don't have any residual physical symptoms, but it was mentally jarring. I now always wear a mask in public, protective eyeglasses, and gloves. I also use lots of hand sanitizer. I practiced these precautionary measures before I was infected, but it apparently wasn't enough. Now I've pretty much become a hermit. I now have my groceries delivered instead of going to the stores. I also have stopped going to the barber shop and hardly ever leave my home. I guess you could say that having COVID-19 was emotionally traumatizing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 6/7/2022 home COVID test negative result; 6/7/2022 PCR COVID-19 test positive result; 6/7/2022 blood work, chest X-ray. EKG heart function normal, lungs clear.
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetes Type II; Facial Acne; Hypertension (Managed); Acid Reflux Disease; Hidradenitis Suppurativa; Grief.
Andere Medikamente: Hydrochlorothiazide; LEVEMIR; HUMALOG; losartan; metformin HCL; omeprazole; RYBELSUS; doxycycline; atorvastatin; adapalene gel; clindamycin gel; ciclopirox olamine cream; FREESTYLE LIBRE blood glucose sensor worn on arm; clonazepam; ciclopi
Allergien: Amoxicillin; tizanidine; codeine; morphine; tetracycline; quinapril; sertraline.
Vorherige Impfungen: -

VAERS 2393680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: HI
Alter: 72,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 13.04.2022
Beginn: 12.07.2022
Tage bis Beginn: 90,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Dyspnoea Fatigue Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Started feeling really worn out and exhausted, with shortness of breath, with a sore throat, and was coughing more than usual. Took a home test and tested positive. Felt severe aches, fever and fatigue. Called Dr. and was prescribed PAXLOVID. Has started taking it and waiting to feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Home COVID test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Arthritis; Fibromyalgia; Osteoporosis.
Andere Medikamente: Metoprolol; DETROL; hydroxyzine; XANAX; naproxen; flexural; butal-acet-caff; benzonatate; losartan; tramadol; hydrochlorothiazide; omeprazole; escitalopram; cetirizine.
Allergien: Sulfa medication; morphine
Vorherige Impfungen: -

VAERS 2379293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 75,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 07.03.2021
Beginn: 23.06.2022
Tage bis Beginn: 473,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: POSITIVE COVID TEST 6/23/22
Aktuelle Erkrankungen: -
Vorgeschichte: Barrett's esophagus Broken foot, right Bronchitis Chronic myelomonocytic leukemia Chemo treatments Chronic pain Gout Compression fracture of L2 lumbar vertebra COPD (chronic obstructive pulmonary disease) Deep vein thrombosis (DVT), left ESBL (extended spectrum beta-lactamase) producing bacteria infection Urine culture E coli GERD (gastroesophageal reflux disease) Heartburn Adenomatous colonic polyps MVA (motor vehicle accident) PONV (postoperative nausea and vomiting) Renal disease Recurrent UTI Vitamin D deficiency Bariatric surgery status Malignant neoplasm of skin Raynaud's syndrome without gangrene Presence of right artificial hip joint COPD Varicose veins of both lower extremities Adenomatous colonic polyps Hydronephrosis concurrent with and due to ureteral stricture Leukocytosis Sweet syndrome Status post placement of ureteral stent Calculus of gallbladder without cholecystitis without obstruction Ureteropelvic junction (UPJ) obstruction Depression with anxiety Osteoporosis Anemia of chronic disease Unspecified urinary incontinence Esophageal pain Pulmonary infiltrates Anasarca Thrombocytopenia Hyponatremia Lethargy Hypocalcemia Generalized weakness Hip fracture, left Symptomatic anemia
Andere Medikamente: acetaminophen (TYLENOL) 325 mg oral tablet albuterol HFA (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler allopurinol (ZYLOPRIM) 300 mg oral tablet calcium carbonate (TUMS) 200 mg calcium (500 mg) oral chew tab
Allergien: Iodinated Contrast Media Metrizamide Penicillins
Vorherige Impfungen: -

VAERS 2376767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: -
Alter: 41,0
Geschlecht: M
Eingang: 21.07.2022
Impfdatum: 05.04.2022
Beginn: 19.07.2022
Tage bis Beginn: 105,0
Dosis: 4
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Chest pain Cough Myalgia Pyrexia

Symptomtext

fever, cough, chest pain, myalgias

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2372485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OH
Alter: 60,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 15.04.2022
Beginn: 28.06.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Exercise tolerance decreased Fatigue Headache Heart rate increased Increased viscosity of upper respiratory secretion Malaise Night sweats Oropharyngeal pain Palpitations Panic attack Paranasal sinus hypersecretion Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sinus congestion

Symptomtext

I received my second Pfizer booster for COVID-19 on 4/15/2022. On 6/28/2022, I developed a sore throat and coughing. The symptoms then progressed to congestion, low-grade fever, runny nose, fatigue, and sneezing; these symptoms lasted over the next several days. On the morning of 7/1/2022, I awoke out of a sound sleep with my heart racing at 109 beats per minute and night sweats. For half an hour, my heartrate wouldn't slow down, despite my best efforts, which consisted of deep breathing and drinking water to cool myself off. My husband then called the doctor, and the doctor said that it sounded like I was having a panic attack. Once my heart resumed its normal rate, my husband and I then took PCR tests; my test result was positive. On 7/2/2022, I began a 5-day course of Paxlovid. I was also prescribed benzonatate to treat my cough. In conjunction with my prescription medications, I also took OTC Sudafed. Before I started using Sudafed, I used Claritin at night, but it didn't help. The Sudafed helped some, but the Paxlovid was very effective; I felt a huge difference the day after I began taking Paxlovid. Before I began taking Paxlovid, I had sweats every night. The last dose of Paxlovid was on 7/6/2022. The Paxlovid helped immensely, but it left a bile-like taste in my mouth that never abated. Not only that, but it gave me abdominal pains that made me feel like I had diarrhea, even though I didn't always have diarrhea. During the time I was taking the Paxlovid, I would have diarrhea just once a day. After I finished taking the Paxlovid, my symptoms were markedly improved. On 7/7/2022, 7/8/2022, and 7/9/2022, I felt much better, but I still had lingering fatigue. On the evening of 7/10/2022, I started to get a sore throat and thickening mucus in the nasal passages. On 7/11/2022, I woke up with a headache, a sore throat, and a runny nose. I took a home test, and it yielded a positive result. From 7/11/2022-7/15/2022, I had a fever of over 100; at its lowest point, the temperature was 99. I woke up every morning with a headache. I had a major cough at this time, so I would sit up in bed at night drinking water and taking Halls Vitamin C Drops. At this point, I also started taking benzonatate again. On 7/12/2022, the sore throat went away and it hasn't returned since then. Throughout the whole experience, I have had extreme fatigue. Before I became ill, I was able to walk about 5 miles a day, but ever since I had COVID-19, I haven't been able to do that. On 7/12/2022, I started taking Claritin and Flonase, and the Flonase helped ease the sneezing and sinus drainage. At the time of this writing, I haven't taken any medicine for the first time since I got sick. However, I think I'll take Flonase later on, because I still have sinus congestion. I took another home test on 7/16/2022, and the result was again positive. I talked with my doctor on 7/17/2022, and we discussed whether I should take antibiotics just in case I have developed a sinus infection. I decided not to take the antibiotics, since my drainage is clear; I have had sinus infections in the past, and I know that thick, opaque drainage and facial pressure are what usually signal infection. I also don't have any facial pressure. As of today, the headache has also disappeared, and it's been 24 hours since I've had a temperature above 99. Although a loss of sense of taste and/or smell is a common symptom of COVID-19, I have never experienced this. I have also not experienced any body aches. I currently feel much better than I did before, but the fatigue continues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: PCR test--7/1/2022. Positive result. At-home antigen tests--7/11/2022 and 7/16/2022. Both positive results.
Aktuelle Erkrankungen: None.
Vorgeschichte: High Cholesterol; Minor Spinal Cord Issues (Resulting from 5 Broken Vertebrae); Artificial Right Hip.
Andere Medikamente: Atorvastatin; Trazodone; Spironolactone; Cymbalta; Vitamin D; Multivitamin.
Allergien: Oxycontin.
Vorherige Impfungen: -

VAERS 2372335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 02.03.2022
Beginn: 17.03.2022
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 COVID-19 pneumonia Endotracheal intubation Lactic acidosis Metabolic encephalopathy Respiratory failure SARS-CoV-2 test positive

Symptomtext

pneumonia due to COVID 10, lactic acidosis, respiratory failure requiring intubation, toxic metabolic encephalopathy

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: covid 19 positive by PCR SARS-CoV-2 (COVID-19) by NAA, Micro detected 7/17/22
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, COPD, CHF, CKF, Diabetes type 2, CAD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2370621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 14.04.2022
Beginn: 01.05.2022
Tage bis Beginn: 17,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypertension Surgery

Symptomtext

Started noticing that my blood pressure was high during routine medical visits for MS. I started noticing that my BP was higher then normal. I had outpatient surgery last week and it was noted that my blood pressure was elevated while I was in recovery. I was told to monitor my BP for a few days. During my follow up with my physician I was prescribed HYZAAR (HBD) medication on 7/12/2022 to control my BP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: MS
Andere Medikamente: NEURONTIN; baclofen; GILENYA; NUEDEXTA; NUVIGIL; PROTONIX; SYNTHROID; KLONOPIN; ZANAFLEX; EFFEXOR; ABILIFY; BUSPAR; simvistatin; AIMOVIG; REQUIP; PEPCID OTC
Allergien: N/A
Vorherige Impfungen: -

VAERS 2367968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NV
Alter: 66,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 20.04.2022
Beginn: 29.06.2022
Tage bis Beginn: 70,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia COVID-19 Dizziness Feeling abnormal Headache Malaise Mobility decreased Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

When I woke up I felt weak and sick and just didn't feel good. I told my girlfriend and she instructed me to take a COVID-19 test and the next day I did and I came back positive and the next day was my worst day. I developed fever, headache, and dizzy. I could barely move and just stayed in bed all day. On the third day I called the after hours physician and was prescribed the Paxlovid for 5 days. The very next day I felt better and by day 5 I felt normal just weak and by day 6 I felt like a million bucks. By the time I finished my last pill I felt great and one or two days after that the symptoms came back and hit me again. I have had headache, weak, sore throat and weak with congestion. I been taking Tylenol to help with the headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID-19 home test 6/30/22 Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tamsulosin; Acyclovir; Famotidine; Rosuvastatin; Finasteride; Allegra; Aspirin
Allergien: Demerol; Amoxicillin
Vorherige Impfungen: -

VAERS 2366208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 08.04.2022
Beginn: 31.05.2022
Tage bis Beginn: 53,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia COVID-19 Cough Dyspnoea Headache Oropharyngeal pain Oxygen saturation decreased Pain Respiratory tract congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

Woke up 5/31 feeling congestion and sore throat. I had body aches and I had low pulse oximeter readings for about 4 days. I experienced shortness of breath, but never asthma. By 6/2 coughing and headache developed. Morning of 5/31 I tested with an At Home COVID 19 Antigen test with a strong positive. 6/5 and 6/6, also positive, but weaker. 6/7 Was first negative test. Telemedicine with doctor on 5/31. Doctor prescribed Paxlovid. Still experiencing a little tickling cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Morning of 5/31 I tested with an At Home COVID 19 Antigen test with a strong positive. 6/5 and 6/6, At Home COVID 19 Antigen test positive, but weaker. 6/7 Was first negative At Home COVID 19 Antigen test.
Aktuelle Erkrankungen: no
Vorgeschichte: Asthma
Andere Medikamente: Lexapro; Strattera; Robaxin; Vitamin C; Potassium; Biotin; Stool Softener
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2366066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 13.04.2022
Beginn: 03.07.2022
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Anxiety Asthenia Blood creatinine increased Blood pressure increased Blood sodium decreased COVID-19 Cough Decreased appetite Diarrhoea Dyspnoea Fatigue Hypophagia Mobility decreased SARS-CoV-2 test positive Urine analysis normal White blood cell count normal

Symptomtext

Discharge Provider: MD, MPH Primary Care Provider: MD Admission Date: 7/3/2022 Discharge Date: Jul 5, 2022 PRESENTING PROBLEM: ARF (acute renal failure) Diarrhea, unspecified type COVID HOSPITAL COURSE: Patient is a 81 y.o. female who presents today with fatigue and diarrhea. pmh copd,htn,pad presenting with co extreme fatigue and generalized weakness. States onset loose stools one week ago . Since that time has been having 2-3 loose not watery stools per day . Initially taking stool softer now stopped . Tested positive for covid 4 days ago and now today completed course of Paxlovid today . No co abdominal Pain , no blood in stool or black stools . Denies fever or chills . She has continued to take medications including cozaar. Co progressive generalized weakness and fatigue. Able to stand and walk short distances . Denies focal weakness , no paraesthesias. Note mild non productive cough . Feels oral intake has declined due to decreased mobility though appetite at baseline . No loss of taste or smell. Feels breathing and her copd are at baseline . Denies dysuria. In ed vitals stable , afebrile , bp was elevated to 240/77 . Given iv hydralazine and ativan with improvement. Per patient she is highly anxious in hospital and not uncommon for her. Labs showing sodium 125.k 3.0,creat 1.65 , nml wbc of 7.47. ua with no infectious findings, tested pos for covid 19. Given x2 liter fluid bolus,zofran , 40 meq kcl Patient symptoms of weakness, shortness of breath are improved by day 2 of admission. Does feel good to ambulate on her own, agreeable to the plan per home with outpatient follow-up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Bilateral carotid artery stenosis COPD (chronic obstructive pulmonary disease) HTN (hypertension) Peripheral vascular disease Hypertension Chest pain Carpal tunnel syndrome, left Carpal tunnel syndrome, right Meningioma Abnormal stress echo Presbyesophagus Hypercholesterolemia Transient ischemic attack Asthma Gastroesophageal reflux disease TIA (transient ischemic attack) Unintentional weight loss Insomnia Intracranial tumor Malignant neoplasm of skin Papilloma of urinary bladder COVID-19 Diabetes mellitus, type II
Andere Medikamente: albuterol (VENTOLIN) 108 (90 BASE) MCG/ACT inhaler atorvastatin (LIPITOR) 40 MG tablet Calcium Carb-Cholecalciferol (CALCIUM 600 + D PO) clopidogrel (PLAVIX) 75 MG tablet docusate (COLACE) 100 MG capsule hydrOXYzine (ATARAX) 25 MG tabl
Allergien: Advair Diskus AspirinNausea/Vomiting/Diarrhea Diuretics Doxycycline HyclateNausea/Vomiting/Diarrhea Hydrochlorothiazide Hydrocodone-acetaminophenRash LatexSkin Rashes/Hives Other PenicillinsOther Tetracyclines Tomato Topamax [Topiramate] Vibramycin
Vorherige Impfungen: -

VAERS 2364725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 31.03.2022
Beginn: 01.06.2022
Tage bis Beginn: 62,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Crepitations Dyspnoea Echocardiogram Electrocardiogram Full blood count Headache Nasal congestion Pain Pyrexia SARS-CoV-2 test positive X-ray

Symptomtext

I had a really bad headache, deep crackling cough, short of breath. labored breathing a stuffy nose, fever. When I blew my nose nothing would come out. I hurt more than when I had open heart surgery. I got home from work on June 1, 2022 and took the COVID-19 test and it was an immediate positive. I went to the county drive through testing PCR COVID-19 test, I received my positive results on June 2, 2022. On June 2, 2022 I went to the Emergency Room because I was so short of breath and I had just had open heart surgery at the end of 2021. I was prescribed Paxlovid for my positive COVID-19 test results I started taking it that evening and am feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Home COVID-19; PCR COVID-19; X-Ray; Echocardiogram; EKG; Complete Blood Panel
Aktuelle Erkrankungen: No
Vorgeschichte: Heart disease
Andere Medikamente: Aspirin
Allergien: Septra
Vorherige Impfungen: -

VAERS 2362738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: KY
Alter: 75,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 20.04.2022
Beginn: 07.07.2022
Tage bis Beginn: 78,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Cough Decreased appetite Dyspnoea Dyspnoea exertional Exposure to SARS-CoV-2

Symptomtext

Patient is a 75-year-old male with history of obesity hypoventilation syndrome, memory impairment, venous insufficiency, hyperglycemia, hyperlipidemia, hypertension who presents to the emergency room with shortness of breath. Patient was actually at the immediate care center earlier today for shortness of breath and was diagnosed with COVID-19, he had sats 88-89 on room air and was dyspneic with exertion so they recommended him come to the emergency room for further evaluation. Patient is fully vaccinated against COVID-19, however he did tell the emergency room provider that he was not vaccinated, his vaccinations are seen in epic. He does have history of memory impairment, and seems to be a somewhat poor historian and changes his story about onset of symptoms. In review of the note from immediate care center he did then that his wife had COVID and his symptoms have been ongoing for a few days. He tell me that he was not aware of any exposure but he has had symptoms for 2 days with shortness of breath and cough. She denies any fever, no nausea or vomiting although he has had a poor appetite the last few days. He states he feels much better since being put on oxygen, at this time he has no complaints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2359597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CO
Alter: 50,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 28.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Asthenia Chest X-ray Chest discomfort Condition aggravated Differential white blood cell count Drooling Electrocardiogram Fatigue Full blood count Hyperhidrosis Hypertension Laboratory test Metabolic function test Myalgia Treatment noncompliance Troponin I

Symptomtext

Patient presented to hospital emergency department with complaints of generalized weakness, fatigue, mylagias, chest tightness, diaphoresis, and uncontrollable drooling one day after receipt of COVID-19 vaccine dose #4. Found to be hypertensive, with initial blood pressures in in the ED of 148/116 and 173/110 mmHg. Patient claimed to have run out of supplies and had not received maintenance blood pressure medicines for approximately one month. Clinic records show documentation of chronic nonadherence. Also present was concern for approximately daily illicit use of methamphetamine. Accordingly, antihypertensive treatment was urgently provided as well as a comprehensive diagnostic workup for other possible cardiovascular disorders. Following counseling on the expected course of events following vaccination and the importance of compliance with all prescribed therapy, he was discharged with stable vital signs, improving symptoms and a temporary supply of antihypertensive medications, along with scheduled follow-up plans with his primary care provider.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Chest X-ray; Basic metabolic panel; Complete blood count with differential; Electrocardiogram; Pulse oximetry; Troponin I
Aktuelle Erkrankungen: Umbilical hernia
Vorgeschichte: Hypertension; Attention Deficit Disorder; Hyperlipidemia; Hashimoto's Thyroiditis; Venous insufficiency; Methamphetamine dependence; Gastroesophageal reflux disease;
Andere Medikamente: Amlodipine; Lisinopril; Atorvastatin; Bupropion XL; Naltrexone
Allergien: Ciprofloxacin; Trimethoprim-Sulfamethoxazole
Vorherige Impfungen: -

VAERS 2347648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: VA
Alter: 72,0
Geschlecht: M
Eingang: 01.07.2022
Impfdatum: 31.03.2022
Beginn: 21.06.2022
Tage bis Beginn: 82,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Dry throat Hypertension Malaise Pain Productive cough Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sinus congestion

Symptomtext

On 3/31/2022, I received my second Pfizer booster for COVID-19. On 6/21/2022, I woke up with a very dry throat, body aches, and head congestion. My oxygen level was 97% or higher. I didn't have a fever or cough, though. That afternoon, I took an at-home COVID-19 test; the result was negative. On 6/22/2022, I still had the same symptoms and felt unwell. I took a second at-home test; this time, the result was positive. I called a clinic at a local pharmacy and got an appointment for 5 PM that day. I took a rapid test at the clinic, and I again got a positive result. The nurse advised me to go to the ER, because my blood pressure was high and so that I could get antiviral medication. The ER doctor prescribed me a 5-day course of molnupiravir. My blood pressure had decreased by 6/23/2022; my hypertension is a pre-existing condition that is unrelated to COVID-19. After I started taking molnupiravir on the evening of 6/22/2022, my congestion got slightly worse, but the dry throat went away. I developed a fever of 100.1 for only a couple of hours, and the only cough I had was a productive one that was related to the head congestion. I was told by both the clinic nurse and the ER doctor that my lungs were clear. Since I have had COVID-19, I have never had any oxygen levels below 96%. At the time of this writing, I feel for the first time like my congestion is almost gone. I have ceased to have any other symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Acid Reflux Disease; Sleep Apnea; Atrial Fibrillation; Enlarged Prostate; Osteoarthritis.
Andere Medikamente: Pravastatin; valsartan; atenolol; dofetilide; JANUVIA; vedolizumab; amlodipine; XARELTO; PENTASA; esomeprazole; finasteride; tamsulosin; XIIDRA; bumetanide; azelastine; fluticasone; vitamin D; zolpidem; hydralazine.
Allergien: Ciprofloxacin.
Vorherige Impfungen: -

VAERS 2344710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: SC
Alter: 45,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 28.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Aphasia Dizziness Hyperhidrosis Hypoaesthesia Panic reaction Paraesthesia Skin warm

Symptomtext

Patient was monitored after vaccine per protocol and after about 14 minutes patient c/o facial numbness tingling, skin sweating, hot to touch, lightheadedness. Patient then lost her ability to speak and became panicked. Patients vitals were stable and no sob or difficulty breathing. Patient was then given 125 mg of Solumedrol and EMS were dispatched. Patient remained stable and vitals were monitored. Patient slowly began to gain ability to speak after about 10 minutes she also received a 24 mg Benadryl and had no trouble swallowing at that time or speaking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known
Vorgeschichte: Type 2 diabetes hx of cerebrovascular accident Vitamin D deficiency Hypertensive Hypercholesterolemia
Andere Medikamente: gabapentin 100 mg capsule 06-28-2022 atorvastatin 20 mg tablet 06-28-2022 lisinopril 10 mg tablet 06-28-2022 metformin 1,000 mg tablet 06-28-2022 Jardiance 10 mg tablet 06-26-2022 ergocalciferol (vitamin D2) 1,250 mcg (50,000 unit) capsule
Allergien: NKA
Vorherige Impfungen: -

VAERS 2342980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fk9894

moderat

Staat: IN
Alter: 25,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 01.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Cough Dyspnoea Headache Laboratory test Oropharyngeal pain Respiration abnormal SARS-CoV-2 test Sleep disorder

Symptomtext

After receiving vaccine, few nights later my husband woke me up panicking over how I was breathing. When woken up I had noticed I had a sore throat which I didn?t hav before going to bed. A headache, pain in sternum, shortness of breath, coughing and to today I am still fighting the symptoms to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Breathing test, covid test, doctors tried to treat me with inhalers and steroid packs to help me fight it off and nothing at all could help.
Aktuelle Erkrankungen: Pulmonary embolism DVT resulting in getting a Thrombectomy procedure done a holiday Day weekend.
Vorgeschichte: Pulmonary embolism
Andere Medikamente: Lovenox 100mg 2x day
Allergien: Penicillin & Latex
Vorherige Impfungen: -

VAERS 2342980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fk9894

moderat

Staat: IN
Alter: 25,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 01.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Cough Dyspnoea Headache Laboratory test Oropharyngeal pain Respiration abnormal SARS-CoV-2 test Sleep disorder

Symptomtext

After receiving vaccine, few nights later my husband woke me up panicking over how I was breathing. When woken up I had noticed I had a sore throat which I didn?t hav before going to bed. A headache, pain in sternum, shortness of breath, coughing and to today I am still fighting the symptoms to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Breathing test, covid test, doctors tried to treat me with inhalers and steroid packs to help me fight it off and nothing at all could help.
Aktuelle Erkrankungen: Pulmonary embolism DVT resulting in getting a Thrombectomy procedure done a holiday Day weekend.
Vorgeschichte: Pulmonary embolism
Andere Medikamente: Lovenox 100mg 2x day
Allergien: Penicillin & Latex
Vorherige Impfungen: -

VAERS 2326793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 29.04.2022
Beginn: 05.05.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Burning sensation Condition aggravated Discomfort Erythema Eyelid rash Facial pain Pyrexia Rash Swelling face Urticaria

Symptomtext

rash trunk; face red; fever; Worsened; Eyelid rash; Burning sensation in face; Swelling of face; Urticaria localized; pain in face; discomfort/Face was stretched to limit and really hurt, Uncomfortable; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): 22K-163-4429208-00. A 44-year-old female patient received BNT162b2 (BNT162B2), on 29Apr2022 as dose 3 (booster), single (Lot number: FK9894) at the age of 44 years intramuscular for covid-19 immunisation; adalimumab (HUMIRA), on 04May2022 (Batch/Lot number: unknown) subcutaneous for rheumatoid arthritis, ankylosing spondylitis; diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (TDAP), on 29Apr2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history included: "Ankylosing Spondylitis" (unspecified if ongoing); "Epilepsy" (unspecified if ongoing); "Rheumatoid Arthritis" (unspecified if ongoing); "Gerd" (unspecified if ongoing); "Interstitial Cystitis" (unspecified if ongoing); "Restless Leg" (unspecified if ongoing). Concomitant medication(s) included: PREGABALIN; ESTRADIOL; KEPPRA [LEVETIRACETAM]; PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; CLARITIN [LORATADINE]; TAGAMET [CIMETIDINE]; PHENOXYMETHYLPENICILLIN POTASSIUM. Past drug history included: Levofloxacin, reaction(s): "Levofloxacin Allergy"; Diltiazem, reaction(s): "Diltiazem allergy"; Furosemide, reaction(s): "Furosemide Allergy". Vaccination history included: comirnaty (dose 1, lot no.EW0151, Intramuscular), administration date: 05Apr2021, for covid-19 immunization; comirnaty (dose 2, lot no. EA6207, Intramuscular), administration date: 15Mar2022, for covid-19 immunization; Zoster vaccine recombinant adjuvanted, reaction(s): "Zoster Vaccine Recombinant Adjuvanted Allergy". The following information was reported: BURNING SENSATION (non-serious) with onset 05May2022, outcome "not recovered", described as "Burning sensation in face"; EYELID RASH (non-serious) with onset 05May2022, outcome "not recovered"; SWELLING FACE (non-serious) with onset 05May2022, outcome "not recovered", described as "Swelling of face"; URTICARIA (non-serious) with onset 05May2022, outcome "not recovered", described as "Urticaria localized"; DISCOMFORT (non-serious) with onset 05May2022, outcome "not recovered", described as "discomfort/Face was stretched to limit and really hurt, Uncomfortable"; FACIAL PAIN (non-serious) with onset 05May2022, outcome "not recovered", described as "pain in face"; RASH (non-serious), outcome "unknown", described as "rash trunk"; ERYTHEMA (non-serious), outcome "not recovered", described as "face red"; PYREXIA (non-serious), outcome "unknown", described as "fever"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "Worsened". Relevant laboratory tests and procedures are available in the appropriate section. The action taken for adalimumab was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: body temperature; Result Unstructured Data: Test Result:104 degree
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Ankylosing spondylitis; Cystitis interstitial; Epilepsy; GERD; Restless legs; Rheumatoid arthritis
Andere Medikamente: PREGABALIN; ESTRADIOL; KEPPRA [LEVETIRACETAM]; PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; CLARITIN [LORATADINE]; TAGAMET [CIMETIDINE]; PHENOXYMETHYLPENICILLIN POTASSIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2323202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 21,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 07.04.2022
Beginn: 16.06.2022
Tage bis Beginn: 70,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Cough Dyspnoea Exposure during pregnancy Vomiting

Symptomtext

Patient arrives to the ED with complaints of cough, shortness of breath and vomiting that all started this morning otherwise healthy female in her 1st pregnancy presents with COVID infection. (7 months pregnant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2319123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 74,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 04.03.2021
Beginn: 16.05.2022
Tage bis Beginn: 438,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Dyspnoea Hypoxia Pyrexia SARS-CoV-2 test positive

Symptomtext

FEVER , COUGH, SHORTNESS OF BREATH, HYPOXIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: POSITIVE COVID TEST 5/20/22
Aktuelle Erkrankungen: -
Vorgeschichte: Basal cell cancer Chronic pain left shoulder COVID-19 Depression Dyslipidemia Multiple sclerosis Neurogenic bladder Seizures ST elevation myocardial infarction involving left anterior descending coronary Spondylosis of lumbar region without myelopathy or radiculopathy TIA Tobacco abuse Urinary tract infection Vertigo
Andere Medikamente: acetaminophen (TYLENOL) 325 mg oral tablet alendronate (FOSAMAX) 70 mg oral tablet atorvastatin (LIPITOR) 20 mg oral tablet baclofen (LIORESAL) 20 mg oral tablet cholecalciferol, vitamin D3, (VITAMIN D3) 1000 uni
Allergien: Mayzent [Siponimod]
Vorherige Impfungen: -

VAERS 2318838

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FK9894

moderat

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 14.03.2022
Beginn: 22.04.2022
Tage bis Beginn: 39,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Balance disorder Fall Laboratory test normal Parkinson's disease Tremor Walking aid user Walking distance test

Symptomtext

I started having trembling in my right hand a lot. I could not keep my balance and I had fallen a few times. The trembling got worse in the right hand and my left hand is started trebling as well. I was using a cane and now am using a walker but I have fallen seven times since this started. My doctor checked my walking and my balance and did a memory test as well. I have a DaT scan coming up as well. After meeting with my medical team and going over what was occurring it was diagnosed as Parkinson's.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: DaT Scan, Memory test, Walking and Balance test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia; Lupus; Dercum's Disease
Andere Medikamente: Diclofenac sodium topical gel; clobetasol propionate foam; COREG; aspirin; valium; FLEXERIL; latanoprost eyedrops; nitroglycerine; ropivacaine; isosorbide
Allergien: Morphine, NEURONTIN, gabapentin, sulfa, PRISTIQ, latex, food allergy to muscles
Vorherige Impfungen: -

VAERS 2317225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 16.01.2021
Beginn: 08.06.2022
Tage bis Beginn: 508,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 COVID-19 pneumonia Cough Dyspnoea Pain

Symptomtext

Pt arrived with shortness of breath and cough. Pt has PMH of CKD stage III and is status post renal transplant, heart failure preserved EF, and type II DM. He has been having these symptoms along with body aches and weakness for 8 days. He is chronically immunosuppressed on antirejection medications for renal transplant. He was admitted for pneumonia due to COVID -19 virus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2316755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 12.06.2022
Impfdatum: 04.05.2022
Beginn: 04.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Dyspnoea Feeling abnormal Malaise Pain in extremity

Symptomtext

Following the shot I felt a bit ill and some arm soreness, but understood that was expected. The arm pain has persisted and is considreable, intermittent pain with occassional loss of strength. It is so sudden and can take my breath away. It is sometimes accompanied by a popping feeling and sound. Prior to the shot my arm was 100% in good shape and I have had no injuries or exceptional use of it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: I am going to Physical Therapy with a referral (starting June 13)
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2315458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 03.05.2022
Beginn: 30.05.2022
Tage bis Beginn: 27,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Diarrhoea Dyspnoea Fatigue Insomnia Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Wheezing

Symptomtext

I contracted COVID-19 on 05/30/2022 with symptoms of fatigue, sore throat, cough, trouble sleeping, fever of 99.5, wheezing, shortness of breath, diarrhea for 2 days, and congestion. On 06/01/2022 I saw my doctor and was prescribed albuterol, benzonatate, and was instructed to take elderberry and zinc supplements. My doctor would not prescribe PAXLOVID and I was not offered the monoclonal antibodies. I am still experiencing lingering symptoms of fatigue, congestion and coughing. I do not feel recovered at this point.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab was positive on 05/31/2022
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; Chronic Lymphocytic Leukemia
Andere Medikamente: Losartan; ALIGNProbiotic
Allergien: No
Vorherige Impfungen: -

VAERS 2313129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 01.04.2022
Beginn: 21.05.2022
Tage bis Beginn: 50,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Asymptomatic COVID-19 Balance disorder Blood culture negative Cellulitis Complication associated with device Erythema Femur fracture Fracture displacement Imaging procedure abnormal Open reduction of fracture Pain Peripheral swelling Periprosthetic fracture SARS-CoV-2 test positive Tachycardia Wound complication Wound secretion

Symptomtext

Patient up to date on COVID vaccinations who had incidental positive COVID test during routine facility placement testing. Asymptomatic throughout stay. Provider d/c note from hospital below: "70 yo F, Hx of L femoral fracture with ORIF on 5/2/2022 (10 screws placed) who was just discharged day before admission who arrived with signs of erythema and green discharge from her wound noted by wound care at home. She was sent to the Hospital for further evaluation. In the ED, she was tachycardic, BP was stable, Imaging showed medially displaced distal femoral fracture with loss of fixation and signs of tissue swelling. Physical exam demonstrated erythema of the skin around the knee. She was started on Vancomycin, Rocephin, and IV fluids. Orthopedic surgery was consulted and evaluated her, and determined need for an attempt for a repeat ORIF with potential for leg amputation of ORIF unable to be performed. She was covered with Zosyn instead of Rocephin for concern for deeper structure infection. The doctor performed ORIF successfully with minimal complications. Surgical and blood cultures were obtained and showed no growth for at least 2 days. Her cellulitis improved with antibiotics, and she was determined to not need Zosyn. She exhibited minimal pain post-surgical. PT/OT recommended rehabilitation and PM&R was consulted who deemed her appropriate for in-patient rehab. On day of discharge, she had one bowel movement without need for lactulose, a COVID test was performed and came back positive. She is fully vaccinated with 2 booster doses obtained before admission. She is asymptomatic. She will need severe respiratory isolation for 10 days. Per Doctor, she will need BID aspirin for 30 days for DVT prophylaxis. She is toe-touch weight bearing on the LLE with dressing changes when the dressing is saturated. She will be discharged to Rehabilitation in stable medical condition. CBC in 2 days to make sure her Hgb remains stable". D/C note from rehab facility below: "70 yo F PMH HTN, obesity, HLD, who presented to the Medical Center 5/2/22 for a periprosthetic supracondylar L femur fracture. She is s/p ORIF and rehabilitation. She was instructed to be NWB on the LLE but states she did intermittently bear weight. She had a loss of balance at home that resulted in her shifting a significant amount of weight to the LLE. Orthopedics was consulted and noted a complete loss of distal fixation on her imaging. She was found to have a medially displaced distal femoral fracture extending to the femoral component of the TKR, S/P repair with plates and screws with the doctor 5/23. Her course was complicated by post operative cellulitis. She was started on Vancomycin and Zosyn. She has a history of SVT and PVCs and is continued on metoprolol. Course at rehab was complicated by asymptomatic course of COVID 19. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: 15,0
Labordaten: COVID detected PCR on 05/25/22
Aktuelle Erkrankungen: -
Vorgeschichte: Essential hypertension, benign Arthralgia of knee borderline diabetes IFG (impaired fasting glucose) BMI 45.0-49.9, adult Sinus tachycardia
Andere Medikamente: Ferrous sulfate HydroDiuril Cozaar Melatonin Toprol XL
Allergien: Enalapril Norvasc
Vorherige Impfungen: -

VAERS 2309664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 05.06.2022
Impfdatum: 27.02.2022
Beginn: 20.05.2022
Tage bis Beginn: 82,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Dizziness Dyspnoea Electrocardiogram Musculoskeletal discomfort Palpitations Transient global amnesia

Symptomtext

Ten days after shot: Transient global amnesia Seven weeks after the shot: Heart palpitations, tightness in breathing, slight burning in chest, tightness in back of neck, lightheaded

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Around March 7: EKG
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2307117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MD
Alter: 51,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 27.04.2022
Beginn: 08.05.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Chest X-ray Chest pain Chills Dyspnoea Electrocardiogram abnormal Fatigue Pain Paranasal sinus discomfort SARS-CoV-2 test positive

Symptomtext

Starting 05/08/2022 I had chills. The next day the chills continued and I developed body aches. On 05/09/2022, I tested positive for COVID. I had a telemedicine visit with urgent care due to risk factors for a severe case of COVID to discuss Paxlovid. On 05/10/2022, I started the Paxlovid. During the next 2 days, I had some body aches, some sinus pressure and some fatigue. I tested negative on 05/14/2022 and I finished Paxlovid on 05/15/2022. The following week I had more fatigue and shortness of breath and mild chest pain. I believe the chest pain and shortness of breath was due to the Paxlovid irritating my acid reflux. On 05/19/2022, I saw my doctor and they did an EKG and told me to see a cardiologist and do a chest x ray. I have had the chest x ray and will follow up to see the cardiologist. The shortness of breath and the mild chest pain has resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG: abnormal (no change since last time). Chest x ray: will get results at next visit.
Aktuelle Erkrankungen: None
Vorgeschichte: Acid Reflux
Andere Medikamente: Pantoprazole; Zyrtec
Allergien: No
Vorherige Impfungen: -

VAERS 2305276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 01.06.2022
Impfdatum: 24.04.2022
Beginn: 24.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Laboratory test Paraesthesia

Symptomtext

A couple of days later, I started to feel numbness/tingliness throughout my body but most in my hands. I saw my dr in May.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Labs to test vitamin
Aktuelle Erkrankungen: None
Vorgeschichte: heart condition, asthma, RA, low thyroid
Andere Medikamente: Potassium chloride, Citroen, Lasik's, dioxin, balquenol, levothyroid, pronazapril, velabutren, singular
Allergien: arythomyacin
Vorherige Impfungen: -

VAERS 2303805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: WI
Alter: 62,0
Geschlecht: M
Eingang: 31.05.2022
Impfdatum: 20.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chondrocalcinosis pyrophosphate Condition aggravated Gait inability

Symptomtext

Two days after my vaccine I started to have a flare up on my right foot. By the next day both feet were bothering me. I didn't take anything for it. 04/25/2022 I ended up having to take an ambulance to the ER because I could not walk. The doctor looked at my history and I told him it was Pseudogout. He prescribed steroids' which seems to help. After taking the steroids' I felt better after about 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type II Diabetic
Andere Medikamente: Fiber Choice Magnesium Vitamin D3 Multivitamin Low Dose Aspirin Furosemide 20mg once daily Colchicine 0.6mg once daily Omeprazole 40mg twice daily Ursodial 300mg twice daily Brilinta 60mg twice daily Atorvastatin Calcium 40mg (2x) once dail
Allergien: N/A
Vorherige Impfungen: -

VAERS 2303337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 25.04.2022
Beginn: 19.05.2022
Tage bis Beginn: 24,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Blood creatinine increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Hypertransaminasaemia Hypoxia Lung opacity Oxygen saturation abnormal SARS-CoV-2 test positive Tachycardia White blood cell count increased

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 5/19/2022 Discharge Date: May 21, 2022 PRESENTING PROBLEM: Pneumonia due to COVID-19 virus [U07.1, J12.82] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 84 y.o. female with PMH significant for CAD, carotid stenosis, a fib, HTN, hypothyroidism, and HLD who presented to the ED on 5/19/22 due to worsening cough and SOB. Patient was initially diagnosed with COVID on 5/16 while visiting friends. She then drove 2.5 hours back. Patient had appointment with her PCP on the day of admission and was found to have spO2 of 87% and was referred to the ED. In the ED, spO2 fluctuated, at times requiring 2L and at times stable on RA. She was also tachycardic in 100-110 range. VS otherwise stable. Labs notable for Cr 1.3 at baseline, mild transaminitis, WBC 12. COVID PCR was repeated and positive. CXR showed patchy indistinct hazy opacities without focal consolidation. She was started on decadron and is being admitted to Blodgett for hypoxia 2/2 covid pneumonia. Patient continued to have fluctuating oxygen saturations with saturating stable on room air at rest but requiring supplemental oxygen with activity. Patient was continued on oral dexamethasone awaiting clinical improvement. She was weaned to room air and discharged to home in stable condition. Will complete 10 days of Decadron.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism Trigger Finger (Bilateral) Mixed hyperlipidemia Essential hypertension PAF (paroxysmal atrial fibrillation) S/P patent foramen ovale closure percutaneously with Septal Amplatzer Device 2-22-11 Chronic coronary artery disease Carotid artery stenosis Primary osteoarthritis involving multiple joints Baker's cyst, left Chronic neck pain Vertigo Mixed Alzheimer's and vascular dementia Cystocele, midline Vaginal atrophy Fecal smearing Incomplete defecation Renal cyst, right Neuropathy Benign paroxysmal positional vertigo due to bilateral vestibular disorder Chronic kidney disease, stage 3b Chronic venous insufficiency
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet allopurinol (ZYLOPRIM) 100 MG tablet amLODIPine (NORVASC) 5 MG tablet atorvastatin (LIPITOR) 40 MG tablet benzonatate (TESSALON) 100 MG capsule dexamethasone (DECADRON) 6 MG tablet (Expired) gabap
Allergien: VenlafaxineShortness of Breath AmoxicillinOther Flagyl [Metronidazole]Other, Headache Lexapro [Selective Serotonin Reuptake Inhibitors]Anxiety Norco [Hydrocodone]Other OxycodoneOther Prozac [Fluoxetine]Diarrhea, Other SerotoninAnxiety
Vorherige Impfungen: -

VAERS 2301551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OR
Alter: 19,0
Geschlecht: F
Eingang: 29.05.2022
Impfdatum: 07.05.2022
Beginn: 10.05.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Back pain Blood test normal Chest pain Electrocardiogram abnormal Laboratory test normal Pain Sinus arrhythmia Urine analysis normal

Symptomtext

Chest pain in center, right and left side of the chest. Pain radiating to right shoulder and back. I went to urgent care on 05/12/2022 where I got multiple lab tests & EKG done. EKG showed a sinus arrhythmia. I was sent home on 05/12/2022 with no treatment plan. The chest pain continues to this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG - sinus arrhythmia 05/12/2022 Blood lab tests - normal 05/12/2022 Urinalysis - normal 05/12/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Gilbert?s syndrome
Andere Medikamente: Retin-A Clindamycin phosphate
Allergien: None
Vorherige Impfungen: -

VAERS 2294403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NJ
Alter: 92,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 18.05.2022
Beginn: 25.05.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypotonia Mobility decreased

Symptomtext

Patient woke up this morning (5/25/22) and her right arm was flaccid, she was unable to use it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, Dementia, Arthritis, HTN, and Bradycardia
Andere Medikamente: Namenda, Pepcid, Pravachol, Lasix, Flonase, ASA, Amaril, Iron, Potassium, Diovan, Glucophage, Januvia, and Melatonin
Allergien: Tramadol, and Penicillin V
Vorherige Impfungen: -

VAERS 2294081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CT
Alter: 79,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 07.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Incorrect dose administered Investigation

Symptomtext

difficulty of breathing; 5th shot of the Pfizer BioNTech covid-19 Vaccine; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. A 79-year-old female patient received BNT162b2 (BNT162B2), on 07Apr2022 as dose 5 (booster), single (Lot number: FK9894) at the age of 79 years for covid-19 immunisation. Relevant medical history included: "COPD" (unspecified if ongoing), notes: COPD Diagnosed before receiving Covid-19 vaccines. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE, 1 SINGLE, NDC: Unknown, Lot: Unknown, Expiration: Unknown), for COVID-19 immunization; Bnt162b2 (DOSE, 2 SINGLE, NDC: Unknown, Lot: Unknown, Expiration: Unknown), for COVID-19 immunization; Bnt162b2 (DOSE 3 (BOOSTER), SINGLE, NDC: Unknown, Lot: Unknown, Expiration: Unknown), for COVID-19 immunization; Bnt162b2 (DOSE 4 (BOOSTER), SINGLE, NDC: Unknown, Lot: Unknown, Expiration: Unknown), for COVID-19 immunization. The following information was reported: INCORRECT DOSE ADMINISTERED (non-serious) with onset 07Apr2022, outcome "unknown", described as "5th shot of the Pfizer BioNTech covid-19 Vaccine"; DYSPNOEA (hospitalization) with onset Apr2022, outcome "unknown", described as "difficulty of breathing". The patient was hospitalized for dyspnoea (hospitalization duration: 5 day(s)). The event "difficulty of breathing" required physician office visit. The patient underwent the following laboratory tests and procedures: Test: (2022) Checked her heart and lungs. Therapeutic measures were taken as a result of dyspnoea with nebulizer, steroids, and oxygen. Clinical course: Caller stated that his wife got the 5th shot of the Pfizer BioNTech Covid-19 Vaccine last 07Apr2022 and stated after a few days, she started to have problems breathing. She went to the pulmonologist to find out if it was caused by the vaccine shot or "part of the problem". After a few days, she went to the hospital and she was there for 5 days and they did every test he could think of to see why she was having difficulty breathing and they couldn't come up with an answer to her condition and they put her on steroids (initially 40mg then changed to 20mg) but she never stops having problems with breathing. It only helped her for a couple of weeks and she was still experiencing difficulty of breathing. Caller stated that he himself got the same shot of the Pfizer Biontech covid-1 vaccine but did not experience the sane side effect with his wife. The patient got all 5 doses of the Pfizer BioNtech covid-19 Vaccine (3rd booster shot). Caller said checked for everything in the hospital and can't find anything and he doesn't know what it was. The only coincidence was after receiving the shot and her breathing kept getting worse. He said he was not saying it was because of the vaccine. He said he was waiting for her doctor to call and if doctor calls he will have to hang up. He said event started the 6th or 7th day after receiving the vaccine. She has been on oxygen since she got home from the hospital. He said oxygen doesn't help and she can walk 10 feet and then she has to sit down and the oxygen doesn't work. He said she can't taste and she is a good cook and it's affecting other part. He said she was on prednisone. He said she has been home for a couple weeks. He asked his wife and she said she has been home for 7 days home from the hospital. He said patient was not real skinny and not real fat and was probably 5' 7" height. They stopped going anywhere since Covid. He said he was calling to see if other people are having problems and if connected to shot? No additional Vaccines Administered on Same Date of the Pfizer Suspect. No prior Vaccinations(within 4 weeks) were received. No family Medical History Relevant to AE(s). Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: Test Date: 2022; Test Name: Test; Result Unstructured Data: Test Result:Checked her heart and lungs.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COPD (COPD Diagnosed before receiving Covid-19 vaccines)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OR
Alter: 93,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 16.05.2022
Beginn: 17.05.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Mobility decreased Vomiting

Symptomtext

Patient vomited after breakfast. She was given ginger tea and bed rest. The vomiting stopped about 30 minutes and she stayed in bed for about 4 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High Blood Pressure.
Andere Medikamente: Lorsartan 100mg, Vitamin D, Multi Vitamin, PreserVision.
Allergien: Penicillin.
Vorherige Impfungen: -

VAERS 2292796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CT
Alter: 74,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dyspnoea Headache Malaise Myalgia Oropharyngeal pain Pain in extremity Pyrexia

Symptomtext

That evening had headache and muscle ache, sore arm. In the middle of the night had sore throat. The next day had a fever over 100.5 felt really sick. Also had SOB. Did not see doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Fibromygia, High Blood Pressure, Cholesterol
Andere Medikamente: Omastattin, Lipitor, Gabapentin
Allergien: Seasonal Allergies
Vorherige Impfungen: -

VAERS 2292753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OH
Alter: 82,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 17.05.2022
Beginn: 17.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Chest pain Mobility decreased Movement disorder Pain

Symptomtext

24 hours after administration: localized pain; 48 hours after: Pain went into upper back and left arm across chest; hard time flexing and moving. 1 week later: still having same symptoms as 48 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis; hypertension
Andere Medikamente: Cyclobenzaprine 5mg up to TID; valsartan-hctz 160-25mg 1qd ; Meloxicam 15mg 1qd; Estradiol 0.5mg 1qd; multivitamin 1qd; Prolia Q6mo
Allergien: codeine: N&V
Vorherige Impfungen: -

VAERS 2290660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: TN
Alter: 94,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 04.05.2022
Beginn: 04.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Musculoskeletal chest pain

Symptomtext

Began to complain of pain on right side of chest below clavicle area, then shortly after initial complaint, the patient stated it was "moving down" . Within approx 5 min patient described the pain as moving down to "bottom rib". No respiratory distress noted. Patient was on her own portable O2. No distress, no palor, no diaphoresis noted. Patient requested ambulance to be called, they arrived within approx 5-8 min.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Patient was transported to local hospital and later released. (per hospital personnel)
Aktuelle Erkrankungen: none that were reported
Vorgeschichte: Currently using O2 by nasal cannula. States has COPD. Family member reports that patient has "anxiety"
Andere Medikamente: Patient stated she had had an B12 shot today as well.
Allergien: unknown
Vorherige Impfungen: -

VAERS 2290606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MA
Alter: 74,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 18.04.2022
Beginn: 10.05.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Dyspnoea Nasal congestion SARS-CoV-2 test positive Throat irritation Vaccine breakthrough infection

Symptomtext

COVID breakthrough case. I received my 2nd booster shot on 04/18/2022 and my adverse event started on 05/10/2022 at night slight stuffy nose. The next day when I woke up I have more of a stuffy nose and a scratchy throat. On the 05/11/2022 I tested positive for COVID. 05/12/2022 I stuffy nose cleared up. 05/13/2022 in the morning I couldn't breathe, I had a dry cough, stuffy nose. On Friday 05/13/2022 I contact my doctor she prescribed me PAXLOVID for 5 days. I started taking PAXLOVID the same night. 05/14/2022 I started to feel better my stuffy nose had gotten better and I still had dry cough but was getting better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID home test.
Aktuelle Erkrankungen: None
Vorgeschichte: Vaginal (when I went to menopause; Clobetasol)
Andere Medikamente: Regular meds; levothyroxine; dorzolamide hydrochloride; (CONSORT) timolol maleate; ophthalmic solution; VALTREX; vitamin D; calcium; artificial tears; CELLUVISC
Allergien: Preceptive use of barium chloride
Vorherige Impfungen: Last fall with the flu shot, my arm was sore.

VAERS 2290450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 21.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Electrocardiogram normal Eye operation Fatigue Laboratory test Nervousness Palpitations Thyroid function test abnormal Weight decreased

Symptomtext

I've been in general good health for my age with the exception of my kidney disease but over the past few weeks, out of nowhere, a few days before Easter, I began to feel very shaky and have lost 7lbs in the past month. I went to see my primary doctor who thought it may be panic attacks since I was also experiencing fatigue and heart pounding. He prescribed an antidepressant but I didn't like that medication. I went to a cardiologist who looked at the recent full work up that was done prior to my recent eye surgery, and added thyroid function test and he informed me that my thyroid function was up and that I would need to see an endocrinologist. I have made that appointment and am waiting to see them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Thyroid function test, elevated levels, EKG normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Polycystic kidney disease
Andere Medikamente: Atenolol twice daily; Valsartan hydrochlorothiazide 320/12.5; nifedipine ER 30mg; ezetimibe simvastatin 10/40mg; Yuvafem; calcium; multivitamin
Allergien: None
Vorherige Impfungen: Flu symptoms after pneumonia vaccine.

VAERS 2289496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: PA
Alter: 81,0
Geschlecht: F
Eingang: 21.05.2022
Impfdatum: 14.04.2022
Beginn: 18.05.2022
Tage bis Beginn: 34,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Migraine Migraine with aura

Symptomtext

Occurred 5 weeks after vaccine and I don't think its related - But you sent me this form anyway. I experienced a possible migraine aura. A colorful kaleidoscope for about 10 minutes. In both eyes. Following I had a mild migraine headache for a day and a half (usual duration of my migraines). I experienced the aura about an hour after eating very ripe pineapple. I think it was a tyramine headache and unrelated to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I was immediately checked out by the optometrist at my ophthalmologist office. She said it was most likely a migraine aura.
Aktuelle Erkrankungen: none
Vorgeschichte: None. I had migraines when I was younger. I haven't had migraines for a long time. But I had just eaten a lot of very ripe pineapple that I think caused the kaleidoscope aura. Lasted 10 minutes. I immediately was checked out by eye doctor. Had only one other possible visual aura about 20 years ago, not kaleidoscope type.
Andere Medikamente: Bystolic, Moduretic, Centrum, Calcium, Salmon Oil, Echinacea, Vit B12, Vit C, Tumeic, CoQ10, Vit D3.
Allergien: Tyramine (migraine headaches), MSG (migraine headaches) Penicillin, Vancomycin (Red Neck syndrome), maybe gentomycin. Statins (heart palpitations)
Vorherige Impfungen: -

VAERS 2287234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 06.04.2022
Beginn: 18.04.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Condition aggravated Exposure to SARS-CoV-2 Facial pain Fatigue Malaise Nasal congestion Nasal discharge discolouration Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive Seasonal allergy Sinusitis Toothache

Symptomtext

I had my fourth Pfizer shot on 4/6/2022. I suffer from seasonal allergies every year. About two weeks after my shot, my allergies worsened and I was concurrently exposed to Covid. My son, husband, daughter, daughter-in-law, cousin and grandson all tested positive between 4/16/2022 and 4/19/2022 (rapid Antigen home test). I tested negative but was having either mild covid symptoms or allergies (sore throat and "stuffed" sinuses. On 4/22/2022 I went for a PCR test which tested positive. On 5/3/2022 I tested negative (home rapid Antigen test). I continued to have mild symptoms and fatigue so called my doctor on 5/6/2022 as my left cheek and teeth hurt and my nose dripped yellow snot. She started me on a Zpack. On 5/10/2022 I flew (for the first time since covid and wore a mask during the journey) During that period I was away, I had mild fatigue, chills at night, sore throat. I went to see the doctor on 5/17/2022. She confirmed the sinus infection still present and started me on a three day course of Prednisone and a new antibiotic (Cefuroxime). I am beginning to feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 4/22/2022 RT PCR
Aktuelle Erkrankungen: none
Vorgeschichte: Controlled Hypertension
Andere Medikamente: Lisinopril, Thiazide, Atorvastatin, Amlodipine, Baby Aspirin, Vitamin C, Calcium, Multivitamin, Glucosamine Chondroitin MSM, Claritin
Allergien: Penicillin Bivalves Walnuts
Vorherige Impfungen: -

VAERS 2286708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OR
Alter: 68,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 12.05.2022
Beginn: 12.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Emotional distress Fatigue Feeling cold Headache Hot flush Hyperhidrosis Insomnia Myalgia Nausea Palpitations

Symptomtext

By 09:00pm I was feeling a little nausea; only to have any sleep I might have had disturbed by heart palpitations which lasted 8 - 10 hours with very little break; All of my muscles were agitated and extremely sore; my feet were freezing; I struggled to get any sleep; completely wiped out all day; I was also emotional most of the day; hotflashes; I expended a little energy and broke out into a drenching sweat; After receiving my 2nd Booster as prescribed for my age group, the symptoms began with a frontal headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old female patient received BNT162b2 (BNT162B2), on 12May2022 at 09:45 as dose 4 (booster), single (Lot number: FK9894) at the age of 68 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Onions" (unspecified if ongoing), notes: Known allergies: Onions; "Known allergies:lactose sensitive" (unspecified if ongoing), notes: Known allergies: lactose sensitive; "Allergy:Wheat" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 3, Batch/Lot No: Lot# FF2589, Location of injection: Arm Right), administration date: 17Oct2021, when the patient was 67-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: Lot# EL9269, Location of injection: Arm Left), administration date: 05Feb2021, when the patient was 67-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: Lot# EL3246, Location of injection: Arm Left), administration date: 16Jan2021, when the patient was 66-year-old. The following information was reported: HEADACHE (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "After receiving my 2nd Booster as prescribed for my age group, the symptoms began with a frontal headache"; MYALGIA (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "All of my muscles were agitated and extremely sore"; HYPERHIDROSIS (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "I expended a little energy and broke out into a drenching sweat"; INSOMNIA (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "I struggled to get any sleep"; EMOTIONAL DISTRESS (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "I was also emotional most of the day"; FATIGUE (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "completely wiped out all day"; HOT FLUSH (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "hotflashes"; FEELING COLD (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "my feet were freezing"; PALPITATIONS (non-serious) with onset 12May2022 at 15:00, outcome "recovering", described as "only to have any sleep I might have had disturbed by heart palpitations which lasted 8 - 10 hours with very little break"; NAUSEA (non-serious) with onset 12May2022 at 21:00, outcome "recovering", described as "By 09:00pm I was feeling a little nausea". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of headache, nausea, palpitations, myalgia, feeling cold, insomnia, fatigue, emotional distress, hot flush, hyperhidrosis. Additional Information: Patient reported that after receiving 2nd Booster as prescribed for my age group, the symptoms began with a frontal headache. By 09:00pm I was feeling a little nausea and at 10:00 pm went to bed, only to have any sleep I might have had disturbed by heart palpitations which lasted 8 - 10 hours with very little break. All of my muscles were agitated and extremely sore and my feet were freezing, even with socks and many blankets. I struggled to get any sleep I could and finally got up at 05:30AM and moved to the sofa. I distracted myself with TV and had a cup of tea. The muscle disturbances and heart palpitations subsided at about 09:00am. I was able to get up and get some breakfast, but was completely wiped out all day. I was also emotional most of the day. I napped and in the evening went to bed. I slept Ok, but had a multitude of hotflashes then I had to be somewhere in the afternoon. I expended a little energy and broke out into a drenching sweat while I was out for only 2 hours. I went home and flopped on the sofa. No covid prior to vaccination. Covid test post vaccination. Normal supplements/vitamins taken daily for years. No other vaccine taken in four weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20220402; Test Name: Nasal Flow; Test Result: Negative; Comments: Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy (Known allergies: Onions); Food allergy; Lactose intolerant (Known allergies: lactose sensitive.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2286627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 14.04.2022
Beginn: 14.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure measurement Dizziness Hypotension

Symptomtext

dizziness; low blood pressure; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team). The reporter is the patient. A 71-year-old female patient received BNT162b2 (COMIRNATY), on 14Apr2022 at 10:45 as dose 4 (booster), single (Lot number: FK9894) at the age of 71 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "little light headed" (unspecified if ongoing), notes: Before she would get a little light headed and once every 4 months; "Pain" (unspecified if ongoing), notes: In the past, she has reacted to a drug supposed to be for pain. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot EN6206 expiration is unknown.Injected in left upper arm.), administration date: 03Mar2021, when the patient was 69-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE, Lot EN6204, expiration is unknown.Injected in left upper arm.), administration date: 24Mar2021, when the patient was 69-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3, SINGLE, Lot FE3590, expiration is unknown.Injected in left upper arm.), administration date: 21Oct2021, when the patient was 70-year-old, for COVID-19 Immunization. The following information was reported: DIZZINESS (non-serious) with onset 14Apr2022 at 13:30, outcome "not recovered"; HYPOTENSION (non-serious) with onset 14Apr2022 at 13:30, outcome "not recovered", described as "low blood pressure". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: Patient was asking whether Pfizer Covid-19 booster, batch FK9894, cause dizziness that won't subside within 3 hours of receiving the drug. It was stated that in a clinical study of participants 18 through 55 years of age, adverse reactions following administration of a first booster dose were pain at the injection site (83.0%), fatigue (63.7%), headache (48.4%), muscle pain (39.1%), chills (29.1%), joint pain (25.3%), lymphadenopathy (5.2%), nausea (0.7%), decreased appetite (0.3%), rash (0.3%), and pain in extremity (0.3%). No information specific to dizziness. A review of the Prescribing Information for <Pfizer Product Name> did not find information regarding dizziness. As the Prescribing Information does not include all adverse reactions that had been reported or that may occur, patient was asked to consult with the doctor/healthcare provider about what she had experienced/are experiencing. Because the doctor/healthcare provider was most familiar with her medical condition, clinical history, how her treatment had been conducted and any relevant information to her specific case, her doctor/healthcare provider was in the best position to advise about the appropriate action to take.Patient stated that she has been experiencing dizziness since then and has been persisting and wanted to know when the dizziness will go away. Patient was Informed that dizziness had not been associated with the vaccine and that the list does not include all possible side effects and was informed that systemic reactions usually lasted 1 day for patients 18 years and older. Patient was advised to consult with her doctor. Patient wanted to know if the serum she received on 14Apr2022 can damage her autoimmune system. Patient later clarified that she was referring to Pfizer COVID-19 Vaccine. Patient stated that she received the Pfizer COVID-19 Vaccine for her 1st and 2nd dose and 1st booster dose. Informed patient that there was no information on the Pfizer COVID-19 Vaccine causing damage to the immune system. Mechanism of action was that the vaccine elicits an immune response to the S antigen, which protects against COVID-19. Informed patient that the vaccine she received for her 2nd booster dose is the same as the ones she received before. Report was not related to a study or programme. No further Investigations. Pfizer COVID vaccine booster manufacturer was unspecified. NDC number of Pfizer COVID vaccine booster was Unknown. Expiry Date of Pfizer COVID vaccine booster was Unknown. Patient stated within 3 hours after receiving it, she was dizzy and so she had to go to bed because it was not safe to walk around and has been dizzy. 4th dose was injected in left upper arm. Patient said since that date, she had low blood pressure and it had not been bothering her. When it did, she would just eat more food. After the injection, she was getting dizzy almost constantly and went to a dietician and said she needed more protein 3 times a day and drink a lot of water. She has been following that method but is still dizzy. She said whenever she goes into her doctor, it has been low but not really diagnosed. When she let her know about the dizziness, she has not gotten back to her yet. Attempted to confirm when the low blood pressure first started when she started to notice it at the doctor's office and caller stated it was 14Apr2022. Attempted to clarify again and unable to clarify when she went to doctor and first noticed it as caller still stated 14Apr2022, which was the date she got the booster. Before she would get a little lightheaded and once every 4 months or so from the low blood pressure. Now it is constant. She wanted to know when will this dizziness will go away. She had been eating protein at least 60 a day for probably the last 3 weeks or so. She listened to a talk, and she talked about low blood pressure and eating protein. Vaccination Facility Type was Pharmacy. No additional Vaccines Administered on Same Date of the Pfizer Suspect. AE(s) does not require a visit to Emergency Room and Physician Office. No other vaccinations were received within four weeks prior to the first administration date of the suspect vaccine(s). No AE(s) following prior vaccinations. In the past, she has reacted to a drug that she cannot remember the name and is supposed to be for pain. It was 15 years ago. It keeps her awake 24 hours. She does not have a name, lot or expiration. Family Medical History Relevant to AE(s) was none. Relevant Tests was None. No follow-up attempts possible. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Date: 20220414; Test Name: Blood pressure; Result Unstructured Data: Test Result:Low; Comments: At 13:30
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Light headedness (Before she would get a little light headed and once every 4 months); Pain (In the past, she has reacted to a drug supposed to be for pain)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2278592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NE
Alter: 15,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 16.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site hypoaesthesia Injection site pain Tremor

Symptomtext

Patient received injection at 1508. Around 1528, patient states pain and numbness in right arm below injection site, along with shakiness in hand. Blood pressure taken at 1529, reading 120/62, pulse at 66, oxygen sat at 98%. Tylenol 500mg given with water and orange..

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2278546

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FK9894

moderat

Staat: WA
Alter: 59,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 05.04.2022
Beginn: 27.04.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Asthma COVID-19 Condition aggravated Laboratory test Pleurisy Vaccine breakthrough infection X-ray

Symptomtext

BREAK THROUGH COVID, 3 weeks after receiving the booster, (hence why I am completing this report) with intense asthma that required Urgent Care and turned into Pleurisy...Ongoing Nebulizer treatments and Prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Went to Urgent Care on 5/14/2022, did X Ray and other tests. Diagnosed with COVID Exacerbated Asthma and Pleurisy.
Aktuelle Erkrankungen: BREAK THROUGH COVID, 3 weeks after receiving the booster, (hence why I am completing this report) with intense asthma that required Urgent Care and turned into Pleurisy...Ongoing Nebulizer treatments and Prednisone.
Vorgeschichte: Diabetes, Chronic Obstructive Asthma, Discoid Lupus, OA, Trigeminal Neuralgia, IBS, Obesity
Andere Medikamente: amlodipine, buproprion, famotidine, hydrodhlorothiazide, hydrozychloroquine, losartan, methocarbamol, montelukast, omeprazole, simvastin, topiramate, trazadone, Symbicort, Albuterol (as needed), ipratropium nasal spray, Tylenol, Vitamin D,
Allergien: ergo derivitive medications, tegritol, some antibiotics, latex, (I couldn't find my list and your form timed out on me)
Vorherige Impfungen: -

VAERS 2273370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 61,0
Geschlecht: M
Eingang: 12.05.2022
Impfdatum: 28.02.2022
Beginn: 11.05.2022
Tage bis Beginn: 72,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Blood creatinine increased Hypotension Nausea Urinary tract infection White blood cell count increased

Symptomtext

Hosp admit for nausea and low blood pressure, no pneumonia, blood pressure dropped with fluids on norepinephrine. Probable UTI WBC in blood 42.6, Creatinine 3.9

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HIV, AIDS most recent CD4 11/21 was 19. CKD, ETOH Cirrhosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2271887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 59,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 13.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood electrolytes normal Dizziness Dyspnoea Electrocardiogram abnormal Supraventricular tachycardia Thyroid function test normal

Symptomtext

Experienced a first time episode of sustained Supraventricular Tachycardia (SVT) on 4/28/22, two weeks after the injection. No history of this previously. Heart rate was 240 and was treated with IV Adenosine in Emergency Room to convert rhythm after over an hour of SVT causing shortness of breath and dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG's - SVT, HR 240 tested electrolytes and Thyroid - all normal
Aktuelle Erkrankungen: None
Vorgeschichte: N/A
Andere Medikamente: Prozac 20 mg qd multivitamin Miralax Vit. D Meltonin
Allergien: Fosamax
Vorherige Impfungen: -

VAERS 2271585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 03.05.2022
Beginn: 04.05.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Cardiac discomfort Dyspnoea Mass Neck mass Pain in extremity

Symptomtext

The patient started developing lumps around her neck/shoulder, difficulty breathing, pressure on heart, and some arm pain the day after she got vaccination. Since these could be possible side effects from COVID19 vaccines, I recommended her to see her PCP as soon as possible and call 911 if breathing problem/pressure on heart get worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2271261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CT
Alter: 53,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 28.02.2022
Beginn: 28.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Breast pain Immediate post-injection reaction Injected limb mobility decreased Injection site pain Joint range of motion decreased Mobility decreased Tenderness

Symptomtext

Immediately after the vaccine, I felt pain at the injection site. The pain went all the way to my breast. It is so painful that I can not lift arms up and limited range of motion. It is very weak and is worse at nights. It is painful to the touch. Eventually the pain went away from breast area. I went to my doctor and waiting for approval from my insurance to get x-rays. The pain still continues to this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Future X-rays
Aktuelle Erkrankungen: None
Vorgeschichte: Psoriasis; Ankle injury
Andere Medikamente: Sertraline one shot every 3 months, Gabapentin, Venlafaxine, Lidocaine
Allergien: None
Vorherige Impfungen: -

VAERS 2270801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: MA
Alter: 68,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 19.04.2022
Beginn: 07.05.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chest pain Cough Fatigue Pain SARS-CoV-2 test positive

Symptomtext

On 05/07/2022 I developed body aches and a bit of a cough. The next day it was worse. I did a COVID-19 at home test that was negative. I did another at home test on 05/09/2022 and it was positive so I called my doctor and they prescribed me Paxlovid. I have been taking that ever since. I am still fatigued but my cough is better and the body aches are better. I was able to sleep last night without coughing. I also have a bit of sore ness in the right side of my chest. It was worse at the beginning but it getting better. I also have a bad taste in my mouth from the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: At Home COVID-19 tests (05/09/2022 & 05/10/2022)
Aktuelle Erkrankungen: None
Vorgeschichte: History of breast cancer
Andere Medikamente: Tamoxifen 20mg, Calcium, Vitamin D
Allergien: Sensitive to narcotic painkillers
Vorherige Impfungen: -

VAERS 2269136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: SC
Alter: 66,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 18.04.2022
Beginn: 03.05.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Eye pain Hypophagia Impaired work ability Migraine Nausea Vertigo Vomiting

Symptomtext

They started in the afternoon. I thought I was getting dizzy. I was working and thought the computer was moving. I thought that eating something would help but then the room started spinning and I was vomiting for the next 4-5 hours and nausea. My doctor suggested that it was migraine related since they are episodic. My eyes were hurting and I couldn't eat anything. The entire week all I ate was Jello and chicken broth. She had me take Advil, Zofran, Benadryl. It helped with the dizziness and I slept through the night. These symptoms have never happened with my migraines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism Osteoporosis
Andere Medikamente: Simvastatin Synthroid Loratadine Omeprazole Probiotic Breztri Inhaler Low Dose Aspirin CoQ10 Calcium with Vitamin D Vitamin D Niacin Advil
Allergien: Penicillin Augmentin Cefaclor
Vorherige Impfungen: -

VAERS 2269016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 10.05.2022
Beginn: 10.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Emotional distress Head discomfort Immediate post-injection reaction Paraesthesia oral

Symptomtext

Pt A&O x4. Communicates verbally. At 11:45AM pt stated she felt "tinging at the back of tongue and pressure on head" right after she received pfizer booster vaccine. Denies SOB. Denies pain. No emotional distress noted. VS taken at 11:48AM. BP 122/84, HR 72, RR 18, SpO2 98% RA. Crackers and water given. Pt recovered w/o difficulties. ER precautions given. Pt acknowledge understanding. Observed pt for another 15 min. Pt left at 11:53AM without assistance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2248066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Mobility decreased Pain in extremity Pain Pyrexia

Symptomtext

My arm got really sore and it still hurts to this day. I had a fever of 100.3 as well and I had some aches and pains. I thought the pain in my arm went away about a week ago, but now it has started back and the pain is going down to my elbow and forearm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: I had a really bad cold 03/17/2022.
Vorgeschichte: Asthma Arthritis Borderline High Cholesterol
Andere Medikamente: Fish oil (Nature Made) Women's 50+ multivitamin (Meijer Brand) Metamucil Tums natural Biotin
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2266574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: HI
Alter: 62,0
Geschlecht: M
Eingang: 07.05.2022
Impfdatum: 23.04.2022
Beginn: 24.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Dizziness

Symptomtext

dizziness, chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2264724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OR
Alter: 23,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood pressure increased Dizziness Hyperhidrosis Pallor Tachycardia Throat tightness Tremor

Symptomtext

PT RECEIVED SECOND DOSE OF PFIZER VACCINE. 10 MINS S/P ADMINISTRATION PT REPORTED FEELING DIZZY, LIGHTHEADED. THIS RN ASSISTED PT TO SUPINE POSITION UNTIL DIZZINESS DISSIPATED. PT POSITION IN BED, HIGH FOWLERS AND ASSISTED DRINKING WATER, APPLE JUICE AND GRANOLA BAR. PT APPEARED MILDLY DIAPHORETIC, WITH PALLOR AND SHAKINESS. PT'S FIANCE REPORTED THIS HAS HAPPENED TO PATIENT SEVERAL TIMES IN THE RECENT PAST. THIS RN ADVISED PT TO ESTABLISH PCP AS SHE DOES NOT CURRENTLY HAVE A PROVIDER. PT SPO2 WNL. TACHYCARDIC BPM 120BPM, ABLE TO REDUCE WITH CALMING TECHNIQUES. NO SOB, CYANOSIS OR DYSPNEA. AIRWAY APPEARS PATENT. PT STATES "IT FEELS LIKE MY THROAT IS SWELLING SHUT BUT I THINK IT IS ANXIETY." PT DID NOT APPEAR TO HAVE ANGIOEDMA, HIVES, CONSTRICTING OF AIRWAYS. PT ABLE TO CONVERSE COHERENTLY AND IS AAOX4. BP ELEVATED TO 188/90, HAS HAPPENED SITUATIONALLY BEFORE. PT STAYED 45 MINS SP VAX AND WAS ABLE TO LEAVE WALKING, UNASSISTED. SHE WAS ADVISED TO RETURN TO ER IF BREATHING BECAME DIFFICULT, HIVES APPEARED OR LOC CHANGED. REFUSED BENADRYL R/T PRIOR ADVERSE REACTION. THIS RN ATTRIBUTES REACTION TO ANXIETY, LACK OF ADEQUATE CALORIC CONSUMPTION THIS DAY AS WELL AS FEAR OF NEEDLES.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety
Andere Medikamente: none
Allergien: NKA
Vorherige Impfungen: -

VAERS 2264604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 44,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 12.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Injected limb mobility decreased Injection site pain Neuralgia Pain Pain in extremity Sensory disturbance Sensory loss

Symptomtext

3 days after her injection at 4/15/22 (10 PM) she had nerve pain down her left arm radiating to the shoulder/spine. Left index finger has continues to have decreased range of motion and sensation. She feels "zings" from her "funny bone" down to the finger.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2263962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: OH
Alter: 76,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood glucose normal Cold sweat Dizziness Hyperhidrosis Hypotension Swollen tongue Yawning

Symptomtext

Patient report being dizzy . The facility nurse took blood pressure and heart rate while I supported patient in her chair. She was sweating and clammy to the touch. I applied an ice pack on her neck and head . She yawned about 8 times in 90 seconds. Her blood pressure was very low. Since she was diabetic we checked her blood sugar and it was 190. She said several times she thought she was feeling better so we transferred her to the wellness center for more observation. The patient reported her tongue was swelling so I decided to administer epinephrine into her left thigh. The nurse called EMS to take over care at this point. The patient reported an improvement within minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: The patient was transported to Clinic . I spoke with patient 5/3/22 and she said she was given steroids and the hospital and they observed to make sure another dose of epinephrine was not needed. She was sent home on oral steroids for 5 days
Aktuelle Erkrankungen: none
Vorgeschichte: diabetes
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2262317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MN
Alter: 51,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 01.04.2022
Beginn: 27.04.2022
Tage bis Beginn: 26,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anxiety Blepharospasm Bowel movement irregularity Chills Diarrhoea Hypoaesthesia oral Paraesthesia Pruritus Tinnitus

Symptomtext

Shivers no fever, head tingling, left eye twitch, lower lip numbness, right ear buzzing, increased anxiety, itching mostly head and face, increased diarrhea and bowel movements

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: IBS Intercystial cystitis mental health
Vorgeschichte: IBS
Andere Medikamente: Pepcid 10mg Elmiron 100mg
Allergien: Sulphonamides
Vorherige Impfungen: Flu vaccine Nov. 2020 severe IBS vertigo flu like muscle fever problems

VAERS 2261915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 28.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Chest pain Chills Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Diarrhoea Extra dose administered Fatigue Fibrin D dimer increased Illness Musculoskeletal chest pain Pain Painful respiration Pyrexia Splenic infarction

Symptomtext

Splenic Infarct Patient is a 74 y.o. female presenting with left sided chest pain. She became very ill after receiving her second Pfizer COVID booster on 4/28 - an hour later, she developed fevers/chills, body aches, diarrhea, and fatigue. By 5/1, she began to develop a pain under her left rib that continued worsen and became unbearable tonight. This pain is worse especially with deep breathing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: d-dimer = 1.27 CT chest/abd/pelvis which showed a medium sized splenic infarct.
Aktuelle Erkrankungen: none
Vorgeschichte: ? Barrett esophagus ? Cataracts, bilateral ? Chronic pain knees ? Complication of anesthesia 2007 morphine caused vomiting x 13 days, sensitive to narcotics pulse oximetry drops, during hyst and knee replacement ? Depression due to pain ? DJD (degenerative joint disease) knees ? Environmental allergies ? Frontal sinus fracture (HCC-CMS) ? Herpes genitalis in women ? Hypertension ? Hypothyroid ? Motion sickness ? Post-operative nausea and vomiting
Andere Medikamente: -
Allergien: morphine, tigan, Bee venom
Vorherige Impfungen: -

VAERS 2261781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: AZ
Alter: 60,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 28.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Epistaxis Fatigue Headache Tendonitis

Symptomtext

Patient reported a nosebleed, starting the night of the vaccine and lasting for a day. Also reports fatigue, headache and exacerbation of tendonitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: none
Allergien: no known allergy
Vorherige Impfungen: reports similar symptoms with the first 2 doses of COVID pfizer vaccine (received on 4/14/2021 and 5/3/2021), received at age 59

VAERS 2260072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NV
Alter: 53,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 15.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Dyspnoea Wheezing

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Shortness of breath, wheezing-Severe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: KS
Alter: 16,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 26.04.2022
Beginn: 26.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Aggression Axillary pain Depressed mood Dyspnoea Injection site rash Irritability Muscular weakness Rash Rash erythematous

Symptomtext

within 2 hours after the shot Mom and pt noted aggressive, depressed, irritable [not suicidal], left armpit felt sore, l. arm felt weak at times, felt short of breath at times. red non-itchy rash across chest/left face/left shoulder today after school.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none, normal exam today in office
Aktuelle Erkrankungen: none
Vorgeschichte: allergic rhinitis, asthma, past allergy shots
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2252298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NV
Alter: 65,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 17.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Electrocardiogram Supraventricular tachycardia

Symptomtext

I developed SVT two days after receiving the vaccine. I have had this before, but it always quit after two doses of metoprolol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: -
Labordaten: EKG on my Watch.
Aktuelle Erkrankungen: Otherwise healthy.
Vorgeschichte: Hypertension, hypertcholesteremia, seasaonal affective disorder, Type 2 DM
Andere Medikamente: Ramipril 20 mg Qday Allopurinol 300 mg Qday Atorvastatin 20 mg Qday Omeprazole 20 mg Qday Escitalopram 5 mg Qday Metformin 1000 mg BID Freestyle Libre 2 Multivitamin Qday Aspirin 81 mg Qday
Allergien: None
Vorherige Impfungen: -

VAERS 2250098

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: IN
Alter: 64,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 22.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Paraesthesia Vision blurred

Symptomtext

Patient states at approximately 9pm on the evening of receiving her Pfizer Covid booster that she begin having blurry vision that lasted approximately 15 minutes. Patient also states that she began having left arm and leg numbness on the same evening. Patient states that the blurry vision resolved, but patient still have some numbness and tingling in the left arm and leg after 3 days. Patient advised to contact PCP today about these issues as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2249690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NJ
Alter: 73,0
Geschlecht: F
Eingang: 24.04.2022
Impfdatum: 20.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injected limb mobility decreased Injection site erythema Injection site swelling Injection site warmth Lymph node pain Lymphadenopathy

Symptomtext

Injection site: 8 inch long by 8 inch wide , bright red, hard, hot, swollen, very painful. Woke me up in the middle of the night. Can?t lift my left arm. Two large painful lymph nodes under my left armpit

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Crestor 10mg
Allergien: None
Vorherige Impfungen: -

VAERS 2248050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NJ
Alter: 78,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 31.03.2022
Beginn: 01.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cardiac flutter Chest X-ray normal Dyspnoea Full blood count normal Haemoglobin decreased Hunger

Symptomtext

Labored breathing, starting early in morning... erratic, on and off throughout the day... Sometimes with "fluttery" chest - like "frantic" when very hungry. Persisted for about 10 days. Note: When outside, visiting doctor, or having dinner with friends had ABSOLUTELY no labored breathing. Steps taken to mitigate/or explain: - tested Pulse-ox frequently - always within 94 to 98 (normal for me) - Used Albuterol occasionally, to no effect. - Visited PCP and Pulmonologist. - Had Chest X-ray and CBC (both within normal limits, no changes from previous tests) - temperature 97.x (normal for me) - BP 129/72 (normal for me) - PCP and resident at office visit said not related to COPD (not a flare) - Pulmonologist agreed - Tried decaf coffee (no change) - Changed Stiolto medication (new on same day as vaccine) BACK to Anoro (no change) - Turned off ionizer in apartment (part of an air filter) - no change - Opened doors and windows in apartment to freshen air - no change Symptom disappeared at about 10 days after onset. Flew to state (no breathing problem on plane) - six days there, no problem. Returned home 4/20, still no problem. Note: had three previous Covid vaccines with only sore arm on third (August 2021), when done with Flu vaccine (other arm) No other Covid vaccine reactions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 4/8/2022 - CBC, Chest X-ray, visits to PCP and Pulmonologist - CBC - normal for me : Hemoglobin 10.2 - Chest X-ray - within normal limits (no change from last, 2021) Had changed Anoro (COPD med) to Stiolto (4/1/2022) for one week or so. Changed back to Anoro 4/8/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Emphysema - MDS-SL (Hemoglobin)
Andere Medikamente: Stiolto (for Emphysema) - Vytorin (statin) - Vitamin D, Vitamin B12, Mucinex, Baby Aspirin, CoQ10
Allergien: None
Vorherige Impfungen: Very sore left arm for a few hours Pfizer -FC3183 8/19/2021 age 77 Same day as Flu vaccine (other arm) also VERY sore for a few

VAERS 2245991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: WA
Alter: 77,0
Geschlecht: M
Eingang: 21.04.2022
Impfdatum: 20.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Computerised tomogram head abnormal Condition aggravated Depressed level of consciousness Peripheral swelling Subdural haematoma Tenderness

Symptomtext

Right hand swelling, mild tenderness to palpation. Had subdural hematoma 2 weeks ago, has been having decline in LOC, sent back to ED, CT showed worsening subdural hematoma. Right arm swelling may not have been related to vaccine. Arm swelling not the main reason he was sent to the ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Subdural hemorrhage, NSTEMI
Vorgeschichte: HTN, CHF, GERD, T2DM, RA, CKD
Andere Medikamente: Glimepiride, Tramadol, Memantine, Sertraline, Risperidone, carvedilol, levetiracetam, hydralazine, omeprazole, acetaminophen, atorvastatin, Vit B
Allergien: Latex, Regadenoson, Sulfa, Nitrates
Vorherige Impfungen: -

VAERS 2245870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: AZ
Alter: 85,0
Geschlecht: M
Eingang: 21.04.2022
Impfdatum: 30.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Hypertension

Symptomtext

I did not noticed anything on 03/30/22 after getting my vaccine. On April 3, 2022 I went to the emergency room. My blood pressure was starting to get high. I measure my blood pressure regularly. I did not have any sick symptoms just the high blood pressure. The doctor at the emergency room stated that he thought it would be related to the booster shot. The doctor did give me a pill at the ER. It brought my blood pressure down in about 30 minutes and I was sent back home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: History of blocked heart arteries (quadruple by-pass and stint placement)
Andere Medikamente: Metoprolol, Lisinopril, Brilinta, Baby Aspirin, Atorvastatin, Levothyroxine, Tamsulosin, Hydrocodone
Allergien: None
Vorherige Impfungen: -

VAERS 2245824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 01.04.2022
Beginn: 12.04.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia Blood glucose normal Brain natriuretic peptide increased Cardiac telemetry Chest X-ray Chest pain Computerised tomogram thorax Dizziness Electrocardiogram Fatigue Feeling abnormal Feeling drunk Haemoglobin decreased Head discomfort Headache Hypertension Influenza A virus test negative Influenza B virus test

Symptomtext

After I got the vaccine, I was really tired more than normal. I didn't feel good at all. I had a headache off and on. Then starting on 4/12/2022, I woke up and I was really lightheaded and dizzy. I felt like I was drunk. I didn't know what to think. My blood pressure was fine when I checked it. I started getting nauseas from the dizziness to the point where I threw up. I took Zofran to stop throwing up. The dizziness continued. I took it easy the rest of the day. The next day I was dizzier and it was worse. I had ordered groceries to be delivered to my home, and I wasn't even able to pick up my groceries because I felt weak. I felt like something was pushing down on my head. That night I had chest pains. On 4/14/2022 I was still having chest pains so I took some Nitro medication, and then the chest pain went away. I called the doctor and they never got back to me. Then I called my family doctor and he told me to call the emergency number because when I checked my blood pressure it was higher than normal. The ambulance came and took me to the hospital. The ER thought I was having a heart attack because they said that my troponin levels in my blood was high, but they actually mixed up my blood work with someone else's results. So, then it was said that I wasn't having a heart attack. The doctor's said that since I been sick with bronchitis the infection could have traveled to my ear which could cause the dizziness. I was at the hospital for 1 night. My blood pressure went up to 185 or 187 over 103. Then it went down to 175 over something. The doctor said I could go home, but I still had a high blood pressure reading so I didn't feel comfortable going home. I'm back home and sometimes my blood pressure reads up to 140 over something. I was prescribed meclizine 12.5mg 3xday up to 10 days as needed for dizziness. I have a home nurse who is going to monitor my blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: Chest X-ray; CT scan of chest and lungs with dye; Cardiac Telemetry; Rapid COVID-19 Test- negative; Influenza A & B Test- negative; EKG; Lab work- brain natriuretic peptide was high at 162 pg/ml when normal range is less than 125 pg/ml but informed not to worry until it's over 1000 or 2000, RBCs was 3.80 when standard range is 4 to 5.2. My hemoglobin HGB was 11.8 g/dL when normal is 12-16 g/dL, my Glucose was high at 132 mg/dL when normal is74/109 mg/dL, my total protein was low at 6.3 mg/dL when normal is 6.4-8.3g/dL
Aktuelle Erkrankungen: Bronchitis
Vorgeschichte: Fibromyalgia; COPD; Emphysema; Interstitial Lung Disease; Mild Heart Failure; Coronary Artery Disease Sclerosis; Obese; Thoracic Aorta Aneurism; GERD; Connective Tissue Disease; Sjogren's Syndrome; High Blood Pressure; Hypothyroidism; Dyslipidemia; Facet Arthritis; Mild Obstructive Sleep Apnea; Depression; Deviated Nasal Septum; Pancreatic Lesion; Degenerative Disc Disease; Cervical Spondylosis; Hypogammaglobulinemia; Fatigue; Elevation of ACTH; Small Intestinal Bacteria Overgrowth; Unspecified Adrenocortical Insufficiency; Vertigo; Osteopenia; Coronary Artery Spasms; Supraventricular Tachycardia; Bowel and Bladder Incontinence
Andere Medikamente: Tylenol 2xday, Potassium 20MEQs 1xday, Myrbetriq 50mg 1xday, Diltiazem ER 240mg 1xday, Evoxac 30mg 3xday, Zyrtec 10mg 1xday, Ecotrin 325mg 1xday, Lyrica 75mg 2xday, Duloxetine Cymbalta 60mg 1xday, Trazadone 75mg 1xday, Chlorthalidone 25mg 1
Allergien: Clindamycin; Augmentin; Dust; Tape Adhesives; Dye
Vorherige Impfungen: COVID-19 (1st dose): I was sick for a week. (2/2/2021)

VAERS 2245722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: TX
Alter: 14,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 18.04.2022
Beginn: 18.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dyspnoea

Symptomtext

evening of injection (4/18) patient also experienced shorntess of breath without increased work of breathing (retractions, accessory muscle use, head bobbing, tripod positioning etc.)- an unexpected reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: IN
Alter: 60,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 12.04.2022
Beginn: 12.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Discomfort Flushing Insomnia Lymph node pain Pain Paraesthesia Swelling Vaccination site mass Vaccination site pain

Symptomtext

Today, the third day the soreness is a little more noticeable, feels like a small knot (that wasn't there before); feels like a small knot (that wasn't there before); slight swelling; weakness; some injection site pain; soreness to the lymph nodes under my right arm (same side as the injection); slight tingling in my forearm; felt flushed; uncomfortable trying to sleep; uncomfortable; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Apr2022 at 12:30 as dose 1, single (Lot number: FK9894) at the age of 60 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Clippers Syndrome" (unspecified if ongoing); "High blood pressure" (unspecified if ongoing); "Diabetes" (unspecified if ongoing); "Food allergies: Fish" (unspecified if ongoing); "Food allergies: Mushrooms" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: FLUSHING (non-serious) with onset 12Apr2022, outcome "not recovered", described as "felt flushed"; DISCOMFORT (non-serious) with onset 12Apr2022, outcome "not recovered", described as "uncomfortable"; INSOMNIA (non-serious) with onset 12Apr2022, outcome "not recovered", described as "uncomfortable trying to sleep"; PARAESTHESIA (non-serious) with onset 12Apr2022 at 18:30, outcome "recovered" (12Apr2022 at 18:35), described as "slight tingling in my forearm"; VACCINATION SITE PAIN (non-serious) with onset 13Apr2022 at 18:30, outcome "not recovered", described as "some injection site pain"; LYMPH NODE PAIN (non-serious) with onset 13Apr2022 at 18:30, outcome "not recovered", described as "soreness to the lymph nodes under my right arm (same side as the injection)"; PAIN (non-serious) with onset 14Apr2022, outcome "not recovered", described as "Today, the third day the soreness is a little more noticeable, feels like a small knot (that wasn't there before)"; VACCINATION SITE MASS (non-serious) with onset 14Apr2022, outcome "not recovered", described as "feels like a small knot (that wasn't there before)"; SWELLING (non-serious) with onset 14Apr2022, outcome "not recovered", described as "slight swelling"; ASTHENIA (non-serious) with onset 14Apr2022, outcome "not recovered", described as "weakness". Therapeutic measures were not taken as a result of paraesthesia, flushing, insomnia, vaccination site mass, swelling, asthenia. Therapeutic measures were taken as a result of discomfort, vaccination site pain, lymph node pain, pain. Additional Information: Patient received no other vaccine in four weeks. Patient received other medications in two weeks. After the shot, patient experienced a slight tingling in forearm, but only for about 5 minutes and it dissipated. That night, patient felt flushed but no fever and was uncomfortable trying to sleep. Upon waking up patient had some injection site pain and noticed soreness to the lymph nodes under right arm (same side as the injection). Today, the third day the soreness is a little more noticeable, feels like a small knot (that wasn't there before) and slight swelling and weakness. Patient was uncomfortable and can't really lay down on that side. Patient took ibuprofen for the discomfort, but it really did not help with the soreness. Patient had no COVID prior vaccination. Patient was not tested for COVID post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; CLIPPERS syndrome; Diabetes; Fish allergy; Food allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2242046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 14.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Blood urine present Migraine Plasmapheresis Platelet count decreased Spinal pain Thrombotic thrombocytopenic purpura

Symptomtext

Migraine, spinal pain, blood in urine, TTP, hospitalization starting 4/17/2022, began plasma dialysis 4/18/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: 10,0
Labordaten: Blood platelet 4/17/2022 - 25 Blood platelet 4/18/2022 - 17 Blood platelet 4/19/2022 - 16
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prozac 40mg
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2242046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 14.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Blood urine present Migraine Plasmapheresis Platelet count decreased Spinal pain Thrombotic thrombocytopenic purpura

Symptomtext

Migraine, spinal pain, blood in urine, TTP, hospitalization starting 4/17/2022, began plasma dialysis 4/18/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: 10,0
Labordaten: Blood platelet 4/17/2022 - 25 Blood platelet 4/18/2022 - 17 Blood platelet 4/19/2022 - 16
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prozac 40mg
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2238845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: ND
Alter: 69,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 08.04.2022
Beginn: 10.04.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Blood test Chest X-ray Computerised tomogram Decreased appetite Dizziness Electrolyte imbalance Fatigue Magnetic resonance imaging head Tremor

Symptomtext

patient presented via ambulance with complaints of generalized weakness and shakiness. decreased appetite, fatigue and lightheadedness. tremors bilateral upper extremities. mild electrolyte imbalance, however Dr. documented that this does not explain the etiology of these symptoms and that this may be vaccination related. patient now is unable to return home and needs nursing home placement related to the change in functional status

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: blood work, CT, CXR, brain MRI
Aktuelle Erkrankungen: none
Vorgeschichte: hyperlipidemia, HTN, CVA, anxiety, depression, bipolar, DMII, hypothyroidism
Andere Medikamente: divalproex sodium 500mg PO bedtime, ubidecarenone (Co-q 10) 400mg PO daily, risperidone 2mg PO Bedtime, lamotrigine 12.5 PO bedtime, atorvastatin 20mg PO daily, amlodipine besylate 10mg PO daily, metformin 500mg BID, potassium Chloride 20m
Allergien: erythromycin base, penicillins, ciprofloxacin, doxycycline, ibuprofen, olanzapine
Vorherige Impfungen: -

VAERS 2238099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 08.04.2022
Beginn: 09.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Hypertension

Symptomtext

Very high blood pressure requiring hospitalization

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: arthritis in both knees
Vorgeschichte: arthritis in both knees depression highbloodpressure hypothyroidism spinal stenosis
Andere Medikamente: aspirin 81mg by mouth daily escitalopram oxalate 20mg by mouth daily levothyroxine 50mcg by mouth daily before breakfast lisinopril 10mg by mouth once daily naproxin 500 mg one tablet twice per day as needed
Allergien: none, but I have had reaction to each of the 3 prior COVID vaccines
Vorherige Impfungen: Reaction of extreme tiredness, feeling ill from other 3 Pfizer covid vaccinations

VAERS 2237993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 11.04.2022
Beginn: 12.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Migraine Pain Vaccination site pain

Symptomtext

Felt sore at site in the morning; gradually got more body soreness; got a migraine headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 58-year-old female patient received BNT162b2 (BNT162B2), on 11Apr2022 at 18:00 as dose 4 (booster), single (Lot number: FK9894) at the age of 58 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (dose number: 3, lot number: Ff2590, administrator route: Intramuscular, administration date: 08Oct2021, vaccine location: Left arm), administration date: 08Oct2021, when the patient was 58-year-old, for Covid-19 immunization; Covid-19 vaccine (Dose 2, Manufacturer Unknown), for Covid-19 immunization; Covid-19 vaccine (Dose 1, Manufacturer Unknown), for Covid-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 12Apr2022, outcome "recovering", described as "Felt sore at site in the morning"; MIGRAINE (non-serious) with onset 12Apr2022, outcome "recovered" (Apr2022), described as "got a migraine headache"; PAIN (non-serious) with onset 12Apr2022, outcome "recovered" (Apr2022), described as "gradually got more body soreness". Therapeutic measures were not taken as a result of vaccination site pain. Therapeutic measures were taken as a result of pain, migraine. Additional information: If covid prior vaccination: No. If covid tested post vaccination: No. Got vaccine at 6PM on 11Apr2022. Felt sore at site in the morning of 12Apr2022, gradually got more body soreness and took Advil at 10AM with good results. At 5PM soreness gradually came back and got a migraine headache. Took Advil at 8PM and slept through the night. Only experiencing site soreness on morning of 13Apr2202 and went to work. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2237861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fk9894

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Balance disorder Decreased appetite Diarrhoea Dizziness Fatigue Headache Malaise Nausea SARS-CoV-2 test Tremor Vaccination site pain

Symptomtext

injection pain; Diarrhea; nausea; weakness; trembling; light headed; loss of appetite; headache; tiredness; loss of balance; feeling unwell; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient received BNT162b2 (BNT162B2), on 07Apr2022 at 13:00 as dose 1, single (Lot number: Fk9894) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes mellitus" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN; ATORVASTATIN; GLIPIZIDE; FAMOTIDINE; BENTYL. The following information was reported: DIARRHOEA (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "Diarrhea"; MALAISE (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "feeling unwell"; HEADACHE (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering"; VACCINATION SITE PAIN (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "injection pain"; DIZZINESS (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "light headed"; DECREASED APPETITE (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "loss of appetite"; BALANCE DISORDER (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "loss of balance"; NAUSEA (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering"; FATIGUE (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "tiredness"; TREMOR (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "trembling"; ASTHENIA (non-serious) with onset 07Apr2022 at 16:00, outcome "recovering", described as "weakness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site pain, diarrhoea, nausea, asthenia, tremor, dizziness, decreased appetite, headache, fatigue, balance disorder, malaise. Additional information: The clinical course was reported as the patient had not other vaccine in 4 weeks. Patient had other medication in 2 weeks with metformin, atorvastatin, glipizide, famotidine and bentyl. Patient had covid prior to vaccination and had covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20220409; Test Name: Self test at home; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Sulfonamide allergy
Andere Medikamente: METFORMIN; ATORVASTATIN; GLIPIZIDE; FAMOTIDINE; BENTYL
Allergien: -
Vorherige Impfungen: -

VAERS 2237664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 78,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 31.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Bone pain Breast pain Breast tenderness Chills Investigation Myalgia Night sweats Tremor

Symptomtext

Breasts feeling sore; She is so weak; Tender breasts; Muscles and bones hurting; Muscles and bones hurting; Night sweats; Chills; Severe shaking; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 78 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 31Mar2022 10:00 (Lot number: FK9894) at the age of 78 years as dose 4 (booster), single for covid-19 immunisation; tamoxifen (TAMOXIFEN) (Lot number: BK4844658, Expiration Date: 20Dec2022) at 20 mg 1x/day for breast cancer. Relevant medical history included: "Breast cancer" (unspecified if ongoing), notes: Breast cancer; "Asthma" (unspecified if ongoing), notes: Asthma; "Drug sensitive" (unspecified if ongoing), notes: Drug sensitive; "Immune compromised" (unspecified if ongoing), notes: Immune compromised, has breast cancer; "Irregular heart beat" (unspecified if ongoing), notes: Irregular heart beat; "COVID-19", start date: 2020 (unspecified if ongoing), notes: She knows that beginning of 2020 all of this came down and she had Covid. Clarified that she had Covid prior to getting the Covid vaccines.; "She didn't have was the taste and smell", start date: 2020 (unspecified if ongoing), notes: The only thing she didn't have was the taste and smell.; "She didn't have was the taste and smell", start date: 2020 (unspecified if ongoing), notes: The only thing she didn't have was the taste and smell.; "Brain fog", start date: Feb2020 (unspecified if ongoing), notes: she has brain fog too which she has had since she got it in Feb2020; "Ill" (unspecified if ongoing), notes: She was ill and in bed for 3 weeks; "Osteoporosis" (unspecified if ongoing), notes: she has to take Prolia every 6 months for osteoporosis; "Sleep" (unspecified if ongoing), notes: Sleep. Concomitant medication(s) included: PRADAXA; METOPROLOL TARTRATE taken for heart rate irregular; SINGULAIR taken for asthma; ADVAIR; REMERON taken for sleep disorder; FLUTICASONE; PROLIA. Vaccination history included: Covid-19 vaccine (Dose: 1, LOT: EL9261, MANUFACTURER UNKNOWN, Route, Anatomical Location: left arm, below the shoulder), administration date: 24Jan2021, when the patient was 77 years old, for COVID-19 Immunization; Covid-19 vaccine (Dose: 2, LOT: EN6701 or EN6201, MANUFACTURER UNKNOWN, Route, Anatomical Location: left arm, below the shoulder), administration date: 15Feb2021, when the patient was 77 years old, for COVID-19 Immunization; Covid-19 vaccine (Dose: 3, First Booster, LOT: 301556A, MANUFACTURER UNKNOWN, Route, Anatomical Location: left arm, below the shoulder), administration date: 04Oct2021, when the patient was 78 years old, for COVID-19 Immunization, reaction(s): "Sore arm". The following information was reported: NIGHT SWEATS (non-serious) with onset 31Mar2022 21:00, outcome "not recovered", described as "Night sweats"; CHILLS (non-serious) with onset 31Mar2022 21:00, outcome "recovering", described as "Chills"; TREMOR (non-serious) with onset 31Mar2022 21:00, outcome "unknown", described as "Severe shaking"; BREAST PAIN (non-serious), outcome "unknown", described as "Breasts feeling sore"; ASTHENIA (non-serious), outcome "unknown", described as "She is so weak"; BREAST TENDERNESS (non-serious), outcome "unknown", described as "Tender breasts"; BONE PAIN (non-serious), MYALGIA (non-serious), outcome "recovered" and all described as "Muscles and bones hurting". Relevant laboratory tests and procedures are available in the appropriate section. The action taken for tamoxifen was unknown. Therapeutic measures were not taken as a result of night sweats, chills, breast pain, asthenia, breast tenderness. Therapeutic measures were taken as a result of tremor, bone pain, myalgia. Additional information : Product Note : Additional Information for Other medicines Metoprolol Tartrate: Start Date: Unknown, when she went to the ER, and everything happened, she had to have these 2 medicines and had atrial fibrillation. RMH Covid-19 note : She knows that beginning of 2020 all of this came down and she had Covid. Clarified that she had Covid prior to getting the Covid vaccines. Caller states she had the fourth vaccine, the booster, last Thursday and she is very drug sensitive. When she had the third one, she had similar side effects but it wasn't that terrible. Her husband had it and nothing happened to him. She had night sweats and just had the chills. She woke up for 3 and a half, our days, ringing out wet hair and her sheets. She was just concerned about the chills and the shaking. Clarified that the vaccine, booster being referred to is the Pfizer Covid vaccine booster. Patient Details: Age adverse event(s) started: Caller states she is 78, 78 and is going to be 79. Weight: 156. Caller states she has to lose 10 pounds before her big trip. Caller states she is going to call him next and find out why she has been having this. She had these night sweats for so long and she had breast cancer and is also taking Tomaxafin. She is just wondering if that might have something to do with this. She has been getting tender breasts and has been taking this medication for a year and hasn't had that before. She states that if someone is going to get something, it is going to be her. She is so drug sensitive. Caller states that the telephone number for this provider is the number for (Facility withheld), and states that she does not have his direct number. Event Details: Night sweats, chills, shaking: Caller states she had her booster Thursday and states they started that night. She had the shot at 10 in the morning, or so. About 9:00pm that night, she just started with severe shaking. She went to bed that night and when she woke up, her hair was all wet, as well as her sheets. Today is the first day it has gotten better. She still has the night sweats but the chills have gotten better. Caller states that Thursday night, Friday and Saturday, she had these symptoms. Last night, she had the sweats but they were not as severe as the night before. Treatment: No, because of the severe shaking and muscles and bones hurting, she took 2 Tylenol. She states she is very careful and took just 2 extra strength Tylenol, only on that Thursday night. Clarified she is not experiencing the muscle and bones hurting anymore. Concomitant Products/medical conditions: Caller states she is just old and is just loaded with those darn pills. She knows they are for her health. She knows that beginning of 2020 all of this came down and she had Covid. The only thing she didn't have was the taste and smell. Clarified that she had Covid prior to getting the Covid vaccines. Suspect Products: Tamoxifen: Caller states this is her cancer medication that she will have to take for 5 years. Clarified that she thinks this might have been the Tomoxifen because, her breasts were feeling sore and states this medication is hormonal and stops the hormones. Start Date: Caller states she started taking it one year ago. LOT: Caller provides the number BK4844658, stating it might be the lot number. NDC: Unknown EXP: Caller provides discard by date of 20Dec 2022 Clarified this medication is in pharmacy prescription bottle. Manufacturer Name: Unknown Caller states that is just states it is generic for Nolvadex. Clarified she is taking the generic medication, the Tamoxifen. Caller states it is a hormone receptor. Caller states there are 2 other medications she takes at night. She knows that it had to do with Covid. That is when she started taking most of this stuff. She states she has brain fog too which she has had since she got it in Feb2020. She was ill and in bed for 3 weeks and was on nebulizers. Clarified she was referring to when she actually had Covid and not regarding the Covid vaccine. Tests: Caller states she has to take Prolia every 6 months for osteoporosis. She just had it a few months ago and has had no problems at all.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: Prolia; Result Unstructured Data: Test Result:Unknown results; Comments: Tests: she has to take Prolia every 6 months for osteoporosis
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Breast cancer; COVID-19; Drug hypersensitivity (Drug sensitive); Foggy feeling in head (she has brain fog too which she has had since she got it in Feb2020); Heartbeats irregular (Irregular heart beat); Illness (She was ill and in bed for 3 weeks); Immune system disorder (Immune compromised, has breast cancer); Osteoporosis (she has to take Prolia every 6 months for osteoporosis); Sleep disorder (Sleep); Smell loss (The only thing she didn't have was the taste and smell.); Taste loss (The only thing she didn't have was the taste and smell.)
Andere Medikamente: PRADAXA; METOPROLOL TARTRATE; SINGULAIR; ADVAIR; REMERON; FLUTICASONE; PROLIA
Allergien: -
Vorherige Impfungen: -

VAERS 2231413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MI
Alter: 51,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 13.04.2022
Beginn: 13.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dyspnoea Feeling abnormal Hyperhidrosis

Symptomtext

10 minutes after administration, client reported feeling strange, describing lightheaded and short of breath. Appeared diaphoretic. Vital signs 154/100, RR 22, HR 82. Client used albuterol rescue inhaler, reported some improvement of breathing. Given snack and water, rested five more minutes, vital signs 141/92, hr 72, rt 20. Encouraged pursed lip breathing and to lean forward to ease respiratory effort. Client stated she needed to catch her bus going home and was advised to contact her doctor if symptoms persisted or seek emergency care if worsening of respiration not eased by her prescribed meds. Client had just seen her doctor, agreed to call the office as needed. Follow up phone call at 3:30 PM, Mailbox full could not leave a voice message

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: BP 154/100 at 2:35 pm, hr 82, rt 22. At 2:50, recheck, 141/92, hr 78, rt 20.
Aktuelle Erkrankungen: None reported
Vorgeschichte: COPD, former smoker, at least 30 years, per Client estimate. Stroke two years ago with some residual sensory deficit on right side, primarily upper extremity. Hypertension and T2DM, under care of her pcp (Whom she saw this morning prior to immunization)
Andere Medikamente: Oral anti-glycemic, client did not remember name medicine; did not take her blood pressure medicine that morning, did not remember the name of it and had albuterol inhaler with her
Allergien: Client Denied
Vorherige Impfungen: -

VAERS 2228608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia Dizziness Extra dose administered Injection site rash Injection site reaction Lethargy Skin lesion Tremor

Symptomtext

Patient described severe body shaking, followed by lethargy and the feeling of imminent loss of consciousness at which time her husband had to help lower her to the floor where she lay while the husband wiped her head with a cold washcloth and contemplated calling 911. Patient gained strength after 30-45 minutes and 911 was not called. Patient went to bed and woke up with lesions/rash encompassing a significant portion of her upper arm around the injection site. All was resolved within a few days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2228558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: UT
Alter: 62,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Headache Heart rate increased Lip swelling Nausea Pain in extremity Peripheral coldness Tremor

Symptomtext

Extreme arm pain, lip swelling, extreme nauseas, bad weakness, extreme head ache, excessive tremors shaking uncontrollably, hands were really cold, high heart rate, took 2 ibuprofen 400mg total

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no
Vorgeschichte: cataracts, glaucoma (close angel)
Andere Medikamente: calcium/D3 1200mg daily, vit. c 500mg daily, turmeric 500mg daily, magnesium 500mg (oxide)
Allergien: bees, fire ants, bull ants, biting bugs, latex, penicillin (amoxicillin), guava
Vorherige Impfungen: Flu vaccine in 1995 (approx)

VAERS 2225423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: IN
Alter: 63,0
Geschlecht: F
Eingang: 10.04.2022
Impfdatum: 08.04.2022
Beginn: 10.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Oedema peripheral Tenderness

Symptomtext

Swollen and sore to touch under left arm which is the arm I received the injection in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteopenia, Arthritis
Andere Medikamente: Sertraline, Famotidine, Meloxicam, Fish Oil, Osteo Bi-Flex, Citracal, Multivitamin, Alendronate
Allergien: Penicillin
Vorherige Impfungen: Swelling under the arm of the injection site arm.

VAERS 2225303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: ME
Alter: 82,0
Geschlecht: M
Eingang: 09.04.2022
Impfdatum: 04.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 1,0
Dosis: 7+
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Fatigue Somnolence Tremor

Symptomtext

Chills, shakes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: diltiazem ER, pantoprazole sodium, potassium chloride, hydrochlorothiazide, isosorbide, doxazosin, losartan potassium and others but running out of time
Allergien: hydrocodone lisinopril milk products
Vorherige Impfungen: Tired and slept most of the day. Which I also had with the most recent shot

VAERS 2219976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 03.04.2022
Beginn: 03.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dyspnoea Hypoaesthesia Tachycardia

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tachycardia-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2219878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: MT
Alter: 40,0
Geschlecht: U
Eingang: 07.04.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40 year-old patient received bnt162b2 (BNT162B2) (Lot number: FK9894) at the age of 40 years as dose number unknown, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: CONDITION AGGRAVATED (non-serious), outcome "not recovered", described as "lot of itching under my skin; I got some itching before the COVID shot very worse, it is reduce some since the COVID shot but it's still pretty bad." Additional information: Consumer stated, I have been learning about, for artificial intelligence since been years for a long time and I'm lot of itching under my skin itself, quite a while I reported it with the last questionnaire (Further clarifications unknown) I have got from you guys but I just also got a COVID shot 'from one' and trying to help with the itching over time (Further clarifications unknown). On paraphrasing: Consumer stated, "I don't have lot of yes, I have had itching before it though too from other things (Further not clarified hence captured as unspecified product) from Pfizer (Hence manufacturer checked). I had, my dad died a few years ago (Further clarifications unknown) and I was, When was it, when was it '2000' that's the case I have, the claim I have right now but I claimed with Pfizer that's what I 'kind of like send you is to' talk somebody with artificial intelligence divisions by the way from Pfizer, so that's kind of who I was trying to talk with but alright (Further clarifications unknown)." When probed to clarify if consumer has any questions regarding it or consumer wants to report it: Consumer stated, "Yes I want to report the issue, yes I got some itching before the COVID shot very worse, it is reduce some since the COVID shot but it's still pretty bad, 'since reported' and I finally got my first one." No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2216689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: TX
Alter: 72,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 25.03.2022
Beginn: 05.04.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Dyspnoea Feeling abnormal Pain Rectal haemorrhage Visual impairment

Symptomtext

Pt said she felt like she "was dying". Said she's always been healthy up until the vaccine. When I talked to her on the phone, she sounded like she had trouble breathing. She said her vision is dim, has rectal bleeding, body aches. I advised she seek medical help immediately, but she said she doesn't have a primary provider. I told her to go to emergency room or urgent care

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2213140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: IN
Alter: 71,0
Geschlecht: M
Eingang: 02.04.2022
Impfdatum: 31.03.2022
Beginn: 01.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Fatigue Mobility decreased Renal pain

Symptomtext

Friday woke up very tired and very sore joints (like i had been packpacking overnight) ... fatigued easily - stayed in bed all day. took ibuprofen at ~ 2am Saturday and felt a little better. by Saturday morning most of symptoms were gone - except sore kidneys. took a steam bath and that helped

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Losartan Potassium; NMN Plus;; Vitamin D; Vitamin B12
Allergien: -
Vorherige Impfungen: -

VAERS 2213064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: GA
Alter: -
Geschlecht: M
Eingang: 02.04.2022
Impfdatum: 08.03.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective Malaise Pneumonia SARS-CoV-2 test

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received bnt162b2 (BNT162B2), administration date 08Mar2022 (Lot number: FK9894) as dose 3 (booster), single for Covid-19 immunisation. Relevant medical history included: "Heart Issue" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose number: Unknown, Manufacture: Unknown, Caller reports her husband has received all of the COVID-19 vaccines.), for Covid-19 immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19"; PNEUMONIA (medically significant), outcome "unknown", described as "Pneumonia"; MALAISE (non-serious), outcome "unknown", described as "did not feel to good". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: positive, notes: he had COVID-19 as well. Clinical course: The reporter reports her husband has received all the COVID-19 vaccines which she and her husband received together, and he had COVID-19 as well. She reports that she received the COVID-19 vaccine booster dose on 08Mar2022. Caller states her husband is 6'2" and her husband is 2 of her. The reporter states her husband is bigger than herself. The reporter states her husband's heart issues was the whole reason behind getting the COVID-19 vaccines. Caller states all of this is trial and error and no one will know unless she calls. The reporter states her husband is like 3 years younger than her. The information regarding, Product strength, count size dispensed and sample of the product available to be returned is not applicable. If packaging sealed and intact is not provided on call. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Test Name: he had COVID-19 as well; Result Unstructured Data: Test Result: Positive; Comments: he had COVID-19 as well.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Heart disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2212149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

moderat

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 31.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Bronchospasm Dyspnoea

Symptomtext

Pt with signs and symptoms of bronchospasm and difficulty breathing approximately 15-30 minutes after receiving vaccine. No prior history of such reaction after previous doses. No relief from albuterol. Pt went to ER and was given magnesium infusion and nebulizer treatments

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2211441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 31.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood pressure increased Chest X-ray Dyspnoea Laboratory test Oxygen saturation decreased Extra dose administered Wheezing

Symptomtext

Shortly after receiving the Pfizer Booster # 2, Patient began to feel SOB. She utilized her Albuterol MDI at [approximately] 4:00 PM. Her breathing worsened and by 5:00 PM, she was audibly wheezing and extremely SOB. She utilized an Albuterol nebulizer at [approximately] 5:30 PM. Her SaO2 on room air was 86%. Normally, her SaO2 on room air is >96%. By 6:30 PM, her breathing condition had worsened even more and she requested to be taken to the ER because she "couldn't breathe." The closest facility was local Urgent Care and her daughter drove her there. The physician placed her on O2 via NC and administered an IM dose of steroids and then instructed her daughter to take her to the local ER for immediate care due to her shortness of breath and decreased SaO2. She was treated in the ER with Magnesium Sulfate 2 G IV; Albuterol + Atrovent nebulizer x 2; Ativan 1 mg; Clonidine PO secondary to increased BP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 3/31/2021: CXR and lab work drew in the ER.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2211267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NY
Alter: 24,0
Geschlecht: M
Eingang: 01.04.2022
Impfdatum: 31.03.2022
Beginn: 01.04.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Burning sensation Chest pain Erythema Skin warm

Symptomtext

He got his vaccine, he didn't feel any reaction at first. About 16 hours later when he woke up this morning, his left armpit is burning and painful, has to keep at a 75 degree angle for the last 3 hours as hoping it will go away. It feels like it is getting worse. One spot has the burning sensation with radiation from underneath his armpit into his chest area. The area is warm to touch, not red to touch. Just has the pain and burning, does look a little swollen. After the first vaccine, he was sick for 2 days and could not leave the house.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma.
Andere Medikamente: None.
Allergien: Bananas and shellfish.
Vorherige Impfungen: -

VAERS 2210252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 31.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure increased Chills Heart rate increased Palpitations Panic attack

Symptomtext

Feeling Chills and palpitations. At first patient couldn't explain symptoms stated they come and go. Blood pressure was taken at 1745 on Left Arm 170/100 P 120, 160/80 P - 108, O2 @ 99%. After 15 minutes BP came down 18:15 Blood pressure was 160/80 P - 94. O2 at 98% 18:25 Heart rate still elevated @ 111. EMS was called and arrived at 18:35. EMS asked Patient if she wanted to go to ER and stated no. EMS explained vital signs were level and didn't see she needed to go to the ER. They confirmed with her they would not transport her. Patient started to have a panic attack while sitting down in chair with family and EMS at her side. Patient was instructed to call PCP if not going to ER. Daughter confirmed she understood the instructions and patient was released. EMS vitals 167/92 BS - 137 HR - 102 retook before leaving and got 136/96 HR - 99

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Type 2 Diabetes
Vorgeschichte: None
Andere Medikamente: Metformin Cetirizine
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 2208859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NJ
Alter: 43,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 17.03.2022
Beginn: 18.03.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Cough Dyspnoea SARS-CoV-2 test Wheezing

Symptomtext

Around 1 am I began to feel shortness of breath/have difficulty breathing at night; cough; chest pain; wheezing; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 43 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 17Mar2022 20:00 (Lot number: FK9894) at the age of 43 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DYSPNOEA (non-serious) with onset 18Mar2022 01:00, outcome "not recovered", described as "Around 1 am I began to feel shortness of breath/have difficulty breathing at night"; COUGH (non-serious) with onset 18Mar2022 01:00, outcome "not recovered", described as "cough"; CHEST PAIN (non-serious) with onset 18Mar2022 01:00, outcome "recovered" (18Mar2022 04:00), described as "chest pain"; WHEEZING (non-serious) with onset 18Mar2022 01:00, outcome "not recovered", described as "wheezing". The events "around 1 am i began to feel shortness of breath/have difficulty breathing at night", "cough", "chest pain" and "wheezing" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of dyspnoea, cough, chest pain, wheezing. Additional information: Patient had no known allergies. The patient was not diagnosed with COVID-19 prior to the vaccination. The patient had tested for COVID-19 after vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20220317; Test Name: PCR Covid test; Test Result: Negative; Comments: covid test type post vaccination=Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: known allergies: no other medical history: no.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2208839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: GA
Alter: 55,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 08.03.2022
Beginn: 01.03.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Dyspnoea Heart rate increased Illness Lethargy Myalgia Pain Pain in extremity

Symptomtext

soreness in left arm; Lethargic; extremely ill; shortness of breath; heart will race; Joint pain; body aches; muscular pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Mar2022 (Lot number: FK9894) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Knee replacement and even that hurts" (unspecified if ongoing), notes: Caller states her knee with the knee replacement aches really bad and even her good knee is bothering her. There were no concomitant medications. Vaccination history included: Bnt162b2 (Pfizer COVID-19 vaccine 1st dose , Date received: 01Aug2021, Lot Number: EWD172, Route, Anatomical Location: Left arm, No. of Previous Doses: n/a, Age at Immunization if date not available: 54), administration date: 01Aug2021, when the patient was 54 years old, for Covid-19 immunization, reaction(s): "Tested positive for COVID-19 and pneumonia", "Tested positive for COVID-19 and pneumonia", "Tested positive for COVID-19 and pneumonia"; Bnt162b2 (Pfizer COVID-19 vaccine 2nd dose, Date received: 02Sept2021, Lot Number: EWD172, Route, Anatomical Location: Left arm, No. of Previous Doses: one, Age at Immunization if date not available: 54), administration date: 02Sep2021, when the patient was 54 years old, for Covid-19 immunization, reaction(s): "Tested positive for COVID-19 and pneumonia", "Tested positive for COVID-19 and pneumonia", "Tested positive for COVID-19 and pneumonia", "Headaches", "Loss of appetite". The following information was reported: ARTHRALGIA (non-serious) with onset Mar2022, outcome "not recovered", described as "Joint pain"; DYSPNOEA (non-serious) with onset 08Mar2022, outcome "not recovered", described as "shortness of breath"; PAIN (non-serious) with onset Mar2022, outcome "not recovered", described as "body aches"; HEART RATE INCREASED (non-serious) with onset 08Mar2022, outcome "not recovered", described as "heart will race"; PAIN IN EXTREMITY (non-serious), outcome "not recovered", described as "soreness in left arm"; LETHARGY (non-serious), outcome "unknown", described as "Lethargic"; MYALGIA (non-serious) with onset Mar2022, outcome "unknown", described as "muscular pain"; ILLNESS (non-serious), outcome "unknown", described as "extremely ill". Therapeutic measures were not taken as a result of arthralgia, dyspnoea. Additional information: Patient stated she couldn't move that arm or lie on that side. Also she was right handed, so she had them give it in her left. She states she was in bed for three days with aches and clarifies the aches were on her back where her lungs are because most people don't know the lungs are not in the front. She reports she was just miserable. She states she usually walks everyday. All symptoms worsen at night. She reports she was not really one for taking meds. She tries to stay as healthy as possible and drinks tons of water and tries to stay hydrated. No test other than after her COVID-19 vaccine 2nd dose. No other vaccines administered on same date with the Pfizer vaccine considered as suspect. No Prior Vaccinations (within 4 weeks). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Knee pain
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2206758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 30.03.2022
Beginn: 30.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Dyspnoea

Symptomtext

Client experienced shortness of breath that resolved after a few minutes, client left with EMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2206612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: UT
Alter: 36,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site hypoaesthesia Paraesthesia

Symptomtext

pins and needles feel starting in heels and moving across legs and arms. It has been a week and pt is still feeling periodically the numbness and pins and needles in the left arm where the shot was given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2206544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 29.03.2022
Beginn: 29.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site paraesthesia Paraesthesia

Symptomtext

TINGLING IN THE FACE AND AROUND THE INJECTION SITE APPROX. 2 HOURS AFTER VACCINE ADMINISTRATION. NO NUMBNESS OR PARALYSIS. TINGLING IS STILL PRESENT 24 HOURS LATER. HAS NOT SEEN A PROVIDER FOR TREATMENT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2204699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CO
Alter: 40,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 25.03.2022
Beginn: 25.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dizziness Dyspnoea Feeling hot Pain in extremity Palpitations Pruritus Rash Sleep disorder

Symptomtext

A few minutes after VX, I started feeling really hot and had pain my right arm that would happen sporadically every few minutes. That night I started feeling lightheaded and my heart was racing and I was having difficulty breathing so I took Benadryl, Advil and using my inhaler. Then overnight I was still having a lot of difficulty breathing and I started getting rashes on the back of my hands. The next morning (3/26/2022) I went to the urgent care and was given an IV of Benadryl, Tylenol and albuterol. When I left they recommended that I take 2 Benadryl every 4 hours. I tried to sleep that night and every 4 hours like clockwork, my hands would started extremely itching with the rash coming back. It was so strong that it woke me from my sleep. As long as I took it exactly every 4 hours it started keeping it at bay. The next day I tried to decrease the dose to 1 pill every 4 hours, then that evening, I woke up again having a hard time breathing. It took me about 2 hours to fall back asleep and was still having a hard time breathing. I am still feeling some effects of it and trying to take it easy and heal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia
Andere Medikamente: None
Allergien: Codeine; Yellow dye
Vorherige Impfungen: -

VAERS 2198709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NC
Alter: 59,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 02.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Dyspnoea Night sweats Rash Rash erythematous Rash papular Rash pruritic Sensation of foreign body

Symptomtext

Patient reported development of rash on right arm 1 day after vaccine. Described as raised, erythematous, pruritic. Rash then spread to left arm and left leg and neck. Rash is still present. Also endorsed 3 weeks of night sweats following vaccination. Also endorsed 1 day of chest discomfort, globus sensation, and difficulty breathing- resolved with albuterol inhaler. Had telephone visit with PCP office- on 3/25/22 for her symptoms. Treatment: 7-10 day course of hydroxyzine 25 mg for rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none known or reported
Vorgeschichte: asthma, hypertension, seasonal allergies
Andere Medikamente: -
Allergien: none reported
Vorherige Impfungen: -

VAERS 2184632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: WA
Alter: 32,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 16.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood electrolytes normal Dyspnoea Electrocardiogram normal Feeling cold Heart rate increased Palpitations

Symptomtext

Pt here for Covid vaccine - first dose. While waiting, developed reaction. Pt felt chilled, short of breath and racing heart. Pulse 170's x several minutes, then 160's. Dr. into evaluate. 25 mg Benadryl given PO - per Dr.'s verbal order. 911 called and arrived in appro x 10-12 minutes. HR remained elevated - decreased over a 15 min period to 140's. HR 124 as pt was being placed on the stretcher and wheeled out. O2 sat remained 98+% during entire episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Patient was transported to the ER for Eval Records reviewed- See below HR in ER was 91, BP 125/84. R- 18 ER EKG normal - HR 79 electrolytes - normal Xray order- no results noted. Received IV fluids. Call to pt at (H), discussed below. Reports she did not have the xray done. Was instructed by ER to f/u with PCP - to discuss future covid vaccine dose, and eval of the elevated HR. Pt will call.
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity Allergies Asthma
Andere Medikamente: Singulair Zyrtec
Allergien: Asprin- Hives, itching, rash ibuprofen- Swelling rash
Vorherige Impfungen: -

VAERS 2184217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 22.02.2022
Beginn: 12.03.2022
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Condition aggravated Cough Dizziness Ear disorder Impaired driving ability Impaired work ability

Symptomtext

woke up dizzy exactly three weeks after booster given same adverse reaction happened after the second vaccine received on: 3/3/2021 (Pfizer, lot # 14371) current event worse I had omicron covid on /13/2022, went to Dr for lingering dry cough. Ears were cloudy with eardrums bulging, but did not hurt. Put on day ZPak and 5 days of 5mg of prednisone. On third day of current event, went to Dr for dizziness. Ears had not cleared up . Put on 10 days 500 mg Amoxicillin TID, 5 days of 20 mg prednisone QID and 12.5 mg Meclizine TID Although dizziness better, have plateaued with symptoms - no better or worse Have been out of work x5 days. Work in Hospital, was forced to get booster or lose my job. Dr feels dizziness much worse this time due to covid complication from a month ago Still not recovered Unable to work Unable to drive

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: physical ear exam: 3/14/2022
Aktuelle Erkrankungen: omicron covid: diagnosed 1/13/2022
Vorgeschichte: none
Andere Medikamente: Levoxyl 50 mcg: one tab QID Kirkland Adult Gummies 500mg Calcium with 25 mcg vitamin D: 4 gummies QID Kirkland 50 mcg vitamin D3 : 2 tabs QID Vitafusion Vitamin C 270mg with 15 mg Zinc: 2 gummies QID
Allergien: NKDA NKA
Vorherige Impfungen: Second Covid Vaccine: Pfizer Lot # 14371, administered: 03/03/2021, age 63, three weeks after receiving vaccine, had 4 days of

VAERS 2177064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 23,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 04.03.2022
Beginn: 01.03.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Cough Dysphagia Dyspnoea Influenza like illness Migraine Productive cough Sneezing

Symptomtext

shortness of breath; Chest pain/feels like sharp pains are stabbing her chest; a lot of dry coughing/dry cough; migraine headaches; flu- like symptoms; sneezing; the cough is bringing up a lot of phlegm; difficult to for to consume harder, more solid foods; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 23 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 04Mar2022 (Lot number: FK9894) at the age of 23 years as dose 2 (booster), single for covid-19 immunisation. Relevant medical history included: "interchange of vaccine products" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Johnson and johnson covid-19 vaccine (Johnson and Johnson Covid-19 vaccine, Date received: 23May2021, Lot: 201A21A, NDC, EXP: unknown, Administered in Left arm; dose unknown), administration date: 23May2021, when the patient was 22 years old, for Covid-19 immunization. The following information was reported: DYSPNOEA (non-serious) with onset 05Mar2022, outcome "not recovered", described as "shortness of breath"; CHEST PAIN (non-serious) with onset 05Mar2022, outcome "not recovered", described as "Chest pain/feels like sharp pains are stabbing her chest"; COUGH (non-serious) with onset 05Mar2022, outcome "not recovered", described as "a lot of dry coughing/dry cough"; MIGRAINE (non-serious) with onset 04Mar2022, outcome "recovering", described as "migraine headaches"; INFLUENZA LIKE ILLNESS (non-serious) with onset 04Mar2022, outcome "not recovered", described as "flu- like symptoms"; SNEEZING (non-serious) with onset Mar2022, outcome "not recovered", described as "sneezing"; PRODUCTIVE COUGH (non-serious) with onset Mar2022, outcome "not recovered", described as "the cough is bringing up a lot of phlegm"; DYSPHAGIA (non-serious) with onset Mar2022, outcome "not recovered", described as "difficult to for to consume harder, more solid foods". Therapeutic measures were taken as a result of dyspnoea, chest pain, cough, migraine, influenza like illness, sneezing, productive cough, dysphagia. Additional information: Received the Covid-19 vaccine booster on Friday and is still experiencing side effects today. She reached out to report side effects to the vaccine. Shortness of breath: Started in the evening. Outcome: She explains it fluctuates. Sometimes feels like its getting better, but then it gets worse after she thinks its getting better. Chest pain: When she is not coughing, it feels okay, but when she is coughing it feels like sharp pains are stabbing her chest. She thinks the chest pain coincided with the dry cough which is also ongoing as well. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Interchange of vaccine products
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2173736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 11.03.2022
Beginn: 11.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Electrocardiogram

Symptomtext

Patient complained of chest pain at 11:14 am N.P. and R.N. began assessing the patient at 11:15am. EMS was radioed at this time by POD director. EMS in to assess patient vitals were obtained, patient described pain as piercing and EKG was initiated at 11:20 am and completed at 11:22am. 11:35 am Patient noted rubbing chest N.P. encouraged patient multiple times to be transported to ER for further evaluation Client denied immediate transport each time she was encouraged to do so. Patient verbally expressed that she was fine and left with accompanied by her boyfriend at 11:41am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: patient denies illness
Vorgeschichte: patient denies
Andere Medikamente: multivitamins
Allergien: no known drug or a food allergies
Vorherige Impfungen: -

VAERS 2170972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: GA
Alter: 18,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 10.03.2022
Beginn: 10.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dizziness Dyspnoea Full blood count normal Hypotension Hypoxia Metabolic function test Tachypnoea

Symptomtext

Pt started feeling short of breath and dizzy at about 10 minutes after her shot, vitals were monitored and initially normal but she became progressively more sob with tachypnea and associated hypoxia and hypotension. at about 30 minutes post covid booster she required administration of an epi pen and transfer to the local hospital via EMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ER did CBC- stable, CMP- stable 3/10/22
Aktuelle Erkrankungen: none known of
Vorgeschichte: Asthma
Andere Medikamente: Miralax, naproxen, ventolin, epi-pen
Allergien: NKDA, seafood allergy
Vorherige Impfungen: -

VAERS 2170740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: TX
Alter: 47,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 05.03.2022
Beginn: 05.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Computerised tomogram Electrocardiogram Fatigue Headache Impaired driving ability Impaired work ability Laboratory test Mobility decreased Nausea Vomiting

Symptomtext

After 24 hours post vaccination I had severe headaches, nausea, and vomiting that wouldn't allow me to drive and so I had to take a next day off work. Monday, day 2 post vaccine, my headache and nausea continued to be an annoyance and I suffered from a lot of fatigue that caused me to go to bed almost immediately after work for the remainder of the week. I tried to sleep in during the weekend however when speaking with healthcare professionals they had no answers for my symptoms. I am now starting to feel a lot better, and my nausea has gone away however my headache comes and goes. But my symptoms are getting better. I still have the headache and some nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: EKG, Lab Work and CAT Scan.
Aktuelle Erkrankungen: COVID-19
Vorgeschichte: Celiac; Insulin Resistance; Atrial Fibrillation; ADHD; Anxiety; Premenopausal; Allergies and Asthma
Andere Medikamente: Cytomel; Metformin; Pravega; Irbesartan; Metoprolol; Probiotic; Vangelia Root; Magnesium and Zyrtec
Allergien: Celiac; Gluten; Corn and Penicillin
Vorherige Impfungen: T-Dap 1990, Flu Shot 2008

VAERS 2155761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: WI
Alter: 16,0
Geschlecht: M
Eingang: 03.03.2022
Impfdatum: 28.02.2022
Beginn: 01.03.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Angiogram Angiogram abnormal Brain natriuretic peptide normal Dyspnoea Electrocardiogram Fatigue Headache Heart rate increased Pain Pyrexia Troponin

Symptomtext

Complaints of severe shortness of breath, headache, body aches, fatigue, fever that started 1 day after getting Pfizer booster. HR increased from 80 bpm to 130 bpm with walking a short distance and O2 sat dropped from 98% to 90%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 3/3/22 - ECG, Troponin, BNP unremarkable. CTA chest negative for PE, infiltrates.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2155008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: IA
Alter: 31,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 02.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site pain Lip swelling Paraesthesia oral

Symptomtext

Swelling and tingling of lips, pain at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2154945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: FL
Alter: 34,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 28.02.2022
Beginn: 28.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Cold sweat Dizziness Hypoaesthesia Myalgia Paraesthesia Vision blurred

Symptomtext

Dizziness, feeling woozy, blurred vision, myalgias, numbness, tingling, weakness, cold sweats,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: None
Vorherige Impfungen: -

VAERS 2154921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 03.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Condition aggravated Dizziness Dyspnoea

Symptomtext

At 10:28 the patient c/o dizziness and SOB o2 99% HR 74, patient mentioned it happened with her previous vaccines and only had coffee in am. At 10:36 temp 97.8 o2 99% HR 72 R 16 B/P 120/80. At 10:45 O2 99% HR 67 B/P 120/80 R16. At 11:00 O2 99% HR 65 B/P 120/80 R 16. Patient mentioned she was feeling better and was cleared to go home. She was educated to hydrate and get something to eat. She was D/C at 11:03.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2117110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

moderat

Staat: NY
Alter: 39,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 14.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Aphasia Chest discomfort Clumsiness Confusional state Discomfort Dizziness Dysarthria Dyspepsia Dyspnoea Feeling abnormal Flushing Headache Limb discomfort Muscle spasms Muscle twitching Muscular weakness Paraesthesia oral Skin warm

Symptomtext

At 13minutes face flushing, lip tingling,chest warm At 26 minutes arm heavy, chest pressure,confusion,dizzy At 7hrs burning in stomach and face throbbing and pressure where previously tingling. Sense of surroundings moving or spinning if eyes closed At 10hrs twitching throughout left arm lips and fingers, vision getting blurry At 19hrs lower ext weak and clumsy,headache,vision blurry continued and more involved twitching in left arm and both legs..speech slurring improving but word finding deficits. 24 to 48hrs pvc ,twitching, brain fog and severe focal cramps in arms and legs, chest pressure reduced but breathing labored and not automatic.. At

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2718036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 90,0
Geschlecht: F
Eingang: 27.11.2023
Impfdatum: 18.11.2022
Beginn: 26.11.2023
Tage bis Beginn: 373,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue

Symptomtext

Tired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2717510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MD
Alter: 71,0
Geschlecht: F
Eingang: 24.11.2023
Impfdatum: 19.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain SARS-CoV-2 test

Symptomtext

each time, only had sore spot to touch; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An elderly female patient received bnt162b2 (BNT162B2), on 19Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 71 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: bnt162b2 (First dose, Lot. EN6200), administration date: 26Feb2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "each time, only had sore spot to touch"; bnt162b2 (Second dose, Lot. EN6206), administration date: 19Mar2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "each time, only had sore spot to touch"; bnt162b2 (Third dose, Lot. FH8027), administration date: 14Nov2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "each time, only had sore spot to touch". The following information was reported: PAIN (non-serious), outcome "unknown", described as "each time, only had sore spot to touch". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Each time, only had sore spot to touch and negative COVID-19 test (PCR) after the vaccinations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test (PCR); Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2687247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 63,0
Geschlecht: F
Eingang: 27.09.2023
Impfdatum: 11.04.2022
Beginn: 02.09.2023
Tage bis Beginn: 509,0
Dosis: N/A
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Headache Oropharyngeal pain Productive cough Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sepsis

Symptomtext

The patient was brought to the ED by EMS on 9/2/23 with 3-4 days of congestion, sore throat, productive cough, headache, and fever of 101.7 F. She had two at-home COVID tests which were both negative, however a COVID-19 PCR test performed in the ED resulted positive. The patient was admitted 9/2/23 - 9/5/23 with sepsis secondary to COVID-19 infection, among other diagnoses. Of note, the patient has received the primary COVID vaccine series and two boosters.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2662911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 29.07.2023
Impfdatum: 02.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Body temperature increased Pain in extremity

Symptomtext

temp and upper arm soreness; temp and upper arm soreness; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An elderly female patient received BNT162b2 (BNT162B2), on 02May2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 73 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Product name/Manufacturer lot number: Pfizer Lot EN6200), administration date: 27Feb2021, when the patient was 71-year-old, for COVID-19 immunization, reaction(s): "temp and upper arm soreness", "temp and upper arm soreness"; BNT162b2 (DOSE 2, SINGLE, Product name / Manufacturer lot number: Pfizer Lot ER8730, Time: 9:25AM), administration date: 23Mar2021, when the patient was 72-year-old, for COVID-19 immunization, reaction(s): "temp and upper arm soreness", "temp and upper arm soreness"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Pfizer Lot: FE3590, Expiration: 30Nov2021), administration date: 15Oct2021, when the patient was 72-year-old, for COVID-19 immunization, reaction(s): "temp and upper arm soreness", "temp and upper arm soreness". The following information was reported: PAIN IN EXTREMITY (non-serious), BODY TEMPERATURE INCREASED (non-serious), outcome "unknown" and all described as "temp and upper arm soreness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity, body temperature increased. Additional information: Patient reported that the side effects were minor (temp and upper arm soreness). Patient had no medicines other than Tylenol taken day 1, 2 of vaccine.; Sender's Comments: Linked Report(s) : US-PFIZER INC-PV202300101946 same patient, different vaccine dose/event;US-PFIZER INC-202300259180 same patient, different vaccine dose/event;US-PFIZER INC-202300259177 same patient, different vaccine dose/event;US-PFIZER INC-202300259176 same patient, different vaccine dose/event;US-PFIZER INC-202300259178 same patient, different vaccine dose/event;US-PFIZER INC-PV202300128433 same patient, different vaccine dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:(Unknown result) had temperature
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2642891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: IN
Alter: 55,0
Geschlecht: F
Eingang: 08.06.2023
Impfdatum: 03.06.2022
Beginn: 12.01.2023
Tage bis Beginn: 223,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain upper COVID-19 Diarrhoea Oropharyngeal pain SARS-CoV-2 test positive Taste disorder

Symptomtext

I had an extremely sore throat and diarrhea and stomach pain so I went to an urgent care clinic and tested poditive for COVID-19. I was prescribed Paxlovid and a Prednezone steroid, cough syrup was prescribed but not taken. Taste disorder is still present at the rtime of this report

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: 12JAN2023 COVID-19 Test-Positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Astmha; Isolated IGA
Andere Medikamente: Daxlansoprazole; Lorazapam; Tramadol; Levothyroxine; Diazepam;
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2631885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 15.05.2023
Impfdatum: 25.02.2021
Beginn: 12.05.2023
Tage bis Beginn: 806,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chills Confusional state Cough Diarrhoea SARS-CoV-2 test positive Vascular device user

Symptomtext

Pt has a PMH of CAD s/p MI and a stent in 2005, chronic diastolic CHF, and chronic A-fib. He returned the previous day from a trip overseas. Last night he was very confused per the wife and could not answer questions appropriately. He has chills, a dry cough, and loose stools and is positive for COVID-19 in the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2628372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 06.05.2022
Beginn: 10.02.2023
Tage bis Beginn: 280,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Decreased appetite Headache Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

On 02/10/2023, from the time I woke up, I did not feel well. I had body aches, fever, loss of appetite, headache, cough. I took Tylenol and went to bed. I took a COVID-19 Test and it was positive, so I called the doctor. I was prescribed Paxlovid, which I took and it helped. I am better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 11FEB2023 - COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart disease
Andere Medikamente: Metoprolol; Crestor; lisinopril
Allergien: N/A
Vorherige Impfungen: -

VAERS 2626723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fk9894

mild

Staat: KS
Alter: 69,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 02.05.2022
Beginn: 17.10.2022
Tage bis Beginn: 168,0
Dosis: 5
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anosmia Apathy Asthenia COVID-19 Pyrexia SARS-CoV-2 test Vaccine breakthrough infection

Symptomtext

I had a covid breakthrough. I had no energy. I had a fever- unknown temp, it lasted less than 24 hours. I lost my sense of smell for 2 days. I did a breathing treatment due to my asthma. I was very apathetic. I was also prescribed paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Covid test
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: metformin; Avastin; Montelukast; Vitamin E and D.
Allergien: Thimerosal
Vorherige Impfungen: RSV booster

VAERS 2624238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 29.04.2022
Beginn: 01.06.2022
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Gastrointestinal disorder

Symptomtext

About a month after being vaccinated, I noticed something wasn't right with my stomach. I went out of town and when I came back, I still had abdominal pain and went to the doctor. They scheduled appointment for a Gastroenterologist. This has been going on for about a year.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Acid Reflux
Andere Medikamente: Omeprazole; Vitamin D3; Vitamin B12; Estradiol; Zyrtec; Montelukast; Famotidine
Allergien: Seasonal Allergies
Vorherige Impfungen: I had a bad reaction to a Shingrix vaccine. I had a bad reaction at the injection site.

VAERS 2619887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 21.04.2022
Beginn: 27.01.2023
Tage bis Beginn: 281,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Atrial fibrillation Blood creatinine increased Blood test abnormal COVID-19 Electrocardiogram ambulatory Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On 1/27/2023 I had a runny nose and slight fever. I tested and the test was positive on 1-27-2023. I called the clinic on a Sunday morning and they referred me to urgent care to get a blood test for Creatinine Test and then they prescribed Paxlovid. My symptoms lasted 5 days. On 04/01/2023 at 11:20AM my watch gave me a notification that I went into A-Fib that night while I was asleep. The clinic recommended I go to Emergency Room and get checked out and everything was normal on 04/02/2023. They sent me home and ordered a heart monitor and I have been wearing it for 14 days. I had a 2nd incidence of the A-fib last week when I was awake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 27JAN2023 - Blood test for Creatinine Test- positive; blood panel - 02APR2023 - Within Normal Ranges
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure; High Cholesterol
Andere Medikamente: Hyzaar; Lipitor
Allergien: N/A
Vorherige Impfungen: -

VAERS 2615252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: GA
Alter: 78,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 11.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Arthralgia Blood test Pain Skin warm X-ray

Symptomtext

Shoulder pain, throbbing, sharp pain that sometimes radiates down to the elbow area, warm/hot to the touch sometimes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Xray, Blood work, steroid injection twice with a little relief but it only lasted 3 days when it should have lasted 4 months
Aktuelle Erkrankungen: No
Vorgeschichte: Pt states this question is irrelevant
Andere Medikamente: Vitamin D, multi vitamin, vitamin E. atenolol, clothalodol, low doses
Allergien: No
Vorherige Impfungen: -

VAERS 2613961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 69,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 11.04.2022
Beginn: 01.01.2023
Tage bis Beginn: 265,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anal incontinence Blood sodium decreased COVID-19 Cough Diarrhoea Malaise SARS-CoV-2 test positive Vomiting

Symptomtext

My COVID-19 symptoms started on 01/01/2023 in the evening. I had a bad cough and diarrhea. The cough was severe and diarrhea was incontinence. I did a home COVID-19 test on the same day which was positive. I called my doctor the next day and my doctor send in prescription for Paxlovid. After 2 days of taking Paxlovid I was feeling sicker and sicker I couldn't told anything down. everything I ate it would come out. So, I went to the hospital on Friday . They took my temperature and gave me intravenous fluids through out the night. The next morning they gave me food to eat I was able to eat it and had no problem. I also had low sodium because I vomited so much. I will going to my doctor's office next week to find out about my low sodium issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 01JAN2023 COVID-19 Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic Kidney Disease ; Arthritis
Andere Medikamente: Flax Seed Oil; Baby Aspirin; Multivitamins; Melatonin; Cranberry Pills; Atenolol; Gabapentin; Atorvastatin; Calcium; Mucinex
Allergien: Penicillin; Codeine; Chicken; Potatoes; Turkey; Injectable Dye; Strawberry
Vorherige Impfungen: -

VAERS 2612342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WA
Alter: 66,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 06.04.2022
Beginn: 06.02.2023
Tage bis Beginn: 306,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

I tested positive for Covid-19 on February 6, 2023, I experienced tiredness. I was prescribed Paxlovid for my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home testing
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Alvesco inhaler; Synthroid; Wellbutrin; Pravachol; Singular; Albuterol
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2611581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CO
Alter: 59,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 04.05.2022
Beginn: 05.05.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood test normal Chills Fatigue Headache Hyperhidrosis Immune system disorder Malaise Pain Pyrexia SARS-CoV-2 test negative

Symptomtext

I received my second COVID-19 booster on 5/4/2022. Within two days, I had mild symptoms of fatigue, body aches, and general malaise. This lasted for maybe a day. For the remainder of the week, I was fine. The following week, though, I had the mild symptoms again, and they lasted a little longer. I then felt fine again. On 5/21/2022, I had a fever of 102. I also had severe headache, chills, sweats, fatigue, malaise, and body aches. I was alarmed enough to seek medical attention, so my husband took me to the emergency room. At the ER, I was put in a hospital bed and given a COVID-19 test, which yielded a negative result. I also underwent bloodwork, and I was given intravenous fluids and possibly acetaminophen. I was under observation for maybe six to eight hours. The doctor told me that I had tested negative for COVID-19. He told me that I had likely had an acute immune response to the booster I had received, which he said sometimes happens. He also advised me that I was likely to have a strong reaction to any future immunizations I received. He told me that I could treat my symptoms with acetaminophen and to take it every four hours, if necessary, and that I should also drink plenty of fluids. He then released me, and I went home. I followed the doctor's orders. I rested, and my situation remained stable. I was able to operate at a satisfactory level by 5/23/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 21MAY2022 - COVID-19 Test - Negative Result; 21MAY2022- Bloodwork - No Anomalies Detected
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C; B Complex; Vitamin D; Allegra; Estrogel; Psyllium Fiber Capsules; Low-Dose Aspirin; Montelukast
Allergien: Tetracycline; Codeine
Vorherige Impfungen: -

VAERS 2611543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 24,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 24.03.2022
Beginn: 01.08.2022
Tage bis Beginn: 130,0
Dosis: 4
Route/Site: - / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Colonoscopy normal Diarrhoea Endoscopy normal Frequent bowel movements Gastrointestinal disorder Laboratory test normal Nausea Stool analysis normal Ultrasound scan normal

Symptomtext

It started around August, I've had intestinal issues such as nausea, diarrhea, frequent needs to go to the bathroom. I initially went to the doctor about a month after the symptoms and they did a bunch of tests, but nothing came up. I've had a bunch of tests since then such as an endoscopy, colonoscopy, and other tests but they haven't found anything. The symptoms have remained the same, the nausea and diarrhea is daily, I go to the bathroom about 10 times a day. There is no vomiting just the constant nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 2022Dec20- Ultrasound; 2022Nov11-Colonoscopy; Endoscopy; 2022Oct07- Stool Samples
Aktuelle Erkrankungen: Latex; Cats
Vorgeschichte: Arthritis; ADHD
Andere Medikamente: Escitalopram; Bupropion; Ozempic; Fish Oil; Vitamin B12; Iron
Allergien: N/A
Vorherige Impfungen: -

VAERS 2611484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TN
Alter: 68,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 06.04.2022
Beginn: 13.08.2022
Tage bis Beginn: 129,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Cough Oropharyngeal pain Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I started having on August 13, I had sore throat and dry cough. On August 14, I had fever, chills, body aches, runny nose and congestion. The next day I went to a clinic to get tested after taking a home test I was positive for COVID-19. I was given a prescription for PAXLOVID. The medicine helped but it didn't, the symptoms did subside but as soon as the script was completely gone the symptoms came right back. On August 28, I tested again and was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Mild Asthma; Arthritis
Andere Medikamente: Levothyroxine; MAXZIDE; ARNUITY ELLIPTA; LATANAPROST eye drops; aspirin; amoxicillin; albuterol HFA; multivitamin; coQ10; turmeric; omega 3; calcium; melatonin; dorzolamide; BUSPAR
Allergien: Cephalexin; sulfa drugs; ZITHROMAX
Vorherige Impfungen: -

VAERS 2611040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: AK
Alter: 71,0
Geschlecht: M
Eingang: 06.04.2023
Impfdatum: 31.03.2022
Beginn: 01.09.2022
Tage bis Beginn: 154,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Feeling abnormal Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Sinus congestion

Symptomtext

After dose 4 I tested positive for COVID-19 in September of 2022. I had a fever and felt really bad with fatigue. My symptoms last about 5 days. After dose 5 I tested positive for COVID-19 in March of 2023. I had fever and fatigue; sinus congestion and sore throat and I developed a cough. I took PAXLOVID with each infection. As of today, I still have a cough and sinus issues.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home, positive, 09/2022 and 03/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: Stage 4 Prostate Cancer; High Blood Pressure; Low Heart Rate; Glaucoma
Andere Medikamente: Losartan; atorvastatin; HCTZ; aspirin; latanoprost
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2609887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: GA
Alter: 67,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 04.04.2022
Beginn: 01.08.2022
Tage bis Beginn: 119,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Exposure to SARS-CoV-2 Malaise SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. I am a nurse and have high exposure to COVID-19. I began feeling symptoms and tested positive for COVID-19 in 08/2022. I got a prescription for Paxlovid. My chef complaint is the awful metallic taste. I did have a rebound and tested positive again on 08/14/2022. As of today, I do not have any lingering symptoms.

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Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: AUG2022 COVID-19 Test - Positive; 14AUG2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes, High Blood Pressure; High Cholesterol
Andere Medikamente: N/A
Allergien: Seasonal Allergies; Benadryl
Vorherige Impfungen: -

VAERS 2609637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MD
Alter: 83,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 02.04.2022
Beginn: 01.02.2023
Tage bis Beginn: 305,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Chest X-ray Fatigue Malaise Oropharyngeal pain Pain Pharyngitis Productive cough Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I experienced COVID-19 on February 2023. I experienced a cough which became very bad, sore throat, body aches, runny nose, fatigued, productive coughing. I went to the ER where chest x-ray was performed and a physical exam. I was told by the ER doctor I had pharyngitis secondary to my COVID symptoms and they gave me a cough medicine. I took a COVID rapid test at home on 02/01/2023 and it was positive. I have recovered from my COVID symptoms.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 01FEB2023 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Atrial Fibrillation; Reynaud's Syndrome; Diverticulosis; Rotator Cuff Tear; Bell Palsy; Pneumonia
Andere Medikamente: Carvedilol; lisinopril; ELIQUIS; rosuvastatin; CENTRUM SILVER; vitamin D3; vitamin B6; PREREVISION A-REDS; ZYRTEC; FLONASE nasal spray
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2609387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 56,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 01.04.2022
Beginn: 01.06.2022
Tage bis Beginn: 61,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dermatitis Imaging procedure abnormal Muscular weakness Rash Skin disorder

Symptomtext

Starting in June 2022, I started to developing rashes on my forehead. The rashes increasing to other parts of my face and neck. I started to develop also skin problems on my hands as well. I also developed muscle weakness, particularly on my legs and my upper extremities, my neck and shoulders. I had medical imaging studies due to my symptoms. My diagnoses was dermatitis. My symptoms are improving but I have not recovered.

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Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Medical imaging studies performed, Dermatitis
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Hypertension; High Cholesterol
Andere Medikamente: Baby ASA; PULMICORT; simvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2609347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 03.04.2022
Beginn: 09.02.2023
Tage bis Beginn: 312,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Chills Concussion Haematoma Pyrexia Respiratory tract congestion Restless legs syndrome SARS-CoV-2 test positive Taste disorder Throat irritation

Symptomtext

I had a scratchy throat, change of taste that has lasted long-term, tremendous amount of congestion, a low-grade fever; initially, the first day, I had body chills even when my temperature was pretty normal. I took TYLENOL to help. I took a rapid antigen COVID-19 test on 02/09/2023 which came back positive. The next day, I was prescribed PAXLOVID the next day. I had a hematoma and concussion at the same time when I contracted COVID-19 which delayed me picking up my prescription for PAXLOVID. By about 36 hours of taking the prescription, I noticed immediate relief. By day 5-6, I made a full recovery; however, I do feel I've been having a long-term COVID-19 effects. It's been triggering restless leg syndrome episodes and additional complications to prior medical illnesses. As of now, I'm trying to determine how long-COVID-19 symptoms affect my medical history.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 09FEB2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Triple Degenerative Disc Disease; Osteoarthritis; Restless Leg Syndrome; Obesity; Asthma; Lymphedema; Lipedema
Andere Medikamente: Valsartan; clonidine; MIRAPEX; tramadol; MONTEX; melatonin; omeprazole; selenium; vitamin D; vitamin E; tizanidine
Allergien: Grass
Vorherige Impfungen: -

VAERS 2606573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 30.03.2023
Impfdatum: 29.03.2022
Beginn: 16.11.2022
Tage bis Beginn: 232,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I positive for COVID-19 on 16NOV2022, I was coughing, I had some fatigue and congestion. I did not have a fever, I contacted my doctor and he prescribed me paxlovid. After taking the medication I started feeling better about 2 days later.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 16NOV2022 COVID-19- Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Reflex; BPH; Arthritis; Enteric neuronal dysfunctions; Erectile dysfunction
Andere Medikamente: Amlodipine; Aspirin; Atorvastatin; Famlodadin; Amlazapam; tadalafil; Alfuzosin; Vitamin D3; Omega 3; Coenzyme Q10; Multi vitamin; Olive oil
Allergien: N/A
Vorherige Impfungen: -

VAERS 2603127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 72,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 25.04.2022
Beginn: 01.10.2022
Tage bis Beginn: 159,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Cough Fatigue Muscle rupture X-ray

Symptomtext

I tore some chest and back muscles from severe coughing; Very exhausted; weak; Cough; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient received BNT162b2 (BNT162B2), on 25Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 72 years intramuscular, in arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "depression" (unspecified if ongoing); "stomach acid" (unspecified if ongoing); "Type 2 Diabetes" (unspecified if ongoing). Concomitant medication(s) included: ENALAPRIL oral taken for hypertension (ongoing); IMIPRAMINE oral taken for depression (ongoing); PANTOPRAZOLE oral taken for hyperchlorhydria (ongoing); METFORMIN oral taken for type 2 diabetes mellitus, stop date: Mar2023. Vaccination history included: BNT162b2 (Dose: 01, Lot number: ER8727, Anatomical site of injection: L. Arm, Route of administration: Intramuscular), administration date: 23Mar2021, when the patient was 71-year-old, for COVID-19 Immunization; BNT162b2 (Dose: 02, Lot number: ER8731, Anatomical site of injection: Arm, Route of administration: Intramuscular), administration date: 13Apr2021, when the patient was 71-year-old, for COVID-19 Immunization; BNT162b2 (Dose: 03, Lot number: FG3527, Anatomical site of injection: Arm, Route of administration: Intramuscular), administration date: 22Nov2021, when the patient was 72-year-old, for COVID-19 Immunization. The following information was reported: COUGH (non-serious) with onset Oct2022, outcome "unknown"; MUSCLE RUPTURE (medically significant), outcome "unknown", described as "I tore some chest and back muscles from severe coughing"; FATIGUE (non-serious), outcome "unknown", described as "Very exhausted"; ASTHENIA (non-serious), outcome "unknown", described as "weak". The patient underwent the following laboratory tests and procedures: X-ray: No Pneumonia, notes: had 2 X-rays. Clinical course: Patient started enalapril, imipramine, and metformin 20 years before. She developed a serious cough in Mid Oct2022, so severe that she tore some chest and back muscles from severe coughing. Patient had 2 X-rays but no pneumonia. Patient was very exhausted and weak from this. Patient did not know if it was RSV, not diagnosed as such. Patient talked to friends and relatives in (Name withheld) who described identical cough, relentless. Patient had 5 Pfizer vaccinations/boosters.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300039609 same patient, different vaccine doses/event;

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: X-Rays; Result Unstructured Data: Test Result:No Pneumonia; Comments: had 2 X-rays
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Hyperacidity; Hypertension; Type 2 diabetes mellitus
Andere Medikamente: ENALAPRIL; IMIPRAMINE; PANTOPRAZOLE; METFORMIN
Allergien: -
Vorherige Impfungen: -

VAERS 2595639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 03.05.2022
Beginn: 06.05.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Deafness Dizziness Ear discomfort Tinnitus

Symptomtext

Intense Ear pressure and pain , dizziness, bilateral tinnitus (new onset) Tinnitus not related to trauma, infection. or hearing loss Continue to experience ear pressure and tinnitus similar to high altitude effect without relief. ENT exam negative for ear disease or TMJ

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Exam by MD on 05/09/22 showed possible ear fluid. Given course of prednisone and antibiotic with no improvement.
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: Symbicort 80/4.5, Levocetirizine Dihydrochloride 5mg
Allergien: allergic to sulfites and chemical preservatives, sulfa,
Vorherige Impfungen: -

VAERS 2593155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 66,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 27.12.2022
Tage bis Beginn: 112,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Malaise Oral pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Went on an 8-day Cruise 12/18/22-12/26/22. Began to experience early symptoms on 12/27/22. Tested with home COVID test which was negative on 12/27, Tested again on 12/28 which was positive. Symptoms developed into cough, oral mucosa pain, general malaise, low-grade fever, tiredness. Called PCP's office and was placed on antiviral (not Paxlovid, the one that starts with O). Symptoms improved by 1/8 but still tested positive. Finally tested negative on 1/15/23.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Abbot Covid-19 Ag 12/27/22 - 12/28/22 + 01/08/23 + 01/15/23 - No lab testing as recent creatinine in doctor's system.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Gout
Andere Medikamente: Losartan 25 mg daily Allopurinol 300 mg daily ASA 81 mg daily Vitamin D3 2,000 units daily Multivitamin 1 tab daily
Allergien: None
Vorherige Impfungen: -

VAERS 2577198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 05.11.2022
Beginn: 06.01.2023
Tage bis Beginn: 62,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Diarrhoea SARS-CoV-2 test positive

Symptomtext

01/08/23 presents to ED for "diarrhea". PMHx of "breast cancer diabetes osteoarthritis hyperlipidemia, hypertension PE on Eliquis"

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Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 01/08/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 09.09.2022
Beginn: 05.01.2023
Tage bis Beginn: 118,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Cough Diarrhoea SARS-CoV-2 test positive

Symptomtext

01/05/23 presents with "cough, diarrhea". PMHx of "dementia, CKD, HTN, DM, psoriasis"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 01/05/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2573428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 01.02.2023
Impfdatum: 05.05.2022
Beginn: 09.01.2023
Tage bis Beginn: 249,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Bacterial test Blood culture negative Blood lactic acid decreased COVID-19 Chest X-ray abnormal Computerised tomogram thorax abnormal Culture urine negative Diverticulitis Emphysema Fatigue Heart rate increased Lactic acidosis Leukocytosis Lung infiltration Magnetic resonance imaging head abnormal Mental status changes Normal pressure hydrocephalus SARS-CoV-2 test positive

Symptomtext

Patient is a 84 y.o. male patient of MD with history of Afib, HTN, CKD, Alzheimer's dementia currently at rehab facility presented to Hospital with altered mentation and elevated HR. found to be septic due to viral etiology most likely with COVID positive status. He remained on room air throughout hospitalization and therefore not a candidate for most therapies and not a candidate for others due to renal function. General surgery consulted to evaluate diverticulitis. Although likely not the underlying cause of sepsis was placed on course of antibiotics. MRI showed no stroke but did reveal likely NPH, from discussion with wife this appears to be a chronic process. Neuro Sepsis Likely due to COVID infection, diverticulitis with possible contribution of aspiration pneumonia CT with findings concerning for aspiration pneumonitis Afebrile, WBC 18k , LA 2.5 on admission UA trace LE, few WBCs, rare bact CXR without new focal consolidation or infiltrate Urine culture with no growth Blood culture 1/2 positive coag negative staph, likely contaminant Repeat blood cultures: NGTD Lactic acidosis and leukocytosis resolved de-escalate to cipro/flagyl No current surgical indication for surgery, plan for 10-14 days of Cipro/Flagyl Covid-19 Virus Infection Date of onset of symptoms: 1/8 Symptoms present on admission: Altered mental status, fatigue Date of covid positive test: 1/9 Imaging: Chest x-ray: Emphysematous changes, no new focal consolidation Oxygen requirements on admission: Room air Current oxygen requirements: Room air Medical therapy: not indicated as not hypoxic also not a candidate for paxlovid due to renal function Anticipated special isolation end date: 10/19

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Praegender Schweregrund: Fatigue
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NH
Alter: 78,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 05.03.2021
Beginn: 01.08.2022
Tage bis Beginn: 514,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Injection site joint pain

Symptomtext

ACUTE PAIN IN RIGHT ARM JOINT TO SHOULDER - SMALL AREA ACUTE PAIN IN RIGHT KNEE JOINT IN MIDDLE FRONT - VERY SMALL AREA

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: no cartilage in left knee
Andere Medikamente: Ator vastatin metaprolol 81 mg aspirin
Allergien: -
Vorherige Impfungen: -

VAERS 2559934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NC
Alter: 71,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 21.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood cholesterol Pain Peripheral swelling Urticaria

Symptomtext

The Second Covid Booster her arm swelled even more with enormous hives.; hives; pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 21Apr2022 as dose 4 (booster), 0.3 ml single (Lot number: FK9894) at the age of 71 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "COVID", start date: 01Jan2021 (unspecified if ongoing), notes: She initially provided she had COVID 01Jan2020, but clarified it was 01Jan2021. She herself had a headache for only one night, but doctor insisted she be tested and she had COVID. She had no other symptoms other than headache one night and a low grade temperature.; "Cancer" (unspecified if ongoing), notes: she had cancer and lymph nodes in both arms.; "Lymph nodes removed", start date: Nov2019, stop date: Nov2019, notes: The lymph nodes removed Nov2019; "Estrogen blocker prevent cancer coming back" (ongoing), notes: Estrogen blocker prevent cancer coming back; "Heartburn" (ongoing). Concomitant medication(s) included: LETROZOLE taken for prophylaxis (ongoing); ESOMEPRAZOLE MAGNESIUM taken for dyspepsia (ongoing). Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), 0.3 ML SINGLE, Batch/lot number: EW0187, Dosage text: .3ml administered in arm; unknown which one, Reaction / Event as Reported by the Primary Source for Translation:First Covid), administration date: 11Oct2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "Hives"; BNT162b2 (DOSE 3 (BOOSTER), 0.3 ML SINGLE, Batch/lot number: EW0187, Dosage text: .3ml administered in arm; unknown which one), administration date: 11Oct2021, when the patient was 70-year-old, for COVID-19 Immunization, reaction(s): "pain"; Covid-19 vaccine (Dose 1 , Unknown Manufacturer), for COVID-19 Immunization; Covid-19 vaccine (Dose 2 , Unknown Manufacturer), for COVID-19 Immunization. The following information was reported: URTICARIA (non-serious) with onset Apr2022, outcome "unknown", described as "hives"; PAIN (non-serious) with onset Apr2022, outcome "unknown"; PERIPHERAL SWELLING (non-serious) with onset 22Apr2022, outcome "unknown", described as "The Second Covid Booster her arm swelled even more with enormous hives.". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller mentioned that she had Pfizer for all of her previous Covid-19 vaccine shots. She had her lymph nodes removed. She was afraid of experiencing lymphadenopathy. she mentioned that she was currently on physical therapy and still experiences pain. Her family care doctor told her to contact Pfizer and tell her if she should still get another booster. Other Conditions and Other Products: Yes. Initially provided she had cancer and lymph nodes in both arms. The second booster, clarified and confirmed as Pfizer. The second COVID Booster her arm swelled even more with enormous hives. Both her and her doctor are afraid of lymphoma. Reporter indicated she was unsure if she reported this to our safety department. Explained, she went on our website which was confusing. She was reading multiple things. She went on to a contact us section and it allowed her to type her information in 500 words or less. She described what happened and was asking for advice. Now she's afraid of getting another booster shot after the reactions she has had. She never received any comments or feedback from us after the submission of details. She confirmed she was not provided with any type of reference number. Therefore, report marked as initial. Started physical therapy and it was helping. Her physical therapist told her he thought the shot that was given in the muscle swelled and pressed on the sciatic nerve which just got worse from there. She added, her physical therapist told her they had three other people come in who had the injection in their arm and had pain for a month long and they were working with them. She's the fourth one with pain. Other Conditions: Reporter later clarified details. She had cancer that had spread to the lymph nodes in both arms. Both of those lymph nodes were removed. The lymph nodes were removed Nov2019. She also added, before any vaccine her husband had COVID. She herself had a headache for only one night, but doctor insisted she be tested and she had COVID. She had no other symptoms other than headache one night and a low grade temperature. She initially provided she had COVID 01Jan2020, but clarified it was 01Jan2021. Investigation: Doctor always checks cholesterol, but no details provided. Declined to continue with report. Wanted to get over to medical information. There is a product complaint to report. Description of Product Complaint: Description of complaint: This is a PC on treatment medications and not the suspect products mentioned during interaction. rednisone and Aleve did not work. Prednisone and Aleve lot and exp are unknown to reporter. Does not have details to provide. Product strength and count size dispensed: Not provided, Additional lot numbers: None. Is a sample of the product available to be returned, if requested (Y/N): Not provided. Packaging sealed and intact? Not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Name: cholesterol; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: Heartburn; Prophylaxis (Estrogen blocker prevent cancer coming back)
Vorgeschichte: Medical History/Concurrent Conditions: Cancer (she had cancer and lymph nodes in both arms.); COVID-19 (She initially provided she had COVID 01Jan2020, but clarified it was 01Jan2021. She herself had a headache for only one night, but doctor insisted she be tested and she had COVID. She had no other symptoms other than headache one night and a low grade temperature.); Lymphadenectomy (The lymph nodes removed Nov2019)
Andere Medikamente: LETROZOLE; ESOMEPRAZOLE MAGNESIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2551449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 11.03.2021
Beginn: 15.11.2022
Tage bis Beginn: 614,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chills Cough Headache Pyrexia SARS-CoV-2 test positive

Symptomtext

11/15/22 presents to EC ED for "worsening HA, cough, fever/chills". PMHx of "DM, HTN, HLP"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 11/15/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2546954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 14.04.2022
Beginn: 29.12.2022
Tage bis Beginn: 259,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia COVID-19 Chest X-ray Pyrexia SARS-CoV-2 test positive

Symptomtext

Admitted with generalized weakness and fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: COVID 19 positive PCR, Chest Xray
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2540722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 12.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Biopsy skin abnormal Blood immunoglobulin E increased Culture positive Eczema Erythema Full blood count abnormal Inflammation Pyrexia Rash SARS-CoV-2 test negative

Symptomtext

One to two weeks after I received my Pfizer vaccine. I began to notice a rash on both of my hands on the dorsal aspect. It became progressively worse. After my 5th dose of my COVID-19 vaccine it progressively became worse still and ascended up my arms to both forearms to dorsal aspect. It was very inflammatory and red. It responded to MOTRIN and TYLENOL. I put steroids on the rash as well. After biopsy, cultures, and blood results were subacute spongiotic dermatitis with eosinophils. Eczematous Dermatitis and its variant, which seem most likely in this case, drug eruptions, and arthropod bite reactions. I also had a low grade fever for about two weeks of about 99.9 degrees. I had elevated IGE to 537 (history of elevated IGE dating back to 7/2016 secondary to ABPA).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 27SEP2022 biopsy to hands; 27SEP2022 cultures; 27SEP2022 CBC; 27SEP202 COVID-19 PR SARS all in one, negative
Aktuelle Erkrankungen: Pneumonia
Vorgeschichte: Allergic Bronchopulmonary Aspergillosis; Bladder Cancer
Andere Medikamente: QNASL steroid; XYZAL; albuterol inhaler
Allergien: Environmental allergies
Vorherige Impfungen: -

VAERS 2539292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WI
Alter: 79,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 27.09.2022
Beginn: 17.11.2022
Tage bis Beginn: 51,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Pyrexia SARS-CoV-2 test positive

Symptomtext

My COVID-19 Infection symptoms started on 11/17/2022 at around 8:00AM in the morning. I had slight fever, cough, and tiredness. I did a home COVID-19 test which was positive. I called my doctor right away after testing positive. He prescribed Legevrio 8 pills per day, pack of 40 pills in total.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 21DEC2022 COVID-19 Test-Positive
Aktuelle Erkrankungen: None
Vorgeschichte: AFIV
Andere Medikamente: Levothyroxine; Potassium Chloride; Vitamin C; Vitamin D
Allergien: Promethean
Vorherige Impfungen: -

VAERS 2538733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CT
Alter: 78,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 12.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Fatigue Headache Influenza like illness Pain in extremity

Symptomtext

1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs; 1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs; 1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs; 1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs; 1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 79-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 78 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Potts" (unspecified if ongoing), notes: Potts. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: EL3248, Location of injection: Arm Left), administration date: 12Jan2021, when the patient was 77-year-old, for COVID-19 Immunization, reaction(s): "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs"; BNT162b2 (Dose Number: 2, Batch/Lot No: N9581, Location of injection: Arm Left), administration date: 02Feb2021, when the patient was 77-year-old, for COVID-19 Immunization, reaction(s): "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs"; Bnt162b2 (Dose Number: 3, Batch/Lot No: FK49894F, Location of injection: Arm Right), for COVID-19 Immunization, reaction(s): "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs", "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs". The following information was reported: INFLUENZA LIKE ILLNESS (non-serious), HEADACHE (non-serious), COUGH (non-serious), FATIGUE (non-serious), PAIN IN EXTREMITY (non-serious) all with onset Apr2022, outcome "unknown" and all described as "1st-5th doses mild flulike: HA, SLcough,fatigue sore arm 48hrs".; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201380992 same patient and different drug dose/events.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pott's disease (Potts)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2535154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 29.10.2021
Beginn: 25.11.2022
Tage bis Beginn: 392,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cardiac pacemaker insertion Malaise Positive airway pressure therapy SARS-CoV-2 test positive Ventricular asystole

Symptomtext

"Patient with 4 COVID vaccines with esophageal cancer admitted to acute care for ventricular asystole and had pacemaker placed. Patient then admitted to Rehab unit and tested detected for COVID prior to discharge. Provider d/c note re COVID: ""1. Symptomatic Covid 19 detected the evening before planned discharge. He was given 3 days of iv remdesivir and had an oncology appt rescheduled. He will be seen next 12/21 by oncology and has f/u with cardiology and sleep medicine. He has remained afebrile and on room air (except for evening cpap/bipap - which is baseline) for over 48 hours. 2. He feels safe and ready to dc home today. He has been room independent for over 48 hours and has done well."" "

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Praegender Schweregrund: Malaise
Hospital-Tage: 14,0
Labordaten: COVID Detected PCR on 12/6/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Hypertension Hyperlipidemia CAD (coronary artery disease) Orthostatic hypotension Digestive Colon cancer (HCC) Esophageal dysphagia Cancer of distal third of esophagus (HCC) Chemotherapy induced nausea and vomiting Endocrine Diabetes mellitus type II Integumentary PYOGENIC GRANULOMA (686.1) Respiratory Obstructive sleep apnea DOE (dyspnea on exertion) Urinary AKI (acute kidney injury) (HCC) Other Chronic back pain History of TIA (transient ischemic attack) Arthritis Morbid obesity (HCC) Blood in the stool Morbid obesity with BMI of 45.0-49.9, adult (HCC) History of colon cancer History of colon polyps History of diabetes mellitus History of coronary artery stent placement Esophageal mass Anxiety Dehydration Syncope and collapse Chemotherapy-induced thrombocytopenia
Andere Medikamente: -
Allergien: Ketorolac Tromethamine
Vorherige Impfungen: -

VAERS 2527926

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NC
Alter: 76,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 06.04.2022
Beginn: 17.11.2022
Tage bis Beginn: 225,0
Dosis: 5
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Cough Influenza virus test negative Oropharyngeal pain Respiratory syncytial virus test negative Rhinorrhoea SARS-CoV-2 test negative Sinusitis

Symptomtext

On 11/17/2022 I had a sore throat, runny nose, and cough. On Monday I went to the urgent care. I tested negative for COVID-19; flu; RSV. The urgent care told me that I had a sinus infection. They prescribed me with antibiotics for 7 days and cough pills as per needed. As of today 12/09/2022 I am feeling better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 09DEC2022 COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetics; Chronic Constipation
Andere Medikamente: Pantoprazole; losartan; metformin; carvedilol; amlodipine; aspirin; vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2521460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 21,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 20.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Contusion Headache Hypertensive crisis Optic nerve disorder Visual impairment

Symptomtext

Hypertensive crisis; headaches; bruising; visual changes; slowing of optic nerve; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from a sales representative. A 21-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 20Apr2022 as dose 1, single (Lot number: FK9894) at the age of 21 years intramuscular for covid-19 immunisation. The patient's relevant medical history included: "If covid prior vaccination: Yes" (unspecified if ongoing). No known allergies. The patient took concomitant medications. Other medications in two weeks included birth control. No other vaccine in four weeks. The following information was reported: HYPERTENSIVE CRISIS (hospitalization, life threatening) with onset Apr2022, outcome "recovered with sequelae"; CONTUSION (non-serious) with onset Apr2022, outcome "recovered with sequelae", described as "bruising"; HEADACHE (non-serious) with onset Apr2022, outcome "recovered with sequelae", described as "headaches"; OPTIC NERVE DISORDER (non-serious) with onset Apr2022, outcome "recovered with sequelae", described as "slowing of optic nerve"; VISUAL IMPAIRMENT (non-serious) with onset Apr2022, outcome "recovered with sequelae", described as "visual changes". The patient was hospitalized for hypertensive crisis (hospitalization duration: 8 day(s)). The events "hypertensive crisis", "headaches", "bruising", "visual changes" and "slowing of optic nerve" required emergency room visit. Therapeutic measures were taken as a result of hypertensive crisis, headache, contusion, visual impairment, optic nerve disorder which included Potassium drip, anti-hypertensive meds. Clinical courses is as follows: The patient received BNT162b2 (BNT162B2), on 11May2022 as dose 2, single (Lot number: FK9894) intramuscular for covid-19 immunisation. The patient experienced hypertensive crisis, requiring emergency hospitalization with 5 days in Intensive Care Unit. headaches, bruising, visual changes, slowing of optic nerve. Covid wasn't tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 29.11.2022
Impfdatum: 13.04.2022
Beginn: 29.11.2022
Tage bis Beginn: 230,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Malaise Pyrexia

Symptomtext

FEVER, NOT FEELING WELL

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Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2516747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 52,0
Geschlecht: F
Eingang: 25.11.2022
Impfdatum: 24.05.2022
Beginn: 07.07.2022
Tage bis Beginn: 44,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Oropharyngeal pain Pain

Symptomtext

I had headache, sore throat, feeling fatigue; I wasn't sure if it was a fibromyalgia flare-up, but I realized my significant other was recovering from COVID-19 so I knew I probably had just contracted it from him. My doctor told me I didn't need to take a test to confirm since my partner had already taken an at-home test and PCR tests, which both came back positive. I'm disabled so I don't work, and having fibromyalgia only worsened the pain of my symptoms. I was in so much physical pain. I took MOTRIN, TYLENOL, and MUCINEX to help subside my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Cancer; Chronic Pain; Chronic Migraine; Chronic Fatigue; IBS; Bladder Spasms; Arrhythmia; Major Depressive Disorder; Arthritis; Chronic Shingles; Chronic Lung Issues
Andere Medikamente: Acyclovir; AIMOVIG; atenolol; BUSPAR; vitamin D3; FLEXURAL; BENADRYL; LEXAPRO; ADVAIR; FLONASE; albuterol; melatonin; SINGULAIR; multivitamin; nortriptyline; PROTONIX; VESICARE; TOPAMAX; vitamin B12; MOTRIN; medical marijuana
Allergien: Dander; mold; mildew; pollen; latex; morphine; opioids; adhesives
Vorherige Impfungen: -

VAERS 2513654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 30.03.2022
Beginn: 09.05.2022
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Alanine aminotransferase Albumin globulin ratio Angiogram Anion gap Atrial fibrillation Basophil count Blood albumin Blood albumin decreased Blood alkaline phosphatase Blood bilirubin Blood calcium Blood calcium decreased Blood chloride Blood cholesterol Blood creatinine Blood creatinine increased Blood glucose Blood glucose increased

Symptomtext

AFib (HR erratic, up to 180 bpm); minimal soreness at injection site; Bumps, rash-like, 50 bumps in total, mostly from very top of thighs up, but some on rt knee. Most on rt side, but not all. A few bumps at first, and then more.; Vaginal Yeast Infection; LDL increased; Diarrhea; Calcium decreased; Creatinine increased; Glucose increased; Albumin decreased; Sodium decreased; BUN increased; Stye in Rt eye; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Mar2022 as dose 4 (booster), single (Lot number: FK9894), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Chest radiograph", start date: 08Apr2016, stop date: 08Apr2016, notes: CLINICAL INDICATION: Chest Pain.; "Breast implant" (unspecified if ongoing); "Shortness of breath" (unspecified if ongoing); "GI pains" (unspecified if ongoing); "Sigmoid colectomy", start date: 22Jun2022, stop date: 22Jun2022, notes: Cancer ruled out.; "TMJ", start date: Oct1980 (unspecified if ongoing); "TMJ arthroplasty", start date: 03Apr1985 (unspecified if ongoing); "hysterectomy", start date: 14Nov1989 (unspecified if ongoing), notes: ovaries not removed; "sentinel node dissection", start date: 07Mar2016 (unspecified if ongoing), notes: port placement (though updated diagnosis changed and no chemo needed); "bilateral mastectomy", start date: 15Apr2016 (unspecified if ongoing); "swap out expander for implants AND port removal", start date: 23Sep2016 (unspecified if ongoing); "bunionectomy", start date: 25Jan2018 (unspecified if ongoing); "arthritis in Rt knee", start date: Dec2018 (unspecified if ongoing), notes: some Hymovis injections and Zilretta injections every 3 months; "flushing" (unspecified if ongoing); "Headache" (unspecified if ongoing); "Insomnia" (unspecified if ongoing); "clogged eye oil glands" (unspecified if ongoing); "bone health" (unspecified if ongoing); "hair health" (unspecified if ongoing); "Joints" (unspecified if ongoing); "breast cancer", start date: 2016 (unspecified if ongoing), notes: diagnosed early 2016; "Hernia" (unspecified if ongoing), notes: the cause of many of the more minor GI pains that resolved w/o antibiotics; "nail health" (unspecified if ongoing); "COVID-19" (unspecified if ongoing); "sentinel node dissection" (unspecified if ongoing); "Robotic surgery" (unspecified if ongoing), notes: undetected hernia (1.5cm x 3 cm), pocket was cleaned out and the tear repaired; "latex (blistering with prolonged contact)" (unspecified if ongoing); "Diverticulitis", start date: 28Apr2017 (unspecified if ongoing); "Subsequent bouts", start date: 15Aug2018 (unspecified if ongoing), notes: (possibly exacerbated by 08Aug2018 Shingrix vaccination),; "bilateral mastectomy", start date: 15Apr2016 (unspecified if ongoing), notes: (right side at my option); "swap out expander for implants AND port removal", start date: 23Sep2016 (unspecified if ongoing); "Chest Pain" (unspecified if ongoing). Concomitant medication(s) included: B12 [CYANOCOBALAMIN], start date: 2017, stop date: 17Jul2022; FISH OIL taken for acne, start date: 01Nov2018, stop date: 17Jul2022; CALCIUM CITRATE taken for bone disorder, start date: Apr2016, stop date: 17Jun2022; D3 taken for bone disorder, start date: 2021, stop date: 17Jul2022; BIOTIN taken for hair disorder, nail disorder, start date: 2017, stop date: 17Jul2022; BIOFLEX CHONDROITIN taken for arthropathy, start date: 01Feb2020, stop date: 17Jul2022; MIDAZOLAM, start date: 22Jun2022 at 07:34; LIDOCAINE HCL, start date: 22Jun2022 at 07:44; DIPRIVAN, start date: 22Jun2022 at 07:44; EXPAREL, start date: 22Jun2022 at 07:59; NAROPIN [ROPIVACAINE], start date: 22Jun2022 at 07:59; DECADRON [DEXAMETHASONE], start date: 22Jun2022 at 08:17; SUBLIMAZE [FENTANYL], start date: 22Jun2022 at 09:10; BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE], start date: 22Jun2022 at 09:18; INDIGO CARMINE, start date: 22Jun2022 at 10:14; ROCURONIUM, start date: 22Jun2022 at 11:27; ZOFRAN [ONDANSETRON], start date: 22Jun2022 at 12:04; EPHEDRINE, start date: 22Jun2022 at 12:09; BRIDION, start date: 22Jun2022 at 12:16; INVANZ. Past drug history included: Danocrine, reaction(s): "significant hives"; Depo-medrol, reaction(s): "severe headache"; Depo-medrol, reaction(s): "insomnia"; Depo-medrol, reaction(s): "several days of hot flushing - red faced"; Arimidex (anastrozole), start date: 2016, stop date: 28Apr2017, reaction(s): "Breast cancer", notes: Cases prior to 16Apr2020 would not resolve until I discontinued Arimidex (anastrozole) that I was taken subsequent to ER+, PR+, HER2- breast cancer diagnosed early 2016.; Flagyl, start date: 17Mar2022, notes: 500 mg, Preop, at 1, 2, and 11 pm; Bactrim, start date: 17Mar2022, notes: 800-160 mg; Zilretta injections for TX for arthritis in Rt knee, notes: every 3 months; Suprep bowel prep, start date: 24May2022, stop date: 24May2022, notes: Prior to colonoscopy. Only half dose needed due to having been on liquid diet.; Miralax, start date: 21Jun2022, stop date: 21Jun2022, notes: Miralax (238 mg) taken day before colectomy. Vaccination history included: coviD-19 vaccine moderna (DOSE 1, SINGLE; Lot number: 029L20A, Dose: 0.5 ml; Site of administration: Right Arm, Time: about 10 am), administration date: 27Jan2021, for COVID-19 immunization, reaction(s): "sore injection site", "slight tenderness at injection site", "red injection site", "swollen arm (injection site reaction)", "sore injection site", "red injection site", "swollen arm (injection site reaction)"; coviD-19 vaccine moderna (DOSE 2, SINGLE; Lot number: 023M20A, Dose: 0.5 ml; Site of administration: Right thigh), administration date: 24Feb2021, for COVID-19 immunization, reaction(s): "sore thigh", "red thigh", "swollen thigh", "Fever", "Chills"; shingrix vaccine (possibly exacerbated by 08Aug2018, Shingrix vaccination), 22Jul2019, 23Mar2021, 23Dec2021, 17Mar2022), administration date: 08Aug2018, reaction(s): "Diverticulitis"; hymovis shots, administration date: 18Mar2021, for arthritis in Rt knee. The following information was reported: HORDEOLUM (non-serious) with onset 09May2022, outcome "recovered" (21May2022), described as "Stye in Rt eye"; BLOOD ALBUMIN DECREASED (non-serious) with onset 11Jun2022, outcome "unknown", described as "Albumin decreased"; BLOOD UREA INCREASED (non-serious) with onset 11Jun2022, outcome "unknown", described as "BUN increased"; BLOOD SODIUM DECREASED (non-serious) with onset 11Jun2022, outcome "unknown", described as "Sodium decreased"; BLOOD CALCIUM DECREASED (non-serious) with onset 23Jun2022, outcome "unknown", described as "Calcium decreased"; BLOOD CREATININE INCREASED (non-serious) with onset 23Jun2022, outcome "unknown", described as "Creatinine increased"; BLOOD GLUCOSE INCREASED (non-serious) with onset 23Jun2022, outcome "unknown", described as "Glucose increased"; ATRIAL FIBRILLATION (hospitalization, medically significant) with onset 26Jun2022, outcome "recovered", described as "AFib (HR erratic, up to 180 bpm)"; DIARRHOEA (non-serious) with onset 26Jun2022, outcome "not recovered", described as "Diarrhea"; LOW DENSITY LIPOPROTEIN INCREASED (non-serious) with onset 26Jun2022, outcome "unknown", described as "LDL increased"; VULVOVAGINAL MYCOTIC INFECTION (non-serious) with onset 29Jun2022, outcome "recovered" (Jun2022), described as "Vaginal Yeast Infection"; RASH (non-serious) with onset 10Jul2022, outcome "recovering", described as "Bumps, rash-like, 50 bumps in total, mostly from very top of thighs up, but some on rt knee. Most on rt side, but not all. A few bumps at first, and then more."; INJECTION SITE PAIN (non-serious), outcome "unknown", described as "minimal soreness at injection site". The patient was hospitalized for atrial fibrillation (start date: 26Jun2022, discharge date: 27Jun2022, hospitalization duration: 2 day(s)). The event "stye in rt eye" required physician office visit. The event "afib (hr erratic, up to 180 bpm)" required emergency room visit. The patient underwent the following laboratory tests and procedures: Alanine aminotransferase: (11Jun2022) 28 Units/L, notes: Standard Range: Standard Range less than 64 Units/L; Alanine aminotransferase (normal high range 64): (21Sep2021) 28, notes: Units/L; Albumin globulin ratio (1.0-2.4): (21Sep2021) 0.8, notes: Flag L; (11Jun2022) 0.8, notes: Standard Range: Standard Range 1.0 - 2.4 Flag: Flag L; Angiogram: (unspecified date) Unknown results; Anion gap (7-19): (21Sep2021) 13 mmol/L; (23Jun2022) 13 mmol/L; Anion gap (10-20): (11Jun2022) 13 mmol/L, notes: Standard Range: Standard Range 10 - 20 mmol/L; Basophil count (0.0-0.3): (unspecified date) 0.0 K/mcL, notes: Standard Range: Standard Range 0.0 - 0.3 K/mcL; Basophil count: (unspecified date) 0 %, notes: Standard Range: Standard Range %; Blood albumin (3.6-5.1): (21Sep2021) 3.3 g/dl, notes: Flag L; (11Jun2022) 3.3 g/dl, notes: Standard Range: Standard Range 3.6 - 5.1 g/dL; Blood alkaline phosphatase (45-117): (21Sep2021) 62, notes: Units/L; (11Jun2022) 62 Units/L, notes: Standard Range: Standard Range 45 - 117 Units/L; Blood bilirubin (0.2-1.0): (21Sep2021) 0.5 mg/dl; (11Jun2022) 0.5 mg/dl, notes: Standard Range: Standard Range 0.2 - 1.0 mg/dL; Blood calcium (8.4-10.2): (21Sep2021) 8.9 mg/dl; (11Jun2022) 8.9 mg/dl, notes: Standard Range: Standard Range 8.4 - 10.2 mg/dL; (23Jun2022) 8.0 mg/dl, notes: Flag L; Blood chloride (98-107): (11Jun2022) 107 mmol/L, notes: Standard Range: Standard Range 98 - 107 mmol/L; Blood chloride (97-110): (21Sep2021) 107 mmol/L; (23Jun2022) 105 mmol/L; Blood cholesterol: (26Jun2022) 199 mg/dl, notes: Standard Range: Standard Range less than 00 mg/dL. Patient is to continue watching diet and exercise; Blood cholesterol (normal high range 00): (unspecified date) 199 mg/dl; (22Oct2021) 199 mg/dl; Blood creatinine (0.51-0.95): (11Jun2022) 0.65 mg/dl, notes: Standard Range: Standard Range 0.51 - 0.95 mg/dL; Blood creatinine (0.51-0.95): (21Sep2021) 0.65 mmol/L; (23Jun2022) 1.07 mmol/L, notes: Flag H; Blood glucose: (11Jun2022) normal at 88 Kidney; Blood glucose (65-99): (11Jun2022) 88 mg/dl, notes: Standard Range: Standard Range 65 - 99 mg/dL; Blood glucose (70-99): (21Sep2021) 88 mmol/L; (23Jun2022) 154 mmol/L, notes: Flag H; Blood potassium (3.4-5.1): (21Sep2021) 4.3 mmol/L; (11Jun2022) 4.3 mmol/L, notes: Standard Range: Standard Range 3.4 - 5.1 mmol/L; (23Jun2022) 4.4 mmol/L; Blood pressure measurement: (11Jun2022) 99/59; Blood sodium (135-145): (21Sep2021) 144 mmol/L; (11Jun2022) 114 mmol/L, notes: Fasting Status: Sodium Standard Range: Standard Range 135 - 145 mmol/L; (23Jun2022) 138 mmol/L; Blood triglycerides: (unspecified date) 66; Blood triglycerides: (26Jun2022) normal at 66, notes: Standard Range: Standard Range less than 150 mg/dL. Patient is to continue watching diet and exercise; Blood triglycerides (normal high range 150): (22Oct2021) 66 mg/dl; Blood urea (6-20): (11Jun2022) 17 mg/dl, notes: Standard Range: Standard Range 6 - 20 mg/Dl; Blood urea (6-20): (21Sep2021) 17 mmol/L; (23Jun2022) 11 mmol/L; Blood urea: (11Jun2022) 26, notes: Standard Range: Standard Range 7 - 25 Flag: Flag H; Carbon dioxide (21-32): (21Sep2021) 28 mmol/L; (11Jun2022) 28 mmol/L, notes: Standard Range: Standard Range 21 - 32 mmol/L; (23Jun2022) 24 mmol/L; Chest X-ray: (unspecified date) Negative; (unspecified date) There is no component information for this result., notes: No suspicious pulmonary infiltrates. Blunting of the right costophrenic angle No pneumothorax The cardio media tinal ilhouette i unremarkable; Computerised tomogram thorax: (21Sep2021) No pulmonary embolus, notes: Small right and trace left pleural effusion with mild atelectasis at the lung bases; Echocardiogram: (unspecified date) unremarkable, notes: Comments from the Doctor's Office: Echocardiogram is unremarkable. Patient is cleared for surgery. Impression: Tran thoracic Echocardiogram (TTE); (unspecified date) Unknown results; (11Jun2022) 2.56; Ejection fraction: (unspecified date) 70 %; (11Jun2022) 70 %; Electrocardiogram: (unspecified date) Abnormal; (25Mar2021) sinus rhythm, notes: with occasional supraventricular premature complexes possible left atrial enlargement incomplete right bundle branch block borderline ecg unconfirmed report confirmed by, (15570) on 29Mar2021 9:23:38 am; (26Jun2022) atrial fibrillation, notes: with rapid ventricular response nonspecific st & t-wave abnormality abnormal rhythm ecg unconfirmed report confirmed by (5049) on 26Jul2022 10:05:34 am; (26Jun2022) atrial fibrillation septal myocardial infarction, notes: of indeterminate age abnormal ecg unconfirmed report confirmed by (5049) on 26Jul2022 10 :05 :37 am; (26Jun2022) sinus rhythm possible left atrial enlargement, notes: [-0.1mv p wave in v1/v2] septal myocardial infarction [40+ m q wave in v1/v2], of indeterminate age abnormal ecg unconfirmed report confirmed by medical on 26Jul2022 10:05:41 am; (25Mar2021) 78; (26Jun2022) 159; (26Jun2022) 85; (26Jun2022) 66; Electrocardiogram QT interval: (25Mar2021) 369; (26Jun2022) 182; (26Jun2022) 318; (26Jun2022) 337; (25Mar2021) 402; (26Jun2022) 271; (26Jun2022) 360; (26Jun2022) 351; Eosinophil count (0.0-0.5): (unspecified date) 0.0 K/mcL, notes: Standard Range: Standard Range 0.0 - 0.5 K/mcL; Eosinophil count: (unspecified date) 0 %, notes: Standard Range: Standard Range %; Full blood count: (unspecified date) Normal; (11Jun2022) normal; Globulin (2.0-4.0): (21Sep2021) 4.1, notes: Flag H; Globulin (2.0-4.0): (11Jun2022) 4.1 g/dl, notes: Standard Range: Standard Range 2.0 - 4.0 g/Dl Flag: Flag H; Glomerular filtration rate: (11Jun2022) 89, notes: Standard Range: Standard Range greater than equals to 60; Glomerular filtration rate (normal low range 60): (21Sep2021) 89, notes: Standard Range greater than equals to 60; (23Jun2022) 55, notes: Standard Range greater than equals to 60 Flag L; Glycosylated haemoglobin: (unspecified date) 5.5 %; (11Jun2022) 5.5 %, notes: Normal. No diabetes seen; Granulocyte count (0.0-0.2): (unspecified date) 0.1 K/mcL, notes: Standard Range: Standard Range 0.0 - 0.2 K/mcL; Granulocyte count: (unspecified date) 1 %, notes: Standard Range: Standard Range %; Haematocrit: (unspecified date) 36.4 %, notes: Standard Range 36 0 46 5 %; Haemoglobin: (unspecified date) 12.0 g/dl, notes: Standard Range: Standard Range 1 0 15 5 g/dL; High density lipoprotein: (unspecified date) 61, notes: Good; High density lipoprotein: (26Jun2022) very good at 61, notes: Standard Range: Standard Range greater than OR 50 mg/dL. Patient is to continue watching diet and exercise; High density lipoprotein (normal low range 50): (22Oct2021) 61 mg/dl; Annulus: (unspecified date) Normal; (unspecified date) Normal; (11Jun2022) 3.00; (11Jun2022) 0.80; (11Jun2022) 6.00; (11Jun2022) 1.24; (unspecified date) 88, notes: Blood sugar is normal at 88 Kidney and liver function is normal; BUN/ Creatinine Ratio (7-25): (21Sep2021) 26; (23Jun2022) 10; (26Jun2022) Unknown results, notes: After intravenous administration of contrast, there is adequate opacification of the pulmonary arteries. No suspicious filling defects to suggest presence of a pulmonary embolus No evidence of right heart strain. The heart size within normal limits. No pericardial effusion. No thoracic aortic aneurysm. No mediastinal or hilar lymphadenopathy; (27Jun2022) Unknown results, notes: No suspicious pulmonary infiltrates. Blunting of the right costophrenic angle No pneumothorax The cardiomediastinal silhouette is unremarkable; CHOL/HDLC RATIO (normal high range 5): (22Oct2021) 3.3, notes: calc; (11Jun2022) 1.2; (unspecified date) Normal; (11Jun2022) 227; (11Jun2022) 17.44; estimated central venous pressure: (unspecified date) 3 mmHg; (unspecified date) 17 mmHg; (unspecified date) Normal; (unspecified date) Normal; (unspecified date) Normal; (11Jun2022) 2.26; (unspecified date) Normal; (11Jun2022) 3.23; (unspecified date) 1.02; (11Jun2022) 24.8; (unspecified date) normal; (unspecified date) 1 mmHg; (unspecified date) 3 mmHg; (unspecified date) Normal; (11Jun2022) 10.9; (11Jun2022) 9.03; (11Jun2022) 7.1650055371; NON HDL CHOLESTEROL (normal high range 130): (22Oct2021) 138 mg/dl, notes: calc; (25Mar2021) 81; (26Jun2022) 75; (unspecified date) 6 mmHg; (unspecified date) 6 mmHg; (unspecified date) Normal; (27Jun2022) 148, notes: Standard Range BPM; (25Mar2021) 159; (26Jun2022) 165; (11Jun2022) 1.26; (25Mar2021) 114; (26Jun2022) 100; (26Jun2022) 92; (26Jun2022) 89; (25Mar2021) 71; (26Jun2022) 60; (26Jun2022) 52; (26Jun2022) 49; (unspecified date) 0.97; respirophasicdiameter (normal high range 50): (unspecified date) normal; (unspecified date) mildly dilated; (unspecified date) Normal; (unspecified date) 17 mmHg; (22Jun2022) Unknown results; (unspecified date) Normal; (25Mar2021) 69; (26Jun2022) 0; (26Jun2022) 43; (26Jun2022) 59; (unspecified date) Normal; (11Jun2022) 17.4; (unspecified date) 3.3cm^2; (unspecified date) 1.96cm^2/m^2; (unspecified date) Normal; Liver function test: (11Jun2022) 18 Units/L, notes: Standard Range: Standard Range less than equals 37 Units/L; Liver function test (normal high range 37): (21Sep2021) 18, notes: Units/L; (11Jun2022) normal; Low density lipoprotein: (unspecified date) 122; Low density lipoprotein: (26Jun2022) slightly elevated at 122, notes: Standard Range: Standard Range mg/dL (calc). Patient is to continue watching diet and exercise; (22Oct2021) 122 mg/dl, notes: Flag H; Lymphocyte count (1.0-4.0): (unspecified date) 1.9 K/mcL, notes: Standard Range: Standard Range 1.0 - 4.0 K/mcL; Lymphocyte count: (unspecified date) 14 %, notes: Standard Range: Standard Range %; Mean cell haemoglobin concentration (30-36.5): (unspecified date) 33.0 g/dl, notes: Standard Range: Standard Range 30 36.5 g/dL; Mean cell volume (78.0-100.0): (unspecified date) 100.6 fl, notes: Standard Range: Standard Range 78.0 100.0 fl Flag: Flag L; Monocyte count (0.3-0.9): (unspecified date) 1.1 K/mcL, notes: Standard Range: Standard Range 0.3 - 0.9 K/mcL Flag: Flag H; Monocyte count: (unspecified date) 8 %, notes: Standard Range: Standard Range %; Neutrophil count (1.8-7.7): (unspecified date) 10.9 K/mcL, notes: Standard Range: Standard Range 1.8 - 7.7 K/mcL Flag: Flag H; Neutrophil count: (unspecified date) 77 %, notes: Standard Range: Standard Range %; Non-high-density lipoprotein cholesterol: (26Jun2022) 138 mg/dl, notes: Standard Range: Standard Range less than 130 mg/dL (calc); Platelet function test (140-450): (unspecified date) 209 K/mcL, notes: Standard Range: Standard Range 140 - 450 K/mcL; Protein total (6.4-8.2): (21Sep2021) 7.4; Protein total (6.4-8.2): (11Jun2022) 7.4 g/dl, notes: Standard Range: Standard Range 6.4 - 8.2 g/dL; Red blood cell count: (unspecified date) 0 /100 WBC, notes: Standard Range: Standard Range less than equals to 0 /100 WBC; (unspecified date) 3.62 mil/mcL, notes: Standard Range: Standard Range 4 00 5 0 mil/mcL Flag: Flag L; Red cell distribution width (11.0-15.0): (unspecified date) 12.6 %, notes: Standard Range: Standard Range 11.0 15.0 %; Red cell distribution width (30 0-50 0): (unspecified date) 46.5 fL, notes: Standard Range: Standard Range 39 0 50 0 fL; SARS-CoV-2 test: (unspecified date) Unknown results; (06Jan2022) Negative; Scan: (11Jun2022) 9.03, notes: Component: MV E Tissue Vel Med; (11Jun2022) 10.9, notes: Component: MV E Tissue Vel Lat; (11Jun2022) 1.26, notes: Component: PV Peak Velocity; (11Jun2022) 17.4, notes: Component: Tricuspid valve annular peak velocity; (11Jun2022) 17.44, notes: Component: Est Right Vent Systolic Pressure by Tricuspid Regurgitation Jet; (11Jun2022) 24.8, notes: Component: LVOT VTI; (11Jun2022) 1.2, notes: Component: DOP Calc LVOT Peak Vel; (11Jun2022) 3.23, notes: Component: Left Ventricular Internal Dimension in Diastole; (11Jun2022) 2.26, notes: Component: Left Internal Dimension in Systole; (11Jun2022) 2.56, notes: Component: Tricuspid Annular Plane Systolic Excursion; Thyroid function test: (unspecified date) Normal; (11Jun2022) normal; Total cholesterol/HDL ratio: (26Jun2022) 3.3 (calc), notes: Standard Range: Standard Range less than 5 0 (calc); White blood cell count: (unspecified date) 14.0 K/mcL, notes: Standard Range: Standard Range 4 11 0 K/mcL Flag: Flag H. Therapeutic measures were taken as a result of diarrhoea, vulvovaginal mycotic infection, rash, hordeolum. Per clinical course, Patient happened to be talking to a MODERNA employee about possible enrollment in a clinical trial for her husband when she happened to mention a drug reaction that she was having a rash. The rash was suspected to be related to a drug (including probiotics) taken in the last year (per the dermatologist); the culprit had not yet been identified, but the current best guess is probiotics: 4 different probiotic challenges have resulted in a rash. Each time, the rash cleared over then subsequent 1-3 weeks. However, that conversation required her to submit an AE report, and Moderna followed up with me. Because she did not particularly think that the crash was caused by the vaccine, please do not bother the medical professionals who have treated her. You do not have my permission to contact my providers without contacting me first. I do not want to waste their time. It was easier to type the information than to fill out the form. Allergic to Danocrin (significant hives), depo-medrol (severe headache, insomnia, several days of hot flushing-red faced), latex (blistering with prolonged contact), and possible other drug (rash that is currently presumed to be due to new probiotics introduced after multiple rounds of antibiotics in the spring, followed by colon surgery for diverticulitis in June. COVID history: On 30Dec2021, she was symptomatic (mild cold symptoms, no loss of taste or smell, no fever), had possibly been exposed to COVID, and so she was tested. The results were not reported for about 2 weeks (and later it was determined that the testing site was somewhat suspect.) With no results available, on 06Jan2022 she tested negative at # (facility name withheld). About 2 weeks later, the first test was reported out as Positive. Given the bad reputation of the first site, it is Unknown whether or not she has had COVID 19. No acute illnesses when vaccinated. Chronic or long-standing health conditions. Diverticulitis started 28Apr2017. Subsequent bouts 15Aug2018 (possibly exacerbated by 08Aug2018. Shingrix vaccination), 22Jul2019, 23Mar2021, 23Dec2021, 17Mar2022. Cases prior to 16Apr2020 would not resolve until I discontinued Arimidex (anastrozole) that she was taken subsequent to ER+, PR+, HER2- breast cancer diagnosed early 2016. Arimidex was stopped on 28Apr2017 due to onset of substantial side effects (hot flashes, feeling awful); my extremely favorable cancer prognosis did not justify continuing the Arimidex and treating the symptoms that drug caused. In addition to treated diverticulitis cases, she had a large number of untreated) GI pains, the frequency and severity of which increased over time. After the 17Mar2022 case, she saw a surgeon, who recommended surgery, but a colonoscopy was to be performed first to rule out cancer (it was ruled out). She was on a 7-day course of flagyl 500 mg and Bactrim 800-160 mg starting 17Mar2022, then an 11-day course of Flagyl and a 7-day course of Bactrim starting 10Jun22. The day before surgery (ie, on 21Jun2022) she had flagyl: 500 mg: Preop, at 1, 2, and 11 pm neomycin: 1 g (2 tabs): Preop, at 1, 2, and 11 pm. Then in surgery she had more antibiotics. Sigmoid colectomy performed 22Jun2022. Cancer ruled out. At the time of (robotic) surgery, a previously undetected hernia (1.5cm x 3 cm) was found; the pocket was cleaned out and the tear repaired. This hernia was almost surely the cause of many of the more minor GI pains that resolved w/o antibiotics. Treated with Tylenol and very little morphine in the hospital (she did not get much relieve from the morphine because she did not think she could push the pump often and she did not know the dose in the bag was so low. But she did not hurt terribly anyhow. Treated with Tylenol and 2 days of Oxycodone at home. Other significant long-standing medical history includes: TMJ (started Oct1980) and TMJ arthroplasty (03Apr1985). No recent changes 14Nov1989 hysterectomy (ovaries not removed) 07Mar2016 sentinel node dissection, port placement (though updated diagnosis changed and no chemo TX needed) 15Apr2016 bilateral mastectomy (right side at my option), 23Sep2016 swap out expander for implants AND port removal, 25Jan2018 bunionectomy, Dec2018 ff: for arthritis in Rt knee: some Hymovis injections and Zilretta injections every 3 months. The knee gets better, then worse, then better, then worse with injection. Recent injections: 21Jan2021, 26Aug2021, 02Dec2021, 09Mar2022, 09Jun2022; 15Sep2022. On 11May2021 had Depo- Medrol instead of Zilretta with reactions of headache, insomnia, flushing (like sunburn) - and it not only didnot help my knee, but it also made it worse for 3 months. (This is another AE - AE #17 below - but not due to moderna. flushing resolved in 4 days, headache in 2-3 days, insomnia in 1 days. pain in knee was not improved) Hymovis shots 11Mar2021 and 18Mar2021. Suprep Bowel Prep taken 24May2022, prior to colonscopy. Only half dose needed due to having been on liquid diet and Miralax for a week prior to procedure. Miralax (238 mg) taken 21Jun2022 day before colectomy. Primary on 14Jul2022 am. Because Eliquis was suspected, went to cardiologist 14Jul2022 pm. Eliquis to Xarelto. She suspect Eliquis was unfairly blamed for rash. Went to Dermatologist 18Jul2022. Biopsy report was suspected bug bite, contact dermatitis, drug reaction, or bullous pemphigoid. Overall rash was not consistent with bite or contact dermatitis. Bullous pemphigoid was later ruled out by biopsy. Medications Given for 22Jun2022 surgery: MIDAZolam (VERSED) Last given 22Jun2022 7:34 AM, lidocaine HCl Last given 22Jun2022 7:44 AM, propofol (DIPRIVAN) Last given 22Jun2022 7:44 AM, bupivacaine liposome (EXPAREL) Last given 22Jun2022 7:59 AM, ropivacaine (NAROPIN) Last given 22Jun2022 7:59 AM, dexAMETHasone (DECADRON) Last given 22Jun2022 8:17 AM, fentaNYL (SUBLIMAZE) Last given 22Jun2022 9:10 AM, diphenhydrAMINE (BENADRYL) Last given 22Jun2022 9:18 AM, indigo carmine Last given 22Jun2022 10:14 AM, rocuronium Last given 22Jun2022 11:27 AM, ondansetron (ZOFRAN) Last given 22Jun2022 12:04 PM, ePHEDrine Last given 22Jun2022 12:09 PM, sugammadex (BRIDION) Last given 22Jun2022 12:16 PM, ertapenem (INVanz) injection (time not given), Current Facility-Administered Medications During ER visit 26Jun2022 for Afib: sodium chloride 0.9 % flush bag 25mL Intravenous PRN, Sodium Chloride (PF) 0.9 % injection 2 mL Intracatheter 2 times per day, last Admin: 2Ml at 26Jun2022 0957, Sodium Chloride (NORMAL SALINE) 0.9 % bolus 500mL Intravenous once, diltiazem 5mg Intravenous once. Report stopping in Sep2022. Just didn't quite get it finalized to send to Moderna at that time. I waited to send it in until / had done the September probiotic challenge to get more confidence that the introduction of new probiotics was the likely cause of the rashes. Given the antibiotic exposure in March and especially June, prior to and during surgery, and given the stress of surgery itself, it is not unreasonable to assume that my gut was stressed. The introduction of new probiotics seems to have been the triggers 4 times for the 4 rounds of rash. It would be interesting to know if there has been an uptick of Afib following non-cardiac surgery since the COVID vaccines have been available but doubt it. It would be interesting to know if there has been an uptick of Afib following non-cardiac surgery since the COVID vaccines have been available but doubt it. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 2,0
Labordaten: Test Date: 20220611; Test Name: GPT/ALT; Result Unstructured Data: Test Result:28 Units/L; Comments: Standard Range: Standard Range less than 64 Units/L; Test Date: 20210921; Test Name: GPT/ALT; Result Unstructured Data: Test Result:28; Comments: Units/L; Test Date: 20210921; Test Name: A/G Ratio; Result Unstructured Data: Test Result:0.8; Comments: Flag L; Test Date: 20220611; Test Name: A/G Ratio; Result Unstructured Data: Test Result:0.8; Comments: Standard Range: Standard Range 1.0 - 2.4 Flag: Flag L; Test Name: CT angiogram; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210921; Test Name: Anion Gap; Result Unstructured Data: Test Result:13 mmol/L; Test Date: 20220623; Test Name: Anion Gap; Result Unstructured Data: Test Result:13 mmol/L; Test Date: 20220611; Test Name: Anion Gap; Result Unstructured Data: Test Result:13 mmol/L; Comments: Standard Range: Standard Range 10 - 20 mmol/L; Test Name: Absolute Basophils; Result Unstructured Data: Test Result:0.0 K/mcL; Comments: Standard Range: Standard Range 0.0 - 0.3 K/mcL; Test Name: Basophils, Percent; Test Result: 0 %; Comments: Standard Range: Standard Range %; Test Date: 20210921; Test Name: Albumin; Result Unstructured Data: Test Result:3.3 g/dl; Comments: Flag L; Test Date: 20220611; Test Name: Albumin; Result Unstructured Data: Test Result:3.3 g/dl; Comments: Standard Range: Standard Range 3.6 - 5.1 g/dL; Test Date: 20210921; Test Name: Alkaline Phosphatase; Result Unstructured Data: Test Result:62; Comments: Units/L; Test Date: 20220611; Test Name: Alkaline Phosphatase; Result Unstructured Data: Test Result:62 Units/L; Comments: Standard Range: Standard Range 45 - 117 Units/L; Test Date: 20210921; Test Name: Bilirubin; Test Result: 0.5 mg/dl; Test Date: 20220611; Test Name: Bilirubin, Total; Test Result: 0.5 mg/dl; Comments: Standard Range: Standard Range 0.2 - 1.0 mg/dL; Test Date: 20210921; Test Name: Calcium; Test Result: 8.9 mg/dl; Test Date: 20220611; Test Name: Calcium; Test Result: 8.9 mg/dl; Comments: Standard Range: Standard Range 8.4 - 10.2 mg/dL; Test Date: 20220623; Test Name: Calcium; Test Result: 8.0 mg/dl; Comments: Flag L; Test Date: 20220611; Test Name: Chloride; Result Unstructured Data: Test Result:107 mmol/L; Comments: Standard Range: Standard Range 98 - 107 mmol/L; Test Date: 20210921; Test Name: Chloride; Result Unstructured Data: Test Result:107 mmol/L; Test Date: 20220623; Test Name: Chloride; Result Unstructured Data: Test Result:105 mmol/L; Test Date: 20220626; Test Name: Total cholesterol; Test Result: 199 mg/dl; Comments: Standard Range: Standard Range less than 00 mg/dL Patient is to continue watching diet and exercise.; Test Name: Total cholesterol; Test Result: 199 mg/dl; Test Date: 20211022; Test Name: Total cholesterol; Test Result: 199 mg/dl; Test Date: 20220611; Test Name: Creatinine; Test Result: 0.65 mg/dl; Comments: Standard Range: Standard Range 0.51 - 0.95 mg/dL; Test Date: 20210921; Test Name: Creatinine; Result Unstructured Data: Test Result:0.65 mmol/L; Test Date: 20220623; Test Name: Creatinine; Result Unstructured Data: Test Result:1.07 mmol/L; Comments: Flag H; Test Date: 20220611; Test Name: Blood sugar; Result Unstructured Data: Test Result:normal at 88 Kidney; Test Date: 20220611; Test Name: Glucose; Test Result: 88 mg/dl; Comments: Standard Range: Standard Range 65 - 99 mg/dL; Test Date: 20210921; Test Name: Glucose; Result Unstructured Data: Test Result:88 mmol/L; Test Date: 20220623; Test Name: Glucose; Result Unstructured Data: Test Result:154 mmol/L; Comments: Flag H; Test Date: 20210921; Test Name: Potassium; Result Unstructured Data: Test Result:4.3 mmol/L; Test Date: 20220611; Test Name: Potassium; Result Unstructured Data: Test Result:4.3 mmol/L; Comments: Standard Range: Standard Range 3.4 - 5.1 mmol/L; Test Date: 20220623; Test Name: Potassium; Result Unstructured Data: Test Result:4.4 mmol/L; Test Date: 20220611; Test Name: Blood pressure; Result Unstructured Data: Test Result:99/59; Test Date: 20210921; Test Name: Sodium; Result Unstructured Data: Test Result:144 mmol/L; Test Date: 20220611; Test Name: Sodium; Result Unstructured Data: Test Result:114 mmol/L; Comments: Fasting Status: Sodium Standard Range: Standard Range 135 - 145 mmol/L; Test Date: 20220623; Test Name: Sodium; Result Unstructured Data: Test Result:138 mmol/L; Test Name: Triglycerides; Result Unstructured Data: Test Result:66; Test Date: 20220626; Test Name: Triglycerides; Result Unstructured Data: Test Result:normal at 66 mg/dl; Comments: Standard Range: Standard Range less than 150 mg/dL Patient is to continue watching diet and exercise.; Test Date: 20211022; Test Name: TRIGLYCERIDES; Test Result: 66 mg/dl; Test Date: 20220611; Test Name: BUN; Test Result: 17 mg/dl; Comments: Standard Range: Standard Range 6 - 20 mg/Dl; Test Date: 20210921; Test Name: BUN; Result Unstructured Data: Test Result:17 mmol/L; Test Date: 20220623; Test Name: BUN; Result Unstructured Data: Test Result:11 mmol/L; Test Date: 20220611; Test Name: BUN/ Creatinine Ratio; Result Unstructured Data: Test Result:26; Comments: Standard Range: Standard Range 7 - 25 Flag: Flag H; Test Date: 20210921; Test Name: Carbon Dioxide; Result Unstructured Data: Test Result:28 mmol/L; Test Date: 20220611; Test Name: Carbon Dioxide; Result Unstructured Data: Test Result:28 mmol/L; Comments: Standard Range: Standard Range 21 - 32 mmol/L; Test Date: 20220623; Test Name: Carbon Dioxide; Result Unstructured Data: Test Result:24 mmol/L; Test Name: Pulmonary embolus; Test Result: Negative ; Test Name: XR CHEST; Result Unstructured Data: Test Result:There is no component information for this result.; Comments: No suspicious pulmonary infiltrates. Blunting of the right costophrenic angle No pneumothorax The cardio media tinal ilhouette i unremarkable; Test Date: 20210921; Test Name: CTA CHEST PULM EMBOLISM; Result Unstructured Data: Test Result:No pulmonary embolus; Comments: Small right and trace left pleural effusion with mild atelectasis at the lung bases.; Test Name: Echocardiogram; Result Unstructured Data: Test Result:unremarkable; Comments: Comments from the Doctor's Office: Echocardiogram is unremarkable. Patient is cleared for surgery. Impression: Tran thoracic Echocardiogram (TTE); Test Name: Transthoracic echocardiography; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220611; Test Name: Tricuspid Annular Plane Systolic Excursion; Result Unstructured Data: Test Result:2.56; Test Name: Ejection fraction; Test Result: 70 %; Test Date: 20220611; Test Name: Ejection Fraction; Test Result: 70 %; Test Name: EKG; Result Unstructured Data: Test Result:Abnormal; Test Date: 20210325; Test Name: Electrocardiogram; Result Unstructured Data: Test Result:sinus rhythm; Comments: with occasional supraventricular premature complexes possible left atrial enlargement incomplete right bundle branch block borderline ecg unconfirmed report confirmed by, (15570) on 29Mar2021 9:23:38 am; Test Date: 20220626; Test Name: Electrocardiogram; Result Unstructured Data: Test Result:atrial fibrillation; Comments: with rapid ventricular response nonspecific st & t-wave abnormality abnormal rhythm ecg unconfirmed report confirmed by (5049) on 26Jul2022 10:05:34 am; Test Date: 20220626; Test Name: Electrocardiogram; Result Unstructured Data: Test Result:atrial fibrillation septal myocardial infarction; Comments: of indeterminate age abnormal ecg unconfirmed report confirmed by (5049) on 26Jul2022 10 :05 :37 am; Test Date: 20220626; Test Name: Electrocardiogram; Result Unstructured Data: Test Result:sinus rhythm possible left atrial enlargement; Comments: [-0.1mv p wave in v1/v2] septal myocardial infarction [40+ m q wave in v1/v2], of indeterminate age abnormal ecg unconfirmed report confirmed by (5049) on 26Jul2022 10:05:41 am; Test Date: 20210325; Test Name: Ventricular Rate EKG/Min (BPM); Result Unstructured Data: Test Result:78; Test Date: 20220626; Test Name: Ventricular Rate EKG/Min (BPM); Result Unstructured Data: Test Result:159; Test Date: 20220626; Test Name: Ventricular Rate EKG/Min (BPM); Result Unstructured Data: Test Result:85; Test Date: 20220626; Test Name: Ventricular Rate EKG/Min (BPM); Result Unstructured Data: Test Result:66; Test Date: 20210325; Test Name: QT Interval (MSEC); Result Unstructured Data: Test Result:369; Test Date: 20220626; Test Name: QT Interval (MSEC); Result Unstructured Data: Test Result:182; Test Date: 20220626; Test Name: QT Interval (MSEC); Result Unstructured Data: Test Result:318; Test Date: 20220626; Test Name: QT Interval (MSEC); Result Unstructured Data: Test Result:337; Test Date: 20210325; Test Name: QTc; Result Unstructured Data: Test Result:402; Test Date: 20220626; Test Name: QTc; Result Unstructured Data: Test Result:271; Test Date: 20220626; Test Name: QTc; Result Unstructured Data: Test Result:360; Test Date: 20220626; Test Name: QTc; Result Unstructured Data: Test Result:351; Test Name: Absolute Eosinophils; Result Unstructured Data: Test Result:0.0 K/mcL; Comments: Standard Range: Standard Range 0.0 - 0.5 K/mcL; Test Name: Eosinophils, Percent; Test Result: 0 %; Comments: Standard Range: Standard Range %; Test Name: CBC; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: CBC; Result Unstructured Data: Test Result:normal; Test Date: 20210921; Test Name: Globulin; Result Unstructured Data: Test Result:4.1; Comments: Flag H; Test Date: 20220611; Test Name: Globulin; Result Unstructured Data: Test Result:4.1 g/dl; Comments: Standard Range: Standard Range 2.0 - 4.0 g/Dl Flag: Flag H; Test Date: 20220611; Test Name: Glomerular Filtration Rate; Result Unstructured Data: Test Result:89; Comments: Standard Range: Standard Range greater than equals to 60; Test Date: 20210921; Test Name: Glomerular Filtration Rate; Result Unstructured Data: Test Result:89; Comments: Standard Range greater than equals to 60; Test Date: 20220623; Test Name: Glomerular Filtration Rate; Result Unstructured Data: Test Result:55; Comments: Standard Range greater than equals to 60 Flag L; Test Name: Hba1c; Test Result: 5.5 %; Test Date: 20220611; Test Name: Hba1c; Test Result: 5.5 %; Comments: Normal No diabetes seen.; Test Name: Absolute Immmature Granulocytes; Result Unstructured Data: Test Result:0.1 K/mcL; Comments: Standard Range: Standard Range 0.0 - 0.2 K/mcL; Test Name: Immature Granulocytes; Test Result: 1 %; Comments: Standard Range: Standard Range %; Test Name: HCT; Test Result: 36.4 %; Comments: Standard Range 36 0 46 5 %; Test Name: HGB; Result Unstructured Data: Test Result:12.0 g/dl; Comments: Standard Range: Standard Range 1 0 15 5 g/dL; Test Name: HDL; Result Unstructured Data: Test Result:61; Comments: Good; Test Date: 20220626; Test Name: HDL; Result Unstructured Data: Test Result:very good at 61 mg/dl; Comments: Standard Range: Standard Range greater than OR 50 mg/dL Patient is to continue watching diet and exercise.; Test Date: 20211022; Test Name: HDL CHOLESTEROL; Test Result: 61 mg/dl; Test Name: Annulus; Result Unstructured Data: Test Result:Normal; Test Name: ATRIAL SEPTUM; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: AV Mean Gradient; Result Unstructured Data: Test Result:3.00; Test Date: 20220611; Test Name: AV Mean Velocity; Result Unstructured Data: Test Result:0.80; Test Date: 20220611; Test Name: AV Peak Gradient; Result Unstructured Data: Test Result:6.00; Test Date: 20220611; Test Name: AV Peak Velocity; Result Unstructured Data: Test Result:1.24; Test Name: Blood sugar; Result Unstructured Data: Test Result:88; Comments: Blood sugar is normal at 88 Kidney and liver function is normal; Test Date: 20210921; Test Name: BUN/ Creatinine Ratio; Result Unstructured Data: Test Result:26; Test Date: 20220623; Test Name: BUN/ Creatinine Ratio; Result Unstructured Data: Test Result:10; Test Date: 20220626; Test Name: chest radiograph; Result Unstructured Data: Test Result:Unknown results; Comments: After intravenous administration of contrast, there is adequate opacification of the pulmonary arteries. No suspicious filling defects to suggest presence of a pulmonary embolus No evidence of right heart strain. The heart size within normal limits. No pericardial effusion. No thoracic aortic aneurysm. No mediastinal or hilar lymphadenopathy.; Test Date: 20220627; Test Name: chest radiograph; Result Unstructured Data: Test Result:Unknown results; Comments: No suspicious pulmonary infiltrates. Blunting of the right costophrenic angle No pneumothorax The cardiomediastinal silhouette is unremarkable; Test Date: 20211022; Test Name: CHOL/HDLC RATIO; Result Unstructured Data: Test Result:3.3; Comments: calc; Test Date: 20220611; Test Name: DOP Calc LVOT Peak Vel; Result Unstructured Data: Test Result:1.2; Test Name: Doppler: Transvalvular velocity; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: E Wave Decelaration Time; Result Unstructured Data: Test Result:227; Test Date: 20220611; Test Name: Est Right Vent Systolic Pressure by Tricuspid Regurgitation Jet; Result Unstructured Data: Test Result:17.44; Test Name: estimated central venous pressure; Result Unstructured Data: Test Result:3 mmHg; Test Name: estimated peak pressure; Result Unstructured Data: Test Result:17 mmHg; Test Name: Leaflet separation; Result Unstructured Data: Test Result:Normal; Test Name: leaflets; Result Unstructured Data: Test Result:Normal; Test Name: LEFT ATRIUM; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: Left Internal Dimenson in Systole; Result Unstructured Data: Test Result:2.26; Test Name: Left ventricle cavity size; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: Left Ventricular Internal Dimension in Diastole; Result Unstructured Data: Test Result:3.23; Test Name: LVOT to aortic valve VTI ratio; Result Unstructured Data: Test Result:1.02; Test Date: 20220611; Test Name: LVOT VTI; Result Unstructured Data: Test Result:24.8; Test Name: main pulmonary artery; Result Unstructured Data: Test Result:normal; Test Name: mean diastolic gradient; Result Unstructured Data: Test Result:1 mmHg; Test Name: mean systolic gradient; Result Unstructured Data: Test Result:3 mmHg; Test Name: Mitral valve; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: MV E Tissue Vel Lat; Result Unstructured Data: Test Result:10.9; Test Date: 20220611; Test Name: MV E Tissue Vel Med; Result Unstructured Data: Test Result:9.03; Test Date: 20220611; Test Name: MV E Wave Vel/E Tissue Vel Med; Result Unstructured Data: Test Result:7.1650055371; Test Date: 20211022; Test Name: NON HDL CHOLESTEROL; Test Result: 138 mg/dl; Comments: calc; Test Date: 20210325; Test Name: P Axis (Degrees); Result Unstructured Data: Test Result:81; Test Date: 20220626; Test Name: P Axis (Degrees); Result Unstructured Data: Test Result:75; Test Name: peak systolic gradient; Result Unstructured Data: Test Result:6 mmHg; Test Name: peak systolic gradient; Result Unstructured Data: Test Result:6 mmHg; Test Name: pericardium; Result Unstructured Data: Test Result:Normal; Test Date: 20220627; Test Name: Predicted HR Max; Result Unstructured Data: Test Result:148; Comments: Standard Range BPM; Test Date: 20210325; Test Name: PR-Interval (MSEC); Result Unstructured Data: Test Result:159; Test Date: 20220626; Test Name: PR-Interval (MSEC); Result Unstructured Data: Test Result:165; Test Date: 20220611; Test Name: PV Peak Velocity; Result Unstructured Data: Test Result:1.26; Test Date: 20210325; Test Name: QRS-Interval (MSEC); Result Unstructured Data: Test Result:114; Test Date: 20220626; Test Name: QRS-Interval (MSEC); Result Unstructured Data: Test Result:100; Test Date: 20220626; Test Name: QRS-Interval (MSEC); Result Unstructured Data: Test Result:92; Test Date: 20220626; Test Name: QRS-Interval (MSEC); Result Unstructured Data: Test Result:89; Test Date: 20210325; Test Name: R Axis (Degrees); Result Unstructured Data: Test Result:71; Test Date: 20220626; Test Name: R Axis (Degrees); Result Unstructured Data: Test Result:60; Test Date: 20220626; Test Name: R Axis (Degrees); Result Unstructured Data: Test Result:52; Test Date: 20220626; Test Name: R Axis (Degrees); Result Unstructured Data: Test Result:49; Test Name: ratio of LVOT to aortic valve peak velocity; Result Unstructured Data: Test Result:0.97; Test Name: respirophasicdiameter; Result Unstructured Data: Test Result:normal %; Test Name: RIGHT ATRIUM; Result Unstructured Data: Test Result:mildly dilated; Test Name: Right ventricle cavity size; Result Unstructured Data: Test Result:Normal; Test Name: RV pressure during systole; Result Unstructured Data: Test Result:17 mmHg; Test Date: 20220622; Test Name: Sigmoid collectomy; Result Unstructured Data: Test Result:Unknown results; Test Name: Systolic function; Result Unstructured Data: Test Result:Normal; Test Date: 20210325; Test Name: T Axis (Degrees); Result Unstructured Data: Test Result:69; Test Date: 20220626; Test Name: T Axis (Degrees); Result Unstructured Data: Test Result:0; Test Date: 20220626; Test Name: T Axis (Degrees); Result Unstructured Data: Test Result:43; Test Date: 20220626; Test Name: T Axis (Degrees); Result Unstructured Data: Test Result:59; Test Name: TRICUSPID VALVE; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: Tricuspid valve annular peak velocity; Result Unstructured Data: Test Result:17.4; Test Name: valve area by pressure half-time; Result Unstructured Data: Test Result:3.3cm^2; Test Name: valve area index by pressure half-time; Result Unstructured Data: Test Result:1.96cm^2/m^2; Test Name: VENTRICULAR SEPTUM; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: GOT/AST; Result Unstructured Data: Test Result:18 Units/L; Comments: Standard Range: Standard Range less than equals 37 Units/L; Test Date: 20210921; Test Name: GOT/AST; Result Unstructured Data: Test Result:18; Comments: Units/L; Test Date: 20220611; Test Name: liver function; Result Unstructured Data: Test Result:normal; Test Name: LDL; Result Unstructured Data: Test Result:122; Test Date: 20220626; Test Name: LDL; Result Unstructured Data: Test Result:slightly elevated at 122 mg/dl; Comments: Standard Range: Standard Range mg/dL (calc) Patient is to continue watching diet and exercise.; Test Date: 20211022; Test Name: LDL-CHOLESTEROL; Test Result: 122 mg/dl; Comments: Flag H; Test Name: Absolute Lymphocytes; Result Unstructured Data: Test Result:1.9 K/mcL; Comments: Standard Range: Standard Range 1.0 - 4.0 K/mcL; Test Name: Lymphocytes, Percent; Test Result: 14 %; Comments: Standard Range: Standard Range %; Test Name: MCHC; Result Unstructured Data: Test Result:33.0 g/dl; Comments: Standard Range: Standard Range 30 36.5 g/dL; Test Name: MCV; Result Unstructured Data: Test Result:100.6 fl; Comments: Standard Range: Standard Range 78.0 100.0 fl Flag: Flag L; Test Name: Absolute Monocytes; Result Unstructured Data: Test Result:1.1 K/mcL; Comments: Standard Range: Standard Range 0.3 - 0.9 K/mcL Flag: Flag H; Test Name: Mono, Percent; Test Result: 8 %; Comments: Standard Range: Standard Range %; Test Name: Absolute Neutrophils; Result Unstructured Data: Test Result:10.9 K/mcL; Comments: Standard Range: Standard Range 1.8 - 7.7 K/mcL Flag: Flag H; Test Name: Neutrophil, Percent; Test Result: 77 %; Comments: Standard Range: Standard Range %; Test Date: 20220626; Test Name: NON HDL CHOLESTEROL; Test Result: 138 mg/dl; Comments: Standard Range: Standard Range less than 130 mg/dL (calc); Test Name: PLT; Result Unstructured Data: Test Result:209 K/mcL; Comments: Standard Range: Standard Range 140 - 450 K/mcL; Test Date: 20210921; Test Name: Protein, Total; Result Unstructured Data: Test Result:7.4; Test Date: 20220611; Test Name: Protein, Total; Result Unstructured Data: Test Result:7.4 g/dl; Comments: Standard Range: Standard Range 6.4 - 8.2 g/dL; Test Name: NRBC; Result Unstructured Data: Test Result:0 /100 WBC; Comments: Standard Range: Standard Range less than equals to 0 /100 WBC; Test Name: RBC; Result Unstructured Data: Test Result:3.62 mil/mcL; Comments: Standard Range: Standard Range 4 00 5 0 mil/mcL Flag: Flag L; Test Name: RDW-CV; Test Result: 12.6 %; Comments: Standard Range: Standard Range 11.0 15.0 %; Test Name: RDW-SD; Result Unstructured Data: Test Result:46.5 fL; Comments: Standard Range: Standard Range 39 0 50 0 fL; Test Name: COVID-19 Test; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220106; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:9.03; Comments: Component: MV E Tissue Vel Med; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:10.9; Comments: Component: MV E Tissue Vel Lat; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:1.26; Comments: Component: PV Peak Velocity; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:17.4; Comments: Component: Tricuspid valve annular peak velocity; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:17.44; Comments: Component: Est Right Vent Systolic Pressure by Tricuspid Regurgitation Jet; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:24.8; Comments: Component: LVOT VTI; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:1.2; Comments: Component: DOP Calc LVOT Peak Vel; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:3.23; Comments: Component: Left Ventricular Internal Dimension in Diastole; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:2.26; Comments: Component: Left Internal Dimension in Systole; Test Date: 20220611; Test Name: Scan; Result Unstructured Data: Test Result:2.56; Comments: Component: Tricuspid Annular Plane Systolic Excursion; Test Name: Thyroid test; Result Unstructured Data: Test Result:Normal; Test Date: 20220611; Test Name: Thyroid test; Result Unstructured Data: Test Result:normal; Test Date: 20220626; Test Name: CHOL/HDLC RATIO; Result Unstructured Data: Test Result:3.3 (calc); Comments: Standard Range: Standard Range less than 5 0 (calc); Test Name: WBC; Result Unstructured Data: Test Result:14.0 K/mcL; Comments: Standard Range: Standard Range 4 11 0 K/mcL Flag: Flag H
Aktuelle Erkrankungen: Sigmoidectomy (Cancer ruled out.)
Vorgeschichte: Medical History/Concurrent Conditions: Bone disorder; Boutonneuse fever ((possibly exacerbated by 08Aug2018 Shingrix vaccination),); Breast cancer (diagnosed early 2016); Breast implant user; Bunionectomy; Capsular contracture associated with breast implant; Chest pain; Chest X-ray (CLINICAL INDICATION: Chest Pain.); COVID-19; Diverticulitis; Flushing; Gastrointestinal disorder; Hair disorder; Headache; Hernia (the cause of many of the more minor GI pains that resolved w/o antibiotics); Hysterectomy (ovaries not removed); Implant removal; Insomnia; Joint arthroplasty; Joint disorder; Knee arthritis (some Hymovis injections and Zilretta injections every 3 months); Latex allergy; Lymph node excision; Mastectomy bilateral ((right side at my option)); Mastectomy bilateral; Meibomian gland obstruction; Nail disorder; Robotic surgery (undetected hernia (1.5cm x 3 cm) pocket was cleaned out and the tear repaired); Sentinel node biopsy (port placement (though updated diagnosis changed and no chemo needed)); Shortness of breath; TMJ syndrome
Andere Medikamente: B12 [CYANOCOBALAMIN]; FISH OIL; CALCIUM CITRATE; D3; BIOTIN; BIOFLEX CHONDROITIN; MIDAZOLAM; LIDOCAINE HCL; DIPRIVAN; EXPAREL; NAROPIN [ROPIVACAINE]; DECADRON [DEXAMETHASONE]; SUBLIMAZE [FENTANYL]; BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE];
Allergien: -
Vorherige Impfungen: -

VAERS 2511983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fk9894

mild

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 28.02.2022
Beginn: 04.05.2022
Tage bis Beginn: 65,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Lip swelling Swelling of eyelid Urticaria chronic

Symptomtext

I have been having chronic hives starting may 5th 2022 all over my body, swollen eye lid, lips. I went to the emergency room at hospital and was told they were chronic hives and was given prednisone and when I left then gave me a prescription for prednisone for 5days with 1 refill. I still have these chronic hives till this day 11/18/2022 and I have tried other medications like Allegra, ibuprofen and Claritin and Zyrtec and the work and then started to not work as much

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria chronic
Hospital-Tage: -
Labordaten: I was at the hospital and they only looked at my body during out break
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2510685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 50,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 10.05.2022
Beginn: 15.08.2022
Tage bis Beginn: 97,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Dysphagia Headache Odynophagia Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

On 8/15/22 at about 5 PM I had a very sore throat and difficulty and painful swallowing accompanied by headache. Tested with an at home COVID-19 test, positive. 08/16 retested at Dr. office rapid COVID-19 test, positive. Returned to see Dr. who prescribed PAXLOVID. 8/17 pain in throat started to improve gradually getting better through about 8/27. Retested with at home COVID-19 test 8/23, faint positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 8/15/22 at home COVID-19 test, positive. 08/16/2022 rapid COVID-19 test, positive. 8/23/2022 at home COVID-19 test, faint positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: AVONEX
Allergien: No
Vorherige Impfungen: -

VAERS 2510634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 11.04.2022
Beginn: 07.10.2022
Tage bis Beginn: 179,0
Dosis: 4
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abdominal pain Constipation Vomiting

Symptomtext

abdominal pain, constipation, vomiting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2508600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 62,0
Geschlecht: F
Eingang: 15.11.2022
Impfdatum: 16.05.2022
Beginn: 07.11.2022
Tage bis Beginn: 175,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Malaise Pain Pain in extremity SARS-CoV-2 test positive Throat irritation

Symptomtext

I had a sore arm for a day after the vaccine and that was it. On 11/07/2022 I wasn't feeling well with a scratchy throat and an achy body. I tested with an expired home test for COVID-19, and it was negative. I tested again for COVID-19 on 11/08/2022 and it was positive. I contacted my doctor on 11/9/2022 and got a prescription for PAXLOVID. As of today, I have a rebound with achy body and scratchy throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 07NOV2022 COVID-19 test negative; 08NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2506893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 13.11.2022
Impfdatum: 10.05.2022
Beginn: 16.08.2022
Tage bis Beginn: 98,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Malaise SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID case w/ Symptons starting on 8/16/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Positive result w/ at-home test on 8/17/22
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Hypertension, Type 2 Diabetes
Andere Medikamente: Prilosec, Tamsulosin, Celexa, Advair, Fenofibrate, Metformin, Ozempic, Atorvastatin, Losartin
Allergien: -
Vorherige Impfungen: -

VAERS 2501948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 68,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 07.05.2022
Beginn: 20.09.2022
Tage bis Beginn: 136,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Feeling abnormal Headache Nasopharyngitis Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I did not have a reaction to the vaccine. I started with symptoms 09/19/2022 of a severe headache, fever, cold symptoms, cough, runny nose and foggy head. I tested positive for COVID-19 with a home test on 09/20/2022. I had a telehealth visit with my doctor on 09/20/2022 and was prescribed PAXLOVID. By the third day I started to feel much better. I tested COVID-19 negative on 09/27/2022. On 10/03/2022 I rebound and tested positive for COVID-19. This time I work up with a runny nose without a fever for a couple of days. I didn't take anything for the symptoms this time. I test negative for COVID-19 on 10/14/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 20SEPT2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; High Blood Pressure
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Shingrix at age 67 in 2020 I had flu like symptoms for a couple days.

VAERS 2496485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 30.04.2022
Beginn: 31.05.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Biopsy Blister Blood test normal Chest X-ray abnormal Computerised tomogram head normal Confusional state Dizziness Headache Hyperhidrosis Pain Pemphigoid Rash Rash pruritic Rash vesicular Rib fracture

Symptomtext

I developed a huge blister on my right inner thigh toward the end of May of 2022. I went to my primary doctor's office on 05/30/2022. The woman I saw stated that she knew what I had but did not know how to treat me. She explained that it was Bullous Pemphigoid and referred me to a dermatologist for further treatment. He performed a biopsy on the area which confirmed the diagnosis. Shortly after that, I started developing a horribly itchy rash, mostly on my torso. On top of the rash, I also get blisters. Still to this day, I get blisters on my stomach, torso, and back. I also get some on my hands, feet, and scalp and there is intense itching as well. I have been taking Doxycycline since receiving this diagnosis and there has been little improvement. On 10/25/2022, I began taking Prednisone which messes with my Diabetes, so I require a prescription of Metformin to counteract the effects of the Prednisone. As of yesterday, 11/01/2022, I have had to increase my dosage of Prednisone because there has been very little improvement. Aside from all of these dermatological issues, on 09/03/2022, I experienced and episode of dizziness, confusion, headache, pain, and sweating. My husband called 911 and I was taken to the emergency room by ambulance. They performed x-rays and discovered that I had two fractured ribs. They also did a CT scan because of the headache I was experiencing but they found nothing there. They advised that I just treat my pain with over-the-counter medication and released me that same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 01JUNE2022- Biopsy- Diagnosis Confirmed; Blood Work- Nothing Abnormal Detected; 03SEPT2022- Chest X-Rays- Fractured Ribs Discovered; CT Scan of Brain- Nothing Found
Aktuelle Erkrankungen: None
Vorgeschichte: Controlled Diabetes
Andere Medikamente: Pravastatin; Lisinopril; Levothyroxine; Benadryl
Allergien: Sulfa; Penicillin; Codeine; Scallops
Vorherige Impfungen: -

VAERS 2496414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 02.11.2022
Impfdatum: 17.02.2021
Beginn: 06.09.2022
Tage bis Beginn: 566,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

09/06/22 presents to ED for "fatigue". PMHx of " AML (diagnosed in 2017), hepatitis C, HLD, HTN, RA and nephrolithiasis"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 09/06/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FK9894

mild

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 21.01.2021
Beginn: 18.06.2022
Tage bis Beginn: 513,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute kidney injury COVID-19 Nausea Vomiting

Symptomtext

Narrative: This patient received four doses of the Pfizer COVID 19 Vaccine in Jan/Feb/Oct 2021/Apr 2022. The patient presented to the ED on nausea and vomiting on 18 June 2022. The patient was admitted with COVID 19 and acute kidney injury. The patient was treated with fluids and was discharged in stable condition on 24 June 2022. Reported per EUA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2487315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NC
Alter: 77,0
Geschlecht: M
Eingang: 24.10.2022
Impfdatum: 22.04.2022
Beginn: 30.08.2022
Tage bis Beginn: 130,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Drainage Dysphagia Pharyngeal swelling Pyrexia SARS-CoV-2 test positive

Symptomtext

I had bad and swollen sore throat, sinus drainage, difficulty swallowing, and fever. I tested positive for COVID-19 at home. My doctor sent me to the ER for an infusion which they did not do anymore. So, they sent me home without doing anything. My doctor sent in a prescription for Paxlovid and my symptoms went away almost immediately.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: COVID-19, Positive, 08/31/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Prostate Cancer; Lymphoma
Andere Medikamente: Simvastatin; Gabapentin; Lisinopril; Metoprolol; Vitamin D; Multiviatin; Corzatin; Q10; Soy; Aspirin; Flonase
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2487045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 59,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 22.04.2022
Beginn: 25.07.2022
Tage bis Beginn: 94,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I had a slight fever and I felt achy for a day after receiving the vaccine. I started feeling symptoms that I was getting sick with feeling very tired, achy and a cough 07/23/2022. I tested positive with a home test for COVID-19 on 07/25/2022. I contacted my doctor and was given the option for Paxlovid, but I did not take it. I took ibuprofen for the fever and achiness and a cough syrup to help with the symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 25JUL2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Hydrochlorothiazide; Levothyroxine
Allergien: Latex
Vorherige Impfungen: -

VAERS 2485151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WA
Alter: 52,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 21.04.2022
Beginn: 17.09.2022
Tage bis Beginn: 149,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Cough Ear infection Fatigue Pyrexia SARS-CoV-2 test Sinusitis Streptococcus test

Symptomtext

I was exhausted and fatigue. I have a fever and chills with a cough. I came down with an ear infection and a sinus infection and the cough continues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19; strep test
Aktuelle Erkrankungen: No
Vorgeschichte: Thyroiditis
Andere Medikamente: Levothyroxine; cimetidine; ALLEGRA
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2483682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 68,0
Geschlecht: M
Eingang: 20.10.2022
Impfdatum: 06.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Bedridden Chills Malaise SARS-CoV-2 test

Symptomtext

he may have had chills that night.; The last one caused me to be in bed for three days, and did not feel good for about a week.; Shot #4 he was in bed 3 days pretty much and didn't feel 100% for a week; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), on 06Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 68 years for covid-19 immunisation. The patient's relevant medical history included: "aortic stenosis" (unspecified if ongoing), notes: he had aortic stenosis, an occlusion causing problems.; "catheter", start date: Nov2021, stop date: Nov2021, notes: Last November he had catheter and they installed in the aortic well,; "heart issue/weak heart" (unspecified if ongoing); "Diastolic Dysfunction" (unspecified if ongoing); "smoking" (ongoing); "Cholesterol" (unspecified if ongoing). Concomitant medication(s) included: ALLOPURINOL; BABY ASPIRIN; BUPROPION taken for ex-tobacco user. Vaccination history included: BNT162b2 (Pfizer Covid 19 vaccine dose #1 on 11Feb2021, lot EN9581), administration date: 11Feb2021, when the patient was 67-year-old, for COVID-19 Immunization, reaction(s): "chills"; BNT162b2 (Pfizer Covid 19 vaccine dose #2 on 04Mar2021, lot EN6198), administration date: 04Mar2021, when the patient was 67-year-old, for COVID-19 Immunization, reaction(s): "Shot #2 he was quite under the weather for a day and a half."; BNT162b2 (Pfizer Covid 19 vaccine dose #3 on 04Oct2021 , on card lot looks like FE or EE, there is a sticker over it, could be FF and numbers 8839), administration date: 04Oct2021, when the patient was 67-year-old, for COVID-19 Immunization, reaction(s): "feeling worse"; Flu shot, reaction(s): "Sensitive"; Vaccine (had tons of shots); Plague, reaction(s): "reaction"; Typhoid (He got a little reaction because he got 5 in 1 shot and they were all different, the plague, typhoid the whole 9 years), reaction(s): "Reaction"; Flu shots, reaction(s): "gets a little chill". The following information was reported: BEDRIDDEN (non-serious) with onset 2022, outcome "recovered" (2022), described as "Shot #4 he was in bed 3 days pretty much and didn't feel 100% for a week"; MALAISE (non-serious) with onset 2022, outcome "recovered" (2022), described as "The last one caused me to be in bed for three days, and did not feel good for about a week."; CHILLS (non-serious) with onset 2022, outcome "recovered" (2022), described as "he may have had chills that night.". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Patient received two shot original vaccine and both booster and was considering getting the Omicron booster. His concern was he had a progressively strong response from each shot. The last one caused him to be in bed for three days and did not feel good for about a week. Patient point was being as the variants are somewhat weaker and oral treatments are available would he foolish to assume that he might be sufficiently protected and were other alternatives available. He had progressively strong response from each shot and the last dose caused him to be in bed 3 days and he didn't feel good for about a week. Patient had questions about Paxlovid and side effects but didn't mention if he was prescribed, they were general questions. Patient stated with shot number 1 he was pretty asymptomatic, he may have had chills that night. Anytime he gets the flu shot he gets a little chill but it's never a problem. After shot 2 he was quite under the weather for a day and a half. Shot 3 was somewhat feeling worse a couple days but cleared up and felt 100% in about 3 days. Shot 4 he was in bed 3 days pretty much and didn't feel 100% for a week. His concern was where is that going. If it wasn't progressive, if it was the same response every time it wouldn't concern him. Patient was not afraid to get omicron one but considering why would he take the chance of 3-4 days in bed sick when he could just take oral medication if he comes down with it, he wouldn't be worse off. His wife tested positive for COVID and was asymptomatic and they slept together forever. He never tested positive, and he has been exposed a couple other times and if he ever had it was very mild or he was asymptomatic. One more caveat with Paxlovid, he takes some medication for his heart, for weak heart, diastolic disfunction. Last November he had catheter and they installed in the aortic well, it's an artificial valve they put in through a catheter through the femoral artery. He was in and out of the hospital and was there 1 night. They have not used this on younger people, he had aortic stenosis, an occlusion causing problems. He feels good but it sounds crazy, but he did hear there were interactions between some heart medications and Paxlovid and was not sure if they are rumor. He takes a couple of different blood pressure medications. He wouldn't have any trouble not using them for a week, he doesn't know. He could probably ask his family physician and suspects he will lay this all out and he will say it's up to him. He was not really looking for strong answers, just trying to sort through. What had got him disturbed was having worse reactions, as progresses more robust reactions. If he was going to be sick 3-5 days he may as well take a chance, he has been exposed. He was trying to establish some kind of level of risk. he just looking to hear if anyone else was having these problems or if we recommend not taking. It's just the response he has, it's not an allergic reaction. In medical sense he was sure it would be labeled as mild reaction but to him it's more toward moderate more like flu. He was sensitive to any flu shot anyways but not like this. After the 4th dose Pfizer COVID-19 vaccine it was about hardest part of it, he doesn't know if he was sick a little earlier. With the other 3 it was about 12 hours after getting the vaccine and the last one may have been 6-8 hours after. Outcome reported as It definitely started improving after 3 days and he felt 100% after a week. He takes several every day including a few blood pressure medications, allopurinol, cholesterol drug, baby aspirin and he just started taking Bupropion. States he started the Bupropion after all of this happened. It's for smoking but he was having blood pressure crisis a few months back and got on extra blood pressure medications and gave him a script for that and it made him calm a little. Declines to provide further details. He would assume that someone would flag his profile if he was getting an interaction and he got a couple through the pharmacy, and no one said anything about interaction. Medical Condition reported as just the heart issue. Had the procedure on 29Nov2021. Additional vaccines administered on Same Date of the Pfizer Suspect reported as none. Patients visit to emergency room and physician office reported as no. Prior Vaccinations (within 4 weeks) reported as none. AE(s) following prior vaccinations reported as Flu vaccine. last 2 he got were for old timers, the bivalent for seniors. Has had every vaccination known to man. Was in # and had tons of shots, got every shot you could think of. He got a little reaction because he got 5 in 1 shot and they were all different, the plague, typhoid the whole 9 years. States nothing reportable or to be concerned about. Had signed up for flu shot and omicron shot when he got there, they said flu but not Omicron their vaccine got too warm. He mentioned really and truly he gets a reaction and was glad it was not both at once. That it might not be bad to wait a couple weeks. The progression of the shot's response has him a little troubled, some people say it's a good thing. He was still looking for data and will contact his family physician. There are no real answers, but this been couple years so someone should. He had sent an email asking are there other alternatives like a lower dose. Apparently, he was the only guy complained about this, it's not offered to ease symptoms for anyone. He questioned if there was an alternative. He will talk over with family physician. He wanted to know if he should get the Omicron booster dose, even if he had "progressively strong responses from each shot (from the Pfizer-BioNTech COVID-19 Vaccine)". Explained that he was eligible for this vaccine, however, we are unable to provide a medical recommendation for individual patients. Referred to HCPs to consult his specific case. Patient described that he had a diastolic, heart condition. He wanted to know if any of the side effects of Paxlovid could affect his heart. He didn't mention that he was sick from COVID or was prescribed this medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: tested; Result Unstructured Data: Test Result:unknown result; Comments: He never tested positive,
Aktuelle Erkrankungen: Smoker
Vorgeschichte: Medical History/Concurrent Conditions: Aortic stenosis (he had aortic stenosis, an occlusion causing problems.); Catheter placement (Last November he had catheter and they installed in the aortic well,); Cholesterol; Diastolic dysfunction; Heart disorder
Andere Medikamente: ALLOPURINOL; BABY ASPIRIN; BUPROPION
Allergien: -
Vorherige Impfungen: -

VAERS 2481711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: ME
Alter: 65,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 14.04.2022
Beginn: 21.09.2022
Tage bis Beginn: 160,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Cough Diarrhoea Pyrexia Respiratory tract congestion SARS-CoV-2 test

Symptomtext

Weakness Cough Diarrhea Fever 101.5 max Congestion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Home Covid test
Aktuelle Erkrankungen: Na
Vorgeschichte: Blood pressure Cholesterol Arthritis
Andere Medikamente: Fenofibrate 48 mg Atorvastatin calcium 10mg Lisinopril mg Voltaren 1% Acetaminophen 1000 mg Cetirizine Hydrocloride 10 mg vitamin D-3 5000iu Iron 18 mg
Allergien: No meds Environmental allergies Food allergies
Vorherige Impfungen: -

VAERS 2481662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: VT
Alter: 72,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 18.04.2022
Beginn: 07.09.2022
Tage bis Beginn: 142,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Limb discomfort Malaise Nasopharyngitis Paranasal sinus discomfort Piloerection Rhinorrhoea SARS-CoV-2 test positive Sinus congestion Throat irritation

Symptomtext

My COVID-19 symptoms were very mild. It started on the 7th with a scratchy throat as if I was coming down with a cold. Next day I had a little sinus congestion which is normal. I tested positive on the 8th. I then had runny nose, sinus pressure, had the sensation that my arm hairs were standing up; my left leg then felt very heavy. Within 5 days all the symptoms had resolved. The sensation with the arm hairs and heavy leg also came after both the vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 test positive
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; GERD; Pre glaucoma
Andere Medikamente: Probiotic; multivitamin; B12; NATURE MADE calcium magnesium & zinc; METAMUCIL; cranberry tablets; vitamin D3; amlodipine; propranolol; ropinirole; famotidine; montelukast; allergy relief; eye drops
Allergien: No
Vorherige Impfungen: My left leg felt heavy and my arms hairs felt like they were standing up after 1st two Covid shots.

VAERS 2478492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: IA
Alter: 58,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 04.05.2022
Beginn: 04.07.2022
Tage bis Beginn: 61,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Diarrhoea Feeling abnormal Headache Malaise Nausea Productive cough Respiratory tract congestion SARS-CoV-2 test positive Sleep disorder

Symptomtext

About 3 days before I tested positive for COVID I started experiencing a very painful headache and I was unable to sleep. On 7/4/2022 I tested positive I was feeling unwell I had a headache; nauseas, diarhea; body chills and brain fog for about 24 hours. I called my Physician however I was not prescribed Paxlovid as treatment. I also want to report that ever since testing positive I have a very bad congested cough and phlegm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: PCR Test
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, High Cholesterol, Genital Herpes, Acid Reflux
Andere Medikamente: OTC Tylenol; Hydroboracite; Zyrtec; Lovastatin; Nasal Spray; Omeprazole, Sucralfate; Valacyclovir
Allergien: None
Vorherige Impfungen: -

VAERS 2478441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OR
Alter: 62,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 14.07.2022
Beginn: 16.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Influenza A virus test negative Influenza B virus test Influenza virus test negative Magnetic resonance imaging abnormal Nausea Respiratory syncytial virus test negative SARS-CoV-2 test positive Sinus pain Sinusitis

Symptomtext

On 7/16/2022, I was nauseous, I felt like I wanted to throw up. I went to clinic on 7/18/2022 to take a COVID-19 test and the result was positive. My daughter tested positive for COVID-19 and that prompted me to test. I was not nauseous on 7/18/2022. I had no other symptoms. I was A-symptomatic. On 9/1/2022, I was having severe sinus pain in my face. I went to the ER on 9/2/2022 and they tested me for COVID-19, and RSV, general flu, influenza A and B. The COVID-19 test came back positive. They did an MRI on my head just to check my sinuses with and without contrast. The doctor said I had a viral sinus infection. I was given pain meds. I was not given any medication for the COVID-19. It took me about a week to recover. I recently took a COVID-19 test and it was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: 9/2/2022 COVID-19- positive 9/2/2022 RSV, general flu test, influenza A and B test -negative lab test 9/2/2022MRI on my head
Aktuelle Erkrankungen: N/A
Vorgeschichte: Spina Bifida; migraines; neuropathy; osteoarthritis; neurogenic bladder and bowel; one atrophy kidney
Andere Medikamente: Lisinopril/Hydrochlorothiazide; Pantoprazole; acetaminophen/butalbital/caffeine; alpha lipoic acid; CBD with THC; Magnesium Glycinate; B12; B1; Centrum Adult multi vitamin; Zinc; Docusate sodium; vitamin C; Krill oil; Milk thistle; Total Re
Allergien: Sulfa; Contrast Dye; latex
Vorherige Impfungen: -

VAERS 2477316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 70,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 13.04.2022
Beginn: 27.07.2022
Tage bis Beginn: 105,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Nausea Pyrexia SARS-CoV-2 test positive

Symptomtext

Approximately 3 months after receiving my fourth dose of the Pfizer vaccine, my husband and I tested positive for COVID-19. My symptoms were a fever for two days, a little nausea and mild fatigue. It felt like allergies with nausea. I don't feel that it was a bad case at all. When we contacted our doctor she prescribed Paxlovid and it helped both of us.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid test at home
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol
Andere Medikamente: Lipitor; multivitamin; Calcium with vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2476939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: KY
Alter: 72,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 14.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body height COVID-19 Cough Drug ineffective Hypersensitivity Magnetic resonance imaging Oropharyngeal pain Pulmonary congestion SARS-CoV-2 test Sinus disorder Skin test Vertigo Vitamin D Vitamin D increased

Symptomtext

still got Covid; still got Covid; Congestion still in throat and down in chest trying to come up; cough; sinus problems; she got allergy; vertigo; sudden increase of Vitamin D; sore throat; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 72-year-old female patient received BNT162b2 (BNT162B2), on 13Feb2021 as dose 1, single (Lot number: EN6201), in right arm, on 06Mar2021 as dose 2, single (Lot number: EN6205), in left arm, on 30Sep2021 as dose 3 (booster), single (Lot number: EN0176), in left arm and on 14May2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 72 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "seasonal allergies" (unspecified if ongoing), notes: She can be susceptible to seasonal allergies. First 10 years in (withheld) had weekly allergy shot; "respiratory illness" (unspecified if ongoing); "compromised immune status" (unspecified if ongoing); "genetic/chromosomal abnormalities" (unspecified if ongoing); "endocrine abnormalities (including diabetes)" (unspecified if ongoing); "endocrine abnormalities (including diabetes)" (unspecified if ongoing); "obesity Illness" (unspecified if ongoing). The patient's family history included: "Mother's whole family was asthmatic" (unspecified if ongoing); "respiratory issues" (unspecified if ongoing), notes: They had some respiratory issues and are all deceased now. Concomitant medication(s) included: SHINGRIX taken for immunisation, in Sep2021 as dose number unknown, single; FLU VACCINE VII taken for immunisation, in Sep2021 as dose number unknown, single. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "still got Covid"; PULMONARY CONGESTION (medically significant), outcome "unknown", described as "Congestion still in throat and down in chest trying to come up"; COUGH (non-serious), outcome "unknown"; SINUS DISORDER (non-serious), outcome "unknown", described as "sinus problems"; HYPERSENSITIVITY (non-serious), outcome "unknown", described as "she got allergy"; VERTIGO (non-serious), outcome "unknown"; VITAMIN D INCREASED (non-serious), outcome "unknown", described as "sudden increase of Vitamin D"; OROPHARYNGEAL PAIN (non-serious), outcome "unknown", described as "sore throat". The patient underwent the following laboratory tests and procedures: Body height: (unspecified date) Little less than 5'2"; Magnetic resonance imaging: (unspecified date) unknown results, notes: She has had 4 years of doing MRI and no need to do it anymore; SARS-CoV-2 test: (unspecified date) Negative, notes: She kept testing negative from last Thursday until Sunday; (unspecified date) Positive, notes: she tested positive for COVID virus; (Feb2022) unknown results, notes: she had a COVID incident in Feb2022; Skin test: (31Jan2022) unknown results, notes: did a patch test 31Jan2022, where she went on Monday, Wednesday and Friday; Vitamin D: (Jul2022) sudden increase of Vitamin D, notes: In Jul2022, when she had physical, sudden increase of Vitamin D. It was a little over 100 and usually they are trying to work on it. Therapeutic measures were taken as a result of drug ineffective, covid-19, cough. Clinical course: Patient had shingles and Flu prior Vaccinations (within 4 weeks). Last fall Sept2021, had one flu shot after that Pfizer COVID 19 vaccine. Then between sep2021 one and may2022 one, had two shingle shot 6 months apart. She does not have the manufacturer, lot or expiration for the flu shot or Shingles shot. Flu shot at doctor's office and shingles. She had some Eczema breakout before the COVID 30Sep2021 vaccine. She got a shot of steroids for that and again 6 weeks later because she broke out again and did a patch test 31Jan2022, where she went on Monday, Wednesday and Friday. Then in Feb2022, she got COVID and thinks it had to do with killing off everything off of her body. She could not Keep having steroid injections and then the chemicals in her body from the test. Name, Lot and expiration of Steroid injection was unknown. The 2nd one was not at potent as the first, he told her that. Felt a little tired and had a sore arm and that was about it. This was with the first Pfizer COVID vaccine she had sore arm. She felt tired and with 2nd one she got in Left arm and went to zoo and stayed active. So, she fared much better. Provide other relevant medical history including but not limited to these conditions: diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity Illness/AE: She can be susceptible to seasonal allergies. First 10 years had weekly allergy shot and finally got immune built up to it. Family Medical History Relevant to AE(s): Mother's whole family was asthmatic. They had some respiratory issues and are all deceased now. Younger brother got COVID but hardheaded and never got the vaccination. Description of Product Complaint: Description of complaint: Got all her Pfizer COVID 19 vaccines and boosters and still got COVID. Additional lot numbers: 1st dose of Pfizer COVID vaccine 13Feb2021, Lot EN6201, expiration was unknown. Injected in Unknown arm. She thinks it was right arm because she was left-handed. 2nd dose date 06 Mar 2021, Lot EN6205, expiration was unknown. Injected in left arm. 3rd dose date 30 Sep 2021, Lot EN0176, expiration was unknown. Injected in left arm. 4th dose 14 May 2022, Lot FK9894, expiration was unknown. Injected in unknown arm. Description of complaint: She got a shot of steroids for that and again 6 weeks later because she broke out again and did a patch test 31Jan2022, where she went on Monday, Wednesday and Friday. Then in Feb2022, she got COVID and thinks it had to do with killing off everything off of her body. She could not Keep having steroid injections and then the chemicals in her body from the test. Name, Lot and expiration of Steroid injection was unknown. The 2nd one was not at potent as the first, her doctor told her. Product strength and count size dispensed: unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:Little less than 5'2"; Test Name: MRI; Result Unstructured Data: Test Result:unknown results; Comments: She has had 4 years of doing MRI and no need to do it anymore; Test Name: COVID-19 Test; Test Result: Negative ; Comments: She kept testing negative from last Thursday until Sunday; Test Name: COVID-19 Test; Test Result: Positive ; Comments: she tested positive for COVID virus; Test Date: 202202; Test Name: COVID-19 Test; Result Unstructured Data: Test Result:unknown results; Comments: she had a COVID incident in Feb2022.; Test Date: 20220131; Test Name: patch test; Result Unstructured Data: Test Result:unknown results; Comments: did a patch test 31Jan2022, where she went on Monday, Wednesday and Friday; Test Date: 202207; Test Name: Vitamin D; Result Unstructured Data: Test Result:sudden increase of Vitamin D; Comments: In Jul2022, when she had physical, sudden increase of Vitamin D. It was a little over 100 and usually they are trying to work on it.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthmatic; Chromosomal abnormality NOS; Diabetes; Endocrine disorder NOS; Immunocompromised; Obesity; Respiratory disorder (They had some respiratory issues and are all deceased now); Respiratory disorder; Seasonal allergy (She can be susceptible to seasonal allergies. First 10 years in (withheld) had weekly allergy shot)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2472451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 08.10.2022
Impfdatum: 02.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache

Symptomtext

mild headache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). Other Case identifier(s): Moderna. A male patient received BNT162b2 (BNT162B2), on 02May2022 as dose 4 (booster), single (Lot number: FK9894) for covid-19 immunisation. The patient's relevant medical history included: "Blood Pressure" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing); "Antidepressant" (unspecified if ongoing); "Digestion" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN taken for blood pressure abnormal; SIMVASTATIN taken for blood cholesterol abnormal; SERTRALINE taken for antidepressant therapy; OMEPRAZOLE taken for dyspepsia; VITAMIN D3. Vaccination history included: BNT162b2 (Dose Number: 1, Manufacturer: Pfizer, Lot number: EN6201), administration date: 10Feb2021, for Covid-19 Immunization, reaction(s): "mild headache"; BNT162b2 (Dose Number: 2, Manufacturer: Pfizer, Lot number: EN6198), administration date: 03Mar2021, for Covid-19 Immunization, reaction(s): "mild headache"; BNT162b2 (Dose Number: 3, Manufacturer: Pfizer, Lot number: EW0186), administration date: 12Oct2021, for Covid-19 Immunization, reaction(s): "mild headache". The following information was reported: HEADACHE (non-serious), outcome "unknown", described as "mild headache".; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201202012 same patient/event, different dose number;US-PFIZER INC-202201202013 same patient/event, different dose number;US-PFIZER INC-202201202011 same patient/event, different dose number;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Antidepressant therapy; Blood cholesterol abnormal; Blood pressure abnormal; Digestion impaired
Andere Medikamente: LOSARTAN; SIMVASTATIN; SERTRALINE; OMEPRAZOLE; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 2471973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: AZ
Alter: 58,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 07.04.2022
Beginn: 03.10.2022
Tage bis Beginn: 179,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Headache Pain Pyrexia SARS-CoV-2 test positive Sneezing Taste disorder

Symptomtext

I tested positive for COVID-19 on October 3, 2022 and I experienced a headache, fever of 101.4; coughing, sneezing; fatigue; body aches; really bad taste. I was prescribed Paxlovid and a cough suppressant and was told to take mucinex.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Lupus; Sjogren's syndrome; Hashimotos;
Andere Medikamente: Levothyroxine; Hydroxychloroquine; Estradiol; Clonidine; Calcium; fish oil; Vitamin D; Multivitamin; Vitamin E; Probiotic
Allergien: Sulfa Drugs; Zithromax;
Vorherige Impfungen: -

VAERS 2471898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OR
Alter: 65,0
Geschlecht: M
Eingang: 07.10.2022
Impfdatum: 22.06.2022
Beginn: 12.09.2022
Tage bis Beginn: 82,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Balance test Cold sweat Computerised tomogram head normal Computerised tomogram normal Differential white blood cell count normal Dizziness Electrocardiogram normal Feeling of body temperature change Full blood count normal Gait inability Impaired work ability Laboratory test normal Metabolic function test normal Nausea Nervousness Retching Vertigo Vomiting

Symptomtext

This was the first Pfizer vaccine I had received after 3 Moderna vaccines. The event itself actually began two days before with a 2 minute severe dizzy and spinning episode that went away in 10 minutes time. Then for the next day and a half, I was fine and didn't have any problems. I didn't know that was part of what was going to happen. This happened on a Saturday afternoon. On Monday 09/12/2022, I went to work and at 8:45 AM, I had another severe nausea spinning episode that lasted 15 to 20 minutes. I waited and calmed down and went back to what I thought was normal. I continued with my work day but watched my vitals throughout the day. At about 12:45PM that afternoon, I had the most severe attack of the dizziness and nausea and felt a strong temperature change in my body. I had to stop work for about 35-45 minutes. I was able to safely drive my vehicle back to work. At that point, I could not walk back inside to where I work because I was spinning and experiencing nausea. I was clammy and dry heaving. I was pretty nervous. A passer by who works in my facility walked by and I asked him to call 911. They got here in 5-6 minutes and assessed my condition. They got me into the emergency vehicle and they brought me to the ER. They ran a series of tests such as blood pressure, pulse, and a mobile CAT scan to assess if I was having a stroke or another kind of health event. During that ride, they mentioned it could be a bout of vertigo. On our way to the ER, I was also vomiting. When we got to the ER, they assessed what was happening and I was admitted into the ER. They kept watch until the next day so I could speak with a physical therapist. Everyone at this point had noted that it could be vestibular neuritis. I was kept there until the spinning had decreased greatly. They prescribed Meclizine and I did feel better. I was not cleared for work for about 3 weeks, and just recently I was released for half days of work. I still feel the effects of wooziness and low level nausea. I can still drive and I'm currently involved in on going assessments with multiple doctor visits and physical therapy visits for the foreseeable future. I have recovered from the event but still have some after effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 1,0
Labordaten: 09/12/2022 Mobile CAT scan - Normal results; 09/12/2022 CBC with Differential - Normal results; 09/12/2022 Comprehensive Metabolic Panel - Normal results; 09/12/2022 CT Scan Head without Contrast - Normal results; 09/12/2022 CT Head and Stroke set - Normal results; 09/12/2022 EKG - Normal results; Performance testing for stability on feet with PCP and PT
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish oil; Garlic extract; Vitamin D3; Vitamin C; Bilberry; Echinacea
Allergien: Coconut
Vorherige Impfungen: Hepatitis B 2nd Vaccine in series 2012 - Abdominal Rash; Moderna COVID-19 1st Vaccine in series 01/22/2021 - Flu like symptoms f

VAERS 2471841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: AK
Alter: 53,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 25.05.2022
Beginn: 24.07.2022
Tage bis Beginn: 60,0
Dosis: 4
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Decreased appetite Headache Memory impairment Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

On 07/24/2022 I had a sore throat for few days since I work in a health care place I tested negative then on 07/28/2022 I tested positive. I had a cough along with a sore throat. I had random headaches went on for a month. I went to the urgent care on 07/29/2022 I was asking for PAXLOVID but they won't give it to me since I wasn't a candidate for it. The doctor recommended to do a nasal wash, vitamin C and vitamin D. Everything resolved slowly. I also had no energy at all. I was extremely tired. I had a lack of appetite. After 1 month my headaches are. I forget things which I never had before after COVID-19 I have to write stuff in order for me to remember.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D3
Allergien: None
Vorherige Impfungen: COVID-19 vaccine does 2, 3 and 4, day after I had chills, fever and muscles aches lasted for 24 hours.

VAERS 2471351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Body temperature Chills Fatigue Malaise Pain in extremity Pyrexia

Symptomtext

She was very sick; temperature of 104.4; woke up very ill that night with chills; she couldn't get out of bed to get a blanket; she had a little soreness in her arm; This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 65-year-old female patient received BNT162b2 (BNT162B2), on 01Oct2021 as dose 3 (booster), single (Lot number: FK9894) at the age of 65 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "diabetes" (unspecified if ongoing); "obesity" (unspecified if ongoing); "She has had reactions in the past to sulfa drugs" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 2, Single; Lot number: FL9262), administration date: 15Mar2021, when the patient was 64-year-old, for COVID-19 immunization, reaction(s): "she had a little soreness in her arm"; BNT162b2 (Dose 1, Single; Lot number: EL9367), administration date: 22Feb2021, when the patient was 64-year-old, for COVID-19 immunization, reaction(s): "she had a little soreness in her arm". The following information was reported: MALAISE (medically significant) with onset 01Oct2021, outcome "recovered" (02Oct2021), described as "She was very sick"; FATIGUE (medically significant) with onset 01Oct2021, outcome "recovered" (02Oct2021), described as "she couldn't get out of bed to get a blanket"; PAIN IN EXTREMITY (medically significant) with onset 01Oct2021, outcome "recovered" (02Oct2021), described as "she had a little soreness in her arm"; PYREXIA (medically significant) with onset 01Oct2021, outcome "recovered" (02Oct2021), described as "temperature of 104.4"; CHILLS (medically significant) with onset 01Oct2021, outcome "recovered" (02Oct2021), described as "woke up very ill that night with chills". The patient underwent the following laboratory tests and procedures: Body temperature: 104. 4 Fahrenheit. Clinical course: After her primary series and her first booster she had a little soreness in her arm. Woke-up very ill that night with chills. She couldn't get out of bed to get a blanket. When she finally got out of bed, her temperature was 104. 4. She never gets temperatures.She was frightened because she lives alone so she didn't know if she should go to the hospital or not. She went back to bed hoping she didn't die during the night, and the next day, her fever was gone. She was fine. She thinks it is very significant. She doesn't get sick and she doesn't have fevers. She has never had a reaction to an injection before in her life. She went with a friend, and her friend didn't have problems. She has had reactions in the past to sulfa drugs and something she can't re-member. She doesn't know the manufacturers or information at this time. Patient not visited to Emergency room and Physician office. No Prior vaccinations within 4weeks. Other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebrospinal fluid culture, bacterial sero-type, diagnostic imaging, (e.g., chest X-ray, MRI) were not performed.; Sender's Comments: As there is limited information in the case provided, the causal association between the events and the suspect drug cannot be excluded. The case will be reassessed once new information is available.,Linked Report(s) : US-PFIZER INC-202201201335 Same product, patient, different AEs, different dose;US-PFIZER INC-202201201336 Same product, patient, different AEs, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: Temperature; Result Unstructured Data: Test Result:104. 4 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Obesity; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2470812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 06.10.2022
Impfdatum: 22.04.2022
Beginn: 23.09.2022
Tage bis Beginn: 154,0
Dosis: 4
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Cough Pyrexia Respiratory tract congestion

Symptomtext

fever, congestion, cough

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2470731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 06.10.2022
Impfdatum: 06.07.2022
Beginn: 23.08.2022
Tage bis Beginn: 48,0
Dosis: 5
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Fatigue Headache Injection site pain Pain in extremity SARS-CoV-2 test positive

Symptomtext

I had a sore arm at injection site, chills, headaches and I needed a nap after the vaccine which lasted a day. The next day I felt fatigued which lasted a couple of days. I tested positive via a home test for COVID-19 on 08/23/2022. I contacted my doctor, and I was prescribed Paxlovid but was advised not to take it because of rebound. I previously tested positive for COVID-19 on 06/01/2022. I was given the prescription for Paxlovid at the time of my first time with COVID-19 which helped with my symtoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home test for COVID-19 was positive on 08/23/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Epilepsy; Multiply Sclerosis; Brain tumor; High blood pressure; Heart valve issues; Hemochromatosis; Dry eye; Sleep apnea; Arthritis; Hearing loss
Andere Medikamente: Levetiracetam; Amlodipine; Vitamin D3; Restasis; Flonase; Allegra; Vitamin B6; Multivitamin; Probiotic; Imvexxy; Biotin
Allergien: Flagyl; Lamictal; Seasonal allergies
Vorherige Impfungen: Shingles vaccine I was sick with chills and body aches.

VAERS 2469852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CT
Alter: 63,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 02.04.2022
Beginn: 06.09.2022
Tage bis Beginn: 157,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Pyrexia SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 via a home test on 09/06/2022. I had a fever, nasal drip and a cough. I had a telehealth visit with my doctor and was prescribed Paxlovid. I'm not sure the Paxlovid really helped but I felt better with a week. I continue to have a cough and I'm tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home test for COVID-19 was positive on 09/06/2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: N/A
Allergien: None
Vorherige Impfungen: The second Shingles really knocked me for a loop. I didn't feel like doing anything for a day.

VAERS 2465654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 31.03.2022
Beginn: 15.08.2022
Tage bis Beginn: 137,0
Dosis: 4
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Myalgia Oropharyngeal pain

Symptomtext

Covid 19 On August 15, 2022 I experienced sore throat, headache and muscle aches, fatigue. I was taking Tylenol for my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol; Glaucoma
Andere Medikamente: Atoravastatin; Timolol; Dorzolamide;
Allergien: N/A
Vorherige Impfungen: -

VAERS 2465246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: -
Geschlecht: U
Eingang: 30.09.2022
Impfdatum: 11.08.2022
Beginn: 11.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Myalgia Poor quality product administered Product administration error

Symptomtext

muscle ache; fatigue; The vaccine was taken from the freezer on 06Apr2022 at 12:00 pm. Vaccine that was administered to 5 patients while the vaccine was expired.; The vaccine was taken from the freezer on 06Apr2022 at 12:00 pm. Vaccine that was administered to 5 patients while the vaccine was expired.; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team, Program ID: A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 11Aug2022 as dose number unknown, single (Lot number: FK9894, Expiration Date: 15Jun2022) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: POOR QUALITY PRODUCT ADMINISTERED (non-serious), PRODUCT ADMINISTRATION ERROR (non-serious) all with onset 11Aug2022, outcome "unknown" and all described as "The vaccine was taken from the freezer on 06Apr2022 at 12:00 pm. Vaccine that was administered to 5 patients while the vaccine was expired."; MYALGIA (non-serious), outcome "unknown", described as "muscle ache"; FATIGUE (non-serious), outcome "unknown". Additional information: Caller was asking about the gray cap vaccine. The vaccine was expired and was administered to 5 patients. Caller mentioned that she was going to report this to VAERS and wants to check on what to do next. She said that this vaccine has an expiration date of 15Jun2022. Caller said at least that helps with one patient and all the patients were similar. 3 patient did report they had several days of side effects- so they thought event though expired that the vaccine had some effect on their sometimes muscle ache, fatigue. Follow-up (18Aug2022): This is a spontaneous follow-up report received from a contactable other HCP. Program ID: Updated information included: Reporter information, lot number and expiry date, therapy start and stop date, and event onset date. Follow-up attempts are completed. No further information is expected. Follow-up (26Sep2022): This is a spontaneous follow-up report received from same contactable Other-HCP. This Other-HCP reported in response to HCP letter sent in cross reference case that included: Updated information included: Reporter details, new events and additional information added. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : PFIZER INC-202201070713 Same reporter/drug/event, different patient; PFIZER INC-202201093830 Same reporter/drug/even, different patient; PFIZER INC-202201070271 Same reporter/drug/even, different patient;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WI
Alter: 76,0
Geschlecht: M
Eingang: 29.09.2022
Impfdatum: 01.04.2022
Beginn: 07.08.2022
Tage bis Beginn: 128,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I had a minor sore throat and a little cough. They lasted about 5 days and were very minor. I was prescribed an antiviral medication by the Nurse, which I took for 5 days, 10 pills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 at home test- positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Pantoprazole sodium; Eliquis; Trazadone HCL; Atorvastatin; Benicar; Detrol
Allergien: No
Vorherige Impfungen: -

VAERS 2464622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 29.09.2022
Impfdatum: 04.04.2022
Beginn: 22.09.2022
Tage bis Beginn: 171,0
Dosis: 4
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Cough Respiratory tract congestion Sinus pain

Symptomtext

congestion, sinus pain, cough

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 10.02.2021
Beginn: 16.08.2022
Tage bis Beginn: 552,0
Dosis: 4
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

Developed Covid with symptoms beginning 8/16/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Home Covid Rapid Antigen test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MO
Alter: 52,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 30.03.2022
Beginn: 01.08.2022
Tage bis Beginn: 124,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Bronchitis COVID-19 Chest X-ray normal Chest discomfort Chills Coagulation time Cough Electrocardiogram normal Feeling abnormal Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

On 07/31/2022, I woke up with a sore scratchy throat. I just kind of generally didn't feel good and it got worse throughout the day. That night I woke up with chills and was shivering. That morning 08/01 I took a home COVID test and tested positive. I then immediately made an appointment with the urgent care to go in. I felt like I had really bad bronchitis, chest discomfort, ran a fever on and off, cough, and runny nose. I never took my temperature but I definitely felt like I had fever. They prescribed an inhaler, they put me on Paxlovid, an antibiotic, and a steroid pack. On 08/03/2022 my chest had gotten worse each day leading up to 08/06/2022. It was hurting more every day. On Saturday 08/06/2022, I called into and went into the ER. They had me start on Mucinex and increase my water. A few days after that I started feeling better every day. On 08/18 I finally tested negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID test - positive EKG - normal Chest X-ray - normal Blood Clot Test - normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Simvastatin; Omeprazole
Allergien: None
Vorherige Impfungen: -

VAERS 2464167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

mild

Staat: OK
Alter: 73,0
Geschlecht: M
Eingang: 29.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ear pain Wrong product administered

Symptomtext

About 5 days after vaccine came down with ear ache; Other vaccine same date dose number=4, lot number=fk9894; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 73-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Sep2022 as dose 5 (booster), single (Lot number: gh9694) at the age of 73 years, in left arm for COVID-19 immunisation; BNT162b2 (BNT162B2), on 08Sep2022 as dose 4 (booster), single (Lot number: fk9894) at the age of 73 years, in left arm for COVID-19 immunisation. The patient's relevant medical history included: "Heart failure" (unspecified if ongoing); "CKD" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: COVID-19 vaccine (Primary immunization complete; Unknown Manufacturer), for COVID-19 Immunization. The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 08Sep2022, outcome "unknown", described as "Other vaccine same date dose number=4, lot number=fk9894"; EAR PAIN (non-serious) with onset 13Sep2022, outcome "recovering", described as "About 5 days after vaccine came down with ear ache". The event "about 5 days after vaccine came down with ear ache" required physician office visit. Therapeutic measures were taken as a result of ear pain. Additional information: The patient had no other vaccine in four weeks and was taking multiple other medications in two weeks. The patient received Amoxicline 870mg as treatment for the events. The patient had no COVID prior vaccination, was not tested for COVID post vaccination, and had no known allergies. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic kidney disease; Heart failure
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2463258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NC
Alter: 31,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Urticaria

Symptomtext

within several minutes of vaccine broke out in hives on extremities and trunk

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: flu vaccine
Vorherige Impfungen: flu vaccine, hives

VAERS 2463184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 73,0
Geschlecht: M
Eingang: 28.09.2022
Impfdatum: 30.03.2022
Beginn: 12.09.2022
Tage bis Beginn: 166,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Nasal congestion Pain in extremity Respiratory symptom SARS-CoV-2 test positive

Symptomtext

I had a little soreness in my arm after receiving the vaccine. On 09/12/2022, I took a home test for COVID-19 and it was positive. I contacted my doctor on 09/16/2022 to get an appointment but was unable. I had a virtual visit with my doctor on 09/20 and my chief complaint was upper respiratory issues. I was informed that if my symptoms got worse to go to the emergency room. As of today I continue to have congestion which is being treated with nasal sprays.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Home test for COVID-19 which was positive on 09/12/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Kidney stones; type 2 diabetic; allergies; high blood pressure
Andere Medikamente: N/A
Allergien: Bicitracin; corn; carrots
Vorherige Impfungen: Every couple of years I get a little under the weather after the flu vaccine with sore throat and sinus drainage.

VAERS 2455668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: DE
Alter: 74,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 28.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature abnormal Burning sensation Chills Decreased appetite Depressed mood Diarrhoea Feeling of body temperature change Hot flush Hyperhidrosis Insomnia Suicidal ideation Visual impairment

Symptomtext

she feels like she wants to die; diarrhea; hot flushes; sweating; chills; a cycle of hot and cold; insomnia/has trouble sleeping; lack of appetite; feels like she is melting from the inside out; She doesn't have a fever, she takes her temperature, but her core body temperature feels like she has got a furnace inside her; feels depressed and hopeless; needing a magnifying glass to read labels is normal for her lately; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 74-year-old female patient received BNT162b2 (BNT162B2), on 28Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 74 years for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose: 1, LOT: EW0151), administration date: 03Apr2021, when the patient was 73-year-old, for Covid-19 immunization, reaction(s): "Diarrhea", "hot flushes", "sweating", "She doesn't have a fever, she takes her temperature, but her core body temperature feels like she has got a furnace inside her"; BNT162b2 (Dose: 1, LOT: EW0151), administration date: 03Apr2021, when the patient was 73-year-old, for Covid-19 Immunization, reaction(s): "a cycle of hot and cold", "insomnia", "lack of appetite"; BNT162b2 (Dose: 2, LOT: FWA72), administration date: 03May2021, when the patient was 73-year-old, for Covid-19 immunization, reaction(s): "Diarrhea", "depressed/feels depressed and hopeless", "does not feel well", "hot flashes", "chills", "she takes her temperature, but her core body temperature feels like she has got a furnace inside her", "sweating", "has trouble sleeping", "needing a magnifying glass to read labels is normal for her lately"; BNT162b2 (Dose: 3, Lot number: 330268D), administration date: 11Nov2021, when the patient was 73-year-old, for Covid-19 immunization, reaction(s): "Diarrhea", "hot flashes", "sweating", "chills", "insomnia/has trouble sleeping", "lack of appetite", "She doesn't have a fever, she takes her temperature, but her core body temperature feels like she has got a furnace inside her", "needing a magnifying glass to read labels is normal for her lately", "feels depressed and hopeless". The following information was reported: SUICIDAL IDEATION (medically significant), outcome "unknown", described as "she feels like she wants to die"; DIARRHOEA (non-serious), outcome "not recovered", described as "diarrhea"; HOT FLUSH (non-serious), outcome "unknown", described as "hot flushes"; HYPERHIDROSIS (non-serious), outcome "unknown", described as "sweating"; CHILLS (non-serious), outcome "unknown"; FEELING OF BODY TEMPERATURE CHANGE (non-serious), outcome "unknown", described as "a cycle of hot and cold"; INSOMNIA (non-serious), outcome "unknown", described as "insomnia/has trouble sleeping"; DECREASED APPETITE (non-serious), outcome "unknown", described as "lack of appetite"; BURNING SENSATION (non-serious), outcome "unknown", described as "feels like she is melting from the inside out"; BODY TEMPERATURE ABNORMAL (non-serious), outcome "unknown", described as "She doesn't have a fever, she takes her temperature, but her core body temperature feels like she has got a furnace inside her"; DEPRESSED MOOD (non-serious), outcome "unknown", described as "feels depressed and hopeless"; VISUAL IMPAIRMENT (non-serious), outcome "unknown", described as "needing a magnifying glass to read labels is normal for her lately". Therapeutic measures were taken as a result of diarrhoea. Clinical course details: The patient reported that she has been experiencing diarrhea since she first got the Pfizer covid-19 vaccine. She would like to know if this has already been reported as a side effect before and wanted information and how to treat it. She asked for information on any ongoing research on how to treat it. She also reported having hot flushes, sweating, chills, a cycle of hot and cold, insomnia, and lack of appetite. She is also aware that diarrhea, fever, and chills are among the most reported side effects from the vaccine so she is assuming there must be something that Pfizer is doing to try and prevent or treat the diarrhea. She mentions that her diarrhea is relieved by Imodium but she asks if there was any other medication she could try to treat her diarrhea, she also asks if we had information on how other patients treat their diarrhea and if other patients have reported it before. Furthermore, the patient was calling about Pfizer COVID-19 vaccines and boosters. The next day after her first vaccine she had diarrhea which she thought was from her other medication. The following month she got another dose of the vaccine, and then she got two boosters. She has been dealing with constant diarrhea, hot flashes, or chills. Her diarrhea started after her first dose, then it stopped and she connected it to her antidepressant medication that she stopped and the diarrhea stopped when she stopped that medication. No further details provided about caller's antidepressant medication. Her diarrhea was constant for about two months after her first vaccine. She feels like she is dying, she is desperate to find out what is going on with her and find out how to get it to stop. She has chills and hot flashes and sweating along with diarrhea, a combination of symptoms, that are relentless. She feels like she is melting from the inside out. She doesn't have a fever, she takes her temperature, but her core body temperature feels like she has got a furnace inside her. She burns and burns, it is hot, so she stops and lays down in front of the AC then she gets cold and covers up because she is feeling chilly. After a certain length of time she overheats. She clarifies her phrase about feeling like she is dying by saying that she feels like she wants to die because she wants it to stop. She feels depressed and hopeless, it affects her in a lot of ways, physically and emotionally. She has been taking Imodium to stop the diarrhea. She has trouble sleeping because it wakes her up at night. She has been taking Imodium and Pepto-Bismol liquid capsules to treat the diarrhea. The Imodium she takes every twelve hours, one capsule, active ingredient Loperamide HCl 2mg. She says her glasses and her eyes are getting, she is crying too now so maybe. Imodium date she started taking unknown, the Pepto-Bismol she started in May or Jun2021, and is sporadically taking Bismuth subsalicylate 262mg, which she takes maybe every 8 hours. She says she needs a magnifying glass to make it bigger for the Bismuth label to read the word subsalicylate, then clarifies that needing a magnifying glass to read labels is normal for her lately.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201173881 same patient/reporter; different vaccine dose/AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 03.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity

Symptomtext

Extreme soreness of her right arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient received BNT162b2 (BNT162B2), on 03Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 70 years for covid-19 immunisation. The patient's relevant medical history included: "ductile carcinoma of the left breast in site 2", start date: 2021 (unspecified if ongoing); "She completed 6 weeks of radiation followed by a year later" (unspecified if ongoing). The patient's family history included: "metastasis of melanoma" (unspecified if ongoing), notes: mother passed away from metastasis of melanoma; "congestive heart failure" (unspecified if ongoing), notes: father passed away at 100 from congestive heart failure. The patient's concomitant medications were not reported. Past drug history included: Tamoxifen, notes: she started a 5 years regimen of tamoxifen. Vaccination history included: BNT162b2 (Dose 1, Single; Lot: EP7534; Expiry: unknown; NDC: unknown. She felt lethargic after the first 2 rounds of the vaccine but nothing earth shattering.), administration date: 15Mar2021, when the patient was 69-year-old, for COVID-19 immunization, reaction(s): "felt lethargic"; BNT162b2 (Dose 2, Single; Lot: EW0151; Expiry: unknown; NDC: unknown. she felt lethargic after the first 2 rounds of the vaccine but nothing earth shattering.), administration date: 05Apr2021, when the patient was 69-year-old, for COVID-19 immunization, reaction(s): "felt lethargic"; BNT162b2 (Dose 3, Single; Lot: FD0810; Expiry: unknown; NDC: unknown), administration date: 25Oct2021, when the patient was 69-year-old, for COVID-19 immunization; Shingles shots (She also had the singles shots a year ago affect her for 24 hours), for Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "unknown", described as "Extreme soreness of her right arm". Additional information: Caller reported that she had extreme soreness of her right arm after the 4th dose, the 2nd booster. The patient did not receive any other vaccines within four weeks prior to the vaccination. Additional vaccines administered on same date was reported as no. Reporter said that she has never had an allergic reaction before. No relevant lab tests. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast ductal carcinoma; Congestive heart failure (father passed away at 100 from congestive heart failure); Metastatic melanoma (mother passed away from metastasis of melanoma); Radiation therapy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2446390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 73,0
Geschlecht: F
Eingang: 15.09.2022
Impfdatum: 14.03.2022
Beginn: 24.05.2022
Tage bis Beginn: 71,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Malaise SARS-CoV-2 test positive

Symptomtext

Tested positive with home test Very mild symptoms,fatigue Dr.prescribed Paxlovid after phone call

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Other than home test none
Aktuelle Erkrankungen: None
Vorgeschichte: Stent in heart,arthritis,scoliosis and COPD
Andere Medikamente: Lantanoprost Atorvastatin Fluoxetine CBD gel Caps 75 mg Low Dose Aspirin Vitamin D
Allergien: Allergic to fentanyl
Vorherige Impfungen: -

VAERS 2440939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TN
Alter: 60,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 10.06.2022
Beginn: 13.08.2022
Tage bis Beginn: 64,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back disorder COVID-19 Ear pain Feeling abnormal Head discomfort Headache Lung disorder Malaise Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I woke up that morning and I noticed I had the worst sore throat I have ever had in my life and both ears were hurting and had extreme congestion that day. I did not have a fever that day but I had a headache with pressure I was blowing a lot of mucus out of my nose and felt it in my back and lungs but did not have short of breath. I had a bad illness that effected my lungs 21 years ago so since then I can feel things is my lungs. So on the 13th it was worse and by the 16th I tested positive for COVID-19 with a home test and it was positive. I contacted my doctor and let her know and she gave me a prescription for Paxlovid. Due to Kidney Function they decreased the dosage. I had rebound symptoms after the Paxlovid prescription was done and felt bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: COVID-19 home test Positive 9/16/22
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Hyperlipidemia; Diabetes Type 2; Heart Arrhythmia; Pacemaker; Common Variable Immunodeficiency;
Andere Medikamente: Lisinopril; Omeprazole; Metformin; Lipitor; Lasix; Zyrtec; Aspirin; Ipratropium Nasal Spray; Flonase; Astroline Nasal Spray; Advair Disks: Atenolol; Vitamin D3; Albuterol; Gammagard Infusion
Allergien: Tropical Fruits; Red Food Dye; Penicillin; Doxycycline; Codeine; Zocor; Decongestion;
Vorherige Impfungen: -

VAERS 2440890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 98,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 28.04.2022
Beginn: 10.09.2022
Tage bis Beginn: 135,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

Patient symptomatic and tested positive for COVID, resulting in hospitalization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: GA
Alter: 18,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 20.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Urticaria

Symptomtext

Diffuse hives developed 12 hours after the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Vasovagal, near syncope; age 16, 3/26/21, Covid-19, Pfizer

VAERS 2433423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 24.02.2021
Beginn: 14.08.2022
Tage bis Beginn: 536,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Exposure to SARS-CoV-2 Micrographic skin surgery Nausea Respiratory tract congestion SARS-CoV-2 test positive Upper respiratory tract congestion

Symptomtext

80-year-old female presented to the hospital with nausea and congestion. Patient played dominoes in her apartment complex with some friends a little over a week ago that friend was positive called her over the weekend to let her know she was positive however patient went for her mohs surgery to her left lateral forehead on the eighth. Patient had mild congestion at that time. Congestion progressed and Wednesday patient tested herself on the 10th and tested positive for COVID. Patient states she thought it was all with cold. She denied any sore throat but she admits to significant head congestion. Patient came to the emergency room on the 14th. Patient spoke with her primary received prescription for Paxlovid. Patient states she took the pills on Wednesday she took half the pills on Thursday and then stopped because they made her nauseated. Patient presented over the weekend. Initially was placed on oxygen but is currently on room air. She received hydration in the emergency room and patient is feeling better infectious disease has been asked to comment. ID service does not recommend steroids or antivirals. Patient stable from a cardiac standpoint without plans for any further cardiac work-up/intervention, follow-up with primary cardiologist upon discharge for further treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: 3,0
Labordaten: 8/14 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2431082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 19,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 21.02.2022
Beginn: 07.09.2022
Tage bis Beginn: 198,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Headache Oropharyngeal pain SARS-CoV-2 test positive Vomiting

Symptomtext

Developed sore throat, headache and vomiting. Tested COVID-19 positive on rapid antigen test 9/7/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2422170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 30.03.2022
Beginn: 30.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Vaccination site pain

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Mar2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 56 years for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "Non-alcoholic fatty liver disease" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE, start date: Mar2021; OMEGA-3-ACID ETHYL ESTER, start date: Mar2021. Past drug history included: Bnt162b2, start date: 07Oct2021, stop date: 07Oct2021, for Covid-19 Immunization, reaction(s): "Treatment of COVID-19", notes: DOSE 3 (BOOSTER), SINGLE; Lot Number: 30145819; Bnt162b2, start date: 19Mar2021, stop date: 19Mar2021, for Covid-19 Immunization, reaction(s): "Treatment of COVID-19", notes: DOSE 2, SINGLE; Lot Number: EN6208; Bnt162b2, start date: 26Feb2021, stop date: 26Feb2021, for Covid-19 Immunization, reaction(s): "Treatment of COVID-19", notes: DOSE 1, SINGLE; Lot Number: EN6203; Bnt162b2, start date: 07Oct2021, stop date: 07Oct2021, for Covid-19 Immunization, reaction(s): "Treatment of COVID-19", notes: DOSE 3 (BOOSTER), SINGLE; Lot Number: 30145819; Bnt162b2, start date: 19Mar2021, stop date: 19Mar2021, for Covid-19 Immunization, reaction(s): "Treatment of COVID-19", notes: DOSE 2, SINGLE; Lot Number: EN6208; Bnt162b2, start date: 26Feb2021, stop date: 26Feb2021, for Covid-19 Immunization, reaction(s): "Treatment of COVID-19", notes: DOSE 1, SINGLE; Lot Number: EN6203. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 30Mar2022, outcome "unknown", described as "sore arm when vaccinated". Additional information: The patient had no known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Non-alcoholic fatty liver
Andere Medikamente: AMLODIPINE; OMEGA-3-ACID ETHYL ESTER
Allergien: -
Vorherige Impfungen: -

VAERS 2417317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 01.04.2022
Beginn: 11.08.2022
Tage bis Beginn: 132,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Abdominal pain Diarrhoea Dizziness Flank pain Nausea

Symptomtext

abdominal pain, diarrhea, nausea, flank pain, dizziness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2415938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PR
Alter: 53,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 20.05.2022
Beginn: 22.05.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Computerised tomogram abdomen Computerised tomogram neck Computerised tomogram pelvis Injection site pain Laboratory test Lymphadenopathy

Symptomtext

Pain in the left arm swelling of lymph nodes in both armpits, neck and Inguinal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: Laboratories May 24 2022, CT scan neck, Abdominal CT and pelvic CT.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Asthma; Hypothyroidism after Hashimoto disease.
Andere Medikamente: Synthroid 137 Monday to Friday and Synthroid 125 Saturday and Sunday.
Allergien: Aspirin, Sulfa, Theophylline.
Vorherige Impfungen: Yes. Joint pain, Fever, tiredness.

VAERS 2415889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 19.05.2022
Beginn: 11.08.2022
Tage bis Beginn: 84,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Lacrimation increased Nasopharyngitis Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

In the night of 08/11/2022 I tested positive for COVID-19. On 08/12/2022 I started experiencing chills; eyes were watery; sore throat. I felt like I had a severe cold. I did a tele health with my doctor she advised me to take Nyquil Cough, Cold & Flu Medicine and Tylenol . I took it approximately for 8 days. I started feeling better afterwards.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 Home Test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Minaers disease; Seasonal Allergies
Andere Medikamente: Multi Mineral; Multi Biotics; CoQ10; Zyrtec
Allergien: Strawberries; Sulfa; Zantac; Gold; Shampoo
Vorherige Impfungen: Dose 1- Rash; Blisters; and Hives for a couple of days. I was admitted in the ER for few hours they gave me Benadryl shot a

VAERS 2415845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 13.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Herpes zoster Pruritus

Symptomtext

Three days after my fourth dose I felt a small itching spot on my leg and thought it was an insect bite. The next day I noticed that it was a pattern and was shingles. I contacted my doctor and by the time she got back to me I was out of the window to use medication but she did give me a prescription of Valtrex incase it comes back again. On June 22, 2022 I had another outbreak and started taking the Valtrex medication. I took the whole course of medication and also have taken the Shingrex vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Metastatic Breast Cancer; High Blood Pressure; High Cholesterol
Andere Medikamente: Herceptin Fam-Transtusamab; Zyrtec; Pepcid; Metoprolol; Exmextame; Zofran; Magnesium; Calcium; Vitamin D3; Tylenol
Allergien: Latex; IV Contrast; Herceptin; Dalara
Vorherige Impfungen: Tetanus antitoxin

VAERS 2405835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 28.04.2022
Beginn: 18.07.2022
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

On 07/18/2022 I took a home test that was negative because I thought I had a chest cold. I had low fever never above 100.3, cough and felt like a chest cold. I spoke with my sister in law and she was positive so I took another test on 07/20/2022 and it was positive. I spoke with my doctor over the phone and he called in PAXLOVID and I started that night. My symptoms started improving within three days. I am having no long term effects now everything went away. I did have a lot of fatigue but it is better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home test negative 07/18/2022, COVID-19 home test positive 07/20/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: SYNTHROID; probiotic; LEVBID; magnesium; WELLBUTRIN; quinapril; LEXAPRO; multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2405822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 14.01.2021
Beginn: 22.06.2022
Tage bis Beginn: 524,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Influenza virus test negative Pyrexia SARS-CoV-2 test positive Streptococcus test negative Throat irritation

Symptomtext

June 22, 2022: scratchy throat, fatigue, slight fever June 23, 2022: same symptoms, negative rapid antigen test for COVID19, telehealth consult, negative strep and influenza tests June 24, 2022: same symptoms, positive COVID19 rapid antigen test. Visited urgent care/obtained Paxlovid and began treatment June25--28, 2022: symptoms improved. Paxlovid caused constant HORRIBLE taste in mouth! June 26, 2022: Tested negative

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 06/24/22: negative rapid test, negative Strep test, negative influenza test 06/25/22: positive COVID19 rapid test
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: fosamax, calcium +D3, colace, claritin, flonase
Allergien: nuts
Vorherige Impfungen: -

VAERS 2404499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CT
Alter: 68,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 06.05.2022
Beginn: 08.07.2022
Tage bis Beginn: 63,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Feeling abnormal Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I had a sore throat and felt kind of yucky on Friday night 07/08/2022. On Saturday, I felt fine when waking up, but about an hour later I felt terrible, so I went back to bed. I tested positive for COVID-19 that day. I had a fever of about 101. My temperature was elevated for 24-36 hours. I also experienced body aches and just felt lousy. I went to a walk-in clinic where they gave me an antiviral medication. Overall, I felt badly for about 3-4 days, but it took around 2 weeks for me to actually test negative for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: At home COVID-19 test positive 07/09/2022.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma.
Andere Medikamente: Multivitamin; vitamin D; vitamin C; magnesium; vitamin D3; calcium; vitamin B12: B complex; probiotic; metoprolol; pantoprazole; CLARITIN; limital; sertraline; rosuvastatin; trazadone; montelukast.
Allergien: Penicillin.
Vorherige Impfungen: Second dose of Pfizer-Covid like symptoms.

VAERS 2404310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 06.05.2022
Beginn: 24.07.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Decreased appetite Fatigue Headache Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

I started getting symptoms of a headache that I thought was a migraine. I got nauseous and vomited. That evening I developed a cough. I took an at home COVID-19 test that was positive. I contacted my doctor and was advised to do over the counter medications and my symptoms we not severe enough for Paxlovid. My symptoms did progress to fatigue and tiredness. My cough got very strong. I had no appetite for about a week. I still cough somewhat at night and experience tiredness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: HTN (controlled); Hypothyroidism; Mild Emphysema
Andere Medikamente: Multivitamins; Probiotics
Allergien: None
Vorherige Impfungen: -

VAERS 2401403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 58,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 01.04.2022
Beginn: 03.08.2022
Tage bis Beginn: 124,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

fever during hospitalization and tested positive for COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2400385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 03.05.2022
Beginn: 19.07.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

7/19/2022 Felt like an allergy attack. 7/20 this felt like a cold Runny nose, shallow cough, aches and pains. 7/21 slight fever. 7/22 Tested with At home COVID 19 test, negative. 7/24 Tested with At home COVID 19 test, positive. Called Doctor's office and left a message. 7/25 televisit with doctor, who advised rest and to treat symptoms as needed with tylenol and cough syrup. Symptoms continued unchanged until time of reporting. 8/3 Tested with At home COVID 19 test, negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 7/22 Tested with At home COVID 19 test, negative. 7/24 Tested with At home COVID 19 test, positive. 8/3 Tested with At home COVID 19 test, negative.
Aktuelle Erkrankungen: No
Vorgeschichte: Afib; Low Thyroid; Acid Reflux; Arthritis
Andere Medikamente: Eliquis; Dofetilide; Tizanidine; Omeprazole; Levothyroxine; Gabapentin; Protandum; Vitamin D3; Bone Up Calcium formula; Osteo Biflex; Lutein; Omega 3; Cetirizine
Allergien: Sulfa; Codeine; Latex
Vorherige Impfungen: -

VAERS 2400371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 61,0
Geschlecht: M
Eingang: 03.08.2022
Impfdatum: 03.05.2022
Beginn: 10.07.2022
Tage bis Beginn: 68,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Pain Paranasal sinus hypersecretion Pyrexia SARS-CoV-2 test positive Sinus congestion Sinusitis

Symptomtext

I received my second Pfizer booster for COVID-19 on 5/3/2022. One evening while I was visiting my son out of state on 7/10/2022, I began running a fever, developed body aches, and had clear nasal drainage. On the morning of 7/11/2022, I still had the same symptoms. I took a home COVID-19 test. The results were inconclusive, though, as we could not tell if there was a second line on the stick. I then went to an urgent care clinic the same day to get a rapid test, and that yielded a positive-abnormal result. I began isolating at my son's house. By 7/14/2022, I was still running a low-grade fever and still had sinus drainage, which was mostly clear. I went back to the urgent care clinic that day to see if I had a sinus infection, but the nurse on duty thought it was just typical COVID-19 drainage. She then prescribed me a 5-day supply of Paxlovid. The fever stabilized, and my temperature returned to normal on 7/15/2022 and 7/16/2022. I returned home on 7/16/2022. I finished the Paxlovid on 7/18/2022. At this point, I was still having sinus congestion and drainage, which continued up to 7/29/2022. On 7/29/2022, I went to my PCP. He determined that I had a sinus infection that had been brought on by the COVID-19, and he prescribed me amoxicillin to treat the sinus infection. At the time of this writing, I am still taking the amoxicillin. The amount of drainage is now greatly reduced, so I believe my PCP's diagnosis was accurate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 7/11/2022--Home COVID-19 Test--Inconclusive Result; 7/11/2022--Rapid COVID-19 Test--Positive Result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Low Bone Density; Deviated Septum; Sinus Polyp.
Andere Medikamente: Montelukast; Allegra; Multivitamin; Calcium with Vitamin D; Vitamin D; Lutein with Zeaxanthin; Aspirin; Tylenol; Aleve; Fish Oil; Airborne Chewable; OTC Eye Drops for Dry Eye; Flonase; Reclast Infusion (Once Annually).
Allergien: None.
Vorherige Impfungen: -

VAERS 2399358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 02.08.2022
Impfdatum: 30.04.2022
Beginn: 25.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: UN / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Chills Fatigue Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Sore throat, fever (101.1), chills, body aches, fatigue Took home rapid test on 7/26/2022 that came back positive, took PCR test at Hospital drive thru facility that came back positive on 7/26/2022 Treated with Paxlovid for 5 days Still tested positive by home rapid test on 5th day of Paxlovid (7/30/2022) Recovered 8/1/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Took home rapid test on 7/26/2022 that came back positive, took PCR test at Hospital drive thru facility that came back positive on 7/26/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxin 50 mcg Vitamin D3 100 mcg Vitamin C 1000 mg Vitamin B Complex Magnesium Citrate 250 mg Acidophilus Probiotic 100 million organisms
Allergien: Thimerosol
Vorherige Impfungen: -

VAERS 2399224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 15.04.2022
Beginn: 21.07.2022
Tage bis Beginn: 97,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood glucose fluctuation COVID-19 Cough Decreased appetite Diarrhoea Exposure to SARS-CoV-2 Headache Hypersensitivity Oropharyngeal pain SARS-CoV-2 test positive Wheezing

Symptomtext

Starting 07/21/2022, I started having more allergy issues and I took ZYRTEC which kind of helped but not much. I got wheezy and used my rescue inhaler and took BENADRYL. These helped a bit but still didn't make it go away. The next day I had the same symptoms. On 07/23/2022, my daughter tested herself and was positive for COVID-19. I tested myself the same day and was negative. By 07/24/2022, I tested myself again with an at-home COVID-19 test which came back positive. At this time, I was also coughing and had a sore throat. I found out the COVID-19 test I had at home was expired by about a week, so when my daughter got home she had brought a new COVID-19 test which I took and confirmed that I was positive. I started isolating myself more into my room and self treated the symptoms. The sore throat, headache and lack of appetite got slightly worse. I started feeling better by 07/30/2022. I decided to wait until today 08/02/2022 to test again and it came back negative. I had diarrhea yesterday but haven't since. I still have a slight cough to this day but no other symptoms. Also, during this infection, my blood sugar was very erratic which is normal for me when I'm sick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: At-home COVID-19 test (07/23/2022): negative; at-home expired COVID-19 test (07/24/2022): positive; at-home COVID-19 test (07/24/2022): positive; at-home COVID-19 test (08/02/2022): negative
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Type II; Allergies; Asthma; COPD; Coronary Artery Disease; Heart Stents; High Blood Pressure; Gastroparesis
Andere Medikamente: Metformin; acarbose; NOVOLIN insulin; insulin; aspirin; omega 3; REPATHA injection monthly; coQ10; vitamin D3; pantoprazole; TENORETIC; ZYRTEC; SINGULAIR; albuterol; BENADRYL; FLEXERIL; ZYRTEC
Allergien: BIAXIN; naproxen; cats; dogs; bananas; pineapple; certain perfumes; grasses
Vorherige Impfungen: -

VAERS 2398094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 29.04.2022
Beginn: 02.05.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Erythema Headache Induration Injection site nodule Injection site rash Injection site warmth Nodule Skin warm

Symptomtext

Starting 05/02/2022, I had a knot on my arm (very hard and hot around it). I had a bad headache (not a migraine). I was more concerned about the knot and heat rash around the injection site. Given I had a reaction similar to this after a flu shot, and its accompanied by an abnormal headache, I was concerned I was having a delayed allergic reaction to the vaccine. I sent a message to my doctor to see if I should come in. She told me to use some compresses on the arm and to take medicine for the headache. I was told to go to the ER if it got worse. The headache lasted for about 12 hours. The redness and heat went down by the next day. The knot gradually worked itself down and was gone in about 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines; Heart murmur
Andere Medikamente: Buspirone; TOPAMAX; levonor/ethestradiol; naratriptan; vitamin D
Allergien: Penicillin
Vorherige Impfungen: Delayed inflammatory response similar to this one after a flu shot.

VAERS 2397682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 61,0
Geschlecht: M
Eingang: 31.07.2022
Impfdatum: 31.03.2022
Beginn: 01.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site mass Injection site pain Injection site swelling

Symptomtext

Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Severe, Additional Details: Pt reported golf ball sized lump on arm at injection site after receiving vaccine as well as some redness and mild pain around injection site initially.Vaccine was given in March as pt's booster, problem is ongoing as of July. Lump on arm is visible and palpable, pain has subsided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2396465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 65,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 21.04.2022
Beginn: 29.05.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Deafness Discomfort Ear infection Exposure to communicable disease Fatigue Herpes zoster Middle ear effusion Oral mucosal eruption Photosensitivity reaction Rash Tympanic membrane perforation Viral upper respiratory tract infection

Symptomtext

The rash developed and there was a lot of pain with the rash. I went into the clinic the next day and was told it was shingles I was given anti-viral. I came home it never blistered bad and open, but it was uncomfortable I got a rash in my mouth and the fatigue was intense. I stayed home and rested I started to lose the fatigue. When I was resting my husband gave me a upper respiratory virus and ended up with an ear infection and my ear drum busted and lost my hearing temporarily. I have been dealing with fluid in the ear and they think that they are allergy related. I just started back with getting the allergy shots. When I would go outside the sun would bother me even through clothing and that lasted 5 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Adeline Efficiency; High Blood Pressure; Depression; Arthritis; Concussions;
Andere Medikamente: Advair; Acetaminophen; Doxepin; Estradiol; Cortef; Claritin; Liftean: Olopatadine; Multi Vitamin; Prilosec; Refresh Eyedrops; Trazadone; Nasacort; Ambien; Vitamin D3; Vitamin E; Fish Oil; Protein Drink; Calm Magnesium Supplement; Calcium; V
Allergien: Environmental Allergies; Antibiotics
Vorherige Impfungen: -

VAERS 2396402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fk9894

mild

Staat: IN
Alter: 70,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 08.04.2022
Beginn: 05.06.2022
Tage bis Beginn: 58,0
Dosis: UNK
Route/Site: - / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ageusia Anosmia COVID-19 Cough Decreased appetite Fatigue Malaise Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I came down with covid on June 5...congestion, extreme fatigue, sick in bed for a week, dry cough, no appetite, loss of taste and smell...then another week but could get out of bed for periods of time

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: home covid tested positive....husband had it a few days later but just a runny nose
Aktuelle Erkrankungen: none
Vorgeschichte: CLL (no sign of disease since 2006 when I finished chemo) Hypothyroid
Andere Medikamente: Omeprazole 20mg Lisinopril2.5mg Sertraline 25mg Levothyroxine 100mcg Rosuvastatin 20mg Calcium with D3 600mg
Allergien: none
Vorherige Impfungen: -

VAERS 2396374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 67,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 27.04.2022
Beginn: 30.06.2022
Tage bis Beginn: 64,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia Anosmia COVID-19 Chills Exposure to SARS-CoV-2 Influenza Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

On June 30 I started with flu symptoms, chills, sore throat. I had been on a Trip and knew that others on the trip had tested positive, so I took an at home Covid test. The results were negative. I tested again on July 2 and got negative result. Since I had worsening symptoms I took another test on July 6 and the results were positive. I called the Health Clinic. Since my positive test was 6 days after my symptoms started I could not get a prescription for Paxlovid. So I just had to live with Covid until it ran it's course. I lost my senses of taste and smell had body aches for several days. I still have not gotten my senses of taste and smell back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: All were at home test kits. June 30, pm July 2, am July 6, am
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Simvastatin 20 mg, Melatonin 10 mg, calcium with D 600 mg
Allergien: -
Vorherige Impfungen: -

VAERS 2395000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NC
Alter: 45,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 26.04.2022
Beginn: 18.06.2022
Tage bis Beginn: 53,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia COVID-19 Diarrhoea Eye pain Fatigue Feeling abnormal Influenza like illness Myalgia Nausea Pruritus Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sleep disorder Sneezing Throat irritation

Symptomtext

I started getting symptoms of tiredness of scratch throat. I had nausea and generally feeling bad. I took a COVID-19 test that was positive. That night I had a fever with mild muscle and joint aches. Then for 4 days, I had flu like symptoms. I had constant sneezing, runny nose, chest congestion, and diarrhea. At nights for 2 straight nights, I experienced odd symptoms of the bottom of my feet was itchy and woke up up at nights and my eye balls ached just until today. I did have a telehealth visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID-19 - positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; Vitamin D; Birth control
Allergien: Iodine; Shellfish; Contrast Dyes
Vorherige Impfungen: -

VAERS 2393677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 23.04.2022
Beginn: 04.07.2022
Tage bis Beginn: 72,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cough Exposure to SARS-CoV-2 Fatigue Feeling abnormal Headache Oropharyngeal pain SARS-CoV-2 test negative

Symptomtext

I was exposed to COVID-19 4 days before feeling bad, but I never tested positive. I had a headache, sore throat, cough, and fatigue. I still have a cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 7/5/2022- PCR COVID-19 Test- Negative; 7/8/2022- At Home COVID-19 Test- Negative; 7/10/2022- At Home COVID-19 Test- Negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2393228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 27.07.2022
Impfdatum: 26.04.2022
Beginn: 24.07.2022
Tage bis Beginn: 89,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal discomfort COVID-19 Decreased appetite Diarrhoea Dysgeusia Dyspepsia Fatigue Feeling abnormal Malaise Pain Parosmia Respiratory tract congestion SARS-CoV-2 test positive Vomiting

Symptomtext

COVID-19 symptoms started on 07/24/22; tested positive on 07/25/2022. It started with a strange taste or smell and I was starting to feel congestion in my throat but I didn't really feel sick. I did a test and it was negative, but then later that day I felt achy and more tired and at night I got bad indigestion and threw up twice and had diarrhea. The next morning I felt terrible as far as achiness and upset stomach and not wanting to eat anything. I did another test and it was positive and I decided at that point to call my doctor to try and get PAXLOVID. I had a telehealth appointment on Tuesday morning and throughout that day I had bad indigestion and achiness and I took some TYLENOL a few times during the day for that and I talked to doctor and the next morning I got a prescription for PAXLOVID and started that 07/26 and my symptoms have gotten better but I still feel tired and achy but no problems with stomach.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 positive 07/24/22.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Testosterone injections; sitosterol; multivitamin; vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 2393162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 26.04.2022
Beginn: 06.07.2022
Tage bis Beginn: 71,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Decreased appetite Disorientation Dizziness Fatigue Feeling abnormal Headache Impaired work ability Malaise Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive Sinus congestion Throat irritation

Symptomtext

Starting 07/06/2022, I developed a scratchy throat, congestion and a headache. I tested that day with an at-home COVID-19 test which came back positive. I called the city COVID HL to see if I needed treatment and she decided to prescribe me PAXLOVID. I started taking that the same day. I continued to feel sick for the next few days (sinus congestion, fatigue, headache and runny nose). I quarantined at home in one room. On 07/09/2022, I started feeling better and it progressively improved as the days went on. On 07/12/2022, the day after I stopped the PAXLOVID, I tested myself at home and was negative. The next day (07/13/2022), I went into the city and got tested with a PCR test and a rapid, both were negative. I thought it was all over so I stopped masking and quarantining. On 07/16/2022, I developed a rebound infection of COVID-19 and experienced all the same symptoms as previously but they lasted longer and were worse than before. I was sick from 07/16/2022 - 07/25/2022. I missed 6 days of work. My nose was running non stop, I was dizzy and disoriented, lost my appetite and just felt poorly. I went back to work after that. I am feeling better now but still am having some congestion and coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: At-home COVID-19 test (07/06/2022): positive; At-home COVID-19 test (07/12/2022): negative; PCR and rapid test (07/13/2022): negative; At-home COVID-19 test (07/16/2022): positive
Aktuelle Erkrankungen: None
Vorgeschichte: Celiac Disease; Hashimoto's Thyroiditis
Andere Medikamente: SYNTHROID; PROZAC; vitamin B12; folate; vitamin D3; progestin-only birth control
Allergien: Gluten
Vorherige Impfungen: -

VAERS 2391044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 22.04.2022
Beginn: 11.07.2022
Tage bis Beginn: 80,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain COVID-19 Cough Exposure to SARS-CoV-2 Herpes zoster Insomnia Malaise Nasal congestion Pain Productive cough Rash Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

We had been traveling out of state. We picked up our grandkids to take them to a museum and then travelled home on 07/07/2022. While vacationing, I noticed some back pain and went to a doctor when I returned home due to a rash. He prescribed prednisone for the rash at that time. That weekend, my husband came down with COVID-19 and I tested positive shortly after him. On 07/11/2022 I had a runny/stuffy nose and a dry cough. I took an at home COVID-19 test and it was positive. I called my doctor for myself and my husband who prescribed PAXLOVID for both of us. He also looked at my rash again and decided that it was shingles. I didn't feel like the PAXLOVID effected my symptoms much but a few days later, my cough became more productive and that lasted for 3 or 4 days. I never ran a fever and my COVID-19 symptoms improved from there. After my symptoms improved, my doctor prescribed LYRICA for the shingles. I'm still experiencing pain from the shingles, more so at night but he also prescribed trazadone for the pain to help me sleep at night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: At home COVID-19 test 07/11/2022 positive.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma; Glaucoma; High Blood Pressure; Glider.
Andere Medikamente: TIMOLOL; AZOPT; bimatoprost; diltiazem; fenofibrate; levothyroxine; pantoprazole; atorvastatin; albuterol; hyoscyamine; estradiol; super B complex; vitamin D3; multivitamin.
Allergien: Sulfa drugs
Vorherige Impfungen: 1st Pfizer/COVID-19. Fever, chills, flu like symptoms for 24 hours.

VAERS 2388341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NC
Alter: 71,0
Geschlecht: M
Eingang: 25.07.2022
Impfdatum: 21.04.2022
Beginn: 15.06.2022
Tage bis Beginn: 55,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Body temperature increased COVID-19 Chills Discomfort Fatigue Feeling hot Insomnia Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

06/15/2022 That evening, I started with a very runny nose and a sore throat. I slept the night and the next morning, I was extremely congested, very sore throat, very tired and I felt I was running a temperature even thought I did not take it. I was very uncomfortable all day. That night I had great difficulty sleeping and had chills, then felt hot and this would go back and forth. I was lying on a tile floor in my bathroom just to try and feel better. The next day, I called my doctor. I felt I had a temperature even though I did not take it. I saw the doctor on 6/17/2022. I was very uncomfortable and very congested. I tested positive for COVID I was given a prescription for Paxlovid. I started the Paxlovid on that evening. I was able to sleep the night, unlike the night before. When I woke up the next morning, I felt better already. I was not well, but much better. At the end of five days , I would almost call myself symptom free. I have recovered, but I do get tired more easily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID tests, positive
Aktuelle Erkrankungen: None
Vorgeschichte: Immune compromised; Rheumatoid Arthritis with Raynaud's
Andere Medikamente: Naproxen; Atorvastatin; Amlodipine; Fildenafil; Daily Multi Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2379232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NJ
Alter: 62,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 04.04.2022
Beginn: 10.06.2022
Tage bis Beginn: 67,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Oropharyngeal pain Rhinorrhoea Sneezing

Symptomtext

I started with a sore throat then came the cough sneezing and a runny nose. I called my dr. for a telehealth visit and I was prescribed a Z-PAK and also cough medicine. I was later given an inhaler & nasal spray, this lasted for over 2 weeks. Finally after about 4 weeks I started feeling better but the symptoms lingered for about another week or so and today I still have the cough sometimes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2376651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 62,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 20.04.2022
Beginn: 12.05.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Malaise SARS-CoV-2 test positive Throat irritation

Symptomtext

I was coming off of a cruise ship and wanted to make sure it was ok. I completed the at home test which was not definitive. I took a PCR COVID-19 test and it was positive. I did not develop symptoms until after I was diagnosed and the symptoms were like seasonal allergies. I had slight scratchy throat. By the 10th day I was feeling fine. I was not prescribed any medicine and I did not take any over the counter medicine. I have completely recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 home test May 12, 2022 result not definitive. COVID-19 PCR test May 14, 2022 positive.
Aktuelle Erkrankungen: Mild Atelectasis in Lungs; Elevated CO2 Levels
Vorgeschichte: Sleep Apnea; Obesity
Andere Medikamente: Olmesartan medoxomil; amlodipine desolate; elderberry gummies
Allergien: Hydrochlorothiazide; latex
Vorherige Impfungen: -

VAERS 2374866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 68,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 15.04.2022
Beginn: 01.07.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Anxiety Atrial fibrillation Dizziness Echocardiogram normal Electrocardiogram abnormal

Symptomtext

On the evening of 7/1/2022, I began to feel lightheaded and woozy. This feeling persisted for a few days, and I thought that maybe I had a sinus or inner ear issue. I even made an appointment to go to an urgent care clinic on 7/6/2022. At midnight or 1 AM on 7/6/2022, I was having trouble. I checked my heartrate, and it was 138. I knew I was in trouble, so I immediately went to the ER. When I got there, I was assessed by triage and immediately hooked up to an EKG. I was diagnosed with atrial fibrillation and given an intravenous supply of diltiazem. About 1.5-2 hours later, my heart went into sinus rhythm, and everything was back to normal. I was discharged with prescriptions for diltiazem and ELIQUIS. I cancelled my urgent care appointment for that morning. I then scheduled an appointment with a NP on my PCP's team, whom I saw on 7/7/2022. The NP ordered an echocardiogram at my request, and I received the echocardiogram on 7/13/2022. The results indicated that my heart function and heart structure were both normal. I scheduled a follow-up with my PCP, and I am due to see her on 7/29/2022. Since I have been on the medication, I have been doing fine and feel reassured by the echocardiogram results, though I am also somewhat anxious, since I wonder if I could have more issues in the future.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: EKG 7/6/2022. Atrial fibrillation detected. Echocardiogram 7/13/2022. No structural or functional abnormalities detected.
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetes Type II; Hypertension; High Cholesterol; Obesity.
Andere Medikamente: Metoprolol; atorvastatin; lisinopril; metformin; multivitamin; fish oil; calcium; vitamin D; vitamin C; potassium; magnesium.
Allergien: Seasonal Allergies.
Vorherige Impfungen: -

VAERS 2374729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 19.04.2022
Beginn: 12.07.2022
Tage bis Beginn: 84,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Cough Exposure to SARS-CoV-2 Fatigue Pain SARS-CoV-2 test positive

Symptomtext

I was coughing and my daughter who is a pharmacist urged me to test for COVID-19. I tested positive with a very faint line on an antigen test. My husband had already tested positive for COVID-19 so I had been wearing a mask. We were out of town at the time that we tested positive, so we isolated in a hotel until we could fly home. I called my doctor while still out of town who called in a prescription for PAXLOVID. My symptoms consisted of a cough, body aches, chills, and fatigue. My cough still persists, primarily at night but after around 2 days the majority of my symptoms went away and I tested negative as of Tuesday 07/19/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Antigen COVID-19 test positive 07/12/2022.
Aktuelle Erkrankungen: None.
Vorgeschichte: None
Andere Medikamente: Lisinopril; pravastatin; calcium citrate.
Allergien: None.
Vorherige Impfungen: -

VAERS 2374702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MT
Alter: 72,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 19.04.2022
Beginn: 13.07.2022
Tage bis Beginn: 85,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dysphonia Fatigue Headache Malaise Oropharyngeal pain SARS-CoV-2 test positive Throat irritation

Symptomtext

On Wednesday, July 13, 2022, I had a scratchy sore throat. I had a lingering mild headache. I thought it was a summer cold. I tested home Thursday and negative. My symptoms continued. I tested at home Friday and was positive. I called the doctor on Friday you discussed PAXLOVID but decided it would not be appropriate. They symptoms also included fatigue. My throat is no longer sore but gravely voice and mild headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test, negative and then positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol
Andere Medikamente: Atorvastatin; REFRESH plus; calcium; vitamin D3; melatonin; SYNTAX night gel; ADVIL
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2283015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 79,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 19.04.2022
Beginn: 10.05.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: SC / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anticoagulant therapy Atrial fibrillation Echocardiogram Electrocardiogram abnormal Light chain analysis increased Fatigue Laboratory test Ventricular extrasystoles

Symptomtext

Diagnosed with new onset atrial fibrillation during pre-admission testing for urologic procedure 5/10/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 5/17/2022 consultation with cardiologist 7/1/2022 echocardiogram 7/5/2022 elevated kappa light chain immunoglobulins 8/16/2022 nuclear medicine cardiac scan scheduled Medications changed: Nifedical DC'd & switched to CardizemCD 180mg qd; Xarelto added 20mg qd; Last EKG (done before scheduled cardioversion 7/15/2022) Normal sinus rhythm with PVCs- cardioversion canceled.
Aktuelle Erkrankungen: Diabetes Hypothyroidism Hypoadrenalism Metastatic melanoma Peripheral neuropathy secondary to diabetes Multiple squamous and basal cell cancers S/P nephrectomy for renal cell carcinoma Nephrolithiasis BPH
Vorgeschichte: See above
Andere Medikamente: Humalog 75/25 tid Synthroid 150mcg qam Hydrocortisone 10mg tid Atorvastatin 00mg qd Lisinopril 20mg qd Potassium chloride 20meq qd Hydrochlorthiazide 25mg qd Nifedipine XL 60mg qd Novolimumab 480mg infusion monthly Ocuvite qd Centrum Silver
Allergien: NKA
Vorherige Impfungen: -

VAERS 2283015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 79,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 19.04.2022
Beginn: 10.05.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anticoagulant therapy Atrial fibrillation Echocardiogram Electrocardiogram abnormal Light chain analysis increased Fatigue Laboratory test Ventricular extrasystoles

Symptomtext

Diagnosed with new onset atrial fibrillation during pre-admission testing for urologic procedure 5/10/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 5/17/2022 consultation with cardiologist 7/1/2022 echocardiogram 7/5/2022 elevated kappa light chain immunoglobulins 8/16/2022 nuclear medicine cardiac scan scheduled Medications changed: Nifedical DC'd & switched to CardizemCD 180mg qd; Xarelto added 20mg qd; Last EKG (done before scheduled cardioversion 7/15/2022) Normal sinus rhythm with PVCs- cardioversion canceled.
Aktuelle Erkrankungen: Diabetes Hypothyroidism Hypoadrenalism Metastatic melanoma Peripheral neuropathy secondary to diabetes Multiple squamous and basal cell cancers S/P nephrectomy for renal cell carcinoma Nephrolithiasis BPH
Vorgeschichte: See above
Andere Medikamente: Humalog 75/25 tid Synthroid 150mcg qam Hydrocortisone 10mg tid Atorvastatin 00mg qd Lisinopril 20mg qd Potassium chloride 20meq qd Hydrochlorthiazide 25mg qd Nifedipine XL 60mg qd Novolimumab 480mg infusion monthly Ocuvite qd Centrum Silver
Allergien: NKA
Vorherige Impfungen: -

VAERS 2373884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 79,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 18.04.2022
Beginn: 15.07.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Diarrhoea Fatigue Hypersomnia Nasopharyngitis Pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On 07/15/2022 at around 03:00PM I began to experience some diarrhea and was really tired. I felt like I needed to lie down, so I did and I ended up sleeping for around 2 hours. The next day, the same thing happened. After being out and about, I came home and had to sleep for another 2 hours. My wife went out to get an at home COVID-19 test which I took that afternoon 07/16 which was positive. I waited 24 hours and took another which was also positive. I began treating my symptoms of runny nose, cough, and body aches with NYQUIL. On Monday, I called my doctor who prescribed an antibiotic, azithromycin. They also advised that I take MUCINEX which I have started. I am still experiencing cold like symptoms but my body aches have gotten a bit better.

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Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: At home COVID-19 test 07/16/2022 positive.
Aktuelle Erkrankungen: None.
Vorgeschichte: High Blood Pressure.
Andere Medikamente: Losartan; amlodipine; glucosamine chondroitin; BAYER aspirin; ZYRTEC; levothyroxine.
Allergien: None.
Vorherige Impfungen: -

VAERS 2372746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WV
Alter: 66,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 13.04.2022
Beginn: 15.07.2022
Tage bis Beginn: 93,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest X-ray Cough Fatigue Increased upper airway secretion SARS-CoV-2 test Wheezing

Symptomtext

I had Upper respiratory drainage, coughing, wheezing, fatigue and i took over the counter medications and after a few days i was feeling better & i also used my inhaler

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Lab testing for covid and chest xray
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Claritin; lexapro; albuterol inhaler;
Allergien: Penicillin; bactrim;
Vorherige Impfungen: -

VAERS 2372525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 16.04.2022
Beginn: 01.07.2022
Tage bis Beginn: 76,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Feeling abnormal Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sinus pain Throat irritation

Symptomtext

I contracted COVID-19 from a co-worker. I started to feel a sensitivity on the back of my throat for about two days. I tested positive on a home test. I had a bit of sore throat and sinus pain. I was feeling like I had a head cold. It was minor sore throat fever and congestion. I never developed a cough. I contacted my PCP and started taking Paxlovid. About 24 hours after starting the medication I started to feel better. I testing positive for about week. I was feeling much better. I had a little fatigue and brain fog but has been subsided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, High Blood Pressure; Sleep Apnea: Type 2 Diabetes: Endometriosis; Myasthenia gravis
Andere Medikamente: Lisinopril; Hydrochlorothiazide; Levothyroxine; Oral Birth Control; Metformin; Vitamin D; Vitamin C; Zinc; Tramadol; Naproxen
Allergien: None
Vorherige Impfungen: -

VAERS 2372356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WA
Alter: 53,0
Geschlecht: M
Eingang: 18.07.2022
Impfdatum: 16.04.2022
Beginn: 11.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Headache Malaise Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 07/11/2022 with symptoms of cough, mild headache, body aches, runny nose, and congestion. I was prescribed PAXLOVID on 07/12/2022. I was ill for 3 days before my symptoms began to resolve. I was feeling feeling recovered, but as of 7/18/2022 my symptoms returned and my cough has worsened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 07/11/2022; COVID-19 rapid nasal home swab was positive on 07/18/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: ALLERCLEAR
Allergien: N/A
Vorherige Impfungen: -

VAERS 2371439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: LA
Alter: 83,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 16.03.2022
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body height Confusional state Eye disorder Frustration tolerance decreased Irritability Neck pain Pain in extremity Vaccination site pain

Symptomtext

Arm soreness at injection after each 3 doses/She then stated that her arms stay sore and still are. This occurred after she got the vaccine.; her arms stay sore and still are. This occurred after she got the vaccine/Her arms hurt./Her left arm hurts all the way; Her left arm hurts all the way to her neck and favors it and rub it with things.; She went to her doctor and he gave shots in back of neck for pain because it hurts so bad.; Caller stated her eyes are so bad. She can't hardy read.; She is frustrated because she cannot make out the numbers on the vaccine card; It is confusing her; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program. The reporter is the patient. An 84-year-old female patient received BNT162b2 (BNT162B2), on 16Mar2022 as dose 2, single (Lot number: FK9894) at the age of 83 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Crippling Arthritis in leg" (unspecified if ongoing), notes: Crippling Arthritis in leg, before getting the Pfizer COVID 19 vaccine. She has had it since 15.; "blood pressure be high" (unspecified if ongoing), notes: her blood pressure be high, She has had that since she was 18.; "nervous" (unspecified if ongoing), notes: her blood pressure be high and she be so nervous, She has had that since she was 18.; "She had eye problems" (unspecified if ongoing), notes: She had eye problems since she was 14 years old. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, Lot number: FK9729, Right arm), administration date: 18Feb2022, when the patient was 83-year-old, for covid-19 immunisation, reaction(s): "Arm soreness at injection". The following information was reported: VACCINATION SITE PAIN (non-serious), outcome "not recovered", described as "Arm soreness at injection after each 3 doses/She then stated that her arms stay sore and still are. This occurred after she got the vaccine."; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "her arms stay sore and still are. This occurred after she got the vaccine/Her arms hurt./Her left arm hurts all the way"; IRRITABILITY (non-serious), outcome "unknown", described as "Her left arm hurts all the way to her neck and favors it and rub it with things."; NECK PAIN (non-serious), outcome "unknown", described as "She went to her doctor and he gave shots in back of neck for pain because it hurts so bad."; EYE DISORDER (non-serious), outcome "unknown", described as "Caller stated her eyes are so bad. She can't hardy read."; FRUSTRATION TOLERANCE DECREASED (non-serious), outcome "unknown", described as "She is frustrated because she cannot make out the numbers on the vaccine card"; CONFUSIONAL STATE (non-serious), outcome "unknown", described as "It is confusing her". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of neck pain. Clinical course included She has a patient calling about booster shot. She already got 3 does of the Pfizer COVID 19 vaccine and saying she has scheduled for booster shot - which is first dose of the vaccine. The HCP who was supposed to give the vaccine did not come to her place, so she is calling to get the 4th dose. She missed her 4th dose. Reporter confirmed information above. She got Crippling Arthritis in leg. That was before getting the Pfizer COVID 19 vaccine. She has had it since 15. She then stated "her blood pressure be high and she be so nervous." She has had that since she was 18. Reporter wanted to know if Pfizer could assist with getting someone to give her the vaccine. Call handler advised caller that Pfizer would not be able to assist with that and to contact her local providers. She then stated that her arms stay sore and still are. This occurred after she got the vaccine. 18Feb2022, 1st one in Right arm Lot FK9729. She later came back and said that it could be RK9729. 16Mar2022, 2nd one in Left arm Lot FK9894, and later said it could be RK9894. She then thought the card said she got two shots on the same day. She started providing 26th of a month and unable to confirm which month. She was not sure about that number and then gave number of RK9729 again when asked when the 3rd dose was given and what that lot number was. She did not remember if she had two on one day and was unable to read the card to see what was given. It is confusing her. She keeps rubbing alcohol on it. Her arms hurt. Her left arm hurts all the way to her neck and favors it and rub it with things. She went to her doctor and he gave shots in back of neck for pain because it hurts so bad. Attempted to confirm name, lot and expiration of injections and she was unable to find it. Some days it doesn't bother her. This morning, after she got shower and was raising hands to change clothes, it hurts on Left side. Caller stated her eyes are so bad. She can't hardy read. She had eye problems since she was 14 years old. She has got one of her eyes she can hardly see out of. She is frustrated because she cannot make out the numbers on the vaccine card and decided to disconnect. The information on the batch/lot number for [BNT162B2] has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200941011 Same patient/drug and different dose/AEs.;

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Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: Test Name: height; Result Unstructured Data: Test Result:5'8"-5'9"; Comments: She said she was tall and provided her height as between 5'8"-5'9".
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis (Crippling Arthritis in leg, before getting the Pfizer COVID 19 vaccine. She has had it since 15.); Blood pressure high (her blood pressure be high, She has had that since she was 18.); Eye disorder (She had eye problems since she was 14 years old.); Nervous (her blood pressure be high and she be so nervous, She has had that since she was 18.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2370613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WV
Alter: 67,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 14.04.2022
Beginn: 09.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Fatigue Feeling abnormal Oropharyngeal discomfort SARS-CoV-2 test positive

Symptomtext

I had a little tickle in my throat, that night I woke up and felt bad I felt like I had a fever. I took a home COIVD-19 test that was positive. I went down to the local hospital and had a PCR COVID-19 test that came positive. I had telehealth with my Asthma doctor who put me on steroids and an antibiotic. I still have some coughing but no temperature, a little fatigue,

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 Test PCR COVID-19 Test
Aktuelle Erkrankungen: No
Vorgeschichte: Allergy induced Asthma
Andere Medikamente: Crestor; Metoprolol Succinate; Amitryliplyne; Estring Vaginal Ring; Arnuita Ellipta; Montelukast; Zyrtec; Fluticasone; Pepcid; Calcium Citrate; Vitamin D3; Vitamin C; CoQ10; Zinc; Magnesium; Melatonin
Allergien: Penicillin; Erythromycin
Vorherige Impfungen: -

VAERS 2370588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: VT
Alter: 67,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 13.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac monitoring Dizziness Vestibular function test normal

Symptomtext

Have had ongoing spells of dizzyness. But after vaccine the dizzyness became more severe. Saw my Dr. and had a vestibular testing and it was negative. Was given a heart monitor to wear for 2 weeks, found that I had 29 events of dizzy reactions. Wasn't any other events in the future.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Vestibular testing, was Negative, heart monitor worn for 2 weeks.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hay fever related Asthma; Acid Reflux; Osteoperosis, previous cancer.
Andere Medikamente: Xolair; Trazadone; Flexapro; Buspar; Advair; Calcium; Vitamin D3; Singular; Claritin; Pepcid; Nexium; Flonase; Multivitamin; Flaxseed; Magnesium; Vitamin C.
Allergien: Biaxin
Vorherige Impfungen: -

VAERS 2368990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WA
Alter: 60,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 13.04.2022
Beginn: 30.06.2022
Tage bis Beginn: 78,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a low grade fever, cough, congestion I had been exposed to COVID-19. I took a home COVID-19 test that came back positive I went to urgent care on July 1, 2022 and had PCR COVID-19 test that also came back positive. I was prescribed PAXLOVID and albuterol nebulizer. I started taking the PAXLOVID immediately, I am still felling fatigue, nasal drainage, and a slight cough.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19; PCR COVID-19.
Aktuelle Erkrankungen: No
Vorgeschichte: Psoriatic Arthritis; Obesity; Asthma
Andere Medikamente: HUMIRA; TYLENOL; multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2368778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WI
Alter: 65,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 13.04.2022
Beginn: 29.06.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Allergy test COVID-19 Cough Fatigue Night sweats Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of fever, night sweats, cough, and sore throat. I took an at home COVID-19 test that was positive. I contacted my doctor and was prescribed Paxlovid. I took Paxlovid for 5 days. During the time course I had fatigue. I don't feel like the Paxlovid helped with they symptoms. I had prolonged COVID-19 and tested positive for 2 weeks. I did also have a persistent cough. I went to get an allergy test on 7/13/2022 and was unable to get testing because none of the controls reacted. I have to be scheduled back to get an allergy test. I'm not for sure if the reason why is because of Paxlovid or COVID-19. I do not have any symptoms now except for some fatigue.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - positive; Allergy test - inconclusive
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal Mild Asthma; Overweight
Andere Medikamente: Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 2367864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: 23,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 04.04.2022
Beginn: 03.05.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Cough Nausea Oropharyngeal pain Vomiting

Symptomtext

sore throat, cough, n/v

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2367739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 72,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 08.04.2022
Beginn: 13.06.2022
Tage bis Beginn: 66,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Dizziness Feeling abnormal Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

6/13/2022 woke up feeling bad experiencing a fever peaking at 101, a cough, runny nose, and dizzy. Took at home COVID 19 rapid antigen test, positive. I reached out to tele visit with doctor. Doctor prescribed molnupiravir. 6/16 fever broke and I started to feel better. Symptoms improved gradually to 6/23 when things returned to normal.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: At home COVID 19 rapid antigen test, positive 6/13/2022.
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; Chronic Kidney Disease; heart condition; High Blood Pressure
Andere Medikamente: PLAVIX; atorvastatin; glipizide; calcium; vitamin D; bicarbonate of soda; lisinopril; amlodipine; carvedilol; chlorthalidone
Allergien: No
Vorherige Impfungen: -

VAERS 2367580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 77,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 08.04.2022
Beginn: 07.07.2022
Tage bis Beginn: 90,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Decreased appetite Fatigue Headache Oropharyngeal pain Polymerase chain reaction positive Pyrexia

Symptomtext

My symptoms started 2 days before testing positive. I had a low grade fever, tiredness, no appetite, & headaches, bad sore throat, with a bad cough. I was prescribed PAXLOVID for my symptoms and after a few days I started to feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: PCR test
Aktuelle Erkrankungen: No
Vorgeschichte: Type 2 diabetes
Andere Medikamente: Vitamin D3; olmesartan; TUMS; CRESTOR
Allergien: Yes
Vorherige Impfungen: -

VAERS 2367480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: IN
Alter: 81,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 11.04.2022
Beginn: 28.06.2022
Tage bis Beginn: 78,0
Dosis: 4
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal discomfort Asthenia Blood test normal COVID-19 Chest X-ray normal Cough Eye pruritus Fatigue Lacrimation increased Pyrexia Renal function test normal Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On 6/28/2022 we were traveling home and I started having symptoms that I thought were allergies. runny nose; cough; itchy runny eyes; then slight fever. Over the next few days it got worse. My fever increased; I felt sick to my stomach and very fatigue. ON the 6/30/2022 I took a COVID-19 at home test and it was positive. We stopped at the urgent care. They took x-ray of my lungs; checked my kidneys; and prescribed me Paxlovid and Benzonatate. Most of my symptoms went away after a few days. However, I still have a cough and feel weak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pruritus
Hospital-Tage: -
Labordaten: 30JUNE2022- COVID-19 Positive; 30JUNE2022- X-ray Clear; 30JUNE2022- Bloodwork- Kidney function was good.
Aktuelle Erkrankungen: Allergies;
Vorgeschichte: Hyperthyroid; obstreperous; High Cholesterol; Diarrhea often; Triple bypass;
Andere Medikamente: Levoxyl; Liothyronine; Setraline; Metoprolol; Omepracol; Low dose Aspirin; Multivitamin; Calcium; Align probiotics; Nexlevol; Imodium as needed.
Allergien: Nexlevol; Cholesterol medication; Trouble eating meat; seasonal allergies- hay fever; cotton wood; cats
Vorherige Impfungen: -

VAERS 2367387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TN
Alter: 64,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 08.04.2022
Beginn: 16.06.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dysphonia Extra dose administered Fatigue Headache Oropharyngeal pain Pain Pyrexia Respiratory symptom Respiratory tract congestion SARS-CoV-2 test positive Sinus disorder

Symptomtext

I started getting symptoms of upper respirator problems like congestions and sore throat. I had fever, body aches, and a headache. I took an at home COVID-19 test that was positive. I contacted my doctor and did a telehealth visit. I was prescribed Paxlovid. I can not tell if Paxlovid helped. It made me dizzy and I had a bad taste for 5 days. I am still experiencing tiredness. I went back to work Monday but I feel fatigued with voice hoarseness and sinus problems.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamins; Lisinopril
Allergien: Morphine; Celebrex
Vorherige Impfungen: Pfizer 2nd dose - chills, fever, achiness

VAERS 2366255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CT
Alter: 76,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 11.04.2022
Beginn: 02.06.2022
Tage bis Beginn: 52,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Decreased appetite Fatigue Headache Nausea Oropharyngeal pain Quarantine SARS-CoV-2 test positive

Symptomtext

Starting 06/02/2022, I had a bad sore throat, a headache, nausea and loss of appetite. I took an at home test on 06/04/2022 which was positive. I called my doctor on 06/06/2022 and they told me to go to Urgent care, where I was tested again and was positive. I was referred to the COVID triage center at the hospital and had a telemedicine visit. I was scheduled for the monoclonal antibodies infusion the next day. My symptoms were starting to get better after the infusion, but I still felt fatigued. By the end of the week, I felt better, tested negative and had my appetite return. I was still fatigued for about a week more. I quarantined at home from 06/06/2022 - 06/11/2022. I did another at home test on 06/14/2022 and it was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At-home COVID-19 test (06/04/2022): Positive; Rapid test at Urgent Care (06/06/2022): Positive; At-home COVID-19 test (06/14/2022): Negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sertraline; Multivitamin; Calcium + Vitamin D
Allergien: None
Vorherige Impfungen: I just get tired and a headache after each COVID vaccine

VAERS 2366216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MS
Alter: 21,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 11.07.2022
Beginn: 11.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Lethargy Muscle spasms Myalgia Pyrexia

Symptomtext

Severe chills/muscle spasms Fever Muscle aches/pain Lethargy All symptoms occurred from 6 hrs post-vaccination to approximately 24 hrs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Zyrtec, 10 mg
Allergien: Singulair (montelukast) allergy
Vorherige Impfungen: Fever, chills, muscle aches following Pfizer COVID19 vaccine series #2 and 3, 20 years old at the time

VAERS 2366211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 71,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 01.04.2022
Beginn: 08.07.2022
Tage bis Beginn: 98,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Fatigue Pain SARS-CoV-2 test Throat irritation

Symptomtext

Approximately 3 months after my 4th dose vaccination I contracted COVID-19 and experienced the following symptoms: scratchy throat, fatigue and body aches. I called my doctor and he did not pick up and I have been taking ibuprofen for now to help improve my symptoms and so far it has been working. As of today 07/12/2022 I am feeling fine and pretty much back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Aspirin; metoprolol; atorvastatin; calcium
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2366023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: IA
Alter: 69,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I didn't know that I had COVID. I had a family member to call and told me that they had COVID-19 and I was exposed. I tested and was positive for COVID-19. I took a test 2 days later and was positive and also went to a drive thru and had a PCR COVID-19 test that was positive. I tested positive for 2 weeks. Then I called my doctor. I had mild symptoms of an occasional cough, sore throat for 1 day, and a headache that was mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test - Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Flu vaccine October 2021 - Flu like symptoms for 2 days

VAERS 2364699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 08.04.2022
Beginn: 03.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest discomfort Fatigue Nasal congestion Oropharyngeal pain Productive cough SARS-CoV-2 test positive

Symptomtext

Starting 07/03/2022, I started having symptoms: sore throat, heavy chest, frequent cough and overall fatigue. 07/04/2022 I called my doctor who said to call in the next day to see if I would qualify for PAXLOVID. Later on 07/05/2022, they got the PAXLOVID ready and I took my first dose then. The sore throat went away quickly after starting it. My last dose was 07/10/2022. I still have productive cough but less frequent and slight nasal congestion. The fatigue and "heavy" chest feeling are better but still bothersome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home COVID-19 tests (07/04/2022): positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Acid reflux; High Blood Pressure; Depression and Anxiety; Lower back pain and sciatica; Arthritis; Asthma; High Cholesterol
Andere Medikamente: Omeprazole; valsartan; hydrochlorothiazide; escitalopram; gabapentin; CELEBREX; WIXELA; rosuvastatin calcium; vitamin D3; multivitamin; calcium
Allergien: AUGMENTIN; BIAXIN; LEVAQUIN; SEPTRA DS; Fluzone High dose 2017-2018 immunization
Vorherige Impfungen: Fluzone High Dose 2017-2018.

VAERS 2364655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 10.04.2022
Beginn: 19.05.2022
Tage bis Beginn: 39,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case. Had vaccine on 04/10/2022. Was around someone who had COVID-19 then 2 days later on 05/19/2022, I started feeling tired and feverish. I tested negative on my home test. Then I went to a clinic the next day and I tested positive. Dr. said symptoms wasn't severe enough so he didn't prescribe anything. Had COVID- 19 for 6 days. Currently, still having a dry cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home test - negative, clinic - positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: GERD; Bipolar; Diabetes; Chronic Kidney Disease; Seasonal Asthma; Peripheral Neuropathy; High Blood Pressure; Obesity
Andere Medikamente: Bariatric vitamins; senior probiotic; lamotrigine; metformin; losartan potassium; atenolol; aripiprazole; vitamin D3; calcium; loratadine; pantoprazole; venlafaxine; atorvastatin; docusate sodium; biotin; TYLENOL; lorazepam
Allergien: NAVANE; bee stings
Vorherige Impfungen: -

VAERS 2364600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WA
Alter: 66,0
Geschlecht: M
Eingang: 11.07.2022
Impfdatum: 07.04.2022
Beginn: 05.06.2022
Tage bis Beginn: 59,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Malaise Nasal congestion Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On 06/05/2022 I woke up feeling a bit stuffy, congested, and had a runny nose. I attended a granddaughter's birthday party that day, but since I wasn't feeling well, I wore a mask and kept my distance from others. My symptoms persisted through the next few days but continued to be mild. By the following Tuesday, I took an at home COVID-19 test which was positive. I took another for confirmation and it was also positive. I called my primary care physician's office and spoke with an on call doctor over a telehealth visit. She prescribed a 5 day round of PAXLOVID. I began taking the medication later that day. After two days, 06/09/2022, I was beginning to feel quite a bit better. By Sunday, 06/12/2022, I began to test negative on at home COVID-19 tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: At home COVID-19 test-multiple days-positive.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Rosuvastatin; CLARITIN; multivitamin; calcium supplement; vitamin D.
Allergien: None.
Vorherige Impfungen: -

VAERS 2364595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: HI
Alter: 74,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 07.04.2022
Beginn: 15.06.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Fatigue Lethargy Oropharyngeal pain SARS-CoV-2 test positive Sinusitis

Symptomtext

sinus infection; cough; very sore throat; lethargy; fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: self test for COVID 19 administered 06/17/2022. COVID test was positive, prescribed PAXLOVID regime. Complete recovery within 7 days. The event was linked to COVID 19 infection.
Aktuelle Erkrankungen: none
Vorgeschichte: afib; high blood pressure; high cholesterol
Andere Medikamente: atorvastatin; amlodipine; calcium supplements; vitamin D; multivitamin
Allergien: sulfa drugs; latex
Vorherige Impfungen: -

VAERS 2364408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CT
Alter: 72,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 08.04.2022
Beginn: 30.05.2022
Tage bis Beginn: 52,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Diarrhoea Disturbance in attention Fatigue Feeling abnormal SARS-CoV-2 test positive Sick relative

Symptomtext

My daughter was married and I went to her rehearsal dinner. I believe that is where I contracted COVID-19. I woke up with diarrhea and my husband was vomiting. He never throws up so I knew something was wrong. What I did first thing was a COVID-19 test on both of us. Both of them came back positive and we had no upper respiratory problems, just lower gastro. Very rapidly we ended up with a positive line on both COVID-19 test. I then called our PCP and explained to him what was going on. He had us take an antiviral that was a five day course. We had a pretty rapid response to the antiviral. Within two days the GI passed. We were extremely fatigued and I had brain fog for about a week after. Concentrating on task was really difficult. After we completed the five day course of the antiviral my brain fog was gone. My husband and I did not require hospitalization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 test 05/31/2022, positive.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma; Arthritis.
Andere Medikamente: WELLBUTRIN; extended relief; albuterol inhaler; FLOVENT; celecoxib; vitamin A; magnesium; vitamin E; glucosamine chondroitin; generic METAMUCIL; PEPCID; vitamin B12; fish oil; vitamin C; coQ10; zinc; lysine
Allergien: Adhesive tape; pollen.
Vorherige Impfungen: -

VAERS 2362811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 62,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 05.04.2022
Beginn: 01.07.2022
Tage bis Beginn: 87,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Malaise Myalgia Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough Covid19 Infection - Headache, sore throat, fatigue, congestion, muscle pain. Started 6/29/22 with mild symptoms, home test negative on 6/30/22, stronger symptoms and positive test 7/1/22. Had video conference with Dr. 7/2/22 (have never seen him otherwise) who prescribed Paxlovid 300/100 5 day treatment. 7/2/22 and 7/3/22 were bad days, as sick as I have been in years though certainly not hospital worthy. Symptoms decreasing 7/4/22 and 7/5/22. Feeling back to normal but took another test 7/6/22 and still showing positive so continuing to isolate. 7/7/22 feeling fine. 7/8/22 fine. Will take another test today but still isolate for 5 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Just the at-home Covid-19 test (Roche lot 53K32L2T1)
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown muscle disease, Gerd, heart disease, hyperlipidemia
Andere Medikamente: Nortriptyline 50mg, Protriptyline 5mg, nexium 40mg, aspirin 81mg, Buprenorphine 100 micrograms, Crestor 5mg, B12 50mcg, Vitamin D 10,000 IU, Tylenol 3000mg (2x500, 3x/day)
Allergien: Amoxycillin
Vorherige Impfungen: -

VAERS 2362656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 87,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 02.04.2022
Beginn: 08.06.2022
Tage bis Beginn: 67,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood test normal COVID-19 Cough Dysphonia Oropharyngeal pain SARS-CoV-2 antibody test positive

Symptomtext

I had a sore throat and hoarseness. A very mild cough. I did not experience fever or chills. I received the monoclonal antibody infusion. They did an antibody test and I didn't have any antibodies. The sore throat and hoarseness lasted about 3 or 4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Antibody test; PCR- positive; at home test- positive; Blood work- normal.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Osteomyelitis; Arthritis; Spinal fusion; BTH prostate; Atrial Fibrillation
Andere Medikamente: LIPITOR; dutasteride; doxycycline; rifampin; furosemide; potassium; XARELTO; NORVASC; valsartan/HCTZ; trazadone; metoprolol; calcium plus D; CENTRUM silver multivitamin; docusate sodium; vitamin D3
Allergien: Albuterol causes arrhythmia; AUGMENTIN causes diarrhea
Vorherige Impfungen: -

VAERS 2362654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

mild

Staat: NH
Alter: 70,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 06.04.2022
Beginn: 20.05.2022
Tage bis Beginn: 44,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Headache Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

COVID-19 case. It was basically a headache, sore throat, and little bit of a runny nose. Two days after going to the Doctor they gave me medication and the next day the sore throat was better. For the next couple of weeks it was just a runny nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 at home test - positive on May 20th
Aktuelle Erkrankungen: No
Vorgeschichte: Osteoarthritis
Andere Medikamente: Zolpidem; Pantoprazole; Meloxicam; Vitamin D; Vitamin B12
Allergien: No
Vorherige Impfungen: -

VAERS 2362646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 07.04.2022
Beginn: 04.07.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dysphonia Malaise Rhinorrhoea SARS-CoV-2 test positive Throat irritation Upper respiratory tract congestion

Symptomtext

I had a scratchy throat and a runny nose but no fever. I was feeling hoarse by Tuesday. I took a COVID-19 home test on July 5th and it came back positive. I reported the positive test on the clinic website and received a phone call. I also self isolated. I got a call from the clinic on Wednesday morning and was prescribed PAXLOVID, though the symptoms were pretty mild. I started to feel better within a day. My throat is fine and I no longer have the stuffiness in my head.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 home test-July 05, 2022-positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Atorvastatin; chlorthalidone; losartan
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2362551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 74,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 06.04.2022
Beginn: 30.06.2022
Tage bis Beginn: 85,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Dizziness Nausea SARS-CoV-2 test positive

Symptomtext

Awoke feeling slightly dizzy and nauseous. Took Covid-19 At Home Test which was positive. Went to Pharmacy for a PCR test that afternoon and eventually received a positive result on Saturday. Spoke to Nurse Practitioner on Monday. Was prescribed a Z pack (prednisone) and an Antibiotic rather than Paxlovid due to risk of aggravating my high blood pressure. After 10 days the symptoms lessened to only occasional dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Covid-19 At home test on June 30th. (POSITIVE) Covid-19 PCR test administered by pharmacy on June 30th. (POSITIVE)
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Arthritis
Andere Medikamente: Lansoprazole 30mg, Lisinopril 20 mg, Aspirin 325 mg, Docusate sodium 100 mg, Lipo Flavonoid 3Xs, Vitamin C 500 mg, Vitamin D2 1000 IU, Vitamin E 400 IU, Metamucil, Omega-3 1000mg, NutraMetrix Isotonix, Naproxen 220mg, Wixela inhaler 2Xs, M
Allergien: None
Vorherige Impfungen: -

VAERS 2361262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 07.07.2022
Impfdatum: 06.04.2022
Beginn: 23.05.2022
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Headache Pyrexia SARS-CoV-2 test

Symptomtext

Cough, but not for long Headache High temperature for 24 hours Given 5 day doses of Pavlovid

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Just Covid test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Centrum for men, sertraline, trazodone, naproxen, levothyroxine, Lipitor, losartan , vitamin d. , baby aspirin, none
Allergien: None
Vorherige Impfungen: -

VAERS 2361249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WA
Alter: 64,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 19.05.2022
Beginn: 23.05.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Ear pain Headache Malaise Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 05/23/2022 with symptoms of headache, sore throat, ear ache, and body aches. I did not seek medical care. I was ill for 6 days before my symptoms began to resolve. I was fully recovered after 7 days with no lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 05/24/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Stage 3 Kidney Disease
Andere Medikamente: Rizatriptan; Tizanidine; Topiramate; Bupropion; Lamotrigine;
Allergien: N/A
Vorherige Impfungen: -

VAERS 2361159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TN
Alter: 77,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 06.04.2022
Beginn: 29.06.2022
Tage bis Beginn: 84,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Bacterial infection Bronchitis COVID-19 Chest X-ray normal Chills Conjunctivitis Cough Decreased appetite Ear congestion Ear discomfort Electrocardiogram normal Exposure to SARS-CoV-2 Fatigue Feeling abnormal Hyperhidrosis Hypersomnia Hypoacusis Mucosal discolouration

Symptomtext

I got my second Pfizer booster for COVID-19 on 4/6/2022. On 5/20/2022, I caught a virus, but it was not COVID-19. I then developed a secondary bacterial sinus infection with bronchitis. Over the holiday, I went to an urgent care clinic, and the NP prescribed doxycycline (6-day course), benzonatate (to use as needed), and an albuterol inhaler. The symptoms improved while I was on the doxycycline. However, about 3 days after the last doxycycline pill, the sinus infection and cough reappeared. On 6/14/2022, I had a telehealth appointment with my PCP. He told me I needed a stronger antibiotic to take for a longer period of time, so he prescribed Augmentin (875 mg), which I was to take twice a day for 10 days. I then began to feel better for a while. On 6/25/2022, I went on a trip abroad. While I was on vacation, I began to feel worse. I had the same symptoms as I did previously. On 6/28/2022, I also developed chills, rigors, fever, and sweats, which I had never had before with the aforementioned current illnesses. I called my doctor while I was on vacation, and he recommended that I see an otolaryngologist, because there was nothing else he could do for me. I then called my ENT and arranged for an appointment on 7/5/2022. It was around this time that my ears became clogged; at the time of this writing, I have a great deal of difficulty hearing. On 6/30/2022, we returned home from vacation. On 7/1/2022, my husband took an at-home test for COVID-19, and the result was positive. Within 15 minutes after he got his result, I also took an at-home test and also got a positive result. On account of my COVID-19-positive status, my appointment with the ENT has had be rescheduled for 7/14/2022. Since I was unable to see a doctor for the treatment of my sinus infection, bronchitis, ear congestion, and COVID-19, I ended up going to the ER on 7/3/2022. At the ER, a chest X-ray was performed, and my lungs were clear. An EKG was also performed, and the results were normal. I explained my situation to the ER doctor, and I was prescribed another 10-day course of Augmentin. I was also given dexamethasone, which has really helped clear my sinus passages. As a result, my coughs and my nose blowing are now more productive. However, I still do have the sinus infection, ear congestion, a deep cough, and chest congestion. On 7/6/2022, I woke up with conjunctivitis in both eyes, with the right eye being the more affected. I called my PCP, and he prescribed me ciprofloxacin. I have at this point only used it a few times, but I am seeing improvement. However, the mucus I expel maintains a greenish color with pus. My ear congestion and loss of hearing still persists. My sense of smell at the time of this writing is tenuous. I have lost 12 lbs. since 5/20/2022, because I've lost much of my appetite. I'm also very fatigued; I'm normally a very active and energetic person, but at this point, I usually have to rest frequently throughout the day. I've also been sleeping 12 hours at night, but whenever I get out of bed, I can easily migrate to the sofa and doze off again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension; Melanoma Survivor; Irritable Bowel Syndrome; Osteoarthritis.
Andere Medikamente: Metoprolol Tartrate; Lisinopril/HCTZ; Sertraline; Solifenacin; Gabapentin; Krill Oil; Calcium with Vitamin D3; Vitamin D3; Biotin; Glucosamine Chondroitin; Low-Dose Aspirin; Phillips Colon Health.
Allergien: Latex.
Vorherige Impfungen: -

VAERS 2361035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MD
Alter: 67,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 06.04.2022
Beginn: 26.06.2022
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Nasopharyngitis Oropharyngeal pain SARS-CoV-2 test positive Sneezing Upper respiratory tract congestion

Symptomtext

I began to have a sore throat on June 26. I tested myself on June 28th and was positive. It was sneezing coughing, a sore throat and upper respiratory congestion like a bad cold. I called my nurse practitioner and was prescribed PAXLOVID. The symptoms continued but I was feeling better the next day. I continued to take it for 5 days and was asked to not take it with my other prescribed medication. I completed the medication on Monday July 4th, I am still tired and coughing at night. I am 90% improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home
Aktuelle Erkrankungen: N/A
Vorgeschichte: Sleep Apnea
Andere Medikamente: Lovastatin; glucosamine; vitamin D; vitamin B12; chondroitin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2360938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 61,0
Geschlecht: M
Eingang: 07.07.2022
Impfdatum: 05.04.2022
Beginn: 28.05.2022
Tage bis Beginn: 53,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Chills Disorientation Fatigue Fibrin D dimer increased Hyperhidrosis Laboratory test abnormal Pyrexia SARS-CoV-2 test positive

Symptomtext

I had a fever and chills after the vaccine for a day. I started feeling symptoms on 05/28/22 and tested positive for COVID-19 on 05/29/22. I had a fever, sweating, tired and disoriented. I spoke to a specialist at my local hospital. At first the doctor did not prescribe anything and advised to wait. I felt worse and then they prescribed molnupiravir. I felt better but it gave me severe diarrhea so I was only able to take it for 2 1/2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home test for COVID-19 which was positive. The doctor at the hospital ordered some test and the D-dimer test was elevated. I was sent to the emergency room to be tested for a blood clot which they did not find anything.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; elevated cholesterol; heart arrhythmia
Andere Medikamente: Diltiazem; pravastatin; multivitamin; aspirin; coQ10
Allergien: Penicillin; gluten
Vorherige Impfungen: -

VAERS 2360917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 79,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 05.04.2022
Beginn: 20.06.2022
Tage bis Beginn: 76,0
Dosis: 4
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Flushing Nasal congestion Nasopharyngitis Pyrexia SARS-CoV-2 test positive

Symptomtext

I had COVID-19. Symptoms were like a head cold. The day after I showed symptoms on the 21st, I felt flush with a fever of 100 degrees so I took the home COVID-19 test and it was positive. I then went to the pharmacy and had their test and it was positive. The hole time I had a very little once in a while cough, and was a bit nasal. Symptoms were very mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: at home COVID-19 - positive COVID-19 test at pharmacy - positive
Aktuelle Erkrankungen: No
Vorgeschichte: Arthritis; CLL
Andere Medikamente: Multivitamin; Tylenol
Allergien: No
Vorherige Impfungen: -

VAERS 2359673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: IA
Alter: 71,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 01.04.2022
Beginn: 18.05.2022
Tage bis Beginn: 47,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Malaise Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 5/17/22. I developed slight fatigue. I developed a fever of 101 over night and felt sick. Woke up w/ body aches and headaches and bit of a sore throat. I called my doctor on 5/17/22 and received paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Losartan; Amlodipine; Terazosin; Multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2359667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 03.04.2022
Beginn: 17.05.2022
Tage bis Beginn: 44,0
Dosis: 4
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Malaise Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

On May 17th I returned from traveling and woke up 2 days after with sore throat and slight cough. I was fatigued. They were mild symptoms. They lasted 3-4 days. The Doctor prescribed Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: at home COVID-19 - positive
Aktuelle Erkrankungen: No
Vorgeschichte: High cholesterol; high blood pressure
Andere Medikamente: Losartan; Ezetimibe; Rosuvastatin
Allergien: No
Vorherige Impfungen: -

VAERS 2359604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 67,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 31.03.2022
Beginn: 14.06.2022
Tage bis Beginn: 75,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Body temperature increased COVID-19 Cough Fatigue Feeling cold Nasal congestion Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

I woke up with a sore throat. I started feeling achy, and chilled. I took my temperature it was at 101. Throughout the day my temp had risen to 102. I took a COVID-19 test that came back positive. I had chills, achenes, and fatigue for the next 3-4 days. On the third day I had nasal congestion, and a slight cough. After 10 days I didn't have any symptoms at all. I had a telephone visit with my doctor the next day after taking the COVID-19 test. She advised me to get an oximeter and make sure that my oxygen levels weren't too low, and if that happened to go to the Emergency Room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril; Lipitor; Vitamin D; Vitamin B 12
Allergien: Penicillin; Codeine
Vorherige Impfungen: -

VAERS 2359565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: IL
Alter: 56,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 03.04.2022
Beginn: 16.06.2022
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Fatigue Headache Nasal congestion Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Starting 06/16/2022, I test positive for COVID. I went to urgent care and was prescribed antibiotics. I had very minimal symptoms: headache, nasal congestion and chest congestion, and very fatigued. These symptoms lasted for about 4 days then resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home COVID-19 test (06/16/2022): positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Sarcoidosis
Andere Medikamente: Omeprazole; lisinopril; ONE A DAY multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2359486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: SC
Alter: 73,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 01.04.2022
Beginn: 14.06.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Eye pain Eye pruritus Fatigue Feeling abnormal Headache Malaise Ocular hyperaemia Pain Pyrexia SARS-CoV-2 test positive Sneezing

Symptomtext

On 6/14/2022, that evening, I noticed a few sneezes but that is not out of the norm for me because I have outdoor allergies. The next morning, I had a new patient appointment at noon with a gynecologist. I took a shower that morning and realized around 10AM that I did not feel well. So I took my temperature and it was slightly elevated at just under 100 degrees. I had a few at home COVID-19 tests, so I took one and the results were positive at which point I cancelled my appointment. Throughout that day, I began to feel progressively worse. The next few days, I felt terrible and was experiencing fever, body aches, headaches, extreme fatigue, and a cough. Leading up to these events, I had been on a trip about 10 days for an out door concert. I did however, ride in a car with 3 other people. Around 2 days after we returned, one of the people that travelled in the car with me, informed me that he was having COVID-19 like symptoms but tested negative for COVID-19 and positive for type 2 Flu and to my knowledge, no one in our group tested positive with the exception of me who tested positive around 10 days after we returned. The Sunday before I tested positive, I visited a exhibit with a friend and wore a mask, but none of the other patrons were wearing masks. We also visited a restaurant and maintained our mask wearing. After testing positive, I called my doctor's office and informed them of my positive results and to ask about a Paxlovid prescription. Within an hour, he called in a prescription for Paxlovid and a Cough medicine. I began taking those the same day that I tested positive. By day 3 my fever was gone and my body aches, headaches, and cough lessened but continued in a more mild capacity for a few more days. The following Monday, 6/20/2022, I took another at home COVID-19 test. The results were still positive, but the line was much lighter. The following Wednesday 06/22/22 I tested myself again and was negative. At this point, all of my symptoms have gotten better with the exception of noticeable fatigue after any activity and a slight cough. Although on Friday, 07/01/2022, I noticed some redness, achiness, and itchiness in my eyes that felt like an allergic reaction or pink eye. I emailed my doctor to inform him that I was using artificial tears and allergy medicine. He called in a prescription for an antibiotics which has helped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: COVID-19 test-multiple dates-positive and negative results.
Aktuelle Erkrankungen: None.
Vorgeschichte: Arthritis; High Blood Pressure (controlled); High Cholesterol (controlled); Degenerative Disk Disease.
Andere Medikamente: Zyac; Naprosyn; Zocor; Pro DHA; CoQ10; D3; Caltrate; Cranberry; Metamucil; Hyaluronic Acid; Voltarin.
Allergien: None.
Vorherige Impfungen: -

VAERS 2358295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 02.04.2022
Beginn: 01.06.2022
Tage bis Beginn: 60,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anosmia COVID-19 Disturbance in attention Fatigue Headache Hypogeusia Hyposmia Impaired work ability Nasal congestion Oropharyngeal pain Parosmia SARS-CoV-2 test positive Vertigo

Symptomtext

6/1 I started to feel a headache, sore throat and fatigue in the evening. Took an at home test which was positive. 6/2 stuffy nose with fatigue and headache. Took a PCR test, positive. 6/3 nasal congestion continued to get worse. 6/5 another at home test positive. 6/6 vertigo happened. 6/7 lost sense of smell and had strange smells that I could smell. Lack of concentration and fatigue. 6/8 this continued. 6/9th tele visit with doctor. Doctor prescribed FLONASE nasal spray. Sense of smell and taste were very limited. 6/10 tested negative for COVID 19. Nasal congestion continued. 6/16 sense of smell returned slowly and fatigue diminished. 6/20 everything returned to normal. Back to work on 6/21st.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home and PCR tests for COVID 19, all positive.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Sesame
Vorherige Impfungen: -

VAERS 2358274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 73,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 03.04.2022
Beginn: 30.06.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Dizziness Exposure to SARS-CoV-2 Feeling abnormal Head discomfort Pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I started to have a runny nose, head congestion and a dry cough. I did not have a fever but I had mild body aches. For the last two days I've been experiencing dizzy spells, and I my cough has loosened up. I took two home COVID-19 test on 6/30/2022 that came back negative. I went to urgent care to have a COVID-19 test done there because both of my sons were positive for COVID-19. On 7/1/2022 my COVID-19 test came back positive. My symptoms have gotten a lot better and I feel almost back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: COVID-19 PCR- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood pressure; A-Fib
Andere Medikamente: Rosuvastatin; Eliquis; Flecainide; Candesartan; Felodipine; Zyrtec; Vitamin D; Co-Q10; Probiotic; Prilosec OTC
Allergien: N/A
Vorherige Impfungen: -

VAERS 2357934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 72,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 01.04.2022
Beginn: 19.06.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Body temperature increased Bronchitis Fatigue Headache Laboratory test abnormal Malaise

Symptomtext

I started thinking I had light Bronchitis on June 19th, I had a headache, and two days later the symptoms got worse June 21. On June 22nd I started getting sick and I was very tired 100.4. June 23, I took an at home test which is came back positive I sent information to my doctor, and they told me to go to the urgent care. When the doctor took my temperature, it read 101.4. The doctor started me on PAXLOVID after rearranging some of my other medications. I took the medication and isolated for 5 days. Then after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Epilepsy; Blood Clots; Factor X Leiden; MTHFR
Andere Medikamente: Atorvastatin; aspirin; losartan; levetiracetam ER; carvedilol; melatonin; niacinamide; vitamin D3; super B complex; multivitamin
Allergien: Dilantin; trazodone HCI
Vorherige Impfungen: -

VAERS 2357908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OR
Alter: 72,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 04.04.2022
Beginn: 09.06.2022
Tage bis Beginn: 66,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Illness SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 06/09/2022 while traveling with symptoms of cough, fatigue but not more than normal during excursions, and only tested due to friend on trip becoming positive. I was not prescribed any medications. I had though these were allergy symptoms until my friend tested positive, due to the cold weather and grasses in the area. I was ill for 5 days before my symptoms resolved. I had a very mild case and have fully recovered with no lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal home test was positive on 06/15/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Overweight; Bone Issues
Andere Medikamente: Multivitamin; Vitamin C; Calcium; Vitamin D; Zyrtec; Eye Vitamins; Montelukast
Allergien: Sulfa; Lactose Intolerant
Vorherige Impfungen: -

VAERS 2357891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 02.04.2022
Beginn: 27.06.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Nasal congestion Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Transient ischaemic attack

Symptomtext

COVID-19 I received my 2nd booster shot on 04/02/2022 and my COVID-19 symptoms started on 06/27/2022 at 12:00PM I started experiencing fatigue I thought it was from the traveling I had. Tested positive for COVID-19 on 06/29/2022. I had fatigue, body ache, fever 100 degrees, sore throat, nasal congestions, headache. I called my doctor he prescribed PAXOVID for 5 days. I started taking medication on 06/30/2022. 07/04/2022 and 07/05/2022 I tested negative;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: none Mini stoke on May 17/2022
Vorgeschichte: Asthma not continues
Andere Medikamente: Losartan; Vitamins B6, vitamin D, Fish oil, Black seed oil, Astatine; Aspirin; Vitamin B12; Multi vitamins;
Allergien: Penicillin; Airborne; Seasonal allergies; Dendron
Vorherige Impfungen: -

VAERS 2357791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 03.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Pyrexia SARS-CoV-2 test positive

Symptomtext

I had previously had Moderna vaccines. Starting 06/29/2022, I had a headache all day that wasn't going away with medicine. The next day I had a fever and a headache. I took an at home COVID-19 test on 06/30/2022 which was positive. I did a telehealth visit with my doctor and I was prescribed PAXLOVID. I have been taking it as instructed. I am feeling better but still fatigued. It has been 3 days since I've had a fever and the headache is gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home COVID-19 test (06/30/2022): positive.
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol
Andere Medikamente: ZETIA; vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2357750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: VA
Alter: 73,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 01.04.2022
Beginn: 14.06.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Diarrhoea Malaise Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I first noticed symptoms for COVID-19 on 06/14/2022. My wife tested positive that day with a PCR test. I tested negative. on 06/15/2022, I was experiencing runny nose, coughing, and diarrhea so I tested again and was positive. We were on a cruise ship at the time. We departed on 06/11. We were placed into isolation on board the vessel. Under guidance for international travel, they recommend a 10 day isolation. So we did 3 days of isolation on the ship and departed from the ship where we completed our isolation. We came out of isolation on 06/25 and returned home. While onboard the ship, we saw the ship's doctor who prescribed pseudoephedrine and Tussin DM for symptoms. My runny nose lasted roughly 2-3 days while the cough lasted a bit longer, but by the time we left the ship my symptoms were declining and they were basically gone after 2 more days in the hotel. Overall though, it just felt like a cold or a mild case of the flu.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 test-negative 06/14/2022; COVID-19 test-positive-06/15/2022
Aktuelle Erkrankungen: None. .
Vorgeschichte: High blood pressure; Type 2 diabetes; High Cholesterol.
Andere Medikamente: Metformin; Doxazosin; Hydralazine; Metoprolol; Lisinopril; Amlodipine; Glipizide; Pantoprazole; Atorvastatin; Iron; Allerclear; Baby Aspirin; Men's Centrum Silver 50+; Kirkland Psyllium Fiber Capsules; Glucosamine with Chondroitin; Vitamin
Allergien: None.
Vorherige Impfungen: -

VAERS 2347978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: AR
Alter: 63,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 15.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Fatigue Headache Insomnia Lymphadenopathy Rash Respiratory tract congestion SARS-CoV-2 test negative Upper respiratory tract infection

Symptomtext

I experienced swollen painful lymph nodes, fatigue, trouble sleeping, congestion, slight cough, and headache. I was examined and prescribed a Z-pack on 06/29/2022 where I was diagnosed with an upper respiratory infection. I was beginning to feel better today 7/1/2022, but the congestion has improved greatly. Around my nostrils on top of my skin I have bumps, but they are also improving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab was negative on 06/29/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetic; Hypertension
Andere Medikamente: Vitamin D; Vitamin C; Vitamin E; Aspirin; Claritin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2347538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 31.03.2022
Beginn: 22.06.2022
Tage bis Beginn: 83,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Headache Nasopharyngitis Pyrexia SARS-CoV-2 test positive

Symptomtext

I started to feel like I had a cold coming on. I had a slight headache and was fatigued. As the day progressed, I had a mild dry cough. The symptoms were more intense the next day so I took a COVID-19 test on Wednesday and it was positive. On Thursday and Friday I developed a mild fever of 100.5 that I treated with TYLENOL. On Saturday I started PAXLOVID. The symptoms improved on Saturday and Sunday. I am still easily tired or fatigued. I am still recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home test positive, June 23rd, 2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Estradiol; vitamin D3; B12; fish oil; CITRACAL calcium
Allergien: N/A
Vorherige Impfungen: -

VAERS 2344829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 30.03.2022
Beginn: 02.06.2022
Tage bis Beginn: 64,0
Dosis: 4
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Fatigue Head discomfort SARS-CoV-2 test positive Throat irritation

Symptomtext

It started on Friday with slight tickle and scratch in my throat with head congestion. I felt really tired. My asthma did not kick in. The first three nights I took cold medicine and was able to sleep. I started feeling better on the fourth day. I tested negative with my home test on Saturday and retested Monday and was positive. I was unable to get into the doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home Nasal Swab COVID-19, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Albuterol; Symbicort; Tolterodine
Allergien: Hay; Lavender; Mesquite; Cat dander
Vorherige Impfungen: -

VAERS 2344807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 30.03.2022
Beginn: 14.06.2022
Tage bis Beginn: 76,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Dysphonia Fatigue Headache Malaise Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 06/14/2022 with symptoms of sore throat, headache, nasal congestion, hoarseness, and extreme fatigue. I was prescribed Paxlovid on 06/15/2022 via a virtual visit. I was ill for 8 days before my symptoms began to resolve. I am fully recovered now with no lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test on 06/15/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vesicare; Zolpidem; Zyrtec; Nasacort; Multivitamin; Eye Health Vitamins; Fish Oil; Cranberry; Prebiotic
Allergien: Sulfa; Pineapple; Lactose Intolerant
Vorherige Impfungen: -

VAERS 2344802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: SD
Alter: 58,0
Geschlecht: M
Eingang: 30.06.2022
Impfdatum: 01.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: SC / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Malaise Myalgia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

COVID-19 symptoms started on 06/21/22; tested positive on 06/25/22. We were on vacationand I wore an N95 mask the entire trip up there and we arrived on Saturday around noon and on Tuesday we were in the car traveling and I started to have quite a bit of coughing and nasal drainage and drainage into lungs which is what I think lead to the coughing. That was late morning and I noticed by 6 PM that evening I was tired and I took a nap and felt crummy. I got up the next morning and didn't feel great but after rest I thought I could function and felt like I had a severe cold and commented that I haven't had a cold since pandemic started because I've been careful. I took Ibuprofen for muscle aches and Zyrtec for the drainage and I stayed pretty steady on those medications until we got home. We got home Friday night and on Saturday morning I took a home test and it was positive and I did another one that was a different brand and it was also positive. At that time I also sent info to my PCP and Monday I got a message back from LPN saying I wasn't a candidate for Paxlovid due to shortages and to take Ibuprofen for the aches and Mucinex and to go to the ER if chest pains occur. They didn't want me to come in and do further testing. I continue, even today, having lots of drainage, coughing, and sneezing. It has improved some but not as much as expected. I will do another home test in a couple of days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Positive 06/25/22
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure; cholesterol
Andere Medikamente: Atorvastatin; metoprolol; losartan/hctz comb; fish oil supplement; multivitamin; low dose aspirin
Allergien: Something in the Penicillin family but we haven't narrowed it down
Vorherige Impfungen: -

VAERS 2344795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 30.03.2022
Beginn: 19.06.2022
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Fatigue Feeling abnormal Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

When I caught COVID-19 I had a dry cough. I had a fever of 101 degrees that lasted for 4 days. I had general malaise, and I felt miserable. I received Paxlovid on 6/21/2021. I'm still a little tired, but I feel much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: PCR COVID-19 Test- Positive (6/19/2022); (2) Home Antigen Tests- Negative (6/19/2022) (6/20/2022); Home Antigen Test- Positive (6/21/2022)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2341975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: KS
Alter: 74,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 08.06.2022
Beginn: 12.06.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest discomfort Chills Dizziness Dysgeusia Fatigue Feeling abnormal Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

COVID-19 symptoms started 06/12/22; tested positive on 06/14/22. It started with sore throat and on the night of the 13th I had a slight chill and a temperature of 98.4. 06/13/22 I had a headache. 06/14/22 I tested positive because of chills and I had a positive result within 2 minutes but at the same time I was testing I had what felt like a constricting band around the lower part of rib cage. I contacted my doctor that morning and he was listening to my symptoms and prescribed me PAXLOVID at that point. By 6:30 PM that night I felt much better but I had an extreme metallic taste from the PAXLOVID. I did 2 doses a day and 2 days I was on PAXLOVID the next morning I was very lightheaded and fuzzy so I called my doctor and they stopped the PAXLOVID because of the reaction. By 2 the next day the fuzzy headedness was gone so it was related to the vaccine. The sore throat continued through the 24th. I also had some fatigue but not extreme fatigue. All symptoms are gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 positive 06/14/22.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Alendronate sodium; multivitamin; vitamin D; chlorthalidone
Allergien: Ampicillin
Vorherige Impfungen: -

VAERS 2341832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 29.06.2022
Impfdatum: 29.04.2022
Beginn: 31.05.2022
Tage bis Beginn: 32,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Lethargy Nasal congestion Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

On that morning, May 31st, I woke up with bad nasal congestion, a cough and 101 fever. I felt achy and tired. This lasted about 2 days. The fever lasted only one day. Still felt lethargic. Congestion lasted longer and has still not gone away completely. I tested positive for COVID-19 on the same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home test, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Post Nasal Drip; Sinusitis.
Andere Medikamente: Lipitor; Ezetimibe; Lisinopril; Baby Aspirin; Benadryl; Multi Vitamin.
Allergien: Seasonal allergies; dust; mold.
Vorherige Impfungen: -

VAERS 2326807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 10.04.2022
Beginn: 17.05.2022
Tage bis Beginn: 37,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Antinuclear antibody increased Arthralgia C-reactive protein increased Joint stiffness Pain in extremity Red blood cell sedimentation rate increased

Symptomtext

Extremity and joint pain and stiffness, elevated CRP, ESR and ANA on 6/7/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: CRP, ESR and ANA on 6/7/2022
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, COPD, A-fib, Hx colectomy, abd incisional hernia, Asthma
Andere Medikamente: Plavix, xarelto, Vit D, Vit C, Slow Mag, Bumetande, Levothyroxine, cardia, Pantoprazole, Potassium, Inspra, Isorbide, simvastin
Allergien: ASA, Bactrim, hydralazine, metoprolol, codeine, Darvon, Erythromycin, propoxyphene, tetracycline,
Vorherige Impfungen: Td

VAERS 2325537

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CO
Alter: 63,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 17.05.2022
Beginn: 09.06.2022
Tage bis Beginn: 23,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Pyrexia Respiratory symptom SARS-CoV-2 test positive

Symptomtext

I tested positive on June 9, 2022 I had fevers and rigors. I spoke with an infectious disease doctor who prescribed PAXLOVID. I started feeling better and by June 14, 2022 I started feeling better and testing negative. By June 17 or 18 I started having upper respiratory symptoms and tested positive for COVID 19 again. I am still testing positive as of today June 21, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: PCR COVID 19 test
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril
Allergien: No
Vorherige Impfungen: -

VAERS 2323903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 18.06.2022
Impfdatum: 11.03.2022
Beginn: 12.03.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness

Symptomtext

dizzy(light headed); This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old male patient received BNT162b2 (BNT162B2), on 11Mar2022 at 11:00 as dose 1, single (Lot number: FK9894) at the age of 63 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: DIZZINESS (non-serious) with onset 12Mar2022, outcome "recovered" (28Mar2022), described as "dizzy(light headed)". Additional information: On 11Mar2022 at 10:00 am (pending clarification), the first dose of the Pfizer vaccine was administered in to patient's left arm. The morning of 12Mar2022 running thru 20Mar2022, the patient found himself very dizzy (light headed) for eight days. The dizzy feeling slowly began dissipating on 21Mar2022 until by the sixteenth day, the morning of 28Mar2022, it was gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: KY
Alter: 44,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 29.04.2022
Beginn: 30.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Burning sensation Erythema Eyelid function disorder Eyelid rash Facial discomfort Facial pain Pyrexia Rash Swelling face Urticaria

Symptomtext

rash on back; face was very red; eyes almost shut; Swelling in face/ face was stretched to limit; facial hives; rash on eyelids; face was stretched to limit and really hurt; burning face; severely uncomfortable; 104 temp; This case was reported by a consumer via other manufacturer and described the occurrence of facial swelling in a 44-year-old female patient who received DTPa (Reduced antigen) (Tdap Vaccine) for prophylaxis. Co-suspect products included PNEUMOCOCCAL VACCINE (PNEUMONIA VACCINE) for prophylaxis, TOZINAMERAN (COVID 19 VACCINE PFIZER) (batch number FK9894, expiry date unknown) for prophylaxis, levetiracetam (Keppra) unknown for product used for unknown indication, pregabalin unknown for product used for unknown indication, estradiol unknown for product used for unknown indication and adalimumab (Humira) unknown for product used for unknown indication. Previously administered products included COVID 19 VACCINE PFIZER (1st dose received on 15th March 2022 at 03.15 pm with batch number EA6207 in left arm), COVID 19 VACCINE PFIZER (2nd dose received on 5th April 2021 at 01.15 pm with batch number EW0151 in right arm), LEVOFLOXACIN with an associated reaction of hypersensitivity, ZOSTER VACCINE RECOMBINANT, ADJUVANTED with an associated reaction of hypersensitivity, FUROSEMIDE with an associated reaction of hypersensitivity, DILTIAZEM with an associated reaction of hypersensitivity and SHINGLES VACCINE (TRADE NAME UNKNOWN) with an associated reaction of hypersensitivity (on an unknown date received shingles vaccine and also experienced hives and facial swelling, refer case US2022AMR091014). Concurrent medical conditions included ankylosis, spondylitis, epilepsy, rheumatoid arthritis, gastroesophageal reflux disease, restless legs and cystitis interstitial. On 29th April 2022 11:30, the patient received the 1st dose of Tdap Vaccine and the 1st dose of PNEUMONIA VACCINE. On 29th April 2022, the patient received the 3rd dose of COVID 19 VACCINE PFIZER. On an unknown date, the patient started Keppra at an unknown dose and frequency, pregabalin at an unknown dose and frequency and estradiol at an unknown dose and frequency. In May 2022, the patient started Humira at an unknown dose and frequency. On 30th April 2022, 1 days after receiving Tdap Vaccine and less than a week after starting Keppra, the patient experienced high temperature. On 5th May 2022, the patient experienced facial swelling, hives, eyelid rash, facial pain, burning sensation in face and facial discomfort. On an unknown date, the patient experienced rash, red face and eyelid function disorder. The patient was treated with cetirizine (Claritin (Cetirizine)), steroids nos (Steroids) and cetirizine hydrochloride (Zyrtec). The action taken with Keppra was unknown. The action taken with pregabalin was unknown. The action taken with estradiol was unknown. The action taken with Humira was unknown. On an unknown date, the outcome of the facial swelling, hives, eyelid rash, facial pain, burning sensation in face, facial discomfort, rash, eyelid function disorder and high temperature were recovering/resolving and the outcome of the red face was not recovered/not resolved. It was unknown if the reporter considered the facial swelling, hives, eyelid rash, facial pain, burning sensation in face, facial discomfort, rash, red face, eyelid function disorder and high temperature to be related to Tdap Vaccine and Keppra. Linked case(s) involving the same patient: US2022AMR091014 Additional Information: Agency Receipt Date: 07-June-2022 Reporter's Comments: The patient self-reported this case. The patient did not receive the other vaccines within 4 weeks prior to the COVID vaccine. The patient received dose of Tdap vaccine into left arm and the Pneumonia vaccine and the Covid 19 vaccine Pfizer on right arm. The Covid 19 vaccine was administered at doctor's office. The patient also started Humira 5 days after shot. The patient received other medications within 2 weeks of vaccination as Pregabalin, Estradiol, Keppra, Pota, Plaquene and experienced swelling in face and facial hives or rash on eyelids. Face was stretched to limit and really hurt and burned where the patient was severely uncomfortable. It starting to occur the next week but got worse on week 2 of shot. The patient had 104 temperature the next day of shot. The Steroids did not respond to the shot. The patient started steroid pills on Monday June 16 (unspecified) and was worse Wednesday (unspecified) morning with eyes almost shut. The patient visited to allergist office and the allergist gave the shot and put on 2 Zyrtec and 2 Claritin and 4 tagments day. Still there was no response. The patient was getting better about four weeks. Had some rash on back. It was a burning sensation on face and face was very red and still red. Rheumatologist said it was not thing related to the patient's RA or Ankylosis Spondylitis. The patient was allergic to the shingles shot severely Hives and facial swelling but different than this. The patient visited doctor office but did not had any adverse events till May 16 (unspecified). The patient was not diagnosed with Covid 19 and since the vaccination the patient not tested for Covid 19. On 30th April 2022, 1 days after receiving Pneumonia vaccine and the Covid 19 vaccine Pfizer and less than a week after starting Pregabalin, estradiol and Humira, the patient experienced high temperature. On 5th May 2022, 6 days after receiving Pneumonia vaccine and the Covid 19 vaccine Pfizer, the patient experienced facial swelling, hives, eyelid rash, facial pain, burning sensation in face, facial discomfort. The time to onset for the events rash, red face and Eyelid function disorder was less than 2 months with respect to Tdap Vaccine, Pneumonia vaccine and the Covid 19 vaccine Pfizer. Less than a week after starting Pregabalin, estradiol and Humira, the patient experienced facial swelling, hives, eyelid rash, facial pain, burning sensation in face, facial discomfort, rash, red face, high temperature and eyelid function disorder. It was unknown if the reporter considered the facial swelling, hives, eyelid rash, facial pain, burning sensation in face, facial discomfort, rash, red face, high temperature and eyelid function disorder to be related to Pneumonia vaccine, the Covid 19 vaccine Pfizer, Pregabalin, estradiol and Humira. The reporter gave permission to contact her and healthcare provider about this report. Additional supportive information: The suspects Pota and plaquene were not captured as they are not available. The vaccination date for the 2nd dose of Covid 19 vaccine Pfizer was reported as 5th April 2021. However, the correct date expected upon follow up.; Sender's Comments: US-GLAXOSMITHKLINE-US2022AMR091014:Same Reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eyelid rash
Hospital-Tage: -
Labordaten: Test Date: 20220430; Test Name: Body temperature; Result Unstructured Data: (Test Result:104,Unit:degree F,Normal Low:,Normal High:)
Aktuelle Erkrankungen: Ankylosis; Cystitis interstitial; Epilepsy; Gastroesophageal reflux disease; Restless legs; Rheumatoid arthritis; Spondylitis
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2322060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: GA
Alter: 62,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 05.05.2022
Beginn: 23.05.2022
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Fatigue Feeling abnormal Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive Throat irritation Vaccine breakthrough infection

Symptomtext

Breakthrough COVID case: 05/28/2022. I started feeling like I had allergies. I experienced congestion, scratchy throat and fatigue. It progressed to a very sore throat, more fatigue, more coughing and brain fog. I did take a rapid test on 5/24/2022 and 05/26/2022 and they both came back negative. I took another rapid test on 05/28/2022 and it came back positive. I went to urgent care and did a PCR test and it came back positive. I was prescribed PAXLOVID. By 06/01/2022 I better but experience some fatigue. On 06/02/2022 I took another rapid test and it came back negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 05/24/2022 and 05/25/2022: Rapid: negative. 05/28/2022: Rapid and PCR: positive. 6/02/2022: Rapid: negative.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Acid reflux
Andere Medikamente: Atenolol; omeprazole; probiotic
Allergien: Sulfa
Vorherige Impfungen: 03/24/2022: Breakthrough COVID-19

VAERS 2320610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 07.06.2022
Beginn: 10.06.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Discomfort Rash Urticaria

Symptomtext

Generalize hives and rash, trunk, torso, arms, and legs. Symptoms on day 3 after vaccination and persist for 7days after vaccination. Employee has taken benadryl and tylenol for discomfort.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Rocephin
Vorherige Impfungen: -

VAERS 2317647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: ND
Alter: 51,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 29.04.2022
Beginn: 30.05.2022
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Nasopharyngitis Oropharyngeal pain Rhinorrhoea Secretion discharge Sensation of foreign body Sleep disorder Throat irritation

Symptomtext

Starting around 05/30/2022, I developed allergy symptoms (sore throat, runny nose, cough which devolved into sticky mucous/saliva and thin mucus). Also, I developed a sticky throat sensation as if something was stuck in my throat. After a few nights of almost no sleep (~2-4hrs a night) and treating myself for cold symptoms, I went to see the Dr. He gave me recommendations for medicine to take and prescribed me an antibiotic, and recommended I continue taking the anti-mucous OTC and OTC sleep medicine. So far, the medicine has been helping me sleep (~6-7 hours of sleep) and I have only had 2 nights where I couldn't sleep since then but have self treated in hopes to go back to sleep. I asked the doctor if I could have medicine to help me sleep and I was given lorazepam but I haven't had to use it yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin, Omega 3 fish oil and ibuprofen as needed
Allergien: None
Vorherige Impfungen: Fatigue and feeling malaise for about 2 days after both Shingles Vaccines

VAERS 2316485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: KY
Alter: 44,0
Geschlecht: F
Eingang: 11.06.2022
Impfdatum: 29.04.2022
Beginn: 29.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Burning sensation Discomfort Erythema Off label use Pain Product use issue Pyrexia Rash Swelling face Urticaria

Symptomtext

Swelling in face and facial hives; Swelling in face and facial hives; rash on eyelids/ Had some rash on back to; Face was stretched to limit and really hurt and burned where I was severely uncomfortable.; Face was stretched to limit and really hurt and burned where I was severely uncomfortable.; Also had 104 temp the next day of shot; It was a burning sensation on face and face was very red and still red; It was a burning sensation on face and face was very red and still red; I took three shots that day TDap one arm and pneumoia and Covid other arm.; I took three shots that day TDap one arm and pneumoia and Covid other arm.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 44-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Apr2022 at 11:30 as dose 3 (booster), single (Lot number: FK9894) at the age of 44 years, in right arm for covid-19 immunisation; diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (TDAP), on 29Apr2022 as dose 1, single (Batch/Lot number: unknown), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Ankylosis Spondylitis" (unspecified if ongoing); "Epilepsy" (unspecified if ongoing); "Rheumatoid Arthritis" (unspecified if ongoing); "Gerd" (unspecified if ongoing); "restless leg" (unspecified if ongoing); "IC" (unspecified if ongoing). Concomitant medication(s) included: PREGABALIN; ESTRADIOL; KEPPRA [LEVETIRACETAM]; POTASSIUM; PLAQUENIL [HYDROXYCHLOROQUINE PHOSPHATE]. Past drug history included: Levofloxacin, reaction(s): "known Allergies: Levofloxacin"; Diltiazem, reaction(s): "known Allergies: Diltiazem"; Zoster vac recomb adjuvanted, reaction(s): "known Allergies: Zoster"; Fursemide, reaction(s): "known Allergies: fursemide". Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: EA6207, Dose administration time: 03:15 pm, Anatomical site: Left arm), administration date: 15Mar2021, when the patient was 43-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE, Lot number: EW0151, Dose administration time: 01:15 pm, Anatomical site: Right arm), administration date: 05Apr2021, when the patient was 43-year-old, for Covid-19 Immunization; Shnigles, for Immunization, reaction(s): "facial swelling", "Severly hives". The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 29Apr2022, outcome "unknown" and all described as "I took three shots that day TDap one arm and pneumoia and Covid other arm."; PYREXIA (non-serious) with onset 05May2022, outcome "recovering", described as "Also had 104 temp the next day of shot"; PAIN (non-serious), DISCOMFORT (non-serious) all with onset 05May2022, outcome "recovering" and all described as "Face was stretched to limit and really hurt and burned where I was severely uncomfortable."; BURNING SENSATION (non-serious), ERYTHEMA (non-serious) all with onset 05May2022, outcome "recovering" and all described as "It was a burning sensation on face and face was very red and still red"; SWELLING FACE (non-serious), URTICARIA (non-serious) all with onset 05May2022, outcome "recovering" and all described as "Swelling in face and facial hives"; RASH (non-serious) with onset 05May2022, outcome "recovering", described as "rash on eyelids/ Had some rash on back to". The events "swelling in face and facial hives", "rash on eyelids/ had some rash on back to", "face was stretched to limit and really hurt and burned where i was severely uncomfortable.", "also had 104 temp the next day of shot" and "it was a burning sensation on face and face was very red and still red" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of swelling face, urticaria, rash, pain, discomfort, pyrexia, burning sensation, erythema. Additional comment: The patient stated swelling in face and facial hives or rash on eyelids. Face was stretched to limit and really hurt and burned where she was severely uncomfortable. It starting to occur the next week but got worse on week 2 of shot. Also started Humira 5 days after shot. Also had 104 temp the next day of shot. Steroids did not respond to the shot. she started steroid pills on Monday June 16 and was worse Wednesday morning with eyes almost shut. Allergist gave her shot and put her on 2 Zyrtec and 2 Claritin and 4 tagments day. Still no response. getting better about four weeks. Had some rash on back to. It was a burning sensation on face and face was very red and still red. Rheumatologist said it was not thing related to her RA or Ankylosis Spondylitis. He took picture. The patient was allergic to the shingles shot severely Hives and facial swelling but different than this. she took three shots that day TDap one arm and pneumonia and Covid other arm. No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20220505; Test Name: temp; Result Unstructured Data: Test Result:104
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cystitis; Epilepsy; GERD; Restless legs; Rheumatoid arthritis; Spondylitis ankylosing
Andere Medikamente: PREGABALIN; ESTRADIOL; KEPPRA [LEVETIRACETAM]; POTASSIUM; PLAQUENIL [HYDROXYCHLOROQUINE PHOSPHATE]
Allergien: -
Vorherige Impfungen: -

VAERS 2315520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 98,0
Geschlecht: M
Eingang: 10.06.2022
Impfdatum: 23.04.2022
Beginn: 14.05.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Eye discharge Eye infection Eye pain Ocular hyperaemia

Symptomtext

He experienced an eye infection in his right eye. He has a lot of mucus and his eye is very red. It was a little painful because of the infection. It lasted for a bout a week before my dad told me and then we went to the doctor. The doctor gave him an antibiotic, Tobramycin. We are going to the doctor next week. It is better but not 100%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Folic Acid Fluoroimide Lisinopril Miralax Timoptic Baby Aspirin Iron Pill Refresh Drops Muro 128
Allergien: N/A
Vorherige Impfungen: -

VAERS 2315067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 10.06.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea

Symptomtext

I am having diarrhea ; even after I eat or drink something; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FK9894) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 IMMUNIZATION; Covid-19 vaccine (first booster, COVID-19 VACCINE [unknown manufacturer]), for COVID-19 IMMUNIZATION. The following information was reported: DIARRHOEA (non-serious), outcome "unknown", described as "I am having diarrhea; even after I eat or drink something". Additional information Reporter stated, I do not want to leave my name but I just wanted to be calling about my side effect that I had from my 2nd booster. So, I have my 2nd booster on May 11th and couple days later I am having diarrhea I still have the once even after I eat or drink something. The first booster did not cause that I don't know why and I take anti- viral (Further clarification unknown hence, captured as unspecified medication) at night so I don't know if that's related to that. Reporter stated, I take it every night anti-viral but the first booster did not do that. So, I don't know why 2nd have like this because doctors aren't really helping me so I thought I am calling you guys may be you guys can explain it to me better. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2311692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 57,0
Geschlecht: M
Eingang: 07.06.2022
Impfdatum: 25.04.2022
Beginn: 14.05.2022
Tage bis Beginn: 19,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Extra dose administered Injection site erythema Injection site streaking Injection site swelling Localised infection Pain in extremity Peripheral swelling Pustule Rash Tenderness Wound secretion

Symptomtext

I received my second Pfizer booster on 4/25/2022. On about 5/14/2022, I saw what appeared to be a swollen, infected area on the knuckle corresponding to my left index finger. Over the course of a week, it increased in size, causing tenderness and pain to the touch and pressure. On about 5/17/2022 or 5/18/2022, I pierced it with a clean needle to relieve the pressure. It emitted a combination of what appeared to be pus and lymphatic fluid. There was no blood, however. Over the course of the following week, the initial bump on the knuckle lessened in size, but it remained an open, weeping wound. I then noticed swelling in between that region and the base of my left thumb. Following that, various other hard swollen subdermal bumps appeared on my left arm. The largest is on top of my left wrist. There are several smaller bumps on the inside of the bend of my left arm, plus another subdermal bump on my left forearm. On the inside of my left upper arm, there appears to be a red streak. Underneath part of the streak there is a subdermal bump. This has persisted to the time of this writing. On 6/3/2022, I went to the doctor. The doctor was unsure about the cause of the bumps, but he guessed that they were symptomatic of a bacteriological infection. On that same day, I began a regimen of amoxicillin. Thus far, I have seen no change in my condition, so I cannot say whether or not the treatment has been effective. I returned to the doctor's office on 6/6/2022. I saw a different doctor, who gave the same diagnosis as the previous one. I was further prescribed a clinically administered injection of Rocephin. I was prescribed additional oral antibiotics. One is doxycycline monohydrate (100 mgs. twice a day) and the other is cephalexin (500mgs three times a day). As of the time of this report, I cannot tell if these have had any effect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension (moderate).
Andere Medikamente: Losartan (75 mg).
Allergien: None.
Vorherige Impfungen: -

VAERS 2298575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 25.05.2022
Beginn: 01.05.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash erythematous Rash Rash pruritic

Symptomtext

I woke up with the diffuse erythematous rash; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old female patient received BNT162b2 (BNT162B2), on 25May2022 as dose number unknown, single (Lot number: FK9894) at the age of 64 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: RASH ERYTHEMATOUS (non-serious) with onset May2022, outcome "unknown", described as "I woke up with the diffuse erythematous rash". Therapeutic measures were taken as a result of rash erythematous. Additional information: The patient did not had any vaccination 4 weeks prior to BNT162B2. The patient was treated with mometasone ointment, Benadryl and metrol dose pack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2298575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 25.05.2022
Beginn: 01.05.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash erythematous Rash Rash pruritic

Symptomtext

I woke up with the diffuse erythematous rash; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old female patient received BNT162b2 (BNT162B2), on 25May2022 as dose number unknown, single (Lot number: FK9894) at the age of 64 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: RASH ERYTHEMATOUS (non-serious) with onset May2022, outcome "unknown", described as "I woke up with the diffuse erythematous rash". Therapeutic measures were taken as a result of rash erythematous. Additional information: The patient did not had any vaccination 4 weeks prior to BNT162B2. The patient was treated with mometasone ointment, Benadryl and metrol dose pack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 04.06.2022
Impfdatum: 19.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain upper Fatigue Heart rate Heart rate increased Malaise COVID-19 Disease recurrence SARS-CoV-2 test Vaccination failure Oxygen saturation

Symptomtext

exhausted; Because of her tachycardia, her heart rate skyrockets when she's sick; Friday felt lousy/ Just felt awful; Had a stomach ache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old female patient received BNT162b2 (BNT162B2), on 19Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 58 years for covid-19 immunisation. The patient's relevant medical history included: "Tachycardia" (unspecified if ongoing), notes: Tachycardia History of heart rate goes through the roof when sick. Racing heart beat. She's had this for a few years at least, a long time.; "Kidney stone removed", start date: 12Apr2022 (unspecified if ongoing), notes: Verbatim: Had Kidney stone removed 12Apr2022. Concomitant medication(s) included: MUCINEX DM. Vaccination history included: BNT162b2 (COVID-19 Vaccine: Dose 3, Manufacturer: Pfizer, Date: 04Oct2021, NDC: Unknown, LOT: 30145BA, EXP: Unknown), administration date: 04Oct2021, when the patient was 58-year-old, for COVID-19 Immunization; BNT162b2 (COVID-19 Vaccine: Dose 2, Manufacturer: Pfizer, Date: 02Apr2021, NDC: Unknown, LOT: EP87534, EXP: 31Jul2021), administration date: 02Apr2021, when the patient was 57-year-old, for COVID-19 Immunization; BNT162b2 (COVID-19 Vaccine: Dose 1, Manufacturer: Pfizer , Date: 12Mar2021, NDC: Unknown, LOT: EN6202, EXP: 30Jun2021), administration date: 12Mar2021, when the patient was 57-year-old, for Covid-19 Immunization. The following information was reported: FATIGUE (non-serious), outcome "unknown", described as "exhausted"; HEART RATE INCREASED (non-serious), outcome "unknown", described as "Because of her tachycardia, her heart rate skyrockets when she's sick"; MALAISE (non-serious), outcome "unknown", described as "Friday felt lousy/ Just felt awful"; ABDOMINAL PAIN UPPER (non-serious), outcome "unknown", described as "Had a stomach ache". Relevant laboratory tests and procedures are available in the appropriate section.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Test Name: Heart rate; Result Unstructured Data: Test Result:104; Comments: heart rate was 104 Her heart rate was 105; Test Name: Heart rate; Result Unstructured Data: Test Result:105; Comments: Her heart rate was 105; Test Name: Oxygen Saturation; Result Unstructured Data: Test Result:93; Comments: Oxygen went down. oxygen went down to 93; Test Date: 20220512; Test Name: Covid-19 test; Test Result: Negative ; Comments: Tested negative on Thursday night; Test Date: 20220514; Test Name: Covid-19 test; Test Result: Positive ; Comments: 14May2022 initially tested positive for COVID-19; Test Date: 20220521; Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID-19 test was 21May2022 was roaring red indicating positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kidney stone (Verbatim: Had Kidney stone removed 12Apr2022); Tachycardia
Andere Medikamente: MUCINEX DM
Allergien: -
Vorherige Impfungen: -

VAERS 2308724

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FK9894

mild

Staat: CA
Alter: 79,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 21.04.2022
Beginn: 20.05.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Rhinorrhoea

Symptomtext

General tired feeling, sniffling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: CholestOff Complete - 2 capsules - Twice daily Centrum Silver 50+ - 1 per day Triamterene-HCTZ 37.5 - 5-25 mg TB - 1 Tablet daily Vitamin D - 25mg -1 Daily Iron- 65mg - 3 times per week Turmeric - 1 daily Simvastatin 40mg - 1 daily Metoprol
Allergien: None
Vorherige Impfungen: -

VAERS 2308524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

mild

Staat: PA
Alter: 87,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 19.05.2022
Beginn: 26.05.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Asthenia Hypoaesthesia Muscular weakness Musculoskeletal pain Pain in extremity

Symptomtext

Systemic: Joint Pain-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Weakness-Mild, Additional Details: Patient went to his doctor on 05/31/2022 with musculoskeletal pain, numbness in his left arm. About a week after vaccination, he developed pain in left hand as well as numbness/weakness. No symptoms at site of injection, only from wrist to fingertip. It is improving slightly, but not normal. Pt picked up prednisolone prescription, stating that numbness disappeared. Patient's hand looked normal without signs of swelling. Patient didn't show any reaction for prior three Pfizer vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2307460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 28.04.2022
Beginn: 09.05.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Biopsy skin Eczema Hypersensitivity Lichenoid keratosis Pain Pruritus Rash Urticaria

Symptomtext

Rash front and back starting on left arm More like welts very itchy and painful

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 05-13-2022 Punch Biopsy "Overall, these findings of a spongiotic and lichenoid dermatitis favor a hypersensitivity reaction, possibly to a medication. However, ecxematous processes are still considered in the histologic differential diagnosis."
Aktuelle Erkrankungen: -
Vorgeschichte: Lichen Planus Gluten Intolerance Osteoporosis
Andere Medikamente: Betamethasone Dipropionate Gel, Ointment and Cream Estrace Loratadine Losartan Potassium PreviDent Prolia SC
Allergien: Sulfa Pistachio Nuts Gluten Xanax Citrus Mint Ginger Vanilla Cinnamon Garlic Licorice TOMATOES Red Wine Non Steroidal anti-inflammatory pain killers
Vorherige Impfungen: -

VAERS 2307407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

mild

Staat: IN
Alter: 84,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 27.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Alanine aminotransferase normal Angiogram pulmonary normal Anion gap Aspartate aminotransferase normal Asthenia Bacterial test negative Band neutrophil count Basophil count decreased Basophil percentage Bilirubin conjugated Bilirubin urine Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin Blood calcium decreased Blood chloride decreased Blood creatine phosphokinase normal Blood creatinine increased

Symptomtext

Basic Information Time Seen: 05/31/2022 09:12 Chief Complaint Weakness or fatigue (Complaint of) Supporting Nursing Comments: pt reports worsening fatigue and weakness over the last month. pt was walking 1 mile a day 1month ago and now cannot walk. Denies SOA or pain anywhere. No change in appetite. "Feels achy" History of Present Illness Pt is an 84 y/o male who presents to the ED secondary to increased weakness and fatigue for the past month that has gradually worsened. Pt states that he used to be able to walk a mile a day but now struggles with 50 feet. Notes having some nausea, decreased appetite, and myalgias; denies dyspnea, CP, abd pain, NVD, and urinary sx. Wife states that pt has had very limited PO intake; mostly eats Jello sporadically over the past week. Denies any acute changes at time of onset such as falls, trauma, or illnesses. Pt notes thought that he had a single fall last week due to the weakness; bent over to pick something up when he fell on his shoulder. Did not hit head or have LOC. pt states that he was able on the ground for 15 minutes and wife was able to get him up; then proceeded to mow the lawn. Denies any changes in medications; compliant with meds. Hx includes DM, HLD, HTN, Aortic regurgitation, ascending aorta dilation, and neuropathy. Review of Systems Constitutional: no fever, no chills, no sweats, mild weakness, + fatigue Skin: no jaundice, no rash, no lesions, no petechiae ENMT: no ear pain, no sore throat, no congestion, no hoarseness Respiratory: no shortness of breath, no cough, no orthopnea, no wheezing Cardiovascular: no chest pain, no palpitations, no edema Gastrointestinal: mild nausea, no vomiting, no diarrhea, no GI bleeding, + decreased PO intake Genitourinary: no dysuria, no hematuria, no discharge, no pain Musculoskeletal: no back pain, no trauma, + myalgias Neurologic: no headache, no dizziness, no numbness, no weakness Psychiatric: no sleeping problems, no irritability, no mood swings/depression Heme/Lymph: no bleeding tendency, no bruising tendency, no petechiae, no swollen nodes Allergy/Immunologic: no seasonal allergies, no food allergies, no recurrent infections, no impaired immunity Additional ROS info: Except as noted in the above Review of Systems and in the History of Present Illness, all other systems have been reviewed and are negative or noncontributory. Physical Exam/Objective Vitals & Measurements last 24 hours VITAL SIGNS Temp C: 36.5 DegC Heart Rate: 72 bpm Resp Rate: 16 br/min BP #1: 135 / 81 mmHg SpO2 (%): 96 % Height CM: 177 cm Weight KG: 80.2 kg Ideal Body Weight: 72.28 kg General: alert, no acute distress Skin: warm, dry Head: no trauma, normocephalic Neck: trachea midline, no adenopathy, no tenderness Eye: normal conjunctiva, clearsclera ENMT: Dry oral mucosa Cardiovascular: regularrate and rhythm, normalperipheral perfusion, soft systolic murmur best heard at apex Respiratory: Lungs CTA, respirations non-labored Chest wall: no deformity Gastrointestinal: soft, non-distended, no tenderness _, no guarding _ Extremities: no deformity, no trauma Neurological: oriented x4 , LOC appropriate for age, CNII-XII intact, motor strength equal and normal bilaterally, sensation equal and normal bilaterally , speech normal Psychiatric: Cooperative , appropriate for ageaffect , normal judgement, normal psychiatric thoughts Medical Decision Making ED Nurse's Notes, Previous Records, and Vital Signs Reviewed DDx includes but is not limited to: dehydration vs electrolyte abnormality vs COVID vs UTI Ordered: Labs, EKG, and Imaging Labs: Reviewed Images: Reviewed 05/31/22 13:23:12 Update: Labs show leukopenia at 1.3 but otherwise baseline blood counts. PTINR is normal. Baseline electrolytes. Baseline renal function. Normal LFTs. Negative Trop, BNP, and lactate. Lipase is elevated at 65. TSH is negative. COVID and Flu negative. CXR and CT abdomen are normal. UA is normal. Will reassess the pt. 05/31/22 13:56:51 Pt is resting on bed comfortably. Updated pt on results of labs and images and recommended admission at this time for observation. Pt is agreeable to be admitted. Dr. Hospitalist, agrees to admit to obs MS w/ tele Condition Stable Disposition 05/31/22 13:57:30 Admitted under Dr. Counseled I have currently counseled the Patient regarding diagnosis, diagnostic results, and treatment plan. Patient indicated understanding of instructions. Scribe Attestation I, acting as scribe for Dr. 05/31/22 09:13:39 . Signed by: 05/31/22 09:13:39 I, DO, attest that the scribe's documentation has been prepared under my direction in person and by me in its entirety. I confirm that the note above accurately reflects all work, treatments, procedures, and medical decision-making performed by me. Assessment/Plan 1. Leukopenia 2. Generalized weakness 3. History of prostate cancer Follow Up No qualifying data available

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Lab Results Hemogram-Platelets-WBC Differential FS LATEST RESULTS HISTORICAL RESULTS WBC 05/31/22 10:10 1.3 Critical 01/20/22 10.0 RBC 05/31/22 10:10 4.98 01/20/22 3.55 Low Hgb 05/31/22 10:10 13.2 Low 01/20/22 10.0 Low Hct 05/31/22 10:10 39.8 Low 01/20/22 29.1 Low MCV 05/31/22 10:10 80 Low 01/20/22 82 MCH 05/31/22 10:10 26.5 Low 01/20/22 28.3 MCHC 05/31/22 10:10 33.2 01/20/22 34.5 RDW 05/31/22 10:10 14.6 High 01/20/22 13.0 Platelet 05/31/22 10:10 163 01/20/22 253 MPV 05/31/22 10:10 7.8 01/20/22 8.3 Neutrophils % 05/31/22 10:10 60 01/20/22 78 Lymphocytes % 05/31/22 10:10 28 01/20/22 11 Monocytes % 05/31/22 10:10 10 01/20/22 10 Eosinophils % 05/31/22 10:10 0 01/20/22 0 Basophils % 05/31/22 10:10 1 01/20/22 0 Absolute Neutrophil 05/31/22 10:10 0.8 Low 01/20/22 7.8 High Absolute Lymphocyte 05/31/22 10:10 0.4 Low 01/20/22 1.1 Absolute Monocyte 05/31/22 10:10 0.1 01/20/22 1.0 Absolute Eosinophil 05/31/22 10:10 0.0 01/20/22 0.0 Absolute Basophil 05/31/22 10:10 0.0 01/20/22 0.0 Band 05/31/22 10:10 9 Neutrophil 05/31/22 10:10 45 Lymphocyte 05/31/22 10:10 31 Monocyte 05/31/22 10:10 15 RBC Morphology 05/31/22 10:10 Normal Platelet Estimate 05/31/22 10:10 Adequate Platelet Morphology 05/31/22 10:10 Normal Routine Coagulation Studies FS LATEST RESULTS PT 05/31/22 10:10 13.1 INR 05/31/22 10:10 1.11 Routine Serum/Plasma Chemistry Tests FS LATEST RESULTS HISTORICAL RESULTS Sodium SerPl QN 05/31/22 10:10 134 Low 01/20/22 134 Low Potassium SerPl QN 05/31/22 10:10 3.6 01/20/22 4.2 Chloride SerPl QN 05/31/22 10:10 97 Low 01/20/22 102 Carbon Dioxide SerPl QN 05/31/22 10:10 28 01/20/22 25 Anion Gap 05/31/22 10:10 9 01/20/22 7 BUN SerPl QN 05/31/22 10:10 24 High 01/20/22 32 High Creatinine SerPl QN 05/31/22 10:10 1.13 01/20/22 1.22 Estimated GFR (CKD-EPI) 05/31/22 10:10 59 Low 01/20/22 54 Low Estimated GFR (CKD-EPI, no race) 05/31/22 10:10 64 Estimated CRCL (CG) 05/31/22 10:10 52 Low 01/20/22 49 Low Glucose SerPl QN 05/31/22 10:10 140 High 01/20/22 196 High Calcium Total SerPl QN 05/31/22 10:10 8.9 01/20/22 8.8 Alkaline Phos SerPl QN 05/31/22 10:10 63 12/30/21 58 ALT SerPl QN 05/31/22 10:10 35 12/30/21 18 AST SerPl QN 05/31/22 10:10 32 12/30/21 17 Bilirubin Direct SerPl QN 05/31/22 10:10 0.1 Bilirubin Total SerPl QN 05/31/22 10:10 0.4 12/30/21 0.6 Total Protein SerPl QN 05/31/22 10:10 6.7 12/30/21 7.5 Albumin SerPl QN 05/31/22 10:10 4.2 12/30/21 4.5 Magnesium SerPl QN 05/31/22 10:10 1.6 Lipase SerPl QN 05/31/22 10:10 65 High CK SerPl QN 05/31/22 10:10 74 Troponin-I High Sensitivity 05/31/22 10:10 16 BNP Pl QN 05/31/22 10:10 28 Lactate Venous Pl QN 05/31/22 10:10 1.6 Endo Serum/Plasma Tests FS LATEST RESULTS HISTORICAL RESULTS TSH 3rd Gen SerPl QN 05/31/22 10:10 3.920 04/27/21 1.855 Urinalysis FS LATEST RESULTS Color 05/31/22 12:02 Yellow Clarity 05/31/22 12:02 Clear Specific Gravity 05/31/22 12:02 >=1.030 pH 05/31/22 12:02 5.5 Protein 05/31/22 12:02 100 Abnormal Glucose 05/31/22 12:02 Negative Ketones 05/31/22 12:02 Negative Bilirubin 05/31/22 12:02 Negative Hgb Ur 05/31/22 12:02 Negative Nitrite 05/31/22 12:02 Negative Urobilinogen 05/31/22 12:02 Normal Leukocyte Esterase Ur 05/31/22 12:02 Negative WBC 05/31/22 12:02 0-5 RBC 05/31/22 12:02 0-2 Bacteria 05/31/22 12:02 None Squamous Epithelial 05/31/22 12:02 Few Mucous 05/31/22 12:02 Present Hyaline Casts 05/31/22 12:02 0-2 Molecular Diagnostic Tests LATEST RESULTS HISTORICAL RESULTS COVID 19 Specimen Source 05/31/22 09:48 Nasopharyngeal 01/16/22 Nasopharyngeal Coronavirus SARS-CoV2 Rapid 05/31/22 09:48 Not Detected 01/16/22 Not Detected Viral FS LATEST RESULTS Rapid Influenza Method 05/31/22 09:48 PCR - Liat Rapid Influenza A PCR 05/31/22 09:48 Not Detected Rapid Influenza B PCR 05/31/22 09:48 Not Detected Diagnostic Results CT Abd/Pelvis W/IV Contrast 05/31/22 13:12:43 IMPRESSION: Negative for bowel obstruction or acute inflammatory process involving the bowel. No overt malignant findings. Hepatic steatosis. No acute diagnostic abnormality identified involving abdomen or pelvis. Thank you for consulting with Radiology. Healthcare providers wishing to discuss this case further can contact the Emergency Radiology reading room. Electronically Signed by: Signed By: MD ************************************************** XR Chest PA or AP Portable 05/31/22 10:46:22 IMPRESSION: No acute cardiopulmonary findings. Electronically Signed by: Signed By: MD EKG Rate: 73 Rhythm: NSR Axis: Normal Conduction: normal ST segments: No changes T waves: Inversion in Lead III Q waves: no q waves Impression: NSR with T wave inversion in Lead III which is nonspecific Comparison to old: 5/23/20 no changes Lab Results Hemogram-Platelets-WBC Differential FS LATEST RESULTS HISTORICAL RESULTS WBC 05/31/22 10:10 1.3 Critical 01/20/22 10.0 RBC 05/31/22 10:10 4.98 01/20/22 3.55 Low Hgb 05/31/22 10:10 13.2 Low 01/20/22 10.0 Low Hct 05/31/22 10:10 39.8 Low 01/20/22 29.1 Low MCV 05/31/22 10:10 80 Low 01/20/22 82 MCH 05/31/22 10:10 26.5 Low 01/20/22 28.3 MCHC 05/31/22 10:10 33.2 01/20/22 34.5 RDW 05/31/22 10:10 14.6 High 01/20/22 13.0 Platelet 05/31/22 10:10 163 01/20/22 253 MPV 05/31/22 10:10 7.8 01/20/22 8.3 Neutrophils % 05/31/22 10:10 60 01/20/22 78 Lymphocytes % 05/31/22 10:10 28 01/20/22 11 Monocytes % 05/31/22 10:10 10 01/20/22 10 Eosinophils % 05/31/22 10:10 0 01/20/22 0 Basophils % 05/31/22 10:10 1 01/20/22 0 Absolute Neutrophil 05/31/22 10:10 0.8 Low 01/20/22 7.8 High Absolute Lymphocyte 05/31/22 10:10 0.4 Low 01/20/22 1.1 Absolute Monocyte 05/31/22 10:10 0.1 01/20/22 1.0 Absolute Eosinophil 05/31/22 10:10 0.0 01/20/22 0.0 Absolute Basophil 05/31/22 10:10 0.0 01/20/22 0.0 Band 05/31/22 10:10 9 Neutrophil 05/31/22 10:10 45 Lymphocyte 05/31/22 10:10 31 Monocyte 05/31/22 10:10 15 RBC Morphology 05/31/22 10:10 Normal Platelet Estimate 05/31/22 10:10 Adequate Platelet Morphology 05/31/22 10:10 Normal Routine Coagulation Studies FS LATEST RESULTS PT 05/31/22 10:10 13.1 INR 05/31/22 10:10 1.11 Routine Serum/Plasma Chemistry Tests FS LATEST RESULTS HISTORICAL RESULTS Sodium SerPl QN 05/31/22 10:10 134 Low 01/20/22 134 Low Potassium SerPl QN 05/31/22 10:10 3.6 01/20/22 4.2 Chloride SerPl QN 05/31/22 10:10 97 Low 01/20/22 102 Carbon Dioxide SerPl QN 05/31/22 10:10 28 01/20/22 25 Anion Gap 05/31/22 10:10 9 01/20/22 7 BUN SerPl QN 05/31/22 10:10 24 High 01/20/22 32 High Creatinine SerPl QN 05/31/22 10:10 1.13 01/20/22 1.22 Estimated GFR (CKD-EPI) 05/31/22 10:10 59 Low 01/20/22 54 Low Estimated GFR (CKD-EPI, no race) 05/31/22 10:10 64 Estimated CRCL (CG) 05/31/22 10:10 52 Low 01/20/22 49 Low Glucose SerPl QN 05/31/22 10:10 140 High 01/20/22 196 High Calcium Total SerPl QN 05/31/22 10:10 8.9 01/20/22 8.8 Alkaline Phos SerPl QN 05/31/22 10:10 63 12/30/21 58 ALT SerPl QN 05/31/22 10:10 35 12/30/21 18 AST SerPl QN 05/31/22 10:10 32 12/30/21 17 Bilirubin Direct SerPl QN 05/31/22 10:10 0.1 Bilirubin Total SerPl QN 05/31/22 10:10 0.4 12/30/21 0.6 Total Protein SerPl QN 05/31/22 10:10 6.7 12/30/21 7.5 Albumin SerPl QN 05/31/22 10:10 4.2 12/30/21 4.5 Magnesium SerPl QN 05/31/22 10:10 1.6 Lipase SerPl QN 05/31/22 10:10 65 High CK SerPl QN 05/31/22 10:10 74 Troponin-I High Sensitivity 05/31/22 10:10 16 BNP Pl QN 05/31/22 10:10 28 Lactate Venous Pl QN 05/31/22 10:10 1.6 Endo Serum/Plasma Tests FS LATEST RESULTS HISTORICAL RESULTS TSH 3rd Gen SerPl QN 05/31/22 10:10 3.920 04/27/21 1.855 Urinalysis FS LATEST RESULTS Color 05/31/22 12:02 Yellow Clarity 05/31/22 12:02 Clear Specific Gravity 05/31/22 12:02 >=1.030 pH 05/31/22 12:02 5.5 Protein 05/31/22 12:02 100 Abnormal Glucose 05/31/22 12:02 Negative Ketones 05/31/22 12:02 Negative Bilirubin 05/31/22 12:02 Negative Hgb Ur 05/31/22 12:02 Negative Nitrite 05/31/22 12:02 Negative Urobilinogen 05/31/22 12:02 Normal Leukocyte Esterase Ur 05/31/22 12:02 Negative WBC 05/31/22 12:02 0-5 RBC 05/31/22 12:02 0-2 Bacteria 05/31/22 12:02 None Squamous Epithelial 05/31/22 12:02 Few Mucous 05/31/22 12:02 Present Hyaline Casts 05/31/22 12:02 0-2 Molecular Diagnostic Tests LATEST RESULTS HISTORICAL RESULTS COVID 19 Specimen Source 05/31/22 09:48 Nasopharyngeal 01/16/22 Nasopharyngeal Coronavirus SARS-CoV2 Rapid 05/31/22 09:48 Not Detected 01/16/22 Not Detected Viral FS LATEST RESULTS Rapid Influenza Method 05/31/22 09:48 PCR - Liat Rapid Influenza A PCR 05/31/22 09:48 Not Detected Rapid Influenza B PCR 05/31/22 09:48 Not Detected Diagnostic Results CT Abd/Pelvis W/IV Contrast 05/31/22 13:12:43 IMPRESSION: Negative for bowel obstruction or acute inflammatory process involving the bowel. No overt malignant findings. Hepatic steatosis. No acute diagnostic abnormality identified involving abdomen or pelvis. Thank you for consulting with Radiology. Healthcare providers wishing to discuss this case further can contact the Emergency Radiology reading room. Electronically Signed by: Signed By: MD ************************************************** XR Chest PA or AP Portable 05/31/22 10:46:22 IMPRESSION: No acute cardiopulmonary findings. Electronically Signed by: Signed By: MD EKG Rate: 73 Rhythm: NSR Axis: Normal Conduction: normal ST segments: No changes T waves: Inversion in Lead III Q waves: no q waves Impression: NSR with T wave inversion in Lead III which is nonspecific Comparison to old: 5/23/20 no changes Lab Results Hemogram-Platelets-WBC Differential FS LATEST RESULTS HISTORICAL RESULTS WBC 05/31/22 10:10 1.3 Critical 01/20/22 10.0 RBC 05/31/22 10:10 4.98 01/20/22 3.55 Low Hgb 05/31/22 10:10 13.2 Low 01/20/22 10.0 Low Hct 05/31/22 10:10 39.8 Low 01/20/22 29.1 Low MCV 05/31/22 10:10 80 Low 01/20/22 82 MCH 05/31/22 10:10 26.5 Low 01/20/22 28.3 MCHC 05/31/22 10:10 33.2 01/20/22 34.5 RDW 05/31/22 10:10 14.6 High 01/20/22 13.0 Platelet 05/31/22 10:10 163 01/20/22 253 MPV 05/31/22 10:10 7.8 01/20/22 8.3 Neutrophils % 05/31/22 10:10 60 01/20/22 78 Lymphocytes % 05/31/22 10:10 28 01/20/22 11 Monocytes % 05/31/22 10:10 10 01/20/22 10 Eosinophils % 05/31/22 10:10 0 01/20/22 0 Basophils % 05/31/22 10:10 1 01/20/22 0 Absolute Neutrophil 05/31/22 10:10 0.8 Low 01/20/22 7.8 High Absolute Lymphocyte 05/31/22 10:10 0.4 Low 01/20/22 1.1 Absolute Monocyte 05/31/22 10:10 0.1 01/20/22 1.0 Absolute Eosinophil 05/31/22 10:10 0.0 01/20/22 0.0 Absolute Basophil 05/31/22 10:10 0.0 01/20/22 0.0 Band 05/31/22 10:10 9 Neutrophil 05/31/22 10:10 45 Lymphocyte 05/31/22 10:10 31 Monocyte 05/31/22 10:10 15 RBC Morphology 05/31/22 10:10 Normal Platelet Estimate 05/31/22 10:10 Adequate Platelet Morphology 05/31/22 10:10 Normal Routine Coagulation Studies FS LATEST RESULTS PT 05/31/22 10:10 13.1 INR 05/31/22 10:10 1.11 Routine Serum/Plasma Chemistry Tests FS LATEST RESULTS HISTORICAL RESULTS Sodium SerPl QN 05/31/22 10:10 134 Low 01/20/22 134 Low Potassium SerPl QN 05/31/22 10:10 3.6 01/20/22 4.2 Chloride SerPl QN 05/31/22 10:10 97 Low 01/20/22 102 Carbon Dioxide SerPl QN 05/31/22 10:10 28 01/20/22 25 Anion Gap 05/31/22 10:10 9 01/20/22 7 BUN SerPl QN 05/31/22 10:10 24 High 01/20/22 32 High Creatinine SerPl QN 05/31/22 10:10 1.13 01/20/22 1.22 Estimated GFR (CKD-EPI) 05/31/22 10:10 59 Low 01/20/22 54 Low Estimated GFR (CKD-EPI, no race) 05/31/22 10:10 64 Estimated CRCL (CG) 05/31/22 10:10 52 Low 01/20/22 49 Low Glucose SerPl QN 05/31/22 10:10 140 High 01/20/22 196 High Calcium Total SerPl QN 05/31/22 10:10 8.9 01/20/22 8.8 Alkaline Phos SerPl QN 05/31/22 10:10 63 12/30/21 58 ALT SerPl QN 05/31/22 10:10 35 12/30/21 18 AST SerPl QN 05/31/22 10:10 32 12/30/21 17 Bilirubin Direct SerPl QN 05/31/22 10:10 0.1 Bilirubin Total SerPl QN 05/31/22 10:10 0.4 12/30/21 0.6 Total Protein SerPl QN 05/31/22 10:10 6.7 12/30/21 7.5 Albumin SerPl QN 05/31/22 10:10 4.2 12/30/21 4.5 Magnesium SerPl QN 05/31/22 10:10 1.6 Lipase SerPl QN 05/31/22 10:10 65 High CK SerPl QN 05/31/22 10:10 74 Troponin-I High Sensitivity 05/31/22 10:10 16 BNP Pl QN 05/31/22 10:10 28 Lactate Venous Pl QN 05/31/22 10:10 1.6 Endo Serum/Plasma Tests FS LATEST RESULTS HISTORICAL RESULTS TSH 3rd Gen SerPl QN 05/31/22 10:10 3.920 04/27/21 1.855 Urinalysis FS LATEST RESULTS Color 05/31/22 12:02 Yellow Clarity 05/31/22 12:02 Clear Specific Gravity 05/31/22 12:02 >=1.030 pH 05/31/22 12:02 5.5 Protein 05/31/22 12:02 100 Abnormal Glucose 05/31/22 12:02 Negative Ketones 05/31/22 12:02 Negative Bilirubin 05/31/22 12:02 Negative Hgb Ur 05/31/22 12:02 Negative Nitrite 05/31/22 12:02 Negative Urobilinogen 05/31/22 12:02 Normal Leukocyte Esterase Ur 05/31/22 12:02 Negative WBC 05/31/22 12:02 0-5 RBC 05/31/22 12:02 0-2 Bacteria 05/31/22 12:02 None Squamous Epithelial 05/31/22 12:02 Few Mucous 05/31/22 12:02 Present Hyaline Casts 05/31/22 12:02 0-2 Molecular Diagnostic Tests LATEST RESULTS HISTORICAL RESULTS COVID 19 Specimen Source 05/31/22 09:48 Nasopharyngeal 01/16/22 Nasopharyngeal Coronavirus SARS-CoV2 Rapid 05/31/22 09:48 Not Detected 01/16/22 Not Detected Viral FS LATEST RESULTS Rapid Influenza Method 05/31/22 09:48 PCR - Liat Rapid Influenza A PCR 05/31/22 09:48 Not Detected Rapid Influenza B PCR 05/31/22 09:48 Not Detected Diagnostic Results CT Abd/Pelvis W/IV Contrast 05/31/22 13:12:43 IMPRESSION: Negative for bowel obstruction or acute inflammatory process involving the bowel. No overt malignant findings. Hepatic steatosis. No acute diagnostic abnormality identified involving abdomen or pelvis. Thank you for consulting with Radiology. Healthcare providers wishing to discuss this case further can contact the Emergency Radiology reading room. Electronically Signed by: Signed By: MD ************************************************** XR Chest PA or AP Portable 05/31/22 10:46:22 IMPRESSION: No acute cardiopulmonary findings. Electronically Signed by: Signed By: MD EKG Rate: 73 Rhythm: NSR Axis: Normal Conduction: normal ST segments: No changes T waves: Inversion in Lead III Q waves: no q waves Impression: NSR with T wave inversion in Lead III which is nonspecific Comparison to old: 5/23/20 no changes XAMINATION: US Abdomen Complete DATE: 05/31/2022 17:31 CLINICAL HISTORY: Nausea and vomiting. COMPARISON: 2/14/2020 and CT of the abdomen and pelvis dated 5/31/2022. DISCUSSION: The pancreas is obscured by overlying bowel gas. There is mild diffuse fatty infiltration of the liver. There are calcified granulomata in the spleen. The gallbladder contains a small, nonmobile or shadowing filling defect suggesting a polyp. The wall is not otherwise thickened. No pericholecystic fluid is identified. The common bile duct is within normal limits at 2 to 3 mm diameter. The right and left kidneys measure 9.5 and 10.7 cm in length, respectively. There are several small cortical cysts in each kidney. The kidneys have lobulated contours but there is no evidence of urinary tract calculus or obstruction. The abdominal aorta and inferior vena cava are obscured by overlying bowel gas. IMPRESSION: Nonvisualization of the pancreas, abdominal aorta and inferior vena cava due to overlying bowel gas. Mild hepatic steatosis. Small, nonmobile filling defect in the gallbladder is probably a polyp. The gallbladder is otherwise unremarkable. Small bilateral renal cysts. EXAM: CT Abd/Pelvis W/IV Contrast DATE: 05/31/2022 13:09 INDICATION: Male, age 84 years; Nausea, weight loss, leukopenia, concern for malignancy; Weakness x 1 month, weight loss, Hx prostate ca 2016 TECHNIQUE: Routine axial CT technique was utilized with coronal and sagittal image reconstruction. This facility uses radiation dose reduction techniques including at least one of the following: automated exposure control, dose modulation, and/or iterative reconstruction. Administered: 100 mL of Isovue 370 COMPARISON: May 23, 2020. FINDINGS: No pathologic free fluid within abdomen or pelvis. The bowel appears unobstructed. The appendix is not seen, however no focal inflammatory process is identified involving the cecum or right lower quadrant. Mesenteric vascular system appears patent. No pneumoperitoneum or extraluminal fluid collections. No focal inflammatory process involving the bowel is identified. Hepatic density compatible with mild-moderate steatosis. Gallbladder and pancreas demonstrate no acute findings. Kidneys appear unobstructed and symmetrically perfused. No AAA. No malignant appearing masses or adenopathy. Visualized lung bases demonstrate no consolidation or pleural effusions. IMPRESSION: Negative for bowel obstruction or acute inflammatory process involving the bowel. No overt malignant findings. Hepatic steatosis. No acute diagnostic abnormality identified involving abdomen or pelvis.
Aktuelle Erkrankungen: -
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VAERS 2282944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 61,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 19.04.2022
Beginn: 22.05.2022
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Oropharyngeal pain Pain Pyrexia SARS-CoV-2 antibody test Vaccination failure SARS-CoV-2 test positive

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Physician) from product quality group. The reporter is the patient. A 61-year-old male patient received BNT162b2 (BNT162B2), on 20Dec2020 at 12:00 as dose 1, single (Lot number: EK5730, Expiration Date: 31Mar2021), in left arm, on 10Jan2021 at 10:00 as dose 2, single (Lot number: EK9231, Expiration Date: 30Apr2021), in left arm, on 25Sep2021 at 17:00 as dose 3 (booster), single (Lot number: 301308A, Expiration Date: 28Feb2022), in left arm and on 19Apr2022 at 18:00 as dose 4 (booster), single (Lot number: FK9894, Expiration Date: 30Sep2022) at the age of 61 years, in left arm, all intramuscular for Covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: NIACINAMIDE, start date: Jan2020, stop date: May2022. Past drug history included: Trimethoprim, reaction(s): "Known allergies: Trimethoprim"; Sulfamethoxazole, reaction(s): "Known allergies: Sulfamethoxazole". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), all with onset 22May2022 at 18:00, outcome "not recovered" and all described as "COVID-19 Infection after immunization". It was reported that COVID rebound after Paxlovid treatment. Treated 13May2022-17May2022, felt well until 21May, then developed recurrent symptoms on 22May. Did home antigen test on 25May, which was positive. Product quality group investigation results included: Lot# (CR): EK5730, EK9231 - The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lots EK5730, EK9231 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EK5730, fill lot EK3313, and the formulated drug product lot EK3312. The final scope included the reported finished goods lot EK9231, fill lot EK9229, and the formulated drug product lot EK9226. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Lot# (CR): 30130BA - The complaint for a Lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot 30130BA was investigated. The investigation included reviewing incoming quality and manufacturing batch records, deviation investigations, an analysis of the complaint history for the reported lot and product type and final release assay testing. This product is received as preformulated bulk, and is manufactured, labeled and packaged by Pfizer (site name withheld). The final scope was determined to be lot 30130BA. No quality issues were identified during the investigation. There is no impact on product quality. An RA was not issued for the complaint. No regulatory notification or SQRTs/AQRTs were held as a result of this complaint. The complaint condition of lack of effect was not confirmed, therefore the root cause cannot be attributed to manufacture or vendor processes. The root cause was not determined to be manufacture or vendor related as incoming quality component testing and the results of all analytical tests performed at the time of lot release confirmed that the batch met potency specifications. No corrective or preventative actions are required as the complaint condition was not determined to be manufacture or vendor related and there are quality systems in place to detect defects prior any lot being released to the market. No further investigation required. Lot# (CR): FK9894 -The complaint for PFIZER BIONTECH COVID-19 VACCINE was investigated. The investigation included reviewing the involved batch records, deviation investigation, an analysis of the complaint history for the reported lot and product type. The final scope was determined to be the associated lot(s) of the reported lot FK9894. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality, regulatory, validation and stability. Regulatory Authority concludes that the reported defect is not representative of the quality of the batch and the batch remains acceptable. The RA process determined that no regulatory notification was required. The reported defect could not be confirmed. No root cause or CAPA were identified as the complaint was not confirmed. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 antibody test: (unspecified date) Unknown result, notes: COVID rebound after Paxlovid treatment; (25May2022) Positive, notes: home antigen test. Therapeutic measures were taken as a result of Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Infection; Result Unstructured Data: Test Result: Unknown result; Comments: COVID rebound after Paxlovid treatment; Test Date: 20220525; Test Name: COVID-19 Infection; Result Unstructured Data: Test Result: Positive; Comments: home antigen test.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: NIACINAMIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2282944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 61,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 19.04.2022
Beginn: 22.05.2022
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Oropharyngeal pain Pain Pyrexia SARS-CoV-2 antibody test Vaccination failure SARS-CoV-2 test positive

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Physician) from product quality group. The reporter is the patient. A 61-year-old male patient received BNT162b2 (BNT162B2), on 20Dec2020 at 12:00 as dose 1, single (Lot number: EK5730, Expiration Date: 31Mar2021), in left arm, on 10Jan2021 at 10:00 as dose 2, single (Lot number: EK9231, Expiration Date: 30Apr2021), in left arm, on 25Sep2021 at 17:00 as dose 3 (booster), single (Lot number: 301308A, Expiration Date: 28Feb2022), in left arm and on 19Apr2022 at 18:00 as dose 4 (booster), single (Lot number: FK9894, Expiration Date: 30Sep2022) at the age of 61 years, in left arm, all intramuscular for Covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: NIACINAMIDE, start date: Jan2020, stop date: May2022. Past drug history included: Trimethoprim, reaction(s): "Known allergies: Trimethoprim"; Sulfamethoxazole, reaction(s): "Known allergies: Sulfamethoxazole". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), all with onset 22May2022 at 18:00, outcome "not recovered" and all described as "COVID-19 Infection after immunization". It was reported that COVID rebound after Paxlovid treatment. Treated 13May2022-17May2022, felt well until 21May, then developed recurrent symptoms on 22May. Did home antigen test on 25May, which was positive. Product quality group investigation results included: Lot# (CR): EK5730, EK9231 - The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lots EK5730, EK9231 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EK5730, fill lot EK3313, and the formulated drug product lot EK3312. The final scope included the reported finished goods lot EK9231, fill lot EK9229, and the formulated drug product lot EK9226. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Lot# (CR): 30130BA - The complaint for a Lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot 30130BA was investigated. The investigation included reviewing incoming quality and manufacturing batch records, deviation investigations, an analysis of the complaint history for the reported lot and product type and final release assay testing. This product is received as preformulated bulk, and is manufactured, labeled and packaged by Pfizer (site name withheld). The final scope was determined to be lot 30130BA. No quality issues were identified during the investigation. There is no impact on product quality. An RA was not issued for the complaint. No regulatory notification or SQRTs/AQRTs were held as a result of this complaint. The complaint condition of lack of effect was not confirmed, therefore the root cause cannot be attributed to manufacture or vendor processes. The root cause was not determined to be manufacture or vendor related as incoming quality component testing and the results of all analytical tests performed at the time of lot release confirmed that the batch met potency specifications. No corrective or preventative actions are required as the complaint condition was not determined to be manufacture or vendor related and there are quality systems in place to detect defects prior any lot being released to the market. No further investigation required. Lot# (CR): FK9894 -The complaint for PFIZER BIONTECH COVID-19 VACCINE was investigated. The investigation included reviewing the involved batch records, deviation investigation, an analysis of the complaint history for the reported lot and product type. The final scope was determined to be the associated lot(s) of the reported lot FK9894. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality, regulatory, validation and stability. Regulatory Authority concludes that the reported defect is not representative of the quality of the batch and the batch remains acceptable. The RA process determined that no regulatory notification was required. The reported defect could not be confirmed. No root cause or CAPA were identified as the complaint was not confirmed. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 antibody test: (unspecified date) Unknown result, notes: COVID rebound after Paxlovid treatment; (25May2022) Positive, notes: home antigen test. Therapeutic measures were taken as a result of Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Infection; Result Unstructured Data: Test Result: Unknown result; Comments: COVID rebound after Paxlovid treatment; Test Date: 20220525; Test Name: COVID-19 Infection; Result Unstructured Data: Test Result: Positive; Comments: home antigen test.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: NIACINAMIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2305582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 01.06.2022
Impfdatum: 29.04.2022
Beginn: 22.05.2022
Tage bis Beginn: 23,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Lacrimation increased Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

Sunday May 22, 2022: sore throat, temp 98.2F Monday May 23: sore throat, temp 98.9F, home covid-19 test positive Tuesday May 24: sore throat, sneezing, runny nose, congestion, deep cough, temp 99.8F Wednesday May 25: deep cough, runny nose, watery eyes, sore throat, temp 99.2F, video Dr appointment, Respiratory Clinic appointment, positive covid test, started on Paxlovid for 5 days Getting better daily till feel much better since Tuesday May 31.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Covid-19 test: May 25, 2022
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, High cholesterol, insomnia
Andere Medikamente: Omeprazole, Lovastatin, Amlodipine, Montelukast, Zyrtec, Ambien, MVI, Turmeric capsule, Calcium, Fosamax
Allergien: none
Vorherige Impfungen: -

VAERS 2305320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OR
Alter: 65,0
Geschlecht: F
Eingang: 01.06.2022
Impfdatum: 19.05.2022
Beginn: 19.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Asthma Chills Coccydynia Decreased appetite Fatigue Headache Lymphadenopathy Malaise Myalgia Nausea Pain in extremity Pyrexia Retching Skin warm Sleep disorder

Symptomtext

She got her vaccine, had a sore arm immediately. She started noticing that she was very very tired about 6 hours later. She developed muscle and joint pain, terrible joint pain to the point that her tailbone hurt. She had severe headache, chills that her fingertips were warm, but she was scrunched up and her teeth were chattering. At one point she realized that she had a fever, which came on during the night and lasted through the night. She did not sleep but realized in the morning the fever had subsided. She had nausea, swollen lymph nodes underneath her ears. She didn't feel like eating, was having dry heaves, and was unable to take her medicines due to be so sick at night. She had never had chills like that ever. She is now fine, but does seem to have a little more asthma components, which has been acting up more than usual. She has been using her medications. The symptoms continued for several days and lasted for about 48-72 hours. She did have some reactions with the other vaccines, the 1st booster had some of the symptoms, but they were much milder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Very bad cold 15 days symptomatic and then asymptomatic a week prior to vaccine.
Vorgeschichte: Arthritis, high blood pressure, acid reflux, asthma.
Andere Medikamente: Losartan, Deloxitine, Anastrozole, Gabapentin, Pantoprazole, Acetamenophen, calcium, zinc, one a day vitamin multivitamin, B-complex vitamin. Alvesco inhaler.
Allergien: Cephalexin.
Vorherige Impfungen: -

VAERS 2305218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 01.06.2022
Impfdatum: 29.04.2022
Beginn: 25.05.2022
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Headache Influenza virus test negative Malaise Nasal congestion Ocular discomfort Oropharyngeal pain Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive Streptococcus test negative Urine analysis normal

Symptomtext

I started with a headache, and I took some Tylenol and it didn?t seem to help. And I thought that maybe I have a UTI or a sore throat or sinus infection because I started with a sore throat as well and it was very sore. The following day it was still there but it wasn?t as prominent. Around 7-8PM, since I wasn?t feeling well. I did a self-rapid test and it came back negative. Between 9-10PM I took my temperature, and it was 100.4. I told my sister I would go to the doctor the next day because I didn?t feel well. I think I took Tylenol or ibuprofen that night. Everything hurt and I was aching. I had a stuffy nose and the reason I thought I might have had a sinus infection was because I had pressure behind my eyes and along my right upper eye brow. In the morning, we left home at about 7:30AM to get to the doctor?s office. They didn?t open until 8am. We had to wait to see the NP. They examined my vitals and said everything was fine. They tested my urine. I was placed into a room where I could be seen by the NP. She went ahead and ordered a strep test and flu test and they all came back negative as well as the urine. I told her I tested myself with a rapid test at home and it was also negative. She did a PCR test and prescribed medication and I was back on my way home. Since then, it started with a runny nose, slightest cough. The following day which was Friday, the doctor?s office called and said I tested positive for COVID. We did a telehealth follow up with another NP and she went ahead and ordered other medications. The first time was the Augmentin and Singulair. For the 2nd visit, she ordered a nebulizer, Paxlovid and the albuterol solution and an albuterol inhaler. I did speak with someone from the local department of health so my 6-day isolation ended yesterday but I?m continuing to isolate until the 10 days. On my own, I started taking Zinc, Vitamin C, Vitamin D, and Vitamin B Complex to help during this time. Still recovering at this time, slightest cough, still a little tired. a little congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 05/25/2022 - At Home COVID Test - Negative 05/26/2022 - Strep Test - Negative 05/26/2022 - Flu Test - Negative 05/26/2022 - Urine sample - Negative 05/26/2022 - PCR COVID TEST - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes High blood pressure Hypothyroidism Cholesterol Asthma Hx of Anxiety Hx of bladder tumor Hx of total hysterectomy and ovaries Hx of uterine tumor - benign Hx of Drusens
Andere Medikamente: Synthroid 125mcg daily Metformin 1000mg twice daily Gemfibrozil 600mg twice daily Hydrochlorothiazide with Lisinopril 20-25mg daily Vitamin D 50,000iu once weekly on Fridays
Allergien: Latex - blistering, redness, itchiness
Vorherige Impfungen: 3rd & 4th Pfizer Vaccines - Finger contractures - painful and joint discomfort all over body. Cold sores on lips

VAERS 2305063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 66,0
Geschlecht: F
Eingang: 01.06.2022
Impfdatum: 06.05.2022
Beginn: 24.05.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Diarrhoea Discomfort Feeling abnormal Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Somnolence Visual impairment

Symptomtext

I did not have an adverse reaction to the vaccine but I did contract Covid 19. I test positive 05/24/2022. I had fever, diarrhea, bad headache, sore throat, brain fog and slept a lot. I took Tylenol and cough drops to help with discomfort. At the time of this report, I'm feeling a little better. I continue to have brain fog, weird stuff with my vision and lingering cough. I had telehealth visit with my doctor who prescribed the anti viral drug but I did not take it. By the time I got my hands on the prescription, I felt like I took a turn for the better and did not take it.

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Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Home Covid 19 test
Aktuelle Erkrankungen: Kidney damage to cancer treatment
Vorgeschichte: Kidney damage to cancer treatment
Andere Medikamente: Multi vitamin Adderall
Allergien: Ciprofloxacin
Vorherige Impfungen: My previous Covid vaccines was Moderna and I felt more flu like symptoms with each one.

VAERS 2303816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 15.04.2022
Beginn: 23.05.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Nasal congestion Oropharyngeal pain SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

tested positive for COVID-19 on 5-23-22 was traveling and sightseeing symptoms started with sore throat and fatigue, then nasal congestion and intermittent cough started treatment with Paxlovid on 5-27-22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: PCR tests on 5-22-22 negative Sofia Antigen test on 5-23-22 positive Sofia Antigen re-test on 5-30-22 positive
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: CoQ10 Red Rice Yeast
Allergien: Ampicillin
Vorherige Impfungen: -

VAERS 2303622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 20,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 31.05.2022
Beginn: 31.05.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dysstasia Hypersensitivity Lip pain Lip pruritus Lip swelling Nausea Skin tightness

Symptomtext

Patient brought into Covid Observation area after reporting dizziness and nausea 15 minutes after receiving 2nd Pfizer vaccination. Patient also reports that her "lips are hurting" 7/10, denies that lips feel tight, itchy or swollen. Lips appear to be slightly swollen. Denies experiencing any of these symptoms with 1st Pfizer vaccination. Alert and oriented, speaking in complete sentences. Patient also denies any swelling, tightness or itchiness to throat. Denies difficulty breathing or swallowing. Patient states she has not had anything to eat this morning, provided with juice. 11:35 am- VS: BP 118/79, HR 77, RR 20, 02 SATs 97% RA Patient reports that she had an allergic reaction to something that she ate last night (smothered chicken dish). States that she felt "lip pain and throat itching". EpiPen administered by her mother. States she did not go to ED last night because symptoms resolved with the Epi. 11:45 am- VS: BP 106/79, HR 92, RR 20, 02 SATs 97% RA. 11:46 am- Call placed to on call provider, Dr., informed of patient symptoms above and allergic reaction that she had last night. Verbal order per Dr. to give patient Zyrtec 10 mg orally x 1 now, continue monitoring vital signs for additional 30 Minutes. 11:48 am- Zyrtec 10 mg ODT x1 given to patient as ordered. 12-noon- Patient states she is feeling better and lip pain is improving. 12:11- Patient reports lip pain is completely resolved; No visible swelling noted to lips. Continues to have nausea and dizziness, but improving. 12:22pm- VS: BP 128/73, HR 67, RR 20, 02 sats 98% RA 12:25- Patient assisted to standing position, ambulated a few steps. Denies feeling lightheaded or dizzy with position change or ambulation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: ASTHMA, UNSPECIFIED CHLAMYDIA INFECTION OF GENITOURINARY TRACT CONTRACEPTIVE METHOD SURVEILLANCE DEPRESSION, UNSPECIFIED MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE W ASSOCIATED FEATURES MEDI-CAL GMC CARE COORDINATION OBESITY, BMI 35-39.9, ADULT POSTTRAUMATIC STRESS DISORDER VACCINATION RECORDS UNAVAILABLE
Vorgeschichte: ASTHMA, UNSPECIFIED CHLAMYDIA INFECTION OF GENITOURINARY TRACT CONTRACEPTIVE METHOD SURVEILLANCE DEPRESSION, UNSPECIFIED MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE W ASSOCIATED FEATURES MEDI-CAL GMC CARE COORDINATION OBESITY, BMI 35-39.9, ADULT POSTTRAUMATIC STRESS DISORDER VACCINATION RECORDS UNAVAILABLE
Andere Medikamente: HYDROcodone-Acetaminophen (NORCO) 5-325 mg Oral Tab Ondansetron (ONDANSETRON) 4 mg Oral Rap Dis Tab Cetirizine (ZyrTEC) 10 mg Oral Tab EPINEPHrine (ADRENACLICK/EPIPEN) 0.3 mg/0.3 mL Inj AutoInjector QUEtiapine (SEROquel) 25 mg Oral Tab
Allergien: Pcn Class [Penicillins Class], Norco [Hydrocodone-acetaminophen], Oxycodone, Tylenol [Acetaminophen
Vorherige Impfungen: -

VAERS 2303469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 43,0
Geschlecht: M
Eingang: 31.05.2022
Impfdatum: 27.04.2022
Beginn: 23.05.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Feeling abnormal Malaise SARS-CoV-2 test positive

Symptomtext

My wife and I drove back from a vacation on 05/23. We both felt a bit tired and out of it. By Tuesday on 5/24, we were still not feeling well so I took an at home Covid test and mine was negative. We went that day to the local county health department and took a PCR test. We received positive results the next day 5/25. I called my doctor's office who advised that I just keep an eye on my respiratory symptoms. By the weekend, I was beginning to feel normal again. I'm still experiencing a bit of cough and fatigue but am feeling mostly better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home Covid test negative 5/25. PCR Covid test positive 5/25.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2303432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 27.05.2022
Beginn: 27.05.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness

Symptomtext

Patient sitting in observation are a and alerted staff she was feeling lightheaded. Vital signs taken: B/P 126/86 P 74 RR 18 O2 98% Patient given a bottle of water. Offered to recline patient but she stated she was okay sitting. Monitored patient for additional 15 minutes. Patient stated she was feeling better. Patient declined offer to repeat vital signs prior to departure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 2298720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: IL
Alter: 50,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 21.05.2022
Beginn: 24.05.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Eye oedema Herpes zoster Rash

Symptomtext

Diagnosed with shingles following eye edema and rash on face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2298654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: IL
Alter: 51,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 09.04.2022
Beginn: 10.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Cough Fatigue Oropharyngeal pain Pain

Symptomtext

The 1st day after I received my 2nd booster shot (4th shot of COVID-19 vaccine), I experienced a sore throat chills, body aches and fatigue. On the 2nd day after the vaccine I began to have a cough on top of all the other symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: I went to my primary care doctor on the following Thursday (April 14, 2022) who prescribed to me Zithromax.
Aktuelle Erkrankungen: NONE
Vorgeschichte: High blood pressure, overactive bladder
Andere Medikamente: Lsinopril/Hydrochlorided 10-12.5 mg - once a day and Oxybutynin Chlorided 10mg - once a day.
Allergien: NONE
Vorherige Impfungen: -

VAERS 2296315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: PR
Alter: 50,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 23.04.2022
Beginn: 13.05.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Nasal congestion Oropharyngeal pain Pain in extremity Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

COVID-19 case: On 05/13/2022 started with sore throat in the morning and felt very fatigued by the evening. The following day by the afternoon felt pain in my calves, hands and experienced a terrible headache. Then I had nasal congestion and allergies and low grade fever. On 05/16/2022 I took a covid test, I also contacted my doctor and had lab work. My covid test resulted positive. If I walk long distances I feel very fatigue and sore throat and have congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid test 05/16/2022; positive, lab work.
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: Acetaminophen
Allergien: Calamari
Vorherige Impfungen: -

VAERS 2295954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OR
Alter: 71,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 28.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Decreased appetite Dizziness Feeling abnormal Headache Pain Vomiting

Symptomtext

Head start hurting; Start getting achy all over; Tried to go to sleep I would take short naps but I felt so achy I would wake up; Start feeling bad; Got really from bad to worse/I am not feeling a 100%; Not have an appetite; Got out of the tub I was so dizzy; Sat on the side of the tub, I do not feel like I could stand without falling; Start throwing up the water; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 28Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 71 years for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing), notes: High blood pressure Consumer stated, "I do have high blood pressure but I went to the doctor and my blood pressure is normal.". Concomitant medication(s) included: HYDROCHLOROTHIAZID taken for hypertension. Vaccination history included: Covid-19 vaccine (Dose:1, Unknown manufacture), for COVID-19 Immunization; Covid-19 vaccine (Dose:2, Unknown manufacture), for COVID-19 Immunization; Covid-19 vaccine (Dose:3, Unknown manufacture, Side effects were worse than the second and the first booster; Side effects lasted longer than before/In the past when I had a side effect, I would be sick for the following day), for COVID-19 Immunization, reaction(s): "Side effects were worse than the second and the first booster; Side effects lasted longer than before/In the past when I had a side effect, I would be sick for the following day". The following information was reported: DIZZINESS (non-serious) with onset 28Apr2022, outcome "unknown", described as "Got out of the tub I was so dizzy; Sat on the side of the tub, I do not feel like I could stand without falling"; HEADACHE (non-serious) with onset 28Apr2022, outcome "unknown", described as "Head start hurting"; DECREASED APPETITE (non-serious) with onset 28Apr2022, outcome "unknown", described as "Not have an appetite"; FEELING ABNORMAL (non-serious) with onset 28Apr2022, outcome "unknown", described as "Start feeling bad; Got really from bad to worse/I am not feeling a 100%"; PAIN (non-serious) with onset 28Apr2022, outcome "unknown", described as "Start getting achy all over; Tried to go to sleep I would take short naps but I felt so achy I would wake up"; VOMITING (non-serious) with onset 28Apr2022, outcome "unknown", described as "Start throwing up the water". Therapeutic measures were taken as a result of headache, pain, feeling abnormal, decreased appetite, dizziness, vomiting. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high.
Andere Medikamente: HYDROCHLOROTHIAZID.
Allergien: -
Vorherige Impfungen: -

VAERS 2294562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: HI
Alter: 73,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 12.04.2022
Beginn: 20.05.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

On May 20, 2022 in the middle of the night, I had a sore throat. I gargled some salt water to alleviate that. The next morning, I took an at home covid test. It showed to be positive so then I went to a clinic and took another covid test. It was positive. I was advised to quarantine. I had some congestion and a couple of sneezing. I had a mild cold nothing severe. I was prescribed Paxlovid. I would say I am 90% recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: At Home Covid Test- positive (5/21/2022), Covid Test- positive
Aktuelle Erkrankungen: none
Vorgeschichte: Nasal polyps (2003), Macular Degeneration (AMD) in my right eye
Andere Medikamente: Brimonidine, Budesonide Inhalation Suspension, 2 or 3 times a week, Atorvastatin, Eye Vitamins
Allergien: Aspirin, Motrin, NSAIDs
Vorherige Impfungen: -

VAERS 2294560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 22.02.2022
Beginn: 14.03.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Dysmenorrhoea Haemorrhage Menstruation irregular Muscle spasms

Symptomtext

Every since I got the vaccine my cycles has been irregular periods. It is coming every two weeks and I cramps more now then before. I hurts in my back like muscles spams. I saw a difference with the dose 2 vaccine. But it got better and now it has started all over again. I had to get on birth control to try and control it but it isn't working. I have to wait 3 months to get it switch to another birth control and that will be in June 2022. So I have to deal with all the bleeding and pain until then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: PCOS, Chron's and Migraines.
Andere Medikamente: Remicade infusion every 8 weeks, Omeprazole 20mg, Norethindrone, Omega 3, Primrose, Vitamin D, Holy Basil, Apple Cider Vinegar, Vitamin A, Muti-Vitamin for women and Tylenol Arthritis, Probiotics and Vitamin E.
Allergien: Sumatriptan & Rizatriptan.
Vorherige Impfungen: -

VAERS 2294545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: OH
Alter: 38,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 25.04.2022
Beginn: 04.05.2022
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dizziness Laboratory test Lethargy Pain in extremity Scan normal Vertigo

Symptomtext

pt stated after she got the vaccine her arm was sore and she became lethargic. She becomes lightheaded and dizzy when trying to do normal activities. The dizziness was intermittent . She became concerned so spoke to the pharmacist about it. They told her to contact her PCP. She had a televisit with PCP and was told it was safe to take second dose. She received her 2nd dose on 5/18/22 which is the same lot number. After 2nd dose she developed these same symptoms immediately except they were back to back continuously. She had to go to the ER where they ran test but could not find anything. She was given motion sickness medicine and to FU w/ PCP. She states it feels like vertigo and she is still experiencing these symptoms at this time. Patient does not wish to disclose her medical records w/ CDC.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: head scan labs
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma seasonal allergies
Andere Medikamente: none
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2294482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 19.04.2022
Beginn: 22.05.2022
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dysgeusia Exposure to SARS-CoV-2 Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

05/22//2022 I tested positive, but no symptoms. Then around 5:00 or 6:00 that evening, I began having aches, runny nose, sneezing, a little bit of fever. The next morning, I ached, but was breathing okay. I called my doctor because my wife had COVID and was prescribed Paxlovid. I took the first dose on 5/23/2022. By the next morning, all the aches were gone. I still have the metallic taste. I still feel weak and sleep a lot. I am feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: COVID, positive
Aktuelle Erkrankungen: Flu, one month before
Vorgeschichte: Valve blockage , Pace Maker, Congestive Heart Failure
Andere Medikamente: Multi Vitamin, Atorvastatin, Mesalamine, Carvedilol, Losartan, Claritin, Vitamin D3
Allergien: Dog and cat hair, Some environmental
Vorherige Impfungen: -

VAERS 2294467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MD
Alter: 64,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 26.04.2022
Beginn: 19.05.2022
Tage bis Beginn: 23,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Oropharyngeal pain Paranasal sinus hypersecretion Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On 05/19/2022, I woke up with a sore throat, congestion, sinus drainage and fatigue. I gave myself a home test that came back positive. 05/20/2022 - I had a confirmation test at the local pharmacy, a rapid antigen test just to confirm it was positive. I spoke to my doctor, and he prescribed Paxlovid, and it worked great. On 05/20/2022, I had to take a few a naps because I was so tired. Right now, I am feeling normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home test on 05/19/2022 - positive, Rapid antigen on 05/20/2022 positive
Aktuelle Erkrankungen: no
Vorgeschichte: recovered from prostate cancer 09/14/2021, in remission
Andere Medikamente: Lipitor 40mg, Tadalafil 5mg, probiotic, Glucosamine 1500mg, Vitamin D
Allergien: no
Vorherige Impfungen: -

VAERS 2294411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

mild

Staat: MI
Alter: 5,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 20.05.2022
Beginn: 20.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Contusion Fatigue Headache Pain in extremity

Symptomtext

Pt experienced fatigue/headaches/sore arm(brusing)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: Allergic to penicillins
Vorherige Impfungen: -

VAERS 2283075

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Headache Visual impairment Vision blurred

Symptomtext

blurred and fuzzy vision; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received BNT162b2 (BNT162B2), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VISION BLURRED (non-serious), outcome "unknown", described as "blurred and fuzzy vision". Additional information: Reporter stated that she had called about the Pfizer Covid vaccine, adult. It was her first vaccine. She had blurred and fuzzy vision. She agrees to complete report. Due to sound quality, she agrees for agent to call her back, to finish report. Two unsuccessful outbound calls made by agent, and voicemail obtained. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 09.05.2022
Beginn: 13.05.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anticoagulant therapy COVID-19 Chills Cough Dizziness Ear pain Fluid retention Oropharyngeal pain SARS-CoV-2 test positive Thirst Vaccine breakthrough infection

Symptomtext

COVID BREAKTHROUGH CASE************** Around May 13, 2022 I set up a video appointment I was having symptoms of allergies or so I thought. Sore throat; Thirsty; Chills; Lightheaded; Earache; Cough; Lots of Fluid buildup. On May 17, 2022 tested positive for Covid 19 with an at home test. Mostly like a allergies. I thought it was due to the high pollen count, but it was COVID. After the video visit my doctor order my prescriptions. Paxlovid I took medication as prescribed. Zithromax 250mg; methylprednisolone 4mg; I could take ibuprofen; Eliquis 5mg. These were the only medications that I was allowed to take because some interact with one another in many different ways.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID
Aktuelle Erkrankungen: -
Vorgeschichte: A fib; Chronic Bronchitis
Andere Medikamente: Ibuprofen 800mg Lyrica 50mg Baclofen 10mg Xyzal 5mg Propol 50mg Tylenol Vitamin D,C,B12 D3,cranberry prebiotic turmeric fish oil Reatha
Allergien: -
Vorherige Impfungen: Flu -my arm blew up for about 5 days.

VAERS 2292858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: AK
Alter: 50,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 18.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Autoimmune disorder Injection site pain

Symptomtext

Soreness at injection site, flared up auto immune disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Connected tissue disorder; mitral atrial valve prolapse; loose valve in stomach
Andere Medikamente: Plaquenil; Singulair; albuterol; Symbicort; Zyrtec; vitamin D; vitamin B; fiber; multivitamin
Allergien: Toradol; inapsine; budesonide; latex; sulfa drugs; dairy; immune health system foods
Vorherige Impfungen: -

VAERS 2292789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

mild

Staat: NC
Alter: 52,0
Geschlecht: M
Eingang: 24.05.2022
Impfdatum: 15.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site erythema Injection site pain Injection site swelling

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2292676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 08.04.2022
Beginn: 17.05.2022
Tage bis Beginn: 39,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Exposure to SARS-CoV-2 Eye pruritus Headache Malaise Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I received my 2nd booster shot on 04/08/2022 and my COVID symptoms started on 05/17/2022. I had runny nose, cough, along with headache and itchy eyes. It felt like allergies. On 05/18/2022 my boss and his wife was positive which made me think to do a COVID test. I went to the urgent care to get COVID test and on 05/19/2022 I was told by the urgent care that I was positive. On the 05/20/2022 I had a Telehealth call with my doctor who prescribed me PAXLOVID for 5 days. My doctor also told me to quarantine for 5 days and wear masks for 5 more days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pruritus
Hospital-Tage: -
Labordaten: urgent care COVID test
Aktuelle Erkrankungen: I had neck surgery on 02/23/2022.
Vorgeschichte: Likepichimus; primary biliary cholangitis; rheumatoid arthritis
Andere Medikamente: ALDACTONE; omeprazole; pentoxifylline; PLAQUENIL; URSO; REMICADE; NORCO; Petra zone
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2290943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 27.04.2022
Beginn: 13.05.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Full blood count Gait disturbance Hyperhidrosis Vertigo Vomiting

Symptomtext

May 13th I woke up to a severe attack of vertigo. I was vomiting, sweating, and I had trouble walking. After 4 days of minimal change that is when I went to see my physician's assistant. My symptoms are moderate now, I am still having dizzy spells but they are steadily improving. My physician's assistant prescribed me meclizine 25mg three times a day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Full blood panel
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis; Fibromyalgia
Andere Medikamente: Atenolol; omeprazole; vitamin D3; furosemide
Allergien: Penicillin; ACE inhibitors; ibuprofen; erythromycin; clindamycin; sulfa; Bactrim; levofloxacin
Vorherige Impfungen: -

VAERS 2290832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 15.04.2022
Beginn: 14.05.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Fatigue Myalgia Ocular discomfort Oropharyngeal pain SARS-CoV-2 test positive Sinus headache Vaccine breakthrough infection

Symptomtext

COVID-19 Breakthrough. I woke up in the middle of the night thinking it was my allergies. I had scratchy eyes, congestion, sore throat, and, sinus headache. I didn't have a fever or chills. I am so tired, I've been having a lot of fatigue. I've also been experiencing muscle aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol Depression Acid Reflux Nerve Pain in Right Arm
Andere Medikamente: Sertraline Omeprazole Pregabalin Slow Release Iron Rosuvastatin Diclofenac Foder
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2290700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WI
Alter: 74,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 20.04.2022
Beginn: 15.05.2022
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ageusia Anosmia COVID-19 Cough Ear congestion Fatigue Headache Pain SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case of Covid 05/15/2022 I started with sx of headaches, loss of taste and smell, stuffiness, my ears were plugged up , cough, aches and a lot of fatigue. It got better on Saturday it got pretty good and it's better everyday and I think I coughed once today. I did not have side effects from any of the vaccinations I got.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 05/19/2022 - Covid Test PCR - positive
Aktuelle Erkrankungen: no
Vorgeschichte: HBP, prostate
Andere Medikamente: lisinopril, finasteride, Tamsulosin
Allergien: no
Vorherige Impfungen: -

VAERS 2290597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: VA
Alter: 57,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 09.04.2022
Beginn: 19.05.2022
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Feeling abnormal Insomnia Nasal congestion Oropharyngeal pain Pain Paranasal sinus discomfort Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Somnolence

Symptomtext

I woke up with a runny nose, stuffed up nose, congested, very mild sore throat with a mild cough. I felt groggy and decided to take a COVID-19 home test. I was not waking up like a normally do. The results were positive and I made a telehealth appointment with my Dr. and he prescribed Paxlovid and I am on my last day of that medication. Thursday night was the worst, I felt ok for most of the day but when evening came around that evening the sinus pressure was bad and I had a hard time sleeping and the body aches had come on. Friday, I had the same symptoms and was tired most of the day. Today I feel pretty much normal. The Dr. said I could leave the house today but not without a mask. I have not taken another home test but plan on doing one tomorrow or Wednesday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Home Test Positive 5/19/22
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia, Osteoarthritis, Hypertension
Andere Medikamente: Losartan, HTZ, Pravastatin, Voltaren, Multivitamin, Fish oil with Omega 3, Glucosamine
Allergien: Penicillin, Ampicillin
Vorherige Impfungen: Polio Vaccine, Age 4, unknown brand, arm turned purple per participant's mother.

VAERS 2290523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: WA
Alter: 53,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 30.01.2022
Beginn: 04.05.2022
Tage bis Beginn: 94,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Bronchitis COVID-19 Cough Decreased appetite Fatigue Headache Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Somnolence Taste disorder

Symptomtext

05/04/2022, I got real achy, had a super bad headache, felt like I wanted to suddenly take a nap, and I had no appetite. I tested negative for COVID. The next morning, I had a low-grade fever, congestion, bad headache and a cough. I spent the next 2 days in bed because I had no energy. I started to feel better pretty quickly. All day on 5/6/2022, everything I ate tasted funny. I tested positive for COVID. My taste resolved. Fever went away on 5/7/2022, but I still had congestion and cough. Then I continued to feel tired, and my cough got worse. I called my doctor on 5/13/2022 and let them know what was going on. They had me go to Urgent Care and I was diagnosed with bronchitis. I was prescribed a 5-day z pack. I am feeling better now, about 95%, but still have a cough and still feel tired, but not as tired as I have felt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID, Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Depression
Andere Medikamente: Citalopram, Wellbutrin, Omega 3, Probiotic
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2290511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: LA
Alter: 50,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 07.04.2022
Beginn: 19.05.2022
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Chills Cough Fatigue Feeling abnormal Insomnia Malaise Nasopharyngitis Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I was at a conference away from home. I flew home on Thursday 5/19. When I returned home that afternoon, I felt like I was coming down with a cold. By midday on 5/20 I was feeling worse, but was testing negative on an at home Covid test. I went for a PCR test and the positive results came back Sunday. But by Friday night I was having a lot of symptoms like fever, chills, achiness, sleeplessness, and cough. That Saturday morning, I called an urgent care who prescribed PAXLOVID which I began taking that morning. I have still been experiencing symptoms, but they have been improving. Other than some fatigue, cough, and achiness, I feel as though I am getting better and am overall out of the woods but I still have a few days left of my antiviral to take.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid test at home, negative 5/19. Covid test PCR, positive 5/20. Covid test at home, positive 5/20.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Multivitamin; lisinopril; fish oil; vitamin D3; baby aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2290367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 13.04.2022
Beginn: 05.05.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Malaise Oropharyngeal pain Productive cough Pyrexia SARS-CoV-2 test positive Throat irritation Upper-airway cough syndrome

Symptomtext

Got Covid symptoms starting on May 5, 2022. Severe burning sore throat, low grade fever, post nasal drip, phlegm, extreme fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home test: positive result on May 5, 2022 Another Home Test: positive on May 7, 2022
Aktuelle Erkrankungen: None
Vorgeschichte: Autoimmune illness (rheumatoid arthritis)
Andere Medikamente: Calcium and Vit D3 tablets
Allergien: None known
Vorherige Impfungen: -

VAERS 2287990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: NY
Alter: 54,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain X-ray normal

Symptomtext

since I got the vacine I'm in pain every single days it's getting worse. I think they gave me the vacine the wrong way from february 17th to now . I can explain the way I feel but it's very very painful.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: I went to the pharmacy to explain that the Pharmacist told me to contact my Doctor. I called my doctor for appt he sent me to the laboratory for an x ray he told me it's negatif I don't remember the date
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: n/a
Allergien: no
Vorherige Impfungen: -

VAERS 2287190

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 14.04.2022
Beginn: 15.05.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Laboratory test abnormal Respiratory tract congestion Throat irritation

Symptomtext

Started feeling fatigued on 5/15 and congestion. Tested positive on 5/16. No fever but scratchy throat. Contact NP on 5/17 and started Paxlovid. Symptoms have rapidly improved since then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; hypertension; high cholesterol
Andere Medikamente: Crestor; Cozaar; hydrochlorothiazide; metformin
Allergien: None
Vorherige Impfungen: -

VAERS 2265868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: MA
Alter: 65,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 21.04.2022
Beginn: 30.04.2022
Tage bis Beginn: 9,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature increased COVID-19 Cough Exposure to SARS-CoV-2 Eye pain SARS-CoV-2 test Vaccination failure Headache Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive Throat irritation

Symptomtext

positive for COVID on 30Apr; positive for COVID on 30Apr; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient received BNT162b2 (BNT162B2), on 18Dec2020 as dose 1, single (Lot number: EK5730), on 08Jan2021 as dose 2, single (Lot number: EK9231), on 08Oct2021 as dose 3 (booster), single (Lot number: FF2580) and on 21Apr2022 as dose 4 (booster), single (Lot number: FK9894) at the age of 65 years for covid-19 immunisation; pneumococcal vaccine conj (PNEUMOCOCCAL CONJUGATE VACCINE), on 25Apr2022 as dose number unknown, single (Batch/Lot number: unknown). The patient's relevant medical history included: "Breast cancer", start date: 2015 (unspecified if ongoing), notes: Breast cancer; "Surgery", start date: 2020 (unspecified if ongoing), notes: I had surgery and radiation and in 2020 I had in the other breast, had surgery and radiation but otherwise no medical condition; "Radiation", start date: 2020 (unspecified if ongoing), notes: I had surgery and radiation and in 2020 I had in the other breast, had surgery and radiation but otherwise no medical condition. The patient took concomitant medications. The following information was reported: COVID-19 (medically significant), VACCINATION FAILURE (medically significant) all with onset 30Apr2022, outcome "unknown" and all described as "positive for COVID on 30Apr". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (30Apr2022) Positive, notes: I did 3 rapid test 30Apr; (30Apr2022) Positive, notes: I did 3 rapid test 30Apr; (30Apr2022) Positive, notes: I did 3 rapid test 30Apr; (06May2022) Negative; (12May2022) Positive, notes: when I did the rapid test today about noon and it was positive within 2 minutes - 1 minutes."; (12May2022) Positive, notes: Date: Not Provided; Result: Positive; Unit: Not Provided. Therapeutic measures were taken as a result of covid-19, vaccination failure. Description of Product Complaint: She stated that she tested positive for COVID on 30Apr, started Paxlovid on 30Apr, she was symptom free by 03May and on 10May she began having rebound COVID. She noted that the symptoms were sinus, headache and running nose, no temperature. Last night she could not sleep and she took two Aleve and did not get any relief. She took a PCR test and it was also positive and she wanted to make report after complete the full course therapy for Paxlovid." Consumer stated, "Almost right, I did not have any temperature. So I took Paxlovid 30Apr through 04May My initial COVID rapid test was 30Apr My symptoms approximately started 30Apr or perhaps 29Apr and official 430Apr, I was symptoms free on 03May I finished the Paxlovid on 04May and on 10May late in the day I began to have nasal sinus symptoms, 11May they become worse no pronounced, I tried Aleve with no relief and the morning on 12May today I also had a headache, sinus congestions, runny nose, headache and I took a rapid test repeated, rapid test today and it was positive and I also did a rapid test on 06May and it was negative and again I was symptom free in that period. when I did the rapid test today about noon and it was positive." No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: Test Date: 20220430; Test Name: COVID-19 Rapid Test; Test Result: Positive ; Comments: I did 3 rapid test 30Apr; Test Date: 20220430; Test Name: COVID-19 Rapid Test; Test Result: Positive ; Comments: I did 3 rapid test 30Apr; Test Date: 20220430; Test Name: COVID-19 Rapid Test; Test Result: Positive ; Comments: I did 3 rapid test 30Apr; Test Date: 20220506; Test Name: COVID-19 Rapid Test; Test Result: Negative ; Test Date: 20220512; Test Name: COVID-19 Rapid Test; Test Result: Positive ; Comments: when I did the rapid test today about noon and it was positive within 2 minutes - 1 minutes."; Test Date: 20220512; Test Name: PCR; Test Result: Positive ; Comments: Date: Not Provided; Result: Positive; Unit: Not Provided
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer; Radiation therapy; Surgery
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2285430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: VA
Alter: 64,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 02.04.2022
Beginn: 19.04.2022
Tage bis Beginn: 17,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

On the evening of 4/19/2022 I developed headache, sore throat, fatigue and low-grade fever (100.4). These symptoms resolved by 4/22/2022. I was on the cruise ship. On the morning of 4/20/2022 I had a rapid Covid-19 PCR test administered by one of the ship nurses. The result was positive and so I and my wife were quarantined to our cabin for the 5 days remaining of the cruise. The ship physician prescribed a 5 day treatment course of molnupiravir, which I took according to directions. I felt well, no longer had symptoms by 4/22/2022. The cruise disembarked on 4/25/2022. We spent the week touring until able to fly back on 5/2/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid-19 rapid PCR test was positive on 4/20/2020. Covid-19 rapid Ag test was negative on 4/24 and again on 4/25. Covid-19 rapid Ag test was positive on 4/25/2020. At home Covid-19 rapid Ag test was negative on 5/4/2020.
Aktuelle Erkrankungen: None
Vorgeschichte: Autoimmune vasculitis (Cogan syndrome), osteoporosis, osteoarthritis
Andere Medikamente: Methotrexate, hydroxychloroquine, folic acid, vit D3
Allergien: None
Vorherige Impfungen: 03/02/2021, Pfizer Covid-19 vaccine #2, rash, fatigue, headache, pain at injection site. Did not require medical care.

VAERS 2285400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: GA
Alter: 71,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 15.03.2022
Beginn: 12.05.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Positive COVID 19; fever and throat congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Positive COVID 19
Aktuelle Erkrankungen: N/a
Vorgeschichte: Lupus
Andere Medikamente: Synthroid
Allergien: N/a
Vorherige Impfungen: -

VAERS 2285150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 16.02.2022
Beginn: 15.05.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Positive COVID 19, sore throat, tired, runny nose and cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Tested positive COVID 19.
Aktuelle Erkrankungen: -
Vorgeschichte: Immunocompromised
Andere Medikamente: Cellcept
Allergien: Cashews
Vorherige Impfungen: -

VAERS 2283147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: KY
Alter: 66,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 08.05.2022
Beginn: 11.05.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Cough Exposure to SARS-CoV-2 Headache Influenza like illness Malaise Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

developed COVID symptoms 3 days after vaccine booster but it was not related to the vaccine; my husband developed COVID the day after my injection and I got COVID from him. All of my symptoms are related to COVID and not the vaccine. -significant flu-like aches all over, headache, chills, fever, cough, congestion...

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: PCR test - May 12th
Aktuelle Erkrankungen: -
Vorgeschichte: lupus, raynauds
Andere Medikamente: citalopram, lansaprazole, calcium, Vitamin D, Multi-vitamin, famotidine, carafate, flexeril hydrocortisone 2.5%, Miralax, tums, beano, probiotics, magnesium, melatonin, preservision, naproxen
Allergien: penicillin, cephalasporins, clindamycin
Vorherige Impfungen: -

VAERS 2283035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: VA
Alter: 68,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 05.04.2022
Beginn: 15.05.2022
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Feeling abnormal Headache Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

My husband tested positive for COVID-19 earlier in May but felt fine and tested negative several times. I felt bad on 05/15/2022 but still tested negative. I had cough, fatigue, headache, and low-grade fever. I tested myself again on 05/16/2022 and tested positive. I called my doctor on 05/16/2022 and asked him to prescribe PAXLOVID. He prescribed it and advised that I stop taking some of my other meds while taking it. I am still testing positive and still have mild symptoms but I am feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Cushing's Disease
Andere Medikamente: Levothyroxine 137mcg; hydrochlorothiazide 25mg; valsartan 80mg; aspirin 81mg; Rosuvastatin 20mg; Vitamin D 3000IU; KORLYM 300mg; Spironolactone 50mg; Isosorbide Mononitrate ER 30mg
Allergien: None
Vorherige Impfungen: -

VAERS 2283031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fk9894

mild

Staat: KY
Alter: 41,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 13.05.2022
Beginn: 14.05.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chills Decreased appetite Dizziness Erythema Fatigue Feeling abnormal Hyperhidrosis Incorrect route of product administration Injection site pain Nausea Pain Pyrexia

Symptomtext

Right after I got the shot which i got at 11am on Friday that evening i was fine. Next day I had 103.6 fever feeling chills and sweating a lot, pain at injection site with pain all over my body. Saturday evening the fever broke, the redness was 3" in diameter at that point and kept growing, fatigue, dizziness, and no appetite is still present. I still have nausea and no appetite. Since the red spot and not feeling better yesterday, I did a virtual visit with the clinic and was told to go to Urgent care. Urgent care said injection was done too low and that I could have gotten a bacterial infection or a bad batch, they gave me an antibiotic cream. And said my immune system is doing what it's suppose to do. I called my Immunologist and they called in an antibiotic pill for me as well. Today red spot is bigger at about 6" in diameter across my arm and I'm very tired, a little achy, no desire to eat, nauseous, and the cognitive fog I normally get is pretty worse right now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: Multiple Scirossis, CVIV common variant immunodeficiency, migranes
Andere Medikamente: Vyvanse, Lyrica, Promethazine,Estradiol patch, Trileptal, Trazodone, Trzanidine, Norco, Essexor, Aimovig, Ocrevus infusion every 6 months, Zytec, Xembify, B12
Allergien: Difluten, Ropack, Mushrooms
Vorherige Impfungen: 2nd dose covid i was sick for about a day and that was it, by the 3rd day I was kind of back to normal

VAERS 2283027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CO
Alter: 75,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 02.05.2022
Beginn: 15.05.2022
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cough Nausea Rash Respiratory tract congestion SARS-CoV-2 test

Symptomtext

I am currently out of town for my grandson's graduation, and I was about to leave to go back home. I had to end up going to the urgent care for severe cough and congestion. I was seen by the doctor and had medication to take. I went back yesterday due to symptoms not getting better at all. I saw the Dr., he prescribed amoxicillin and nausea medication. I was also seen by another Dr. the second time I went back. I also had a COVID test as well yesterday and I am waiting on the results. All my other dose were Moderna. I still have the rash on my scalp that I previously reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: COVID test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes Type II
Andere Medikamente: AREDS medication (vision medication); metformin; pravastatin; potassium citrate
Allergien: Cipro; Demerol; prednisone
Vorherige Impfungen: -

VAERS 2283010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FK9894

mild

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 03.05.2022
Beginn: 09.05.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Headache Malaise SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

***********************COVID BREKTHROUGH CASE******************* I have allergies so I got tested just because the symptoms are similar and I got tested (positive) I had a headache. Video visit given Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID TEST
Aktuelle Erkrankungen: Eye infection
Vorgeschichte: Asthma, Allergies, Depression
Andere Medikamente: Wants to skip
Allergien: NO
Vorherige Impfungen: -