VAERS Reports FD 0809

VAERS 2712523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 10.11.2023
Impfdatum: 16.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Catheterisation cardiac abnormal Coronary artery stenosis Troponin increased

Symptomtext

NSTEMI and subsequent STEMI later in the week. Not Fatal . Overall good health 2 years later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 4,0
Labordaten: Elevated Troponin. Cardiac Cath LAD and LCX stenosis
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MN
Alter: 98,0
Geschlecht: F
Eingang: 02.10.2023
Impfdatum: 02.11.2022
Beginn: 30.09.2023
Tage bis Beginn: 332,0
Dosis: 3
Route/Site: IM / RA

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

Death

Symptomtext

Patient expired 9/30/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Aortic stenosis, DM type 2, CAD
Andere Medikamente: Unknown
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2640256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 02.06.2023
Impfdatum: 30.08.2021
Beginn: 22.11.2022
Tage bis Beginn: 449,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Hypersensitivity

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE ALLERGIC REACTION, INIT

Weitere VAERSDATA-Felder

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

VAERS 2637360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 26.05.2023
Impfdatum: 17.12.2021
Beginn: 24.04.2022
Tage bis Beginn: 128,0
Dosis: 5
Route/Site: IM / LA

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

Acute respiratory failure Chronic respiratory failure Respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE CHRONIC HYPERCAPNIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2635469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 23.05.2023
Impfdatum: 05.01.2022
Beginn: 30.05.2022
Tage bis Beginn: 145,0
Dosis: 3
Route/Site: - / -

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

Cerebrovascular accident

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2634856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 93,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 28.10.2021
Beginn: 09.07.2022
Tage bis Beginn: 254,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Anxiety Aortic arteriosclerosis Hypoxia Lacunar stroke Pain in extremity Pneumonia aspiration

Symptomtext

ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY 7/19/2022 UNSPECIFIED ANXIETY ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/18/2022 UNSPECIFIED ANXIETY HYPOXIA 10/10/2022 UNSPECIFIED ANXIETY ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY 7/19/2022 ASPIRATION PNEUMONIA ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/18/2022 ASPIRATION PNEUMONIA HYPOXIA 10/10/2022 ASPIRATION PNEUMONIA ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY 7/19/2022 ATHEROSCLEROSIS OF AORTA RIGHT ARM PAIN ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/18/2022 ATHEROSCLEROSIS OF AORTA RIGHT ARM PAIN HYPOXIA 10/10/2022 ATHEROSCLEROSIS OF AORTA RIGHT ARM PAIN

Weitere VAERSDATA-Felder

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

VAERS 2618341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 29.10.2021
Beginn: 01.09.2022
Tage bis Beginn: 307,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Asthenia COVID-19 Chronic obstructive pulmonary disease Condition aggravated Death Decreased appetite Dyspnoea Mobility decreased Pneumonia Positive airway pressure therapy Respiratory failure

Symptomtext

pt brought to ED 9/13/22 with dyspnea; found to be positive for COVID; acute on chronic hypoxic respiratory failure; pneumonia; acute COPD exacerbation; given ABX, breathing tx and steroids; pt's condition improved where she was dc'd on 9/19/22 with home O2 via NC during the day and BiPAP at night; back to hospital on 9/21/22 with poor appetite and generalized weakness, with difficulty getting around; was dc'd to a rehab center; she passed away in the SNF

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, AKI, COPD, DMT2, DIASTOLIC HEART FAILURE, CKD, TOBACCO ABUSE, ON HOME O2
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2610058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

kritisch

Staat: TN
Alter: 64,0
Geschlecht: M
Eingang: 05.04.2023
Impfdatum: 17.12.2021
Beginn: 20.03.2023
Tage bis Beginn: 458,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Death Vaccine breakthrough infection

Symptomtext

COVID-related death, breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 30,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DMT2, thrombocytopenia, meningioma brain, CHF, HTN, hypothyroidism, CKD4, seizure disorder, dementia, chronic DVT
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2590278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MN
Alter: 54,0
Geschlecht: M
Eingang: 02.03.2023
Impfdatum: 25.10.2022
Beginn: 09.12.2022
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Cough Dyspnoea Fatigue Malaise Oxygen saturation decreased Pneumonia bacterial SARS-CoV-2 test positive Sepsis Superinfection

Symptomtext

Patient with history of asthma, seizures, and HIV. He was brought to the ED by EMS on 12/9/22 for cough for the past 10 days, along with shortness of breath, fatigue and malaise for the past 2 days. EMS noted his O2 sats were at 88% so was placed on 2L O2 NC. He tested positive for COVID by PCR that same day. He was admitted 12/9/22 - 12/15/22 for further management of COVID-19 and superimposed bacterial pneumonia. Discharge diagnoses include acute hypoxic respiratory failure, COVID-19 pneumonia with superimposed bacterial pneumonia, severe sepsis at presentation due to bacterial pneumonia, COVID-19 infection, among other diagnoses.

Weitere VAERSDATA-Felder

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

VAERS 2578135

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FD0809

kritisch

Staat: KY
Alter: 87,0
Geschlecht: F
Eingang: 08.02.2023
Impfdatum: 18.11.2021
Beginn: 05.10.2022
Tage bis Beginn: 321,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient had a breakthrough infection and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID test on 9/29/2022.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2566862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MN
Alter: 64,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 20.12.2021
Beginn: 09.11.2022
Tage bis Beginn: 324,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure Body temperature increased COVID-19 Dyspnoea Hypotension Hypoxia SARS-CoV-2 test positive Sepsis Skin warm

Symptomtext

Patient with history of ischemic left MCA stroke, chronic respiratory failure and tracheostomy dependence, G-tube dependence. Patient was brought to the ED via EMS on 11/9 for evaluation of difficulty breathing. Patient was noted by nursing facility staff to be hypotensive in the 80/40s, hypoxic in the 80s, and hot to touch with a temperature of 101.2F. There were concerns for sepsis, prompting staff to call 911. In the ED, patient was tested for COVID by PCR and was positive; he was placed on 6L FiO2. At baseline, patient chronically on 0-2L via trach. Ultimately patient was admitted 11/9 - 11/18 for sepsis, suspect secondary to COVID-19 and acute hypoxic respiratory failure. Patient has received COVID primary vaccine series.

Weitere VAERSDATA-Felder

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

VAERS 2545812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

kritisch

Staat: MN
Alter: 75,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 18.05.2022
Beginn: 28.12.2022
Tage bis Beginn: 224,0
Dosis: 3
Route/Site: IM / RA

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

Death

Symptomtext

Patient expired 12/28/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: PMH CAD, STEMI, CKD Stage 3, HTN, hyperlipidemia, asthma, baseline dementia, epilepsy.
Andere Medikamente: Unknown
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2520897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: KY
Alter: 59,0
Geschlecht: M
Eingang: 01.12.2022
Impfdatum: 19.12.2021
Beginn: 16.03.2022
Tage bis Beginn: 87,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient had breakthrough infection and later passed away from complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: Positive COVID test on 2/8/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: DM type 2 COPD Colon/rectal cancer Asthma Emphysema CAD HTN MI Angina Hyperlipidemia
Andere Medikamente: Montelukast Dofetilide Albuterol sulfate Clopidogrel Omeprazole Apixaban Nitroglycerin aspirin Symbicort Metoprolol succinate Atorvastatin Cholecalciferol Digoxin Furosemide Loratadine Tizanidine Zolpidem Ranolazine Hydromorphone
Allergien: Codeine Flu virus vaccine
Vorherige Impfungen: -

VAERS 2501866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: NY
Alter: 56,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 21.12.2021
Beginn: 30.05.2022
Tage bis Beginn: 160,0
Dosis: 3
Route/Site: IM / RA

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

Anticoagulant therapy Aortic aneurysm repair COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Chest pain Intensive care Lung infiltration Pulmonary oedema SARS-CoV-2 test positive Septic shock Urine analysis abnormal White blood cells urine positive

Symptomtext

5/30/2022-Presents to ED, c/o of abrupt chest pain. AAA repair done on 5/3/2022. Covid + test. Afebrile BP 86/62. Resp 24. Admit septic shock and b/l Covid PNA. Not hypoxic on 2 mic of Levophed. Maintaining 02 on RA. UA revealed WBC above 180. CXR: multilobar r lung infiltrate. Cardiomegaly with signs of pulmonary edema: Ordered Lasix, prednisone, bebtelovima, cefepime and Doxy. Urology consulted continue with IV antibiotics. 5/31/2022- On heparin gtt, off Levophed. Continue cefepime and doxy. 6/1/2022- Transfer out of ICU. Continue IV lasix, Follow up with Urology for stent outpatient. Off pressors. VSS stable on RA. D/C home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HFrEF 20%, CHF, CAD, PCI and AICD placement, DVT, AAA, HTN and HLD, ureteral stent placement
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2470767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 06.10.2022
Impfdatum: 03.01.2022
Beginn: 26.09.2022
Tage bis Beginn: 266,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Bronchial wall thickening COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest pain Computerised tomogram thorax abnormal Cough Dyspnoea Emphysema Fibrin D dimer increased Fungal test negative Hypoxia Leukocytosis Lung opacity Mycobacterium tuberculosis complex test Pulmonary mass SARS-CoV-2 test positive

Symptomtext

Discharge Provider:MD Primary Care Provider: MD Admission Date: 9/26/2022 Discharge Date: 10/4/22 PRESENTING PROBLEM: Shortness of breath [R06.02] Cough [R05.9] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 73-year-old male with a history of chronic obstructive pulmonary disease, myeloid neoplasm, BPH, GERD, peripheral arterial disease and prior COVID infection who presented with right-sided chest pain and dyspnea. Patient tested positive for COVID in early August and had completed a course of PAC Slo-bid. In the ER he was found to be tachypneic and hypoxic requiring 2 L of oxygen. COVID-19 test was positive. Chest x-ray showed increased bronchial thickening in the posterior lung bases which could represent inflammatory or infectious bronchitis. CT chest was obtained that showed severe emphysema as well as nodal a past Cities in the right upper lobe with central cavitation which could be infectious or inflammatory. It was felt patient had acute hypoxic respiratory failure secondary to COVID-19 pneumonia and there was also concern for secondary bacterial pneumonia. Pulmonology was consulted and patient was started on remdesivir and Decadron. He completed 5 day course of remdesivir. Also placed on ceftriaxone and azithromycin and completed a 7 day course. Fungal studies were negative, TB screening indeterminate. Patient then developed worsening hypoxia with increasing oxygen needs. He was placed on scheduled nebs as well as Symbicort and Spiriva. He was placed on Solu-Medrol and once his respiratory status had improved, he was transitioned back to dexamethasone. Oxygen needs decreased and he was only requiring 1-2 L of oxygen. As D-dimer was elevated, lower extremity Dopplers were obtained which did not reveal any evidence of DVT Patient did have leukocytosis but had elevated WBC at baseline due to his underlying myeloid neoplasm. Hematology was consulted and they noted that there was no transformation to acute leukemia and no indication to start inpatient therapy. As WBCs did increase to over 100, he was given 1 dose of Hydrea 1000 mg and white coun did improve to 96.76. Pulmonology recommended that patient complete a total of 10 days of dexamethasone. Patient was weaned off oxygen to room air. Patient was seen by pulmonary rehab and was not felt to require oxygen therapy. He was to be followed by Medical Group bridging Older Adult Care program after discharge. Patient discharged home in stable condition 10/4/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Centrilobular emphysema (HCC); Benign prostatic hyperplasia with weak urinary stream Hyperlipidemia; Gastroesophageal reflux disease with esophagitis without hemorrhage Congestive heart failure (HCC); Chronic myelomonocytic leukemia not having achieved remission (HCC); Status post laparoscopic colectomy; Insomnia, unspecified type Chronic low back pain, unspecified back pain laterality, unspecified whether sciatica present Smoker; Neuropathy; Migraine with aura and without status migrainosus, not intractable Pre-diabetes; PAD (peripheral artery disease) (HCC); COVID-19; Acute respiratory insufficiency; Cavitary nodule of lung; Neck pain.
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler; Aspirin; Atorvastatin (LIPITOR); Benzonatate (TESSALON); Cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) capsule; D2000 ULTRA STRENGTH 50 MCG (2000 UT); De
Allergien: None
Vorherige Impfungen: -

VAERS 2451010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: OH
Alter: 80,0
Geschlecht: M
Eingang: 19.09.2022
Impfdatum: 30.09.2021
Beginn: 17.07.2022
Tage bis Beginn: 290,0
Dosis: 3
Route/Site: IM / RA

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

Acute myocardial infarction Acute respiratory failure Anticoagulant therapy Aspiration pleural cavity Atrial fibrillation Benign prostatic hyperplasia Bladder catheterisation Blood creatinine increased Brain natriuretic peptide increased COVID-19 Cardiac failure Cardiac failure congestive Chest X-ray abnormal Chronic kidney disease Condition aggravated Device intolerance Dyspnoea Echocardiogram

Symptomtext

Patient is a 81 y.o. male patient of MD with history of Cardiomyopathy, CAD, DM, HLD, HTN, Renal Disease. Patient presented with shortness of breath and hypoxia. Assessment and Plan Acute HFrEF exacerbation Acute hypoxic respiratory failure Ischemic cardiomyopathy s/p ICD Bilateral pleural effusion COVID-19 infection Shortness of breath and dyspnea resolved after thoracentesis bipap not well tolerated currently on room air; not on home oxygen Initial chest x-ray with bilateral pneumonia. WBC 12=> 7 Tested positive for COVID-19 on 7/16; vaccinated x3 Discontinue dexamethasone 6 mg daily, day 6 Large pleural effusion s/p thoracentesis; removed 1 L from the right side and 250 ml from the left side Postprocedure chest x-ray: small bilateral left greater than right pleural effusions isolation through 7/26 Monitor input and output Incentive spirometry BNP 10,294 Continue home Lasix EKG paced rhythm; 2D echo on 4/5/2022 with EF of 39% Discharge after Foley removal and trial of void Follow-up with cardiology clinic within 1 week NSTEMI type II Elevated troponin due to acute illness and CHF No chest pain Troponin 38=> 105=> 153 Continue metoprolol CKD stage III/IV CRT 2 => baseline 1.8-2.50 Avoid nephrotoxic agents Continue to follow-up with nephrology clinic A. fib without RVR Currently rate controlled Continue metoprolol 100 mg Continue Xarelto Hypertension, benign. BP controlled. Continue home metoprolol, amlodipine Diabetes mellitus type 2 Hemoglobin A1C 7.4 % on 4/5/22 Continue home regimen Gout Continue home allopurinol BPH Continue home finasteride and Flomax.

Weitere VAERSDATA-Felder

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

VAERS 2404619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MI
Alter: 52,0
Geschlecht: M
Eingang: 08.08.2022
Impfdatum: 29.11.2021
Beginn: 27.07.2022
Tage bis Beginn: 240,0
Dosis: 3
Route/Site: - / -

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

Alcohol abuse Alcoholic ketoacidosis Angiogram pulmonary abnormal Anion gap Anticoagulant therapy Antithrombin III decreased Asthenia Atrial fibrillation Atrial flutter Blood alcohol normal Blood bicarbonate decreased Blood glucose decreased Blood ketone body Blood lactic acid COVID-19 Chest X-ray normal Coagulation test abnormal Condition aggravated

Symptomtext

Discharge Provider: Private MD Primary Care Provider: Private, MD Admission Date: 7/27/2022 Discharge Date: 08/01/2022 PRESENTING PROBLEM: Lactic acidosis [E87.2]- Alcoholic ketoacidosis [E87.2]- Hypomagnesemia [E83.42]- Alcohol abuse [F10.10]- Microcytic anemia [D50.9]- Generalized weakness [R53.1]- Polysubstance abuse (HCC) [F19.10]- Typical atrial flutter (HCC) [I48.3]- COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 53-year-old male with PMH significant for severe esophagitis (EGD 6/19 and 2/16), Mallory-Weiss tear in past, history of duodenal ulcer, chronic microcytic anemia, iron deficiency, chronic alcohol abuse, history of DVT/PE (02/2022), depression/anxiety and homelessness who presents to the ED for generalized malaise, cough and SOB. Found to be Covid positive. CXR is negative and SPO2 stable on RA. While in the ER he was noted to have transient a flutter/RVR with HR 140s, otherwise vitals within normal limits, labs consistent with anion gap metabolic acidosis with gap 25, bicarb 13, lactate 4.2. D-dimer elevated at 1100. He was also hypoglycemic at 55, elevated beta hydroxybutyrate 5.2 UA was negative overall but positive for ketones. Blood alcohol level at 0.045. He was started on IVF for alcoholic ketoacidosis and admitted to internal medicine service for supportive treatment. CTA thorax was obtained and revealed acute subsegmental pulmonary embolism in the left upper lobe, no evidence of right heart strain. He had PE/DVT and 02/2022. Was previously on Eliquis but was poorly compliant. During admission in June previous PE noted to have resolved but had residual small chronic DVT in posterior tibial vein. Hypercoagulable workup revealed--low protein C 62% and low AT III 49 %. Hematology recommended continued prophylactic dosing of Eliquis which the patient refused at discharge. Discussed with hematology again this admission who advised life long anticoagulation given recurrence. He was started back on Eliquis at starter dose. He had no further episodes of AFib/flutter in her heart rate remained stable. Echo obtained and was unremarkable. Acidosis quickly resolved with IV fluids and anion gap closed. IV fluids are stopped and he tolerated diet although notably has poor appetite. He had some mild hypokalemia and hypomagnesemia which were replaced. Patient continued to feel poorly due to COVID 19 symptoms but vitals remained hemodynamically stable on room air. He received 1 dose of remdesivir but declined further dosing because patient advocate had concerns about side effects. He was otherwise treated with supportive care. Discharged was delayed due to homeless status until he completed 5 day isolation period, at which point he could be discharged back to local shelter. Patient was strongly advised to be compliant with Eliquis and follow up with PCP for refills of this medication. Patient in agreement with discharge plan and discharged in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: 11/27/2021 ED Visit to hospital for Alcoholic Ketoacidosis 11/25/2021 ED Visit to alternate health clinic for Alcohol Abuse 11/11/2021 Hospital Visit to alternate hospital for Upper GI Bleed 11/11/21-11/14/21 11/09/2021 ED Visit to alternate hospital for Alcohol Abuse
Vorgeschichte: Hiatal hernia Anxiety and depression SVT (supraventricular tachycardia) (HCC) Esophageal ulceration Mallory-Weiss tear Idiopathic, histamine-mediated angioedema Alcohol abuse Marijuana use Depression with suicidal ideation GERD (gastroesophageal reflux disease) Plantar fasciitis Esophagitis Alcohol-induced acute pancreatitis Single subsegmental pulmonary embolism without acute cor pulmonale (HCC) Hematemesis Lung nodules COVID-19 virus infection Microcytic hypochromic anemia
Andere Medikamente: apixaban (ELIQUIS) 5 MG tablet benzonatate (TESSALON) 100 MG capsule busPIRone (BUSPAR) 5 MG tablet escitalopram (LEXAPRO) 20 MG tablet guaiFENesin (MUCINEX) 600 MG 12 hr tablet ondansetron (ZOFRAN-ODT) 4 MG disintegrating tablet pant
Allergien: Compazine [Phenothiazines]Angioedema MetoclopramideSwelling
Vorherige Impfungen: -

VAERS 2398125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MI
Alter: 49,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 12.01.2022
Beginn: 22.07.2022
Tage bis Beginn: 191,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Anticoagulant therapy Asthma Blood gases abnormal COVID-19 Carbon dioxide abnormal Condition aggravated Diuretic therapy Dyspnoea Haematuria Hyperkalaemia Hypoxia Klebsiella infection Multiple-drug resistance Positive airway pressure therapy Proteus infection Respiratory failure

Symptomtext

Discharge Provider: MD Primary Care Provider: NP Admission Date: 7/22/2022 Discharge Date: Jul 26, 2022 PRESENTING PROBLEM: Hyperkalemia [E87.5] AKI (acute kidney injury) (HCC) [N17.9] Urinary tract infection due to Proteus [N39.0, B96.4] Urinary tract infection with hematuria, site unspecified [N39.0, R31.9] UTI due to Klebsiella species [N39.0, B96.89] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 50 year-old female with PMHx for restrictive lung disease secondary to obesity, CKD stage 3, diabetes type 2, CHF, bipolar disorder, depression, neuropathy, morbid obesity presenting with shortness of breath. The patient was found to have COVID-19 and a severe persistent asthma exacerbation with acute on chronic hypoxic respiratory failure. She uses 2 L by nasal cannula at baseline at home. The patient was treated with IV Solu-Medrol with improvement. She was switched back to Decadron to finish a 10-day course for COVID 19. She was also treated supportively with nebulizer treatment, Mucinex and subcutaneous heparin. Of note she had acute kidney injury on admission in the setting of acute urinary tract infection and hypoxia. This resolved. She does have chronic kidney disease stage 3. Her diuretics were resumed. She was treated with IV ertapenem due to multi-drug resistant urinary tract infection. Infectious Disease evaluated the patient with recommendations for 7 days of therapy. The patient received a midline to complete IV antibiotic therapy at home. Pulmonary rehab ordered a home BIPAP device as she qualified due to her CO2 levels on ABG. They also provided the patient with a nebulizer machine. Ultimately the patient was discharged home with home health care in improved and stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: 1/7/2022- ED Visit for Shortness of Breath to Emergency Room. DIAGNOSIS at time of disposition: 1. Shortness of breath 2. Moderate persistent asthma with acute exacerbation 3. COVID-19 virus not detected 1/4/2022- UTI Symptoms; Prescribed Keflex by Urologist 1/3/2022- CT Detected Renal Mass by Urologist 12/16/2021- Yeast Infection; Prescribed Diflucan by Urologist 12/15/2021-UTI Symptoms; Prescribed Keflex by Urologist
Vorgeschichte: CHF (congestive heart failure) (HCC) Chronic diastolic heart failure (HCC) Morbid obesity with BMI of 50.0-59.9, adult (HCC) Type 2 diabetes mellitus with diabetic neuropathy, with long-term current use of insulin (HCC) Secondary oligomenorrhea Recurrent UTI Chronic respiratory failure with hypoxia (HCC) Restrictive lung disease secondary to obesity Obesity hypoventilation syndrome (HCC) Renal mass Schizoaffective disorder (HCC) Severe persistent asthma without complication Essential hypertension, benign Dyslipidemia Acute UTI COVID-19 virus infection
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 10 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet BD PEN NEEDLE NANO 2ND GEN busPIRone (BUSPAR) 30 MG tablet chlorhexidine (P
Allergien: Singulair [Montelukast] Tetanus Toxoids
Vorherige Impfungen: Tetanus- Unknown Reaction

VAERS 2391013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 16.12.2021
Beginn: 14.07.2022
Tage bis Beginn: 210,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Blood gases Blood pH decreased COVID-19 Chronic obstructive pulmonary disease Condition aggravated Confusional state Dyspnoea Hypercapnia Intensive care Legionella test PCO2 increased Positive airway pressure therapy Respiratory failure Streptococcus test negative

Symptomtext

Admission Date: 7/14/2022 Discharge Date: 7/23/2022 PRESENTING PROBLEM: COPD exacerbation (HCC) [J44.1] COPD with acute exacerbation (HCC) [J44.1] Acute respiratory failure with hypercapnia (HCC) [J96.02] Respiratory tract infection due to COVID-19 virus [U07.1, J98.8] COVID-19 [U07.1] Acute on chronic respiratory failure with hypoxia and hypercapnia (HCC) [J96.21, J96.22] Patient is a 73-year-old woman admitted for COPD exacerbation w/ resultant acute on chronic respiratory failure with hypercapnia and hypoxia post recent COVID19 infection. She has a PMH of very severe COPD on 2-3L NC at baseline, chronic systolic heart failure with recovered EF 2/2 NICM,AFIB, depression and anxiety. Patient presented w/ dyspnea and developed confusion w/ severe hypercapnia noted with blood gas showing PH 7.04 with pCO2 of 130. She was admitted to the intensive care unit with BiPAP. She underwent an infectious workup with negative strep pneumo and Legionella antigens. She was not felt to have bacterial superinfection. She improved and IV steroids were transitioned to PO taper. She completed remdesivir. She was discharged to SAR when back to baseline respiratory status.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: 12/03/2022 call to Pulmonologist office for Respiratory Symptoms. Negative Covid> Treated with Z-pack.
Vorgeschichte: Physical deconditioning Very severe COPD Osteoporosis Depression with anxiety Vitamin D deficiency Osteoarthritis Former cigarette smoker History of Apical ballooning syndrome Dyspnea Nonischemic cardiomyopathy Sinus tachycardia Hypoxemia Mixed simple and mucopurulent chronic bronchitis (HCC) Atrophic vaginitis Supplemental oxygen dependent Weak antibody response to pneumococcal vaccine Nicotine abuse Chest pain Recurrent stress-induced cardiomyopathy Acute on chronic respiratory failure with hypoxia (HCC) Anxiety Constipation Goals of care, counseling/discussion Paroxysmal atrial fibrillation Long term current use of antiarrhythmic drug Acute on chronic respiratory failure with hypoxia and hypercapnia (HCC) COVID-19 COPD with acute exacerbation (HCC) Rib pain on right side
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet amiodarone (PACERONE) 200 MG tablet ascorbic acid (VITAMIN C) 1000 MG tablet B Complex Vitamins (B-COMPLEX/B-12) LIQD beta carotene 10000 units capsule bisacodyl (DULCOLAX) 10 MG suppository budes
Allergien: None
Vorherige Impfungen: -

VAERS 2366114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: IL
Alter: 81,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 13.10.2021
Beginn: 10.02.2022
Tage bis Beginn: 120,0
Dosis: 2
Route/Site: IM / -

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

Bladder catheterisation Blood urine present COVID-19 Cerebrovascular accident Cognitive disorder Communication disorder Computerised tomogram head normal Dysarthria Facial paralysis Inappropriate schedule of product administration SARS-CoV-2 test positive Urinary incontinence

Symptomtext

Pfizer Dose 1 1/7/21 (EL0142); Pfizer Dose 2 10/13/21 (FD0809); COVID Positive 2/14/22. 2/14/22: 81-year-old male patient with a history of type 2 diabetes, depression, COPD, CAD, BPH, hypertension lives at a local nursing home where he was moved recently from another nursing home. Over the last couple of days, the patient was visited by his family members who noticed slurred speech becoming worse this morning. When the family spoke with him on 02/13 over the phone, they noticed some difference in his communication and the nursing staff at the nursing home mentioned that the patient could be having some infection and is daily reassess. But this morning when the patient was seen by the family, he had significant slurred speech which concerned them and hence he was brought to the hospital for further evaluation. The noticed that his left-sided facial droop which became more evident this morning. Patient is also scheduled for a neuro psychological evaluation at the Administration in May of this year as the family wanted clear diagnoses for his cognitive dysfunction. Neurology consultation was obtained from the emergency room for evaluation of his slurred speech. CT of the head was negative and the patient is admitted for further evaluation and treatment. A Foley catheter was placed in the emergency room which is draining the noon tinged with blood. The patient denies any abdominal pain. He does have urinary incontinence and wears depends but the family has not noticed any blood in the urine and the nursing staff at the nursing home did not inform them of any new onset of hematuria. 2/24/22: 2019 novel coronavirus detected. Acute cerebrovascular accident (CVA), Acute cerebrovascular accident (CVA). Dysarthria, Dysarthria

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM type 2; depression; COPD; CAD; BPH; HTN; resident of nursing home
Andere Medikamente: APAP; Albuteorl; Aspirin; Atorvastatin; Bisacodyl; Clopidogrle; Dextromethorphan-guaifenein; Donepezil; Fluticasone nasal spray; Furosemide; Hydralazine; Insulin aspart sliding scale; Insulin glargine; Ipratropium; Isosorbide mononitrate ER
Allergien: morphine - unknown
Vorherige Impfungen: -

VAERS 2263211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: TN
Alter: 75,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 03.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction Asthenia Atrial fibrillation COVID-19 Death Diarrhoea Intensive care Loss of consciousness Malnutrition SARS-CoV-2 test positive

Symptomtext

Pfizer vaccine #1 given 5/15/21, lot # EW0185; Pfizer vaccine #2, lot # EW0178; pt was admitted to the medical center from 1/11/22 - 2/11/22 after LOC while transferring to toilet; c/o diarrhea; found to be positive for COVID; pt has malnutrition and debility; A Fib with RVR; NSTEMI; transferred to PCU; comfort focused; DNR/DNI; pt never required O2; was given remdesivir; transferred to hospice facility where she passed away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 31,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple strokes/TIA; HTN, OA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2234249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: WA
Alter: 61,0
Geschlecht: M
Eingang: 14.04.2022
Impfdatum: 10.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Cardio-respiratory distress Death Resuscitation Sinus arrhythmia

Symptomtext

His wife awoke to the patient moving around in distress in the bed at about 6:30am. She called emergency and started CPR and continued until the paramedics arrived and they took over. Paramedics performed CPR both manual and mechanical and used paddles to try and restart a normal sinus rhythm. The paramedics also gave the patient 2 shots of Epinephrine. They were unsuccessful and declared the patient dead after about 50 minutes of trying to revive the patient.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Being treated for high blood pressure and high cholesterol. Both controlled by medication
Andere Medikamente: Advil PM
Allergien: none
Vorherige Impfungen: -

VAERS 2206112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: -
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 30.11.2021
Beginn: 26.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Arthralgia Back pain Blood test Blood uric acid Blood uric acid increased Borrelia test Borrelia test positive Chest pain Chiropractic Computerised tomogram Computerised tomogram abnormal Condition aggravated Feeling abnormal Feeling hot Gait disturbance Gait inability Hordeolum Intervertebral disc protrusion

Symptomtext

slowly got worse; felt like he put his foot in bucket of warm water; sensations that he was getting in his right foot was very strange; Sciatica was increased and got worse; veins in his foot again; uric acid was elevated in blood test/ blood uric acid increased; left eye was closed (swelling of eyelid); had a style (hordeolum); swelling in his right foot (peripheral swelling); swelled up and had a purple tint (skin discolouration); experience serve pain in hips and buttocks (gait inability); Pain in extremity; computerized tomogram abnormal; chest pain; pain in chest, more pain while inhaling (painful respiration); Bilateral pulmonary embolisms; Spinal Spondylosis and Disc herniations; magnetic resonance imaging spinal abnormal; back spine pain (Spinal pain); Lyme Disease; borrelia test positive; pinched nerve (nerve compression); back pain; pain in shoulders and hips; spinal osteoarthritis; could not walk; chiropractic; polymyalgia rheumatica; musculoskeletal pain; he really complained about his foot and sent a picture; limb discomfort; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from Regulatory Authority. The reporter is the patient. Regulatory number: 2132210. Other Case identifier(s): 20220312707(0) (Janssen Research & Development). A 55 year-old male patient received bnt162b2 (BNT162B2), administration date 30Nov2021 (Lot number: FD0809) as dose 2 (booster), single for covid-19 immunisation; janssen covid-19 vaccine (JANSSEN COVID-19 VACCINE), administered in arm left, administration date 06Mar2021 (Lot number: 1805022) as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: OMEPRAZOLE; SHINGRIX, administration date 04Aug2021. The following information was reported: POLYMYALGIA RHEUMATICA (hospitalization, medically significant) with onset Apr2021, outcome "not recovered", described as "polymyalgia rheumatica"; LYME DISEASE (hospitalization, medically significant) with onset 08Oct2021, outcome "unknown", described as "Lyme Disease"; PULMONARY EMBOLISM (hospitalization, medically significant) with onset 05Dec2021, outcome "not recovered", described as "Bilateral pulmonary embolisms"; MUSCULOSKELETAL PAIN (hospitalization) with onset Apr2021, outcome "not recovered", described as "musculoskeletal pain"; ARTHRALGIA (hospitalization) with onset 24May2021, outcome "not recovered", described as "pain in shoulders and hips"; SPINAL OSTEOARTHRITIS (hospitalization) with onset 09May2021, outcome "not recovered", described as "spinal osteoarthritis"; GAIT DISTURBANCE (hospitalization) with onset 09May2021, outcome "not recovered", described as "could not walk"; CONDITION AGGRAVATED (hospitalization), outcome "unknown", described as "slowly got worse"; FEELING HOT (hospitalization), outcome "unknown", described as "felt like he put his foot in bucket of warm water"; FEELING ABNORMAL (hospitalization), outcome "unknown", described as "sensations that he was getting in his right foot was very strange"; SPINAL PAIN (hospitalization) with onset 28Oct2021, outcome "not recovered", described as "back spine pain (Spinal pain)"; NERVE COMPRESSION (hospitalization) with onset Oct2021, outcome "not recovered", described as "pinched nerve (nerve compression)"; SCIATICA (hospitalization), outcome "not recovered", described as "Sciatica was increased and got worse"; INTERVERTEBRAL DISC PROTRUSION (hospitalization) with onset 17Nov2021, outcome "not recovered", described as "Spinal Spondylosis and Disc herniations"; PAINFUL RESPIRATION (hospitalization) with onset 05Dec2021, outcome "not recovered", described as "pain in chest, more pain while inhaling (painful respiration)"; GAIT INABILITY (hospitalization) with onset 10Feb2022, outcome "not recovered", described as "experience serve pain in hips and buttocks (gait inability)"; LIMB DISCOMFORT (hospitalization) with onset 26Mar2021, outcome "not recovered", described as "he really complained about his foot and sent a picture"; SKIN DISCOLOURATION (hospitalization) with onset 17Feb2022, outcome "not recovered", described as "swelled up and had a purple tint (skin discolouration)"; BLOOD URIC ACID INCREASED (hospitalization) with onset 19Feb2022, outcome "not recovered", described as "uric acid was elevated in blood test/ blood uric acid increased"; SWELLING OF EYELID (hospitalization) with onset 19Feb2022, outcome "not recovered", described as "left eye was closed (swelling of eyelid)"; HORDEOLUM (hospitalization) with onset 19Feb2022, outcome "not recovered", described as "had a style (hordeolum)"; PERIPHERAL SWELLING (hospitalization) with onset 19Feb2022, outcome "not recovered", described as "swelling in his right foot (peripheral swelling)"; PERIPHERAL VASCULAR DISORDER (hospitalization), outcome "unknown", described as "veins in his foot again"; CHIROPRACTIC (hospitalization) with onset 09Apr2021, outcome "not recovered", described as "chiropractic"; BACK PAIN (hospitalization) with onset Aug2021, outcome "not recovered", described as "back pain"; CHEST PAIN (hospitalization) with onset 05Dec2021, outcome "not recovered", described as "chest pain"; BORRELIA TEST POSITIVE (hospitalization) with onset 08Oct2021, outcome "not recovered", described as "borrelia test positive"; COMPUTERISED TOMOGRAM ABNORMAL (hospitalization) with onset 05Dec2021, outcome "not recovered", described as "computerized tomogram abnormal"; MAGNETIC RESONANCE IMAGING SPINAL ABNORMAL (hospitalization) with onset 17Nov2021, outcome "not recovered", described as "magnetic resonance imaging spinal abnormal"; LIMB DISCOMFORT (hospitalization) with onset 26Mar2021, outcome "not recovered", described as "limb discomfort"; PAIN IN EXTREMITY (hospitalization) with onset 13Jan2022, outcome "not recovered", described as "Pain in extremity". The patient was hospitalized for pulmonary embolism (start date: 06Dec2021). The events "polymyalgia rheumatica", "lyme disease", "bilateral pulmonary embolisms", "musculoskeletal pain", "pain in shoulders and hips", "spinal osteoarthritis", "could not walk", "slowly got worse", "felt like he put his foot in bucket of warm water", "sensations that he was getting in his right foot was very strange", "back spine pain (spinal pain)", "pinched nerve (nerve compression)", "sciatica was increased and got worse", "spinal spondylosis and disc herniations", "pain in chest, more pain while inhaling (painful respiration)", "experience severe pain in hips and buttocks (gait inability)", "he really complained about his foot and sent a picture", "swelled up and had a purple tint (skin discolouration)", "uric acid was elevated in blood test/ blood uric acid increased", "left eye was closed (swelling of eyelid)", "had a style (hordeolum)", "swelling in his right foot (peripheral swelling)", "veins in his foot again", "chiropractic", "back pain", "chest pain", "borrelia test positive", "computerized tomogram abnormal", "magnetic resonance imaging spinal abnormal", "limb discomfort" and "pain in extremity" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood test: (09May2021) unknown results; blood uric acid: (19Feb2022) increased; borrelia test: (08Oct2021) positive; computerised tomogram: (05Dec2021) abnormal, notes: Show Bilateral Pulmonary embolism; laboratory test: (Oct2021) pinched nerve compression, notes: Indicated probably pinched nerve (nerve compression); magnetic resonance imaging spinal: (17Nov2021) abnormal, notes: MRI-Spinal Spondylosis and Disc herniation (intervertebral disc protrusion) at various levels; nerve conduction studies: (18Nov2021) unknown results. Therapeutic measures were taken as a result of polymyalgia rheumatica, lyme disease, pulmonary embolism, musculoskeletal pain, arthralgia, spinal osteoarthritis, gait disturbance, condition aggravated, feeling hot, feeling abnormal, spinal pain, nerve compression, sciatica, intervertebral disc protrusion, painful respiration, gait inability, limb discomfort, skin discolouration, blood uric acid increased, swelling of eyelid, hordeolum, peripheral swelling, peripheral vascular disorder, chiropractic, back pain, chest pain, borrelia test positive, computerised tomogram abnormal, magnetic resonance imaging spinal abnormal, limb discomfort, pain in extremity; patient was given Xarelto (Rivaroxaban) possibly 35 mg (milligram), 20 mg and 15 mg per day, gabapentin 300 mg per day increased to 600 mg per day, epidural steroid injection in back, methotrexate 12.5 mg once per week, folic acid 1 mg daily, prednisone from 10 mg (milligram) to 30 mg for 2 days, then taper down to 20 mg for 2 days and then back to 10 mg, allopurinol, cephalexin 500mg 2 times per day along with an eye ointment 4 times per day. Clinical Information: Causality for Janssen Covid-19 Vaccine and the events Polymyalgia Rheumatica, Pulmonary Embolism, Back pain, Chest pain, Chiropractic, Gait Disturbance, Gait Inability, Hordeolum, Intervertebral Disc Protrusion, Nerve Compression, Painful respiration, Peripheral Swelling, Sciatica, Skin Discolouration, Spinal Osteoarthritis, Spinal Pain, Swelling of eyelid, Borrelia Test Positive, Computerized Tomogram Abnormal, Blood Uric Acid Increased, Magnetic Resonance Imaging Spinal Abnormal, Arthralgia, Limb Discomfort, Pain Extremity and Musculoskeletal Pain per reporter and manufacturer was possible. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Test Date: 20210509; Test Name: Blood Work; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220219; Test Name: Blood Uric Acid; Result Unstructured Data: Test Result:Increased; Test Date: 20211008; Test Name: Borrelia test; Test Result: Positive ; Test Date: 20211205; Test Name: Computerized Tomogram; Result Unstructured Data: Test Result:Abnormal; Comments: Show Bilateral Pulmonary embolism; Test Date: 202110; Test Name: Laboratory test; Result Unstructured Data: Test Result:Pinched nerve compression; Comments: Indicated probably pinched nerve (nerve compression).; Test Date: 20211117; Test Name: Magnetic resonance imaging spinal; Result Unstructured Data: Test Result:Abnormal; Comments: MRI-Spinal Spondylosis and Disc herniation (intervertebral disc protrusion) at various levels.; Test Date: 20211118; Test Name: Nerve Conduction Test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: OMEPRAZOLE; ZOSTER
Allergien: -
Vorherige Impfungen: -

VAERS 2155083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: OH
Alter: 100,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 19.10.2021
Beginn: 13.01.2022
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: IM / RA

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

Asymptomatic COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Patient tested positive for Covid on 01/04/2022 and was asymptomatic. No other records were charted except that there were unspecified underlying health conditions. Patient died.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: SARS-CoV-2 antigen test-positive 01/04/2022
Aktuelle Erkrankungen: -
Vorgeschichte: No pre-existing conditions listed in database
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2151018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: WI
Alter: 54,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 30.09.2021
Beginn: 17.02.2022
Tage bis Beginn: 140,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Asthenia COVID-19 Cough Dyspnoea Dyspnoea exertional Hyperhidrosis Pyrexia SARS-CoV-2 test positive Sinus congestion Throat irritation

Symptomtext

Patient admitted as inpatient on 2/18 due to acute respiratory failure with hypoxia. Patient was tested for COVID-19 and was positive on 1/31 and again on 2/17. history of recurrent multiple myeloma on chemotherapy who presented to hospital with complaint of shortness of breath. She reports that she initially developed fevers on the evening of 2/15/22, measured 100.5? with subsequent diaphoresis. This continued although with less severe diaphoresis over the last couple days. Additionally noted to be very weak at rest with worsened DOE yesterday, ultimately prompting ED visit. Diagnosed with covid 19 infection on 1/31/22, 18 days ago, which was reportedly a mild case with only slight worsening of chronic "tickle" in her throat, sinus congestion, cough. Receiving chemotherapy with teclistamab/dara/Pom, most recently on 1/17/22 with daratumumab.

Weitere VAERSDATA-Felder

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

VAERS 2129050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: KY
Alter: 55,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 12.11.2021
Beginn: 17.02.2022
Tage bis Beginn: 97,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Patient received his third dose of Pfizer on 11/12/2021, was admitted to the hospital on 02/07/2022, Diganosed with COVID19 on 02/07/2022, and passed away on 02/17/2022. Patients death is currently being investigated by the Mortality Review team to determine if this death was COVID19 related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: metastatic squamous cell carcinoma of the larynx
Vorgeschichte: metastatic squamous cell carcinoma of the larynx
Andere Medikamente: Unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2109401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: ID
Alter: 83,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 28.12.2021
Beginn: 09.02.2022
Tage bis Beginn: 43,0
Dosis: 2
Route/Site: IM / RA

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

Acute myocardial infarction Brain natriuretic peptide Cardiac failure acute Catheterisation cardiac Chest X-ray Coronary arterial stent insertion Echocardiogram Ejection fraction decreased Full blood count Metabolic function test Troponin

Symptomtext

USA, NSTEMI, acute on chronic HF with reduced EF (25-30%) s/p stents x2 to the RCA and LAD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: LHC, TTE, CXR, CBC, BMP, BNP, troponin
Aktuelle Erkrankungen: -
Vorgeschichte: CAD with stents (left circumflex and kissing stents to the LAD diagonal in 2019), ischemic cardiomyopathy, biventricular HF with improved EF (50-55%), mod-severe MR, Aflutter on apixaban, narcotic dependence with related sleep apnea, moderate pulmonary HTN, h/o NSAID induced UGIB (3/2021), CKD 3a, mild cognitive impairment
Andere Medikamente: ? acetaminophen (TYLENOL) 325 MG tablet Take 2 tablets (650 mg total) by mouth every 6 (six) hours as needed for Fever, mild pain or moderate pain. Do not exceed 4,000 mg in a 24 hour period. ? amiodarone (PACERONE) 200 MG tablet Take 1
Allergien: Grass pollen
Vorherige Impfungen: -

VAERS 2079546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: OH
Alter: 78,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 14.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Hospitallization due to COVID and resulting death due to COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: RNA COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2074531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MN
Alter: 63,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 11.11.2021
Beginn: 11.01.2022
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Anticoagulant therapy Dizziness Dyspnoea Dyspnoea exertional Myocardial strain imaging abnormal Pulmonary embolism

Symptomtext

From patient discharge summary: "Patient is a 63 year old female with a past medical history of lichen planus, and asthma that mostly was problematic as a child. She presented to the emergency department with increasing shortness of breath. She reports her symptoms began about 2 weeks ago. At this time she was working at her brother's house who had recently passed. She was busy cleaning out the house in preparation to listed on the market. She noticed being a little more short of breath than usual, when going up stairs. At times she would have to sit and rest a little. She did not think much of it at that time. The house was very dusty, she felt like maybe her shortness of breath was being triggered by the dust or mold in the air. She does have a history of asthma but has not had recent triggers, it was mostly as a child. She traveled back to town, and contacted her primary care to get a refill on her albuterol inhaler, thinking that that may help her symptoms. She said it did help her breathing some. She went to visit her daughter, and noticed that she was much more short of breath going up the stairs there. She traveled back to home on Saturday 1/22 to continue to clean out her brother's house. She states on 1/24 when she was brushing the snow off her car, she felt extremely winded and started to feel "dizzy", she had to sit in the car for a while because she felt like she could pass out. She then decided to be seen in the ED. She reports even with her driving back and forth from town to town recently, she makes frequent stops along the way and gets out and walks. She does not live a very sedentary life. She reports no history of lower leg or calf swelling, no pain. She has had no personal history of clots, there is no family history of clotting disorder that she is aware of. She reports her brother who had recently passed away had clots in the past, but he was also wheelchair-bound. She recently had her annual appointment with her primary care provider, she has had recent mammograms with no abnormal findings, Pap smears have all been normal, she has had colon cancer screening with a benign polyp found, she is due for repeat colonoscopy in the next couple of years. She does use a topical estrogen cream for her lichen planus, but does not use it frequently, and has not used it recently. She has family members who are currently sick with covid but she has not been around them recently, she received her most recent covid vaccine in November. CTA was performed, findings of acute bilateral pulmonary emboli and right heart strain, as described above. Treated with heparin drip, with switch to Eliquis. She had resolution in her shortness of breath, was not requiring oxygen. RT performed a home O2 evaluation, she did not require at home oxygen. Will need to continue Eliquis for at least 3 months. Recommend coagulation studies at future follow up with PCP. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: See item 18.
Aktuelle Erkrankungen: None.
Vorgeschichte: Mild intermittent asthma. Generalized anxiety disorder. Lichen planus.
Andere Medikamente: Albuterol inhaler. Estriol vaginal cream.
Allergien: No known allergies.
Vorherige Impfungen: -

VAERS 2062195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 03.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Anticoagulant therapy COVID-19 Computerised tomogram thorax abnormal Condition aggravated Cor pulmonale acute Deep vein thrombosis Dyspnoea Echocardiogram abnormal Inflammatory marker increased Lung opacity Pulmonary embolism Respiratory syncytial virus test positive SARS-CoV-2 test positive Suspected COVID-19 Thrombectomy Ultrasound Doppler abnormal Ventricular dysfunction

Symptomtext

Hospitalized 01/17/2022; COVID-19 positive 01/17/2022; fully vaccinated plus booster Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 1/17/2022 Discharge Date: 1/19/2022 PRESENTING PROBLEM: Acute respiratory failure with hypoxia [J96.01] Other acute pulmonary embolism with acute cor pulmonale [I26.09] Acute pulmonary embolism with acute cor pulmonale, unspecified pulmonary embolism type [I26.09] Suspected COVID-19 virus infection [Z20.822] HOSPITAL COURSE: The patient is a 71-year-old male with a history of essential tremor as well as diabetes mellitus type 2, mild obesity and dyslipidemia who presented with increasing shortness of breath on 1/17. At the time of admission, CT showed bilateral ground-glass infiltrates as well as large PE with evidence of right heart strain. Patient was started on heparin and admitted to the hospital service. Film array was positive for COVID as well as RSV. The patient was started on remdesivir and dexamethasone. An echocardiogram was performed as biomarkers were elevated. Ultrasound of the lower extremities did show residual clot in the left lower extremity in the popliteal vein. Echocardiogram showed significant right heart strain and medical team was activated. After evaluation it was felt the patient would benefit from a thrombectomy, but no need for IVC filter. Thrombectomy was performed by IR on 01/18/2022. After undergoing thrombectomy the patient's hypoxia resolved. The patient was continued on heparin, and transition to Xarelto prior to discharge. With clinical improvement, it was felt that he did not require further treatment with remdesivir, but was prescribed dexamethasone at the time of discharge. Patient's thrombosis was considered precipitated by his COVID infection and recent long automobile trip, with 3-6 months of anticoagulation being recommended. Pulmonary does recommend a repeat echocardiogram to reassess pulmonary hypertension in the next 90 days. As patient was clinically stable, he was discharged to home on 01/19/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Acute pulmonary embolism with acute cor pulmonale, unspecified pulmonary embolism type Acute deep vein thrombosis of left popliteal vein Class 1 obesity in adult Tremor, essential Hyperlipidemia, unspecified hyperlipidemia type Type 2 diabetes mellitus without complication, without long-term current use of insulin Primary osteoarthritis of right knee Chronic fatigue
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler allopurinol (ZYLOPRIM) 100 MG tablet cetirizine (ZYRTEC) 10 MG tablet dexamethasone (DECADRON) 6 MG tablet metFORMIN (GLUCOPHAGE) 500 MG tablet multivita
Allergien: NKA
Vorherige Impfungen: -

VAERS 2059247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD 0809

kritisch

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 07.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 8,0
Dosis: N/A
Route/Site: - / AR

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

Abdominal X-ray Abdominal pain upper Appendix disorder Blood bilirubin increased Chest X-ray Dyspnoea Enteritis Enteritis infectious Hepatic infection Kidney infection Laboratory test Malaise Nausea Pulmonary oedema Pyrexia Septic shock

Symptomtext

Fell sick fever morning of 12/15 - started with nausea stomach pains fever rise within hours to 104.5, went to er where was told blood pressure was 88/40, hard to breath. Was in septic shock- small intestine full of infection which moved to kidneys, liver and appendix, fluid on lungs . Was in hospital 4 days and duscharged on the fourth . They said it wasn?t bacterial infection mite viral and couldn?t really pinpoint what the cause was but said it was enteritis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 4,0
Labordaten: I have multiple tests done 3 times a day along with X-rays of lungs abdomen and heart . When I left the hospital bilirubin was high and liver they wanted checked the following week snd then had to go back again for blood work 2 weeks later
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: Lisiniprol 20 mg
Allergien: None
Vorherige Impfungen: -

VAERS 2054415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MN
Alter: 92,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 13.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Died on 12/15/21 of what is believed to be natural causes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UTI
Vorgeschichte: Breast cancer, arthritis, constipation, dementia, esophageal reflux, essential hypertension, hyperlipidemia, depression, hip pain, urinary incontinence.
Andere Medikamente: Aspirin, lexapro, estrace, glucosamine, remeron, polyethylene glycol, metamucil.
Allergien: Amoxicillin, ciprofloxacin, nitrofurantoin, sulfa, simvastatin
Vorherige Impfungen: -

VAERS 2039641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: WI
Alter: 69,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 20.08.2021
Beginn: 30.10.2021
Tage bis Beginn: 71,0
Dosis: 2
Route/Site: IM / UN

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

Cerebrovascular accident Computerised tomogram head abnormal Death Neurological symptom Subarachnoid haemorrhage

Symptomtext

Patient arrived to hospital with stroke like symptoms on 10/31/2021, LKW 10/30. Stroke (subarachnoid hemorrhage) confirmed via CToH. Patient expired 11/5/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: vascular dementia, COPD, DDD, HTN, MI (1997), prior left occipital stroke, HLD, COVID-19 (08/2021), and recurrent pulmonary emboli
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1985282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: PA
Alter: 78,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Angiogram Chills Computerised tomogram Cough Death Dyspnoea Heart rate decreased Laboratory test Pain in extremity Pneumonia Pyrexia Skin discolouration Stent placement Thrombectomy Thrombosis

Symptomtext

Oct. 21, started out with chills and fever that went up to 102.7. Fever lasted 5 days. Monday, Oct. 25. we called PCP, He said it was a side affect of booster, it should pass. Monday night Mom started to have a cough and hard time breathing. she could not catch her breath after coughing. she was getting worse. Oct. 26, her left hand and fingers started to turn black and very painful, while getting worse with the breathing and coughing. Took her to ER. she had multifocal pneumonia and very low pulse in left arm and wrist. So then she was transfered to Medical Center OCt. 27, had angiogram done then Life flighted Oct. 28. then died Nov. 2, 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: ct. scans, labs were done daily, angiogram was done. Surgery to try and remove clots from arm and collarbone area. Stint was placed in Collarbone area. Clot was to big to remove.
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure, fibromalgia , degeberatuve disc disease
Andere Medikamente: Losarten/hctz 100-25MG, Laryca 100mg 3x day. Hydrcodone 7.5mg
Allergien: morphine and novicane
Vorherige Impfungen: -

VAERS 1981036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 15.11.2021
Beginn: 25.12.2021
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Arterial disorder Catheterisation cardiac abnormal Chest discomfort Coronary angioplasty Coronary arterial stent insertion Coronary artery dilatation Coronary artery stenosis Intensive care

Symptomtext

70-year-old man with no significant cardiac history. He was visiting relatives for the holidays today when he developed acute onset chest discomfort. He presented to the local ER and was found to have inferior STEMI. He was emergently transferred directly to the Hospital. There was noted to be a subtotal lesion in the distal right coronary artery. The right coronary artery is a moderate caliber dominant vessel which supplies a moderate area of myocardium and is 99% stenosed in the distal segment. The lesion was predilated with a 2.5 mm balloon, stented with a 2.5 mm drug-eluting stent, and postdilated with a 2.75 mm noncompliant balloon with multiple inflations to burst rated atmospheres. There was excellent angiographic result with reduction in stenosis from 99% to 0% residual and continued TIMI-3 flow down the vessel. Admitted to ICU for recovery.

Weitere VAERSDATA-Felder

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

VAERS 1952066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: TX
Alter: 97,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 18.10.2021
Beginn: 06.12.2021
Tage bis Beginn: 49,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death General physical health deterioration Inappropriate schedule of product administration SARS-CoV-2 test positive

Symptomtext

Tested positive for COVID on 12/6/21. Expired on 12/13/21. Patient was on palliative care services with significant decline in functioning prior to becoming covid positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 12/6/21: BINAX NOW COVID 19 AG CARD- Positive result
Aktuelle Erkrankungen: Malnutrition, weakness
Vorgeschichte: CVA, dementia, herpes, COPD, severe protein- calorie malnutrition
Andere Medikamente: -
Allergien: Aspirin, Penicillin, NSAIDs, Garlic, Pork
Vorherige Impfungen: -

VAERS 1948162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: GA
Alter: 76,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 10.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Death Unresponsive to stimuli

Symptomtext

Resident became unresponsive 911 called transported to the hospital but patient expired

Weitere VAERSDATA-Felder

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

VAERS 1933072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: WI
Alter: 91,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 22.09.2021
Beginn: 04.10.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: - / -

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

Death

Symptomtext

Patient was admitted to hospital 12 days after receiving covid vaccine dose #3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1921178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: NC
Alter: 88,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 09.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Chest X-ray abnormal Condition aggravated Death Lethargy Pulmonary congestion Respiratory tract congestion SARS-CoV-2 test negative

Symptomtext

11/9 Booster administered- No fever, negative Covid test, Chest xray mild pulmonary venous congestion. Seen by Attending physician and stated OK to receive vaccine. 11/11 lethargy, chest congestion, Telehealth visit, Had MOST form for DNR and do not hospitalize, Family requested to go to ED 11/11 To ED 11/12 Returned from ED with DNR and Hospice ordered. Seen by NP. Orders for IV fluids and IV antibiotic 11/13 Resident expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 11/6 Chest xray mild pulmonary venous congestion
Aktuelle Erkrankungen: mild pulmonary venous congestion via chest xray with negative covid test
Vorgeschichte: A. fib Hypertension CHF Hypothyroidism DVT Cholecystitis Past Surgical History: Cholecystectomy Permanent pacemaker placement Tubal ligation Right hip intramedullary hip screw 3-4 years ago Left hip repair
Andere Medikamente: Atropine Sulfate Sol 1%, Azithromycin 500mg, Ceftriaxone IV, Exelon , Fentanyl, , Ativan Liq po, Morphine Sublin, IV flushes
Allergien: Clavlanic Acid, Codeine, Fexafenadine, Ketaconazole, Ofloxacin, Bactrim, Trimethoprim, Flexeril, Hydrocodone, Penicillin, Toradol, Tramadol
Vorherige Impfungen: -

VAERS 1906144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Bradycardia Death Pyrexia Respiratory distress Tachycardia

Symptomtext

Respiratory distress - Tachycardia, with periods of bradycardia, fever observed at approx 3:09 pm - call to MD who gave order to send to ER for Eval and Treat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Sent to the hospital for Eval and Treat - Hospital called facility with notification of death of Patient
Aktuelle Erkrankungen: PNA treated within the last 30 days
Vorgeschichte: Seizure Disorder, COPD, CVA, Hypertension, GERD, Dementia, HLD, Aphasia, Anxiety, Depression,
Andere Medikamente: Pepcid,
Allergien: none
Vorherige Impfungen: -

VAERS 1891018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: OR
Alter: 44,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 02.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: - / LA

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

Delivery Exposure during pregnancy Foetal death Ultrasound scan abnormal

Symptomtext

I received the first shot on November 2, 2021. On Nov 9th I went in for an ultrasound (17 weeks pregnant). My son's heartbeat stopped. They confirmed he died. We know for sure he was alive on my last appointment Oct. 29, 2021. He was diagnosed prior to the vaccine as having Trisomy 18. The doctors strongly encouraged me to get the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Foetal death
Hospital-Tage: 1,0
Labordaten: Delivery of deceased child was on November 11, 2021 at the hospital.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Celexa, Prenatal vitamin, iron supplement
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1831764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Arteriogram coronary normal Arthralgia Chest pain Chills Computerised tomogram abdomen normal Computerised tomogram thorax abnormal Dyspnoea Ear pain Electrocardiogram T wave inversion Neck pain Pain Pain in extremity Pain in jaw Pulmonary embolism Pyrexia Troponin normal Ultrasound Doppler normal

Symptomtext

Within 12 hours after receiving dose #3 of the COVID vaccine, the patient reports sharp pain in ear/jaw/neck and knee and toes. The patient also reports body aches and chills/fevers 100.4. The patient took her BP (192/117) and messaged her PCP and rested at home. Patient took her own benazepril 40mg and hydrochlorothiazide 12.5mg. On 10/13, the patient went to Urgent Care per MD instructions and was taken by ambulance from urgent care to Hospital as EKG showed inverted T waves in urgent care and patient reported onset of chest pain. She was given nitroglycerin 0.4mg SL x 1 and aspirin 81mg x 4 by ambulance. She was treated and discharged on 10/15. She rested at home and on 10/16, the chest pain returned and new onset shortness of breath. She drives to a facility. A CT chest showed a tiny nonocclusive pulmonary embolism in a left upper lobe segmental pulmonary artery. CT abd/pelvis showed no DVT. Ultrasound doppler negative for DVTs. CT angiogram is performed and coronary arteries are clear. Troponins are negative. She was treated with Eliquis 10mg BID (10/17-10/23) and then 5mg BID x 3 months. She is discharged on 10/19/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: hyperlipidemia w predominanthypertriglycerides, uncontrolled hypertension, uncontrolled type 2 diabetes
Vorgeschichte: -
Andere Medikamente: -
Allergien: Fluticasone (mood changes), morphine (nausea/vomiting), grass/pollen (dermatitis), oat (dermatitis)
Vorherige Impfungen: -

VAERS 1804672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 10.09.2021
Beginn: 07.10.2021
Tage bis Beginn: 27,0
Dosis: UNK
Route/Site: - / -

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

Blood osmolarity decreased Death Hyponatraemia

Symptomtext

death E87.1 - Hypo-osmolality and hyponatremia

Weitere VAERSDATA-Felder

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

VAERS 1797961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 06.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Death Gastrointestinal haemorrhage Syncope

Symptomtext

death K92.2 - GI bleed I95.1 - Orthostasis K92.2 - Gastrointestinal hemorrhage, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1778995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 03.09.2021
Beginn: 16.09.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory distress syndrome COVID-19 COVID-19 pneumonia Fatigue Pulmonary embolism Respiratory symptom SARS-CoV-2 test positive

Symptomtext

Saw PCP for annual physical on 9/3/2021. Felt generally well at that appointment other than some mild ongoing fatigue, nothing specific. Administered first dose of Pfizer Covid-19 vaccine that day and tolerated it well. Patient reported significant increase in fatigue on 9/6/2021. Came in to be tested for Covid-19 on 9/10/2021 and tested positive. Insidious onset of respiratory symptoms which progressively got worse around this time. Came in to Emergency Department on 9/16/2021 and was found to have Covid-19 pneumonia, acute respiratory distress and pulmonary embolism but main factor for admission to hospital was the pulmonary embolism.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: As above.
Aktuelle Erkrankungen: Vaccine given 9/3/2021. Covid-19 positive diagnosis made on 9/10/2021. Symptom onset including severe fatigue on 9/6/2021 with respiratory symptoms to follow. Diagnosed with Covid-19 pneumonia, ARDS, and pulmonary embolism on 9/16/2021. It is unclear if the administration of the Covid-19 vaccine contributed to development of pulmonary emboli or if this was related to Covid-19 illness itself, and/or if oral contraceptive pill was contributing factor.
Vorgeschichte: None known other than foot pain which she was seeing podiatry for. Patient is otherwise very healthy.
Andere Medikamente: desogestreL-ethinyl estradioL (Apri) 0.15-0.03 mg per tablet - Take 1 tablet by mouth daily for menstrual cycle regulation
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1768504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 90,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 24.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / -

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

Cerebral haemorrhage Death

Symptomtext

death I61.9 - Cerebral parenchymal hemorrhage (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1765317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: WI
Alter: 77,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 30.09.2021
Beginn: 03.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

My dad had a physical 9/30/2021 and received a clean bill of health complete with lab work. He then received his second covid vaccine. sunday 10/3/2021 my dad got up went to the store..called my mother around noon had lunch and went back to work. two hours later he had an event and DIED. he was In perfect tip top health. he was taken from us way to soon

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: multi vitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1723558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 22.09.2021
Impfdatum: 27.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / -

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

Acute myocardial infarction Acute respiratory failure Death Dyspnoea

Symptomtext

death SHORTNESS OF BREATH Non-ST elevation (NSTEMI) myocardial infarction Acute respiratory failure with hypoxia

Weitere VAERSDATA-Felder

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

VAERS 1693148

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 09.09.2021
Beginn: 09.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Death Life support Pulse absent

Symptomtext

Death Patient was being prepared for discharge. Found pulseless in room around 1845 which was roughly 3 hours post vaccination. Additional therapies given during ED stay were IV fluids and IV acetaminophen. ACLS initiated and continued for ~45 minutes. Time of death called at 1928

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Patient was being seen in emergency department for abdominal pain status post a fall, being treated for UTI (with cefdinir) since previous week
Vorgeschichte: 3 abdominal hernias, hypertension, diabetes, neuropathy, hyperlipidemia
Andere Medikamente: Cefdinir 300 mg capsule BID Duloxetine 30 mg DR capsule daily Ergocalciferol (Vitamin D-2) 50,000 capsule weekly Fenofibrate 145 mg tablet daily Insulin aspart 25 units SQ TID before meals Lisinopril 5 mg tablet daily Pravastatin 20 mg
Allergien: Ibuprofen (unknown) Morphine (headache)
Vorherige Impfungen: -

VAERS 1689283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

kritisch

Staat: ID
Alter: 42,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 03.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

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

Anticoagulant therapy Back pain Blood cholesterol normal Dyspepsia Laboratory test abnormal Myocardial infarction Pain in extremity

Symptomtext

Patient woke Tuesday, 4 days after her second dose of Pfizer, and had terrible arm and back pain and what felt like really bad heart burn in her chest. Her mother called Wednesday and told me about her symptoms and I suggested getting to a doctor and getting an EKG. The patient came in today and was feeling much better but she was getting nitrogylcerin SL tabs and baby aspirin because cardiologist said she had minor heart attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Pt reported that her labs had been indicative of a heart attack. She didn't have any other risk factors- she is thin, cholesterol normal, bp normal and no sign of any other clots, etc.
Aktuelle Erkrankungen: Hypothyroidism
Vorgeschichte: Hypothyroidism
Andere Medikamente: NP Thyroid, Multivitamin
Allergien: no known
Vorherige Impfungen: -

VAERS 2713219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 13.11.2023
Impfdatum: 03.01.2022
Beginn: 10.09.2023
Tage bis Beginn: 615,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Asthenia COVID-19 Cardiac telemetry normal Fall Syncope

Symptomtext

BRIEF OVERVIEW: Admission Date: 9/10/2023 Discharge Date: Sep 11, 2023 Discharge Disposition: home or self care Active Issues Requiring Follow-up: None No future appointments. DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Weakness generalized [R53.1] AKI (acute kidney injury) (HCC) [N17.9] Syncope, unspecified syncope type [R55] COVID-19 [U07.1] HOSPITAL COURSE: Patient was admitted for observation and evaluation for her falls. On telemetry there was no a arrhythmias noted. PT was not performed, but OT saw patient and found her to be strong enough to go home. Her diet was improved while she was here in the hospital. IV fluids were again not required. No symptomatic treatments were necessary for COVID as she had no pulmonary or GI symptoms. This patient was medically stable at discharge to go home. She will have a tenuous course of caution with mobilization and daughter will be with. Would consider her contagious for a 7 day. Which is nearly up at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Constipation, slow transit Anxiety and depression Acquired hypothyroidism Advanced care planning/counseling discussion Complaints of memory disturbance Generalized weakness Compression fracture of body of thoracic vertebra (HCC) Syncope and collapse AKI (acute kidney injury) (HCC) COVID-19
Andere Medikamente: ALPRAZolam (XANAX) 0.25 mg tablet aspirin 81 MG chewable tablet donepezil (ARICEPT) 10 MG tablet escitalopram (LEXAPRO) 10 mg tablet furosemide (LASIX) 20 MG tablet levothyroxine (SYNTHROID) 50 MCG tablet magnesium oxide (MAG-OX) 400 mg tab
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 2647213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 20.06.2023
Impfdatum: 16.12.2021
Beginn: 08.03.2022
Tage bis Beginn: 82,0
Dosis: 3
Route/Site: IM / LA

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

Deep vein thrombosis

Symptomtext

ACUTE DVT OF LEFT POPLITEAL VEIN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2570036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: NY
Alter: 57,0
Geschlecht: M
Eingang: 29.01.2023
Impfdatum: 11.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: SYR / AR

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

Angiogram cerebral normal Anti-muscle specific kinase antibody Antibody test Antinuclear antibody Borrelia test negative C-reactive protein normal Diplopia Full blood count normal Magnetic resonance imaging head normal Metabolic function test Red blood cell sedimentation rate normal Scan with contrast normal Thyroid function test normal VIth nerve paralysis

Symptomtext

Patient developed double vision beginning 5-6 weeks after the booster; diagnosed as isolated Trochlear nerve (Cranial nerve IV) palsy. Symptoms persistent 1 year later. All labs and imaging normal. Evaluated and confirmed by general ophthalmologist, neurologist, neuro-ophthamologist, ENT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: MRI Brain/IAC with and without contrast (2/24/2022) - normal. MR Angiogram Head (10/19/2022) - normal All bloodwork normal (4/15/2022) including: CBC, BMP, CMP, TFT's, Lyme titers, ESR, CRP, ANA, ACRM binding Ab, MuSK Ab
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Multivitamin, vitamin D, Fish oil, vitamin C
Allergien: none
Vorherige Impfungen: -

VAERS 2560091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FD0809

schwer

Staat: WI
Alter: 74,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 15.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 49,0
Dosis: 3
Route/Site: SC / RA

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

Agitation Balance disorder Basedow's disease Blood thyroid stimulating hormone Condition aggravated Dizziness Feeling abnormal Food allergy Heart rate irregular Loss of personal independence in daily activities Syncope Thyroxine Tri-iodothyronine Vertigo Vestibular migraine

Symptomtext

Date Event 2021-03-14 Covid vaccine Pfizer EN6207 2021-04-06 Covid vaccine Pfizer EW0150 2021-11-15 Covid Booster Pfizer Lot FD0809 2022-01-03 Graves disease episode onset manifested by aggitation, 120 bpm pulse, irregular heart rate; successfully treated with methimazole and beta blocker. However, for appoximately 3 weeks after treatment began, had a complete shutdown consisting of brain fog, dizziness, inertia. After emerging had to "relearn" various skills that had been in place for 20 years. 2023-01-14 Continue treatment of 2022-01-03 episode. Am hoping for a remission. Initial onset of Graves disease 1996 diagnosed with radioactive iodine uptake and scan. Since that time I have had short episodes treated successfully with methimozole for about 12 weeks or less followed with remission. Was already taking a beta blocker for migraine in the earlier years. However, the 01-03-2022 episode has been dramatically different and is still on-going after more than a year. The difference is the duration and the dramatic difference in symptoms, including the bodily shutdown for just under 3 weeks. Also new is the tree nut allergy to pecans and walnuts triggering vestibular/syncopal migraine. 2021-10-01 Vestibular/syncopal migraine triggered by pecans. Within months walnuts would be added to list.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: TSH/T3/T4 testing. 01/03/2022 and continuing throughout 2022 and 2023 at regular intervals.
Aktuelle Erkrankungen: -
Vorgeschichte: 1996 diagnosed with Graves disease. Since that time have had infrequent short episodes lasting maybe 12 weeks at most. Treatment with methimazole and beta blockers.
Andere Medikamente: none
Allergien: Latex Tetracycline Timolol Latanoprost Travoprost Carboxymethylcellulose Pecans, walnuts (syncope, vertigo) Apraclonidine solution (headache, dizzy) Penicillin
Vorherige Impfungen: -

VAERS 2546413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 57,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 12.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Paralysis Transient ischaemic attack

Symptomtext

Per pt call on 12.29.22. pt started having half body paralyzed on and off about 7-8 days after injection. After discussing with regular MD was rushed to ER. Pt ok know, but per pt a neurologist said that he had many mini strokes. per pt around 21 mini strokes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: don't have access to pt hospital file
Aktuelle Erkrankungen: unknown
Vorgeschichte: non known
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2537866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 27.01.2022
Beginn: 11.12.2022
Tage bis Beginn: 318,0
Dosis: 3
Route/Site: - / -

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

Acute pulmonary oedema COVID-19 Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Computerised tomogram thorax abnormal Condition aggravated Dyspnoea Echocardiogram Ejection fraction decreased Goitre Hypoxia Pulmonary oedema SARS-CoV-2 test positive Scan myocardial perfusion normal Thyroid mass Tracheal disorder Wall motion score index abnormal

Symptomtext

Discharge Provider: PRIVATE, MD Primary Care Provider: PRIVATE, MD Admission Date: 12/11/2022 Discharge Date: Dec 16, 2022 COVID positive Date 12/11/2022 PRESENTING PROBLEM: Flash pulmonary edema (HCC) [J81.0] Hypoxia [R09.02] Acute on chronic congestive heart failure, unspecified heart failure type (HCC) [I50.9] HOSPITAL COURSE: Patient is a 88 y.o. female with past medical history of chronic diastolic CHF, Crohn's disease, CKD stage IIIA, permanent atrial fibrillation on Xarelto, hyperthyroidism and pulmonary hypertension who presented with shortness of breath. She was brought in by EMS and in the ER was found to have COVID-19, CXR with pulmonary edema, and started on HFNC and Lasix. She was admitted to medicine for further evaluation. Oxygen was able to wean down to nasal cannula. Continued on steroids while on oxygen. Continued Lasix to diurese. She underwent TTE to further evaluate which showed a newly decreased EF to 43% with minor RWMA. Cardiology was consulted. She underwent a Lexiscan which showed no myocardial ischemia, and return of EF to normal. Lasix was switch to oral dosing. On initial CXR in ER there was note of a thyroid mass with unclear nature. A CT thorax was completed to further evaluate this and showed a goiter that is causing mass effect on the trachea. This is a chronic problem the patient is well aware of. She follows closely with Dr. (Endocrinology) to monitor this and wants to avoid further interventions if possible. She was in stable condition and discharged home on 12/16/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute pulmonary oedema
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Flash pulmonary edema (HCC) Symptomatic spider varicose vein, left Varicose veins of leg with complications, left Permanent atrial fibrillation (HCC) Chronic heart failure with preserved ejection fraction (HCC) Pulmonary hypertension (HCC) Hypertension Ileitis UTI (urinary tract infection) Other specified anemias Platelets decreased (HCC) CKD stage G3a/A1, GFR 45-59 and albumin creatinine ratio <30 mg/g (HCC) Hyperthyroidism with goiter Toxic multinodular goiter Prediabetes Crohn's disease (HCC) of terminal ileum Gram negative sepsis (HCC) Hemorrhage
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet budesonide (ENTOCORT EC) 3 MG delayed release capsule cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) capsule ferrous sulfate 325 (65 FE) MG tablet furosemide (LASI
Allergien: NKA
Vorherige Impfungen: -

VAERS 2444784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: IL
Alter: 48,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 20.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Amenorrhoea Feeling abnormal Heavy menstrual bleeding Thrombosis

Symptomtext

Patient has reported feelings of "brain fog". Additionally, she has reported a heavy menses with clot/s following the vaccination followed by amenorrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GERD, Chronic Kidney Disease, Hypertension, Anxiety
Andere Medikamente: Protonix, Celexa, Buspar, Cozaar, MVI
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2399274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: VA
Alter: 67,0
Geschlecht: M
Eingang: 02.08.2022
Impfdatum: 24.09.2021
Beginn: 26.06.2022
Tage bis Beginn: 275,0
Dosis: 4
Route/Site: IM / LA

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

Anticoagulant therapy Computerised tomogram abnormal Pain in extremity Thrombosis

Symptomtext

I started having pain in my left leg in late June 2022. I went to see my Primary Care Physician who had a leg CT Scan and found a blood clot behind my knee going down my lower leg. He sent me to see my blood doctor who took me off Xarelto and had me start using Enoxaparin 0.4mg injections and I will be going back August 8, 2022. My blood doctor had referred me to the hospital who wants to scan my veins because I have been on Xarelto for years and have still got a clot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: CT Scan
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure; High Cholesterol; Sleep Apnea
Andere Medikamente: Xarelto; Lisinopril/hctz; Atorvastatin; Multivitamin; Vitamin C; Vitamin D
Allergien: No
Vorherige Impfungen: -

VAERS 2308371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: OR
Alter: 13,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 29.11.2021
Beginn: 01.02.2022
Tage bis Beginn: 64,0
Dosis: 2
Route/Site: IM / LA

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

Facial paralysis

Symptomtext

In Feb. 2022, my daughter came to me to tell me she could not wrinkle her nose of move the side of her face. I called the doctor the next morning. She had noticed she had that longer than that night. She for sure had it a week before and just thought to finally tell me. The doctor was not sure if it was due to infection on a tooth. He gave her an antibiotic and acyclovir and prednisone. She is good now and it took about a week to clear up from that date. She has braces, also so I called her dentist to see if something of that nature could have created that effect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None; Sensitivity to morphine
Vorherige Impfungen: -

VAERS 2093638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MA
Alter: -
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 24.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / AR

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

Cerebral venous sinus thrombosis Cerebral venous thrombosis Headache Jugular vein thrombosis Magnetic resonance imaging head abnormal Magnetic resonance imaging Phonophobia Photophobia Sigmoid sinus thrombosis Superior sagittal sinus thrombosis Transverse sinus thrombosis Vomiting

Symptomtext

[Pfizer Vaccine] use for COVID-19 under Emergency Use Authorization (EUA): booster given on 12/14/2021. On pt noticed headache on Sunday (1/16) described as generalized, aching and constant with associated photophobia and phonophobia. The headache continued, with associated daily vomiting. on 1/25 Brain MRI showed CVST. Potential etiologies include occult malignancy and exposure to the Covid 19 vaccine. This has been very rarely associated with thrombocytopenia and extensive VST, although there are very few cases in which this occurred without thrombocytopenia. Extensive venous sinus thrombosis involving the middle third and posterior third of the superior sagittal sinus, the paramedian aspects of multiple draining cortical veins at the vertex, the medial left transverses sinus the entire right transverse sinus, right sigmoid sinus, right jugular bulb and proximal right jugular vein.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous thrombosis
Hospital-Tage: -
Labordaten: BRAIN MRI, 24-Jan-2022, Cerebral venous thrombosis
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperuricemia, Benign paroxysmal positional vertigo, Osteopenia of multiple sites, Intermittent urinary incontinence, History of vesicoureteral reflux, History of renal stone, History of basal cell carcinoma (BCC) of skin, History of tonsillectomy, At high risk for breast cancer, Chronic bilateral low back pain without sciatica, Acute cystitis without hematuria, Vitamin D deficiency, Stage 3a chronic kidney disease, Pulmonary nodules
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2093638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

schwer

Staat: MA
Alter: -
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 24.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

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

Cerebral venous sinus thrombosis Cerebral venous thrombosis Headache Jugular vein thrombosis Magnetic resonance imaging head abnormal Magnetic resonance imaging Phonophobia Photophobia Sigmoid sinus thrombosis Superior sagittal sinus thrombosis Transverse sinus thrombosis Vomiting

Symptomtext

[Pfizer Vaccine] use for COVID-19 under Emergency Use Authorization (EUA): booster given on 12/14/2021. On pt noticed headache on Sunday (1/16) described as generalized, aching and constant with associated photophobia and phonophobia. The headache continued, with associated daily vomiting. on 1/25 Brain MRI showed CVST. Potential etiologies include occult malignancy and exposure to the Covid 19 vaccine. This has been very rarely associated with thrombocytopenia and extensive VST, although there are very few cases in which this occurred without thrombocytopenia. Extensive venous sinus thrombosis involving the middle third and posterior third of the superior sagittal sinus, the paramedian aspects of multiple draining cortical veins at the vertex, the medial left transverses sinus the entire right transverse sinus, right sigmoid sinus, right jugular bulb and proximal right jugular vein.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous thrombosis
Hospital-Tage: -
Labordaten: BRAIN MRI, 24-Jan-2022, Cerebral venous thrombosis
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperuricemia, Benign paroxysmal positional vertigo, Osteopenia of multiple sites, Intermittent urinary incontinence, History of vesicoureteral reflux, History of renal stone, History of basal cell carcinoma (BCC) of skin, History of tonsillectomy, At high risk for breast cancer, Chronic bilateral low back pain without sciatica, Acute cystitis without hematuria, Vitamin D deficiency, Stage 3a chronic kidney disease, Pulmonary nodules
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2183822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 30.08.2021
Beginn: 02.09.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / LA

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

Antinuclear antibody Arthralgia Blood calcium Blood cortisol Blood creatine phosphokinase Blood creatinine Blood lactate dehydrogenase Blood thyroid stimulating hormone Blood uric acid Bone pain C-reactive protein Condition aggravated Disturbance in attention Dyspepsia Dyspnoea Feeling abnormal Full blood count Gastrointestinal disorder

Symptomtext

because of this I've had to reduce to only working one day a week; This has prevented me from performing normal daily functions; neurological issues; felt like she was going to faint; chronic abdominal digestive issues gotten worse/side effects have progressed to really bad; difficulty breathing; really bad head pain in back of head; tail bone pain; brain fog; difficulty focusing; blurry vision slightly; hasn't been driving; chronic abdominal digestive issues gotten worse and heartburn; chronic abdominal digestive issues gotten worse and heartburn; muscle fatigue; I have had joint pain/joint pain in fingers, knees and ankles; swelling; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Physician) from medical information team for a Pfizer sponsored program. The reporter is the patient. Other Case identifier(s): MIQ-02032022-344. A 26 year-old female patient received bnt162b2 (COMIRNATY), intramuscular, administered in deltoid left, administration date 30Aug2021 12:09 (Lot number: FD0809) at the age of 26 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Chronic Digestive Issues" (ongoing), notes: Started about 10 Years Ago and haven't really been diagnosed; "Allergic to Shellfish" (ongoing); "Irritable bowel syndrome" (ongoing); "Dyspepsia", start date: 2013 (ongoing); "GERD" (unspecified if ongoing). Concomitant medication(s) included: PANTOPRAZOLE taken for gastrooesophageal reflux disease, dyspepsia, start date: 15Jul2021. The following information was reported: ARTHRALGIA (non-serious) with onset 02Sep2021, outcome "not recovered", described as "I have had joint pain/joint pain in fingers, knees and ankles"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "unknown", described as "This has prevented me from performing normal daily functions"; NERVOUS SYSTEM DISORDER (non-serious), outcome "unknown", described as "neurological issues"; MUSCLE FATIGUE (non-serious) with onset 02Sep2021, outcome "not recovered", described as "muscle fatigue"; IMPAIRED WORK ABILITY (non-serious), outcome "unknown", described as "because of this I've had to reduce to only working one day a week"; HEADACHE (non-serious) with onset 30Jan2022, outcome "not recovered", described as "really bad head pain in back of head"; BONE PAIN (non-serious) with onset 30Jan2022, outcome "not recovered", described as "tail bone pain"; FEELING ABNORMAL (non-serious) with onset Jan2022, outcome "not recovered", described as "brain fog"; DISTURBANCE IN ATTENTION (non-serious) with onset Jan2022, outcome "not recovered", described as "difficulty focusing"; VISION BLURRED (non-serious) with onset Jan2022, outcome "not recovered", described as "blurry vision slightly"; GASTROINTESTINAL DISORDER (non-serious), DYSPEPSIA (non-serious) all with onset Dec2021, outcome "not recovered" and all described as "chronic abdominal digestive issues gotten worse and heartburn"; PRESYNCOPE (non-serious), outcome "not recovered", described as "felt like she was going to faint"; IMPAIRED DRIVING ABILITY (non-serious) with onset Jan2022, outcome "not recovered", described as "hasn't been driving"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "chronic abdominal digestive issues gotten worse/side effects have progressed to really bad"; SWELLING (non-serious) with onset 02Sep2021, outcome "unknown", described as "swelling"; DYSPNOEA (non-serious), outcome "unknown", described as "difficulty breathing". The event "i have had joint pain/joint pain in fingers, knees and ankles" was evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of arthralgia, loss of personal independence in daily activities, nervous system disorder, muscle fatigue, impaired work ability, headache, bone pain, feeling abnormal, disturbance in attention, vision blurred, gastrointestinal disorder, dyspepsia, presyncope, impaired driving ability, condition aggravated, swelling. Additional information: It was reported that the patient experienced joint pain in fingers, knees and ankles, really bad head pain in back of head, tail bone pain, brain fog, difficulty focusing, blurry vision slightly, hasn't been driving, muscle fatigue, chronic abdominal digestive issues gotten worse and heartburn, felt like she was going to faint, back pain, chest pain, difficulty breathing which were worsened except neurological issues and prevented her from performing normal daily functions and because of this she had to reduce to only working one day a week. She stated that it had been 6 months, and she had to see a rheumatologist and neurologist, and she still had joint pain and her side effects have progressed. Stated that she had an MRI taken the other day and the doctors are clueless right now on what to do. Caller stated that neurologist recommend her to go on an antidepressant to see if it was a nerve issue to calm her nerves down and stated that her rheumatologist wants her to try an anti-seizure medication called gabapentin where the events brain fog, fatigue, chest pain started on gabapentin. She was kept on prednisone on 3Oct2021, it was the general pack of prednisone and she didn't felt much different, but when she stopped taking it, she felt like a truck hit her and she was in a lot of pain. Since the rheumatologist thought the prednisone helped a bit, he upped the dosage to 10mg (NDC: 0054-0017-25 Lot: AB4663A Expiration: May2023) and she had to take it again on 16Nov2021 and that was when she had a lot of side effects from the Prednisone she was on it for a week and a half. Caller stated that she went to the emergency room for the Joint Pain on 24Oct2021 and on 24Nov2021 for prednisone reaction and they said to cut the prednisone cold turkey and the next week she struggled with getting back to normal. No additional vaccines were administered on same date of the Pfizer suspect. The patient had received no Prior Vaccinations (within 4 weeks) and no AE(s) following prior vaccinations. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20210917; Test Name: ANA; Result Unstructured Data: Test Result:NL/Neg; Test Date: 20220113; Test Name: calcium; Result Unstructured Data: Test Result:NL; Test Date: 20220210; Test Name: cortisol; Result Unstructured Data: Test Result:NL; Test Date: 20220113; Test Name: CK; Result Unstructured Data: Test Result:NL; Test Date: 20211024; Test Name: CR; Result Unstructured Data: Test Result:NL; Test Date: 20220113; Test Name: LDH; Result Unstructured Data: Test Result:NL; Test Date: 20220210; Test Name: TSH; Result Unstructured Data: Test Result:NL; Test Date: 20210917; Test Name: Uric acid; Result Unstructured Data: Test Result:NL/Neg; Test Date: 20210917; Test Name: CRP; Result Unstructured Data: Test Result:NL/Neg; Test Date: 20211024; Test Name: CBC; Result Unstructured Data: Test Result:NL; Test Date: 20220210; Test Name: Aldo/resin cation; Result Unstructured Data: Test Result:NL; Test Date: 20210917; Test Name: CCP160; Result Unstructured Data: Test Result:NL/Neg; Test Date: 20211024; Test Name: LFT; Result Unstructured Data: Test Result:NL; Test Name: MRI; Result Unstructured Data: Test Result:Normal; Comments: MRI brain normal; Test Date: 20210917; Test Name: RF; Result Unstructured Data: Test Result:NL/Neg; Test Date: 20220113; Test Name: Vit B12; Result Unstructured Data: Test Result:NL; Test Date: 20220113; Test Name: Vit D; Result Unstructured Data: Test Result:NL
Aktuelle Erkrankungen: Dyspepsia; Gastrointestinal disorder (Started about 10 Years Ago and haven't really been diagnosed); Irritable bowel syndrome; Shellfish allergy
Vorgeschichte: Medical History/Concurrent Conditions: GERD
Andere Medikamente: PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2127971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: NY
Alter: 18,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 02.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: - / RA

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

Paralysis Pelvic pain SARS-CoV-2 test

Symptomtext

Severe pelvic pain; Inability to move legs; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 18 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 02Jan2022 17:30 (Lot number: FD0809) at the age of 18 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Lyme disease" (unspecified if ongoing); "Soy allergy" (unspecified if ongoing); "COVID-19" (not ongoing), notes: covid prior vaccination. Concomitant medication(s) included: ZOLOFT; WELLBUTRIN; PROPRANOLOL; AMANTADINE. Vaccination history included: Bnt162b2 (First dose received in the right arm, at 05:30 PM. Lot. FH8027), administration date: 10Dec2021, when the patient was 18 years old, for COVID-19 immunisation. The following information was reported: PELVIC PAIN (hospitalization, disability) with onset 12Jan2022 07:00, outcome "not recovered", described as "Severe pelvic pain"; PARALYSIS (hospitalization, disability) with onset 12Jan2022 07:00, outcome "not recovered", described as "Inability to move legs". The patient was hospitalized for pelvic pain, paralysis (hospitalization duration: 15 day(s)). The events "severe pelvic pain" and "inability to move legs" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (26Jan2022) negative. Therapeutic measures were taken as a result of pelvic pain, paralysis. Treatment: Gabapentin, magnesium, morphine, Toradol, Tylenol. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Paralysis
Hospital-Tage: 15,0
Labordaten: Test Date: 20220126; Test Name: COVID 19 Test (Nasal Swab); Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (covid prior vaccination); Lyme disease; Soy allergy
Andere Medikamente: ZOLOFT; WELLBUTRIN; PROPRANOLOL; AMANTADINE
Allergien: -
Vorherige Impfungen: -

VAERS 1696291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 03.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Condition aggravated Deep vein thrombosis Hypoaesthesia Pain Pain in extremity Paraesthesia Peripheral swelling Tenderness Swelling Ultrasound Doppler Vaccination site pain

Symptomtext

My arm aches and is sore to the touch; Pain; swelling; numbness; tingling in left arm; pinching pain at injection site; sometimes it is worse; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Other HCP). The reporter is the patient. A 44 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Sep2021 12:30 (Lot number: FD0809) at the age of 44 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "moderate persistent asthma without complication" (unspecified if ongoing), notes: moderate persistent asthma without, complication, Asthma as a child; "bananas, mellons" (unspecified if ongoing); "Fur" (unspecified if ongoing); "chickenpox" (unspecified if ongoing), notes: Chickenpox as a child. Family history included: "churg-strauss" (unspecified if ongoing), notes: Mother; "HTN" (unspecified if ongoing), notes: Mother; "Hypothyroid" (unspecified if ongoing), notes: Mother; "hypothyroid-col cancer" (unspecified if ongoing), notes: maternal grandmother. There were no concomitant medications. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 03Sep2021 13:30, outcome "recovered" (2021), described as "My arm aches and is sore to the touch"; PAIN (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "Pain"; SWELLING (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "swelling"; HYPOAESTHESIA (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "numbness"; PARAESTHESIA (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "tingling in left arm"; VACCINATION SITE PAIN (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "pinching pain at injection site"; CONDITION AGGRAVATED (non-serious) with onset Sep2021, outcome "recovering", described as "sometimes it is worse". The events "my arm aches and is sore to the touch", "pain", "swelling", "numbness", "tingling in left arm", "pinching pain at injection site" and "sometimes it is worse" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, pain, swelling, hypoaesthesia, paraesthesia, vaccination site pain, condition aggravated. Additional information: Adverse events resulted in Pharmacy or Drug Store visit. The patient did not received any other vaccines within four weeks prior to the vaccination. No other medications in two weeks. The patient was not tested positive for covid 19 prior to vaccination as well as post vaccination. COVID-19 injection given. Had pinching pain at injection site immediately. Then a few minutes numbness started mid upper arm to hand, affecting entire surface of hand, wrist (down arrow) arm. Got worse the following week and now stable. Severity of numbness changes. Distraction helps. No pain or weakness in arm, shoulder or neck. See neurology 16Sep2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210914; Test Name: DVT; Result Unstructured Data: Test Result:absent; Test Date: 20210914; Test Name: doppler ultrasound; Result Unstructured Data: Test Result:Negative; Comments: Left Arm
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to wool; Asthma (moderate persistent asthma without complication Asthma as a child); Chickenpox (Chickenpox as a child); Churg Strauss syndrome (Mother); Colon cancer (maternal grandmother); Fruit allergy; Hypertension (Mother); Hypothyroidism (Mother)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1696291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 03.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Deep vein thrombosis Hypoaesthesia Pain Pain in extremity Paraesthesia Peripheral swelling Tenderness Swelling Ultrasound Doppler Vaccination site pain

Symptomtext

My arm aches and is sore to the touch; Pain; swelling; numbness; tingling in left arm; pinching pain at injection site; sometimes it is worse; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Other HCP). The reporter is the patient. A 44 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Sep2021 12:30 (Lot number: FD0809) at the age of 44 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "moderate persistent asthma without complication" (unspecified if ongoing), notes: moderate persistent asthma without, complication, Asthma as a child; "bananas, mellons" (unspecified if ongoing); "Fur" (unspecified if ongoing); "chickenpox" (unspecified if ongoing), notes: Chickenpox as a child. Family history included: "churg-strauss" (unspecified if ongoing), notes: Mother; "HTN" (unspecified if ongoing), notes: Mother; "Hypothyroid" (unspecified if ongoing), notes: Mother; "hypothyroid-col cancer" (unspecified if ongoing), notes: maternal grandmother. There were no concomitant medications. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 03Sep2021 13:30, outcome "recovered" (2021), described as "My arm aches and is sore to the touch"; PAIN (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "Pain"; SWELLING (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "swelling"; HYPOAESTHESIA (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "numbness"; PARAESTHESIA (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "tingling in left arm"; VACCINATION SITE PAIN (non-serious) with onset 03Sep2021 13:30, outcome "not recovered", described as "pinching pain at injection site"; CONDITION AGGRAVATED (non-serious) with onset Sep2021, outcome "recovering", described as "sometimes it is worse". The events "my arm aches and is sore to the touch", "pain", "swelling", "numbness", "tingling in left arm", "pinching pain at injection site" and "sometimes it is worse" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, pain, swelling, hypoaesthesia, paraesthesia, vaccination site pain, condition aggravated. Additional information: Adverse events resulted in Pharmacy or Drug Store visit. The patient did not received any other vaccines within four weeks prior to the vaccination. No other medications in two weeks. The patient was not tested positive for covid 19 prior to vaccination as well as post vaccination. COVID-19 injection given. Had pinching pain at injection site immediately. Then a few minutes numbness started mid upper arm to hand, affecting entire surface of hand, wrist (down arrow) arm. Got worse the following week and now stable. Severity of numbness changes. Distraction helps. No pain or weakness in arm, shoulder or neck. See neurology 16Sep2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210914; Test Name: DVT; Result Unstructured Data: Test Result:absent; Test Date: 20210914; Test Name: doppler ultrasound; Result Unstructured Data: Test Result:Negative; Comments: Left Arm
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to wool; Asthma (moderate persistent asthma without complication Asthma as a child); Chickenpox (Chickenpox as a child); Churg Strauss syndrome (Mother); Colon cancer (maternal grandmother); Fruit allergy; Hypertension (Mother); Hypothyroidism (Mother)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2076956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD-0809

schwer

Staat: PA
Alter: 54,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Dizziness Haemorrhage Heavy menstrual bleeding Thrombosis

Symptomtext

Immediately after first dose experienced unusual menstrual symptoms. Two days after second dose experienced severe menorrhagia. Bled for 4 hours straight first day with larger and more clots than I have ever experienced before. Have been bleeding since, and am now experiencing chest pains and lightheadedness - I'm guessing from how much blood I've lost. I started saving the clots I could salvage in a pint-sized container and put them in the freezer. The container is almost full. I believe I've lost over two pints of blood over the past four days. This has never, ever, ever happened to me. I know that menorrhagia is one of the side effects of Pfizer's vaccines. This was not an informed decision that I was able to make. If I end up having to go to the hospital, Pfizer should pay for this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: None yet.
Aktuelle Erkrankungen: NONE.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Allergic to amoxicillin, naprosyn, micins, and certain food preservatives.
Vorherige Impfungen: -

VAERS 2063055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MI
Alter: 30,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 22.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Asthenia Blood lactic acid normal Blood magnesium normal Brain natriuretic peptide normal COVID-19 Chest X-ray Computerised tomogram head normal Computerised tomogram spine Drug screen negative Electrocardiogram abnormal Fall Fatigue Feeling abnormal Full blood count normal Loss of consciousness Mental status changes Metabolic function test normal

Symptomtext

Hospitalized (1.12.22); COVID-19 positive (1.12.22); fully vaccinated (no booster) Admitted 1.12.22 - 1.13.22 (32 hours - observation) CHIEF COMPLAINT: ALTERED MENTAL STATUS (per ems: found by coworkers on scene unreponsive on ground by them, last thing he remembers was feeling weak, inspiratory wheeze, was given duoneb in route that seemed to improve his symptoms, inititially Aox2 and is currently Aox4 with delays in respoinding, bs 162) DIAGNOSIS at time of disposition: 1. Syncope and collapse 2. COVID MEDICAL DECISION MAKING: Patient seen evaluated by myself. Electronic medical record was reviewed. I did review prior emergency department visits for similar complaints. I see that he were a ZIO patch in November 2021 for 14 days which was unremarkable. At this time patient appears somewhat groggy. Will do routine labs, urine drug screen, EKG, chest x-ray as well as CT head and neck and x-rays of the right shoulder from his fall. EKG shows sinus mechanism with sinus arrhythmia. No ST elevation, depression or signs of acute ischemic change. Urine drug screen is negative Lactic acid is normal Troponin is normal BNP is normal Complete blood count and CMP are unremarkable Magnesium is normal CT head does not show any acute process CT cervical spine does not show any acute fracture Chest x-ray is unremarkable X-rays right shoulder did not show any fracture. At this time patient is re-evaluated. His vital signs have been stable in the emergency department. There has been no signs of significant cardiac ectopy. I discussed the findings with patient. It is my concern that since he has had serial episodes of the last few months these potentially could be seizure in etiology. The fact that he was altered after this last episode would further collaborate that. He has remained neurovascularly intact in the emergency department during my observation as well as has stable vital signs. I placed a call the observation unit for admission for likely echo/EEG/ MRI. Patient's COVID-19 screen did come back positive. I did reinterview him. Again he has had no cough, congestion or shortness of breath. No fevers or chills. He states he feels back to normal currently. He denies any recent upper respiratory infection symptoms over the last few weeks. He denies testing positive previously. He is vaccinated. I did speak with the observation unit regarding this COVID-19 positive finding. They have agreed still to take him for above workup. Blood Pressure Screening: Based on last blood pressure taken in the ED of 112/66, BP <120/80, routine follow up with PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: 12.16.21 - ED visit - CHIEF COMPLAINT: SYNCOPE (Patient coming from work at GR foam, patient had syncopal episode unwitnessed found by co worker around 1530 BG 130 , + LOC, A&O4 for EMS pain from right shoulder radiating down arm, feeling weak and tired, not normal, reports simular event 1 month a go and was told he had a TIA.) 12.28.21 - ED visit - abscessed tooth 01.02.22 - ED visit - dental pain s/p tooth extraction
Vorgeschichte: Bipolar disorder (HCC) Moderate persistent asthma with acute exacerbation Attention deficit hyperactivity disorder (ADHD), predominantly hyperactive type Syncope and collapse
Andere Medikamente: acetaminophen-codeine (TYLENOL #3) 300-30 MG per tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler beclomethasone Diprop HFA (QVAR REDIHALER) 80 MCG/ACT inhaler clindamycin (CLEOCIN) 150 MG capsule
Allergien: AmoxicillinSwelling IbuprofenGI Upset PenicillinsSwelling Steroids [Corticosteroids]Palpitations
Vorherige Impfungen: -

VAERS 2062400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 30.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain Abnormal faeces Activated partial thromboplastin time shortened Aphasia Asymptomatic COVID-19 Back pain Biopsy Blood albumin decreased Blood glucose normal Colonoscopy abnormal Computerised tomogram abdomen abnormal Computerised tomogram head normal Computerised tomogram spine Computerised tomogram thorax abnormal Dizziness Exposure to SARS-CoV-2 Faecal volume decreased Fall

Symptomtext

49 yo F w PMH of DCIS managed w mastectomies, hyperthyroidism (overactive thyroid nodules) >10 years currently managed by Physician--never requiring medications--managed with nodular drainage and biopsies for years. She presents after having a colonoscopy @ surgery CTR by yesterday or eval of recent hematochezia and change in stools. He biopsied a rectal mass and colon polyps--path pending (findings detailed below.) She ate pizza last evening following this and developed sweating, abd cramps, nausea, and tenesmus. She then passed a large amount of hematochezia @ 8pm with bright and dark blood with clots and has had #3-4 episodes overnight. She did not sleep. At 5a she again felt tenesmus-- am ambulated to the bathroom, felt sweaty and lightheaded and next think that she recalls was being helped in the bathroom by her husband. He recalls hearing a thud in the bathroom at 5a and finding her partially standing but bending forward holding herself on the door then sliding down to the floor. He witnessed her eyes being open but that she was nonverbal w/ a blank stare when he spoke to her. She had a bleeding laceration to her central forehead. She had 10 seconds of tremorous upper extremities (also had when fainted years ago postop) but no head arching back, no eyes rolling back, no tongue biting, and no urinary incontinence . She was incontinent of about 2 liters of rectal blood on the floor and between her thighs. She eventually responded to him and EMS was summoned. She does not recall falling or hitting her head but it is presumed that she hit it on the toilet. She has intermittent abd cramping. She has nausea but no vomitting, no hematochezia, no focal abd or rectal pain. She has had low back pian x 2weeks ands noticed R>L groin lymphadenopathy 1 week ago. She developed increased fatigue 3 months ago with recent change in her BMs to smaller caliber, more explosive evacuation, foul smelling, and noticed that they float. She had an episode about 1 week ago of hematochezia followed by a few episodes of melena. This is what prompted yesterday's colonoscopy. In the ED, she has been hypotensive (90/50s--a few MAPs <65) with no tachycardia and no respiratory depression. Afebrile. She has a mid forehead superficial lac (nonsuturable) w/ dried blood, mild swelling. She is calm, pale, and in NAD. She has had no further hematochezia since 05am. Labs: WBC 13, Hgb 8.8, PLts nl. CMP unremarkable except: gluc 198 (AIC in am), albumin 3.3, LFTS nl. PT/INR 14/1.2, PTT 25. I spoke w Dr who plans to observe for further bleeding and if occurs wil do flex sig. Dr had also seen pt in the ED. CT c/a/p: "pelvic congestion, multinodular goiter; minimal intramural air at the rectosigmoid junction and along the hepatic flexure of the colon related to recent procedure. There is no free air to suggest colonic perforation." NCCT Head, CT c-spine no acute fractures or acute IC abn. She received 1 liter NS IVF in the ED and is on 125cc/h maintenance. Her BP is still soft at times but overall fld responsive. She has had no further hematochezia when seen at 8am since 5am. Hospitalist has been asked to admit the pt. NOTE re: COVID positive (asymptomatic : She was exposed to her positive COVID daughter on 1/9/22; Patient tested positive on 1/12/22-- she needs COVID room neg pressure placement x10 days post testing positive which will be until tomorrow. DISCHARGE SUMMARY HAS NOT BEEN UPLOADED AT THIS TIME.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: GA
Alter: 17,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Blood test Body temperature C-reactive protein Diagnostic aspiration Echocardiogram Electrocardiogram Electrocardiogram T wave inversion Erythema Full blood count Immunisation Myocarditis Pyrexia Rash Troponin Troponin increased X-ray

Symptomtext

t-wave inversion; The rash was like tiny red dots that kids get when they were little.; Cardio Myositis; 3rd booster shot with Pfizer COVID 19 vaccine; Slight rash on truncal and thoracic area; Fever of 103 degrees Fahrenheit; His Troponin levels were increased; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 17 year-old male patient received bnt162b2 (BNT162B2), administration date 28Dec2021 (Lot number: FD0809, Expiration Date: 31Jan2022) at the age of 17 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "He is heavy but not obese" (unspecified if ongoing). There was no family medical history relevant to AE(s). There were no concomitant medications. Prior vaccinations (within 4 weeks), the patient did not receive other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s). The patient did not have any adverse event following prior vaccinations. Vaccination history included: Bnt162b2 (Dose: 01, Lot Number: EN6204 expiration is unknown and it could say EW6204, Anatomical location; left deltoid), administration date: 09Apr2021, when the patient was 16 years old, for COVID-19 immunization, reaction(s): "No adverse event"; Bnt162b2 (Dose: 02, Lot Number: EW OR EN0161, Anatomical location; left deltoid), administration date: 30Apr2021, when the patient was 16 years old, for COVID-19 immunization, reaction(s): "No adverse event". The following information was reported: IMMUNISATION (medically significant) with onset 28Dec2021, outcome "unknown", described as "3rd booster shot with Pfizer COVID 19 vaccine"; MYOCARDITIS (medically significant) with onset 03Jan2022, outcome "recovering", described as "Cardio Myositis"; ELECTROCARDIOGRAM T WAVE INVERSION (medically significant), outcome "unknown", described as "t-wave inversion"; RASH (medically significant) with onset 28Dec2021, outcome "recovering", described as "Slight rash on truncal and thoracic area"; PYREXIA (medically significant) with onset 28Dec2021, outcome "recovering", described as "Fever of 103 degrees Fahrenheit"; TROPONIN INCREASED (non-serious) with onset 2021, outcome "unknown", described as "His Troponin levels were increased"; ERYTHEMA (non-serious), outcome "unknown", described as "The rash was like tiny red dots that kids get when they were little.". The events "cardio myositis", "slight rash on truncal and thoracic area", "fever of 103 degrees fahrenheit", "his troponin levels were increased" and "the rash was like tiny red dots that kids get when they were little." were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood test: (unspecified date) unknown result; body temperature: (28Dec2021) 103 degrees; c-reactive protein: (unspecified date) unknown result; diagnostic aspiration: (unspecified date) unknown result; echocardiogram: (unspecified date) fine; electrocardiogram: (unspecified date) t-wave inversion, notes: which suggests he has some problems still; full blood count: (unspecified date) unknown result; troponin: (unspecified date) increased; x-ray: (unspecified date) unknown result. Therapeutic measures were taken as a result of myocarditis, electrocardiogram t wave inversion, rash, pyrexia, troponin increased, erythema. The patient had slight rash on truncal and thoracic in the evening of 28Dec2021, and throughout the next day. He also had fever of 103 degrees Fahrenheit in the evening of 28Dec2021 post vaccination. That was the only time he got either of those and it was after the third dose as well. The rash was like tiny red dots that kids get when they were little. They just thought he was having a robust immune response. He had a fever of 103 degrees Fahrenheit for 4 days. The rash was on his stomach and back, his truncal and thoracic region. His symptoms started New Years Eve. It was very serious when he had it on 31Dec2021, but she thought he was having reflux. He had cardio myositis first thing on 03Jan2022, Monday morning. His troponin levels were already going down by the time he was seen on Monday. It had improved, but he had a t-wave inversion, which suggests he has some problems still. But he was mean as ever and would probably be fine. The patient did not visit to an emergency room. The patient had several physicians and lab visits. She did not know all of it, CBC, Tropin, Cardiac, C Reactive Protein monitoring. He also received palliative care, Ibuprofen, rest and monitoring. He had been seeing a cardiologist. They had been caught up being sick, so today was the first day they have not had an appointment or anything. The reporter's assessment of causality for the events Cardio Myositis, Slight rash on truncal and thoracic area, Fever of 103 degrees Fahrenheit was related with the suspect bnt162b2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Name: Blood test; Result Unstructured Data: Test Result:Unknown result; Test Date: 20211228; Test Name: Temperature; Result Unstructured Data: Test Result:103 degrees Fahrenheit; Test Name: C Reactive Protein monitoring; Result Unstructured Data: Test Result:Unknown result; Test Name: Radiograph; Result Unstructured Data: Test Result:Unknown result; Test Name: Echo; Result Unstructured Data: Test Result:fine; Test Name: EKG; Result Unstructured Data: Test Result:t-wave inversion; Comments: which suggests he has some problems still.; Test Name: CBC; Result Unstructured Data: Test Result:Unknown result; Test Name: Troponin; Result Unstructured Data: Test Result:increased; Test Name: Xrays; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High weight
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: GA
Alter: 18,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 28.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac imaging procedure abnormal Chest pain Chills Cough Echocardiogram abnormal Echocardiogram Electrocardiogram Magnetic resonance imaging heart Myocarditis Ejection fraction decreased Right ventricular ejection fraction decreased Sneezing Tricuspid valve incompetence Pericarditis Troponin increased

Symptomtext

Chest pain, hospitalized with Myocarditis/Pericarditis, released on anti inflammatory meds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: EKG, ECCO, MRI cardiac
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1935708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: GA
Alter: 18,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 28.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / LA

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

Cardiac imaging procedure abnormal Chest pain Chills Cough Echocardiogram abnormal Echocardiogram Electrocardiogram Magnetic resonance imaging heart Myocarditis Ejection fraction decreased Right ventricular ejection fraction decreased Sneezing Tricuspid valve incompetence Pericarditis Troponin increased

Symptomtext

Chest pain, hospitalized with Myocarditis/Pericarditis, released on anti inflammatory meds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: EKG, ECCO, MRI cardiac
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2039806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: WI
Alter: 68,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 10.09.2021
Beginn: 05.01.2022
Tage bis Beginn: 117,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 COVID-19 pneumonia Intensive care SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 3/3, 3/24, 9/9/21 COVID-19 positive by PCR on 1/5/22 admitted to hospital 1/13/22 to ICU for pneumonia d/t COVID 19 pt s/p lung transplant May 19, 2019; h/o DM, CAD

Weitere VAERSDATA-Felder

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

VAERS 2032030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: PR
Alter: 49,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 28.08.2021
Beginn: 28.08.2021
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 Diarrhoea Fatigue Nausea Oedema peripheral Pain in extremity Panic attack Presyncope Rectal haemorrhage Swelling Vomiting

Symptomtext

The patient refers that three days after vaccination (Pfizer) he began experiencing vasovagal episodes, nausea, vomiting, diarrhea, and panic attacks. The next day he began experiencing severe fatigue, and a week later he noticed severe pitting edema and swelling of bilateral lower extremities, up to the level of the knee. Now, in January, he refers he is experiencing rectal hemorrhage, severe chest pain, and pain in his left arm (contralateral to that of vaccination). The patient visited his primary doctor who suggested it was associated to vaccination event, and recommended he fill out a report. Recommendation by us was to visit a specialist, and undergo further more exhaustive and comprehensive testing, before reaching such a conclussion.

Weitere VAERSDATA-Felder

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

VAERS 2021038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

schwer

Staat: MA
Alter: 20,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Dyspnoea Myocarditis

Symptomtext

Patient started to exhibit chest pain on 12/31/21. Mom said he felt like he was having a heart attack and trouble breathing. He was taken to ER and diagnosed and treated for Myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 7,0
Labordaten: not given any tests or lab results
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE LISTED
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2020751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MN
Alter: 58,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 05.03.2021
Beginn: 07.01.2022
Tage bis Beginn: 308,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Immunosuppression Intensive care Vaccine breakthrough infection

Symptomtext

Fully vaccinated and boosted 11/17/21. Symptomatic COVID infection breakthrough with inpatient hospital stay to ICU. Immunosuppressed

Weitere VAERSDATA-Felder

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

VAERS 2019553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: TX
Alter: 12,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 08.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

Fainted about 2 minutes after getting the vaccine. She regained consciousness immediately. Patient was monitored while the ambulance arrived. Patient was assessed by the EMT and mom took patient home. She said she'll consult with her PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2018338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MI
Alter: 27,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Dizziness Seizure

Symptomtext

Seizure, dizziness, weakness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Seizure disorder, bipolar disorder, cigarette smoker, Horizon 14 Disease
Andere Medikamente: -
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2010442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 02.02.2021
Beginn: 31.12.2021
Tage bis Beginn: 332,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Hypoxia SARS-CoV-2 test positive Seizure

Symptomtext

Pt received Pfizer booster on 12/30 and was sent to the hospital due to a seizure on 12/31. Pt was hypoxic and found to be COVID positive.

Weitere VAERSDATA-Felder

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

VAERS 2010298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

schwer

Staat: OH
Alter: 18,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Grimacing Headache Heart rate irregular Loss of consciousness Musculoskeletal stiffness Nausea

Symptomtext

Patient winced upon injection, stiffened up for approximately 1 to 2 seconds then passed out. Woke up immediately. Felt nauseous which passed then developed a headache. EMS was called. Vitals good except irregular heartbeat detected. Went home with family, advised to follow-up with physician.

Weitere VAERSDATA-Felder

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

VAERS 1999422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Aphonia Throat tightness Thrombosis

Symptomtext

On 12/28/21 patient received first dose pfizer shot, after about 5 minutes patient reported losing her voice and throat starting to close up. Patient stated she did not need epipen. She was given dose of benadryl. After approximately 30 minutes, patient stated she was feeling better and comfortable leaving. We advised that she call us next day with an update and she did call us stating she was back to normal and her voice also had returned to normal. Patient called 1/3/22 to let us know she was admitted to hospital on 12/30/21 and just released 1/3/22. She was diagnosed with a blood clot in hospital but not confirmed if it was covid related. On 1/3/22 patient stated she was feeling well and following up with her PCP and a cardiologist

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: shellfish, iodine salt
Vorherige Impfungen: -

VAERS 1982183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: NC
Alter: 70,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

Patient experienced syncope and fell down while shopping in the store following vaccination. Patient had sat in a chair for 15 minutes following her booster shot, had been jovial and in good spirits post-vaccine. When asked how she was feeling, after waiting , she said she felt fine, but was ready to go home. She was provided with a small bottle of water, not at her request, but as a courtesy. Pharmacy staff did not witness her fall, but her husband said she fell quietly and he only heard her fountain drink hit the ground. EMS was called. Her sister, who was a nurse, was with her as well. BP was taken and was 144/83 and HR was 76. Her husband reported that those values were low for her normal BP. She did not go to hospital and ambulated out of the warehouse on her own.

Weitere VAERSDATA-Felder

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

VAERS 1981548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MI
Alter: 32,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram normal Computerised tomogram head normal Confusional state Electroencephalogram normal Encephalopathy Enterovirus test negative Exposure to communicable disease Headache Herpes simplex test negative Hypoaesthesia Laboratory test normal Lumbar puncture abnormal Magnetic resonance imaging abnormal Magnetic resonance imaging head normal Meningitis aseptic Seizure Seizure like phenomena Tremor

Symptomtext

Patient was hospitalized following COVID vaccination (12.21.21); 3 ED visits prior to hospitalization (12.16.21; 12.17.21; 12.21.21); fully vaccinated PLUS booster (12.15.21); Admission Date: 12/21/2021 - Encephalopathy Discharge Date: Dec 25, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Seizure (HCC) [R56.9] Seizure-like activity (HCC) [R56.9] HOSPITAL COURSE: Patient is a 32 y.o. male with no significant PMH who presented on the 16th with complaints of numbness and shaking his head on the right leg that moved up to his right arm and then to his left side of the body, presented with acute onset headache. At the time he was evaluated by a CT of the head which was normal and was discharged home. Reports that the episodes recurred 12/22 early morning with - "numbness of the entire body". Initial workup was negative including CT angiogram head and neck, MRI brain, an EEG. Prior to DC, he had recurrence of symptoms. He was admitted for further evaluation. MRI 12/22 showed a diffuse sulcal flair hyperintense signal abnormalities with corresponding leptomeningeal enhancement most concerning for meningitis/encephalitis. Patient was put on emperic abx with vanc,rocephin,acyclovir while awaiting an LP to rule out meningitis. Prior to symptom onset on 16th - wife added that there had been illness including within the family - Their 4 -year-old son was recently diagnosed with hand-foot-mouth disease and RSV.Neurology had been consulted and They recommended long-term EEG, showed slowing, but no evidence of epileptiform abnormalities or seizures. Patient underwent an LP procedure on 12/24, results indicated aseptic viral meningitis w/ negative HSV and enterovirus PCRs. Patient was transitioned off of antibiotics as well as acyclovir. He was discharged in his baseline mental state w/ follow up with neurology as outpatient in 1-2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 4,0
Labordaten: Emergency department history: Patient is a 32 y.o. male presenting to the emergency department with concern for possible seizure activity. Patient was evaluated in the emergency department a couple of days ago for concern of seizure with having convulsive movements. He completed CT imaging of the brain which showed no acute abnormality. Patient had another episode early this morning where he felt numbness over his entire body and then developed confusion that eventually cleared. No complaint of fever, sweats, or chills. He had a mild headache prior to this episode this morning. No complaint of visual disturbance, facial droop, aphasia, or neck stiffness. Patient denies chest pain, pleuritic pain, or shortness of breath. No abdominal pain, nausea, or vomiting. No complaint of tongue injury or incontinence. Basic laboratory studies unremarkable. Urology service requested admission to the observation unit for MRI of the brain and EEG."
Aktuelle Erkrankungen: N/A
Vorgeschichte: Knee pain, right
Andere Medikamente: clobetasol (TEMOVATE) 0.05 % cream clobetasol (TEMOVATE) 0.05 % ointment diclofenac potassium (CATAFLAM) 50 MG tablet metoclopramide (REGLAN) 10 MG tablet tretinoin (RETIN-A) 0.05 % cream
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1971889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: TN
Alter: 18,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Feeling hot Loss of consciousness Vision blurred

Symptomtext

Patient experienced lightheadedness, overheating, blurry vision, and blacking out approximately 10 minutes post vaccination. Patient was awake and alert with normal breathing shortly before EMS arrived.

Weitere VAERSDATA-Felder

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

VAERS 1967365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: OH
Alter: 21,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

Bell's Palsy - symptoms started 8 hours after first vaccine. Treated with prednisone and Valtrex on DOS 12/16/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: PCN
Vorherige Impfungen: -

VAERS 1958359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: MA
Alter: -
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Atrial fibrillation Electrocardiogram abnormal Seizure

Symptomtext

Patient had an observed seizure that lasted about 30 seconds. Patient had a full evaluation by a medical provider. Provider did an EKG that showed patient in Atrail fibrillation. Patient transported via ambulance to the emergency department at this time in stable condition.

Weitere VAERSDATA-Felder

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

VAERS 1947149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: VA
Alter: 36,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anaphylactic reaction Dyspnoea Heart rate Heart rate abnormal Rash Tachycardia

Symptomtext

within 30 minutes she had started experiencing anaphylaxis; She was tachycardic and remained tachycardic for 5 days; breathing problems; having trouble with her heart rate while moving around; Within 10 minutes of receiving the vaccine rashes appeared; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 36 year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 10Nov2021 11:00 (Lot number: FD0809) at the age of 36 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulfa drugs" (unspecified if ongoing). There were no concomitant medications. The following information was reported: RASH (life threatening) with onset 10Nov2021 11:10, outcome "unknown", described as "Within 10 minutes of receiving the vaccine rashes appeared"; ANAPHYLACTIC REACTION (life threatening) with onset 10Nov2021 11:30, outcome "unknown", described as "within 30 minutes she had started experiencing anaphylaxis"; TACHYCARDIA (life threatening) with onset 10Nov2021 11:30, outcome "unknown", described as "She was tachycardic and remained tachycardic for 5 days"; DYSPNOEA (life threatening) with onset 10Nov2021 11:30, outcome "unknown", described as "breathing problems"; HEART RATE ABNORMAL (life threatening) with onset 10Nov2021 11:30, outcome "unknown", described as "having trouble with her heart rate while moving around". The events "within 10 minutes of receiving the vaccine rashes appeared", "within 30 minutes she had started experiencing anaphylaxis", "she was tachycardic and remained tachycardic for 5 days", "breathing problems" and "having trouble with her heart rate while moving around" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: heart rate: (10Nov2021) trouble with her heart rate while moving around, notes: trouble with her heart rate while moving around. Therapeutic measures were taken as a result of rash, anaphylactic reaction, tachycardia, dyspnoea, heart rate abnormal as the patient received steroid. Clinical course details: Within 10 minutes of receiving the vaccine rashes appeared, within 30 minutes she had started experiencing anaphylaxis. She was tachycardic and remained tachycardic for 5 days. The long lasting steroid administered helped with the breathing problems but still 20 days post vaccine having trouble with her heart rate while moving around. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:trouble with her heart rate while moving around; Comments: trouble with her heart rate while moving around
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1947124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: NJ
Alter: 43,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Loss of consciousness Syncope

Symptomtext

Fainting; Blacking out; Booster; This is a spontaneous report received from a contactable Consumer. The reporter is the patient. A 43 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 27Nov2021 12:00 (Lot number: FD0809) at the age of 43 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3248, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 25Feb2021, when the patient was 42 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EK4176, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 04Feb2021, when the patient was 42 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (medically significant) with onset 27Nov2021 12:00, outcome "unknown", described as "Booster"; SYNCOPE (medically significant) with onset 28Nov2021 06:00, outcome "unknown", described as "Fainting"; LOSS OF CONSCIOUSNESS (medically significant) with onset 28Nov2021 06:00, outcome "unknown", described as "Blacking out". The events "fainting" and "blacking out" were evaluated at the emergency room visit. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1944314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: AL
Alter: 19,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Condition aggravated Palpitations Seizure

Symptomtext

Patient had racing heart, tightness of chest, and a seizure following vaccine administration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: History of seizures
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 1940693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CO
Alter: 25,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness postural Hypoaesthesia Loss of consciousness Nausea

Symptomtext

12/2/21 @6:33 LOC while seated at post-vaccine table for < 1min. No head impact. Patient reported hand numbness, nausea. Laid flat and elevated legs. Vitals WNL : 104/70, HR 78, Pulse ox 99%. Patient accompanied with partner who reports this type of thing happens about every 2 weeks. Patient is alert and oriented x 3. Patient reports hx of dissociative seizures, POTS, and notes she had increased anxiety prior in the day. She reports she may have had a seizure earlier in the day. She notes she had very little to eat or drink today. She appears extremely thin - she states she has ongoing issues with nausea that prevent her from eating well. She is followed by a neurologist. Carpopedal symptoms resolved within 15 minutes. Offered patient sips of water, she tolerated this well. Vitals remained stable throughout observation. Took laying/sitting readings as follows: 100/72, HR 60 o2 99%; 102/70 HR 62 O2 99%. Patient denied dizziness with position changes. She left the clinic by 7:15 pm, accompanied by her partner who drove her home. They were advised to call 911 with any concerns. Advised f/u with neurologist to discuss recent seizures and work with a provider regarding nausea issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: Per patient: dissociative seizure disorder, POTS.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1928835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: IA
Alter: 46,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 28.08.2021
Beginn: 03.09.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Eyelid ptosis

Symptomtext

Client verbalized that she develops Bell's Palsy after all vaccinations. Her physician has placed her on steroids prior to receiving any vaccine due to this. Patient received her 1st dose on 8/28 and had started steroids and benadryl onFriday, 8/27 in preparation to receiving her vaccine. On September 3, upon coompleting the steroid dose, she developed Bell's Palsy and still has a droopy L eye as residual.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Controlled DM2 Menopause
Andere Medikamente: Steroids; Benadryl; Low dose Estrogen; Lisinopril-HCTZ
Allergien: PCN; Keflex; MS04; Ibuprofen
Vorherige Impfungen: Bell's Palsy after all vaccinations

VAERS 1924919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: NH
Alter: 44,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 30.11.2021
Beginn: 06.12.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac telemetry Chest pain Dyspnoea Heart rate abnormal Hemiparesis Hypoaesthesia Injection site pain Loss of consciousness Migraine Paraesthesia

Symptomtext

Employee reported that eleven hours after receiving the vaccine, she "passed out" while at home. States she has a history of vasovagal events and has not had one for some time. Employee was seen by provider and referred to the ED the next day for further evaluation due to some left sided weakness, heart rate fluctuation, severe migraine, numbness in her feet, pain and burning at injection site (left arm) and tingling in fingers in left hand. Also experienced some shortness of breath and left upper chest pain which resolved. Employee was discharged to home from ED same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Received IV fluids and heart was monitored on telemetry.
Aktuelle Erkrankungen: -
Vorgeschichte: Bronchitis History of vasovagal episodes - last one many years ago Anxiety
Andere Medikamente: baby aspirin daily
Allergien: Anaphylaxis x2 - Bee stings, Bees wax
Vorherige Impfungen: -

VAERS 1904109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Crying Fall Fear Hypersensitivity Syncope

Symptomtext

About one to two minutes after the patient walked out of the vaccination room, she fainted and fell backwards. The patient cried out and was scared. The patient seemed to be able to talk and breath normally during this time. We called 911 emergency while keeping her laying on her back in the same position that she fell to the ground in. We tried to calm her down while looking for signs of any allergic reactions. 911 emergency services personal then arrived and took over the entire situation. The patient decided not to get into the ambulance. She sat on a chair in front of the pharmacy under the observation of her boyfriend for about 30 minutes. Then she left our facility

Weitere VAERSDATA-Felder

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

VAERS 1885591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 18.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 14,0
Dosis: UNK
Route/Site: - / -

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

Hyponatraemia Hypoosmolar state Seizure Systemic inflammatory response syndrome

Symptomtext

E87.1 - Hypo-osmolality and hyponatremia R65.10 - Systemic inflammatory response syndrome (sirs) of non-infectious origin without acute organ dysfunction R56.9 - Unspecified convulsions

Weitere VAERSDATA-Felder

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

VAERS 1885532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 15.10.2021
Beginn: 11.11.2021
Tage bis Beginn: 27,0
Dosis: UNK
Route/Site: - / -

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

Pericarditis

Symptomtext

I30.9 - Acute pericarditis, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1873584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

schwer

Staat: MN
Alter: 57,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Deep vein thrombosis Ultrasound Doppler abnormal

Symptomtext

the next day a small blood clot (DVT) was found in my left calf

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: ultrasound, and blood work to prepare
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1855557

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
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 Laboratory test normal Unresponsive to stimuli Urinary incontinence Electrocardiogram Fatigue Syncope

Symptomtext

Pt. states that after receiving the 3rd Booster of Phizer 11/08/2021 (High-Dose Influenza also) , started experiencing symptoms 10 minutes after of fainting *few seconds. Paramedics evaluated *BP, EKG transported to local Emergency Room Department for observation. Discharged 2 hours after evaluation = Normal. Still experiencing fatigue with no other underlying symptoms. Primary visit scheduled for Follow-Up 11/12/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG 11/08/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levoxyl, Atorvastatin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1857567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: -
Alter: 44,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 04.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / RA

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

Chest X-ray Chest pain Dyspnoea Electrocardiogram Fibrin D dimer Full blood count Metabolic function test Pericarditis SARS-CoV-2 test negative Troponin

Symptomtext

The patient developed chest pain and some shortness of breath on 10/13/2021. He was seen in the and discharge with instructions to follow up with Cardiology, Dr. Appointment with Dr. on 10/15 diagnosed with pericarditis. Dr. recommended Motrin for treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: CBC - unremarkable CMP - unremarkable D-Dimer - within normal limits Troponin - within normal limits COVID-19 - negative EKG - sinus rhythm CXR
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1821554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: -
Alter: 12,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 23.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / -

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

Seizure

Symptomtext

Seizures

Weitere VAERSDATA-Felder

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

VAERS 1821127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

schwer

Staat: MA
Alter: 77,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 22.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

The patient was found unconscious - ambulance was called and pt was hospitalized. Her BP (according to the patient) was 80/50

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1809370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: GA
Alter: 38,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 12.09.2021
Beginn: 13.09.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Amnesia Back pain Cognitive disorder Condition aggravated Inflammation Injected limb mobility decreased Injection site inflammation Seizure

Symptomtext

Inflammation in right arm and right shoulder. Could not lift arm above shoulder and head for several days. Severe pain in upper right back muscles. Triggered return of seizures, which previously were absent 6 years. Severe memory loss, cognitive damage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: epilepsy
Andere Medikamente: Zoloft b12 magnesium vitamin e & d ashwaganda
Allergien: penicillin codeine shellfish
Vorherige Impfungen: -

VAERS 1806164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dizziness Syncope

Symptomtext

AT APPROXIMATELY 3:53 PM, PATIENT EXPERIENCED DIZZINESS AND FAINTING AND IT WAS NOTIFIED TO PHARMACY STAFF BY THE PATIENT'S SISTER. PATIENT WAS ABLE TO SIT UP AND THEN PROCEED TO LAY DOWN ON A COT. VITALS WERE TAKEN AT 3:54 PM AND REASSESSED AT 4:07 PM. PATIENT'S DIZZINES SYMPTOM RESOLVED AND WAS ABLE TO LEAVE WITH HIS SISTER. A PHONE CALL WAS MADE TO THE PATIENT AT 5:15 PM AND PATIENT STATED THAT HE IS NO LONGER FEELING ANY DIZZINESS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 3:54 PM SYSTOLIC BP 109 DIASTOLIC BP 66 HR 69 O2 SAT 98 4:07 PM SYSTOLIC BP 89 DIASTOLIC BP 72 HR 70
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 1799335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Fall Hyperhidrosis Syncope

Symptomtext

The Patient walked out of the vaccination room and sat down for the 15-minute observation period but fall off his chair and fainted. He had pulse and was breathing but sweeting profusely. I wanted to call 911 but he got up and signaled me not to call 911.RR was 68 and BP 110/70. Gave him a bottle of cold water and he later admitted that he had not eaten breakfast yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: HIP PROBLEM
Vorgeschichte: HIP PAIN
Andere Medikamente: N/A
Allergien: NONE
Vorherige Impfungen: -

VAERS 1765114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 33,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anaphylactic reaction Electrocardiogram Headache Pain

Symptomtext

Anaphylactic Reaction, was resolved, took patient to ER; next day follow up reports headache/body aches but otherwise well

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Lexapro, Testosterone
Allergien: Miralax
Vorherige Impfungen: -

VAERS 1759812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: ID
Alter: 22,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 16.09.2021
Beginn: 02.10.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: SYR / LA

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

Generalised tonic-clonic seizure

Symptomtext

Two weeks after receiving my second dose of the Pfizer vaccine I had a grand mal seizure for the first time in 8 years. With no medication changes and no major life changes I believe the only thing that could have caused the seizure was the vaccine. I received my first dose of Pfizer just 3-4 weeks after testing positive for the virus itself, which I later found out you?re supposed to wait a minimum of 90 days after testing positive for the virus to get the vaccine. After going to my nurse with the new information I found out about having COVID and waiting to get the second shot, I was advised I would be okay and should complete the series, in hindsight I wish I would not have received the vaccine when I did.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: None at this time. Appointments are being scheduled at this time with multiple specialists.
Aktuelle Erkrankungen: Tested positive for covid 19 virus 4 weeks before receiving my first shot of the Pfizer vaccine.
Vorgeschichte: Epilepsy
Andere Medikamente: Keppra (seizure medication) and Falmina (birth control)
Allergien: Benadryl, latex
Vorherige Impfungen: October 25, 1999 - First MMR vaccine, Pt was 9 months old, 104.1 degree fever, full body rash, weight loss.

VAERS 1740852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD 0809

schwer

Staat: PA
Alter: 42,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 25.09.2021
Beginn: 25.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Hypertension Migraine Respiratory rate increased Syncope

Symptomtext

Increased respiration; headache evolving to migraine; increase in BP (109/78-183/113) syncope 15-20 min post vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Migraine; Sinus; Hypothyroidism.
Andere Medikamente: Synthroid; Vit D prescription; Sngulair; Advair ; Flonase; B12; Zomig; Naratriptan; Benadryl.
Allergien: Latex; Seafood; Shellfish; Silk tape; Iodine.
Vorherige Impfungen: -

VAERS 1737010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: WI
Alter: 46,0
Geschlecht: M
Eingang: 27.09.2021
Impfdatum: 31.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Balance disorder Computerised tomogram head Concussion Dizziness Head injury Loss of consciousness Nausea Vomiting

Symptomtext

Patient reports he felt dizzy on Day 2 to the point of losing balance. On day 3 he was still, feeling dizzy, blacked out, hit his head on concrete, and got a concussion. After that he continued to have dizziness, nausea, vomiting. Continued for at least 7 days. Still has some mild sporadic dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: CT Scan 09/02/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: bee stings
Vorherige Impfungen: -

VAERS 1939068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CT
Alter: 12,0
Geschlecht: F
Eingang: 26.09.2021
Impfdatum: 01.09.2021
Beginn: 12.09.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / -

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

Chest X-ray normal Chest pain Electrocardiogram P wave abnormal Electrocardiogram ST segment elevation Electrocardiogram abnormal Immunoglobulin therapy Myocarditis Sinus tachycardia Troponin increased

Symptomtext

Per records - Patient presented to ER with complaints of chest pain that started 9/12/21, worse at bedtime. Admitted to hospital for observation. Per Post COVID vaccine myocarditis pathway patient treated with 1 dose IVIG on 09/22/21 and 1IV Solumedrol. At time of discharge patient her usual state of health w/out complaints of headache, nausea, and was afebrile, tolerating good PO intake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: In ER troponin 0.36 on 9/20/21. Troponin normal 9/21/21. Chest x-ray normal. 9/21/21 EKG sinus tachycardia w/borderline P wave depression in lead II and ST elevations.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA/NKA
Vorherige Impfungen: -

VAERS 1719101

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FD0809

schwer

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 25.09.2021
Impfdatum: 03.09.2021
Beginn: 03.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Injection site pain Somnolence Tremor Headache Loss of consciousness Seizure

Symptomtext

Patient reports experiencing a seizure 45 minutes after she received the 1st dose of the COVID-19 vaccine while at home. She reports being unconscious for 3 minutes, and does not remember much from that episode. However, her granddaughter witnessed the event, and believes that it was a seizure. Denies incontinence. She denies any history of seizures, and says that she has been genetically tested for conditions that cause seizures as she has a family history of seizures. She denies any other episodes of seizures since that first episode. She does report some headaches but attributes it to all of the smoke from the recent wildfires.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Did not receive medical attention same day, came to my office on the 21st and reported no subsequent seizures. It is thought that this was a reversible cause. EEG ordered for future time.
Aktuelle Erkrankungen: *fell and hit her head 2/21/21 ER visit with normal head CT COPD with exacerbations
Vorgeschichte: COPD Tobacco use disorder prediabetes GERD Lumbar DDD
Andere Medikamente: QNASL 80 mcg/actuation nasal aerosol spray spray 2 spray by intranasal route every day in each nostril Vitamin D3 50 mcg (2,000 unit) capsule take 1 capsule by oral route every day loratadine 10 mg tablet TAKE 1 TABLET BY MOUTH EVERY DAY
Allergien: CHLORPHENIRAMINE hives CLINDAMYCIN HCL CORTISONE Anaphylaxis (moderate to severe) swelling, rash, turned beat red FLUTICASONE PROPIONATE burning sensation in nostrils Flonase GABAPENTIN rash NEURONTIN IBUPROFEN Anaphylaxis IBUPROFEN hives ADVIL, swelling of face PANTOPRAZOLE SODIUM diarrhea Protonix PREDNISONE Breathing Trouble;Numbness (moderate to severe) PSEUDOEPHEDRINE HCL hives
Vorherige Impfungen: -

VAERS 1719101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 25.09.2021
Impfdatum: 03.09.2021
Beginn: 03.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Injection site pain Somnolence Tremor Headache Loss of consciousness Seizure

Symptomtext

Patient reports experiencing a seizure 45 minutes after she received the 1st dose of the COVID-19 vaccine while at home. She reports being unconscious for 3 minutes, and does not remember much from that episode. However, her granddaughter witnessed the event, and believes that it was a seizure. Denies incontinence. She denies any history of seizures, and says that she has been genetically tested for conditions that cause seizures as she has a family history of seizures. She denies any other episodes of seizures since that first episode. She does report some headaches but attributes it to all of the smoke from the recent wildfires.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Did not receive medical attention same day, came to my office on the 21st and reported no subsequent seizures. It is thought that this was a reversible cause. EEG ordered for future time.
Aktuelle Erkrankungen: *fell and hit her head 2/21/21 ER visit with normal head CT COPD with exacerbations
Vorgeschichte: COPD Tobacco use disorder prediabetes GERD Lumbar DDD
Andere Medikamente: QNASL 80 mcg/actuation nasal aerosol spray spray 2 spray by intranasal route every day in each nostril Vitamin D3 50 mcg (2,000 unit) capsule take 1 capsule by oral route every day loratadine 10 mg tablet TAKE 1 TABLET BY MOUTH EVERY DAY
Allergien: CHLORPHENIRAMINE hives CLINDAMYCIN HCL CORTISONE Anaphylaxis (moderate to severe) swelling, rash, turned beat red FLUTICASONE PROPIONATE burning sensation in nostrils Flonase GABAPENTIN rash NEURONTIN IBUPROFEN Anaphylaxis IBUPROFEN hives ADVIL, swelling of face PANTOPRAZOLE SODIUM diarrhea Protonix PREDNISONE Breathing Trouble;Numbness (moderate to severe) PSEUDOEPHEDRINE HCL hives
Vorherige Impfungen: -

VAERS 1726841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: WI
Alter: 20,0
Geschlecht: F
Eingang: 23.09.2021
Impfdatum: 23.09.2021
Beginn: 23.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope

Symptomtext

Immediately after receiving vaccine pt developed syncopal episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Denies
Vorgeschichte: Denies
Andere Medikamente: IUD.
Allergien: Sulfa drugs
Vorherige Impfungen: Syncopal event with dental procedure.

VAERS 1726588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 23.09.2021
Impfdatum: 30.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction

Symptomtext

Anaphylaxis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: acetaminophen, covid vaccine Pfizer-Biontech
Vorherige Impfungen: -

VAERS 1725530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: ND
Alter: -
Geschlecht: F
Eingang: 23.09.2021
Impfdatum: -
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Loss of consciousness

Symptomtext

Passed out; This is a spontaneous report from a contactable consumer (Patient's parent). A female patient of an unknown age received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number FD0809 ), on Sep2021 as single dose for COVID-19 immunization. Medical history and concomitant drugs were unknown. The patient received the vaccine dose in Sep2021 and she just passed out for like 10 minutes. The outcome of the event was unknown. Follow up (17Sep2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1715825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: VA
Alter: 28,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 14.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Blood glucose decreased Blood test Chest X-ray Chest pain Dizziness Fatigue Heart rate abnormal Migraine Muscle twitching Nausea Pain Pain in extremity Pyrexia Syncope Ultrasound scan Urine analysis Vomiting

Symptomtext

severe migraine, light headedness, fever, nausea, vomiting, extreme fatigue, arm soreness, twitching fingers in hand of arm Vaccine given, low blood sugar, chest pains through into the back, abnormal heart rate, fainting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: chest x-ray, urine specimen, blood work, ultrasound of internal organs; All in the ED on 09/16/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Escitalopram, ClonazePam, Seroquil, Woman's Daily Multi-Gummy
Allergien: N/A
Vorherige Impfungen: -

VAERS 1711581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: LA
Alter: 63,0
Geschlecht: F
Eingang: 18.09.2021
Impfdatum: 31.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Chills Fall Hyperhidrosis Loss of consciousness

Symptomtext

blackout (falling to the floor and unable to get up on my on); weakness; blackout (falling to the floor and unable to get up on my on); sweats; Chills; This is a spontaneous report from a contactable consumer (patient). A 63-year-old female (not pregnant) patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number FD0809, on 31Aug2021 08:15 at single dose in left arm (at the age of 63-year-old) for COVID-19 immunization. Medical history was not reported. The patient was not diagnosed with COVID-19 prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. Concomitant medication included unspecified medication. The patient received other medications within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received first dose of BNT162B2 lot number= FC3180 on 10Aug2021 10:45 AM in left arm for COVID-19 Immunization. The patient previously received olmesartan medoxomil (BENICAR) and experienced allergy. On 31Aug2021, the patient experienced Chills on the day of second vaccine. The following morning (01Sep2021 02:30), the patient experienced weakness, blackout (falling to the floor and unable to get up on her on), sweats. No treatment was received for all events. The outcome of all events was resolving.

Weitere VAERSDATA-Felder

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

VAERS 1705276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: LA
Alter: 43,0
Geschlecht: F
Eingang: 16.09.2021
Impfdatum: 16.09.2021
Beginn: 16.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Discomfort Ear discomfort Ear pain Eyelid disorder Headache Hypoaesthesia Pain in extremity Paralysis

Symptomtext

20 min after injection the left side of my face went numb and felt heavy. My left eye lid was hard to open and the pressure in left ear was intense and painful. It took three hours for the paralysis / numbness to subside. Resting heart rate continues to be ielevated (between 120-188). Other side effects (sore arm and headache seem reasonable).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: None to date I was if I showed signs of worsening to go to the emergency room
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1696341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 09.09.2021
Beginn: 11.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood glucose normal Condition aggravated Dizziness Electrocardiogram normal Fear Feeling abnormal Gait disturbance Hyperhidrosis Loss of consciousness Nausea Respiratory rate increased

Symptomtext

Suddenly got weak and felt very faint, nausea and profuse sweating, rapid breathing . I crawled to phone called 911 and was barely able to get my words out then I passed out twice while lying on kitchen floor, holding on to the phone with dispatcher while waiting for EMT's to arrive). I felt like I was dying. My blood sugar was 150, my BP was 150/59 and they checked me out thoroughly. Oxygen levels okay and EKG fine.. We discussed possible Anxiety attack but that did not make sense as i was going about my normal routine and was not upset about anything. I have passed out a couple times in my life but I've never felt like that or had anything like this happen to me before! It's hard to know with all my other conditions exactly what happened but this event was nothing like anything I've experienced before. I am following up with my doctor and seeing if I need medication adjustments but I don't think there is any definitive answer and I'm afraid to get the second dose of the vaccine now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EMT's did the following. EKG normal BP 150/59 Blood sugar 150
Aktuelle Erkrankungen: Type 1 Insulin Dependent Diabetes Hashimoto's Hypothyroidism Hypertension Sciatica
Vorgeschichte: Type 1 Insulin dependent Diabetes Hashimoto's Hypothyroidism Hypertension peripheral neuropathy in feet
Andere Medikamente: Insulin Humalog and Lantus, Verapamil, Lisinopril, VitaminD3, Synthroid, Alpha Lipoic Acid
Allergien: Sulfa and Iodine
Vorherige Impfungen: -

VAERS 1695515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD 0809

schwer

Staat: -
Alter: 32,0
Geschlecht: F
Eingang: 13.09.2021
Impfdatum: 10.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Presyncope

Symptomtext

32 year old female attendee with preexisting condition of vasovagal response to needles, reacted within 4 minutes of receipt of vaccination. She was assisted to gurney, exhibited a lower muscle tone which initiated EMS. EMS arrived 5 minutes and monitored until event self resolved to point Attendee was able to stand and ambulate without assistance 55 minutes later. Discharged self to home with brother driving, declined EMS.

Weitere VAERSDATA-Felder

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

VAERS 1693788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: WI
Alter: 53,0
Geschlecht: F
Eingang: 12.09.2021
Impfdatum: 30.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Back pain Computerised tomogram Electrocardiogram Head injury Headache Hyperhidrosis Hypoaesthesia Injection site pain Laboratory test Lethargy Loss of consciousness Mobility decreased Musculoskeletal stiffness Nausea Neck pain Pain in jaw

Symptomtext

Woke at 6am the day after the 2nd covid dose, headache, numbness jow-neck-head pain, lathargic, nauseated, back pain, RHR 90, painful at injection site, stiff hands. Around 10 am ate 1/2 bagel, 1/2 banana and had been drinking water even though just rolling over in bed was a challenge. 1pm got up and walked 20 feet, stood and talked to daughter for a bit, began to sweat profusely, walked towards bathroom because thought to vomit and passed out and hit my head. Tried to rest back in bed and the head and neck pain was to bad and PCP recomended to go to ER. Temp 99 degree at ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: At ER, CT, labs, EKG, 2 sets of pain meds and sent home once no fever and pain improved
Aktuelle Erkrankungen: none
Vorgeschichte: March 2020 diagnosed with Breast cancer, ended chemo July 2020, ended immunotherapy treatment March 2021, last surgery May 2021
Andere Medikamente: anastrozole, vitamin D, zinc, multivitamin
Allergien: sulfa, kiwi
Vorherige Impfungen: -

VAERS 1686431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 22,0
Geschlecht: F
Eingang: 09.09.2021
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Hypotension Paraesthesia Syncope

Symptomtext

Client reported a history of syncope after vaccinations to RN prior to receiving the vaccine today. The client was vaccinated while seated in the anti-gravity chair. At 7:35 PM the client reported feeling lightheaded. RN responded. RN reclined the anti-gravity chair to a low-fowler's position. RN noted the client close her eyes and her body relax for about one second. The client opened her eyes and RN provided the client with an alcohol swab to smell. The client reported "dizziness, tingling on ears, and seeing spots." The client stated all of these symptoms are normal for her after receiving and injection. Vitals obtained at 7:35PM were as follows: automatic BP 93/58, HR 68, O2 99%. The client reported a history of hypotension. The client stated that her systolic blood pressure is usually under 100. Repeat vitals obtained at 7:45 PM were as follows: BP 111/66, HR 70, O2 99%. The client denied any symptoms at that time. RN provided education regarding s/s of anaphylaxis and when to seek EMS. The client voiced understanding of this education. RN adjusted the anti-gravity chair to a high fowler's position. Repeat vitals obtained at 8:01PM were as follows: BP 105/70, HR 75, O2 99%. The client denied any symptoms at that time. The client left the vaccination site at 8:05PM. The client ambulated unassisted with a steady gait.

Weitere VAERSDATA-Felder

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

VAERS 1679028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 08.09.2021
Impfdatum: 03.09.2021
Beginn: 03.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SC / LA

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

Blood creatinine normal Blood urea normal Chest pain Electrocardiogram ST segment elevation Electrocardiogram T wave inversion Brain natriuretic peptide normal Echocardiogram normal Full blood count normal Metabolic function test normal Fatigue Haematocrit normal Haemoglobin normal Myalgia Myocarditis Oropharyngeal pain Painful respiration Pyrexia Respiratory viral panel

Symptomtext

16 year old male with no significant PMH who presented with a 2 day history of worsening substernal chest pain that gets worse with inspiration and radiates to left shoulder. Patient reports received Pfizer covid vaccine #2 on Friday and subseqently develop mild fevers, fatigue, myalgias, and throat pain. Saturday started to have some chest pain that would worsen with inspiration and sometimes radiated to the left shoulder. Patient previously felt similar symptoms with first vaccine dose however, it was worse this time.Initially seen and was found to have slightly elevated troponin of 0.03 so was transferred to ED for further evaluation. In ED, patient was found to have worsening troponin to 1.4 as well as slight T wave inversions and ST elevation noted on EKG. Cardiology consulted whom recommended CVICU admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: 9/7/21 Progress Note: Progress Note Today's Date: 09/07/2021 Date of Admission: 09/06/2021 Hospital stay: 1 days Subjective No acute events overnight. Troponins downtrending. Chest pain improving. Objective Vitals & Measurements Admit Wt: 51 kg (09/06/21) Current Wt: 49.8 kg (09/06/21) Chg from Admit Wt -1.2 kg (from 51 kg on 09/06/21) Dose Calc Wt: 49.8 kg Last VS: 09/07/21 0600 Tmax: 37.2 deg C (09/06/21 16:00) Tcurr: 37.2 deg C SaO2: 98% (96-100%) HR: 81 (58-107) RR: 16 (12-27) BP: 118/70 (106-126/61-80) I&O 24hr Summary (Ending 09/07/21 @ 06:59:59) -v2 In: 720.00 mL = 14.5 mL/kg/24hrs 720 mL oral Out: 275.00 mL = 0.23 UOP mL/kg/hr 275 mL UOP 0 mL drains 0 mL other Bal: 445.00 mL Total: 0 kCal/24hrs =0 kCal/kg/24hrs Parenteral: 0 kCal/24hrs =0 kCal/kg/24hrs Enteral: 0 kCal/24hrs =0 kCal/kg/24hrs Physical Exam General:Awake, alert, no acute distress, very thin/tall male HEENT:NC/AT, PERRL, Moist mucous membranes, oropharynx clear without erythema or exudate, no LAD Respiratory:No nasal flaring or retractions, No tachypnea, Lungs CTAB Cardiovascular:Regular rate and rhythm, normal S1, S2, no murmurs, rubs or gallops, 2+ brachial and femoral pulses Gastrointestinal:Soft, non-tender, non-distended, normoactive bowel sounds, no hepatosplenomegaly, no masses. Extremities:Warm and well perfused, Cap refill <2 sec, No cyanosis, clubbing or edema. Musculoskeletal:Normal range of motion, no tenderness, no swelling, no deformity. Integumentary:Warm, dry, no rash or lesions. No bruising. Neurologic:No facial asymmetry. Normal strength and normal tone Lab Results No qualifying data (09/06@22:29): Trop: 0.82 Diagnostic Results ECHO 9/6/21: Summary: 1. There is qualitatively normal left ventricular size and systolic function. 2. There is qualitatively normal right ventricular size and systolic function. 3. No evidence of pericardial effusion. 4. No prior echocardiographic images are available for comparison. Diagnoses Chest pain Myopericarditis Elevated troponin Assessment/Plan Patient is a 16 year old male with no significant PMH who presented with a 2 day history of worsening substernal chest pain and found to have evidence of troponin leak concerning for possible myocarditis vs. ischemia vs. vaccine induced pericarditis. EKG reviewed with no significant evidence of ST segment changes however, given thin lengthy nature of body habitus, would need close evaluation for possible aortic dilatation as a cause of coronary ischemia. ECHO on admission with normal appearing aorta, coronaries (although LCx unable to be visualized), and function. Troponins now downtrending which could be consistent with possible post-vaccine myocarditis. CV: - Continue CR monitoring - ECHO on admission with normal BV function - Trend troponins Q8H - downtrending - Repeat EKG today - Cardiology consulted Pulm: - Sat 99% on RA FEN/GI: - Regular diet - Monitor strict I/Os - Baseline CMP wnl Renal: -BUN and Cr stable - Monitor strict I/Os ID: - Afebrile - Will continue to monitor - Covid antibodies pending - RP-PCR Negative - ID consulted, will follow up regarding possible myocarditis workup Heme: - H/H stable Neuro: - PRN tylenol 16 year old with chest pain and elevated troponin Now 4 days post COVID vaccine second dose Troponin 1.4 ->0.55 Agree with exam above Alert, NAD CTA bilaterally RRR no murmur WWP Presume post COVID vaccine myocarditis ECHO reassuring Will make VAERS notification D/c home with close outpatient follow-up in 2 days Discussed at length with patient and mother The patient is critically ill due to possible myocarditis and is at risk of life-threatening deterioration from potential arrhythmias that requires critical care nursing, monitoring, management and treatment.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1678835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 02.09.2021
Beginn: 02.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Nausea Pallor Presyncope Somnolence

Symptomtext

RN stat called for patient due to near syncopal episode after receiving the 1st dose of the Pfizer vaccine. With in 3 minutes of receiving vaccine at 1:28pm, patient became pale, diaphoretic, drowsy, ammonia used but patient did not loose consciousness. Ice pack placed to her neck, fan facing patient, legs elevated on chair and vitals assessed. BP checked and low. Patient became nauseous but no vomiting. Mother remained with patient. Patient rested, vitals repeated and stable, Dr. cleared for discharge home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: BMI greater than 95 percentile, bilateral sensorineural hearing loss
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1642256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: -
Alter: 14,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 27.08.2021
Beginn: 27.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Feeling jittery Loss of consciousness

Symptomtext

Loss of consciousness, anxious, jittery

Weitere VAERSDATA-Felder

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

VAERS 1632640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

schwer

Staat: WI
Alter: 19,0
Geschlecht: M
Eingang: 25.08.2021
Impfdatum: 25.08.2021
Beginn: 25.08.2021
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 Muscle rigidity Syncope Urinary incontinence Vision blurred

Symptomtext

C/o blurred vision, lightheaded, diaphoretic. Became rigid and syncopal episode occurred x 10-15 seconds. Pt was incontinent of urine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None known.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2716061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NC
Alter: 61,0
Geschlecht: M
Eingang: 21.11.2023
Impfdatum: 04.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Hip fracture Pneumonia

Symptomtext

broke a hip; pneumonia; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 63-year-old male patient received bnt162b2 (BNT162B2), on 04Jan2022 as dose 3 (booster), single (Lot number: FD0809) at the age of 61 years for covid-19 immunisation. The patient's relevant medical history included: "COPD" (ongoing), notes: on COPD medication; "anxiety" (ongoing), notes: on anti anxiety medication; "blood pressure" (ongoing), notes: on blood pressure medication. Concomitant medication(s) included: FLU VACCINE VII taken for influenza immunisation as dose number unknown, single. Vaccination history included: bnt162b2 (DOSE 2, SINGLE), administration date: 06Apr2021, for COVID-19 immunisation; Bnt162b2 (DOSE 1, SINGLE, Expiry date: 31Jul2021), for COVID-19 immunisation. The following information was reported: HIP FRACTURE (hospitalization, medically significant) with onset 2023, outcome "unknown", described as "broke a hip"; PNEUMONIA (hospitalization) with onset 2023, outcome "unknown". The patient was hospitalized for hip fracture, pneumonia (start date: 10Nov2023). Therapeutic measures were taken as a result of hip fracture. Clinical course: Caller asked if being in the hospital should he take the fourth dose of the vaccine. Caller said he has COPD, he has been in the hospital twice and broke a hip a month a half ago. Caller currently in hospital for pneumonia, that he had about a week before being admitted to hospital, the symptoms were not as bad. Carries oximeter, his numbers just crashed, went way down. Clarified, he was admitted to hospital 10Nov2023. Had hip surgery about a month and a half ago, they put his hip back together. Patient was currently on COPD medication, anti anxiety medication, blood pressure medication. Prior vaccination included flu shot and pneumonia shot.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300372632 same reporter/patient, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anxiety (on anti anxiety medication); Blood pressure abnormal (on blood pressure medication); COPD (on COPD medication)
Vorgeschichte: -
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 2712016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 09.11.2023
Impfdatum: 21.12.2021
Beginn: 13.08.2023
Tage bis Beginn: 600,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Condition aggravated Dementia Dysphagia Lethargy Mental status changes Metabolic encephalopathy Sepsis

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 8/13/2023 Discharge Date: 08/17/2023 Discharge Disposition: Home PRESENTING PROBLEM: AMS & Lethargy HOSPITAL COURSE: Patient is a 77 year-old male who was admitted on 8/13/23 for sepsis 2/2 COVID-19 infection with metabolic encephalopathy. Patient was given fluid hydration, he was not hypoxic so no steroids or Remdesivir was given. Due to AMS he was having difficulties following commands to eat and was made NPO for 2 days. Yesterday 8/16 he has fully returned to baseline dementia mentation, he passed RN swallow screen and has tolerated dental soft diet. SLP evaluated 8/17 and notes mild dysphagia, but can continue with thin liquid and dental soft (bite-sized foods) diet. Vitals are stable, medically cleared for discharge. No changes to medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Essential hypertension Hyperlipidemia Coronary artery disease Diabetes Mellitus Type II PAD (peripheral artery disease) Back pain Vitamin B12 deficiency Bilateral Numbness and Tingling of Feet Elevated prostate specific antigen (PSA) Bilateral leg weakness Bilateral carotid artery stenosis Frontotemporal dementia Trauma Chest pain, unspecified type Advanced care planning/counseling discussion Altered mental status Acute ischemic right MCA stroke Metabolic encephalopathy COVID-19 virus infection
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet ALPRAZolam (XANAX) 0.25 mg tablet amLODIPine (NORVASC) 5 mg tablet aspirin 81 MG chewable tablet carvedilol (COREG) 3.125 MG tablet cholecalciferol (VITAMIN D3) 125 MCG (5000 UT) tablet divalproex (DEPA
Allergien: NiacinHives Bee Omega-3 [Ascorbate Dl-lysine] Pneumovax [Pneumococcal Polysaccharides] StatinsMyalgia
Vorherige Impfungen: Pneumovax- He stated that this was given at the same time as the FLU vaccine in 1994. So not sure what vaccine cause it? He got

VAERS 2638404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 20,0
Geschlecht: M
Eingang: 30.05.2023
Impfdatum: 22.12.2021
Beginn: 06.05.2022
Tage bis Beginn: 135,0
Dosis: 3
Route/Site: IM / LA

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

Hypotension

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2623180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 28.04.2023
Impfdatum: 09.03.2022
Beginn: 12.08.2022
Tage bis Beginn: 156,0
Dosis: 4
Route/Site: IM / RA

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

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2622350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 27.04.2023
Impfdatum: 18.12.2021
Beginn: 24.05.2022
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: IM / LA

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

Hypotension

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2594858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FD0809

moderat

Staat: MS
Alter: 53,0
Geschlecht: F
Eingang: 10.03.2023
Impfdatum: 04.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: - / LA

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

Bundle branch block left Catheterisation cardiac Chest X-ray Chest pain Dyspnoea Echocardiogram Ejection fraction Electrocardiogram Fluid retention Laboratory test Oedema Pulmonary hypertension

Symptomtext

Shortness of breath, chest pain, dyspnea, Pulmonary HTN, Left Bundle Branch Block, Edema, Fluid Retention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: EKGx5: 2021, 2022, 2023 Chest xraysx3: 2021, 2022 EF Fraction: 2021, 2022, 2023 Echo: 2022, 2023 Left heart cath: 2021 Labs: 2021, 2022, 2023 Right heart cath: 2022
Aktuelle Erkrankungen: HTN, Hypothyroidism, Depression, GERD
Vorgeschichte: HTN
Andere Medikamente: Armour Thyroid, Losartan, Sertraline, Prevacid, Amytriptiline.
Allergien: KNDA
Vorherige Impfungen: -

VAERS 2564570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 20.01.2023
Impfdatum: 17.05.2022
Beginn: 22.12.2022
Tage bis Beginn: 219,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain Dyspnoea Gastrointestinal haemorrhage Pyrexia Red blood cell transfusion SARS-CoV-2 test positive

Symptomtext

12/22/22 presents to ED for "fever, sob, chest pain". PMHx of "CHF, COPD (on home O2), severe AS s/p AVR on Warfarin, HTN, T2DM, CVA, Anemia, recent GI bleed (Dec 2022 requiring 1U PRBC), Asthma, Tobacco Dependence, Neuropathy, Anxiety, and Depression"

Weitere VAERSDATA-Felder

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

VAERS 2561960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: VA
Alter: 38,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 23.09.2022
Beginn: 25.09.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / AR

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

Arthralgia Dyspnoea Heart rate increased Hypertension Palpitations

Symptomtext

extreme heart palpataions, racing pounding heart felt throughout my body and visibly noticeable, Joint pains that worsened following the last vaccine 09/23/2022 started after the first vaccine 2021.shortness of breath. My heart rate was so high that i went to local emergency dept and my resting heart rate was 175 beats per minute, blood pressure has been high ever since. Seeing a cardiologist tomorrow for an echocardiogram and a holter monitor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Joint pain from first vaccine 03/2021
Andere Medikamente: flu vaccine
Allergien: NO
Vorherige Impfungen: folowwing the first covid vaccines I had joint pains

VAERS 2533283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 05.01.2022
Beginn: 08.12.2022
Tage bis Beginn: 337,0
Dosis: 3
Route/Site: - / -

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

Asthma Bronchial wall thickening COVID-19 Chest X-ray abnormal Condition aggravated Laboratory test normal Malaise Musculoskeletal pain SARS-CoV-2 test positive Suicidal ideation

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 12/8/2022 Discharge Date: 12/13/2022 COVID positive Date 12/8/2022 PRESENTING PROBLEM: Suicidal ideation [R45.851] COVID-19 [U07.1] HOSPITAL COURSE: Pt is a 68 y.o. female with a past medical history of schizoaffective disorder, depression, anxiety, PTSD, hypertension, hyperlipidemia, type 2 diabetes mellitus who presented on 12/13 with acute complain of suicidal ideation. Pt was admitted for suicidal ideation for a plan to ingest her medications at home with the intention to overdose. Pt was evaluated and called a high suicide risk with need to transfer to a psychiatric hospital. Pt was put with a 1:1 sitter for the entirety of her stay. Labs on admission were unremarkable save for a positive COVID-19 PCR and a CXR remarkable for LLL bronchial thickening consistent with possible pneumonia. Pt had some symptoms of COVID infection that started 2 weeks prior, however they were minor and pt did not need Oxygen, so there was no indication for steroid or remdesivir treatment. Pt was noted to have some symptoms of possible tardive dyskinesia on admission, however Seroquel was continued as pt has acute disease state with SI. Pt's stay at hospital was largely unremarkable, save for occasional MSK pain amenable to tylenol and lidocaine, and some treatments with Duo-nebs due to underlying asthma with her COVID infection. Patient remained stable until 12/13/2022 when she was accepted for further psychiatric care at facility. She was transferred in stable medical condition for further psychiatric care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Allergic rhinitis Asthma Cerebrovascular accident (HCC) GERD (gastroesophageal reflux disease) BPPV (benign paroxysmal positional vertigo) Hyperlipidemia Type 2 diabetes mellitus (HCC) Suicidal ideation Depressive disorder Schizoaffective disorder (HCC
Andere Medikamente: atorvastatin (LIPITOR) 20 MG tablet hydroCHLOROthiazide (MICROZIDE) 12.5 MG capsule losartan (COZAAR) 50 MG tablet metFORMIN (GLUCOPHAGE) 1000 MG tablet montelukast (SINGULAIR) 10 MG tablet prochlorperazine (COMPAZINE) 5 MG tablet QUEtiapin
Allergien: Cranberry Motrin [Ibuprofen] Yellow Dye Zofran [Ondansetron
Vorherige Impfungen: -

VAERS 2502800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 33,0
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 15.10.2021
Beginn: 01.09.2022
Tage bis Beginn: 321,0
Dosis: 3
Route/Site: - / LA

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

Blood testosterone Blood testosterone abnormal Chest pain Discomfort Fatigue COVID-19 SARS-CoV-2 test Vaccination failure Lymph gland infection Lymph node calcification Lymphadenopathy Musculoskeletal chest pain Pain Pulmonary pain

Symptomtext

Covid 19 Nasal Swab/ Positive/ Sep2022; Covid 19 Nasal Swab/ Positive/ Sep2022; 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 34-year-old male patient received BNT162b2 (BNT162B2), on 21Jan2021 as dose 1, single (Lot number: EL9262), in left arm, on 11Feb2021 as dose 2, single (Lot number: EN6201), in left arm and on 15Oct2021 as dose 3 (booster), single (Lot number: FD0809) at the age of 33 years, in left arm for COVID-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Past drug history included: Morphine, reaction(s): "known allergies". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Covid 19 Nasal Swab/ Positive/ Sep2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Sep2022) Positive, notes: Nasal Swab. Additional information: Facility type vaccine: Pharmacy or Drug Store. There were no other vaccine in four weeks and no other medications in two weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 202209; Test Name: COVID-19 TEST; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: n/a
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2481640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 68,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 04.12.2021
Beginn: 23.02.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Cartilage injury Hypoaesthesia Injection site pain Magnetic resonance imaging abnormal Muscle atrophy Muscular weakness Neuralgic amyotrophy Osteoarthritis Paraesthesia Radiculitis brachial Synovial cyst Tendon disorder X-ray limb abnormal

Symptomtext

Patient had first COVID-19 Booster vaccination (3rd total Pfizer vaccine) on 12/04/2021. This injection was given into the Right arm. He reported typical pain at the injection site with no other issues. Then 2.5 months later, toward the end of February 2022 he began to have intense Right shoulder pain, numbness, tingling, and frank weakness in the right arm and shoulder. Patient was seen in our orthopedic walk-in clinic on 3/4/22 and was prescribed a methylprednisolone oral steroid taper (Medrol Dosepak). This relieved his shoulder pains within days and he has not had return of pain since. But Patient had continued to experience weakness and atrophy in muscles innervated by C5-C6 nerve roots. This included his supraspinatus, infraspinatus, deltoid, and biceps muscles. He also had some decreased cutaneous sensation in the axillary nerve distribution on the lateral right upper arm. His constellation of symptoms after a vaccination with no other injury, trauma, medication change, illness, is consistent with Parsonage-Turner Syndrome (Brachial neuritis/neuralgic amyotrophy).

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: X-rays of the right shoulder from 3/4/2022 with some moderate AC joint and glenohumeral joint OA. MRI Right shoulder from 3/31/22 with chronic labral tear and paralabral cyst, rotator cuff tendinosis, supraspinatus muscle atrophy.
Aktuelle Erkrankungen: Surgery on 11/10/2021: ROBOTIC ASSISTED LAPAROSCOPIC LEFT INGUINAL HERNIA REPAIR WITH MESH (Left)
Vorgeschichte: None
Andere Medikamente: Ibuprofen
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2468356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 04.01.2021
Beginn: 29.09.2022
Tage bis Beginn: 633,0
Dosis: 3
Route/Site: - / -

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

COVID-19 COVID-19 pneumonia Cough Haemarthrosis SARS-CoV-2 test positive

Symptomtext

Pt was admitted on 9/23 for a nontraumatic hemarthrosis of the left knee. She had a COVID test on 9/29 for discharge to rehab that was positive. Pt had COVID pneumonia with a nonproductive cough and required 2L nasal canula.

Weitere VAERSDATA-Felder

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

VAERS 2460574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NH
Alter: 67,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 19.11.2021
Beginn: 24.05.2022
Tage bis Beginn: 186,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Blood test Cardiac flutter Cardiac monitoring abnormal Differential white blood cell count abnormal Electrocardiogram abnormal Electrocardiogram ambulatory Full blood count abnormal Heart rate increased Hypotension Metabolic function test abnormal Palpitations Tinnitus Vision blurred

Symptomtext

On 05/24/2022 around 01:00AM, I woke up to urinate and my heart was racing. I have pulsating tinnitus, so I can hear my heart rate regularly and I could hear it beating really fast and I had a vail of white over my vision. I went back to sleep and woke up at 04:00AM and it was still racing. I put on a cuff, and it read up in the 150 range and my blood pressure was down in the 90 over 50 something range. I didn't go to the hospital immediately but ended up there around 11:00AM the following day with my pulse still elevated and my blood pressure still low. They took me into the emergency room and attempted to bring my heart rate down to get a more effective idea of what was going on. They had me on a medication drip as well and were doing blood work along with prepping me for the possible need of an cardioversion. They admitted me for the night for continuing monitoring. Around 02:00AM my heart rate finally reached a normal level. They continued to check things in my blood and monitor things but eventually determined that I was experiencing a heart flutter and not A-fib. I was discharged in the afternoon of 05/25/2022. They prescribed Eliquis and Metoprolol. I no longer needed the Metoprolol after around 6 weeks and was off of the Eliquis after around 2 months. I wore a halter monitor for around a week around June 27th of 2022 and will have a follow up appointment with a cardiologist in October 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 1,0
Labordaten: 05/24/2022- ECG 12 lead-Abnormal results; CBC and Differential-Abnormal Results; Basic Metabolic Panel-abnormal results; 006/27/2022-Heart Monitoring-atrial flutter
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Osteopenia
Andere Medikamente: Vitamin D; Flax Seed Oil; Calcium/Magnesium; Multivitamin
Allergien: Azithromycin
Vorherige Impfungen: -

VAERS 2440912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AK
Alter: 51,0
Geschlecht: M
Eingang: 12.09.2022
Impfdatum: 09.09.2021
Beginn: 09.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia Asthenia Burning sensation COVID-19 Cough Dyspnoea Fatigue Headache Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I experienced a breakthrough case of COVID-19, burning in my nose, cough, fever, shortness of breath, headaches, fatigue, weakness, loss of taste, loss of smell, symptoms lasted for 9 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 Test Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic
Andere Medikamente: Lantus; Metformin; Lisinopril; Atorvastatin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2425347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CO
Alter: 78,0
Geschlecht: M
Eingang: 31.08.2022
Impfdatum: 08.02.2021
Beginn: 24.08.2022
Tage bis Beginn: 562,0
Dosis: 1
Route/Site: IM / RA

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

C-reactive protein COVID-19 Dysphonia Dyspnoea Fibrin D dimer Full blood count Inflammatory marker increased Liver function test Metabolic function test Oropharyngeal pain Oxygen saturation decreased Pyrexia Respiratory symptom SARS-CoV-2 test positive

Symptomtext

Hospitalization for COVID-19 infection after COVID-19 immunization is a reportable event. This 79 year-old male with a history of advanced prostate cancer presented to the outpatient clinic with complaints of sore throat, hoarseness, and symptoms of an upper respiratory infection. Upon examination he was febrile with breathing difficulties requiring O2 at 2 L/min. Upon ambulation to the bathroom he desaturated to 82%. PCR testing for SARS-CoV-2 was positive. He was transferred to hospital and admitted. He was treated with dexamethasone 6mg daily for a total of 10 days and IV remdesivir for 5 days. Improvement in symptom severity and decrements of inflammatory markers ensued. With minimal symptoms he was discharged medically stable after 5 days with detailed follow-up healthcare plans in place.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: CBC BMP CRP LFTs D dimer
Aktuelle Erkrankungen: Prostate cancer Hematuria
Vorgeschichte: Prostate cancer Hematuria
Andere Medikamente: Abiraterone
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 2418333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 57,0
Geschlecht: M
Eingang: 23.08.2022
Impfdatum: 27.12.2021
Beginn: 18.04.2022
Tage bis Beginn: 112,0
Dosis: 3
Route/Site: IM / LA

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

Alanine aminotransferase increased Aspartate aminotransferase increased COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Fibrin D dimer Hypertransaminasaemia Lung infiltration Positive airway pressure therapy SARS-CoV-2 test positive Tachycardia

Symptomtext

4/18/2022-Presents to ED, c/o SOB. Tachy at 138, O2 sat 89% on 4L, placed on Bipap. Covid + on admission. CXR-bibasilar infiltrates. Transaminits: AST 154 ALT 129. D Dimer 848. Start Remdesivir. Admit COPD exacerbaton in the setting of Covid 19. 4/20/2022-Transmanitis improving. Currently on RA. 4/22/2022- Weaned to RA. Improved AST 55 and ALT 104. D/C to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2377054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AK
Alter: 35,0
Geschlecht: M
Eingang: 21.07.2022
Impfdatum: 09.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Chest discomfort Palpitations Pharyngeal swelling Swelling face

Symptomtext

Severe facial swelling for 24 hours, throat swelling for 24 hours. throat still swells from time to time for up to 24 hours, heart palpations that last for a few minutes that continue until this very day, Chest tightness that continues from time to time but doesn't persist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: I've been seen at the local clinic several times. No treatment. Please contact the clinic ask for PA.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2366144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 64,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 22.12.2021
Beginn: 15.03.2022
Tage bis Beginn: 83,0
Dosis: 3
Route/Site: IM / RA

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

Anticoagulant therapy Anxiety COVID-19 Dyspnoea Flushing Hyperhidrosis Malaise Oxygen saturation decreased Productive cough Respiratory failure Sinus tachycardia Wheezing White blood cell count increased

Symptomtext

3/15/2022- Presents to ED, c/o feeling sick, SOB, wheezing and productive cough. Recent PCP visit and completed 14 days of Doxycycline. Afebrile, BP:183/98, P-122 and RR 20. O2 93% on RA, on walking sat drops to 85%, on 2L via NC. WBC :13. Admit hypoxemic respiratory failure d/t Covid 19. Received IV ceftriaxone and doxy in ED. Ordered IV azithromycin, Decadron and Lovenox. 3/16/2022-AM: Sinus tach 120's consistent. Anxious, flushed and diaphoretic. On 1.5 L NC sating 93%. Atarax ordered and given. HR decreased to 110's. PM; HR consistently in the 100-110's. 3/17/2022- Wheezing significantly improved. Weaned off oxygen to RA with o2 sat levels above 90. 3/18/2022- Improved, on RA for 24 hours. Discharged to home, with additional 4 days of dexamethasone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, GERD, Type 2 DM, IBS, Obesity,
Andere Medikamente: -
Allergien: Corticosteroids
Vorherige Impfungen: -

VAERS 2329074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 13.03.2021
Beginn: 16.05.2022
Tage bis Beginn: 429,0
Dosis: 3
Route/Site: - / -

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

Cough Dyspnoea Fatigue

Symptomtext

Shortness of breath, fatigue, and cough ongoing over 2 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD (chronic obstructive pulmonary disease) (CMS/HCC) Pneumonia due to COVID-19 virus Pleural effusion Gastroesophageal reflux disease without esophagitis Type 2 diabetes mellitus without complication (CMS/HCC) Acquired hypothyroidism Secondary hyperparathyroidism of renal origin (CMS/HCC) PAD (peripheral artery disease) (CMS/HCC) Mixed hyperlipidemia Fracture of humerus, proximal, left, closed Renal failure STEMI (ST elevation myocardial infarction) (CMS/HCC) S/P CABG (coronary artery bypass graft) Renal failure (ARF), acute on chronic (CMS/HCC) Altered mental status Cerebrovascular accident (CMS/HCC) Impending cerebrovascular accident (CMS/HCC) S/P carotid endarterectomy Bradycardia Syncope and collapse AKI (acute kidney injury) (CMS/HCC) Normocytic anemia Vitamin D deficiency Acute renal failure with acute renal cortical necrosis superimposed on stage 4 chronic kidney disease (CMS/HCC) Anemia in stage 4 chronic kidney disease (CMS/HCC) Proteinuria Metabolic encephalopathy Acute cystitis with hematuria Paroxysmal atrial fibrillation (CMS/HCC) Gait instability History of cardiac monitoring Essential hypertension, malignant Toxic metabolic encephalopathy Concussion Hypertensive urgency Recurrent syncope Syncope Paroxysmal A-fib (CMS/HCC) NSTEMI (non-ST elevated myocardial infarction) (CMS/HCC) Acute exacerbation of congestive heart failure (CMS/HCC) Body mass index (BMI) 24.0-24.9, adult Anemia due to stage 4 chronic kidney disease (CMS/HCC) Elevated brain natriuretic peptide (BNP) level Hypocalcemia Hyponatremia Acute blood loss anemia D-dimer, elevated Hyperphosphatemia Class 1 obesity due to excess calories with serious comorbidity and body mass index (BMI) of 31.0 to 31.9 in adult
Andere Medikamente: acetaminophen (TYLENOL) 650 MG PO CR tablet albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln apixaban (ELIQUIS) 2.5 MG PO Tab aspirin EC (HALFPRIN) 81 MG PO Tablet Delayed Response atorvastatin (LIPITOR)
Allergien: Clindamycin/lincomycin Succinylcholine Chloride
Vorherige Impfungen: -

VAERS 2322056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 45,0
Geschlecht: M
Eingang: 16.06.2022
Impfdatum: 08.12.2021
Beginn: 08.05.2022
Tage bis Beginn: 151,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Dyspnoea Eye pruritus Fatigue Feeling abnormal Lacrimation increased Lethargy Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

I started out with allergy like symptoms. Runny nose, itchy and watery eyes, scratchy throat. When I woke up the next morning, I felt achy. Didn?t have a cough yet but had some difficulty breathing. Allergy symptoms were still there. Much more of a sore throat but the biggest change was the strong aches and pains that I woke up with. It didn?t prevent me from doing much, and I was able to function at least. But it prompted me to take an at home test and came back positive quickly. I called my doctor with the 24-hour nurse line. Because of my asthma and my BMI, they prescribed me Paxlovid and I started that immediately on Monday, May 9 for a 5 day course. I isolated from my family and I took the medicine and by Thursday, my symptoms had disappeared. Didn?t have tightness in my chest or the cough. No itchy eyes or allergy symptoms. By Sunday I was symptom free and tested negative on an at home test. I would say for about 2 weeks after, I felt tired. A little lethargic and then after about 2 weeks I felt completely normal like I did before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 05/09/2022 - At Home COVID Test - Positive 05/15/2022 - At Home COVID Test - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Bupropion XL, Top Care OTC Allergy Relief
Allergien: None
Vorherige Impfungen: -

VAERS 2052259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: FL
Alter: 34,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Blood test Chest pain Dyspnoea Dyspnoea exertional Gait disturbance Inflammation Fatigue Palpitations Tachycardia SARS-CoV-2 test Scan

Symptomtext

Chest pain; tachycardia; dyspnea; Scans and blood tests are showing inflammation; unable to do more than a slow walk; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35-year-old male patient received BNT162b2 (BNT162B2), on 16Dec2021 at 09:30 as dose 3 (booster), single (Lot number: FD0809) at the age of 34 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing); "Known allergies: cephalosporins" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Previous dose details:, Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Prev dose administration date: 27Apr2021, Prev dose administration time: 09:30 AM, Prev dose lot number=ER8732, Prev dose dose number=2, Prev dose vaccine location=Left arm), administration date: 27Apr2021, when the patient was 34-year-old, for COVID-19 immunization; BNT162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Prev dose administration date: 05Apr2021, Prev dose administration time: 09:30 AM, Prev dose lot number=ER8729, Prev dose dose number=1, Prev dose vaccine location=Left arm), administration date: 05Apr2021, when the patient was 34-year-old, for COVID-19 immunization. The following information was reported: CHEST PAIN (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered"; INFLAMMATION (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered", described as "Scans and blood tests are showing inflammation"; DYSPNOEA (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered", described as "dyspnea"; TACHYCARDIA (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered"; GAIT DISTURBANCE (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered", described as "unable to do more than a slow walk". The patient was hospitalized for chest pain, tachycardia, dyspnoea, inflammation, gait disturbance (hospitalization duration: 6 day(s)). The events "chest pain", "tachycardia", "dyspnea", "scans and blood tests are showing inflammation" and "unable to do more than a slow walk" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood test: (16Dec2021) inflammation, notes: Scans and blood tests are showing inflammation; SARS-CoV-2 test: (Jan2022) Negative, notes: Nasal Swab; (Feb2022) Negative, notes: Nasal Swab; (Mar2022) Negative, notes: Nasal Swab; (Apr2022) Negative, notes: Nasal Swab; (May2022) Negative, notes: Nasal Swab; Scan: (16Dec2021) inflammation. Therapeutic measures were taken as a result of chest pain, tachycardia, dyspnoea, inflammation, gait disturbance. Clinical course: As reported no other vaccine in four weeks and no medication in two weeks was administered to patient. Facility type for vaccine was Pharmacy or drug store. He was an active 35 year old male who does a lot of running and cycling, but had been unable to do more than a slow walk since receiving the vaccine. Symptoms began hours after receiving the booster shot. The treatment was given in form of fluids and medications. No covid prior to vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 6,0
Labordaten: Test Date: 20211216; Test Name: Blood test; Result Unstructured Data: Test Result:inflammation; Comments: Scans and blood tests are showing inflammation; Test Date: 202201; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202202; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202203; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202204; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202205; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211216; Test Name: Scans; Result Unstructured Data: Test Result:inflammation
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to antibiotics; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2052259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: FL
Alter: 34,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Blood test Chest pain Dyspnoea Dyspnoea exertional Gait disturbance Inflammation Fatigue Palpitations Tachycardia SARS-CoV-2 test Scan

Symptomtext

Chest pain; tachycardia; dyspnea; Scans and blood tests are showing inflammation; unable to do more than a slow walk; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35-year-old male patient received BNT162b2 (BNT162B2), on 16Dec2021 at 09:30 as dose 3 (booster), single (Lot number: FD0809) at the age of 34 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing); "Known allergies: cephalosporins" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Previous dose details:, Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Prev dose administration date: 27Apr2021, Prev dose administration time: 09:30 AM, Prev dose lot number=ER8732, Prev dose dose number=2, Prev dose vaccine location=Left arm), administration date: 27Apr2021, when the patient was 34-year-old, for COVID-19 immunization; BNT162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Prev dose administration date: 05Apr2021, Prev dose administration time: 09:30 AM, Prev dose lot number=ER8729, Prev dose dose number=1, Prev dose vaccine location=Left arm), administration date: 05Apr2021, when the patient was 34-year-old, for COVID-19 immunization. The following information was reported: CHEST PAIN (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered"; INFLAMMATION (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered", described as "Scans and blood tests are showing inflammation"; DYSPNOEA (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered", described as "dyspnea"; TACHYCARDIA (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered"; GAIT DISTURBANCE (hospitalization) with onset 16Dec2021 at 18:00, outcome "not recovered", described as "unable to do more than a slow walk". The patient was hospitalized for chest pain, tachycardia, dyspnoea, inflammation, gait disturbance (hospitalization duration: 6 day(s)). The events "chest pain", "tachycardia", "dyspnea", "scans and blood tests are showing inflammation" and "unable to do more than a slow walk" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood test: (16Dec2021) inflammation, notes: Scans and blood tests are showing inflammation; SARS-CoV-2 test: (Jan2022) Negative, notes: Nasal Swab; (Feb2022) Negative, notes: Nasal Swab; (Mar2022) Negative, notes: Nasal Swab; (Apr2022) Negative, notes: Nasal Swab; (May2022) Negative, notes: Nasal Swab; Scan: (16Dec2021) inflammation. Therapeutic measures were taken as a result of chest pain, tachycardia, dyspnoea, inflammation, gait disturbance. Clinical course: As reported no other vaccine in four weeks and no medication in two weeks was administered to patient. Facility type for vaccine was Pharmacy or drug store. He was an active 35 year old male who does a lot of running and cycling, but had been unable to do more than a slow walk since receiving the vaccine. Symptoms began hours after receiving the booster shot. The treatment was given in form of fluids and medications. No covid prior to vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 6,0
Labordaten: Test Date: 20211216; Test Name: Blood test; Result Unstructured Data: Test Result:inflammation; Comments: Scans and blood tests are showing inflammation; Test Date: 202201; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202202; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202203; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202204; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202205; Test Name: Home Tests; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211216; Test Name: Scans; Result Unstructured Data: Test Result:inflammation
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to antibiotics; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2284784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 53,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 17.12.2021
Beginn: 17.05.2022
Tage bis Beginn: 151,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Received Moderna vaccines on 12/31/20, 1/28/21; Pfizer vaccine on 12/17/21; tested positive COVID home test on 5/17/22, positive COVID PCR on 5/18/22; admitted to hospital on 5/18/22 d/t SOB, COVID infection. Underlying morbid obesity, sleep apnea, asthma, Type II DM

Weitere VAERSDATA-Felder

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

VAERS 2282898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 88,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 23.11.2021
Beginn: 14.05.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Cough Dyspnoea Pyrexia Respiratory symptom

Symptomtext

89 year old male with a past medical history significant for hypertension hyperlipidemia coronary artery disease history of pulmonary embolism diabetes type 2, obstructive sleep apnea chronic renal failure and congestive heart failure who presents emergency department from a residential facility complaining of cough, shortness of breath fever. Patient has had mild upper respiratory symptoms but developed increasing shortness of breath and coughing with low-grade fevers and complained of some abdominal pain when arriving in the ED

Weitere VAERSDATA-Felder

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

VAERS 2277704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 14.05.2022
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Psychomotor hyperactivity Tinnitus Tremor

Symptomtext

First dose 3/13/21: next day feeling "not normal". Difficult to describe. Usual side effects - tired, slight headache, slight nausea Second dose 4/3/21: Less usual side effects - essentially no problems ***First booster shot 12/15/2021: Next morning "intense hyperactivity - lasted 12 hours". Left hand shook Uncontrolled - lasted ~2minutes. Intense and extremely loud periodic ringing in ears - happened 4 times. each episode lasting 10-15 minutes ****Since the first booster December 15, 2021 have experienced continuous tinnitus, varying degrees, day to day. Worse at night when it is quiet.****

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Prediabetes
Andere Medikamente: Lisinopril 10mg daily Magnesium 400 mg daily Zyrtec 10mg daily Tylenol ES Arthritis PRN Motrin 400mg PRN
Allergien: Sulfa Morphine Ceftin
Vorherige Impfungen: -

VAERS 2270842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 19.01.2021
Beginn: 22.02.2022
Tage bis Beginn: 399,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Confusional state Hypotension Hypoxia SARS-CoV-2 test positive

Symptomtext

02/22/22 presents to ED for "hypoxia, hypotension as well as confusion". PMHx of "Alzheimer dementia"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: 02/22/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NC
Alter: 46,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 05.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: UN / AR

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

Cardiac flutter Cardiac monitoring Cardiac stress test normal Electrocardiogram normal Palpitations

Symptomtext

Three weeks after my booster, I started having heart palpitations/fluttering. My Primary Care Dr's referred me to a Cardiologist. I was given a Stress test and an EKG, both came back normal. I was given a heart monitor for 2 weeks. They added 2 meds Magnesium Oxide 400mg, Metoprolol 25mg and they adjusted my prescription of Amlodipine from 5mg to 2.5mg

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Primary Care, Cardiologist
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Amlodipine 5mg Allegra 180mg Vitamin D 50mcg Culturelle Probiotic Flonase
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2266080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 23.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 159,0
Dosis: 3
Route/Site: IM / -

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

Acquired diaphragmatic eventration Acute kidney injury Anion gap Asthenia Blood bicarbonate normal Blood chloride normal Blood creatinine increased Blood potassium increased Blood sodium normal Blood urea increased Chills Chronic kidney disease Condition aggravated Decreased appetite Diarrhoea COVID-19 COVID-19 pneumonia Chest X-ray abnormal

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 5/1/2022 Discharge Date: 5/3/2022 PRESENTING PROBLEM: Pneumonia due to COVID-19 virus COVID-19 HOSPITAL COURSE: Patient is a 74 y.o. female with past medical history significant for hypertension, hyperlipidemia, hypothyroidism, coronary artery disease, HFrEF with ejection fraction 25%, ischemic cardiomyopathy, history of myocardial infarction, diabetes mellitus type 2, history of CVA/TIA, CKD stage IIIB, obstructive sleep apnea on CPAP, parkinson's disease, dementia, mixed anxiety and depression, additional comorbidities who presented to the emergency department for generalized weakness. Per family at bedside patient initially had chest discomfort on Friday 4/29/2022 midsternal radiating to her left neck; patient was given nitroglycerin with mild relief. Throughout the night patient developed fever and chills, family went to urgent care and was tested for COVID and was found to be COVID-19 positive on April 30, 2022. Per family at bedside she has had low-grade fevers, generalized weakness, decreased appetite and decreased intake of fluids. Daughter also states she has had loose stools. Patient is vaccinated against COVID-19 with booster. In the ED, vital signs reviewed in the emergency department, patient was mildly hypertensive, otherwise within acceptable range. Patient extensive diagnostic workup consisting of complete blood count: WBCs 4.5, hemoglobin 11.7, hematocrit 38.2, platelets 189, differential within acceptable limits. CMP: Sodium 140, potassium 5.2, chloride 106, bicarb 25, anion gap 9, creatinine 1.63, BUN 42, GFR 31, liver enzymes within acceptable limits. Initial troponin 123, 2nd troponin 116. One-view chest x-ray: No acute pulmonary infiltrate with chronic elevation of left hemidiaphragm. Rapid COVID-19 positive. Limited echocardiogram reveals ejection fraction 25%, right ventricle function cannot be assessed due to poor imaging quality. NM lung perfusion was negative for PE. She was given 324 mg of aspirin, normal saline 250 bolus, and supportive treatment. Emergency room department provider spoke with Cardiology concerning elevated troponins and EKG changes, which felt at this time the patient is not a candidate for interventional therapy. Patient mildly improved in the emergency department treatment plan. She was admitted for further medical management. Home lasix was held and AKI on CKD 3 improved. She was evaluated by Cardiology and recommended outpatient follow up and they will arrange outpatient palliative care as well. She was evaluated by PT/OT and home health services were arranged. It was recommended that the patient hold lasix until 5/6/2022 as her oral intake improves as she recovers from COVID 19. She should follow up with her PCP as well. She was discharged home in stable condition on 5/3/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: 11/3/2021-Pain in left toe(s) (Primary) Ulcer of toe of left foot, with fat layer exposed (HCC) Diabetic nephropathy associated with type 2 diabetes mellitus (HCC) Status post left foot surgery
Vorgeschichte: Type 2 diabetes mellitus with other specified complication, unspecified whether long term insulin use (HCC) Family history of colon cancer Dyslipidemia Essential hypertension Cardiomyopathy, ischemic (clinic) CAD (coronary artery disease) Single ICD (implantable cardiac defibrillator) in place Peripheral artery disease (HCC) Depression Thyroid disease Dementia (HCC) Carotid artery bruit TIA (transient ischemic attack) CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) Parkinsonism (HCC) Counseling regarding advanced care planning and goals of care Stenosis of right carotid artery Parkinson's disease (HCC) Carotid artery stenosis, asymptomatic, bilateral HFrEF (heart failure with reduced ejection fraction) (HCC) Hallucinations Essential tremor ACC/AHA stage B congestive heart failure due to ischemic cardiomyopathy (HCC) Cardiomyopathy (HCC) Chronic foot ulcer (HCC) Cognitive communication deficit Diabetic nephropathy associated with type 2 diabetes mellitus (HCC) Diabetic retinopathy (HCC) Diabetic neuropathy (HCC) Arthritis of elbow Arthritis Hyperlipidemia OSA (obstructive sleep apnea) Nausea and vomiting Muscle weakness (generalized) Minimal cognitive impairment Migraine headache Dysphagia, oropharyngeal phase Dysuria Legal blindness, as defined Major depressive disorder, single episode, unspecified Menopause AKI (acute kidney injury) (HCC) Disruption of external surgical wound, initial encounter Diabetic ulcer of toe of left foot associated with type 2 diabetes mellitus, with fat layer exposed (HCC) Protein-calorie malnutrition, moderate (HCC) COVID-19 NSTEMI (non-ST elevated myocardial infarction) (HCC) Chest pain Acute on chronic combined systolic and diastolic heart failure (HCC)
Andere Medikamente: aspirin 81 MG tablet atorvastatin (LIPITOR) 40 MG tablet Bacillus Coagulans-Inulin (PROBIOTIC FORMULA PO) buPROPion (WELLBUTRIN SR) 200 MG 12 hr tablet carbidopa-levodopa (SINEMET) 25-100 MG per tablet carbidopa-levodopa ER (SINEMET CR
Allergien: Ambien CrAnxiety, Dizziness CaffeineNausea and Vomiting CodeineNausea and Vomiting Cymbalta [Duloxetine Hcl]Nausea Only LoratadineAgitation MorphineAnxiety PseudoephedrineAnxiety Duloxetine TramadolOther ExcedrinNausea and Vomiting
Vorherige Impfungen: -

VAERS 2259941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WA
Alter: 29,0
Geschlecht: F
Eingang: 01.05.2022
Impfdatum: 04.12.2021
Beginn: 22.04.2022
Tage bis Beginn: 139,0
Dosis: 3
Route/Site: IM / LA

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

Cough Dyspnoea Ear pain Fatigue Headache Night sweats Pyrexia Respiratory tract congestion SARS-CoV-2 test

Symptomtext

I had a fever, congestion, cough, night sweats, headache, ear pain, and fatigue. I congestion was heavy enough that I couldn't breath and I still have a bad cough. This lasted for 7-8 days.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 2 Rapid Antigen Test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Gianvi; B12; Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 2259874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD 0809

moderat

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 01.05.2022
Impfdatum: 28.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Dysstasia Inflammatory marker increased Injected limb mobility decreased Laboratory test Musculoskeletal disorder Neck pain Pelvic girdle pain Polymyalgia rheumatica

Symptomtext

Gradual loss of use of vaccinated (left) arm Increasing pain in shoulders/neck area & pelvic girdle Eventual loss of ability to stand from sitting position & loss of function of left arm 02/11/2022 ER Visit local clinic -6 day prednisone taper given-symptoms lessoned till end of taper 02/11/2022 local Urgent care- 15 mg prednisone prescribed-symptoms lessoned 03/05/2022 local Urgent Care- prednisone prescribed 03/07/2022 local Health Neurology- Polymyalgia Rhuematica diagnosis 03/10/2022 local Health clinic- 15mg prednisone prescribed 04/07/2022 local Dr.- 3 month prednisone prescribed

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Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Local Clinic lab tests results -high inflamatory markers Local Health lab test results- same as above
Aktuelle Erkrankungen: -
Vorgeschichte: polio at age 5 (1953) right arm disability (deltoid muscle)
Andere Medikamente: Lisinipril,Flomax,Wellbutrin,81mg aspirin,
Allergien: -
Vorherige Impfungen: Myalgia after 1st 2 Covid doses Pfizer 03-09-21 & 03-30-21

VAERS 2258614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: TN
Alter: 71,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 01.11.2021
Beginn: 29.04.2022
Tage bis Beginn: 179,0
Dosis: 3
Route/Site: IM / RA

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

Burning sensation Injection site pain Limb discomfort Pain in extremity Paraesthesia

Symptomtext

A patient presented for her 2nd COVID booster, but complained of arm pain in the arm where her previous three doses were given. The patient stated the pain was an ocassional twinge that lasted a few seconds then went away. The patient reported no shoulder involvement or loss in range of motion. The patient also reported no burning, tingling, or numbness in the arm or extremeties. The patient stated the pain was isolated in the area the shots were given in the right arm.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Atorvastatin, Bystolic, Doxepin, Duloxetine, Fluticasone, Glycopyrolate, Hydralazine
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2255233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 02.12.2021
Beginn: 04.04.2022
Tage bis Beginn: 123,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 COVID-19 pneumonia Chills Cough Fatigue Nasal congestion Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I started with a low-grade fever of 100 or 101. Some nasal congestion. I also had upper chest congestion and a cough. I had COVID-19 before that turn into pneumonia. Fatigue and chills I also had. I took a PCR test that conformed it was COVID-19. I did get a prescription to help with my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; High Cholesterol
Andere Medikamente: Losartan; Amlodipine; Atorvastatin; Mucinex
Allergien: Sudafed
Vorherige Impfungen: -

VAERS 2254656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 06.12.2021
Beginn: 25.04.2022
Tage bis Beginn: 140,0
Dosis: 3
Route/Site: IM / RA

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

Computerised tomogram spine Computerised tomogram thorax abnormal Condition aggravated Fall Gait disturbance COVID-19 Cerebral cavernous malformation Chest X-ray normal Computerised tomogram abdomen abnormal Computerised tomogram head abnormal Haemangioma of bone Haemoglobin decreased Intracranial mass Lip injury Magnetic resonance imaging head abnormal Neutropenia Retroperitoneal mass SARS-CoV-2 test positive

Symptomtext

Hospitalized 04/25/2022-04/26/2022; COVID-19 positive 04/25/2022; fully vaccinated plus booster BRIEF OVERVIEW: Admission Date: 4/25/2022 Discharge Date: 4/26/2022 DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: Patient is an 87 y.o female, hx of HTN, dyslipidemia, seizures, breast cancer s/p mastectomy, who presented to the ED following a mechanical fall. Previously known family members recently tested positive for COVID. Also noted to have unsteady gait. In the emergency department, she was noted have a laceration above her left lateral are broad left upper lip which was repaired. She was found to be COVID positive. She underwent a CT head which showed a right uncal mass. She also underwent a CT cervical spine which showed a C4 vertebral body lesion favored to represent a hemangioma. X-ray of her ribs and knee showed no acute abnormality. The case was discussed with Neurosurgery who recommended MRI of the brain. Due to her history of breast cancer, it was also recommended to obtain a CT of the chest abdomen and pelvis. She was admitted for further evaluation and management. CT of the chest abdomen and pelvis showed a retroperitoneal mass which was unchanged from previous examination in 2019 with a stable appearance of the remainder of the abdomen and pelvis. She also was noted to have a chronic T12 vertebral compression fracture. She underwent MRI of the brain which showed a 1.5 cm right mesial temporal lobe lesion most consistent with a cavernous hemangioma. Imaging was reviewed by Neurosurgery and recommended outpatient follow-up with no acute surgical intervention. She was seen by PT/OT who recommended home with assist and outpatient therapies. She was discharged home in stable condition. Of note, hemoglobin drop from 11.3 to 9.9 without overt bleed, suspect dilutional with IVF given. Also with chronic mild neutropenia that could be contributed to her lamictal. Recommend follow up with PCP to discuss further.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN (hypertension), benign Nonrheumatic aortic valve stenosis Mild concentric left ventricular hypertrophy (LVH) Benign hypertensive heart and CKD, stage 3 (GFR 30-59), w CHF Carotid disease, bilateral Chronic diastolic heart failure Disorder of arteries and arterioles, unspecified Cavernous hemangioma of brain Rectocele COVID-19 Anemia in chronic kidney disease Seizure, petit mal Benign essential tremor Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus Cystocele with prolapse Hyperlipidemia, unspecified Mass of psoas muscle Osteoporosis HX OTHER MEDICAL S/P mastectomy Wedge compression fracture of T11 vertebra Basal cell carcinoma (BCC) of scalp Age-related osteoporosis without current pathological fracture Age-related osteoporosis without current pathological fracture Hx of breast cancer Unsteady gait when walking Lip laceration
Andere Medikamente: aspirin 81 MG chewable tablet Cholecalciferol (VITAMIN D3) 2000 units CAPS docusate (COLACE) 100 MG capsule lamoTRIgine (LAMICTAL) 100 MG tablet lisinopril (PRINIVIL,ZESTRIL) 10 MG tablet
Allergien: Actonel Alendronic Acid Bisphosphonates Evista Fosamax Pfizer
Vorherige Impfungen: -

VAERS 2249662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: PA
Alter: 72,0
Geschlecht: M
Eingang: 24.04.2022
Impfdatum: 05.01.2022
Beginn: 01.03.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure increased Condition aggravated Electrocardiogram ambulatory abnormal Extrasystoles Supraventricular extrasystoles Supraventricular tachycardia Ventricular extrasystoles

Symptomtext

Chronic effects from series of vaccines 1, 2 & 3. Substantial increase in PVC?s / PAC?s following vaccine doses 2 and 3 in February and March 2021. Then following booster in January 2022 significant jump in blood pressure which is now unable to control through blood pressure medicine (Verapamil). Also prevalence following booster dose. These are chronic effects not short term.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Holter monitor: Ectopics jumped from 5652 to 12,927 following Vaccine administration in February and March of 2022.
Aktuelle Erkrankungen: None
Vorgeschichte: History of PVC?s dating back to my early 1920
Andere Medikamente: Multi vitamin Vitamin C -1000 mg Fish oil- 1200 mg Vitamin B12 Flax seed Oil - 1200 mg Cranberry pills - 4200
Allergien: Cortisone Lisinopril TamaFlu Hydroxichloroquin (Placquinil) Cipro Doxycycline
Vorherige Impfungen: -

VAERS 2233689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 74,0
Geschlecht: M
Eingang: 14.04.2022
Impfdatum: 08.11.2021
Beginn: 25.01.2022
Tage bis Beginn: 78,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Decreased appetite Diarrhoea Dyspnoea Pneumonia

Symptomtext

Patient presented to the hospital with diarrhea, low appetite, SOB, and was diagnosed with COVID-19. Patient acquired PNA and need to be on levaquin and steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 31,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, GERD, HF, hypothyroidism, Depression, leukemia, HTN, ashtma, diabetes, anemia
Andere Medikamente: APAP, ventolin, symbicort, asa 81mg, wellbutrin xl, calcium, vit b12, cymbalta, zetia, ferrous sulfate, lasix, mucinex norco, fish oil,, nizoral, synthroid, claritin, myrbetriq, nexium, nitrostat, ditropan, crestor, ozempic, desyrel.
Allergien: Latex, metformin, biaxin, gabapentin, imipramine, lisinopril.
Vorherige Impfungen: -

VAERS 2235914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 17.08.2021
Beginn: 28.09.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / RA

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

Electrocardiogram abnormal Sinus tachycardia Supraventricular tachycardia

Symptomtext

Multiple recurrent episodes of supraventricular tachycardia noted on 09/28/2021, 10/22/2021, 12/15/2021, 02/21/2022, 03/09/2022 x 3 episodes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus tachycardia
Hospital-Tage: -
Labordaten: ER visit 09/28/21- EKG Sinus Tachycardia results Vitals HR-141 EKG 3/01/224- Sinus Tachycardia 03/09/22-Pulse 152
Aktuelle Erkrankungen: None
Vorgeschichte: Schizophrenia paranoia, constipation, hyperlipidemia, history of traumatic brain injury
Andere Medikamente: Lipitor, Cogentin, Clozapine, Depakote, Luvox, Invega Sus, Dss,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2225988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: SC
Alter: 52,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 30.12.2021
Beginn: 14.02.2022
Tage bis Beginn: 46,0
Dosis: 3
Route/Site: IM / LA

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

Asthma Blood test COVID-19 Lung disorder Malaise Migraine Nasal congestion Nasopharyngitis Pleural effusion Pulmonary pain Respiratory disorder SARS-CoV-2 test positive

Symptomtext

I started to feel unwell on weekend before I had the symptoms of a cold for a couple of days. I had a stuffy nose for two days mild cold however now I am now having long issues with asthma and migraines after being diagnosis with COVID Positive 02/15/2022. I have just seen a doctor for a six month checkup and he put me on Singulair and that helped with lungs and I was put on prednisone for migraines and the lungs. I am scheduled to see a neurologist in May 2022. I am recovered from COVID but not the side effects of COVID symptoms breathing, lungs, and asthma. No physical exercise and this cause issue with lung filling up, and pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Blood work as apart of regular check, observation and Stethoscope.
Aktuelle Erkrankungen: No
Vorgeschichte: Blood Pressure
Andere Medikamente: Losartan daily; Lexapro daily
Allergien: No food; Sulfa Drugs
Vorherige Impfungen: -

VAERS 2220355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 42,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 16.08.2021
Beginn: 23.08.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Head discomfort Heart rate increased Nasopharyngitis Palpitations SARS-CoV-2 test positive Sneezing

Symptomtext

When I caught COVID I had really mild cold symptoms. I had a lot of sneezing and a very stuffy head. I had no fever. My cold symptoms lasted about 5 days. 2 weeks after that I had heart palpitations that lasted about 5 days. When I walk my heart would get up to a certain number of beats. When I would do cardio exercises I would get heart palpitations. I didn't have any coughing or lung involvement issues. My primary care doctor said I should get the monoclonal antibody infusion but I ended up not getting one because it was too much of a hassle. Some people were saying that it wasn't necessary to get. On 1/5/2022 I had a consultation with my PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: COVID Test- 1/3/2022.
Aktuelle Erkrankungen: No
Vorgeschichte: Rheumatoid Arthritis
Andere Medikamente: Enbrel 25mg once a week
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2220354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MS
Alter: 72,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 05.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: SYR / RA

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

Heart rate increased Nasal congestion Nasopharyngitis Palpitations SARS-CoV-2 test Sneezing

Symptomtext

I had really mild cold symptoms I had a lot of sneezing and a very stuffy head. No fever, cold symptoms lasted about 5 days 2 weeks after had about a 5 days of week of heart palpitations. It wouldn't stop for 5 days. When I walk my heat would get up to a certain number of beats. When I would do cardio exercises I would get heart palpitations. I didn't have any coughing or lung involvement issues. My primary care said I should get an infusion monoclonal antibody doctor recommended but would did get it setup for me and I should set it up. I was not able to get it because were saying it wasn't necessary. 1/5/2022 I had a consultation with my PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Covid Test- 1/3/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Emphysema
Andere Medikamente: Multivitamin; Vitamin C; Turmeric; Calcium with D; Magnesium; Lisinopril; Ezetimibe
Allergien: None
Vorherige Impfungen: -

VAERS 2209303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 17.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Back injury Back pain Condition aggravated Heavy menstrual bleeding Intervertebral disc protrusion Magnetic resonance imaging abnormal Menstruation irregular Spinal disorder Uterine spasm X-ray

Symptomtext

So I got the vaccine 12/17/2021 the next day I was fine. I woke up Sunday morning with extreme lower back pain and uterine cramping. The lower back pain went up my spine to mid back. My old injury it has never gone up that far. I felt really unstable like my spine was not happy. That whole next week up to the holiday, I iced and used Tylenol and Advil alternating and took it easy. On the holiday morning I woke up with my period and it was more intense that normal. It usually lasts 3 days and lasted 5 days. I went on vacation my back pain persisted but my period stopped. Normally my back pain stops after my period stops. I was not able to see my doctor until I came back from vacation on 1/20/2022. I got an x-ray and MRI and she wanted to compare to my old injury. It showed two new injuries that showed two herniated discs that were higher up. All the way up to about 3/15/2022 I had the back pain. I did start on physical therapy for 2 days a week to strengthen my core. The disc pain went away but my lower back pain continued. The discs are still herniated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: MRI; X-ray
Aktuelle Erkrankungen: None
Vorgeschichte: Low Back Pain
Andere Medikamente: Armour Thyroid medication Amitriptyline
Allergien: Advil; Tylenol; Capers
Vorherige Impfungen: Flu vaccine 2008. I broke out in hives several hours afterwards. It lasted about 3 days.

VAERS 2202396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 23.09.2021
Beginn: 15.10.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: IM / RA

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

Arthritis Blood test abnormal Joint instability Mobility decreased Neuropathy peripheral Pain in extremity Peripheral swelling Tinnitus X-ray limb abnormal

Symptomtext

Both arms from my shoulder to finger tips felt pain, my hands swollen up couldn't lift arm, felt like rubber bands in joints could not function neuropathy in hands.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: GP referred Rheumatologists ordered shoulder x-rays and blood test showed arthritis and tinnitus.
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure High Cholesterol and Thyroid medication
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2201645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 08.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Areflexia Asthenia Autoimmune neuropathy Blood immunoglobulin G increased CSF cell count increased Cerebellar atrophy Electromyogram abnormal Hypoaesthesia Magnetic resonance imaging head abnormal Magnetic resonance imaging spinal abnormal Meningioma Muscle contractions involuntary Nerve conduction studies abnormal Nervous system disorder Paraesthesia Protein total increased Spinal disorder

Symptomtext

The symptoms were a progressive polyneuropathy. Starting in the feet and progressing fully from head to toe. Included fasciculations in muscles in all regions, loss of position sense, loss of reflex in left ankle, numbness and tingling in feet and legs and progressing to same over whole body. Some loss of strength in the feet and toes bilaterally. Test suggest chronic autoimmune polyneuropathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI of spine revealed enhancements of nerve roots of the cauda equina. Brain MRI, left occipital incidental 6mm meningioma. mildly prominent lateral ventricals. mild cerebellar atrophy. Nerve conduction showed delay through the reflex suggesting delay at spinal nerve roots. No demyelination. EMG confirmed fasciculations in most muscle groups. CSF had elevated opening pressures, increased protein, increased IgG. No oligoclonal bands. No elevation in cells. Clear fluid.
Aktuelle Erkrankungen: No
Vorgeschichte: History of thyroid cancer with resection more than 2 years ago now on thyroxin
Andere Medikamente: Thyroxin
Allergien: Latex allergy
Vorherige Impfungen: Fasciculations transiently after 1st and second pfizer doses but resolved. 3rd dose progressive condition.

VAERS 2057615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 10.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: - / LA

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

Antinuclear antibody negative Arthralgia Blood creatine phosphokinase Blood thyroid stimulating hormone Burning sensation C-reactive protein Chest X-ray normal Chest pain Costochondritis Differential white blood cell count normal Dyskinesia Dyspnoea Feeling abnormal Full blood count normal Glycosylated haemoglobin HIV test negative Headache Heart rate increased

Symptomtext

Neuropathy type of issues; Constant muscle twitches; Pins and needles in arms and legs; Burning pains; Tinnitus; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Sep2021 (Lot number: FD0809) at the age of 38 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "SVT" (unspecified if ongoing); "gerd" (unspecified if ongoing); "gastritis" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL; PROTONIX [OMEPRAZOLE]. Past drug history included: Bactrim, reaction(s): "known allergies: bactrim"; Cipro, reaction(s): "known allergies: Cipro"; Macrobid, reaction(s): "known allergies: Macrobid" and multivitamins. The following information was reported: NEUROPATHY PERIPHERAL (medically significant) with onset 27Sep2021, outcome "not recovered", described as "Neuropathy type of issues"; MUSCLE TWITCHING (non-serious) with onset 27Sep2021, outcome "not recovered", described as "Constant muscle twitches"; PARAESTHESIA (non-serious) with onset 27Sep2021, outcome "not recovered", described as "Pins and needles in arms and legs"; PAIN (non-serious) with onset 27Sep2021, outcome "not recovered", described as "Burning pains"; TINNITUS (non-serious) with onset 27Sep2021, outcome "not recovered", described as "Tinnitus". The events "neuropathy type of issues", "constant muscle twitches", "pins and needles in arms and legs", "burning pains" and "tinnitus" were evaluated at the physician office visit and emergency room visit. Clinical course: Neuropathy type of issues, constant muscle twitches, pins and needles in arms and legs, burning pains and tinnitus. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine The adverse event result in doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. 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: Gastritis; GERD; Supraventricular tachycardia
Andere Medikamente: METOPROLOL; PROTONIX [OMEPRAZOLE]
Allergien: -
Vorherige Impfungen: -

VAERS 2057615

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge FD0809

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 10.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: IM / LA

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

Antinuclear antibody negative Arthralgia Blood creatine phosphokinase Blood thyroid stimulating hormone Burning sensation C-reactive protein Chest X-ray normal Chest pain Costochondritis Differential white blood cell count normal Dyskinesia Dyspnoea Feeling abnormal Full blood count normal Glycosylated haemoglobin HIV test negative Headache Heart rate increased

Symptomtext

Neuropathy type of issues; Constant muscle twitches; Pins and needles in arms and legs; Burning pains; Tinnitus; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Sep2021 (Lot number: FD0809) at the age of 38 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "SVT" (unspecified if ongoing); "gerd" (unspecified if ongoing); "gastritis" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL; PROTONIX [OMEPRAZOLE]. Past drug history included: Bactrim, reaction(s): "known allergies: bactrim"; Cipro, reaction(s): "known allergies: Cipro"; Macrobid, reaction(s): "known allergies: Macrobid" and multivitamins. The following information was reported: NEUROPATHY PERIPHERAL (medically significant) with onset 27Sep2021, outcome "not recovered", described as "Neuropathy type of issues"; MUSCLE TWITCHING (non-serious) with onset 27Sep2021, outcome "not recovered", described as "Constant muscle twitches"; PARAESTHESIA (non-serious) with onset 27Sep2021, outcome "not recovered", described as "Pins and needles in arms and legs"; PAIN (non-serious) with onset 27Sep2021, outcome "not recovered", described as "Burning pains"; TINNITUS (non-serious) with onset 27Sep2021, outcome "not recovered", described as "Tinnitus". The events "neuropathy type of issues", "constant muscle twitches", "pins and needles in arms and legs", "burning pains" and "tinnitus" were evaluated at the physician office visit and emergency room visit. Clinical course: Neuropathy type of issues, constant muscle twitches, pins and needles in arms and legs, burning pains and tinnitus. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine The adverse event result in doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. 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: Gastritis; GERD; Supraventricular tachycardia
Andere Medikamente: METOPROLOL; PROTONIX [OMEPRAZOLE]
Allergien: -
Vorherige Impfungen: -

VAERS 2182251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: TN
Alter: 61,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Ophthalmic migraine Photophobia

Symptomtext

Starting 3 hours after receiving the vaccine, I developed an ocular migraine in my line of sight. Normally they would last 15 min in the dark, but this one lasted for over an hour (which made me very concerned). When I came out of the bedroom into the light, it came back again. Normally I would only get one episode, but this time it was re-occurring all day. I ended up having to put my sunglasses on indoors to tolerate light. Also, I took Excedrin migraine to alleviate the symptoms. This lasted for about 24 hours. By the next day, I felt better, and the ocular migraines were no longer present. I have not gotten the booster due to my side effects from the first two doses, and prior COVID infection (08/2020). Also, per my doctor's recommendation I have been taking turmeric for my inflammation as a response to previous COVID infection and arthritis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ophthalmic migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Turmeric, Omega-3D, Multivitamin
Allergien: Wasps and Bees
Vorherige Impfungen: 1st covid vaccine (VAERS report done)

VAERS 2181895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NH
Alter: 14,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Chest pain

Symptomtext

Chest pain approximately 5 minutes post vaccination; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 14 year-old female patient received bnt162b2 (BNT162B2), administration date 07Jan2022 (Lot number: FD0809, Expiration Date: 10Jan2022) at the age of 14 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: CHEST PAIN (non-serious) with onset 07Jan2022, outcome "unknown", described as "Chest pain approximately 5 minutes post vaccination". Additional information: The reporter stated that vaccine was administered at one of their specific fixed vaccination site and that particular day, 3 of their individuals between ages of 14 and 16 had adverse reaction, 3 which were 'about the 10% reactive' for that day'. The reporter stated the vaccine was administered for provision not for treatment. Further stated that 1st patient was a 14 years old female which reported chest pain approximately 5 minutes post vaccination. The reporter stated that immediately after vaccination on 07Jan2022, these vaccines were pulled '"from use" to "for do not use". The reporter stated that 2 of the 3 did seek emergency room care and was unaware of the outcome and for evaluation yes for the 2 that had chest pain for both of them. Follow-up attempts completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2181640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Hyperaesthesia Muscular weakness Pain Pain in extremity Paraesthesia Vaccination site pain

Symptomtext

pain continued to elbow; arm of injection continued to feel sore and weak; Injection site was sore to the touch; injection site was sore to the touch; arm of injection continued to feel sore and weak; arm is weak and sometimes tingly; 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 (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 17Nov2021 (Lot number: FD0809) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, start date: 2021, stop date: 2021. Vaccination history included: Bnt162b2 (Prev dose product: COVID-19, Prev dose brand: Pfizer, Prev dose Lot number: ER8730,, Prev dose dose number: 2, Prev dose vaccine location: Left arm), administration date: 21Mar2021, when the patient was 55 years old, for COVID-19 immunization; Bnt162b2 (Prev dose product: COVID-19, Prev dose brand: Pfizer, Prev dose Lot number: EM9809,, Prev dose dose number: 1, Prev dose vaccine location: Left arm), administration date: 28Feb2021, when the patient was 55 years old, for COVID-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 17Nov2021, outcome "not recovered", described as "Injection site was sore to the touch"; HYPERAESTHESIA (non-serious) with onset 17Nov2021, outcome "not recovered", described as "injection site was sore to the touch"; PAIN (non-serious) with onset 20Nov2021, outcome "not recovered", described as "pain continued to elbow"; PAIN IN EXTREMITY (non-serious) with onset 17Nov2021, outcome "not recovered", MUSCULAR WEAKNESS (non-serious) with onset 2021, outcome "not recovered" and all described as "arm of injection continued to feel sore and weak"; PARAESTHESIA (non-serious) with onset 2021, outcome "not recovered", described as "arm is weak and sometimes tingly". Therapeutic measures were not taken as a result of vaccination site pain, hyperaesthesia, pain, pain in extremity, muscular weakness, paraesthesia. Additional information: Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination, has the patient was not been tested for COVID-19. Follow-Up (07Dec2021): Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history : None
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 2176212

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AL
Alter: 51,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / LA

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

Anxiety Insomnia Palpitations Panic attack Thinking abnormal

Symptomtext

Heart racing; Anxiety; Trouble sleeping; Panic attacks; Thought process is not clear; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 22Oct2021 11:00 (Lot number: FD0809) at the age of 51 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), intramuscular, administered in deltoid right, administration date 21Oct2021 (Batch/Lot number: unknown) as dose number unknown, single. Relevant medical history included: "known allergies: Penicillin" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1,single, Lot number:EP6955, Dose administration time:12:00, Vaccine location:Left arm (Left deltoid), Route of administration: Intramuscular), administration date: 24Mar2021, when the patient was 50 years old, for Covid-19 immunization; Bnt162b2 (Dose 2,single, Lot number:EW015D, Dose administration time:10:00, Vaccine location:Right arm (Right deltoid), Route of administration: Intramuscular), administration date: 14Apr2021, when the patient was 50 years old, for Covid-19 immunization. The following information was reported: PALPITATIONS (non-serious) with onset 23Oct2021, outcome "not recovered", described as "Heart racing"; ANXIETY (non-serious) with onset 23Oct2021, outcome "not recovered", described as "Anxiety"; INSOMNIA (non-serious) with onset 23Oct2021, outcome "not recovered", described as "Trouble sleeping"; PANIC ATTACK (non-serious) with onset 23Oct2021, outcome "not recovered", described as "Panic attacks"; THINKING ABNORMAL (non-serious) with onset 23Oct2021, outcome "not recovered", described as "Thought process is not clear". Therapeutic measures were not taken as a result of palpitations, anxiety, insomnia, panic attack, thinking abnormal. Additional Information: If covid prior vaccination was reported as no. if covid tested post vaccination was reported as no. Concomitant drugs was reported as none. Patient's Medical History (including any illness at time of vaccination) was reported none. Relevant Tests was reported was none. Specific Relevant Test For Thromboembolic Events With Thrombocytopenia was reported as None. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2175387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 28.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / LA

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

Dizziness Migraine SARS-CoV-2 test Speech disorder Visual impairment Vomiting

Symptomtext

dizziness; distortion of vision; migraine headache accompanied by vomiting; migraine headache accompanied by vomiting; distortion of Speech; 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), administered in arm left, administration date 28Aug2021 08:30 (Lot number: FD0809) at the age of 57 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "lupus" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Erythromycin, reaction(s): "Allergy: erythromycin", notes: Allergy: erythromycin; Hydroxychloroquine, reaction(s): "Allergy: hydroxychloroquine", notes: Allergy: hydroxychloroquine. The following information was reported: DIZZINESS (non-serious) with onset 31Aug2021, outcome "recovered" (2021), described as "dizziness"; VISUAL IMPAIRMENT (non-serious) with onset 31Aug2021, outcome "recovered" (2021), described as "distortion of vision"; MIGRAINE (non-serious), VOMITING (non-serious) all with onset 31Aug2021, outcome "recovered" (2021) and all described as "migraine headache accompanied by vomiting"; SPEECH DISORDER (non-serious) with onset 31Aug2021, outcome "recovered" (2021), described as "distortion of Speech". The events "dizziness", "distortion of vision", "migraine headache accompanied by vomiting", "migraine headache accompanied by vomiting" and "distortion of speech" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of dizziness, visual impairment, migraine, vomiting, speech disorder. Additional information: The patient did not receive any other vaccine in four weeks and other medications in two weeks. It was reported that shot received on Saturday (28Aug2021), Tuesday (31Aug2021) morning experienced dizziness distortion of vision and speech which accelerated into a migraine headache accompanied by vomiting. AE treatment with iv fluids and pain killer. The patient had no covid prior vaccination. The patient tested covid post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20210831; Test Name: COVID-19 test; Test Result: Negative ; Comments: Nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Lupus erythematosus
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2175381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 13.09.2021
Beginn: 13.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood cholesterol Blood cholesterol increased Fatigue Headache Heart rate abnormal Hypertension Pain Visual impairment

Symptomtext

Hers is high / total cholesterol is 217; high blood pressure; her glasses to provide lot number; irregular heart beat; Headache; body ache; tired; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 70 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 13Sep2021 (Lot number: FD0809) at the age of 70 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "irregular heartbeat" (unspecified if ongoing), notes: Chronic; "high blood pressure" (unspecified if ongoing), notes: Takes metroprolol, Chronic; "Diabetes" (unspecified if ongoing), notes: It is under control with her diet. Diagnosed about 4 years ago. Her number has never been higher than 7 but the last time the number was 8.; "chronic arthritis" (unspecified if ongoing), notes: Sometimes she get steroid injection in her knees, For two or three months she gets very bad body; "she got kind of sick" (unspecified if ongoing), notes: but it went away. Concomitant medication(s) included: METOPROLOL taken for hypertension. The following information was reported: HEART RATE ABNORMAL (non-serious), outcome "unknown", described as "irregular heart beat"; HEADACHE (non-serious) with onset 13Sep2021, outcome "recovered" (Sep2021), described as "Headache"; PAIN (non-serious) with onset 13Sep2021, outcome "recovering", described as "body ache"; BLOOD CHOLESTEROL INCREASED (non-serious), outcome "unknown", described as "Hers is high / total cholesterol is 217"; HYPERTENSION (non-serious), outcome "unknown", described as "high blood pressure"; VISUAL IMPAIRMENT (non-serious), outcome "unknown", described as "her glasses to provide lot number"; FATIGUE (non-serious) with onset 13Sep2021, outcome "recovering", described as "tired". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient stated that the time of the first vaccination was given in the morning around 09:30 or 09:45. She stated she has an irregular heartbeat but that has been for ages, and she takes metoprolol for high blood pressure. She stated this comes and goes sometimes after the vaccine, but she was having this way before the vaccine, it is chronic but not that bad. She has always had it. She stated she started getting body aches within an hour of the vaccine and they are still there but not as much. She also got a headache that began the same day and time as the body aches, but she has no more headache. She wants to know if the vaccine contains cholesterol. Hers is high, and she is concerned about that. States her total cholesterol is 217. She is tired and has been on the phone for a half hour trying to get her questions answered. No prior vaccinations within 4 weeks. Patient neither visited to emergency room nor physician office for AE. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: total cholesterol; Result Unstructured Data: Test Result:217
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic arthritis (Sometimes she get steroid injection in her knees For two or three months she gets very bad body); Diabetes (It is under control with her diet. Diagnosed about 4 years ago.); Heartbeats irregular (Chronic); Hypertension (Takes metroprolol Chronic); Sickness (but it went away)
Andere Medikamente: METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1840718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Chills Cough Decreased appetite Fatigue Headache Dyspnoea Influenza like illness Lymph node pain Lymphadenopathy Pain Pain in extremity Pyrexia

Symptomtext

cough; Painful swollen lymph node in armpit near injection site size of a large gumball; Painful swollen lymph node in armpit near injection site size of a large gumball; flu-like symptoms; fatigue for 4 days; shortness of breathe; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48 year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), administered in arm left, administration date 01Nov2021 (Lot number: FD0809) at the age of 48 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "IBS" (unspecified if ongoing); "Allergy" (unspecified if ongoing). Concomitant medication(s) included: ZINC; PHYTOESTROGEN; MAGNESIUM. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: 30155BA, Location of injection: Arm Left, 1st dose: mouth sores/blisters (1+ week), metallic taste (2 days)), administration date: 11Oct2021, when the patient was 48 years old, for COVID-19 immunization, reaction(s): "mouth sores/blisters", "mouth sores/blisters"; Bnt162b2 (Dose Number: 1, Batch/Lot No: 30155BA, Location of injection: Arm Left, 1st dose: mouth sores/blisters (1+ week), metallic taste (2 days)), when the patient was 48 years old, for COVID-19 immunization, reaction(s): "metallic taste". The following information was reported: COUGH (non-serious) with onset 02Nov2021, outcome "recovered", described as "cough"; LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 02Nov2021, outcome "recovered" and all described as "Painful swollen lymph node in armpit near injection site size of a large gumball"; INFLUENZA LIKE ILLNESS (non-serious) with onset 02Nov2021, outcome "recovered", described as "flu-like symptoms"; FATIGUE (non-serious) with onset 02Nov2021, outcome "recovered" (04Nov2021), described as "fatigue for 4 days"; DYSPNOEA (non-serious) with onset 02Nov2021, outcome "recovered", described as "shortness of breathe". The events "cough", "painful swollen lymph node in armpit near injection site size of a large gumball", "flu-like symptoms", "fatigue for 4 days", "shortness of breathe" and "painful swollen lymph node in armpit near injection site size of a large gumball" were evaluated at the physician office visit. Additional information: Patient did not receive any other vaccine in four weeks, Other medications in two weeks include multi-vitamin, Patient did not had covid prior vaccination, patient not tested for covid post vaccination. Clinical course: After 1st dose mouth sores/blisters (1+ week), metallic taste (2 days), After 2nd dose Painful swollen lymph node in armpit near injection site size of a large gumball, flu-like symptoms and fatigue for 4 days, & shortness of breathe and cough for a month. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101849397 similar report from same reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy NOS; Irritable bowel syndrome
Andere Medikamente: ZINC; PHYTOESTROGEN; MAGNESIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1840718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Cough Decreased appetite Fatigue Headache Dyspnoea Influenza like illness Lymph node pain Lymphadenopathy Pain Pain in extremity Pyrexia

Symptomtext

cough; Painful swollen lymph node in armpit near injection site size of a large gumball; Painful swollen lymph node in armpit near injection site size of a large gumball; flu-like symptoms; fatigue for 4 days; shortness of breathe; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48 year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), administered in arm left, administration date 01Nov2021 (Lot number: FD0809) at the age of 48 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "IBS" (unspecified if ongoing); "Allergy" (unspecified if ongoing). Concomitant medication(s) included: ZINC; PHYTOESTROGEN; MAGNESIUM. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: 30155BA, Location of injection: Arm Left, 1st dose: mouth sores/blisters (1+ week), metallic taste (2 days)), administration date: 11Oct2021, when the patient was 48 years old, for COVID-19 immunization, reaction(s): "mouth sores/blisters", "mouth sores/blisters"; Bnt162b2 (Dose Number: 1, Batch/Lot No: 30155BA, Location of injection: Arm Left, 1st dose: mouth sores/blisters (1+ week), metallic taste (2 days)), when the patient was 48 years old, for COVID-19 immunization, reaction(s): "metallic taste". The following information was reported: COUGH (non-serious) with onset 02Nov2021, outcome "recovered", described as "cough"; LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 02Nov2021, outcome "recovered" and all described as "Painful swollen lymph node in armpit near injection site size of a large gumball"; INFLUENZA LIKE ILLNESS (non-serious) with onset 02Nov2021, outcome "recovered", described as "flu-like symptoms"; FATIGUE (non-serious) with onset 02Nov2021, outcome "recovered" (04Nov2021), described as "fatigue for 4 days"; DYSPNOEA (non-serious) with onset 02Nov2021, outcome "recovered", described as "shortness of breathe". The events "cough", "painful swollen lymph node in armpit near injection site size of a large gumball", "flu-like symptoms", "fatigue for 4 days", "shortness of breathe" and "painful swollen lymph node in armpit near injection site size of a large gumball" were evaluated at the physician office visit. Additional information: Patient did not receive any other vaccine in four weeks, Other medications in two weeks include multi-vitamin, Patient did not had covid prior vaccination, patient not tested for covid post vaccination. Clinical course: After 1st dose mouth sores/blisters (1+ week), metallic taste (2 days), After 2nd dose Painful swollen lymph node in armpit near injection site size of a large gumball, flu-like symptoms and fatigue for 4 days, & shortness of breathe and cough for a month. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101849397 similar report from same reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy NOS; Irritable bowel syndrome
Andere Medikamente: ZINC; PHYTOESTROGEN; MAGNESIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2173751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 27.08.2021
Beginn: 27.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Confusional state Dizziness Dry mouth Fatigue Feeling abnormal Glossodynia Headache Lymph node pain Lymphadenopathy Maternal exposure during breast feeding Menstruation delayed Myalgia Nasal congestion Nausea Night sweats Pain Paraesthesia Peripheral coldness

Symptomtext

Night sweats Lymph node swelling & painful Body aches, sore muscles Extreme fatigue Foggy brain / mixing words up/ birthday confusion Dizzy Nausea headache Stuffy nose Tongue pain Tingling hands /cold Elbow - tendinitis? Dry mouth Late period Lost milk supply (breastfeeding) 10 days post vaccine: Dizzy Headache Dry mouth Nausea Tired Brain fog Lymph node swelling Overall yucky feeling Night sweats Low grade Fevers nightly (continued for more than 3 months)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, Infertility
Andere Medikamente: Levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 2157788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: FL
Alter: 20,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 22.01.2022
Beginn: 27.02.2022
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: IM / LA

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

Lethargy Muscle twitching Tremor

Symptomtext

Severe twitching and trembling. Tremoring. Lethargy

Weitere VAERSDATA-Felder

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

VAERS 2154852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AR
Alter: -
Geschlecht: U
Eingang: 03.03.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Blindness Chest pain Computerised tomogram Dizziness Headache Magnetic resonance imaging Migraine Tachycardia

Symptomtext

Chest pain, tachycardia, severe head pain, dizziness, loss of vision, and continued headaches/migraines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CT scan- Jan 4, 2022, MRI- Jan 27, 2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2140881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 25.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: UN / LA

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

Hypoaesthesia Injection site pain Paraesthesia

Symptomtext

Numbness and tingling all down my left arm all the way down to my finger tips on two of my fingers. The injection hurt more than a normal shot and it feels as though there is nerve damage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None. I was hoping it would go away but it hasn?t.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Clyndomiacin
Vorherige Impfungen: -

VAERS 2130089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: PR
Alter: 45,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 30.08.2021
Beginn: 05.10.2021
Tage bis Beginn: 36,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Palpitations

Symptomtext

Severe palpitations. Pain in the shoulder joints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Protein shakes. BCAA amino acids.
Allergien: No
Vorherige Impfungen: Yes. Severe palpitations. Age 45

VAERS 2123164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 14.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / -

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

Chest pain

Symptomtext

Mild chest pain on left side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2122750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 09.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Abdominal pain upper Blister Blood test Dyspnoea Feeling abnormal Gingival pain Gingival swelling Illness Lip swelling Loss of personal independence in daily activities Oral mucosal eruption Pyrexia Vomiting

Symptomtext

I had rash in my mouth; swelling in my nose and lips; I had fever; I had lot of pain in my gums; I started to have like blister types in my mouth, in my nose, in my cheeks; My gums were very swollen; I had a lot of pain in my stomach; I was vomiting; I couldn't eat or drink possibly; I feel like somebody is punching on my face; I was very sick; I am short of breath when I walk; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 61 year-old female patient received bnt162b2 (BNT162B2), administered in deltoid left, administration date 09Sep2021 19:00 (Lot number: FD0809) at the age of 61 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Blood pressure high" (unspecified if ongoing), notes: Verbatim: Blood pressure high; "High cholesterol" (unspecified if ongoing), notes: Verbatim: High cholesterol. Concomitant medication(s) included: METOPROLOL. The following information was reported: PYREXIA (non-serious) with onset 10Sep2021 08:00, outcome "recovered" (2021), described as "I had fever"; GINGIVAL PAIN (non-serious) with onset 10Sep2021 08:00, outcome "recovered" (2021), described as "I had lot of pain in my gums"; BLISTER (non-serious) with onset 10Sep2021 08:00, outcome "recovered" (2021), described as "I started to have like blister types in my mouth, in my nose, in my cheeks"; GINGIVAL SWELLING (non-serious) with onset 10Sep2021 08:00, outcome "recovered" (2021), described as "My gums were very swollen"; ABDOMINAL PAIN UPPER (non-serious) with onset 10Sep2021 08:00, outcome "recovered" (2021), described as "I had a lot of pain in my stomach"; VOMITING (non-serious) with onset 10Sep2021 08:00, outcome "recovered" (2021), described as "I was vomiting"; ORAL MUCOSAL ERUPTION (non-serious) with onset 13Sep2021, outcome "recovered" (2021), described as "I had rash in my mouth"; DYSPNOEA (non-serious) with onset 2021, outcome "not recovered", described as "I am short of breath when I walk"; FEELING ABNORMAL (non-serious) with onset Sep2021, outcome "recovered" (Sep2021), described as "I feel like somebody is punching on my face"; LIP SWELLING (non-serious) with onset 13Sep2021, outcome "recovered" (2021), described as "swelling in my nose and lips"; ILLNESS (non-serious) with onset Sep2021, outcome "recovered" (2021), described as "I was very sick"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 10Sep2021 08:00, outcome "recovered" (2021), described as "I couldn't eat or drink possibly". The events "i had fever", "i had lot of pain in my gums", "i started to have like blister types in my mouth, in my nose, in my cheeks", "my gums were very swollen", "i had a lot of pain in my stomach", "i was vomiting", "i had rash in my mouth", "i feel like somebody is punching on my face" and "swelling in my nose and lips" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, gingival pain, blister, gingival swelling, abdominal pain upper, vomiting, oral mucosal eruption, feeling abnormal, lip swelling, loss of personal independence in daily activities. Additional information: The patient had vaccine previously. She stated that her primary doctor never recommended, her allergy doctor allowed her to do, but her employee doctor pushing her to do. Nurse stated that she had not had second shot of Pfizer Covid 19 vaccine. The nurse stated that she was healthy and good, she had no problem before vaccine. The nurse stated that Last 2 weeks, no but after the vaccine, She went to my doctor cause she could not eat or drink so told her to do blood test. Then she had her blood test, 13Sep2021. Nurse stated that, it was a general blood test and then it showed she thought that was the abnormalities. Nurse stated that she was not experiencing anything now it was 2 months later. So, she do not know if it was related to vaccine. Nurse stated that, doctor prescribed her the Acyclovir. She gave me something else, she do not remember now. Nurse further stated that, she had a lot of pain in her gum, she felt like her gum gonna break, her whole mouth, it was for 3-4 days, she felt like somebody was punching on her face that how much pain she had, also, Friday and Saturday. No Prior vaccinations within 4 weeks. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101705943 similar report from same reporter

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210913; Test Name: Blood test; Result Unstructured Data: Test Result:elevated LFT, abnormal pigmentation; Comments: and something with the protein
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Verbatim: Blood pressure high); High cholesterol (Verbatim: High cholesterol)
Andere Medikamente: METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2118414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 41,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 22.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Cardiac monitoring Electrocardiogram normal Goitre Gynaecological examination normal Heart rate increased Hypertension Menstruation delayed Nodule Palpitations Ultrasound thyroid abnormal Uterine haemorrhage

Symptomtext

Delayed menstruation (1 week) Abnormal Uterine Bleeding (for 19/23 days) Heart Palpitations & increased heart rate (resting & active) Enlarged Thyroid, Cystic Nodule

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: EKG 2/7/22 (normal) Bloodwork 2/7/22 & 2/8/22 (mostly unremarkable) High Blood pressure (142/74) 2/8/22 Thyroid Ultrasound 2/15/22 (large cystic nodule) Heart Monitor (24 hour) 2/8/22-2/9/22 (results not yet available) Genital exam (unremarkable) 2/8/22
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: No prescription medications
Allergien: None
Vorherige Impfungen: -

VAERS 2113118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CO
Alter: 74,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 27.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Blood culture negative Chest X-ray abnormal Fatigue Hypotension Influenza Influenza A virus test positive Pyrexia SARS-CoV-2 test negative

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient hospitalized with fatigue, fevers, and hypotension, and influenza A. Received oseltamivir and intravenous fluids. Discharged to home medically stable.

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Praegender Schweregrund: Hypotension
Hospital-Tage: 2,0
Labordaten: Chest x-ray: no radiographic evidence of pneumonia Influenza A positive, blood cultures negative, SARS-CoV-2 negative
Aktuelle Erkrankungen: poor oral intake, enterocolitis
Vorgeschichte: pancreatic cancer, leukocytosis, nausea, vomiting, diarrhea, fatigue
Andere Medikamente: acetaminophen, Boost High protein, Creon, Dulcolax, guaifenesin, loperamide, Narcan, omeprazole, ondansetron, prochlorperazine, senna, Tums
Allergien: None
Vorherige Impfungen: -

VAERS 1869277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: TN
Alter: 81,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Cough Pain Pollakiuria Pyrexia Rash erythematous Rash Tremor Urinary incontinence

Symptomtext

shaking; experienced fever; chills; a bright red rash on face; a bright red rash on face; uncontrollable urine; aching; cough; This is a spontaneous report received from contactable reporter(s) (Pharmacist). A 81 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 12Nov2021 11:45 (Lot number: FD0809) at the age of 81 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Coronary Artery Disease" (unspecified if ongoing); "Kidney disease" (unspecified if ongoing); "Urinary Infection", stop date: Jan2011; "Pecans" (unspecified if ongoing), notes: Known allergies: Pecans. Concomitant medication(s) included: CLOPIDOGREL (ongoing); LISINOPRIL (ongoing); EXEMESTANE (ongoing); METOPROLOL TARTRATE (ongoing); AMLODIPINE (ongoing); EZETIMIBE (ongoing). Past drug history included: Haldol, reaction(s): "known allergies: Halodol"; Sulfa, notes: Known allergies: Sulfa. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL9269, Route of Administration: Intramuscular), administration date: 03Mar2021, when the patient was 81 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN5318, Route of Administration: Intramuscular), administration date: 10Feb2021, when the patient was 81 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (2021), described as "experienced fever"; CHILLS (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (Nov2021), described as "chills"; RASH ERYTHEMATOUS (non-serious), RASH (non-serious) all with onset 13Nov2021 03:00, outcome "recovered" (Nov2021) and all described as "a bright red rash on face"; POLLAKIURIA (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (Nov2021), described as "uncontrollable urine"; PAIN (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (2021), described as "aching"; COUGH (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (2021), described as "cough"; TREMOR (non-serious), outcome "recovered" (Nov2021), described as "shaking". Therapeutic measures were taken as a result of pyrexia, chills, rash erythematous, rash, pollakiuria, pain, cough, tremor. Additional Information: About 12-15 hours post booster dose, patient experienced fever/chills, a bright red rash on face, uncontrollable urine, aching, and cough. Patient took tylenol and benadryl to alleviate symptoms. Symptoms resolved about 24-36 hours post onset. It was unknown that the patient had covid prior vaccination and not tested for Covid post vaccination. It was unknown that the patient received prior vaccination (within 4 weeks). Patient started experiencing chills, shaking and a red rash on her face approximately 12 hours post Injection. She also had trouble controlling her urine during this time as well. She took some Benadryl and her symptoms subsided around 36 hrs post Injection. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Coronary artery disease; Kidney disorder; Peanut allergy (Known allergies: Pecans); Urinary infection
Andere Medikamente: CLOPIDOGREL; LISINOPRIL; EXEMESTANE; METOPROLOL TARTRATE; AMLODIPINE; EZETIMIBE
Allergien: -
Vorherige Impfungen: -

VAERS 1869277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: TN
Alter: 81,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / RA

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

Chills Cough Pain Pollakiuria Pyrexia Rash erythematous Rash Tremor Urinary incontinence

Symptomtext

shaking; experienced fever; chills; a bright red rash on face; a bright red rash on face; uncontrollable urine; aching; cough; This is a spontaneous report received from contactable reporter(s) (Pharmacist). A 81 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 12Nov2021 11:45 (Lot number: FD0809) at the age of 81 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Coronary Artery Disease" (unspecified if ongoing); "Kidney disease" (unspecified if ongoing); "Urinary Infection", stop date: Jan2011; "Pecans" (unspecified if ongoing), notes: Known allergies: Pecans. Concomitant medication(s) included: CLOPIDOGREL (ongoing); LISINOPRIL (ongoing); EXEMESTANE (ongoing); METOPROLOL TARTRATE (ongoing); AMLODIPINE (ongoing); EZETIMIBE (ongoing). Past drug history included: Haldol, reaction(s): "known allergies: Halodol"; Sulfa, notes: Known allergies: Sulfa. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL9269, Route of Administration: Intramuscular), administration date: 03Mar2021, when the patient was 81 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN5318, Route of Administration: Intramuscular), administration date: 10Feb2021, when the patient was 81 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (2021), described as "experienced fever"; CHILLS (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (Nov2021), described as "chills"; RASH ERYTHEMATOUS (non-serious), RASH (non-serious) all with onset 13Nov2021 03:00, outcome "recovered" (Nov2021) and all described as "a bright red rash on face"; POLLAKIURIA (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (Nov2021), described as "uncontrollable urine"; PAIN (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (2021), described as "aching"; COUGH (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (2021), described as "cough"; TREMOR (non-serious), outcome "recovered" (Nov2021), described as "shaking". Therapeutic measures were taken as a result of pyrexia, chills, rash erythematous, rash, pollakiuria, pain, cough, tremor. Additional Information: About 12-15 hours post booster dose, patient experienced fever/chills, a bright red rash on face, uncontrollable urine, aching, and cough. Patient took tylenol and benadryl to alleviate symptoms. Symptoms resolved about 24-36 hours post onset. It was unknown that the patient had covid prior vaccination and not tested for Covid post vaccination. It was unknown that the patient received prior vaccination (within 4 weeks). Patient started experiencing chills, shaking and a red rash on her face approximately 12 hours post Injection. She also had trouble controlling her urine during this time as well. She took some Benadryl and her symptoms subsided around 36 hrs post Injection. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Coronary artery disease; Kidney disorder; Peanut allergy (Known allergies: Pecans); Urinary infection
Andere Medikamente: CLOPIDOGREL; LISINOPRIL; EXEMESTANE; METOPROLOL TARTRATE; AMLODIPINE; EZETIMIBE
Allergien: -
Vorherige Impfungen: -

VAERS 2095510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OK
Alter: 49,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 14.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Blood thyroid stimulating hormone Cardiac monitoring Full blood count Metabolic function test Palpitations Sleep disorder

Symptomtext

Heart palpitations and heart racing intermittently, often waking from sleep at night.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: CBC, TSH, CMP, EKG, Cardiac Event monitor
Aktuelle Erkrankungen: KNDA
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: -
Vorherige Impfungen: -

VAERS 2093619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 60,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 26.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Feeling abnormal Headache Hypoaesthesia Malaise Nausea Paraesthesia

Symptomtext

Vaccine received 1000 on 1/26/2022. I felt a little foggy as the evening progressed. I awoke with a headache at 0345 on 1/27/2022 and my face was numb. I did not note any drooping or facial paralysis and this episode lasted 30-45 minutes. At 1415 on 1/27/2022 I had a feeling of pins and needles in my left chest and under my left armpit radiating down to my hip area that lasted approximately 30 minutes. This episode repeated at 2045 on 1/27/2022 lasting approximately the same amount of time. Aside from nausea and malaise lasting 36-48 hours, I have still been getting frequent headaches that seem worse when I lie down. Treatment has been either Motrin, Tylenol, or Alleve.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: No further testing completed with events.
Aktuelle Erkrankungen: None known.
Vorgeschichte: MTHFR gene mutation.
Andere Medikamente: Vitamin D-2000-4000U daily; Stress B complex vitamin daily; Quercitin with Zinc daily; ASA 81 mg daily.
Allergien: Sulfa.
Vorherige Impfungen: -

VAERS 2092470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MD
Alter: 36,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 14.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blood pressure increased Blood test Chest X-ray Chest discomfort Chest pain Condition aggravated Dyspnoea Myalgia Pyrexia

Symptomtext

The booster shot initially caused a severe fever (much more robust than after the second shot which in itself caused a 3-day fever), very strong muscle aches, etc.Following the initial recovery I found that taking a deep satisfying breath is an new and still ongoing experience. I wake up in the mornings with a sense that someone is sitting on my chest. On bad days I need to take a break in speaking after a few sentences. These side effects peaked in January (about 4-6 weeks after the shot), and are still ongoing to a lesser extent (speaking is easier, but chest pains and difficulty taking a satisfying breath is an issue). The quality of life is objectively impacted. I would like to note that there were no long-term chest pains after the initial 2-shot of Pfizer vaccines.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: In late-January to early-February I have had a series of doctor visits and had chest x-ray, a test breathing rapidly into a tube to measure air flow, blood test for allergens, and an ENT exam. My understanding from the doctors that nothing usual detected. My blood pressure has been quite elevated since the booster shot.
Aktuelle Erkrankungen: None. Same day's morning work-mandated COVID-19 test came negative.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Penicillin; none otherwise.
Vorherige Impfungen: -

VAERS 2090910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: PA
Alter: 44,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Breath holding Chest discomfort Chest pain Dyspnoea Echocardiogram Full blood count Glycosylated haemoglobin Heart rate Heart rate increased Metabolic function test Palpitations

Symptomtext

The initial safety information received was reporting only non-serious adverse drug reactions, Upon receipt of follow-up information on 31Jan2022, this case now contains serious adverse reactions. Information processed together. This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Other HCP). The reporter is the patient. A 44 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 13Dec2021 09:30 (Lot number: FD0809) at the age of 44 years as dose 1, single for Covid-19 immunisation. Relevant medical history included: "achalasia" (unspecified if ongoing); "GERD" (ongoing); "fatty liver" (unspecified if ongoing); "penicillin" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing), notes: Medicine controlled high blood pressure; "Hypertension" (ongoing); "Anxiety" (ongoing); "Thyroid goiter" (ongoing); " Gestational diabetes mellitus", stop date: 2011. Family history included: "Hypertension" (unspecified if ongoing), notes: Father; "Type 2 diabetes mellitus" (unspecified if ongoing), notes: Father. Concomitant medication(s) included: LABETALOL taken for hypertension, anxiety (ongoing); PREVACID; LANSOPRAZOLE taken for gastrooesophageal reflux disease (ongoing). Past drug history included: Codeine, reaction(s): "Drug allergy"; Morphine, reaction(s): "Drug allergy"; Sulfates, reaction(s): "Drug allergy"; Amoxicillin, reaction(s): "Drug allergy". Patient did not receive other vaccine in four weeks prior to the COVID vaccine. Patient had no COVID prior vaccination. The following information was reported: PALPITATIONS (hospitalization) with onset 15Dec2021, outcome "recovering", described as "Palpitation"; DYSPNOEA (hospitalization) with onset 15Dec2021, outcome "recovering", described as "Shortness of breath"; HEART RATE INCREASED (non-serious) with onset 14Dec2021 09:00, outcome "not recovered", described as "Rapid heart rate"; CHEST PAIN (non-serious), CHEST DISCOMFORT (non-serious) all with onset 14Dec2021 09:00, outcome "not recovered" and all described as "chest pressure and pain". The events "palpitation", "shortness of breath", "rapid heart rate", "chest pressure and pain" and "chest pressure and pain" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: breath holding: (12Dec2021) 0.993; echocardiogram: (unspecified date) scheduled; full blood count: (12Dec2021) within normal limits; glycosylated haemoglobin: (12Dec2021) 6.1; heart rate: (14Dec2021) rapid; metabolic function test: (12Dec2021) elevated LFTS (Liver function test), notes: Stable for patient. Therapeutic measures were not taken as a result of palpitations, dyspnoea. It was unknown if therapeutic measures were taken as a result of heart rate increased, chest pain, chest discomfort. Clinical course: No COVID tested post vaccination. The other health care professional confirmed that patient provided information regarding the reported events and considered that suspect product had a causal effect to the adverse events. Sender's Comments: Based on available information and the drug temporal relationship, the causality between the events - Palpitations, dyspnea, and the suspect drug "BNT162B2" cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211212; Test Name: BH; Result Unstructured Data: Test Result:0.993; Test Name: Echocardiogram; Result Unstructured Data: Test Result: scheduled; Test Date: 20211212; Test Name: CBC; Result Unstructured Data: Test Result: within normal limits; Test Date: 20211212; Test Name: HbA1c; Result Unstructured Data: Test Result:6.1; Test Date: 20211214; Test Name: Heart Rate; Result Unstructured Data: Test Result: Rapid; Test Date: 20211212; Test Name: CMP; Result Unstructured Data: Test Result: Elevated LFTS; Comments: Stable for patient.
Aktuelle Erkrankungen: Anxiety; GERD; Goitre; Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: Achalasia; Blood pressure high (Medicine controlled high blood pressure); Fatty liver; Gestational diabetes mellitus; Hypertension (Father); Penicillin allergy; Type 2 diabetes mellitus (Father).
Andere Medikamente: LABETALOL; PREVACID; LANSOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2090054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: TX
Alter: -
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Blood pressure measurement Dizziness Fatigue Headache Hypertension Lymphadenopathy Migraine Nausea Pain Pyrexia Tachycardia

Symptomtext

migraine; body aches; fatigue; tachycardia; fever; swollen lymphnode; blood pressure started to elevate; nauseous; bad headache; dizzy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 07Sep2021 14:30 (Lot number: FD0809) as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (1st dose , Date: 16Aug2021, Time: 14:20 , Site and Route of injection:, Anatomical site of injection: Right Arm, Route of administration: Intramuscular, Batch number: EW0171 (Pfizer)), administration date: 16Aug2021, for COVID-19 Immunization, reaction(s): "Headaches", "Lightheadness", "Dizziness", "Nausea", "Tachycardia". The following information was reported: HYPERTENSION (non-serious) with onset 07Sep2021, outcome "unknown", described as "blood pressure started to elevate"; NAUSEA (non-serious) with onset 07Sep2021, outcome "unknown", described as "nauseous"; HEADACHE (non-serious) with onset 07Sep2021, outcome "unknown", described as "bad headache"; DIZZINESS (non-serious) with onset 07Sep2021, outcome "unknown", described as "dizzy"; MIGRAINE (non-serious) with onset 08Sep2021, outcome "unknown", described as "migraine"; PAIN (non-serious) with onset 08Sep2021, outcome "unknown", described as "body aches"; FATIGUE (non-serious) with onset 08Sep2021, outcome "unknown", described as "fatigue"; TACHYCARDIA (non-serious) with onset 08Sep2021, outcome "unknown", described as "tachycardia"; PYREXIA (non-serious) with onset 08Sep2021, outcome "unknown", described as "fever"; LYMPHADENOPATHY (non-serious) with onset 08Sep2021, outcome "unknown", described as "swollen lymphnode". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of nausea, headache. Additional information: On 07Sep2021 at 02:30pm I received the second COVID-19 vaccine LOT# FD0809 at the same location after waiting 30 minutes with a nurse that was monitoring me my blood pressure started to elevated to high very high number and I started to feel super nauseous with a really bad headache. Once my time was up I left and started to drive home when I had to stop and pull over because I felt dizzy. On 08Sep2021 I began to have a migraine severe nausea, body aches, dizziness, fatigue tachycardia, fever, and swollen lymph node under my right arm that continued until 09Sep2021. I still have headaches, nausea and slight headaches as of 11Sep2021 that I have to take medication that was prescribed after the first vaccine on 16Aug2021. Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210907; Test Name: Blood pressure; Result Unstructured Data: Test Result:High
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2090006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 44,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 25.08.2021
Beginn: 29.08.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / LA

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

Blepharospasm Chest pain

Symptomtext

Chest pain for 5 days, 4 days after the first dose of Pfizer Covid 19 vaccine.; Left lower eyelid involuntary twitching; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 25Aug2021 12:45 (Lot number: FD0809) at the age of 44 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Seasonal Bronchitis." (unspecified if ongoing), notes: Other medical history: Seasonal Bronchitis.; "Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin. The patient's concomitant medications were not reported. The following information was reported: BLEPHAROSPASM (non-serious) with onset 29Aug2021, outcome "recovering", described as "Left lower eyelid involuntary twitching"; CHEST PAIN (non-serious) with onset 29Aug2021 12:00, outcome "recovering", described as "Chest pain for 5 days, 4 days after the first dose of Pfizer Covid 19 vaccine.". Therapeutic measures were not taken as a result of blepharospasm, chest pain. Additional information: The patient received bnt162b2 (BNT162B2), administered in arm left, on unspecified date (Lot number: FF2587) as dose 2, single for covid-19 immunisation. The patient had Chest pain for 5 days, 4 days after the first dose of Pfizer Covid 19 vaccine and left lower eyelid involuntary twitching,4 days after first dose of Pfizer COVID-19 vaccine, which up to the second dose persisted. The patient did not receive any other vaccine within 4 weeks. The patient did not have any other medications the patient received within 2 weeks of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bronchitis (Other medical history: Seasonal Bronchitis.); Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NJ
Alter: 74,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 28.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Decubitus ulcer General physical condition abnormal Hypoxia Pneumonia SARS-CoV-2 test positive

Symptomtext

75-year-old frail chronically ill-appearing female brought in by daughter for treatment of COVID 19. patient tested positive on Friday and was being seen in the ER for IV monoclonal antibodies however In ER eval found to have bilateral pneumonia and hypoxemia. She is being admitted for treatment of cope with. Patient is unable to provide history history is taken from the daughter. The daughter states she was tested on Friday and was negative. Patient also has a decubitus ulcer that she was getting treatment at home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 3,0
Labordaten: 01/28/2022 - pre admission SARS-CoV-2 Antigen (+), then after admission on 02/01/2022 - SARS-CoV-2 Antigen (-) and PCR (++) - no antibodies done
Aktuelle Erkrankungen: -
Vorgeschichte: Parkinson's, HTN, recent fall, with L olecranon fx and left hip fracture and repair in September bed-bound. Significant Surg Hx As Listed Addt'l Surgical History Recent left hip sx. Smoking Status Never Smoker. Alcohol Use Denies.
Andere Medikamente: amantadine HCl 100 mg Tablet Directions: 1 tablet oral twice a day (Active) lamoTRIgine (LaMICtal) 25 mg Tablet Directions: 1 tablet oral twice a day (Active) mirtazapine 45 mg Tablet Directions: 1 tablet oral daily every evening (Ac
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2079244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: ID
Alter: 67,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Heart rate increased Nausea Tachycardia

Symptomtext

At 11:55 pm the day of my Covid Booster, I woke with tachycardia, feeling of nausea. I checked my heart rate and it was 116-120 and remained that for a few hours. I felt weak and drank water and continued to try and rest but the fast heart rate lasted for 2-3 hours. Nausea eventually subsided as well. Next morning heart rate was normal. Never developed temperature.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis, Osteopenia, HTN, Ankylosing Spondylitis, "Fibromyalgia", L5 Disc Bulge, chronic Scoliosis
Andere Medikamente: Prescriptions: Meloxicam, Carvedilol, Amlodipine, Acyclovir. Supplements: Vitamin D, Lysine, Calcium
Allergien: Sulfa allergy
Vorherige Impfungen: -

VAERS 2074820

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: RI
Alter: 68,0
Geschlecht: M
Eingang: 30.01.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Haemorrhage Incorrect route of product administration Mobility decreased Pain Pain in extremity

Symptomtext

Shot was injected high on left arm towards the back of arm. It bled quite a bit and the pharmacist took awhile to stop it. (compared to any other shot I ever received. The arm has not stopped hurting since. When I raise my arm over my head or ben elbows and pull arms back it hurts. It feels like it is locking up and I'm restricting my movement to avoid the pain. Looked up info and I've seen it could be it hit a nerve?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: I have not visited a medical professional regarding this. I do not know if my medical will cover this.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 2071826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: ND
Alter: 42,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Breast pain Fatigue Headache Injection site warmth Joint stiffness Mammogram normal Mobility decreased Musculoskeletal stiffness Nasopharyngitis Pain Pain in extremity Rash Rash papular Rash pruritic Swelling Tenderness Urticaria

Symptomtext

11/2/2021-14:00-1st Covid-19 Pfizer shot, Warm to the touch that evening. 11/03/2021- 07:00, Rash all over body. Not raised or itchy faded within hours. Tired and feeling of exhaustion around 15:00. 11/04/2021 07:00, Arm was sore could only raise it halfway in the air. Tender on top of shoulder near neck, in the arm pit, and inner elbow. 11/05/2021- 05:00, Any movement of my arm felt like I hit my funny bone. Developed hives on neck, behind ears, chest, stomach, behind legs, buttocks. Took Benadryl tablet and that relieved itching. 11/06/2021- 08:00, Rash appeared. Raised and itchy patches on chest, arm pit, stomach, hips, face and ears. Took Benadryl tablet @ 18:00. 11/13/2021, Rash continued daily with little to no relief with Benadryl. 11/15/2021- 08:00, Went to the walk in clinic. Prescription hydroxyzine and Zyrtec daily and nightly helped. Gradually getting better. Not completely cleared up. Some days have flare up of hives but it's tolerable. 11/22/2021- 13:00, Visited Primary Physician about the reaction and receiving 2nd dose. He did not think it had to do with the vaccine. 11/27/2021- Rash and hives out breaks continue. 11/30/2021- 13:00, 2nd Covid-19 Pfizer shot. Developed cold like symptoms. Body aches, headache, fever (low grade) (99-100), and fatigue. Rash and hives continued and taking Zyrtec and hydroxyzine daily. 01/06/2022- 10:00, Went to women's clinic to be sure I was just having hives and reaction and not a yeast infection. 01/10/2022- 05:00, Continued rash and hives not much relief with antihistamines. Fingers knees and shoulders seem tight. Best way to describe is I feel like I'm swollen on the inside. 01/14/2022- 15:00, Seen by another doctor. Prescribed Zyrtec 1 dose am, Hydroxyzine 2 dose bed time, Medrol Dosepak, Calamine clear, and/ or Benadryl cooling gel. Referred to a Dermatologist. 01/15/2022- 23:00, Pain in left breast mammogram scheduled. 01/19/2022- 08:00, No rash or hives. 01/21/2022- 20:00, Rash on stomach. Still daily use of Zyrtec 1 dose am, Hydroxyzine 2 dose bed time and Calamine clear, and/ or Benadryl cooling gel. Mammogram was normal. 01/27/2022- 09:10, Dermatologist appointment, Continue with antihistamine treatment and assess in 1 month. He believes it is a reaction to the Pfizer Covid-19 vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Mirena birth control IUD 2nd implant
Allergien: None
Vorherige Impfungen: -

VAERS 2062339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cough Headache Nausea Pharyngeal paraesthesia Throat irritation

Symptomtext

COVID VACCINE REACTION Patient presented for second Pfizer/Covid vaccination; about 10 minutes post-injection she started to cough. She complained of throat tingling. VS: Pulse 81, BP 130/75, P02 98%. She was given water to drink and expressed that she wanted to lay down on a stretcher. She was attended by the charge nurse and a vaccinator. The cough persisted and she developed pruritus in the throat but without dyspnea, as well as nausea and headache, and was administered diphenhydramine 25 mg by IM (per policy, 65 year old). VS: 10 minutes after diphenhydramine: Pulse 74, BP 120/17, P02 97% Patient stated she was feeling better. Was offered transport by ambulance to hospital but refused. The patient is ESRD on dialysis. She has a history of anaphylaxis to ACE inhibitors. her rheumatologist, recommended she take the Covid vaccination while still on prednisone. Advised her to follow up with rheumatologist prior to next dose of Covid vaccine regarding any pre-medication. The patient decided to leave on her own in satisfactory condition, approximately 1 hour after onset of symptoms. VS: Blood pressure 120/75, pulse 79 P02 99%. ADDENDUM: At 11:00 am patient decided to be transported to hospital due to recurring throat symptoms. EMS called. She was administered second dose of diphenhydramine 25 mg prior to transport at 11:13 am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: Vital signs as noted above
Aktuelle Erkrankungen: ESRD on dialysis Osteoporosis Polioarthrosis Obesity
Vorgeschichte: As above
Andere Medikamente: Eliquis, prednisone, Tylenol
Allergien: ACE inhibitors - anaphylaxis Amlactin
Vorherige Impfungen: -

VAERS 2061879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NH
Alter: 16,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Chest pain

Symptomtext

Chest pain, approximately 5 minutes post vaccination; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 16 year-old male patient received bnt162b2 (BNT162B2), administration date 07Jan2022 (Lot number: FD0809, Expiration Date: 10Jan2022) at the age of 16 years as dose number, unknown, single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: CHEST PAIN (non-serious) with onset 07Jan2022, outcome "unknown", described as "Chest pain, approximately 5 minutes post vaccination". The event "chest pain, approximately 5 minutes post vaccination" was evaluated at the emergency room visit. Therapeutic measures were taken as a result of chest pain. Follow-Up (18Jan2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History:Patient Other Relevant History 1: None.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 02.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Allergy to vaccine Amnesia Anxiety Blood pressure measurement Blood test Cardiac stress test Chest X-ray Chest discomfort Computerised tomogram Dysphemia Electrocardiogram Fall Fatigue Feeling abnormal Hyperhidrosis Hypertension Hypoaesthesia Mental fatigue

Symptomtext

she could feel was a rushing. It felt like someone was squeezing her heart/feels like it was hit with a jackhammer; she was falling off of a mountain; high blood pressure/160/110; Her left arm is going numb; tingling/left arm tingling; allergic to the vaccine; brain is completely fried; Migraine headache; She has no memory; nasty sweat; light sensitivity; anxiety attacks; she couldn't speak for 10 minutes; panic attack; collapse across the kitchen floor; extreme fatigue; stuttering; had tremors; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 58 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02Sep2021 (Lot number: FD0809) at the age of 58 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Past drug history included: Epinephrine, reaction(s): "allergic to epinephrine", notes: She is allergic to epinephrine. The following information was reported: PANIC ATTACK (medically significant) with onset 02Sep2021, outcome "unknown", described as "panic attack"; HYPERTENSION (medically significant), outcome "unknown", described as "high blood pressure/160/110"; SPEECH DISORDER (non-serious) with onset 02Sep2021, outcome "unknown", described as "she couldn't speak for 10 minutes"; CHEST DISCOMFORT (non-serious), outcome "unknown", described as "she could feel was a rushing. It felt like someone was squeezing her heart/feels like it was hit with a jackhammer"; FEELING ABNORMAL (non-serious), outcome "unknown", described as "she was falling off of a mountain"; AMNESIA (non-serious) with onset 24Dec2021, outcome "unknown", described as "She has no memory"; DYSPHEMIA (non-serious) with onset 2021, outcome "unknown", described as "stuttering"; TREMOR (non-serious) with onset 2021, outcome "unknown", described as "had tremors"; MIGRAINE (non-serious) with onset 24Dec2021, outcome "unknown", described as "Migraine headache"; ANXIETY (non-serious) with onset 09Sep2021, outcome "unknown", described as "anxiety attacks"; HYPOAESTHESIA (non-serious), outcome "unknown", described as "Her left arm is going numb"; PARAESTHESIA (non-serious), outcome "unknown", described as "tingling/left arm tingling"; FALL (non-serious) with onset Sep2021, outcome "unknown", described as "collapse across the kitchen floor"; PHOTOPHOBIA (non-serious) with onset 05Oct2021, outcome "unknown", described as "light sensitivity"; MENTAL FATIGUE (non-serious) with onset 24Dec2021, outcome "unknown", described as "brain is completely fried"; HYPERHIDROSIS (non-serious) with onset 05Oct2021, outcome "unknown", described as "nasty sweat"; FATIGUE (non-serious) with onset 2021, outcome "unknown", described as "extreme fatigue"; ALLERGY TO VACCINE (non-serious), outcome "unknown", described as "allergic to the vaccine". The events "panic attack", "high blood pressure/160/110", "she couldn't speak for 10 minutes", "she was falling off of a mountain", "she has no memory", "stuttering", "had tremors", "migraine headache", "anxiety attacks", "her left arm is going numb", "tingling/left arm tingling", "collapse across the kitchen floor", "light sensitivity", "brain is completely fried", "nasty sweat" and "extreme fatigue" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (2021) 160/110; blood test: (2021) negative; (05Oct2021) whole series of blood work which was clean; cardiac stress test: (07Oct2021) it came back negative; chest x-ray: (05Oct2021) that was clean; computerised tomogram: (27Dec2021) negative; electrocardiogram: (2021) negative; (2021) nothing; (11Sep2021) everything was normal, notes: They ran an EKG and did all vitals; (15Sep2021) negative; (05Oct2021) ekg which came back clean; sars-cov-2 test: (09Sep2021) negative; (20Sep2021) negative. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:160/110; Test Date: 2021; Test Name: blood tests; Result Unstructured Data: Test Result:Negative; Test Date: 20211005; Test Name: blood tests; Result Unstructured Data: Test Result:whole series of blood work which was clean; Test Date: 20211007; Test Name: Stress test; Result Unstructured Data: Test Result:It came back negative; Test Date: 20211005; Test Name: chest x-ray; Result Unstructured Data: Test Result:that was clean; Test Date: 20211227; Test Name: CT Scan; Result Unstructured Data: Test Result:Negative; Test Date: 2021; Test Name: EKG; Result Unstructured Data: Test Result:Negative; Test Date: 2021; Test Name: EKG; Result Unstructured Data: Test Result:Nothing; Test Date: 20210911; Test Name: EKG; Result Unstructured Data: Test Result:Everything was normal; Comments: They ran an EKG and did all vitals; Test Date: 20210915; Test Name: EKG; Result Unstructured Data: Test Result:Negative; Test Date: 20211005; Test Name: EKG; Result Unstructured Data: Test Result:EKG which came back clean; Test Date: 20210909; Test Name: COVID test; Result Unstructured Data: Test Result:Negative; Test Date: 20210920; Test Name: COVID test; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WV
Alter: 51,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 07.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: IM / RA

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

Mobility decreased Pain in extremity X-ray

Symptomtext

About a week after the vaccine I started with pain in the right arm to the point of being unable to move my arm. This lasted over a week. I also started having catching in my right upper arm near the deltoid muscle. I saw my healthcare provider and had an X-ray with no findings. Now going to PT which isn't really helping with the catching in my arm. Requesting an MRI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-ray
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, history of MI due to blood clot
Andere Medikamente: Wellbutrin, synthroid, magnesium, protonix, metoprolol, atorvastatin, celexa, vitamin D, aspirin, probiotics, singulair
Allergien: Penicillin and sulfa
Vorherige Impfungen: -

VAERS 2047962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Back pain Bone pain Chills Diarrhoea Flushing Headache Hepatic enzyme Hepatomegaly Intermenstrual bleeding Muscle spasms Palpitations Rash Swelling of eyelid Swollen tongue

Symptomtext

Swelling of eyelids and tongue. Benadryl helps. Later in the week- rash, flushing, chills, achy joints, ache of bones, liver swelled under ribcage (visible to the eye as well), diarrhea, heart palpitations, headache, lower back ache by kidney, green sludge bowel movement after 2 1/2 days, headache. Continued all prescribed medications and increased Benadryl. Now experiencing cramping and breakthrough bleeding. Already through menopause.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Liver enzyme tests on 1/8/22.
Aktuelle Erkrankungen: Mast Cell Activation Syndrome, Eosinophilic Esophagitis, Allergies, Cough, Laryngitis and sore throat
Vorgeschichte: Mast Cell Activation Syndrome, Eosinophlic Esophagitis, Sleep Apnea, Schatzki's Ring, Dysphagia, Gastritis, GERD, Liver Disease, Epstein Barr Virus, Asthma, Allergies, Chronic Fatigue Syndrome, Dysphagia, Dysrhythmias (SVT), Endometriosis
Andere Medikamente: Celecoxib; Cromolyn Sodium; Lansoprazole, Cetirizine; Benzonatate; Famotidine; Prednisone; Triamcinalone; Albuterol Inahler; Benadryl; Multiple Vitamin; Calcium; Magnesium; Vitamin C; Vitamin D
Allergien: Clindamyacine, floxin, acetamenophine, vicodin, morphine, septra, omeprazole, singulair, peanuts, tree nuts, eggs, milk, cheese, mango, sunflower, sesame seeds, soy, mold, trees, grass, cats, dogs, horses.
Vorherige Impfungen: Flu Shot in 2000 - Bedridden for two weeks - Started Chronic Fatigue

VAERS 2039955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 13,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pharyngeal paraesthesia Throat irritation

Symptomtext

Tingling in the back of throat; "feels like I need to spit something out" Mother gave her loratidine 10mg

Weitere VAERSDATA-Felder

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

VAERS 2034994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 21.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: UN / UN

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

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

Symptomtext

chills, fatigue, cough, short of breath

Weitere VAERSDATA-Felder

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

VAERS 2028614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: PA
Alter: 41,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 24.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Mobility decreased Neck pain Pain Peripheral swelling Tremor

Symptomtext

Severe swelling of upper arm persisting 7 days total, immobilizing arm and neck pain with severe headache. Body shakes due to chills, full body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: AFib, hypothyroid, mitral valve prolapse, social anxiety and depression
Vorgeschichte: -
Andere Medikamente: Levothyroxine 25mcg, sotalol 80, alprazolam 1mg, atorvastatin 20mg...citalopram 20mg....OTC nothing
Allergien: Penicillin, hot peppers
Vorherige Impfungen: -

VAERS 2027666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Paraesthesia

Symptomtext

Dose received: 3; Approximately 3 hours after receiving the injection, I experienced paresthesia in my left arm as a tingling feeling in my fingertips and hand, which makes using a keyboard difficult as I cannot feel the keys; This is a spontaneous report from a non-contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 34-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jan2022 (Lot number: FD0809) at the age of 34 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Migraine with aura" (unspecified if ongoing); "Acne" (unspecified if ongoing); "Hypoglycemia" (unspecified if ongoing) and "Fruit allergy" (unspecified if ongoing), notes: Known allergies: Strawberries. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EW0162; Anatomical location: left arm; Route of administration: unspecified), administration date: 14Apr2021, when the patient was 33 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EW0172; Anatomical location: left arm; Route of administration: unspecified), administration date: 05May2021, when the patient was 33 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 07Jan2022, outcome "unknown", described as "Dose received: 3"; PARAESTHESIA (non-serious) with onset 07Jan2022, outcome "unknown", described as "Approximately 3 hours after receiving the injection, I experienced paresthesia in my left arm as a tingling feeling in my fingertips and hand, which makes using a keyboard difficult as I cannot feel the keys". Therapeutic measures were not taken as a result of paraesthesia.Additional Information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19.No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acne; Fruit allergy (Known allergies: Strawberries); Hypoglycemia; Migraine with aura.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 29.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Injection site erythema Injection site pruritus Injection site swelling Injection site warmth Neuralgia Pain in extremity Paraesthesia Pruritus Sleep disorder

Symptomtext

The side effects I am reporting that have not gone away are two things. Since the evening of December 30, 2021, I have outer thigh leg pain that is best described as nerve pain. It wakes me up at night and most times it is an intense itching sensation and also a tingling and numbness feeling. I've never had anything like this ever. It mainly occurs while I'm sleeping but has occasionally happened when I'm on the treadmill walking. The other issue is after the initial swelling and redness at the injection site, the swelling had gone away but the warmth and redness area has increased in size to about 5" diameter and it also itched. It is now 2 weeks out and the rednes is still there though the itching has disappeared

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Metoprolol, lisinopril/hydrochlorothiazide, tamoxifen, multivitamin, vitamin D, vitamin C, zinc, magnesium, B complex, docusate sodium.
Allergien: None
Vorherige Impfungen: -

VAERS 2024568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia oral

Symptomtext

Lip tingling

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, stroke (residual affects), clotting disorder, Chronic Respiratory Failure, DVT
Andere Medikamente: -
Allergien: adhesive tape, aspirin
Vorherige Impfungen: -

VAERS 2018364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AL
Alter: 44,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Burning sensation Dizziness Immunisation Lymphadenopathy Paraesthesia Peripheral swelling Rash

Symptomtext

Pfizer COVID 19 and this was for her Booster; Experienced like burning and tingling in her leg and it''s only her right leg; Tingling is pretty bad; Very swollen arm like her entire arm and kind of go within into her chest belly area; Slight dizziness; Normal swollen lymph nodes; Rash; Experienced like burning and tingling in her leg and it''s only her right leg; Tingling is pretty bad; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 44 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 10Dec2021 16:30 (Lot number: FD0809, Expiration Date: 19Dec2021) at the age of 44 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1), for COVID-19 immunization; Bnt162b2 (Dose: 2), for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 10Dec2021 16:30, outcome "unknown", described as "Pfizer COVID 19 and this was for her Booster"; PARAESTHESIA (non-serious), BURNING SENSATION (non-serious) all with onset 2021, outcome "unknown" and all described as "Experienced like burning and tingling in her leg and it''s only her right leg; Tingling is pretty bad"; PERIPHERAL SWELLING (non-serious) with onset 2021, outcome "unknown", described as "Very swollen arm like her entire arm and kind of go within into her chest belly area"; DIZZINESS (non-serious) with onset 2021, outcome "unknown", described as "Slight dizziness"; LYMPHADENOPATHY (non-serious) with onset 2021, outcome "unknown", described as "Normal swollen lymph nodes"; RASH (non-serious) with onset 2021, outcome "unknown", described as "Rash". Therapeutic measures were taken as a result of rash. Additional information: Pharmacist stated, I am a pharmacist calling to report the adverse effect to the vaccine. My name is (Name) (first name further not clarified phonetically hence captured as UNKNOWN in tab). So, the main thing the patient is complaining about is she has experienced like burning and tingling in her leg and it's only her right leg, she had the vaccine in her left arm, I don't know if that's important. But the tingling is pretty bad, and she has also had a very swollen arm like her entire arm and kind of go within into her chest belly area as well and then slight dizziness and then the normal swollen lymph nodes. When confirmed the name of the vaccine as Pfizer COVID 19 Vaccine, Pharmacist stated, Yeah Pfizer COVID 19 and this was for her Booster, she did not have any reaction to the first 2 Pfizer doses. Pharmacist stated, the date was 9Dec (09Dec2021) yes actually let me make sure, she had the vaccine given on 10Dec (10Dec2021). Treatment: Pharmacist stated, she no she took Benadryl for the rash, but that was it (further not clarified hence captured rash as event conservatively). Other medical condition or Concomitant medication: Pharmacist stated, no other condition that I am aware, let me see on her profile. This is all we have ever filled for her, so I am going to say unknown but no (further clarification unknown). Pharmacist stated, she is 44-year-old (further not clarified hence not captured in tab) and vaccine was given to her at 4:30 PM. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2014106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NH
Alter: 16,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain

Symptomtext

Pain on sternum O 5 mins P no R to right side of chest Q dull, pressure S 3

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: NP listened to chest and found everything WNL Sitting P76 BP 110/50 Stand P92 BP 112/50
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Ibuprofen, Claritin
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2010227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 16,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 28.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal pain Chest X-ray Chest pain Diarrhoea Electrocardiogram Myalgia Pain in extremity Pyrexia SARS-CoV-2 test negative Vomiting

Symptomtext

The next morning he had a fever for 24hrs, I gave him Advil, didn't work, he complained about arm and muscle pain for at least 36 hours. On 01/02/2022 he had chest pain as well. This continued until 01/05/2022. As of today he still has pain in his chest pain. On 01/05/2022 around 2:30 AM he got up in the middle of the night vomiting and diarrhea. He still has abdominal pain but the diarrhea has stopped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Covid test which was negative, X-ray of the chest, as well as a EKG. Monday 01/03/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma, ADHD, Autism spectrum disorder, DMDD, Anxiety.
Andere Medikamente: Concerta ER 18mg tablet, Escitalopram 20mg Tablet, Guanfacine HCL extended release 3mg tablet, Hydroxyzine HCL 25 mg twice a day, Singular 10mg Seroquel XR 300mg Loratadine 10 mg. Lansoprazole 15mg . Vitamin D 3 50 MCG.
Allergien: Amoxicillin, Feathers, dust mites. Summer pollen and outdoors.
Vorherige Impfungen: -

VAERS 2005954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: PA
Alter: 36,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 02.10.2021
Beginn: 20.12.2021
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Discomfort Exposure to SARS-CoV-2 Fatigue Headache Heart rate increased Lymphadenopathy Malaise Muscular weakness Myalgia Nasopharyngitis Pain Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive Sleep disorder Tremor

Symptomtext

I had no AE to the vaccine but on 12/18 I was exposed to a Covid positive individual. On 12/20 I began having various mild cold symptoms a headache, muscles and body ache and my legs and body just felt very heavy, so I took a rapid Covid test on 12/21, but it was negative. On 12/21 later that evening I developed a 99.8 fever that didn't last too long. 12/22 I took another rapid Covid test that was positive at that time. I had a PCR test that I performed as well on 12/29 which confirmed the rapid test. I only had one night of fever which subsided. Fatigue, muscle weakness, the feeling of being very tired and body heaviness and not just not feeling well overall has been experienced since. The lymph nodes under my arms were a little swollen. And today when returning from the restroom my body got super shaky, my HR elevated, my hands were trembling and it feels as if my whole body has a mild tremor so I am currently laying on the flood to help my body relax and hopefully these symptoms will subside soon. This has affected my sleep patterns resulting in me not being able to sleep well and I'm startled at the slightest of noises I hear. It feels as if my body has a high level of adrenaline running through me at times. My usual resting HR has usually between 60-70 BPM, but since the day after my Covid exposure my HR has elevated over that 70 mark near the 80's which remained elevated until after about a week then finally started lowering on its own, but is still slightly above normal but has lowered since the exposure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: COVID-19-negative/positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Birth Control
Allergien: No
Vorherige Impfungen: -

VAERS 2005943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 70,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 22.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: IM / RA

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

Blood creatinine increased Blood potassium decreased Blood urea increased COVID-19 Dizziness Dyspnoea Full blood count Glomerular filtration rate decreased Laboratory test abnormal Metabolic function test SARS-CoV-2 test positive

Symptomtext

Patient was initially referred to the ED following routine labs as his creatinine had tripled since 12/1 accompanied with elevated BUN and decreased potassium. Patient visited the ED earlier today but left without being seen after triage and having labs done. Patient did have CBC and CMP done with creatinine of 3.09, BUN of 63, and eGFR of 21. Patient was called and instructed to return to the ED for admission. Currently, patient reports he feels lightheaded. He denies abdominal or back pain. He states he has been urinating normally. He denies fever, chills, chest pain, or cold/flu symptoms. He does report some shortness of breath, but indicates this is normal for him. Patient reports that he has had normal LVAD numbers and currently they are: RPM 5300, 4.0 flow, 4.5 PI, and 3.9 PWR. He denies any source of bleeding. He denies any new leg swelling within the past week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID-19 PCR 1/5/22
Aktuelle Erkrankungen: -
Vorgeschichte: Nonischemic cardiomyopathy secondary to doxorubicin toxicity s/p HeartMate 3 LVAD placement in 2018 for destination therapy, CHF, recurrent GI bleeds, V. fib s/p ICD placement (anticoagulated on warfarin), and prior Pseudomonas driveline infection on chronic antibiotics
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1263964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 20.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Confusional state Dizziness Feeling abnormal Magnetic resonance imaging Migraine Headache Magnetic resonance imaging head Motion sickness Nausea Ophthalmological examination Photophobia Tinnitus Vertigo

Symptomtext

SIDE EFFECTS FROM ALL VACCINATIONS NASEAU, MIGRANES, DIZZINESS, MOTION SICKESS, VERITGO, RINGING IN EARS, EXTREME SENSATIVITY TO LIGHT, CONFUSSION, BRAIN FOG, FEELS LIKE SOMEONE TOOK BRAIN OUT AND SHOOK IT UP. SIDE EFFECTS FROM FIRST TWO VACCINATION 8 WEEKS OF MORE, BOOSTER SIDE EFFECT STILL ON GOING

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: SERVERAL DOCTORS VISITS, CHIROPRACTOR, MASSAGE THERAPHY, MRI, EYE DOCTOR
Aktuelle Erkrankungen: non3
Vorgeschichte: born with Cerbral palsey, mild only causes mild limb in left leg due to muscle shorter
Andere Medikamente: Vita, Multi,D, probotics,benedryl, nitrofurantoinpost coitally
Allergien: Sulfur
Vorherige Impfungen: -

VAERS 1999249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 13.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Back pain Chest pain Computerised tomogram Ear pain Electrocardiogram Headache Oropharyngeal pain

Symptomtext

From patient Two weeks ago today, I had the Covid 19 booster in my right arm in your office. The pain level in the right side of my head, right ear, and throat is still the same. The pain in the right side of my head is like a bad headache, but hurts when touched or when the shower water hits my head. The pain in my right chest and back has increased.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, CT, office visit
Aktuelle Erkrankungen: -
Vorgeschichte: AF (paroxysmal atrial fibrillation) Altered mental status Arthritis At risk for falls BPH (benign prostatic hypertrophy) CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min Coronary artery disease of native artery of native heart with stable angina pectoris Dyslipidemia ED (erectile dysfunction) Essential hypertension GERD (gastroesophageal reflux disease) Hypogonadotropic hypogonadism Insomnia OA (osteoarthritis) OSA (obstructive sleep apnea) Polio
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG EC tablet atorvastatin (LIPITOR) 20 MG tablet Calcium Carbonate-Vitamin D (CALCIUM 600 + D PO) cholecalciferol (CHOLECALCIFEROL) 1000 units Coenzyme
Allergien: Betadine, Codeine, Vicodin, Hydrocodone
Vorherige Impfungen: -

VAERS 1997855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

moderat

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Hypoaesthesia Palpitations

Symptomtext

Heart palpitation Shortness of breath numbness in one side of arm

Weitere VAERSDATA-Felder

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

VAERS 1941867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: ND
Alter: -
Geschlecht: U
Eingang: 31.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chills Dizziness Fatigue Feeling of body temperature change Headache Feeling cold Feeling hot Hyperhidrosis Insomnia Immunisation Nausea Palpitations Sleep disorder

Symptomtext

Heart palpitation; I get a lot of nausea, comes and goes; I have hot and cold, not totally chills but cold one moment and hot the next and sweating; I have hot and cold, not totally chills but cold one moment and hot the next and sweating; I have hot and cold, not totally chills but cold one moment and hot the next and sweating; Dizziness; Waking up at night and not being able to sleep due to this nausea.; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 63 year-old patient received bnt162b2 (BNT162B2) (Batch/Lot number: unknown) as dose 1, single and (Batch/Lot number: unknown) as dose 2, single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: PALPITATIONS (non-serious), outcome "recovering", described as "Heart palpitation"; NAUSEA (non-serious), outcome "recovering", described as "I get a lot of nausea, comes and goes"; FEELING COLD (non-serious), FEELING HOT (non-serious), HYPERHIDROSIS (non-serious), outcome "recovering" and all described as "I have hot and cold, not totally chills but cold one moment and hot the next and sweating"; DIZZINESS (non-serious), outcome "recovering", described as "Dizziness"; INSOMNIA (non-serious), outcome "recovering", described as "Waking up at night and not being able to sleep due to this nausea.". Therapeutic measures were taken as a result of palpitations, nausea. Additional information: It was reported that, the nurse concerned and stated that, the patient had the Pfizer booster shot, the patient already had the booster shot. Stated that, patient had the 4 vaccination, got the first shot, the second shot and 8 months after that second shot they had Covid booster just 5 days ago. Stated that, most of the times the symptoms go away in 2 to 3 days. But the patient was having some different symptoms now still hanging on day 5. Stated that, the patient was just kind of wondering whether what the patient feeling here was kind of normal. Stated that, the patient had hot and cold, not totally chills but cold one moment and hot the next and sweating, dizziness, waking up at night and not being able to sleep due to this nausea. Stated that, the patient got a lot of nausea, come and go. The patient did have a little bit of heart palpitation. Stated that, was there anything the patient can take or was it normal to hang on that long. Stated that, a home self-test was done twice to see whether patient had Covid before if the patient could had got exposed before the patient got the shot or something, but it came out negative (further clarification unknown about the tests). The reporter seriousness for the events was reported as unspecified. Other medical condition and other medications, nurse stated, no, not really after the shot the patient took some Tylenol (clarified as treatment). Nurse confirmed the name of the product as Covid-19 vaccine of Pfizer. Stated that, the nurse was informed the role of Pfizer Drug Safety and about Pfizer Medical Information Department for the concern. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1993252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 05.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray Palpitations

Symptomtext

Palpitations that lasted about 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Chest X-ray 12/8/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium supplements and multivitamin. Occasional Advil.
Allergien: Allergic to eggplant.
Vorherige Impfungen: -

VAERS 1992203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 29,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Chills Injection site pain Palpitations

Symptomtext

Chest pain intermittent over the course of 5 days, heart palpations intermittent over the course of 3 days, pain at injection site for 2 days after injection, Chills 16 hours after injection lasting 5 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zyrtec 10mg, b12 1000mg, D3 1000 IU
Allergien: None
Vorherige Impfungen: -

VAERS 1985151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Cough Headache Immediate post-injection reaction Pain in extremity Rhinorrhoea Sleep disorder Somnolence

Symptomtext

Immediate histamine response with this one just like the first 2 doses. This time I got a very bad cough that interrupted my sleep and was causing a bad mucus to build up. I did go to the doctor for this one as well but there was nothing they could do. I also had horrible leg pain like someone had taken a meat tenderizer and banged up my lower back all the way to the bottom of my legs. The headache and not being able to stay awake was much worse than the first 2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Sinus, Upper Respiratory
Vorgeschichte: Diabetes, Autism
Andere Medikamente: Clonazepam, Pramipexol, Amlodipine, Atorvastatin, Montelukast, Basaglar, Ozempic
Allergien: Prochlorperazine, Sulfa, Prednisone, Oxycodone, Hydrocodone, Bupropion, Lorazidone, Lamotrigine, Metformin, Ziprasidone, Ondansetron, Glipizide, Tramadol, Doxycycline, Lorazepam
Vorherige Impfungen: -

VAERS 1985129

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FD0809

moderat

Staat: NV
Alter: 69,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 26.02.2021
Beginn: 20.09.2021
Tage bis Beginn: 206,0
Dosis: 3
Route/Site: IM / LA

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

Arrhythmia Arteriogram coronary abnormal Atrial fibrillation Atrial hypertrophy Cardiac flutter Condition aggravated Congenital cardiovascular anomaly Echocardiogram abnormal Electrocardiogram abnormal Electrocardiogram ambulatory abnormal Fatigue Magnetic resonance imaging heart Myocardial bridging Pain in extremity Scan with contrast abnormal

Symptomtext

The first 2 shots I had very little issue with. A sore arm and some tiredness. The third shot (booster) I had no significant reactions except a sore arm for less than 12 hours. June 26, 2021 I had a flutter of my heart that was anomalous lasting 20 minutes or more. This was different because it lasted more than the usual few seconds to a couple of minutes. On September 21, 2021, I was admitted to emergency room after a flutter/afib event lasting ~2 hours. An EKG was anomalous and I was transferred to the hospital for an Echo and angiogram. The diagnosis was miocardial bridging and atrial hypertrophy believed to be congenital in nature. After getting back home I have worn a heart monitor for 30 days. and completed an MRI for my heart. Between the heart monitor and MRI I suffered another event that lasted over 3 hours. This event came after the booster shot I received on 09/26/2021. I apparently have clean arteries, but the arrhythmia appears to be electrical in nature. The increased time intervals of afib/flutter may be coincidental to the timing of the injection and more related to my age heart defects that I didn't know I had until the recent hospitalization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: 3,0
Labordaten: Angiogram 09/22/2021 - Miocardial bridging and apical hypertrophy, no significant plaque 2 Echo Cardiograms one with contrast - helped diagnose the apical hypertrophy
Aktuelle Erkrankungen: none
Vorgeschichte: heart flutter for 20 years, but not for significant lengths of time, erratic intervals up to 6 months between events
Andere Medikamente: D-3 (5000), Symvistatin (40), asprin (81), Zyrtec (10)
Allergien: Most antibiotics except cephalosporins
Vorherige Impfungen: -

VAERS 1981621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fd0809

moderat

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 26.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

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

Feeling hot Pain in extremity Palpitations

Symptomtext

Arm hurts really bad, woke up heart racing and really warm in the middle of the night about 10 hours after shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control oral yaz brand taken daily
Allergien: None
Vorherige Impfungen: -

VAERS 1979393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: GA
Alter: 52,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 24.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Hypertension Vaccine positive rechallenge

Symptomtext

Patient had extreme high blood pressure, up to 160/108. also had high bp with second dose, pt sat still until felt okay, on blood pressure meds, told to take regular bp med and contact pcp

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: High blood pressure
Vorgeschichte: High blood pressure
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Pfizer- high blood pressure

VAERS 1974306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WA
Alter: 56,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Angina pectoris Axillary mass Axillary pain Breast mass Chest pain Dyspnoea Headache Immunisation Lethargy Neoplasm Pain assessment Product use issue SARS-CoV-2 test

Symptomtext

Swollen lumps; Left armpit and left breast had engorged lumps; Left armpit and left breast had engorged lumps; Headache; lethargy; shooting pain started deep inside chest - felt like it originated from the heart & radiated outward toward armpit; shooting pain started deep inside chest - felt like it originated from the heart & radiated outward toward armpit; shooting pain started deep inside chest - felt like it originated from the heart & radiated outward toward armpit; Difficult to breathe when shooting pain occurred; bnt162b2 (BNT162B2), administration date 26Nov2021 16:00; influenza vaccine (INFLUENZA), administration date 26Nov2021; Booster; 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 (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 26Nov2021 16:00 (Lot number: FD0809) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA), administered in arm right, administration date 26Nov2021 (Batch/Lot number: unknown) as dose number unknown, single for immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "known allergis: Yes" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0153, Location of injection: Arm Right, Vaccine Administration Time: 04:00 PM), administration date: 09Apr2021, when the patient was 56 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER2613, Location of injection: Arm Left, Vaccine Administration Time: 04:00 PM), administration date: 18Mar2021, when the patient was 56 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 26Nov2021 16:00, outcome "unknown", described as "Booster"; ANGINA PECTORIS (medically significant), CHEST PAIN (medically significant), AXILLARY PAIN (medically significant) all with onset 27Nov2021, outcome "recovered" and all described as "shooting pain started deep inside chest - felt like it originated from the heart & radiated outward toward armpit"; DYSPNOEA (non-serious) with onset 27Nov2021, outcome "recovered", described as "Difficult to breathe when shooting pain occurred"; AXILLARY MASS (non-serious), BREAST MASS (non-serious) all with onset 27Nov2021 19:00, outcome "recovered" and all described as "Left armpit and left breast had engorged lumps"; NEOPLASM (non-serious), outcome "recovered", described as "Swollen lumps"; HEADACHE (non-serious) with onset 27Nov2021, outcome "recovered" (28Nov2021), described as "Headache"; LETHARGY (non-serious) with onset 27Nov2021, outcome "recovered" (28Nov2021), described as "lethargy"; PRODUCT USE ISSUE (non-serious) with onset 26Nov2021 16:00, outcome "unknown", described as "bnt162b2 (BNT162B2), administration date 26Nov2021 16:00; influenza vaccine (INFLUENZA), administration date 26Nov2021". The patient underwent the following laboratory tests and procedures: pain assessment: (27Nov2021) 7/10, notes: Shooting pain intensity 7/10 (10 being most painful); sars-cov-2 test: (26Nov2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of angina pectoris, chest pain, axillary pain, dyspnoea, axillary mass, breast mass, neoplasm, headache, lethargy. Shooting pain intensity 7/10 (10 being most painful). Shooting pain started Saturday around 8-9 pm. Swollen lumps (lympth nodes) subsided between 01Dec2021 and 02Dec2021. AE treatment includes took 2x 500mg acetaminophen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211127; Test Name: Shooting pain; Result Unstructured Data: Test Result:7/10; Comments: Shooting pain intensity 7/10 (10 being most painful); Test Date: 20211126; Test Name: PCA; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 29.11.2021
Beginn: 06.12.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / LA

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

Hypoaesthesia Injected limb mobility decreased Injection site pain Pain Pain in extremity Paraesthesia X-ray

Symptomtext

When I received the shot it was very painful and I made a comment to the pharmacist that it hurt really bad. Exactly 1 week later (12/6/21) I woke up and had numbness and tingling in my left forearm, top and outside of hand, and pinky and ring finger. It was not painful but worrisome that I could not feel. I went to the doctor and they said they though it could be due to how the shot was administered. On 12/6 I was working and felt sharp and intense radiating pain in my left top hand. That weekend the sharp pain moved to my forearm, but was no longer in my hand. On 12/21 I woke up at 3 am to intense and sharp pain in my upper arm and shoulder pain. I could not lift my arm. I took Advil and this did not help much. The only position I could get comfortable in was childs pose. I called my doctor and they sent me for x-rays which showed nothing wrong (as I knew it would because I did not injure my arm). On 12/22 I again woke up and had intense sharp pain in my shoulder blade at 3 am and could not move my arm. OTC pain meds do not touch the intense sharp pain. During the day the pain is still there but subsides so I can at least use my arm and hands. Meanwhile, I still have numbness and tightness in my left 2 outer fingers and wrist as well as tingling but it is not as intense as it was initially when this began.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: 12/21 - Was sent to get x-rays and they came back normal. Was on my left arm (Shoulder, upper arm, and lower arm and hand).
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Macrobid
Vorherige Impfungen: -

VAERS 1963645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OR
Alter: 15,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 12.11.2021
Beginn: 06.12.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: IM / LA

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

Antibody test negative Blood albumin decreased Blood fibrinogen increased Brain natriuretic peptide increased C-reactive protein increased Campylobacter test Dehydration Diarrhoea Electrocardiogram QT prolonged Electrolyte imbalance Escherichia test negative Fatigue Fibrin D dimer increased Haemoglobin decreased Headache Hyponatraemia International normalised ratio increased Leukopenia

Symptomtext

Presumed MIS-C. beginning 24d after 2nd vaccine: severe headache, fatigue, then 2d later fever, then 2d later N/V/D, very high fevers 105F. Presented d8: elevated procal, CRP, nl ESR/ferritin, elevated troponin, BNP, neutrophilia, leukopenia, thrombocytopenia, hyponatremia. no rash, but ++diarrhea, some nausea, stool NAAT negative for Salmonella, Shigella, Ecoli, Campy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: PCT 40, BNP 248, Trop 139, ESR 43, CRP 21.8 Neg nucleocapsid AB, but spike AB pos after vaccination neg COVID test and no history of COVID diarrhea, dehydration, electrolyte imbalance, prolonged QTc Ferritin 135, Alb 2.5, LFTs normal D-dimer 2.5 peak, INR 1.2, fibrinogen 495 WBC 10.2 0-10%bands, 87% N, ALC 1000-- >400; platelets 77-- >143, Hgb 10.8
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: topical acyclovir tylenol (paracetamol) 1000mg PO TID ondansetron 8mg PRN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1942156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: IL
Alter: 5,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect dose administered Lethargy Mobility decreased Pyrexia

Symptomtext

I was called and informed that my daughter received the adult dose of the second COVID 19 vaccine. She experienced fever up to 102-103 F, was lethargic, could not move her left arm (where it was administered for 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1962442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: ID
Alter: 62,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 25.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Blood test normal Dyspnoea Electrocardiogram normal Fatigue Headache Irritable bowel syndrome Lymphadenopathy Musculoskeletal chest pain Neck pain Palpitations Pyrexia Tachycardia Vertigo

Symptomtext

The day after my 3 shoot I had fatigue, headache, fever, severe joint pain, shortness of breath, tachycardia, swollen lymph nodes in my neck, pain in my right rib cage, neck pain, bouts of vertigo, and IBS. These systems have lasted six weeks. I have been to the E.R. 3 times for shortness of breath and tachycardia and severe joint pain and I was send home to rest. I went to my primary care doctor and his said lets just wait and see if the systems go away. I can not walk the grocery store without being short of breath. I exert my self at all and I feel my heart pounding in my chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG was good. I did not have any marker for a blood clot. All blood work was good.
Aktuelle Erkrankungen: c-diff
Vorgeschichte: obesity, high blood pressure,
Andere Medikamente: Armour 1.5 gr 1 daily, prozac 5 mg daily, valium 8 mg daily, quetiapine 25 mg daily, amlodipine besylate 10 mg, losartan 100mg daily, Multivitamin 1 daily, align probiotic 1 daily, actaminophen 650 daily.
Allergien: Penicillin, keflex, z-pack, iodine, sulfur drugs, methylparaben. walnuts, strawberries, carrots, green beans, shell fish, herbs and spices
Vorherige Impfungen: -

VAERS 1961947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WI
Alter: 18,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 11.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Echocardiogram normal Electrocardiogram Magnetic resonance imaging head normal Muscle contractions involuntary Palpitations Paraesthesia

Symptomtext

One week after the second dose of Covid 19 Pfizer vaccination. presented palpitations, tingling and fasciculations of the four extremities. Cardiologist did an echocardiogram and results were normal. On December 4th 2021 the symptoms persisted and were more frequent. Neurologist Dr. ordered a Brain MRI and the results were normal. Today 18 th December finally the symptoms are starting to fade.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: ECG Echocardiogram Brain MRI
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1961947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WI
Alter: 18,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 11.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / -

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

Echocardiogram normal Electrocardiogram Magnetic resonance imaging head normal Muscle contractions involuntary Palpitations Paraesthesia

Symptomtext

One week after the second dose of Covid 19 Pfizer vaccination. presented palpitations, tingling and fasciculations of the four extremities. Cardiologist did an echocardiogram and results were normal. On December 4th 2021 the symptoms persisted and were more frequent. Neurologist Dr. ordered a Brain MRI and the results were normal. Today 18 th December finally the symptoms are starting to fade.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: ECG Echocardiogram Brain MRI
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1959282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 74,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 10.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Positive airway pressure therapy

Symptomtext

CHIEF COMPLAINT: pt brought to ER by EMS for sob that started 3 weeks ago. started getting worse today neg wheezing noted pt on cpap by EMS pt switched to hospital cpap. medicated with solumedrol. HISTORY OF PRESENT ILLNESS: Patient brought into the ER by EMS for shortness of breath that started 3 weeks ago. It seems to be getting worse. Patient was put on CPAP by EMS. Patient was not given Solu-Medrol in the ambulance. Patient states that he just feels like he cannot catch his own breath. He has been on CPAP before. He denies any expressed history of heart failure. Does have a history of pulmonary hypertension and bad COPD. He denies any fever chills. No cough cold or congestion is vaccinated against Covid. No leg pain or swelling history of blood clots. No other complaints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Acute respiratory failure with hypoxia, COPD type B, Diabetes mellitus, Hypertension, Stroke, Pacemaker.
Andere Medikamente: Unknown
Allergien: N/A
Vorherige Impfungen: -

VAERS 1958056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 32,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 10.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Back pain Cardiac discomfort Headache Muscle tightness Nasal congestion Paraesthesia Skin burning sensation

Symptomtext

pain and soreness in back behind heart and in left shoulder; pain and soreness in back behind heart and in left shoulder; pricking and burning all over body; pricking and burning all over body; congestion; tightness in neck; feeling like heart is being squeezed from back; headache; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 32 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Dec2021 12:30 (Lot number: FD0809) at the age of 32 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: VITAMIN D [COLECALCIFEROL]; B12 [CYANOCOBALAMIN]. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: 3203080, Location of injection: Arm Left, Vaccine Administration Time: 07:00 PM), administration date: 04Nov2021, when the patient was 32 years old, for COVID-19 Immunization, reaction(s): "Diagnosed with Covid after first dose", "Diagnosed with Covid after first dose", "numbness in face", "pricking sensation all over body including face", "headache", "chest discomfort", "feeling like heart is being squeezed". The following information was reported: ARTHRALGIA (non-serious), BACK PAIN (non-serious) all with onset 11Dec2021 08:00, outcome "not recovered" and all described as "pain and soreness in back behind heart and in left shoulder"; PARAESTHESIA (non-serious), SKIN BURNING SENSATION (non-serious) all with onset 11Dec2021 08:00, outcome "not recovered" and all described as "pricking and burning all over body"; NASAL CONGESTION (non-serious) with onset 11Dec2021 08:00, outcome "not recovered", described as "congestion"; MUSCLE TIGHTNESS (non-serious) with onset 11Dec2021 08:00, outcome "not recovered", described as "tightness in neck"; CARDIAC DISCOMFORT (non-serious) with onset 11Dec2021 08:00, outcome "not recovered", described as "feeling like heart is being squeezed from back"; HEADACHE (non-serious) with onset 11Dec2021 08:00, outcome "not recovered", described as "headache". Therapeutic measures were not taken as a result of arthralgia, back pain, paraesthesia, skin burning sensation, nasal congestion, muscle tightness, cardiac discomfort, headache. Additional information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, patient did not test for COVID-19. Second dose- pricking and burning all over body, feeling like heart is being squeezed from back (has happened once so far after second dose on 10Dec), pain and soreness in back behind heart and in left shoulder, congestion, headache, tightness in neck. Patient did not received treatment for events. Device Date: 11Dec2021 No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: VITAMIN D [COLECALCIFEROL]; B12 [CYANOCOBALAMIN]
Allergien: -
Vorherige Impfungen: -

VAERS 1954699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: VA
Alter: 36,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 05.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Blood pressure increased Disturbance in attention Dizziness Dyspnoea Electrocardiogram normal Heart rate increased Impaired work ability Malaise Troponin normal

Symptomtext

My normal heart rate is 60. After my booster shot, my heart rate is at least 80 when I sit. When I stand up and walk slowly, the heart rate will go to 120. My regular blood pressure is 120/80. Now my blood pressure is 150/90 all the time. I also feel short of breath and dizzy. It is very hard to focus and cannot go to work. I went to the urgent care (12/7) and cardiology (12/9) last week. They checked the ECG and troponin level. They looked normal. The doctors said it may be just the response from the vaccine and it will go away eventually. But after a week, I have the same symptoms and I am not feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ECG and troponin level were normal at 12/9.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1954302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: LA
Alter: 52,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 29.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chest pain Chills Decreased appetite Dyspnoea Headache Illness Pain in extremity Pyrexia Sleep disorder

Symptomtext

Headache; Got extremely ill; His arm hurt for days; Shortness of breath; He had chills; Fever; Was sleeping like a vampire / didn't wake up until 07:00PM to 08:00PM at night; No appetite; Felt chest pains; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52 year-old male patient received bnt162b2 (BNT162B2), administered in arm, administration date 29Oct2021 03:00 (Lot number: FD0809) at the age of 52 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN IN EXTREMITY (hospitalization) with onset Oct2021, outcome "unknown", described as "His arm hurt for days"; DYSPNOEA (hospitalization) with onset Oct2021, outcome "unknown", described as "Shortness of breath"; CHILLS (hospitalization) with onset Oct2021, outcome "unknown", described as "He had chills"; PYREXIA (hospitalization) with onset Oct2021, outcome "unknown", described as "Fever"; SLEEP DISORDER (hospitalization) with onset Oct2021, outcome "unknown", described as "Was sleeping like a vampire / didn't wake up until 07:00PM to 08:00PM at night"; DECREASED APPETITE (hospitalization) with onset Oct2021, outcome "unknown", described as "No appetite"; CHEST PAIN (hospitalization) with onset Oct2021, outcome "unknown", described as "Felt chest pains"; HEADACHE (hospitalization) with onset 30Oct2021 03:00, outcome "unknown", described as "Headache"; ILLNESS (hospitalization) with onset Oct2021, outcome "unknown", described as "Got extremely ill". The patient was hospitalized for pain in extremity (start date: 31Oct2021). Therapeutic measures were taken as a result of pain in extremity, sleep disorder, headache. Clinical course: Patient says his arm hurt for days after the shot and for treatment he put ice on it. He says he was put into the hospital 31Oct2021 as a result of that injection and went home a couple hours later. He says the hospital gave him meds for the headache he had had for four days. He says at first he tried to take Motrin for the headache but that didn't do nothing, and the hospital gave him something then told him to take Tylenol from now on, which he took over the counter extra strength for the dose. he was in perfect health before he got the vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1952844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 36,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Dyspnoea Fear Flushing Immediate post-injection reaction Tachycardia Tremor

Symptomtext

Almost immediately after injection, the patient stated she was dizzy. I had her sit down. She turned a bright shade of red, said she felt faint, tachycardic, short of breath, and was shaking. She was frightened. We called EMS and they came to the pharmacy. She did not leave with them and elected to drive herself home. The episode passed after about 10 to 12 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none reported
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: doxycycline, minocycline
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1952132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 18.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Cardiac failure congestive Chest pain Condition aggravated Dyspnoea Hypertension Hypoxia Pneumonia Sepsis Tachycardia Unresponsive to stimuli

Symptomtext

Patient sent to ER on 10/27 r/t SOB and CP, admitted 10/27-11/2 with Dx: Sepsis, hypoxia, pneumonia. Sent back to ER for CP, SOB, and tachycardia and hospitalized 11/3-11/15 r/t pneumonia, hypoxia, CHF, A-Fib. ER visit on 11/19/21 r/t unresponsiveness. Sent to ER for hypertension and SOB and Hospitalized 11/21-12/2. Sent to ER for SOB and CP and hospitalized 12/7- present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 30,0
Labordaten: -
Aktuelle Erkrankungen: Cellulitis
Vorgeschichte: Asperger's syndrome, Type 2 DM, Acute Kidney Failure, Seizures, Chronic Ischemic Heart Disease, CVA, Hypertension, Acute Respiratory Failure
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1951808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: GA
Alter: 21,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia Throat irritation

Symptomtext

After speaking to patient about reactions to allergies listed, it was advised that patient wait in Covid-19 seating area, after about 15 minutes patient informed pharmacist of tingling along the jaw line, had patient wait a little longer she then reported having a scratchy throat-no swelling and no trouble breathing. She said she has a scratchy throat with peanut allergy in the past and nothing else(no use of EpiPen ever needed). Pharmacist gave one dose of 50mg Benadryl and patient continued to wait (total wait for observation 1 hr) no additional reaction or intervention required

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: PEANUTS, CORN, RICE, WHEAT, DAIRY, SHRIMP
Vorherige Impfungen: -

VAERS 1947118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 57,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Cardiomyopathy Chest pain Dyspepsia Immunisation Laboratory test Muscle spasms

Symptomtext

weird pain in the middle of her chest; feels like heartburn; Third Dose: muscle spams in the heart; Third Dose: Back muscle spasms; Pfizer covid vaccine the third dose, the booster dose; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57 year-old female patient received bnt162b2 (BNT162B2), administered in arm left (upper left arm), administration date 19Nov2021 14:30 (Lot number: FD0809) at the age of 57 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "food intolerances like gluten" (unspecified if ongoing); "food intolerances like dairy" (unspecified if ongoing); "food intolerances like corn" (unspecified if ongoing). Family history included: "genetic blood clotting: thrombophilia" (unspecified if ongoing), notes: genetic blood clotting, the caller only has one of 2 genes. There were no concomitant medications. Vaccination history included: Bnt162b2 (First Dose: lot ER2613, NDC and expiration date unknown.), administration date: 18Mar2021, when the patient was 56 years old, for COVID-19 Immunization, reaction(s): "sore arm" and "lightheaded"; Bnt162b2 (Second Dose: lot ER8737, NDC and expiration date unknown.), administration date: 08Apr2021, when the patient was 56 years old, for COVID-19 Immunization, reaction(s): "sore arm" and "lightheaded", reported as the only thing that happened after the first two doses of the Pfizer covid vaccine is that the caller got lightheaded like she got unplugged and plugged back in. This happened 3 days after getting the vaccines and that was the only thing that happened other than the sore arm. The following information was reported: IMMUNISATION (medically significant) with onset 19Nov2021, outcome "unknown", described as "Pfizer covid vaccine the third dose, the booster dose"; CARDIOMYOPATHY (medically significant) with onset 29Nov2021 07:50, outcome "recovering", described as "Third Dose: muscle spams in the heart"; MUSCLE SPASMS (medically significant) with onset 21Nov2021, outcome "not recovered", described as "Third Dose: Back muscle spasms"; CHEST PAIN (non-serious), outcome "unknown", described as "weird pain in the middle of her chest"; DYSPEPSIA (non-serious), outcome "unknown", described as "feels like heartburn". The events "third dose: muscle spams in the heart" and "third dose: back muscle spasms" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: laboratory test: unknown result, notes: They did a lot of tests on the caller today and didn't find anything of concern. Therapeutic measures were taken as a result of cardiomyopathy, muscle spasms. Clinical courses: The caller just got back for the emergency room because she had muscle spams in the heart, it was gripping. The caller has been dealing with back spasms all last week and chocked it up to throwing out her back. The back muscle spasms go up her back and along her spine. They did all sorts of tests at the hospital. It seemed really strange that this happened because she is otherwise healthy. The doctors didn't see any abnormal heart activity and the caller has 3 baby aspirins just in case. The caller doesn't know if the back and heart muscle spasms are related. On 19Nov2021 the caller got her third dose and its strange that something like this would happen 10 days later and it may not be related to the vaccine. The caller has been standing because when she sits on a hard surface that's when the spasms go up her back, its really painful its worse than childbirth. The caller's heart muscle spasms happened at 7:50 this morning, it happened every minute for approximately 15 minutes and had someone drive her to the hospital. The caller was never admitted as a patient but was seen in the emergency room. The caller still feels some weird pain in the middle of her chest and it feels like heartburn even though she didn't eat anything spicy.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101686201 similar report from same reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: Test; Result Unstructured Data: Test Result:unknown result; Comments: They did a lot of tests on the caller today and didn't find anything of concern.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Dairy intolerance; Food intolerance; Gluten intolerance; Thrombophilia (genetic blood clotting, the caller only has one of 2 genes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1947091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Immunisation Mobility decreased Pain in extremity

Symptomtext

difficulty lifting her arm; sore arm; Stated that she received the booster at 4pm on 19 Nov; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 27 year-old female patient received bnt162b2 (BNT162B2), administered in arm, administration date 19Nov2021 16:00 (Lot number: FD0809, Expiration Date: 22Jan2022) at the age of 27 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (First dose, Lot: EP6955 , Expiration date: 30Jun2021, Route: Intramuscular), administration date: 20Mar2021, when the patient was 26 years old, for Covid-19 immunization; Bnt162b2 (Second dose, Lot: EP6955 , Expiration date: 30Jun2021, Route: Intramuscular), administration date: 10Apr2021, when the patient was 26 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021 16:00, outcome "unknown", described as "Stated that she received the booster at 4pm on 19 Nov"; MOBILITY DECREASED (non-serious) with onset 20Nov2021, outcome "recovering", described as "difficulty lifting her arm"; PAIN IN EXTREMITY (non-serious) with onset 19Nov2021 21:00, outcome "recovering", described as "sore arm". Therapeutic measures were taken as a result of mobility decreased, pain in extremity. Additional information: There was no patient history. It was reported that the patient could lift her arm more easily last night and that she took Tylenol on 19Nov2021 and she iced her arm on Saturday. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1944078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 02.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Computerised tomogram Inappropriate schedule of product administration Migraine

Symptomtext

Patient also received flu shot but was not given information on the lot #, brand, etc. On December 6, at 2:30pm patient started experiencing symptoms of migraine (onset within 30 minutes). This is patient's first migraine. Patient was seen at the ER on December 8 and administered sodium chloride, dexamethasone PF, diphenhydramine, ketorolac, metoclopramide, and olanzapine. Pain was reduced some but not resolved and client was discharged. Patient saw PCP on 12/10 and was given Fioricet and Zofran, which was taken from 12/10 until 12/13 but did not resolve the migraine. On 12/13 patient was given Imitrex, Verapamil and Fioricet; treatment results are pending. Patient does not have a history of migraines or significant headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: a CT scan was given on 12/9 in the ER but was unremarkable
Aktuelle Erkrankungen: low back/gluteal pain from sports injury (musculoskeletal in nature)
Vorgeschichte: NA
Andere Medikamente: flu shot received at the same time, Vitamin D3, women's multivitamin and cod liver oil supplement also taken regularly by patient
Allergien: NA
Vorherige Impfungen: -

VAERS 1941854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: IN
Alter: 77,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 25.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Amnesia Blood test Chest X-ray Culture urine Decreased appetite Dyspnoea Electrocardiogram Feeling jittery Immunisation Investigation Irritability Nervousness Psychomotor hyperactivity SARS-CoV-2 test Tremor Urinary tract infection Ventilation/perfusion scan Weight decreased

Symptomtext

Urinary tract infection; Booster; Lost appetite; Nervous; Memory not as good; I'm grasping for breath; Trembling; Grumpy; Fidgety; Jittery; Lost 10-15 pounds; 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 77 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 25Oct2021 (Lot number: FD0809) at the age of 77 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "lymphedema" (unspecified if ongoing), notes: The therapy is lymphedema for lymphedema from breast cancer.; "blood clots", start date: 2009 (unspecified if ongoing); "diagnosed allergies" (unspecified if ongoing); "compromised immune status" (unspecified if ongoing); "respiratory illness" (unspecified if ongoing); "genetic/chromosomal abnormalities" (unspecified if ongoing); "endocrine abnormalities" (unspecified if ongoing); "diabetes" (unspecified if ongoing); "obesity" (unspecified if ongoing). Concomitant medication(s) included: ELIQUIS taken for haemorrhage urinary tract, start date: 2009 (ongoing); LOSARTAN taken for hypertension, start date: 2015; CARVEDILOL taken for hypertension, start date: 2015; SERTRALINE taken for restlessness, start date: 2015. Vaccination history included: Bnt162b2 (Dose: 1, Lot: ZTC2948, Expiration: Unknown. , Anatomical Location: left arm), administration date: 16Mar2021, when the patient was 77 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2, Lot: ZTL5384026 , Expiration: Unknown. , Anatomical Location: left arm), administration date: 13Apr2021, when the patient was 77 years old, for COVID-19 immunization; Flu shot (She had a flu shot 2 weeks before the last dose.), administration date: 2021. The following information was reported: IMMUNISATION (non-serious) with onset 25Oct2021, outcome "unknown", described as "Booster"; DECREASED APPETITE (non-serious) with onset Oct2021, outcome "not recovered", described as "Lost appetite"; NERVOUSNESS (non-serious) with onset Oct2021, outcome "not recovered", described as "Nervous"; AMNESIA (non-serious) with onset Oct2021, outcome "not recovered", described as "Memory not as good"; DYSPNOEA (non-serious) with onset Oct2021, outcome "not recovered", described as "I'm grasping for breath"; TREMOR (non-serious) with onset Oct2021, outcome "unknown", described as "Trembling"; IRRITABILITY (non-serious) with onset Oct2021, outcome "unknown", described as "Grumpy"; PSYCHOMOTOR HYPERACTIVITY (non-serious) with onset Oct2021, outcome "unknown", described as "Fidgety"; FEELING JITTERY (non-serious) with onset Oct2021, outcome "unknown", described as "Jittery"; WEIGHT DECREASED (non-serious) with onset Oct2021, outcome "not recovered", described as "Lost 10-15 pounds"; URINARY TRACT INFECTION (non-serious) with onset 12Nov2021, outcome "unknown", described as "Urinary tract infection". The event "i'm grasping for breath" was evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Follow-up (18Nov2021): This is a follow-up spontaneous report received from a contactable consumer. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown result; Test Date: 202111; Test Name: chest X-ray; Result Unstructured Data: Test Result:All were normal; Test Date: 202111; Test Name: urine culture; Result Unstructured Data: Test Result:All were normal; Test Date: 202111; Test Name: EKG; Result Unstructured Data: Test Result:All were normal; Test Date: 202111; Test Name: Some other kind of machine that she cannot remember; Result Unstructured Data: Test Result:Unknown result; Test Date: 202111; Test Name: COVID test; Result Unstructured Data: Test Result:Unknown result; Test Date: 202111; Test Name: Lung scan; Result Unstructured Data: Test Result:All were normal; Test Date: 202111; Test Name: Lost 10-15 lbs; Result Unstructured Data: Test Result:Lost 10-15 lbs
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Chromosomal abnormality NOS; Clot blood; Diabetes; Endocrine disorder; Immune system disorder; Lymphedema (The therapy is lymphedema for lymphedema from breast cancer.); Obesity; Respiratory disorder
Andere Medikamente: ELIQUIS; LOSARTAN; CARVEDILOL; SERTRALINE
Allergien: -
Vorherige Impfungen: -

VAERS 1940489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 8,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Headache Incorrect dose administered Skin warm

Symptomtext

8 year old patient was administered a covid 19 vaccine for patients 12 years and older. Patients mother was contacted by the provider and support staff the day this was discovered. Patients mother reports patient has experienced headache and felt warm. Mother denies fever. Patients mother has office contact info in the case of any worsening symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: For at least 1 month prior to vaccine date patient has been experiencing stomach aches and headaches.
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1937037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Mobility decreased Pain Pain in extremity Product administered at inappropriate site

Symptomtext

Severe arm pain. Unable to lift arms up resulting in severe pain. Patient touched her skin and there was no pain. Muscles felt good. No pain. The pain localized to shoulders and the lifting mechanism that caused pain. When she twisted her wrist it caused pain too. Patient concerned the pain is because the shot was given too high in the arms (compared to the first two doses she received previously). Arm soreness after the first 2 doses but not like this pain. Patient instructed to see a doctor to diagnose if the pain is due to the shot being too high in the arm causing injury, or if it is due to the COVID-19 vaccination, which normally causes arm pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 1936750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 85,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 24.11.2021
Beginn: 08.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Hyponatraemia Hypotension Unresponsive to stimuli

Symptomtext

Patient had an episode of 1 minute unreponsiveness days after receiving COVID vaccine. Was hospitalized and admitted. More than likey due to hyponatremia which led to hypotension.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 2,0
Labordaten: n/a
Aktuelle Erkrankungen: Failure to THrive Cachexia
Vorgeschichte: afib dementia
Andere Medikamente: There is a black box warning associated with this order. Please click to view details. There is a potential drug interaction with another medication. Please click to view details. Eliquis Tablet 2.5 MG (Apixaban) Give 1 tablet by mouth two
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1929095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Dizziness Palpitations Peripheral coldness

Symptomtext

Patient received the first dose of pfizer COVID 19 vaccine in pharmacy at 12PM. After given first dose of pfizer vaccine, pt was waiting for 15 minutes as precaution. Patient felt heart palpitation after 10 minutes of receiving vaccine. She was given water and sat on the chair for few minutes. She developed dizziness on top of palpitation. When pharmacist measured the blood pressure, her first blood pressure measured at 12:15 PM was 192/99 with hear rate of 86. According to patient, she never had high blood pressure before. We offered patient to call ambulance but patient refused to call ambulance. At 12: 18, second blood pressure was measured with result of 182/88 with heart rate of 76. At a time, she experienced cold extremities. Manager called an ambulance after pharmacist measured second blood pressure. While waiting for paramedics, third blood pressure was measured with 153/97 with heart rate of 94 at 12:30. At 12:35, patient left pharmacy with paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: No other illness at the time and up to one moth prior to vaccination
Vorgeschichte: Asthma
Andere Medikamente: No medication listed
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1921445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: VA
Alter: 24,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Hypoaesthesia Palpitations Paraesthesia

Symptomtext

3 minutes after receiving first dose of Pfizer vaccine, patient complaints of numbness and tingling all over his body, shortness of breath, racing heart and he asked multiple times that we call Emergency which we did. on evaluation, patient was in no distress, was calm,. BP was checked and initially was 180/103 and repeated reading was 170/92; heart rate was 92 initially then 103. Denied history of hypertension but admitted to history of anxiety, Paramedics arrived and patient walked and sat in the truck but was later release when he felt better then he left with his wife.

Weitere VAERSDATA-Felder

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

VAERS 1920866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WV
Alter: 48,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 29.10.2021
Beginn: 07.11.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac discomfort Cardiac flutter Cardiac monitoring Cardiac stress test Chest discomfort Chest pain Computerised tomogram Dyspnoea Echocardiogram Electrocardiogram Electrocardiogram ambulatory Fatigue Fibrin D dimer Myocardial necrosis marker Neck pain Pain Pain in extremity Pain in jaw

Symptomtext

About 6-7 days after the second vaccine I began having palpitations, fluttering, pounding heart, increased SOB, chest tightness, severe fatigue, arm/leg tingling that seemed to increase in intensity and frequency over about 2-3 weeks, then chest pain that felt like I was having a heart attach on Thanksgiving Day (severe SOB, chest pain into my left jaw/neck/arm) and went to the ED. Symptoms remain but less frequent and intense.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Cardiology appointment, 2D Echo, EKG, Stress Test, Holter Monitor, Coronary CT, PFT, Pulmonary Appointment, Covid Testing, ED visit, D-dimer testing, cardiac enzymes, monitoring.
Aktuelle Erkrankungen: Had Covid August 2021
Vorgeschichte: History of Ovarian Cancer
Andere Medikamente: Pepcid, multivitamin, citracal
Allergien: Bactrim-severe reaction
Vorherige Impfungen: -

VAERS 1910036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 53,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 08.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / RA

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

Cold-stimulus headache Feeling abnormal Headache Paraesthesia Pyrexia Sensitive skin Sluggishness

Symptomtext

I had the normal side effects of sluggish/ slight fever on Tuesday and was feeling better Wednesday morning. At this point I noticed areas of my skin to feel very tingly and sensitive. I also started getting a worse headache that felt like a brain freeze. It felt a lot like the one time I had shingles years ago. I have been vaccinated for shingles but this felt super similar and mainly on left side of body along foot, left side of genitalia, left torso under arm, and left side of neck and scalp. It wasn't super severe but it went on for several days and the headache lingered as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: I did not seek medical help. Just self-monitored.
Aktuelle Erkrankungen: None known
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergies known only to lobster, crab, shrimp foods
Vorherige Impfungen: Well, what is "adverse"? I occasionally have stronger reactions to the flu vaccine and did not enjoy the shingles vaccine at all

VAERS 1895560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: VA
Alter: 52,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Paraesthesia Paraesthesia oral

Symptomtext

Tingling in tongue, lips, hands

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism GERD IBS Fibromyalgia DJD/DDD/Osteoarthritis Frequent urination Cystitis Hematuria Iatrogenic Liver Disease
Andere Medikamente: Synthroid Omeprazole Vitamin D3 Iron Cetirizine Diclofenac Tylenol
Allergien: -
Vorherige Impfungen: Severe flu with hospitalization

VAERS 1889764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: IL
Alter: 45,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 01.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: IM / RA

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

Fatigue Heavy menstrual bleeding Hot flush Hyperhidrosis Impaired work ability Menstruation delayed Neck pain Paraesthesia Paraesthesia oral Urticaria

Symptomtext

Hives on chest ,severe neck pain for weeks ,1st dose notified doctor Claritin, pepcid recommended for 2nd dose ,symptoms lasted 2 weeks missed work due to side effects sweats hot flashes parasethsta around mouth fingers period late then severe clotts when it came ,fatigue severe neck pain to side of injection on going

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None just notified primary MD
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: None
Allergien: Doxycycline ,pcn,,flu vaccine
Vorherige Impfungen: Flu vaccine in late 90's

VAERS 1877072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AK
Alter: 51,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 27.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Erythema Hypoaesthesia Injection site pain Pain in extremity Paraesthesia Peripheral swelling Sensory disturbance Sleep disorder

Symptomtext

With my second shot my arm got very red painful and swollen, That lasted about 10 days and since then I've had tingling in my left arm along with pain and some swelling. So much so that I mostly sleep on the couch due to being woken up from the pain and burning feeling in my upper arm around the injection site, All that has caused me to have numbness and tingling in several of my fingers as well as what feels like fluid rushing through that area as well. At first I thought maybe it was a pinched nerve but its been happening pretty much since my second shot so I'm leaning more towards a side effect from the vaccine. Before I go to the doctor to spend thousands of dollars on tests I may not need I was hoping there might be a cheaper way to go... Like maybe this is common and I just haven't heard about this side effect. But I also don't want to be having a reaction that cold impact my health or possibly kill me. I would love to know if this is something that will go away or if I need to fly to get treatment since our medical here is less than desirable. And if I do need to be seen... Who's paying for this?

Weitere VAERSDATA-Felder

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

VAERS 1876730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NM
Alter: 41,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Chills Dizziness Fatigue Feeling hot Flushing Head discomfort Headache Hypertension Inflammation Joint range of motion decreased Menstruation irregular Myalgia Pain Pain in extremity Polymenorrhoea

Symptomtext

Instant wave from head to toe of dizziness. Headache began within a few minutes of injection as a dull but constant headache with pressure of entire head. Headache worsened off and on the next 3-4 days but the pressure headache has always remained constant. OTC did not work. High blood pressure started with the headache following initial injection. Blood pressure has been high since 11/3/2021. Arm soreness for about a week, very painful and difficult to raise above shoulder but only limited to right bicep. Dizziness and fatigue was very strong for first 2 weeks, both continue now. Major fatigue, chills, body/muscle/joint aches continue. Chills continue along with feeling hot and flushed (fever-like but not high temperature). Menstrual cycle changes: cycle began 11/3/21, and one week after cycle, on 11/15/21 I get another cycle (on 3rd day now). This began one month prior, when my husband received his first dose of Covid-19 mandated vaccine21 days +/- previous to my first dose. Menstrual cycle changes have changed the last two months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Doctor monitoring blood pressure, headaches are likely from inflammation and high blood pressure as a result of first dose of Covid-19 mandated vaccine. I am monitoring at home and it fluctuates at rest from 120s to above 140s. Doctor visit 11/16/21: blood pressure was 165/98. Doctor visit 11/5/2021: blood pressure was 140/90. Blood work to try to find reason for inflammation.
Aktuelle Erkrankungen: Positive ANA (antinuclear antibody): Diagnosed with Fibromyalgia August 2021; in the process of obtaining second opinion since my primary doctor and I do not concur with the Rheumatologist. No chronic pain, only limited to wrists/hands.
Vorgeschichte: Bilateral carpal tunnel syndrome. Primary concern and hesitance to get Covid-19 mandated vaccine was due to worsening of inflammation, which as predicted has now occurred since the moment the shot was administered 11/3/21 at 10am.
Andere Medikamente: Spiranolactone 100mg (50mg AM/50mg PM) for acne.
Allergien: Penicillins, Sulfas
Vorherige Impfungen: -

VAERS 1874651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Echocardiogram Electrocardiogram

Symptomtext

While I had some stronger initial symptoms following the first 36 hours of the 3rd dose of vaccine, I had very noticeable shortness of breath for days afterward, to which I connected the timing of the symptom with the vaccine. I asked my doctor if it was possible to have had this as a side-effect, and she said yes. I asked her what supplement I could take to help with the symptoms, and she recommended BCQ. Taking BCQ three times a day alleviates the symptoms. If I forget a dose, the shortness of breath returns. I have had a chest xray within the last year, a cardio workup (including EKG and Echo) -- post Pfizer 3, plus regular labs, nothing else shows up as causing this shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG, ECHO 10-21-21.
Aktuelle Erkrankungen: none.
Vorgeschichte: hashimoto's thyroidits
Andere Medikamente: levothyroxine, cytomel, ashwaghanda, brahmi, vit C, vit D, vit E, NAC, CBD.
Allergien: acetaminophen, cisatracurium, bacitracin, neosporin, all pain killers with acetaminophen.
Vorherige Impfungen: -

VAERS 1873257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: VA
Alter: 46,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Dizziness Dyspnoea Fatigue Heart rate increased Hepatic enzyme increased Laboratory test Night sweats Thyroid function test Tremor Herpes zoster Rash

Symptomtext

shingles outbreak rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: bronchitis and sinus infection
Vorgeschichte: fibromyalgia, HTN, chronic pain, migraines, allergies, TBI, PTSD, neuropathy
Andere Medikamente: venlafaxine, HCTZ/lisinopril combo 12.5/10, allegra, topamax, pantaprazole, atarax, oraphedrine, prebiotic
Allergien: latex, iodine, ketamine, hydrocodone, codeine, shellfish, benadryl, penicillin
Vorherige Impfungen: -

VAERS 1872304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AL
Alter: 54,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Back pain Chills Diarrhoea Immunisation Migraine Myalgia Nausea Pyrexia Vaccination site pain

Symptomtext

Site pain; Back pain; Muscle ache; Migraines; Fever; Diarrhea; Nausea; Chills-temporary; The patient received third/booster dose of BNT162b2; This is a spontaneous report from a contactable consumer, the patient. A 54-year-old non-pregnant female patient received third (booster) dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FD0809) via an unspecified route of administration in the right arm on 05Nov2021 at 12:15 (at the age of 54-years-old) as a single dose for COVID-19 immunisation. Medical history included mitral valve prolapse (MVP) and migraines. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Concomitant medications included atenolol (TENORMIN), acetylsalicylic acid (ASPIRIN), paracetamol (TYLENOL), hydrocodone bitartrate, paracetamol (NORCO) and ketorolac tromethamine (SPRIX); all for unknown indication from an unknown date and unknown if ongoing. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6205) via an unspecified route of administration in the right arm on 26Mar2021 at 12:00 (at the age of 53-years-old) and second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8732) via an unspecified route of administration in the right arm on 16Apr2021 at 12:00 (at the age of 53-years-old), as single dose for COVID-19 immunisation. The patient previously took promethazine hydrochloride (PHENERGAN), moxifloxacin hydrochloride (AVELOX) and butorphanol tartrate (STADOL) and experienced drug allergy. On 05Nov2021 at 20:00, the patient experienced site pain, back pain, muscle ache, migraines, fever, diarrhea, nausea and chills-temporary. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event chills-temporary was resolved on an unknown date in Nov2021; while that of events site pain, back pain, muscle ache, migraines, fever, diarrhea, nausea and was resolving at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine (Migraines); Mitral valve prolapse (MVP)
Andere Medikamente: TENORMIN; ASPIRIN [ACETYLSALICYLIC ACID]; TYLENOL; NORCO; SPRIX
Allergien: -
Vorherige Impfungen: -

VAERS 1867842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MA
Alter: 60,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Bed rest Condition aggravated Headache Impaired driving ability Migraine Mobility decreased Nausea Vomiting

Symptomtext

Symptom onset 12 hours after injection. Rapid growing headache to migraine + status Inability to leave bed for next (11/12/2021 1:30 AM - 11/12/2021 5:30 PM except 1 assisted trip to the bathroom) due to intense head pain, weakness and nausea. Attempted 2 Tylenol caplets at 11/12/2021 at 5:45 PM Nausea persisted most of the day resulting in vomiting at 11/12/2021 6:00 PM Headache started to abate around 11/12/2021 7:30 PM Weakness and continued headache pain (though much milder that previous day ) encouraged bedrest until 11/13/2021 at 11:00 AM. Continued weakness until this present time (11/13/2021 3:35 PM) however able to walk safely through my home. I do not feel it would be safe to drive (for myself and others) or be alone at this time due to the weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Sjogren's syndrome Raynaud's syndrome
Andere Medikamente: 11/11/2021 10:00 AM Levothyroxine 11/11/2021 10:30 AM Alendronate Sodium
Allergien: Latex Most nuts Celery (mild) Tomatoes (mild)
Vorherige Impfungen: Shingrix - headaches, age 59 further details unknown

VAERS 1855097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 14,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Blood creatine phosphokinase Blood test Clonus Condition aggravated Feeling abnormal Full blood count Intrusive thoughts Metabolic function test Red blood cell sedimentation rate Rhabdomyolysis Tic Troponin

Symptomtext

Within 24 hours of receiving dose 2 of COVID, patient experienced an enormous upswing in his tics, to the point where some of his muscles were in a clonic state. His developmental neurologist attempted to control these tics with Klonopin, with minimal success. The severity of these tics increased to the point that he experienced rhabdomyolysis. He also had an increase in intrusive thoughts, stating that he was going to die, and that he would be dead by Thanksgiving. He also was stating that he wasn't himself, he had been replaced.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CBC, CK, CMP, CRP, ESR, Troponin, evaluation for immune encephalopathy. Multiple blood draws from 11/3-11/9/2021.
Aktuelle Erkrankungen: Ingrown toenail
Vorgeschichte: Autism; ADHD; OCD; Tic Disorder, All of these were well controlled
Andere Medikamente: Risperdone 1mg; Guanfacine ER 1mg; Methylphenidate ER 18mg (ongoing); Keflex 1000mg BID (10/18-1/28)
Allergien: None
Vorherige Impfungen: -

VAERS 1855057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

moderat

Staat: TN
Alter: 37,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Chest pain Dyspnoea Paraesthesia oral Pharyngeal paraesthesia Tremor

Symptomtext

tingly feeling in tongue and throat, chest pain, shortness of breath, shaky legs

Weitere VAERSDATA-Felder

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

VAERS 1854919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 27.09.2021
Beginn: 03.11.2021
Tage bis Beginn: 37,0
Dosis: 3
Route/Site: IM / LA

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

Chills Cough Eye infection Fatigue Heart rate increased Nasopharyngitis Palpitations Sinusitis Upper respiratory tract congestion

Symptomtext

Cold started 7 days ago with chills, cough, upper airway congestion, no fever. Progressed to sinus infection and eye infection. Within one day of receiving the booster, I experienced heart palpitations with elevated heart rate (110 range) and feelings of exhaustion that lasted approximately one week with no medical intervention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Type II Diabetes (diet controlled)
Andere Medikamente: Meloxicam Crestor
Allergien: Compazine Vicodin Tramadol
Vorherige Impfungen: -

VAERS 1850954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Angiocardiogram Angiogram Arthralgia Back pain Blood glucose increased Blood pressure increased Chest X-ray Chest pain Computerised tomogram abdomen Computerised tomogram thorax Ear pain Echocardiogram Eczema Electrocardiogram Electrocardiogram T wave inversion Insulin resistance Lymph node pain Lymphadenopathy

Symptomtext

10/12/2021 at 1:15 am Sharp Left ear pain, left jaw pain, neck pain chest pain extreme pounding of the left side of heart sharp left wrist pain, extreme itching then noticed new eczema rash left arm and left axilla enlarged painful burning lymph node. Sharp right knee pain and left and right big toes. Chest pain began to pierce through to left side of back when inhaling and exhaling. Blood pressure 190s over 120s and blood sugars in high 200s low 300s blood pressure, and insulin medication not working. Chest pain never went away Tylenol and Ibuprofen did not work and blood pressure continued to be high. 10/12/2021 Notified PCP at 11 am. PCP replied on 10/13/2021 at 8:30 am giving instructions to go to Urgent Care went to Urgent care and ECG had inverted T waves paramedics called. 1st admission 10/13/2021-10/15/2021 2nd Admission 10/17-10/19/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: 10/13/2021, 10/16/2021 Chest xrays 10/13/2021, 10/16/2021 ECGs 10/14/2021 2D Echo 10/16/2021 CT Chest Angiogram 10/18/2021 Ultrasound Duplex Bilateral Legs 10/18/2021 CT Coronary Angiogram 10/19/2021 CT Abdomen and Pelvis Angiogram 10/20/2021 Right Knee xray Right knee and calf pain 10/27/2021 2D echo at Cardiology office
Aktuelle Erkrankungen: No
Vorgeschichte: HTN, DM II Overweight and uterine fibroids
Andere Medikamente: Benazepril, HCTZ, Lantus and Humalog
Allergien: Oats, animal hair and grass
Vorherige Impfungen: -

VAERS 1849663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 18.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Flank pain Hypoaesthesia Muscular weakness Paraesthesia

Symptomtext

Severe chest pain graduated to the right side of my body. Right arm and leg numbness, tingling and weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: ibuprofen
Vorherige Impfungen: -

VAERS 1849354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AR
Alter: 23,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Cold sweat Dizziness Fatigue Injection site swelling Migraine Peripheral swelling Pharyngeal swelling

Symptomtext

SWELLING IN THROAT, SWELLING IN INJECTION SITE DOWN TO WRIST, MIGRAINE, DIZZINESS, EXHAUSTION, COLD SWEATS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: SHELLFISH
Vorherige Impfungen: -

VAERS 1849224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AR
Alter: 63,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 01.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / -

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

Chest discomfort Condition aggravated Hypertension

Symptomtext

Hypertension, chest pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension, obesity, postsurgical DVT/PE, arthritis, degenerative disc disease
Andere Medikamente: amlodipine 5mg, prolensa 0.07% eye drops, hydrochlorothiazide 25mg, olmesartan 40mg, vitamin c, vitamin d3, aspirin 81mg
Allergien: N/A
Vorherige Impfungen: -

VAERS 1840227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: IA
Alter: 39,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Extra dose administered Heart rate increased Tremor

Symptomtext

Patient received the shot and was doing fine. Then got up after waiting for 15 min, took 10 steps and sat on the floor because she was dizzy, shaking, and had an elevated heart rate. She had said that this had happened before with the second COVID shot but that it happened the day after. EMS was called and checked her out but she did not go with them. Spouse of patient took patient to the emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Not known.
Allergien: NKDA
Vorherige Impfungen: Same reaction but to the second COVID vaccine and it did happen a day later the previous time. Patient discussed with her docto

VAERS 1832951

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: LA
Alter: 42,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Chest pain Dizziness Dyspnoea Headache Injection site erythema Injection site pain Somnolence

Symptomtext

Patient reported that he has a non stop headache, dizziness, shortness of breath, always sleepy, chest pains, Injection site red and painful...

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10/31/2021 went to ER was given medicine for side effects
Aktuelle Erkrankungen: no
Vorgeschichte: allergies
Andere Medikamente: Singular 10mg Levothyroxine Flowmax 0.4mg Reglan 10mg
Allergien: Celbrix
Vorherige Impfungen: -

VAERS 1830894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: -
Beginn: 04.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Abdominal pain upper Dyspnoea Rash erythematous SARS-CoV-2 test Swelling face

Symptomtext

Facial swelling; red rash on face; short of breath for 2 weeks; stomach cramping; This is a spontaneous report from a non-contactable other healthcare professional, the patient. A 53-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FD0809) via an unspecified route of administration on an unknown date (at the age of 53-years-old) as a single dose for COVID-19 immunisation. The medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The concomitant medications were not reported. On 04Sep2021, the patient experienced facial swelling, red rash on face, short of breath for 2 weeks and stomach cramping. On an unknown date, the patient underwent SARS-CoV-2 test and the result was not reported. The adverse events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were not taken as a result of the reported events. The clinical outcome of the events facial swelling, red rash on face, short of breath for 2 weeks and stomach cramping were resolving at the time of this report. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: SARS-CoV-2 test; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1828707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: KY
Alter: 25,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Chills Nausea Pain Pyrexia

Symptomtext

PT received 1st dose of the Pfizer at 5:00PM (10/28/2021) from our facility. PT. called the Health Dept. at around 9:30 AM (10/29/2021). PT. stated that they experienced Nausea, Fever (103 F), Body aches, chills, and chest pain at 1 am this morning (approximately 8 hrs after receiving the first COVID-19 Pfizer vaccine.) PT stated that they took Tylenol and Zofran, but symptoms still persist. As of 10:45 AM we have referred the PT to seek their primary care physician for further assistance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: At this moment 10:47 AM (10/29/2021) the PT has not received any Medical tests or laboratory tests.
Aktuelle Erkrankungen: No acute illness. 5 wks prior to vaccination Pt. stated having a child
Vorgeschichte: None stated by PT
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1825830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AZ
Alter: 31,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Adverse event Anxiety Chest pain Palpitations Tearfulness

Symptomtext

Anxious, tearful, chest pain, palpitations - onset about 3 hours after injection. Vaccine required by employer, patient reluctantly received it near deadline to meet work requirement. Stated she "wished she didn't have to get it." Paramedics called, patient then refused medical evaluation or transport to a hospital ER for further evaluation. She stated her usual BP was 160/100 but her "PCP is OK with it and said I could stop my meds." During adverse event BP 156/116. Patient strongly advised to go to ER but refused. Advised to make sure she called 911 for any worsening or if she changes her mind.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Depression, anxiety, hypertension
Vorgeschichte: Depression, anxiety, depression
Andere Medikamente: Patient can't remember names of meds for anxiety and depression.
Allergien: None known
Vorherige Impfungen: -

VAERS 1825504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: ID
Alter: 34,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Blood pressure increased Cough Dyspnoea Extra dose administered Feeling hot Productive cough Retching Secretion discharge Sensation of foreign body

Symptomtext

Pt was in waiting room after her COVID booster vaccine. She received the COVID booster about 10-15 minutes after her flu shot. About 10 minutes after the COVID booster., she reported becoming hot and feeling like she "needed to get some air". She began coughing and stated it felt like something "hard" was stuck in her throat. She coughed very hard to point she was gagging and throwing up mucous. After throwing up small amount of phlegm she reported feeling better. BP during cough was elevated but came back down. O2 sats normal. Patient denied feeling like throat was swelling or any mouth tingling. Denied itching. No rash. Was held 1 hour and was feeling herself again with normal VS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: nka
Vorherige Impfungen: Pt described having a non-immediate skin reaction to her axilla following her 3/31/21 2nd Pfizer vaccine.

VAERS 1825359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: ID
Alter: 57,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 16.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Dyspnoea Electrocardiogram normal Fear Laboratory test normal Malaise SARS-CoV-2 test negative Troponin

Symptomtext

CHEST PAIN, SHORT OF BREATH, OVERALL FELT VERY UNWELL. I WOKE UP AT 1AM FEELING THIS WAY, IT PROGRESSED THROUGH THE MORNING. FINALLY I WAS SCARED ENOUGH TO GO TO THE EMERGENCY DESPITE THE COVID RISK. AT THE HOSPITAL THEY DID AN EKG, TOOK LABS, AND DID A COVID TEST. THEY PERFORMED 2 TRONPONIN TESTS TO INSURE THAT I HAD NOT HAD A HEART ATTACK. BOTH TESTS WERE NORMAL. COVID CAME BACK NEGATIVE. THE EMERGENCY ROOM NEVER CAME TO A DEFINITIVE DIAGNOSIS BUT SUGGESTED MY COVID VACCINATION MAY HAVE CAUSED THIS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: TROPONIN - X2 2019 NOVEL CORONAVIRUS SARS-COV-2 BY PCR
Aktuelle Erkrankungen: NONE
Vorgeschichte: ATRIAL FIBRILLATION, HIGH BLOOD PRESSURE, OBESITY
Andere Medikamente: SPIRONOLACTONE, WARFFARIN, OMEPRAZOLE, GABAPENTIN, DILTAZEM, DOFETILIDE, LOSARTAN, ZINC GLUCONATE, VITAMIN D3, MAGNESIUM OXIDE, VITAMIN B12, MULTI-VITAMIN
Allergien: VANCOMYCIN, METFORMIN, DICLOFENAC SODIUM
Vorherige Impfungen: -

VAERS 1825351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: IN
Alter: 38,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 20.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / RA

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

Arrhythmia Blood pressure increased Blood test Echocardiogram Electrocardiogram Electrocardiogram ambulatory Extrasystoles Supraventricular tachycardia Tachycardia

Symptomtext

Sudden onset of tachycardia and heart dysrhythmias. On or around Monday September 27th while lying in bed I felt my heart skip a beat and then has some tachycardia. On Friday October 1st while driving my heart again went into tachycardia and I was seen in the ER and upon arrival my heart rate was 172 and my BP was elevated and I was told by the ER staff that they believed I had a run of SVT. Had another episode on 10/08/21, 10/09/21 and 10/21/21. I made an appointment with a cardiologist and he has diagnosed it as AV nodal re-entry tachycardia or PSVT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Holter monitor 10/07/21-10/14/21 EKG 10/01/21 Echocardiogram 10/18/21 Blood work 10/01/21
Aktuelle Erkrankungen: UTI
Vorgeschichte: None
Andere Medikamente: Nitrofurantoin Mono/Mac 100 mg Caps
Allergien: None
Vorherige Impfungen: -

VAERS 1821882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: GA
Alter: 26,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 12.09.2021
Beginn: 23.10.2021
Tage bis Beginn: 41,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Back pain Chest pain Muscular weakness

Symptomtext

loss of strength in my left arm, back pain, and mild chest pains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Tylenol
Allergien: -
Vorherige Impfungen: -

VAERS 1820576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 07.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Anaemia Breast pain Lymph node pain Lymphadenopathy Menstrual disorder Migraine Taste disorder

Symptomtext

mensuration started early; left lymph node under her arm pit was painful; Taste in her mouth right after injection; migraines; breasts are sore under her arm; anemic; her left lymph node was swollen; This is a spontaneous report from a contactable consumer (patient). A 45-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number FD0809), via an unspecified route of administration, administered in Arm Left on 07Sep2021 10:30 (at the age of 45-year-old) as dose 1, single for covid-19 immunisation. On 29Sep2021, the patient took second vaccination dose. No prior Vaccinations (within 4 weeks). Medical history included ongoing anaemia Verbatim: Severe Anemia had it for Years, ongoing migraine Verbatim: Migraine had it for Years, but she hasn't had them like this in a long time. AEs following prior vaccinations was none. There were no concomitant medications. The patient previously took morphine and experienced drug hypersensitivity. On an unknown date in Sep2021 the patient experienced anemic, her left lymph node was swollen, migraines, breasts are sore under her arm. On 07Sep2021 taste in her mouth right after injection. On 09Sep2021 mensuration started early, left lymph node under her arm pit was painful. She reported that her doctor checked her vaginal area and the nurse asking about taking the Tetanus shot and they offered her Provera to stop the bleeding, but she didn't want to add any more medications. She was anemic but cleared up after 7 days. Patient reported that her first vaccine was on 07Sep2021 and a couple of days later, her left lymph node under her arm pit was painful and she started her menstrual cycle early. She is severely anemic, so she could not afford to lose any additional blood. She went to see her doctor, and she wanted to prescribe Provera to stop the bleeding, but caller said no, because she did not want to add any additional medications to the vaccine. She stated her period did stop. On 29Sep2021, she had her second vaccination, and this time the left arm pit is swollen and it has traveled to her breast and it is painful and it is radiating to her left arm and shoulder. She also had migraines, behind her left eye, her whole left side is affected. She reported that she did not know if this is okay or normal. Therapeutic measures were taken as a result of, migraines (migraine). The patient was treated with Tylenol (Lot: AHA044 Expiration: 02May2025). She reported that she was taking Tylenol and it was not working. UPC: Unknown, she doesnt have the box. Lot: AHA044 Expiration: 02May2025. Caller stated she thought about going to the ER for her headache, but she did want to add any medication to the vaccine. On an unknown date in Sep2021 the outcome of anemic and her left lymph node was swollen was recovered. On 07Sep2021 the outcome of taste in her mouth right after injection was recovered. On 13Sep2021 the outcome of left lymph node under her arm pit was recovered. On 15Sep2021 the outcome of mensuration started early was recovered. The outcome of migraines and breasts are sore under her arm was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anemia (Verbatim: Severe Anemia Had it for Years); Migraine (Verbatim: Migraine Had it for Years, but she hasn't had them like this in a long time.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1818102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AR
Alter: 27,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chills Fatigue Hypoaesthesia Injection site pain Injection site swelling Joint range of motion decreased Nausea Neck pain Pain Paraesthesia Pyrexia

Symptomtext

Fever, Chills, Nausea, Extreme fatigue, pain in injection site, pain in both shoulders radiating down into both elbows and wrists, neck pain, left arm going numb occasionally, slight tingling in fingers during numb periods with the arm, swelling at injection site for 3-4 days, limited mobility in left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 1807793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WV
Alter: 67,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Paraesthesia

Symptomtext

PATIENT REPORTED ABOUT 2 HOURS AFTER RECEIVING VACCINATION A TINGLING SENSATION IN ARM THAT RADIATED DOWN THAT OCCURS INTERMITTENTLY. HE REPORTS THAT IT WAS MORE FREQUENT IN THE DAYS IMMEDIATELY AFTER THE SHOT & HAS NOW DECREASED IN FREQUENCY TO MAYBE ABOUT 4 TO 5 TIMES DAILY LASTING 2 MINUTES EACH TIME BUT HAS PLATEAUED. HE DOES NOT NOTICE ANYTHING THAT PRECIPITATES THE TINGLING SUCH AS PHYSICAL ACTIVITY, AS HE IS PHYSICIALLY ACTIVE MULTIPLE DAYS A WEEK. HE DOES NOT REPORT PAIN, JUST A WEIRD SENSATION. HE HAS HIS YEARLY APPOINTMENT WITH HIS PRIMARY CARE DOCTOR MONDAY NOVEMBER 1ST & WILL DISCUSS WITH HIS PROVIDER THEN AS IT IS NOT CAUSING HIM ANY SIGNIFICANT ISSUE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: OSTEO BI FLEX
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1967179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: IL
Alter: 88,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Delusion Lymphoedema Peripheral swelling Sensory disturbance

Symptomtext

Patient states her"Right & Left thigh are feeling like air is being pumped into them." States "yes" "to do you legs feel like they are getting more swollen?" VSS, Ptable to walk independently w steady gait 30feet. AOX3. States"demonic forces I am battling right now." States the above mentioned leg feelings & demonic forces are not different from in her past, Doctor called & spoke with patient. Pt bilat LE lymphedema.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Signs remained state, leg sensation remains better after sitting down. Patient able to ambulate will. Patient discharged to home after 30 minutes per Doctor.
Aktuelle Erkrankungen: Lymphedema; Thyroid problems
Vorgeschichte: Lymphedema; Thyroid problems; Demonic Ideations
Andere Medikamente: Not taking any meds
Allergien: NKA
Vorherige Impfungen: -

VAERS 1806376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 20,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Disorientation Dizziness Hyperhidrosis Immediate post-injection reaction Impaired driving ability Influenza Insomnia Lethargy Mental impairment Nausea

Symptomtext

Pt received one Pfizer vaccination, and right afterwards got severe flu symptoms, chest pains, dizzy, nausea, sweating, mentally very disoriented, and severe lethargy but difficult to sleep. He was unable to drive that night. These severe symptoms lasted for 7 days. Pt continues to have episodic mental impairments and difficulty sleeping.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Chronic Lyme Syndrome History Bartonella infection History Babesia infection Asthma Malignant melanoma of face
Vorgeschichte: see answers in item 11 Also patient has had multiple vaccine adverse reactions to DTaP, meningococcal, and influenza vaccines
Andere Medikamente: Albuterol MDI for asthma; NutramedX; One a day Multivitamin; Vitamin B 12; Magnesium
Allergien: No known allergies
Vorherige Impfungen: TDaP age 12 was bedridden for 2 months followed by persistent cognitive impairments and disorientation; meningococcal age 18 had

VAERS 1801053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AK
Alter: 39,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 28.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Palpitations Sleep disorder

Symptomtext

Patient stated that she had an episode of palpitations that woke her from sleep. She said that this occurred over 2-3 minutes in the middle of the night while she was sleeping. Pt denies having chest pain, dizziness, SOB, or other cardiac symptoms. Pt denies increased caffeine use or performing activities that may increase HR or cause chest discomfort. Pt stated that after episode, she went back to bed and it has not happened again. She did not seek out advise from PCP or vaccine-administering clinic. Pt denies any cardiac symptoms on day of 2nd dose. Pt requested to have 2nd dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Patient did not seek medical attention for this episode and did not feel it necessary to have any testing done. Episode was discovered at her 2nd dose appointment. Pt declines vitals signs stating issue has resolved. Pt still wanted to get 2nd dose since she was not sure if the 2 events are related.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes II
Andere Medikamente: Metformin, glimepiride
Allergien: Unknown Anaphylactic reaction as a child, required epipen, but has not happened since. No other known allergies.
Vorherige Impfungen: -

VAERS 1800369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chest pain Eye pain Headache Lymph node pain Lymphadenopathy Migraine Pain in extremity Peripheral swelling Swelling Taste disorder

Symptomtext

pain behind left eye; after second dose she is experiencing left arm lymph node swollen radiating to her breast causing pain in left arm and chest; after second dose she is experiencing left arm lymph node swollen radiating to her breast causing pain in left arm and chest; migraines/Migraines; behind her left eye; whole left side is affected; left arm pit is swollen and it has traveled to her breast and it is painful and it is radiating to her left arm and shoulder; after second dose she is experiencing left arm lymph node swollen radiating to her breast causing pain in left arm and chest; left arm pit is swollen and it has traveled to her breast and it is painful and it is radiating to her left arm and shoulder; the arm is more swollen, she can see the swelling.; headache; Second Dose: Felt the vaccine going in; This is a spontaneous report from a contactable consumer (Patient). A 45-year-old female patient received second dose of bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: FD0809), dose 2 via an unspecified route of administration, at Arm Left on 29Sep2021 08:30 as dose 2, single for COVID-19 immunization. The patient's medical history included ongoing Severe Anaemia, ongoing migraine. There were no concomitant medications. The patient's historic vaccine included first dose of bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: FD0809), for COVID-19 immunisation on 07Sep2021 at 10:30 and experienced left lymph node was swollen, Started her menstrual cycle early, taste disorder, she has migraines since both doses, Breasts are sore under arm and anaemia. No other Vaccines Administered on Same Date of the Pfizer Suspect and no Prior Vaccinations taken. She was Allergic to Morphine. On 29Sep2021, she had her second vaccination, and this time the left arm pit was swollen and it has travelled to her breast and it was painful and it is radiating to her left arm and shoulder. The patient Felt the vaccine going in on 29 sep2021; she experienced pain behind left eye, left arm pit is swollen and it has travelled to her breast and it is painful and it is radiating to her left arm and shoulder, migraines with pain behind her left eye; whole left side is affected on 30Sep2021. Caller stated she also had migraines, behind her left eye, her whole left side is affected. after the second dose, the arm was more swollen, she could see the swelling. Caller reports after second dose she is experiencing left arm lymph node swollen radiating to her breast causing pain in left arm and chest. Caller is also experiencing migraines with pain behind left eye. MI agent did not gather callers age, realized after call. she could see a difference in her arms when she extends her arms. The patient felt that with the second vaccine she felt it go in, but it was not as noticeable as the first one. she was taking Tylenol and it is not working. . Caller states her doctor checked her vaginal area and the nurse asking about taking the Tetanus shot and they offered her Provera to stop the bleeding, but she didn't want to add any more medications. The patient stated that her eyes were not that good. Events resulted in physician office visit. The outcome of pain behind left eye, Pain in arm, chest pain, migraines, swelling, Swollen lymph nodes,lymph node pain, headache was not recovered; Felt the vaccine going in was recovered on 29Sep2021 and the arm is more swollen, she can see the swelling was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anemia (Verbatim: Severe Anemia); Migraine (Verbatim: Migraine)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1765465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: 74,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 10.02.2021
Beginn: 03.10.2021
Tage bis Beginn: 235,0
Dosis: 3
Route/Site: IM / -

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

Cough Fatigue Influenza like illness Laboratory test abnormal Myalgia COVID-19 pneumonia Dyspnoea Pain Oropharyngeal pain SARS-CoV-2 test positive Somnolence

Symptomtext

BODY ACHES, COUGH, SHORTNESS OF BREATH, FATIGUE, SLEEPING MORE, COVID PNEUMONIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST 10/3/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Bladder disease COVID-19 Acute hypoxic respiratory failure due to covid-19 Colonic polyps Hematuria Hyperlipidemia Mantle cell lymphoma of lymph nodes of axilla Prostate disease
Andere Medikamente: acyclovir (ZOVIRAX) 400 mg oral tablet albuterol HFA (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler benzonatate (TESSALON) 100 mg oral capsule dexAMETHasone (DECADRON) 6 mg oral tablet dextromethorphan
Allergien: -
Vorherige Impfungen: -

VAERS 1795749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test Computerised tomogram Hypertension Hypoaesthesia Nausea Paraesthesia Urine analysis X-ray

Symptomtext

Numbness and tingling in arms, legs, and face. High blood pressure and nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: CT scan X-Ray Bloodwork Urinary analysis 10/16/2021
Aktuelle Erkrankungen: I had COVID a couple weeks before first vaccination.
Vorgeschichte: Seizures
Andere Medikamente: Lamictal
Allergien: NSAIDS
Vorherige Impfungen: -

VAERS 1795069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: IN
Alter: 20,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain Fatigue Migraine Pyrexia

Symptomtext

Fever of 101.3, intense migrane, back pain, and fatigue. Treated with 3 doses of over the counter acetaminophen.

Weitere VAERSDATA-Felder

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

VAERS 1794333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AK
Alter: 37,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 11.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Electrocardiogram Full blood count Laboratory test Palpitations Troponin

Symptomtext

Heart palpitations began morning of 10/14, sporadic until 2am 10/15 when they became consistent and problematic. Visited ER and observed PVCs. Returned to ER as instructed when symptoms continued, was given ZioXT patch for monitoring.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG, CBC, chem, triponin - all 10/15
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Femara, Claritin, Metamucil, prenatal multivitamin, DHA, vitamin D, bee pollen
Allergien: Latex, lactose intolerant
Vorherige Impfungen: -

VAERS 1791210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: LA
Alter: 31,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 22.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / RA

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

Chest discomfort Chest pain Fatigue Inappropriate schedule of product administration Pain Pain in extremity Palpitations

Symptomtext

dose 1 on 08Sep2021 and dose 2 on 22sep2021; chest tightness; heart palpitations; dull aches on the left side of my chest and sometimes in my left arm; I had aches and fatigue; I had aches and fatigue; aches on the left side of my chest and sometimes in my left arm; This is a spontaneous report from a contactable consumer or other non-health care professional reported for herself (patient). A 31-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA vaccine, Solution for injection), dose 2 via an unspecified route of administration, administered in arm right on 22Sep2021 (Batch/Lot Number: FD0809) (at the age of 31-years-old) as dose 2, single for covid-19 immunisation. The patient medical history was reported as none. The patient had no known allergies. The patient concomitant medication(s) included vitamins nos (DAILY VITAMINS) taken for an unspecified indication, start and stop date were not reported and probiotics (PROBIOTICS) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within 4 weeks prior to the Covid 19 vaccine. The patient had not been diagnosed with COVID-19 prior to vaccination and had been tested for Covid-19 since the vaccination. The patient received daily vitamins, probiotics, birth control medications within 2 weeks of vaccination. The patient had previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA vaccine, Solution for injection), dose 1 via an unspecified route of administration, administered in arm right on 08Sep2021 (Batch/Lot Number: FD0809) as dose 1, single for covid-19 immunization and experienced soreness in her right arm. The patient received inappropriate schedule of vaccine administration. On 24Sep2021, the patient experienced aches and fatigue; aches in other parts of her body went away but aches in her chest did not. She started to have chest tightness, heart palpitations, and dull aches on the left side of her chest and sometimes in her left arm. She went to the urgent care and her EKG looked normal. They prescribed a low dosage of pain meds and muscle relaxers but it didn't help. She finally went to see a cardiologist yesterday, 04Oct2021 because she was considered she developed a heart issue but her heart looked fine and strong, but they have no idea why she still have adverse aches in her chest area. The heart doctor kept her on some strong Ibuprofen and steroids and she will see him again in a week. The doctor does feel like this was temporary and it's just prolonged autoimmune reactions from the shot. The patient hope he was right. The patient was visited to doctor or other healthcare professional office/clinic and emergency room/department or urgent care. The patient received treatment of anti-inflammatory drugs and steroids for the events. The patient underwent lab tests and procedures which included electrocardiogram resulted in normal on an unspecified date, nasal swab test (sars-cov-2 test) resulted in negative on 01Oct2021. The outcome of the event pain was recovered on 24Sep2021 and for the remaining events was recovering. Follow-Up (12Oct2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20211001; Test Name: Sars-Cov-2 Test; Test Result: Negative ; Comments: 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: None.
Andere Medikamente: DAILY VITAMINS; PROBIOTICS.
Allergien: -
Vorherige Impfungen: -

VAERS 1789488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: ID
Alter: 42,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 27.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / -

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

Axillary pain Breast pain Hypoaesthesia Paraesthesia

Symptomtext

Extreme armpit and breast pain on injection side for 2weeks. Numbness to legs, mostly the left side which was the side of my injection. Legs and feet feel numb and tingle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine 25 mcg daily
Allergien: None
Vorherige Impfungen: -

VAERS 1788917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OR
Alter: 69,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 13.09.2021
Beginn: 15.09.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Balance disorder Chest pain Chills Condition aggravated Dizziness Fatigue Feeling abnormal Flushing Laboratory test Musculoskeletal stiffness Neuralgia Pulmonary pain Pyrexia

Symptomtext

Sore joints, becoming much more sore over the first 5 days after vaccination. Very sore joints lasted about 2 weeks. Then, extremely tired, and required four days to recover from a partial day of canning (extreme tired for me). Still ill with exhaustion, I developed a fever of about +1.5 degrees F, for about 12 hours. Quite lightheaded, with pain around my left lung. Often this signals a systemic fungal flare (for me). Strong chest wall pains went on for about 5 days, and were then joined by what I believe are Epstein-Barr flare symptoms, and CMV flare symptoms. As of today, 10/15/21 I still have the EBV and CMV flare symptoms. Current symptoms include chills, lightheadedness, brain fog, feeling flushed, stiffness, sore joints, some minor pain around left lung, nerve pain in groin, exhaustion, unsteady on feet. (FYI: I have been tested numerous times with the left chest wall muscle pain, and know to rest with it until it subsides.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None yet. I have new orders for EBV and CMV blood levels, but the lab isn't open until Monday. Orders are from my cardiology folks.
Aktuelle Erkrankungen: Not known to have any acute infections. See below,
Vorgeschichte: Chronic systemic fungus, adrenal insufficiency (Addisons), chronic Epstein-Barr virus (EBV), chronic Cytomegalovirus (CMV). Arthritis, asthma,
Andere Medikamente: Rx: Oral hydrocortizone, Flow-vent, nasal mometazone, armor thyroid, estradiol-progesterone-testosterone, albuterol. Also DHEA, hawthorn extract, multivitamins, calcium, magnesium, zinc, phosphatidylserine, milk thistle, CoQ10, glusocamin
Allergien: Lactose, dairy, citrus, nightshades, strawberries, shrimp, peanuts. Latex, fluoroquinoles, sulfa drugs, flagyl, augmentin, fluconazole, possibly cephalexin, possibly doxycycline.
Vorherige Impfungen: Influenza vaccine in 1998

VAERS 1785209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 12.10.1979
Beginn: 14.10.2021
Tage bis Beginn: 15.343,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Dizziness Dysstasia Headache

Symptomtext

Prior to vaccination patient reported dizziness and headache to nurse that started approximately 20 minutes before her appointment. Appointment was at 11:30. Heart Rate and oxygen in normal range. Blood pressure 144/90. Patient could not stand, headache and dizziness not subsiding. Patient taken by ambulance to nearest Emergency Department at approximately 1:25pm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none per patient
Vorgeschichte: none per patient
Andere Medikamente: none per patient
Allergien: none per patient
Vorherige Impfungen: -

VAERS 1768842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MI
Alter: 32,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 30.09.2021
Beginn: 03.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Acoustic stimulation tests abnormal Audiogram abnormal Chills Deafness unilateral Dizziness Deafness neurosensory Vertigo Headache Hot flush Mobility decreased Pain Sudden hearing loss

Symptomtext

09/30/21 at 800am, pfizer covid booster vaccine given. 10/1/21 all day body aches, dizziness, head aches, chills and hot flashes. These continued until 10/3/21. 10/3/21 at 800pm sudden hearing loss in right ear. 10/4/21 at 600am unable to get out of bed, spinning room, right ear deafness, dizzy and vertigo. Contacted Occupation Health and was directed to see Dr, ENT. 10/4/21 at 300pm consult with Dr at ENT and told that I had a rare side effect from the booster that is covid related and known. Sent to Audiology for hearing test and was confirmed 100% deaf in right ear, Went back over to ENT where Dr administered a steroid injection in to my right ear drum. 10/7/21 at 300pm back to Dr ENT for a second steroid injection and at this point no changes in my hearing. He sent me to another ENT for additional injections as he was out of the office, 10/11/21 Dr ENT, administered a third steroid injection in to my right ear drum. Also put on a weeks worth of combination oral medications to help. While in the office Dr performed another Audiology test, At this point I am still 100% deaf in my right ear. I am still having ongoing treatment but told that it is unlikely that my hearing will come back at all. 10/25/21 - MRI will be completed 11/3/21 - Dr, ENT and Audiology Appointments are scheduled.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1779555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 09.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Cognitive disorder Condition aggravated Headache Neck pain Oropharyngeal pain Pyrexia SARS-CoV-2 test negative

Symptomtext

I began having low grade fever and joint aches on pains on 09/10/21. Due to a recent brain injury, I had been having trouble with processing thought. On 09/12/21, I noticed that those symptoms getting worse for about one week. On 10/05/2021, I had a fever of 99.6 and the next day no fever but a sore throat. I took a home covid test and it was negative. Thursday, 10/07/2021, stayed home to rest. On 10/8/2021, my temp went to 102.2 and had severe neck pain for a day. By morning it had improved. 10/09/21, I developed a headache during the day. I took a second test 10/12/2021, it came back negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: Mild head injury
Vorgeschichte: No
Andere Medikamente: None
Allergien: Sulfa drugs; iodine; shellfish; insect bites (bees)
Vorherige Impfungen: -

VAERS 1768346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cough Paraesthesia oral Throat tightness

Symptomtext

0838 Patient received vaccine Pfizer 3rd dose in right arm. Patient waited observation time for 15 minutes, and at approx. 17 mins past, 0901 patient complained throat was abnormally tight, cough was present, and tongue was slightly tingling . Denied itchiness, complained that a abnormal feeling of tightness was accompanied the vaccine. At approx 0903 Benadryl 50mg was given PO. RN stat notified, and patient was wheelchaired over to urgent care for further evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1765890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OR
Alter: 57,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 27.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Rash Rash erythematous Rash pruritic Rheumatoid arthritis

Symptomtext

Itchy Red Rash-consisting of small red bumps, on front of shins and forearms--started 3 days after first dose of vaccine. Rash on shins healed within 3 days, rash on forearms is still present after 7 days. Took pictures of forearms and sent to my PCP, also made appointment for an office visit. Also noticed a flare up with my RA--seemed to only last about 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No medical testing at this time.
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis--diagnosis in 2020
Andere Medikamente: Levothyroxine-88mcg/Daily Predinsone --2 MG/Daily
Allergien: Eggs, Dairy, Sulfur, Penicillin
Vorherige Impfungen: Flu Vaccine-2009

VAERS 1763687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Heart rate increased Malaise Tachycardia

Symptomtext

Patient initially experienced tachycardia (HR >110 bpm). She reported that she's not feeling too well and that her heart is beating so fast. This occurred within the 15 min monitoring period post vaccination. Checked her bp and reading was 199/100. checked it once again after 15 mins and it was at 188/89. 15 mins after paramedics came, her bp was still at 190/89 and HR of 117bpm, O2 sat 99%. Patient was still not feeling too well, although conscious and was able to communicate with me and the paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: BP: 199/100, 188/89, 190/89 HR: 117bpm O2 sat: 99%
Aktuelle Erkrankungen: no known illnesses
Vorgeschichte: no known health conditions
Andere Medikamente: Losartan
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1762192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 25.09.2021
Beginn: 25.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Axillary pain Feeling abnormal Laboratory test normal Pain Pain in extremity Tremor Urine analysis normal Vaccination site pain

Symptomtext

MY DAUGHTER STARTED WITH ARM PAIN PULSING ON VACCINE SITE A FEW HRS AFTER RECEIVING THE VACCINE. SHECONTINUED LIKE THAT FOR THE REAT OF THE DAY. ON SUNDAY HER ARM WAS STILL SORE AND ARM PAIN HAD RADIATED TO LEFT UNDERARM. PULSING WAS STIILL PRESENT, BUT NOW IT WAS RADIATING TO LOWER ARM, TO THE ELBOW. ON MONDAY SHE WAS STILL COMPLAING OF PAIN AND SHE WAS NOW FEELING A KIND OF VIBRATION ON HER ELBOW AREA. IT WAS CONTINIOUSLY, IT WOULDN'T STOP. TUESDAY SHE WOKE UP WITH A STRONGER VIBRATION FEELING ON HER ARM, NOT JUST THE ELBOW AREA. BY THE EVENING HER ARM WAS HAVING A TIC/ UNCONTROLABLE SHAKING. WEDNESDAY HER ARM WAS SHAKING UNCONTROLABLY AND NOW IT WAS VERY NOTICIBLE. THAT IS WHEN I TOOK HER TO THE ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: LAB WORK ONLY 09/29/2021 URINE TEST 09/29/2021 EVERYTHING WAS NORMAL
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: EGGS, PEANUTS
Vorherige Impfungen: -

VAERS 1762064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WI
Alter: 56,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 16.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Dizziness Fatigue Full blood count Pain in extremity Tremor

Symptomtext

Lightheadedness, worsened fatigue, shaky-intermittent, lower extremity achiness-bilateral

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CBC
Aktuelle Erkrankungen: Some fatigue, lightheadedness Ankylosing spondylitis- on Humira
Vorgeschichte: Ankylosing spondylitis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1761605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: IL
Alter: 50,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Biopsy Dyspnoea Haemorrhage Headache Hot flush Hypoaesthesia Impaired work ability Pain Paraesthesia Spinal disorder

Symptomtext

After Dose 1 08/26/2021 was in menopause and she noticed that she had some bleeding after Dose1, biopsy for two weeks later and informed that it was a side effect of the vaccination. Felt like a rod went down her spin Really bad head ache and numbness with feet. Hot flash like fever, warm and flush and numbness tingled, short of breath like a wait on her and numbness and hands and body aches and computer work was getting worst and saw a occupational health and primary health provider and did not miss work but felt miserable and upcoming Neurology test coming up. 10/07/2021 appoint with PA and urgent care on the Saturday 09/25/2021 Urgent care visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Biopsy, MRI scheduled 10/09/201, EMG Electro Muscled trying to determine Auto Immune Issue next week of 10/10/2021.
Aktuelle Erkrankungen: No
Vorgeschichte: Tremor; Sensitivity to cold.
Andere Medikamente: Primidone; Zyrtec
Allergien: Sessional allergies
Vorherige Impfungen: -

VAERS 1761522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: UT
Alter: 42,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Aphasia Disturbance in attention Dyspnoea Epistaxis Feeling abnormal Headache Injection site pain Irritability Nasal congestion Oropharyngeal discomfort

Symptomtext

About an hour after the shot, was extremely irritated and couldn't really speak. The words were just not coming out. Then my brain was foggy, really couldn't keep focus. Around 3pm, I started to get a clearer head. Had a normal night. Around 7pm, my right arm started to hurt at the injection site. Around 10:30pm, I started to get a headache. I took ibuprofen to help deal with the pain in the arm and my headache. Around 6am, I woke up on my right side, not able to breathe. My nose was completely full of stuff, my throat was clogged. I rolled over on my back to see it would help and felt my nose starting to bleed. I got up and rushed to the bathroom, where my nose continued to run. I would call it a steady stream of blood coming out of my left nostril. I blew my nose hoping it would stop, it didn't. Around 7am, I shoved a tampon up my nose, hoping it would stop. Around 7:30am, took the tampon out and blew my nose again. Got more blood clots. Stoved another tampoon up my left nostril. Around 8am, I could taste the blood dripping down my throat. I took out the tampon, my nose was no longer bleeding, but now it was dripping down my throat. At 9:30am, called the clinic, where I talked to a nurse, where she advised me to go to urgent care to have them stop the bleeding. As of 10am, it is still dripping down my throat. I am not going to the urgent care to have them burn the vessels.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Herpes
Andere Medikamente: Perscription:Valtrex-1GM Vitamins: Hair, Skin & Nails Gummies-5000mcg, Super Collagen-36g, Vitamin D3-1000IU, Vitamin C-2000mg, Fish Oil-2400mg, Potassium-99mg, B12-1000mcg, Vitamin E-400IU, Cranberry-8400mg, B6-100mg
Allergien: I am allergic to cajun seasoning
Vorherige Impfungen: -

VAERS 1759681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 01.09.2021
Beginn: 01.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / AR

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

Chest pain Dizziness Dyspnoea Fatigue Headache Heart rate increased Heart rate irregular Paraesthesia

Symptomtext

Shortness of breath, chest pain, rapid and irregular heart rate, headache, dizziness, fatigue, lightheadedness, pins and needles in extremities

Weitere VAERSDATA-Felder

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

VAERS 1757045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: AK
Alter: 36,0
Geschlecht: M
Eingang: 02.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Abdominal pain lower Arthralgia Back pain Chills Feeling cold Migraine Pain Pyrexia

Symptomtext

Fever (102), unable to control body temperature (always cold), migrain, intense joint pain, periodic stabbing pain in right lower abdomen and right lower back. Obtained second dose of vaccine at 0900, 30 Sep 21. Pain and chills started at 0230, 1 Oct 21. Checked into ER at 1300, 1 Oct 21. Released from at 2030, 1 Oct 21 after testing, Toradol, Zofran, and 100ml IV Tylonal. 2 Oct 21, abdominal pain continued. After the first dose I experienced 72 hours of fever, chills, migrain, vomiting, and body aches. This was the same as when I had covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Viral tests negative, CT normal, area of appendix tender in abdominal exam.
Aktuelle Erkrankungen: None
Vorgeschichte: pinched C6, TBI
Andere Medikamente: Daily Multivitimen
Allergien: Penicilin
Vorherige Impfungen: -

VAERS 1754517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Dyspnoea Feeling jittery Throat tightness

Symptomtext

Patient reported dizziness, brought back to observation room, vital signs b/p: 202/104, pulse: 92, began to be jittery and stated she felt her throat closing and having trouble to breathe. 1535 administered epi pen 0.3 mg to left thigh, b/p: 210/122, pulse; 129, 911 called, also put her on oxygen, 1542 911 services got here and took over care and transferred patient out to nearest emergency room.

Weitere VAERSDATA-Felder

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

VAERS 1754132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fd0809

moderat

Staat: TX
Alter: 36,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain Arthralgia Cold sweat Dizziness Extra dose administered Flushing Migraine Myalgia Nausea Pain Pyrexia

Symptomtext

Dizzy, light headed, facial flushing, cool/clammy, fever, severe body aches/ joint pain/ muscle pain/ migraines/ nausea/ abdominal pain Home care with rest/fluids/meds Today 10/1 is the first back to normal day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Virus about 3 weeks prior
Vorgeschichte: Migraines Back injury
Andere Medikamente: Birth control Women?s multivitamin Naproxen
Allergien: Pork Soy
Vorherige Impfungen: Pfizer Covid vaccine 1 & 2- same as listed above 12/27/20 and 1/7/21 35 years of age

VAERS 1753427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 26,0
Geschlecht: M
Eingang: 01.10.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Extra dose administered Pharyngeal paraesthesia

Symptomtext

Patient was in office and receive his 3rd dose of Pfizer vaccine. patient started having tingling in his throat and lightheaded 3 to 4 minutes after the vaccine was given. Patient was give 1 tablet of Allegra 60 mg . Patient started feeling better after he took the Allegra. Patient was kept in observation for additional 30 min.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Crohn's Disease
Andere Medikamente: adalimumab (HUMIRA,CF, PEN) 40 mg/0.4 mL pen, cetirizine-pseudoephedrine (ZYRTEC-D) 5-120 mg per tablet, cholecalciferol, vitamin D3, (VITAMIN D3 ORAL), and PROAIR HFA 90 mcg/actuation inhaler
Allergien: Nut and Latex
Vorherige Impfungen: -

VAERS 1750280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MS
Alter: 17,0
Geschlecht: M
Eingang: 30.09.2021
Impfdatum: 28.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Chest X-ray normal Chest pain Electrocardiogram normal Fatigue Full blood count Liver function test Metabolic function test Pain Pyrexia Troponin

Symptomtext

Onset of fatigue, body aches, low grade fever, and chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG and Cxray Normal Pending CBC, BMP/Liver Profile, Troponin
Aktuelle Erkrankungen: None
Vorgeschichte: ADHD, Allergic Rhinitis
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 1745407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 29.09.2021
Impfdatum: 14.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Chest pain Dyspnoea Heart rate increased

Symptomtext

Heart beating fast, shortness of breath, chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, high blood pressure, fatty liver, enlarged ovarian cysts, umbilical hernia, polyp
Andere Medikamente: metformin, lisinopril, atorvastatin, metropolol, vitamin d, baby aspirin, insulin, victoza, multivitamin, calcium
Allergien: levoquin
Vorherige Impfungen: -

VAERS 1741729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 11.09.2021
Beginn: 11.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Discomfort Grip strength decreased Pain Paraesthesia

Symptomtext

Employee calling to report a reaction after receiving a COVID-19 vaccine. Vaccine Name - Pfizer Vaccine Date - ? 9/11/2021 Is this your first or second dose- 2nd Date of symptom onset - ? 9/11/2021 Symptoms - ? heavy feeling, pain all over, joint pain in big joints all over the body, parasthesia of hands and feet (so bad she drops objects), employee states she can still walk and do things but it is hard. employee also stated that she has psoriatic arthritis and takes biologics for it but it was a month before the first dose COVID-19 vaccine as recommended. Last day of work and shift - ? NA Home remedies-Employee stated she has been taking 1 gram of Tylenol twice a day for pain Any improvement- Tylenol helps the pain only Recommendation- Advised employee to follow treatment plan of phycisian. Employee voiced understanding Employee of information ? Yes Employee voiced any concerns ? No Employee?s questions answered to employee?s satisfaction -Yes

Weitere VAERSDATA-Felder

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

VAERS 1741676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WI
Alter: 69,0
Geschlecht: M
Eingang: 28.09.2021
Impfdatum: 23.09.2021
Beginn: 23.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Balance disorder Dizziness Fall Hypotension Pallor Unresponsive to stimuli

Symptomtext

Patient states that he was feeling dizzy after he waited in observation for 15 minutes. Patient became unsteady, pale, and started to fall and was lowered to the ground by staff. Patient was talking and then became unresponsive for 15-30 seconds. Patient had a pulse and was breathing and 911 was called. Patient became responsive and states that he fell asleep and was dreaming. Blood pressure was 86/49. States blood pressure is usually low. Patient drank 2 apple juices and 2 waters. EMS arrived took blood pressure and patient's pressure returned to his baseline and was responding appropraitely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: History of vasovagel response
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1740870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WI
Alter: 49,0
Geschlecht: M
Eingang: 28.09.2021
Impfdatum: 20.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Diplopia Headache Magnetic resonance imaging Paraesthesia

Symptomtext

9/24/21 12:00pm dull head ache, numb tingling feeling on the right side of scalp. 9/25/21 woke up around 8am with binocular double vision, continues through 9/27. 9/27/21 sought care at Clinic. Saw NP who referred the client to the emergency room. There the client reports he had an MRI and blood work. No abnormalities were found. He was scheduled for a neurologist appointment next week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 9/27/21 Client reports normal MRI and blood work.
Aktuelle Erkrankungen: No.
Vorgeschichte: No.
Andere Medikamente: Simvastatin.
Allergien: No known allergies.
Vorherige Impfungen: -

VAERS 1735454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 34,0
Geschlecht: F
Eingang: 26.09.2021
Impfdatum: 16.09.2021
Beginn: 17.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Dyspnoea Limb discomfort

Symptomtext

Shortness of breath, heaviness in arms, lightheadedness, weakness.

Weitere VAERSDATA-Felder

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

VAERS 1731870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 23.09.2021
Beginn: 23.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Adverse reaction Erythema Face oedema Paraesthesia oral Swelling face

Symptomtext

-Patient received Pfizer vaccine on 9/23/21. Patient reports the following adverse reactions: facial swelling/redness and tingling. Tongue tingling and arm redness. No sob or difficulty swallowing. I did have pt wait 30 minutes after the vaccine was given. Vitals taken and recorded. Pt was given 25mg of Benadryl after she reported tongue tingling. Pt then returned to the office 30 minutes later with facial edema,redness and tingling. Pt was given another Benedryl 25mg -Pt was advised to continue to take Benadryl 25-50mg q 4-6 hours as needed. Pt will continue to monitor symptoms and will go to the ER if any difficulty breathing or chest tightness. Pt was advised to follow up with her PCP tomorrow. Covid Pfizer vaccine added to pt allergy list.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: acyclovir, multivitamin
Allergien: valium, sulfa, penicillin, vancomycin, erythromycin, fluconazole, EE
Vorherige Impfungen: -

VAERS 1731779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: 24.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia oral

Symptomtext

pt complained of tingling of lips

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: HX OF BILAT HIP ARTHROPLASTY FHX OF BRAIN ANEURYSM HX OF DVT HX OF ADENOMATOUS COLONIC POLYPS PREDIABETES
Andere Medikamente: Plavix 75 mg daily
Allergien: NA
Vorherige Impfungen: -

VAERS 1727117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 23.09.2021
Impfdatum: 27.08.2021
Beginn: 27.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Immediate post-injection reaction Neck pain

Symptomtext

Patient states that immediately after the vaccine he had chest pain for approximately 15 minutes and then it resolved without any interventions. The next day he reports he had a sore neck. The sore neck lasted approximately 1 week in duration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None reported.
Vorgeschichte: None reported.
Andere Medikamente: Vitamin B 12 and other supplements. No prescription medications.
Allergien: None reported
Vorherige Impfungen: -

VAERS 1726390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 37,0
Geschlecht: M
Eingang: 23.09.2021
Impfdatum: 10.09.2021
Beginn: 11.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram pulmonary normal Blood test normal Chest X-ray normal Chest pain Computerised tomogram thorax Dyspnoea Pain

Symptomtext

Patient experienced chest pain, shortness of breath and diffuse body pain for 2 weeks following vaccination with Pfizer vaccine on 9/10/21. Seen in outside hospital ED on 9/21/21. No evidence of pulmonary embolism, deep vein thrombosis nor myocardial infarction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 9/21/21 - tests performed including CT pulmonary angiogram, chest x-ray, blood tests. . No evidence of pulmonary embolism, deep vein thrombosis nor myocardial infarction.
Aktuelle Erkrankungen: none
Vorgeschichte: left popliteal deep venous thrombosis
Andere Medikamente: Xarelto 20 mg by mouth daily
Allergien: none
Vorherige Impfungen: -

VAERS 1722857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 16.09.2021
Beginn: 16.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Fatigue Headache Palpitations Rash Rash pruritic Urticaria Vaccination complication Vomiting

Symptomtext

racing heart (pulse 115), shortness of breath, vomiting, headache, itchy painful rash/hives. Both #1 and #2 injections gave me the COVID arm. Have ongoing headache still since these events, and extreme tiredness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic bronchitis
Andere Medikamente: 75 mg Effexor XR 600 mg Gabapentin
Allergien: Aspirin Erythromycin Pollen
Vorherige Impfungen: -

VAERS 1722776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: OH
Alter: 60,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Paraesthesia oral Swollen tongue

Symptomtext

Patient experienced a reaction post COVID vaccination Vaccine brand PFIZER Lot # FD0809 Type of reaction TINGLING Symptoms Patient had vaccine and was in the observation area. She experienced tingling of her lips and tongue. Patient felt like her tongue was beginning to feel swollen. Denied trouble breathing or difficulty swallowing. No swelling noted. Vital signs: BP 149/76 | Pulse 71 | Resp 16 | LMP (LMP Unknown) Interventions (Fexofenadine 60 PO given per standing order) Was a code blue called -No How long was patient monitored in observation area -30 minutes after the Fexofenadine was given Final outcome - Tingling subsided. Instructed to call PCP for further instructions and to proceed to nearest ER or call the emergency line for difficulty breathing or swallowing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: HTN, hyperlipidemia, hypothyroidism
Vorgeschichte: -
Andere Medikamente: -
Allergien: PCN, Egg Yolk
Vorherige Impfungen: -

VAERS 1718946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

moderat

Staat: TX
Alter: 47,0
Geschlecht: F
Eingang: 21.09.2021
Impfdatum: 20.09.2021
Beginn: 20.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Headache Nausea Pain Paraesthesia Sleep disorder Vomiting

Symptomtext

EE received 1st dose of Pfizer vaccine on 9/20/2021, at vaccine event at . Went home feeling really tired an fatigue, had a headache and body Aches, had wired tingling on the left side of body were vaccine was administered. Woke up in middle of night feeling nausea and small amount of vomit did eat a light meal before she laid down. Report she is feeling a little better today

Weitere VAERSDATA-Felder

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

VAERS 1714516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: ID
Alter: 15,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Decreased appetite Fatigue Headache Loss of personal independence in daily activities Mobility decreased Nausea Pain Pyrexia

Symptomtext

body aches / fever of 101.5 for 48 hours / tired / headache / unable to move from bed without help / chills / nausea / loss of appetite received the vaccine on a Tuesday (9-7-21) - went to bed the evening after the vaccine at 6:00 pm - missed school the two next days - stayed in bed until Friday morning and was able to go to school but didn't feel fully recovered until Saturday. Gave Tylenol and Advil alternating every 4-8 hours to help with symptoms -

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: migraines and hypermobility syndrome
Andere Medikamente: -
Allergien: amoxicillin
Vorherige Impfungen: -

VAERS 1709224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 17.09.2021
Impfdatum: 13.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Aphasia CSF cell count normal Cerebral disorder Condition aggravated Diplopia Gait disturbance Magnetic resonance imaging head abnormal Speech disorder

Symptomtext

Technically symptoms had started 1 mo prior to vaccination, but patient was admitted to hospital for workup and treatment of these symptoms AFTER vaccination. He and his mom denies worsening of his symptoms after vaccination. Symptoms-- intermittent diplopia, speech/word finding difficulties, and gait instability (but no falls). MRI brain on admission was abnormal for patchy/nodular densities in multiple parts of the brain. He was hospitalized 9/14 (1 day after vaccination) for workup, and on 9/15 after significant workup sent, started on a 5-day course of high dose steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 6,0
Labordaten: MRI brain as described above. CSF studies nonrevealing thus far.
Aktuelle Erkrankungen: Symptoms had been happening for about 1 mo prior to admission to hospital (admission date 9/14). Symptoms were diplopia, word finding difficulties, and gait instability.
Vorgeschichte: scoliosis.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1704566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 16.09.2021
Impfdatum: 10.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Chest discomfort Condition aggravated Confusional state Decreased appetite Dyspnoea Fatigue Insomnia Mental fatigue Nausea Nervousness Peripheral coldness Tachycardia Tremor

Symptomtext

On Friday September 10, at 7:00 pm, I began having symptoms of anxiety which triggered shortness of breath , heaviness in chest. I been feeling nauseous, confused, body tremors, difficulty falling asleep, tachycardia, nervousness cold feet and hands, mental exhaustion, loss of appetite that have not subsided until this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: As of now I have not gone in person because I have no stamina, nor strength nor the will to go out because I am concerned of not being able to breathe if I travel away from home
Aktuelle Erkrankungen: tachycardia, anxiety, stress, fear of needles.
Vorgeschichte: Long covid lingering symptoms such as anxiety, tachycardia, stress shortness of breath and fatigue.
Andere Medikamente: Magnesium, vitamin C
Allergien: gluten sensitivity to carbs
Vorherige Impfungen: -

VAERS 1704503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 80,0
Geschlecht: F
Eingang: 16.09.2021
Impfdatum: 02.09.2021
Beginn: 02.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Full blood count Metabolic function test Pain in extremity Pyrexia Tachycardia Urinary incontinence Urine analysis

Symptomtext

Chills, Loss of Bladder control (5 episodes). Presented to the Emergency Room the following day and was found to febrile to 101 and tachycardic at 120 bpm. labwork was drawn, but pt did not want to wait in the emergency room. she presented to me 9/16/21 in follow up and reported that bladder issues resolved as did the fever. she developed Left arm pain the same day and it still feels weak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: CBC 9/3/21, CMP, UA
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Lymphoid Leukemia Fatty Liver MTHR mutation, homozygous
Andere Medikamente: Arimidex 1mg, Calcium, Vit C
Allergien: Alendronate, Actonel, Clindamycin, Cephalexin, Epinephrine, Penicillin, Sulfa
Vorherige Impfungen: -

VAERS 1700891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 15.09.2021
Impfdatum: 14.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain

Symptomtext

Health worker came in to report a dull pain to center area of chest. states it happened the day after 2nd dose Pfizer and lasted for about half hour. Pain was 3/10 and happened while at rest (sitting). No medication taken to alleviate pain. States that it went away on its own. He also rubbed his chest and states that it seemed to help. HCW states that not too long ago (sometime within the year) he was seen by his PCP and they had ruled out angina. HCW came in at approx. 1230 pm 9/15/21 and states he is not experiencing the pain and that it has subsided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: DM, HTN, High cholesterol
Vorgeschichte: DM, HTN, High cholesterol
Andere Medikamente: Lisinopril, Amlodipine, Terazosin, Metformin and a cholesterol medication that he is unable to recall the name.
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1697214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 14.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Adverse reaction Allergy to vaccine Auscultation Chest discomfort Chest pain Feeling abnormal Feeling hot Flushing Pharyngeal hypoaesthesia

Symptomtext

Situation 2/21/1962 Patient is here for first dose of covid vaccination Background History of hypertension Assessment Pt has completed a 60 minute-minute observation period with the following signs and symptoms of an adverse reaction: other - chest pain/pressure and throat numbness and flushing. Pfizer-BioNTech COVID-19 vaccine #1 in series administered. Action(s) taken: Other - Vital signs, MD evaluation, O2 2lnc Allergy to COVID-19 vaccine documented in Allergies activity: Yes Patient advised to discuss second dose considerations with a clinician 1339: Patient awake, alert, ambulatory, reporting mid chest pressure 8/10, and throat feeling "different," pt fanning herself and feeling hot. Denies SOB, nausea, dizziness, palpitations or any other symptoms. 1340: Pt taken to procedure. Pt is able to speak in full sentences. VS taken BP 174/106 HR 77 SpO2 97% RA RR 20. No angio edema, no rash, no reports of itching, BS clear to auscultation. Denies history of anxiety and states she has never had this pain before. Does report feeling nervous prior to getting vaccinated. Pt reports hx of HTN which she takes lisinopril 1/2 tab daily (she took today's dose), pt did not know dosage. 1342: BP recheck 172/99 HR 80. 1346: I have called Dr., incident to for the covid vaccine clinic, and given report. Received VO to transport pt to ER via ALS, read back completed. 1350: Pt now reporting pain is traveling to abdomen and is intermittent. Dr. notified. Received VO to administer O2 2lcn and aspirin 325 mg PO x 1 now. Readback completed. 1400: Pt is agreeable to being transported to ER via ambulance. Pt also reported she had taken aspirin this morning, she did not know the dose. Dr. notified and ordered to hold aspirin 325 mg PO x 1, read back completed. Pt placed on O2 2lnc. 1411: Called to request ambulance transportation to Hospital. 1414: Pt denies any chest pain or any other symptoms. BP 157/105 HR 78 SpO2 97% RA Recommendation/Action: 1440: Paramedics have arrived. Report given. While report was being given to paramedics pt stated she started having the chest pain 5 minutes after vaccine was administered and reported it 14 minutes after vaccine administration.

Weitere VAERSDATA-Felder

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

VAERS 1695235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 13.09.2021
Impfdatum: 13.09.2021
Beginn: 13.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Dizziness Fall Headache Nausea Pain in extremity Sitting disability Vomiting

Symptomtext

Patient became dizzy lightheaded, fell over, N&V, Headache pain 8/10. BP 179/102, HR 93, SaO2 100 %. Unable to sit up. Began to complain of chest pain 3/10 lt arm pain, called 911 for transport

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: denies any previous illness
Vorgeschichte: NA
Andere Medikamente: Prozac, unknown other meds
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1693414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: NJ
Alter: 32,0
Geschlecht: F
Eingang: 12.09.2021
Impfdatum: 09.09.2021
Beginn: 09.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Headache Migraine Pain in jaw Vision blurred

Symptomtext

severe headache with intermittent migraines, blurry vision, joint pain, jaw pain,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: none yet
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: unknown
Vorherige Impfungen: -

VAERS 1693229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 08.09.2021
Beginn: 08.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Dyspnoea Headache Hypoaesthesia oral Paraesthesia Paraesthesia oral Pharyngeal hypoaesthesia Pharyngeal paraesthesia

Symptomtext

At 1645 client she was feeling tingling in her nose, cheeks and legs. Client denied any allergies to medication/food/environment and denied any pertinent medical history or regular medication use. Client denied any shortness of breath (SOB), difficulty breathing, headache (HA), chest pain (CP), or numbness and tingling in mouth, lips or throat. Client ambulated to zero gravity chair without assistance or incidence. At 1647 a first set of vitals taken: BP 118/80, HR 88, RR 20, skin warm, dry and normal color for ethnicity, A&Ox4. Lead RN visualized client's oropharyngeal area and noted no swelling or redness, capillary refill <2 seconds. Client stated the numbness and tingling in her legs was resolving and stated she could, "swallow ok". At 1650 client stated tingling in her legs had subsided, she reported a decrease in the tingling of her nose and cheeks, stated the feeling was "minor" and rated it a 1/10. Client continued to deny SOB, CP, HA, dizziness and numbness or swelling of mouth, lips or throat. At 1655 vitals taken: BP 118/78, HR 78, RR 18, client states she, "feels better". At 1705 vitals taken: 118/76, HR: 76, RR 18, client stated tingling of legs, cheeks and nose had resolved. She denied any SOB, difficulty swallowing or breathing, denied CP, HA, and numbness of mouth, throat or lips. At 1710 client educated on ED precautions. Client verbalized understanding and ambulated away from the observation site on her own accord and with a steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None stated
Allergien: None reported
Vorherige Impfungen: -

VAERS 1689221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: WI
Alter: 40,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 10.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Dizziness Hypertension

Symptomtext

patient c/o dizziness at 10:45 Patient was noted to be hypertensive 168/101, VS monitored for an additional 15 minutes with improvement in BP 136/84 patient without further symptom development, released to home at 11:10

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none known
Vorgeschichte: BMI > 40
Andere Medikamente: albuterol 108 (90 Base) MCG/ACT inhaler Inhale 2 puffs into the lungs every 4 hours as needed for Shortness of Breath or Wheezing. cetirizine (ZyrTEC Allergy) 10 MG tablet Take 1 tablet by mouth daily. tiZANidine (ZANAFLEX) 4 MG tablet Take
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1685986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 33,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Blood pressure increased Cold sweat Condition aggravated Hyperhidrosis

Symptomtext

Client reported "sweating" to EMT. RN responded. The client ambulated and sat down in the anti-gravity chair. The client denied any other s/s of anaphylaxis. The client stated he "started sweating cold." RN provided the client with two cold packs, which the client placed underneath his arms in his armpits. Vitals obtained at 4:18PM were as follows: BP 168/99, HR 96, O2 98%. RN educated the client regarding elevated blood pressure. The client stated he was "feeling better." The client reported a history of anxiety and high cholesterol. The client was unsure the name of the medication he takes for high cholesterol. The client stated that when he experiences anxiety he "just tries to stay calm." The client denied a history of hypertension. The client was unsure of his normal blood pressure. At 4:21 the client requested water, RN provided him with a water bottle, and the client began drinking water. Repeat vitals obtained at 4:24PM were as follows: BP 171/99 and HR 92. The client denied any current symptoms. RN checked in with the client around 4:27PM. The client denied any current symptoms. The client stated he wanted to stay sitting in the anti-gravity chair for a little while longer. The client ambulated unassisted with a steady gait. The client was alert and oriented to person, place, time, and situation. Approximately around 6:45 PM RN asked the client if he was experiencing any symptoms. The client reported "sweating" and stated that he was "anxious for his wife." The client denied any other signs or symptoms at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Anxiety and high cholesterol
Andere Medikamente: Unknown
Allergien: -
Vorherige Impfungen: -

VAERS 1685345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fd0809

moderat

Staat: OR
Alter: 60,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 07.09.2021
Beginn: 08.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Cardiac disorder Chills Condition aggravated Pyrexia Respiratory disorder

Symptomtext

Chills from fever-like Heart muscle tighten (excessive caffeine effects) , difficult breathing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: In progress
Aktuelle Erkrankungen: Chills from fever-like/ Respiratory or heart muscle irregularity (excessive Caffein -like to the heart)
Vorgeschichte: Unknown
Andere Medikamente: None
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1683317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Balance disorder Chest discomfort Dizziness Dyspnoea Eye movement disorder Fall Feeling cold Hyperhidrosis Lacrimation increased Palpitations Paraesthesia Tremor Unresponsive to stimuli

Symptomtext

RN noted the client's husband asking the client if she was okay. RN responded to the client. RN noted the client seated in her seat but leaning forward. The client stated that her "heart is racing." The client reported a history of hyperthyroidism and stated that sometimes she feels her heart racing in the middle of the night. EMT responded. O2 was 99%. The client denied any shortness of breath or itching. The client reported shaking. RN noted shaking of the client's right hand. The client reported feeling "dizzy." RN left the scene to obtain the anti-gravity chair. RN responded with the anti-gravity chair. RN observed the client attempt to stand and fell back into the chair. No injury was noted by RN. RN responded. EMT prepared to assist the client into the anti-gravity chair. The client stood up partially, became unsteady, and EMT supported her into the anti-gravity chair. The anti-gravity chair was reclined to low-fowler's position. RN noted the client's eyes rolling back in her head and her head rolling to the side. The client was not verbally responsive for a few seconds. The client's husband responded. The client's husband said the client's current state was abnormal for the client. The client was oriented to person, place, time, but not situation. RN noted the client's speech was interrupted with periods of non-verbal responsiveness. RN activated EMS at 4:28PM. RN Responded. The client reported chest pressure to RN. The client and her husband denied any history of anxiety. The client reported history of allergy to "something blue." The client's husband stated the client has an allergy to contrast dye. RN inquired if the client's current symptoms felt similar to her previous reaction to contrast dye. The client said "no." The client was intermittently squeezing RN hand and telling RN about her day in incomplete sentences. The phrases included "cooked chicken and rice" and "for kids." RN noted the client arching her neck and back intermittently trying to adjust her position in the chair. The client reported chest pressure radiating into her abdomen. Denied feeling nauseas or the urge to defecate or urinate. RN noted tears in the client's eyes. Vitals obtained at 16:35PM were as follows: HR 104, O2 99%. The client reported tingling all over her face. The client requested to be sat up and reported "I can't breathe." RN noted the client's hand on her chest and the client gasping for breath. RN noted the client's cheek and ear were cold. The client stated she felt like she was sweating. RN recommended administration of Epinephrine per CoSD Emergency Life Support Manual. RN educated the client that she was about administer Epinephrine. The client was not verbally responsive. RN administered Epinephrine Injection, USP Auto-Injector 0.3mg into the anterolateral aspect of the right thigh at 4:37PM. RN noted the client verbally responsive. Client stated her breathing was improving. Chula Vista Fire Department assumed care at 4:38PM. RN was unable to administer Benadryl 50mg prior to the Fire Department assuming care. Client transported to. The exact time the client left the facility was not noted. VAERS completed. VAERS confirmation number.

Weitere VAERSDATA-Felder

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

VAERS 1682643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: UT
Alter: 56,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 01.09.2021
Beginn: 01.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood glucose normal Dizziness Dyspnoea Fatigue Labile blood pressure Pharyngeal swelling

Symptomtext

After receiving COVID-19 vaccine, patient experienced lightheadedness, dizziness, extreme fatigue, blood pressure was labile, throat swelling and shortness of breath. RRT called, patient was monitored, vitals taken, glucose monitored, O2 administered at 2 L/min. Pt reported feeling dizzy and fatigued, but other symptoms improved. No medication interventions noted. patient discharged and scheduled for 2nd COVID vaccine 9/20.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 9/1/21 - Glucose wnl
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Sulfa antibiotics
Vorherige Impfungen: -

VAERS 1680300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 13,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Dyspnoea Nausea Pain Vomiting

Symptomtext

Throwing up, body aches, nauseous, weakness and trouble breathing. It started about 1.5 hours after injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No test, given Zofran at urgent care at 8:42 on 9/7/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergic to a specific psych medication
Vorherige Impfungen: -

VAERS 1679396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Muscle spasms Tremor Unresponsive to stimuli

Symptomtext

At approximately 1318, security guard alerted facility staff that medical personnel are needed outside. At approximately 1318, 2 nurses responded to security and ran patient to outside. RN saw patient sitting inside vehicle in driver's seat. Patient's eyes were closed. Patient was unresponsive to verbal and physical stimuli. At approximately 1318, RN notified Lead RN. At 1319, RN activated EMS. Lead RN arrived on scene and assessed patient. Patient was responsive to verbal and physical stimuli. Patient was oriented to person, place, and situation. Patient denied itchiness, rashes, and difficulty swallowing. Patient's husband reported patient was driving out of parking space and patient asked "do your muscles hurt". Patient then parked car. Patient's left and right hands started "cramping" and "shaking". Patient then closed eyes and became unresponsive to verbal stimuli. Patient's husband alerted security guard and said he "needs to see a nurse". RN educated patient's husband on signs/symptoms of when to seek care, to follow up with primary care provider, and to sign up on v-safe. At approximately 1322 patient vomited on asphalt. At approximately 1325, paramedics arrived on scene and assumed care. At approximately 1345, patient transported to hospital for further care. At approximately 1345, patient left facility via ambulance.

Weitere VAERSDATA-Felder

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

VAERS 1678929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 03.09.2021
Beginn: 03.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Pharyngeal paraesthesia Vaccine positive rechallenge

Symptomtext

At approximately 1626, patient reported tingling of throat to RN. Patient denied difficulty breathing, difficulty swallowing, itchiness and rashes. RN offered to take vital signs. Patient denied vitals signs. RN offered diphenhydramine. Patient denied diphenhydramine. Patient reported "I'm fine". Patient given water. Patient able to drink water. Patient reported similar reaction to the first dose of Pfizer Covid Vaccine (LOT# EW0168, exp. 08/2021) administered on 08/10/21. Patient reported she felt the "same thing" and "didn't say anything". Patient reported it "felt like a panic attack starting". At 1634, RN reassessed patient. Patient reported "it didn't get any worse". Patient denied itchiness, rashes, difficulty breathing and difficulty swallowing. RN offered diphenhydramine. Patient denied diphenhydramine. RN offered to take vital signs. Patient denied vital signs. At 1642, RN reassessed patient. Patient reported the symptom had "gone down". Patient denied itchiness, rashes, difficulty breathing, difficulty swallowing. RN offered diphenhydramine. Patient denied diphenhydramine. RN offered to take vital signs. Patient denied vitals signs. At 1645, RN reassessed patient. Patient reported the symptom is "gone". Patient denied itchiness, rashes, difficulty breathing and difficulty swallowing. RN educated patient on signs/symptoms of when to seek emergency care, to follow up with primary care provider, and to sign up on v-safe. At 1647, patient left facility with steady gait and unlabored respirations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: Penicillin
Vorherige Impfungen: On 8/10/2021, patient received the first dose of Pfizer. Patient reported she felt "tingling of the throat" a "few minutes" afte

VAERS 1670633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: -
Alter: 12,0
Geschlecht: F
Eingang: 03.09.2021
Impfdatum: 02.09.2021
Beginn: 02.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chromatopsia Fall Headache Pallor Tinnitus Tremor Urinary incontinence

Symptomtext

Pt received the second dose of Pfizer Covid Vaccine (LOT# FD0809, exp. 10/2021) at 1602. At approximately 1606, patient fell from chair to the floor. RN turned patient onto her left side. RN observed minimal shaking for approximately 10 seconds. Patient opened her eyes and sat up. RN assessed patient. RN saw urine on the floor and noted pallor of the face. Patient was alert and oriented to person, place, situation and time. Patient stated "my head hurts". Patient reported 6/10 head pain. Patient reported "I heard my ears ringing" and "saw colorful stuff" before she fell. Patient's father reported patient has no history of seizures, no current medical conditions, and no current medications. At approximately 1607, EMT activated EMS. Patient denied seizures after the first dose of Pfizer (LOT# EW0187, exp. 08/2021) administered on 08/12/2021. At 1610, RN assessed patient vital signs: blood pressure 120/88 mmHg, pulse 101 beats/minute, and SpO2 99%. RN educated patient and patient's father on signs/symptoms of when to seek emergency care, to follow up with primary care provider, and to sign up on v-safe. At approximately 1620, RN reassessed patient. Patient reported 1/10 head pain. At 1622, EMS arrived and assumed care. At approximately 1635, patient was transported to a hospital for further care. At 1635, patient left facility with unlabored breathing.

Weitere VAERSDATA-Felder

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

VAERS 1663184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 36,0
Geschlecht: M
Eingang: 01.09.2021
Impfdatum: 28.08.2021
Beginn: 28.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Dizziness Dyspnoea Headache Paraesthesia Paraesthesia oral Pharyngeal paraesthesia Skin warm Vision blurred

Symptomtext

Client stated he was having blurry vision and mild dizziness, he denied any other symptoms such as chest pain (CP), shortness of breath (SOB), tingling or mouth, face or throat and headache (HA). Client was A&Ox4, skin normal color for ethnicity, warm and dry. Client denied any allergies to medications/foods/environment and stated that other than a fractured back 6 years prior for which he takes Advil and Tylenol as needed for pain, he had no other pertinent medical history or medication use. At 1048 a first set of vitals taken: BP 120/70, HR: 68, RR: 12. Client stated he was "feeling nervous" about receiving the vaccination. He ambulated to the zero gravity chair without assistance or incidence. Client stated last oral intake was the evening prior at dinner. He was given a juice and granola bar which he ate and drank. Client stated he felt, "warm and tingling" in the left arm, that his vision was improving and the dizziness was gone. He continued to deny SOB, CP, HA or tingling in mouth, throat and face. At 1057 a second set of vitals were taken: BP 120/80, HR 62, RR 16, A&Ox4, skin normal color for ethnicity, warm and dry. Client reported he was, "feeling much better". He denied having any CP, SOB, HA or tingling of mouth, throat, and face. At 1105 a third set of vitals were taken: BP 120/78, HR 62, RR 16, A&O x4. Client continued to deny SOB, CP, HA or any other symptoms. He stated symptoms of dizziness, arm tingling and blurry vision had resolved. Lead RN educated client on ED precautions and client ambulated away from the observation site on his own accord with a steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Advil, Tylenol as needed for pain
Allergien: None
Vorherige Impfungen: -

VAERS 1662601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 01.09.2021
Impfdatum: 31.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

Approximately 5 minutes after client's vaccine, he stated he needed water. Then he stated he was having trouble breathing. This lasted abut 20 seconds. The client then reported it had passed. Vitals taken. Observed for 30 minutes.

Weitere VAERSDATA-Felder

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

VAERS 1662238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: MN
Alter: -
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 31.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Pain Pyrexia Tachycardia

Symptomtext

Fever to 101.6F, chills, headache, body aches, tachycardia to 140

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Depression, hyperlipidemia, closed patent foremen ovale , GERD , obesity, anxiety
Andere Medikamente: Potassium, omeprazole, seroquel,asa, plavix,cymbalta,simvastatin,Wellbutrin,
Allergien: None
Vorherige Impfungen: -

VAERS 1656395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 30.08.2021
Impfdatum: 30.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Chest pain

Symptomtext

Client received the 1st COVID vaccine (Pfizer Lot # FD0809 expiration date 09/24/2021) at 1125. At 1140, client notified that she "felt two sharp pains on the left side of her chest. The pain came and went and only lasted a few seconds." Client denied SOB, dizziness, and current chest pain. Client was alert and oriented times four and skin was dry and appropriate to ethnicity. Vital signs taken at 1145 (blood pressure 101/80, oxygen 98%, heart rate 66). Client stated "I was anxious before and after receiving the vaccine today." Client denies any allergies, medical conditions, or current medications. They provided education to client on when to seek emergency services, and to follow up with her primary care provider. Client left the site at 1155 unassisted and with a steady gait.

Weitere VAERSDATA-Felder

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

VAERS 1638249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

moderat

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 26.08.2021
Beginn: 26.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Chest discomfort Dyspnoea Palpitations

Symptomtext

At 1841 client stated "I feel something in my heart." RN responded immediately. Client was already sitting on anti-gravity, alert and oriented x4. PHN arrived at 1842. First vitals at 1842: blood pressure 107/70, pulse 94, oxygen sat 98%. Client stated she "felt palpitations, some pressure on chest and shortness of breath for a few seconds." Client denied dizziness, headache, chest pain, or blurry vision. Mother was primary historian and stated this is normal for client with anything that involves pain. Mother stated client has very low tolerance to pain. Per Mother the symptoms client stated were "her normal course". Medical history of anxiety, medication: birth control, could not recall name at this time, and allergy to Keflex. At 1844 client stated chest pressure was improving. Client denied chest pain or shortness of breath. Client alert and oriented x4, answering all questions. Vitals at 1847: blood pressure 100/68, pulse 88, oxygen sat 99%. Per client, "feeling normal." Vitals at 1852: blood pressure 103/73, pulse 90, oxygen sat 99%. Per client "feeling fine." Vitals at 1902: blood pressure 98/65, pulse 82, oxygen sat 99%. Per client ready to stand and walk to observation area to meet rest of family. Client walked to observation area with steady gait. EMTstayed with client. Last vitals at 1912: blood pressure 99/61, pulse 85, oxygen sat 99%. EMT advised client and client's Mother on following up with medical provider and gave ER precautions. Client left facility with steady gait at 1915.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: anxiety, low tolerance to pain
Andere Medikamente: birth control, could not recall name and vitamins
Allergien: keflex
Vorherige Impfungen: -

VAERS 1637590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

moderat

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 25.08.2021
Beginn: 25.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Palpitations Throat tightness

Symptomtext

Patient reported sensation of throat closure and palpitations. Patient has history of A-fib and stroke. Patient given 50 mg of benadryl IM and improved until stable and discharged from facility.

Weitere VAERSDATA-Felder

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

VAERS 2000025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MA
Alter: 87,0
Geschlecht: M
Eingang: 23.09.2023
Impfdatum: 13.01.2021
Beginn: 23.09.2023
Tage bis Beginn: 983,0
Dosis: 3
Route/Site: UN / UN

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

Body temperature increased COVID-19 SARS-CoV-2 test positive Vomiting Productive cough Pyrexia

Symptomtext

Resident vomited x 1, temp of 102

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Covid Rapid test with Positive results.
Aktuelle Erkrankungen: Nontraumatic chronic subdural hemorrhage, Paroxysmal Atrial Fibrillation, Old Myocardial infarction, Atherosclerosis heart disease of native coronary artery without angina pectoris. hyperlipidemia, hypothyroidism. Alzheimer's disease with late onset, retention of urine, restlessness and agitation, vascular dementia, severity with behavioral disturbance, Vit B deficiency.
Vorgeschichte: see above
Andere Medikamente: Unknown
Allergien: Levofloxacin, Prevagen
Vorherige Impfungen: -

VAERS 2651112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MA
Alter: 54,0
Geschlecht: F
Eingang: 29.06.2023
Impfdatum: 15.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Nausea

Symptomtext

feeling yucky; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 56-year-old female patient received BNT162b2 (BNT162B2), on 15Dec2021 as dose 3 (booster), single (Lot number: FD0809) at the age of 54 years for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, LOT: ER8731), administration date: 15Apr2021, when the patient was 54-year-old, for COVID-19 immunization, reaction(s): "feeling yucky"; BNT162b2 (DOSE 2, SINGLE, LOT: EW0199), administration date: 08May2021, when the patient was 54-year-old, for Covid-19 immunization, reaction(s): "feeling yucky". The following information was reported: NAUSEA (non-serious), outcome "recovered", described as "feeling yucky". Additional information: Had three or 4 other injections prior and had no other side effects other than feeling yucky for a day but never had rashes. Clarified injections as all Pfizer COVID-19 Vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
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 2605744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: WI
Alter: 67,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 24.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered Pain in extremity Product preparation issue

Symptomtext

Patient was given 0.4ml of undiluted Pfizer vaccine. Patient contacted, denies any adverse or local effects, merely a sore arm for 1 1/2 days after receiving vaccine. No treatment needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Anxiety, fatigue
Vorgeschichte: Anxiety, Dorsalgia, Fatigue, Hyperlipidemia
Andere Medikamente: Sertraline, Venlafaxine, Lidocaine patches
Allergien: None
Vorherige Impfungen: -

VAERS 2585976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: SC
Alter: 62,0
Geschlecht: F
Eingang: 23.02.2023
Impfdatum: 05.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / RA

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

Dizziness Hypersomnia Lethargy Sleep apnoea syndrome

Symptomtext

very lethargic; sleep apnea; severe dizziness; slept many more hours than I normally do, in bed 12-14 hours after injection - normally 6-8 hours; 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 received BNT162b2 (BNT162B2), on 05Jan2022 at 13:00 as dose 3 (booster), single (Lot number: FD0809) at the age of 62 years intramuscular, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Osteoarthritis", start date: 01Jan2017 (unspecified if ongoing); "Spinal fusion" (unspecified if ongoing); "TKA Lt. Knee/TKA Rt. Knee" (unspecified if ongoing), notes: TKA Lt. Knee/TKA Rt. Knee. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Single time: 10:00 am, Anatomical site of injection: Right upper arm, Route of administration: Intramuscular, Batch\lot number: ER8733), administration date: 26Mar2021, for COVID-19 Immunization, reaction(s): "Severe dizziness", "Very lethargic"; BNT162b2 (Dose 1, Single time: 10:00 am, Anatomical site of injection: Right upper arm, Route of administration: Intramuscular, Batch\lot number: ER8733), administration date: 26Mar2021, for COVID-19 immunisation, reaction(s): "Sleep apnea", "Every time she bends over, if her head gets below her shoulders to pick something up she will black out", "Fever", "queasy", "everything in her body ached", "she had vertigo", "very tired"; BNT162b2 (Dose 2, Single, Anatomical site of injection: Right upper arm, Route of administration: Intramuscular, Batch\lot number: EW0158), administration date: 16Apr2021, for COVID-19 immunisation, reaction(s): "Very lethargic", "Severe dizziness", "Sleep apnea", "She fell asleep in her sunroom and got up around 3:00PM/ Went to bed early plus slept many more hours", "COPD", "She felt like she was on a boat/ she was not feeling", "had soreness in her arm", "has zero energy", "fever", "everything in her body ached ", "She felt like she was on a boat/ she was not feeling right". The following information was reported: LETHARGY (non-serious), outcome "unknown", described as "very lethargic"; SLEEP APNOEA SYNDROME (non-serious), outcome "unknown", described as "sleep apnea"; DIZZINESS (non-serious), outcome "unknown", described as "severe dizziness"; HYPERSOMNIA (non-serious), outcome "unknown", described as "slept many more hours than I normally do, in bed 12-14 hours after injection - normally 6-8 hours". Clinical course: After each injection, he experienced severe dizziness, very lethargic. Went to bed early and slept many more hours than he normally do. In bed 12-14 hours. After injection - normally 6-8 hours. He had been diagnosed with sleep apnea plus COPD since he had the injections. Sender's Comments: Linked Report(s): US-PFIZER INC-2021435489 same patient/drug, different dose/event; US-PFIZER INC-2021435657 same patient/drug, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Osteoarthritis; Spinal fusion; Total knee replacement (TKA Lt. Knee/TKA Rt. Knee)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2578155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: AL
Alter: 22,0
Geschlecht: F
Eingang: 08.02.2023
Impfdatum: 23.08.2021
Beginn: 21.04.2022
Tage bis Beginn: 241,0
Dosis: 2
Route/Site: IM / LA

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

Chills Discomfort Dysmenorrhoea Influenza like illness Menstrual disorder Menstruation delayed Nausea Pyrexia

Symptomtext

Late menstration cycle. Terrible cramps, deep pressure before menstration occurs, flu like symptoms with period that have never occurred before. Chills, fever, nausea right before menstration starts.

Weitere VAERSDATA-Felder

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

VAERS 2570123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NY
Alter: 35,0
Geschlecht: M
Eingang: 29.01.2023
Impfdatum: 02.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Blood test Inflammatory marker test Joint swelling

Symptomtext

Developed joint pain in both hands 5-7 days after second dose. Pain is worse in the left hand. Pain still ongoing since receiving vaccine. 1st dose got me into the Emergecy room due to sever headaches that lasted all day and night for several months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Blood work done at PCP to check inflammatory markers. Swollen around painful jount 4th digit. CT scan of head was done at a local hospital due to the headaches after first dose.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Joint pain in both hands 5-7 days after second done. 1st dose got me to the Emergeny room of a local HCF due to severe headaches that lasted several months.
Allergien: None
Vorherige Impfungen: -

VAERS 2557627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MN
Alter: 80,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 07.06.2022
Beginn: 31.10.2022
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia COVID-19 Diarrhoea Heart rate irregular SARS-CoV-2 test positive Sepsis

Symptomtext

Patient brought to the ED on 10/31 with generalized weakness that started the same morning. He lives at an assisted living facility, and the nurse checked his vitals and found that this heart was irregular so advised he come to the ED. Additionally the patient reported about 2 episodes of diarrhea per day for the past two weeks. In the ED, he was found to have a fever of 100.3 F and oxygen saturations at 88-90% on room air. He tested positive for COVID-19 by PCR. He was admitted to the hospital 10/31 - 11/3 for sepsis with COVID-19 infection resulting in acute diarrhea. Patient has received the primary vaccine series and two boosters.

Weitere VAERSDATA-Felder

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

VAERS 2549066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MI
Alter: 40,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 30.12.2021
Beginn: 28.12.2022
Tage bis Beginn: 363,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Ear pain Malaise Paranasal sinus discomfort Respiratory symptom SARS-CoV-2 test positive

Symptomtext

12/28/2022 in the morning participant woke up not feeling well with upper respiratory symptoms. Tested positive on an at home COVID-19 test. Televisit with doctor. Doctor prescribed PAXLOVID, but not able to take due to medication interference. Advised to treat symptomatically. Symptoms gradually eased and felt better. 12/30 experienced bad sinus pressure and ear pain. Consulted with doctor again who advised decongestant. Symptoms continue to diminish, but still lingering. Participant has not recovered yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Tested positive on an at home COVID-19 test 12/28.
Aktuelle Erkrankungen: No
Vorgeschichte: Hashimoto's; Bipolar
Andere Medikamente: SEROQUEL; TEGRETOL; ARMOUR THYROID; ADDERALL XR; WELLBUTRIN XL; VALTREX
Allergien: Mushroom
Vorherige Impfungen: -

VAERS 2533201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: FL
Alter: 51,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 07.12.2021
Beginn: 28.03.2022
Tage bis Beginn: 111,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test abnormal Chemotherapy Leukaemia Neck pain White blood cell count increased

Symptomtext

I started feeling some neck pain for three tests so I went to urgent care and a blood test showed a high white blood count a few days later leukemia was diagnosed. I have started Chemotherapy for eight months and treatments at home and this is the current standing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: Blood tests diagnosis was Leukemia
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2520109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MD
Alter: 31,0
Geschlecht: M
Eingang: 30.11.2022
Impfdatum: 29.11.2021
Beginn: 01.08.2022
Tage bis Beginn: 245,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Feeling abnormal Malaise Oropharyngeal pain Pain in extremity Pyrexia SARS-CoV-2 test positive Sleep disorder

Symptomtext

After receiving the vaccine, I had a fever, chills and pain in the arm for about 60 hours. On 08/01/2022, I started not feeling well with a sore throat that got progressively worse for the next two days. On 08/03/2022 I tested positive with a home test for COVID-19. I contacted my doctor's office and talked to the nurse practitioner who is in charge of the COVID-19 cases. I took an analgesic to help with my symptoms and rested. As of today, I continue to have brain fog and my sleep cycle is off. If I am exhausted, I can fall asleep easy. When I try to go to bed for the night, I'm wide awake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 03AUG2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2492579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: -
Alter: 24,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 14.09.2022
Beginn: 20.10.2022
Tage bis Beginn: 36,0
Dosis: 1
Route/Site: IM / RA

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

Angina pectoris Arthralgia Pain in extremity

Symptomtext

Slight pain in wrists, toes, fee, ankles, fingers; sharp pain in heart

Weitere VAERSDATA-Felder

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

VAERS 2486899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 14.12.2021
Beginn: 16.10.2022
Tage bis Beginn: 306,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Chest X-ray normal Fall Malaise SARS-CoV-2 test positive Urine analysis abnormal

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 10/16/2022 Discharge Date: Oct 17, 2022 PRESENTING PROBLEM: Weakness [R53.1] COVID-19 virus detected [U07.1] HOSPITAL COURSE: 88 y.o. female with PMH Endometrial Ca s/p TLH/BSO, cognitive impairment presented with weakness. In emergency department patient saturating well on room air, hemodynamically stable. Lab significant for COVID-19 positive PCR, urinalysis with 15 squamous cells, chest x-ray negative for acute abnormality. Patient was given 1 L IV fluid bolus. Patient admitted for weakness, recurrent falls and likely placement following PT OT evaluation and care management evaluation. Continue him monitor COVID-19 symptoms for progression. Patient stayed in hospital for approximately 24 hours. Patient was monitored and did well. Stable throughout the 24 hours of stay without any episodes of hypoxia or fevers. PTOT evaluation completed and recommended home health care. With patient stable and home safety confirmed, patient was discharged home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis Cognitive impairment Advanced care planning/counseling discussion COVID-19 virus detected
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet Dextromethorphan HBr (VICKS DAYQUIL COUGH PO) ibuprofen (MOTRIN) 200 MG tablet
Allergien: Ami-texRash Bactrim [Sulfa Drugs]Nausea and Vomiting LatexSwelling, Other, Rash ProcaineOther, Palpitations Sulfamethoxazole W-trimethoprimRash
Vorherige Impfungen: -

VAERS 2485583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MN
Alter: 59,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 18.10.2021
Beginn: 19.08.2022
Tage bis Beginn: 305,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Exposure to SARS-CoV-2 Fatigue Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On day one, I had a runny nose, sinus drainage, and a sore throat. I took a COVID-19 test due to exposure. The result was negative. It felt like seasonal allergies. The next day, the symptoms continued, but they increased in severity. I took another COVID-19 test. The result was positive. On day three, I called the clinic line and left a message for my doctor detailing symptoms and test result. On day four, I was given a prescription for Paxlovid. I started the meds that night. That day, I noticed I was more tired than usual. I finished the prescription. My symptoms didn't get worse while taking it. I went back to work the following Monday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 08/19/2022 At Home COVID-19 Test - Negative; 08/20/2022 At Home COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes; GERD
Andere Medikamente: Atorvastatin; Pantoprazole; Baby Aspirin; Magnesium; Vitamin C; Vitamin D; Cetirizine; Metformin; Victoza
Allergien: Seasonal; Penicillin; Amoxycillin; Sulpha Drugs
Vorherige Impfungen: -

VAERS 1894923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac monitoring Chest discomfort Dizziness Hypoaesthesia oral

Symptomtext

Patient reported that her chest was feeling tight and she was feeling dizzy. The tightness in her chest persisted and got worse. Patient then reported that her tongue went numb. Vital signs were taken and all WNL. EMS were called and paramedics assessed her, including heart monitoring. Patient was sent to the ER for further treatment and observation. She remained alert and conscious the entire time.

Weitere VAERSDATA-Felder

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

VAERS 2471969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: FL
Alter: 90,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 19.10.2021
Beginn: 29.09.2022
Tage bis Beginn: 345,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dizziness SARS-CoV-2 test positive

Symptomtext

Hospitalization: 9/29/2022 - 10/4/2022 Presentation to the ED: DIZZINESS. COVID-19 + date: 9/29/22. Treatment: NO TREATMENT SPECIFIC TO COVID. Discharge to: HOME W/ HEALTHCARE SERVICES.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM T2, GERD, AFIB.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2471969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: FL
Alter: 90,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 19.10.2021
Beginn: 29.09.2022
Tage bis Beginn: 345,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Dizziness SARS-CoV-2 test positive

Symptomtext

Hospitalization: 9/29/2022 - 10/4/2022 Presentation to the ED: DIZZINESS. COVID-19 + date: 9/29/22. Treatment: NO TREATMENT SPECIFIC TO COVID. Discharge to: HOME W/ HEALTHCARE SERVICES.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM T2, GERD, AFIB.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2467146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: LA
Alter: 65,0
Geschlecht: M
Eingang: 03.10.2022
Impfdatum: 30.09.2021
Beginn: 01.03.2022
Tage bis Beginn: 152,0
Dosis: 3
Route/Site: - / RA

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

Laboratory test Ligament pain Magnetic resonance imaging Myalgia Spondylitis Tendon pain

Symptomtext

I started experience muscle, ligament and tendon pain in March of 2022. I went to to see my Primary Care Physician. He ordered many test that were inconclusive. I was referred to a Rheumatologist who ordered test, including a MRI the diagnosis is Axial Spondyloarthritis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ligament pain
Hospital-Tage: -
Labordaten: MRI
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2422843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 29.08.2022
Impfdatum: 30.12.2021
Beginn: 20.08.2022
Tage bis Beginn: 233,0
Dosis: 2
Route/Site: UN / UN

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

Chills Myalgia Oropharyngeal pain

Symptomtext

chills, sore throat, myalgias

Weitere VAERSDATA-Felder

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

VAERS 2407311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CO
Alter: 55,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 10.05.2022
Beginn: 27.07.2022
Tage bis Beginn: 78,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia COVID-19 Diarrhoea Fatigue Feeling abnormal Feeling hot Hypersomnia Impaired work ability Nausea Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

On July 26, 2021 I had a mild sore throat and fatigue, did a home test and was negative. At 3 am on the 27th of July, I woke up and felt worse, achy, hot, took a home test and was positive. I also took a PCR test and was positive. For the next few days I slept a lot, had a mild fever of 99-100 degrees, achy, fatigue. I contacted my doctor and she prescribed Paxlovid, which I took the full course. It caused some nausea and mild diarrhea. After 5 days I was cleared to go back to work, still felt tired and fatigued, but no other symptoms. I tested positive on a home test on day 6, and negative on a home test on day 8. I am now feeling well and have my energy back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 7/27 positive home covid test (ihealth brand, lot number 20211126 positive PCR test at facility on 7/27 (results received 2 days later)
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: vitamin d 7,000 units
Allergien: no
Vorherige Impfungen: -

VAERS 2338938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MN
Alter: 87,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 27.11.2021
Beginn: 30.05.2022
Tage bis Beginn: 184,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Cough Malaise Pyrexia

Symptomtext

Patient seen in the emergency department on 5/30 for generalized weakness, rigors, fever, cough, and malaise. She has medical history of CKD. Patient admitted to the hospital from 5/30-6/4. This meets criteria for VAERS reporting.

Weitere VAERSDATA-Felder

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

VAERS 2335272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: UT
Alter: 62,0
Geschlecht: F
Eingang: 25.06.2022
Impfdatum: 09.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Joint range of motion decreased Joint swelling Joint warmth

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Physician). A 62-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Jun2022 as dose 3 (booster) , single (Lot number: FD0809) at the age of 62 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "lichen sclerosis et atrophicus" (unspecified if ongoing); "osteoarthritis" (unspecified if ongoing); "atrophic vaginitis" (unspecified if ongoing); "penicillin" (unspecified if ongoing), notes: known allergies: dairy, codeine, penicillin, scallops; "scallops" (unspecified if ongoing), notes: known allergies: dairy, codeine, penicillin, scallops; "known allergies: dairy" (unspecified if ongoing), notes: known allergies: dairy. Concomitant medication(s) included: COMBIPATCH; CLOBETASOL; METRONIDAZOLE; VIT D [VITAMIN D NOS]; CALCIUM; PATANOL. Past drug history included: Codeine, reaction(s): "known allergies: codeine", notes: known allergies: dairy, codeine, penicillin, scallops. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer), for Covid-19 Immunization. The following information was reported: JOINT RANGE OF MOTION DECREASED (non-serious) with onset 16Jun2022 at 03:00, outcome "unknown", described as "joint motion limitation"; JOINT SWELLING (non-serious), JOINT WARMTH (non-serious) all with onset 16Jun2022 at 03:00, outcome "unknown" and all described as "joints very painful, hot, swollen"; ARTHRALGIA (non-serious) with onset 16Jun2022 at 03:00, outcome "unknown", described as "severe arthralgia/ joints very painful". The events "severe arthralgia/ joints very painful", "joint motion limitation" and "joints very painful, hot, swollen" required physician office visit. Therapeutic measures were not taken as a result of arthralgia, joint range of motion decreased, joint swelling, joint warmth. Additional information: No other vaccine in four weeks: No If other vaccine in four weeks. No covid tested prior or post vaccination. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : PFIZER INC-202200887057 Same patient and drug, different event;

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to animal (known allergies: dairy, codeine, penicillin, scallops); Atrophic vaginitis; Food allergy (known allergies: dairy); Lichen sclerosis atrophicus; Osteoarthritis; Penicillin allergy (known allergies: dairy, codeine, penicillin, scallops.)
Andere Medikamente: COMBIPATCH; CLOBETASOL; METRONIDAZOLE; VIT D [VITAMIN D NOS]; CALCIUM; PATANOL.
Allergien: -
Vorherige Impfungen: -

VAERS 2329436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 23.06.2022
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Feeling abnormal Headache

Symptomtext

Headache in the frontal lobe region of head lasting about 1 week in duration with episodic headaches throughout entire head lasting approximately 2-4 hours in duration for the next 3 weeks. Physical sensation of ?cloudiness? throughout the head associated with the headache described above. The ?cloudiness? lasted about 1 week starting 11/17/2021.

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

VAERS 2328392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: TN
Alter: 45,0
Geschlecht: M
Eingang: 23.06.2022
Impfdatum: 24.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: - / LA

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

Blood test Rash

Symptomtext

I have rash that keeps spreading on my face, it is limited to my face only, it started 2 weeks after I got my Booster shot; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old male patient received BNT162b2 (BNT162B2), on 24Nov2021 as dose number unknown (booster), single (Lot number: FD0809, Expiration Date: 31Jan2022) at the age of 45 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Primary immunization completed; Manufacturer unknown), for COVID-19 Immunization. The following information was reported: RASH (non-serious) with onset Dec2021, outcome "not recovered", described as "I have rash that keeps spreading on my face, it is limited to my face only, it started 2 weeks after I got my Booster shot". The event "i have rash that keeps spreading on my face, it is limited to my face only, it started 2 weeks after i got my booster shot" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash. Additional information: The patient called and stated that he was trying to narrow down, he have gone to his family doctor, have gone to dermatologist, also have gone to an allergist and he have this rash that keeps spreading on his face, it was limited to his face only and they all told me to contact Pfizer, it has been ongoing since Dec, but it started 2 weeks after he got Booster shot (Pfizer COVID-19 Vaccine) and nothing else that he tried it was helping and they recommended to contact Pfizer to see if there was anything in there that he might be allergic to or it was because of his immune system to act funky and cause the outbreak or they could tell him what was it. When asked for any treatment for the event occurred the patient stated, "Yes, he was doing the treatment, but it was not working, so the treatment medicine was Itraconazole". When asked for any other medication conditions or taking any concomitant medications, the patient stated, "At this time no". When asked for any laboratory test, the patient stated, "Yes, he did have blood work done on 02Jun2022 in the beginning of Jun this month, so about 3 weeks ago".

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Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Date: 20220602; Test Name: blood work; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2324211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 20.06.2022
Impfdatum: 02.02.2021
Beginn: 12.06.2022
Tage bis Beginn: 495,0
Dosis: UNK
Route/Site: IM / LA

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

Abdominal distension Abdominal pain upper COVID-19 Cough Infrequent bowel movements Intestinal obstruction Nausea SARS-CoV-2 test positive Sinus disorder Vomiting

Symptomtext

2 nights ago tested positive for covid on a home test. Saturday morning started vomiting. Cough and sinus. vaxxed and boosted.Tested at home and positive for COVID 6/11. Began having nausea and vomiting yesterday into this am, no diarrhea, no BM for a few days Today, his upper abdomen became more swollen and painful so presented to the ED States had bowel obstruction due to colon cancer, had "18 inches" of colon removed Had followup colonoscopy 4.5 years ago and told needs repeat in December of this year. Discharged on 06/16/2022

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Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 28.08.2021
Beginn: 28.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Dizziness Fear Impaired driving ability Refusal of vaccination Vertigo

Symptomtext

Client 53 y/o, female, , presented as a walk in to the vaccination site on 06/17/2022. The client appears alert and oriented x4, no visible s/ sx of illness, no symptoms nor allergies reported, cooperative, friendly, talkative and well dressed. Client reported to have experienced severe dizziness (lightheaded) after around ~15 minutes from her discharge from the clinic after her 2nd shot of Pfizer lot # FD0809 given on 08/28/2021. She experienced sudden dizziness while drive home after discharged from clinic (aprox. ~45-60 minutes from the given Pfizer 2nd shot). She recalls that she felt scared while driving home and was able to make it home safely. Her son, an EMT, help her get into the house and called 911 due to her dizziness "it felt like the room was spinning". Client mentioned that she refused hospitalization. Client reports a medical hx of: Allergies, asthma, TIA (01/1999), Myocarcinoma (2003), migranes, high cholesterol, Surgeries: sinus, tonsillectomy, tumor. Current Rx.: EpiPen, Buproprion, Statins, Inhalers: Fluvent and albuterol, Claritin. RN consulted site's supervisor RN. RN submitted a medical consult via text to Dr. at 12:54 pm on 6/17/2022 to inquire on approval to proceed with COVID Booster. Dr. approved at 12:55 pm to proceed with the booster shot for the client. RN informed the client and vaccinator of the approval immediately. The patient seemed hesitant and reported some anxiety. RN offered to give client extra time to ask questions, read paperwork on vaccine information , reactions and side effects, and suggested to consult with her PCP. The vaccinator RN: proceeded to continue with the intake questionnaire, gather paperwork, educated client and provided information regarding side effects, allergic reactions, and when to seek medical care or 911 and to register with V-Safe. prepare client for administration. The client was given time to read the CDC Vaccine information. The client decided to leave the clinic and to consult her PCP before her 1st booster and walked out the clinic at 13:20 showing no s/sx of acute distress, alert and orientedrnted x4, talkative, no reporting any s/sx, and smiling.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: High cholesterol, anxiety, cancer (2003), TIA (1999), allergies, asthma,
Vorgeschichte: asthma,
Andere Medikamente: Statins, EpiPen, Claritin, Albuterol inhaler, Fluvent inhaler, Bupropion
Allergien: Environmental allergies, dust, pets, sulfa, iodine contrast,
Vorherige Impfungen: -

VAERS 2315060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 18.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Pain in extremity

Symptomtext

First Booster dose: Arm hurt/Second Booster Dose: Arm hurting; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP), Program ID. The reporter is the patient. A 45-year-old female patient received BNT162b2 (BNT162B2), on 18Nov2021 as dose 3 (booster), single (Lot number: FD0809) at the age of 45 years, in right arm for covid-19 immunization. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (First dose: 20Mar2021, lot: ER2613, NDC: Unknown , expiration: unknown, route of administration: upper right arm), administration date: 20Mar2021, when the patient was 44-year-old, for COVID-19 Immunization; BNT162b2 (second dose: 10Apr2021 , lot: ER8731, NDC: unknown, expiration: unknown , route of administration: upper right arm), administration date: 10Apr2021, when the patient was 44-year-old, for COVID-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "recovering", described as "First Booster dose: Arm hurt/Second Booster Dose: Arm hurting". Additional information: it was noted that after the second booster dose, the arm hurt; it barely hurt as of the reporting, however if the shoulder is raised up, the arm pain would be felt. Otherwise, it was not bothersome. If moves arm really high would only be doing it to find out if arm hurts or not. Arm hurting was improving.

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Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NJ
Alter: 29,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 02.12.2021
Beginn: 30.05.2022
Tage bis Beginn: 179,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Headache Oropharyngeal pain Pain Productive cough Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Started having symptoms on 5/30/22. Tested positive for COVID-19 on 6/1/22. I had a very sore throat, feverish, chills, body aches, headaches, congestion, nasal drip, phlegm, and a cough. The cough is productive. I am still dealing with these symptoms at this time.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Rapid COVID-19 Test- Negative- 5/31/22; Rapid COVID-19 Test- Positive- 6/1/22
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Fibromyalgia; Endometriosis; Migraines
Andere Medikamente: Albuterol; Elderberry; Turmeric; CBD
Allergien: Amoxicillin; Ciprofloxacin; Seasonal Allergies
Vorherige Impfungen: -

VAERS 2306942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: WA
Alter: 28,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 01.12.2021
Beginn: 25.04.2022
Tage bis Beginn: 145,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Nasal congestion Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Sinus congestion Sinus operation Sneezing Vaccine breakthrough infection

Symptomtext

Breakthrough case of Covid - Sx began on 04/25/2022. I woke up with a very sore throat and was coughing throughout the day. The following day I was quite tired, had a sore throat and coughing continued. On 05/27/2022 I tested positive on a home rapid antigen test. I had a sore throat, I was fatigued, sneezing and had a runny nose, this continued for several days including sleeping a lot with a stuffy nose. I was not eligible to take Paxlovid. My sx started to relieve around 05/04/2022. I was feeling mostly better, sore throat and cough dissipated and I was still having fatigue, sinus drainage and congestion. On 05/12/2022 I saw my doctor and was prescribed a nasal spray. These were resolved by about 05/20/2022. I still have some fatigue, it is not affecting work, but still noticeable.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 05/27/2022 - tested positive on a home rapid antigen test.
Aktuelle Erkrankungen: No
Vorgeschichte: Herniated disc for about a year, polycystic ovulary syndrome
Andere Medikamente: Vitamin D3, Woman's multi Vitamin
Allergien: Tree pollen
Vorherige Impfungen: -

VAERS 2303849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: OR
Alter: 60,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Axillary pain Lymphadenopathy Skin tightness Swelling Tenderness

Symptomtext

A few hours after receiving my booster, I started having significant right armpit pain. This was the same arm that I had received the booster. My inner armpit lymph nodes started swelling up a great deal, and the skin felt very tight and very painful to the touch. My armpit pain and swelling lasted for several weeks, and was quite intense for 3 weeks before very slowly going down. I did not experience this symptom on my first two shots

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Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: I did not seek medical attention because I figured there was nothing they could do.
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: 20mg citalopram 5mg rosuvastatin calcium
Allergien: Sulfa drugs Slight shellfish when peeling raw
Vorherige Impfungen: -

VAERS 2303174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MD
Alter: 76,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 30.10.2021
Beginn: 17.04.2022
Tage bis Beginn: 169,0
Dosis: 3
Route/Site: - / -

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

Gait inability Pain in extremity Weight Weight decreased

Symptomtext

onset severe pain in her left foot and until now she is still unable to walk/ Very abrupt onset of severe pain in left foot; Unable to walk; when went in hospital caller was 195 pounds and is probably considerably less than that now; 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 76-year-old female patient received BNT162b2 (BNT162B2), on 30Oct2021 as dose 3 (booster), single (Lot number: FD0809) at the age of 76 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "Heart disease", start date: 16Feb2016 (ongoing), notes: heart disease Major health condition is heart disease. Had three stents placed on 16Feb2016.; "Cancer", start date: 2013 (unspecified if ongoing), notes: Cancer Clear of cancer, diagnosed with 9 years ago. There were no concomitant medications. Vaccination history included: BNT162b2 (Second dose: 09Feb2021, lot: EL3247, NDC: Unknown , expiration: unknown, Route of administration: arm, doesn't remember if left or right arm, Caller had no reaction where administered, second dose.), administration date: 09Feb2021, when the patient was 75-year-old, for Covid-19 immunization; BNT162b2 (First dose: 19Jan2021 , lot: EL0142, NDC: Unknown , expiration: Unknown , Route of administration: arm, doesn't remember if left or right arm), administration date: 19Jan2021, when the patient was 75-year-old, for Covid-19 immunization. The following information was reported: GAIT INABILITY (caused and prolonged hospitalization) with onset 17Apr2022, outcome "not recovered", described as "Unable to walk"; PAIN IN EXTREMITY (caused and prolonged hospitalization) with onset 17Apr2022, outcome "not recovered", described as "onset severe pain in her left foot and until now she is still unable to walk/ Very abrupt onset of severe pain in left foot"; WEIGHT DECREASED (non-serious) with onset 17Apr2022, outcome "unknown", described as "when went in hospital caller was 195 pounds and is probably considerably less than that now". The patient was hospitalized and prolonged hospitalization for pain in extremity, gait inability (start date: 17Apr2022, discharge date: 28Apr2022, hospitalization duration: 11 day(s)). The events "onset severe pain in her left foot and until now she is still unable to walk/ very abrupt onset of severe pain in left foot" and "unable to walk" required emergency room visit. The patient underwent the following laboratory tests and procedures: Weight: (17Apr2022) Less, notes: when went in hospital caller was 195 pounds and is probably considerably less than that now. Therapeutic measures were taken as a result of pain in extremity, gait inability. Clinical course: Patient had the Pfizer COVID-19 Vaccine first, second and booster dose. Patient experienced an onset severe pain in her left foot and until now she is still unable to walk. Patient stated that she was hospitalized for 12 days with morphine, and after that her foot continues to be swollen and she can't walk. Patient wanted to know if this adverse reaction was reported before? Patient stated that there is no definitive diagnosis as to what could have caused that, and patient wanted to make this report to help people in case someone else had this adverse reaction. Time the vaccination was given: First dose: unknown, second dose: scheduled through hospital on 09Feb2021 at 13:00, but was not given at that exact time, reported and stood in line at 1300 to receive second dose, booster dose: unknown. Anatomical Location of Administration of Pfizer vaccine considered as suspect: arm, doesn't remember if left or right arm. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Pain in extremity
Hospital-Tage: 11,0
Labordaten: Test Date: 20220417; Test Name: weight; Result Unstructured Data: Test Result:Less; Comments: when went in hospital caller was 195 pounds and is probably considerably less than that now
Aktuelle Erkrankungen: Heart disease, unspecified (heart disease Major health condition is heart disease. Had three stents placed on 16Feb2016.)
Vorgeschichte: Medical History/Concurrent Conditions: Cancer (Cancer Clear of cancer, diagnosed with 9 years ago.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2295942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: VA
Alter: 62,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 05.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Fatigue

Symptomtext

fatigue/ felt a little fatigued; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID: A 62-year-old female patient received BNT162b2 (BNT162B2), on 05Nov2021 as dose 3 (booster), single (Lot number: FD0809) at the age of 62 years, in left arm for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (First Dose:, LOT: EJ1686, NDC, EXP: Unknown), administration date: 14Jan2021, when the patient was 61-year-old, for Covid-19 immunization; BNT162b2 (Second Dose:, LOT: EL8982, NDC, EXP: Unknown), administration date: 04Feb2021, when the patient was 61-year-old, for Covid-19 immunization. The following information was reported: FATIGUE (non-serious), outcome "unknown", described as "fatigue/ felt a little fatigued". Additional information: Caller is calling on behalf of his wife (patient), who received the second Pfizer Covid-19 booster dose. Caller wants to know the "initial period after receiving the vaccine" if there is a greater risk for putting down the immune system and mentioned caller's wife is working in a facility as a Physical Therapist. Caller mentioned his wife experienced fatigue 48 hours after the second booster shot. Caller wants to know if these will affect her wife's immune response. Caller states that the "immune system engage the vaccine causing immunity to drop" and a day or two after getting booster dose, Does her (wife) immune response drop, while pushing the immune system to make antibodies. The caller is asking if the vaccine would weaken their immune system since his wife is working at a hospital and is being exposed to Covid-19, with a lot of patients. Caller stated they have already received their first vaccines are supposed to be going to get their second booster dose. Caller states that it is really a kind of simple question. There are a lot of people there who have had it and she has been dealing with people every day who have it. Caller stated that he knows that when they first get the vaccines, that are mrna vaccines, and in this case, would be the booster, there is a period of a day or two when the person might feel a little funk and that varies from person to person. It is engaging the immune system to build antibodies for the disease. Caller stated, his wife was concerned about the time during that period, the 3 days after the booster shot, or something like that. Asked is her immunity to Covid reduced and Is the immunity reduced for that couple of days before everything kind of comes back and she is feeling back to normal. He stated that it is a really weird question and in so many instances, people get the booster shots and 2 or 3 days later, they test positive for Covid, It just ends up happening to some people within those first couple of days. They got their first booster, and his wife is over 60. There is that period of time where the immune system is being engaged and she might have felt a little fatigued and had a little side effect because the immune system is being engaged, to produce antibodies. During that period of time, during tomorrow or Wednesday, is she at greater risk during that time, while it puts down the immune system after taking the vaccine. Clarified that the caller's wife took the first 3 doses of the Pfizer Covid-19 vaccine. He states they are going for their second booster this afternoon. Description of Product Complaint: Caller stated that in so many instances, people get the booster shots and 2 or 3 days later, they test positive for Covid. Product strength and count size dispensed was not provided. Additional lot numbers were Unknown. sample of the product available to be returned was not provided. Packaging sealed and intact was not provided

Weitere VAERSDATA-Felder

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

VAERS 2294586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CO
Alter: 60,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 23.11.2021
Beginn: 15.05.2022
Tage bis Beginn: 173,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Respiratory tract congestion SARS-CoV-2 test positive Taste disorder

Symptomtext

Postive Covid Test/treated with Paxlovid on 3 day after test/Negative test on 5/25/22. Symptoms-cough, fatigue, congestion, off taste in mouth

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 1 Diabetes
Andere Medikamente: Levothyroxine, Atrovastatin, Insulin Lispro
Allergien: None
Vorherige Impfungen: -

VAERS 2279001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NJ
Alter: 47,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 03.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / RA

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

Allergy test Blood test Chiropractic Pruritus Rash Rash erythematous Rash macular Toxicologic test

Symptomtext

Extreme rashes and itchiness lasting about 4 months. These were from scalp to toe, different parts of the body had rashes, but they were not connected rashes. Red bumps that came and went. Under arms had blotches. For a few days ears, eyes and cheeks displayed the rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Ran detox panel, allergy panel, chiropractic maneuvers and blood work.
Aktuelle Erkrankungen: Cold
Vorgeschichte: No
Andere Medikamente: Multivitamin; low estrogen birth control
Allergien: Penicillin; nickel; wheat; ragweed; dust mites
Vorherige Impfungen: -

VAERS 2267433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CT
Alter: 68,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 11.11.2021
Beginn: 05.05.2022
Tage bis Beginn: 175,0
Dosis: 3
Route/Site: SYR / UN

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

Asthenia Diarrhoea Mental status changes SARS-CoV-2 test

Symptomtext

mental status changes, diarrhea, weakness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 4,0
Labordaten: rapid test
Aktuelle Erkrankungen: none stated
Vorgeschichte: hydrocephalus, back injury, joint pain, Alzheimer's early onset, hyperlipidemia
Andere Medikamente: unavailable
Allergien: dog hair
Vorherige Impfungen: -

VAERS 2265004

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Musculoskeletal stiffness Periarthritis Rotator cuff syndrome X-ray limb abnormal

Symptomtext

The next day 11/6/2021, my left shoulder got stiff and seemed to painfully lock up. This lasted for 2 solid weeks, so my Dr. sent me for an X-ray and it showed that I have an Impingement. I'm currently going to Physical Therapy. The 10 sessions I've had now has really helped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D3, Fish Oil, Multivitamin, Biotin, Iron, Calcium
Allergien: None
Vorherige Impfungen: -

VAERS 2264721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CT
Alter: 86,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 12.11.2021
Beginn: 05.05.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

Routine testing identified Covid, low grade fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Rapid test.
Aktuelle Erkrankungen: None reported
Vorgeschichte: Pacemaker; AFib; Hyperlipidemia; Macular degeneration; Sarcoidosis; Osteopenia; Cognitive impairment.
Andere Medikamente: Atenolol; Atorvastatin Calcium; Donepezil HCL; Eliquis; Vitamin D3.
Allergien: NKA
Vorherige Impfungen: -

VAERS 2261821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MD
Alter: 58,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 01.12.2021
Beginn: 03.04.2022
Tage bis Beginn: 123,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Eye pruritus Nasal congestion Pyrexia SARS-CoV-2 test positive Throat irritation

Symptomtext

Nasal congestion, scratchy throat, itchy eyes, a very low fever never over 100.3. Mild in severity and lasted 4 or 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pruritus
Hospital-Tage: -
Labordaten: At home COVID-19 test - positive.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Nexium, Magnesium, Fish oil, D3, Cinnamon, Cholestoff
Allergien: No
Vorherige Impfungen: -

VAERS 2258936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: GA
Alter: 31,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 20.11.2021
Beginn: 02.02.2022
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Cough Exposure during pregnancy Fatigue Herpes zoster Malaise Night sweats Oropharyngeal pain Pain Parosmia Respiratory tract congestion SARS-CoV-2 test positive Taste disorder

Symptomtext

I had shingles 12/19/2021 I was given medication for the symptom it was Valacyclovir. So, I just had COVID-19 symptoms for I guess two weeks, sore throat, very congestion. The first couple of days I had an elevated temperature of about 99. I had a cough and it impacted taste and smell. I was achy and tired, I took Tylenol, night sweats. That continued on until the following weekend like 02/13/2022. It seems the duration of the symptoms were longer due to the pregnancy. Pregnancy Info Due 07/24/2022, normal pregnancy to this point, I followed up with OB and they told me what to look for and I will be doing an additional ultra sound in the third trimester.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Rapid test & PCR - COVID-19 tests - both came back positive
Aktuelle Erkrankungen: No
Vorgeschichte: PCOS - Polycystic ovary syndrome
Andere Medikamente: Prenatal vitamin, Magnesium, Allertec
Allergien: Bacterium
Vorherige Impfungen: -

VAERS 2256941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Pyrexia

Symptomtext

I started experiencing a fever in the middle of the night with severe joint pain in every joint in my body. I took Tylenol. That morning I still felt pain until this day. I have an appointment with my doctor next week due to still experiencing this issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, Heart Valve Disease
Andere Medikamente: Kilodyne, Metoprolol, Spironolactone, Herbal tea
Allergien: Penicillin, Myacins, Gadolinium, Fish allergy
Vorherige Impfungen: Pfizer 2nd dose - blood clot.

VAERS 2248092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: IN
Alter: 55,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 18.10.2021
Beginn: 17.04.2022
Tage bis Beginn: 181,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Oropharyngeal pain Pain Productive cough SARS-CoV-2 test positive

Symptomtext

On April 17 I started having a sore throat and coughing I drank warm tea , It felt like I had allergies. On Monday I felt really tired and achiness. On Tuesday the 19th I went to get tested for COVID-19 and the test came back positive . I drank plenty of water and tea. I stayed home for 3 days and I still have a productive cough .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: NA
Vorgeschichte: Diabetes Type 1
Andere Medikamente: Calcium Aspirin Multivitamins
Allergien: Bandaids
Vorherige Impfungen: -

VAERS 2248001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: AZ
Alter: 65,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 12.10.2021
Beginn: 01.05.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Blood creatine phosphokinase increased Dysstasia Exercise tolerance decreased Gait disturbance Laboratory test Muscular weakness Neurological examination normal Pain in extremity

Symptomtext

In June 2021, I developed weakness and pain in both legs. It became difficult to stand from sitting w/o using my arms. I tried exercising to reduce the pain but it only got worse. In Sept I had trouble walking up a hill. I saw my PCP in Oct 2021 and they did some labs and everything was normal except my CK levels were high. I saw a rheumatologist in Nov 2021 who confirmed I didn't have a rheumatologic problem. I saw a neurologist in Nov 2021 and she didn't think it was from the vaccine or long COVID. She did extensive test but all tests were normal. I'm currently in the middle of a genetic workup.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine, D3, Estradiol cream
Allergien: None
Vorherige Impfungen: -

VAERS 2245717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: VA
Alter: 47,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 15.11.2021
Beginn: 18.03.2022
Tage bis Beginn: 123,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Cough Diarrhoea Headache Influenza like illness Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Swelling

Symptomtext

I was COVID-19 positive in March. It was a pretty severe flu, body ache, fever, diarrhea, sore throat, head ache, cough. It lasted severe for 7 days and started dwelling off for 8/9 days. Then I started feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 test, positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Hypothyroidism
Andere Medikamente: Synthroid; Metformin
Allergien: None
Vorherige Impfungen: -

VAERS 2241998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: WA
Alter: 23,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 28.10.2021
Beginn: 27.03.2022
Tage bis Beginn: 150,0
Dosis: 1
Route/Site: SYR / LA

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

Erythema Pruritus Rash Skin irritation Urticaria

Symptomtext

Skin irritation, hives, bumps, itching, redness, rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2238061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: GA
Alter: 47,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 14.09.2021
Beginn: 18.09.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / RA

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

Anti-thyroid antibody Antinuclear antibody negative Basophil count decreased Basophil percentage decreased Blood thyroid stimulating hormone normal Eosinophil count normal Eosinophil percentage Haematocrit normal Haemoglobin normal Helicobacter test Hepatitis B core antibody negative Hepatitis B surface antibody positive Hepatitis B surface antigen negative Immature granulocyte count Induration Lymphocyte count Lymphocyte percentage Mean cell haemoglobin concentration decreased

Symptomtext

approximately 4 days following my first injection, I began having what appears to be breakouts of what look like hives, globally around my body. Spoke with my Dr, who spoke with infection control specialist who said get second shot and I was to take Claritin. Continued having global break following second shot, some causing large hard lumps on buttocks, face, arms and neck. Referred to Allergy and test run. Told to take Zyrtec for 30 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Component Your value Standard range ESR 2 mm/hr 0 - 10 mm/hr Component Your value Standard range TPO AB 13 IU/mL <9 IU/mL THYROGLOBULIN AB <1 IU/mL <=1 IU/mL HEP B SURFACE AG Nonreactive HEP B SURFACE AB Reactive HEP B CORE AB, EIA Nonreactive T4 FREE 1.04 ng/dL TSH 2.24 uIU/ml UNIVERSAL MISCELLANEOUS FLEXITEST 1 FLEXITEST 1 HELICOBACTER PYLORI, UREA BREATH TEST H. PYLORI,UREA BREATH TEST NOT DETECTED Reference range: NOT DETECTED Antimicrobials, proton pump inhibitors, and bismuth preparations are known to suppress H. pylori, and ingestion of these prior to H. pylori diagnostic testing may lead to false negative results. If clinically indicated, the test may be repeated on a new specimen obtained two weeks after discontinuing treatment. However, a positive result is still clinically valid. Test Performed NEUTROPHILS %, AUTOMATED COUNT 54.1 % % LYMPHOCYTES %, AUTOMATED COUNT 32.4 % % MONOS %, AUTO 9.0 % % EOSINOPHILS %, AUTOMATED COUNT 4.0 % % BASOPHILS %, AUTOMATED COUNT 0.0 % % IMMATURE GRANULOCYTES %, AUTOMATED COUNT 0.50 % % NEUTROPHILS, ABSOLUTE, AUTOMATED COUNT 3.4 10*3uL 1.3 - 6.1 10*3uL LYMPHOCYTES, AUTOMATED COUNT 2.0 10*3uL 0.8 - 3.2 10*3uL MONOCYTES, AUTOMATED COUNT 0.6 10*3uL 0.2 - 1.1 10*3uL EOSINOPHILS, AUTOMATED COUNT 0.2 10*3uL 0.0 - 0.4 10*3uL BASOPHILS, AUTOMATED COUNT 0.0 10*3uL 0.0 - 0.1 10*3uL IMMATURE GRANULOCYTES, AUTOMATED COUNT 0.03 10*3uL 0.00 - 0.03 10*3uL WBC'S AUTO 6.2 10*3 uL 3.1 - 10.0 10*3 uL RBC, AUTO 5.49 10*6uL 3.90 - 6.00 10*6uL HGB 15.3 g/dl 11.4 - 17.1 g/dl HCT, AUTO 48.1 % 35.7 - 51.3 % PLATELETS, AUTOMATED COUNT 263 10*3 uL 126 - 362 10*3 uL MPV 9.8 fL 8.6 - 12.3 fL MCV 87.6 fL 76.9 - 98.6 fL MCH 27.9 pg 24.5 - 33.0 pg MCHC 31.8 g/dl 30.4 - 35.0 g/dl RDW, RATIO, RBC, QN, AUTO 13.6 % 11.7 - 14.7 % NUCLEAR AB, SER, QL NEGATIVE
Aktuelle Erkrankungen: NKI
Vorgeschichte: N/A
Andere Medikamente: Omeprazole Dr. 20 Mg Cap Krem
Allergien: Wellbutrin
Vorherige Impfungen: -

VAERS 2219895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 76,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 29.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Investigation Pain in extremity

Symptomtext

sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 76-year-old female patient received bnt162b2 (BNT162B2), administration date 29Oct2021 (Lot number: FD0809) at the age of 76 years as dose 3 (booster), single, administration date 31Mar2021 (Lot number: EW0150) as dose 2, single and administration date 10Mar2021 (Lot number: EN6208) as dose 1, single for covid-19 immunisation. Relevant medical history included: "Blood pressure" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN taken for blood pressure measurement; NORVASC taken for blood pressure measurement. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "sore arm". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: She reports last night but states she hasn't had any problems from her previous doses. Caller states she never had these side effects before except a sore arm that she has had before. Patient details: Caller states she thinks that she has shrunk. Caller states weight is unknown, but she is not big and fat. She states she tells the doctor she does not want to be weighed as she is not fooling with that. She states maybe 170 pounds. Caller states she has shrunk over the years and clarifies many years. Caller states the phone broke up. Caller confirms the call is about the COVID-19 vaccine. She states her vaccination card is in her purse. Caller reports the pharmacy gave her some paperwork yesterday maybe her vaccination information will be there. She states the pharmacy gave her a lot of papers. Caller reports all her COVID-19 vaccinations were Pfizer. Caller reports the date is hard to read due to the writing on her card but confirms the date is 31Mar2021. Caller states the date does not sound right. Caller asks does that sound right. Caller states the vaccination took like 3 seconds in her left arm. Indication: Caller states she saw on TV that if greater than 5 months since her last vaccination and if she is immune compromised, she should get a booster dose of the COVID-19 vaccine. She states she does not know if she is immune compromised, but she is old. She reports her granddaughter comes to her house and her granddaughter is not vaccinated. Caller states all her test results came back fine but she needs her physical this month. She reports that she hasn't had her physical since last year, but all her tests were fine last year. Caller declined to complete supplemental form as she states she has someone calling on the other line. No further details to provide. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: lab test; Result Unstructured Data: Test Result:all her test results came back fine
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure.
Andere Medikamente: LOSARTAN; NORVASC.
Allergien: -
Vorherige Impfungen: -

VAERS 2214147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: GA
Alter: 56,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 18.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site pain Injection site reaction Rash Skin texture abnormal Urticaria Vaccine positive rechallenge

Symptomtext

After both shots, had reaction with bumps and hives. Took benadryl. Started having pain in area of arm where shots were given. Still today pain is consistent and when patient feels the area where shot was given, it has a spongy feeling, per patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2212354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 15.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / AR

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

Biopsy Laboratory test Metabolic function test Rheumatoid factor Urine analysis Urticaria

Symptomtext

Hives first appeared on 11/25/21. Increased in frequency and severity through January. Saw Primary Care Doc early Feb. Then referred to Allergist, Rheumatologist, Dermatologist and Immunologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Complete lab work up for autoimmune, rheum, basic metabolic, biopsies, and urinalysis. Lab tests occurred between February 2022 and March 2022.
Aktuelle Erkrankungen: Post op DVT in R femoral/saphenous junction. Surgery was 9/2/2021.
Vorgeschichte: Anxiety. Herpes.
Andere Medikamente: Sertraline, Valacyclovir, Famotadine, multi vitamin, Eliquis
Allergien: None known
Vorherige Impfungen: -

VAERS 2206423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: WV
Alter: 61,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 04.11.2021
Beginn: 02.01.2022
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: SYR / RA

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

Pruritus Psoriasis

Symptomtext

11/21/2021. I noticed my skin started itching and I had psoriasis come up out of the blue. No stress related issues. Went back to dermatologist last month, and he looked at the new psoriasis on my body. He had prescribed medication to use on my head. The treatment plan was to use medication on my body every day, if that doesn't work, we would try the injectable. Psoriasis covers 20% of my body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fiber, B Complex with Vitamin C, Benadryl, Venlafaxine, Escitalopram, Atorvastatin, Enstiliar
Allergien: Penicillin
Vorherige Impfungen: Flu shot, red and swollen arm. No medical attention needed.

VAERS 2204326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: UT
Alter: 56,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 24.09.2021
Beginn: 25.12.2021
Tage bis Beginn: 92,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Pain in extremity Peripheral swelling Rheumatoid factor negative X-ray normal

Symptomtext

12/25/2021 I woke to swelling and pain in my left hand and a week later the right swelled but went back down. The left kept on hurting but right was back and forth with arthritic pain across the last few months. Last Friday, 3/25/2022, I had a rheumatoid test done and just today on 3/29/2022 I discussed the negative results and was told there was an arthritis that wouldn't show up on this test. So the doc offered to go ahead to try and treat it as if it was positive. If no help through this then my doctor will know it will be the new type and treat it as such.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Rheumatoid test (Normal); X-Ray (No joint damage).
Aktuelle Erkrankungen: None
Vorgeschichte: RAD (Reactive Airway Disease); Mild AI (Aortic Insufficiency); Intractable Migraines; Bilateral Extremity Edema; Depression
Andere Medikamente: Amoxicillin, Nurtec, Singular, Zyrtec, Azelastine, Rhinocort, aspirin 81mg, Atorvastatin, Prozac, Lasix, Potassium Chloride, Neurontin, Relafen, Verapamil, Allopurinol, Botox, Nature's Power Solutions Acidophilous, Premium Max Q core, Bena
Allergien: CECLOR; BIAXIN; morphine; perfume
Vorherige Impfungen: -

VAERS 2204221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 29.03.2022
Impfdatum: 17.05.2021
Beginn: 23.01.2022
Tage bis Beginn: 251,0
Dosis: UNK
Route/Site: - / -

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

Abdominal pain upper COVID-19 Constipation Decreased appetite SARS-CoV-2 test positive

Symptomtext

01/23/22 presents to ED for "epigastric abdominal pain, constipation and decreased appetite". PMHx of "CAD s/p DES (2018), Uncontrolled DM II, and HTN"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: 01/24/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2203528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MN
Alter: 75,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 29.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Biopsy Rash macular

Symptomtext

Then she got the booster shot and the rash spread again; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 75-year-old female patient received bnt162b2 (BNT162B2), administration date 29Nov2021 (Lot number: FD0809) at the age of 75 years as dose 3 (booster), single for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose1, LOT: EN6198), administration date: 24Feb2021, when the patient was 74 years old, for COVID-19 immunization, reaction(s): "she had kind of like a rash where every pore at the bottom part of her leg was red", "She says then she noticed she had two spots, one on her upper right leg thigh and that was red spots also the size of maybe a half dollar and she also had one spot on her stomach that was about the same size."; Bnt162b2 (Dose2, LOT: ER8730), administration date: 24Mar2021, when the patient was 74 years old, for COVID-19 immunization, reaction(s): "She says she had red spots on her back and then red blotchy stuff.", "rash started to spread and went to all of her leg upper, with some on her back that spread really bad", "Granuloma annulare", "she is still taking it simply because everything gets so dry, that this keeps it so it is moist.". The following information was reported: RASH MACULAR (non-serious) with onset 2021, outcome "not recovered", described as "Then she got the booster shot and the rash spread again". The event "then she got the booster shot and the rash spread again" was evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash macular. She got her first COVID-19 shot 24Feb2021 then approximately a week and a half later, though she thinks sooner than when she noticed it, she had kind of like a rash where every pore at the bottom part of her leg was red. She said then she noticed she had two spots, one on her upper right leg thigh and that was red spots also the size of maybe a half dollar and she also had one spot on her stomach that was about the same size. She says her second Pfizer COVID-19 vaccine dose was 24Mar2021, and then the rash started to spread and went to all of her leg upper, with some on her back that spread really bad. She says she had red spots on her back and then red blotchy stuff. She says it was at that time she went to the dermatologist who gave her some ointment to take. She was given the ointment in Jul first by her primary care doctor who gave her a couple of small tubes to put on the two little spots, and this didn't really do anything. She says her dermatologist gave her the same thing as a bigger container, which by that time she had the rash all over her body. Patient said the ointment, she was given for treatment was Triamcindlon (documented as provided), NDC/LOT/EXP: unknown. she was still taking it simply because everything gets so dry, that this keeps it so it was moist. She says she doesn't put it on as she was supposed to as two times a day, though she did in the beginning. She says after Nov they just decided she really didn't need to put it on twice a day, just once or whenever it was needed to keep it moist. She says it didn't show any sign of doing anything. She stated that other treatment she was taking a pill, which then the rash started to kind of go away, but then she got the booster shot and the rash spread again. She says the pills she was taking was Hydroxychloroquine 200mg tablets, she takes one twice a day by mouth and that has seemed to help. On 14Jul2021 was when she took that the first day, when she had also seen the dermatologist. The rash started in Mar2021, but it didn't really do anything really at the time, she hadn't seen anybody and didn't think anything of where it came from. She says what they have diagnosed her with is somewhat related to a medicine change, but she hasn't changed anything. She says that her primary care doctor took some biopsies, and also her doctor sent her what explained it could be Granuloma annulare. She said she sees her doctor in Apr, so that was given to her in Apr, and they took one biopsy of her arm, which at that time it was on her arm too. She clarifies that it was sometime in Apr that she got this paper that says what they think it was. She says the only other thing was when she got the booster shot after the rash had started to go away, with her spots fading and stuff a little bit. She says she got the booster dose and it spread again to areas it hadn't been prior. She says it was on her arms before this and also kinda on her back but was more or less back and back of her arms. She says thank goodness it didn't itch, the dermatologist, took pictures and told her when she was there last month that she has everything documented. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: Test Name: biopsy; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2201781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CT
Alter: 80,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 24.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Arthritis Blood test abnormal Joint swelling Osteoarthritis

Symptomtext

Starting one week after receiving the vaccine, I developed joint swelling in my hands, fingers, wrists, neck and knees. As the inflammation increased, my symptoms increased. It progressed to most of the joints in my body. I was referred to rheumatology immediately which took about 3 months to get in. The pain had gotten extremely severe by that point. The doctor diagnosed me with osteoarthritis after a full workup and I was prescribed prednisone to alleviate the symptoms. At the moment, they are still determining the best dosage of prednisone for me. So, she is trying to get me onto Hydroxychloroquine in order to hopefully get me off prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Rheumatology work up: osteoarthritis
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin and Cranberry supplements
Allergien: Drug Sensitive: Antibiotics (lower the dosage)
Vorherige Impfungen: Shingles shot: Severe inflammation of the shoulder

VAERS 2196564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 25.08.2021
Beginn: 25.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Colonoscopy Computerised tomogram abdomen Helicobacter test Oesophagogastroduodenoscopy

Symptomtext

Persistent left sided abdominal pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: H.Pylori, Colonoscopy, CT Abdomen, EGD
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PORTIA-28 0.15-30M TAB TEVA
Allergien: -
Vorherige Impfungen: -

VAERS 2196564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 25.08.2021
Beginn: 25.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Colonoscopy Computerised tomogram abdomen Helicobacter test Oesophagogastroduodenoscopy

Symptomtext

Persistent left sided abdominal pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: H.Pylori, Colonoscopy, CT Abdomen, EGD
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PORTIA-28 0.15-30M TAB TEVA
Allergien: -
Vorherige Impfungen: -

VAERS 2194304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: FL
Alter: 49,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 18.02.2021
Beginn: 23.03.2022
Tage bis Beginn: 398,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Cough Decreased appetite Lower respiratory tract infection Lower respiratory tract inflammation Lung opacity Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 01/26/2021. 50 y/o with PMHX of CADASIL dementia, bradycardia, depression, Dysthymic disorder, memory loss, vascular dementia, G-tube and non-verbal per baseline presents to ED via EMS from a HCF and Rehab with cough, abnormal CXR, decreased appetite and fever x1 day. CXR with stable moderate patchy opacities involving left lower lobe likely infectious/inflammatory. Pt on O2 2L NC sats 98%, febrile per rehab reports. Pt started on IV steroids/ABX and Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19-Detected on 03/23/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Bradycardia, CADASIL Dementia, depression, Dysthymic disorder, memory loss, vascular dementia
Andere Medikamente: -
Allergien: Depakote
Vorherige Impfungen: -

VAERS 2179245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: TN
Alter: -
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 13.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Overdose Pain in extremity

Symptomtext

administered a full vial of the purple cap covid vaccine as a single dose; sore arm; This is a spontaneous report received from contactable reporter(s) (Pharmacist and Consumer or other non HCP) from medical information team for a Pfizer sponsored program (159558). A male patient in his 50's received bnt162b2 (BNT162B2), administered in deltoid left, administration date 13Nov2021 (Lot number: FD0809) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: OVERDOSE (non-serious) with onset 13Nov2021, outcome "unknown", described as "administered a full vial of the purple cap covid vaccine as a single dose"; PAIN IN EXTREMITY (non-serious) with onset Nov2021, outcome "recovered" (Nov2021), described as "sore arm". Additional information: Reporter reported that Patient was inadvertently administered a full vial of the purple cap covid vaccine as a single dose. What are the recommendations for proceeding with the second vaccination in series? the nurse had not done these vaccines before and didn't want to wait for the other nurse to come explain it, so she just grabbed a vial and administered the full vial without diluting. The patient reported he had a sore arm for only a day and then it was fine. No other AEs reported. He was planning on getting the second dose at the scheduled interval. She has not heard anything new from the patient and he has not gotten his second dose yet. He was due for it, but since he has not come in yet she's not sure if he was waiting. The patient had not reported any adverse events to them since the overdose event. Phone answered by reporter who provided an update. She said the patient is still doing well so no new adverse events to report. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: KS
Alter: 49,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Dysphonia Laryngitis Pain in extremity

Symptomtext

Laryngitis or Hoarse voice set in 27 hours following booster along with congestion.; Laryngitis or Hoarse voice set in 27 hours following booster along with congestion.; sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Other HCP). The reporter is the patient. A 49 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Nov2021 17:45 (Lot number: FD0809) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU), administered in arm right, administration date 05Nov2021 (Batch/Lot number: unknown). The patient had no relevant medical history. Concomitant medication(s) included: NYQUIL. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Unknown. Unable to locate or read the details, Location of injection: Arm Right, Vaccine Administration Time: 03:30 PM), administration date: 02Apr2021, when the patient was 49 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: Unknown. Unable to locate or read the details, Location of injection: Arm Left, Vaccine Administration Time: 03:30 PM), administration date: 10Mar2021, when the patient was 48 years old, for COVID-19 immunization. The following information was reported: LARYNGITIS (non-serious), DYSPHONIA (non-serious) all with onset 06Nov2021 20:00, outcome "not recovered" and all described as "Laryngitis or Hoarse voice set in 27 hours following booster along with congestion."; PAIN IN EXTREMITY (non-serious) with onset 06Nov2021 20:00, outcome "not recovered", described as "sore arm". Therapeutic measures were not taken as a result of laryngitis, dysphonia, pain in extremity. Additional information: The patient had no known allergies. The patient had no covid prior vaccination and not tested for covid post vaccination. No other vaccines within 4 weeks of vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: NYQUIL
Allergien: -
Vorherige Impfungen: -

VAERS 1903750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 25.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Blood test Body temperature Cellulitis Feeling abnormal Immunisation Pain Pyrexia

Symptomtext

body aches; 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), administration date 25Feb2021 (Lot number: 3247) as dose 2, single and administration date 04Feb2021 (Lot number: 3247) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN (non-serious), outcome "unknown", described as "body aches". Additional information: Patient received booster dose on 12Nov2021, 30mcg/0.3ml, injection in the right arm (Batch/lot number: FD0809). NDC number of Covid-19 Booster was 59267-1000-01. Reporter was a Pfizer Colleague that was calling about the Pfizer Covid-19 booster dose. Patient experienced really bad side effects, high fever 102.5, fever she could not get under control. She called the doctor yesterday 15Nov2021 and stated that she developed cellulitis at the vaccine site. She said that it had nothing to do with the vaccine itself, but how it was administered. She also had body aches. Reporter said that body aches was a known side effect. She had body aches with the first 2 doses. She felt obligated to update what occurred with the cellulitis. The reporter clarified that she previously reported the body aches and the fever in the initial report. She was put on antibiotics because the cellulitis was traveling down her arm. Her arm was throbbing today, but she was feeling better and was on the mend. She felt back to herself and was able to do her job today. She received her first 2 doses on site and that the lot numbers did not have any letters or anything at the beginning of the numbers that were written on her card. At 102.5 fever, her mind was very foggy. She had already reported her concomitant medications, medical conditions, and relevant tests in the initial report. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2176126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: AK
Alter: 63,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 15.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Pain in extremity SARS-CoV-2 test

Symptomtext

just a sore arm.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 15Oct2021 11:00 (Lot number: FD0809) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Arthritis" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (prev dose lot number=EL9265, prev dose administration date=24Feb2021, prev dose administration time=10:00 AM, prev dose dose number=2, prev dose vaccine location=Left arm), administration date: 24Feb2021, when the patient was 63 years old, for COVID-19 Immunization; Bnt162b2 (prev dose lot number=EL1284, prev dose administration date=14Jan2021, prev dose administration time=10:00 AM , prev dose dose number=1, prev dose vaccine location=Left arm), administration date: 14Jan2021, when the patient was 63 years old, for COVID-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "recovered", described as "just a sore arm.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity. Additional information: Patient was not received any other vaccine four weeks prior vaccination and patient did not receive any medication two weeks prior vaccination. Patient not diagnosed with covid-19 prior to vaccination and patient was tested for COVID-19 post vaccination. The patient had no known allergies. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Date: 20211005; Test Name: nasal swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 06.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Vaccination site erythema Vaccination site pruritus Vaccination site rash Vaccination site swelling Vaccination site warmth

Symptomtext

it started itching and had a slight rash; it started itching and had a slight rash; it 'kinda' swell; it got red and was like hot also in the area below the injection site; it got red and was like hot also in the area below the injection site; 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 78 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 06Oct2021 13:00 (Lot number: FD0809) at the age of 78 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), administered in arm left, administration date 27Sep2021 (Batch/Lot number: unknown) as dose number unknown, single. Relevant medical history included: "allergic to a lot of antibiotics" (unspecified if ongoing), notes: She is allergic to a lot of antibiotics.; "Blood pressure" (unspecified if ongoing); "Sinuses" (unspecified if ongoing). Concomitant medication(s) included: FLONASE [MOMETASONE FUROATE] taken for sinus disorder; NASONEX taken for sinus disorder. Vaccination history included: Bnt162b2 (Dose:1,Lot Number EN9581, Route, Anatomical Location: Left arm), administration date: 05Feb2021, when the patient was 78 years old, for COVID-19 Immunisation, reaction(s): "little swelling"; Bnt162b2 (Dose: 2, Lot Number EN6203, Route, Anatomical Location: Left arm), administration date: 26Feb2021, when the patient was 78 years old, for COVID-19 Immunisation, reaction(s): "little swelling". The following information was reported: VACCINATION SITE SWELLING (non-serious) with onset 09Oct2021, outcome "recovered" (12Oct2021), described as "it 'kinda' swell"; VACCINATION SITE ERYTHEMA (non-serious) with onset 09Oct2021, outcome "recovered" (12Oct2021), VACCINATION SITE WARMTH (non-serious) with onset Oct2021, outcome "recovered" (2021) and all described as "it got red and was like hot also in the area below the injection site"; VACCINATION SITE RASH (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 12Oct2021, outcome "recovered" and all described as "it started itching and had a slight rash". Additional information: Caller stated that the patient had the booster dose of the Pfizer BioNTech COVID-19 vaccine last 06Oct2021, and "few days after, it 'kinda' swell and a few days after that, it got red and was like hot also in the area below the injection site which lasted for a while, maybe 5 or 6 days, somewhere in there". Caller also stated that "it started itching and had a slight rash" Caller stated that the "itching and the rash is better, the redness is gone". Caller wanted to know how long would her "slight rash" last. Caller stated that she did not have "any severe thing like breathing problem". She's not taking anything else besides medication for her blood pressure. She confirms this is not something new she began within the 2 weeks leading up to her symptoms, she has been on this medication for about a year. Sometimes, she does take Flonase or Nasonex for her sinuses.The caller states that the patient taken the third COVID shot. She took the third one on 06Oct2021. She mentioned that she didn't have any problems with her other two doses, maybe a little swelling but it didn't last very long. After she took her third dose, she of course was swollen a little bit, but then it became real red below the injection site which lasted a while. She mentioned that she wrote it all down, but she can't even read her own handwriting. She wrote on 09Oct2021, she started to have swelling and redness around the site and underneath where the person had given the shot. Near the middle of her upper arm, it started getting real red and stayed that way until about the 12Oct2021. On 12Oct2021, she started to get a little bit of a rash and started itching. When probed for the outcome of these symptoms, the caller explains her arm is not red anymore. It's still broken out a little bit, there is a little rash still there. She states if she scratches her arm, it itches a little bit. There is slight itching. Caller clarifies further her arm is better. It's not breaking out anymore, there is no additional breaking out. It's just taking a while for the break out/rash to disappear. She just has a slight breakout, nothing real thick. There is still itching but its not there like it was and its not breaking out any further. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient received other vaccine within four weeks prior to the vaccination. The caller states she had gotten her flu shot 8 days prior to the COVID shot and she got each injection in different arms so if something happened she would know which shot did it. She confirms she had the regular flu shot in her left arm. She mentions she has a lot of allergies which is part of her problem. She had the flu shot in Withheld. AE(s) following prior vaccinations: The caller states she usually might get a little bit of swelling but never has she had it where the area is real red and feels real hot before. She clarifies where the injection area and underneath got red, it also go hot. She states once the redness left, she then developed a little bit of a rash. She states it was in the middle of her upper arm and it was itchy, it has subsided now. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic (She is allergic to a lot of antibiotics.); Blood pressure; Sinus disorder
Andere Medikamente: FLONASE [MOMETASONE FUROATE]; NASONEX
Allergien: -
Vorherige Impfungen: -

VAERS 2175944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: IN
Alter: 30,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Pain SARS-CoV-2 antibody test negative

Symptomtext

Not adverse just soreness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Oct2021 15:15 (Lot number: FD0809) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: CELEXA [CELECOXIB]; ADDERALL. Vaccination history included: Bnt162b2 (Dose 1, single, Batch/Lot No: Er8736, Anatomical location: Left Arm, Vaccine Administration Time: 12:00 PM), administration date: 16May2021, when the patient was 30 years old, for Covid-19 immunization; Bnt162b2 (Dose 2, single, Batch/Lot No: Ew968, Anatomical location: Left Arm, Vaccine Administration Time: 12:00 PM), administration date: 13Jun2021, when the patient was 30 years old, for Covid-19 immunization. The following information was reported: PAIN (non-serious) with onset 14Oct2021 10:00, outcome "recovering", described as "Not adverse just soreness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain. Additional information: The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. patient received Celexa, adderall within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. The vaccine was administered at Public Health Clinic. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101374795 similar report from same reporter

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CELEXA [CELECOXIB]; ADDERALL
Allergien: -
Vorherige Impfungen: -

VAERS 2175702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: LA
Alter: 31,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 01.09.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Blood creatine phosphokinase Blood test Echocardiogram Electrocardiogram Pain in extremity SARS-CoV-2 test

Symptomtext

I have no issues with the first shot- other than soreness in my right arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old female patient (not pregnant) received bnt162b2 (COVID19 Vaccine- Solution for injection), administered in arm right, administration date 01Sep2021 15:00 (Lot number: FD0809) at the age of 31 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "chest pains", start date: 23Sep2021 (ongoing); "upper back pain", start date: 23Sep2021 (ongoing). Concomitant medication(s) included: IBUPROFEN taken for pain, inflammation, start date: 04Oct2021, stop date: 18Oct2021; NAPROXEN taken for pain, start date: 27Oct2021 (ongoing); FAMOTIDINE taken for gastrooesophageal reflux disease, start date: 27Oct2021 (ongoing); OMEPRAZOLE taken for abdominal discomfort, start date: 27Oct2021 (ongoing); DAILY VITAMINS; PROBIOTICS. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "unknown", described as "I have no issues with the first shot- other than soreness in my right arm". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Narrative case summary: Patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: FD0809), via an unspecified route of administration, administered in arm right on 22Sep2021 15:00 (at the age of 31-year-old) as Dose 2, Single for COVID-19 immunization. The patient medical history was reported as none including no known allergies. The patients concomitant medications included daily vitamins, probiotics, birth control medications received within 2 weeks of vaccination. Historical vaccination included the patient had previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation:Solution for injection, lot number: FD0809), via an unspecified route of administration, administered in arm right on 01Sep2021 15:00 (at the age of 31-year-old) as Dose 1,Single for COVID-19 immunization and experienced soreness in her right arm.The patient did not receive any other vaccines within 4 weeks prior to the COVID 19 vaccine. The patient had not been diagnosed with COVID-19 prior to vaccination and had been tested for Covid-19 since the vaccination. On 24Sep2021, the patient experienced body aches and fatigue; Eventually the aches were in her chest - both sides, aches in other parts of her body went away but aches in her chest did not. She started to have chest tightness, upper back discomfort (that would worsen when she laid on her back or sat back), heart palpitations and dull aches on the left side of her chest and sometimes in her left arm. On 01Oct2021, the patient went to urgent care and the EKG was normal. They prescribed a low dosage of pain med and muscle relaxers toradal but it didn't help. She finally went to see a cardiologist yesterday. On 04Oct2021 (Monday) because she considered she developed a heart issue, echo done & heart looked fine and strong, but they have no idea why she still have adverse aches in her chest area. The heart doctor kept her on some strong ibuprofen (IBUPROFEN, strength: 800 mg) for pain, inflammation and steroids and started feeling better by Thursday. The doctor felt like this was temporary and it was just prolonged autoimmune reactions from the shot. The patient hoped he was right. On 07Nov2021 the patients heart palpitations stopped (as well as caffeine). On 11Oct2021 the doctor told her to stay on ibuprofen as needed or seen herself off. She did another EKG - looked fine. The patient had a few bad days, but overall, it did seem to be slowly improving. She started to do muscle stretches. heating pad and bath with Epsom. She even took 3 turmeric pills dally, omega 3, a folic acid. On 22Oct2021- reduced medicines to 200 mg felt just fine. She stopped turmeric & other supplements earlier in the week for a break Saturday. Felt fine Sunday the 24Oct2021 she forgot to take medicine all together until that even, but she was okay. On 25Oct2021 (Monday)- Felt achy around 11:00 even though she took med that morning and around 13:00. These aches and upper back pain persist off and on all day. Around 19:00 she took 800 mg. On 26Oct2021 (Tuesday)- 800mg Ibuprofen and omega 3 and folic acid. Did some aches. been laying on heating pad. Aches here and there but evening was better. On 27Oct2021 (Wednesday), took medicine at 07:00 very few eggs, took folic acid Omega 3, plus quercetin. Drank tea with ginger and honey. Did not feel better until 16:30, after visit, took medicine famotidine (FAMOTIDINE, strength: 20 mg) taken for acid reflux and omeprazole (OMEPRAZOLE, strength: 40mg) taken to protect stomach Lining. Then 1/2 of ibuprofen at bedtime took magnesium and Benadryl. She also took naproxen (NAPROXEN, strength: 500 mg) taken for pain. On 28Oct2021, Thursday woke up had few aches. Took her antacid, folic acid, omega-3 and quercetin. Had blood work done and then came home and took magnesium pill at 09:30 and she was feeling fine. Took 2nd pepcid and magnesium. Her back hurt but felt ok most of the evening took magnesium and Benadryl at night-time. On 29Oct2021, (Friday), felt good this morning took pepcid, stomach protector, magnesium, quercetin, Zinc, omega-3, folate. Drank some coffee felt a great most of the day. Took a leave around lunchtime. Had a few aches come night-time but she laid on heating pad and was ok! took magnesium and Benadryl. On 30Oct2021 05:00, took same medicines. Felt ok this morning but these three doses seem to give more aches in her upper back lately much better than her chest but still annoying. Took Aleve at lunch and the better spending lot of time on the heating pad. she had also had two rounds of IV vitamin infusions, which have helped significantly. On 31Oct2021 (Saturday) felt great all day continued with the same medications omega 3, folic acid, pepcid, quercetin, omeprazole, naproxen at lunchtime only. Doing the same today 01Nov2021, it does seem improving but it seems very slow. The patient was visited to doctor or other healthcare professional office/clinic and emergency room/department or urgent care for her events. The patient underwent lab tests and procedures which included on 30Sep2021 EKG: normal, 01Oct2021 EKG: fine, on 04Oct2021 echocardiogram: heart looked fine but did see heart palpitations, on 28Oct2021 CK blood test: came back normal, on an unspecified date regular blood test: result unknown, on 11Oct2021 EKG: looked fine and on 01Oct2021 nasal swab test (sars-cov-2 test) resulted in negative. The outcome of the event body aches and I had aches and fatigue/ body aches was recovered on 24Sep2021 and the outcome of the event Heart palpitations was recovered on 07Nov2021 while the outcome of the remaining events was recovering and the outcome of the Aches in my upper back was not recovered. No hospitalization prolonged, treatment received for the event. No follow-up attempts are possible. No further information is expected. Follow-up (09Nov2021): This is a follow-up spontaneous report received from a contactable consumer (patient). This consumer reported in response to non-hcp letter sent which included: Updated Clinical information, treatment medication and the outcome of the events. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Date: 20211028; Test Name: c.k blood test; Result Unstructured Data: Test Result:Normal; Comments: came back normal; Test Name: Regular blood test; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211028; Test Name: Regular blood test; Result Unstructured Data: Test Result:Unknown results; Comments: Had blood work done; Test Date: 20211004; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Fine; Comments: Heart looked fine but did see heart palpitations; Test Date: 20210930; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20211001; Test Name: EKG; Result Unstructured Data: Test Result:Fine; Test Date: 20211011; Test Name: EKG; Result Unstructured Data: Test Result:Fine; Comments: looked fine; Test Date: 20211001; Test Name: Sars-Cov-2 Test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211028; Test Name: Sars-Cov-2 Test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: Chest pain; Upper back pain
Vorgeschichte: -
Andere Medikamente: IBUPROFEN; NAPROXEN; FAMOTIDINE; OMEPRAZOLE; DAILY VITAMINS; PROBIOTICS
Allergien: -
Vorherige Impfungen: -

VAERS 2175601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Fatigue Headache Inappropriate schedule of product administration Lymphadenopathy Nausea Pain Pain in extremity Vaccination site pain

Symptomtext

Body aches; Very Achy; Swollen Lymph nodes; Nausea; Pain at injection site; Prev dose administration date: 25Apr2021/ Administration date: 02Oct2021; Horrible headache; Extreme fatigue; Had sore left arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 01Oct2021 14:45 (Lot number: FD0809) at the age of 59 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "High blood pressure" (unspecified if ongoing), notes: High blood pressure; "Hypothyroid" (unspecified if ongoing), notes: Hypothyroid; "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin. Concomitant medication(s) included: POTASSIUM. Vaccination history included: Bnt162b2 (Prev dose Brand: Pfizer BioNTech, Prev dose Administration time: 11:30 AM, Prev dose Vaccine location: Left arm, Route of administration: Intramuscular, Lot Number : misplaced/discarded), administration date: 25Apr2021, when the patient was 59 years old, for COVID-19 Immunization. The patient received medication within 2 weeks of vaccination were hypothyroid med, thyroid med. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 02Oct2021 14:30, outcome "unknown", described as "Prev dose administration date: 25Apr2021/ Administration date: 02Oct2021"; FATIGUE (non-serious) with onset 01Oct2021 16:00, outcome "recovered" (04Oct2021), described as "Extreme fatigue"; HEADACHE (non-serious) with onset 01Oct2021 17:00, outcome "recovered" (05Oct2021), described as "Horrible headache"; VACCINATION SITE PAIN (non-serious) with onset 02Oct2021 16:00, outcome "not recovered", described as "Pain at injection site"; PAIN (non-serious) with onset 03Oct2021 16:00, outcome "recovered" (05Oct2021), described as "Very Achy"; NAUSEA (non-serious) with onset 02Oct2021 16:00, outcome "not recovered", described as "Nausea"; LYMPHADENOPATHY (non-serious) with onset 03Oct2021 09:00, outcome "recovered" (11Oct2021), described as "Swollen Lymph nodes"; PAIN IN EXTREMITY (non-serious) with onset 01Oct2021, outcome "recovered" (04Oct2021), described as "Had sore left arm"; PAIN (non-serious), outcome "unknown", described as "Body aches". Therapeutic measures were not taken as a result of fatigue, headache, vaccination site pain, pain, nausea, lymphadenopathy, pain. Additional information: Seriousness criteria was not Results in death, Life threatening Caused/prolonged hospitalization and Congenital anomaly/birth defect. Prior to vaccination, patient did not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine.After 2nd dose 01Oct2021 also had sore left arm for 3 days was nauseated 1st day fatigue started after a few hours lasted 3 days, very achy like non over started 03Oct2021 lasted 2 days. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (High blood pressure); Hypothyroidism (Hypothyroid); Penicillin allergy (Known allergies: Penicillin.)
Andere Medikamente: POTASSIUM.
Allergien: -
Vorherige Impfungen: -

VAERS 2175326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 14.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Breast pain Off label use Pain in extremity Product use issue Suppressed lactation

Symptomtext

I am currently Breastfeeding; I am currently Breastfeeding; my left breast was very sore to the touch and hurt; I have significantly decreased my milk supply in my left breast only. I was producing 4-5 oz per breast, now my left breast is only producing less than 1 oz.; my left arm pit; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 36 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Sep2021 13:15 (Lot number: FD0809) at the age of 36 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: PROZAC. Past drug history included: Known allergies: none. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 14Sep2021 17:00, outcome "unknown" and all described as "I am currently Breastfeeding"; BREAST PAIN (non-serious) with onset 14Sep2021 17:00, outcome "not recovered", described as "my left breast was very sore to the touch and hurt"; SUPPRESSED LACTATION (non-serious) with onset 14Sep2021 17:00, outcome "not recovered", described as "I have significantly decreased my milk supply in my left breast only. I was producing 4-5 oz per breast, now my left breast is only producing less than 1 oz."; PAIN IN EXTREMITY (non-serious) with onset 14Sep2021 17:00, outcome "not recovered", described as "my left arm pit". The events "i am currently breastfeeding", "i am currently breastfeeding", "my left breast was very sore to the touch and hurt", "i have significantly decreased my milk supply in my left breast only. i was producing 4-5 oz per breast, now my left breast is only producing less than 1 oz." and "my left arm pit" were evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of breast pain, suppressed lactation, pain in extremity. Additional information: The patient had not received any other vaccine within 4 weeks prior to COVID vaccine. Prior to vaccination the patient was not diagnosed with COVID 19. Since the vaccination the patient had not tested for COVID 19. No follow-up attempts are possible. No further information is expected. Follow-up (18Oct2021): Follow-up attempts completed. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101243499 mother/baby case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: PROZAC
Allergien: -
Vorherige Impfungen: -

VAERS 2175235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NM
Alter: 42,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 30.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Fatigue Feeling abnormal Headache Heart rate irregular Hyperhidrosis Myalgia Nausea

Symptomtext

Irregular heart beat/racing; Fatigue; Nausea; Headache; Muscle aches; Just don't feel good; Sweeping in my legs and hands; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 30Aug2021 10:00 (Lot number: FD0809) at the age of 42 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: ARMOUR THYROID; ALEVE. The following information was reported: HEART RATE IRREGULAR (non-serious) with onset 30Aug2021 20:00, outcome "not recovered", described as "Irregular heart beat/racing"; FATIGUE (non-serious) with onset 30Aug2021 20:00, outcome "not recovered", described as "Fatigue"; NAUSEA (non-serious) with onset 30Aug2021 20:00, outcome "not recovered", described as "Nausea"; HEADACHE (non-serious) with onset 30Aug2021 20:00, outcome "not recovered", described as "Headache"; MYALGIA (non-serious) with onset 30Aug2021 20:00, outcome "not recovered", described as "Muscle aches"; FEELING ABNORMAL (non-serious) with onset 30Aug2021 20:00, outcome "not recovered", described as "Just don't feel good"; HYPERHIDROSIS (non-serious) with onset 30Aug2021 20:00, outcome "not recovered", described as "Sweeping in my legs and hands". Therapeutic measures were not taken as a result of heart rate irregular, fatigue, nausea, headache, myalgia, feeling abnormal, hyperhidrosis. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: ARMOUR THYROID; ALEVE
Allergien: -
Vorherige Impfungen: -

VAERS 2173480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: IN
Alter: 50,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 08.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: SYR / RA

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

Eyelid disorder Psoriasis Urticaria

Symptomtext

a couple of. months after my booster I developed hives, psoriasis along my skalp and a horrible reaction on my eyelids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: None
Andere Medikamente: blood orange and apple cider vinegar supplements
Allergien: none that I am aware of
Vorherige Impfungen: -

VAERS 2162058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: PA
Alter: 59,0
Geschlecht: M
Eingang: 06.03.2022
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / UN

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

Dizziness Illness Nausea Pain

Symptomtext

nausea, lightheadedness, body aches. I was sick for about 2 days after the onset of symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety
Andere Medikamente: Sertraline, Omeprazole, Men's multi-vitamin
Allergien: -
Vorherige Impfungen: flu-like symptoms, nausea, hot/cold chills, dizziness/lightheadedness - age 58, 4/9/21, 4/30/21 - COVID19 Pfizer

VAERS 2151596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MI
Alter: 56,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 03.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 14,0
Dosis: UNK
Route/Site: IM / LA

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

Axillary pain Breast pain Dizziness Fatigue Lichen planus Lymphadenopathy Vertigo

Symptomtext

Approx. 2 weeks after my booster shot, I started having very noticeable vertigo, which was persistent. Whenever I move my head suddenly, I get dizziness. It was very significant for over 2 weeks and is still noticeable to this date, but less severe. I also had unusual fatigue and a very large, swollen walnut-sized lymph node just above my left clavicle. This was very hard (like a rock) and was present for over a week. Once that resolved, I started having sharp pains in my breasts and under my armpits down my side. I am still having some of this pain and the vertigo. I have been diagnosed with the autoimmune condition, Lichen Planus, which I am being treated for.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Clobetasol Topical
Allergien: Mangos, cashews
Vorherige Impfungen: I had a reaction to the 2nd dose of the Shingrix shingles vaccine.

VAERS 2141540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: PR
Alter: 61,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Feeling hot Interchange of vaccine products Off label use Pain Swelling Vaccination site swelling

Symptomtext

swelling in the left armpit; Little pain when touching the area; hot and with little pain,; I had the area of the vaccine swollen; recieved first and second dose of moderna and third dose of comirnaty; recieved first and second dose of moderna and third dose of comirnaty; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 11Nov2021 14:45 (Lot number: FD0809) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "diabetes" (unspecified if ongoing); "High Blood Pressure" (unspecified if ongoing); "Arthritis" (unspecified if ongoing). Concomitant medication(s) included: SIMVASTATIN; AMLODIPINE BESYLATE. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: 031B21A, Location of injection: Arm Right, Vaccine Administration Time: 01:30 PM), administration date: 07Apr2021, when the patient was 60 years old; Moderna (Dose Number: 1, Batch/Lot No: 013A21, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM), administration date: 12Mar2021, when the patient was 60 years old. The following information was reported: OFF LABEL USE (non-serious) with onset 12Nov2021, outcome "unknown", INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 11Nov2021, outcome "unknown" and all described as "recieved first and second dose of moderna and third dose of comirnaty"; SWELLING (non-serious) with onset 13Nov2021, outcome "recovering", described as "swelling in the left armpit"; PAIN (non-serious) with onset 13Nov2021, outcome "recovering", described as "Little pain when touching the area"; FEELING HOT (non-serious) with onset 12Nov2021, outcome "recovering", described as "hot and with little pain,"; VACCINATION SITE SWELLING (non-serious) with onset 12Nov2021, outcome "recovering", described as "I had the area of the vaccine swollen". Therapeutic measures were taken as a result of swelling, pain, feeling hot, vaccination site swelling. Additional information: No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination. No known allergies. Facility type vaccine : Pharmacy or perfumery. Adverse event: swelling in the left armpit with a little pain when touching the area. I noticed this on 13Nov2021, when I started to touch the area. I don't know If I had it before and I didn't notice it then as I had not touched myself there. By 12Nov2021 I had the area of the vaccine swollen, hot and with little pain, but only if I touched myself there. AE treatment : continued taking Panadol. No follow-up attempts are possible. No further information was expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Blood pressure increased; Diabetes
Andere Medikamente: SIMVASTATIN; AMLODIPINE BESYLATE
Allergien: -
Vorherige Impfungen: -

VAERS 2140183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Rash SARS-CoV-2 test positive

Symptomtext

Employee experienced a generalized rash to arm and chest/breast area several hours after receiving the 2nd dose of COVID19 vaccine PFIZER. Employee subsequently tested positive for COVID-19 on 01/20/22 and experienced same rash.

Weitere VAERSDATA-Felder

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

VAERS 2124208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: AK
Alter: 45,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 01.10.2021
Beginn: 15.11.2021
Tage bis Beginn: 45,0
Dosis: UNK
Route/Site: IM / RA

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

Eye pruritus Lacrimation increased Pruritus Throat irritation

Symptomtext

usual monthly allergy shot with systemic response of watery itchy eyes, itchy hands, itchy throat. Happened again 2/17/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: Vitamin D, fish oil, sam-e, monthly allergy shot for cats/dogs/dust/cockroaches
Allergien: none
Vorherige Impfungen: -

VAERS 2119460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 20.12.2021
Beginn: 28.01.2022
Tage bis Beginn: 39,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Blood calcium decreased Blood test Chest X-ray Communication disorder Computerised tomogram Confusional state Fatigue Gait disturbance Influenza virus test negative Magnetic resonance imaging Meningitis viral Protein total decreased Pyrexia SARS-CoV-2 test negative

Symptomtext

Pt.'s Daughter states that after receiving the 1st dose of Pfizer 12/20/2022 (Booster - Previous J&J 01/15/2021), started experiencing symptoms 01/28/2022 of fatigue, fever, and weakness. Urgent Care 01/29/2022 visit/ tested for Flu & Covid = Negative. 01/31/2022 Confusion, fever, difficulty walking and communicating/ Transported to Hospital admitted for Viral Meningitis, IV treatment followed with Discharged 02/05/2022 to Rehabilitation 02/05/2022 - 02/11/2021 discharged. Primary visit 02/17/2021 protein and calcium levels low. Infectious Disease appt. 03/01/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 5,0
Labordaten: Blood Panel 01/31/2022 MRI 01/31/2022 Cat Scan 01/31/2022 Chest X-Ray 01/31/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Calcium x2, Amlodipine, Atorvastatin, Ezetimibe
Allergien: Ciproflozion, Amoxicillin, Latex, Benadryl
Vorherige Impfungen: -

VAERS 2119055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MI
Alter: 34,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia

Symptomtext

Joint Pain began 1 day post immunization. Pt still has intermittent joint pain to date.

Weitere VAERSDATA-Felder

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

VAERS 2118574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: UT
Alter: 87,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 07.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: OT / RA

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

Dry skin Hypersensitivity Insomnia Rash Rash pruritic Urticaria

Symptomtext

couldn't sleep; dry skin; allergic reaction; rash on his chest, arms, and back that was itchy (like hives); the rash had become painful; rash on his chest, arms, and back that was itchy (like hives); This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 87 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 07Oct2021 15:30 (Lot number: FD0809) at the age of 87 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "A-fib" (unspecified if ongoing); "low thyroid" (unspecified if ongoing), notes: Hypothyroid; "milk intollerance" (unspecified if ongoing). Family history included: "history of Polyps" (unspecified if ongoing), notes: history of Polyps (his dad had colon cancer). Concomitant medication(s) included: ELIQUIS taken for atrial fibrillation (ongoing); LEVOTHYROXIN taken for hypothyroidism (ongoing); METAMUCIL [PLANTAGO OVATA]; CALCIUM; GLUCOSAMINE; FISH OIL; IODINE; METOPROLOL taken for atrial fibrillation (ongoing). Vaccination history included: Bnt162b2 (prev dose product=COVID 19, prev dose brand=Pfizer, prev dose brand unknown=False, prev dose lot number= EM9809, prev dose lot unknown=False, prev dose administrator route=Intramuscular, prev dose administration date=10Feb2021 , prev dose dose number=2, Anatomical site of injection: Arm), administration date: 10Feb2021, when the patient was 86 years old, for Covid-19 immunization; Bnt162b2 (prev dose product=COVID 19, prev dose brand=Pfizer, prev dose brand unknown=False, prev dose lot number= =EL8982, prev dose lot unknown=False, prev dose administrator route=Intramuscular, prev dose administration date=21Jan2021 , prev dose dose number=1, Anatomical site of injection: Arm), administration date: 21Jan2021, when the patient was 86 years old, for Covid-19 immunization. The following information was reported: INSOMNIA (non-serious) with onset 10Oct2021, outcome "not recovered", described as "couldn't sleep"; DRY SKIN (non-serious) with onset 10Oct2021, outcome "not recovered", described as "dry skin"; HYPERSENSITIVITY (non-serious) with onset 10Oct2021, outcome "not recovered", described as "allergic reaction"; RASH PRURITIC (non-serious) with onset 10Oct2021, outcome "not recovered", URTICARIA (non-serious) with onset 09Oct2021, outcome "recovered" (31Oct2021) and all described as "rash on his chest, arms, and back that was itchy (like hives)"; RASH (non-serious) with onset 10Oct2021, outcome "not recovered", described as "the rash had become painful". The events "couldn't sleep", "dry skin", "allergic reaction", "rash on his chest, arms, and back that was itchy (like hives)", "rash on his chest, arms, and back that was itchy (like hives)" and "the rash had become painful" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of insomnia, dry skin, hypersensitivity, rash pruritic, urticaria, rash. Additional information: Patient was received his recent Covid-19 vaccine in Public Health Clinic/Veterans Administration facility. Patient did not received any other vaccine in four weeks of covid-19 vaccination. Patient did not tested for Covid-19 since vaccination. patient was not diagnosed with Covid-19 before vaccination. Patient did not have any known allergies. in other medication's Multivitamin also reported. The Physician there gave patient a Methopredinsolone (6 day) and thought it was something ingested as an allergic reaction. Patient also received Prednisone for treatment. Patient went to the urgent care the next day as the welts & itchy got progressively worse & covered more of his body. Urgent care gave prednisolone pack (4mg 21 tablets (6,5,4,3,2,1). Hives kept spreading & only got marginally better on the prednisolone. Patient went a few days after to Dermatologist who prescribed a full prednisolone 10 mg (4,3,2,1 4 days) and steroid cream (2weeks) after that the hives did not come back. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Hypothyroidism (Hypothyroid); Lactose intolerance; Polyps (history of Polyps (his dad had colon cancer))
Andere Medikamente: ELIQUIS; LEVOTHYROXIN; METAMUCIL [PLANTAGO OVATA]; CALCIUM; GLUCOSAMINE; FISH OIL; IODINE; METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2139624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MN
Alter: 53,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Arthralgia Back pain Headache Injection site pain Magnetic resonance imaging Myalgia Neck pain Pain in extremity

Symptomtext

PT EXPERIENCED SEVERE PAIN AT INJECTIONS SITE THAT SPREAD INTO BACK/SHOULDER, DELTOID, NECK, UPPER AND LOWER ARM, AND HAND. PT HAS HAD TO SEEK MEDICAL CARE AND CONTINUE TO USE OTC MEDS. PERSISTENT HEADACHE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: MRI
Aktuelle Erkrankungen: SORE THROAT
Vorgeschichte: A-FIB, FIBROMYALGIA, CHRONIC PAIN, DIABETES TYPE 2, PTSD, TBR
Andere Medikamente: -
Allergien: NKA/NKDA
Vorherige Impfungen: MODERNA DOSE LOT # 046A21A 3/13/2021

VAERS 2116336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MI
Alter: 54,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 06.01.2021
Beginn: 15.02.2022
Tage bis Beginn: 405,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Back pain SARS-CoV-2 test

Symptomtext

Pt was admitted on 2/13 due to hip and low back pain. He was scheduled for the OR for neurosurgery, but had a pre-operative COVID test on 2/15.

Weitere VAERSDATA-Felder

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

VAERS 2109567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: AK
Alter: 36,0
Geschlecht: F
Eingang: 13.02.2022
Impfdatum: 23.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / RA

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

Adverse event Exercise tolerance decreased Fatigue

Symptomtext

Beginning within 24hrs past second dose on 10/14/21, severe physical exhaustion that improved roughly 72 hours later. Post 72 hours dramatic decline in physical performance that has persisted through current date, 02/2022. Pre-vaccine, long distance runner comfortably running 20+ miles at once. Post- vaccine, struggle to run 5+ miles. Have run 10+ miles once since vaccine and experienced exhaustion early in the activity that remained throughout. Performance stats demonstrate slower speeds and working harder. Reporting as an adverse event here because it has felt like a continuation of the immediate post- vaccine exhaustion that I've been waiting to improve. Nothing I've done has seemed to improve it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None that I'm aware of
Vorgeschichte: Anxiety
Andere Medikamente: 10 mg fluoxetine, CBD or Ibuprofen prn.
Allergien: All PCNs
Vorherige Impfungen: -

VAERS 2107438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: SC
Alter: 27,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Injection site pain Off label use Product use issue Pruritus Skin disorder

Symptomtext

itchy hands and feet; Her skin is like she is digging in her skin; Left arm hurting at injection; Caller reports having her first dose of the vaccine on 07DEC2021. Caller reports on 08DEC2021 having itchiness; Caller reports having her first dose of the vaccine on 07DEC2021. Caller reports on 08DEC2021 having itchiness; 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 27 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Dec2021 10:30 (Lot number: FD0809) at the age of 27 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Diabetic", start date: 2019 (unspecified if ongoing). There were no concomitant medications. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 07Dec2021, outcome "unknown" and all described as "Caller reports having her first dose of the vaccine on 07DEC2021. Caller reports on 08DEC2021 having itchiness"; PRURITUS (non-serious) with onset 08Dec2021 12:00, outcome "not recovered", described as "itchy hands and feet"; SKIN DISORDER (non-serious) with onset 08Dec2021, outcome "unknown", described as "Her skin is like she is digging in her skin"; INJECTION SITE PAIN (non-serious) with onset 08Dec2021, outcome "not recovered", described as "Left arm hurting at injection". The patient had itchy hands and feet. Her skin was like the patient was digging in her skin. The patient had the first dose on 07Dec2021 and just had a baby so she got it for prevention. The patient normally did not get vaccines, but got it because of her daughter. The patient then asked if they can pass antibodies through breast milk. The patient was breastfeeding her daughter. Since then, her daughter had been extremely fussy. The patient was crying all day yesterday and today and then stated she cries all the time anyway. Separate report created for her daughter. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101761084 maternal/child case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetic
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2107304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 17,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Body temperature Pyrexia

Symptomtext

This is a spontaneous report received from noncontactable consumer or other non-HCP (patient). A 17-year-old male patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, batch/lot# FD0809), at the age of 17, in right arm, on Oct 4, 2021, at 14:45, single dose, for COVID-19 immunisation. No medical history or concomitant medications reported. The patient developed pyrexia (fever of 100.6 and climbing), onset Oct 5, 2021, at 13:00, with outcome of not recovered. Relevant laboratory tests and procedures available in the appropriate section. Additional information: Patient did not receive any other vaccine within four weeks of vaccination. Patient did not have COVID-19 prior vaccination and has not tested positive post vaccination. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result: 100.6 and climbing.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No allergies reported.
Vorherige Impfungen: -

VAERS 2107259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 30.09.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Body temperature Dizziness Fatigue Gingival swelling Headache Menstruation delayed Oral herpes Oral mucosal blistering Pyrexia Swollen tongue Vertigo

Symptomtext

No Menstrual yet (late); Vertigo; Dizziness; Headache; Tongue and gum swelling; gum swelling; Fever; Fever blisters in my mouth; Fever blisters in my mouth; Tiredness; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 30Sep2021 14:45 (Lot number: FD0809) at the age of 38 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FD0809, Location of injection: Arm Left, Vaccine Administration Time: 3:00 PM,Dose Number: 1, Batch/Lot No: FD0809, Location of injection: Arm Left, Vaccine Administration Time: 3:00 PM), administration date: 09Sep2021, when the patient was 38 years old, for COVID-19 immunization, reaction(s): "Injection site pain", "No Menstrual yet (late)", "Vertigo", "Dizziness", "Headache", "Tongue and gum swelling", "Tongue and gum swelling", "Fever"; Bnt162b2 (Dose Number: 1, Batch/Lot No: FD0809, Location of injection: Arm Left, Vaccine Administration Time: 3:00 PM), administration date: 09Sep2021, when the patient was 38 years old, for Covid-19 Immunization, reaction(s): "Fever blisters in my mouth", "Injection site pain". The following information was reported: MENSTRUATION DELAYED (non-serious) with onset 2021, outcome "not recovered", described as "No Menstrual yet (late)"; VERTIGO (non-serious) with onset 2021, outcome "not recovered", described as "Vertigo"; DIZZINESS (non-serious) with onset 2021, outcome "not recovered", described as "Dizziness"; HEADACHE (non-serious) with onset 2021, outcome "not recovered", described as "Headache"; SWOLLEN TONGUE (non-serious) with onset 2021, outcome "not recovered", described as "Tongue and gum swelling"; GINGIVAL SWELLING (non-serious) with onset 2021, outcome "not recovered", described as "gum swelling"; PYREXIA (non-serious) with onset 2021, outcome "not recovered", described as "Fever"; ORAL HERPES (non-serious), ORAL MUCOSAL BLISTERING (non-serious) all with onset 2021, outcome "not recovered" and all described as "Fever blisters in my mouth"; FATIGUE (non-serious) with onset 2021, outcome "not recovered", described as "Tiredness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of menstruation delayed, vertigo, dizziness, headache, swollen tongue, gingival swelling, pyrexia, oral herpes, oral mucosal blistering, fatigue. Additional information: The patient did not receive any other vaccine within 4 weeks prior to COVID vaccine. No other medications the patient received within 2 weeks of vaccination. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101302213 same reporter/patient/product, different dose/event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's Medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2107242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 09.09.2021
Beginn: 09.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dizziness Fatigue Gingival swelling Headache Menstruation delayed Oral herpes Pyrexia Swollen tongue Vaccination site pain Vertigo

Symptomtext

No Menstrual yet (late); Vertigo; Dizziness; Headache; Tongue and gum swelling; gum swelling; Fever; Fever blisters in my mouth; Tiredness; Injection site pain (only w/the 1st doze); This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 09Sep2021 15:00 (Lot number: FD0809) at the age of 38 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: MENSTRUATION DELAYED (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "No Menstrual yet (late)"; VERTIGO (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "Vertigo"; DIZZINESS (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "Dizziness"; HEADACHE (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "Headache"; SWOLLEN TONGUE (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "Tongue and gum swelling"; GINGIVAL SWELLING (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "gum swelling"; PYREXIA (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "Fever"; ORAL HERPES (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "Fever blisters in my mouth"; FATIGUE (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "Tiredness"; VACCINATION SITE PAIN (non-serious) with onset 09Sep2021 15:30, outcome "not recovered", described as "Injection site pain (only w/the 1st doze)". Therapeutic measures were not taken as a result of menstruation delayed, vertigo, dizziness, headache, swollen tongue, gingival swelling, pyrexia, oral herpes, fatigue, vaccination site pain. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101303886 same reporter/patient/product, different dose/event.

Weitere VAERSDATA-Felder

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

VAERS 2101483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 23.03.2021
Beginn: 09.02.2022
Tage bis Beginn: 323,0
Dosis: 3
Route/Site: - / -

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

Asthenia Fatigue Interchange of vaccine products

Symptomtext

weakness and fatigue admit to hospital.

Weitere VAERSDATA-Felder

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

VAERS 2096033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 17.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain

Symptomtext

patient described pain in the deltoid/shoulder in which she received her vaccination beginning 3 days post vaccination. The pain has remained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2093164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NY
Alter: 18,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 02.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / RA

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

Back pain Electromyogram Headache Laboratory test Magnetic resonance imaging Movement disorder Pelvic pain

Symptomtext

Severe pelvic pain, inability to move legs, feet, headache, back pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: 12,0
Labordaten: MEI, EMG, labs
Aktuelle Erkrankungen: -
Vorgeschichte: Lyme disease
Andere Medikamente: Wellbutrin, Zoloft, propranolol, Amantadine
Allergien: Soy
Vorherige Impfungen: -

VAERS 2092761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 04.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Blood urine present Cold sweat Vomiting

Symptomtext

Patient called pharmacy and reported throwing up, cold sweats, bleeding during urination, severe abdominal pain. Symptoms started after she went home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Trazodone 50MG, Carisoprodol 350MG, Oxycodone Hcl 30MG, Alprazolam XR 3MG, Clonidine 0.2 patch, Rabeprazole dr 20MG, Diltiazem 30MG, Prempo 0.45-1.5, Clopidogrel 75MG, Rizatriptan 10MG ODT,
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2019323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NJ
Alter: 57,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pyrexia Tinnitus

Symptomtext

A few hour after being vaccinated the patient experience tinnitus and still has it. It fluctuates in intensity. Patient also had a slight fever the same day as vaccination but was gone the next day.

Weitere VAERSDATA-Felder

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

VAERS 2089899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NY
Alter: 39,0
Geschlecht: U
Eingang: 05.02.2022
Impfdatum: 03.09.2021
Beginn: 04.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Arthralgia Chills Dry skin Fatigue Headache Lymphadenopathy Malaise Myalgia Nausea Pain Pain in extremity Pruritus Pyrexia Vaccination site erythema Vaccination site pain Vaccination site swelling

Symptomtext

Feeling unwell; Fever; My body was aching; I am very itchy all over my body; It is just a continuous itch, all over my body from head to toe/not getting red but it's just itching; under my boobs it's itching it's irritating; muscle pain; chills; joint pain; injection site swelling; injecting site redness; nausea; swelling in lymph nodes; arm pain; slight headache; tiredness; injection site pain; skin is so dry; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old patient received bnt162b2 (BNT162B2), administration date 03Sep2021 (Lot number: FD0809) at the age of 39 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "High cholesterol" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "Allergy" (unspecified if ongoing). There were no concomitant medications. The following information was reported: MALAISE (non-serious) with onset 04Sep2021, outcome "not recovered", described as "Feeling unwell"; PYREXIA (non-serious) with onset 04Sep2021, outcome "not recovered", described as "Fever"; PAIN (non-serious) with onset 04Sep2021, outcome "not recovered", described as "My body was aching"; PRURITUS (non-serious) with onset 04Sep2021, outcome "not recovered", described as "I am very itchy all over my body; It is just a continuous itch, all over my body from head to toe/not getting red but it's just itching; under my boobs it's itching it's irritating"; MYALGIA (non-serious) with onset 04Sep2021, outcome "not recovered", described as "muscle pain"; CHILLS (non-serious) with onset 04Sep2021, outcome "not recovered", described as "chills"; ARTHRALGIA (non-serious) with onset 04Sep2021, outcome "not recovered", described as "joint pain"; VACCINATION SITE SWELLING (non-serious) with onset 04Sep2021, outcome "not recovered", described as "injection site swelling"; VACCINATION SITE ERYTHEMA (non-serious) with onset 04Sep2021, outcome "not recovered", described as "injecting site redness"; NAUSEA (non-serious) with onset 04Sep2021, outcome "not recovered", described as "nausea"; LYMPHADENOPATHY (non-serious) with onset 04Sep2021, outcome "not recovered", described as "swelling in lymph nodes"; PAIN IN EXTREMITY (non-serious) with onset 04Sep2021, outcome "not recovered", described as "arm pain"; HEADACHE (non-serious) with onset 04Sep2021, outcome "not recovered", described as "slight headache"; FATIGUE (non-serious) with onset 04Sep2021, outcome "not recovered", described as "tiredness"; VACCINATION SITE PAIN (non-serious) with onset 04Sep2021, outcome "not recovered", described as "injection site pain"; DRY SKIN (non-serious) with onset 04Sep2021, outcome "not recovered", described as "skin is so dry". Additional information: A 39-year-old patient of an unspecified gender received bnt162b2 (BNT162B2) via unspecified route of administration. It was reported that the patient took the vaccine on Friday, the 03Sep2021 (Clarified as Pfizer COVID 19 vaccine) on Friday, last Friday, don't know what date that was but it's Friday that past and the night, it seems like, the patient was feeling unwell like the patient had a fever and patent body was aching but the very next day, which was the 4th, the patient noticed that patient body was 'getting lot of the side effects but one of them 'is today', it is itchy, itchy all over my body, itch was not getting worse but it was just a continuous itch, all over my body from head to toe. The patient was just trying to figure out what to do because the patient have to go to work today. The patient also reported that one was lingering most of all was itchiness; itching all over my body, my face, my head, my arm, my leg everything; not getting red but it's just itching; under my boobs it's itching it's irritating me. It was reported that patent getting most of the side effect (later clarified) and patient just wanted to know one was lingering most of all which was itchiness. Reportedly the patient was getting itching all over body so patient wanted to know what do. The patient queried that do like I go back to site where patient took the vaccine. What the patient can take to stop the itchiness because patient was itching all over body." Reportedly the patient work in the hospital. The patient job provided it to patient a nurse in patient hospital gave it to reporter. Patient don't have email for them. It was reported that the patient experienced most of the side effects. The patient was experiencing muscle pain, chills, joint pain, fever, injection site swelling, injecting site redness, nausea, start feeling unwell, have swelling in lymph nodes, had arm pain and had slight headache, had tiredness and had injection site pain, had most of them. It was reported that on 04Sep2021 the patient experienced all of these things." (Further not clarified). Scheduled date for second dose: Consumer stated, patient think it's schedule for end of the month, later end of the month it's 20th of September. "Consumer further stated, "For allergies patient was taking over the counter drugs. Patient haven't took any in a while." Patient added, "For high cholesterol doctor prescribed something new which patient never picked it up. He prescribed like 2-3 months ago but never took it. But patent was taking simvastatin. (further not clarified), haven't took simvastatin, haven't took medical, haven't took drug for in years. So doctor say as if patient have high cholesterol but not taking new kind of medication. It was reported that the patient can't give a diagnose but it's been years. It's have been over 5 years that have had a high cholesterol, allergies also but like last 3-4 years patient was diagnosed patient can't give you the back date and year. Patient stated, patient would take a Tylenol if had a headache, Aleve, Ibuprofen for pain that's it." (further not clarified hence not captured in tab). Still experiencing the events: Consumer stated, "just getting a lot of itchiness on my body just itching all over my body, my face, my head, my arm, my leg everything itching me. patient was not getting red but it's just itching, patient skin was so dry." Outcome of event: Consumer stated, "It's persisting. It's just persisting under my boobs it's itching it's just irritating me." No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Asthma; High cholesterol
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2087757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MS
Alter: 61,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 17.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / LA

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

Blood test normal Fatigue Heart rate increased Infectious mononucleosis Lip swelling Mononucleosis heterophile test positive Myalgia Oropharyngeal pain Pyrexia Sinusitis Swelling face Throat irritation

Symptomtext

On 1/17/2022 I felt very fatigue, muscle pain, sore throat, swelling of my lips and nose. Low grade fever. I went to the doctor because I thought I had COVID, but it was Mononucleosis. I had sinus infection. I was given antibiotic for this sinus infection, but I still feel very fatigue. Muscle ache, throat throat. Fast heart rate. Feb 10, 2022, I had to go back to the doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Blood test was normal but Mononucleosis Test was positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Depression; Seasonal Allergies (grass; pollen)
Andere Medikamente: Nortriptyline; Azelastine Nasal Spray
Allergien: Erythromycin; Minocycline; Seasonal Allergies (grass; pollen)
Vorherige Impfungen: COVID Pfizer 2nd dose 1/12/2021

VAERS 2077190

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fd0809

mild

Staat: NJ
Alter: 47,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 14.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal distension Amenorrhoea Axillary pain Blood test normal Discomfort Fear Fungal infection Heavy menstrual bleeding Infection Injection site lymphadenopathy Menstruation delayed Mood swings Pelvic discomfort Pelvic pain Polymenorrhoea Pregnancy test negative

Symptomtext

Sever pain left armpit and horribly enlarged lymphonode at the injection site. 5 days early menstrual cycle start with extremely heavy bleeding to the point to go to emergency room. ( i have a very regular 28 days period and never experienced any changes though my all life). After that menstrual cycle no period at all. Negative pregnancy test done in the lab ( blood work checked by my doctor) today my period is 15 days late. Never happened to me before in all my life!!! Every day I experience pain and unpleasant sensations at the pelvic era. Hurts a lot and feels like period should start but it doesn?t. Mood swings ( never had related to mensural cycle before). Reoccurring yeast infection on and off. My belly feels inflated and very heavy like a soccer ball. As of today no signs of period starting. I am very scarred, conserved as I never had any kind of go ecological issues before or any history with menstrual irregularities. Reported this to my family doctor and was told that a lot of females in her practice experience exactly the same issues and some of them were admitted to emergency with heavy bleeding and had blood transfusion done. All these women still do not have their periods return ( yang and old). The recommendations are not clear ( seat and wait for 2 months ). as doctors don?t know what is triggering menstrual problem. What is it???? What should i do?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: 01/24/2022 blood work. No abnormalities. Hormones were not checked.
Aktuelle Erkrankungen: None
Vorgeschichte: Bipolar disorder 2, pre-diabetes, arthritis
Andere Medikamente: Celebrex, vitamin d, fish oil, metformin
Allergien: Gluten, Cypro, z- pack
Vorherige Impfungen: Only Covid vaccinations

VAERS 2075761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: ID
Alter: 15,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 21.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Pain Product preparation issue Pyrexia SARS-CoV-2 test negative

Symptomtext

The vaccine was mixed incorrectly: The 12+ vial that should have been diluted with 1.8 ml's of 0.9% sodium chloride was instead diluted with 1.8 ml's of sterile water. Patient was still given 0.3 ml's but we spoke with Pfizer and they stated they could not clarify validity or stability because they have not run any tests regarding diluting with sterile water. Basically to review it with the medical director of the clinic and that dose is invalid so revaccination is necessary. Patient's mother was notified and patient did have fever of 102 degrees and body aches that lasted 3 days. He was seen 3 days later by his PCP due to these symptoms. A Covid test was done which was negative. Supportive treatment recommended.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Covid test done - negative result.
Aktuelle Erkrankungen: -
Vorgeschichte: Depression Obesity
Andere Medikamente: Albuterol Inhaler as needed Escitalopram 20 mg once daily
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2074873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NE
Alter: 33,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Urticaria

Symptomtext

Staff member was receiving her booster of Pfizer after receiving Janssen COVID19 vaccination 05/27/2021. Was observed by nursing staff x 15 minutes with no issues and was dismissed to home from work. About 1 hour post vaccination, staff member called their supervisor to report hives over their face, no problems breathing or swelling of lips or tongue. Staff member was told to report to urgent care, who then told the staff member to report to the emergency room. At the emergency room the staff member was given Benadryl and steroids, the hives resolved. No further issues reported. Staff member never reported swelling of the face, lips, tongue or problems breathing.

Weitere VAERSDATA-Felder

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

VAERS 2065462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MI
Alter: 41,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 22.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Headache Injection site swelling Injection site warmth Peripheral swelling Pruritus Pyrexia

Symptomtext

Patient developed left arm swelling/swelling of fingers of left hand about 14 hours post injection. Shortly after receiving injection, patient developed itching of both arms. She reported HA, swelling, warmth at injection site, fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: bee pollen, codeine
Vorherige Impfungen: -

VAERS 2058684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MT
Alter: 37,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chest X-ray normal Chest discomfort Dyspepsia Electrocardiogram normal Full blood count normal Gastrooesophageal reflux disease Influenza A virus test negative Influenza B virus test Metabolic function test normal Nausea SARS-CoV-2 test negative

Symptomtext

Approximately 34 hours following my Pfizer/BioNTech Booster, I began experiencing intense nausea (no vomiting). The nausea/GERD-like symptoms have lasted 5+ weeks (until present day). Patient (self) has no prior history of acid-reflux, GERD, etc. Patient (self) completed a two week Prilosec regimen (at the request of her doctor). It helped the nausea, however, symptoms have now shifted to heartburn, acid reflux, GERD (not previously experienced pre-Prilosec with the nausea). Patient (self) will be seeing a GI specialist on January 28, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: Patient (self) visited the ER around midnight on January 23, 2022. Suffering from heaviness towards center of chest. Concerned with breathing. ER doctor determined it was GERD (although no heartburn or acid reflux was present). Tests completed (all normal/negative/clear): -Xray Chest Portable -Comprehensive Metabolic Panel -Lab Only - Complete Blood Count -Influenza A+B and Sars Cov-2 -EKG
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: -Duloxetine - 5mg (tapering) (1 - 1x day) -Gaia Herbs Ashwagandha Root (1 - 1x day) -Ortho Molecular Products OrthoBiotic (1 - 1x day) -Pure Encapsulations OptiFerin C (1 - 1x day) -RLC Labs a-Drenal (1 - 1x day) -Integrative Therapeutics V
Allergien: Sulfa, Codeine, Gluten
Vorherige Impfungen: -

VAERS 2057997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fd0809

mild

Staat: GA
Alter: 25,0
Geschlecht: F
Eingang: 23.01.2022
Impfdatum: 01.03.2021
Beginn: 01.03.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Impaired work ability Lymphadenopathy Pain

Symptomtext

Armpit/lymph node swelling with sharp pains upon moving arm. Started around 5-6 hours after each vaccine (all 3) and lasted 3-5 days. The first time I contacted my doctor who said to just take ibuprofen and tylenol. It did help the pain slightly but it did not go away. I was unable to do my usual work on days 2-3 due to pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety and depression. IBS-M.
Andere Medikamente: Fluoxetine 40mg SID Junel 1/20 SID Alazopram 0.5mg PRN
Allergien: None known
Vorherige Impfungen: -

VAERS 2057069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 10.12.2021
Beginn: 25.04.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Eczema Immunisation Rash SARS-CoV-2 test

Symptomtext

Dose Number: 3; Eczema-like lesions as well as red raised bumps on torso; entire body rash; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 10Dec2021 13:00 (Lot number: FD0809) at the age of 59 years as dose 3 (booster), single, administered in arm left, administration date 09Apr2021 13:30 (Lot number: EW0162) as dose 2, single and administered in arm left, administration date 19Mar2021 12:00 (Lot number: ER8727) 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: IMMUNISATION (non-serious) with onset 10Dec2021, outcome "unknown", described as "Dose Number: 3"; ECZEMA (non-serious) with onset 25Apr2021, outcome "not recovered", described as "Eczema-like lesions as well as red raised bumps on torso"; RASH (non-serious) with onset 25Apr2021, outcome "not recovered", described as "entire body rash". The events "eczema-like lesions as well as red raised bumps on torso" and "entire body rash" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of eczema, rash. Additional information: Patient was administered most recent Covid-19 vaccine in facility: Pharmacy or Drug store. Patient did not received any other vaccines within 4 weeks prior to the Covid-19 vaccine. Patient did not received any other medications within 2 weeks of vaccination. Patient was started experiencing events with the 1st dose, and escalating BADLY after the 2nd dose, it was Began to subside (though faintly with getting better and worse intermittently) and now EXTREMELY bad again after the booster. Patient have had treatments continuously including Prednisone, Cyclosporin, UV light treatments and multiple antihistamines. All to very little effect. Patient was not diagnosed with Covid-19 prior to vaccination. Patient was not tested for Covid-19 since vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Date: 20210923; Test Name: Quest SARS-COV-2 RNA; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: None.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2053827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Diarrhoea Feeling cold Illness Musculoskeletal stiffness Vaccination site mass Vaccination site pain Vaccination site swelling Vomiting

Symptomtext

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 57 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 27Dec2021 (Lot number: FD0809) at the age of 57 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "torn rotor cuff" (unspecified if ongoing), notes: She states her rotor cuff has not been healed and she was supposed to have operations all the time but she messed up her arm and they didn't end up doing the operation. The following information was reported: ILLNESS (non-serious) with onset 28Dec2021, outcome "recovered" (Dec2021), described as "sick"; VACCINATION SITE MASS (non-serious) with onset 27Dec2021, outcome "unknown", described as "She doesn't feel a bump on there but still feels lumps."; FEELING COLD (non-serious) with onset 28Dec2021, outcome "unknown", described as "cool"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 27Dec2021, outcome "unknown", described as "Her arm gets real stiff"; VACCINATION SITE PAIN (non-serious) with onset 27Dec2021, outcome "unknown", described as "Caller stated she took a Tylenol last night to ease the pain"; VACCINATION SITE SWELLING (non-serious) with onset 27Dec2021, outcome "not recovered", described as "swelling at the injection site"; VOMITING (non-serious) with onset 28Dec2021, outcome "recovered" (Dec2021), described as "throwing up"; DIARRHOEA (non-serious) with onset 28Dec2021, outcome "recovered" (Dec2021), described as "diarrhea". Therapeutic measures were taken as a result of vaccination site pain, vaccination site swelling, vomiting, diarrhoea. Additional information: Concomitant medication included blood pressure pill. She received the first dose of the Pfizer covid 19 vaccine yesterday in the left arm (Time the Vaccination Was Given: 6:30-7:00pm). Caller stated she still had swelling at the injection site and she put ice on it and a warm compress on it and heat on it. Caller stated she took a Tylenol last night to ease the pain. Caller stated she moved it around as instructed too. Caller stated she was sick this morning throwing up and diarrhea and then she was cool noting she was told she would be sick for 24 hours. Caller wanted to know how long this side effect would last. She said the arm she had the shot in has a torn rotor cuff. Caller wanted to know if they can put the vaccine in the right arm the next shot. The caller clarifies she threw up this morning. The vaccine made her sick. She was throwing up and having diarrhea. She states she drank Pepto-Bismol and drank some water, and she is alright now. She did everything she could do. . She states her rotor cuff has not been healed and she was supposed to have operations all the time, but she messed up her arm and they didn't end up doing the operation. The caller states she put ice on her arm and a hot towel. She doesn't feel a bump on there but still feels lumps. Her arm gets really stiff and she has a torn rotor cuff in her arm which takes time to heal but she hasn't had surgery on it. The caller explains she took a blood pressure pill, stating it was hydro something. Caller was unable to provide the spelling or any product information as she did not have her blood pressure pills with her. Caller stated she started her blood pressure pills since they gave them to her. Patient did not do emergency room or physician office due to the event. Patient did not receive any additional vaccines on same date of the Pfizer. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient wanted to know if she can put alcohol on her arm. She was going to ask them to administer the next shot in her right arm. Relevant tests were none. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Rotator cuff injury (She states her rotor cuff has not been healed and she was supposed to have operations all the time but she messed up her arm and they didn't end up doing the operation.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2050330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fd0809

mild

Staat: CO
Alter: 18,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Immunisation Lymphadenopathy Malaise Pain in extremity Pyrexia

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 18 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 22Dec2021 (Lot number: Fd0809) at the age of 18 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Ew0172, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 05May2021, when the patient was 17 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: Ew0158, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 11Apr2021, when the patient was 17 years old, for Covid-19 immunization.The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021, outcome "unknown", described as "Dose Number 3"; PAIN IN EXTREMITY (non-serious) with onset 23Dec2021 09:00, outcome "recovering", described as "Left arm pain"; LYMPHADENOPATHY (non-serious) with onset 23Dec2021 09:00, outcome "recovering", described as "swollen lymph nodes left under arm"; PYREXIA (non-serious) with onset 23Dec2021 09:00, outcome "recovering", described as "fever"; MALAISE (non-serious) with onset 23Dec2021 09:00, outcome "recovering", described as "general malaise". Therapeutic measures were taken as a result of pain in extremity, lymphadenopathy, pyrexia, malaise.No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2038299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Headache

Symptomtext

Chronic severe headache all day 24/7 Dizziness comes and goes more often

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Self reporting
Aktuelle Erkrankungen: NONE
Vorgeschichte: Chiari Malformation I
Andere Medikamente: Fish oil, MVI, Vit D3, tumeric, apple cider vinegar pill, probiotic, zinc.
Allergien: NONE
Vorherige Impfungen: -

VAERS 2034890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NJ
Alter: 47,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / -

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

Lymph node pain Lymphadenopathy Tenderness

Symptomtext

B/L armpit swelling, L side of neck tender and sore for over a month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1854931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 7,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered Pain in extremity Tenderness Overdose Product administered to patient of inappropriate age

Symptomtext

inadvertently got the adult dose of Pfizer Covid19 vaccine; inadvertently got the adult dose of Pfizer Covid19 vaccine; sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 7 year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in arm left, administration date 08Nov2021 14:45 (Lot number: FK5127) at the age of 7 years as dose 1, single for covid-19 immunization. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), OVERDOSE (non-serious) all with onset 08Nov2021, outcome "unknown" and all described as " inadvertently got the adult dose of Pfizer Covid19 vaccine"; PAIN IN EXTREMITY (non-serious) with onset 08Nov2021, outcome "unknown", described as "sore arm". Additional information: patient inadvertently got the adult dose of Pfizer Covid19 vaccine. The pediatric sticker was put on the vaccine card, but that is not what patient received. The one she got was clear and the pediatric one is supposed to be orange. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: SC
Alter: 77,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Dysphonia Influenza Nasopharyngitis Pain Respiratory tract congestion Swelling Tenderness

Symptomtext

Within 24 hours arm started to swell, became tender and sore, cold/flu symptoms, a change in the voice, and congestion. Healthcare professional advised not to get 2nd dose of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Grass.
Vorherige Impfungen: -

VAERS 2027863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MI
Alter: 27,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 10.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: UN / LA

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

Chills Fatigue Pain in extremity Pyrexia

Symptomtext

Fever. Chills, arm pain, tiredness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: I had a cold
Vorgeschichte: Back pain
Andere Medikamente: zyrtec, prednisone, singular, Tylenol
Allergien: Rae eggs, Red apples, Sulfa, cherries
Vorherige Impfungen: -

VAERS 2024221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: GA
Alter: 37,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Allergy test Blood test Erythema Feeling hot Immunisation Investigation Pain Product use issue Pruritus Urticaria

Symptomtext

Large red hot hives; The hives appear for 24hr and go from small to large, raised, hot, itchy, and if itched - painful; The hives appear for 24hr and go from small to large, raised, hot, itchy, and if itched - painful; The hives appear for 24hr and go from small to large, raised, hot, itchy, and if itched - painful; Large red hot hives; Flulaval quadrivalent was administered on 22Sep2021; Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 22Sep2021 (Lot number: FD0809) at the age of 37 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine inact split 4v (FLULAVAL QUADRIVALENT), administered in arm left, administration date 22Sep2021 (Lot number: 2579B) as dose 1, single. The patient's relevant medical history was not reported. Concomitant medication(s) included: BUPROPION; DEXTROAMPHETAMINE [DEXAMFETAMINE]; AMPHETAMINE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8734, Location of injection: Arm Left), administration date: 02Apr2021, when the patient was 36 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6202, Location of injection: Arm Left), administration date: 05Mar2021, when the patient was 36 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 22Sep2021, outcome "unknown", described as "Booster"; URTICARIA (medically significant), ERYTHEMA (non-serious) all with onset 09Oct2021, outcome "not recovered" and all described as "Large red hot hives"; FEELING HOT (non-serious), PRURITUS (non-serious), PAIN (non-serious) all with onset 09Oct2021, outcome "not recovered" and all described as "The hives appear for 24hr and go from small to large, raised, hot, itchy, and if itched - painful"; PRODUCT USE ISSUE (non-serious) with onset 22Sep2021, outcome "unknown", described as "Flulaval quadrivalent was administered on 22Sep2021". The events "large red hot hives", "the hives appear for 24hr and go from small to large, raised, hot, itchy, and if itched - painful", "the hives appear for 24hr and go from small to large, raised, hot, itchy, and if itched - painful", "the hives appear for 24hr and go from small to large, raised, hot, itchy, and if itched - painful" and "large red hot hives" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: allergy test: (2021) unknown results; blood test: (2021) unknown results; investigation: (2021) unknown results. Therapeutic measures were taken as a result of urticaria, feeling hot, pruritus, pain, erythema. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Two weeks after the booster on 09Oct2021, the patient developed large red hot hives and they have continued daily until this very day. Three months. The only new variable at the time was the booster shot. The last dermatologist the patient spoke with told that others have experienced the same. The hives appear for 24hr and go from small to large, raised, hot, itchy, and if itched - painful. There was no prolonged hospitalization. The adverse event resulted in doctor or other healthcare professional office/clinic visit. Steroids, antihistamine were the treatment received for the adverse event and nothing worked. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: allergy tests; Result Unstructured Data: Test Result:Unknown results; Test Date: 2021; Test Name: blood tests; Result Unstructured Data: Test Result:Unknown results; Test Date: 2021; Test Name: Patch test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: BUPROPION; DEXTROAMPHETAMINE [DEXAMFETAMINE]; AMPHETAMINE
Allergien: -
Vorherige Impfungen: -

VAERS 2021764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: AZ
Alter: 57,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 04.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Cough Headache Nasal discharge discolouration Pain in extremity Pyrexia Respiratory tract congestion

Symptomtext

Arm pain for a few days; fever 103; on and off low grade few; headache; chest congestion in the morning; coughing yellowish mucus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Covid test - negative; influenza A & B - negative
Aktuelle Erkrankungen: Congestions
Vorgeschichte: Psoriasis; Low Thyroid; neuropathy
Andere Medikamente: Cetirizine; multivitamin; vitamin D; vitamin B12; lysine; alpha lipoic acid
Allergien: Insects; milk; corn; narcotics
Vorherige Impfungen: Measles - I was around the age of 10

VAERS 2020830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: LA
Alter: 57,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 01.10.2021
Beginn: 29.12.2021
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: SYR / LA

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

Cough Headache Oropharyngeal pain Respiratory tract congestion Rhinorrhoea Sinusitis

Symptomtext

12/29/2021 I woke up with a sore throat congested all night , one side was congested, one side running, headache, cough, but I was not coughing anything up. I went to clinic, the doctor checked me there, my lungs were clear, she offered me antibiotics. She told me to treat it like a sinusitis. And said it was too early to test me for COVID-19. I wasn't feeling worse, so I did not go back to the clinic. So I never got tested. I'm still stuffed up and coughing. I think it's the weather. I get the sinus stuff every year.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: not at all
Vorgeschichte: high blood pressure
Andere Medikamente: Micardis 40 mg/ 12 1/2 hctz od Effexor 37 1/2 mg at night
Allergien: no
Vorherige Impfungen: -

VAERS 2019318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 14.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Injection site pain

Symptomtext

Lingering arm pain at injection site. Patient has been feeling dizzy, especially when getting up from bed in the night. She made appointment with PCP and was told dizziness could be due to BP medications. Arm pain is normal side effect of vaccine and should reduce with time. Dizziness has reduced, however patient still experiencing lingering arm pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Famotidine, Diazepam, Metoprolol, Atorvastatin, Bromocriptine, Glipizide, Mycophenolate
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 2018524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

COVID-19 Cough Fatigue Headache Immunisation Nasal congestion Pain Polymerase chain reaction Rhinorrhoea SARS-CoV-2 test Vaccination failure

Symptomtext

Breakthrough Covid-19 infection; 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 27 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administration date 19Nov2021 (Lot number: FD0809) at the age of 27 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: No. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Route of Administration: Intramuscular), administration date: 10Apr2021, when the patient was 27 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP6955, Route of Administration: Intramuscular), administration date: 20Mar2021, when the patient was 27 years old, for Covid-19 immunization. The following information was reported: immunization, vaccination failure, pain, fatigue, headache, cough, nasal congestion and rhinorrhea all not recovered with onset 19Dec2021. Therapeutic measures were taken as a result of immunisation, covid-19, vaccination failure, pain, fatigue, headache, cough, nasal congestion, rhinorrhoea. Additional information: Patient was treated with Dayquil every 4 hours. Patient was not Covid prior vaccination. Investigational results of RA: 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 EP6955, fill lot EP6954, and the formulated drug product lot EP6953. 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20211217; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211220; Test Name: PCR; Result Unstructured Data: Test Result:Unknown result; Comments: Nasal Swab; Test Date: 20211217; Test Name: Rapid; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211220; Test Name: Rapid; Test Result: Positive ; Comments: Nasal Swab; Test Date: 20211222; Test Name: Rapid; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MO
Alter: 62,0
Geschlecht: U
Eingang: 08.01.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Asthenia Chills Illness Immunisation Interchange of vaccine products Nausea Off label use SARS-CoV-2 test Urticaria

Symptomtext

I have been nauseated every time I eat I have nausea; I have been sick ever since I got this shot; This medicine this booster made me sick; I feel weak; cold chills; hives; booster shot; my other two shots were Moderna; my other two shots were Moderna; 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 patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Dec2021 (Lot number: FD0809) at the age of 62 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Rheumatoid arthritis" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "sleep disorder" (unspecified if ongoing); "breast cancer" (unspecified if ongoing); "bronchitis" (unspecified if ongoing); "Breast cancer surgery" (unspecified if ongoing). Concomitant medication(s) included: IBUPROFEN taken for arthritis, start date: 2009; TRAZODONE taken for sleep disorder. Vaccination history included: Moderna (Dose:1), for COVID-19 Immunization; Moderna (Dose:2), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 08Dec2021, outcome "unknown", described as "booster shot"; OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 08Dec2021, outcome "unknown" and all described as "my other two shots were Moderna"; NAUSEA (non-serious) with onset 16Dec2021, outcome "unknown", described as "I have been nauseated every time I eat I have nausea"; ILLNESS (non-serious) with onset 16Dec2021, outcome "unknown", described as "I have been sick ever since I got this shot; This medicine this booster made me sick"; ASTHENIA (non-serious) with onset 16Dec2021, outcome "unknown", described as "I feel weak"; CHILLS (non-serious) with onset 16Dec2021, outcome "unknown", described as "cold chills"; URTICARIA (non-serious) with onset 16Dec2021, outcome "unknown", described as "hives". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of nausea, illness, asthenia, chills, urticaria. Additional information: Patient stated, patient had been nauseated every time patient ate patient had nausea in the stomach and felt weak. When patient first got the shot patient had cold chills and hives (Further clarifications unknown hence event captured as per verbatim) when patient laid down you know patient had been sick ever since patient got this shot and did not have COVID. Had been tested 6 times and all the tests came out negative. Patient talked about Pfizer, yes because patient was the other two shots were Moderna and patient really had problem with this. Patient was informed about Pfizer drug safety department. Patient wanted to report, need no medical assistance if patient was getting sicker patient knew patient had to go to the hospital. Start date of Adverse Event: patient stated, about three days ago, about 17Dec2021 or 16Dec2021. Start date for nasal inhaler patient stated no, 2008 something like this when patient first started. Treatment for AE: Patient stated, No, I have no. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Covid test; Test Result: Negative ; Comments: have been tested 6 times and all my tests came out negative.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer; Bronchial asthma; Bronchitis; Rheumatoid arthritis; Sleep disorder; Surgery
Andere Medikamente: IBUPROFEN; TRAZODONE
Allergien: -
Vorherige Impfungen: -

VAERS 2018352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: OH
Alter: 21,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 04.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Rash Swelling face

Symptomtext

patient woke up saturday morning with rash on left arm , leg and puffy face. mother gave benadryl for the allergic reaction. i suggested if symptoms get worse or difficulty in breathing or swallowing to go to emergency department for further treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: larin fe 1/20 tablet
Allergien: none
Vorherige Impfungen: -

VAERS 2018307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NH
Alter: 63,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 11.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Body temperature Chills Fatigue Headache Immunisation Nasal congestion Pain Pyrexia Somnolence

Symptomtext

Fever; Chills; Body aches; Dull headache; booster; Stuffy nose; Tired; Sleeping a bit more; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63 year-old male patient received bnt162b2 (BNT162B2), administered in arm, administration date 11Dec2021 (Lot number: FD0809) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (LOT: ER8730, Anatomical Location: Arm), administration date: 31Mar2021, when the patient was 62 years old, for COVID-19 immunization; Bnt162b2 (LOT: EW0169, Anatomical Location: Arm), administration date: 22Apr2021, when the patient was 62 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 11Dec2021, outcome "unknown", described as "booster"; PYREXIA (non-serious) with onset 12Dec2021, outcome "not recovered", described as "Fever"; CHILLS (non-serious) with onset 12Dec2021, outcome "recovered" (Dec2021), described as "Chills"; PAIN (non-serious) with onset 12Dec2021, outcome "recovered" (Dec2021), described as "Body aches"; HEADACHE (non-serious) with onset 12Dec2021, outcome "recovered" (Dec2021), described as "Dull headache"; NASAL CONGESTION (non-serious) with onset Dec2021, outcome "not recovered", described as "Stuffy nose"; FATIGUE (non-serious) with onset Dec2021, outcome "unknown", described as "Tired"; SOMNOLENCE (non-serious) with onset Dec2021, outcome "unknown", described as "Sleeping a bit more". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, headache, nasal congestion. Therapeutic measures were not taken as a result of chills, pain. Additional information: Patient stated that his Pfizer COVID-19 vaccine booster Saturday and the following day he had more side effects than last time he had any. Patient told he was getting better but he has the booklet they gave out that says the booster doesn't give you COVID, but tomorrow patient had an appointment with someone to get his toenails cut and wanted to make sure it is ok to keep that appointment. Patient told his side effects were that had a fever that has been coming and going, and most of his other symptoms were gone. Patient told had chills and body aches on Sunday and a dull headache that was almost gone, and a stuffy nose that was getting a little better. Patient said that temp was 102 degrees Fahrenheit at the highest, it has come and gone, it was sometimes 101 or 100 and now it was 99.3 degrees Fahrenheit. patient told it comes and goes too, so patient was wondering if it would be ok to wear a mask and keep this appointment tomorrow in the morning? Patient said that he was tired and sleeping a bit more. Patient said he took aspirin for the fever, dose unknown, he just took one and then later he maybe took another after a few hours. He said after a while it went away, and this afternoon then it came back. He said his temp was 98.5 now or 98.9, it goes back and forth he guesses, he has a handheld thing to take his temperature that you put on or near forehead. Patient said he had chills mostly on Sunday afternoon, and he did no treatment other than being bundled up, drinking water, using a heating pad type thing that put in a microwave to warm it up, a bag type thing. He said he only had chills on Sunday though he did feel a little cool today, it was not chills, he just felt cold again, so he did the same thing, got in the bed and warmed up. He said the body aches were Sunday afternoon or early evening maybe. He said for treatment he just heated up and keep warm, and warm up. Patient said for the dull headache he had the Aspirin and would blow his nose and take Flonase to try to help his sinuses, he was a little stuffed up still. He said the dull headache was not as bad, and it started Sunday. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: Body Temperature; Result Unstructured Data: Test Result:102 degrees degrees Fahrenheit; Comments: At the highest, it has come and gone; Test Name: Body Temperature; Result Unstructured Data: Test Result:101; Comments: It is sometimes 101 or 100; Test Name: Body Temperature; Result Unstructured Data: Test Result:99.3 degrees Fahrenheit; Comments: Now it is 99.3 degrees Fahrenheit; Test Name: Body Temperature; Result Unstructured Data: Test Result:100; Comments: It is sometimes 101 or 100
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 06.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Chills Diarrhoea Immunisation Myalgia Nausea Pain in extremity Pyrexia Vomiting

Symptomtext

had arm pain; muscle aches; fever; chills; Booster; had severe nausea; vomiting; diarrhea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administration date 06Dec2021 (Lot number: FD0809) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Allergies: PCN" (unspecified if ongoing), notes: known allergies: PCN, codeine. Concomitant medication(s) included: ELIQUIS. Past drug history included: Codeine, reaction(s): "Allergy: Codeine", notes: known allergies: PCN, codeine. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0153), administration date: 08Apr2021, when the patient was 64 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER2613), administration date: 18Mar2021, when the patient was 64 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 06Dec2021, outcome "unknown", described as "Booster"; PAIN IN EXTREMITY (non-serious) with onset 07Dec2021, outcome "recovered" (Dec2021), described as "had arm pain"; MYALGIA (non-serious) with onset 07Dec2021, outcome "recovered" (Dec2021), described as "muscle aches"; PYREXIA (non-serious) with onset 07Dec2021, outcome "recovered" (Dec2021), described as "fever"; CHILLS (non-serious) with onset 07Dec2021, outcome "recovered" (Dec2021), described as "chills"; NAUSEA (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "had severe nausea"; VOMITING (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "vomiting"; DIARRHOEA (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "diarrhea". Therapeutic measures were not taken as a result of pain in extremity, myalgia, pyrexia, chills, nausea, vomiting, diarrhoea. Additional information: Facility where the most recent COVID-19 vaccine was administered was public health clinic/veterans administration facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (known allergies: PCN, codeine)
Andere Medikamente: ELIQUIS
Allergien: -
Vorherige Impfungen: -

VAERS 2017450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 18.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Body temperature COVID-19 Chills Fatigue Feeling abnormal Headache Hyperhidrosis Immunisation Pyrexia SARS-CoV-2 test Vaccination failure Interchange of vaccine products Loss of personal independence in daily activities Off label use

Symptomtext

had a very high fever to 104; severe chills; couldn't get her head off of the pillow; bad headaches; extreme fatigue; 1st dose- 15Mar2021 Manufacture: Johnson and Johnson/had her booster dose on Saturday; 1st dose- 15Mar2021 Manufacture: Johnson and Johnson/had her booster dose on Saturday; had her booster dose on Saturday; sweating profusely; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Local reference (HZNR65AB). A 58 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 18Dec2021 10:30 (Lot number: FD0809) at the age of 58 years as dose 2 (booster), single for covid-19 immunisation. Relevant medical history included: "COVID", start date: 24Nov2021 (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Johnson and johnson covid vaccine (1st dose, Route, Anatomical Location: Left upper arm, Lot Number: 1805022, unknown expiry), administration date: 15Mar2021, when the patient was 57 years old, for COVID-19 Immunization. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 18Dec2021 10:30, outcome "unknown" and all described as "1st dose- 15Mar2021 Manufacture: Johnson and Johnson/had her booster dose on Saturday"; IMMUNISATION (non-serious) with onset 18Dec2021 10:30, outcome "unknown", described as "had her booster dose on Saturday"; PYREXIA (non-serious) with onset 18Dec2021 22:30, outcome "recovered" (Dec2021), described as "had a very high fever to 104"; CHILLS (non-serious) with onset 18Dec2021 22:30, outcome "recovered" (Dec2021), described as "severe chills"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 18Dec2021 22:30, outcome "recovered" (Dec2021), described as "couldn't get her head off of the pillow"; HEADACHE (non-serious) with onset 18Dec2021 22:30, outcome "recovering", described as "bad headaches"; FATIGUE (non-serious) with onset 18Dec2021 22:30, outcome "recovering", described as "extreme fatigue"; HYPERHIDROSIS (non-serious) with onset Dec2021, outcome "unknown", described as "sweating profusely". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller says that on her information sheet it says that if she were to have an adverse reaction that she should call this number and she had the Pfizer booster on Saturday. Product clarified to the Pfizer COVID vaccine, booster dose. Event Details: She had her booster dose on Saturday and then 12 hours later she had a very high fever to 104, severe chills, she couldn't get her head off of the pillow, bad headaches and extreme fatigue. Confirmed that she had her booster dose on 18Dec2021 around 10:30 AM so her side effects all began at 10:30 PM on the same day, 18Dec2021. Inquired if her side effects went away and she says that she is very tired still today. Her fever probably broke in the middle of the night last night because she was sweating profusely. She still has the headache and the tiredness, but they are better. Lot Number: FD0809, the 0 could be an "O" but they put slashes through them. History: She had COVID the day before thanksgiving and she doesn't know if that has anything to do with this. She was tested on 24Nov2021. Nonadditional vaccines administered on same date of the Pfizer suspect. Prior Vaccinations (within 4 weeks) If applicable, No other vaccinations within four weeks prior to the first administration date of the suspect vaccine, No AEs following prior vaccinations. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211218; Test Name: Fever; Result Unstructured Data: Test Result:104; Comments: very high fever to 104
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2017450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 18.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Body temperature COVID-19 Chills Fatigue Feeling abnormal Headache Hyperhidrosis Immunisation Pyrexia SARS-CoV-2 test Vaccination failure Interchange of vaccine products Loss of personal independence in daily activities Off label use

Symptomtext

had a very high fever to 104; severe chills; couldn't get her head off of the pillow; bad headaches; extreme fatigue; 1st dose- 15Mar2021 Manufacture: Johnson and Johnson/had her booster dose on Saturday; 1st dose- 15Mar2021 Manufacture: Johnson and Johnson/had her booster dose on Saturday; had her booster dose on Saturday; sweating profusely; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Local reference (HZNR65AB). A 58 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 18Dec2021 10:30 (Lot number: FD0809) at the age of 58 years as dose 2 (booster), single for covid-19 immunisation. Relevant medical history included: "COVID", start date: 24Nov2021 (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Johnson and johnson covid vaccine (1st dose, Route, Anatomical Location: Left upper arm, Lot Number: 1805022, unknown expiry), administration date: 15Mar2021, when the patient was 57 years old, for COVID-19 Immunization. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 18Dec2021 10:30, outcome "unknown" and all described as "1st dose- 15Mar2021 Manufacture: Johnson and Johnson/had her booster dose on Saturday"; IMMUNISATION (non-serious) with onset 18Dec2021 10:30, outcome "unknown", described as "had her booster dose on Saturday"; PYREXIA (non-serious) with onset 18Dec2021 22:30, outcome "recovered" (Dec2021), described as "had a very high fever to 104"; CHILLS (non-serious) with onset 18Dec2021 22:30, outcome "recovered" (Dec2021), described as "severe chills"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 18Dec2021 22:30, outcome "recovered" (Dec2021), described as "couldn't get her head off of the pillow"; HEADACHE (non-serious) with onset 18Dec2021 22:30, outcome "recovering", described as "bad headaches"; FATIGUE (non-serious) with onset 18Dec2021 22:30, outcome "recovering", described as "extreme fatigue"; HYPERHIDROSIS (non-serious) with onset Dec2021, outcome "unknown", described as "sweating profusely". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller says that on her information sheet it says that if she were to have an adverse reaction that she should call this number and she had the Pfizer booster on Saturday. Product clarified to the Pfizer COVID vaccine, booster dose. Event Details: She had her booster dose on Saturday and then 12 hours later she had a very high fever to 104, severe chills, she couldn't get her head off of the pillow, bad headaches and extreme fatigue. Confirmed that she had her booster dose on 18Dec2021 around 10:30 AM so her side effects all began at 10:30 PM on the same day, 18Dec2021. Inquired if her side effects went away and she says that she is very tired still today. Her fever probably broke in the middle of the night last night because she was sweating profusely. She still has the headache and the tiredness, but they are better. Lot Number: FD0809, the 0 could be an "O" but they put slashes through them. History: She had COVID the day before thanksgiving and she doesn't know if that has anything to do with this. She was tested on 24Nov2021. Nonadditional vaccines administered on same date of the Pfizer suspect. Prior Vaccinations (within 4 weeks) If applicable, No other vaccinations within four weeks prior to the first administration date of the suspect vaccine, No AEs following prior vaccinations. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211218; Test Name: Fever; Result Unstructured Data: Test Result:104; Comments: very high fever to 104
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2647055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: ID
Alter: 67,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 27.08.2021
Beginn: 30.10.2021
Tage bis Beginn: 64,0
Dosis: 3
Route/Site: SYR / LA

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

Blood donor Head discomfort Headache Rash Tension headache

Symptomtext

Jan 2021 -First vaccine after still having antibodies after giving convalescent plasma 7 weeks of Covid headaches. Tried HBOT to treat headaches. Chronic fatigue after Covid 19 in March 2020 August 27, 2021 2nd vaccine Pfizer Oct 6, 2021, 3rd vaccine Pzizer Oct 30 began severe head pressure, as though temples are being squeezed and brain is too large for skull. Full body rash after all 3 vaccines. Just received a referral to Long Covid Clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: n Long Covid
Andere Medikamente: Vitamin, C,D3, E, selenium, zinc, quercetin, magnesium,
Allergien: none
Vorherige Impfungen: -

VAERS 2014854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NH
Alter: 14,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Dizziness Hyperhidrosis Mydriasis Nausea Pallor Throat irritation

Symptomtext

Within 1 minute of giving the vaccine, patient became pale,diaphoretic, dizzy, nauseous, and had dilated pupil. She was helped to a chair. She complained of a tickling and scratching of her throat and was given 25 mg of Benadryl. After another 3-4 min her color came back and all symptoms resolved. She sat with us for another 20 min to rule out any immediate allergic reactions. Pulse 60 bpm. Blood pressure 110/50 sitting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prescription for hyperhydrosis
Allergien: No known
Vorherige Impfungen: -

VAERS 2010277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: PA
Alter: 30,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 01.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain Pregnancy test negative Urinary tract infection Urine analysis

Symptomtext

Extreme dizziness (1/6/22 onset, lasting for hours at a time) Back pain (7/10 pain scale, 1/4/22 onset, lasting for 3 days) UTI (asymptomatic, unknown onset, prescribed cephalexin for 7 days) Determined that the dizziness was from starting buspirone on 1/1/22 immediately after stopping Zoloft. Patient instructed to stop buspirone and restart Zoloft on 1/6/22. Back pain was attributed to PMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Urinalysis. Pregnancy test (negative).
Aktuelle Erkrankungen: Ear infection beginning in October 2021 until present.
Vorgeschichte: -
Andere Medikamente: Prenatal vitamin once per day, buspirone 5 mg twice per day.
Allergien: Cats, dust.
Vorherige Impfungen: -

VAERS 2006166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: OH
Alter: 46,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Chills Decreased appetite Dizziness Malaise Pain

Symptomtext

Started to feel ill night of vaccination. Had chills, weakness and aches, dizziness and some loss of appetite. Symptoms were worst the next day (Friday). Each day the symptoms got lighter, by Sunday I felt almost back to normal. By Monday symptoms were gone. Used Advil to treat symptoms Thursday and Friday, by Saturday no longer needed Advil. All in all, felt like a small replay of many of the symptoms I had back in mid November when I tested positive for COVID itself.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: DEPRESSION, ANXIETY
Andere Medikamente: PANTOPRAZOLE 20MG, ESCITALOPRAM 20MG
Allergien: N/A
Vorherige Impfungen: -

VAERS 2002924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: MI
Alter: 34,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Malaise

Symptomtext

Patient received vaccination without any issues. Asked him to stay the 15 minutes after vaccination to make sure that he doesn't have side effects. A few minutes after he sat down, he got my attention and said he was not feeling well, dizzy. Had him sit down, drink water. Took his blood pressure which was 148/105, repeated in 10 minutes and it was 146/108 via electronic cuff. Switched to manual to ensure correct values and manual pressure was 145/105. Called 911 to evaluate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None that were discussed
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2002372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MD
Alter: 16,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 27.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain upper Cough Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative Streptococcus test negative Vomiting

Symptomtext

12/31- started with vomiting, cough/congestion, belly pain, and sore throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Rapid strep/rapid Covid-19 negative 1/4/22.
Aktuelle Erkrankungen: none
Vorgeschichte: Migraines
Andere Medikamente: OCP
Allergien: none
Vorherige Impfungen: -

VAERS 2001997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 75,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 29.09.2021
Beginn: 21.12.2021
Tage bis Beginn: 83,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fall Vertigo positional

Symptomtext

I was extremely dizzy and fell back into bed after getting up on the morning of 12/21. After this event found it only happened when getting up or laying down. Positional Vertigo seems to be what I have but I have yet to see my doctor. I am scheduled to see my doctor on 01/18 about this issue. Seems that everything I do goes toward the left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None yet.
Aktuelle Erkrankungen: None
Vorgeschichte: COPD; GERD
Andere Medikamente: Trilogy; ProAir; Zyrtec; Nasacort; Omeprazole; Mucinex; Instaflex Advanced Joint Support; Citrucel; Lorazepam; Zoloft; Metoprolol Succinate; Yin Chiao; Olive Leaf Tea
Allergien: Contrast dye; Narcotic Opioid Family; Kiwi; Scent or Perfumes
Vorherige Impfungen: -

VAERS 1999106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: LA
Alter: 47,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 30.09.2021
Beginn: 30.12.2021
Tage bis Beginn: 91,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Fatigue Pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I started off with a runny nose. I had been exposed at work on Monday and Tuesday. When I got home from work on Thursday I contacted my insurance provider. They did not answer so I tested myself at home and it tested positive. I also tested with a PCR and it was positive as well. I only had the runny nose. I had very little soreness. Thursday I blew my nose a couple of times but I did not have anything else, so I think I was asymptomatic. I took Zinc, Vitamin C, Ginger, and Tylenol one day. I still feel kind of tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid test 12/30/2021 positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Synthroid; Lipitor; Vitamin D; Claritin
Allergien: Latex; Clindamycin
Vorherige Impfungen: -

VAERS 1998011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CO
Alter: 36,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Pain

Symptomtext

Pain at soft palate. Began morning following initial dose. Duration: 10 days. Pain scale: 6/10.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Liletta IUD. Insertion date 2/14/2020; Biotin soft gel 2500mcg PO QD
Allergien: NKA, NKDA
Vorherige Impfungen: -

VAERS 1998007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 13.09.2021
Beginn: 04.10.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Erythema Malaise Scleroderma Skin discolouration

Symptomtext

On October 18, 2021, lilac and bright red spots of 0.5 centimeters - 7 centimeters appeared in the abdomen, under the arms, and between the legs. I began to feel unwell, dizziness and weakness appeared. I went to the doctors and was diagnosed with Scleroderma. I am sure that the immediate development of this dangerous disease was provoked by the Pfizer Covid19 vaccine. I am ready to undergo an examination to clarify the disease caused by the Pfizer Covid19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1997453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: GA
Alter: 63,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 31.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Peripheral swelling Pruritus

Symptomtext

Itching and swelling of palms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Essential tremor
Andere Medikamente: Magnesium Zinc Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1985275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: IL
Alter: 68,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 10.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site erythema Injection site pain Injection site swelling Injection site warmth

Symptomtext

48 Hours after the injection I woke up on 12/12/2021 early AM with pain soreness and redness in my left upper arm where I received the booster third shot of the COVID vaccine the swelling and redness was about the size of a quarter and as the day went on the swelling increased and redness to the area increased and the site became more painful the area had become the size of an orange and more painful and the area was hot to touch I made an appointment with the Dr to show her my left arm and she prescribed Keflex after taking the Keflex for two days the swelling started to go down and I was on medication for 5 days and by the 5th day of medication the pain was relieved the area was hardly swelled and it wasn't hot to touch any more

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma Allergies
Vorgeschichte: Asthma Lymphedema Failure Back Surgery since 2010 Seasonal Allergies
Andere Medikamente: Flonase Singulair Torsemide Potassium
Allergien: Fish Iodine IVP Dye Contrast Z Pak Clindamycin Azithromycin
Vorherige Impfungen: -

VAERS 1985245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 29.11.2021
Beginn: 21.12.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Oropharyngeal pain SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

I developed a sore throat on the evening of 21 December, and it became significant enough to warrant concern during the morning of 23 December. I tested positive for COVID on the morning of 24 December, and the sore throat continued before symptoms lessened starting 28 December.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 21 Decemeber: Negative 22 December: Negative 23 December: Negative 24 December: Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Concerta, Focalin, Zoloft, NAC, Melatonin, Multivitamin, Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 1981912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Blood urine present Computerised tomogram abdomen abnormal Computerised tomogram thorax Culture urine positive Gait disturbance Gallbladder disorder Gallbladder enlargement Groin pain Headache Immediate post-injection reaction Influenza A virus test negative Influenza B virus test Influenza virus test negative Lymphadenopathy Nausea Pain Pain in extremity Pyrexia

Symptomtext

I experienced pain in my left arm right after the shot. Also, both sides of my groin were already hurting at that point. I saw lumps on both sides of my groin that evening (lymph nodes were swollen). The pain was becoming more severe and I felt I would not be able to walk. I went to the ER and they told me to take Tylenol and ibuprofen. They did not do any tests at that time but they examined the legs to see if there was any injuries but didn't see anything of note. Fever continued for a few more days and I experienced a headache with nausea. I went to the ER on 12/25/2021 and they ran tests on me (noted below). I was hospitalized overnight (woke up with a fever), and they assumed it was likely another virus because they hadn't seen somebody react like that after the booster. I got some nausea medicine and I was told to follow up with my PCP if I didn't get better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Groin pain
Hospital-Tage: 1,0
Labordaten: Urine culture: had some blood in it, were going to send that off. CT scan of chest/pelvis/abdomen: Saw some fluid in the gallbladder which was concerning. Ultrasound: Saw thickening of gallbladder lining but no stones. Did a dye test: surgeons reported gallbladder ok/no need for surgery. I got a rapid test for FLU A/B, RSV and COVID and all were negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control
Allergien: Penicillin; another antibiotic (possibly Oxycycline)
Vorherige Impfungen: -

VAERS 1981852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fd0809

mild

Staat: VA
Alter: 45,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 07.09.2021
Beginn: 23.12.2021
Tage bis Beginn: 107,0
Dosis: 3
Route/Site: SYR / AR

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

Ageusia Anosmia Arthralgia Chills Cough Exposure to SARS-CoV-2 Fatigue Hyperhidrosis Myalgia Nausea Oropharyngeal pain Pain in extremity

Symptomtext

Sunday December 19 husband and kids started getting sick, kids tested negative Tuesday 12/21 in AM for flu & Covid, husband tested positive for tuesday afternoon - was told to assume everyone in the house is positive. Thursday 12/23 woke up with a sore throat and coughing, as day progressed got worse, friday 12/24 started having the sweats/chills. Saturday 12/25 - extreme joint & muscle pain - couldn't bend certain fingers due to pain, nausea and exhaustion along with the sore throat & coughing.. Sunday 12/26 - started losing sense of taste and some sense of smell. Monday 12/27 - no improvement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia, spina bifida occulta, IBS, PCOS, asthma, OCD, anxiety, depression, TMJ
Andere Medikamente: Cymbalta - 30 mg, Prevacid - 15 mg, Vitamin E - 400 IU, Magnesium - 250 mg (twice daily), Vitamin D - 2000 IU, Junel 1.5, Zyrtec - 10 mg, B-12 injections
Allergien: anaprox/naproxin - lung issues penicillin and amoxicillin - no longer work - need stronger antibiotics
Vorherige Impfungen: -

VAERS 1981358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD 0809

mild

Staat: VA
Alter: 63,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 02.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Insomnia Myalgia Pain Pain in extremity

Symptomtext

Minor constant pain in my left arm muscle. Pain worsen significantly stretching my arm and lifting. Pain severity restricts motion like bending my left arm to put on a coat. Pain bothers me while sleeping if I lay on the arm. I lived with this a while thinking it would go away over time. I do moderate exercise to use the arm muscle. The pain is now seeming to get worst and wider into my lower shoulder so I filed this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: I reported some pain in the arm during my last doctor's physical on 11/12/21.
Aktuelle Erkrankungen: None
Vorgeschichte: Prehypertension Prediabetes High cholesterol
Andere Medikamente: Simvastatin 40 Mg Tablet - one a day Metformin 500 Mg Tablet - two a day Lisinopril 20 Mg Tablet - one a day
Allergien: None
Vorherige Impfungen: -

VAERS 1981033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Decreased appetite Dizziness Eye pain Feeling abnormal Gingival pain Headache Heart rate increased Injection site erythema Injection site pain Injection site swelling Joint stiffness Lymph node pain Lymphadenopathy Myalgia Nausea Pain Pyrexia

Symptomtext

12/21/2021, 5:00PM generalized muscle aches started; swelling, redness, and increased pain at injection site; approximately 9:00PM increased heart rate, headache, and increased joint pain and tightness noticed. 12/22/2021 3:00AM lymph nodes in left clavicle, left armpit, and left groin area painful with/without touch; visual check of said lymph nodes at approximately 5:00AM, all are visibly swollen, pain intensified; 11:00AM, headache, dizziness, "fogginess," eye pain, gum pain, intensified body aches, loss of appetite, fever of 100.1 degrees F, pulse 100+BPM (baseline is 80-86); required assistance ambulating; 6:00PM blood pressure 136/88 (baseline is 114-120/74-80, no medication was missed). 12/25/2021 9:00AM: signs and symptoms noticeably decreased; lymph nodes still swollen, but have decreased approximately 50% in size, not visible, but palpable and painful with/without touch; headache; body aches (minimized, but present); fatigue and joint tightness remain, especially in right total knee replacement; occasional nausea secondary to headache; temperature 98.8 degrees F; heart rate 80; blood pressure 120/84.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I did not feel that I needed to seek higher level care because my symptoms could be, and were, managed at home.
Aktuelle Erkrankungen: N/A
Vorgeschichte: asthma, hypertension, type 2 diabetes; degenerative joint disease, total right knee replacement (circa 2013).
Andere Medikamente: amlodipine, hydrochlorothiazide, fexofenedine, albuterol HFA, potassium, gabapentin, vitamin E, multi-vitamin for women over 50
Allergien: lisinopril, erythromycin
Vorherige Impfungen: -

VAERS 1980833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MD
Alter: 24,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Immunisation Neck pain

Symptomtext

Sharp pain in the underarm area; Sharp pain in the neck where the trap muscle is; Dose number: 3; This is a spontaneous report from a contactable reporter (consumer or other non HCP). The reporter is the patient. A 24 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 13Dec2021 at 17:00 (Lot number: FD0809) at the age of 24 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: ER2613, Anatomical location: Arm Left, Administration Time: 10:00, Route of administration: Unspecified), administration date: 18Mar2021, when the patient was 23 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EW0151, Anatomical location: Arm Left, Administration Time: 11:45, Route of administration: Unspecified), administration date: 13Apr2021, when the patient was 23 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 13Dec2021 at 17:00, outcome "unknown", described as "Dose number: 3"; AXILLARY PAIN (non-serious) with onset 14Dec2021 at 09:00, outcome "recovering", described as "Sharp pain in the underarm area"; NECK PAIN (non-serious) with onset 14Dec2021 at 09:00, outcome "recovering", described as "Sharp pain in the neck where the trap muscle is". Therapeutic measures were not taken as a result of axillary pain and neck pain. Additional information: It was reported that patient had researched it and it said lymph nodes could be a cause, the supraclavicular and axillary lymph nodes. The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1980830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: GA
Alter: 28,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Arthralgia Immunisation Joint range of motion decreased Product administered at inappropriate site

Symptomtext

Pt reported terrible shoulder pain 2 days after receiving 3rd dose; Loss of range of motion; Vaccine was administered in the left leg; Dose received: 3; This is a spontaneous report from a contactable reporter (pharmacist). A 28-year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in left leg, administration date 16Dec2021 at 09:45 (Lot number: FD0809) at the age of 28 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was reported as unknown. Concomitant medications were not reported. Other vaccinations included: FLUCELVAX taken for Immunisation, start date: 09Dec2021, stop date: 09Dec2021. Vaccination history included: Covid 19 vaccine (DOSE 1, SINGLE, MANUFACTURER UNKNOWN, Lot Number: UNKNOWN), and Covid 19 vaccine (DOSE 2, SINGLE, MANUFACTURER UNKNOWN, Lot Number: UNKNOWN), administration date: 24Apr2021, when the patient was 28 years old, for COVID-19 immunisation. The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 16Dec2021 at 09:45, outcome "unknown", described as "Vaccine was administered in the left leg"; IMMUNISATION (non-serious) with onset 16Dec2021 at 09:45, outcome "unknown", described as "Dose received: 3"; ARTHRALGIA (non-serious) with onset 18Dec2021, outcome "unknown", described as "Pt reported terrible shoulder pain 2 days after receiving 3rd dose"; JOINT RANGE OF MOTION DECREASED (non-serious) with onset 18Dec2021, outcome "unknown", described as "Loss of range of motion". It was unknown whether therapeutic measures were taken as a result of the events arthralgia and joint range of motion decreased. Additional information: The patient had no known allergies. Prior to vaccination, it was unknown whether the patient was diagnosed with COVID-19. Since the vaccination, it was unknown whether the patient had been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1980789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: OR
Alter: 69,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Confusional state Delirium Disorientation Headache Immunisation Memory impairment Mental status changes SARS-CoV-2 test Vomiting

Symptomtext

Onset of delirium; altered mental status; confusion; vomiting; headache; Completely disoriented; has no memory of events.; Booster; This is a spontaneous report received from a contactable reporter(s) (Physician). A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 09Dec2021 14:15 (Lot number: FD0809) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetes" (unspecified if ongoing); "obesity" (unspecified if ongoing); "chronic pain" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "hyperlipidemia" (unspecified if ongoing); "Hashimoto's thyroiditis" (unspecified if ongoing); "GERD" (unspecified if ongoing). Patient didn't have Covid prior vaccination. Concomitant medication(s) included: FUROSEMIDE; GABAPENTIN; GLIPIZIDE; AZITHROMYCIN; IRBESARTAN; PRALUENT; ESOMEPRAZOLE MAGNESIUM. No other vaccine in four weeks. Vaccination history included: Bnt162b2 (Dose 2, lot number: EW0153, administrator route: Intramuscular, administration time: 02:15 PM, location: Left arm.), administration date: 09Apr2021, when the patient was 68 years old, for COVID-19 immunization; Bnt162b2 (Dose 1, lot number: ER2613, administrator route: Intramuscular, administration time: 02:15 PM, location: Left arm), administration date: 19Mar2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (hospitalization) with onset 09Dec2021 14:15, outcome "unknown", described as "Booster"; DELIRIUM (hospitalization) with onset 10Dec2021 01:00, outcome "recovering", described as "Onset of delirium"; MENTAL STATUS CHANGES (hospitalization) with onset 10Dec2021 01:00, outcome "recovering", described as "altered mental status"; CONFUSIONAL STATE (hospitalization) with onset 10Dec2021 01:00, outcome "recovering", described as "confusion"; VOMITING (hospitalization) with onset 10Dec2021 01:00, outcome "recovering", described as "vomiting"; HEADACHE (hospitalization) with onset 10Dec2021 01:00, outcome "recovering", described as "headache"; DISORIENTATION (hospitalization) with onset 10Dec2021 01:00, outcome "recovering", described as "Completely disoriented"; MEMORY IMPAIRMENT (hospitalization) with onset 10Dec2021 01:00, outcome "recovering", described as "has no memory of events.". Clinical course: Onset of delirium, altered mental status, confusion, vomiting, headache within about 10-12 hours of vaccine. Completely disoriented for 24 hours and has no memory of events. The patient was hospitalized for immunisation, delirium, mental status changes, confusional state, vomiting, headache, disorientation, memory impairment (hospitalization duration: 1 day(s)). The events "onset of delirium", "altered mental status", "confusion", "vomiting", "headache", "completely disoriented" and "has no memory of events" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of delirium, mental status changes, confusional state, vomiting, headache, disorientation, memory impairment, which included: IV fluids, observation, imaging, labs. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (10Dec2021) negative, notes: Nasal Swab.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the events and BNT162B2. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: 1,0
Labordaten: Test Date: 20211210; Test Name: Respiratory pathogens PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic pain; Diabetes; GERD; Hashimoto's thyroiditis; Hyperlipidemia; Hypertension; Obesity
Andere Medikamente: FUROSEMIDE; GABAPENTIN; GLIPIZIDE; AZITHROMYCIN; IRBESARTAN; PRALUENT; ESOMEPRAZOLE MAGNESIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1980776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 25.12.2021
Impfdatum: 09.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / -

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

Axillary pain Immunisation Lymphadenopathy Pain in extremity

Symptomtext

Yes, so I got the Pfizer booster; Underneath my arm and my armpit was sore; its very swollen like in the lymph nodes; its only in one side of my arm or one arm that I got the shot in; Underneath my arm and my armpit was sore; its only in one side of my arm or one arm that I got the shot in; Underneath my arm and my armpit was sore; 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), administration date 09Dec2021 (Lot number: FD0809) as dose 3 (booster) , single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose:1), for Covid-19 Immunization; Bnt162b2 (Dose:2), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "Yes, so I got the Pfizer booster"; LYMPHADENOPATHY (non-serious) with onset 11Dec2021, outcome "unknown", described as "Underneath my arm and my armpit was sore; its very swollen like in the lymph nodes; its only in one side of my arm or one arm that I got the shot in"; PAIN IN EXTREMITY (non-serious) with onset 11Dec2021, outcome "unknown", described as "Underneath my arm and my armpit was sore; its only in one side of my arm or one arm that I got the shot in"; AXILLARY PAIN (non-serious) with onset 11Dec2021, outcome "unknown", described as "Underneath my arm and my armpit was sore". Additional information: The patient got the Pfizer booster on the 09Dec2021 and the day before reporting on 11Dec2021 the patient woke up and underneath patient's arm and armpit was sore and so, the following morning on 12Dec2021 which was on the day of reporting morning the patient woke up and its very swollen like in the lymph nodes the patient mentioned. So, the patient was assuming this was a side effect because its only in one side of my arm or one arm that I got the shot in. So, the patient was wondering what should be the next course of action. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1980761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 20.09.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Abdominal pain Flatulence Gastritis Helicobacter test

Symptomtext

possible gastritis; Abdominal Pain worsened immediately after second dose/Pain was always constant and would get extremely painful at times.More pain in the morning and night.; Lots of gas is associated with the pain; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 41 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 20Sep2021 09:13 (Lot number: FD0809) at the age of 41 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose:1, Anatomical site of injection: Left arm, Route of administration: Intramuscular, Lot No: FD0809), administration date: 25Aug2021, when the patient was 41 years old, for COVID-19 immunization, reaction(s): "Abdominal pain". The following information was reported: GASTRITIS (non-serious), outcome "unknown", described as "possible gastritis"; ABDOMINAL PAIN (non-serious), outcome "not recovered", described as "Abdominal Pain worsened immediately after second dose/Pain was always constant and would get extremely painful at times.More pain in the morning and night."; FLATULENCE (non-serious), outcome "not recovered", described as "Lots of gas is associated with the pain". The events "possible gastritis", "abdominal pain worsened immediately after second dose/pain was always constant and would get extremely painful at times. more pain in the morning and night." and "lots of gas is associated with the pain" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of gastritis, abdominal pain, flatulence. Additional information: The patient provided information regarding the reported adverse events with the use of the product and reporter consider the Pfizer product had a casual effect to the adverse event and was willing to be contacted again by Pfizer on the reported adverse event. The patient took PRILOSEC [OMEPRAZOLE] tablet orally from 13Oct2021 to 30Oct2021 for abdominal pain and possible gastritis. The patient went to see physician on 29Oct2021, and started possibly gastritis. The patient was given Rx for gastritis and did an H.pylori test which was negative. Took Rx for two weeks which did not seem to help too much. Pain was still there with no current definition of cause or diagnosis. Will be following of with treating MD on Monday 13Dec2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Test Date: 20211030; Test Name: H.pylory; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1978801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NM
Alter: 57,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Rash

Symptomtext

Rash on chest and arms.; Dose received: 3/ Dose number= 3; This is a spontaneous report from a contactable reporter (consumer or other non hcp). The reporter is the patient. A 57-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 14Dec2021 at 14:30 (batch number: FD0809) at the age of 57 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Penicillin allergy" (unspecified if ongoing), notes: Known allergies: Penicillin. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: ER8731; Anatomical location: Left Arm), administration date: 14Apr2021, when the patient was 57 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EW0165; Anatomical location: Left Arm), administration date: 06May2021, when the patient was 57 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 14Dec2021 at 14:30, outcome "unknown", described as "Dose received: 3/ Dose number= 3"; RASH (non-serious) with onset 16Dec2021, outcome "not recovered", described as "Rash on chest and arms". Therapeutic measures were taken as a result of rash. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Therapeutic measures for RASH included treatment with Benadryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1975234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 10.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blood urine present Chills Fatigue Pyrexia

Symptomtext

I had fever, chills, tired and blood in urine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Paranoucturnal Anemia
Andere Medikamente: Multivitamins
Allergien: N/A
Vorherige Impfungen: -

VAERS 1975142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: NE
Alter: 76,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Pain Pain in extremity Pyrexia

Symptomtext

Sore arm, body aches,fever, headache, chills for entire day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Blood pressure
Allergien: No
Vorherige Impfungen: -

VAERS 1974869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fd0809

mild

Staat: NJ
Alter: 36,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 01.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 19,0
Dosis: 2
Route/Site: IM / LA

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

Back pain

Symptomtext

Severe upper back pain for 3 days. Worse on left side which was injection side. I'm a nurse, I've never had a pain like this before and nothing else in my life is different.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Wellbutrin, Seroquel
Allergien: None
Vorherige Impfungen: -

VAERS 1924756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Immunisation Pain Pain in extremity

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 female patient received bnt162b2 (BNT162B2) (Batch/Lot number: unknown) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 01), for COVID-19 Immunization, reaction(s): "1st and 2nd dose did not result in any adverse reactions"; Bnt162b2 (Dose: 02), for COVID-19 Immunization, reaction(s): "1st and 2nd dose did not result in any adverse reactions". The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "Booster dose"; HEADACHE (non-serious), outcome "unknown", described as "Headache"; PAIN (non-serious), outcome "unknown", described as "full body ache"; CHILLS (non-serious), outcome "unknown", described as "chills". The lot number for bnt162b2 was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

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

VAERS 1967775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 10,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered Pain in extremity

Symptomtext

Patient accidentally received adult dose of Pfizer covid vaccine. Patient is only 10 years old and only pediatric Pfizer is approved for her age. Followed up with patient for 3 days. Mother reported no adverse events other than sore arm. Pediatrician has been notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1967696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: CA
Alter: 13,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pain in extremity Product administered to patient of inappropriate age

Symptomtext

A child aged 13 was given a booster dose after being brought in by his parent for a booster dose. The child has a sore arm, and no other reported symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1967536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: VA
Alter: 14,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Nausea

Symptomtext

Severe nausea and dizziness

Weitere VAERSDATA-Felder

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

VAERS 1967484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MA
Alter: 28,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 29.11.2021
Beginn: 08.12.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

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

Audiogram Dizziness Tinnitus

Symptomtext

Dizziness after 3 weeks of initial covid shot with onset of tinnitus approximately 9 days after 2nd vaccination shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Audiology test on 12/21/21 came back normal.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: MiniPill - birth control
Allergien: N/A
Vorherige Impfungen: -

VAERS 1967414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: TN
Alter: 42,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Pain in extremity

Symptomtext

I was very tired and had a lot of pain in my left arm. I took Tylenol and had plenty of rest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: No medical test were performed.
Aktuelle Erkrankungen: No illnesses at the time of vaccination.
Vorgeschichte: I have fibroids and obese.
Andere Medikamente: I was taken Allegra 81mg, Aspirin, Sambucol Elderberry and a multivitamin.
Allergien: I am allergic to Augmentin.
Vorherige Impfungen: -

VAERS 1966958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CT
Alter: 35,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Abdominal discomfort Body temperature Immunisation Pain in extremity Pyrexia

Symptomtext

I began to develop a fever since early morning of 13 Dec 2021.; My left arm, where the injection took place, was exceedingly sore; I felt pressure in my stomach as if the food I ate was stuck there and not being digested; Dose received: 3; This is a spontaneous report received from contactable reporter (consumer or other non-HCP). The reporter is the patient. A 35 year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 12Dec2021 at 12:30 (Lot number: FD0809) at the age of 35 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Bowel obstruction" (unspecified if ongoing); "Thyroid nodule" (unspecified if ongoing), notes: Thyroid nodules; "Circumcision" (unspecified if ongoing) and "Allergy to antibiotic" (unspecified if ongoing), notes: Known allergies: Cephalosporins. The patient did not take any concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EL3247), administration date: 09Mar2021, when the patient was 34 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EP6955), administration date: 30Mar2021, when the patient was 34 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 12Dec2021 at 12:30, outcome "unknown", described as "Dose received: 3"; PYREXIA (non-serious) with onset 13Dec2021 at 01:00, outcome "recovering", described as "I began to develop a fever since early morning of 13 Dec 2021"; PAIN IN EXTREMITY (non-serious) with onset 13Dec2021 at 01:00, outcome "recovering", described as "My left arm, where the injection took place, was exceedingly sore"; ABDOMINAL DISCOMFORT (non-serious) with onset 13Dec2021 at 01:00, outcome "recovering", described as "I felt pressure in my stomach as if the food I ate was stuck there and not being digested". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, pain in extremity and abdominal discomfort. Additional Information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. It was reported that the fever lasted through the day, and in the evening his body temperature was still 99.5 F. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Date: 20211213; Test Name: Body temperature; Result Unstructured Data: Test Result:99.5 F
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic (Known allergies: Cephalosporins); Bowel obstruction; Circumcision; Thyroid nodule (Thyroid nodules)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1913504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD 0809

mild

Staat: CO
Alter: 56,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Acoustic stimulation tests abnormal Mixed deafness Sensory disturbance Tinnitus Balance disorder Diarrhoea Ear discomfort Fatigue Flushing Nausea

Symptomtext

Tinnitus bilateral ears, vibration sensations in his body

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Audiology testing 12/16/21, Mixed conductive and sensorineural hearing loss of right ear with unrestricted hearing of left ear -unchanged from previous testing
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Arthritis; Arthritis of carpometacarpal (CMC) joint of left thumb; Chronic bilateral low back pain; Chronic neck and back pain; Fatigue; Generalized weakness; Hemangioma of skin and subcutaneous tissue; History of multiple concussions; Hypertension; Hypothyroidism; Muscle weakness; Polyneuropathy; Sensation disorder; Spinal stenosis
Andere Medikamente: amitriptyline (ELAVIL) 25 mg tablet; hydrOXYchloroQUINE (PLAQUENIL) 200 mg tablet; lisinopriL (PRINIVIL,ZESTRIL) 10 mg tablet; methocarbamoL (ROBAXIN) 750 mg tablet; multivitamin capsule; pregabalin (LYRICA) 75 mg capsule
Allergien: None
Vorherige Impfungen: -

VAERS 1913504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CO
Alter: 56,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Acoustic stimulation tests abnormal Mixed deafness Sensory disturbance Tinnitus Balance disorder Diarrhoea Ear discomfort Fatigue Flushing Nausea

Symptomtext

Tinnitus bilateral ears, vibration sensations in his body

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Audiology testing 12/16/21, Mixed conductive and sensorineural hearing loss of right ear with unrestricted hearing of left ear -unchanged from previous testing
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Arthritis; Arthritis of carpometacarpal (CMC) joint of left thumb; Chronic bilateral low back pain; Chronic neck and back pain; Fatigue; Generalized weakness; Hemangioma of skin and subcutaneous tissue; History of multiple concussions; Hypertension; Hypothyroidism; Muscle weakness; Polyneuropathy; Sensation disorder; Spinal stenosis
Andere Medikamente: amitriptyline (ELAVIL) 25 mg tablet; hydrOXYchloroQUINE (PLAQUENIL) 200 mg tablet; lisinopriL (PRINIVIL,ZESTRIL) 10 mg tablet; methocarbamoL (ROBAXIN) 750 mg tablet; multivitamin capsule; pregabalin (LYRICA) 75 mg capsule
Allergien: None
Vorherige Impfungen: -

VAERS 1886891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CT
Alter: 34,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 21.09.2021
Beginn: 21.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Acoustic stimulation tests normal Disorientation Ear discomfort Feeling abnormal Headache Hyperacusis Physical examination normal Tinnitus

Symptomtext

ear fullness; sensitivity to noise at normal volumes; tinnitus in both ears and head; brain fog; disorientation; headache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21Sep2021 12:30 (Lot number: FD0809) at the age of 34 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. The patient took concomitant medications. The following information was reported: FEELING ABNORMAL (non-serious) with onset 21Sep2021 20:00, outcome "not recovered", described as "brain fog"; DISORIENTATION (non-serious) with onset 21Sep2021 20:00, outcome "not recovered", described as "disorientation"; HEADACHE (non-serious) with onset 21Sep2021 20:00, outcome "not recovered", described as "headache"; EAR DISCOMFORT (non-serious) with onset 28Sep2021, outcome "not recovered", described as "ear fullness"; HYPERACUSIS (non-serious) with onset 28Sep2021, outcome "not recovered", described as "sensitivity to noise at normal volumes"; TINNITUS (non-serious) with onset 28Sep2021, outcome "not recovered", described as "tinnitus in both ears and head". The events "brain fog", "disorientation", "headache", "ear fullness", "sensitivity to noise at normal volumes" and "tinnitus in both ears and head" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of feeling abnormal, disorientation, headache, ear discomfort, hyperacusis, tinnitus. Additional information: The patient received daily multivitamin within 2 weeks of vaccination (as reported). The patient has no known allergies. The patient did not receive any other vaccine within 4 weeks prior to COVID-19 vaccine. Prior to vaccination, the patient was not been diagnosed with COVID-19 and since the vaccination, the patient has not been tested for COVID-19. It was reported that the brain fog and disorientation subsided after two weeks. One week after vaccination (as reported), ear fullness, sensitivity to noise at normal volumes, and tinnitus in both ears and head occurred. Events were still present at the time of the report. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1886891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CT
Alter: 34,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 21.09.2021
Beginn: 21.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Acoustic stimulation tests normal Disorientation Ear discomfort Feeling abnormal Headache Hyperacusis Physical examination normal Tinnitus

Symptomtext

ear fullness; sensitivity to noise at normal volumes; tinnitus in both ears and head; brain fog; disorientation; headache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21Sep2021 12:30 (Lot number: FD0809) at the age of 34 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. The patient took concomitant medications. The following information was reported: FEELING ABNORMAL (non-serious) with onset 21Sep2021 20:00, outcome "not recovered", described as "brain fog"; DISORIENTATION (non-serious) with onset 21Sep2021 20:00, outcome "not recovered", described as "disorientation"; HEADACHE (non-serious) with onset 21Sep2021 20:00, outcome "not recovered", described as "headache"; EAR DISCOMFORT (non-serious) with onset 28Sep2021, outcome "not recovered", described as "ear fullness"; HYPERACUSIS (non-serious) with onset 28Sep2021, outcome "not recovered", described as "sensitivity to noise at normal volumes"; TINNITUS (non-serious) with onset 28Sep2021, outcome "not recovered", described as "tinnitus in both ears and head". The events "brain fog", "disorientation", "headache", "ear fullness", "sensitivity to noise at normal volumes" and "tinnitus in both ears and head" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of feeling abnormal, disorientation, headache, ear discomfort, hyperacusis, tinnitus. Additional information: The patient received daily multivitamin within 2 weeks of vaccination (as reported). The patient has no known allergies. The patient did not receive any other vaccine within 4 weeks prior to COVID-19 vaccine. Prior to vaccination, the patient was not been diagnosed with COVID-19 and since the vaccination, the patient has not been tested for COVID-19. It was reported that the brain fog and disorientation subsided after two weeks. One week after vaccination (as reported), ear fullness, sensitivity to noise at normal volumes, and tinnitus in both ears and head occurred. Events were still present at the time of the report. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1964013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: TN
Alter: 41,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Deafness unilateral Dizziness Gait disturbance Maternal exposure during pregnancy Middle ear effusion Tinnitus Vertigo

Symptomtext

Vertigo, fluid in right ear, loss of hearing in right ear for 3 weeks, whooshing and high pitched noises in ear during hearing loss; varying degrees of dizziness 1-2 days after booster I needed help to walk; 2 weeks after booster needed to hold on to things when walking; 3-4 weeks after booster still dizzy. it feels like the room is tipping down left and right

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 11/22/2021 noted fluid in ear, prescribed Ipratropium Bromide; 11/29 began acupuncture treatment (still under care); 12/17/2021 was referred by doctor for physical therapy for possible ear crystals; 12/21 begin physical therapy treatment
Aktuelle Erkrankungen: sinusitis around 9/27/2021 and 10/07/2021; conjunctivitis around 10/22/2021 and 11/10/2021
Vorgeschichte: patient is breastfeeding a baby
Andere Medikamente: Zyrtec, Flonase, Post natal vitamin, Sunflower Lecithin
Allergien: penecillin; dairy sensitivity
Vorherige Impfungen: both previous PFIZER vaccines had mild adverse events: sore arm and fatigue, symptoms gone by the next day; patient age 40 at ti

VAERS 1963938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: TN
Alter: 59,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Burning sensation Erythema Oral discomfort Pruritus Urticaria

Symptomtext

Patient experience hives 30 minutes after shot, and then 1 week later red, itchy burning spots appeared around her joints and inside of her mouth, disappeared within 30 minutes after taking benadryl

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1963261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: PA
Alter: 41,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 16.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Lymphadenopathy Nausea Pain Peripheral swelling Swelling

Symptomtext

Per 12/20/21 email: "I had my booster Thursday afternoon. Friday I woke up with achiness and a little nausea, which isn?t abnormal considering how I reacted to the second vaccine. However, Saturday morning I had swelling in my arm as well as my armpit into my chest. It feels like someone stuck a knife in my armpit for lack of a better description and I still have it today"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Sulfa drugs, doxycycline
Vorherige Impfungen: -

VAERS 1962439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Epistaxis Fall Headache

Symptomtext

Patient was just given the Pfizer BioNtech Vaccine> Prior to vaccination, Patient informed us that she has experienced dizziness for vaccines before specifically prior to giving birth but has a reaction to her 2nd dose due to being nervous about getting her shot. After giving her the vaccine, we stayed at the area seated for few minutes and she was given instructions to sit down still at the waiting area for 15 minutes. She said she felt good so she decided to roam at the pharmacy area, bumped into one of the shelves, got lightheaded then fell down. She also started having nose bleeds. We called 911 but she decided not to go to them and just waited until she's fine. Called patient today and she said she was fine after and just experienced a headache the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: Patient was just given the Pfizer BioNtech Vaccine> Prior to vaccination, Patient informed us that she has experienced dizziness for vaccines before specifically prior to giving birth but has a reaction to her 2nd dose due to being nervous
Allergien: na
Vorherige Impfungen: 2ND DOSE

VAERS 1962355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fd0809

mild

Staat: PA
Alter: 73,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Pain Product administered at inappropriate site

Symptomtext

Patient says that the immunization was received too high in the arm and experienced extreme pain the day of and the next day. She followed up with her physician and is still experiencing pain. She iced the area and it helped with the pain.

Weitere VAERSDATA-Felder

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

VAERS 1961876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MD
Alter: 41,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Pharyngeal swelling Tongue pruritus

Symptomtext

Five minutes after receiving the Pfizer vaccine shot at 9:40a on 12/17/21 my tongue got really itchy. I took an allergy pill and right after that I got might headed and my throat began to swell. The ambulance was called and I was taken to the emergency department. They watch me for about 4 hours and gave me benadryl and prednisone and also prescribed me 4 days of prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Birth control tri fenynor
Allergien: All seafood, hazelnut, strawberries
Vorherige Impfungen: -

VAERS 1958042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 08.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Bedridden Chills Immunisation Productive cough Pyrexia

Symptomtext

he has received the booster dose yesterday; He got fever; Experienced some chills; Had some Phlegm in throat and nose; I was in bed for three hours; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 70 year-old male patient received bnt162b2 (BNT162B2), administration date 08Dec2021 (Lot number: FD0809) at the age of 70 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Covid-19" (unspecified if ongoing), notes: he had covid 2 years ago. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (1st Dose), administration date: 2021, when the patient was 70 years old, for COVID-19 Immunization; Bnt162b2 (2nd Dose), administration date: 2021, when the patient was 70 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 08Dec2021, outcome "unknown", described as "he has received the booster dose yesterday"; PYREXIA (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "He got fever"; CHILLS (non-serious) with onset Dec2021, outcome "not recovered", described as "Experienced some chills"; PRODUCTIVE COUGH (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "Had some Phlegm in throat and nose"; BEDRIDDEN (non-serious) with onset Dec2021, outcome "unknown", described as "I was in bed for three hours". Therapeutic measures were taken as a result of pyrexia, chills, productive cough. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (he had covid 2 years ago.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1957995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 24.09.2021
Beginn: 13.10.2021
Tage bis Beginn: 19,0
Dosis: 2
Route/Site: - / RA

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

Blister Pain in extremity Peripheral swelling Rash Skin exfoliation Urticaria

Symptomtext

had pain and swelling in my left hand; had pain and swelling in my left hand/swollen rash covering my limbs.; It developed into hive rash on finger. Now it has developed into swollen hives on my scalp, ears, chest, arms, back, legs, and feet.; finger then started blistering up with open sores and peeling skin.; finger then started blistering up with open sores and peeling skin.; That then developed into a complete swollen rash covering my limbs.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 24Sep2021 14:00 (Lot number: FD0809) at the age of 37 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. No known allergies. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FD0808, Location of injection: Arm Right, Vaccine Administration Time: 02:00 PM), administration date: 03Sep2021, when the patient was 37 years old, for COVID-19 immunization. The following information was reported: PAIN IN EXTREMITY (disability, medically significant) with onset 13Oct2021 01:00, outcome "not recovered", described as "had pain and swelling in my left hand"; PERIPHERAL SWELLING (disability, medically significant) with onset 13Oct2021 01:00, outcome "not recovered", described as "had pain and swelling in my left hand/swollen rash covering my limbs"; URTICARIA (disability, medically significant) with onset 13Oct2021 01:00, outcome "not recovered", described as "It developed into hive rash on finger. Now it has developed into swollen hives on my scalp, ears, chest, arms, back, legs, and feet"; BLISTER (disability, medically significant), SKIN EXFOLIATION (disability, medically significant) all with onset 13Oct2021 01:00, outcome "not recovered" and all described as "finger then started blistering up with open sores and peeling skin."; RASH (disability, medically significant) with onset 13Oct2021 01:00, outcome "not recovered", described as "That then developed into a complete swollen rash covering my limbs". The all the events were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of all events (antibiotic, steroid topical, 7 different). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1957989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: PA
Alter: 35,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Arthralgia Back pain Body temperature Chills Chromaturia Fatigue Immunisation Measles Muscular weakness Otorrhoea Pyrexia

Symptomtext

brown urine; 'brown ear end'; received the Pfizer Covid 19 Vaccine Booster on Wednesday 01Dec2021; General Measles; muscle weakness; tiredness; achy joint/achiness in knees; temperature 101.3/Fever; Chills; Achiness in back; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP) from medical information team. The reporter is the patient. A 35-year-old female patient received BNT162B2 (COMIRNATY, solution for injection), administered in arm left, administration date 01Dec2021 (Lot number: FD0809) at the age of 35 years as dose number unknown (booster), single for COVID-19 immunisation. Relevant medical history included: "Chronic migraine" (unspecified if ongoing). Concomitant medication included: EMGALITY [GALCANEZUMAB]. Vaccination history included: COVID-19 vaccine (Manufacturer unknown), for COVID-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 01Dec2021, outcome "unknown", described as "received the Pfizer Covid 19 Vaccine Booster on Wednesday 01Dec2021"; MEASLES (medically significant) with onset Dec2021, outcome "recovering", described as "General Measles"; MUSCULAR WEAKNESS (non-serious) with onset Dec2021, outcome "recovering", described as "muscle weakness"; FATIGUE (non-serious) with onset Dec2021, outcome "recovering", described as "tiredness"; ARTHRALGIA (non-serious) with onset Dec2021, outcome "recovering", described as "achy joint/achiness in knees"; PYREXIA (non-serious) with onset Dec2021, outcome "recovering", described as "temperature 101.3/Fever"; CHROMATURIA (non-serious) with onset 03Dec2021, outcome "unknown", described as "brown urine"; CHILLS (non-serious) with onset Dec2021, outcome "recovering", described as "Chills"; BACK PAIN (non-serious) with onset Dec2021, outcome "recovering", described as "Achiness in back"; OTORRHOEA (non-serious) with onset 03Dec2021, outcome "unknown", described as "'brown ear end'". The patient underwent the following laboratory tests and procedures: body temperature: (Dec2021) 101.3. Clinical course: Per caller she received the Pfizer COVID-19 Vaccine Booster on 01Dec2021. Per caller, she experienced the common side effects muscle weakness, tiredness, achy joint, temperature 101.3. She felt much better today. She started voiding brown urine on 03Dec2021. Patient stated that she is well hydrated. Patient also reported having fever, chills, general measles, achiness in her knees and back especially. But on 03Dec2021, she was presented with like a 'brown ear end' (further not clarified) all day and she had not seen that as common side effect, so was not sure if it could be something more serious. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: Fever; Result Unstructured Data: Test Result:101.3
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic migraine
Andere Medikamente: EMGALITY [GALCANEZUMAB]
Allergien: -
Vorherige Impfungen: -

VAERS 1957820

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Asthenia Axillary pain Chills Fatigue Headache Injection site pain Lymphadenopathy

Symptomtext

12/13/21 mild pain at injection site (left arm), sensitive stomach 12/14/21 mild pain at injection site, moderate pain in left armpit, sensitive stomach, low energy/exhaustion, chills 12/15/21 severe pain in left armpit, swollen lymph nodes, low energy/exhaustion, mild headache 12/16/21 moderate pain in left armpit, swollen lymph nodes, mild headache, low energy/exhaustion,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diarrhea and upset stomach the night before vaccination
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1954340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Joint range of motion decreased Pain Pain in extremity

Symptomtext

Ongoing and progressively worsening left arm pain that is also causing limited range of motion of the arm that begin a few days ago. Left arm pain has ongoing since vaccination date with no relief of symptoms. Client has tried OTC Tylenol with mild relief. Even with limited range of motion of the left arm, client reports continued arm pain. Encouraged client to seek medical evaluation for further follow-up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Gold, silver
Vorherige Impfungen: -

VAERS 1955049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction

Symptomtext

Immediately post vaccination pt c/o dizziness Vitals: 126/86, 79, 16, 97% -- > 119/83, 80, 16, 97% Pt given water and orange juice for hydration. Pt stable and released from the vaccination site @11:15

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Endometriosis w/ endometrioma, Uterine anomaly, PCOS, Fatty Liver, subclinical hypothyroidism, Vitamin D deficiency, liver hemangioma, hx of acute appendicitis s/p appendectomy, iron def. anemia, postpartum anxiety, GAD, OCD
Andere Medikamente: Medications: Fluoxetine 60mg PO Daily Buspar 10mg PO Daily
Allergien: Allergies: Sertraline (Anxiety)
Vorherige Impfungen: -

VAERS 1951969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FD0809

mild

Staat: KY
Alter: 24,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 13.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Rash

Symptomtext

Patient c/o whole body rash on 12/ 15 after recieving pfizer on 12/13/21. Patient seen by primary care center on 12/15/21 given benedryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: grey matter heteroptopia seizures
Andere Medikamente: Kepra
Allergien: Pencillin
Vorherige Impfungen: -