VAERS Reports FH8027

VAERS 2674252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 21.08.2023
Impfdatum: 21.10.2021
Beginn: 18.02.2023
Tage bis Beginn: 485,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Symptom recurrence

Symptomtext

ACUTE NON ST ELEVATION MI 2/20/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2672426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 16.08.2023
Impfdatum: 15.10.2021
Beginn: 13.04.2023
Tage bis Beginn: 545,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Interstitial lung disease Obstructive sleep apnoea syndrome Pericardial effusion

Symptomtext

ACUTE ON CHRONIC RESPIRATORY FAILURE 3/27/2023 INTERSTITIAL LUNG DISEASE ACUTE ON CHRONIC RESPIRATORY FAILURE 3/27/2023 ADULT OBSTRUCTIVE SLEEP APNEA, SEVERE ACUTE ON CHRONIC RESPIRATORY FAILURE 3/27/2023 PERICARDIAL EFFUSION

Weitere VAERSDATA-Felder

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

VAERS 2658334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FH8027

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 19.07.2023
Impfdatum: 22.11.2021
Beginn: 03.05.2023
Tage bis Beginn: 527,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Aortic aneurysm Aortic stenosis COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Computerised tomogram thorax Delirium Echocardiogram Ejection fraction decreased Hypertension Hypoxia Lethargy Lung infiltration Mental status changes Metabolic encephalopathy Mitral valve incompetence

Symptomtext

Patient is a 84 y.o. male past medical history of severe aortic stenosis, COPD who presented from home on 5/3/2023 with 1 day of fever, altered mental status and subsequently tested positive for COVID-19. Patient noted to have delta positive troponins and hypoxia Acute Hypoxic Respiratory Failure -Due to COVID-19 infection with suspected viral pneumonia -No evidence of PE on CTPA -Clinically does not appear volume overloaded on admission. Viral pneumonia COVID-19 Infection - Presented with: lethargy, fever - Symptom onset: 5/3 - Positive COVID-19: 5/4/23 at facility - Vaccination status: yes - CXR on admission showed bibasilar infiltrates - Oxygen status: 2L NC - PO Decadron for 10 days total - Seen by Pulmonology - Treated with Remdesivir x3 days hererecommended by Pulm Elevated troponin -Possibly demand ischemia from hypoxia, and infection. No chest pain, syncope, dyspnea noted. -Troponin 52-- >92 - CTPA show pneumonia - Seen by Cardiology (Dr) - TTE show EF45-50%, mod/severe AR, pulm htn - Recommend close outpatient f/u with Cardiology (follows with Dr) Acute Metabolic Encephalopathy - Mild, waxing/waning - Likely multifactorial due to covid infection, hospital delerium - Nonfocal neuro exam - CT head non-acute - Resolved COPD -Per history. No wheezing appreciated during my exam though noted by EMS and while in the emergency department. -PFTs 4/2023: Moderate to severe obstructive disease, normal DLCO -Patient has been initiated on steroids for COVID-pneumonia as above which would also provide management for COPD -Continue home bronchodilator regimen -Follows with pulmonary, Dr. Severe Aortic Stenosis Bicuspid AV Thoracic Aortic Aneurysm -Does not appear volume overloaded on admission -TTE 5/22: EF 56%, severe AS with AVA 0.7, mean gradient 39, mild to moderate MR, RVSP 59 -BNP 10,500 -TTE ordered -Resume home beta-blocker -Patient undergoing work-up for possible TAVR and is due for repeat echo. Follows with cardio, Dr HTN -Continue home Lopressor, ACE inhibitor -No leukocytosis -CXR: Mild bilateral lower lung infiltrates vs. Edema, trace bilateral pleural effusions -CTPA with premedication for contrast allergy ordered -Decadron for COVID infection -Hypoxic on room air, currently with adequate oxygenation on 2 L nasal cannula V

Weitere VAERSDATA-Felder

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

VAERS 2639752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 01.06.2023
Impfdatum: 21.10.2021
Beginn: 20.12.2021
Tage bis Beginn: 60,0
Dosis: 3
Route/Site: IM / RA

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

Acute myocardial infarction Angina pectoris

Symptomtext

STABLE ANGINA ACUTE NON ST ELEVATION MI

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

VAERS 2629774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 28.06.2022
Beginn: 27.09.2022
Tage bis Beginn: 91,0
Dosis: 4
Route/Site: IM / LA

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

Acute respiratory failure Hypoxia

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA

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

VAERS 2626509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 22.11.2021
Beginn: 09.03.2022
Tage bis Beginn: 107,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Adenocarcinoma metastatic Hypoxia Metastases to lung Sepsis

Symptomtext

ACUTE RESPIRATORY FAILURE 4/28/2022 ADENOCARCINOMA METASTATIC TO LEFT LUNG HYPOXIA 4/28/2022 ADENOCARCINOMA METASTATIC TO LEFT LUNG ACUTE RESPIRATORY FAILURE 4/28/2022 SEPSIS WO ACUTE ORGAN DYSFUNCTION HYPOXIA 4/28/2022 SEPSIS WO ACUTE ORGAN DYSFUNCTION

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

VAERS 2625760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 08.04.2022
Beginn: 27.07.2022
Tage bis Beginn: 110,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2620039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 21.11.2021
Beginn: 29.03.2022
Tage bis Beginn: 128,0
Dosis: 3
Route/Site: - / LA

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 2618439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 20.04.2023
Impfdatum: 13.10.2021
Beginn: 26.01.2022
Tage bis Beginn: 105,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Angina unstable Hypoxia

Symptomtext

UNSTABLE ANGINA ACUTE ON CHRONIC RESPIRATORY FAILURE HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2618418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 28.10.2021
Beginn: 26.03.2022
Tage bis Beginn: 149,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Liver function test increased Organ failure Sepsis

Symptomtext

J96.00 ACUTE RESPIRATORY FAILURE 3/30/2022 SEVERE SEPSIS W ACUTE ORGAN DYSFUNCTION J96.00 ACUTE RESPIRATORY FAILURE 3/30/2022 ELEVATED LIVER FUNCTION TEST

Weitere VAERSDATA-Felder

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

VAERS 2557583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FH8027

kritisch

Staat: GA
Alter: 48,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 19.11.2021
Beginn: 07.10.2022
Tage bis Beginn: 322,0
Dosis: 3
Route/Site: IM / AR

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

Cardiac monitoring normal Cerebrovascular accident Coagulation test normal Echocardiogram normal Hemiparesis Hypoaesthesia Implantable cardiac monitor insertion Laboratory test normal Ultrasound Doppler normal

Symptomtext

Right temporal lobe stroke on 10/7/22, symptoms included left hand numbness, and weakness in left arm and left leg through 10/10/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Hospitalized from 10/8/22-10/10/22 for testing to determine cause. All labs for hypercoagulability were negative, bilateral Doppler scans of lower extremities negative, transthoracic echo unremarkable, trans esophageal echo also unremarkable, implanted cardiac monitor has shown no arrhythmias so far. All testing was done during hospitalization.
Aktuelle Erkrankungen: None
Vorgeschichte: Mild controlled hypertension
Andere Medikamente: Synthroid, Lo-Estrin, lisinopril, cetirizine, Citracal
Allergien: None
Vorherige Impfungen: -

VAERS 2550173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 02.12.2021
Beginn: 01.11.2022
Tage bis Beginn: 334,0
Dosis: 3
Route/Site: - / -

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

Abdominal distension Acute respiratory failure Atelectasis Blood creatinine increased COVID-19 Cardiac failure Chest X-ray abnormal Chronic obstructive pulmonary disease Colectomy Colonoscopy abnormal Condition aggravated Constipation Culture urine Diuretic therapy Dyspnoea Echocardiogram normal Ejection fraction normal Gastrointestinal decompression

Symptomtext

Patient is a 75 y.o. male patient of an MD with history of COPD, chronic respiratory failure on 4 L, HFpEF, GERD, chronic hepatitis C, HLD, chronic pain syndrome, and PAH who presented to the Medical Center with shortness of breath and found to have acute on chronic respiratory failure due to COPD exacerbation. Hospitalization complicated by COVID with worsening respiratory failure requiring bipap and transfer to ICU 11/21. Acute on chronic respiratory failure - improving Hypoxia on admission due to COPD exacerbation Wears 5L O2 at home Worsening hypoxia requiring max bipap 11/12 due covid Pulm following, appreciate assistance Started on Veletri, completed 11/30 Weaned from HHF to nasal cannula, now on 4L Diuresed with IV lasix, now on PO Covid-19 Virus Infection Bacterial pneumonia Worsening hypoxia; covid positive 11/12 Vaccinated with CXR showing bibasilar atelect vs PNA Completed course of rocephin/doxy Completed 10d decadron (done 11/26) No remdesivir due to CKD Out of isolation on 11/24 Acute COPD exacerbation Pulmonary fibrosis Acute COPD exacerbation POA Completed course of decadron and azithromycin IV solumedrol started 11/26 Weaned back to chronic home dose prednisone 10mg 11/28 Continue bronchodilators and symbicort Follows with pulm outpt UTI U/A consistent with infection; rocephin started 12/2 Urine culture contaminated Switched Rocephin to Keflex 12/3 Ileus - resolved Chronic constipation Distention increased 11/21 S/p decompression from above GI consulted; on linzess, relistor, reglan (stopped 12/5), and miralax; signed off 12/6 Neostigmine 11/25-11/26 BMs daily, decrease BR Repeat KUB 12/7 with improved ileus Tolerating diet C-scope 12/8 with multiple polyps s/p resection and significant looping secondary to severely redundant, tortuous and elongated colon. GI recs repeat C-scope in 3 years and Barium enema in 2 weeks to evaluate R colon. Pulmonary hypertension Chronic HFpEF Elevated troponin Echo 11/2021 with EF 50-55% Elevated troponin likely due to demand ischemia Follows with Dr. out pt; consulted Continue home toprol and lasix Lasix changed to IV; increased 11/28; Change to PO Lasix 12/7 CKD stage III Baseline Cre ~1.25 Stable DMT2 A1c 6.5 On SSI; stop 11/29

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 37,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2543814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 23.12.2021
Beginn: 07.12.2022
Tage bis Beginn: 349,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Blood sodium decreased COVID-19 Chest X-ray normal Culture negative Fall Hypertension Hyponatraemia Hypoxia Illness Liver function test increased Mental status changes Obesity Pyrexia SARS-CoV-2 test positive Speech disorder Subarachnoid haemorrhage Subdural haematoma

Symptomtext

FINAL DIAGNOSIS: 1. Covid-19 Virus Infection 2. Acute hypoxemic respiratory failure 2/2 COVID 3. Mild Hyponatremia - 130 on admission - repeating CMP today 4. HTN 5. Hx frontotemporal dementia 6. Hx of CVA and TIA with aphasia 7. Obesity with BMI 31.44 Elevated LFTs REASON FOR HOSPITALIZATION AND ADMITTING DIAGNOSIS: Illness Hypoxia Fever, unspecified fever cause COVID-19 virus infection HOSPITAL COURSE: Date of onset of symptoms: Unknown Symptoms present on admission: Hypoxemia Date of covid positive test: 12/7/2022 Unknown when SNF test was positive Vaccination status: Vaccinated Imaging: 12/7/2022 CXR no acute process Oxygen requirements on admission: no home oxygen - 3-4LPM/NC Current oxygen requirements: 4LPM/NC Medical therapy: Decadron started 12/7/2022 Consultants following: NA Anticipated special isolation end date 12/17/2022 Obtained from EMR as patient is aphasic Patient is a 65 y.o. year-old male, who presented with illness. From ECF with known positive COVID, hypoxemia, increased AMS, and fever. Patient is there for rehab after having a fall. Per records patient was discharged from hospital on 12/1 where he had subdural hematoma and subarachnoid hemorrhage. Per records patient also has frontotemporal dementia and Parkinson's likely. Per report patient has been getting IV fluids/hydration at nursing facility and has diagnosis of COVID. Per report patient is full code. Per report patient running fever and more altered therefore sent to the ER. Patient is awake but has difficulty speaking/giving history. He is able to give yes and no answers. No family present at this time. Upon arrival to the ER patient was found to have fever of 101.6, tachycardia of 114 respiratory rate of 20. Patient now on room air. Improving with current therapy being provided. We will discharge to skilled nursing facility for continued PT/OT. Patient in agreement with plan. All cultures have remained negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2494980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 01.04.2021
Beginn: 06.09.2022
Tage bis Beginn: 523,0
Dosis: 2
Route/Site: - / -

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

Death Pyrexia

Symptomtext

09/06/22 presents to ED for "fever". PMHx of "afib not on thinners, HTN, HLD"

Weitere VAERSDATA-Felder

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

VAERS 2491467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 02.12.2021
Beginn: 22.10.2022
Tage bis Beginn: 324,0
Dosis: 3
Route/Site: IM / -

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

Acute respiratory failure Atrial flutter COVID-19 Chest X-ray normal Chest discomfort Chest pain Chronic kidney disease Computerised tomogram abdomen abnormal Dyspnoea Hypoxia Lung opacity Magnetic resonance cholangiopancreatography Muscle twitching Nodule Pancreatic disorder Pneumonia Pneumonia bacterial Pulmonary embolism

Symptomtext

COVID+ 10/22/22 - Vaccination status - Moderna x2 + 1 pfizer booster BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: PA Admission Date: 10/22/2022 Discharge Date: Oct 24, 2022 Discharge Disposition: home or self care Active Issues Requiring Follow-up: Acute respiratory insufficiency with hypoxia COVID-19 - Home oxygen, 2L with activity, can try to be off oxygen at rest - Dexamethasone, sent with 7 days to complete 10 day course as she is going home with oxygen - Enrolled in transition to home monitoring program Incidental imaging findings: Nodular opacities 7-8mm - Incidental finding on CT abd/pelvis - Most likely 2/2 infectious process - Consider repeat imaging to ensure resolution Patchy heterogenicity in region of uncinate process of pancreas - MRCP recommended to exclude underlying mass DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Community acquired bacterial pneumonia [J15.9] Paroxysmal atrial flutter (HCC) [I48.92] Other pulmonary embolism without acute cor pulmonale, unspecified chronicity (HCC) [I26.99] Community acquired pneumonia of left lower lobe of lung [J18.9] Stage 3 chronic kidney disease, unspecified whether stage 3a or 3b CKD (HCC) [N18.30] HOSPITAL COURSE: Patient is a 74 y.o. female with PMH significant for COPD, h/o PE, CAD with h/o MI s/p stenting, atrial fibrillation, h/o v fib, h/o NSVT, CHF and hypothyroidism who presented to the ED on 10/22 with chest pain and SOB. Symptoms started 3 days beforehand, but continued to progress and she developed sharp right sided chest pain. In the ED, patient was hypoxic at 88% requiring 2L oxygen. CXR without any acute changes. CT abd/pelvis showed no acute abdominal findings but did demonstrate patchy left basilar airspace opacities suspicious for pneumonia with incidental findings as noted above. Patient was started on Rocpehin/zithromax and admitted to medicine for CAP. Shortly after COVID testing returned positive. Pneumonia was attributed to viral etiology and abx were stopped. She was started on dexamethasone and remdesivir. She continued requiring 2L nasal cannula, but later weaned to room air. She was concerned about twitching in her chest and CXR to evaluate ppm/ICD lead placement, which was reviewed and stable, and twitching resolved on its own. Given her stability and mild improvement in oxygenation, we discussed COVID at home program. She was agreeable to this. Rehab consulted and recommended 2L with activity, though at times, she may also need oxygen while at rest. Given home oxygen, and COVID at home transition program, she was discharged in stable condition on 10/24/2022. CONSULTS / RECOMMENDATION: Rehab - home oxygen Transition to home program

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Acute anterior wall MI (HCC) 2/17/2009 DES LAD ? Apnea, sleep ? Atrial flutter (HCC) coumadin- ? Breast cancer (HCC) 02/2008 radiation ? Bronchiectasis without complication (HCC) 8/28/2019 ? CAD (coronary artery disease) BMS RCA 2003. DES LAD 2009 after anterior wall MI ? Carotid disease, bilateral (HCC) 07/21/2020 Mild B/L CCA/Bulb/ICA dz <50% ? Congestive heart failure (CHF) (HCC) ? COPD (chronic obstructive pulmonary disease) (HCC) ? Depression ? Dyslipidemia ? Emphysema (subcutaneous) (surgical) resulting from a procedure ? History of GI diverticular bleed 2011 recurrent bleed May 2012 ? HTN (hypertension) ? Hypothyroidism ? Ischemic cardiomyopathy EF 31.5% by MUGA ? Left bundle branch block ? Osteoporosis ? Pulmonary embolism (HCC) 10/11 off coumadin due to GI bleed ? Rectal polyp 01/27/2020 15mm rectal polyp ? S/P ICD (internal cardiac defibrillator) procedure 2/14/2013 BI-V ICD ? Tobacco abuse ? Vasospasm (HCC)
Andere Medikamente: Albuterol Sulfate 108 (90 Base) MCG/ACT 1-2 puffs Inhalation Every 4 hours PRN Atorvastatin Calcium 80 mg Oral Daily, for cholesterol Budesonide-Formoterol Fumarate 160-4.5 MCG/ACT 2 puffs Inhalation 2 times daily, rinse mouth after use Ch
Allergien: CodeineNausea Only Elavil [Amitriptyline Hcl] Morphine
Vorherige Impfungen: -

VAERS 2480593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: IL
Alter: 45,0
Geschlecht: M
Eingang: 17.10.2022
Impfdatum: 23.03.2021
Beginn: 17.08.2022
Tage bis Beginn: 512,0
Dosis: 3
Route/Site: IM / AR

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

Acute myocardial infarction Anticoagulant therapy Arteriogram coronary normal C-reactive protein normal Chest pain Echocardiogram normal Ejection fraction normal Electrocardiogram ST segment depression Electrocardiogram abnormal Haemoglobin decreased Hyperhidrosis Hypoaesthesia Intensive care Low density lipoprotein increased Magnetic resonance imaging heart Myocarditis Pain Sinus bradycardia

Symptomtext

8/17/22 Myocarditis. Had 12+ months of dull pain in center of chest following 2nd dose. Nearly 9+ months after third dose, was intensely exercising and sat down 11:15pm with acute chest pain, bilateral arm numbness and diaphoresis (full body sweat). No coughing, nausea, diarrhea or headaches. No history of heart issues or Covid19 infection. Went to ED, RHR 45bpm. Labs were significant for troponin 11,111.8 (went up to 25,000 a few hours later), elevated WBC 11.58, low Hgb 13, CRP<1, LDL 167. EKG showed sinus bradycardia, ST depression in I, aVL, and V4-V6, with no STEMI present. No CXR. Given ASA load, atorvastatin, and started on heparin gtt and admitted to CCU for NSTEMI. Vitals: BP 118/71 | Pulse 85 | Temp 97.5 ?F (36.4 ?C) | Resp 19 | Ht 182.9 cm (6') | Wt 70.3 kg (154 lb 15.7 oz) | SpO2 95% | BMI 21.02 kg/m?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: 8/18/22 Angiogram which was negative for significant coronary artery obstruction. Transthoracic echo was then obtained which showed normal ejection fraction 55-60% and no regional wall motion abnormalities. 9/13/22 Cardiac MRI showed late gadolinium enhancement was diffuse in nature. Of obstructive coronary disease this was consistent with myocarditis.
Aktuelle Erkrankungen: Similar sharp chest pain with nausea experienced 1-2 months prior.
Vorgeschichte: Crohn's Disease, Ileocecal Resectioning, General Anxiety Disorder, ADHD
Andere Medikamente: Vyvanse, 20mg; Viibryd 20mg; Strattera, 80mg ; Finasteride, 1mg; Fish Oil supplement
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2436943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: SD
Alter: 56,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 11.12.2021
Beginn: 17.07.2022
Tage bis Beginn: 218,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 COVID-19 pneumonia Death Dyspnoea Hypoxia Inappropriate schedule of product administration Pneumonia mycoplasmal Pulmonary embolism SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Pfizer product on 03/30/2021, 04/21/2021, and 12/11/2021. They were admitted to hospital on 06/24/2022 with a primary complaint of shortness of breath. COVID-19 test on 06/24/2022 was negative. They were found to be experiencing complications of hypoxia and acute bilateral pulmonary thromboembolic tic disease. They were also diagnosed with mycoplasma pneumonia. A second test on 07/17/2022 was positive. They were also diagnosed with COVID-19 pneumonia. They remained hospitalized until their death on 07/18/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 24,0
Labordaten: Negative COVID-19 test on 06/24/2022. Positive COVID-19 test on 07/18/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Mycoplasma Pneumonia, Severe Pulmonary Hypertension, Hypothyroidism, GERD, heparin-induced thrombocytopenia, Unspecified Anemia,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2416134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: WI
Alter: 97,0
Geschlecht: M
Eingang: 19.08.2022
Impfdatum: 07.12.2021
Beginn: 05.08.2022
Tage bis Beginn: 241,0
Dosis: 1
Route/Site: UN / UN

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

Asthenia Atrial fibrillation Blood creatinine increased Blood urea increased Brain natriuretic peptide increased COVID-19 Computerised tomogram head normal Condition aggravated Death Dementia Dysstasia Electrocardiogram abnormal Fall Full blood count normal Glomerular filtration rate decreased Hypoxia Presyncope Prohormone brain natriuretic peptide increased

Symptomtext

8/5/2022: Presented to ED after fall x2, unable to stand after second fall at facility where he lives. No other contributing symptoms noted at the time. A pelvic x-ray is normal. Head CT reassuring. No signs of a stroke or definitive weakness. He has A. fib on his EKG. He has mild renal insufficiency. BNP noted to be elevated but nothing to suspect florid congestive heart failure. At this point it is unclear why he is weak. 8/9/2022 transitioned to Hospice with a terminal diagnosis of covid 19 virus infection. Evaluation revealed hypoxia and covid 19 infection. His hospital course was complicated by worsening dementia, atrial fibrillation with RAPID VENTRICULAR RESPONSE and an episode of presyncope. Passed away on 8/11/2022 Submitter does not have access to further medical records or information on hospital course. If further information is needed, please contact Hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: 8/5/2022: Covid-19 positive per PCR T-max of 97.7, heart rate 60s, respiratory rate 16, blood pressure 152/71, saturating 96% on room air. Chemistry notable for creatinine of 2.09, BUN of 36, GFR of 26, proBNP 1197. High-sensitivity troponin within normal limits. CBC unremarkable. UA negative for UTI. CT head unremarkable. Pelvis x-ray negative for any acute fractures. CXR pending
Aktuelle Erkrankungen: unknown
Vorgeschichte: new onset atrial fibrillation, AKI (acute kidney injury), dementia, expressive aphasia, diabetes
Andere Medikamente: unknown
Allergien: Penicillins Anaphylaxis ? Naproxen Unknown Reaction
Vorherige Impfungen: -

VAERS 2391408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: ND
Alter: 51,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 09.03.2021
Beginn: 22.06.2022
Tage bis Beginn: 470,0
Dosis: 3
Route/Site: SYR / -

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

Arteriogram coronary abnormal Echocardiogram abnormal Electrocardiogram abnormal Myocardial infarction Myocarditis

Symptomtext

Heart attack, myocarditis. Life flight to hospital, 6 days in hospital, numerous tests and appointments once released.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 6,0
Labordaten: 6/22/22 to 6/27/22 EKG, echocardiogram, angiogram Too many to list without submitting full medical records.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2357620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: IA
Alter: 75,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 04.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: IM / -

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

Abdominal pain Acute myocardial infarction Anticoagulant therapy Atrial fibrillation COVID-19 Catheterisation cardiac normal Chest pain Condition aggravated Diarrhoea Electrocardiogram abnormal Nausea Pain SARS-CoV-2 test positive Troponin increased Upper respiratory tract infection Vomiting

Symptomtext

Pfizer Dose 1 2/25/21 (EN6200) Pfizer Dose 2 3/19/21 (EN6208) Pfizer Dose 3 12/4/21 (FH8027) COVID Positive 1/5/22 1/12/22: A 75-year-old female with a past medical history of paroxysmal atrial fibrillation on anticoagulation with Eliquis, COPD, chronic hypoxic respiratory failure on home oxygen, hypertension, hyperthyroidism, thoracic aortic aneurysm and chronic HFpEF comes to ED complaining of chest pain. Patient complains of left-sided chest pain radiating across to the right, started this morning, not associated with shortness of breath or palpitations or nausea or vomiting. Denies cough or fever or chills. States that she had some abdominal pain with nausea and vomiting and diarrhea a couple of days ago which is resolved. Patient had recent upper respiratory infection, was tested positive for COVID-19 on 01/05/2022. In the ED, she was afebrile, vital signs stable, pulse ox 98% on room air. Troponin is positive 0.12. EKG showed atrial fibrillation, rate controlled. ED provider has discussed the case with on-call cardiologist, patient is started on nitro drip. She is seen by me on the medical floor, states that she does not have any chest pain at this time. 1/15/22: Patient is a 75-year-old female with a past medical history of paroxysmal atrial fibrillation on anticoagulation with Eliquis, COPD, chronic hypoxic respiratory failure on home oxygen, hypertension, hyperthyroidism, thoracic aortic aneurysm, chronic HFpEF adn recent diagnosis of COVID 19 came to ED complaining of chest pain. Patient admitted for NSTEMI. Patient was noted to have elevated troponin with no acute EKG changes. Patient was started on heparin drip. Cardiology was consulted. Patient had cardiac catheterization but did not require any intervention. Continue medical management. On discharge patient is chest pain-free. Patient will follow-up with Cardiology as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: A fib COPD chronic hypoxic respiratory failure HTN hyperthyroidism thoracic aortic aneurysm chronic HFpEF
Andere Medikamente: albuterol 2 puffs Q6h PRN alendronate 70 mg PO QWeek amlodipine 10 mg PO QD aspirin 81 mg PO Q atorvastatin 40 mg PO QD apixaban 5 mg PO QD Trelegy Ellipta 1 puff inh QD furosemide 40 mg PO QD omeprazole 20 mg PO QD sotalol 40 mg PO QD
Allergien: ACE inhibitors - nausea, vomiting metoprolol - cramp in lower leg
Vorherige Impfungen: -

VAERS 2242039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: PA
Alter: 60,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 29.11.2021
Beginn: 01.04.2022
Tage bis Beginn: 123,0
Dosis: 3
Route/Site: IM / UN

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

Death Dyspnoea Influenza like illness Malaise SARS-CoV-2 test negative

Symptomtext

He hadn?t felt well, with flu like symptoms, he took an at home covid test to be sure which came back negative. He called his PCP and they sent in a prescription for dexamethasone 4mg and Azithromycin 250mg, and he died within 24 hours of treatment. He was having trouble breathing in prior conversations with him and flu like symptoms, starting Friday April 1st, and died on Tuesday April 5th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: Acetaminophen 500mg -prescription Albuterol sulfate 90 mcg- prescription Aripiprazole 5mg- prescription Budesonide-formoterol 160-4.5 mcg- prescription Gabapentin 300 mg- prescription Meloxicam 15 mg- prescription Naproxen 500 mg- pre
Allergien: None
Vorherige Impfungen: -

VAERS 2218367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 13.12.2021
Beginn: 21.01.2022
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Catheterisation cardiac abnormal Coronary arterial stent insertion Coronary artery occlusion Electrocardiogram ST segment elevation Hyperhidrosis Nausea Sinus rhythm Thrombectomy

Symptomtext

Patient admitted for STEMI. November. She does reports associated diaphoresis and nausea, worse with exertion. ECG showed sinus rhythm with inferior ST elevations and she was taken emergently to cath lab which revealed distal RCA occlusion which was treated with thrombectomy and placement of a 3.0 x 48 mm DES. She did require pressor support for a short period post procedure, resolved. Discharged home. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2209515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: WI
Alter: 93,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 18.11.2021
Beginn: 30.03.2022
Tage bis Beginn: 132,0
Dosis: UNK
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Death related to COVID-19 infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Other significant conditions: COPD, HTN, A-Fib, Dementia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1984578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 10.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: - / -

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

Bradycardia COVID-19 Confusional state Cough Death Vaccine breakthrough infection Dyspnoea Endotracheal intubation Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

pt brought to ED via EMS with c/o SOB, fever, non-productive cough; pt confused; O2 sats 40% on RA; O2 supplementation; positive for COVID in ED; bilateral pneumonia; given decadron; O2 needs increased requiring intubation; pt had worsening bradycardia; vasopressors given; DNAR/DNI; transitioned to comfort care and pt died in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: sarcoidosis, HLD, obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1984578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 10.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / -

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

Bradycardia COVID-19 Confusional state Cough Death Vaccine breakthrough infection Dyspnoea Endotracheal intubation Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

pt brought to ED via EMS with c/o SOB, fever, non-productive cough; pt confused; O2 sats 40% on RA; O2 supplementation; positive for COVID in ED; bilateral pneumonia; given decadron; O2 needs increased requiring intubation; pt had worsening bradycardia; vasopressors given; DNAR/DNI; transitioned to comfort care and pt died in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: sarcoidosis, HLD, obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2171030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: OH
Alter: 80,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 10.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / UN

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

Death Loss of consciousness Syncope

Symptomtext

Patient as a lively 80 year old who took the Pfizer booster (after having 2 Moderna vaccines in her vaccination series.) She had the booster on December 10 . She collapsed in her home on December 14, 2021, and was found unconscious on December 15, 2021., by a family member. She never regained consciousness and died in an ambulance on the way to the hospital. The cause of death was not really explained -- and she died very close in time to her Covid booster shot.

Weitere VAERSDATA-Felder

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

VAERS 2203722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 24.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Death Unresponsive to stimuli

Symptomtext

Narrative: Patient was found unresponsive at home on 11:40 AM on 11/26/21 and was pronounced deceased at 12:10PM.

Weitere VAERSDATA-Felder

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

VAERS 2006570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Death Loss of consciousness Malaise

Symptomtext

Patient became sick within an hour of receiving her 2nd dose of the phiser vaccine & never recovered she died a couple of days later on 11/25/2021 after being found unconsious at home she was rushed by ambulance to doctors hospital where she was pronounced dead

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Information was not given to me by this hospital and has never been offered by her doctor or hospital she was in very good health until the day she received this Vaccine
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: valsatran
Allergien: none
Vorherige Impfungen: -

VAERS 2006570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / UN

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

Death Loss of consciousness Malaise

Symptomtext

Patient became sick within an hour of receiving her 2nd dose of the phiser vaccine & never recovered she died a couple of days later on 11/25/2021 after being found unconsious at home she was rushed by ambulance to doctors hospital where she was pronounced dead

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Information was not given to me by this hospital and has never been offered by her doctor or hospital she was in very good health until the day she received this Vaccine
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: valsatran
Allergien: none
Vorherige Impfungen: -

VAERS 2031907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: ND
Alter: 69,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 07.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: IM / AR

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

Angiogram pulmonary abnormal Echocardiogram abnormal Hypoxia Myocardial strain imaging abnormal Pulmonary embolism

Symptomtext

Large Saddle Pulmonary embolism with right heart strain and hypoxia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CTA, eecho,
Aktuelle Erkrankungen: -
Vorgeschichte: osteopenia, anxiety
Andere Medikamente: calcium, vitamin D, tylenol prn
Allergien: nickel
Vorherige Impfungen: -

VAERS 2010274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: NY
Alter: 78,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Death General physical health deterioration

Symptomtext

Resident was on Hospice Care due to declining health. Resident expired at 9:30am on 1/6/2022

Weitere VAERSDATA-Felder

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

VAERS 1972082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Myocardial infarction Neck pain Pain in jaw Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Patient received L arm Covid-19 injection and R arm Flu injection. Had onset of jaw and neck pain shortly following. Went to ED and was Diagnosed with Heart attack. Was hospitalized from 12/11 to 12/14. Tested negative for Covid on 12/11 but positive PCR on 12/20 with runny nose from 12/14 to 12/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes and Coronary Artery Disease
Andere Medikamente: Metformin, Hydrochlorothiazide
Allergien: Ibuprofen
Vorherige Impfungen: -

VAERS 1919645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 16.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Myocardial infarction

Symptomtext

I suffered a life threatening heart attack; This is a spontaneous report received from a contactable reporter (Consumer). The reporter is the patient. A 43 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 16Nov2021 10:00 (Lot number: FF8027) at the age of 43 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE: 1, Lot: FF2593, Anatomical location: Left arm, Time: 1 PM, took Tylenol), administration date: 26Oct2021, when the patient was 43 years old, for COVID-19 immunization, reaction: "Carpal tunnel", and "had pain down my arm". The following information was reported: MYOCARDIAL INFARCTION (medically significant, life threatening) with onset 2021, outcome "unknown", described as "I suffered a life threatening heart attack". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
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 1923944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: VT
Alter: 40,0
Geschlecht: M
Eingang: 05.12.2021
Impfdatum: 20.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Chest X-ray abnormal Chest pain Electrocardiogram Painful respiration Chest X-ray Differential white blood cell count Fibrin D dimer Full blood count Prohormone brain natriuretic peptide Prothrombin time Pulmonary embolism Pulmonary thrombosis Scan with contrast abnormal Troponin

Symptomtext

Pain while breathing- taking a deep breath on left side Started on Saturday evening and went to ER on Sunday 28Nov2021. Diagnosed with pulmonary embolisms in both lungs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: 28Nov: Basic metabolic panel, d-dimer, differential, hemogram, prothrombin time, troponin, pro-brain natriuretic peptide performed 2 times CT angiogram chest pulmonary embolus with contrast EKG 12 lead XR chest one view
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Advil occasionally and multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1923944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: VT
Alter: 40,0
Geschlecht: M
Eingang: 05.12.2021
Impfdatum: 20.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 8,0
Dosis: UNK
Route/Site: IM / -

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

Angiogram pulmonary abnormal Chest X-ray abnormal Chest pain Electrocardiogram Painful respiration Chest X-ray Differential white blood cell count Fibrin D dimer Full blood count Prohormone brain natriuretic peptide Prothrombin time Pulmonary embolism Pulmonary thrombosis Scan with contrast abnormal Troponin

Symptomtext

Pain while breathing- taking a deep breath on left side Started on Saturday evening and went to ER on Sunday 28Nov2021. Diagnosed with pulmonary embolisms in both lungs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: 28Nov: Basic metabolic panel, d-dimer, differential, hemogram, prothrombin time, troponin, pro-brain natriuretic peptide performed 2 times CT angiogram chest pulmonary embolus with contrast EKG 12 lead XR chest one view
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Advil occasionally and multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1921012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: MI
Alter: 51,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 20.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure Atelectasis Blood creatinine increased Blood pH decreased Brain natriuretic peptide increased Chills Cough Dyspnoea Dyspnoea exertional Echocardiogram COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest discomfort Chest pain Electrocardiogram normal Endotracheal intubation Fatigue

Symptomtext

Hospitalized (11.26.21): Acute Respiratory failure due to COVID-19 pneumonia; COVID positive (11.26.21) Patient is still admitted to hospital; rapid response event this AM (12.3.21) - patient is now intubated HISTORY OF PRESENT ILLNESS: Patient is a 51 y.o. male with a past medical history of CHF, dilated cardiomyopathy, type 2 diabetes, hypertension, hyperlipidemia and GERD who presents today with chest tightness. History and physical were performed in the emergency department where patient will board until a bed becomes available, patient's wife was present at bedside. Patient states that he has been feeling poorly since the dual administration of his 1st COVID vaccination and flu shot on November 20th. He has been feeling fevers, chills and fatigue. States that measured home temperatures were never elevated. However, after the 1st few days post vaccination administration, patient reports worsening cough, shortness of breath and chest tightness that worsens with deep inspiration. He reports intermittent sputum production which is yellow, denies presence of blood. Patient does endorse that for the past 2 days he has been working on clearing land in building a new home, for which his shortness of breath and fatigue has been a hindrance to his work. Patient's wife states that patient requested the route to the hospital when his chest tightness was severe in nature, given his cardiac history. Patient's wife is fully vaccinated. Patient states he is unaware of any known exposures. He does not wear home oxygen. Patient denies headaches, dizziness, abdominal pain, dysuria, hematuria, numbness or tingling in his extremities. In the emergency department patient was afebrile. He was tachycardic and hypoxic requiring supplemental oxygen saturation. Initially patient was started on 4 L via nasal cannula, at the time of our conversation he had been increased to 6 L via nasal cannula. Pertinent lab findings include an elevated creatinine of 2.22. BNP was within normal limits at 195. Troponins were within normal limits at 20 and then 21 at recheck. EKG showed normal sinus rhythm. Chest x-ray showed abnormal opacity in the left upper lobe extending from the hilum, abnormal patchy opacity in the retrocardiac left lung base. Probable areas of left-sided pneumonia. Suspect minimal strandy atelectasis in the right lung base as well. Rapid COVID PCR was positive. Due to concerns of acute respiratory failure with hypoxia secondary to COVID pneumonia, as well as acute kidney injury, patient was admitted to hospitalist service. Patient is a full code. Discussed with patient our intention to admit to the hospital, which will include judicious fluid administration, and COVID treatment including Decadron and remdesivir. I did discuss with patient and his wife at bedside his code status, and his comfort level with respiratory escalation should it be needed. Patient is agreeable to are all respiratory intervention including mechanical intubation if needed. Patient states he already feels better and would like to go home, at the encouragement and urging of his wife, patient agreed to stay to be admitted to undergo fluid administration and COVID treatment. All questions and concerns answered at this time. Brief history and medical decision making: 51-year-old man with dilated cardiomyopathy type 2 diabetes, dyslipidemia and heart failure preserved ejection fraction, presented with shortness of breath. Patient just received his 1st COVID vaccination and influenza vaccination 7 days ago. Patient presented with cough sputum production and shortness of breath. This is accompanied with worsening dyspnea on exertion. In the emergency department he was hypoxemic and tachycardic. Chest x-ray revealed left upper lobe opacification as well as patchy opacification in the left lung base. Procalcitonin elevated. COVID-19 positive. Will start treatment for COVID-19 respiratory failure with superimposed bacterial community-acquired pneumonia. Will start ceftriaxone/azithromycin. Progress note 12.3.21: Assessment & Plan 12/3 - intubation/mechanical ventilation Requiring norepinephrine, likely due large of the effects of sedation and positive pressure ventilation Check echocardiogram Acute respiratory failure due to COVID-19 Assessment & Plan Tested positive 11/26/2021 Status post remdesivir, finished course Dexamethasone 6 mg/day 11/27 - 12/3 - intubation/mechanical ventilation Lung protective mechanical ventilation, goal tidal volume 4-6 mL/kg ideal body weight Permissive hypercapnia, tolerate pH approximately 7.25 - 7. 40 range Goal plateau pressure less than 30, driving pressure less than 15 Wean FiO2, as tolerated Deep sedation, paralysis Prone position for P/F ratio < 150 Severe COVID pneumonia, severe acute hypoxemic respiratory failure, prior history of cardiomyopathy (ejection fraction normalized on most recent outpatient echocardiogram last month.) Unfortunately, patient required intubation and mechanical ventilation overnight due to refractory hypoxemia and increased work of breathing. Continue deep sedation with propofol/fentanyl; this monitor in place for guidance Continue paralysis Try prone positioning, after patient has central line in place Lung protective mechanical ventilation underway. Given pH 7.19, increased respiratory rate from 26-32. Continue peep 16, wean FiO2 as able (currently 100% with PO2 134) Ultrasound upper/lower extremities and perform CT angiogram, rule out clot. If present, would begin systemic anticoagulation Given history of viral cardiomyopathy, would consider checking echocardiogram to evaluate function Lasix, goal even to negative fluid balance, as tolerated Holding CHF medications, given norepinephrine requirement Continue dexamethasone 6 mg daily, as per protocol Status post empiric ceftriaxone/azithromycin--no indication to resume antibiotics

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: 11.23.21; Called Nurse Triage line: Patient had first dose of Pfizer vaccine on Saturday. Patient did not have any symptoms until yesterday( over 1-2 days from vaccine) including intermittent cough after walking and standing , HA, chills, muscle body aches, feeling hot, fatigue, and intermittent chest pressure. Per caller lying on stomach and chest pressure is not there. Sp02 has dropped from baseline per caller usually 95-100% per OV 96 % Spo2 from writer looking it up. SP02 93 % and and lowest point was 86 %, but currently is back up to 93 %. Possibly for possible exposure. 11.26.21: Called cardiology after hours line; Chest pain --Patient has been experiencing chest pain since Monday --has progressively gotten worse over the last several days and his wife endorses that today it has been the worst --he is currently chest pain and not feeling too well --he has a history of nonischemic dilated cardiomyopathy --instructed to go to ED
Vorgeschichte: Erectile dysfunction Low testosterone Chronic systolic CHF (congestive heart failure) Kidney stone Diabetic neuropathy Sleep disorder Back spasm Prolapsed internal hemorrhoids, grade 3 Acute respiratory failure with hypoxia Viral cardiomyopathy Congestive heart failure
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet cyclobenzaprine (FLEXERIL) 5 MG tablet dapagliflozin (FARXIGA) 10 MG TABS tablet DULoxetine (CYMBALTA) 30 MG delayed release capsule furosemide (LASIX) 40 MG tablet gabapentin (NEURONTIN) 800 MG tablet
Allergien: Oxycontin [Oxycodone]Itching
Vorherige Impfungen: -

VAERS 1897678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: OH
Alter: 62,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Activated partial thromboplastin time Anticoagulant therapy Burning sensation Chest X-ray Chills Constipation Coronary arterial stent insertion Coronary artery thrombosis Cough Dizziness Echocardiogram Electrocardiogram Fatigue Full blood count Headache Hyperhidrosis Intensive care Lipids

Symptomtext

11/20/2021 headache, chills, fever, aches, soe muscles, shallow cough, twinges, dizzy, nausea, fatigue. Much worse than either of the first two doses of the Pfizer vaccine. All day, all night. 11/21/2021 at approximately 6am nausea, need to have BM without success, profuse full-body sweating. Went to ER. Had a heart attack. Emergency heart surgery found blood clot in the RCA. Implanted two stents in the RCA. Recovered in coronary ICU. Given aspirin, heparin, ticagrelor, metoprolol tartrate, plus some sedative during surgery. 11/22/2021 moved from ICU to coronary ward, recovery continued 11/23/2021 echocardiogram, lipid, and EKG results sufficient to release from hospital. New prescriptions set up - continued Prescribed metoprolol tartrate 25mg daily, repatha 1ml every 14 days, ticagrelor 90mg 2 times a day, aspirin 81mg daily, cholecalciferol 25mcg daily, nitroglycerin PRN. Prescribed 12 weeks of 3x/week cardio rehabilitation. 11/24/2021 recovering at home. Sore, fatigue, but no chest pain. Skin of legs and arms burning. I got my seasonal flu vaccine at the pharmacy and got the standard quadrivalent shot. I am assuming that it was the Afluria Quadrivalent but I do not have the paperwork any longer. I assume the records could be obtained from the pharmacy is needed. I got the flu vaccine 15 days before the booster COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: In hospital ER, surgery, and ICU conducted, multiple blood tests (lipid, CBC w/o Diff, basic metabolic panel, Troponin, activated clotting time, ) chest x-ray, echocardiogram, EKG,
Aktuelle Erkrankungen: none
Vorgeschichte: heart problems: MI in 2014, lifelong paroxysmal atrial tachycardia triggered by stimulants.
Andere Medikamente: low dose aspirin
Allergien: statins, floxin antibiotics, cephalosporin antibiotics, etc. Robaxal, stimulants like caffeine, cleaning chemicals and air fresheners, beta blockers
Vorherige Impfungen: -

VAERS 1889448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: IA
Alter: 87,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 18.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Death General physical health deterioration

Symptomtext

Resident had significant decline in condition on 11/21/2021, Resident passed away the morning of 11/22/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None due to Hospice level of care.
Aktuelle Erkrankungen: History of GI bleed, On Hospice at the time of vaccine administration
Vorgeschichte: History of GI bleeds, Alzeimer's disease, COPD, CVA, HTN, CHF, Lyme Disease, PVD
Andere Medikamente: Morphine Sulfate Concentrate 20mg/ml, Tylenol 325mg, Med Pass supplement, Diltiazem 60mg,
Allergien: Propoxyphene, Animal Dander
Vorherige Impfungen: -

VAERS 1873132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: MA
Alter: 81,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Pt received pfizer booster on 11/3/21 in L deltoid, received seasonal flu vaccine on 11/4/21 in R deltoid with HCP consent. No reactions identified at the time of either administration. Pt current status at time of vaccination was non verbal with late stage dementia, which is his baseline. Initiation of hospice services had been discussed with HCP prior to both vaccines. Pt expired on 11/6/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Alzheimer's disease with early onset Dementia in other diseases classified elsewhere without behavioral disturbance Anxiety disorder, unspecified Major depressive disorder, single episode, unspecified Essential (primary) hypertension Gastro-esophageal reflux disease without esophagitis Dysphagia, oral phase Muscle weakness (generalized) Difficulty in walking, not elsewhere classified Alzheimer's disease with late onset Non-verbal
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1865333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: NJ
Alter: 42,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 16.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / LA

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

Death Pericarditis

Symptomtext

I am the epidemiologist reporting on behalf of 42 year-old male patient. Patient received three doses of the Pfizer vaccine, according to immunization records. The first dose was on 02/13/21, the second on 03/06/21, and the third was on 10/16/2021. According to death certificate, patient was found dead on 10/31/21 at home (15 days post dose 3). Immediate cause of death listed is ?complications of pericarditis.? Interval between onset and death is listed as ?unknown.? I do not have any further details on underlying health conditions that may have contributed to this fatality.

Weitere VAERSDATA-Felder

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

VAERS 1804258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

kritisch

Staat: MA
Alter: 103,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Cerebrovascular accident Chest X-ray Computerised tomogram Condition aggravated Hypovolaemia Magnetic resonance imaging Meningioma Toxic encephalopathy Urinary tract infection Urine analysis

Symptomtext

Resident was admitted to the hospital with diagnoses of toxic metabolic encephalopathy likely related to hypovolemia which was resolved after fluid resuscitation. A brain Ct was done and showed chronic occipital infarct with chronic meningioma. A follow up MRI done which did not show any hemorrhage. There was also left occipital lobe acute infarction measuring 3.2 cm in dimension from the CT scan. A new medication Eliquis 2.5 mg twice a day was started in the hospital per Neurologist recommendations and to discontinue ASA 81mg. She also has supraventricular tachycardia with A-fib, cardiologist recommended Lopressor 25 mg twice a day. She was also found to have UTI on admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Chest X-ray, UA and C&S, CT Scans and MRI
Aktuelle Erkrankungen: Xerosis Cutis and some fungal rash
Vorgeschichte: Supra ventricular Tachycardia, Afib, Chronic occipital lobe infarct, urinary incontinence, Macular degeneration
Andere Medikamente: Lopressor, Aspirin, Colace, Magnesium Oxide, Gabapentin, Miralax
Allergien: Bactrim, ciprofloxacin, Levaquin, Macrobid
Vorherige Impfungen: -

VAERS 2634859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: -
Alter: 21,0
Geschlecht: M
Eingang: 22.05.2023
Impfdatum: 14.12.2021
Beginn: 24.05.2022
Tage bis Beginn: 161,0
Dosis: 2
Route/Site: IM / LA

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

Myocarditis Pericarditis

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE PERICARDITIS, UNSPECIFIED MYOCARDITIS

Weitere VAERSDATA-Felder

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

VAERS 2624930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: -
Alter: 34,0
Geschlecht: M
Eingang: 02.05.2023
Impfdatum: 28.11.2021
Beginn: 06.04.2022
Tage bis Beginn: 129,0
Dosis: 3
Route/Site: IM / LA

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

Cardiogenic shock

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE CARDIOGENIC SHOCK

Weitere VAERSDATA-Felder

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

VAERS 2619325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: -
Alter: 90,0
Geschlecht: M
Eingang: 21.04.2023
Impfdatum: 15.10.2021
Beginn: 27.01.2022
Tage bis Beginn: 104,0
Dosis: 3
Route/Site: IM / RA

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

Aortic aneurysm Ischaemic stroke Lacunar stroke

Symptomtext

ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY 1/28/2022 ABDOMINAL AORTIC ANEURYSM, UNSPECIFIED PART ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 1/27/2022 ABDOMINAL AORTIC ANEURYSM, UNSPECIFIED PART

Weitere VAERSDATA-Felder

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

VAERS 2121147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: FL
Alter: 69,0
Geschlecht: M
Eingang: 30.03.2023
Impfdatum: 08.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Biopsy peripheral nerve Chronic inflammatory demyelinating polyradiculoneuropathy Computerised tomogram Electric shock sensation Hypoaesthesia Magnetic resonance imaging Nerve conduction studies abnormal Pain Paraesthesia Polyneuropathy X-ray

Symptomtext

Started having reactions that were later determined to be autoimmune in nature and I was diagnosed with chronic inflammatory demyelinating polyneuropathy (CDIP); 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), on 08Dec2021 as dose 3 (booster), single (Batch/Lot number: unknown) at the age of 69 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for COVID-19 immunisation; Bnt162b2 (DOSE 2, SINGLE), for COVID-19 immunisation. The following information was reported: CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY (medically significant), outcome "unknown", described as "Started having reactions that were later determined to be autoimmune in nature and I was diagnosed with chronic inflammatory demyelinating polyneuropathy (CDIP)". The patient underwent the following laboratory tests and procedures: Biopsy peripheral nerve: Unknown results. Therapeutic measures were taken as a result of chronic inflammatory demyelinating polyradiculoneuropathy. Clinical Course: Patient received Pfizer COVID-19 monovalent booster on 08Dec2021 and started having reactions that were later determined to be autoimmune in nature and he was diagnosed with chronic inflammatory demyelinating polyneuropathy (CDIP). He did not have any trouble with the first two Pfizer COVID-19 injections. Patient doctor prescribed IVIG as treatment but his insurance does not cover it. He was working with a couple of neurologists that did a biopsy of the nerves on the ankle and prescribed a Rituxan protocol but that did not work. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300133556 same patient, different product and event;US-PFIZER INC-202300134288 same patient, different drug/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Name: biopsy of the nerves on the ankle; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2585074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 21.02.2023
Impfdatum: 01.02.2021
Beginn: 17.10.2022
Tage bis Beginn: 623,0
Dosis: 2
Route/Site: SYR / AR

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

Back pain Chest pain Laboratory test abnormal Myocarditis Pain in extremity

Symptomtext

Arms, chest & back began to ache. No signs prior, felt fine, standing checking into my Dr.?s office for a regular checkup. . I was sent to urgent care & then to hospital . Many tests were given. Diagnosis was myocarditis. My Heart Dr. issued another text & the result is apparently it has healed itself. Very odd considering I have been extremely healthy only bring in a hospital 3 times. Which were elective. No heath issues whatsoever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: All are documented with my primary Dr. Too many tests to text. I was in the hospital from the 10/17/22 & discharged 10/18/22.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Alprazolam, Celexa, Flonase, Zyrtec, simvastatin
Allergien: Some antibiotics., that?s it
Vorherige Impfungen: -

VAERS 2560047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Alopecia Anxiety Arthralgia Attention deficit hyperactivity disorder Autonomic nervous system imbalance Body temperature Body temperature abnormal Cellulitis Chest pain Chills Decreased appetite Depression Disturbance in attention Dizziness Dry eye Dry mouth Dyspnoea Dysphagia

Symptomtext

rapid muscle mass loss; tachycardia; hypertension; anxiety; depression; palpitations; ADHD; ptsd; insomnia; shingles; rash; tremors/zaps and shocks of fingers / Shaking; internal vibrations; shob on exertion; pots; dysautonomia; head pressure; hot flashes; cold chills; tinnitus; runny nose; parenthesis; hair loss; dry eyes and mouth; dry eyes and mouth; mouth and nasal ulcers; mouth and nasal ulcers; vertigo; unable to control body temperature; swollen painful joints; gi problems; chest pains; cellulitis; mcas; neuropathy in hands and feet; dizziness; fatigue; pain in muscles and joints; pain in muscles and joints; headache; nausea; syncope / near syncope; Interchange of vaccine products; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 36-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Dec2021 at 15:45 as dose 3 (booster), single (Lot number: FH8027) at the age of 36 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Pollen allergy" (unspecified if ongoing). Concomitant medication(s) included: CLARITIN [LORATADINE]. Vaccination history included: moderna (DOSE 1, SINGLE, Batch/Lot No: 011J20A, Anatomical location: Arm Right), administration date: 23Dec2020, when the patient was 35-year-old, for COVID-19 immunization; moderna (DOSE 2, SINGLE, Batch/Lot No: 028L20A, Anatomical location: Arm Right), administration date: 25Jan2021, when the patient was 35-year-old, for COVID-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 29Dec2021 at 15:45, outcome "unknown"; DIZZINESS (disability) with onset 29Dec2021 at 23:45, outcome "not recovered"; FATIGUE (disability) with onset 29Dec2021 at 23:45, outcome "not recovered"; HEADACHE (disability) with onset 29Dec2021 at 23:45, outcome "not recovered"; NAUSEA (disability) with onset 29Dec2021 at 23:45, outcome "not recovered"; MYALGIA (disability), ARTHRALGIA (disability) all with onset 29Dec2021 at 23:45, outcome "not recovered" and all described as "pain in muscles and joints"; SYNCOPE (disability, medically significant) with onset 29Dec2021 at 23:45, outcome "not recovered", described as "syncope / near syncope"; ATTENTION DEFICIT HYPERACTIVITY DISORDER (disability) with onset Jan2022, outcome "not recovered", described as "ADHD"; ANXIETY (disability) with onset Jan2022, outcome "not recovered"; CELLULITIS (disability, medically significant) with onset Jan2022, outcome "not recovered"; CHEST PAIN (disability) with onset Jan2022, outcome "not recovered", described as "chest pains"; CHILLS (disability) with onset Jan2022, outcome "not recovered", described as "cold chills"; DEPRESSION (disability) with onset Jan2022, outcome "not recovered"; DRY EYE (disability), DRY MOUTH (disability) all with onset Jan2022, outcome "not recovered" and all described as "dry eyes and mouth"; AUTONOMIC NERVOUS SYSTEM IMBALANCE (disability) with onset Jan2022, outcome "not recovered", described as "dysautonomia"; GASTROINTESTINAL DISORDER (disability) with onset Jan2022, outcome "not recovered", described as "gi problems"; ALOPECIA (disability) with onset Jan2022, outcome "not recovered", described as "hair loss"; HEAD DISCOMFORT (disability) with onset Jan2022, outcome "not recovered", described as "head pressure"; HOT FLUSH (disability) with onset Jan2022, outcome "not recovered", described as "hot flashes"; HYPERTENSION (disability) with onset Jan2022, outcome "not recovered"; INSOMNIA (disability) with onset Jan2022, outcome "not recovered"; NERVOUSNESS (disability) with onset Jan2022, outcome "not recovered", described as "internal vibrations"; MAST CELL ACTIVATION SYNDROME (disability, medically significant) with onset Jan2022, outcome "not recovered", described as "mcas"; MOUTH ULCERATION (disability), NASAL ULCER (disability) all with onset Jan2022, outcome "not recovered" and all described as "mouth and nasal ulcers"; NEUROPATHY PERIPHERAL (disability, medically significant) with onset Jan2022, outcome "not recovered", described as "neuropathy in hands and feet"; PALPITATIONS (disability) with onset Jan2022, outcome "not recovered"; PARAESTHESIA (disability) with onset Jan2022, outcome "not recovered", described as "parenthesis"; POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME (disability) with onset Jan2022, outcome "not recovered", described as "pots"; POST-TRAUMATIC STRESS DISORDER (disability) with onset Jan2022, outcome "not recovered", described as "ptsd"; MUSCLE ATROPHY (disability) with onset Jan2022, outcome "not recovered", described as "rapid muscle mass loss"; RASH (disability) with onset Jan2022, outcome "not recovered"; RHINORRHOEA (disability) with onset Jan2022, outcome "not recovered", described as "runny nose"; HERPES ZOSTER (disability) with onset Jan2022, outcome "not recovered", described as "shingles"; DYSPNOEA (disability) with onset Jan2022, outcome "not recovered", described as "shob on exertion"; JOINT SWELLING (disability) with onset Jan2022, outcome "not recovered", described as "swollen painful joints"; TACHYCARDIA (disability) with onset Jan2022, outcome "not recovered"; TINNITUS (disability) with onset Jan2022, outcome "not recovered"; TREMOR (disability) with onset Jan2022, outcome "not recovered", described as "tremors/zaps and shocks of fingers / Shaking"; BODY TEMPERATURE ABNORMAL (disability) with onset Jan2022, outcome "not recovered", described as "unable to control body temperature"; VERTIGO (disability) with onset Jan2022, outcome "not recovered". The event "shob on exertion" required emergency room visit. The events "syncope / near syncope", "cellulitis", "mcas", "neuropathy in hands and feet", "dizziness", "fatigue", "pain in muscles and joints", "headache", "nausea", "rapid muscle mass loss", "tachycardia", "hypertension", "anxiety", "depression", "palpitations", "adhd", "ptsd", "insomnia", "shingles", "rash", "tremors/zaps and shocks of fingers / shaking", "internal vibrations", "pots", "dysautonomia", "head pressure", "hot flashes", "cold chills", "tinnitus", "runny nose", "parenthesis", "hair loss", "dry eyes and mouth", "mouth and nasal ulcers", "vertigo", "unable to control body temperature", "swollen painful joints", "gi problems" and "chest pains" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Body temperature: (Jan2022) unable to control body temperature. Therapeutic measures were taken as a result of syncope, cellulitis, mast cell activation syndrome, neuropathy peripheral, dizziness, fatigue, myalgia, arthralgia, headache, nausea, muscle atrophy, tachycardia, hypertension, anxiety, depression, palpitations, attention deficit hyperactivity disorder, post-traumatic stress disorder, insomnia, herpes zoster, rash, tremor, nervousness, dyspnoea, postural orthostatic tachycardia syndrome, autonomic nervous system imbalance, head discomfort, hot flush, chills, tinnitus, rhinorrhoea, paraesthesia, alopecia, dry eye, dry mouth, mouth ulceration, nasal ulcer, vertigo, body temperature abnormal, joint swelling, gastrointestinal disorder, chest pain. Clinical course: The patient was not pregnant at the time of vaccination. The patient had no known allergies. No other vaccine in four weeks. No covid prior vaccination and covid not tested post vaccination. Facility type vaccine: Hospital. Stated that, 8 hours post vaccination, the patient experienced dizziness, fatigue, pain in muscles and joints, headache, nausea and syncope. Two weeks later rapid muscle mass loss, tachycardia, hypertension, anxiety, depression, near syncope, palpitations, adhd, ptsd, insomnia each month new symptoms appeared including shingles, cellulitis, rash, tremors, internal vibrations, zaps and shocks of fingers, shob on exertion, pots, mcas, dysautonomia, head pressure, hot flashes, cold chills, shaking, tinnitus, runny nose, neuropathy in hands and feet, parenthesis, hair loss, dry eyes and mouth, mouth and nasal ulcers, vertigo, unable to control body temperature, swollen painful joints, GI problems and chest pains. All new onset of symptoms and diagnosis. AE resulted in: (Doctor or other healthcare professional office clinic visit, Emergency Room department or urgent care, Disability or permanent damage).; Sender's Comments: Based on the available information in the case, an association between the reported events and The suspected drug cannot be ruled out. 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: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Date: 202201; Test Name: Body temperature; Result Unstructured Data: Test Result:unable to control body temperature
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pollen allergy
Andere Medikamente: CLARITIN [LORATADINE]
Allergien: -
Vorherige Impfungen: -

VAERS 2560047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Alopecia Anxiety Arthralgia Attention deficit hyperactivity disorder Autonomic nervous system imbalance Body temperature Body temperature abnormal Cellulitis Chest pain Chills Decreased appetite Depression Disturbance in attention Dizziness Dry eye Dry mouth Dyspnoea Dysphagia

Symptomtext

rapid muscle mass loss; tachycardia; hypertension; anxiety; depression; palpitations; ADHD; ptsd; insomnia; shingles; rash; tremors/zaps and shocks of fingers / Shaking; internal vibrations; shob on exertion; pots; dysautonomia; head pressure; hot flashes; cold chills; tinnitus; runny nose; parenthesis; hair loss; dry eyes and mouth; dry eyes and mouth; mouth and nasal ulcers; mouth and nasal ulcers; vertigo; unable to control body temperature; swollen painful joints; gi problems; chest pains; cellulitis; mcas; neuropathy in hands and feet; dizziness; fatigue; pain in muscles and joints; pain in muscles and joints; headache; nausea; syncope / near syncope; Interchange of vaccine products; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 36-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Dec2021 at 15:45 as dose 3 (booster), single (Lot number: FH8027) at the age of 36 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Pollen allergy" (unspecified if ongoing). Concomitant medication(s) included: CLARITIN [LORATADINE]. Vaccination history included: moderna (DOSE 1, SINGLE, Batch/Lot No: 011J20A, Anatomical location: Arm Right), administration date: 23Dec2020, when the patient was 35-year-old, for COVID-19 immunization; moderna (DOSE 2, SINGLE, Batch/Lot No: 028L20A, Anatomical location: Arm Right), administration date: 25Jan2021, when the patient was 35-year-old, for COVID-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 29Dec2021 at 15:45, outcome "unknown"; DIZZINESS (disability) with onset 29Dec2021 at 23:45, outcome "not recovered"; FATIGUE (disability) with onset 29Dec2021 at 23:45, outcome "not recovered"; HEADACHE (disability) with onset 29Dec2021 at 23:45, outcome "not recovered"; NAUSEA (disability) with onset 29Dec2021 at 23:45, outcome "not recovered"; MYALGIA (disability), ARTHRALGIA (disability) all with onset 29Dec2021 at 23:45, outcome "not recovered" and all described as "pain in muscles and joints"; SYNCOPE (disability, medically significant) with onset 29Dec2021 at 23:45, outcome "not recovered", described as "syncope / near syncope"; ATTENTION DEFICIT HYPERACTIVITY DISORDER (disability) with onset Jan2022, outcome "not recovered", described as "ADHD"; ANXIETY (disability) with onset Jan2022, outcome "not recovered"; CELLULITIS (disability, medically significant) with onset Jan2022, outcome "not recovered"; CHEST PAIN (disability) with onset Jan2022, outcome "not recovered", described as "chest pains"; CHILLS (disability) with onset Jan2022, outcome "not recovered", described as "cold chills"; DEPRESSION (disability) with onset Jan2022, outcome "not recovered"; DRY EYE (disability), DRY MOUTH (disability) all with onset Jan2022, outcome "not recovered" and all described as "dry eyes and mouth"; AUTONOMIC NERVOUS SYSTEM IMBALANCE (disability) with onset Jan2022, outcome "not recovered", described as "dysautonomia"; GASTROINTESTINAL DISORDER (disability) with onset Jan2022, outcome "not recovered", described as "gi problems"; ALOPECIA (disability) with onset Jan2022, outcome "not recovered", described as "hair loss"; HEAD DISCOMFORT (disability) with onset Jan2022, outcome "not recovered", described as "head pressure"; HOT FLUSH (disability) with onset Jan2022, outcome "not recovered", described as "hot flashes"; HYPERTENSION (disability) with onset Jan2022, outcome "not recovered"; INSOMNIA (disability) with onset Jan2022, outcome "not recovered"; NERVOUSNESS (disability) with onset Jan2022, outcome "not recovered", described as "internal vibrations"; MAST CELL ACTIVATION SYNDROME (disability, medically significant) with onset Jan2022, outcome "not recovered", described as "mcas"; MOUTH ULCERATION (disability), NASAL ULCER (disability) all with onset Jan2022, outcome "not recovered" and all described as "mouth and nasal ulcers"; NEUROPATHY PERIPHERAL (disability, medically significant) with onset Jan2022, outcome "not recovered", described as "neuropathy in hands and feet"; PALPITATIONS (disability) with onset Jan2022, outcome "not recovered"; PARAESTHESIA (disability) with onset Jan2022, outcome "not recovered", described as "parenthesis"; POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME (disability) with onset Jan2022, outcome "not recovered", described as "pots"; POST-TRAUMATIC STRESS DISORDER (disability) with onset Jan2022, outcome "not recovered", described as "ptsd"; MUSCLE ATROPHY (disability) with onset Jan2022, outcome "not recovered", described as "rapid muscle mass loss"; RASH (disability) with onset Jan2022, outcome "not recovered"; RHINORRHOEA (disability) with onset Jan2022, outcome "not recovered", described as "runny nose"; HERPES ZOSTER (disability) with onset Jan2022, outcome "not recovered", described as "shingles"; DYSPNOEA (disability) with onset Jan2022, outcome "not recovered", described as "shob on exertion"; JOINT SWELLING (disability) with onset Jan2022, outcome "not recovered", described as "swollen painful joints"; TACHYCARDIA (disability) with onset Jan2022, outcome "not recovered"; TINNITUS (disability) with onset Jan2022, outcome "not recovered"; TREMOR (disability) with onset Jan2022, outcome "not recovered", described as "tremors/zaps and shocks of fingers / Shaking"; BODY TEMPERATURE ABNORMAL (disability) with onset Jan2022, outcome "not recovered", described as "unable to control body temperature"; VERTIGO (disability) with onset Jan2022, outcome "not recovered". The event "shob on exertion" required emergency room visit. The events "syncope / near syncope", "cellulitis", "mcas", "neuropathy in hands and feet", "dizziness", "fatigue", "pain in muscles and joints", "headache", "nausea", "rapid muscle mass loss", "tachycardia", "hypertension", "anxiety", "depression", "palpitations", "adhd", "ptsd", "insomnia", "shingles", "rash", "tremors/zaps and shocks of fingers / shaking", "internal vibrations", "pots", "dysautonomia", "head pressure", "hot flashes", "cold chills", "tinnitus", "runny nose", "parenthesis", "hair loss", "dry eyes and mouth", "mouth and nasal ulcers", "vertigo", "unable to control body temperature", "swollen painful joints", "gi problems" and "chest pains" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Body temperature: (Jan2022) unable to control body temperature. Therapeutic measures were taken as a result of syncope, cellulitis, mast cell activation syndrome, neuropathy peripheral, dizziness, fatigue, myalgia, arthralgia, headache, nausea, muscle atrophy, tachycardia, hypertension, anxiety, depression, palpitations, attention deficit hyperactivity disorder, post-traumatic stress disorder, insomnia, herpes zoster, rash, tremor, nervousness, dyspnoea, postural orthostatic tachycardia syndrome, autonomic nervous system imbalance, head discomfort, hot flush, chills, tinnitus, rhinorrhoea, paraesthesia, alopecia, dry eye, dry mouth, mouth ulceration, nasal ulcer, vertigo, body temperature abnormal, joint swelling, gastrointestinal disorder, chest pain. Clinical course: The patient was not pregnant at the time of vaccination. The patient had no known allergies. No other vaccine in four weeks. No covid prior vaccination and covid not tested post vaccination. Facility type vaccine: Hospital. Stated that, 8 hours post vaccination, the patient experienced dizziness, fatigue, pain in muscles and joints, headache, nausea and syncope. Two weeks later rapid muscle mass loss, tachycardia, hypertension, anxiety, depression, near syncope, palpitations, adhd, ptsd, insomnia each month new symptoms appeared including shingles, cellulitis, rash, tremors, internal vibrations, zaps and shocks of fingers, shob on exertion, pots, mcas, dysautonomia, head pressure, hot flashes, cold chills, shaking, tinnitus, runny nose, neuropathy in hands and feet, parenthesis, hair loss, dry eyes and mouth, mouth and nasal ulcers, vertigo, unable to control body temperature, swollen painful joints, GI problems and chest pains. All new onset of symptoms and diagnosis. AE resulted in: (Doctor or other healthcare professional office clinic visit, Emergency Room department or urgent care, Disability or permanent damage).; Sender's Comments: Based on the available information in the case, an association between the reported events and The suspected drug cannot be ruled out. 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: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Date: 202201; Test Name: Body temperature; Result Unstructured Data: Test Result:unable to control body temperature
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pollen allergy
Andere Medikamente: CLARITIN [LORATADINE]
Allergien: -
Vorherige Impfungen: -

VAERS 2560227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: FL
Alter: 50,0
Geschlecht: F
Eingang: 15.01.2023
Impfdatum: 24.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Antiacetylcholine receptor antibody Arthralgia Blood copper Blood test Borrelia test Cardiac stress test Chest X-ray Chest pain Cognitive disorder Computerised tomogram abdomen Computerised tomogram head Computerised tomogram spine Confusional state Diplegia Dysphemia Electric shock sensation Electrocardiogram

Symptomtext

After 1st and 2nd doses of Pfizer COVID vaccine I experienced ringing in ears, joint pain, headache, fatigue, swollen joints, and nausea that never went away. After Booster shot I experienced all of the above plus additional symptoms that have slowly added over time. My symptoms are constantly changing and now include but are not limited to: Widespread debilitating burning and aching pain in my arms, legs, neck and chest. Weight Loss, Cognitive issues, brain fog and confusion. Abdominal pain, pain in jaw and all teeth. Left side face paralysis of eye and mouth causing a sneering look. In June 2022 I began stuttering when I talk and starting having seizure like myoclonic jerking of both arms, legs and neck. New symptoms since include: Tremors, falling, intermittent paralysis of arms. Tingling, numbness, electric shocks throughout body. muscle twitching and spasms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: 2022 CT and MRI of brain and spinal cord CT scan of abdomen Heart stress test EKG EEG Chest xrays spine xrays sleep test Multiple blood panels repeated throughout the year: CBC Thyroid Metabolic panel Hepatitis HIV STD Rheumatoid factors SED rate Iron, TIBC Hemoglobin D-Dimer Hepatic HLA-B27 DNA typing Lyme screen Celiac Heavy Metal Copper Acetylcholine receptor binding
Aktuelle Erkrankungen: none
Vorgeschichte: psoriasis and psoriatic arthritis
Andere Medikamente: Cosentyx
Allergien: none
Vorherige Impfungen: -

VAERS 2493175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: AR
Alter: 30,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 23.11.2021
Beginn: 03.03.2022
Tage bis Beginn: 100,0
Dosis: 2
Route/Site: - / RA

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

Bell's palsy

Symptomtext

Bell(s) palsy on right side of my face.; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Nov2021 at 12:00 as dose 2, single (Lot number: FH8027) at the age of 30 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing); "Anxiety" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: FF2593, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 28Oct2021, when the patient was 30-year-old, for Covid-19 immunization. The following information was reported: BELL'S PALSY (medically significant) with onset 03Mar2022 at 14:00, outcome "recovering", described as "Bell(s) palsy on right side of my face.". The event "bell(s) palsy on right side of my face." required physician office visit and emergency room visit. Therapeutic measures were taken as a result of bell's palsy. Clinical course: Patient did not have any known allergies. Patient did not receive any other vaccine in four weeks and not received other medications in two weeks. Patient did not had covid prior vaccination and not tested covid post vaccination. Received treatment for AE with Steroids and Viral medicine.; Sender's Comments: Based on the known safety profile and Limited information in the case report a casual association between reported serious event Bell's Palsy and the suspect drug BNT162B2 cannot be 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

Weitere VAERSDATA-Felder

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

VAERS 2450819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: PA
Alter: 61,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 18.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Fibrin D dimer Oxygen saturation decreased Thrombosis

Symptomtext

I had low oxygen , shortness of breath and blood clots

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: d-dimer test, rushed through emergency room
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: PROPAFENONE: B12: VITAMIN D:
Allergien: IODINE
Vorherige Impfungen: -

VAERS 2425737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: TX
Alter: 30,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 14.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 48,0
Dosis: 1
Route/Site: SYR / AR

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

Heavy menstrual bleeding Menstruation irregular Thrombosis Ultrasound scan normal

Symptomtext

I got first and second dose of vaccines of Pfizer, First dose november 14, and second dose December 05, 2021. On December 2021 after two days of my vaccines I got my period, it was spotting for 4 days, After that, In January, I dont have period at all, by February I only got spotting for 9 days, Its was weird because for many years I always have period. By March for some reason I got heaviest period in my life, I feel the blood its like pee, it last for 15 days, because I took advil to help it decreased. By end of April my period start again, but at first I got spotting at like 3 to 4 days before actual period start April 24 to May 10, its like 17 days bleeding, I know it was not normal at all Im taken advil for this also to help me stop the bleeding. In May I went to have check up the doctor advice me to get a transvaginal ultrasound, and I'm glad it went, normal result. That time, the doctor prescribed me a traxenemic acid. In June, It seem it was lighter and I have 9 days period but in the 7th day, I took traxenemic and stop in 9 days. So I thought, and hoping by July will go back to normal but it wasnt. In July I got my period again start July 04 to July 18, its 15 days bleeding, before the period start, I had spotting again by 4 days before start, this time my period, has a lot of clots and there are some days i'ts lighter and for some reason the next day it will be heavier. I took the traxenemic and advil, I only allowed 5 days for traxenemic so when its end after a day, I took advil. So in August I got my period.I didnt spotting but my period start August 17 but stop for 2 days. And then August 20 start again, its lighter some days, and next days it heavier its been like 12 days up to now it didnt stop. For many years I never experienced this before I got the vaccine. I have only like 4 days of period and like 28 days of cycle before. I'm hoping that one day it will go back to normal, i'ts been like almost 6 months, and I still dealing with it. I dont have any cramps, but I do have like more clotty period, and heavier some days, some days lighter, and for some reason I feel it won't stop unless I took some medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: May 06 2022, I got check up and the doctor prescribed me Traxenimic Acid after two weeks I got my transvaginal Ultrasound, I forgot the exact date of it.
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2344753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: IA
Alter: 63,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 11.01.2022
Beginn: 23.03.2022
Tage bis Beginn: 71,0
Dosis: 3
Route/Site: IM / -

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

Abdominal X-ray Abdominal discomfort Alanine aminotransferase normal Alcohol use Alcohol withdrawal syndrome Alcoholic seizure Aspartate aminotransferase increased Blood bilirubin increased Blood creatinine increased Blood lactic acid Blood pressure increased COVID-19 Flatulence Full blood count normal Pyrexia SARS-CoV-2 test positive Substance use Tachycardia

Symptomtext

Pfizer Dose 1 4/13/21 (Er8732) Pfizer Dose 2 5/5/21 (ER8736) Pfizer Dose 3 1/11/22 (FH8027) COVID Positive 3/23/22 3/23/22: Patient is a 65-year-old female with past medical history of alcoholism, cirrhosis, chronic hepatitis C, rheumatoid arthritis, spinal stenosis, and history of smoking. She presented to ED on 03/23/2022 after having an alcohol withdrawal seizure at home. This is her 5th or 6th alcohol withdrawal seizure in total. She has been unable to drink as much alcohol the last few days as her stomach has been upset. Her last alcoholic drink was yesterday. She has been vomiting recently. No blood in her vomit. No blood in her stools or dark stools. She denies history of being told that she has esophageal varices. She otherwise denies fever, chills, sweats. No chest pain or shortness of breath. After her seizure, her significant other brought her to the emergency department. Her blood pressure was elevated on arrival. She was also mildly tachycardic. Abdominal x-ray showed a moderate amount of gas and stool throughout the colon and rectum but was otherwise unremarkable. She denies any abdominal pain so CT was held. Her lab work was notable for creatinine of 1.23 which is actually about her baseline. ALT was 36 and AST was 119. Total bilirubin 2.5. Lactic acid was 10.6. Her CBC was unremarkable. Patient was administered Benadryl, morphine, Zofran, Phenergan, and normal saline, and thiamine in the ED. She was admitted for further management of her alcohol withdrawal. The patient wants to get sober. She has previously been able to stay sober for about 6 months, but relapsed when her mom got sick. She does not want to pursue inpatient treatment facility for her alcoholism. She feels that she will be okay at home with her significant other as she does feel she has support at home. She did try to smoke some marijuana to settle her stomach, but otherwise denies any illicit drug use. No current smoking history. Her family history was reviewed and is noncontributory. 3/25/22: The patient was admitted with alcohol withdrawal seizure, had recurrent episodes of alcohol withdrawal seizures, and actually she is on Keppra. Unfortunately, patient continues to drink. She was admitted, monitored on a CIWA scale. Patient was seen and examined on the day of discharge. She was awake, alert, and oriented. Not exhibiting any alcohol withdrawal symptoms. She had a slight fever. She had a mild fever overnight. Otherwise, no source of infection other than her COVID-19 positive test, no respiratory symptoms, no difficulty breathing nor requiring any oxygen. She was instructed to self isolate at home for 10 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alcoholic seizure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: alcoholism cirrhosis chronic hepatitis C RA spinal stenosis h/o smoking
Andere Medikamente: folic acid 1 mg PO QD hydroxyzine 10 mg Po HS levetiracetam 500 mg PO BID metoprolol 25 mg PO BID omeprazole 20 mg PO QD KCl 10 mEq Po QD K phos 1 tab PO QD rifaximin 550 mg PO BID spironolactone 50 mg PO QD thiamine 100 mg PO QD
Allergien: triple antibiotic ointent - swelling
Vorherige Impfungen: -

VAERS 2335445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 26.06.2022
Impfdatum: 29.11.2021
Beginn: 12.12.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / RA

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

Angiogram pulmonary abnormal Chest X-ray normal Chest pain Echocardiogram abnormal Head injury Headache Hypotension Laboratory test Lymphadenopathy mediastinal Pericardial drainage Pericardial effusion Pericardial excision Syncope Tachycardia

Symptomtext

Woke up on 12/12/21 with chest pain and headache. Went to dr on 12/13/21, had chest xray, nothing could be seen. This continued until pericardial window procedure on 12/17/21. Had a syncope episode and hit head about 5:45 am on 12/16/21. Went to ER as I take Eliquis. After running numerous tests, a moderate pericardial effusion was found on a CT scan. Was admitted to the hospital and a pericardial window procedure was performed the next morning on 12/17/21 with a chest drain tube. Transthoracic echo demonstrates moderate-large pericardial effusion. There are no signs of tamponade physiology at this time. However the patient is tachycardic and relatively hypotensive

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 4,0
Labordaten: 12/16/21 - CT ANGIOGRAM CHEST - moderate pericardial effusion present. Mild mediastinal lymphadenopathy is also identified;
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2315477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: LA
Alter: 73,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 19.05.2022
Beginn: 20.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Abdominal pain upper Asthenia Blood test abnormal Chest X-ray normal Chest pain Chills Echocardiogram Electrocardiogram normal Headache Nausea Pericarditis Protein total increased Pyrexia Stress Troponin increased

Symptomtext

I woke up the next day and had a headache, stomach pain, and nausea and when I tried to get up I was really weak later in the day I felt like I had a fever and checked my temperature and had fever of 100.1. So I took some Tylenol and later in the day began to have chills off and on for the next 3 days. I started having chest pains on the 22nd and I called the Dr. and they advised for me to go to the ED to get checked out I started feeling better the next day while I was in the hospital. I stayed in the hospital for 4 days. When I was in the ED they said I had heart stress and later on that day he stated I had Pericarditis and that I had high levels of Troponin and they were thinking it was from the booster shot. My pain is more on the right side of my chest than my left side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 4,0
Labordaten: Blood work-abnormal Troponin level elevated, elevated Protein levels, EKG- normal, Echocardiogram, Chest X-Ray-normal
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis, COPD, Hypertension
Andere Medikamente: Amlodipine 10 mg, Atarax, Atorvastatin, Atrovent Inhaler, Azelastine, Desloratine, Flovent Disk Inhaler, HTZ, Ipratropium Nebulizer, Meclizine, Mobic, Nitroglycerin, Omeprazole 40 mg, Singular Tetracycline, Valacyclovir, Eye Drops Refresh,
Allergien: Penicillin, Codeine, Corn and Corn products, Red dye
Vorherige Impfungen: Every Vaccine gives an reaction with mild symptoms.

VAERS 2000564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 28.05.2022
Impfdatum: 23.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: - / LA

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

Anxiety Back pain Blood test Cardiac stress test Computerised tomogram Biopsy skin Insomnia Lumbar puncture Palpitations Echocardiogram Electrocardiogram Electrocardiogram ambulatory Feeling hot Lipids Muscle tightness Myocarditis Neck pain Pain in extremity

Symptomtext

Heart Palpitations; Insomnia; Small fiber neuropathy; Anxiety; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Nov2021 at 12:15 as dose 3 (booster), single (Lot number: FH8027) at the age of 53 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Past drug history included: Codeine, reaction(s): "Drug allergy"; Augmentin, reaction(s): "Drug allergy". Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EW0176, Location of injection: Arm Left, Vaccine Administration Time: 12:15 PM), administration date: 07May2021, when the patient was 52-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EW0158, Location of injection: Arm Left, Vaccine Administration Time: 12:15 PM), administration date: 16Apr2021, when the patient was 52-year-old, for COVID-19 immunization. The following information was reported: ANXIETY (hospitalization, disability, life threatening) with onset 29Nov2021 at 09:30, outcome "not recovered"; PALPITATIONS (hospitalization, disability, life threatening) with onset 29Nov2021 at 09:30, outcome "recovered", described as "Heart Palpitations"; INSOMNIA (hospitalization, disability, life threatening) with onset 29Nov2021 at 09:30, outcome "recovered"; SMALL FIBRE NEUROPATHY (hospitalization, disability, life threatening) with onset 29Nov2021 at 09:30, outcome "not recovered", described as "Small fiber neuropathy". The patient was hospitalized for palpitations, insomnia, small fibre neuropathy, anxiety (hospitalization duration: 1 day(s)). The patient underwent the following laboratory tests and procedures: Biopsy skin: Unknown results; Lumbar puncture: Small fiber neuropathy. Therapeutic measures were taken as a result of palpitations, insomnia, small fibre neuropathy, anxiety. Clinical course: Other medication in 2weeks: No. Adverse event: Heart Palpitations Insomnia (5 weeks) Small fiber neuropathy (as detected by the lumbar puncture and skin biopsy) Anxiety. AE resulted in: [Hospitalization, Life threatening illness (immediate risk of death from the event), Disability or permanent damage]. AE treatment: Gabapentin 600 mg 3/day, Propafenone 225mg 2/day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: Test Name: skin biopsy; Result Unstructured Data: Test Result:Unknown results; Test Name: lumbar puncture; Result Unstructured Data: Test Result:Small fiber neuropathy
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2266085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: MD
Alter: 31,0
Geschlecht: M
Eingang: 06.05.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

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

Asthma Bronchitis Cardiac failure Cardiomegaly Computerised tomogram thorax Dyspnoea Eating disorder Echocardiogram abnormal Electrocardiogram abnormal Fatigue Influenza like illness Insomnia Loss of personal independence in daily activities Myocarditis Pneumonia Viral infection X-ray abnormal

Symptomtext

I had severe flu like symptoms following the third dose of Pfizer. I took both a rapid at home test and a PCR test for COVID-19 which both came back negative. I went to urgent care and was diagnosed with pneumonia. I took a 10 day course of antibiotics. About a week later, I went back to urgent care because the symptoms had returned. I was prescribed antibiotics again and was told that it was either bronchitis or asthma. My fatigue and shortness of breath continued to get worse which was interfering with my ability to perform normal daily activities. I was unable to even sleep or eat properly. On one of my follow ups at urgent care, the doctor suggested that I may have cardiomegaly and referred me to a cardiologist who advised that I get an echocardiogram. The echocardiogram found that I had heart failure at which point I was hospitalized for 4 days. The cardiologist I saw after believed that the cause was viral infection induced myocarditis which he attributed to the third dose of the vaccine. I am currently being treated for heart failure and none of the cardiologists have been able to definitively determine the cause as of yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: Echocardiogram-Heart Failure Discovered-04/15/2022 Multiple X-Rays-Cardiomegaly Found Multiple EKGs-Heart Failure Found Cardiac CT Scan-Results Unknown-05/05/2022
Aktuelle Erkrankungen: Cold/Flu Like Symptoms
Vorgeschichte: Heart Failure
Andere Medikamente: Adderall 15mg ER Escitalopram 15mg Dayquill/Nyquill
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2255256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: AK
Alter: 69,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 26.04.2022
Beginn: 26.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Bone contusion Contusion Joint injury Loss of consciousness Syncope

Symptomtext

8 hours after receiving the vaccine, Patient got up from couch, stepped forward and momentarily lost consciousness (fainted). She recovered right away. It took several moments to gather her wits and then was able to stand up. She did not seek treatment. She twisted her ankle, bruised ribs, and bruised right hand. She did call primary care physician and is going to follow up with them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None yet. She is going to follow up with physician.
Aktuelle Erkrankungen: -
Vorgeschichte: SPINAL STENOSIS
Andere Medikamente: GABAPENTIN, IBUPROFEN, ROSUVASTATIN, TRAZODONE
Allergien: -
Vorherige Impfungen: -

VAERS 2194655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: ND
Alter: 50,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 24.11.2021
Beginn: 30.12.2021
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: SYR / AR

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

Blood test abnormal Peripheral artery thrombosis

Symptomtext

I developed a Blood Clot in My Artery in my right leg. Dr's could not officially diagnose why the blood clot happened by my blood tests. I asked them if it could have been caused by my booster shot and they told me they could not say but it was unlikely but that I should report it anyways.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Peripheral artery thrombosis
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Losartan - 100MG Hydrochlorothiazide - 50MG Amlodipine - 10MG
Allergien: Environmental
Vorherige Impfungen: -

VAERS 2162571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: OH
Alter: 73,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 28.11.2021
Beginn: 25.01.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory distress syndrome COVID-19 Chest X-ray abnormal Cough Dyspnoea Oropharyngeal pain Pneumonia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Patient tested positive for Covid on 01/17/2022. Admitted to hospital on 01/25/2022 with symptoms: runny nose, sore throat, cough, shortness of breath. Patient develop pneumonia and was in acute respiratory distress. Patient did have an abnormal chest xray. Patient has multiple underlying health conditions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: 7,0
Labordaten: SARS-CoV-2 Antigen tested positive 01/17/2022
Aktuelle Erkrankungen: diabetes, cardiovascular disease, hypertension
Vorgeschichte: diabetes, cardiovascular disease, hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2157607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: MO
Alter: 63,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood magnesium Blood test Chills Electrocardiogram Fatigue Metabolic function test Pain in extremity Pyrexia SARS-CoV-2 test Sleep disorder Syncope

Symptomtext

I had pain in my arm. In the evening I was fatigued and had chills and fever that same night. I got up in the middle of the night and I briefly passed out. I went to urgent care the same day but they just sent me to the ER. They ran some tests and gave me fluids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Covid-19 test, blood work, EKG, CBC, PCR, mag LVL, metabolic basic. .
Aktuelle Erkrankungen: None
Vorgeschichte: Severe dermatitis
Andere Medikamente: Omeprazole, Tylenol
Allergien: Sulfur drugs
Vorherige Impfungen: -

VAERS 2091357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: MD
Alter: 81,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Fall Loss of consciousness Pruritus Skin lesion Swelling Urticaria

Symptomtext

Blacked out; fell to ground; swelling; sores / Right wrist, Right arm underarm back; itching / Itching is intense; outbreaks of hives; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 81 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 07Dec2021 (Lot number: FH8027) at the age of 81 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Anaphylaxis bee sting", start date: 1980 (unspecified if ongoing), notes: Other medical history: Anaphylaxis bee sting 1980 ER. Concomitant medication(s) included: FIORICET; TYLENOL; BENICAR. Vaccination history included: Bnt162b2 (lot number: ER2613, dose number: 2, vaccine location: Right arm), administration date: 26Mar2021, when the patient was 81 years old, for Covid-19 immunization; Bnt162b2 (lot number: EN6199, administration route: Intramuscular, dose number: 1, vaccine location: Right arm), administration date: 05Mar2021, when the patient was 81 years old, for Covid-19 immunization. The following information was reported: LOSS OF CONSCIOUSNESS (medically significant) with onset 08Dec2021, outcome "not recovered", described as "Blacked out"; FALL (medically significant) with onset 08Dec2021, outcome "not recovered", described as "fell to ground"; URTICARIA (non-serious) with onset 08Dec2021, outcome "not recovered", described as "outbreaks of hives"; PRURITUS (non-serious) with onset 08Dec2021, outcome "not recovered", described as "itching / Itching is intense"; SWELLING (non-serious) with onset 08Dec2021, outcome "not recovered", described as "swelling"; SKIN LESION (non-serious) with onset 08Dec2021, outcome "not recovered", described as "sores / Right wrist, Right arm underarm back". The events "blacked out", "fell to ground", "outbreaks of hives", "itching / itching is intense", "swelling" and "sores / right wrist, right arm underarm back" were evaluated at the physician office visit. Therapeutic measures were taken as a result of loss of consciousness, fall, urticaria, pruritus, swelling, skin lesion. Therapeutic measures were taken as a result of loss of consciousness, urticaria, pruritus, swelling, arthralgia, pain in extremity, axillary pain, back pain, fall. Clinical course: The patient had no other vaccine in four weeks and no known allergies. As of the time of report, the patient was still having outbreaks of hives, itching, swelling and sores two months after last dose in the right wrist, right arm, underarm and back. Doctor's prescription of Triamcinolone Acetonide cream .5% was not helping. Blacked out 08Dec2021 briefly and fell to ground. Itching was intense. The patient had no COVID prior vaccination and was not tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anaphylaxis (Other medical history: Anaphylaxis bee sting 1980 ER)
Andere Medikamente: FIORICET; TYLENOL; BENICAR
Allergien: -
Vorherige Impfungen: -

VAERS 2080290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: VA
Alter: -
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 17.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: - / -

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

Chest pain Costochondritis Dysphagia Insomnia Musculoskeletal stiffness Electrocardiogram Hypoaesthesia Magnetic resonance imaging Neck pain Pain Palpitations Panic attack Pericarditis Oropharyngeal pain SARS-CoV-2 test Thyroid cyst Ultrasound scan

Symptomtext

Pericarditis; Pain and numbness of left side of brain; Neck Stiffness and Pain; Neck stiffness and pain; pain that casually radiated to left jaws and left side of the brain the pain was on the left side of the throat, neck, jaw and head; Nocturnal panic attack and heart palpitation; Nocturnal panic attack and heart palpitation; Small thyroid cyst; Chest Pain; The initial case was missing the following minimum criteria: unspecified adverse event. Upon receipt of follow-up information on (18Jan2022), this case now contains all required information to be considered valid. A 33-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administration date 17Oct2021 (Lot number: FH8027) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "tooth extraction" (unspecified if ongoing). Concomitant medication(s) included: FLU, administration date 03Oct2021; IBUPROFEN taken for tooth extraction, start date: 01Oct2021, stop date: 03Oct2021; AMOXICILLIN taken for tooth extraction, start date: 01Oct2021, stop date: 05Oct2021. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Anatomical site of injection: Lot: Pfizer ER8737), administration date: 28Mar2021, for COVID-19 Immunization; Bnt162b2 (DOSE 2, SINGLE, Anatomical site of injection: Lot: Pfizer ER8736), administration date: 18Apr2021, for COVID-19 Immunization. The following information was reported: PERICARDITIS (medically significant), outcome "unknown", described as "Pericarditis"; CHEST PAIN (medically significant) with onset 24Oct2021 14:00, outcome "not recovered", described as "Chest Pain"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 15Nov2021, outcome "not recovered", described as "Neck Stiffness and Pain"; NECK PAIN (non-serious) with onset 15Nov2021, outcome "not recovered", described as "Neck stiffness and pain"; PAIN (non-serious) with onset 15Nov2021, outcome "not recovered", described as "pain that casually radiated to left jaws and left side of the brain the pain was on the left side of the throat, neck, jaw and head"; HYPOAESTHESIA (non-serious) with onset 20Nov2021, outcome "not recovered", described as "Pain and numbness of left side of brain"; PANIC ATTACK (non-serious), PALPITATIONS (non-serious) all with onset 01Nov2021, outcome "recovered with sequelae" and all described as "Nocturnal panic attack and heart palpitation"; THYROID CYST (non-serious) with onset 01Nov2021, outcome "recovered with sequelae", described as "Small thyroid cyst". The events "chest pain", "nocturnal panic attack and heart palpitation", "nocturnal panic attack and heart palpitation" and "small thyroid cyst" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: electrocardiogram: (24Oct2021) unknown, notes: No abnormalities found; (26Oct2021) unknown, notes: No abnormalities found; (12Nov2021) unknown, notes: No abnormalities found; (05Jan2022) unknown, notes: Historic changes in EKG; magnetic resonance imaging: (05Jan2022) unknown, notes: Clinical Follow-ups MRI; sars-cov-2 test: (14Oct2020) negative; (15Dec2020) negative; ultrasound scan: (unspecified date) unknown, notes: Small thyroid cyst. Therapeutic measures were taken as a result of chest pain included Ibuprofen for anti-inflammatory. Therapeutic measures were not taken as a result of musculoskeletal stiffness, pain, hypoaesthesia, panic attack, palpitations. Clinical course: Few days after the vaccination the patient started to develop severe chest pain. After visiting ER for three time on 24Oct2021, 26Oct2021 and 12Nov2021, no abnormalities in the EKG were found however on 05Jan2022 a cardiologist diagnosed possible mild pericarditis based on historic changes in the EKG and other clinical follow ups (MRI) were ordered. In addition, a month after the vaccine the patient started to have some neck stiffness and pain that casually radiated to left jaws and left side of the brain the pain was on the left side of the throat, neck, jaw and head. Ultrasound showed a small thyroid cyst (nodule) that according to doctors was unlikely to create any pain further Duplex/Carotid ultrasound was ordered to check the blood flow in the neck area and the test are not done yet. For a while the patient had nocturnal panic attacks and heart palpitation. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Date: 20211024; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: No abnormalities found; Test Date: 20211026; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: No abnormalities found; Test Date: 20211112; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: No abnormalities found; Test Date: 20220105; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: Historic changes in EKG; Test Date: 20220105; Test Name: MRI; Result Unstructured Data: Test Result:Unknown; Comments: Clinical Followups MRI; Test Date: 20201014; Test Name: COVID test; Test Result: Negative ; Test Date: 20201215; Test Name: COVID test; Test Result: Negative ; Test Name: ULTRA SOUND; Result Unstructured Data: Test Result:Unknown; Comments: Small thyroid cyst
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Tooth extraction
Andere Medikamente: IBUPROFEN; AMOXICILLIN
Allergien: -
Vorherige Impfungen: -

VAERS 2080290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: VA
Alter: -
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 17.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Costochondritis Dysphagia Insomnia Musculoskeletal stiffness Electrocardiogram Hypoaesthesia Magnetic resonance imaging Neck pain Pain Palpitations Panic attack Pericarditis Oropharyngeal pain SARS-CoV-2 test Thyroid cyst Ultrasound scan

Symptomtext

Pericarditis; Pain and numbness of left side of brain; Neck Stiffness and Pain; Neck stiffness and pain; pain that casually radiated to left jaws and left side of the brain the pain was on the left side of the throat, neck, jaw and head; Nocturnal panic attack and heart palpitation; Nocturnal panic attack and heart palpitation; Small thyroid cyst; Chest Pain; The initial case was missing the following minimum criteria: unspecified adverse event. Upon receipt of follow-up information on (18Jan2022), this case now contains all required information to be considered valid. A 33-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administration date 17Oct2021 (Lot number: FH8027) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "tooth extraction" (unspecified if ongoing). Concomitant medication(s) included: FLU, administration date 03Oct2021; IBUPROFEN taken for tooth extraction, start date: 01Oct2021, stop date: 03Oct2021; AMOXICILLIN taken for tooth extraction, start date: 01Oct2021, stop date: 05Oct2021. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Anatomical site of injection: Lot: Pfizer ER8737), administration date: 28Mar2021, for COVID-19 Immunization; Bnt162b2 (DOSE 2, SINGLE, Anatomical site of injection: Lot: Pfizer ER8736), administration date: 18Apr2021, for COVID-19 Immunization. The following information was reported: PERICARDITIS (medically significant), outcome "unknown", described as "Pericarditis"; CHEST PAIN (medically significant) with onset 24Oct2021 14:00, outcome "not recovered", described as "Chest Pain"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 15Nov2021, outcome "not recovered", described as "Neck Stiffness and Pain"; NECK PAIN (non-serious) with onset 15Nov2021, outcome "not recovered", described as "Neck stiffness and pain"; PAIN (non-serious) with onset 15Nov2021, outcome "not recovered", described as "pain that casually radiated to left jaws and left side of the brain the pain was on the left side of the throat, neck, jaw and head"; HYPOAESTHESIA (non-serious) with onset 20Nov2021, outcome "not recovered", described as "Pain and numbness of left side of brain"; PANIC ATTACK (non-serious), PALPITATIONS (non-serious) all with onset 01Nov2021, outcome "recovered with sequelae" and all described as "Nocturnal panic attack and heart palpitation"; THYROID CYST (non-serious) with onset 01Nov2021, outcome "recovered with sequelae", described as "Small thyroid cyst". The events "chest pain", "nocturnal panic attack and heart palpitation", "nocturnal panic attack and heart palpitation" and "small thyroid cyst" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: electrocardiogram: (24Oct2021) unknown, notes: No abnormalities found; (26Oct2021) unknown, notes: No abnormalities found; (12Nov2021) unknown, notes: No abnormalities found; (05Jan2022) unknown, notes: Historic changes in EKG; magnetic resonance imaging: (05Jan2022) unknown, notes: Clinical Follow-ups MRI; sars-cov-2 test: (14Oct2020) negative; (15Dec2020) negative; ultrasound scan: (unspecified date) unknown, notes: Small thyroid cyst. Therapeutic measures were taken as a result of chest pain included Ibuprofen for anti-inflammatory. Therapeutic measures were not taken as a result of musculoskeletal stiffness, pain, hypoaesthesia, panic attack, palpitations. Clinical course: Few days after the vaccination the patient started to develop severe chest pain. After visiting ER for three time on 24Oct2021, 26Oct2021 and 12Nov2021, no abnormalities in the EKG were found however on 05Jan2022 a cardiologist diagnosed possible mild pericarditis based on historic changes in the EKG and other clinical follow ups (MRI) were ordered. In addition, a month after the vaccine the patient started to have some neck stiffness and pain that casually radiated to left jaws and left side of the brain the pain was on the left side of the throat, neck, jaw and head. Ultrasound showed a small thyroid cyst (nodule) that according to doctors was unlikely to create any pain further Duplex/Carotid ultrasound was ordered to check the blood flow in the neck area and the test are not done yet. For a while the patient had nocturnal panic attacks and heart palpitation. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Date: 20211024; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: No abnormalities found; Test Date: 20211026; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: No abnormalities found; Test Date: 20211112; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: No abnormalities found; Test Date: 20220105; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: Historic changes in EKG; Test Date: 20220105; Test Name: MRI; Result Unstructured Data: Test Result:Unknown; Comments: Clinical Followups MRI; Test Date: 20201014; Test Name: COVID test; Test Result: Negative ; Test Date: 20201215; Test Name: COVID test; Test Result: Negative ; Test Name: ULTRA SOUND; Result Unstructured Data: Test Result:Unknown; Comments: Small thyroid cyst
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Tooth extraction
Andere Medikamente: IBUPROFEN; AMOXICILLIN
Allergien: -
Vorherige Impfungen: -

VAERS 2086226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: MD
Alter: 52,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 30.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Antinuclear antibody positive Dizziness Magnetic resonance imaging head normal Magnetic resonance imaging neck Seizure Tremor

Symptomtext

Dizziness, tremulousness, seizures/convulsions started 12/10/2021 and have not ceased to date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: brain MRI 1/3/2022 - normal result; cervical spine MRI 1/10/2022 - normal result; blood work 1/8/2022 - positive result for ANA
Aktuelle Erkrankungen: -
Vorgeschichte: Long COVID
Andere Medikamente: Rosuvastatin, diltiazem, low dose aspirin, tylenol
Allergien: None
Vorherige Impfungen: -

VAERS 1921138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NJ
Alter: 12,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 31.10.2021
Beginn: 25.11.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal lymphadenopathy Abdominal pain lower Asthenia Computerised tomogram abdomen abnormal Conjunctivitis Abdominal pain Alanine aminotransferase normal Albumin globulin ratio Anion gap Aspartate aminotransferase normal Basophil percentage Blood albumin decreased Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatinine increased Blood culture negative

Symptomtext

This patient was admitted 11/30/2021 because of concern for septic shock. Patient is a 12 yo female previously healthy, s/p surgery for right wrist fracture on 10/13 (pin removed), now presenting with a 6 day history of abdominal pain and febrile illness. Per parents, patient received the 2nd dose of her Pfizer COVID-19 vaccine on Nov 21. On Nov 26, she started developing b/l lower abdominal pain. The following day, she started having other symptoms including fever, sore throat, headaches, and weakness/dizziness. She was seen at the hospital on Nov 27th and had a CT scan of her abdomen which revealed mesenteric adenopathy (appendix not well visualized) and she was discharged home. Yesterday, she developed a non-pruritic sh over her abdomen, conjunctivitis, and worsening fevers, neck pain and headaches so they presented to the ED. No nausea, vomiting, diarrhea, cough, congestion, dysuria, bone pain or other complaints. She was treated for MIS-C.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Shock
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2082711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: VT
Alter: 62,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Dehydration Impaired driving ability Malaise Syncope Vomiting

Symptomtext

Fainted in chair right after the booster. Threw up several times within minutes of the vaccine. Was held at facility for several hours and got sick several times after. Husband picked me up as I could not drive. Was sick for several days, contacted my physician and she recommended I go to the ER on 11/25/2021 as I could not hold down water and was dehydrated - directly attributable to being sick from the Booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Was given IV Fluids in the ER on 11/25/2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2068939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NC
Alter: 40,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Alcohol test negative Alcoholic seizure Blood ethanol normal Blood magnesium normal Blood thyroid stimulating hormone normal Computerised tomogram head Computerised tomogram normal Confusional state Drug screen negative Full blood count normal Interchange of vaccine products Metabolic function test Postictal state Urine analysis normal Vomiting

Symptomtext

Patient presented to our facility for detox pertinently for alcohol use of 2 pints vodka daily. 5 days into admission patient received Pfizer booster to initial J&J vaccine at 1224. At 2048 patient walked out of his hospital room with vomit in his hair. He appeared confused and post-ictal which persisted for 15-20 minutes, raising concern for an unwitnessed seizure or syncopal episode. He appeared in his normal state of health within several hours. He was transferred out to an ED for medical evaluation and after labs and head imaging returned normal he returned to our facility without incident. An alcohol withdrawal seizure was considered the most likely cause of this episode, although there were atypical elements for this being an alcohol withdrawal seizure, including that he had no reported prior history of withdrawal seizures, had not complained of alcohol withdrawal symptoms for at least 2 days prior to this episode, and that he was 5 days out from his last drink at the time of this episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alcoholic seizure
Hospital-Tage: -
Labordaten: All done 1/26/22: CT head, UA, UDS, Mg level, TSH, CMP, CBC w/ diff, alcohol, Ethyl level
Aktuelle Erkrankungen: Acute alcohol withdrawal Opioid detox
Vorgeschichte: Alcohol use disorder, severe, dependence Opioid use disorder, severe, dependence History of pancreatitis Tobacco use IVDU (intravenous drug user) GERD
Andere Medikamente: Baclofen, dicyclomine, famotidine, folic acid, gabapentin, ibuprofen, methadone, daily multivitamin, nicotine patch, pantoprazole, thiamine , eucerin cream
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2065456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 18.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / -

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

Angiogram Computerised tomogram Dizziness Headache Magnetic resonance imaging head Magnetic resonance imaging neck Neck pain Syncope Vertebral artery dissection

Symptomtext

Left vertebral artery dissection C2-C7. Had syncopal episode on 12/19/2021, called ambulance, but not taken to ER. Had persistent headache/dizziness/left neck pain for 3 weeks. Seen in clinic on 1/7/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: On 1/7/2022, CT stroke study and sent to ER. On 1/24/2022, MRI/MRA of head and neck.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Altavera (28) one tab PO daily
Allergien: None
Vorherige Impfungen: -

VAERS 2647081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NC
Alter: 79,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 28.01.2021
Beginn: 24.12.2021
Tage bis Beginn: 330,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain COVID-19 Carditis Chest X-ray normal Chest pain Echocardiogram Electrocardiogram Pericarditis X-ray limb normal

Symptomtext

had COVID mid September before received booster shot. chest and backpain 12/24/2021. Hopitalized 12/26/201 - 12/27/2021 with inflammation around the heart, diagnosed with pericarditis. Hospitalized again 1/6-1-7/2022 with chest pains, same diagnoses. Taking heart med for 90 days and then I will be reevaluated to see long term affects or effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 4,0
Labordaten: numerous EKG's, ECHO's, xrays of legs and lungs for blood clots (none) 12/26-27/2021 & 1//6-1/7/2022
Aktuelle Erkrankungen: none
Vorgeschichte: kidney disease, high blood pressure, high cholesterol
Andere Medikamente: simvastatin, cavedilol, losartan, amlodipine, vit. d, multi-vi
Allergien: codene
Vorherige Impfungen: -

VAERS 2053869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 20.01.2022
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: ja

Condition aggravated Syncope

Symptomtext

fainting vitals checked Patient reported history of fainting after recovery, Patient also reported history of low HR after recovery lie flat feet elevated, candy, Gatorade

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Vital signs BP 127/63 HR 55 (her normal)
Aktuelle Erkrankungen: History of fainting low HR
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: No
Vorherige Impfungen: Blood work

VAERS 2043678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

schwer

Staat: VA
Alter: 67,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 04.11.2021
Beginn: 19.12.2021
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

Bells Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Went to Emergency Room - Neurologist made diagnosis after examination.
Aktuelle Erkrankungen: None
Vorgeschichte: Treated for prostate cancer in 2018 (Proton Radiation)
Andere Medikamente: Silodosin 8mg/day Tadalafil 5mg/day Sildenafil 20Mg As needed Centrum Silver Vitamin /daily
Allergien: Ceclore
Vorherige Impfungen: -

VAERS 2023733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: -
Alter: 13,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 07.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fall Feeling hot Hyperhidrosis Nausea Presyncope Vision blurred Vomiting

Symptomtext

About 2 days after vaccination, patient reported feeling hot and sweaty; he then felt dizzy and had some nausea with blurring of his vision. He was standing during this episode. fell back onto father, recovered and went to the bathroom and had an episode of vomiting. Felt better subsequently and has been doing well. Denies loss of consciousness. Likely brief vasovagal episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin, Vitamin C
Allergien: None
Vorherige Impfungen: -

VAERS 1996744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: PA
Alter: 29,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

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

Cold sweat Immunisation Interchange of vaccine products Syncope Urinary incontinence Inappropriate schedule of product administration Off label use

Symptomtext

Fainted; Cold sweat; Urinated himself while getting a haircut; patient received one dose of COVID-19 vaccine, one dose of Janssen vaccine, and now a booster with Pfizer; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), administered in arm left, administration date 21Dec2021 14:00 (Lot number: FH8027) at the age of 29 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the vaccination. Vaccination history included: Janssen vaccine (2nd dose; Lot number: 1805022; at 18:00 in the left arm), administration date: 17Mar2021, when the patient was 29 years old, for COVID-19 Immunization; COVID-19 vaccine (1st dose; MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 21Dec2021 14:00, outcome "unknown", described as "patient received one dose of COVID-19 vaccine, one dose of Janssen vaccine, and now a booster with Pfizer"; IMMUNISATION (medically significant) with onset 21Dec2021 14:00, outcome "unknown", described as "booster"; SYNCOPE (medically significant) with onset 22Dec2021 11:30, outcome "recovering", described as "Fainted"; COLD SWEAT (non-serious) with onset 22Dec2021 11:30, outcome "recovering", described as "Cold sweat"; URINARY INCONTINENCE (non-serious) with onset 22Dec2021 11:30, outcome "recovering", described as "Urinated himself while getting a haircut". The events "fainted", "cold sweat" and "urinated himself while getting a haircut" were evaluated at the emergency room visit. Therapeutic measures were not taken as a result of syncope, cold sweat, urinary incontinence. It was also reported that since the vaccination, the patient had not been tested for COVID-19. Additional information: On 21Dec2021, the patient received a "booster with Pfizer." On 22Dec2021, the patient broke out into cold sweat, fainted and urinated on himself in his barber's chair while getting a haircut.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
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 1996744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: PA
Alter: 29,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Cold sweat Immunisation Interchange of vaccine products Syncope Urinary incontinence Inappropriate schedule of product administration Off label use

Symptomtext

Fainted; Cold sweat; Urinated himself while getting a haircut; patient received one dose of COVID-19 vaccine, one dose of Janssen vaccine, and now a booster with Pfizer; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), administered in arm left, administration date 21Dec2021 14:00 (Lot number: FH8027) at the age of 29 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the vaccination. Vaccination history included: Janssen vaccine (2nd dose; Lot number: 1805022; at 18:00 in the left arm), administration date: 17Mar2021, when the patient was 29 years old, for COVID-19 Immunization; COVID-19 vaccine (1st dose; MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 21Dec2021 14:00, outcome "unknown", described as "patient received one dose of COVID-19 vaccine, one dose of Janssen vaccine, and now a booster with Pfizer"; IMMUNISATION (medically significant) with onset 21Dec2021 14:00, outcome "unknown", described as "booster"; SYNCOPE (medically significant) with onset 22Dec2021 11:30, outcome "recovering", described as "Fainted"; COLD SWEAT (non-serious) with onset 22Dec2021 11:30, outcome "recovering", described as "Cold sweat"; URINARY INCONTINENCE (non-serious) with onset 22Dec2021 11:30, outcome "recovering", described as "Urinated himself while getting a haircut". The events "fainted", "cold sweat" and "urinated himself while getting a haircut" were evaluated at the emergency room visit. Therapeutic measures were not taken as a result of syncope, cold sweat, urinary incontinence. It was also reported that since the vaccination, the patient had not been tested for COVID-19. Additional information: On 21Dec2021, the patient received a "booster with Pfizer." On 22Dec2021, the patient broke out into cold sweat, fainted and urinated on himself in his barber's chair while getting a haircut.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
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 1999336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: OH
Alter: 41,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Blood test Electrocardiogram Feeling cold Headache Loss of consciousness Nausea Pain in extremity Pallor Vertigo

Symptomtext

A couple hours after 2nd dose, my arm was sore. The next morning around 8 am, I started feeling nauseous and freezing cold. No fever. The second dose was November 19, 2021. I am still feeling the same. On December 8, 2021, my boyfriend found me on the floor pale/white. He stated like a piece of paper. He called 911. I was going in and out of consciousness, even in the emergency room. The only thing the ER did was bloodwork and an EKG. They treated me for vertigo. Since December 9, 2021, I have been feeling like my brain is throbbing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood work and EKG.
Aktuelle Erkrankungen: -
Vorgeschichte: Myasthenia gravis, SLE lupus, tachycardia, vitamin D deficiency, iron deficiency, seizures
Andere Medikamente: Soliris; Iron (over-the-counter); Folic acid (over-the-counter); Vitamin D (over-the-counter); Lamotrigine 200mg twice daily; Metoprolol succinate 25mg ER; Diphenhydramine HCL 25mg; Lidocaine 2.5% (put on before Soliris treatment); Heparin
Allergien: Penicillin; Sulfa; Chloroquine and peanuts
Vorherige Impfungen: -

VAERS 1992741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: -
Alter: 55,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 17.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / UN

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

Deep vein thrombosis Ultrasound Doppler abnormal

Symptomtext

Patient with otherwise unprovoked lower extremity DVT. started on anticoagulation today

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: +US doppler right LE vein on 12/30/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: triamcinalone cream PRN
Allergien: -
Vorherige Impfungen: -

VAERS 1989034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: MI
Alter: 16,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 05.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / -

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

Arrhythmia Blood test Chest discomfort Chest pain Electrocardiogram abnormal Pericarditis Ultrasound scan X-ray

Symptomtext

Swelling of the heart, chest pressure/pain and arrhythmia. Took to the ER on 12/13. Seen by Doctor. Symptoms are still on going.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 12/13 X-ray? Ultrasound?, bloodwork and ekg. Ekg found issues. 12/20 follow up- told not to exercise 12/28 ultrasound 12/29 follow up, pain and pressure gone but significant arrhythmia still on going Has appointment Jan 6 for stress test follow up Jan 10
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sertraline 100mg
Allergien: Codeine
Vorherige Impfungen: -

VAERS 1958013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

schwer

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Angioedema Chest pain Eye swelling Immunisation Pericarditis SARS-CoV-2 test Swelling face Swollen tongue Urticaria

Symptomtext

my face and eyes were swollen; my face and eyes were swollen; chest pain; Pericarditis; angioedema; swelling to my tongue; hives all over my body / continuous hives all over my body/urticaria; dose number=3; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 64-year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in arm left, administration date 01Dec2021 10:00 (Lot number: Fh8027) at the age of 64 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Hyperlipidemia" (unspecified if ongoing); "osteoporosis" (unspecified if ongoing). Concomitant medications included: lovastatin (MANUFACTURER UNKNOWN). Vaccination history included: bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (Dose Number: 1, Batch/Lot No: En6208, Location of injection: Arm Left, Vaccine Administration Time: 12:15 AM), administration date: 14Mar2021, when the patient was 63 years old, for COVID-19 immunization; bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (Dose Number: 2, Batch/Lot No: Ew0150, Location of injection: Arm Left, Vaccine Administration Time: 11:45 AM), administration date: 04Apr2021, when the patient was 63 years old, for COVID-19 immunization. The following information was reported: SWOLLEN TONGUE (hospitalization, life threatening) with onset 02Dec2021 14:00, outcome "not recovered", described as "swelling to my tongue"; URTICARIA (hospitalization, life threatening) with onset 02Dec2021 14:00, outcome "not recovered", described as "hives all over my body / continuous hives all over my body/urticaria"; CHEST PAIN (hospitalization, life threatening) with onset 04Dec2021, outcome "not recovered", described as "chest pain"; PERICARDITIS (hospitalization, medically significant, life threatening) with onset 04Dec2021, outcome "not recovered", described as "Pericarditis"; ANGIOEDEMA (hospitalization, medically significant, life threatening) with onset 04Dec2021, outcome "not recovered", described as "angioedema"; SWELLING FACE (hospitalization, life threatening), EYE SWELLING (hospitalization, life threatening) all with onset 06Dec2021, outcome "not recovered" and all described as "my face and eyes were swollen"; IMMUNISATION (hospitalization, medically significant, life threatening) with onset 01Dec2021 10:00, outcome "unknown", described as "dose number=3". The patient was hospitalized for swollen tongue, urticaria, chest pain, pericarditis, angioedema, swelling face, eye swelling, immunisation (hospitalization duration: 2 days). The events "swelling to my tongue", "hives all over my body / continuous hives all over my body/urticaria", "chest pain", "pericarditis", "angioedema", "my face and eyes were swollen" and "my face and eyes were swollen" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test (PCR): (04Dec2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of swollen tongue, urticaria, chest pain, pericarditis, angioedema, swelling face, eye swelling which included steroids, famotidine (PEPCID), diphenhydramine hydrochloride (BENADRYL), colchicine, ibuprofen. Clinical course: The patient did not have COVID prior to vaccination. The patient did not have any known allergies. On 02Dec2021, the patient experienced swelling to her tongue and hives all over her body, treated with steroids in the emergency room (ER) and was sent home. On 04Dec2021, the patient had chest pain and went to the ER again. The patient was admitted for pericarditis, angioedema, and urticaria. On 06Dec2021, the patient's face and eyes were swollen with continuous hives all over my body. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: Test Date: 20211204; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hyperlipidemia; Osteoporosis
Andere Medikamente: LOVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1948399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Electric shock sensation Headache Immediate post-injection reaction Migraine Oral discomfort Oral pain Rash Toothache

Symptomtext

headache immediately, pain in mouth similar to tooth ache, after using mouthwash mouth felt like it was on fire, saturday night feeling of electrical shocks throughout body, small circles appeared on arm , monday a migraine headache developed on left temple

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes
Andere Medikamente: -
Allergien: codeine
Vorherige Impfungen: -

VAERS 1947952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8027

schwer

Staat: VA
Alter: 69,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 09.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Seizure like phenomena

Symptomtext

Presented with seizure like activity, was sent to ER for evaluation/treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: Admitted to hospital after evaluation/treatment in ER.
Aktuelle Erkrankungen: DVT of LLE, NHL, Parkinson's Disease, Major Depressive Disorder, Anxiety Disorder, HTN, Dementia, A Fib, Osteoarthritis
Vorgeschichte: DVT of LLE, NHL, Parkinson's Disease, Major Depressive Disorder, Anxiety Disorder, HTN, Dementia, A Fib, Osteoarthritis
Andere Medikamente: Buspirone, Vitamin D, Colace, Drisdol capsule, Eliquis, Mucinex, Hydrochlorothiazide, Lasix, Metoprolol, MVI, Namenda, Norco, Nystatin Cream, Paroxetine, Potassium, Senna, Sinemet, Tizanidine, Tramadol, Tylenol, Voltaren Gel.
Allergien: Azithromycin
Vorherige Impfungen: -

VAERS 1933828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

schwer

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

Fainted three times hours after receiving the booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Preservision. HRT
Allergien: None
Vorherige Impfungen: -

VAERS 1932684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Anaphylactic reaction Autoimmune disorder Bell's palsy Blood disorder Chest discomfort Chest pain Chills Confusional state Diarrhoea Dizziness Dysphagia Dyspnoea Eye swelling Fatigue Flushing Headache Hyperhidrosis

Symptomtext

Site: Bruising at Injection Site-Mild, Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Anaphylaxis-Mild, Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Itch Generalized-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash Generalized-Mild, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Mild, Systemic: Abdominal Pain-Mild, Systemic: Autoimmune Disease (diagnosed by MD)-Mild, Systemic: Bell's Palsy-Mild, Systemic: Blood Disorder (diagnosed by MD)-Mild, Systemic: Body Aches Generalized-Mild, Systemic: Cardiac Disorder (diagnosed by MD)-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Chills-Mild, Systemic: Confusion-Medium, Systemic: Diarrhea-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Fever-Mild, Systemic: sweating-Medium, Systemic: Flushed / Sweating-Severe, Systemic: Headache-Mild, Systemic: Heart Attack-Mild, Systemic: Hypertension-Mild, Systemic: Hyperventilation-Mild, Systemic: Hypotension-Mild, Systemic: Joint Pain-Mild, Systemic: Lymph Node Swelling-Mild, Systemic: MIS (Multisystem Inflammatory Syndrome)(diagnosed by MD)-Mild, Systemic: Nausea-Medium, Systemic: Neurological Disorder (diagnosed by MD)-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Seizure-Mild, Systemic: Shakiness-Mild, Systemic: Stroke-Mild, Systemic: Tachycardia-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Systemic: Tinnitus-Mild, Systemic: Unable to Sleep-Mild, Systemic: Visual Changes/Disturbances-Mild, Systemic: Vomiting-Mild, Systemic: Weakness-Mild, Additional Details: after giving him the pfizer shot and the flu shot, he suddenly said he didnt feel well, as I was grabbing a water and blood pressure machine, he fainted and was not responsive. we called 911 but after about 7 to 10 seconds, he woke up and his color was flushed and he had profuse sweating. we gave him water and had him stay in observation till he was feeling ok to leave, i called him today and hes is feeling fine. He did mention that before he had come to get his shots, he had thrown up that am.

Weitere VAERSDATA-Felder

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

VAERS 1929876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: WA
Alter: 49,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Seizure

Symptomtext

Family members report that patient had multiple seizures in the evening approximately 3 hours after receiving his vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type2 DM, Tonic-clonic seizures, hyperlipidemia, hypertension
Andere Medikamente: Amlodipine 5mg, Atorvastatin 40mg, Chlorthalidone 25mg, Divalproex 250mg, Glipizide 10mg, Losartan 100mg, Metformin ER 500mg, Phenytoin ER 300mg
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 1928378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 06.12.2011
Beginn: 06.12.2021
Tage bis Beginn: 3.653,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Nausea Syncope Tremor Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium, Systemic: Shakiness-Medium, Systemic: Vomiting-Medium, Additional Details: Called 911 and parametics arrive within minutes. Upon arrival, paramedics examined patient and results were normal. Parametics offered to take patient to hospital, but patient refused. Patient stated that he had a fear of needles. He stated that he suffers from chronic migraines. Patient called a friend to pick him up from the pharmacy. Patient rested for 20 minutes, left the pharmacy feeling better and back to normal.

Weitere VAERSDATA-Felder

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

VAERS 1928311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: VA
Alter: 12,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Flushing Hyperhidrosis Speech disorder Syncope Tinnitus Tremor Unresponsive to stimuli Visual impairment

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Shakiness-Severe, Systemic: Tinnitus-Severe, Systemic: Visual Changes/Disturbances-Severe, Additional Details: pt with syncopal episode following vaccine but initially unable to speak so epi pen was given.

Weitere VAERSDATA-Felder

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

VAERS 1923606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: AZ
Alter: 32,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 29.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Headache Muscular weakness Pain Pyrexia Hypoaesthesia Imaging procedure Laboratory test Palpitations Physical examination Syncope Tachycardia

Symptomtext

Pt report she also had an adverse reaction with the first PFizer vaccine given on 11/8/2021 lot number FJ8768 in to right deltoid. Pt report she is currently having tachycardia, headache, generalized weakness, right arm/hand (dominant) weakness, body aches, fevers, a syncopal episode yesterday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: referred to emergency room
Aktuelle Erkrankungen: reaction to first pfizer vaccine given on 11/8/2021
Vorgeschichte: ADHD
Andere Medikamente: adderal
Allergien: none known
Vorherige Impfungen: pfizer covid vaccine as mentioned above

VAERS 1923606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: AZ
Alter: 32,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 29.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Headache Muscular weakness Pain Pyrexia Hypoaesthesia Imaging procedure Laboratory test Palpitations Physical examination Syncope Tachycardia

Symptomtext

Pt report she also had an adverse reaction with the first PFizer vaccine given on 11/8/2021 lot number FJ8768 in to right deltoid. Pt report she is currently having tachycardia, headache, generalized weakness, right arm/hand (dominant) weakness, body aches, fevers, a syncopal episode yesterday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: referred to emergency room
Aktuelle Erkrankungen: reaction to first pfizer vaccine given on 11/8/2021
Vorgeschichte: ADHD
Andere Medikamente: adderal
Allergien: none known
Vorherige Impfungen: pfizer covid vaccine as mentioned above

VAERS 1917505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: IN
Alter: 44,0
Geschlecht: F
Eingang: 02.12.2021
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: nein

Fall Head injury Seizure like phenomena

Symptomtext

I was told by front staff that the patient had fallen down and was exhibiting signs of seizures. This was about 5 minutes after receiving the vaccine. I rushed up there and found patient conscious of her surroundings and following verbal instructions. There were no signs of anaphylactic reactions. She had a bump on the back of her head as a result of the fall. I applied ice on it while waiting for EMT to arrive. EMT arrived with 5 minutes and took her away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: taking Prozac for mood .
Andere Medikamente: rizatriptan, fluoxtine
Allergien: none
Vorherige Impfungen: -

VAERS 1917212

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NC
Alter: 51,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Muscle spasms Pain Palpitations Syncope Vision blurred

Symptomtext

About 5-10 minutes after Pfizer vaccine was administered, she reported heart pounding, muscle spasms, blurred vision, and feeling light-headed and body pain. While in the wheelchair, patient had a witnessed syncopal episode that lasted about 45 seconds. EMS was called and patient taken to Medical Center for further evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 12/2/2021 Done at Medical Center where she was seen and discharged.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1915965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: VA
Alter: 60,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / RA

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

Blood pressure increased Blood pressure measurement Burning sensation Chest pain Dizziness Feeling abnormal Feeling jittery Headache Loss of consciousness Pain in extremity Palpitations Throat tightness Tunnel vision

Symptomtext

about to pass out; BP 189/128; tunnel vision; Light headed/dizzy; jittery; head ache; heart pounding; pain in chest; pain in left arm; burning across chest and left arm; burning across chest and left arm; throat closing; feeling bad continued until 19Nov2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 09Nov2021 12:00 (Lot number: FH8027) at the age of 60 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Treatment for high blood pressure" (unspecified if ongoing); "known allergies: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL; METOPROLOL TARTRATE. Past drug history included: Tetanus, reaction(s): "Allergy"; Morphin, reaction(s): "Allergy"; Keflex, reaction(s): "Allergy". The following information was reported: LOSS OF CONSCIOUSNESS (medically significant) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "about to pass out"; BLOOD PRESSURE INCREASED (medically significant) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "BP 189/128"; TUNNEL VISION (medically significant) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "tunnel vision"; DIZZINESS (non-serious) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "Light headed/dizzy"; FEELING JITTERY (non-serious) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "jittery"; HEADACHE (non-serious) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "head ache"; PALPITATIONS (non-serious) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "heart pounding"; CHEST PAIN (non-serious) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "pain in chest"; PAIN IN EXTREMITY (non-serious) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "pain in left arm"; CHEST PAIN (non-serious), BURNING SENSATION (non-serious) all with onset 11Nov2021 09:00, outcome "recovered with sequelae" and all described as "burning across chest and left arm"; THROAT TIGHTNESS (non-serious) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "throat closing"; FEELING ABNORMAL (non-serious) with onset 11Nov2021 09:00, outcome "recovered with sequelae", described as "feeling bad continued until 19Nov2021". The events "about to pass out", "bp 189/128", "tunnel vision", "light headed/dizzy", "jittery", "head ache", "heart pounding", "pain in chest", "pain in left arm", "burning across chest and left arm", "burning across chest and left arm", "throat closing" and "feeling bad continued until 19nov2021" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: 189/128 mmHg. It was unknown if therapeutic measures were taken as a result of loss of consciousness, blood pressure increased, tunnel vision, dizziness, feeling jittery, headache, palpitations, chest pain, pain in extremity, chest pain, burning sensation, throat tightness, feeling abnormal. No follow up attempts are needed . No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:189/128 mmHg
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy; Hypertension
Andere Medikamente: LISINOPRIL; METOPROLOL TARTRATE
Allergien: -
Vorherige Impfungen: -

VAERS 1913860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: CA
Alter: 42,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 22.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: - / LA

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

Bell's palsy Facial paralysis Facial paresis

Symptomtext

Starting 11/27/21, patient noted left sided facial droop and facial weakness - diagnosed with Bells Palsy 12/1/21

Weitere VAERSDATA-Felder

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

VAERS 1913167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: AL
Alter: 21,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Confusional state Cough Dizziness Dyspnoea Heart rate irregular Hypersensitivity Hypopnoea Immediate post-injection reaction Loss of consciousness Panic reaction

Symptomtext

Immediately after injection patient c/o feeling very dizzy. We elevated her legs immediately. within seconds she lost consciousness. Rph safely lowered patient to the floor and tried to wake patient. She was breathing very shallow, and eventually made a huge gasp for air. She was coughing and very confused. Patient began stating she was having trouble breathing and was reaching up for me and holding her neck at the same time. her head was extended all the way back as if she was trying to straighten her airway. Epi 0.3 was administered. Patient began to control her breathing again, but also began having symptoms of panic. Ambulance arrived. Spoke to patient today and she informed me that the ER believes she had an allergic reaction. Also was experiencing an irregular heartbeat and she has been referred to a cardiologist for further evaluation, Patient was asked to stay overnight in hospital, but she declined.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Patient had pneumonia 2 weeks prior.
Vorgeschichte: -
Andere Medikamente: -
Allergien: Tramadol
Vorherige Impfungen: -

VAERS 1909716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 30.11.2021
Beginn: 30.11.2021
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 received Pfizer Covid-19 Booster and fainted. She fell off bench and I immediately came to her assistance. Patient was alert and responsive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EMS was called and the evaluated patient. Checked her glucose levels and heart was monitored.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: n/a
Allergien: nkda
Vorherige Impfungen: -

VAERS 1909335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 21.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / -

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

Hyperhidrosis Loss of consciousness Nausea Pain in extremity Palpitations Vomiting

Symptomtext

heart palpitation, sweating, nausea, sore arm, collapsed on floor, throwing up

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: went to dr and said she shouldnt have been vaxed
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: MO
Alter: 24,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: Patient fainted about 1 minute after vaccination. She was unconcious for 5-10 seconds before recovering. She was given ice water and about 15 minutes later said she felt much better.

Weitere VAERSDATA-Felder

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

VAERS 1907143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: OK
Alter: 18,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Fall Seizure Somnolence Syncope

Symptomtext

Syncope following immunization seconds after administering, then had brief convulsion causing him to fall to floor. No hitting of head or other injury. Patient finally became responsive to calling him by name and recovered quickly after. Directly monitored patient for about 5 minutes to assess symptoms and coherence. Only had some slight somnolence. Patient also informed me that he consumed cannabis "edibles" before coming in to curb anxiety to shots. Patient was instructed to remain in waiting area for 10 more minutes. Patient did not drive home; he had a ride to and from home with friends.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety
Andere Medikamente: Cannabis (edible) from dispensary
Allergien: NKDA
Vorherige Impfungen: Lightheadedness from TDaP many years ago

VAERS 1904092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Presyncope Syncope

Symptomtext

Patient had a fainting vasovagal episode a couple minutes post vaccine administration while sitting in the recovery area. Patient was laid on her back on the floor into a recovery position. Mask was removed for better airway and water after awaking. Paramedics/EMS were called and patient was brought out of the building by them. At the time she was alert, awake, and talking.

Weitere VAERSDATA-Felder

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

VAERS 1902113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: GA
Alter: 20,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood glucose normal Syncope

Symptomtext

Syncope the morning after vaccination. Called 911. Received vital check from EMTs and decided not to go to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Blood glucose test after fasting on 11/26/2021 (reading of 83 mg/dL).
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety, depression
Andere Medikamente: Sertraline HCL 75mg tablet, Junel FE, Acetaminophen 500mg
Allergien: Peanut allergy (anaphylactic)
Vorherige Impfungen: Severe muscle cramps/pain at injection site that lasted approximately a week; left patient to walk with great difficulty; 16 yea

VAERS 1901939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: WA
Alter: 53,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Guillain-Barre syndrome Joint swelling Muscular weakness

Symptomtext

Guillain-Barre syndrome Muscle weakness and joints swelling

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: NKA
Vorherige Impfungen: -

VAERS 1897279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: MN
Alter: 26,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 27.10.2021
Beginn: 22.11.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / -

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

Chest X-ray Chills Dizziness Headache Laboratory test Malaise Pain Pyrexia Syncope

Symptomtext

After vaccine - normal body aches, headache. 14 hours after vaccine had a syncopal event. Dizziness afterwards, Feeling unwell afterwards with subjective fever and chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Chest xray and labs on 11/24
Aktuelle Erkrankungen: -
Vorgeschichte: Migraine, ADHD
Andere Medikamente: Migraine medication - zomeg, birth control, adderall
Allergien: Ancef and amoxicillin
Vorherige Impfungen: -

VAERS 1896976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: MN
Alter: 25,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Confusional state Fall Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Seizure-Mild, Additional Details: I administered two vaccines (pfizer covid then fluzone quad), upon receipt of the 2nd vaccine, the patient lost conciosness/fainted and fell off the chair she was sitting on. The patient came to within 5 seconds, and she was confussed as why she was on the floor. she said she felt fine, but we had called 911. The EMT arrived and took her out to vehicle to check her out. The patient returned 20-30 minutes later and she said she had cleared the EMT visit.

Weitere VAERSDATA-Felder

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

VAERS 1884968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: IN
Alter: 39,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Blood test normal Computerised tomogram normal Hyperhidrosis Loose tooth Loss of consciousness Pyrexia Skin laceration Sleep disorder Syncope Tooth fracture

Symptomtext

Fever / chills began at bedtime. Barely slept, alternating between chills and profusely sweating all night. In morning, took a shower and fainted / lost consciousness without any warning in shower. Impacted side of tub and impact caused large laceration in chin (lower incisors cut all the way through) and loosened/mobile lower teeth, including small lower tooth fracture discovered by dentist x-rays. (Patient is healthy with clean medical records. Never fainted or abruptly lost consciousness before; no history of such events.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: ER visit within 30 minutes of event. All CT / blood tests came back negative. ER Doc implied that it was part of an extreme immune reaction to the Pfizer Booster shot, and possibly dehydration due to lost fluids overnight (fever sweats). Dentist estimates 4-6 weeks for fracture to heal. Cannot bite with front teeth until then.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1881377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Seizure

Symptomtext

patient had seizure, became alert but still dizzy,

Weitere VAERSDATA-Felder

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

VAERS 1877045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / UN

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

Autoimmune disorder Bell's palsy Chills Dizziness Eye swelling Fatigue Injection site pain Injection site swelling Lethargy Mouth swelling Pruritus Pyrexia Swelling face Swollen tongue

Symptomtext

Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe, Systemic: Autoimmune Disease (diagnosed by MD)-Medium, Systemic: Bell's Palsy-Medium, Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Additional Details: swelling of the eyes and itchiness.

Weitere VAERSDATA-Felder

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

VAERS 1873515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: NY
Alter: 70,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Seizure Speech disorder Vision blurred

Symptomtext

Patient felt dizzy and vision was blurry, began to seize for 10 seconds and then came to and was unable to speak for 5 minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Heart disease
Vorgeschichte: Heart disease
Andere Medikamente: Sildenafil, Levetiracetam, Eliquis, Metoprolol Succinate, Furosemide, Atorvastatin, Lamotrigine, Diltiazem ER, Gabapentin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1870423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: IA
Alter: 43,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Anaphylactic reaction Chest discomfort Interchange of vaccine products Pain Pain in extremity Throat irritation Tongue disorder

Symptomtext

Patient stated she had received the Janssen vaccine in April and had an anaphylactic reaction that she was taken to the hospital for and given epinephrine. She spoke with her MD who recommended she get a different brand for her second dose. She chose Pfizer. She had no other allergies that she shared with us. About 2-3 minutes after receiving the Pfizer dose she felt her throat was scratchy and her tongue felt thick, I gave her 50 mg of Benadryl po. At about 4 minutes after she said she definitely felt like she did after the J&J vaccine. At this point EMS was called, her BP and pulse were WNL, I gave her epi via Epi-pen in her right thigh. She had no difficulty breathing but felt like her chest was a bit tight. EMS arrived about 10 minutes after her dose. She was talking, BP and pulse remained stable, O2 sat was 100% per EMS oximeter. She was transported to our local ER. I spoke with her today and she was feeling well except for a sore arm and a bit achy overall. She reported the ER did not repeat epi but gave her Solumedrol and a nebulizer treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Allergic reaction per her report to the Janssen vaccine.
Vorherige Impfungen: Janssen brand in April 2021

VAERS 1867777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: IL
Alter: 56,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered Loss of consciousness Refusal of treatment by patient Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient passed out shortly after receiveing the vaccine. Patient has a history of passing out when blood is taken but this is the first time after receiveing a vaccination. Ambulance was called, he was responsive shortly before the EMS arrived. They checked him out ans he was ok. Patient refused to go to the ER. I called him about 2-3 hours later and his wife said he was doing well.

Weitere VAERSDATA-Felder

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

VAERS 1867488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: IN
Alter: 20,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Chest discomfort Chest pain Confusional state Dizziness Flushing Hyperhidrosis Seizure

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Severe, Systemic: Seizure-Severe, Systemic: Weakness-Severe

Weitere VAERSDATA-Felder

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

VAERS 1860550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NV
Alter: 29,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium.

Weitere VAERSDATA-Felder

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

VAERS 1855320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope Vomiting

Symptomtext

SHE FAINTED AND WHEN SHE CAME THROUGH STARTED VOMITING .

Weitere VAERSDATA-Felder

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

VAERS 1831697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: ME
Alter: 26,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Angiogram normal Arrhythmia Arthritis Bradycardia Chest X-ray normal Computerised tomogram head normal Electrocardiogram ambulatory Erythema Fibrin D dimer normal Fluid replacement Heart rate abnormal Palpitations Rash macular Supraventricular tachycardia Syncope Tachycardia Troponin normal

Symptomtext

SVT- two separate runs. 10/12/21 for approx 30 mins and 10/22/21 for approx 20 mins. Syncopal episode 10/22/21. Heart palpitations- off and on since 10/12/21 Tachycardia/ bradycardia arrhythmias, which include rapid heart rate changes upon changing positions- current since 10/12/21 Joint inflammation Redness/ blotchy was on face Was hospitalized, fluid resuscitated to rule out dehydration, and have received a holter monitor. Will be having an echocardiogram as well as possible other tests and have not ruled out POTS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: D dimer-negative (10/12, 10/21,10/22) Trop-negative (10/12, 10/21, 10/22) Chest X-ray-negative (10/12, 10/22) Ct head and CT angio negative (10/23)
Aktuelle Erkrankungen: None.
Vorgeschichte: Anxiety
Andere Medikamente: Fluoxetine-20mg qday Pantoprazole-20mg qday Fexofenadine 180mg qday Multivitamin Probiotic
Allergien: Amoxicillin, Levaquin, Codeine, Benzoyl Peroxide Animal dander, tree pollens, mold, apples, carrots, celery, tree nuts, cherries, cantaloupe.
Vorherige Impfungen: 10/20, flu vaccination, urticaria, age 25.

VAERS 1831616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: OH
Alter: 15,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Patient passed out in store about 1 hour after his vaccines. Patient was assessed by EMS and it was determined patient had only eaten noodles a few hours before vaccines and was light-headed due to not having eating in combination with vaccines. Patient left with parents on his own accord.

Weitere VAERSDATA-Felder

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

VAERS 1814375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: NJ
Alter: 17,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

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

Abdominal pain Abdominal pain upper Crying Diarrhoea Fatigue Screaming Thrombosis Uterine pain Uterine spasm

Symptomtext

Cramping and pain began on Friday during the day, tiredness and some aching. (10/22) Severe Cramping and pain in uterus and abdomen. Worse than anything she has ever experienced before screaming and crying in pain. clots as big as 25c not ususal (usually dime size) Severe diarrhea and stomach pain. Lasted all day Saturday . Given tylenol and later ibubrofen to relieve pain, hot water bottle applied and rest. 10/23

Weitere VAERSDATA-Felder

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

VAERS 1967175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: MD
Alter: 51,0
Geschlecht: M
Eingang: 24.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Posture abnormal

Symptomtext

The patient passed out after receiving his first Pfizer vaccine on 10/15/2021, a Friday evening. He slumped in the chair in the Observation area, and was quickly attended to by the Pharmacist and the Store manager. We immediately called 911, and then laid him down across the chairs to get his head and feet at the same elevation, at which time he quickly regained consciousness. We stayed by his side until the EMS arrived, and he was taken away on their stretcher. Hi wife reported that they took him to a medical facility and he had a follow-up with his Dr on the following Monday.

Weitere VAERSDATA-Felder

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

VAERS 1814068

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge fh8027

schwer

Staat: WA
Alter: 33,0
Geschlecht: M
Eingang: 24.10.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Seizure like phenomena

Symptomtext

Patient experienced a seizure like activity for about 2 to 3 minutes after receiving 1st dose of pfizer. He was helped to the floor, and left on his right side until the activity subsided for about 4 minutes. Reported lightheadedness, and no pain. Was given a bottle of water and a protein bar. He was helped up to the chair for a minute, then he wanted to go back on the floor. Stayed in that position for about 20 minutes, before he went back to the chair, and was advised to sit for at least 15 minutes. He left after 35 minutes, and neither lightheadedness no pain was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1785461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

schwer

Staat: CA
Alter: 40,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Dizziness Hyperhidrosis Syncope

Symptomtext

Injection given at 3:56. Pt seated in chair at 4:05, Pt complained of dizziness, became diaphoretic, fainted. Regained consciousness. Alert and oriented x3. At 4:05 -Vital Signs- 113/57-56-20 Pulse Ox 100% At 4:25- 130/83 - 59 - 20 patient eating and drinking without difficulty. At 4:50- 131/91-64-20 Temp 97.1

Weitere VAERSDATA-Felder

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

VAERS 1783120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

schwer

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 13.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

patient was observed to have fainted after receiving the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: report of patient fainted after receiving vaccination .
Allergien: -
Vorherige Impfungen: -

VAERS 2672819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 17.08.2023
Impfdatum: 27.11.2021
Beginn: 09.02.2023
Tage bis Beginn: 439,0
Dosis: 2
Route/Site: IM / LA

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

Facial paresis Hypotension

Symptomtext

HYPOTENSION LEFT FACIAL MUSCLE WEAKNESS

Weitere VAERSDATA-Felder

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

VAERS 2639197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: FL
Alter: 64,0
Geschlecht: M
Eingang: 31.05.2023
Impfdatum: 21.03.2021
Beginn: 13.07.2022
Tage bis Beginn: 479,0
Dosis: 3
Route/Site: - / -

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

Atrial fibrillation Blood pressure inadequately controlled Brain natriuretic peptide normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Dyspnoea exertional Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Heart rate increased Imaging procedure abnormal Oedema Pneumonia viral Pulmonary congestion SARS-CoV-2 test positive

Symptomtext

BREAKTHROUGH COVID: FULLY VACCINATED WITH BOOSTER. Pt states he tested positive for COVID 3 wks ago, since than pt has had a cough, and increase SOB at night. DX post COVID pneumonia. PT REQUIRED 2L OF OXYGEN. Patient was given nebulizers, ceftriaxone, azithromycin, Decadron for presumed post viral pneumonia. Patient is being admitted for further evaluation. Upon further evaluation, patient states that he ha5-year-old gentleman who presented with complaint of shortness of breath, cough and dyspnea on exertion. Chest imaging revealed evidence of likely edema. Patient responded well to IV Lasix. Echocardiogram revealed decreased ejection fraction roughly 35-40% EF.s noticed that his heart rate had been elevated since COVID a and his blood pressure has been uncontrolled.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Troponin x1 is negative. POSITVE COVID. hest x-ray shows pulmonary vascular congestion. EKG shows atrial fibrillation with controlled ventricular rate.A BNP level is negative.
Aktuelle Erkrankungen: UNKNONWN
Vorgeschichte: hypertension, hyperlipidemia, obesity and diabetes mellitus.
Andere Medikamente: UNKNOWN
Allergien: IODINE
Vorherige Impfungen: -

VAERS 2619072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 12.06.2022
Beginn: 13.07.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / -

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

Hypotension Respiratory failure

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION RESPIRATORY FAILURE, UNSPECIFIED ACUITY

Weitere VAERSDATA-Felder

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

VAERS 2595007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 17.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Blood pressure measurement Pain in extremity Weight Body temperature COVID-19 Palpitations SARS-CoV-2 test Vaccination failure

Symptomtext

all booster shots she takes she gets sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. An 80-year-old female patient received BNT162b2 (BNT162B2), on 17Dec2021 as dose 3 (booster), single (Lot number: FH8027) at the age of 79 years for covid-19 immunization. The patient's relevant medical history included: "Blood pressure", start date: 2012 (unspecified if ongoing); "pacemaker", start date: 2012 (ongoing). Concomitant medication(s) included: VALSARTAN taken for blood pressure abnormal, start date: 2012 (ongoing). Vaccination history included: BNT162b2 (DOSE 1, SINGLE, lot ER8729), administration date: 15Apr2021, when the patient was 78-year-old, for Covid-19 immunization, reaction(s): "heart started racing", "She took a test and she caught the virus", "She took a test and she caught the virus"; BNT162b2 (DOSE 2, SINGLE, Lot: EW0175), administration date: 20May2021, when the patient was 78-year-old, for Covid-19 immunization, reaction(s): "all booster shots she takes she gets sore arm"; Flu shot (Also had a Flu shot unknown date. Manufacturer unknown.), for Covid-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "recovered", described as "all booster shots she takes she gets sore arm". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: arm soreness - when she takes any vaccine her arm is sore for a little bit and goes away. When queried what vaccines cause arm soreness caller states all booster shots, she takes she gets sore arm. Unable to clarify further. Pfizer Covid 19 vaccine booster on 17Nov2022. lot GH9703 in her left side arm in the afternoon, after going to the gym. late evening at (Withheld).; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300100075 same reporter/patient, different dose number/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result: Unknown results; Test Name: weight; Result Unstructured Data: Test Result: weight is 140 something.
Aktuelle Erkrankungen: Pacemaker insertion (cardiac)
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal
Andere Medikamente: VALSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2591880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 20.11.2021
Beginn: 01.12.2022
Tage bis Beginn: 376,0
Dosis: 3
Route/Site: - / -

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

Abdominal distension Acute kidney injury Atrial fibrillation Behaviour disorder Blood folate normal Bradycardia COVID-19 Chest X-ray abnormal Chest pain Constipation Dementia Diastolic dysfunction Disorientation Echocardiogram Ejection fraction normal Electrocardiogram abnormal Fall Hyperkalaemia

Symptomtext

Patient is a 84 y.o. male with history of dementia, CAD, CHF, Afib, HTN transferred from Psych facility to with chest pain radiating to left arm, work-up unremarkable. Hospital course complicated by COVID and prolonged due to placement issues. Presumed Dementia with behavioral disturbances Toxic metabolic encephalopathy - (Resolved) Approximately 4-5 months of disorientation, marked paranoia resulting in psychiatric admission. Family does admit to some memory changes prior Has had several changes in setting from home, jail, medical hospital, psych hospital, son's house BH consulted: unlikely primary psychological disorder given age, no need for inpatient psych Workup generally unrevealing Old strokes/microvascular changes on MRI, at risk for vascular dementia Remains no AMA, Wife is surrogate decision maker but currently in SNF Patient is not able to consistently name a POA Continue donepezil, memantine, nightly olanzapine Patient needs outpatient neurocognitive evaluation Discharging to the Facility on Tuesday 2/14 at 11 am Falls Twice this admit Fall precautions, E companion in place PT/OT-- AM-PAC 19 Recommend out of bed TID with nursing B12 and folate normal Vitamin D insufficiency Vitamin D: 29, started replacement Insomnia Scheduled melatonin nightly PRN trazodone Stable/Chronic or Resolved Medical Conditions Covid 19 infection with Hypoxia (Resolved) -- Required 2L NC, weaned to RA (12/14); treated with Decadron 6 mg (12/12 - 12/22). Isolation ended 12/19 Chest pain -- Troponin negative; EKG a.fib. Cardio c/s, no ischemic testing recommended CAD S/p CABG (2005) subsequent PCI 2015 Chronic HFpEF -- euvolemic. TTE (10/2022): EF 60%, diastolic dysfunction. Continue Toprol, Cardura, Lisinopril. Lasix stopped d/t AKI, resumed at 20 mg (12/29). Check weekly weights Bradycardia (Resolved) -- HR down ~30's while sleeping / soft pressures Toprol reduced, stopped clonidine Essential HTN -- Continue home cardura, lisinopril and Toprol w/ hold parameters. Dose of lisinopril reduced (parameters added) for soft pressures Chronic A. Fib -- Continue home Toprol and Xarelto Abdominal Distention (Resolved) -- KUB no acute, PVR WNL (12/21) Leukocytosis (Resolved) AKI and Hyperkalemia - (Resolved) -- Baseline Cr ~1.0; Renal/bladder US (12/25): without obstruction. Follow RFP intermittently. Hypophosphatemia-- (Resolved) -- supplement given Pleural Calcifications CXR (12/22/22): Extensive bilateral calcified pleural plaquing consistent with asbestos related pleural disease Currently stable on RA Can follow with PCP OP for PFTs and referral to pulmonology as needed Constipation Continue bowel regimen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 75,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2587921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 27.02.2023
Impfdatum: 20.11.2021
Beginn: 12.02.2023
Tage bis Beginn: 449,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/12/23 presents to EC ED for "shortness of breath". PMHx of "emphysema on 3.5 L O2 NC (4 L at bedtime), non-insulin-dependent diabetes mellitus, hypertension, dyslipidemia and BPH"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/12/23 SARS-CoV-2 (COVID-19) by detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2572324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NM
Alter: 38,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 08.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Arthralgia Blood test Cardiac monitoring Chest pain Dizziness Electrocardiogram Headache Heart rate increased Hypoaesthesia Impaired driving ability Insomnia Magnetic resonance imaging Mammogram Muscle tightness Muscle twitching Neck pain Pain

Symptomtext

Chest pain (achy, sometimes sharp, all-over chest but mostly middle and left; radiates into left arm (numbness), ribs, back, neck). Chest palpitations, anxiety attacks, pins and needles down back. Insomnia. Head zaps Pain in neck (left side) felt like straining Difficulty driving Extreme muscle tension in back, neck, chest and legs Knots in neck on left side Leg pain (achy, hurts where leg meets torso) Dizzy feeling Headaches Muscle twitching TMJ/tinnitus After Booster: Rapid heartbeat Feel heartbeat in left arm Pain/achy left arm Prickly feeling in head Headaches Sharp pain in chest with rapid heart beat Sharp pain in fingers and achy wrists

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Physical Therapy to relieve headaches and left side numbness in arm. Seen primary care physician, neurologist, cardiologist, obgyn, endocrinologist, rheumatologist: Bloodwork, X-rays, 48hr heart monitor, ekg?s, breast ultrasound, mri and mammogram.
Aktuelle Erkrankungen: Postpartum Depression
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin/gluten intolerance
Vorherige Impfungen: -

VAERS 2572155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 31.01.2023
Impfdatum: 16.11.2021
Beginn: 01.01.2023
Tage bis Beginn: 411,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain Cough Pyrexia SARS-CoV-2 test positive

Symptomtext

01/01/23 presents to ED for "chest pain, fever, cough". PMHx of "HLD, ulcerative colitis, former tobacco use"

Weitere VAERSDATA-Felder

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

VAERS 2565125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 21.01.2023
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

Chest pain Lymph node pain Lymphadenopathy

Symptomtext

Intermittent chest pains for about 4-5 days. Swelling and pain of the lymph nodes under my arm lasting several months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None, I did not have a primary care physician at the time and didn?t go to urgent care.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2564150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: RI
Alter: 30,0
Geschlecht: F
Eingang: 20.01.2023
Impfdatum: 12.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chest pain Chills Dizziness Headache Pyrexia COVID-19 SARS-CoV-2 test Vaccination failure Rash Tremor

Symptomtext

Covid test result: Positive; Covid test result: Positive; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 15Apr2021 as dose 1, single (Lot number: EW0161), in left arm, on 06May2021 as dose 2, single (Lot number: EW0171), in right arm and on 12Jan2022 as dose 3 (booster), single (Lot number: FH8027) at the age of 30 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Fatty liver" (unspecified if ongoing); "Known allergies: Yes" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Covid test result: Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Clinical course: The patient was covid tested post vaccination; covid test type post vaccination was Nasal Swab; and Covid test result was Positive. The patient had no other vaccine in four weeks. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300024971 Same reporter/patient/product, different dose/event.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test (Nasal Swab); Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Fatty liver
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2562262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 03.12.2021
Beginn: 27.12.2022
Tage bis Beginn: 389,0
Dosis: 3
Route/Site: - / -

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

Cough Dyspnoea Pneumonia Procalcitonin increased Respiratory failure COVID-19 Chills Chronic obstructive pulmonary disease Chronic respiratory failure Condition aggravated Sepsis Sputum abnormal

Symptomtext

Patient is a 72 y.o. male admitted to the hospital on 12/27/2022 for complaints of cough, dyspnea, chills and was subsequently found to have COVID with suspected CAP and COPD exacerbation. He was noted on admission to have a severe sepsis without shock as well. Given his oxygen requirements he was started on steroids and an E consult was placed to infectious disease who recommended initiation of remdesivir. He had a trace elevated Pro-Cal and given his complaints of thick sputum he has been treated for community-acquired pneumonia as well. He did have signs of COPD exacerbation on admission in which was also started on appropriate regimen. Of note, he does have chronic hypoxic respiratory failure with suspected prescribed continuous 2 L of oxygen but reports wearing 2-3 only in the evening hours and at night. He has a average SPO2 around 90% at rest and reports his oxygen levels normally are in the low 80s with activity and takes about 10 minutes for full recovery at baseline. He was weaned off of supplemental oxygen and a walking oxygen test does reflect his home oxygen levels. He has no respiratory distress on discharge and has no signs of continued acute exacerbation. He will continue on oral prednisone for 6 additional days for COVID as well as COPD treatment. He only has 1 more additional day of Zithromax and Omnicef for CAP coverage. I recommended that he follow-up with his primary care provider and also pulmonary. I recommend that he have follow-up for full explanation of prescribed home O2 needs and anything additional from a pulmonary perspective for chronic home regimen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2554559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 12.03.2021
Beginn: 17.11.2022
Tage bis Beginn: 615,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

11/17/22 presents to EC ED for "cough and dyspnea". PMHx of "HTN, CAD s/p LAD stent placement (2006), T2DM, base of tongue cancer s/p R tonsillectomy and excision of base of tongue (2012) followed by chemo/radiation therapy(2015) s/p PEG tube placement, diverticulitis with abscess and colovesical fistula s/p sigmoid colectomy (2011), atrial fibrillation, bilateral DVT, and carotid artery stenosis s/p R endarterectomy (2013)"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/17/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2546970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 03.02.2021
Beginn: 17.12.2022
Tage bis Beginn: 682,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Culture urine positive Enterococcus test positive Fall Mobility decreased Urinary tract infection White blood cell count abnormal

Symptomtext

Hospital Course and Significant Findings: Patient is a 79 year old male with a history of dementia, NPH who lives alone with part time caregiver who presented with fall and inability to get up. Daughter called emergency number. In the ER patient found to have UTI and COVID. For his UTI he was treated with cipro with improvement in WBC and no fever. Urine culture grew Enterococcus. In terms of his COVID, he was not hypoxic so received no decadron. He did receive Remdesivir while in the hospital. He will go home on COVID isolation through 12/26/22.

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

VAERS 2529037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: AZ
Alter: 67,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 07.12.2021
Beginn: 01.03.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: SYR / LA

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

Anal cyst Biopsy Erythema Haemorrhage Haemorrhoids Infected cyst Mass Mobility decreased Pain Surgery

Symptomtext

It started with a cyst on my butt near the anus. The doctor called it a lesion. It hurt so much I couldn't sit down. I noticed it when I wiped myself. It appeared to be infected. It was red, and by the time I made an appointment to see the doctor, it was bleeding. He prescribed BACTRIM. I couldn't finish them because they made me ill. It seemed to go away on its own, but I had another one a couple of weeks later. It really hurt also. The next time I went to the doctor, he prescribed a different antibiotic. It seemed to get better. Then, a third one appeared. The doctor prescribed ciprofloxacin. Because of the location and my age, he didn't want to do an incision to drain it. He suggested I see a general surgeon. The surgeon found four of the cysts on the left and a hemorrhoid. He also found a mass on the right perineum. He said he would remove them. I had the surgery on November 9, 2022. The mass was sub fascial, 2x2cm, and was completely excised off the side. They sent samples to the lab to screen for cancer. They were negative. I am still recovering.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 11/09/2022 samples for Cancer screen negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zolpidem
Allergien: Sulfa drugs
Vorherige Impfungen: 1991 Flu vaccine (Seasonal), lump in armpit. Age: 37, other info unknown.

VAERS 2526773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 07.12.2021
Beginn: 06.01.2022
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Chills Condition aggravated Dizziness Fatigue Headache Impaired work ability Nausea Oropharyngeal pain Pain Postural orthostatic tachycardia syndrome SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

I received the Pfizer booster for COVID-19 on 12/7/2021. On 1/6/2022, I woke up with headache, body aches, fatigue, and sore throat. I self-isolated in case I had COVID-19. I took a home test that day and got a negative result. I then arranged to get a PCR test later that day; when I got the PCR results back a few days later, they indicated a negative result. On 1/8/2022, I took another home antigen test and got a positive result. The headache, body aches, fatigue, and sore throat persisted for about 7 days, and I ended up being off from work for a week and half. I also developed chills and nausea at one point, and those lasted for about 3 days. I never vomited, though. I treated my symptoms with TYLENOL, which helped a little, but not much. The COVID-19 exacerbated some of the symptoms of my pre-existing conditions. For example, the dizziness and fatigue associated with POTS were exacerbated for about a week or two after I became infected.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 1/6/2022 home antigen test negative result; 1/6/2022 PCR test negative result; 1/8/2022 home antigen test positive result; 1/10/2022(?) home antigen test negative result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Mast Cell Activation Syndrome; Postural Orthostatic Tachycardia Syndrome; Asthma; Gastroesophageal Reflux Disease; Endometriosis; Irritable Bowel Syndrome; Periodic Paralysis.
Andere Medikamente: Cromolyn; ADVAIR DISKUS inhaler; vitamin D3; vitamin B12; PREVACID; levalbuterol.
Allergien: Latex; corn; ZOFRAN.
Vorherige Impfungen: -

VAERS 2526613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: AZ
Alter: 64,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 06.12.2021
Beginn: 14.08.2022
Tage bis Beginn: 251,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Chills Computerised tomogram normal Disturbance in attention Dyspnoea Feeling abnormal Headache Lethargy Malaise Mobility decreased Pain Parosmia Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I started experiencing symptoms on 08/14/2022 and tested positive for COVID-19 on 8/16 and 8/17. I had a really high fever at 102.5 and just total lethargy. I didn't move out of the chair much unless I needed to go to the bathroom or drink some fluid. It hit me a lot harder than the first time as far as fevers. I had headaches, congestion, and some shortness of breath. From the first round of COVID-19, that's when I started with my heart and lung symptoms. So for this infection, I already knew what was going on with my symptoms. I was just unable to function at all. I talked to my doctor via telehealth and told her I wasn't feeling well. She said she would send a prescription of Paxlovid just in case. I didn't take it because I didn't want to add to some of the problems I already have. I just stuck to fluids. I felt really bad for a full week. Out of commission and it was really tough. Most of it was fever, body aches, and chills. The headache did not go away, and I thought it would with the infection. I tried Tylenol and other medications, but nothing would knock it down. I didn't go to the hospital or anything, but it was not a nice experience. All other symptoms subsided but the headache persisted 24/7. I talked to my doctor and mentioned that my headache would not go away and nothing helped. I was having trouble focusing and I couldn't keep track of the things I was doing because it was distracting. My doctor said to get a CT because of the aneurysm. She also wanted to check to see if there was anything else causing this headache. I walked in to get my first CT done and compared to my old CTs and they saw no changes with the aneurysm. There was no sinus infection, so it was bizarre. Many health care providers noted that sometimes people with an autoimmune factor, after getting the COVID-19 infection, may get horrible headaches because the body cannot handle the spike protein. My PCP put me on Neurontin, which was 100mg one week, 200mg the next week, and 300mg the third week. It didn't help too much. I'm currently taking 900mg of Neurontin a day and the pain is now actually under control. I take that 3 times a day. I've been on that for a while now. I don't know what could happen if I get off of the medication because I'm not sure if the headache will come back or not. I started taking the medication on October 5, 2022. My biggest fear is I don't want to be on this medication for the rest of my life. We don't know what's going on. All of my doctors have said the same thing with the protein. I'm going back to the doctor in January and they may attempt to lower my dosage and get me off it and see the results. The sense of smell from the infection is getting better. I had smelled some perfume and it smelled different. With cooking, there was some things that I didn't smell well either. I think the smelling symptoms are getting better.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 08/16/2022 COVID-19 At Home Test - Positive; 08/17/2022 COVID-19 At Home Test - Positive; 09/20/2022 CT Scan without Contrast - Nothing in relation to aneurysm or sinus infection; 09/21/2022 CT Scan with Contrast - Nothing in relation to aneurysm or sinus infection
Aktuelle Erkrankungen: None
Vorgeschichte: PACs; Arrhythmias; Breathing Challenges; Aneurysm; Rheumatoid Arthritis; Unspecified Autoimmune Disease
Andere Medikamente: Carvedilol; Flecainide; Calcium; Vitamin D3; Actonel
Allergien: Gluten Intolerance; Steroids; Penicillin; Flovent
Vorherige Impfungen: -

VAERS 2501856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 10.12.2021
Beginn: 15.05.2022
Tage bis Beginn: 156,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Blood creatinine increased COVID-19 Dehydration Dyspnoea Oropharyngeal pain SARS-CoV-2 test positive White blood cell count increased

Symptomtext

5/15/2022- Presents to ED, c/o of SOB and sore throat, tested Covid + at home. Had fever of 100 at home. VSS in ED afebrile. WBC-15.7 , creatnine 1.91 and covid + test. Ordered Decadron , azithromycin and Bebtelovimab. Admit Covid 19. 5/16/2022- AKI s/t to dehydration d/t sore throat. Follow up with Nephro outpatient. Creatnine stable 1.6. WBC-12.6 Complete Zithromax and d/c home.

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Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, hyperlipidemia, Type 2 DM and CKD.
Andere Medikamente: -
Allergien: Procardia,Ampicillin, Latex, PCN and Tetracyclins.
Vorherige Impfungen: -

VAERS 2489480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 07.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Chest pain Costochondritis Lymphadenopathy Menstrual disorder Swelling

Symptomtext

chest pain that she describes as severe, constant, in the breast tissue, hard to move, hard to pick things up, hurt constantly; chest swelling; monthly cycles have been very effected and are still 'pretty bad'.; chest swelling that her doctor thought might be relayed to lymph node issues and under her arm lymph nodes; chest swelling that her doctor thought might be relayed to lymph node issues and under her arm lymph nodes; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. The reporter is the patient. A 34-year-old female patient received BNT162b2 (BNT162B2), on 07Dec2021 as dose 3 (booster), single (Lot number: FH8027) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE: 01, Lot number: unknown), administration date: Apr2021, for COVID-19 immunization, reaction(s): "chest pain that she describes as severe, constant, in the breast tissue, hard to move, hard to pick things up, hurt constantly", "chest swelling might be relayed to lymph node issues and under her arm lymph nodes", "monthly cycles have been very effected and are still 'pretty bad'", "chest swelling might be relayed to lymph node issues and under her arm lymph nodes"; Bnt162b2 (DOSE: 02, Lot number: unknown), administration date: May2021, for COVID-19 immunization, reaction(s): "chest pain that she describes as severe, constant, in the breast tissue, hard to move, hard to pick things up, hurt constantly", "chest swelling might be relayed to lymph node issues and under her arm lymph nodes", "monthly cycles have been very effected and are still 'pretty bad'", "chest swelling might be relayed to lymph node issues and under her arm lymph nodes". The following information was reported: CHEST PAIN (medically significant), outcome "unknown", described as "chest pain that she describes as severe, constant, in the breast tissue, hard to move, hard to pick things up, hurt constantly"; COSTOCHONDRITIS (non-serious), outcome "unknown", described as "chest swelling"; MENSTRUAL DISORDER (non-serious), outcome "unknown", described as "monthly cycles have been very effected and are still 'pretty bad'."; SWELLING (non-serious), LYMPHADENOPATHY (non-serious), outcome "unknown" and all described as "chest swelling that her doctor thought might be relayed to lymph node issues and under her arm lymph nodes".

Weitere VAERSDATA-Felder

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

VAERS 2468438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FH8027

moderat

Staat: CO
Alter: 70,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 01.10.2021
Beginn: 01.06.2022
Tage bis Beginn: 243,0
Dosis: 3
Route/Site: - / -

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

Axillary pain Hypertension Injection site pain Muscle injury Overweight Pain Pain in extremity

Symptomtext

It has been a while since I got my third dose and my arm started bothering me months down the road. When I went to have my fourth dose my left arm where I had taken all 3 doses before was hurting so I had the fourth shot in my right arm. The pain can be acute and it comes when moving my arm a certain way. Something in there is damaged and I blame it on the Covid vaccine since I have never had a muscle problem like this in my life and the area where it hurts is right over the injection area. It is a pain that I hoped I could work out, but it feels as if the muscle itself is damaged and will not repair itself. It doesn't hurt all the time and I still use the arm. Only certain stretches I make to reach or wash the opposite armpit lets say, I get a sharp pain there. (I will say that you might find another report on me for a full body rash from the covid. My personal opinion is the vaccine may have interacted with a prescription drug I took during the same period, but that was the other report I did to you on the rash. And, I sent you a follow-up after we got the rash under control with a mild form of steroids.) So, this report is on the muscle which seems to have been damaged. I lay on the left side where the first 3 doses were given. I am quite heavy at this time and losing but the weight could have something to do with it. I also have high blood pressure.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: none so far except Dr. checked it and she wasn't concerned.
Aktuelle Erkrankungen: no
Vorgeschichte: obese
Andere Medikamente: HCTZ 25/Triamterene 35.5MG tab Cholecalcif 25 MCG (D3-1000 unit) TAB Docusate Sodium 100mg Simvastatin 20MG TAB Fish Oil 1000MG (500MG DHA/EPA) CAP
Allergien: possibly rare strain of penicillian
Vorherige Impfungen: As I said before, I had a full body rash from the 2nd shot.

VAERS 2450723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MD
Alter: 61,0
Geschlecht: M
Eingang: 18.09.2022
Impfdatum: 18.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Angiogram cerebral Dehydration Dizziness Laboratory test Magnetic resonance imaging head Nystagmus Vertigo Visual impairment Vomiting

Symptomtext

Severe vertigo/vomiting that started 2-3 days after vacccination, and lasted 2-3 days, resulting in severe dehydration and required taking an ambulance to the hospital. Long term sequelae lasted a number of months and included dizziness, nystagmus, and brain/vision ?asymchrony?

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Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Various tests conducted at hospital on 21 or 22 Nov 2021. Multiple follow-up visits over a number of months invluded ENT, physical therapy, optometrist/opthamologist, and neurologist. Brain MRI and Brain MRA.
Aktuelle Erkrankungen: None
Vorgeschichte: GERD
Andere Medikamente: Protonix, Lipitor
Allergien: None
Vorherige Impfungen: -

VAERS 2442885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OH
Alter: 89,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 10.11.2021
Beginn: 01.06.2022
Tage bis Beginn: 203,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Tested COVID positive. Symptoms include shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: Nasopharyngeal specimen collected 6/03/2022 tested positive for 2019 Novel Coronavirus RNA on 6/03/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular disease, hypertension, and dementia.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2418304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: RI
Alter: 51,0
Geschlecht: M
Eingang: 23.08.2022
Impfdatum: 01.12.2021
Beginn: 28.06.2022
Tage bis Beginn: 209,0
Dosis: 3
Route/Site: SYR / AR

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

Asthenia Dyspnoea Exercise tolerance decreased Impaired quality of life Impaired work ability Laboratory test Malaise Respiration abnormal Sudden onset of sleep

Symptomtext

I got sick from something my family was exposed to and since I have been having serious trouble breathing. I have less energy and I fall asleep randomly (assume this is from lack of oxygen). I have trouble with strenuous physical exertion. I have raspy breath. Last fall we ran every test my PCP could imagine to discover a known problem as I was having breathing issues to some degree from July 2021 through February 2022. Then it cleared up from March to June and came back after I got sick. I do not get sick and I have never had breathing problems until July 2021 a month after the COVID vaccine. The current flare up continues today and I am afraid to get exposed to COVID or other viruses. I am very cautious in public and have been since the start of the COVID-19 pandemic. As far as I know since testing started,I have never contracted COVID-19. I test when any potential exposure or illness. I may have contracted it in January of 2020 in state but it was not reported to be in the country at that time. We discovered no way to treat the symptoms that I have chronically been experiencing. This is a serious impact on my quality of life and productivity at my employment working to help responsibly develop the offshore wind industry in the country to combat climate change - working for the State.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No tests related to the recent occurrence. Prior tests were reported here c. Nov or Dec 2021 or Jan | Feb 2022. I do not have the last report here with me.
Aktuelle Erkrankungen: Would need to confirm with PCP but nothing that I recall as a significant illness at that time.
Vorgeschichte: none prior to COVID-19 vaccinations starting in May 2021
Andere Medikamente: no
Allergien: Penecillin, earlier in childhood allergic to hydrocortisone, triaminic X, illisone (have not had a chance to test the latter two since childhood)
Vorherige Impfungen: as mentioned, I received the Pfizer COVID-19 max May 2021 - June 2021 and had a respitory problem starting July 2021. It began m

VAERS 2407461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: TX
Alter: 25,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / AR

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

Blood test normal Cardiac discomfort Condition aggravated Exercise tolerance decreased Feeling abnormal Loss of personal independence in daily activities Raynaud's phenomenon Tremor

Symptomtext

I also made a report for my first vaccine (J&J). The problems started with that vaccination, but they began to accelerate a lot faster after getting this booster. Increase in tremor strength, and faster spread. More pressure on my heart. Raynaud's worsened. I can no longer write. I can't exercise anymore, because my heart feels like it's going to explode. At all hours of the day, it feels like my internal organs are vibrating. I don't know if it's a coincidence, and it was caused by my J&J vaccine, and Pfizer booster has nothing to do with this or not. I just thought I'd send in information about this stuff. I've been wanting to for a while, but I don't know. I haven't been able to find any information about people who have mixed J&J with Pfizer.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood work is normal. ~ April 2022
Aktuelle Erkrankungen: None
Vorgeschichte: Narcolepsy (Type-2)
Andere Medikamente: Adderall
Allergien: No
Vorherige Impfungen: Janssen COVID-19 Vaccine, Lot 1805029, 24 years old at vaccination, March 11th, 2021. Like I said, I don't know if the Pfizer

VAERS 2397388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: DC
Alter: 41,0
Geschlecht: F
Eingang: 30.07.2022
Impfdatum: 10.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Vaccination failure Crying Dyspnoea Headache Hypersomnia Illness Irritability Malaise Mental disorder Moaning Motor dysfunction Muscle disorder Myalgia Nausea Pain Pain in extremity Vomiting

Symptomtext

insane; body wasn't working; throwing up; muscle aches; muscles felt like they were going to melt off the bones; headaches; nausea; moaning and whining and crying; moaning and whining and crying; moaning and whining and crying; slept for 12 hours; arm was a little sore and nothing to shake a stick at; did not feel good/from 9 in the morning till 9 at night she didn't feel good and she was out; intense pain; very sick; couldn't breath; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient received BNT162b2 (BNT162B2), on 10Nov2021 as dose 3 (booster), single (Lot number: FH8027) at the age of 41 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: BNT162b2 (DOSE 1, SINGLE, Lot: EN6204, Expiration: Jun2021, Time given: afternoon, Anatomical location: Left shoulder non dominant shoulder. She said the doctor scribbled over the NDC. She got vaccinated during her third trimester of pregnancy and that when they said pregnant women can get vaccinated.), administration date: 13Mar2021, when the patient was 41-year-old, for COVID-19 Immunization, reaction(s): "Maternal Exposure During Pregnancy, third trimester"; BNT162b2 (DOSE 2, SINGLE, Lot: ER8729, Expiration: Jul2021, Time given: Afternoon, Anatomical location: Left arm), administration date: 03Apr2021, when the patient was 41-year-old, for COVID-19 Immunization, reaction(s): "Maternal Exposure During Pregnancy, third trimester". The following information was reported: MENTAL DISORDER (non-serious), outcome "unknown", described as "insane"; MOTOR DYSFUNCTION (non-serious), outcome "unknown", described as "body wasn't working"; VOMITING (non-serious), outcome "unknown", described as "throwing up"; MYALGIA (non-serious), outcome "unknown", described as "muscle aches"; MUSCLE DISORDER (non-serious), outcome "unknown", described as "muscles felt like they were going to melt off the bones"; HEADACHE (non-serious), outcome "recovered", described as "headaches"; NAUSEA (non-serious), outcome "recovered"; MOANING (non-serious), CRYING (non-serious), IRRITABILITY (non-serious), outcome "recovered" and all described as "moaning and whining and crying"; HYPERSOMNIA (non-serious), outcome "unknown", described as "slept for 12 hours"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "arm was a little sore and nothing to shake a stick at"; MALAISE (non-serious), outcome "recovering", described as "did not feel good/from 9 in the morning till 9 at night she didn't feel good and she was out"; PAIN (non-serious), outcome "unknown", described as "intense pain"; ILLNESS (non-serious), outcome "unknown", described as "very sick"; DYSPNOEA (non-serious), outcome "unknown", described as "couldn't breath". Therapeutic measures were taken as a result of dyspnoea. Additional information: Time the booster vaccination was given: Afternoon. She said the booster took her out for 12 hours. She said was insane and her body wasn't working and she was throwing up and had muscle aches and her muscles felt like they were going to melt off the bones and she never felt anything like this. She had headaches and nausea, she was moaning and winning and crying and slept for 12 hours and woke and she was fine. He arm was a little sore and nothing to shake a stick at. She did not feel good and then it hit her and she was out for the count for 12 hours. She said around 8pm or 9pm she started feeling better. She said from 9 in the morning till 9 at night she didn't feel good and she was out. She said intense pain and very sick all that and she couldn't breath and she did a breathing treatment. The only difference with the vaccine she was pregnant with those two shots and the booster she had the baby and not sure if the baby help offset and the third shot did something special. Follow-Up (28Jul2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2344777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / AR

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

Condition aggravated Eczema Erythema Food allergy Hypersensitivity Mouth swelling Pruritus

Symptomtext

I had a reaction resembling an allergic reaction to food. My eczema patches turned red and began to itch, there was some swelling around the mouth. The reaction seemed to subside 30 minutes after it appeared.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Zyrtec, Benadryl, albuterol
Allergien: Peanuts, soy, corn, oral allergy syndrome, codeine, and sulfa drugs
Vorherige Impfungen: -

VAERS 2331917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IA
Alter: 82,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 08.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / -

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

Abdominal X-ray Abdominal discomfort Abdominal distension Acute kidney injury Anticoagulant therapy Anticoagulation drug level above therapeutic Atrial fibrillation Bladder catheterisation Bladder scan Blood calcium normal Blood creatinine increased Blood glucose normal Blood urine present Bowel preparation Bradycardia Chest X-ray normal Chronic obstructive pulmonary disease Colonoscopy abnormal

Symptomtext

Pfizer Dose 1 2/9/21 (el3302) Pfizer Dose 2 3/3/21 (EN6199) Pfizer Dose 3 12/8/21 (FH8027) COVID Positive 12/14/21 12/19/21: Patient is an 82 year old with a past medical history of COPD, CKD stage 3B, CAD, chronic CHF, HTN, HLD, AFib with pacemaker, and BPH who presented to the ED with shortness of breath and sore throat. The sore throat started today and his shortness of breath he has had for about 1 week. He also endorses a non-productive cough. Denies fever, chest pain, diarrhea, loss of sense of taste or smell. He has a decreased appetite and says he has been trying to drink PO fluids but his throat hurts too much. He was recently evaluated in the ED on 12/14 when he presented with shortness of breath for 3-4 days. He was discharged with a diagnoses of COPD exacerbation. He was given prescriptions for Prednisone 50mg PO daily for 5 days which he completed today and Levaquin 750mg PO daily for 7 days. He has 3 tablets remaining. During that hospital visit he was found to have a supratherapeutic INR and was told to contact the Coumadin clinic. He states that they told him to continue taking his Coumadin. Denies active bleeding. During that ED visit he was also found to be COVID-19 positive. He received 2 doses of the Pfizer vaccine and the Pfizer booster. In the ED: VSS. Labs remarkable for glc 112, cr 2.48, ca 10.3, ProBNP 2418, WBC 12.98, INR > 9. CXR no acute findings. U/A demonstrated moderate blood and leuk esterase. He was given one duo-neb treatment, 1g ceftriaxone, methylprednisolone OT, 500mL NS bolus x2, and vitamin K. 1/2/22: Patient initially saturating well on room air. Treated with Mucinex and respiratory therapy. Respiratory status was relatively stable throughout hospital course and did not require COVID protocol treatment. Nephrology was consulted on 12/22 for AKI they believed to be due to cardiorenal syndrome. Bladder scan showed urinary retention and Foley catheter was placed. Was attempted to be removed on 12/22, urinary retention continued and was placed back in. Blood pressure was closely monitored in fluids were started. Kidney function was closely monitored throughout hospital course. Nephrology continued to follow along with patient's kidney function. He was continued on Bumex drip, D5 at low rate, and cinacalcet. Nephrology had continued discussion with patient about dismal kidney function and concern for dialysis or CRRT. Patient was interested in neither. His Bumex drip was stopped late in hospitalization. Nephrology subsequently signed off. Daily INR checks were in place. Warfarin was given only 2X in 1 mg doses when INR return to therapeutic range, but patient was very responsive to this and cause it to increase again. Pharmacy recommend consideration of alternate form of anticoagulation once back in the outpatient setting. Daily INR checks were continued throughout admission and INR was noted to rise despite warfarin being held. No anticoagulation was restarted on discharge secondary to patient's desire to stop workup of GI bleed and no definitive treatment being made. On 12/24, patient developed bradycardia, and so an inquiry was run on patient's device. It was found that on 12/19 he had an episode of VFib that resulted in an ICD shock. Patient was unaware of this. It was then found that patient was in ventricular bigeminy and amiodarone was started in an attempt to suppress his ventricular ectopy. This was effective and bigeminy was improved, amiodarone was switched to oral and decreased throughout hospital course. Cardiology consult was recommended by EP. Curbside consult on 12/27 was done and it was recommended to restart patient on metoprolol 12.5 b.i.d. for AFib. Official consult was not warranted. Metoprolol was intermittently discontinued due to low blood pressures but ultimately restarted. Per EP recommendations patient was continued on amiodarone 400 mg daily as an outpatient with close follow-up scheduled. Covid protocols discontinued on 12/25 due to patient being outside the 10 day window since testing positive. Continued to remain stable in terms of his respiratory status. On 12/26, a rapid response was called on patient due to shortness of breath after getting up to use the restroom. He was started on supplemental O2. Abdominal distention was noted on physical exam, blood pressure 95/70, heart rate in the 70s. Telemetry reported paced rhythm, no redness. Chest x-ray showed fluid in the right lower lung, otherwise no acute changes. Respiratory therapy placed BiPAP on patient. Lasix and Solu-Medrol given at that time. Breathing improved. KUB was ordered which showed possible volvulus with gaseous distension. CT the abdomen was ordered and showed gaseous distention of the cecum and transverse colon but no obvious volvulus or obstruction. Surgery was not indicated, but continue to follow for couple days. GI was consulted and a decompressive colonoscopy was performed on 12/26. Report showed Ogilvie syndrome, sessile polyp 3 cm x 2 cm, ulcerations in the cecum. Repeat abdominal x-ray showed resolution of bowel gas distention. Because there was no bowel prep, GI recommended repeat colonoscopy after patient was properly prepped before hand. The patient felt clinically better the next morning, noted resolution of abdominal discomfort. On 12/28 hemoglobin dropped to 9 and was more closely monitored. Warfarin was continued to be held. When hemoglobin continued to fall and dark stools were noted by nursing staff, GI recommended upper and lower scope after bowel prep was done. Patient had significant difficulty doing this, and by 12/30 was still unable to complete this, while hemoglobin dropped to 7.4. Multiple discussions were had with patient by GI, Family Medical Clinic team, nursing staff, and his daughter regarding the importance of completing bowel prep so this study can be done. Patient attempted to complete prep the following several days, however, was unable to. His hemoglobin remained stable at over 7.0. After further discussion with patient he decided to forego any further evaluation of suspected GI bleed. He requested discharge on 01/01, however, there was a snowstorm and discharge was unsafe. He agreed to stay another night. He was seen and examined the morning of 01/02 and his exam was unchanged. He continued to endorse desire to be discharged. His hemoglobin was stable on discharge. He was agreeable for a home hospice consult given his decline in renal function and refusal to undergo further medical workup for GI bleed. He was discharged home in guarded condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD CKD stabe 3B CAD chronic CHF HTN HLD A fib with pacemaker BPH
Andere Medikamente: alprazolam 0.5 mg PO TID PRN amiodarone 400 mg PO QD metoprolol ER 25 mg PO QD pantoprazole 40 mg PO QD Spiriva 18 mcg inh QD albuterol 2 puffs Q4h PRN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2329199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IA
Alter: 72,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 01.12.2021
Beginn: 24.02.2022
Tage bis Beginn: 85,0
Dosis: 3
Route/Site: IM / -

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

Aortic stenosis Blood creatinine increased Blood urea increased COVID-19 Chest X-ray abnormal Dyspnoea Echocardiogram Ejection fraction Haemodialysis Haemoglobin normal Hypervolaemia Mitral valve incompetence Oedema peripheral Peripheral swelling Prohormone brain natriuretic peptide SARS-CoV-2 test positive Troponin

Symptomtext

Pfizer Dose 1 3/5/21 (EN6199); Pfizer Dose 2 3/31/21 (EN6207); Pfizer Dose 3 12/1/21 (FH8027); COVID Positive 3/10/22; 3/10/22: This is a 72-year-old female with history of type 2 diabetes mellitus, chronic kidney disease stage 4, hyperlipidemia, hypertension, sick sinus syndrome status post pacemaker placement in the past and monoclonal gammopathy who presented to the emergency department with shortness of breath and swelling in both legs. Patient states that her symptoms started about 2 weeks ago. She has been getting worsening dyspnea and she noted more edema in her legs than usual. She has no associated fever, chills, chest pain, nausea or vomiting. In the emergency department, patient was found to have a blood pressure of 168/92. Labs showed a creatinine of 6.4, BUN of 68, proBNP of 32636, troponin level of 0.79 with repeat of 0.74 hemoglobin of 9.1. Chest x-ray showed fluid overload. Patient received nebulizer treatment, p.o. aspirin, IV Lasix 80 mg. 3/16/22: Patient is a 72-year-old female who presented on 03/10/2022 with chief complaint of shortness of breath and bilateral lower extremity edema. Symptoms had been progressing for 2 weeks. Creatinine was 6.4 on arrival. Patient was noted to be in fluid volume overload. Echocardiogram showed EF of 60-65%. There was also mention of severe aortic stenosis and moderate to severe mitral regurg. On admission, it was thought that her symptoms were secondary to progression of her baseline stage IV CKD. She already had had a fistula placed in her right forearm prior to admission in anticipation that she would need dialysis in the near future. Patient was started on HD. She tolerated this well. Patient felt overall improved from time of admission. An outpatient dialysis chair was arranged. She was therefore discharged on 03/16/2022. Prior to her discharge, we did have a risks/benefits discussion about staying in the hospital for cardiology consultation and workup for possible TAVR. Through shared decision making, it was felt reasonable to have the patient follow-up as an outpatient within the next week or so since she was overall doing better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM type 2; CKD IV; HLD; HTN; sick sinus sydrome s/p pacemaker placement; monoclonal gammopathy.
Andere Medikamente: APAP ER ; Albuterol; Atorvastatin; Calcium acetate; Calcium-vitamin D;Cyanocobalamin; Diclofenac topical; Epoetin alfa; Ferrous sulfate; Insulin aspart; Sliding scale insulin aspart insulin; Insuli detemir; Metoprolol ER.
Allergien: Adenosine - respiratory distress; Darvocet N - swelling of throat; Keflex - hives, nausea, vomiting, swelling.
Vorherige Impfungen: -

VAERS 2329086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IA
Alter: 75,0
Geschlecht: M
Eingang: 23.06.2022
Impfdatum: 30.11.2021
Beginn: 18.01.2022
Tage bis Beginn: 49,0
Dosis: 3
Route/Site: IM / -

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

Anticoagulant therapy Atrial fibrillation Bladder catheterisation Blood creatinine increased Blood glucose normal Blood potassium increased Blood urea increased COVID-19 Cardiac failure Cardiac failure congestive Chest X-ray normal Condition aggravated Dyspnoea Dyspnoea paroxysmal nocturnal Electrocardiogram abnormal Electrolyte imbalance Hypervolaemia Hypoxia

Symptomtext

Pfizer Dose 1 3/9/21 (EN6199) Pfizer Dose 2 3/31/21 (EN6207) Pfizer Dose 3 11/30/21 (FH8027) COVID Negative 2/1/22 COVID Positive 2/8/22 2/1/22: Patient is 75-year-old male with history of nonobstructive CAD and severe systolic dysfunction and EF 25%, history of severe aortic stenosis s/p bioprosthetic valve replacement, history of permanent AFib on Coumadin, history of sustained V-tach s/p AICD, OSA on CPAP, CKD stage 3, history of hypertension, diabetes mellitus, presenting to the emergency depart with a complaint of worsening shortness of breath of 2 weeks duration. Patient reports orthopnea and paroxysmal nocturnal dyspnea. Increased weight and lower extremity swelling. Denies any fever or chills, no cough or sputum production, no chest pain or palpitations, no changes in his bowel movements or urinary habits. Reports compliance with his medications and diuretics. Compliance with diet. His primary cardiologist Dr., was last time seen prior to Christmas time. Apart from noted he denies any complaints. In ED, EKG shows atrial fibrillation his heart rate was 118, he was placed on 2 L by nasal cannula but was with no hypoxia, reported shortness of breath, his potassium 5.1, glucose 199, BUN 39, creatinine 2.3 which seems to be at baseline, proBNP 11947, troponin 0.04, INR 4.3, he was given Lasix 80 mg IV x1, Dr. from Cardiology consulted and he recommended starting Lasix drip at 20 mL an hours. 2/12/22: 75-year-old male with history of nonobstructive CAD and severe systolic dysfunction and EF 25%, history of severe aortic stenosis s/p bioprosthetic valve replacement, history of permanent AFib on Coumadin, history of sustained V-tach s/p AICD, OSA on CPAP, CKD stage 3, history of hypertension, diabetes mellitus, presenting to the emergency depart with a complaint of worsening shortness of breath of 2 weeks duration. In ED, EKG shows atrial fibrillation his heart rate was 118, he was placed on 2 L by nasal cannula but was with no hypoxia, reported shortness of breath, his potassium 5.1, glucose 199, BUN 39, creatinine 2.3 which seems to be at baseline, proBNP 11947, troponin 0.04, INR 4.3, he was given Lasix 80 mg IV x1, Dr. from Cardiology consulted and he recommended starting Lasix drip at 20 mL an hours. Subsequently the patient was managed with IV Bumex GTT that has been tapered down. To oral Bumex dose. Electrolyte abnormalities were corrected He is anticoagulated on Coumadin and INR which is therapeutic. Both Cardiology and Nephrology assisted with management of patient's care during admission, patient will need longitudinal follow-up with PCP and possible referral to Nephrology as outpatient. Renal function stabilized, Foley left in place for retention. May need urology follow-up at some point Incidentally tested positive for COVID 19 during discharge planning, patient is on 3 L, upper 90s not working hard to breathe. X-ray without infiltrate, did not qualify for remdesivir/Actemra. Suspect hypoxia mostly related to fluid overload/CHF supportive care for COVID-19 he was placed on dexamethasone will taper, vitamin-C, vitamin-D, zinc, 3 days of azithromycin. Patient will need INR check in 3 days, BMP within 7 days ideally follow-up with PCP within 7 days of discharge. Follow-up with Cardiology for heart failure as discussed. All ED in RTC precautions provided to patient endorse understanding and initiate with plan as outlined.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: nonobstructive CAD severe systolic dysfunction EF 25% severe aortic stenosis s/p bioprosthetic valve replacement a fib sustained V-tach s/p AICD OSA on CPAP CKD III HTN DM
Andere Medikamente: APAP 650 mg Po Q4h PRN aspirin 81 mg PO QD atorvastatin 40 mg PO QD bumetanide 2 mg PO BID vitamin D 25 mcg PO QD dexamethasone taper docusate 100 mg Po BId duloxetie ER 60 mg PO QD ferrous sulfate 325 mg Po QD finasteride 5 mg PO QD gabape
Allergien: NKA
Vorherige Impfungen: -

VAERS 2324240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 20.06.2022
Impfdatum: 28.11.2021
Beginn: 11.06.2022
Tage bis Beginn: 195,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury COVID-19 Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Diuretic therapy Dyspnoea Dyspnoea exertional Echocardiogram abnormal Ejection fraction Exposure to SARS-CoV-2 Hyperkalaemia Hypokinesia Left ventricular failure Prohormone brain natriuretic peptide increased SARS-CoV-2 test positive Weight increased

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 6/11/2022 Discharge Date: Jun 14, 2022 PRESENTING PROBLEM: Acute on chronic heart failure, unspecified heart failure type (HCC) [I50.9] Systolic congestive heart failure, unspecified HF chronicity (HCC) [I50.20] COVID-19 [U07.1] HOSPITAL COURSE: 64 y.o. male with a history of of NICM s/p ICD, HFrEF, sardoidosis of heart and lung who presented with shortness of breath. He had exposure to a family friend who tested positive for COVID. HE then developed dyspnea on exertion of less than 15 feet. Admits not adhering to recommended 2 gram and 2L diet and had gained about 3 pounds in the past day. On arrival he had normal and stable vitals, mild AKI with hyperkalemia, proBNP >10,000 and CXR concerning for fluid overload. One dose of IV lasix improved his symptoms, and COVID testing was positive. He was admitted to internal medicine team for further evaluation treatment. Entresto was held due to AKI. Cardiology was consulted on admission. AKI improved with diuretic holiday and his shortness of breath resolved by day 2 admission. He never developed hypoxia. He was able to ambulate for more than 50 ft without assistance without developing any dyspnea or hypoxia. Echocardiogram was updated which showed global hypokinesis and ejection fraction of 11%. On 06/14/2022 he was discharged in stable condition with instruction to follow up with Cardiology on June 22. Torsemide was held on discharge, as well as Entresto.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Sarcoidosis Cardiomyopathy (HCC) COPD (chronic obstructive pulmonary disease) (HCC) Cardiomyopathy, nonischemic (HCC) Shortness of breath ICD (implantable cardioverter-defibrillator), dual, in situ Non-sustained ventricular tachycardia (HCC) RBBB Acute on chronic systolic (congestive) heart failure (HCC) Precordial pain
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet allopurinol (ZYLOPRIM) 100 MG tablet atorvastatin (LIPITOR) 40 MG tablet carvedilol (COREG) 25 MG tablet clobetasol (TEMOVATE) 0.05 % cream colchicine (COLCRYS) 0.6 MG tablet diphenhydrAMINE (BENA
Allergien: Jardiance [Empagliflozin]Hives LatexHives LisinoprilCough Losartan Potassium [Losartan]Dizziness, GI Upset MetoprololNausea Only SeasonalSneezing Seasonal Allergies, Unspecified SpironolactoneGI Upset
Vorherige Impfungen: -

VAERS 2313228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MO
Alter: 56,0
Geschlecht: M
Eingang: 08.06.2022
Impfdatum: 16.12.2021
Beginn: 11.04.2022
Tage bis Beginn: 116,0
Dosis: 3
Route/Site: - / -

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

Cytology Dyspnoea Magnetic resonance imaging Non-small cell lung cancer Paracentesis Positron emission tomogram

Symptomtext

Patient seen for SOB and susequently found to have Non-Small Cell Cancer, LLL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Paracentesis with cytology, MRI, PET scan
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety, depression
Andere Medikamente: alprazolam, venlafaxine
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2311416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MA
Alter: 57,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 05.04.2022
Beginn: 01.05.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: OT / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure Insomnia Palpitations Pyrexia

Symptomtext

Temperature of 102 degrees; Racing heart; could not fall back to sleep; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Apr2022 at 10:00 as dose 4 (booster), single (Lot number: FH8027) at the age of 57 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Right, Vaccine Administration Time: 01:00 PM, Route of Administration: Intramuscular), administration date: 12Apr2021, when the patient was 57-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM, Route of Administration: Intramuscular), administration date: 24Mar2021, when the patient was 57-year-old, for covid-19 immunization; Bnt162b2 (DOSE 3 (BOOSTER), SINGLE), for covid-19 immunization. The following information was reported: PALPITATIONS (non-serious) with onset May2022, outcome "recovering", described as "Racing heart"; PYREXIA (non-serious) with onset May2022, outcome "recovering", described as "Temperature of 102 degrees"; INSOMNIA (non-serious) with onset May2022, outcome "recovering", described as "could not fall back to sleep". The events "temperature of 102 degrees", "racing heart" and "could not fall back to sleep" required emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, palpitations, insomnia. Additional information: Patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. Patient did not on any other medications within 2 weeks of vaccination. Patient received 2 Pfizer Covid vaccines plus 2 Pfizer Covid boosters. On the day of her last booster, 05Apr2022, she also had a dentist appointment. She told to dentist at the start of visit that she had just received a Covid booster. He said that he was only going to give her no vacaine, so it would not be an issue. She went to sleep early that evening and woke up at 3am with a racing heart. She could not fall back to sleep. At around 7am her heart had been racing for hours, so she went to the emergency room. They confirmed that heart was racing and that she had a temperature of 102 degrees. They gave to patient IV fluids and lots of tests and sent to home after several hours. Treatment received for the adverse event with IV fluids, Advil. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has been tested for COVID-19. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200793055 similar report from same reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20220521; Test Name: pyrexia; Result Unstructured Data: Test Result:102 f; Comments: 102 F; Test Date: 20220521; Test Name: covid-19; Result Unstructured Data: Test Result:Positive; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2303364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NC
Alter: 38,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 27.11.2021
Beginn: 23.05.2022
Tage bis Beginn: 177,0
Dosis: 3
Route/Site: SYR / RA

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

Ageusia Anosmia Aphasia Back pain COVID-19 Chest pain Chills Cough Feeling abnormal Headache Initial insomnia Memory impairment Myalgia Nasal congestion Nausea Oropharyngeal pain Pain Pain in extremity

Symptomtext

On the evening of May 23 after dinner, I started getting a scratchy throat. Felt as if my throat was swollen, like I was trying to swallow something, but it wouldn?t go down. Swollen feeling and scratchy. Did not really sleep well that night. Next morning, I woke up with postnasal drip, sore throat, and felt off. Took two Advil at this point. By the afternoon, I still had the scratchy throat and a little bit of a cough. I took an at-home COVID test and it came back positive. So I went to pharmacy and went to get a PCR test and it also came back positive by the next day. The evening of the 24th, I had a fever of 100.2. I was achy especially my legs. Sore and scratchy throat, cough, runny nose, postnasal drip. Muscle aches, chills, low grade fever around 99 degrees, brain fog. Took more Advil at this point. Going into the 25th, didn?t wake up as bad. But was stuffy, coughing, phlegmy. Started to get bad again. Fever at 100.5, cough, sore throat, achy, chills, etc. was alternating between Tylenol and Advil. Also had a headache. Poking pain in the mid back, legs were sore and skin was highly sensitive. When my ankles rubbed together, felt like rubbing sandpaper. Went back and forth between Tylenol and Advil every 4-6 hours. Still had a fever the night of the 26th. Sensitive skin, stuffy, congestion, aches. On the 27th, woke up really sore in the legs, slight nausea, still sore throat. My chest did get sore from coughing at one point and throat was swollen and sore. The afternoon of the 27th was starting to not have a fever but would still get the leg aches. Still taking Advil and Tylenol. But fever had broken and haven?t had one since. Took me a while to fall asleep because of the pain in my legs. On the 27th around 11:20AM ? I did take another rapid COVID test because it had been 24 hours since my fever and that rapid test was still positive. I did start to notice on that day on the 28th in the afternoon, I was losing my sense of smell and taste. My lunch tasted off and dinner couldn?t taste at all. On the 29th, the pain in my legs was still on going, but fever was no longer present. Took another test the next day and it still came back positive. Was able to sleep through the night of the 30th. Haven?t had any Advil and Tylenol since the night of the 29th. Feeling much better, still some congestion and phlegm occasionally. Brain fog was pretty bad. I would forget why I walked into rooms and trying to find the right words were harder than usual. Psychologically, felt pretty down at the moment because of the positive test after 5 days. Sense of taste and smell started returning the day of the 30th. Have been isolating in my bedroom and have been wearing an N-95 mask around the house as well. Have not fully recovered, but in the process of recovery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 05/24/2022 - At-Home COVID Test - positive 05/24/2022 - COVID PCR Test - positive 05/28/2022 - At Home COVID Test (After 5 days) - positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Women?s One-A-Day Multivitamin Vitamin D Pantoprazole
Allergien: Dust Dust Mites
Vorherige Impfungen: -

VAERS 2281018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 02.12.2021
Beginn: 10.05.2022
Tage bis Beginn: 159,0
Dosis: 3
Route/Site: IM / AR

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

Anticoagulant therapy COVID-19 Chest pain Cough Dialysis Diarrhoea Echocardiogram abnormal Ejection fraction Electrocardiogram ST segment depression Hypertension Hypertensive emergency Interchange of vaccine products Myalgia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Troponin increased Ventricular hypertrophy

Symptomtext

Hospitalized 05/10/2022-05/13/2022; COVID-19 positive 05/10/2022; fully vaccinated plus booster BRIEF OVERVIEW: Discharge Provider: Primary Care Provider: Admission Date: 5/10/2022 Discharge Date: May 13, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Chest pain [R07.9] Hypertensive emergency [I16.1] HOSPITAL COURSE: A 62 y.o. male with PMHx including ESRD on HD (MWF), HTN, HOCM, CAD s/p PCIx2, not on anti-platelet therapy, presenting with chest pain and hypertensive emergency. Upon arrival to the emergency department he was noted to be hypertensive at 228/97, remainder of his vitals were stable. Initial EKG showed some ST depression in the inferior leads. Troponin elevated at 63, repeat 2 hour troponin 69. He was started on nitroglycerin drip for his blood pressure, with subsequent resolution of his chest pain. Repeat EKG showed resolution of the ST changes. Cardiology was contacted who recommended echocardiogram and starting heparin drip for possible ACS. He was incidentally found to be positive for COVID, with symptoms including mild diarrhea and rhinorrhea x 1 week, myalgias, cough with congestion using OTC mucinex and coricidin. He had SpO2 >90% on room air. He was also found to have vitamin D deficiency, and was started on vitamin D supplementation. Cardiology recommended starting carvedilol, and patient was weaned off clonidine, and stopped metoprolol, and subsequently weaned off nitroglycerin gtt. Repeat echo with evidence of LVEF 75%, unchanged from prior, with septal thickening to 14mm. Nephrology was consulted, and he received dialysis on his scheduled days, MWF. Patient was discharged in stable condition, with chest pain resolved, in no acute distress, O2Sat >92% on room air.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Pneumonia; Hypertrophic cardiomyopathy (HCC); Coronary artery disease involving native heart without angina; pectoris, unspecified vessel or lesion type; Essential hypertension, malignant; Chronic hepatitis C without hepatic coma (HCC); COVID-19 Anemia in chronic kidney disease; Pain from fibrosis of arteriovenous fistula (HCC); Renal insufficiency; Chronic kidney disease, unspecified CKD stage; Stage 5 chronic kidney disease (HCC); Renal osteodystrophy; End stage renal disease (HCC); Dyslipidemia; Family history of prostate cancer; Dependence on renal dialysis (HCC); Genetic testing for HCM (DO NOT EDIT); Encounter for fitting and adjustment of extracorporeal; dialysis catheter (HCC); Pain management; Trigger middle finger of right hand; History of cocaine abuse (HCC); Personal history of tobacco use, presenting hazards to health
Andere Medikamente: Amlodipine (NORVASC); Aspirin; Atorvastatin (LIPITOR); B Complex-C-Folic Acid (DIALYVITE 800); Carvedilol (COREG); Cinacalcet (SENSIPAR); Ergocalciferol (VITAMIN D2); Hydralazine (APRESOLINE); Hydrocodone-acetaminophen (NORCO); Isosorbide m
Allergien: NKA.
Vorherige Impfungen: -

VAERS 2263534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MO
Alter: 54,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 21.04.2021
Beginn: 30.04.2022
Tage bis Beginn: 374,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain Dyspnoea Respiratory tract congestion

Symptomtext

Symptom onset was 04/29/2022, SOB, congestion and chest pain/pressure. Admitted to hospital 04/30/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Chronic Kidney and Urinary Tract Infections
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2260225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 51,0
Geschlecht: F
Eingang: 02.05.2022
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

Balance disorder Cardiac monitoring Chest pain Dyspepsia Laboratory test Vertigo

Symptomtext

Employee states after receiving her first dose of Pfizer BioNtech COVID 19 vaccine, she has had vertigo and when she turns quickly, she loses her balance, along with chest pain and acid indigestion. All symptoms worse after receiving second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Heart Event Monitor, Laboratory testing Unknown results
Aktuelle Erkrankungen: none known
Vorgeschichte: none known
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2260225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 51,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 26.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / UN

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

Balance disorder Cardiac monitoring Chest pain Dyspepsia Laboratory test Vertigo

Symptomtext

Employee states after receiving her first dose of Pfizer BioNtech COVID 19 vaccine, she has had vertigo and when she turns quickly, she loses her balance, along with chest pain and acid indigestion. All symptoms worse after receiving second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Heart Event Monitor, Laboratory testing Unknown results
Aktuelle Erkrankungen: none known
Vorgeschichte: none known
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2260099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: VA
Alter: 51,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 29.10.2021
Beginn: 03.04.2022
Tage bis Beginn: 156,0
Dosis: 2
Route/Site: SYR / LA

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

Chest pain Dyspnoea Echocardiogram Electrocardiogram Fatigue

Symptomtext

Approximately 6 months after my 2nd dose I experienced the following symptoms: Fatigue, Shortness of breath, Massive centralized chest pain. I have no family history of having a heart attack but due to my existing health conditions such as (overweight and hypertension) it could be a contributing factor. I went to see my primary care physician and was advised to take a cardiology exercise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Echocardiogram; Cardiac rehab; EKG; ECG
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Valsartan, Hydrochlorothiazide, Amlodipine
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2255258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 01.03.2021
Beginn: 01.02.2022
Tage bis Beginn: 337,0
Dosis: 3
Route/Site: IM / LA

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

Asthma Condition aggravated Dyspnoea Palpitations

Symptomtext

About February I noticed my heart would be racing for little or no reason. I also would hear myself breathing like I was out of breath just climbing stairs. I started having these symptoms more and more often. Even waking up gasping for air at night. My husband asked me to see a doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I had a wellness test on March 1, 2022. Dr. prescribed Metoprolol succ er 25 mg tabs for my heart. I have been taking them 2 months and I am feeling better. I did have some issues with my asthma last week and got a z-pack and a shot and some new asthma inhaler and am feeling much better than I have in weeks.
Aktuelle Erkrankungen: NOTHING
Vorgeschichte: ASTHMA
Andere Medikamente: ACYCLOVIR 400 MG
Allergien: SULFER
Vorherige Impfungen: -

VAERS 2252210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 05.10.2021
Beginn: 01.02.2022
Tage bis Beginn: 119,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Hypoaesthesia Naprapathy Pain Paraesthesia Swelling

Symptomtext

I had the booster in Oct. It started with a localized swelling. Then 3 months later, I started having numbness and tingling in my left side of my foot. It became progressively worst. I started having pain in late Feb. but couldn't get an appointment until April. I saw my doctor on April 7,2022 she tested my foot and diagnosed me with perirhinal naprapathy. She also ordered blood work to find the source. Bloodwork was inconclusive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Mass in pelvic area Removed in Feb 8,2022
Vorgeschichte: Fibromyalgia; Chronic Fatigue; SIBO; Type 2 Diabetes; Thrombocytopenia; Obstructive Sleep; Apnea; IBS; Perifocal Naprapathy; Mix Hyper Lipedema
Andere Medikamente: Crestor Cymbalta Klonopin Lexapro Metformin Mobic Motegrity Neurontin Norvasc Singulair Soma Valtrex Calcium D3 Vitamin D3 Zyrtec
Allergien: IV Gamma Globulin; Levofloxacin; Ace Inhibitors; Flu Vaccine; DPT Vaccine; Adhesive and Tape; Bee Vitim; Fish allergy; other
Vorherige Impfungen: Flu Vaccine - I got really sick, nauseas, vomiting, hallucination, high fever; DPT Vaccine - allergic to the pertussis in the va

VAERS 2236047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 15.04.2022
Impfdatum: 22.11.2021
Beginn: 02.04.2022
Tage bis Beginn: 131,0
Dosis: 2
Route/Site: UN / UN

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

Chills Cough Dyspnoea Fatigue Respiratory tract congestion

Symptomtext

chills, fatigue, congestion, cough, SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2226056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 37,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 12.11.2021
Beginn: 10.01.2022
Tage bis Beginn: 59,0
Dosis: 2
Route/Site: SYR / LA

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

Back pain COVID-19 Chills Cough Fatigue Headache Lymphadenopathy Migraine Myalgia Pyrexia SARS-CoV-2 test positive

Symptomtext

COVID breakthrough, back pain, muscle aches, slight cough, headache, swollen lymph nods, exhaustion fatigue, migraines and slight fever and shivers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: COVID test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control norethisterone ethanol estradiol
Allergien: None
Vorherige Impfungen: -

VAERS 2220457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: ND
Alter: 41,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 07.12.2021
Beginn: 11.01.2022
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: IM / UN

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

Migraine Sepsis

Symptomtext

Patient presented to the ED for migraine without status migrainosus on 1/11/22. Patient presented to the ED on 1/16 and was subsequently hospitalized for sepsis. These visits are within 6 weeks of receiving covid vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2219983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 22.12.2021
Beginn: 23.01.2022
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Condition aggravated Malaise Mental status changes Metabolic encephalopathy SARS-CoV-2 test positive

Symptomtext

patient presented to emergency department on 1/23/22 with toxic metabolic encephalopathy patient was admitted for further management of altered mental status patient did not require treatment for symptoms associated with covid-19 patient was discharged to home on 1/25/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: tested at hospital - covid-19 test positive on 1/23/22
Aktuelle Erkrankungen: none known
Vorgeschichte: Advanced Directives and General Issues Medical marijuana use Cardiac and Vasculature Hypertension Endocrine and Metabolic Controlled type 2 diabetes mellitus without complication, without long-term current use of insulin Overweight (BMI 25.0-29.9) Gastrointestinal and Abdominal Gastroesophageal reflux disease Barrett's esophagus without dysplasia Genitourinary and Reproductive Hyponatremia Other male erectile dysfunction Infectious Diseases Osteomyelitis, right thumb COVID-19 Mental Health Panic attack Alcohol abuse, in remission Depression with anxiety Musculoskeletal and Injuries Gout, unspecified cause, unspecified chronicity, unspecified site Neuro RLS (restless legs syndrome) Toxic metabolic encephalopathy Symptoms and Signs Paresthesias
Andere Medikamente: buPROPion (WELLBUTRIN) 100 MG tablet buPROPion (WELLBUTRIN-XL) 150 MG XL tablets clonazePAM (KLONOPIN) 0.5 MG tablet doxycycline hyclate (VIBRAMYCIN) 100 MG capsule DULoxetine (CYMBALTA) 60 MG DR capsule losartan-hydrochlorothiazide (H
Allergien: penicillins
Vorherige Impfungen: -

VAERS 2218095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 06.04.2022
Impfdatum: 16.11.2021
Beginn: 15.12.2021
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / LA

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

Haemoglobin normal Pancytopenia Pneumonia Thrombocytopenia Transfusion

Symptomtext

Pancytopenia, new diagnosis; community-acquired pneumonia - Transfused x3, Hg stable signs without bleeding. Thrombocytopenia, transfused x1 unit before discharge. Complete antibiotic course, Levaquin for CAP. Will follow up with oncology. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2213988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: GA
Alter: 59,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Fatigue Interchange of vaccine products Lymph node pain Lymphadenopathy Neck pain

Symptomtext

Next morning I woke up, neck was sore and the lymph nodes across my neck were painful and swollen again. Was extremely tired that weekend after the booster. I was in the hospital with my son at that time, so I didn't call anybody about it. May have taken some Aleve or my meloxicam for the pain. I don't remember exactly but it took about 2 weeks for the swelling to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Sciatic Arthritis
Andere Medikamente: Apple cider vinegar gummy vitamin daily, meloxicam occasionally for arthritis relief, B complex daily
Allergien: Dust, Seasonal Pollen
Vorherige Impfungen: swollen lymph nodes in neck and arm for first a second dose of Moderna vaccine

VAERS 2198314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 41,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 28.10.2021
Beginn: 07.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / LA

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

Lymphadenopathy Pain Palpitations

Symptomtext

palpitations; upper body aches (arms, shoulders, chest, upper back); "reactive" lymph node under left axillary/left chest area; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 41 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 28Oct2021 (Lot number: FH8027) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation; calcium (VIACTIV [CALCIUM]) (Batch/Lot number: unknown). Relevant medical history included: "Eczema" (unspecified if ongoing); "Acne" (unspecified if ongoing). Concomitant medication(s) included: FLU taken for immunisation, administration date 19Oct2021; VIT B COMPLEXE [VITAMINS NOS]; VIT D [VITAMIN D NOS]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EK9231, Location of injection: Arm Left), administration date: 13Jan2021, when the patient was 40 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL5730, Location of injection: Arm Left), administration date: 23Dec2020, when the patient was 40 years old, for COVID-19 immunization. The following information was reported: PALPITATIONS (non-serious) with onset 07Nov2021, outcome "recovered" (Nov2021), described as "palpitations"; PAIN (non-serious) with onset 07Nov2021, outcome "not recovered", described as "upper body aches (arms, shoulders, chest, upper back)"; LYMPHADENOPATHY (non-serious) with onset 07Nov2021, outcome "not recovered", described as ""reactive" lymph node under left axillary/left chest area". Therapeutic measures were not taken as a result of palpitations, pain, lymphadenopathy. 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: Acne; Eczema.
Andere Medikamente: VIT B COMPLEXE [VITAMINS NOS]; VIT D [VITAMIN D NOS]; VIACTIV [CALCIUM]
Allergien: -
Vorherige Impfungen: -

VAERS 2194437

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WI
Alter: 46,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood disorder Blood test Computerised tomogram thorax Condition aggravated Feeling abnormal Fibrin D dimer increased Pruritus Urticaria

Symptomtext

CLIENT REPORTS HIVES AND INTENSE ITCHING AFTER LEAVING THE FACILITY. CLIENT ALSO REPORTED 2 DAYS ALTER (FRIDAY), THE CLIENT WENT INTO MEDICAL PROVIDER AFTER FEELING "WEIRD. CLIENT HAD BLOOD DRAWN AND WAS ALTER CALLED BACK TO THE HOSPITAL TO HAVE SCANS OF LUNGS TO EB SURE SHE DIDN'T HAVE BLOOD CLOTS. D-DIMER WAS HIGH (5 OR HIGHER). CLIENT REPORTED HAVING ISSUES WITH BLOOD FOR WEEKS AFTER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: BLOOD TESTS. CT SCAN.
Aktuelle Erkrankungen: NONE.
Vorgeschichte: BLOOD DISORDER (HIT).
Andere Medikamente: BLOOD THINNERS, OTHER EMDICATIONS UNKOWN
Allergien: REPORTS ALLERGY TO ANTIBIOTIC (-CYN). NONE OTHER SPECIFIED.
Vorherige Impfungen: FLU VACCINE UNKNOWN.

VAERS 2191462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: -
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 27.01.2022
Beginn: 29.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: OT / LA

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

Lymphadenopathy Palpitations

Symptomtext

Swelling of lymph node in left armpit; Heart palpitations; 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 male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 27Jan2022 13:30 (Lot number: FH8027) as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: VITAMIN D3. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3248, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 10Feb2021, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3248, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 22Jan2021, for COVID-19 immunization. The following information was reported: LYMPHADENOPATHY (non-serious) with onset 29Jan2022, outcome "unknown", described as "Swelling of lymph node in left armpit"; PALPITATIONS (non-serious) with onset 29Jan2022, outcome "unknown", described as "Heart palpitations". The events "swelling of lymph node in left armpit" and "heart palpitations" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of lymphadenopathy, palpitations. Additional information: Prior to the vaccination, the patient was 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 four weeks prior to the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: No other medical history: No
Andere Medikamente: VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 2188115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: SC
Alter: 49,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 18.02.2022
Beginn: 04.03.2022
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Erythema Psoriasis Rash papular Rash pruritic

Symptomtext

2 Weeks after receiving my booster - it appears it overstimulated my immune system and caused psoriasis on my knee which has be resolved the past 5 years in been in remission. Redness covering my knee, swollen-raised rash, pruritus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Treated with steroid cream and monitoring for any additional flare ups
Aktuelle Erkrankungen: none
Vorgeschichte: After pregnancy - had psoriasis on my knees and it has resolved for past 5 years.
Andere Medikamente: multivitamin
Allergien: none to medicines and foods Gluteraldehyde and Propylene glycol - mid reaction on dermatology allergy test. Not sure if a true allergy.
Vorherige Impfungen: -

VAERS 2186232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: HI
Alter: 44,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 30.10.2021
Beginn: 01.12.2021
Tage bis Beginn: 32,0
Dosis: 2
Route/Site: - / LA

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

Chest discomfort Fatigue Pain Palpitations

Symptomtext

Chest pressure & palpitations, entire body feeling sore/fatigue since getting vaccine and continued over the course of months since getting shot!

Weitere VAERSDATA-Felder

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

VAERS 2183802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 54,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Dyspnoea Fatigue Malaise

Symptomtext

Fatigue; Shortness of Breath; Didn''t Feel so Well; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. A 54 year-old male patient received bnt162b2 (BNT162B2), administration date 23Dec2021 (Lot number: FH8027) at the age of 54 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Long COVID", start date: 2020 (ongoing); "He got sick", start date: Jun2021 (unspecified if ongoing), notes: He got sick and went to the hospital; "Pneumonia", start date: Jun2021 (unspecified if ongoing), notes: He wound up getting pneumonia again and his organs were shutting down; "Organs were shutting down", start date: Jun2021 (unspecified if ongoing), notes: He wound up getting pneumonia again and his organs were shutting down; "Infection through his entire body", start date: Jun2021 (unspecified if ongoing), notes: He had pneumonia and infection through his entire body and organs were shutting down.; "He had to learn to walk and talk all over again", start date: Jun2021 (unspecified if ongoing), notes: He had to learn to walk and talk all over again. The patient took concomitant medications. The following information was reported: FATIGUE (non-serious) with onset 23Dec2021, outcome "recovered" (25Dec2021), described as "Fatigue"; DYSPNOEA (non-serious) with onset 23Dec2021, outcome "recovered" (25Dec2021), described as "Shortness of Breath"; MALAISE (non-serious) with onset 23Dec2021, outcome "recovered" (25Dec2021), described as "Didn''t Feel so Well". Additional information: Dates for Concomitant Products Blood Pressure Medication: (Start: Unspecified Stop: Ongoing). Caller states her husband had Covid in 2020 and then he became a long hauler. Caller states then last year, he was in the hospital and his organs were shutting down and he wound up getting Covid again and he was transferred from one hospital to another. Caller states they had to wait and wait to see when he could get a vaccine. Caller states he got his first vaccine 23Dec2021, and he recently got his second one on 14Jan2022. Caller states because he has long hauler Covid, he always has fatigue and shortness of breath but they were a little more and he didn't feel so good but that passed in 2 days and they didn't think much of it. Caller states with the second dose it was different. Caller states he does not have a rash on his body, but he is continuously itchy and his insides are shaky and his blood pressure has been escalated more than normal. Caller states the last 2 days his blood pressure has been coming down. Caller states the recording said the itching could be a side effect from the vaccine, is it. Treatment: Lotion. Caller's husband received the first dose of the Pfizer COVID-19 Vaccine on Dec2021 and Second dose on Jan2022 but experienced serious side effects specially after the second dose and so she wanted to know if her husband should get the booster dose. Her husband has had both COVID-19 vaccine doses. He experienced side effects from both vaccines and the second vaccine was worse. 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: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Long COVID
Vorgeschichte: Medical History/Concurrent Conditions: Activities of daily living impaired (He had to learn to walk and talk all over again); Infection (He had pneumonia and infection through his entire body and organs were shutting down.); Multiorgan failure (He wound up getting pneumonia again and his organs were shutting down); Pneumonia (He wound up getting pneumonia again and his organs were shutting down); Sickness (He got sick and went to the hospital)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2178293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 36,0
Geschlecht: M
Eingang: 14.03.2022
Impfdatum: 01.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Blood test Cardiac failure Cardiac imaging procedure normal Cardioversion Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Dyspnoea exertional Echocardiogram abnormal Lymphadenopathy Muscular weakness Pericardial effusion Pleural effusion Ultrasound scan normal

Symptomtext

After within a week of the vaccination I had a lymph node on left armpit wore really swollen. After a week that went away. Then in December I started feeling shortness of breath very simple task will leave me out of breath and that had prompted me to see a doctor on January 10th and we had an ultrasound and the ultrasound didn't show anything. On January 13th I went and got a CT scan of chest and abdomen and it show some lymph and show I had small amount of fluid around my heart and lung. The 14th I went in and had blood work done and in the afternoon I had an Echocardiogram and it showed I was having heart failure atrial fibrillation. I had to go to ER and they shocked my heart to its normal rhythm. I stayed in the hospital for 3 days. Before I went home, I had an MRI on my heart, and I didn't have any inflammation on my heart it looked normal but it was really weak. They put me on medication to help support my heart so it can build itself back up to normal strength. I went to an appointment it my heart is building his way up to his strength.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: 3,0
Labordaten: Ultrasound, CT, Blood work, MRI, Echocardiogram.
Aktuelle Erkrankungen: Cold.
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2178006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 14.03.2022
Impfdatum: 16.11.2021
Beginn: 11.12.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / RA

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

Bladder catheterisation Dyspnoea Polyuria

Symptomtext

patient with shortness of breath. Patient was tested at her facility was negative. Patient does have a history of hypertension and dyslipidemia. Patient is a status post bilateral below the knee amputation- this was due to recurrent blood clots in her lower extremities and complications from those blood clot she is not currently anticoagulated. She has been given Levaquin and Lasix in the ED, Foley has been placed and has been diuresing well. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2177990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NH
Alter: 67,0
Geschlecht: F
Eingang: 14.03.2022
Impfdatum: 22.11.2021
Beginn: 25.12.2021
Tage bis Beginn: 33,0
Dosis: 3
Route/Site: SYR / LA

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

Asthma COVID-19 Condition aggravated Dyspnoea Fatigue Headache Oxygen saturation decreased SARS-CoV-2 test positive Sinusitis

Symptomtext

When I caught COVID I had extreme fatigue. I had headaches and difficulty breathing. I was dropping down to 80% and 90% of oxygen. The breathing difficulty continued for about 5 weeks. If I didn't use an inhaler I had issues with my breathing. I was put on a Z-Pak for a 6 day course because the doctors couldn't tell if I had a sinus infection or not because normally I would get bronchitis or asthma when I get a sinus infection. So they prescribed the Z-Pak just to be safe to make sure a sinus infection wasn't the cause for my difficulty breathing. I was behaving as if I had asthma. I had to use an inhaler everyday. The rest of the symptoms went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Cancer Survivor; Recurrent Hernia; Bronchial Induced Asthma
Andere Medikamente: Pantoprazole; Mobic as needed
Allergien: High number of Antibiotics; Dilaudid; Bactrim; Spring Allergies
Vorherige Impfungen: -

VAERS 2168109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 18.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac failure congestive Condition aggravated Dyspnoea Dyspnoea exertional Pneumonia Productive cough Sleep disorder Sputum discoloured

Symptomtext

Patient got her COVID-19 booster shot 1 week prior to admission. Since that point the patient has become gradually more short of breath. She admitted to a positive productive cough that was mostly clear with occasional yellow amounts. The shortness of breath became severe enough that she developed dyspnea walking 10 feet. The patient was unable to sleep at night because laying flat caused her shortness of breath to worsen. Found to have left lower lobe pneumonia which may have contributed congestive heart failure exacerbation. Patient was hospitalized for total of 9 days for IV diuresis as well as treatment for the community-acquired pneumonia. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 22.11.2021
Beginn: 29.01.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Condition aggravated Decreased appetite Disorientation Influenza A virus test negative Influenza B virus test Lethargy Mental status changes Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

Chief Complaint: Patient presents with Altered Mental Status per EMS, pt coming from nursing care facility for AMS, pt is A&Ox1-2 at this time, pt is not eating and lethargic. HPI. Patient is a 64-year-old female presenting to our ED via EMS from her ECF with chief complaint of altered mental status. Patient has a past medical history significant for multiple myeloma in remission, CHF with preserved ejection fraction, CKD, seizure disorder on Keppra, hypertension, hyperlipidemia, CVA. Patient has a mentation baseline of A&Ox2 per EMS report. Patient was recently admitted to hospital for unknown etiology. Review of Systems. Review of systems is limited due to patient's dementia, developmental delay, altered mental status and/or inability to communicate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 20,0
Labordaten: HEALTH SYSTEM; LABORATORY. Chart Review Copy (64 yrs)PT CLASS: Inpatient DEPT: PATIENT STATUS: Discharged GENDER: female BED: ORD DR: AUTH DR: Results Covid-19, Flu, RSV; Contains abnormal data Covid-19, Flu, RSV Status: Final result; Visible to patient: Yes (seen) Next appt: None; Specimen Information: Nasopharyngeal; Swab;0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) Micro Not Detected Detected Abnormal. Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified under CLIA to perform high complexity testing. This test has not been FDA cleared or approved.Specimen Collected: 01/27/22 7:21 PM Last Resulted: 01/27/22 8:29 PM Order Details View Encounter Lab and Collection Details Routing Result History Result Care Coordination Patient Communication
Aktuelle Erkrankungen: Asthma; Bell's palsy; Cancer; Chronic kidney disease; CVA (cerebrovascular; accident); Diastolic dysfunction; Hyperlipidemia; Hypertension; Lower extremity edema Mild; Syncope.
Vorgeschichte: Asthma; Bell's palsy; Cancer; Chronic kidney disease; CVA (cerebrovascular accident) ;Diastolic dysfunction; Hyperlipidemia; Hypertension; Lower extremity edema Mild;Multiple myeloma;Syncope
Andere Medikamente: Aspirin; Azithromycin 1 % OPHTH Solution; Azithromycin 1 % OPHTH Solution; Hydrochlorothiazide (HYDRODIURIL); Mometasone Furo-Formoterol Fum (Dulera) 200-5 MCG/ACT INHAL Aerosol; Senna (SENOKOT); valacyclovir (VALTREX);Albuterol (PROVENTIL,
Allergien: No Known Drug Allergy;
Vorherige Impfungen: -

VAERS 2151097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: FL
Alter: 36,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Palpitations

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Tachycardia-Mild, Additional Details: Patient reported feeling dizzy and heart was racing. She says she suffers from anxiety and it was probably that. She took Clonazepam prescribed by her doctor and wanted rescue called. Rescue arrived and said it was anxiety. She reported feeling better and left with her dad

Weitere VAERSDATA-Felder

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

VAERS 2150994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 34,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 18.10.2021
Beginn: 19.12.2021
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: IM / LA

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

Bronchial disorder COVID-19 Cardiac stress test normal Cough Echocardiogram normal Exposure to SARS-CoV-2 Nasopharyngitis Non-cardiac chest pain Oropharyngeal pain Productive cough SARS-CoV-2 test negative SARS-CoV-2 test positive Sinus disorder

Symptomtext

I was exposed to COVID 12/18/21 by someone who was fully vaccinated, and their only symptom was a runny nose. On 12/19/21 and 12/20/21 I only experienced a sore throat. On 12/21/21 it felt like I had bronchitis with no nasal drip or discharge. On 12/22/21 felt like I had bad cold and sinus symptoms, I did not have a barking cough anymore just a mild wet cough. On 12/23/21 through 12/27/21 I had decreasing cold symptoms. I was nasal symptoms free from the 28th and 29th and on. I did start experiencing chest pains for about a month and half and since then it has gone away. As far as testing I tested negative on the 12/20/21 and 12/22/21 and tested positive on 12/23/21. I followed up with my doctor for chest pains and was ordered an Echocardiogram and Stress Test and my results looks normal and no concerns.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Non-cardiac chest pain
Hospital-Tage: -
Labordaten: Echocardiogram; Stress Test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Mirena IUD
Allergien: Cefaclor
Vorherige Impfungen: -

VAERS 2149537

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 14.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 79,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Back pain Dyspnoea Fatigue

Symptomtext

Extreme joint pain. Lower back pain. Fatigue in January 2022 and current. Intermittent Shortness of breath noticed around January 2022.

Weitere VAERSDATA-Felder

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

VAERS 2137296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NV
Alter: 62,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 27.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Hypoaesthesia Injection site pain Muscle spasms Neck pain Neuralgia Pain Pain in extremity Paraesthesia Pyrexia

Symptomtext

Day after injection, high fever that lasted for 48 hours. 3 days after injection nerve pain radiating from right side of neck, right shoulder and down right arm. Symptoms included severe pain, numbness, tingling, spasms. I believe I have autoimmune nerve damage due to the booster of the Pfizer Covid-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: An MRI has been scheduled. Initially insurance denied the MRI and have to submit to x-ray prior to authorization from insurance.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism
Andere Medikamente: Atorvastatin, levothyroxine, Liothyronine Sodium, Lisinopril-Hydrochlorothiazide
Allergien: Tramadol
Vorherige Impfungen: -

VAERS 2134280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 29,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 19.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: SYR / LA

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

Asthma Condition aggravated

Symptomtext

I have been having asthma flair ups since about a month after the vaccine. I has Sport's induced asthma my entire life and after the 3rd dose of the vaccine, my asthma has been more extreme. I was prescribed a steroid inhaler when I went to the doctor on February 16, 2022 for my asthma to try and control my flair up. I have never had an asthma flair up before this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Common cold.
Vorgeschichte: Asthma.
Andere Medikamente: Adderall XR; Ventolin HFA; Mirena IUD; Women's multivitamins; Biotin; Vitamin D.
Allergien: NKDA; Shrimp allergy.
Vorherige Impfungen: -

VAERS 2131372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: KY
Alter: 30,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 23.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / RA

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

Chest pain Headache Myalgia Oropharyngeal pain

Symptomtext

Chest pain, headache, sore throat, sore muscle

Weitere VAERSDATA-Felder

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

VAERS 1837424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Blood pressure measurement Blood test Burning sensation Condition aggravated Gait inability Drug ineffective Suspected COVID-19 Gait disturbance Hypoaesthesia Musculoskeletal stiffness Hypertension Myalgia Pain in extremity Movement disorder Neuralgia

Symptomtext

not able to move her right leg.; 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 female patient received bnt162b2 (BNT162B2) (Batch/Lot number: unknown) 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, SINGLE), for Covid-19 immunization. The following information was reported: MOVEMENT DISORDER (non-serious), outcome "unknown", described as "not able to move her right leg.". Additional information: Patient was a consumer who received the second dose for Pfizer-BioNTech COVID-19 vaccine 3 months ago and is not able to move her right leg. Patient thought Pfizer is not doing anything about side effects of the vaccine and that other people have been reporting this adverse event on the internet. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2113090

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge FH8027

moderat

Staat: WI
Alter: 63,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 06.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Aphasia Chest X-ray normal Cough Dyspnoea SARS-CoV-2 test negative

Symptomtext

In the morning around 8:00 Chronic cough all day long. I could not sing. I slept ok but I couldn't breath properly, I took home remedies to feel better. It lasted 7 weeks. It cleared up at last week of January.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: covid19 test and chest x-ray. The result were fine.
Aktuelle Erkrankungen: None
Vorgeschichte: N/A
Andere Medikamente: Hydrochlorothiazide 25mg. multivitamins
Allergien: None
Vorherige Impfungen: -

VAERS 2101391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: VA
Alter: 29,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 29.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / -

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

Anxiety Balance disorder Chest discomfort Chest pain Palpitations Paraesthesia Troponin increased

Symptomtext

Patient is a 29-year-old female with no significant past medical problems who presents emergency department complaining of a 1 month history of chest pain. Patient states symptoms started about 6 days after she got her Pfizer Covid booster. She states the following week she started to have some heart palpitations like her heart was beating out of her chest. States she went to the emergency department due to some chest pain and her heart rate was found to be in the 140s. States that the run emergency department told her that all of her lab work was fine and thought it might be due to anxiety and was advised to follow up with cardiology. Patient states she did not follow-up with cardiology and has had persistent symptoms since then. She states that symptoms occur randomly and are not exertional. Her most recent episode was this morning. States she was driving home after night shift and felt like the chest pain came back with bilateral arm tingling. She states she does not necessarily feel lightheaded or dizzy but feels like she is going to fall down and die. She states she still has some persistent chest pressure but the sensation of dying has passed. States it never feels like "an elephant on (her) chest." No more tingling. She denies any diaphoresis, shortness of breath, vomiting. Patient denies any history of heart problems. Denies any family history of heart problems under the age of 65. She has a ParaGard IUD. No history of blood clots. No other complaints today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 31-Jan-2022 TROPONIN: <6 Test Unit NANOGRAMS PER MILLILITRE <6 High Test Range 19 31-Jan-2022 TROPONIN: 17 Test Unit NANOGRAMS PER MILLILITRE <6 High Test Range 19 Sudden rise in troponin, though not above normal upper limit.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2096035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 13.12.2021
Beginn: 05.02.2022
Tage bis Beginn: 54,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain Headache SARS-CoV-2 test positive

Symptomtext

chest pain, headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: 2/5/22 +covid test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2076400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WI
Alter: 17,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Dyspnoea Illness Pain Rash

Symptomtext

Spoke to mother, by phone on 01/21/2022. She reported that patient had been ill for 2 days following her vaccine. She experienced body aches, shortness of breath and a fine rash on her chest the evening following her vaccine. At the time that mother reported this, her symptoms had all resolved. It was recommended that she get written approval from a medical provider prior to her receiving her second dose. Spoke to mother by phone on 01/25/22 and she reported that their pediatrician was fine with her getting the second dose however upon further questioning, she had spoke with the nurse on the Nurse Advice Line and not the medical provider. When patient presented for second vaccine, she reported that she also had chills. Vaccine was not given at this appointment.

Weitere VAERSDATA-Felder

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

VAERS 2075549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 59,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 20.10.2021
Beginn: 28.01.2022
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Cardiac ablation Dyspnoea SARS-CoV-2 antibody test SARS-CoV-2 test positive

Symptomtext

This is a 60-year-old male patient with a past medical history of coronary artery disease a recent diagnosis of atrial fibrillation status post ablation a month ago started having shortness of breath after ablation. Shortness of breath was initially off and on. It got worse in last 2 days Patient denies any chest pain Shortness of breath was worse on laying down

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: 01/28/2022 - SARS-CoV-2 Antigen (++) 01/29/2022 - SARS-COV-2 PCR (++), IgM 0.11, IgG 0.07
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, Myocardial Infarction; Addt'l Med History Atrial fibrillation. Significant Surg Hx As Listed Common Appendectomy. Smoking Status Former Smoker.
Andere Medikamente: apixaban (Eliquis) 5 mg Tablet Directions: 1 tablet oral twice a day (Active) aspirin (Adult Low Dose Aspirin) 81 mg tablet,delayed release (DR/EC) Directions: 1 tablet oral daily (Active) atorvastatin 40 mg Tablet Directions: 1 tabl
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2075513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: KY
Alter: 82,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 31.01.2021
Beginn: 28.01.2022
Tage bis Beginn: 362,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

pt vaccinated/boosted admitted for covid pna on dexamethasone/remdesivir

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: 1/28 COVID positive
Aktuelle Erkrankungen: none
Vorgeschichte: no known
Andere Medikamente: Magnesium, acetaminophen, albuterol sulfate HFA, allopurinol, amiodarone, aspirin, atorvastatin, carvedilol, erythromycin, folic acid, levETIRAcetam, multivitamin with minerals, mupirocin, nitroglycerin, omeprazole, and oxybutynin XL
Allergien: nkda
Vorherige Impfungen: -

VAERS 2029249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 03.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Asthenia Condition aggravated Muscular weakness Neuropathy peripheral Sensory disturbance Pain Small fibre neuropathy

Symptomtext

weakness/difficulty lifting left foot; small fiber neuropathy shocking/stabbing sensations; Difficulty lifting left foot; Shocking/Stabbing sensation; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 03Jan2022 (Lot number: FH8027) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "amyloidosis polyneuropathy including small fiber neuropathy" (unspecified if ongoing), notes: amyloidosis polyneuropathy including small fiber neuropathy; "amyloidosis polyneuropathy including small fiber neuropathy" (unspecified if ongoing), notes: amyloidosis polyneuropathy including small fiber neuropathy. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 2, Batch/Lot No: ER8737, Location of injection: Arm Left), administration date: 05Apr2021, when the patient was 41 years old, for Covid-19 Immunization; Bnt162b2 (Dose 1, Batch/Lot No: EN6206, Location of injection: Arm Left), administration date: 15Mar2021, when the patient was 41 years old, for Covid-19 Immunization. The following information was reported: MUSCULAR WEAKNESS (non-serious) with onset 04Jan2022, outcome "not recovered", described as "weakness/difficulty lifting left foot"; SMALL FIBRE NEUROPATHY (non-serious) with onset 04Jan2022, outcome "not recovered", described as "small fiber neuropathy shocking/stabbing sensations"; PAIN (non-serious) with onset 04Jan2022, outcome "not recovered", described as "Difficulty lifting left foot"; SENSORY DISTURBANCE (non-serious) with onset 04Jan2022, outcome "not recovered", described as "Shocking/Stabbing sensation". Therapeutic measures were not taken as a result of muscular weakness, small fibre neuropathy, pain, sensory disturbance. Additional Information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not diagnosed with COVID-19 since the vaccination. Increase in neuropathy symptoms the next day following vaccine including small fibre neuropathy shocking/stabbing sensations and weakness/difficulty lifting left foot. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Polyneuropathy (amyloidosis polyneuropathy including small fiber neuropathy); Small fibre neuropathy (amyloidosis polyneuropathy including small fiber neuropathy)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2029249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 03.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Condition aggravated Muscular weakness Neuropathy peripheral Sensory disturbance Pain Small fibre neuropathy

Symptomtext

weakness/difficulty lifting left foot; small fiber neuropathy shocking/stabbing sensations; Difficulty lifting left foot; Shocking/Stabbing sensation; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 03Jan2022 (Lot number: FH8027) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "amyloidosis polyneuropathy including small fiber neuropathy" (unspecified if ongoing), notes: amyloidosis polyneuropathy including small fiber neuropathy; "amyloidosis polyneuropathy including small fiber neuropathy" (unspecified if ongoing), notes: amyloidosis polyneuropathy including small fiber neuropathy. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 2, Batch/Lot No: ER8737, Location of injection: Arm Left), administration date: 05Apr2021, when the patient was 41 years old, for Covid-19 Immunization; Bnt162b2 (Dose 1, Batch/Lot No: EN6206, Location of injection: Arm Left), administration date: 15Mar2021, when the patient was 41 years old, for Covid-19 Immunization. The following information was reported: MUSCULAR WEAKNESS (non-serious) with onset 04Jan2022, outcome "not recovered", described as "weakness/difficulty lifting left foot"; SMALL FIBRE NEUROPATHY (non-serious) with onset 04Jan2022, outcome "not recovered", described as "small fiber neuropathy shocking/stabbing sensations"; PAIN (non-serious) with onset 04Jan2022, outcome "not recovered", described as "Difficulty lifting left foot"; SENSORY DISTURBANCE (non-serious) with onset 04Jan2022, outcome "not recovered", described as "Shocking/Stabbing sensation". Therapeutic measures were not taken as a result of muscular weakness, small fibre neuropathy, pain, sensory disturbance. Additional Information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not diagnosed with COVID-19 since the vaccination. Increase in neuropathy symptoms the next day following vaccine including small fibre neuropathy shocking/stabbing sensations and weakness/difficulty lifting left foot. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Polyneuropathy (amyloidosis polyneuropathy including small fiber neuropathy); Small fibre neuropathy (amyloidosis polyneuropathy including small fiber neuropathy)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2068060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OH
Alter: 33,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain upper Chest pain Dyspnoea Fatigue Headache Immunisation SARS-CoV-2 test Vaccination site pain Vomiting

Symptomtext

headache; Injection site pain; stomach ache; vomiting; extreme fatigue; chest pain; difficulty breathing in mask; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33 year-old male patient received bnt162b2 (BNT162B2), administration date 08Dec2021 (Lot number: FH8027) at the age of 33 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "ADHD" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "Known allergies: Cat" (unspecified if ongoing); "Known allergies: Dog" (unspecified if ongoing). Concomitant medication(s) included: ADDERALL; CRESTOR; XYZAL; PROTONIX [OMEPRAZOLE]. Past drug history included: Known allergies: penicillin, reaction(s): "drug hypersensitivity"; Known allergies: gadolinium, reaction(s): "Known allergies: gadolinium". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0158, Location of injection: Arm Left), administration date: 21Apr2021, when the patient was 32 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Arm Left), administration date: 31Mar2021, when the patient was 32 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 08Dec2021, outcome "unknown", described as "booster"; HEADACHE (non-serious) with onset 09Dec2021, outcome "unknown", described as "headache"; VACCINATION SITE PAIN (non-serious) with onset 09Dec2021, outcome "unknown", described as "Injection site pain"; ABDOMINAL PAIN UPPER (non-serious) with onset 09Dec2021, outcome "unknown", described as "stomach ache"; VOMITING (non-serious) with onset 09Dec2021, outcome "unknown", described as "vomiting"; FATIGUE (non-serious) with onset 09Dec2021, outcome "unknown", described as "extreme fatigue"; CHEST PAIN (non-serious) with onset 09Dec2021, outcome "unknown", described as "chest pain"; DYSPNOEA (non-serious) with onset 09Dec2021, outcome "unknown", described as "difficulty breathing in mask". The events "headache", "injection site pain", "stomach ache", "vomiting", "extreme fatigue", "chest pain" and "difficulty breathing in mask" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Facility type vaccine was Pharmacy or Drug Store. No other vaccine in four weeks. No covid prior vaccination. Tested post vaccination for covid. Other medications in two weeks included MULTIVITAM. If covid prior vaccination: No. If covid tested post vaccination: Yes. Covid test post vaccination. Covid test type post vaccination=Nasal Swab. Covid test name post vaccination=SARS-COV2-INFLUENZA A&B, RSV PCR, Covid test date=14Dec2021, Covid test result=Negative. Covid test type post vaccination=Nasal Swab, Covid test name post vaccination= PCR, Covid test date=06Jan2022, Covid test result=Pending. Covid test type post vaccination=Nasal Swab, Covid test name post vaccination=SARS-COV-2 RNA, QL NAAT, RTPCR/TMA, Covid test date=27Dec2021, Covid test result=Negative No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20220106; Test Name: PCR; Result Unstructured Data: Test Result:Pending; Comments: Nasal Swab; Test Date: 20211227; Test Name: SARS-COV-2 RNA, QL NAAT, RT PCR/TMA; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211214; Test Name: SARS-COV2-INFLUENZA A'||CHR(38)||'B, RSV PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD; Allergic to dogs; Allergy to animal; High cholesterol.
Andere Medikamente: ADDERALL; CRESTOR; XYZAL; PROTONIX [OMEPRAZOLE].
Allergien: -
Vorherige Impfungen: -

VAERS 2065927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OR
Alter: 52,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 23.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

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

Chest X-ray Chest discomfort Echocardiogram normal Electrocardiogram Exercise tolerance decreased Laboratory test Pain Palpitations Swelling Tremor

Symptomtext

pt stated after getting his 2nd dose of the covid vaccine he started having palpitations, he had shaking and quivering in his chest. The shooting pain caused him to go to the ER where they did a EKG and chest X-Ray. They discharged him to go home where he continued to have these symptoms. Next day he went back to the ER and they did more test. He started having a feeling of swelling around his heart, like there was a bubble inside his chest. He was referred to the Cardiologist where they performed a echocardiogram but could not find anything wrong. He continues to have these symptoms so was put on betablockers. He was very athletic before getting vaccinated and now he cannot do anything physical. He went to a second cardiologist which did nothing for him. He now has a third cardiologist that is trying to treat him and figure out what is going on with him. He continues to have the same pressure on his chest and quivering of his heart just like he had a few days after getting his second vaccine. He is not able to train or run and is still in pain daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: lab work EKG Chest XRAY echocardiogram TMT
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: none
Allergien: nka
Vorherige Impfungen: -

VAERS 2058861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Chills Headache Injected limb mobility decreased Injection site warmth Neuralgia Pain Pain in extremity Pyrexia Swelling Tenderness

Symptomtext

with administration felt a slight nerve twinge that went up the right side of my neck near the carotid, after waiting 15 minutes nothing more; after about an hour felt warm at injection site and swelling and tenderness to the right side of my clavicle, joint pain, feeling feverish but temp was wnl, headache and generalized achiness. At approx. 2300, had chills for about 2 hours; On Saturday, still had swelling and tenderness on the right side clavicle and could barely move right arm; Sunday still had tenderness and swelling but able to move right arm a little more but still having soreness. Monday still having tenderness and swelling at right clavicle and soreness in right arm. Did take aleve on Sunday for pain. On Monday, did notify workplace and my PCP of adverse reactions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: December 30 had flu symptoms, achy, muscle aches, headache, no fever; was tested for covid was negative
Vorgeschichte: hypothyroid
Andere Medikamente: synthroid ASA
Allergien: tylenol with codeine, mobic
Vorherige Impfungen: -

VAERS 2057048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WI
Alter: 54,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Feeling abnormal Hypoaesthesia Immunisation Paraesthesia

Symptomtext

mild numbness above face area upper lip; tingling in cheeks; brain fog for 5 days; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Dec2021 11:30 (Lot number: FH8027) at the age of 54 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: some sulfa" (unspecified if ongoing), notes: Known allergies: some sulfa; "Mold allergy" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0183, Location of injection: Arm Left), administration date: 18May2021, when the patient was 53 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0175, Location of injection: Arm Left), administration date: 27Apr2021, when the patient was 53 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 21Dec2021 11:30, outcome "unknown", described as "booster"; HYPOAESTHESIA (non-serious) with onset 21Dec2021 11:45, outcome "not recovered", described as "mild numbness above face area upper lip"; PARAESTHESIA (non-serious) with onset 21Dec2021 11:45, outcome "not recovered", described as "tingling in cheeks"; FEELING ABNORMAL (non-serious) with onset 21Dec2021 11:45, outcome "recovered" (26Dec2021), described as "brain fog for 5 days". Therapeutic measures were not taken as a result of hypoaesthesia, paraesthesia, feeling abnormal. Additional information: It was reported that patient administer vaccine at Doctor's office/urgent care. The patient did not receive any other vaccine in four weeks and received multi vitamin medications in two weeks. It was also reported that patient did not suffer from covid prior vaccination and did not underwent covid tested post vaccination. The patient had experienced mild numbness above face area upper lip and tingling in cheeks 20 min after shot on drive home, continued mild for 2 more days, brain fog for 5 days. Face numbness tingling issue reappeared 05Jan2022. 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: Allergy to molds; Sulfonamide allergy (Known allergies: some sulfa)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2050565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 17.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Condition aggravated Contusion Fibromyalgia Heart rate increased Inflammation Myalgia

Symptomtext

Increased heart rate. Heart rate of 100 at all times after vaccine. Excessive bruising on arms and legs. Widespread inflammation and pain in muscles in joints. Fibromyalgia pain increase with little help by using medication . Never had to use medication to treat this condition prior to COVID-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Fibromyalgia and IBS
Andere Medikamente: None.
Allergien: Flagyl
Vorherige Impfungen: -

VAERS 2047876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

moderat

Staat: MA
Alter: 69,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 16.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: IM / RA

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

Blood test normal Chest X-ray normal Condition aggravated Costochondritis Electrocardiogram normal Musculoskeletal chest pain

Symptomtext

Costochondritis, recurring ( developed same day as 2nd shot and lasted 4 months), this time more severe sharp chest wall pain ribs and sternum, 2 weeks after booster. ,Continuous, does not subside, to date, no easing of pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 6/17/21 after 2nd vaccine, had workup ekg, chest X-ray, blood work, exam by Dr. all normal. First episode of costochondritis in my life.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, IBS, Ostio arthritis,
Andere Medikamente: Zyrtec, singulare, protonix, Wellbutrin, Prozac, trazadone, nasonex, astelin, citracal with vit. D, multivitamin
Allergien: Sulfur, ampicillin
Vorherige Impfungen: 3/29/21 after 2nd Pfizer shot.

VAERS 2024299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OH
Alter: 15,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain Asthenia Cough Dizziness Dyspnoea Arthralgia Decreased appetite Fatigue Headache Myalgia Nausea Sinus disorder Pain Pyrexia Somnolence Vomiting

Symptomtext

fever, fatigue, dizzy, nausea, sleepy, achy all over, abd pain, short of breath and weakness with cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Autism, ADHD, anemia, chronic constipation, chronic urticaria, chronic constipation,
Andere Medikamente: Azelasatine, zyrtec, melatonin 5, omeprazole 20, sertraline 25, ziprasidone 40,
Allergien: docusate, dander, grass pollen, house dust, latex, metamucil, nickel, mold, miralax.
Vorherige Impfungen: -

VAERS 2024299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OH
Alter: 15,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal pain Asthenia Cough Dizziness Dyspnoea Arthralgia Decreased appetite Fatigue Headache Myalgia Nausea Sinus disorder Pain Pyrexia Somnolence Vomiting

Symptomtext

fever, fatigue, dizzy, nausea, sleepy, achy all over, abd pain, short of breath and weakness with cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Autism, ADHD, anemia, chronic constipation, chronic urticaria, chronic constipation,
Andere Medikamente: Azelasatine, zyrtec, melatonin 5, omeprazole 20, sertraline 25, ziprasidone 40,
Allergien: docusate, dander, grass pollen, house dust, latex, metamucil, nickel, mold, miralax.
Vorherige Impfungen: -

VAERS 2035830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 29,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 02.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: - / RA

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

Asthenia Computerised tomogram Disturbance in attention Dizziness Electroencephalogram Feeling abnormal Migraine Muscle twitching Tremor Vision blurred

Symptomtext

Severe tremors, muscle twitches, occasional blurred vision, sudden weakness, light headed, foggy clouded mind, difficulty concentrating, and migraines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: EEG, CAT.
Aktuelle Erkrankungen: -
Vorgeschichte: PTSD, Tinnitus, Degraded Disc
Andere Medikamente: NONE
Allergien: NKA
Vorherige Impfungen: -

VAERS 2031204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Burning sensation Dysphagia Dyspnoea Hypoaesthesia Paraesthesia Similar reaction on previous exposure to drug

Symptomtext

Similar to what happened in April, almost like clockwork, about 10 hours after receiving the shot, the first thing I noticed, I was having trouble swallowing. Then I had pins and needles and burning that started from my feet and spread throughout my whole body. After some time, the numbness and tingling was then more prominent on the left side of my body. (I had received second shot in left arm, but the booster shot in right arm, so this was strange). I had trouble breathing, don't know whether this was anxiety or a reaction. I immediately took a Benadryl and 1/2 a Xanax. It subsided after a couple of hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Xanax 0.5 MG Tablet Taking CeleXA 10 MG Tablet Taking Valtrex 500 MG Tablet Taking Vagifem 10 MCG Tablet Taking Levothyroxine Sodium 100 MCG Tablet
Allergien: Amoxicillin: hives Levaquin: lower extremity pain Latex: rash
Vorherige Impfungen: pfizer Covid vaccine 04/09/2021

VAERS 2029038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

moderat

Staat: VA
Alter: 45,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Hypertension Vertigo

Symptomtext

High blood pressure lasting 2 days self monitored beginning before I got home from the facility. Starting day 2 vertigo that lasted for 8 days (severe for the first 5). Treated at home with rest and limited movement, no medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None. Did not seek medical help because the symptoms were similar to dose 2 and no medication was given then.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothroid
Allergien: None known
Vorherige Impfungen: Pfizer covid vaccine (1/23/2021 and 2/11/2021)

VAERS 2018530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CT
Alter: 36,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 20.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Fatigue Headache Immunisation Migraine Nausea Pain assessment Pain in extremity Paraesthesia Photophobia Sensitive skin Sleep disorder Vomiting

Symptomtext

light sensitivity; nausea; vomiting; full migraine/severe migraine persisted for 9 hours; severe headache/Light headache in the morning and a more severe headache returning; Severe arm pain preventing sleep when sleeping on opposite side/pain 6/10; severe arm pain preventing sleep when sleeping on opposite side (left arm injection, sleeping on right side); skin sensitivity with tingling sensation on any touch to the skin; skin sensitivity with tingling sensation on any touch to the skin; Dose number: 3; fatigue; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 36 year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), administered in arm left, administration date 20Dec2021 14:00 (Lot number: FH8027) at the age of 36 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Occipital Neuralgia" (unspecified if ongoing); "exercise-induced asthma" (unspecified if ongoing); "chronic bronchitis" (unspecified if ongoing); "Covid" (unspecified if ongoing), notes: if covid prior vaccination: Yes. Concomitant medication(s) included: ETONOGESTREL. Past drug history included: Aspartame, reaction(s): "Allergy: aspartame (Headaches, Nausea)", notes: known allergies: aspartame (headaches, nausea); Aspartame, reaction(s): "Allergy: aspartame (Headaches, Nausea)", notes: known allergies: aspartame (headaches, nausea); Percocet, reaction(s): "Allergy: Percoset (Nausea, vomiting, hives)", notes: known allergies: Percoset (nausea, vomiting, hives),; Percocet, reaction(s): "Allergy: Percoset (Nausea, vomiting, hives)", notes: known allergies: Percoset (nausea, vomiting, hives),; Percocet, reaction(s): "Allergy: Percoset (Nausea, vomiting, hives)", notes: known allergies: Percoset (nausea, vomiting, hives),. Vaccination history included: Comirnaty (First Dose, lot number: EL3247, vaccine location: Left arm), administration date: 10Mar2021, when the patient was 35 years old, for Covid-19 Immunization; Comirnaty (Second Dose, lot number: EP6955, vaccine location: Left arm), administration date: 31Mar2021, when the patient was 35 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 14:00, outcome "unknown", described as "Dose number: 3"; PAIN IN EXTREMITY (non-serious) with onset 21Dec2021 03:00, outcome "unknown", described as "Severe arm pain preventing sleep when sleeping on opposite side/pain 6/10"; SLEEP DISORDER (non-serious) with onset 21Dec2021 03:00, outcome "unknown", described as "severe arm pain preventing sleep when sleeping on opposite side (left arm injection, sleeping on right side)"; HEADACHE (non-serious) with onset 21Dec2021 12:00, outcome "recovered" (22Dec2021 18:00), described as "severe headache/Light headache in the morning and a more severe headache returning"; MIGRAINE (non-serious) with onset 21Dec2021 14:00, outcome "recovered" (21Dec2021 23:00), described as "full migraine/severe migraine persisted for 9 hours"; PHOTOPHOBIA (non-serious) with onset 21Dec2021 15:00, outcome "recovered" (21Dec2021 16:00), described as "light sensitivity"; NAUSEA (non-serious) with onset 21Dec2021 15:00, outcome "recovered" (21Dec2021 16:00), described as "nausea"; VOMITING (non-serious) with onset 21Dec2021 15:00, outcome "recovered" (21Dec2021 16:00), described as "vomiting"; FATIGUE (non-serious) with onset Dec2021, outcome "unknown", described as "fatigue"; PARAESTHESIA (non-serious), SENSITIVE SKIN (non-serious) all with onset 21Dec2021, outcome "recovered" (Dec2021) and all described as "skin sensitivity with tingling sensation on any touch to the skin". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, sleep disorder, headache, migraine, photophobia, nausea, vomiting, fatigue, paraesthesia, sensitive skin. The patient didn't received any other vaccines within 4 weeks prior to the COVID vaccine List of any other medications the patient received within 2 weeks of vaccination:Etonogestrel - EE Vaginal Ring .12/.015. Reported Event: 13 Hours post vaccination (3am) severe arm pain preventing sleep when sleeping on opposite side (left arm injection, sleeping on right side) - pain 6/10. 22 hours (12p) post vaccination severe headache onset worsening to full migraine by 24 hours (2p) with light sensitivity and nausea, vomiting at 25 hours (3p) lasted for 1 hour (until 4p), severe migraine persisted for 9 hours until Hour 33 (11p). 22H post vaccination also experienced skin sensitivity with tingling sensation on any touch to the skin, lasted approximately 1-2 hours. Mild headache and fatigue remained on 2nd day after booster, with a light headache in the morning and a more severe headache returning 48-51 hours/2-5p before ending around 6p. Yes, reported that covid prior vaccination. The patient had been tested for COVID-19 was no, Device Date : 22Dec2021 Follow-Up (04Jan2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20211221; Test Name: pain; Result Unstructured Data: Test Result:6/10
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma exercise induced; Chronic bronchitis; COVID-19 (if covid prior vaccination: Yes); Occipital neuralgia
Andere Medikamente: ETONOGESTREL
Allergien: -
Vorherige Impfungen: -

VAERS 2018321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CT
Alter: 55,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Arthralgia Body temperature Body temperature decreased Chills Condition aggravated Feeling abnormal Grip strength decreased Immunisation Lymphadenopathy Pain Pain in extremity

Symptomtext

Sore arm; Joint aches; Swollen lymph nodes; No hand grip strength; Can't get warm; Chills; Not feeling great; lymphnode swelling got worse; Aches; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 13Dec2021 11:30 (Lot number: FH8027) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Breast Cancer", start date: 2018 (unspecified if ongoing), notes: other medical history: Breast Cancer - 2018; "Known allergies: Sulfa drugs" (unspecified if ongoing), notes: Verbatim: Known allergies: Sulfa drugs. Concomitant medication(s) included: TAMOXIFEN; LIPITOR; CELEBREX; TYLENOL. Past drug history included: Levequin, reaction(s): "Known allergies: Levequin", notes: Verbatim: Levequin. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Right), administration date: 23Mar2021, when the patient was 54 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Right), administration date: 01Mar2021, when the patient was 54 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 13Dec2021 11:30, outcome "unknown", described as "Booster"; PAIN IN EXTREMITY (non-serious) with onset 14Dec2021 10:00, outcome "recovering", described as "Sore arm"; ARTHRALGIA (non-serious) with onset 14Dec2021 10:00, outcome "recovered" (Dec2021), described as "Joint aches"; LYMPHADENOPATHY (non-serious) with onset 14Dec2021 10:00, outcome "not recovered", described as "Swollen lymph nodes"; GRIP STRENGTH DECREASED (non-serious) with onset 14Dec2021 10:00, outcome "recovering", described as "No hand grip strength"; BODY TEMPERATURE DECREASED (non-serious) with onset 14Dec2021 10:00, outcome "recovering", described as "Can't get warm"; CHILLS (non-serious) with onset 14Dec2021 10:00, outcome "recovered" (Dec2021), described as "Chills"; PAIN (non-serious) with onset 14Dec2021, outcome "unknown", described as "Aches"; FEELING ABNORMAL (non-serious) with onset 14Dec2021 10:00, outcome "recovering", described as "Not feeling great"; CONDITION AGGRAVATED (non-serious) with onset 14Dec2021 10:00, outcome "not recovered", described as "lymphnode swelling got worse". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, arthralgia, lymphadenopathy, grip strength decreased, body temperature decreased. Additional Information: Patient received 3 doses. She did not receive other vaccine in 4 weeks. She received multivitamins in last two weeks. She had swollen lymph nodes (more severe in right arm, but she had fewer lymph nodes on the left), joint aches, no hand grip strength, can't get warm. She did not have covid prior vaccination and not tested positive after covid vaccination. Device timestamp: 15Dec2021. She received her booster around 11:30 am on 13Dec21. She was not feeling great around 10 am on 14Dec2021 and the aches, chills, lymph node, swelling got worse throughout the day, so she went to bed. She reported first thing (8 am) 15Dec2021 at which point she still wasn't feeling great, but better than the afternoon before. She still had lymph node swelling (8 am 16Dec2021) but the joint aches and chills were gone. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20211214; Test Name: body temperature; Result Unstructured Data: Test Result:decreased
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer (other medical history: Breast Cancer - 2018); Sulfonamide allergy (Verbatim: Known allergies: Sulfa drugs)
Andere Medikamente: TAMOXIFEN; LIPITOR; CELEBREX; TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 2014783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: GA
Alter: 54,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 26.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

C-reactive protein Chest pain Cough Dyspnoea Electrocardiogram Exercise tolerance decreased Joint swelling Palpitations Troponin

Symptomtext

Racing Heartbeat, cough not related to any type of chest congestion etc., unable to tolerate exercise, chest pain which was much worse when laying down, occasional shortness of breath and swelling of ankles. Current treatment: 650mg aspirin TID for 7 days, then 650mg daily for 7 days colchicine 0.6 mg tablet 1 by mouth 2 (two) times a day. (180 tablets) omeprazole (PRILOSEC) 40 MG capsule 1 capsule (40 mg total) by mouth daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Taken 12/29- ECG 12 lead Blood Tests (HIGH SENSITIVITY CRP, TROPONIN)
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Women vitamins, melatonin, liquid zinc, liquid magnesium, emergenC, fish oil, collagen pills
Allergien: none
Vorherige Impfungen: 2nd dose Pfizer Covid-19 Vaccine 4/17/2021 Age 54 Heart related issues primarily palpitations and PVCs

VAERS 2010641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 06.01.2022
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: unbekannt Erholt: nein

Chest discomfort Fatigue Feeling abnormal Headache Heavy menstrual bleeding Hypoaesthesia Menstruation irregular Mobility decreased Muscle disorder Nausea Palpitations Premenstrual syndrome Vomiting

Symptomtext

heart palpitation started couple minutes after the shot, last for couple minutes. couple hours later, left leg felt expanding, numb, legs felt uneven. vomit at lunch next day, and felt nausea got zofran , HA , brain fog, fatigue. Day 3 woke up with chest tightness, stayed in bed almost whole day, heavy cycle came on day 3 afternoon with lots PMS. I had IUD, heavy cycle and PMS is not expected. Spent 5 days in bed after 1st shot. Got 1 wk break, cycle started again and became heavy after 2nd shot. Similar, but more severe symptoms after 2nd shot, my legs still felt uneven, and continuously frequent HA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamin D, vitamin C, Zinc
Allergien: alcohol
Vorherige Impfungen: -

VAERS 2008810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: TN
Alter: 47,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Axillary mass Chest pain Fear Influenza like illness Pain in extremity

Symptomtext

I have had so many side effects after getting the third vaccine shot. First, I feel like I have had the flu for several weeks. Second, I feel like the left side of my body has been beaten up (with pain throughout my left arm and the left side of my chest), and finally I now have lumps the size of grapes in my left arm pit. The lumps in my arm pit are the most concerning and scary. How do others deal with this? I'm really concerned and scared!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: None
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: Slight pain at the injection point, cold and fever, and pain

VAERS 2006410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MN
Alter: 62,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 13.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Atrial fibrillation Atrial flutter Supraventricular tachycardia

Symptomtext

Paroxysmal atrial fib with flutter with RVR. Wide-complex tachycardia suspect supraventricular with aberrancy. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2005476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 16.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / RA

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

Blood pressure increased Chest pain Electrocardiogram

Symptomtext

Chest pain Increased blood pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG sent to cardiologist 1/3/2022 Increase in medications 1/3/2022
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension COVID-19 in June 2020
Andere Medikamente: Metoprolol Norvasc Vitamin D
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2005468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 84,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 13.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Atrial fibrillation Cardioversion Dyspnoea Dyspnoea exertional Electrocardiogram

Symptomtext

Patient first received J&J vaccine 3/3/21 then received Pfizer dose in December 2021. Two days after receiving vaccine, patient reported dyspnea. She reported that she now gets short of breath with minimal activity such as going to the bathroom. She was found to have atrial fibrillation with rapid ventricular rate. She was hospitalized and chemically cardioverted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: -
Vorgeschichte: a 84 y.o. female with a past medical history significant for nonischemic cardiomyopathy, left bundle branch block, biventricular defibrillator implantation in 2019, paroxysmal atrial fibrillation, chronic anticoagulation, hypertension and hyperlipidemia.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Hypersensitivity Pharyngeal swelling Vomiting

Symptomtext

Patient described mild symptoms of allergic reaction with 1st COVID-19 dose. She states that she did not require an epinephrine pen with her 1st dose. Given concerns for shortness of breath with 1st dose, she had epinephrine pen ready. After her COVID-19 vaccine she went to the bathroom and started having emesis. She also appeared short of breath. She had some visible throat swelling on exam. Given concerning symptoms for anaphylaxis, an epinephrine pen was administered to her left thigh. She immediately felt relief after the epinephrine pen and no longer had any further emesis or shortness of breath. 911 was contacted. Ambulance arrived and she was transported to the emergency room for further evaluation. Told patient she is no longer to have the COVID-19 vaccination due to her adverse allergic reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Patient transported via ambulance to the hospital.
Aktuelle Erkrankungen: Adult obesity; asthma; depression; diabetes; hypertension
Vorgeschichte: Adult obesity; asthma; depression; diabetes; hypertension
Andere Medikamente: Glucophage (metformin) 1,000mg tablet; Singulair (montelukast) 10mg tablet; Actos (pioglitazone) 30mg tablet; Humulin R U-500 "concentrated" (insulin regular human U-500 "concentrated") 500 unit/mL; Hydrodiuril (hydrochlorothiazide) 25mg ta
Allergien: Morphine
Vorherige Impfungen: -

VAERS 1989551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: UT
Alter: 31,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 23.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / -

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

Angina pectoris Cardiac discomfort Dyspnoea Heart rate increased

Symptomtext

Heart pain, felt like somebody grabbing your heart and squeezing so that you can?t breathe. Had rapid heart rate while resting higher than 110, when testing heart rate is 60. Symptoms lasted for two hours. Since the first dose of the vaccine in March and second dose in April, have had an attack in April and one in July.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: family clinic 12/28/2021
Aktuelle Erkrankungen: Nope
Vorgeschichte: Nope
Andere Medikamente: Fish oils, biotin. Had heart issues after each vaccination, it wasn?t until my booster I made the connection.
Allergien: None
Vorherige Impfungen: Last vaccine dose, did not make the connection till third dose

VAERS 1988945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: VA
Alter: 16,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 17.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / AR

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

C-reactive protein normal Cardiac ablation Cardiac imaging procedure normal Ejection fraction decreased Electrocardiogram abnormal Inflammatory marker test Palpitations Red blood cell sedimentation rate normal Tachycardia Ventricular hypokinesia

Symptomtext

Vaccine 12/17, developed palpitations and narrow complex tachycardia on 12/22. No elevated inflammatory markers and no evidence of myocarditis on cardiac MRI. Underwent ablation of atrial ectopic focus on 12/28.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 8,0
Labordaten: Ekg 12/22-narrow complex tachycardia 12/22 CRP normal (0.6 mg/dl) and ESR normal (5mm/hr) Cardiac MRI 12/24: moderate to severe global hypothesis of left ventricle with an ejection fraction of 30%. No evidence of myocardial, myocardial scar, or infiltrative disease
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1984648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WI
Alter: 42,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Epistaxis Fatigue Headache Migraine Neck pain Vertigo Vomiting

Symptomtext

Headache, vomiting, nose bleed 12/7 3am-2pm Vertigo, neck pain, migraine, fatigue 12/19-ongoing

Weitere VAERSDATA-Felder

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

VAERS 1982017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 01.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Mass Mobility decreased Pain Pain in extremity Sleep disorder

Symptomtext

I noticed on 12/17/2021 until 12/24/2021 I couldn't put my right arm down. If I would drive and try to turn left or sleep it would hurt. I also noticed a lump, which was sensitive and hurting. Also my left arm was hurting. Body was also sore and fatigued. Also still have the lump.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Went to PCP on 12/23/2021- She looked at my lump. Treatment Plan= Ultrasound will be scheduled
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Constipation, Osteoarthritis and Bone Spur in heels
Andere Medikamente: Pantoprazole 40mg 1xday, Stool softeners 100mg 1xday, Metamucil capsules 2xday
Allergien: None
Vorherige Impfungen: -

VAERS 1980847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CT
Alter: 43,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Arthralgia Chills Hyperhidrosis Immunisation Migraine Nausea

Symptomtext

Migraine; joint pain; chills; sweating; nausea; Dose number:3; This is a spontaneous report from a contactable reporter (consumer or other non HCP). The reporter is the patient. A 43-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 09Dec2021 at 11:45 (Lot number: FH8027) at the age of 43 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Colitis ulcerative" (unspecified if ongoing) and "Migraine" (unspecified if ongoing), notes: migraines. Concomitant medication(s) included: MESALAMINE; FLUTICASONE and MIRENA IUD. Past drug history included: Cecloretta, reaction(s): "Drug allergy", notes: known allergies: ceclore. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE; Lot number: EP6955; Anatomical location: Arm Right ; Vaccine Administration Time: 15:00), administration date: 06Apr2021, when the patient was 42 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 1, SINGLE; Lot number: EP6955; Anatomical location: Arm Right; Vaccine Administration Time: 13:00), administration date: 16Mar2021, when the patient was 42 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 09Dec2021 at 11:45, outcome "unknown", described as "dose number: 3"; MIGRAINE (non-serious) with onset 09Dec2021 at 21:00, outcome "recovered" (an unknown date in Dec2021), described as "migraine"; ARTHRALGIA (non-serious) with onset 09Dec2021 at 21:00, outcome "recovered" (an unknown date in Dec2021), described as "joint pain"; CHILLS (non-serious) with onset 09Dec2021 at 21:00, outcome "recovered" (an unknown date in Dec2021), described as "chills"; HYPERHIDROSIS (non-serious) with onset 09Dec2021 at 21:00, outcome "recovered" (an unknown date in Dec2021), described as "sweating"; NAUSEA (non-serious) with onset 09Dec2021 at 21:00, outcome "recovered" (an unknown date in Dec2021), described as "nausea". Therapeutic measures taken as a result of migraine, joint pain, chills, sweating, nausea was unknown. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive other vaccines within four weeks prior to 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Colitis ulcerative; Migraine (migraines)
Andere Medikamente: MESALAMINE; FLUTICASONE; MIRENA
Allergien: -
Vorherige Impfungen: -

VAERS 1979252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MD
Alter: 50,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure increased Chest pain Contusion Lymphadenopathy Musculoskeletal pain Pain Pyrexia Swelling

Symptomtext

Dec 18 & 19: 101-102 F fever + swollen lymph nodes under left armpit size and shape of a mango + pain radiating in left chest and behind left shoulder blade + spike in blood pressure (140/90+) Dec 20: blood pressure rising: 150/high 90 Dec 21: blood pressure rising: 160/103 Dec 22: lymph nodes reduced in swelling but replaced by bruising (yellow/greenish in color). blood pressure normal Dec 24: still some swelling and bruising appearance. blood pressure normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: could not see a physical doctor. only virtual visit on 12/21 @ 9pm. increased Lisinopril from 20mg to 40mg daily. no tests performed.
Aktuelle Erkrankungen: none
Vorgeschichte: elevated high blood pressure.
Andere Medikamente: lisinopril 20 mg daily levothyroxine 150 mcg daily Lo loestrin FE daily
Allergien: none
Vorherige Impfungen: -

VAERS 1979216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IN
Alter: 44,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 09.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Chest X-ray Chest discomfort Chills Computerised tomogram Discomfort Echocardiogram Electrocardiogram ambulatory Fatigue Heart rate increased Impaired work ability Laboratory test Migraine Nervous system disorder Pneumonia Sinus congestion Sleep disorder

Symptomtext

Started with Migraines that led into sinus congestion. Rapid heart beat 122-132 waking me in the middle of the night. Chest pressure led into pneumonia. Chills off and on still, still having chest pressure, glands in armpit, side of chest and above chest on vaccine administered side have bothered me ever since the vaccine. Autonomic nervous system has been in hyper drive ever since. Chest pressure still, very fatigued, Lots of anxiety due to all of this. Have been to ER 3x, family Doctor, Cardiologist, Pulmonologist . Chest X-rays, labs, CT, Echocardiogram, holter monitor. Still have more testing along with Cardiac Even monitor for a month. Ongoing treatment now on Medication to lower heart rate, inhalers, anxiety meds . I had no health issues prior to this vaccine and have now been out of work since 10-27-21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Ongoing since vaccine still out of work. There needs to be more help or specialists in the area that are seeing the adverse reactions to these vaccines as I?m not the only person going through this as I know many others. We all could use the help to stop this vaccine from still actively effecting our autonomic nervous system overload.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1978700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: GA
Alter: 28,0
Geschlecht: U
Eingang: 24.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Immunisation Migraine with aura Thyroid hormones test

Symptomtext

booster; had a horrible Aura migraine; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 28 year-old patient received bnt162b2 (BNT162B2), administered in deltoid right, administration date 08Dec2021 (Lot number: FH8027) at the age of 28 years as dose 3 (booster), single , single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing), notes: "I have Asthma. I am taking albuterol as emergency inhaler, (unclear voice) and Singulair."; "Migraine" (unspecified if ongoing), notes: I usually get them once every couple years. Concomitant medication(s) included: ALBUTEROL [SALBUTAMOL SULFATE] taken for asthma; SINGULAIR taken for asthma. Vaccination history included: Covid-19 vaccine (Manufacturer: Unknown), for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 08Dec2021, outcome "unknown", described as "booster"; MIGRAINE WITH AURA (non-serious) with onset 08Dec2021, outcome "unknown", described as "had a horrible Aura migraine". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of migraine with aura. Additional info- Patient did not receive any vaccination within 4 weeks prior to vaccination. It was reported that patient need to know if I need to go a doctor for some sort of like cardiovascular issue (Further not clarified) or it's a normal side effect to get a migraine afterwards .Therapeutic measure were taken as AE and treatment was taken with 200 milligrams pills of Ibuprofen but no it usually doesn't, it helps a little bit but not enough. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine with aura
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: hormone check; Result Unstructured Data: Test Result:Normal; Comments: hormone check, with my hormones like my thyroid
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma ("I have Asthma. I am taking albuterol as emergency inhaler, (unclear voice) and Singulair."); Migraine (I usually get them once every couple years)
Andere Medikamente: ALBUTEROL [SALBUTAMOL SULFATE]; SINGULAIR
Allergien: -
Vorherige Impfungen: -

VAERS 1971754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NM
Alter: 13,0
Geschlecht: F
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

Paraesthesia oral Rash

Symptomtext

30min later had facial rash, lip tingling and possible lip swelling. No SOB, cough, tongue/throat swelling, nausea/vomit/abdominal pain , confusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: ance vulgaris, abscess under breast fold, s/p Course of clindamycin started 12/10/21 for associated cellulitis, now with resolution.
Vorgeschichte: Obesity,.
Andere Medikamente: none
Allergien: Ibuprofen allergy in past. Lip swelling/face rash.
Vorherige Impfungen: -

VAERS 1970961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 19.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arrhythmia Blood creatine phosphokinase Electrocardiogram abnormal Full blood count Laboratory test Palpitations Ventricular extrasystoles

Symptomtext

Developed heart arrhythmia within 24 hours of the vaccination. Went to Dr (my primary) and was given an ECG which showed PVC's. Am currently on a 24 hour Holter monitor. Still having symptoms palpitations but no dizziness or chest pain or such.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: ECG. Multiple labs including CPK (results pending), blood chemistry, CBC
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D3
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1970655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

moderat

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 22.12.2021
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: nein

Body temperature Cold sweat Dyspnoea Headache Immunisation Nausea Pain Pyrexia

Symptomtext

High temp 102 degrees; Shortness of breath; Severe headache; sweats chills; nausea; Body ache; Dose Number: 3; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 26Nov2021 13:45 (Lot number: Fh8027) at the age of 66 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 Number: 2, Batch/Lot No: er2613, Location of injection: Arm Left, Vaccine Administration Time: 02:30 PM), administration date: 19Mar2021, when the patient was 65 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: en2603, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM), administration date: 26Feb2021, when the patient was 65 years old, for COVID-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset 27Nov2021, outcome "not recovered", described as "High temp 102 degrees"; DYSPNOEA (non-serious) with onset 27Nov2021, outcome "not recovered", described as "Shortness of breath"; HEADACHE (non-serious) with onset 27Nov2021, outcome "not recovered", described as "Severe headache"; COLD SWEAT (non-serious) with onset 27Nov2021, outcome "not recovered", described as "sweats chills"; NAUSEA (non-serious) with onset 27Nov2021, outcome "not recovered", described as "nausea"; PAIN (non-serious) with onset 27Nov2021, outcome "not recovered", described as "Body ache"; IMMUNISATION (non-serious) with onset 26Nov2021 13:45, outcome "unknown", described as "Dose Number: 3". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, dyspnoea, headache, cold sweat, nausea, pain. 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-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. At the time of report, no known allergies were reported. The patient was administered vaccine in a pharmacy. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: High temp; Result Unstructured Data: Test Result:102 degrees
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1970635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MA
Alter: 59,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 20.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Bedridden Cheilitis Condition aggravated Headache Illness Immunisation Lip blister Lip swelling Lymphadenopathy Nausea Oral herpes Pain Pyrexia

Symptomtext

The swelling of her lips/inflammation has worsened; lips swelled up/inflamed and blistered; lips swelled up/inflamed and blistered; lips swelled up/inflamed and blistered; in bed for two days; sick for four days; headache; fever; nausea; achy; swollen lymph nodes on her whole left side-arm, breast, legs; Booster dose of the purple cap Pfizer Covid-19 vaccine on 20Nov2021; cold sores that have gotten really bad; 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 20Nov2021 11:45 (Lot number: FH8027) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "developed allergies over the years and with certain foods" (unspecified if ongoing), notes: she has developed allergies over the years and with certain foods, she has anaphylactic reactions.; "Developed allergies over the years and with certain foods; anaphylactic reactions" (unspecified if ongoing), notes: she has developed allergies over the years and with certain foods, she has anaphylactic reactions. There were no concomitant medications. Vaccination history included: Bnt162b2 (Vaccine Name: First dose of the Pfizer COVID-19 vaccine, Lot Number / Expiry Date: EL9261/ Unknown, Route, Anatomical Location: Left arm, Date: 22Jan2021, She had no reactions the first dose), administration date: 22Jan2021, when the patient was 58 years old, for Covid-19 immunization; Bnt162b2 (Vaccine Name: Second dose of the Pfizer COVID-19 vaccine, Lot Number / Expiry Date: EN5318/ Unknown , Route, Anatomical Location: Left arm , Date: 12Feb2021, 3 weeks after she got her second dose, she developed a golf ball size lymph node on her left arm, it was huge.), administration date: 12Feb2021, when the patient was 58 years old, for Covid-19 immunization, reaction(s): "3 weeks after she got her second dose, she developed a golf ball size lymph node on her left arm, it was huge". The following information was reported: IMMUNISATION (non-serious) with onset 20Nov2021, outcome "unknown", described as "Booster dose of the purple cap Pfizer Covid-19 vaccine on 20Nov2021"; HEADACHE (non-serious) with onset 21Nov2021 00:45, outcome "not recovered", described as "headache"; PYREXIA (non-serious) with onset 21Nov2021 00:45, outcome "recovered", described as "fever"; NAUSEA (non-serious) with onset 21Nov2021 00:45, outcome "recovered", described as "nausea"; PAIN (non-serious) with onset 21Nov2021 00:45, outcome "recovered", described as "achy"; LYMPHADENOPATHY (non-serious) with onset 21Nov2021, outcome "not recovered", described as "swollen lymph nodes on her whole left side-arm, breast, legs"; LIP SWELLING (non-serious), CHEILITIS (non-serious), LIP BLISTER (non-serious) all with onset 23Nov2021, outcome "not recovered" and all described as "lips swelled up/inflamed and blistered"; BEDRIDDEN (non-serious) with onset 21Nov2021 00:45, outcome "recovered" (23Nov2021), described as "in bed for two days"; ILLNESS (non-serious) with onset 21Nov2021 00:45, outcome "recovered" (25Nov2021), described as "sick for four days"; ORAL HERPES (non-serious) with onset Nov2021, outcome "not recovered", described as "cold sores that have gotten really bad"; CONDITION AGGRAVATED (non-serious), outcome "not recovered", described as "The swelling of her lips/inflammation has worsened". Relevant laboratory tests and procedures are available in the appropriate section. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: body temperature; Result Unstructured Data: Test Result: Unknown result.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anaphylactic reaction to food (she has developed allergies over the years and with certain foods, she has anaphylactic reactions); Food allergy (she has developed allergies over the years and with certain foods, she has anaphylactic reactions).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1963951

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

moderat

Staat: VT
Alter: 55,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Disturbance in attention Insomnia Tinnitus

Symptomtext

Upon waking the morning after the booster shot, I immediately noticed the ringing in my ears/tinnitus was markedly louder. It remains consistent and loud, a month later, like a hive of bees with a high pitch tone as well. It is challenging to sleep and to concentrate with this condition. I reported, at the suggestion of doctor, this symptom after the 2nd vaccine, note e report 560886 and ID 1406331. I have seen an ENT and an audiologist after the first report, no hearing loss of structural problems. I now take medication to sleep, run an air purifier on high for white noise. Doctor requested I report this incident as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Had been experiencing tinnitus since COVID vaccine via Moderna #2, please see report 560886 , ID 1406331. Upon waking the morning after the booster , this time Pfizer, tinnitus was louder and continues to be loud and constant. Like a hive of bees with a high pitched tone as well.
Vorgeschichte: -
Andere Medikamente: Multivitamins, over the counter sleep aid Diphenhydramine.
Allergien: Azithromyacin
Vorherige Impfungen: I reference the Moderna vaccine and prior report/ ID In this form

VAERS 1963372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IL
Alter: 41,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 02.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest discomfort Dyspnoea Electromyogram Influenza like illness Muscular weakness Pain in extremity

Symptomtext

Chronic flu like symptoms, weakness/pain in left arm, chest tightness and shortness or breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest x-ray; bloodwork and EMG test. Prescribed various medications; Folic Acid; Vitamin B12; Lipid Profile with reflex 2LDL; Albuterol inhaler; Zithromax; Medrol dose pack
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1962447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MD
Alter: 45,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain Arthralgia Blood test Dyspnoea exertional Fatigue Muscle spasms Muscle tightness Sleep disorder Trismus

Symptomtext

For the first dose I got extreme cramping in my jaw in front of my left and right ear. It would tighten really bad then pop. The left side was a little worse than the right side. This went away after about a week. I also got tightness on the left side of my neck. The tightness felt like it was in the muscles used to swallow. It did not hinder me from swallowing so I did not go to the doctor. The neck tightness went away about a week after the shot. The second dose (administered on 11/16/21) is where I had and am still having bad side effects. About a day after the second dose I the jaw tightness came back to only the left side. It is less extreme, but has not gone away. When I whistle it tightens then pops. So it is mostly an annoyance. The main problems is that from my belt line to my belly button (all the way around my core) I get very severe pain when I lay down. It affects my sleep causing me to wake up during the night. Likewise, I have a raw (like tendonitis) pain on the inner side of my left elbow. I get cramping in my left wrist (especially when playing guitar which I never had before). And worse of all I seem to fatigue very quickly, like my muscles are not getting enough oxygen. I was running before the first shot, so I know this was not an issue before. Now I breath hard when walking. This has continued till today and has not lessened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: I just had blood work done last week. I am still waiting on test results.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1959541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

moderat

Staat: IA
Alter: 47,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Chest pain Condition aggravated Dehydration Dyspnoea Laboratory test Migraine Pyrexia

Symptomtext

Chest pain , fever , breathing issues , migraines that didn't respond to meds two rd visits. Five day migraine and ongoing breathing issues at time over two weeks later. Dehydration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Labs Nov.30 and 31 ivs for pain and fever breathimg.
Aktuelle Erkrankungen: Migraines
Vorgeschichte: Ibs, fibromyalgia, asthma non treated , migraines, ankle issues , kidney disease, fatty liver
Andere Medikamente: Propranolal, esomeaprazole magnesium, magoxide,esclitapram,montelukast , momentasone nasal spray, miralax, potassium, vitamin d, calcium and vitamin k eletriptan, promenthazine,
Allergien: Allergic to most pain meds and antibiotics
Vorherige Impfungen: -

VAERS 1959159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IN
Alter: 35,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 09.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test normal Dizziness Electrocardiogram normal Heart rate increased Hypertension Nausea

Symptomtext

I had elevated heart rate of 125, High blood pressure, light headed, nausea. I went to ER, at the ER they gave me IV with anxiety meds and anti nausea medicine. It lasted about 3 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: EKG- normal Bloodwork- normal
Aktuelle Erkrankungen: Virus 2 weeks prior
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1958752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: VA
Alter: 43,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 30.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Paraesthesia

Symptomtext

Pt. states that after receiving the 1st dose of Phizer 11/30/2021, started experiencing symptoms 12/04/2021 of Right arm pain in the shoulder throughout and tingling in the fingers. Emergency Room visit 12/17/2021 (Currently).

Weitere VAERSDATA-Felder

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

VAERS 1955211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MA
Alter: 51,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Excessive granulation tissue Injection site erythema Injection site induration Injection site pain Injection site reaction Injection site vesicles Neuralgia Pain Pain in extremity Paraesthesia Sensory disturbance Skin exfoliation Urticaria

Symptomtext

12-03-2021 3:13 PM: I spoke with patient she received her Pfizer booster on Wednesday and this is the progression of the reaction she had , Please review all 5 pictures and advise , She is currently on an antibiotic for sinusitis. Her skin as she described was like she had gotten burnt and started to peel. (pin to top) 12-03-2021 5:31 PM: called patient- rest of her skin outside of injection area has remained normal. patient informed that VAERS system report is needed. patient consents. Denies that any expansion of blistered and peeling area. Induration is also not spreading. patient already on Augmentin for sinusitis. She denies fever, chills, facial rash or swelling, SOB, or sensation of throat closing. ER precautions for Steven-Johnson's syndrome, anaphylaxis or worsening angioedema reviewed. advised patient keep petrolatum and sterile gauze on base of blister until healed. Will call patient on 12/6 to check on condition (pin to top) 12-06-2021 3:08 PM: called patient. patient reports pain, "yucky" appearance to blister, and went to dr. office. patient denies spread of reaction beyond right arm, however patient has new sensation discrepancy between forearms. patient significantly distressed by pain in reaction site, feels like pins and needles. patient denies SOB, fever, dyspnea, expanding redness, nausea. reviewed with patient that symptoms appear related to superficial irritation of nerves, similar to burn victims. patient would like call back on 12/10/21 to follow symptoms (pin to top) 12-06-2021 3:25 PM :patient gives verbal consent to send in patient's pictures to VAERS system (pin to top) 12-10-2021 5:38 PM: called patient for update: -remains in pain -patient has kept arm covered up until yesterday was continuing to have goey granulation tissue -pain radiates down the arm (dorsal and ventral) and up to shoulder, but not into neck -blistered, desquamated area is same size -no border of redness has spread away from the blister -icing did not help the welt that formed before the blister 12-16-2021 1:33 PM: patient has not showed to visit or answered call today

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none ordered
Aktuelle Erkrankungen: J01.00 Acute maxillary sinusitis, unspecified
Vorgeschichte: acid reflux K21.9 Gastro-esophageal reflux disease without esophagitis acquired spondylolysis of lumbosacral spine M43.07 Spondylolysis, lumbosacral region L5 agoraphobia with panic attacks F40.01 Agoraphobia with panic disorder atypical squamous cells of undetermined significance on cervical Papanicolaou smear R87.610 Atypical squamous cells of undetermined significance on cytologic smear of cervix body mass index 30+ - obesity Z68.34 Body mass index [BMI] 34.0-34.9, adult bulimia nervosa F50.2 Bulimia nervosa concussion injury of brain S06.0X0D Concussion without loss of consciousness, subsequent encounter decreased thyroid stimulating hormone level R94.6 Abnormal results of thyroid function studies essential hypertension I10 Essential (primary) hypertension heart failure with normal ejection fraction I50.32 Chronic diastolic (congestive) heart failure history of attempted suicide Z91.5 Personal history of self-harm impaired fasting glycemia iron deficiency anemia D50.9 Iron deficiency anemia, unspecified lumbosacral spondylolisthesis M43.17 Spondylolisthesis, lumbosacral region L5-S1 migraine G43.909 Migraine, unspecified, not intractable, without status migrainosus mild persistent allergic asthma J45.30 Mild persistent asthma, uncomplicated nodular adrenal cortex E27.8 Other specified disorders of adrenal gland right side obesity osteoarthritis of right knee joint M17.11 Unilateral primary osteoarthritis, right knee seasonal allergic rhinitis J30.2 Other seasonal allergic rhinitis severe major depression F32.2 Major depressive disorder, single episode, severe without psychotic features smoker F17.200 Nicotine dependence, unspecified, uncomplicated social phobia F40.10 Social phobia, unspecified thyroid nodule E04.1 Nontoxic single thyroid nodule left lobe
Andere Medikamente: albuterol sulfate HFA 90 mcg/actuation aerosol inhaler Inhale 2 puffs every 4 hours by inhalation route for 30 days. Alli 60 mg capsule TAKE 1 CAPSULE BY MOUTH UP TO 3 TIMES A DAY WITH MEALS ARIPiprazole 5 mg tablet Take 1 tablet every
Allergien: duloxetine (nausea), propranolol (acid reflux), ferrous sulfate (nausea)
Vorherige Impfungen: -

VAERS 1955092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NY
Alter: 52,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure increased Hypoxia Inappropriate schedule of product administration Lethargy Pyrexia Tachycardia

Symptomtext

Elevated B/P and lethargy, upon assessment, patient was observed with fever (T 103), hypoxia (O2Sat 85 - 88), and tachycardia (HR 115),

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: 12/12/2021 - Flucelvax Quad 2021-2022 60 mcg (15 mcg x 4)/0.5 mL intramuscular
Vorgeschichte: Multiple sclerosis
Andere Medikamente: acetaminophen 325 mg tablet baclofen 20 mg tablet glatiramer 40 mg/mL subcutaneous syringe metoprolol tartrate 50 mg tablet mirtazapine 15 mg tablet
Allergien: NKA
Vorherige Impfungen: -

VAERS 1950910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NV
Alter: 17,0
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

Dizziness Dyspnoea Flushing Hyperhidrosis

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium

Weitere VAERSDATA-Felder

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

VAERS 1948623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 14.12.2021
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: ja

Chest discomfort Chills Dyspnoea Headache Nausea Palpitations

Symptomtext

Nausea, headache, chills, and the very scary racing of my heart and pressure on my chest like it was hard to breathe. It lasted for about 3 hours starting almost exactly 24 hours after the shot. And it came on slow and steady, it then got very intense for a good 30 mins. And then it slowly waned.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/14/2021.
Aktuelle Erkrankungen: No
Vorgeschichte: Drugs / Alcohol.
Andere Medikamente: Pristiq, vitamin D, Zyrtec
Allergien: No
Vorherige Impfungen: 04/18/2021.

VAERS 1945325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MD
Alter: 42,0
Geschlecht: F
Eingang: 13.12.2021
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: ja Erholt: nein

Breast discharge Chest pain Pain Rash Scab

Symptomtext

Severe rash and discharge from breasts- took Benadryl and am monitoring now. The rash has gone but the skin is scabbed over and is painful. Developed chest pain on day 3 going to hospital now

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Bipolar disorder Trigeminal Neuralgia
Andere Medikamente: Effexor Xr, gabapentin, lamictal, tegratol
Allergien: None
Vorherige Impfungen: -

VAERS 1944871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Biopsy skin Blood pressure increased Chills Gait disturbance Hypoaesthesia Lichenoid keratosis Mobility decreased Pruritus Rash Skin burning sensation Skin exfoliation Skin fissures

Symptomtext

Within 2 weeks after the 2nd shot the rash began on my torso. It then spread to my back, legs, arms and eventually my hands and feet. In July numbness happened in my feet and shoulders. I was not able to feel my feet or move my arms. In September the skin on my hands and feet began cracking and peeling. Walking and using my hands was nearly impossible. The symptoms resolve with steroids, however the exacerbation happen immediately after discontinuing use of the steroid. Severe itching. Skin feeling on fire causing chills. No fever. Causes blood pressure to increase.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Skin biopsy impression: Lichenoid dermatitis, compatible with lichenoid drug eruption
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Zoloft, Vesicare, Premrin, Flonaze, Macrobid,
Allergien: Ironman dextron
Vorherige Impfungen: -

VAERS 1943450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Bone pain Dehydration Epistaxis Fatigue Headache Injection site erythema Injection site swelling Lymphadenopathy Pyrexia Tinnitus Vision blurred

Symptomtext

severe joint/bone pain, blurry vision, tinitis, headache, fever, dehydration, bloody nose, tired, swollen lymph nodes. Symptoms started about 6 hours after receiving booster and lasted 48 hours. Headache continued for another eight hours beyond. Injection site turned red and swollen 48 hours after receiving shot. Swollen lymph nodes persisting 72 hours after shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroidism
Andere Medikamente: birth control pills, Levothyroxine
Allergien: penicillin, sucralose, Ace-K, xylitol, milk, mushrooms, adhesives
Vorherige Impfungen: Pfizer Covid 19 vaccine second dose

VAERS 1939298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 10.12.2021
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: ja Erholt: nein

Dizziness Fall Hypotension Nausea Paraesthesia

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Hypotension-Severe, Systemic: Nausea-Medium, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: pt got shot 6:26pm was fine until nurse asked how he was feeling at 6:30 said was feeling dizzy, nurse brough pt insode pharamcy and had pt lay on back with feet elevated took bp at 6:35pm 100/50 pulse=49, monitored bp for over 1 hour, but when pt was sitting upright bp and hr would fall. At 7:05pm called EMS they came in around 715pm and advised mom to take pt to er to get checked out or they can take with abulance but it would be more cost effective to take pt to er themselves.

Weitere VAERSDATA-Felder

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

VAERS 1938784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NC
Alter: 54,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chills Diarrhoea Headache Immunisation Interchange of vaccine products Migraine Nausea Off label use Ophthalmic migraine

Symptomtext

Headache that has lasted six days, evolving into ocular migraine then regular migraine; Headache that has lasted six days, evolving into ocular migraine then regular migraine; Headache that has lasted six days, evolving into ocular migraine then regular migraine; Chills; Nausea; Diarrhea persisting the same length oftime.; Dose received: 3 / dose number = 3; Off label use; Interchange of vaccine product; This is a spontaneous report received from contactable reporter (consumer or other non-HCP). The reporter is the patient. A 54 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 29Nov2021 at 14:00 (Lot number: FH8027) at the age of 54 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Celiac disease" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Moderna covid-19 vaccine (DOSE 1, SINGLE, Lot Number: 019821A, Route of Administration: Unknown, Anatomical Location: Right arm), administration date: 24Mar2021, when the patient was 54 years old, for COVID-19 immunisation and Moderna covid-19 vaccine (DOSE 2, SINGLE, Lot Number: 045b21A, Route of Administration: Unknown, Anatomical Location: Left arm), administration date: 21Apr2021, when the patient was 54 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 29Nov2021 at 14:00, outcome "unknown", described as "Dose received: 3 / dose number = 3"; OFF LABEL USE (non-serious) with onset 29Nov2021 at 14:00, outcome "unknown", described as "Off label use"; INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 29Nov2021 at 14:00, outcome "unknown", described as "Interchange of vaccine product"; HEADACHE (non-serious), OPHTHALMIC MIGRAINE (non-serious), MIGRAINE (non-serious), CHILLS (non-serious), NAUSEA (non-serious), DIARRHOEA (non-serious) all with onset 29Nov2021 at 15:00, outcome "not recovered", and all described as "Headache that has lasted six days, evolving into ocular migraine then regular migraine". Therapeutic measures were not taken as a result of headache, ophthalmic migraine, migraine, chills, nausea and diarrhoea. 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. 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: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Celiac disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1936393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 04.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / LA

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

Arthritis Bruxism Condition aggravated Dysstasia Wheelchair user

Symptomtext

Started with intense jaw-clenching--still ongoing. Then 3 weeks later intense arthritis flare-up involving both knees, left shoulder, elbow, thumbs. Unable to leave my house and am using a wheelchair as I can't stand for more than 10 -15 seconds at a time-Ongoing. I was ambulatory, using a cane for assistance, prior to receiving the 3rd covid booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes Polyarthritis Heart Failure
Andere Medikamente: Losartan Torsimide Carvedilol Spironalactone metformin Basaglar Novalog Vitamin D Calcium Multi Vitamin Aleve Omeprazole Potassium
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1936217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Dyspnoea Headache Hyperhidrosis Nausea Pain in extremity

Symptomtext

shortness of breath. left leg pain, HA, Dizzy, nauseated, HA, sweaty, dizzy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: referred to the ER
Aktuelle Erkrankungen: back pains
Vorgeschichte: hypertension hx of lung fungal infection
Andere Medikamente: lisinopril amlodipine norethindrone/ethinyl estradiol nabumetone
Allergien: -
Vorherige Impfungen: leg cramping after 2nd covid vaccine on 4/16/21

VAERS 1933943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MN
Alter: 49,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

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

Back pain Chest X-ray Chest discomfort Chest pain Electrocardiogram Gait disturbance Hypersomnia Hypertension Insomnia Mobility decreased Oropharyngeal pain Pain Pharyngeal swelling Respiratory tract congestion Respiratory tract inflammation SARS-CoV-2 test negative

Symptomtext

10 hours after and through 2 days later Extreme pain all over body so much that I couldn?t walk and husband had to help me out of bath. 3rd day slept all day and could wake up, 3 rd day started extreme congestion that is still continuing after day 10. 1 week in started prednisone for respiratory inflammation which then started high blood pressure issues. So congested couldn?t sleep at night. Same symptoms that I had back in March 2021 when I did have Covid. I have taken 2 Covid tests which were negative and have been to Dr that included ekg and chest X-ray for pressure in chest. I had a really bad reaction to both vaccines. First I had throat swelling and sore throat for a week and 2nd worst pain and congestion/chest pain/lower back pain for 10 days plus now. Hopefully this will pass but it still isn?t over and I am still experiencing symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12/1 Covid test negative , Dr on demand 12/5, 12/7 Covid test negative , Dr visit EKG (ok), Chest X-ray. Prednisone, Antibiotic, abuterol inhaler.
Aktuelle Erkrankungen: Zero
Vorgeschichte: Migraine, Raynauds
Andere Medikamente: Only zomig as needed for migraines
Allergien: Lots of food allergies (carrot, egg, broccoli, peanuts, bean . Sulfa and seasonal
Vorherige Impfungen: Pfizer 1st dose

VAERS 1933602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 52,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Body temperature increased Hyperhidrosis Influenza virus test negative Myalgia Pain Pain of skin Paraesthesia SARS-CoV-2 test negative Tendon pain

Symptomtext

Friday, December 3, I felt tingling in my right shoulder and then down into my forearm. Drank 100oz of water. Awakened Saturday morning and my body ached all over, it hurt to make a fist, it hurt everywhere, my skin felt like it had been rubbed with coarse sand paper all over. I checked my temp and I had a 101 temp (normal is 97.8). I took 500mg of Tylenol every 6 hours and that lowered my temp to 99.1. I was still uncomfortable and no sweating occurred. I woke on Sunday and the discomfort had intensified and my temp was reading 103. I took 1000mg of Tylenol and 2 hours later I began to sweat and the temp was dropped to 101. My skin, muscles and tendons hurt. I took 500mg at 1pm and alternated to Motrin (200mg) at 4pm and lastly Tylenol (500mg at 9pm with a 101 temp remaining. On Monday, I woke to a 101 temp and the only place where muscle pain existed was on the sides of my neck and right below my rib cage on my back. Continued 500mg of Tylenol at 7am, 1pm, Motrin (200mg) at 5pm and Tylenol (500mg)at 11pm. Tuesday I woke to no pain and no need to take any pain meds. Wednesday I woke to body skin aches and started the Tylenol again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Monday, December 6: PCR COVID test, Antigen COVID test and the results were negative, Flu Test with a negative result.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Valsartan/HCTZ = 160/25; Multivitamin; Potassium (90 mg / day); Statin for Cholesterol; Omeprazole
Allergien: Augmentin
Vorherige Impfungen: Tifoid at 24 years old 1995 or 1996

VAERS 1932114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: GA
Alter: 47,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Axillary pain Condition aggravated Headache Injection site pain Oedema peripheral

Symptomtext

I received booster shot on Monday 12/6/2021. The next morning while working (stilling in front of a computer) I noticed a headache. It wasn't until around 2pm that I thought it could be related to the booster shot. The injection site (left arm) also sore, But I also have soreness on my left arm pit, but I didn't equate that to the shot. Wednesday 12/8/2021 morning after showering I checked my left arm pit because it is extremely sore and noticed it's swollen. As I'm filling out this form (Wed. 12/8/2021 @ 8:30am) I have the headache, injection site soreness and soreness and swelling on arm pit

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: high-blood pressure, diabetes
Andere Medikamente: Amlodipine Besylate 10mg (1x), Lisinopril - HCTZ 20-12.5mg (2x), Pravastatine Sodium 80mg (1x), Metformn HCL 500mg (2x), Dextroamp-Amphetamin 30mg (1x)
Allergien: lactose intolerant
Vorherige Impfungen: Pfizer (EW0151) on 4/30/2021, (EW0165) on 5/21/2021; headaches the following days

VAERS 1929173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: GA
Alter: 55,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Extra dose administered Fatigue Feeding disorder Feeling cold Headache Injection site pain Nausea Pain Somnolence Tremor

Symptomtext

Dec 1 - vaccination at 3:30pm. Slight headache starting at 4pm Dec 2 -7am upon waking felt generally achy, but not terrible. By 10:30am symptoms had increased such that I was freezing cold, unable to get warm, shaking, headache, tired. Took Tylenol PM at 1pm hoping to sleep through the reaction as this is similar to what I experienced with the 2nd dose of Moderna. Continued with chills, aches, headache, sleepiness, added dizziness throughout the day, sleeping off and on, not able to eat any food. At 6pm ate some saltine crackers, had nausea upon standing, chills began to lessen. Dec 3 - 7am upon waking felt much better, no chills, mild body aches, resolved pretty by 11am aside from pain at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: penicillin, NSAIDs
Vorherige Impfungen: COVID-19 Moderna 2nd dose - similar to the currently reported incident - uncontrolloable shaking, chills, dizziness, body aches,

VAERS 1928870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8027

moderat

Staat: NY
Alter: 44,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Electrocardiogram Tachycardia

Symptomtext

Tachycardia with pulse rate 126

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: had MRSA S/P chochlear implant removal
Vorgeschichte: HTN/HLD, asthma, obesity, hyperglycemia, conductive hearing loss, GERD, NAFLD
Andere Medikamente: on OBC, pepcid, asmanex, phentermine,
Allergien: Sulfa/Sulfate, trimethorim
Vorherige Impfungen: -

VAERS 1925114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NC
Alter: 72,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Chest pain Interchange of vaccine products Palpitations

Symptomtext

Patient received Moderna vaccine for her primary series. After her 2nd dose of Moderna vaccine, patient experienced chest tightness and EMS was called. Patient informed RN of this previous adverse event to vaccination prior to being vaccinated today. Patient received her 3rd (booster) dose of Pfizer vaccine today. About 5 minutes into her observation period, patient began experiencing chest pain and her heart was racing. Patient was evaluated by on-site RN/provider staff who deemed it necessary to take patient to the ED for further evaluation, assessment, and monitoring. Patient left the vaccine clinic site on stretcher to go to on-site ED.

Weitere VAERSDATA-Felder

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

VAERS 1924100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NE
Alter: 56,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 27.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Confusional state Dehydration Diarrhoea Fibrin D dimer increased Lethargy Nausea Oxygen saturation decreased SARS-CoV-2 test positive Vomiting

Symptomtext

Severe lethargy, confusion, dehydration 12/2-3. Low oxygen saturation of 78% on 12/4 and increased confusion along with nausea, vomiting, diarrhea. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: ER visit covid swab was positive 12/4. Along with elevated d-dimer >1000.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic pain, vasovagal syncope
Andere Medikamente: Lyrica, cymbalta, lasix, dilaudid infusion
Allergien: Aspirin, penicillin, sulfa, doxycycline
Vorherige Impfungen: -

VAERS 1923742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: FL
Alter: 52,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Fatigue Hyperhidrosis Lymph node pain Lymphadenopathy Malaise Nausea Pyrexia Tremor

Symptomtext

CHILLS, SWEATS, TEMPERATURE, FEVER RANGING FROM 99.5 TO 102.5, SHAKES, GENERAL MALAISE, TIREDNESS, NAUSEA, SWOLLEN LEFT ARM LYMPH NODES WITH PAIN, FEVER LASTED 2 AND A HALF DAYS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: OTC Multivitamin, Lisinopril 5mg 1 tab daily, Amlodepine Besylate 5mg 1 tab daily
Allergien: Penicillin, Latex, Tree Nuts
Vorherige Impfungen: 04/02/2021

VAERS 1923264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IN
Alter: 52,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Headache Pain Pyrexia Tremor

Symptomtext

Extreme headache, full body aches, uncontrollable chills/shaking and slight fever

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Metoprolol 25mg one/day Pregabalin 150mg two/day
Allergien: None
Vorherige Impfungen: Slight fever 51 yrs old 3/12/2021 first dose 4/2/2021 second dose Pfizer

VAERS 1923131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: NJ
Alter: 52,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Hypertension

Symptomtext

Systemic: chest pain and high blood pressure-Mild, Systemic: Hypertension-Mild

Weitere VAERSDATA-Felder

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

VAERS 1923022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 23,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 27.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Chills Decreased appetite Hyperhidrosis Immunisation Malaise Migraine Myalgia Pain Pain in extremity Pyrexia

Symptomtext

Dose number: 3; Fever; Aches; Chills / Shivers; Sweats; Migraine; Muscle aches; Loss of appetite; Arm soreness; Started feeling sick that night / Too sick to leave bed the entire day; This is a spontaneous report received from a non-contactable reporter (consumer). The reporter is the patient. A 23-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in right arm, administration date 27Nov2021 at 11:00 (Batch/Lot number: FH8027) at the age of 23 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. Concomitant medication included: CLARAVIS. Vaccination history included: COVID-19 vaccine (DOSE 1, SINGLE; Lot Number: UNKNOWN; Route of administration: Unspecified; MANUFACTURER UNKNOWN), administration date: unknown, single for COVID-19 immunisation and COVID-19 vaccine (DOSE 2, SINGLE; Lot Number: UNKNOWN; Route of administration: Unspecified; MANUFACTURER UNKNOWN), administration date: unknown, single for COVID-19 immunisation. The following information was reported: PYREXIA (non-serious), PAIN (non-serious), CHILLS (non-serious), HYPERHIDROSIS (non-serious), MIGRAINE (non-serious), MYALGIA (non-serious), DECREASED APPETITE (non-serious), PAIN IN EXTREMITY (non-serious), all with onset 28Nov2021 at 04:00, outcome "recovered" (an unknown date in Nov2021), all described as "fever, aches, chills / shivers, sweats, migraine, muscle aches, loss of appetite, arm soreness"; MALAISE (non-serious) with onset an unknown date in Nov2021, outcome "recovered" (an unknown date in Nov2021), described as "started feeling sick that night / too sick to leave bed the entire day". Therapeutic measures were not taken as a result of pyrexia, pain, chills, hyperhidrosis, migraine, myalgia, decreased appetite, pain in extremity, malaise. Additional information: The patient had no known allergies. 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 vaccine. This was the patient's booster shot which happened on the 27Nov2021 at 11:00, it was not until late in the night at 04:00 in which it really took a turn for the worse. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctors 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: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: CLARAVIS
Allergien: -
Vorherige Impfungen: -

VAERS 1921244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 53,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Erythema Pain Paraesthesia

Symptomtext

Patient experienced tingling in her right arm, followed by redness and pain on right side of body, as well as chest pain. Redness lasted 4-5 days, chest pain lasted 2-3 days per patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol, diabetes, high blood pressure, hypothyroidism
Andere Medikamente: Patient does not want to provide
Allergien: Shellfish and an unknown antibiotic
Vorherige Impfungen: -

VAERS 1916756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Chills Decreased appetite Fatigue Feeling abnormal Headache Impaired driving ability Impaired work ability Insomnia Migraine Myalgia Nausea Pain Pain in extremity Pyrexia Tremor

Symptomtext

First dose done Sunday, 12/27/2020- same day was fine. Sxs started that evening in middle of night- arm sore, headache, fever (would fluctuate from 100-101), chills, scatterbrained, joint pain, muscle aches, fatigue that lasted over 2 weeks. Second dose done Friday, 01/15/2021- same day was fine. Sxs started that evening in middle of night- same sxs as above but more intensified. Literally could not get out of bed, chills were so bad- I was shaking look like I was convulsing. Fever went up to 103, Headache was more of a migraine but medication would somewhat subside it. Booster done Friday, 11/26/2021- same day started feeling fatigue cpl hrs after I recv'd it. Sxs started that night as above (extreme joint and muscle aches as if I have Restless Leg Syndrome), fever, chills, headache, fatigue, scatterbrained BUT there were more side effects to add to the mix: loss of appetite and nausea. This headache NOTHING will help subside the pain and makes it very difficult to function at work and home. Had to call out work bc I was unable to sleep night before nor drive. It is now Thursday, 12/02 and I still have this headache with not much of an appetite and nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Endometriosis
Andere Medikamente: Birth control-Errin Adderall XR 25mg (last dose taken was Wed, 11/24) Tylenol 500mg (to prepare for future sxs from booster shot)
Allergien: NKA NKDA
Vorherige Impfungen: Just this one flu shot (never before). Only had headache

VAERS 1912949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 28.03.2021
Beginn: 30.11.2021
Tage bis Beginn: 247,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Hospitalized with shortness of breath and treated for COVID

Weitere VAERSDATA-Felder

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

VAERS 1910685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: TN
Alter: 25,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 28.09.2021
Beginn: 10.11.2021
Tage bis Beginn: 43,0
Dosis: 2
Route/Site: SYR / LA

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

Anxiety Heart rate increased Hypertension

Symptomtext

Rapid Heart Rate, Anxiety, High Blood Pressure. All began for the first time after vaccination. Approximately 10 weeks after vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Was recently diagnosed with high blood pressure as of November 30, 2021. I am currently taking 10mg of Lisinopril daily.
Aktuelle Erkrankungen: N/A
Vorgeschichte: -
Andere Medikamente: N/A
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1909965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: AR
Alter: 39,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 15.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Cognitive disorder Confusional state Disorientation Headache Impaired driving ability Mobility decreased Mouth haemorrhage Nausea Visual impairment

Symptomtext

SEVERE HEADACH AND NAUSEA THAT MOVED TO COGNITIVE EFFECTS OF DISORIENTATION, VISUAL PROCESSING ISSUES, INABILITY TO DRIVE, DECREASE REACTION TIME, CONFUSION, BLEEDING ORAL MUCOSA. PATIENT DID NOT GO TO THE DOCTOR BUT DID TAKE ASPIRIN 81MG ONCE DAILY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: valtrex, fish oil, multivitamin,
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1909421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WI
Alter: 61,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Chest pain Headache Neck pain Pain Pain in extremity

Symptomtext

Patient called today (11/30/21) to report that on the evening he received his pfizer booster vaccine (11/24) he started experiencing severe pains in his arm that radiated to his shoulder, neck, and across his chest. He also reports on and off headaches in the days since he received his vaccine. He reports only mild improvement from the initial symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Patient reported that prior to coming for his vaccination, he had an appointment to get a root canal done at his dentist
Vorgeschichte: diabetes, high blood pressure,
Andere Medikamente: Patients daily medication regimen: losartan, tresiba flextouch, Trulicity, chlorhaltidone, sprionolactone, metoprolol succinate, farxiga, citalopram, gabapentin
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2633971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WI
Alter: -
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: UN / UN

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

Feeling abnormal Feeling of body temperature change Fluid retention Injected limb mobility decreased Injection site erythema Injection site induration Injection site pain Injection site swelling Injection site warmth Pruritus

Symptomtext

I received my Covid booster on Thursday, November 18. All three doses were Pfizer. On Friday and Saturday, I was in a daze and alternately way too hot and way too cold. Then on Sunday morning I couldn't move my arm. The entire outer half of my upper arm where I had received the injection was extremely swollen, red, hot, hard, and painful. Monday it was still bad, so I called my doctor's office and the nurse said to come in. The doctor said to switch from Tylenol to Aleve and to keep applying a cold pack and that it would go away in less then two weeks. She said maybe get Moderna if we have to get more boosters in the future, but I've read that covid arm is more common with Moderna. I don't know when I've had a bad a pain as that (9/10) for 2 whole days. It has been slowly getting better every day. Range of motion was back by Wednesday the 24th. Now its Monday the 29th, and my arm is still hot, itchy, and retaining some water.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure well controlled with medication
Andere Medikamente: hydrochlorothiadize, potassium chloride, vitamin D, Aleve
Allergien: peaches, almonds
Vorherige Impfungen: -

VAERS 1905734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IL
Alter: 55,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Blood glucose normal Dizziness Hypertension

Symptomtext

Ten minutes after the shot I felt like I was going to pass out. Felt very similar to an experience I had where I passed out shortly after giving blood. I was dizzy and light headed and called for help. Pharmacist took my BP which was high so paramedics were called.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Glucose test was normal Heart was normal BP was elevated
Aktuelle Erkrankungen: Slight cold a few days before booster
Vorgeschichte: Hashimotos disease Cavernous angioma
Andere Medikamente: Synthroid Liothyronine Zyrtec D3 B12 Calcium
Allergien: Bactria, sulfa drugs Milk Wheat Corn Soy
Vorherige Impfungen: -

VAERS 1905612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 26.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Chills Fatigue Headache Hypoaesthesia Lip swelling Paraesthesia oral

Symptomtext

Numbness in face. Not completely numb, but enough that it is noticeable. Also, lips feel full and tingly, but are not noticeably larger. I first noticed this event approximately 72 hours post injection. I experienced the usual chills, fatigue, headache for approximately 36 hours following injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: No tests - just keeping an eye on it.
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Junel
Allergien: n/a
Vorherige Impfungen: -

VAERS 1905012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: FL
Alter: 36,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 27.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chest pain Electrocardiogram normal Laboratory test normal Limb discomfort Lymphadenopathy

Symptomtext

1 week after getting 2nd COVID vaccine, developed chest pain, and left arm heaviness. Reports intermittent sharp chest pain and chest heaviness for 1 week prior to going to Emergency room. Patient states he still developed intermittent chest pain, that has not resolved. Reports left arm heaviness for 3 days and left lymph node swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Patient reports he went to the local Emergency room. Does not have ER notes or treatment received. Patient states he underwent. EKG, lab work- reporting test "normal." Patient states he was informed by ER doctor if chest pain continues, he will need to return for further treatment.
Aktuelle Erkrankungen: no
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1904295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IL
Alter: 33,0
Geschlecht: M
Eingang: 28.11.2021
Impfdatum: 17.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / RA

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

Atrial fibrillation Blood magnesium normal Blood thyroid stimulating hormone normal Cardiac flutter Chest discomfort Drug screen negative Echocardiogram Echocardiogram normal Ejection fraction decreased Extrasystoles Fatigue Full blood count normal General physical health deterioration Heart rate increased Hypotension Metabolic function test normal

Symptomtext

2nd shot: woke up one night with heart fluttering for about 10-15 minutes. Went back to sleep without any further issues. 3rd shot: 11/21 woke up at 10:45pm with a rapid heartbeat and fluttering. I had my smartwatch with me and my heartbeat was at 160-180bpm. I waited about an hour and a half prior to checking myself into the hospital. I travel for work, working in a specific city that weekend and check myself into hospital around 12:30a.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 1,0
Labordaten: Hospital notes: Attestation signed by MD at 11/26/2021 4:16 PM I saw and evaluated the patient. I have reviewed the resident's/fellow's findings and agree. Yes - I provided critical care for this patient. Critical care was necessary because there was a high probability of imminent or life-threatening deterioration and this patient required continuous observation and interventions to respond to emergent changes in their medical condition and prevent further deterioration in their clinical state. The critical care I provided included: managing hypotension or other hemodynamic instability, management of electrolyte/metabolic abnormalities, consultation with specialists, and review of medical records Critical Care Time: I spent a total of (30-74 minutes) 56 minutes personally providing critical care to patient. This does not include time spent teaching or performing any separately billable procedures. Patient is a 33-year-old male with no significant past medical history who presents to the ED in atrial fibrillation with rapid ventricular response. His initial HR was 181; he is hemodynamically stable with SBP in the 140s and is satting well on room air without other symptoms related to the fibrillation. Labwork including CBC, BMP, TSH, magnesium, utox sent. Labs all within normal limits and utox negative. No clear trigger for atrial fibrillation for this patient, given normal labs, no substance use. Patient given 5mg metoprolol initially with decrease in rates from 180s to 140s. Additional 5mg x2 metoprolol IV given without further significant response. Discussed cardioversion with patient; he prefers to avoid at this time and requests other pharmaceutical options. Patient given .0.25mg/kg diltiazem IV with good response with HR decrease to the 90s; patient remains in atrial fibrillation. Cardiology consulted for admission and recommend initiation of 5mg apixaban and 120mg ER diltiazem PO. At 4am, patient Hrs back between 130s and 150s and he was given an additional 0.35mg/kg diltiazem. TTE ordered. Patient was transferred to the inpatient floor in stable condition. (My notes) 7am converted to normal sinus rhythm was released at 10:30am on Monday 11/22 and traveled back home to another city that evening. (Post Hospital visit) Saw my personal doctor back in my city and as recommended by the cardiologists at the other city's hospital they recommended an Eco. My doctor order an Eco and it was performed at a local hospital on 11/24 notes are below. (Eco Results) PHYSICIAN INTERPRETATION: Left Ventricle: Normal LV systolic function. Left ventricular ejection fraction, by visual estimation, is 60 to 65%. Spectral Doppler shows normal pattern of LV diastolic filling. The left ventricular cavity size is normal. Right Ventricle: The right ventricular cavity is normal in size and structure. Global RV systolic function is normal. Left Atrium: The left atrium is normal in size and structure. Right Atrium: The right atrium is normal in size and structure. Mitral Valve: The mitral valve is structurally normal with normal leaflet excursion. Tricuspid Valve: The tricuspid valve is structurally normal with normal leaflet excursion. Aortic Valve: The aortic valve is trileaflet and structurally normal with normal leaflet excursion. The aortic valve is tricuspid. Pulmonic Valve: The pulmonic valve is trileaflet without evidence of stenosis or insufficiency. Aorta: The aortic root and ascending aorta are structurally normal with no evidence of dilitation. Pericardium: No evidence of pericardial abnormalities. There is no pleural effusion in either the left or right lateral region. In comparison to the previous echocardiogram(s): There are no prior studies on this patient for comparison purposes. ECHO/TEE --- Final --- 11/28- still feeling very tired and experiencing chest tightness at times especially when laying down when trying to sleep. Have had a few skipped beats/flutters in the past week but nothing more than a couple of beats and not for an extended period of time.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Azelastine, Benadryl, Claritin D
Allergien: Tree nuts, sesame seeds, Aleve, Advil, NSAIDs
Vorherige Impfungen: Pfizer 5/3

VAERS 1904108

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: ID
Alter: 56,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Chest discomfort Cough Dry mouth Eye irritation Fatigue Nausea Paraesthesia Pyrexia Rhinorrhoea

Symptomtext

Woke up entire body was still. Extreme dry mouth. Nausea. Every joint aching (wrists, ankles, neck, elbows, knees, and shoulders. Fever over 100. Runny nose and cough. Extreme fatigue, especially when standing. Burning sensation in eyes (possibly related to the fever). Got tired when walking short distances, taking deep breaths because of chest tightness. Pins and needles sensation in no particular location (felt like I was being poked). Need to mention that this injection was painful and the other two were not, I wonder if it had something to do with the technician not injecting in the right sport or hitting nerve).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: Type II Diabetes
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1903467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WA
Alter: 60,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 23.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Dizziness Dyspnoea Heart rate increased Nausea Pyrexia

Symptomtext

Short of breath, chest pain. heart beats fast with little movement. Dizziness with Nausea. Fever on face and head

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: 3 times of stent insertion of surgery cardiovascular expansion. But recent heart check-up, dated October 2021, with cardiologist resulted fine. Test included EKG, treadmill test etc.
Vorgeschichte: Heart disease.
Andere Medikamente: N/A
Allergien: No known allergy
Vorherige Impfungen: -

VAERS 1902261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CO
Alter: 43,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Fatigue Gaze palsy Injection site pain Lymphadenopathy Paraesthesia Pyrexia Tenderness

Symptomtext

Day 1:Left Arm pit became tingly evening of the injection. Sore injection site Day 2: Lymph node started to swell. Skin tender in armpit. Fatigue. Sore injection site. Day 3: fatigue, more swelling and tenderness in armpit. Woke with headache. Day 4: headache woke me during the night. Left armpit still swollen and tender. Fever, tingly feeling in face, slightly dizzy feeling. Fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Obese
Andere Medikamente: -
Allergien: Eurythromyicine
Vorherige Impfungen: -

VAERS 1900005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IN
Alter: 36,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Injection site pain Middle ear effusion Movement disorder Pain Pyrexia Tremor

Symptomtext

103.9 fever, chills, shaking, chattering teeth, full body pains and aches, I was unable to move I was in so much pain, fluid in ears felt like boiling wax. Very sore arm of injection site. Fever took 12 hours to break but then came back on 11/25/21 at 11am. Currently taking ibuprofen and Tylenol every 4 hours and fever is is at 101.1 right now. I only had a sore arm with the first two shots, something isn?t right with this one or this lot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None so far, will see dr tomorrow if fever doesn?t go away or stay away.
Aktuelle Erkrankungen: None
Vorgeschichte: Dry eye disease and allergies
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1899714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: TX
Alter: 82,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac disorder Chest discomfort Chest pain Flushing Hyperhidrosis Interchange of vaccine products

Symptomtext

Systemic: Cardiac Disorder (diagnosed by MD)-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Flushed / Sweating-Medium, Additional Details: pt received moderna series and pfizer booster

Weitere VAERSDATA-Felder

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

VAERS 1899362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: FL
Alter: 40,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 14.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Chest discomfort Dyspnoea Fatigue Pain in extremity SARS-CoV-2 test

Symptomtext

shortness of breath/ can't take full breath; Sore arm; tightness in chest; fatigue; This is a spontaneous report from a contactable consumer (Patient). A 40 years-old non-pregnant female patient received bnt162b2 (BNT162B2, Lot Number: FH8027), via Intramuscular on arm left on 14Nov2021 10: 00 AM (at the age of 40 years-old) as dose 1, single for COVID-19 immunization at a Pharmacy or drug store. The patient's medical history was not reported. The patient did not take any other medications in two weeks. 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 has been tested for COVID-19. On 15Nov2021, the patient experienced shortness of breath/ can't take full breath, sore arm, tightness in chest and fatigue. On 15Nov2021 08: 00 AM, the patient underwent lab tests and procedures which included Nasal Swab: Pending. The patient did not receive any treatment for adverse event. The outcome of events was recovering. Follow-Up (18Nov2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211115; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Pending
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1893997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Angioedema Facial discomfort Facial pain Pain in jaw Paraesthesia oral

Symptomtext

Tongue tingling, tightness in face, right side of face droopy, smile crooked, jaw and chin sore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Sertraline Trazodone Vitamins
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 1893663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: IL
Alter: 20,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest discomfort Chest pain Dizziness Dyspnoea Nausea Pruritus Throat irritation

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: itchty throat-Medium, Systemic: Nausea-Mild, Additional Details: Patient stated self administer benadryl after arriving home

Weitere VAERSDATA-Felder

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

VAERS 1888794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain upper Burning sensation Dizziness Dysstasia Hypoaesthesia Migraine Muscle spasms Pain in extremity Uterine spasm Vaginal haemorrhage

Symptomtext

I woke up the following morning covered in blood. I am not on my period my period is not due for another 7 days. Vaginal bleeding confined for over the day until now it?s been 2 days of heavy bleeding. My legs are hurting almost feel like they are on fire. Cramping and numbness at times. My stomach and uterus are also cramping to the point I can?t stand straight. Dizziness and a terrible migraine

Weitere VAERSDATA-Felder

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

VAERS 1884984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: VA
Alter: 86,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Dizziness Erythema Flushing Hyperhidrosis Tachycardia

Symptomtext

Systemic: Abdominal Pain-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: face was not swollen but very red-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Tachycardia-Mild

Weitere VAERSDATA-Felder

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

VAERS 1884185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NC
Alter: 53,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Cardiac flutter Fatigue Palpitations Ventricular extrasystoles

Symptomtext

fluttering; heart started racing; diagnosed with MVPC, multiple ventricular premature complexes; fatigue; same heart issue.; This is a spontaneous report from a contactable consumer (patient). A 53-year-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on 29Oct2021 16:45 (Lot Number: FH8027) at age of 53-year-old as single dose for covid-19 immunisation. Medical history included asthma, allergy to sulfur drugs, latex, guillain-barre syndrome, fibromyalgia. The patient was not pregnant at time of vaccination. No covid prior vaccination. The other medications in two weeks included normal prescriptions. The patient previously took bnt162b2 (lot number=FF2587) dose 1 on 08Oct2021 04:45 PM at Left arm at age of 53-year-old for covid-19 immunisation, azithromycin (Z-PAK). Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Within 30 minutes (29Oct2021 17:15), heart started racing, fluttering, palpitations. Patient went to the ER Saturday morning, diagnosed with MVPC, multiple ventricular premature complexes- V complexes w/ short R-R. A week later she was still feeling the same, now with fatigue, still have same heart issue. She cannot get into a cardiologist as ER doctor recommended until 24Nov2021. All event onset date was 29Oct2021 17:15. The adverse event result in Emergency room/department or urgent care. No treatment received for the events. The covid was not tested post vaccination. The outcome of events was not recovered. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Fibromyalgia; Guillain-Barre syndrome; Latex allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1881272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MI
Alter: 31,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dyspnoea Throat irritation

Symptomtext

Client complained of itching of the throat, tightness of chest, shortness of breath after receiving 1st dose of Pfizer. 25mg of Benadryl was given. 2 doses of epinephrine 0.3ml at 11:35am and 11:45am. Vitals were monitored. EMS was called . After assessment by EMS client was transported to the hospital.

Weitere VAERSDATA-Felder

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

VAERS 1880081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Hypertension Oropharyngeal pain

Symptomtext

Systemic: Chills-Mild, Systemic: throat pain- no swelling. Just pain-Mild, Systemic: Hypertension-Mild, Additional Details: Checked patient's BP was 143/82 then 135/78 5 mins later. Could be due to anxiety

Weitere VAERSDATA-Felder

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

VAERS 1876567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 50,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
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 Fatigue Headache Malaise Nausea Pain Pyrexia

Symptomtext

Mild Fever, Fatigue, Body Aches, Headache, Malaise, Nausea all on Tuesday November 16th. Mild Body Aches, Mild Headache on Wednesday November 17th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Mitral Valve Prolapse
Andere Medikamente: Woman's One-a-Day, St. John's Wort, Glucosamine, Vitamin C
Allergien: Percocet
Vorherige Impfungen: Malaise, Body Aches after 1st Covid vaccine, Age 49, vaccine on 3/17/2021 (Pfizer)

VAERS 1869804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

moderat

Staat: IL
Alter: 38,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Dyspnoea Fatigue Hypertension Troponin increased

Symptomtext

Blood pressure of 185/150 .. chest pain, shortness of breath, and fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Troponin level high19
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D 3
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1865678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OH
Alter: 29,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Urticaria

Symptomtext

WITHIN 2 MINUTES SHE HAD BROKEN OUT IN HIVES AND ONLY SECONDS LATER, SHE BEGAN HAVING DIFFICULTY BREATHING

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: IVP DYE
Vorherige Impfungen: -

VAERS 1857161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: PA
Alter: 19,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Chills Dizziness Hyperventilation Hypoaesthesia Tardive dyskinesia Tremor

Symptomtext

Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Hyperventilation-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Shakiness-Mild, Systemic: Weakness-Medium, Additional Details: After 15 minutes from injection she slumped to the floor, lips were quivering, c/o weakness and numbness in arms, hyperventilating, BP 130/82, pulse regular at 82. Called 911.

Weitere VAERSDATA-Felder

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

VAERS 1857142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

moderat

Staat: IN
Alter: 65,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Diarrhoea Dyspnoea Injection site pain Sleep disorder

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Chills-Medium, Systemic: Diarrhea-Medium, Systemic: Unable to Sleep-Mild

Weitere VAERSDATA-Felder

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

VAERS 1855347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: MO
Alter: 29,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Heart rate increased Hypertension Palpitations

Symptomtext

Patient reported heart pounding and like someone was twisting her chest. She had a high blood pressure and pulse about 15 minutes after getting shot

Weitere VAERSDATA-Felder

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

VAERS 1854920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: GA
Alter: 23,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 04.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Cough Dyspnoea Pyrexia Respiratory tract congestion

Symptomtext

PATIENT FEELING DIFFICULTY IN BREATHING, CHEST CONGESTION AND COUGHING A LOT AFTER 2 DAYS OF FEVER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: paliperidone, Buspirone, Divalproex 500 mg, Amanatadine
Allergien: none
Vorherige Impfungen: -

VAERS 1853636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: OR
Alter: 85,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysphagia Dyspnoea Eye swelling Mouth swelling Swelling face Swollen tongue Throat tightness

Symptomtext

Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe, Additional Details: symptom onset after patient left pharmacy, after the 15minute observation was over

Weitere VAERSDATA-Felder

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

VAERS 1835590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 49,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Chills Dysgeusia Dyspnoea Hyperhidrosis Lymphadenopathy Myalgia Pyrexia

Symptomtext

difficulty breathing; Swelling of lymph node under left armpit and left jaw.; Metal taste in mouth; fever (99.6 F); chills; sweats; muscle aches; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 49-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot Number was FH8027,e xpiry date was not reported), via an unspecified route of administration, administered in Arm Left on 15Oct2021 12:45 as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation. Medical history included,drug hypersensitivity from an unknown date and unknown if ongoing. There were no concomitant medications. The patient did not receive any other vaccines within four weeks prior to the 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. The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number was EN6207, Expiry date was not reported) via an unspecified route of administration on 14Mar2021 08:00AM, administered in Left arm as dose 1, single for covid-19 immunisation and on 04Apr2021 08:00AM patient had received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number was ER8733, Expiry date was not reported) via an unspecified route of administration, administered in Left arm as dose 2, single for covid-19 immunisation. On 15Oct2021 21:00 the patient experienced difficulty breathing, swelling of lymph node under left armpit and left jaw, metal taste in mouth, fever (99.6 f), chills, sweats, muscle aches. On 15Oct2021 the patient underwent lab tests and procedures which included body temperature was 99.6 fahrenheit. Events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of difficulty breathing, swelling of lymph node under left armpit and left jaw, metal taste in mouth,fever (99.6 f),chills, sweats,muscle aches included Advil and drink water. The clinical outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211015; Test Name: temparature; Result Unstructured Data: Test Result:99.6 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1833636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: WA
Alter: 34,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Chills Dyspnoea Eye swelling Feeling abnormal Headache Nausea Pain Pyrexia Vomiting

Symptomtext

Around 8pm, I started having chills. Around 10pm, I started having body aches, joint pain, and headaches. The next morning had a low-grade fever. On Monday, I was almost symptom free. On Monday night, my symptoms came back. On Tuesday night, I nausea and vomiting. My symptoms continued on Wednesday and Thursday. On Friday, I was symptom free. On Saturday, my symptoms came back. On Sunday, I had difficulty breathing and had brain fog. My eye started swelling.

Weitere VAERSDATA-Felder

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

VAERS 1821397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 52,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Condition aggravated Eye swelling Eyelid ptosis Hypersensitivity Interchange of vaccine products Lymphadenopathy Swelling of eyelid Throat tightness

Symptomtext

When I took my 1st Pfizer dose on 6/2/21, I suffered an allergic reaction (lymph glands swelled & my throat closed, making it difficult to swallow). This made it very difficult to use my CPAP, which my job requires me to use for my sleep apnea. The CDC website recommends not taking Pfizer or Moderna for the 2nd dose if you had an allergic reaction to the 1st dose. So, I delayed receiving another dose. However now, as a federal employee, I am required to become fully vaccinated. I have a family history of blood clotting (my mother suffered a massive stroke as a result), so the J&J vaccine is not a viable option due to the multitude of reports of blood clotting as a side effect. I consulted with my FAA medical examiner who I go to for my annual physical (for my job) and he recommended taking the 2nd Pfizer dose, but to also take 50mg of Benadryl before and after, which I did. I took the 2nd dose two days ago and had an even worse allergic reaction. In addition to my lymph glands swelling and throat closing, my left eyelid is swollen and drooping. I went to the doctor yesterday for a diagnosis, which is outlined in Item 19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I went to my primary care physician yesterday (10/26/21) because of the allergic reaction I suffered from the 2nd Pfizer dose. He believed it is an allergic reaction, and initially recommended Benadryl. However, after a full day of taking Benadryl, my condition has worsened. My left eyelid is drooping to a point where it is nearly fully closed. The swelling around my eye has also worsened. The doctor still believes it is an allergic reaction, but I fear it could be Bells Palsy. The doctor prescribed Prednisone, and he wants me to follow up with him tomorrow. If my condition has not improved, he wants to see me in his office again.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes (Type 2) and Severe Obstructive Sleep Apnea
Andere Medikamente: Metformin, Finasteride
Allergien: None known (however, I did suffer an allergic reaction after my first Pfizer COVID-19 dose)
Vorherige Impfungen: Pfizer EW0178, 06/02/2021

VAERS 1813988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: NJ
Alter: 77,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Tremor Vomiting

Symptomtext

About 15 minutes after the patient received her 3rd dose (booster) of covid 19 Phizer vaccine, the patient vomited and her hands started to shake. The patient was in another room being observed by the patient care techs of the facility when this occurred. This was a memory care facility for the mentally ill. I did not witness the occurrence first hand. We sat the patient down where she relaxed and notified the medical physician on staff who would come to evaluate her. There was no signs of difficulty breathing or allergic reaction. Patient seemed tired when I left where she was being observed by the facility staff until the physician arrived. Side note: she was administered the vaccine shortly after eating lunch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None that I am aware of, not sure what was preformed once physician arrived.
Aktuelle Erkrankungen: Mental Illness, UTI infection treated 10/4/21
Vorgeschichte: Mental Illness, Cholesterol, GI Issues (constipation/diarrhea)
Andere Medikamente: Alprazolam 0.25mg, Atorvastatin 20mg, AZO cranberry, Divalproex DR 125mg caps, Colace 100mg, Loperamide 2mg, Mirtazipine 15mg, Quetiapine 25mg, Trazadone 100mg, Vit B12, C and D2 50,000. Zinc 50mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1813869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: TN
Alter: 16,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Headache Hypersensitivity Hypoaesthesia Lip erythema Lip swelling Paraesthesia

Symptomtext

20 minutes after receiving her second COVID dose, patient began having symptoms of an allergic reaction. We were in the car, and her hands began tingling and getting numb, her lips got red and a bit swollen, and she began to have a throbbing headache. Within 10 minutes of symptoms, I gave her 15 ml Benadryl. She slept for an hour and woke feeling better with none of previous symptoms. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Exactly one month ago she had an allergic reaction to something she ate. I took her to the ER and she was given IV antihistamines and steroids.
Vorgeschichte: None
Andere Medikamente: Vitamin C Vitamin D
Allergien: Histamine intolerance
Vorherige Impfungen: -

VAERS 1806519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

moderat

Staat: WA
Alter: 55,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Dehydration Headache Vomiting

Symptomtext

Vomiting, headache, dehydration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine, anxiety
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1804581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: VA
Alter: 21,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 18.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chest pain Dizziness Dyspnoea Nausea

Symptomtext

Extreme shortness of breath, dizziness, nausea, chest pain. All symptoms lasted 48 hours.

Weitere VAERSDATA-Felder

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

VAERS 1798342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 12.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Asthma Choking Condition aggravated Cough Diarrhoea Dyspnoea Fatigue Headache Injection site erythema Injection site pain Injection site swelling Pain Productive cough Sputum discoloured

Symptomtext

I got the shot and I didn't feel anything until the next day and it might have been because it took that long until the next morning. I was extremely tired and my body ached. I had redness and swollenness on my arm where the shot was. Redness, swollen, and pain. And then the next day (Wednesday) those were the same effects. I was tired all day long. Thursday, I was still very exhausted and I felt like my body was beaten up with a baseball bat and was achy all over. Friday I was exhausted and achy all over. At night at 10:50pm on Friday, I got the asthmatic attack. I kept coughing and choking and I couldn't catch my breath. Luckily I had my nebulizer next to me, and I had all the medications readily available. Ipratropium bromide 0.5 mg and the Albuterol sulfate inhalation solution 3mg, Use 3mL vile nebulizer 4 times daily. Saturday and Sunday and yesterday, I've been coughing up yellow and green phlegm. So I called my doctor on Saturday for the asthmatic attack and she said if it gets worse, to go to ER but I just did the nebulizer. Monday 10/18, I called her again about the phlegm and that it was yellow and sometimes green and over the phone, she said that she would send a prescription for amoxicillin clav. I did have diarrhea on 10/18/21 as well. Headaches after vaccination. Currently still tired and achy (10/19/2021).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: asthma because of the fire smoke - breathing treatments on nebulizer and inhaler
Vorgeschichte: asthma; sleep apnea; chronic back pain - degenerative disc disease; osteoarthritis; scoliosis; 5 bulging discs; spin stenosis; fibromyalgia; GERD; acid reflux; migraines
Andere Medikamente: Pantoprazole 40mg daily; Dicyclomine 10mg 4 times daily before meals; Fluoxetine 60mg (3 20mg tabs) once daily; Bupropion 150mg 24-hour tab ? once daily; Atenolol 25mg 12.5 mg daily; Medical cannabis as needed; Flaxseed oil 1 tab daily; Vit
Allergien: time release morphine; time release methadone; codeine; Vicodin; azithromycin; abilify; latex; roses
Vorherige Impfungen: 1st Pfizer COVID-19 Shot: 2/8/2021 Lot#EN9581 2nd Pfizer COVID-19 Shot: 3/1/2021 Lot#EN6203 Tiredness for both and achy body,

VAERS 1795398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: VA
Alter: 44,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Paraesthesia

Symptomtext

IMMEDIATELY AFTER RECEIVING THE VACCINE PATIENT REPORTED FEELING TINGLING IN THE ARM THAT RECEIVED THE INJECTION. PATIENT SAID IT FELT LIKE THEIR ARM FELL ASLEEP. THERE WAS NO REDNESS AT THE INJECTION SITE. NO INDICATION OF HIVES, SWOLLEN LIPS OR TONGUE, OR DIFFICULTY BREATHING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NO KNOWN HEALTH CONDITIONS
Vorgeschichte: NO KNOWN HEALTH CONDITIONS
Andere Medikamente: NO PRESCRIPTIONS, OR OTC MEDICATIONS ON PATIENT PROFILE
Allergien: NO KNOW ALLERGIES
Vorherige Impfungen: -

VAERS 1795383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: VA
Alter: 45,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

IMMEDIATELY AFTER RECEIVING THE VACCINE PATIENT REPORTED FEELING TINGLING IN THE ARM THAT RECEIVED THE INJECTION. PATIENT SAID IT FELT LIKE THEIR ARM FELL ASLEEP. THERE WAS NO REDNESS AT THE INJECTION SITE. NO INDICATION OF HIVES, SWOLLEN LIPS OR TONGUE, OR DIFFICULTY BREATHING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO KNOWN HEALTH CONDITIONS
Vorgeschichte: NO KNOWN HEALTH CONDITIONS
Andere Medikamente: PHENTERMINE 37.5 MG TABELTS
Allergien: PENICILLIN
Vorherige Impfungen: -

VAERS 1793850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

moderat

Staat: IN
Alter: 35,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Dyspnoea Hyperventilation Panic attack

Symptomtext

PATIENT STATED SHE HAS BEEN DIZZY SINCE SHE RECEIVED HER FIRST PFIZER VACCINATION 9/21/21, THE VACCINE IS REQUIRED FOR HER EMPLOYMENT AND SHE WISHED TO GET HER SECOND DOSE, ABOUT 15 MINUTES AFTER HER DOSE SHE CAME BACK TO THE PHARMACY HYPERVENTALATING OR HAVING A PANIC ATTACK (WE CALLED 911) AFTER ABOUT 5 MINUTES OF ATTEMPTING TO CALM THE PATIENT SHE CLAIMED SHE COULD NOT BREATHE, WE ADMINSTERED A DOSE OF EPINEPHRINE, SHE CALMED FOR ABOUT 5 MINUTES AND STARTED HYPERVENTALATING AGAIN, THE PARAMEDICS THEN ARRIVED AND STABALIZED THE PATIENT AND TRANSPORTED HER TO THE HOSPITAL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma
Andere Medikamente: meclizine
Allergien: none
Vorherige Impfungen: -

VAERS 2726698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 21.12.2023
Impfdatum: 16.02.2021
Beginn: 25.08.2023
Tage bis Beginn: 920,0
Dosis: 3
Route/Site: IM / RA

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

Bronchitis COVID-19 Chills Hypokalaemia Pyrexia SARS-CoV-2 test positive Sepsis Urinary tract infection Urine odour abnormal

Symptomtext

Reported Symptoms: 10011232:COUGHING; 10016558:FEVER; 10021018:HYPOKALEMIA; 10040047:SEPSIS; 10084401:COVID-19 RESPIRATORY INFECTION; Narrative: Patient received five doses of Pfizer COVID 19 Vaccine (Feb/Mar/Dec 2021) and (May/Dec 2021). The patient presented to the ED on 25 Aug 23 with fever, chills, and foul-smelling urine. The patient tested positive for COVID-19 on 25 August 23. The patient was admitted to the hospital on 25 Aug 23 with sepsis, covid 19, hypokalemia, and UTI. The patient was treated with antibiotics and electrolytes and discharged on 28 August 2023 in stable condition. Patient did develop post covid bronchitis and was seen in the ED on 6 Sep 23. Reported per EUA. Other Relevant HX: Other: sepsis, covid 19, hypokalemia

Weitere VAERSDATA-Felder

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

VAERS 2717509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MD
Alter: 70,0
Geschlecht: F
Eingang: 24.11.2023
Impfdatum: 14.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Pain SARS-CoV-2 test

Symptomtext

each time, only had sore spot to touch; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An elderly female patient received bnt162b2 (BNT162B2), on 14Nov2021 as dose 3 (booster), single (Lot number: FH8027) at the age of 70 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: bnt162b2 (First dose, Lot. EN6200), administration date: 26Feb2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "each time, only had sore spot to touch"; bnt162b2 (Second dose, Lot. EN6206), administration date: 19Mar2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "each time, only had sore spot to touch". The following information was reported: PAIN (non-serious), outcome "unknown", described as "each time, only had sore spot to touch". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Each time, only had sore spot to touch and negative COVID-19 test (PCR) after the vaccinations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test (PCR); Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2715869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NJ
Alter: 36,0
Geschlecht: F
Eingang: 20.11.2023
Impfdatum: 17.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Back pain Body temperature Chills Headache Nausea Pain Pain in extremity Pyrexia

Symptomtext

headache; body aches; nausea; shooting pain through back; 101.1 fever; chills; Sore arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). An adult female patient (unknown if pregnant) received bnt162b2 (BNT162B2), on 17Oct2021 as dose 3 (booster), single (Lot number: FH8027) at the age of 36 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ELINEST taken for contraception (ongoing). Vaccination history included: bnt162b2 (Dose 1, Lot number: EK9231, Time: 13:00, Vaccination site: left arm upper), administration date: 30Dec2020, when the patient was 35-year-old, for COVID-19 immunisation, reaction(s): "headache", "Sore arm"; bnt162b2 (Dose 2, Lot number: EL8982, Time: 13:00, Vaccination site: left arm upper), administration date: 20Jan2021, when the patient was 35-year-old, for COVID-19 immunisation, reaction(s): "Headache", "Body aches", "Sore arm", "nause", "Slight fever". The following information was reported: HEADACHE (non-serious), outcome "unknown"; PAIN (non-serious), outcome "unknown", described as "body aches"; NAUSEA (non-serious), outcome "unknown"; BACK PAIN (non-serious), outcome "unknown", described as "shooting pain through back"; PYREXIA (non-serious), outcome "unknown", described as "101.1 fever"; CHILLS (non-serious), outcome "unknown"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Sore arm". Relevant laboratory tests and procedures are available in the appropriate section.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201152033 same patient and reporter, different dose and event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:101.1 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ELINEST
Allergien: -
Vorherige Impfungen: -

VAERS 2627025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AL
Alter: 61,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 22.09.2022
Beginn: 07.02.2023
Tage bis Beginn: 138,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Illness Impaired work ability Influenza virus test Insomnia Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a hard time sleeping, nose was running, so I stayed home from work. On the third day I woke up with an extremely sore throat, and I went to the doctor, and he tested me and told me that I had COVID. He prescribed LAGEVRIO (MOLNUPIRAVIR) 200 MG. I started taking it and within 3-4 days felt much better. I still quarantined at home for 10 days after the onset of my illness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID / Flu test on 02/09/2023
Aktuelle Erkrankungen: -
Vorgeschichte: Sleep apnea, depression, bipolar disorder, high blood pressure, gout, obese.
Andere Medikamente: allopurinol amlodipine Azelastine Hydrocline Nasal Spray bupropion XL lamotrigine Latuda lisinopril Lithium Carbonate montelukast Multivitamin Tamsulosin HCL Ventoiin HFA Zyrtec Vitamin B6 Multivitamin
Allergien: Allergic to Biaxin antibiotic.
Vorherige Impfungen: -

VAERS 2588123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: RI
Alter: 51,0
Geschlecht: F
Eingang: 28.02.2023
Impfdatum: 16.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Pain in extremity Vaccination site pain

Symptomtext

My arm where it was administered has been painful to touch/Sometimes just sitting I feel pain in the arm.; My arm where it was administered has been painful to touch; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP), Program ID: The reporter is the patient. A 51-year-old female patient received BNT162b2 (BNT162B2), on 16Oct2021 at 10:30 as dose 3 (booster), single (Lot number: FH8027) at the age of 51 years, in arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1st, Time (24hr): 11:30 AM, Batch/Lot number: Not available / Provided at time of report completion), administration date: 13Mar2021, when the patient was 50-year-old, for COVID-19 Immunization; BNT162b2 (Dose 2nd, Time (24hr): 11:00 AM, Batch/Lot number: Not available / Provided at time of report completion), administration date: 10Apr2021, when the patient was 50-year-old, for COVID-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset Oct2021, outcome "unknown", described as "My arm where it was administered has been painful to touch"; PAIN IN EXTREMITY (non-serious) with onset Oct2021, outcome "unknown", described as "My arm where it was administered has been painful to touch/Sometimes just sitting I feel pain in the arm.". Additional information: Ever since the third dose (Booster) on 16Oct2021, her arm where it was administered has been painful to touch as well as whenever she carries anything heavy in that hand/arm. Sometimes just sitting she feel pain in the arm. In addition, 6 weeks after the 4th booster of 10Nov2022 she tested positive for COVID-19.

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 2585070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MD
Alter: 65,0
Geschlecht: F
Eingang: 21.02.2023
Impfdatum: 04.11.2021
Beginn: 22.12.2021
Tage bis Beginn: 48,0
Dosis: 3
Route/Site: IM / LA

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

Biopsy uterus abnormal Dysmenorrhoea Endometriosis Fatigue Hysterectomy Laparoscopic surgery Menstrual disorder Pathology test Ultrasound scan Uterine dilation and curettage Uterine haemorrhage

Symptomtext

I feel there is an association of my post-menopausal diagnosis of endometriosis with the receiving mRNA COVID shots/boosters. After a dozen years of menopause, I began having a period and cramping on 12.22.21. I had a uterine biopsy and no cancer was found, but much bleeding was present. The cramping and exhaustion from the symptoms became worse over the months following, and I had diagnostic sonograms and exams by a GYN. I had laparoscopic surgery on 5/31/22 and was diagnosed with endometriosis at age 65 and 9 months. I noticed the initiation of this uterine abnormal reactivity was after my first booster shot (Pfizer 11.4.21). The doctor removed endometriosis from my bladder, ovaries, and fallopian tubes and performed uterine curettage. I recovered from this surgery, and --reluctantly-obtained my 2nd booster (Moderna 6.23.22). About two weeks later, on 7/9/22 I started bleeding and cramping again! I couldn't believe it and this time the association really clicked. This pain (and associated fatigue) continued for 3 months. I had a complete hysterectomy on 10/11/22. Even after the laparascopic surgery and D/C, there was endometriosis present and my uterus was 2x normal size with hyper-proliferative lining.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Intrauterine sonograms - Radiology Hospital Outpatient surgery and Pathology Uterine biopsy - negative for cancer Pathology- endometriosis tissue found on bladder, pelvic floor, ovaries and Fallopian tubes (laparascopy) Pathology - endometriosis found on Fallopian tubes, hyper proliferative uterine lining (hysterectomy)
Aktuelle Erkrankungen: None
Vorgeschichte: Glaucoma
Andere Medikamente: Atorvastatin 20 mg 3x/week, Dorzolamine/timolol eye drops 1x/day/primidone 50mg/day
Allergien: Quinolones, Adhesive
Vorherige Impfungen: -

VAERS 2577198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 05.11.2022
Beginn: 06.01.2023
Tage bis Beginn: 62,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Diarrhoea SARS-CoV-2 test positive

Symptomtext

01/08/23 presents to ED for "diarrhea". PMHx of "breast cancer diabetes osteoarthritis hyperlipidemia, hypertension PE on Eliquis"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 01/08/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2572762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: ID
Alter: 14,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 26.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Chills Headache

Symptomtext

headache; chills; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 15-year-old female patient received BNT162b2 (BNT162B2), on 26Jan2022 as dose 3 (booster), single (Lot number: FH8027) at the age of 14 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot#EW0164), administration date: 19May2021, when the patient was 14-year-old, for Covid-19 immunization, reaction(s): "headache", "chills"; BNT162b2 (DOSE 2, SINGLE, Lot#EW0172), administration date: 09Jun2021, when the patient was 14-year-old, for Covid-19 immunization, reaction(s): "headache", "chills". The following information was reported: HEADACHE (non-serious), outcome "unknown"; CHILLS (non-serious), outcome "unknown". Additional information: The mother calling on behalf of her daughter (patient) who received Pfizer covid-19 vaccines; the mother stated that after the first three Pfizer doses everything was ok, aside from headache and chills. Fourth dose on 24Jan2023 Lot#GK1337: Pfizer bivalent.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300039503 same product, event and patient, different dose;

Weitere VAERSDATA-Felder

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

VAERS 2568670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 17.12.2022
Beginn: 29.12.2022
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

12/29/22 presents to ED for "fever". PMHx of "CKD stage III, hypertension and DVT on anticoagulation"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 12/29/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2551442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: KY
Alter: 31,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 04.01.2022
Beginn: 03.11.2022
Tage bis Beginn: 303,0
Dosis: 3
Route/Site: SYR / RA

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

Fatigue Influenza virus test negative Lymphadenopathy Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative Upper respiratory tract infection

Symptomtext

An upper respiratory infection that started with congestion and and a sore throat it lasted for two weeks then came back for two more weeks even worse this time with swollen lymph nodes and fatigue. It was actually three different occasions where this would return the last time being the worst.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 and Influenzas tests done results were negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2548860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NC
Alter: 66,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 30.12.2021
Beginn: 18.12.2022
Tage bis Beginn: 353,0
Dosis: 3
Route/Site: IM / LA

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

Cough Headache Influenza virus test negative Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative

Symptomtext

On 12/18/22 I started having a stuffy head and headache, it progressed to congestion and coughing that hurt, runny nose I went in to see the doctor and I was prescribed steroids, Z-PAK and something to help with the cough. I still have a slight cough and a bit of a runny nose, but I am feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test negative, influenza test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Egg; bee venom
Vorherige Impfungen: -

VAERS 2543640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NC
Alter: 57,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 23.12.2021
Beginn: 14.12.2022
Tage bis Beginn: 356,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Chills Decreased appetite Diarrhoea Fatigue Headache Middle insomnia Pain Paranasal sinus discomfort SARS-CoV-2 test positive Sneezing

Symptomtext

12/14/22 I got chills, never had a fever on my thermometer, tired, some body aches, and some sneezing. At 7:00 that evening I was in bed, which is unusual for me, and slept okay. The next morning, I called my doctor, and they told me to do a home COVID test, that he would not see me if I was positive. I did a home COVID test which was positive. I called my doctor back and he called in a prescription for PAXLOVID. The pharmacy did not have my prescription, called the doctor and they called the prescription in. On 12/15/22 I had a bad case of diarrhea. On 12/16/22 I started on PAXLOVID. During the night of 12/16/22, I woke up with a bad headache and very bad sinus pressure and it continued the next day. I took MOTRIN and sinus spray which took care of it. I never had much of an appetite throughout it. 12/20/22 I began to feel better. I finished my PAXLOVID and now feel pretty good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home COVID test, positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: LIPITOR; spironolactone; aspirin; coQ10
Allergien: None
Vorherige Impfungen: -

VAERS 2543626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 72,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 07.08.2022
Beginn: 01.10.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Pain Pain in extremity X-ray normal

Symptomtext

I had no real rection to the first 4 shots. Just a little soreness in the arm for a couple of days. I had the 5 short at the same time and in the same artm as the flu short. No pain at all for 2-3 days. I now have significant pain: sometimes in the shoulder, sometimes halfway between the shoulder and the elbow. Sometimes dull, sometimes sharp. Pain only comes when I hold or move my arm in certain positions and particularly when i try to lift something relatively heavy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I had the arm x-rayed today and there was nothing unusual for someone my age (72).
Aktuelle Erkrankungen: none
Vorgeschichte: atrial fibrilation
Andere Medikamente: Metoprolo 100 mg daily Xarelto, 20 mg daily Rosuvastatin, 5 mg, 5 times per week Amiodarone, 200 mg, 5X/week Levothyroxine, 75mg, dail
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2530914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MA
Alter: 35,0
Geschlecht: M
Eingang: 14.12.2022
Impfdatum: 19.11.2021
Beginn: 11.07.2022
Tage bis Beginn: 234,0
Dosis: 3
Route/Site: IM / RA

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

Ageusia Anosmia COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

Covid-19. Fatigue, loss of smell and taste. Took naproxen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home testing of COVID-19. Positive for 20 days after.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Metamucil, Omeprazole, fish oil, multivitamin, rogaine
Allergien: -
Vorherige Impfungen: -

VAERS 2522976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 03.12.2021
Beginn: 26.04.2022
Tage bis Beginn: 144,0
Dosis: 3
Route/Site: SYR / LA

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

Food allergy Rash

Symptomtext

I started to develop rashes on my neck after eating certain items. I had never had any rashes prior to being vaccinated with COVID-19. Wine, dairy products, chocolate, would cause me to break out again and never had allergies to these items before and occasionally just break out having eaten nothing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Allergies; Leg cramps
Andere Medikamente: FLOVENT; FLONASE; gabapentin; ZYRTEC
Allergien: Penicillin; sulfa; cephalosporin
Vorherige Impfungen: -

VAERS 2520035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 29.11.2021
Beginn: 15.12.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / RA

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

Blood test abnormal Bone pain Heart rate increased Myalgia Pain Thyroid disorder

Symptomtext

I had intense bone and muscle aches. I had a lot of pain in my hips as well. I was thinking that had Arthritis. This continued to progress, and I started to have this in my arms, legs, knees, and all over. My hip was hurting so bad that I went to an urgent care clinic, and she did an X-Ray and said I had an old hairline fracture and prescribed 7 days' worth of steroids. I started taking a supplement for joint pain and my heartrate skyrocketed. I went to the ER, and they admitted me because my Thyroid went crazy. I had to stay in the hospital for 4 days. That happened in April. They put me on a Beta Blocker to slow my heartrate. I explained to the doctor why I started taking the supplement and this started happening shortly after taking the supplement. The doctor seemed to think that this could have been booster related. Now, am I seeing an Endocrinologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: 4,0
Labordaten: 31OCT2022 Blood panel abnormal
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: EMERGEN-C; ADVIL
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2515860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: HI
Alter: -
Geschlecht: F
Eingang: 24.11.2022
Impfdatum: 02.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure Fatigue Pain in extremity

Symptomtext

Sore arm; fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An elderly female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Jun2022 as dose 4 (booster), single (Lot number: FH8027), in left arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "brain aneurysm" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Sensitive to aspirin for Known allergies: Sensitive to aspirin, notes: Sensitive to aspirin and ibuprofen; Ibuprofen for Known allergies: ibuprofen. Vaccination history included: BNT162b2 (Pfizer/BioNTech, lot number was EW0153, dose 1, left arm), administration date: 14Apr2021, for Covid-19 Immunization, reaction(s): "Sore arm", "fatigue"; BNT162b2 (Pfizer/BioNTech, lot number was EW0167, dose 2, left arm.), administration date: 05May2021, for Covid-19 Immunization, reaction(s): "Sore arm", "fatigue"; BNT162b2 (Pfizer/BioNTech , administration time was 10:15 AM, lot number was FN2908, dose 3, left arm), administration date: 18Nov2021, for Covid-19 Immunization, reaction(s): "Sore arm", "fatigue". The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Sore arm"; FATIGUE (non-serious), outcome "unknown". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Negative, notes: tested negative for two days; (unspecified date) Negative, notes: tested negative for two days; (unspecified date) Positive, notes: Then on third day, tested positive for covid again; (08Nov2022) Positive, notes: Tested positive for Covid on 08Nov2022. Therapeutic measures were taken as a result of pain in extremity, fatigue. Additional information: Adverse events for the Pfizer Covid shots and boosters was Sore arm and fatigue. Tested positive for Covid on 08Nov2022: fever, headache, body aches and fatigue. For Paxlovid: Metallic taste that distorted sense of taste Completed the 5 day regimen and then tested negative for two days. Then on third day, tested positive for covid again. Symptoms was sneezing, nasal congestion, runny nose, cough, some fatigue. Even eight days after completing Paxlovid, still testing positive with sneezing, coughing, nasal congestion. Took Paxlovid from 08Nov2022 to 12Nov2022 as COVID 19 treatment. Other medication details: Amlodipline-Benazepril, clopidogrel 75 mg, Raloxifene, Multi for Her 50+ from 01Nov2022 to 21Nov2022 and Rosuvastatin from 01Nov2022 to 07Nov2022. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Negative ; Comments: tested negative for two days; Test Name: COVID-19 Test; Test Result: Negative ; Comments: tested negative for two days; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Then on third day, tested positive for covid again; Test Date: 20221108; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Tested positive for Covid on 08Nov2022
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Aneurysm cerebral; Blood pressure high; High cholesterol
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2513891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: TN
Alter: 47,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 21.11.2021
Beginn: 07.07.2022
Tage bis Beginn: 228,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia COVID-19 Headache Myalgia Pyrexia SARS-CoV-2 test positive

Symptomtext

I caught Covid 19, positive; I have a fever with horrible headache as well as much muscle aches and join aches; I saw my doctor and he gave me antibiotics to keep me from getting an infection.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Covid- 19 positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: ALLEGRA D; WELLBUTRIN; PRILOSEC; birth control; AMBIEN; vitamin D
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2509526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 45,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 15.11.2021
Beginn: 06.09.2022
Tage bis Beginn: 295,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Chills Fatigue Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Somnolence

Symptomtext

I did not have a reaction to the vaccine. I tested positive for COVID-19 with a home test on 09/06/2022 without prior symptoms. I had a sore throat and a fever. I got a PCR test at my doctor's office which was positive for COVID-19. My doctor recommended aspirin and ibuprofen for the fever. I was given a prescription for PAXLOVID but never got it filled. The fever, sore throat, aches and chills lasted for three days. The fatigue and grogginess lasted about fifteen days.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 06SEPT2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Albuterol inhaler
Allergien: N/A
Vorherige Impfungen: -

VAERS 2497153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AL
Alter: 37,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 21.10.2021
Beginn: 10.02.2022
Tage bis Beginn: 112,0
Dosis: 3
Route/Site: - / -

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

Biopsy skin Echocardiogram Heart valve incompetence Rash

Symptomtext

Full body rash covering 95% of my body.; 3 valve heart regurgitation.; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 38-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Oct2021 as dose 3 (booster), single (Lot number: FH8027) at the age of 37 years for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "depression" (unspecified if ongoing); "HTN" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Ambien, reaction(s): "Known allergies: Ambien", notes: Known allergies: Ambien. Vaccination history included: BNT162b2 (Prev dose lot Number: LL8982, Prev dose administration date: 28Jan2021, Prev dose dose number: 2), administration date: 28Jan2021, when the patient was 36-year-old, for COVID-19 immunization; BNT162b2 (Prev dose lot Number: EJ1685, Prev dose administration date: 07Jan2021, Prev dose dose number:1), administration date: 07Jan2021, when the patient was 36-year-old, for COVID-19 immunization. The following information was reported: HEART VALVE INCOMPETENCE (disability) with onset 10Feb2022, outcome "recovered with sequelae" (2022), described as "3 valve heart regurgitation."; RASH (disability) with onset 10Feb2022, outcome "recovered with sequelae" (2022), described as "Full body rash covering 95% of my body.". The event "full body rash covering 95% of my body." required physician office visit. The patient underwent the following laboratory tests and procedures: Biopsy skin: Unknown results, notes: Multiple skin biopsies; Echocardiogram: Unknown results. Therapeutic measures were taken as a result of rash, heart valve incompetence.; Sender's Comments: As there is limited information in the case provided, the causal association between the events and the suspect drug cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer drug 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: Rash
Hospital-Tage: -
Labordaten: Test Name: skin biopsies; Result Unstructured Data: Test Result:Unknown results; Comments: Multiple skin biopsies; Test Name: echocardiograms; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Depression; Hypertension; Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2492595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MN
Alter: 80,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 09.03.2021
Beginn: 26.10.2022
Tage bis Beginn: 596,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram thorax abnormal Lung consolidation Respiratory viral panel SARS-CoV-2 test Sputum culture COVID-19 Malaise Vaccine breakthrough infection

Symptomtext

Patient hospitalized and had breakthrough COVID-19 that was symptomatic

Weitere VAERSDATA-Felder

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

VAERS 2478483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NJ
Alter: 51,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 15.11.2021
Beginn: 04.01.2022
Tage bis Beginn: 50,0
Dosis: 3
Route/Site: - / -

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

Acoustic stimulation tests Balance disorder Dizziness Ear discomfort Electronystagmogram Feeling abnormal Neck pain Tinnitus

Symptomtext

Approximately 6 weeks after receiving my booster on 11/15/21, I woke up with a clogged left ear, tinnitus in left ear, balance and dizziness, terrible neck pain and brain fog . I still have these symptoms almost 11 months later. This vaccine is poison and you ruined the lives of so many.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Hearing test and Vng test conducted in January and February which has cost me 1000s. You guys ruined me
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zyrtec
Allergien: None
Vorherige Impfungen: -

VAERS 2447837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 32,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 10.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test normal Diarrhoea Dizziness Dysmenorrhoea Headache Hypercoagulation Impaired work ability Menstrual disorder Nausea Vomiting

Symptomtext

5 days after receiving my recent booster, I started my menstrual cycle for September. My cramps were so painful that I quickly became nauseous and vomited. I also had diarrhea. Shortly after this episode, the cramps subsided enough that I could rest, but I was truly concerned I would have to call 9-1-1 as I live alone and felt like I would pass out. I had to call out of work from the pain. The rest of the day I had a horrible headache. My period has not been flowing regularly and I?ve had a lot of coagulation occurring.

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Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: I had a routine check up with blood work on 8/29 (all came back normal) and a routine OBGYN check up on 9/6 which, so far, has come back normal as well.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Probiotic, Magnesium supplement, Ashwaganda supplement, B-Complex supplement
Allergien: Dust mites
Vorherige Impfungen: -

VAERS 2436353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MN
Alter: 95,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 14.04.2022
Beginn: 28.08.2022
Tage bis Beginn: 136,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Balance disorder COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

WEAKNESS, BALANCE ISSUES, FEVER,

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Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST 8/31/22
Aktuelle Erkrankungen: -
Vorgeschichte: ? Cancer (HCC) ? CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) 10/9/2018 ? HTN (hypertension) pt denies ? Stroke (HCC) 5/31/2020 ? Syncope ? Vertebral compression fracture (HCC) - L1L2 ? Syncope R55 ? Arthritis M19.90 ? Glaucoma H40.9 ? Closed compression fracture of L2 lumbar vertebra (HCC) S32.020A ? CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) N18.30 ? Diarrhea, unspecified type R19.7 ? Bilateral low back pain without sciatica - reported L1/2 compression fractures M54.50 ? Generalized weakness R53.1 ? Stroke (HCC) I63.9
Andere Medikamente: acetaminophen (TYLENOL) 500 mg oral tablet latanoprost 0.005% (XALATAN) 0.005 % Opht Drop ophthalmic (EYE) solution multivitamin oral tablet timolol (TIMOPTIC) 0.5% ophthalmic (EYE) drops UNKNOWN MEDICATIONS
Allergien: Chocolate Flavor
Vorherige Impfungen: -

VAERS 2426581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 23,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 04.12.2021
Beginn: 29.08.2022
Tage bis Beginn: 268,0
Dosis: 3
Route/Site: UN / UN

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

Chills Cough Fatigue Headache Hyperhidrosis Pyrexia Respiratory tract congestion

Symptomtext

chills, diaphoresis, fatigue, fever, congestion, cough, headaches

Weitere VAERSDATA-Felder

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

VAERS 2422163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 20.12.2021
Beginn: 17.08.2022
Tage bis Beginn: 240,0
Dosis: 3
Route/Site: OT / LA

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

Body temperature Cough Nasal congestion Pain Pyrexia COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Positive COVID test; Positive COVID test; fever of 102F; coughing; congestion; body aches; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 41-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Apr2021 as dose 1, single (Lot number: ER8731), on 12May2021 as dose 2, single (Lot number: EW0172) and on 20Dec2021 as dose 3 (booster), single (Lot number: FH8027) at the age of 40 years, in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "High blood pressure" (unspecified if ongoing). Concomitant medication(s) included: MONTELUKAST; DHEA; ZINC; IODINE; FISH OIL; PREGNENOLONE; ASHWAGANDHA; VITEX AGNUS CASTUS; IRON; B12-VITAMIIN. Past drug history included: Marcaine, reaction(s): "Known allergies: Marcaine"; Lidocaine, reaction(s): "Known allergies: lidocaine"; Augmentin, reaction(s): "Known allergies: Augmentin". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 17Aug2022, outcome "unknown" and all described as "Positive COVID test"; PAIN (non-serious) with onset 17Aug2022, outcome "unknown", described as "body aches"; NASAL CONGESTION (non-serious) with onset 17Aug2022, outcome "unknown", described as "congestion"; COUGH (non-serious) with onset 17Aug2022, outcome "unknown", described as "coughing"; PYREXIA (non-serious) with onset 17Aug2022, outcome "unknown", described as "fever of 102F". The events "positive covid test", "fever of 102f", "coughing", "congestion" and "body aches" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Aug2022) Positive, notes: Nasal Swab; Body temperature: (17Aug2022) 102F, notes: fever. Therapeutic measures were taken as a result of vaccination failure, covid-19, pyrexia, cough, nasal congestion, pain. AE treatment included with Paxlovid. Facility type vaccine was workplace clinic. No other vaccine in four weeks. No covid prior vaccination. Covid was tested post vaccination.

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20220817; Test Name: body temperature; Result Unstructured Data: Test Result:102F; Comments: fever; Test Date: 20220819; Test Name: Bionax; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Blood pressure high
Andere Medikamente: MONTELUKAST; DHEA; ZINC; IODINE; FISH OIL; PREGNENOLONE; ASHWAGANDHA; VITEX AGNUS CASTUS; IRON; B12-VITAMIIN
Allergien: -
Vorherige Impfungen: -

VAERS 2421118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 30.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Amnesia Bedridden Biopsy Blood test Colitis microscopic Colonoscopy Disturbance in attention Fatigue Full blood count Hot flush Impaired work ability Inflammation Irritable bowel syndrome Mammogram Oesophagogastroduodenoscopy Pyrexia Stool analysis Thyroid function test

Symptomtext

Each vax resulted in one week bedridden, fever only first 3 days, inflammation since first vaccination. Extreme fatigue, memory fog, hot flashes (previously went away by 2018). Two major health conditions arose after vaccinating between the first and second: undiagnosed IBS diarrhea (unable to work full time, 25+ visits to toilet per day); bloodwork, thyroid and fecal tests at lab; diagnostic and excision biopsies both EGD and colonoscopy; diagnosed collagenous colitis 4/29/2022; undiagnosed breast tumor from mammogram 4/25/2022; primary dr referred me to oncologist for more scans and another outpatient diagnostic excision biopsy on one breast. I am unable to work full time despite Collagenous Colitis drug therapy, I?m always tired, I?m unable to focus at work and home, I?ve been healthy without disease prior to 2018 having one bad cold November 2019 which is rare.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Diagnostic lab tests: cbc thyroid fecal 3/11/2022 Diagnostic EGD and colonoscopy both with biopsies 4/29/2023 Mammogram 8/25/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Exercise induced asthma.
Andere Medikamente: Sertraline, albuterol inhaler
Allergien: Penicillin erythromycin clindamycin sulfa bactrim
Vorherige Impfungen: Extreme fatigue lasting 2 yrs from seasonal flu shot quad I was age 50 intramuscular arm side unknown brand unknown 09/2012

VAERS 2399332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: GA
Alter: 59,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 20.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

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

Eye infection Eye irritation Eye pain Photophobia

Symptomtext

right eye became infected, which included stabbing pain and over sensitivity to light and severe burning sensation. treatment included neomycin eye ointment which was applied to right eye for 10 days.

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Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes
Andere Medikamente: One A Day Women's multivitamin, 70/30 Humulin/Novolin insulin
Allergien: severve stomach pains with ibuprophen over 600 mg
Vorherige Impfungen: -

VAERS 2374036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AR
Alter: 19,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 05.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Heavy menstrual bleeding Muscle spasms Pain Product preparation issue

Symptomtext

Patient was given 0.3 mL of Pfizer that had not been diluted

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Patient stopped taking her birth control pills after being notified that her vaccine was not diluted. On 07/07/2022 she went to the ER for heavy menstrual flow and body aches with cramping.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2357646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 19,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 02.12.2021
Beginn: 29.06.2022
Tage bis Beginn: 209,0
Dosis: 3
Route/Site: IM / -

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

Fatigue Headache SARS-CoV-2 test

Symptomtext

Headache, Fatigue

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Rapid 6/29/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2356194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IL
Alter: 79,0
Geschlecht: M
Eingang: 03.07.2022
Impfdatum: 22.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Arthralgia Blood glucose increased Blood test Depression Electromyogram Glycosylated haemoglobin Investigation Magnetic resonance imaging Muscle disorder Myalgia Pain Peripheral swelling Stress Weight Weight decreased

Symptomtext

EMG; fluid around muscle around left bicep and swelling in left hand /his left hand started swelling; muscle was abnormal; severe progressively worsening pain after the Pfizer COVID-19 Vaccine booster dose/started having a lot of pain all over; asked for reports with problems with muscles or muscle pains after the Pfizer COVID-19 Vaccine booster dose.; lost a lot of weight on Jardience; Stress; depression; she tried to help him he would scream out in pain,especially in left shoulder.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. An 80-year-old male patient received BNT162b2 (BNT162B2), on 22Nov2021 as dose 3 (booster), single (Lot number: FH8027) at the age of 79 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "diabetes type 2" (unspecified if ongoing), notes: diabetes type 2 diagnosed years ago. Concomitant medication(s) included: JARDIANCE taken for type 2 diabetes mellitus, start date: Jan2022; SHINGRIX, on 07Oct2021. Past drug history included: Metformin, notes: Patient had been taking Metformin for Type 2 diabetes for years. Vaccination history included: BNT162b2 (Second dose administered on 23Feb2021, LOTEN6202), administration date: 23Feb2021, when the patient was 79-year-old, for COVID-19 Immunization; BNT162b2 (First dose administered on 05Feb2021, LOT- EL9269), administration date: 05Feb2021, when the patient was 79-year-old, for COVID-19 Immunization. The following information was reported: ELECTROMYOGRAM (medically significant) with onset 2021, outcome "unknown", described as "EMG"; STRESS (non-serious) with onset 2021, outcome "not recovered"; MYALGIA (non-serious) with onset 2021, outcome "not recovered", described as "asked for reports with problems with muscles or muscle pains after the Pfizer COVID-19 Vaccine booster dose."; DEPRESSION (non-serious) with onset 2021, outcome "not recovered"; PERIPHERAL SWELLING (medically significant) with onset 2021, outcome "not recovered", described as "fluid around muscle around left bicep and swelling in left hand /his left hand started swelling"; WEIGHT DECREASED (non-serious) with onset 2021, outcome "unknown", described as "lost a lot of weight on Jardience"; MUSCLE DISORDER (non-serious) with onset 2021, outcome "not recovered", described as "muscle was abnormal"; PAIN (non-serious) with onset 2021, outcome "not recovered", described as "severe progressively worsening pain after the Pfizer COVID-19 Vaccine booster dose/started having a lot of pain all over"; ARTHRALGIA (non-serious) with onset 2021, outcome "not recovered", described as "she tried to help him he would scream out in pain,especially in left shoulder.". The events "fluid around muscle around left bicep and swelling in left hand /his left hand started swelling", "muscle was abnormal", "severe progressively worsening pain after the pfizer covid-19 vaccine booster dose/started having a lot of pain all over", "asked for reports with problems with muscles or muscle pains after the pfizer covid-19 vaccine booster dose.", "lost a lot of weight on jardience", "stress", "depression" and "she tried to help him he would scream out in pain,especially in left shoulder." required physician office visit. The patient underwent the following laboratory tests and procedures: Blood glucose increased: (2021) blood sugar was then high., notes: blood sugar was then high; (2021) dropped significantly very fast; Blood test: (2021) range or normal, notes: Caller confirmed that husband had no ALS; Electromyogram: (2021) muscle was abnormal, notes: EMG", a procedure where "they put needles in muscles, starts at the tip of his fore finger all the way up to arm, to elbow" was performed on her husband. Caller mentioned that the procedure "was painful" and her husband "couldn't take anymore of it"; Glycosylated haemoglobin: (2021) down to below 7; Test: (2021) normal; Magnetic resonance imaging: (2021) found he had fluid around bicep muscle in the left, notes: did an MRI and found he had fluid around bicep muscle in the left arm; Weight: (2021) Loss. Therapeutic measures were taken as a result of peripheral swelling, muscle disorder, pain, myalgia, stress, depression, arthralgia. Clinical course:Caller called on behalf of her husband and asked if anyone else had reported "severe progressively worsening pain after the Pfizer COVID-19 Vaccine booster dose". Caller also asked for reports with problems with muscles or muscle pains after the Pfizer COVID-19 Vaccine booster dose. Caller stated that her husband was seen by different doctors/HCPs. Caller was seen by a neurologist "trying to get relief from pain". "EMG", a procedure where "they put needles in muscles, starts at the tip of his fore finger all the way up to arm, to elbow" was performed on her husband. Caller mentioned that the procedure "was painful" and her husband "couldn't take anymore of it". Caller also mentioned that the neurologist said "all" her husband's "muscle was abnormal". The HCP thought it was ALS but couldn't diagnose as they don't have the training. Caller's husband was then seen by his primary care physician and other doctors. Tests including blood test were done on husband. Caller confirmed that husband had no ALS and results "were in range or normal". Caller mentioned that they've been seeking guidance from HCPs for "months now". Husband was seen by "spine doctor, 2 neurologist, orthopedist, a diabetic doctor, and now going to see a rheumatologist".Patient had been taking Metformin for Type 2 diabetes for years and the doctor put him on Jardiance also for diabetes. Clarifies the Jardiance was prescribed in Jan2022, states the pain started prior to taking this medication. Patient lost a lot of weight on Jardience, doctor said it could be normal to lose 15 or so pounds, but also told them his blood sugar could have dropped significantly very fast and caused neuropathy which would ex-plain the pain possibly, Jardience.Doctors took patient off the Jardiance and cut in half his metformin, blood sugar was then high. First neurologist said that he was sure the patient had ALS and caller states her husband just gave up at this point because he was in so much pain was on sofa and bed all the time with the stress of that diagnosis Caller states her husband went to see another neurologist and this doctor confirmed the patient did not have ALS, and they began looking for other autoimmune diagnosis and doing a lot of tests, states they took 8 vials of blood and all the tests look normal and came back within range, specific details of tests not provided. Husband went back to the primary care provider and he prescribed him medication for pain and depression, caller states the patient just started these. In the meantime he was to the point he could not put on clothes or do anything, if she tried to help him he would scream out in pain, especially in left shoulder. States then his left hand started swelling, did an MRI and found he had fluid around bicep muscle in the left arm. Doctors are currently debating starting the patient on steroids.Patient received the Shingles shot within a week of the COVID booster, clarifies that the shingles shot was administered on 07Oct2021. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: blood sugar; Result Unstructured Data: Test Result:blood sugar was then high.; Comments: blood sugar was then high.; Test Date: 2021; Test Name: blood sugar; Result Unstructured Data: Test Result:dropped significantly very fast; Test Date: 2021; Test Name: blood test; Result Unstructured Data: Test Result:range or normal; Comments: Caller confirmed that husband had no ALS; Test Date: 2021; Test Name: EMG; Result Unstructured Data: Test Result:muscle was abnormal; Comments: EMG", a procedure where "they put needles in muscles, starts at the tip of his fore finger all the way up to arm, to elbow" was performed on her husband. Caller mentioned that the procedure "was painful" and her husband "couldn't take anymore of it".; Test Date: 2021; Test Name: A1C; Result Unstructured Data: Test Result:down to below 7; Test Date: 2021; Test Name: Test; Result Unstructured Data: Test Result:normal; Test Date: 2021; Test Name: MRI; Result Unstructured Data: Test Result:found he had fluid around bicep muscle in the left; Comments: did an MRI and found he had fluid around bicep muscle in the left arm; Test Date: 2021; Test Name: Weight; Result Unstructured Data: Test Result:Loss
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes (diabetes type 2 diagnosed years ago)
Andere Medikamente: JARDIANCE
Allergien: -
Vorherige Impfungen: -

VAERS 2317411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 38,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 11.12.2021
Beginn: 29.05.2022
Tage bis Beginn: 169,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Cough Fatigue Headache Impaired work ability Loss of personal independence in daily activities Myalgia Nausea Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sneezing Vaccine breakthrough infection

Symptomtext

I received a phone call from a representative of the CDC's V-safe program, on June 13, 2022, to follow up to my six-month post-vaccination V-safe check-in. During our discussion he advised me to report a breakthrough COVID-19 case (which I experienced since my booster) via the VAERS. The adverse event was a clinically mild case of COVID-19 for which I tested positive on May 29, 2022 using the Abbot COVID-19 BinaxNOW at-home test kit product. Signs and symptoms included fever (up to 103 degrees Fahrenheit), muscle aches, headache, fatigue, nausea, congestion, sneezing, and coughing. The time course was 2+ weeks, as I have some lingering symptoms that are clearing up (fatigue, congestion, coughing). I did not require in-person medical care and simply coordinated with my PCP's office via telephone and electronically, but I did miss a week of work and could not complete most normal daily activities due to being ill. The December 11, 2021 vaccination was a booster after I had previously received the first two courses of the Pfizer-BioNTech vaccine on April 3, 2021 and April 24, 2021.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: No tests administered by a physician's office or lab, only the aforementioned at-home Abbott COVID-19 BinaxNOW test kit product.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Anxiety, depression, GERD, gastroparesis, partially obstructed bladder neck, tendinitis, arthropathy, vision field floaters, anemia.
Andere Medikamente: Men's daily multivitamin, Tamsulosin 0.4 mg daily
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2314154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: TX
Alter: 33,0
Geschlecht: M
Eingang: 09.06.2022
Impfdatum: 06.12.2021
Beginn: 30.05.2022
Tage bis Beginn: 175,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Exposure to SARS-CoV-2 Headache Nasal congestion Respiratory tract congestion SARS-CoV-2 test positive Throat irritation Vaccine breakthrough infection

Symptomtext

Breakthrough COVID case: I found out about exposure on Monday, the 30th. That night, I began to feel a scratchy throat. The scratchy throat continued until at least Thursday. I also began to have nasal congestion and a brief slight headache. I tested 5 times between Monday night and Thursday. Every result was negative until Thursday morning when I got a positive result. I had a doctor's appointment where I was prescribed PAXLOVID. I received my prescription and started treatment on the evening of Friday, the 3rd. For the next day and a half or 2 days, I continued to have congestion but less of it. Symptoms disappeared for the most part by Monday, the 6th. I began to test negative on the evening of the 6th. I completed the PAXLOVID treatment on June 8th and I've continued to test negative since June 7th.

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: At home test x10 negative (dates vary). At home test x7 positive (dates vary).
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fluoxetine 20mg 2xday
Allergien: Not that I know of
Vorherige Impfungen: -

VAERS 2313472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IL
Alter: 33,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 03.12.2021
Beginn: 28.05.2022
Tage bis Beginn: 176,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Fatigue Feeling cold Oropharyngeal pain Pain Paranasal sinus discomfort Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Sinus pressure. Congestion. Runny nose. Body aches. Fatigue. Fever like chills. Sore throat

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID positive on 05/31/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Loestrin
Allergien: None
Vorherige Impfungen: -

VAERS 2313145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: OR
Alter: 45,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 07.12.2021
Beginn: 01.03.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: SYR / LA

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

Apathy Constipation Cough Disturbance in attention Fatigue Feeling abnormal Irritability Night sweats Thyroid function test Weight increased

Symptomtext

I've been extremely tired the last few months, I've had unexpected weight gain (12 lbs) even though I eat very healthy and exercise regularly, problems concentrating, constipation, loss of motivation, memory loss, irritability, night sweats and this weird feeling like I'm going to wake up and be sick, but then I don't get sick. It's hard to explain, but it feels like I'll wake up with a dry, barking cough. I haven't had even the slightest cold in over 3 years so this is strange.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Still waiting on results to check thyroid and B levels(?). Blood drawn on Friday, June 3.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Valacyclovir 500 mg per day
Allergien: vicodin, norco
Vorherige Impfungen: Flu shot in 2012, legs felt heavy, achy and I couldn't walk for a few hours

VAERS 2313009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 63,0
Geschlecht: M
Eingang: 08.06.2022
Impfdatum: 07.12.2021
Beginn: 23.05.2022
Tage bis Beginn: 167,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia COVID-19 Chest discomfort Chills Dysphonia Exposure to SARS-CoV-2 Feeling abnormal Headache Insomnia Nasopharyngitis Oropharyngeal pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

5/23/2022 I attended a wedding the week-end before where there was a COVID outbreak. I began getting a sore throat and head ache. My wife tested positive and I tested negative. I scheduled a PCR test. On 5/25/2022 I tested positive. I had chills, low grade fever and pressure on my chest. The next day I spoke with my PCP. He prescribed Paxlovid. I took that for 5 days. After the first day, the pressure in my chest went away. After 3 days I started feeling better. Then 2 days later I had lack of energy, my sore throat came back and by 06/04/2022 I had congestion, runny nose, fever, chills and a tremendously bad head cold. I felt crappy. 06/05/2022 I started taking Sudafed in the daytime and Alka Seltzer Cold relief at night that helped me sleep for the first time in weeks. Then I started feeling better. Yesterday, I felt better. The runny nose has stopped. Today my voice is affected, have fever and feel crappy. I tested positive on 06/07/2022 I tested positive.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 3 COVID tests, 2 positive and 1 negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Potassium Citrate ER Vitamin D3
Allergien: Wool
Vorherige Impfungen: -

VAERS 2312065

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: OH
Alter: 34,0
Geschlecht: M
Eingang: 07.06.2022
Impfdatum: 04.12.2021
Beginn: 27.05.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Feeling abnormal Headache Imperception Malaise SARS-CoV-2 test positive

Symptomtext

Symptoms started on May 27, 2022 in the evening right after work. I had a headache that was very bothersome from the middle of my head. I felt off, my perception was off but not dizzy. On Saturday, I had a dry cough, no fever, getting was an issue, the headache was there all over my head and my perception was still off. I took a home COVID-19 test, it came back positive in two minutes. I got online and scheduled a telehealth visit, I spoke with a Nurse Practitioner who prescribed PAXLOVID that I picked up later the evening of May 28, 2022. Once I started taking the PAXLOVID, on Sunday I started experiencing a bad taste in my mouth. I tested negative on Monday June 06, 2022 although my symptoms were completely gone by June 04, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Compazine
Vorherige Impfungen: -

VAERS 2310306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WA
Alter: 14,0
Geschlecht: M
Eingang: 06.06.2022
Impfdatum: 27.11.2021
Beginn: 16.05.2022
Tage bis Beginn: 170,0
Dosis: 2
Route/Site: IM / LA

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

Diplopia Eye pain Neck pain

Symptomtext

He has had double vision that started three weeks ago. He is under the care of an Ophthalmologist. He is also having mild eye and neck pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Seasonal Allergies
Andere Medikamente: Vitamin D; multivitamin; cetirizine 10mg once daily.
Allergien: N/A
Vorherige Impfungen: -

VAERS 1995230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: -
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 01.12.2021
Beginn: 25.05.2022
Tage bis Beginn: 175,0
Dosis: 3
Route/Site: - / -

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

Chills Fatigue Immunisation Pain Vaccination site pain COVID-19 Nasal congestion SARS-CoV-2 test Vaccination failure

Symptomtext

tested positive for COVID (developing mild congestion, a mild headache, and diarrhea); tested positive for COVID (developing mild congestion, a mild headache, and diarrhea); mild congestion; This is a spontaneous report received from a contactable reporter (Consumer). The reporter is the patient. A 46-year-old female patient received BNT162b2 (COMIRNATY), on 18Feb2021 as dose 1, single (Lot number: EL3247, Expiration Date: May2021), on 11Mar2021 as dose 2, single (Lot number: EN6203, Expiration Date: Jun2022) and on 01Dec2021 as dose 3 (booster), single (Lot number: FH8027) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: NASAL CONGESTION (non-serious) with onset 25May2022, outcome "unknown", described as "mild congestion"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 25May2022, outcome "unknown" and all described as "tested positive for COVID (developing mild congestion, a mild headache, and diarrhea)". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (05Oct2021) Positive, notes: previously tested positive for COVID; (25May2022) Positive, notes: at approximately 10:30 p.m. Clinical details: On 25May2022, she began developing mild congestion, a mild headache, and diarrhea. She took a BinaxNow home test at approximately 10:30 p.m. and it showed a positive result. She mentioned that she previously tested positive for COVID on 05Oct2021.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101326549 same patient/suspect drug, different dose, similar events (previous LOE)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211005; Test Name: BinaxNow home test/tested/COVID; Test Result: Positive ; Comments: previously tested positive for COVID; Test Date: 20220525; Test Name: BinaxNow home test/tested/COVID; Test Result: Positive ; Comments: at approximately 10:30 p.m.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1995230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: -
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 01.12.2021
Beginn: 25.05.2022
Tage bis Beginn: 175,0
Dosis: 3
Route/Site: OT / -

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

Chills Fatigue Immunisation Pain Vaccination site pain COVID-19 Nasal congestion SARS-CoV-2 test Vaccination failure

Symptomtext

tested positive for COVID (developing mild congestion, a mild headache, and diarrhea); tested positive for COVID (developing mild congestion, a mild headache, and diarrhea); mild congestion; This is a spontaneous report received from a contactable reporter (Consumer). The reporter is the patient. A 46-year-old female patient received BNT162b2 (COMIRNATY), on 18Feb2021 as dose 1, single (Lot number: EL3247, Expiration Date: May2021), on 11Mar2021 as dose 2, single (Lot number: EN6203, Expiration Date: Jun2022) and on 01Dec2021 as dose 3 (booster), single (Lot number: FH8027) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: NASAL CONGESTION (non-serious) with onset 25May2022, outcome "unknown", described as "mild congestion"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 25May2022, outcome "unknown" and all described as "tested positive for COVID (developing mild congestion, a mild headache, and diarrhea)". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (05Oct2021) Positive, notes: previously tested positive for COVID; (25May2022) Positive, notes: at approximately 10:30 p.m. Clinical details: On 25May2022, she began developing mild congestion, a mild headache, and diarrhea. She took a BinaxNow home test at approximately 10:30 p.m. and it showed a positive result. She mentioned that she previously tested positive for COVID on 05Oct2021.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101326549 same patient/suspect drug, different dose, similar events (previous LOE)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211005; Test Name: BinaxNow home test/tested/COVID; Test Result: Positive ; Comments: previously tested positive for COVID; Test Date: 20220525; Test Name: BinaxNow home test/tested/COVID; Test Result: Positive ; Comments: at approximately 10:30 p.m.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2633938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: TN
Alter: 39,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 12.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / LA

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

Blood iron decreased Fatigue Haematocrit decreased Haemoglobin decreased Hot flush SARS-CoV-2 test positive Serum ferritin decreased Transfusion Ultrasound scan Vaginal haemorrhage

Symptomtext

Jan 12, 2022 Pfizer Booster administered Jan 12, 2022 hot flash after being administered Pfizer and reported to nurses who observed me for additional time (30minutes) and checked my vital signs - all in normal limits no fever. Jan 12-28 fatigue; managing PTSD symptoms stemming from racial sexual trauma from years ago and attempting to manage case Jan 27, 2022 stressful meeting with work director supervisor in which my integrity was questioned when I reported being sick with COVID first week of January, 2022; did not get two or three weeks off away from work like other demographics. I had to be at work the next week. March 18 Provider instructed me to go to ER, admitted for hospital blood transfusion Jan 2022 detected SAR CoV 2 symptomatic sick Jan 2022 work discriminated against required additional reporting not typical for me to have to call the director when I've talk to those I report to; integrity called into question Jan 2022 went into work after a week; I would learn weeks later males and other demographics were allowed two and some three weeks off Jan 27 2022, meeting with director brought up the week I was sick and my integrity was questioned Jan 28, 2022 went to provider to ask for sick call slip - 24 hours off work Jan 28, 2022, large vaginal clots in toilet first time ever March 18, 2022 provider office called instructed me to have someone drive me to ER for critical low feritin, hemoglobin, hematocrit, iron; admitted to hospital for blood transfusion (first time in my life I required blood transfusion) March 19, 2022 April 2022 : two more infusion sessions (first time in life) May 2022, more large vaginal clots requested quarters - provider gave me 3 days off work Hospital has inaccurate had inaccurate errors in my medical records that I requested to be corrected to include: 1. Ultrasound order reason is incorrect: I DID NOT present to the ER with vaginal bleeding and SOB. I was not vaginally bleeding 2. ER disposition was admitted to the hospital in patient and I was not discharged 3. I do not have a chronic history of vaginal large clots 4. Clarification: I WAS NOT pregnant and DID NOT have a miscarriage or other

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID PCR Jan 2022 highly detected; March 18th labs critical low feritin, iron, hemoglobin, hematocrit.; first time blood transfusion and large vaginal blood clots
Aktuelle Erkrankungen: PTSD
Vorgeschichte: PTSD; March 2021 normal blood lab results first vaccine 25 May 2021
Andere Medikamente: -
Allergien: Mango; Latex; Fragrances; Dyes
Vorherige Impfungen: -

VAERS 2298745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AZ
Alter: 71,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 23.11.2021
Beginn: 17.05.2022
Tage bis Beginn: 175,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Chills Cough Dysgeusia Headache Nasal congestion Nasopharyngitis Pain SARS-CoV-2 test positive Sinus operation Sneezing

Symptomtext

I woke up at 2:30AM with a headache and stuffy nose. The next morning I was achy with some chills. I took an at home COVID-19 test which was positive. I called my doctor and was prescribed Paxlovid. I only took 2 of the pills due to kidney issues and the pharmacist took the one out. I did get the side effect of a metal taste. I took that 5/17/2022. I did take some Sudafed. I did feel kind of normal, like 90 percent asymptomatic for 6 days. On 5/26/2022, I felt like I had a cold with a lot of sinus drainage, coughing, and sneezing. This continued until this morning. My symptoms rebounded. I took another COVID-19 test which was positive.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 2 COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine; carbidopa; levodopa; atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2292746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MA
Alter: 61,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 20.11.2021
Beginn: 22.04.2022
Tage bis Beginn: 153,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia COVID-19 Chills Fatigue Feeling abnormal Malaise Nasal congestion Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

I was outdoors for an event talking and engaged with people, completely outdoors and very windy. In the afternoon I started feeling scratchy throat and a bit tired. On Saturday I was a bit tired and had a lot to do, had a busy day. Sunday was probably the same but because I had a lot to do I continued. Sunday evening I started feeling chills and body ache and went to bed. In the morning I got the rapid Covid test and one that was sent and it came out positive. I spoke to my Dr. on virtual appt and sent me Paxlovid. I took it for 5 days. The symptoms continued to be the same on Monday I had stuffy nose. Tuesday was terrible stuffy nose and body ache. 3-4 days I didn't feel well at all but never really had a fever, though I was feverish in the evening. By the weekend I walked a bit and felt tired. For 2 weeks I wasn't very energetic but by the time I finished taking Paxlovid I was ok without much congestion and now I'm pretty ok. Monday/Tuesday April 27th I felt very very bad. On the 5th of May I took another Covid test and it was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid test - positive; May 5th Covid test - negative
Aktuelle Erkrankungen: No
Vorgeschichte: Multiple sclerosis
Andere Medikamente: Calcium, Probiotics, Vitamin C, Bone strength tablets, weekly vaginal estradiol
Allergien: Penicillin
Vorherige Impfungen: 2nd and 3 dose of Pfizer.

VAERS 2292728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 22.11.2021
Beginn: 13.05.2022
Tage bis Beginn: 172,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Exposure to SARS-CoV-2 Fatigue Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

11/22/2021 vaccination. 5/13/2022 I started to feel symptoms to include scratchy throat, nose was running a lot. The day before, a co-worker had tested positive. He left immediately. I tested that day and tested positive; COVID positive. I did a home test and through the pharmacy. 5/24/2022 Still feeling residual fatigue.

Weitere VAERSDATA-Felder

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

VAERS 2292608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WI
Alter: 64,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 29.12.2021
Beginn: 06.05.2022
Tage bis Beginn: 128,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Decreased appetite Hyperkalaemia Laboratory test abnormal Large intestine perforation Malaise Muscular weakness Nausea

Symptomtext

64 y.o. female with significant comorbidities of essential hypertension, T2DM, moderate COPD (PFTs 2020), restrictive lung disease of obesity with OHS, chronic right-sided heart failure, VTE on rivaroxaban, and more recent history of spontaneous colonic perforation in March 2022. Presented to ED with nausea, poor appetite, generalized malaise and muscular weakness and was found to have severe hyperkalemia and AKI. Tested positive upon admission

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

VAERS 2290971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MD
Alter: 29,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 28.10.2021
Beginn: 04.12.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: SYR / LA

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

Abortion spontaneous Blood test Malaise Menstruation irregular Pain in extremity Pregnancy Pyrexia Ultrasound scan

Symptomtext

None at the time that the shot was given for shot #1. After shot #2 I had a sore arm and a couple days later I did get weird sickness. I got a fever that went on and off for days as well as other varying symptoms that were so random and inconsistent. The MAJOR side effect I experienced is that my period was thrown off in the month of December 2021. I actually didn't get it so I decided to take a pregnancy test. It was positive but I was on birth control at the time so this was very interesting because I am really good about taking my pill every evening, Come the end of January 2022, I was diagnosed with a miscarriage at week 4-5 timeframe. Fast forward a couple months after my body and period was able to naturally clear and reset, I then found out I was pregnant again in beginning of April 2022. But unfortunately I was once again diagnosed with a miscarriage mid-May 2022 where I was told I was around 4-5 week timeframe once again. I am 100% convinced this is happening because of the stupid covid vaccine that I was forced to get in order to keep my job.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: I have gotten a lot of blood work and ultrasounds over the last 5 months.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2290910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IL
Alter: 39,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 21.11.2021
Beginn: 14.05.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Chills Cough Fatigue Feeling abnormal Lacrimation increased Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID-19 Breakthrough. I think my son had it first. I started feeling bad that Saturday. I had fever , chills, congestion, sore throat and cough. I also had watery eyes. I have also been experiencing a lot of fatigue. I lost my taste and smell capabilities about 3 days into my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2290716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AZ
Alter: 65,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 12.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Biopsy thyroid gland Bladder catheterisation Computerised tomogram Electromyogram Insomnia Magnetic resonance imaging Nerve conduction studies Pain Pelvic pain Quality of life decreased Sciatica Sleep disorder Therapeutic product ineffective Ultrasound Doppler Ultrasound thyroid Urinary retention Walking aid user X-ray limb

Symptomtext

severe pain initiated as sciatica, seeked out physician care, MRI and CT performed. Seeked out pain control. Couldnt get appointment until Dec 20,2021. received pain shot on 12/23/21. Successful injection. Then started to have severe pelvic pain. Pelvic x-rays. made 2 trips to ER Received another shot and was successful. Then more severe pelvic pain started. was unable to sleep in bed, had to walk with cane. went to ER for a urinary retention issue. Had to wear leg bag for 2 weeks until that issue turned around. My PCP was trying to figure out what was going on and had started me on Vicodin which in turn caused constipation. Many sleepless nights, much pain and a decreased life .Had an appt at a Center for Neurosciences. Took 2.5 months to get appt. Had an EMG/NCT. of right leg. Was negative and neurologist said nothing wrong dont need to return. Went to a new pain place and had a bilateral superior hypogastric plexus block. Was unsuccessful so far. Still seeking answers..

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: MRI, CT, Pelvic x-ray Pelvic ultrasound. Ankle x-rays, thyroid ultrasound ,thyroid biopsy leg ultrasound, EMG/NCT
Aktuelle Erkrankungen: NONE
Vorgeschichte: None other than medication controlled high blood pressure.
Andere Medikamente: Lisinopril/HCTZ 20-25,, Omeprazole 20mg, Cetirizine 10 mg, Amabelz 0.5mg/0.1 mg, Naprosyn 220 mg, Vit D 5000 units, Acetaminophen 500 mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2290689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MN
Alter: 60,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 18.11.2021
Beginn: 29.12.2021
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: IM / RA

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

Headache Magnetic resonance imaging head Magnetic resonance imaging spinal Swelling

Symptomtext

Approximately 3 weeks after receiving vaccine began having intense headaches. Tried Tylenol with no effect. Headaches continued gaining in intensity and frequency. March I had 18 episodes with 4 being major. In April I had 20 episodes with 6 major episodes. The length varies 3-4 hours up to the entire day. Went to see doctor at the end of April. Doctor prescribed Neurontin and Compazine. Doctor also has me charting my headaches. Neurontin has improved symptoms and I have not needed Compazine. Neck circumference has increased by an inch and a quarter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: MRI of Brain-TBD; MRI of C-Spine-TBD
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; Hyperlipidemia; Diabetes Type 2; Peripheral Arterial Disease
Andere Medikamente: Baby aspirin; turmeric; amlodipine; atorvastatin; PAXIL; lisinopril; metformin; metoprolol succinate
Allergien: CHANTIX
Vorherige Impfungen: -

VAERS 2287237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IA
Alter: 91,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 02.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / -

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

Aerococcus urinae infection Asthenia COVID-19 Chest X-ray abnormal Fatigue Malaise Pyuria Renal impairment Respiratory failure SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 2/15/21 (en6201) Pfizer Dose 2 3/11/21 (EN6205) Pfizer Dose 3 12/2/21 (FH8027) COVID Positive 12/21/21 12/21/21: The patient complaining from generalized weakness and fatigue, decline fever or chills or cough or shortness of breath or abdominal pain or nausea or vomiting or diarrhea, no chest pain or palpitation. The patient is vaccinated for COVID-19. His labs show stable CKD, he does have pyuria, chest x-ray show possible pneumonia. COVID-19 test is positive. 12/27/21: The patient admitted for worsening COVID symptoms and Aerococcus UTI s/p Ceftriaxone course The patient is vaccinated for COVID-19. Patient not requiring oxygen during hospitalization but had respiratory insufficiency while ambulating He was managed with IV steroids. No remdesivir given because of kidney function Patient's symptoms improved. He is hemodyanmiclly stable Patient accepted at home and will be discharged today

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Praegender Schweregrund: Fatigue
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: h/o TIA; h/o prostate CA; CKD; partial hearing loss; macular degeneration; h/o skin cancer; HLD.
Vorgeschichte: h/o TIA; h/o prostate CA; CKD; partial hearing loss; macular degeneration; h/o skin cancer HLD.
Andere Medikamente: Vitamin D; Clopidogrel; Vitamin B-12; HCTZ; multivitamin; Simvastatin.
Allergien: NKA.
Vorherige Impfungen: -

VAERS 2282964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WI
Alter: 62,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 16.11.2021
Beginn: 20.04.2022
Tage bis Beginn: 155,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Diarrhoea Exercise tolerance decreased Exposure to SARS-CoV-2 Fatigue Feeling abnormal Head discomfort Hypersomnia Malaise SARS-CoV-2 test positive

Symptomtext

My husband and I took a trip on April 15, 2022 which is probably where we got our exposure. We did use masks but we ate at crowded restaurants several times. On Sunday, my husband started to experience symptoms and he did an At-home test on Monday, April 18 and came back positive and confirmed with a PCR test. He was symptomatic and we did our best and I still did not avoid infection either from exposure over the weekend or exposure from him. I began testing myself every 2 days starting on the 18 of April. I was symptomatic on Wednesday April 20, and tested myself but still came back negative. The symptoms I felt were fatigue, head congestion which was very much like bad allergy symptoms. Mild diarrhea which was a slight disruption from usual GI patterns. I believe I felt a little better on the 23rd then felt bad on the 24th again. I finally got a positive test on the 24th. Because I have asthma and approaching 65 years old and I knew Paxlovid was available, I sought out help from a clinic on Sunday the 24th. They did a PCR test. I also looked into government testing, and I was referred to a pharmacy. And the timing was off, so I was looking to see if I was still eligible for Paxlovid. I was able to make the window and I was able to take Paxlovid on April 25-29. My respiratory and GI symptoms started abating around the 27th. They were pretty much gone by that point. I still experience some fatigue that?s unusual for me. Less frequency over the month. At first I would even get tired running up the stairs and I haven?t been able to resume my exercise routine. I have been wanting to take naps, but that?s lessening as well. During the time when I had more symptoms from COVID, I had one day where I slept all day. Main symptoms were fatigue (moderate) and other symptoms such as respiratory and GI were mild. I would say I?m almost recovered but not fully. Around 90-95% recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 04/18/2022 - At home COVID test - negative 04/20/2022 - At home COVID test - negative 04/22/2022 - At home COVID test - negative 04/24/2022 - At home COVID test - positive 04/24/2022 - PCR COVID test - positive (results came back 04/26/2022 04/24/2022 - 2nd PCR COVID test - positive (results came back on 04/25/2022)
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal allergies Mild Asthma
Andere Medikamente: Claritin as needed
Allergien: None
Vorherige Impfungen: -

VAERS 2280546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: -
Beginn: 13.08.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Asthenia Dermatomyositis Rash erythematous Vaccination site erythema

Symptomtext

have been diagnosed with Dermatomyositis; had red rashing everywhere; I also had a red ring around the injection site for 4.5 months; I began to lose strength in my arms and legs; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 66-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 3 (booster), single (Lot number: FH8027) intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Other medical history: hypothyroidism" (unspecified if ongoing), notes: Other medical history: hypothyroidism; "Other medical history: hashimotos" (unspecified if ongoing), notes: Other medical history: hashimotos; "Other medical history: vitiligo" (unspecified if ongoing), notes: Other medical history: vitiligo; "Known allergies: pollen" (unspecified if ongoing), notes: Known allergies: pollen. Concomitant medication(s) included: PANTOPRAZOLE; LEVOTHYROXINE; ZYRTEC [CETIRIZINE HYDROCHLORIDE] taken for hypersensitivity. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EN6202, Route of Administration: Intramuscular), administration date: 08Mar2021, when the patient was 65-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL3247, Route of Administration: Intramuscular), administration date: 12Feb2021, when the patient was 65-year-old, for COVID-19 immunization. The following information was reported: VACCINATION SITE ERYTHEMA (disability) with onset 13Aug2021, outcome "not recovered", described as "I also had a red ring around the injection site for 4.5 months"; ASTHENIA (disability) with onset 13Aug2021, outcome "not recovered", described as "I began to lose strength in my arms and legs"; RASH ERYTHEMATOUS (disability) with onset 13Aug2021, outcome "not recovered", described as "had red rashing everywhere"; DERMATOMYOSITIS (disability, medically significant) with onset 13Aug2021, outcome "not recovered", described as "have been diagnosed with Dermatomyositis". The events "have been diagnosed with dermatomyositis", "had red rashing everywhere", "i also had a red ring around the injection site for 4.5 months" and "i began to lose strength in my arms and legs" required physician office visit and emergency room visit. Therapeutic measures were taken as a result of dermatomyositis, rash erythematous, vaccination site erythema, asthenia included lots of medical care. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's disease (Other medical history: hashimotos); Hypothyroidism (Other medical history: hypothyroidism); Pollen allergy (Known allergies: pollen); Vitiligo (Other medical history: vitiligo)
Andere Medikamente: PANTOPRAZOLE; LEVOTHYROXINE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2274088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WI
Alter: 61,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 28.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Chills Erythema Periarthritis Pyrexia Swelling

Symptomtext

Shoulder pain with redness and swelling, fever, chills, and eventually a frozen shoulder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Metoprolol, levothyroxine, multi-vitamin
Allergien: Penicillin, Sulpha
Vorherige Impfungen: -

VAERS 2267643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 08.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / UN

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

COVID-19 Delivery Exposure during pregnancy Headache Rhinorrhoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID-19 case: 12/30/2021. I was 37 weeks pregnant. My daughter had a runny nose and I was testing her and she was testing negative. I went to a drive up COVID-19 testing site and I received my positive COVID-19 results two days later. The only symptoms I experienced was the running nose and a headache. Birth Weight: 8lbs 5oz.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 Test: 12/30/2021 Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Right Shoulder Pain
Andere Medikamente: Prenatal St Johns wort
Allergien: None
Vorherige Impfungen: -

VAERS 2265741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 17.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / -

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

Asthenia Hyperhidrosis Illness Nausea Pain in extremity Pruritus Throat tightness

Symptomtext

sweats appeared with terrible itching; throat closing; sick over 1.5 weeks; nausea; weak; sore arm; day 2 woke up with itching; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old female patient received BNT162b2 (BNT162B2), on 17Oct2021 as dose 2, single (Lot number: FH8027) at the age of 72 years for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE , Anatomical site of injection: shoulder, Batch/lot number: 30130BA), administration date: 01Sep2021, for COVID-19 immunization, reaction(s): "Tired". The following information was reported: PRURITUS (non-serious) with onset 19Oct2021, outcome "unknown", described as "day 2 woke up with itching"; PAIN IN EXTREMITY (non-serious) with onset 19Oct2021, outcome "unknown", described as "sore arm"; NAUSEA (non-serious) with onset 20Oct2021, outcome "unknown"; ILLNESS (non-serious) with onset 20Oct2021, outcome "unknown", described as "sick over 1.5 weeks"; HYPERHIDROSIS (non-serious) with onset 20Oct2021, outcome "unknown", described as "sweats appeared with terrible itching"; THROAT TIGHTNESS (non-serious) with onset 20Oct2021, outcome "unknown", described as "throat closing"; ASTHENIA (non-serious) with onset 20Oct2021, outcome "unknown", described as "weak". Therapeutic measures were taken as a result of throat tightness. Additional Information: Dose 1, administered on 01Sep2021, Anatomical site of injection: shoulder, Batch/lot number: 30130BA. Dose 2, administered on 17Oct2021, Anatomical site of injection: shoulder, Batch/lot number: FH8027. No Prior vaccination within 4 weeks. No Concomitant drugs. No Patient's medical history. Comments/Narrative: 1st Pfizer vaccine part A: No reaction, tired after 2 days. 2nd Pfizer vaccine part B: sore arm-day 2 woke up with itching. Day 3 very sore arm of well appeared with terrible itching. Day 3-night time throat closing urgent care said- don't come here- we cannot help you. Go where you got vaccine. Pharm at (facility name withheld) gave the Benadryl and took my report. Sick over 1.5 weeks and weak. Nausea 3 days. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2258141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 52,0
Geschlecht: M
Eingang: 29.04.2022
Impfdatum: 07.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Nausea Pain Pain in extremity

Symptomtext

Nausea; aches; sore arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) received via COVID-19 Adverse Event Self-Reporting Solution. The reporter is the patient. A 52-year-old male patient received BNT162b2 (BNT162B2), on 07Apr2022 as dose 4 (booster) single (Lot number: FH8027) at the age of 52 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Cipro, reaction(s): "Allergy to Cipro". Vaccination history included: Covid-19 vaccine (Dose: 1, MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (Dose: 2, MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (Dose: 3, MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: NAUSEA (non-serious) with onset 08Apr2022, outcome "recovered" (Apr2022); PAIN (non-serious) with onset 08Apr2022, outcome "recovered" (Apr2022), described as "aches"; PAIN IN EXTREMITY (non-serious) with onset 08Apr2022, outcome "recovered" (Apr2022), described as "sore arm". Therapeutic measures were not taken as a result of nausea, pain, pain in extremity. Additional information: Patient did not receive other vaccine in four weeks. Patient had no COVID prior vaccination and was not COVID tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

mild

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 23.11.2021
Beginn: 06.04.2022
Tage bis Beginn: 134,0
Dosis: 3
Route/Site: SYR / RA

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

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

Symptomtext

I had a breakthrough case of covid in early April. I have since recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Got a positive PCR test the day after the symptoms started.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Slynd (birth contorl) 4mg
Allergien: Bactrium
Vorherige Impfungen: -

VAERS 2256515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

mild

Staat: NY
Alter: 55,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 19.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Arthropathy Magnetic resonance imaging joint

Symptomtext

Extreme pain and weakness in both shoulders and left knee, followed by arthritic feeling in both hands. The joints affected had previously been operated on. The knee in 1983, the right shoulder in 2013 and the left shoulder in 2015.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: MRI done on left knee and right shoulder. Left knee was given two cortisone shots. I also met with a Rhumatoligist.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Trintelix 20mg. Natesto 2* a day
Allergien: Aspirin, sulfur
Vorherige Impfungen: -

VAERS 2254810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MD
Alter: 53,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 13.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fatigue Impaired work ability Nausea Pain Pain in extremity

Symptomtext

Pain radiating down left arm fatigue dizziness, nausea next morning, missed work

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: high cholesterol GERD hx concussions, head injury
Andere Medikamente: tylenol 2 tabs
Allergien: bactrim
Vorherige Impfungen: -

VAERS 2254694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NJ
Alter: 74,0
Geschlecht: M
Eingang: 27.04.2022
Impfdatum: 09.11.2021
Beginn: 11.04.2022
Tage bis Beginn: 153,0
Dosis: 3
Route/Site: IM / AR

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

Asthenia COVID-19 Decreased appetite Fatigue Influenza like illness Pyrexia SARS-CoV-2 test positive

Symptomtext

I got symptoms of flu like symptoms with tired, loss of energy, loss of appetite, weakness, and low grade fever. I got a positive COVID-19 test. I went to the hospital and received an antibody infusion. I was also prescribed Pavlovic. My symptoms lasted for 7-10 days. I do feel that the infusion did help. I did call my doctor and did a follow up telehealth visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test, antibody infusion
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin
Allergien: None
Vorherige Impfungen: 1st and 2nd dose Pfizer - weakness, tiredness - not severe

VAERS 2245733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 28.11.2021
Beginn: 01.04.2022
Tage bis Beginn: 124,0
Dosis: 3
Route/Site: SYR / LA

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

Bronchitis Chest X-ray normal Cough Cyst Electrocardiogram normal Influenza A virus test negative Influenza B virus test Magnetic resonance imaging Pain Peripheral swelling SARS-CoV-2 test negative Streptococcus test negative Ultrasound Doppler abnormal

Symptomtext

I first noticed cysts on my lower left legs on my calf. I noticed swelling in my leg, around the calf and ankle. By the following morning, they were even more swollen despite elevation and icing. On 04/02/2022 I went to urgent care where they did X-rays and I also still had a cough. I had been to a clinic on 03/17/2022 I did go to a Clinic for cough and they some testing and all test were negative. They treated me for Bronchitis. Ultrasound ordered but it was a weekend and could not be performed until that Tuesday 04/05/2022. I went I have the Ultrasound 5.5 cm fluid filled cysts interior of the left lower leg only shin bone. The second cyst is behind left knee 3.1cm. They did not refer to it as a bakers cyst. Two fluid filled cysts were found. No additional orders they referred me to an Orthopedic doctor. I have not yet seen that specialist because I am awaiting to return home for continued care. I was advised to follow up with Orthopedic that the cysts have two alternatives. The first is it would resolve itself and reabsorb and the second choice was if it continued to cause pain to have needle aspiration. It is giving me some pain and can feel it when I walk. I did have a pre-existing condition of blood clotting in the the left leg in September 2020 18 months prior. That was not observed on the recent Ultrasound. They were clear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 03/17/2022 Urgent Care for Cough. Strep, Type A/B Flu and COVID-19 Test all results -Negative. 04/02/2022 ordered Chest X-ray results Negative for Pneumonia and no clotting. Ultrasound was ordered MRI. EKG Normal.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Aleve Naproxen for pain 220mg 3 tablets PRN.
Allergien: Tylenol and Ibuprofen.
Vorherige Impfungen: -

VAERS 2243693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 48,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 16.04.2021
Beginn: 07.04.2022
Tage bis Beginn: 356,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Headache Myalgia Pyrexia SARS-CoV-2 test positive Sneezing

Symptomtext

Severe Covid. Fever, muscle aches, cough, sneezing, headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Rapid test (at home) and rapid test at CVS
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Zyrtec, vitamin D, calcium
Allergien: -
Vorherige Impfungen: Arm swelled after a flu vaccine in 1998 or 1999.

VAERS 2243665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia

Symptomtext

Shoulder pain after 5 months of receiving the COVID-19 vaccine. I still have the pain and it is getting worst.

Weitere VAERSDATA-Felder

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

VAERS 2241487

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 29.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Autoimmune disorder Blister Blood test Onychomadesis Pain Psoriasis Skin exfoliation Vitamin D decreased

Symptomtext

About 10 days later around 12/10/2021, I was travelling and I had: I was hiking and had what I thought was environmental issues, I was hiking and there were cacti and all these plants I was not used to be around. I had contact with a cactus flower, I thought I had a reaction to this plant. December came and went, then January and in February I had continued having blisters and pealing on the palms of my hands and bottom of my feet. I thought it was triggered by the cactus. My regular doctor did not know what it was so he sent me to my dermatologist, He stated you do not have a reaction to the plant, it is an auto immune disease that you will probably have forever. It is called Palmoplantar Psoriasis. The problem is not the plant it is your immune system. He is treating me for this condition I did not know about. I don't know if you need to know this but I am loosing my fingernails also. My concern is that this all happened within close proximity to the vaccine. The doctor is currently treating me with strong topical cortisone cream which has helped with the pain and has caused everything to calm down some. This is all very embarrassing with loosing my fingernails.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: PCP sent me for blood work, everything was perfect except for my vitamin D was low.
Aktuelle Erkrankungen: None
Vorgeschichte: HBP
Andere Medikamente: Metoprolol 50mg
Allergien: None
Vorherige Impfungen: -

VAERS 2225909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: GA
Alter: 54,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Immunisation reaction Injection site erythema Injection site nodule Injection site pain Injection site swelling Injection site warmth Pyrexia

Symptomtext

We had an employee get their 2nd booster on Friday and had a reaction. She stated the shot hurt very badly during administration which she had never experienced before. Then that night she had a raised knot appear at the injection site. She stated that the raised knot could be seen through a shirt and that it was very painful and had ?fever.? She took Tylenol throughout the weekend to help. Today I looked at it and the knot is gone but there is still a still a red circular area where the injection was given and it is still warm to touch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NO
Vorgeschichte: HIGH BLOOD PRESSURE PRE-DIABETES ANXIETY
Andere Medikamente: OZEMPIC WOMENS MULTI BLACK COHOSH MAGNESIUM CLONIDINE PAXIL LISINOPRIL
Allergien: PENCILLIN BENADRYL SULFA DRUGS
Vorherige Impfungen: -

VAERS 2225466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AZ
Alter: 36,0
Geschlecht: F
Eingang: 10.04.2022
Impfdatum: 20.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: UN / LA

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

Acoustic stimulation tests normal Laboratory test abnormal Laboratory test normal Lymph node pain Lymphadenopathy Neck pain Nervous system disorder Pain Vertigo Vestibular disorder

Symptomtext

I received a Pfizer COVID booster on 11/20/2021. (My first two COVID vaccines were Moderna, so this was my first time receiving a Pfizer vaccine.) I had typical side effects: body aches without fever for about 24 hours after the vaccination, and pain and swelling in the lymph node of my left armpit and pain up the left side of my neck that subsided after about a week. On 12/3/2021, I noticed a persistent feeling of vertigo. It started a day or two earlier, but at first I thought it was caused by anxiety. 12/3 was the day I first noticed it was not going away. The vertigo feels like I am slightly tilted to the right. It is slightly aggravated by bending forward and leaning to the right. One week after I noticed the persistent vertigo, on 12/10/2021, I had a telehealth visit with my doctor, and he recommended trying the Epley maneuver. I tried this several times over the next few days and it made no difference. On 1/3/2022 I again visited Health clinic and was referred to ENT. I visited ENT on 1/5/2022 and was seen by the NP. She conducted tests that ruled out BVVP. I visited ENT again on 1/27/2022 for visual nystygmography testing. This test determined that I had a vestibular nerve imbalance, with borderline weakness in the left vestibular nerve. At this appointment it was suggested to me that the nerve weakness might have been caused by my COVID booster. Various providers at ENT told me that multiple other patients had reported ringing in the ears after their COVID boosters, which made them suspect a possible relationship between COVID boosters and inner ear issues. After the visit on 1/27/2022, I began vestibular rehabilitation therapy (VRT). I performed a series of exercises three times per day for about 10-15 minutes each session, increasing the difficulty of the exercises each week. I had a follow-up on 2/3/2022 and another follow-up on 4/7/2022. At each follow-up, NP performed the same vertigo tests, and the scores for both appointments were similar--in fact the score was slightly higher (worse) at the second follow-up. After more than four months of experiencing vertigo and 10 weeks of doing VRT exercises 3 times daily, I have not observed any improvement in my symptoms since I first noted them on 12/3/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: BPPV test and hearing test (both normal; 1/5/2022), visual mystygmography (identified nerve imbalance and borderline weakness in left vestibular nerve; 1/27/2022)
Aktuelle Erkrankungen: N/A
Vorgeschichte: menstrual migraines
Andere Medikamente: Vitamin D 25 mcg/day, Jasmiel 3 mg/day, rizatriptan as needed
Allergien: N/A
Vorherige Impfungen: -

VAERS 2223184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

mild

Staat: IL
Alter: 57,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 12.01.2022
Beginn: 07.04.2022
Tage bis Beginn: 85,0
Dosis: 1
Route/Site: SYR / -

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

Abdominal pain Diarrhoea

Symptomtext

Abdominal pain and diarrhea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2220002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 04.01.2021
Beginn: 12.01.2022
Tage bis Beginn: 373,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Asthenia COVID-19 Hyponatraemia Hypophagia Nausea SARS-CoV-2 test positive

Symptomtext

Narrative: The patient received three doses of COVID 19 Vaccine (two doses Moderna Jan/Feb 2021 and one dose Moderna Nov 2021). The patient tested positive on 12 Jan 2022. The patient presented to the ED with weakness, nausea, and not eating. The patient was admitted with covid hyponatremia and acute kidney failure. The patient was discharged in stable condition on 25 Jan 2022.

Weitere VAERSDATA-Felder

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

VAERS 2218176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain lower Fungal infection Hydronephrosis Renal colic Stent placement

Symptomtext

ED to hospital admission on 1/2 for lower abdominal pain. Acute left renal colic, caused by the above + yeast encrusted left lower pole stent/ left upper and lower pole hydronephrosis, improved post urology intervention, stent replaced, cleared by urology to dc. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2216414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AZ
Alter: 43,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 22.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / UN

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

Arthralgia Blood thyroid stimulating hormone Fatigue Fluid retention Full blood count Gait disturbance Hypersomnia Low density lipoprotein Metabolic function test Myalgia Oedema Pain Swelling

Symptomtext

I had swelling and fluid retention that started in my stomach and then lower legs then thighs arms and face. The edema is worse when I am active. It has gotten so significant that it effects the way I walk. I also then feel extreme fatigue after exertion. For example after working three 12s I will sleep for 24 hours straight which is not at all normal. I also have muscle pain when the edema starts to subside. And shooting pain in joints especially.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: CBC, CMP, TSH LDLs March 9th, 2022
Aktuelle Erkrankungen: Post surgical from procedure in October
Vorgeschichte: Depression, anxiety, atopic dermatitis, psoriasis, eczema, rosacea
Andere Medikamente: Buspar, cymbalta, hydroxizine
Allergien: Shellfish, latex
Vorherige Impfungen: -

VAERS 2216025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 19.11.2021
Beginn: 19.12.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

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

Abscess drainage Pain in extremity Pelvic abscess Pelvic mass Peripheral swelling

Symptomtext

ED visit for left leg pain and swelling - treated and released. Admission to the hospital with a left hemipelvic mass. She underwent CT-guided drainage and fortunately the mass was found to be an abscess rather than a malignancy as we were originally concerned. Drainage was uneventful and patient was placed on vancomycin and Zosyn. Treated and discharged. ED visit and hospital admission were within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2200757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 34,0
Geschlecht: M
Eingang: 27.03.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Dizziness Fatigue Feeling cold Headache Malaise Muscular weakness Photophobia Vision blurred

Symptomtext

Around 11:15, 45 minutes after my injection. I started to feel a little bit weak and dizzy. This gradually got worse and worse, until I lost the ability to see because it was so blurry, and anything bright would cause me an agonizing headache. Later, I started to lose functionality in my legs and arms, I just felt weak. This weakness continued and grew to exhaustion. The feeling ill, weakness, and exhaustion continued for a little bit over 48 hours. And my blurry vision, sensitivity to brightness, and agonizing headache continued for about 72 hours. The worst part about the whole ordeal is that the physiological changes the vaccine did to my body. I typically am not cold, yet I continuously felt cold for about 2 months, not only my weakness and loss of functionality continued for about 2 months as well yet not regular.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: When I called local clinics they stated that they can just analyze and make sure I don't get worse. They stated that this is all normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Military injuries.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2183890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NM
Alter: 69,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 17.11.2021
Beginn: 14.01.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: - / RA

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

Computerised tomogram Headache Magnetic resonance imaging SARS-CoV-2 test

Symptomtext

Severe headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 17Nov2021 15:30 (Lot number: FH8027) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Yogurt" (unspecified if ongoing), notes: Known allergies: Yogurt. Concomitant medication(s) included: LEVOTHYROXINE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0158, Location of injection: Arm Left, Vaccine Administration Time: 16:00 PM), administration date: 21Apr2021, when the patient was 68 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8734, Location of injection: Arm Left, Vaccine Administration Time: 17:00 PM), administration date: 31Mar2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 14Jan2022 13:30, outcome "recovering", described as "Severe headache". The event "severe headache" was evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache. Additional information: The patient was not pregnant during the vaccination. The most recent COVID-19 vaccine was administered in Pharmacy or Drug Store Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient had been tested COVID-19. The patient received treatment for the adverse events with Toradal shots, muscle relaxer, gabapentin. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Name: CT Scan; Result Unstructured Data: Test Result:unremarkable and normal; Test Name: MRI; Result Unstructured Data: Test Result:unremarkable and normal; Test Date: 20220119; Test Name: Rapid; Test Result: Negative; Comments: Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy (Known allergies: Yogurt.)
Andere Medikamente: LEVOTHYROXINE.
Allergien: -
Vorherige Impfungen: -

VAERS 2183845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 31.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / RA

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

Blood test Bone pain Breast swelling Feeling abnormal Pain Pain in extremity Polymerase chain reaction Pyrexia

Symptomtext

soreness in my arm, bone in my under arm; soreness in my arm, bone in my under arm; right side of my breast is swollen; body ache; Fever; I just don''t feel good; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46 year-old female patient received bnt162b2 (BNT162B2), administered in deltoid right, administration date 31Jan2022 (Lot number: FH8027) at the age of 46 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "Polycystic disease" (unspecified if ongoing), notes: Verbatim: polycystic disease; "Hypertension" (unspecified if ongoing), notes: Verbatim: Hypertension; "Blood pressure" (unspecified if ongoing), notes: Verbatim: Blood pressure. Concomitant medication(s) included: NORVASC taken for blood pressure measurement; LOZOL taken for blood pressure measurement; HCTZ taken for blood pressure measurement. Vaccination history included: Covid-19 vaccine (Manufacturer Unknown, Dose number : Unknown), for COVID-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious), BONE PAIN (non-serious) all with onset 2022, outcome "unknown" and all described as "soreness in my arm, bone in my under arm"; BREAST SWELLING (non-serious) with onset 2022, outcome "unknown", described as "right side of my breast is swollen"; PAIN (non-serious) with onset 2022, outcome "unknown", described as "body ache"; PYREXIA (non-serious) with onset 2022, outcome "unknown", described as "Fever"; FEELING ABNORMAL (non-serious) with onset 2022, outcome "unknown", described as "I just don''t feel good". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity, bone pain, breast swelling, pain, pyrexia, feeling abnormal. Additional Information: It was reported that the patient took the Pfizer booster on Monday, was having like soreness in her arm, bone in her under arm, right side of her breast was swollen, she was having body ache, she was having fever,she just didn't feel good. It was further reported that she just had her blood work done. she got the blood work done, everything was fine. They did the PCR testing and it was negative, she was fine beside those things. she had Tylenol, she was taking, every 6 hours. There was no Prior vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: Test Date: 2022; Test Name: Blood work; Result Unstructured Data: Test Result:Fine; Test Date: 2022; Test Name: PCR test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure (Verbatim: Blood pressure); Hypertension (Verbatim: Hypertension); Polycystic kidney (Verbatim: polycystic disease)
Andere Medikamente: NORVASC; LOZOL; HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 2181613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 19.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Asthenia Chills Fatigue Feeling abnormal Feeling cold Headache Influenza like illness Pain

Symptomtext

Achiness; Feel achy; Chills; Headache; I feel tired/fatigue; I am not having much energy as I normally would; Felt kind of really bad as if I am coming down with the flu; I felt cold; Felt kind of really bad as if I am coming down with the flu; I felt cold; Felt kind of really bad as if I am coming down with the flu; I felt cold; 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 received bnt162b2 (BNT162B2), administration date 19Nov2021 (Lot number: FH8027) at the age of 57 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU VACCINE VII, administration date 01Nov2021. Vaccination history included: Bnt162b2 (1st Dose), for Covid-19 Immunization; Bnt162b2 (2nd Dose), for Covid-19 Immunization. The following information was reported: PAIN (non-serious) with onset Nov2021, outcome "unknown", described as "Achiness; Feel achy"; CHILLS (non-serious) with onset Nov2021, outcome "unknown", described as "Chills"; HEADACHE (non-serious) with onset Nov2021, outcome "unknown", described as "Headache"; FATIGUE (non-serious) with onset Nov2021, outcome "unknown", described as "I feel tired/fatigue"; ASTHENIA (non-serious) with onset Nov2021, outcome "unknown", described as "I am not having much energy as I normally would"; FEELING ABNORMAL (non-serious), INFLUENZA LIKE ILLNESS (non-serious), FEELING COLD (non-serious) all with onset Nov2021, outcome "unknown" and all described as "Felt kind of really bad as if I am coming down with the flu; I felt cold". Therapeutic measures were taken as a result of headache, fatigue. Additional Information: The patient was calling in today because as had the Pfizer booster shot this past Friday and the patient just experiencing some side effects like achiness, chills, headache and everything as if it was coming down with the cold or flu, like tiredness, fatigue and the patient not having much energy as normally would. So, the patients husband the patient were reading that those are some side effects and you just have to just take Tylenol and see how long, if it is lasting too long, go to urgent care or something. Actually, started like on Friday, had a headache and yesterday, did go out and do some errands, The patient came back home and felt kind of really bad as if the patient was coming down with the flu and then this morning, the same thing, felt tired and just feel achy, don't feel too good, don't really look too good either. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2179332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 52,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 18.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Vaccination site pain

Symptomtext

pain at injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 18Nov2021 (Lot number: FH8027) at the age of 52 years as dose 1, 0.3 ml single for covid-19 immunisation. Relevant medical history included: "Verbatim: Chemotherapy" (unspecified if ongoing), notes: Verbatim: Chemotherapy, Received chemotherapy 5 years ago for a duration of 1 year. There were no concomitant medications. Vaccination history included: measles (In college there was a measles outbreak. She got the vaccine for it and had no problems). The following information was reported: VACCINATION SITE PAIN (non-serious) with onset Nov2021, outcome "recovered" (Nov2021), described as "pain at injection site". Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chemotherapy (Verbatim: Chemotherapy Received chemotherapy 5 years ago for a duration of 1 year)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IL
Alter: 57,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Dry mouth Feeling abnormal Hypoaesthesia Hypoaesthesia oral Nausea Nervousness

Symptomtext

dry mouth; feels numbness at the top of his mouth and tongue; He stated it is a funny feeling in his mouth; He was a little nauseated; little numbness on the top of the jaw; nervous; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Physician) from medical information team. The reporter is the patient. A 57 year-old male patient received bnt162b2 (BNT162B2), administration date 15Nov2021 10:55 (Lot number: FH8027, Expiration Date: Dec2022) at the age of 57 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "cancer survivor" (unspecified if ongoing); "heartburn and stuff" (unspecified if ongoing). Concomitant medication(s) included: FLU, administration date 2021; PANTOPRAZOLE taken for dyspepsia (ongoing). Vaccination history included: Bnt162b2 (First Dose , LOT: EN6207,, EXP: 30Jun2021,, NDC: Unknown, Anatomical Location: right arm), administration date: 11Mar2021, when the patient was 57 years old, for COVID-19 Immunization; Bnt162b2 (Second Dose , LOT: EW0150, EXP: 31Jul2021, NDC: unknown, Anatomical Location: right arm), administration date: 01Apr2021, when the patient was 57 years old, for COVID-19 Immunization. The following information was reported: DRY MOUTH (non-serious) with onset 15Nov2021, outcome "recovered" (15Nov2021), described as "dry mouth"; HYPOAESTHESIA ORAL (non-serious) with onset 15Nov2021, outcome "recovering", described as "feels numbness at the top of his mouth and tongue"; FEELING ABNORMAL (non-serious) with onset 15Nov2021, outcome "unknown", described as "He stated it is a funny feeling in his mouth"; NAUSEA (non-serious) with onset 15Nov2021, outcome "recovered", described as "He was a little nauseated"; HYPOAESTHESIA (non-serious) with onset 15Nov2021, outcome "unknown", described as "little numbness on the top of the jaw"; NERVOUSNESS (non-serious) with onset 15Nov2021, outcome "unknown", described as "nervous". Therapeutic measures were taken as a result of dry mouth, hypoaesthesia oral, feeling abnormal, nausea, hypoaesthesia, nervousness. Additional information: The caller stated he took the booster dose 30 minutes ago and got a dry mouth and feels numbness at the top of his mouth and tongue. He stated he took pantoprazole 40 mg this morning and did not know if he was supposed to. He stated he he did not have any other symptoms and the top of his mouth is starting to resolve. He stated he was in home care and a cancer survivor. After the verbal response he stated he was not experiencing swelling in his throat or face, just was a funny feeling in his mouth. He wanted to know if these symptoms were normal. No investigation assessment was done. Clarified that he is referring to the booster shot, stated that he was a cancer patient, he had cancer in the past and his doctor said he should have it. Caller stated that the dryness was gone and there was just a little numbness on the top of the jaw and mouth. Treatment: He just took some Tylenol. Caller stated he had a separate card for the first two doses. He stated he had to put his glasses on to read it. The patient did not visit emergency room and physician office. Prior Vaccinations (within 4 weeks): yes, the Flu shot. No Relevant Tests was done. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer; Heartburn.
Andere Medikamente: PANTOPRAZOLE.
Allergien: -
Vorherige Impfungen: -

VAERS 2179217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 12,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Bedridden Dizziness Nausea Vomiting

Symptomtext

nauseous; dizzy; Threw up 3 times; could not get out of bed for 24 hours; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 12 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 12Nov2021 15:30 (Lot number: FH8027) at the age of 12 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU, administration date 01Oct2021; ALIGN. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FF2590, Vaccine Administration Time: 03:30 PM), administration date: 19Oct2021, when the patient was 12 years old, for COVID-19 Immunization. The following information was reported: NAUSEA (non-serious) with onset 13Nov2021 03:00, outcome "recovering", described as "nauseous"; DIZZINESS (non-serious) with onset 13Nov2021 03:00, outcome "recovering", described as "dizzy"; VOMITING (non-serious) with onset 13Nov2021 03:00, outcome "recovering", described as "Threw up 3 times"; BEDRIDDEN (non-serious) with onset 13Nov2021 03:00, outcome "recovered" (14Nov2021), described as "could not get out of bed for 24 hours". Therapeutic measures were not taken as a result of nausea, dizziness, vomiting, bedridden. Additional Information: Facility type vaccine was other. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. Other medications in two weeks were OTC Accentrate. Known allergies: Not that we are aware. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2176695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / LA

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

Axillary pain Swelling Vaccination site pain

Symptomtext

Pain to left arm injection site; Swelling & pain to left armpit; swelling & pain to left armpit; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 08Dec2021 01:15 (Lot number: FH8027) at the age of 42 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: Pfizer (DOSE 2, SINGLE, Batch/Lot No: EL3246, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 09Jan2021, when the patient was 42 years old, for Covid-19 immunization; Pfizer (DOSE 1, SINGLE, Batch/Lot No: EH9899, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 19Dec2020, when the patient was 42 years old, for Covid-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 09Dec2021 07:00, outcome "unknown", described as "Pain to left arm injection site"; SWELLING (non-serious) with onset 09Dec2021 07:00, outcome "unknown", described as "Swelling & pain to left armpit"; AXILLARY PAIN (non-serious) with onset 09Dec2021 07:00, outcome "unknown", described as "swelling & pain to left armpit". Therapeutic measures were not taken as a result of vaccination site pain, swelling, axillary pain. 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 2176498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 12.03.2022
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

Tenderness Vaccination site pain

Symptomtext

our arms (right rear) continues to be very tender; very painful, and our arms (right rear) continues to be very tender and painful 20 hours later; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 65 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 05Nov2021 19:00 (Lot number: FH8027) at the age of 65 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU taken for immunisation, administration date 05Nov2021; LANTUS; METFORMIN; EXFORGE. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL9265, Location of injection: Arm Left, Vaccine Administration Time: 08:00 PM), administration date: 25Feb2021, for Covid-19 immunization, reaction(s): "No reaction on previous exposure to vaccine"; Bnt162b2 (Dose Number: 2, Batch/Lot No: EP7534, Location of injection: Arm Left, Vaccine Administration Time: 08:00 PM), administration date: 22Mar2021, for Covid-19 immunization, reaction(s): "No reaction on previous exposure to vaccine". The following information was reported: TENDERNESS (non-serious) with onset 05Nov2021 21:00, outcome "not recovered", described as "our arms (right rear) continues to be very tender"; VACCINATION SITE PAIN (non-serious) with onset 05Nov2021 21:00, outcome "not recovered", described as "very painful, and our arms (right rear) continues to be very tender and painful 20 hours later". Therapeutic measures were not taken as a result of tenderness, vaccination site pain. Additional information: The patient was vaccinated at the same times and locations for all three doses. The first two doses to let to a mild sore shoulder for her. The Booster injection for BOTH OF US were very painful, and her arms (right rear) continues to be very tender and painful 20 hours later. Also note that we also received our Senior dose Flu shot in the same right (front) arms. This injection site was also a little tender (2 out of 10), but nothing like the Pfizer site (7-8 out of 10) No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101531727 Same reporter/ drug/ event for different patients

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
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: LANTUS; METFORMIN; EXFORGE
Allergien: -
Vorherige Impfungen: -

VAERS 2176497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 12.03.2022
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

Vaccination site pain

Symptomtext

very painful, and our arms (right rear) continues to be very tender and painful 20 hours later; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 05Nov2021 19:00 (Lot number: FH8027) at the age of 68 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU), administered in arm right, administration date 05Nov2021 (Batch/Lot number: unknown) for immunisation. Relevant medical history included: "Diabetis" (unspecified if ongoing). Concomitant medication(s) included: LANTUS; METFORMIN; EXFORGE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP7534, Location of injection: Arm Left, Vaccine Administration Time: 08:00 PM), administration date: 22Mar2021, when the patient was 68 years old, for COVID-19 Immunization, reaction(s): "first two doses to let to a mild sore shoulder for me"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL9265, Location of injection: Arm Left, Vaccine Administration Time: 08:00 PM), administration date: 25Feb2021, when the patient was 67 years old, for COVID-19 Immunization, reaction(s): "first two doses to let to a mild sore shoulder for me". The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 05Nov2021 21:00, outcome "not recovered", described as "very painful, and our arms (right rear) continues to be very tender and painful 20 hours later". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site pain. Additional information: The Booster injection were very painful, and our arms (right rear) continues to be very tender and painful 20 hours later. Also note that we also received our Senior dose Flu shot in the same right (front) arms. This injection site is also a little tender (2 out of 10), but nothing like the Pfizer site (7-8 out of 10). 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 and not tested for COVID-19 since vaccination. The patient had no known allergy. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101531728 Same reporter/ drug/ event for different patients

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: Test Date: 20211105; Test Name: This injection site is also a little tender; Result Unstructured Data: Test Result:7-8 out of 10; Comments: 2 out of 10 but nothing like the Pfizer site (7-8 out of 10)
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetic
Andere Medikamente: LANTUS; METFORMIN; EXFORGE
Allergien: -
Vorherige Impfungen: -

VAERS 1795562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Asthenia Headache Inappropriate schedule of product administration Pain Pain in extremity

Symptomtext

had no energy; body aches; arm was sore; mild headache; she inadvertently received her second dose on 14OCT2021; 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 (159558). The reporter is the patient. A 59 year-old female patient received bnt162b2 (BNT162B2), administration date 14Oct2021 (Lot number: FH8027) at the age of 59 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: 1st, Lot Number: FF2589), administration date: 30Sep2021, when the patient was 59 years old, for Covid-19 immunization. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 14Oct2021, outcome "unknown", described as "she inadvertently received her second dose on 14OCT2021"; ASTHENIA (non-serious), outcome "unknown", described as "had no energy"; PAIN (non-serious), outcome "unknown", described as "body aches"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "arm was sore"; HEADACHE (non-serious), outcome "unknown", described as "mild headache". Additional information: Reporter was stated she received her first dose of Comirnaty on 30Sep2021. Caller states she inadvertently received her second dose on 14Oct2021, thinking the second dose should have been two weeks after the first dose. Caller states she just received a notification on her phone that her second dose is coming up on 21Oct2021. From this caller realized that she got her second dose one week too early. Caller states she is "afraid for her life" and wants to know if Pfizer has any additional information on the timing of the second dose of Comirnaty. The initial primary vaccination series of Comirnaty (COVID-19 Vaccine, mRNA) and the Pfizer BioNTech COVID-19 Vaccine are to be administered as a 2-dose series, 3 weeks apart. In the Pfizer-BioNTech COVID-19 Vaccine clinical study, the second dose was allowed to be given 19-23 days after the first dose. Initial primary series of Pfizer-BioNTech COVID-19 Vaccine consists of 2 doses given 3 weeks (21 days) apart. The second dose of Pfizer-BioNTech vaccine should be given as close to the recommended interval (3 weeks after the first dose) as possible, but not earlier than 3 weeks. However, individuals who receive the second dose up to 4 days before or at any time after the recommended date can be considered fully vaccinated. Advised caller that she does not fall into this timeframe. Informed caller that no additional untoward side effects should be expected other than those listed in the Fact Sheet for Recipients and Caregivers. Advised caller that this timing is more related to vaccine efficacy. Advised caller to notify her vaccination provider of what has occurred and have the vaccination provider contact Pfizer or the CDC for guidance moving forward on whether or not she will need revaccination. Provided caller with Case Number. Sending attached document via email fulfillment for patient to review with vaccination provider. Advised caller to contact her HCP if she experiences any side effects that bother her or do not go away. Transfer agent has a consumer on the line who had the 1st dose of the Pfizer COVID vaccine on 30Sep2021 and the 2nd dose 14Oct2021, so the caller did get the 2nd dose a week early and the caller is specifically asking if she has any medical liability for that early dose. Caller asks, so she is the only person in the whole world that this has happened to? She has been overdosed, or at least she feels like she has been and she is trying not to cry. She doesn't understand the question but she has taken her thyroid medication daily. Reworded question and caller states that she had the normal side effects to the COVID vaccine. She had her vaccine on Thursday and then on Friday she had no energy, she had body aches, her arm was sore and she had a mild headache so to the question, no, not at this time. She is unsure about the future though and what was going to happen to her. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1795562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Headache Inappropriate schedule of product administration Pain Pain in extremity

Symptomtext

had no energy; body aches; arm was sore; mild headache; she inadvertently received her second dose on 14OCT2021; 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 (159558). The reporter is the patient. A 59 year-old female patient received bnt162b2 (BNT162B2), administration date 14Oct2021 (Lot number: FH8027) at the age of 59 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: 1st, Lot Number: FF2589), administration date: 30Sep2021, when the patient was 59 years old, for Covid-19 immunization. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 14Oct2021, outcome "unknown", described as "she inadvertently received her second dose on 14OCT2021"; ASTHENIA (non-serious), outcome "unknown", described as "had no energy"; PAIN (non-serious), outcome "unknown", described as "body aches"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "arm was sore"; HEADACHE (non-serious), outcome "unknown", described as "mild headache". Additional information: Reporter was stated she received her first dose of Comirnaty on 30Sep2021. Caller states she inadvertently received her second dose on 14Oct2021, thinking the second dose should have been two weeks after the first dose. Caller states she just received a notification on her phone that her second dose is coming up on 21Oct2021. From this caller realized that she got her second dose one week too early. Caller states she is "afraid for her life" and wants to know if Pfizer has any additional information on the timing of the second dose of Comirnaty. The initial primary vaccination series of Comirnaty (COVID-19 Vaccine, mRNA) and the Pfizer BioNTech COVID-19 Vaccine are to be administered as a 2-dose series, 3 weeks apart. In the Pfizer-BioNTech COVID-19 Vaccine clinical study, the second dose was allowed to be given 19-23 days after the first dose. Initial primary series of Pfizer-BioNTech COVID-19 Vaccine consists of 2 doses given 3 weeks (21 days) apart. The second dose of Pfizer-BioNTech vaccine should be given as close to the recommended interval (3 weeks after the first dose) as possible, but not earlier than 3 weeks. However, individuals who receive the second dose up to 4 days before or at any time after the recommended date can be considered fully vaccinated. Advised caller that she does not fall into this timeframe. Informed caller that no additional untoward side effects should be expected other than those listed in the Fact Sheet for Recipients and Caregivers. Advised caller that this timing is more related to vaccine efficacy. Advised caller to notify her vaccination provider of what has occurred and have the vaccination provider contact Pfizer or the CDC for guidance moving forward on whether or not she will need revaccination. Provided caller with Case Number. Sending attached document via email fulfillment for patient to review with vaccination provider. Advised caller to contact her HCP if she experiences any side effects that bother her or do not go away. Transfer agent has a consumer on the line who had the 1st dose of the Pfizer COVID vaccine on 30Sep2021 and the 2nd dose 14Oct2021, so the caller did get the 2nd dose a week early and the caller is specifically asking if she has any medical liability for that early dose. Caller asks, so she is the only person in the whole world that this has happened to? She has been overdosed, or at least she feels like she has been and she is trying not to cry. She doesn't understand the question but she has taken her thyroid medication daily. Reworded question and caller states that she had the normal side effects to the COVID vaccine. She had her vaccine on Thursday and then on Friday she had no energy, she had body aches, her arm was sore and she had a mild headache so to the question, no, not at this time. She is unsure about the future though and what was going to happen to her. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2161518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AL
Alter: 54,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 08.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Blood test Glycosylated haemoglobin increased Illness Limb discomfort Nodule Peripheral swelling Pyrexia

Symptomtext

Elevated A1C; COVID arm; Sick for like 3 weeks; Knot in her arm for 3 weeks; COVID arm with swelling; Fever; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. A 54 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 08Nov2021 15:00 (Lot number: FH8027) at the age of 54 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "allergies" (unspecified if ongoing); "obesity" (unspecified if ongoing); "prediabetic" (unspecified if ongoing), notes: she has been prediabetic for several years now. She said her numbers were at a 6 for several years. There were no concomitant medications. The following information was reported: GLYCOSYLATED HAEMOGLOBIN INCREASED (non-serious) with onset 09Nov2021, outcome "not recovered", described as "Elevated A1C"; LIMB DISCOMFORT (non-serious) with onset 09Nov2021, outcome "unknown", described as "COVID arm"; ILLNESS (non-serious) with onset 09Nov2021, outcome "recovered" (Nov2021), described as "Sick for like 3 weeks"; NODULE (non-serious) with onset 09Nov2021, outcome "recovered" (2021), described as "Knot in her arm for 3 weeks"; PERIPHERAL SWELLING (non-serious) with onset 09Nov2021, outcome "unknown", described as "COVID arm with swelling"; PYREXIA (non-serious) with onset Nov2021, outcome "unknown", described as "Fever". The events "elevated a1c", "covid arm", "sick for like 3 weeks", "knot in her arm for 3 weeks", "covid arm with swelling" and "fever" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: A caller stated that she had her first dose of covid adult vaccine on 08Nov at her left arm. She had COVID arm with swelling, she had a fever and was sick for like 3 weeks. She had a knot in her arm for 3 weeks. She went to the doctor, and he checked her blood work. Her A1C levels were elevated was the only thing he could find. They have been monitoring it for the last 5 years. She is calling about the COVID vaccine. The first dose was on 08Nov2021, given in her Left arm, around 3pm. Her second one was given 30Nov2021 with lot FF2593, in her left arm, around 2pm. She didn't get it for any particular reason. After the first dose is when she experienced all of these side effects. Her A1C is still elevated. 54-year-old female said she has been prediabetic for several years now. She said her numbers were at a 6 for several years. Then after receiving the 1st dose of the Pfizer-BioNTech Covid-19 Vaccine, her A1C levels became elevated. Patient wants to know if this is normal. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Name: Blood work; Result Unstructured Data: Test Result:prediabetic; Comments: numbers were at a 6 for several years; Test Date: 202111; Test Name: Blood work; Result Unstructured Data: Test Result:CBC A1C elevated
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Diabetic (she has been prediabetic for several years now. She said her numbers were at a 6 for several years); Obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2161506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 15,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 23.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: OT / RA

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

Mechanical urticaria

Symptomtext

receiving the 1st dose of the vaccine the patient developed urticaria dermatographia on the left hip; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 15 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 23Nov2021 17:00 (Lot number: FH8027) at the age of 15 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: No. The following information was reported: MECHANICAL URTICARIA (non-serious) with onset 29Nov2021 19:00, outcome "not recovered", described as "receiving the 1st dose of the vaccine the patient developed urticaria dermatographia on the left hip". Therapeutic measures were not taken as a result of mechanical urticaria. Additional information:: 6 days after receiving the 1st dose of the vaccine the patient developed urticaria dermatographia on the left hip. adverse event start date 29Nov2021. adverse event start time 07:00 PM No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2161492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NJ
Alter: 14,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Fatigue Lymphadenopathy Pain in extremity

Symptomtext

left armpit gland swelling and pain; Fatigue; left arm soreness; left armpit gland swelling and pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 14-year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 26Nov2021 16:00 (Lot number: FH8027) at the age of 14 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Juvenile idiopathic arthritis" (unspecified if ongoing). Concomitant medication(s) included: HUMIRA. Past drug history included: Morphine, reaction(s): "Known allergies: Morphine"; Sulfasalazine, reaction(s): "Known allergies: sulfasalazine". Vaccination history included: Bnt162b2 (Dose 2, single; Lot Number: Ew0173), administration date: 16Jun2021, when the patient was 13 years old, for Covid-19 immunization; Bnt162b2 (Dose 1, single; Lot Number: Ew0179), administration date: 29May2021, when the patient was 13 years old, for Covid-19 immunization. The following information was reported: AXILLARY PAIN (non-serious), LYMPHADENOPATHY (non-serious) all with onset 27Nov2021, outcome "recovering" and all described as "left armpit gland swelling and pain"; FATIGUE (non-serious) with onset 27Nov2021, outcome "recovering", described as "Fatigue"; PAIN IN EXTREMITY (non-serious) with onset 27Nov2021, outcome "recovering", described as "left arm soreness". Therapeutic measures were not taken as a result of axillary pain, fatigue, pain in extremity, lymphadenopathy. Additional information: Non-healthcare professional reporting for a patient. Prior to the vaccination, the patient was 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 four weeks prior to the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Juvenile arthritis
Andere Medikamente: HUMIRA
Allergien: -
Vorherige Impfungen: -

VAERS 2161406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

mild

Staat: MO
Alter: 66,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 12.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Vaccination site rash

Symptomtext

rash at site of injection; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Other HCP). The reporter is the patient. A 66 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 12Nov2021 (Lot number: Fh8027) at the age of 66 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: VACCINATION SITE RASH (non-serious) with onset 14Nov2021, outcome "recovering", described as "rash at site of injection". Therapeutic measures were not taken as a result of vaccination site rash. Additional information: The patient had not received any other vaccine within 4 weeks. Patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2148779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MO
Alter: 80,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 16.02.2021
Beginn: 08.02.2022
Tage bis Beginn: 357,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Pyrexia

Symptomtext

fever, severe fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 1,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2146531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IL
Alter: 56,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / RA

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

Arthralgia Headache Lymphadenopathy

Symptomtext

Joint aches; Headache; Lump swelling under right armpit; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 18Nov2021 16:00 (Formulation: solution for injection, Lot number: FH8027) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Ankylosing spondylitis" (unspecified if ongoing). Concomitant medication(s) included: HUMIRA; ATORVASTATIN; OMEPRAZOLE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EK5730, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 23Mar2021, when the patient was 55 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EJ1685, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 02Mar2021, when the patient was 55 years old, for COVID-19 immunization. The following information was reported: ARTHRALGIA (non-serious) with onset 19Nov2021 17:00, outcome "recovered" (Nov2021), described as "Joint aches"; HEADACHE (non-serious) with onset 19Nov2021 17:00, outcome "recovered" (Nov2021), described as "Headache"; LYMPHADENOPATHY (non-serious) with onset 19Nov2021 17:00, outcome "recovered" (Nov2021), described as "Lump swelling under right armpit". Therapeutic measures were not taken as a result of arthralgia, headache, lymphadenopathy. Additional information: The patient had not received any other vaccine within 4 weeks. Before being vaccinated he did not have COVID and had not been tested COVID post vaccination. 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: Ankylosing spondylitis
Andere Medikamente: HUMIRA; ATORVASTATIN; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2141995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: VA
Alter: 64,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 06.03.2021
Beginn: 25.01.2022
Tage bis Beginn: 325,0
Dosis: 2
Route/Site: OT / -

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

Blood test Decreased appetite Hepatitis Nausea Suspected COVID-19 Vaccination failure Weight Weight decreased

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; LIVER INFLAMMATION; SEVERE LOSS OF APPETITE; WEIGHT LOSS OF AROUND 18 LBS; MODERATE NAUSEA; This spontaneous report received from a patient and concerned a 64 year old male of unspecified ethnicity. The patient's weight was 86.18 kilograms, and height was 183 centimeters. The patient's concurrent conditions included: cancer and immunocompromised. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805022 expiry: 25-MAY-2021) dose was not reported, 1 total administered on 06-MAR-2021 at left arm for prophylactic vaccination. The patient additionally received non-company suspect vaccine BNT 162 (dose number in series 2) (batch number: FH8027 expiry: unknown, form of admin, route of admin, and were not reported) dose was not reported, administered on 18-NOV-2021 at left arm for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient developed covid virus (suspected clinical vaccination failure, suspected covid-19 infection) (dose number in series 1) with associated symptoms. On 10-JAN-2022, the patient was treated with Paxlovid tablet (2 different tablets) for covid virus to minimize result of covid and his associated symptoms with the medication. Around 25-JAN-2022, the patient experienced severe loss of appetite, weight loss of around 18 lbs, and moderate nausea (dose number in series 2). On an unspecified date, the patient experienced slightly jaundiced. On 08-FEB-2022, the patient experienced liver inflammation (dose number in series 2). The loss of appetite had improved slightly at a very slow rate. He did have an oncology appointment and they did blood work. He was called 3 days ago with results and they said he did have liver inflammation. He had no problem with the vaccines. Moderate nausea improved significantly, but the rate of improvement was very slow. He first noticed being slightly jaundiced 2 weeks ago. He did not have an exact date. His oncologist had scheduled for more labs in a week and a half. He also reported that associated with lack of appetite was weight loss of around 18 lbs., which had then stabilized. The action taken with covid-19 vaccine ad26.cov2.s, and bnt 162 was not applicable. The patient recovered from suspected covid-19 infection, was recovering from severe loss of appetite, moderate nausea, and weight loss of around 18 lbs, and the outcome of suspected clinical vaccination failure and liver inflammation was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000218644.; Sender's Comments: V0: 20220242568- covid-19 vaccine ad26.cov2.s- liver inflammation. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). Therefore, this event(s) is considered unassessable. 20220242568- covid-19 vaccine ad26.cov2.s-Suspected Clinical Vaccination failure. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: Test Date: 20220125; Test Name: Weight; Result Unstructured Data: loss of around 18 lbs; Test Name: Blood test; Result Unstructured Data: liver inflammation
Aktuelle Erkrankungen: Cancer; Immunocompromised
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1857986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Breast swelling Oedema peripheral Rash erythematous Swelling Fluid retention

Symptomtext

Swelling with accumulation of fluid in from left armpit, down side of left breast to top of left side torso; Swelling with accumulation of fluid in from left armpit, down side of left breast to top of left side torso; Red rash from left shoulder, across chest and to top of torso; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP and Physician). The reporter is the patient. A 61-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Nov2021 10:15 (Lot number: FH8027) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ESCITALOPRAM. Vaccination history included: Bnt162b2 (Dose 1, single, Lot no: EP7534, vaccination location: left arm), administration date: 23Mar2021, when the patient was 60 years old, for Covid-19 immunization; Bnt162b2 (Dose 2, single, Lot no: EW0161, vaccination location: left arm), administration date: 13Apr2021, when the patient was 60 years old, for Covid-19 immunization. The following information was reported: SWELLING (non-serious), FLUID RETENTION (non-serious) all with onset 07Nov2021, outcome "not recovered" and all described as "Swelling with accumulation of fluid in from left armpit, downside of left breast to top of left side torso"; RASH ERYTHEMATOUS (non-serious) with onset 07Nov2021, outcome "recovered", described as "Red rash from left shoulder, across chest and to top of torso". The events "swelling with accumulation of fluid in from left armpit, downside of left breast to top of left side torso", "swelling with accumulation of fluid in from left armpit, downside of left breast to top of left side torso" and "red rash from left shoulder, across chest and to top of torso" were evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of swelling, fluid retention, rash erythematous. Additional information: Patient has not taken any other vaccines within four weeks. Rash subsided but fluid seems to be migrating downside. Will be making a doctor appt. Prior to vaccination patient was not tested for covid-19 and not been tested since the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: ESCITALOPRAM
Allergien: -
Vorherige Impfungen: -

VAERS 1857986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Breast swelling Oedema peripheral Rash erythematous Swelling Fluid retention

Symptomtext

Swelling with accumulation of fluid in from left armpit, down side of left breast to top of left side torso; Swelling with accumulation of fluid in from left armpit, down side of left breast to top of left side torso; Red rash from left shoulder, across chest and to top of torso; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP and Physician). The reporter is the patient. A 61-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Nov2021 10:15 (Lot number: FH8027) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ESCITALOPRAM. Vaccination history included: Bnt162b2 (Dose 1, single, Lot no: EP7534, vaccination location: left arm), administration date: 23Mar2021, when the patient was 60 years old, for Covid-19 immunization; Bnt162b2 (Dose 2, single, Lot no: EW0161, vaccination location: left arm), administration date: 13Apr2021, when the patient was 60 years old, for Covid-19 immunization. The following information was reported: SWELLING (non-serious), FLUID RETENTION (non-serious) all with onset 07Nov2021, outcome "not recovered" and all described as "Swelling with accumulation of fluid in from left armpit, downside of left breast to top of left side torso"; RASH ERYTHEMATOUS (non-serious) with onset 07Nov2021, outcome "recovered", described as "Red rash from left shoulder, across chest and to top of torso". The events "swelling with accumulation of fluid in from left armpit, downside of left breast to top of left side torso", "swelling with accumulation of fluid in from left armpit, downside of left breast to top of left side torso" and "red rash from left shoulder, across chest and to top of torso" were evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of swelling, fluid retention, rash erythematous. Additional information: Patient has not taken any other vaccines within four weeks. Rash subsided but fluid seems to be migrating downside. Will be making a doctor appt. Prior to vaccination patient was not tested for covid-19 and not been tested since the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: ESCITALOPRAM
Allergien: -
Vorherige Impfungen: -

VAERS 2122743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: -
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 21.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Asthenia Feeling abnormal Headache Nasopharyngitis Oropharyngeal pain Pyrexia

Symptomtext

Had a fever; fever was terrible/ Had fever again; I had so many blankets on top of me still I was cold; Headache; Weakness; I had a terrible experience last night; Sore throat; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A male patient received bnt162b2 (BNT162B2), administration date 21Nov2021 21:00 (Lot number: FH8027) 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), for COVID-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset 21Nov2021 21:00, outcome "recovering", described as "Had a fever; fever was terrible/ Had fever again"; NASOPHARYNGITIS (non-serious) with onset 21Nov2021 21:00, outcome "recovering", described as "I had so many blankets on top of me still I was cold"; HEADACHE (non-serious) with onset 21Nov2021 21:00, outcome "recovering", described as "Headache"; ASTHENIA (non-serious) with onset 21Nov2021 21:00, outcome "recovering", described as "Weakness"; OROPHARYNGEAL PAIN (non-serious) with onset Nov2021, outcome "recovering", described as "Sore throat"; FEELING ABNORMAL (non-serious) with onset 21Nov2021, outcome "recovered" (Nov2021), described as "I had a terrible experience last night". Additional information: Consumer stated, he had second dose of Pfizer (COVID 19 Vaccine) yesterday noon, he got the second done noon, by 9 pm had a fever, headache, weakness, the fever was terrible though like had so many blankets on top of me still I was cold. So, by 5 am the fever was out, was gone and then now had fever again since lets say 5 am like as of now he had a fever and a sore throat. The patient asked what he needs to do. Consumer further stated, he cannot have, he had a terrible experience last night, cannot have it again. He does not know what to take, should he take Nyqul, Tylenol, Ibuprofen. Consumer was suggested to visit Emergency room in case of emergency and informed the role of Pfizer Drug Safety and Pfizer Medical Information again. consumer who stayed he has not fully recovered. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2121123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MD
Alter: 63,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 10.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 19,0
Dosis: UNK
Route/Site: IM / -

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

Arthralgia Bursitis Magnetic resonance imaging abnormal Neck pain Rotator cuff syndrome Vaccination site pain

Symptomtext

PAIN in upper arm, neck, shoulder, progressively worsening on the left side at the site of vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: MRI showed bursitis of the subacromial and subdeltoid bursa, likely reactive, and a full-thickness supraspinatus tear.
Aktuelle Erkrankungen: none
Vorgeschichte: osteoporosis claustrophobia
Andere Medikamente: Sertraline 25mg daily, VitaminD 1000mg daily
Allergien: none
Vorherige Impfungen: -

VAERS 2118741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 22,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Maternal exposure during pregnancy Rash

Symptomtext

Patient pregnant, last menstrual date: 13May2021, administration date: 22Oct2021; Rash all over face,arms,and chest.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 22 year-old female patient (pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 22Oct2021 11:30 (Lot number: FH8027) at the age of 22 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. Date of last menstrual period: 13May2021. The patient was 23 weeks pregnant at the time of exposure to bnt162b2. The patient was 23 weeks pregnant at the event onset. The patient is expected to deliver a baby(s) on 17Feb2022. Concomitant medication(s) included: PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Ff2587, Location of injection: Arm Left, Vaccine Administration Time: 11:30), administration date: 01Oct2021, when the patient was 22 years old, for Covid-19 immunization. The following information was reported: MATERNAL EXPOSURE DURING PREGNANCY (non-serious), outcome "unknown", described as "Patient pregnant, last menstrual date: 13May2021, administration date: 22Oct2021"; RASH (non-serious) with onset 22Oct2021 13:00, outcome "recovering", described as "Rash all over face,arms,and chest.". Therapeutic measures were not taken as a result of rash. Additional information: The patient had past drug history included: (unspecified) drug name and reaction(s): "Allergy".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2115976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 28,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 01.01.2022
Beginn: 26.01.2022
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / UN

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

Fibrin D dimer Inflammation Livedo reticularis Pyrexia Rash Skin discolouration

Symptomtext

Patient (employee) experienced inflammation in bilateral legs, fever overnight Also had discoloration/rash of lower extremeties - per PA, consistent with livedo reticularis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: D-dimer - negative (rule out blood clot)
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2110516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: GA
Alter: 66,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LL

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

Breast pain Breast swelling Electrocardiogram Laboratory test Lymphadenopathy Sleep disorder Tenderness

Symptomtext

The next morning, I noticed swelling and hardening of my lymph nodes in my left armpit. A lot of tenderness. It lasted probably a week. Each day being a little better than the first day. After about maybe 2 weeks after the shot, I noticed that my left breast implant felt hard. It was swollen and it was very painful. I got an MRI to see what was going on and I went and saw (plastic surgeon). The swelling of the implant, it was swelling on the top of the implant. She was not familiar with this happening to anyone else. They were shocked when they saw my breast in the office. When sleeping at night, it would be so painful it would wake me up. In addition, after the booster, my left lateral side of my implant started to swell and extremely painful. Instead of being at the top of the implant, this was on the side, close to the armpit. For procedures, I'm going to have a surgical explant of breast implants for both. Dr. said that she would recommend that I would not have new implants at this time and to have my body try to get back to normal since I'm having this side effects. Surgery for explant 03/09/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: Labs for pre surgery EKG for pre surgery Once surgery is complete, implants will be inspected for specimens.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure High cholesterol
Andere Medikamente: Simvastatin 40mg 1xday Valtrex 500mg 1xday Irbesartan 150mg 1xday Progesterone 100mg 1xday Estradiol patch 0.0375mg 2xweekly Align probiotic Vitamin C 500mg 2xday Vitamin D3 50mg 2xday Calcium 500mg 1xday
Allergien: One episode with Dilaudid after surgery
Vorherige Impfungen: 1st COVID Pfizer vaccination 01/22/2021 - The next morning, I noticed swelling and hardening of my lymph nodes in my left armpit

VAERS 2105903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NC
Alter: 65,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Angioedema Erythema Hypersensitivity Pain Pruritus Rash Urticaria

Symptomtext

severe allergic reaction with rash and large welts ...angio edema....had 4 prescriptions of steroids over 6 weeks and Benadryl, Allegra, Pepcid. Welts are large, painful, itchy, red and have not gone away. Was referred to Dr. Had a video conference. Her treatment was the same as, prednisone, antihistimines, and Pepcid. Suggested an experimental drug called Xolair. Have not take it. $2300 and shot and adverse effects too dangerous.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: hypothyroidism mitral valve regurgitation
Andere Medikamente: metoprolol, lexapro, armor thyroid, multi vitamin, vitamin D, omega 3, vitamin B, vitamin K, glucosamine
Allergien: sulfa drugs sometimes shrimp
Vorherige Impfungen: -

VAERS 2101970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: GA
Alter: 55,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Fatigue Malaise

Symptomtext

I woke up the next day feeling dizzy, exhausted and not well. My BP was 90/50. I did a nebulizer treatment at home and it popped back up to normal (110/70).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HBP, Asthma
Andere Medikamente: Zoloft, Wellbutrin, Lisinopril, Simvistatin
Allergien: Eggs
Vorherige Impfungen: -

VAERS 2099032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AL
Alter: 52,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 01.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Influenza virus test Lymph node pain Myalgia Pain in extremity SARS-CoV-2 test

Symptomtext

I had very tinder lymph nodes. I had a very sore arm, fatigue, and leg muscle pain. These other symptoms lasted for about 3 days but the leg muscle pain are still ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid-19 flu
Aktuelle Erkrankungen: N/a
Vorgeschichte: Kidney disease
Andere Medikamente: N/a
Allergien: N/a
Vorherige Impfungen: shingles

VAERS 2098892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WA
Alter: 58,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 28.01.2022
Beginn: 29.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cold sweat Fatigue Headache Hot flush Muscle spasms Pain in extremity Vomiting

Symptomtext

Side effects started 3am Sat morning including: HA, cold sweets, hot flashes, cramping and vomiting. Intensity peaked around 3pm. Symptoms decreased by 530 pm leaving fatigue/sore arm. By Sunday Noon symptoms resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypercholesteremia Hashimoto's thyroiditis (Chronic)
Andere Medikamente: diazePAM (VALIUM) levothyroxine rizatriptan rosuvastatin
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2093164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

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: 1
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 2092790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 15.10.2021
Beginn: 16.01.2022
Tage bis Beginn: 93,0
Dosis: 3
Route/Site: SYR / -

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

COVID-19 Malaise SARS-CoV-2 test

Symptomtext

Contracted the COVID virus after all three doses of the vaccine. Received the antibody infusion. Still sick going on four weeks now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID test
Aktuelle Erkrankungen: No
Vorgeschichte: Heart problem, Thyroid, depression, anxiety
Andere Medikamente: Celexa, Centroid, Conzpan, Crestar, Vitamin C, Probiotic, Vitamin D, Iron pill, Vitamin D3, Zinc, Calpret, Colas
Allergien: No
Vorherige Impfungen: -

VAERS 2091290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Neck pain Pain in extremity SARS-CoV-2 test

Symptomtext

Severe pain in left arm; Severe pain in left arm that radiated to neck and shoulder; Severe pain in left arm that radiated to neck and shoulder; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 65 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Dec2021 14:00 (Lot number: FH8027) at the age of 65 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 03Dec2021, outcome "recovering", described as "Severe pain in left arm"; NECK PAIN (non-serious), ARTHRALGIA (non-serious) all with onset 03Dec2021, outcome "recovering" and all described as "Severe pain in left arm that radiated to neck and shoulder". The events "severe pain in left arm", "severe pain in left arm that radiated to neck and shoulder" and "severe pain in left arm that radiated to neck and shoulder" 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, neck pain, arthralgia. Additional information: Patient did not receive any other vaccine in four weeks of vaccination and other medications in two weeks. Patient was not diagnosed with COVID-19 prior to vaccination, underwent COVID nasal swab test with negative result. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20220110; Test Name: Nasal Swab; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2090970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: OK
Alter: 37,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Pruritus Rash SARS-CoV-2 test Scab

Symptomtext

Rash and itching at the injection site which is still present after 4 weeks, as well as scabbing.; Rash and itching at the injection site which is still present after 4 weeks, as well as scabbing.; Rash and itching at the injection site which is still present after 4 weeks, as well as scabbing.; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 37 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 15Dec2021 (Lot number: FH8027) at the age of 37 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Allergies: Cephalosporins" (unspecified if ongoing); "Allergies: wasp sting" (unspecified if ongoing); "Allergies: latex" (unspecified if ongoing); "Allergies: nickel" (unspecified if ongoing); "Allergies: tree pollen" (unspecified if ongoing); "depression" (unspecified if ongoing); "anxiety" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID; LIOTHYRONINE; WELLBUTRIN; LEXAPRO; ZYRTEC [CETIRIZINE HYDROCHLORIDE]. Vaccination history included: Bnt162b2 (COVID 19, lot number EN6202, administration date 26Feb2021, dose number 2, vaccine location Left arm), administration date: 26Feb2021, when the patient was 36 years old, for COVID-19 immunization; Bnt162b2 (COVID 19, lot number EM9809, administration date 05Feb2021, dose number 1, vaccine location Left arm), administration date: 05Feb2021, when the patient was 36 years old, for COVID-19 immunization; Flu shot (other vaccine 4weeks product=Flu shot, vaccine date 09Nov2021, dose number 1, vaccine location left deltoid), administration date: 09Nov2021, when the patient was 37 years old, for Immunization. The following information was reported: RASH (non-serious), PRURITUS (non-serious), SCAB (non-serious) all with onset 15Dec2021, outcome "not recovered" and all described as "Rash and itching at the injection site which is still present after 4 weeks, as well as scabbing.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of rash, pruritus, scab. Additional Information: Facility type vaccine Doctor's office/urgent care, other vaccine in four weeks: Yes. Other vaccine 4weeks product was Flu shot on left deltoid on 09Nov2021 as dose 1.other medications in two weeks: Synthroid, Liothyronine, Wellbutrin, Lexapro, Zyrt. Known allergies to Cephalosporins, wasp sting, latex, nickel, tree pollen. Other medical history included Hypothyroidism, depression, anxiety The lot number for bnt162b2 was not provided and will be requested during follow up.

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Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Test Date: 20211222; Test Name: Abbott BinaxNOW home test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211227; Test Name: Abbott BinaxNOW home test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to wasp sting; Allergy to antibiotic; Anxiety; Depression; Hypothyroidism; Latex allergy; Nickel sensitivity; Pollen allergy
Andere Medikamente: SYNTHROID; LIOTHYRONINE; WELLBUTRIN; LEXAPRO; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2076141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WI
Alter: 45,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Rash Rash papular

Symptomtext

Client called the Health Department on 01/05/2022 to report that she had a "big, bumpy rash"on her lower back, right side breast and right buttock. She reported that it was not itchy and she was feeling fine otherwise. The rash was continuing to get worse. Recommended that client be seen by a medical provider and requested that she get written approval from a medical provider prior to receiving her 2nd vaccine. Spoke to client again on 01/21/2022. She reports that she saw a provider and took some Zyrtec and Benadryl. At the time of our conversation on 01/21/2022, she reported the rash had not resolved.

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

VAERS 2072305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: FL
Alter: 54,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac stress test Electrocardiogram Pain Pain in extremity

Symptomtext

sore arm with pain radiating towards the heart

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: EKG 1/11/22 stress test 1/13/22
Aktuelle Erkrankungen: none
Vorgeschichte: blood pressure, cholesterol
Andere Medikamente: Atorvostatin, Lisinipro/HCTZ, Vit D, methyl folate
Allergien: none
Vorherige Impfungen: -

VAERS 2071988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 07.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Hypoxia Malaise

Symptomtext

12/15/2021: Symptoms of COVID started on 12/08. Pt began decadron 6mg x 10 days. Start albuterol inhaler and pulmicort 12/16-12/17: Hypoxic on 3L. Began on IV remdesivir. Continuing IV decadron 12/18/2021-: Pt doing better. Supplemental oxygen currently at 2L. continuing medications 12/20/2021: Finished course of remdesivir 12/22/2021: Pt discharged. Continue dexamethasone

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

VAERS 2067861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MO
Alter: 51,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Dizziness Flushing Immunisation Nausea Rash Rash pruritic

Symptomtext

itched after it faded; nausea; dizziness; developed a rash on her back and stomach/Rash moved to neck; felt flush; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 51-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 13Nov2021 15:00 (Lot number: FH8027) at the age of 51 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: VITAMIN D NOS; KARIVA taken for contraception (ongoing). Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8734, Location of injection: Arm Left, Route of Administration: Intramuscular, time: 01:00 pm), administration date: 03Apr2021, when the patient was 51 years old, for Covid-19 Immunization, reaction(s): "No known adverse events"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP7534, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 13Mar2021, when the patient was 51 years old, for COVID-19 Immunization, reaction(s): "No known adverse events". The following information was reported: IMMUNISATION (non-serious) with onset 13Nov2021 15:00, outcome "unknown", described as "Booster"; NAUSEA (non-serious) with onset 14Nov2021 03:00, outcome "recovering", described as "nausea"; DIZZINESS (non-serious) with onset 14Nov2021 03:00, outcome "recovering", described as "dizziness"; RASH (non-serious) with onset 14Nov2021 03:00, outcome "recovering", described as "developed a rash on her back and stomach/Rash moved to neck"; FLUSHING (non-serious) with onset 14Nov2021 03:00, outcome "recovering", described as "felt flush"; RASH PRURITIC (non-serious) with onset 15Nov2021, outcome "recovering", described as "itched after it faded". Therapeutic measures were not taken as a result of nausea, dizziness, rash, flushing. Adverse event: 12 hours post 3rd vaccine booster, patient experienced nausea and dizziness. The nausea and dizziness subsided and then 12 hours later patient developed a rash on her back and stomach and felt flush. 3rd BNT162B2 booster received the afternoon of 13Nov2021. Early morning (02:00 AM) of 14Nov2021 experienced nausea and dizziness. Subsided a few hours later on 14Nov2021 mid-afternoon, a rash formed on stomach/back which itched as it faded. Rash moved to neck on 15Nov2021 which itched after it faded. After all rashes faded, no other known event occurred. No known adverse events occurred with the first 2 dosed (dose 1 and 2). Other medications in two weeks: Birth control, vitamin D supplement and multivitamin supplement. Known allergies: None. Other medical history: None. Patient did not receive any other vaccine in four weeks. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Birth control; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: VITAMIN D NOS; KARIVA
Allergien: -
Vorherige Impfungen: -

VAERS 2065638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

mild

Staat: MD
Alter: 54,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 26.01.2022
Beginn: 26.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysphagia Feeling hot Hyperhidrosis Nausea Throat clearing Vomiting

Symptomtext

Patient confirmed 2nd dose of Pfizer received on 5/22/21. 3rd dose of Pfizer 0.3ml was administered to LA on 1/26/22 at 11:35AM. Patient denies allergies to medications, vaccines or foods. Patient reported that she tested positive for COVID-19 4 weeks ago, tested negative yesterday and feels well. Patient was asked to wait 15 minutes for observation. 10 minutes into observation, it was noticed patient trying to clear her throat and complained of feeling hot. Patient was asked if she was Ok, Patient at that time reports that she is feeling hot, having nausea and having difficulty swallowing. Patient said she has allergies to shrimp and is encouraged to wait 30 mins for observation. V ital Signs BP 130/80, HR 58 RR20, O2sat 98%. Patient sweating and vomiting, cold compress applied and patient continued to be monitored. Patient continues to have difficulty clearing her throat , vomiting and sweating, at that point 911 was called 02sat at 97%. Patient continued to be monitored by staff until EMT arrived and transferred to hospital. Patient was accompanied by daughter.

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Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: COVID-19 four weeks ago without hospitalization
Vorgeschichte: None Reported
Andere Medikamente: unknown
Allergien: Shrimp
Vorherige Impfungen: -

VAERS 2059518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

Pt reported hives 2 hrs after receiving the vaccine. He was treated with benadryl 50 mg IM and Solu-Medrol 125 mg IM. Pt was kept under close observation.

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Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: NONE.
Vorgeschichte: NONE.
Andere Medikamente: NONE.
Allergien: NONE.
Vorherige Impfungen: -

VAERS 2057738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Burning sensation Fungal infection Hypersensitivity Loss of personal independence in daily activities Rash Rash pruritic

Symptomtext

I developed a rash about 24 hours after my booster injection. The rash started in both arm pits and started traveling across my left breast, into the right neck, on to my right and left trunk and mid lower back. The spread to these areas progressed over a week. The rash is EXTREMELY itchy and burns. It is disrupting my day to day activities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: I was seen by my PCP about 7 days after injection and given Nystatin powder for a fungal infection. This made it worse. I was seen by urgent treatment clinic on 12/23/2021 and given a steroid cream. I used this every day for 2 weeks and the rash improved but did not completely go away. I was seen by a dermatologist on 1/13/2021 and given more creams include steroid and non-steroids. The dermatologist told confirmed that it was a hypersensitivity reaction from the covid vaccine. I was told in may take 2-3 months to calm down.
Aktuelle Erkrankungen: none
Vorgeschichte: seasonal allergies
Andere Medikamente: Vitamin D3 2000mg /day
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2057176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: TN
Alter: 74,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / LA

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

Blood test Dry skin Immunisation Pruritus Skin disorder

Symptomtext

I had the Pfizer COVID booster vaccine; breaking out; Itching; It seems to be drying up some on, I got it on my hands and on legs and on my back; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 01Nov2021 (Lot number: FH8027) at the age of 74 years as dose number unknown (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: LASIX [FUROSEMIDE]. Vaccination history included: Covid-19 vaccine (Unknown Manufacturer), for COVID-19 Immunization. The following information was reported: IMMUNISATION (medically significant) with onset 01Nov2021, outcome "unknown", described as "I had the Pfizer COVID booster vaccine"; SKIN DISORDER (medically significant) with onset Nov2021, outcome "unknown", described as "breaking out"; PRURITUS (medically significant) with onset Nov2021, outcome "unknown", described as "Itching"; DRY SKIN (non-serious) with onset Nov2021, outcome "unknown", described as "It seems to be drying up some on, I got it on my hands and on legs and on my back". The events "breaking out" and "itching" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood test: (Oct2021) unknown results, notes: I had a lab test just a draw blood for 6 months check up the end of October." (Further clarifications unknown). Therapeutic measures were taken as a result of skin disorder, pruritus, dry skin. Clinical course information: reporter stated, that just wanted to call and report that on 01Nov he had the Pfizer COVID booster vaccine, On 06Nov he went to the hospital because he had a breaking out and itching and the doctors saw that there was sought of puzzled they gave me a steroid shot and put on a series of steroids and it helped it some (Further clarification unknown, hence captured suspect as Unspecified shot conservatively) but then patient saw my doctor it started about two weeks later and he saw my doctor and he was sought of puzzled with himself, we were not (Incomplete sentence) we just not connected into the Pfizer Booster but anyhow patient had two more incidents (Further clarification unknown) doctor seen again on Tuesday, patient got the purple cap COVID booster shot and it seems to be drying up some on, and got it on my hands and on legs and on my back, and taken Benadryl tablets (Intent treatment) for about three times a day and also applied Benadryl gel (Intent treatment) on my hands and back and legs and also taken steroids."When asked taking steroids and Benadryl Gel after the side effect reporter stated, "Yes, he was not having steroids for two weeks ago today." (Further clarification unknown), "The expiration date for the shot all they got here is date is 01Nov2021 (Further not clarified) there is no expiration date on this." Patient have not had any lab test since end of October, I had a lab test just a draw blood for 6 months checkup the end of October." (Further clarifications unknown) Consumer stated, that he don't have the information, and know the steroid packet that he took was the something Prednisolone, Prednisone." No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Test Date: 202110; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown Results; Comments: I had a lab test just a draw blood for 6 months check up the end of October." (Further clarifications unknown)
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Medical Conditions: Consumer stated, "No."
Andere Medikamente: LASIX [FUROSEMIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2054169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 15.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

Two days after the booster dose of the Pfizer vaccine, the patient developed hives over chest and hands for eight days. Treatment required two Prednisone injections.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Codeine Phosphate
Vorherige Impfungen: -

VAERS 2050306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 51,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Back pain Body temperature Chills Headache Heart rate Heart rate abnormal Immunisation Lymph node pain Lymphadenopathy Pain in extremity Pyrexia SARS-CoV-2 test

Symptomtext

fever/ by 3pm fever was to 102.3/ fever went below 101 by 9pm/ termperature was 100.3 around 10pm/ 99.3/ 101.3; heart rate was 128 bpm/heart rate was under 100 bpm/heat rate is approx 102 bpm; chills; headache; aches and pains (esp in lower back and legs).; aches and pains (esp in lower back and legs).; lymph nodes in my left arm pit are swollen and sore; lymph nodes in my left arm pit are swollen and sore; dose number: 3; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Dec2021 13:45 (Lot number: FH8027) at the age of 51 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "High Blood pressure" (unspecified if ongoing); "stroke" (unspecified if ongoing); "migraines" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing); "Known allergies: latex" (unspecified if ongoing). Concomitant medication(s) included: VICTOZA; PRAVASTATIN SODIUM; LISINOPRIL. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left, Vaccine Administration Time: 11:30 AM), administration date: 26Mar2021, when the patient was 50 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 02:30 PM), administration date: 04Mar2021, when the patient was 50 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 13:45, outcome "unknown", described as "dose number: 3"; PYREXIA (non-serious) with onset 21Dec2021 13:00, outcome "recovering", described as "fever/ by 3pm fever was to 102.3/ fever went below 101 by 9pm/ termperature was 100.3 around 10pm/ 99.3/ 101.3"; HEART RATE ABNORMAL (non-serious) with onset 21Dec2021 13:00, outcome "recovering", described as "heart rate was 128 bpm/heart rate was under 100 bpm/heat rate is approx 102 bpm"; CHILLS (non-serious) with onset 21Dec2021 13:00, outcome "recovering", described as "chills"; HEADACHE (non-serious) with onset 21Dec2021 13:00, outcome "recovering", described as "headache"; PAIN IN EXTREMITY (non-serious), BACK PAIN (non-serious) all with onset 21Dec2021 13:00, outcome "recovering" and all described as "aches and pains (esp in lower back and legs)."; LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 21Dec2021 13:00, outcome "recovering" and all described as "lymph nodes in my left arm pit are swollen and sore". The events "fever/ by 3pm fever was to 102.3/ fever went below 101 by 9pm/ termperature was 100.3 around 10pm/ 99.3/ 101.3", "heart rate was 128 bpm/heart rate was under 100 bpm/heat rate is approx 102 bpm", "chills", "headache", "aches and pains (esp in lower back and legs).", "aches and pains (esp in lower back and legs).", "lymph nodes in my left arm pit are swollen and sore" and "lymph nodes in my left arm pit are swollen and sore" 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, heart rate abnormal, chills, headache, pain in extremity, back pain, lymphadenopathy, lymph node pain. Additional info-It was reported that patient did not receive any vaccine in four weeks. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Test Date: 20211221; Test Name: Temp; Result Unstructured Data: Test Result:102.3; Comments: By 3pm fever was to 102.3; Test Date: 20211221; Test Name: Temp; Result Unstructured Data: Test Result:101; Comments: Fever went below 101 by 9pm; Test Date: 20211221; Test Name: Temp; Result Unstructured Data: Test Result:100.3; Comments: Temp was 100.3 around 10pm; Test Date: 20211222; Test Name: Temp; Result Unstructured Data: Test Result:99.3; Comments: at 7am; Test Date: 20211222; Test Name: Temp; Result Unstructured Data: Test Result:101.3; Comments: by 11 am fever was back 101.3; Test Date: 20211222; Test Name: Temp; Result Unstructured Data: Test Result:Normal; Comments: by 09 AM; Test Date: 20211221; Test Name: heart rate; Result Unstructured Data: Test Result:128 Bpm; Comments: resting heart rate was 128 bpm.; Test Date: 20211221; Test Name: heart rate; Result Unstructured Data: Test Result:100 Bpm; Comments: heart rate was under 100 bpm.; Test Date: 20211222; Test Name: heart rate; Result Unstructured Data: Test Result:102; Comments: heat rate is approx. 102 bpm; Test Date: 20211029; Test Name: COVID test: PCR; Test Result: Negative ; Comments: Post vaccination: Nasal Swab; Test Date: 20201201; Test Name: COVID test: PCR/NAAT; Test Result: Negative ; Comments: Post vaccination: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Latex allergy; Migraine; Penicillin allergy; Stroke.
Andere Medikamente: VICTOZA; PRAVASTATIN SODIUM; LISINOPRIL.
Allergien: -
Vorherige Impfungen: -

VAERS 2042312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 52,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Arthralgia Chills Headache Immunisation Myalgia Vaccination site pain

Symptomtext

Booster; Mild injection site pain (started date of booster dose); headache; muscle/joint aches; muscle/joint aches; chills; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 20Dec2021 10:30 (Lot number: FH8027) at the age of 52 years as dose 3(booster)single for covid-19 immunisation. Relevant medical history included: "Oysters" (unspecified if ongoing). Concomitant medication(s) included: SHINGRIX, administration date 02Dec2021. Vaccination history included: Pfizer (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left, Vaccine Administration Time: 02:15 PM, Route of Administration: Intramuscular), administration date: 01Apr2021, when the patient was 51 years old, for Covid-19 immunization; Pfizer (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM, Route of Administration: Intramuscular), administration date: 11Mar2021, when the patient was 51 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 17:00, outcome "recovering", described as "Booster"; VACCINATION SITE PAIN (non-serious) with onset 20Dec2021 17:00, outcome "recovering", described as "Mild injection site pain (started date of booster dose)"; HEADACHE (non-serious) with onset 20Dec2021 17:00, outcome "recovering", described as "headache"; MYALGIA (non-serious), ARTHRALGIA (non-serious) all with onset 20Dec2021 17:00, outcome "recovering" and all described as "muscle/joint aches"; CHILLS (non-serious) with onset 20Dec2021 17:00, outcome "recovering", described as "chills". Therapeutic measures were not taken as a result of immunisation. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seafood allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2036068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IA
Alter: 38,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 23.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Lymphadenopathy Pain Swelling

Symptomtext

After vx, lymph nodes under arm became swollen. Was very large and sore for about a week or so, has remained a little swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Multi-vitamin
Allergien: Amoxicillin, bacterium
Vorherige Impfungen: -

VAERS 2032082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NJ
Alter: 45,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 25.10.2021
Beginn: 24.12.2021
Tage bis Beginn: 60,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Headache Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

12/24/2021 Covid symptoms started with runny nose, mild headache, a bit of a fever but very mild, very bad cough, and congestion. Symptoms lasted 6-7 days. Tested positive on 12/24/21 with a home test and then went to a pharmacy to get tested through PCR which was positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Covid (12/24/21)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamins
Allergien: None
Vorherige Impfungen: Pfizer Dose 2 2021

VAERS 2025505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: VT
Alter: 60,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 23.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Arthritis Dysstasia Gait disturbance Joint stiffness Movement disorder Muscular weakness Musculoskeletal stiffness Neuropathy peripheral Pain in extremity Sciatica Sitting disability

Symptomtext

Three days after vaccine administration, I woke with stiffness / arthritic tips of fingers on right hand and toes on right foot. The joint stiffness continued to get worse on my right side and on the eleventh day after vaccination, I developed sciatica so badly that my right leg was so weak and could not be used to go up stairs; walking and sitting / standing were extremely painful. The sciatica and neuropathy / arthritic joint pain went away on my right side at approximately eighteen days after vaccination. But then the joint stiffness / neuropathy emerged on my left side (in the tips of fingers on my left hand and in the toes on my left leg). Within a few days I then also developed intense pain in my left hip joint which made it difficult to move my left leg. These symptoms went away as of six weeks after vaccination. Today is my seventh week after vaccination and the only lingering symptoms are slight neuropathy / stiffness in the tips of my fingers and toes on my right side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None but overweight
Andere Medikamente: None
Allergien: I had an allergic reaction to my most recent flu shot in January 2021. Shortly after receiving the flu shot, I developed rash down the vaccinated arm and within a few days, I developed rash down the opposite arm as well as on the backs of both knees
Vorherige Impfungen: Rash on the backs of both arms and legs following flu shot in Jan 2021

VAERS 2021353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: VT
Alter: 52,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Hypoaesthesia Immediate post-injection reaction Nerve compression Nerve injury Pain Pain in extremity Radiculopathy

Symptomtext

12/14/21 Left arm pain, with immediate onset after injection of Covid vaccine, and has evidence for nerve injury or compression by the vaccine. Discussed the possibility of pursuing an EMG to further elucidate, but he declines. Symptoms are improving over time. 12/23/21 Left-sided radiculopathy pain and numbness thought possibly to be early zoster at last office visit, but never manifested rash. Question now of T4-T5 radiculopathy. Not worsening over time, but not getting better. Reviewed his literature citation of concern, and given lack of evidence of zoster, and also very rare case reports of zoster after Covid vaccine as an indicator of inflammatory arthritis, overall risks for this appeared to be very low. He is okay monitoring the left-sided dermatomal pain and potentially pursue physical therapy if persistent. EMG discussed, but declined given the painful nature of the procedure.

Weitere VAERSDATA-Felder

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

VAERS 2020799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PR
Alter: 42,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Exposure during pregnancy Pelvic pain

Symptomtext

A patient with 7-month-old gestation/pregnant reported dizziness and pain in the pelvic area. At 2:30 90/50, 99%, 80P, 100 dxt, Doctor indicated rest and elevation of the lower extremities. After 15 min 110/80 BP, 98%, 83P, after several minutes he refers to feeling good and wants to go. The pulse is evaluated again and normal.

Weitere VAERSDATA-Felder

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

VAERS 2020364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MI
Alter: 53,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Blood glucose increased Chills Headache Pain

Symptomtext

After the chills and aches (headache and body) my blood sugar level has elevated to upwards of 400 consistently every day since 12/1/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Daily Glucose Meter readings
Aktuelle Erkrankungen: N/a
Vorgeschichte: Type 2 Hypertension
Andere Medikamente: Lisinopril Vitamin D (extra strength D^3 5000IU)
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2019631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 09.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / RA

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

Arthralgia Inflammation Pain in extremity Peripheral swelling

Symptomtext

Two days after receiving my third Pfizer dose my left shoulder, left hand and left hip became painful, inflamed and swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Appointment with GP, Xray scheduled and app with Ortho scheduled.
Aktuelle Erkrankungen: None
Vorgeschichte: Bone spurs in knee, hips, feet. Neck problems,
Andere Medikamente: Flexeril, Tylenol, Cardizem, otc sinus meds
Allergien: Naproxen, sulfa drugs
Vorherige Impfungen: Left side of face became slightly numb after second and third dose

VAERS 2018605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 51,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Fatigue Headache Immunisation Myalgia 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 51 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 20Dec2021 14:00 (Lot number: FH8027) at the age of 51 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 Number: 2, Prev dose product: COVID 19,, Prev dose brand: Pfizer,, Prev dose brand unknown: False,, Prev dose lot number: EL3247,, Prev dose lot unknown: False,, Prev dose administrator route: Intramuscular,, Prev dose administration date: 19Feb2021,, Prev dose administration time: 02:00 PM, Prev dose dose number: 2,, Prev dose vaccine location: Left arm,), administration date: 19Feb2021, when the patient was 50 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Previous dose details: , Prev dose product: COVID 19,, Prev dose brand: Pfizer,, Prev dose brand unknown: False,, Prev dose lot number: EL3247,, Prev dose lot unknown: False,, Prev dose administrator route: Intramuscular , Prev dose administration date: 29Jan2021,, Prev dose administration time: 12:45PM, Prev dose dose number: 1,, Prev dose vaccine location: Left arm), administration date: 29Jan2021, when the patient was 50 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 14:00, outcome "recovered" (2021), described as "booster"; PAIN IN EXTREMITY (non-serious) with onset 20Dec2021 17:00, outcome "recovered" (2021), described as "Sore arm - 72 hours"; MYALGIA (non-serious) with onset 20Dec2021 17:00, outcome "recovered" (2021), described as "muscle aches - 48 hours"; HEADACHE (non-serious) with onset 20Dec2021 17:00, outcome "recovered" (2021), described as "intense headache - 24 hours/mild headache - 54 hours"; FATIGUE (non-serious) with onset 20Dec2021 17:00, outcome "recovered" (2021), described as "fatigue - 54 hours". Therapeutic measures were not taken as a result of immunisation, pain in extremity, myalgia, headache, fatigue. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2018574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 56,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Chills Headache Immunisation Myalgia Vaccination site pain

Symptomtext

Mild pain at site of injection; Mild pain at site of injection which switched to intense muscle aches; chill.; Intense headaches; dose received: 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 20Dec2021 10:45 (Lot number: FH8027) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: IBUPROFEN. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Right), administration date: 16Feb2021, when the patient was 55 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Right), administration date: 26Jan2021, when the patient was 55 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 10:45, outcome "unknown", described as "dose received: 3"; VACCINATION SITE PAIN (non-serious) with onset 20Dec2021 19:00, outcome "recovered" (Dec2021), described as "Mild pain at site of injection"; MYALGIA (non-serious) with onset 20Dec2021 19:00, outcome "recovered" (Dec2021), described as "Mild pain at site of injection which switched to intense muscle aches"; CHILLS (non-serious) with onset 20Dec2021 19:00, outcome "recovered" (Dec2021), described as "chill."; HEADACHE (non-serious) with onset 20Dec2021 19:00, outcome "recovered" (Dec2021), described as "Intense headaches". Therapeutic measures were not taken as a result of vaccination site pain, myalgia, chills, headache. Additional information: The patient had mild pain at site of injection which switched to intense muscle aches and chill. This occurred the first 24 hours after injection. Intense headaches 24-48 hours post injection. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received ibuprofen within 2 weeks of vaccination. The patient known allergies was reported as unknown. Prior to the 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; information about lot/batch provided.

Weitere VAERSDATA-Felder

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

VAERS 2018511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 27,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Body temperature Immunisation Influenza like illness Pain Pyrexia Somnolence

Symptomtext

Flu like symptoms; aches; Drowsiness; fever; dose received: 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 27 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 20Dec2021 11:45 (Lot number: FH8027) 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 (Dose Number: 2, Batch/Lot No: EL3247, brand=Pfizer), administration date: 16Feb2021, when the patient was 26 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, brand=Pfizer), administration date: 26Jan2021, when the patient was 26 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 11:45, outcome "unknown", described as "dose received: 3"; INFLUENZA LIKE ILLNESS (non-serious) with onset 20Dec2021 22:00, outcome "recovering", described as "Flu like symptoms"; PAIN (non-serious) with onset 20Dec2021 22:00, outcome "recovering", described as "aches"; SOMNOLENCE (non-serious) with onset 20Dec2021 22:00, outcome "recovering", described as "Drowsiness"; PYREXIA (non-serious) with onset 20Dec2021 22:00, outcome "recovering", described as "fever". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of influenza like illness, pain, somnolence, pyrexia. Additional information: The patient had no known allergies.The patient did not receive any other vaccine in four weeks.The patient did not receive any other medications in two weeks.The patient was not diagnosed with COVID-19 prior and post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20211220; Test Name: Fever; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 46,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Immunisation Nausea Pain Pain in extremity

Symptomtext

Sore arm; body aches; nausea; Dose number 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46 year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), intramuscular, administered in arm left, administration date 20Dec2021 14:30 (Lot number: FH8027) at the age of 46 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hyperthyroidism" (unspecified if ongoing). Concomitant medication(s) included: METHIMAZOLE; VITAMIN D [COLECALCIFEROL]. Vaccination history included: Comirnaty (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 08Apr2021, when the patient was 45 years old, for Covid-19 immunization; Comirnaty (Dose Number: 1, Batch/Lot No: EP6955, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 18Mar2021, when the patient was 45 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 14:30, outcome "unknown", described as "Dose number 3"; PAIN IN EXTREMITY (non-serious) with onset 21Dec2021 06:00, outcome "recovering", described as "Sore arm"; PAIN (non-serious) with onset 21Dec2021 06:00, outcome "recovering", described as "body aches"; NAUSEA (non-serious) with onset 21Dec2021 06:00, outcome "recovering", described as "nausea". Therapeutic measures were not taken as a result of pain in extremity, pain, nausea. Additional information: Patient was not diagnosed with covid prior to vaccination. Patient was not tested for covid post vaccination. Patient did not receive any other vaccine in four weeks. Other medications in two weeks: FLO PMS Gummy Vitamins;Hair Skin & nails 5,000 mcg Biotin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hyperthyroidism
Andere Medikamente: METHIMAZOLE; VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2018466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 63,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Body temperature Chills Fatigue Headache Immunisation Pyrexia Vaccination site pain Vaccination site warmth

Symptomtext

fatigue; low-grade fever (101 F); chills; headache; booster; injection site soreness/warmth starting 20Dec2021; injection site soreness/warmth starting 20Dec2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 20Dec2021 14:15 (Lot number: FH8027) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "known allergies: peanuts" (unspecified if ongoing); "known allergies: blueberries" (unspecified if ongoing), notes: known allergies: blueberries; "known allergies: CT scan dye" (unspecified if ongoing), notes: known allergies: CT scan dye. Concomitant medication(s) included: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; CALCIUM CITRATE/VITAMIN D. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left, Vaccine Administration Time: 10:30 AM, Route of Administration: Intramuscular), administration date: 25Mar2021, when the patient was 62 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 12:45 PM, Route of Administration: Intramuscular), administration date: 03Mar2021, when the patient was 62 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 14:15, outcome "unknown", described as "booster"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE WARMTH (non-serious) all with onset 20Dec2021, outcome "recovering" and all described as "injection site soreness/warmth starting 20Dec2021"; FATIGUE (non-serious) with onset 21Dec2021 08:00, outcome "recovering", described as "fatigue"; PYREXIA (non-serious) with onset 21Dec2021 08:00, outcome "recovering", described as "low-grade fever (101 F)"; CHILLS (non-serious) with onset 21Dec2021 08:00, outcome "recovering", described as "chills"; HEADACHE (non-serious) with onset 21Dec2021 08:00, outcome "recovering", described as "headache". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site pain, vaccination site warmth, fatigue, pyrexia, chills, headache. Additional Information: The patient had no other vaccines in 4 weeks. The patient did not have COVID-19 prior to vaccination and since the vaccination was not tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211221; Test Name: fever; Result Unstructured Data: Test Result:101 Fahrenheit; Comments: low-grade fever (101 F)
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy (known allergies: CT scan dye); Fruit allergy (known allergies: blueberries); Peanut allergy
Andere Medikamente: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; CALCIUM CITRATE/VITAMIN D
Allergien: -
Vorherige Impfungen: -

VAERS 2018465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 23,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Axillary pain Body temperature Chills Dyskinesia Headache Immunisation Myalgia Pyrexia Vaccination site pain Vaccination site rash

Symptomtext

Intense pain at the injection site and at the armpit.; Intense pain at the injection site and at the armpit.; Could barely move it; Severe chills; Muscle aches; Low grade fever of 99.4 degrees; Headache; rash around the injection site; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 20Dec2021 10:30 (Lot number: FH8027) at the age of 23 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing), notes: Note: Asthma; "Birth control" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Amoxicillin, reaction(s): "Known allergies: Amoxicillin"; Ibuprofen, reaction(s): "known allergies: Ibuprofen"; Advil, reaction(s): "known allergies: Advil". Vaccination history included: Bnt162b2 (Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: EL3247,, Previous dose lot unknown: False,, Previous dose Administrator route: Intramuscular,, Previous dose administration date: 18Feb2021, Previous dose Administration time: 02:30 PM,, Previous dose number: 2, Previous dose Vaccine location: Left arm), administration date: 18Feb2021, when the patient was 23 years old, for Covid-19 immunization; Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: EL3247,, Previous dose lot unknown: False,, Previous dose Administrator route: Intramuscular,, Previous dose administration date: 28Jan2021, Previous dose Administration time: 10:15 AM,, Previous dose number: 1, Previous dose Vaccine location: Left arm), administration date: 28Jan2021, when the patient was 23 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 10:30, outcome "unknown", described as "booster"; AXILLARY PAIN (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 20Dec2021 22:15, outcome "not recovered" and all described as "Intense pain at the injection site and at the armpit."; DYSKINESIA (non-serious) with onset 20Dec2021 22:15, outcome "not recovered", described as "Could barely move it"; CHILLS (non-serious) with onset 20Dec2021 22:15, outcome "not recovered", described as "Severe chills"; MYALGIA (non-serious) with onset 20Dec2021 22:15, outcome "unknown", described as "Muscle aches"; PYREXIA (non-serious) with onset 20Dec2021 22:15, outcome "not recovered", described as "Low grade fever of 99.4 degrees"; HEADACHE (non-serious) with onset 20Dec2021 22:15, outcome "not recovered", described as "Headache"; VACCINATION SITE RASH (non-serious) with onset 20Dec2021 22:15, outcome "not recovered", described as "rash around the injection site". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of axillary pain, vaccination site pain. Additional information: on 20Dec2021, the patient's body temperature was Low grade fever of 99.4 degrees Fahrenheitt. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Test Date: 20211220; Test Name: Body temperature; Result Unstructured Data: Test Result:99.4; Comments: Low grade fever of 99.4 degrees Fahrenheitt
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (Note: Asthma); Birth control
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 53,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Chills Fatigue Headache Immunisation Nausea Pyrexia Vaccination site pain

Symptomtext

tiredness; headache; fever; nausea; chills; Pain at injection site; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 15Dec2021 13:30 (Lot number: FH8027) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: PANTOPRAZOLE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left), administration date: 25Mar2021, when the patient was 52 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left), administration date: 03Mar2021, when the patient was 52 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021 13:30, outcome "not recovered", described as "Booster"; FATIGUE (non-serious) with onset 16Dec2021, outcome "recovered" (20Dec2021), described as "tiredness"; HEADACHE (non-serious) with onset 16Dec2021, outcome "recovered" (20Dec2021), described as "headache"; PYREXIA (non-serious) with onset 16Dec2021, outcome "recovered" (20Dec2021), described as "fever"; NAUSEA (non-serious) with onset 16Dec2021, outcome "recovered" (20Dec2021), described as "nausea"; CHILLS (non-serious) with onset 16Dec2021, outcome "recovered" (20Dec2021), described as "chills"; VACCINATION SITE PAIN (non-serious) with onset 15Dec2021 18:00, outcome "recovered" (20Dec2021), described as "Pain at injection site". Therapeutic measures were not taken as a result of immunisation, fatigue, headache, pyrexia, nausea, chills, vaccination site pain. Additional information: Patient was not received 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 not tested for COVID-19. No known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
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 known allergies: No
Andere Medikamente: PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2018295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 33,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Immunisation Lymphadenopathy Myalgia

Symptomtext

sever fatigue; swollen lymph nodes in left arm pit and behind right ear; Myalgia; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Dec2021 11:30 (Lot number: FH8027) at the age of 33 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: 1, Batch/Lot No: EW0150, Location of injection: Arm Left), administration date: 31Mar2021, when the patient was 32 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0158, Location of injection: Arm Left), administration date: 21Apr2021, when the patient was 32 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 07Dec2021 11:30, outcome "unknown", described as "Booster"; FATIGUE (non-serious) with onset 08Dec2021 06:30, outcome "recovered" (Dec2021), described as "sever fatigue"; LYMPHADENOPATHY (non-serious) with onset 08Dec2021 06:30, outcome "recovered" (Dec2021), described as "swollen lymph nodes in left arm pit and behind right ear"; MYALGIA (non-serious) with onset 08Dec2021 06:30, outcome "recovered" (Dec2021), described as "Myalgia". Therapeutic measures were not taken as a result of fatigue, lymphadenopathy, myalgia. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. The patient was not diagnosed with covid-19 prior and post to vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: No other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 44,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 15.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Angina pectoris Chest discomfort Fatigue

Symptomtext

Fatigue on first day. On second day, I started to experience pains and tightness around my heart area. These pains continue to re-occur as of today, January 7, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: GERD
Andere Medikamente: Omeprazol 20 mg daily
Allergien: Allergy to raw tree fruit such as apple and plum
Vorherige Impfungen: -

VAERS 2014252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MN
Alter: 56,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 18.03.2021
Beginn: 05.01.2022
Tage bis Beginn: 293,0
Dosis: 3
Route/Site: - / -

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

Cough Headache Rhinorrhoea Throat irritation

Symptomtext

runny nose, scratchy throat, headache, cough. starting 1/5/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Hernia repair, herniated disc April '93, Lumbar disc surgery 2006; residual neuropathy, Lumbar disc surg 2010, Depression, Colonoscopy 2010, RLS-Dr., Hypercholesterolemia, Elevated CK , Sleep apnea--relieved with mandibular advancement device.
Andere Medikamente: Taking Neupro 4 MG/24HR Patch 24 Hour 1 patch to skin Transdermal Once a day, Taking Lyrica 150 MG Capsule 4 capsules Orally Once a day, Not-Taking traMADol HCl 50 MG Tablet 1 tablet as needed Orally every 6 hrs, Notes: PRN, Not-Taking Albu
Allergien: Remeron: SOB - Allergy, Trazodone HCl: SOB - Allergy
Vorherige Impfungen: -

VAERS 2010440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 50,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain upper Dizziness Fatigue Headache Malaise Pyrexia Vertigo

Symptomtext

Felt unwell, feverish the next day and had a bad headache, fatigue that lasted 4 days. I also had pain under right rib cage. Headache was bad and later had also dizziness and vertigo. I took Tylenol a few times and one dose of Benadryl. Things subsided but vertigo I had it for a few more days, requiring /motivating a medical telehealth appointment. Things improved and subsided. But I had vertigo/dizziness again recently ( past 4 days), better today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: gerd
Vorgeschichte: Hypothyroidism, chronic. Obesity. GERD ( new)
Andere Medikamente: Synthroid, Vit D and B complex, Prilosec
Allergien: I previously had a reaction to the flu vaccine
Vorherige Impfungen: Dose 1 and 2 of same vaccine. at age 49 ,1/23/21 and 2/23/21

VAERS 2006198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: TX
Alter: 22,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Full blood count Metabolic function test Pruritus Throat irritation Urticaria

Symptomtext

Advised to go to ER: symptoms included hive to face, itching to face an d body and itchy throat aproximatley 30 minutes after getting Pfizer Vaccine Was prescribed benadryl and prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: CBC, CMP
Aktuelle Erkrankungen: -
Vorgeschichte: ASTHMA
Andere Medikamente: -
Allergien: LATEX, LETTUCE, PINEAPPLE
Vorherige Impfungen: -

VAERS 2006183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NC
Alter: 62,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 28.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Oropharyngeal pain Pain in extremity Pharyngeal swelling Pruritus Rash Secretion discharge Urticaria

Symptomtext

Severe Rash/Hives - Head causing secretions from hair to matte hair, Neck, Upper Thighs on Back and Lower Hips, Under each arm, Both Groins, Genital Area. Then hands and feet started itching uncontrollably. Left Arm hurt Throat hurt like it was too big for the area

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Urgent Care Shot of Cortizone 6 day course of Prednisone Pills HydroCortizone Cream 2.5%
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine Headaches (on occasion)
Andere Medikamente: Metropolol, Protonix, Tylenol, Melatonin, B12, D3, Elderberry, Dramamine, 81mg Aspirin
Allergien: No Food Allergies Allergic to all Coedine, Fentynal, Morphine, Dilaudid pain meds
Vorherige Impfungen: -

VAERS 1971553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MO
Alter: 61,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Peripheral swelling Pyrexia Skin exfoliation Rash

Symptomtext

Fever (102), Skin Peeling, Redness under eyes, Swelling in arm.

Weitere VAERSDATA-Felder

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

VAERS 1971553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MO
Alter: 61,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Erythema Peripheral swelling Pyrexia Skin exfoliation Rash

Symptomtext

Fever (102), Skin Peeling, Redness under eyes, Swelling in arm.

Weitere VAERSDATA-Felder

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

VAERS 2001829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MO
Alter: 52,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Cough Fatigue Headache Injection site pain Lymph node pain Lymphadenopathy Myalgia Pain Pyrexia Rhinorrhoea

Symptomtext

The evening of the day of the shot I developed a sore arm at the injection site. My lymph nodes under that arm were extremely swollen and very painful. I woke up approx 4am the morning after the shot (12/30) in excruciating body pain. My joints and muscles hurt. On a scale of 1-10 with 10 being the most pain, I was at a 12. I ran a fever the day after, with a cough, running nose, extreme headache that lasted 2 days. Headache is still present but not as bad. Finally feeling a little better on Jan 2. Today, Jan 4, still have a running nose, headache and persistent cough and fatigue.

Weitere VAERSDATA-Felder

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

VAERS 1997653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IN
Alter: 64,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 01.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Axillary mass Eye pruritus Fatigue Headache Injection site pruritus Pain Pruritus Rash Urticaria

Symptomtext

December 1, 2021 I got the Pfizer booster. Got a headache three hours after. 12/2 was achy, tired. On 12/3 woke up with an egg shaped mass under my arm and itchy feeling at that site. 12/4 broke out with a rash with welts going down my left side. 12/5 rash with welts moved to my back at shoulder area. 12/6 rash was in same areas as prior days + moved to private areas. 12/7 rash with welts were also on lower back. Rash with welts have been on my elbows, hands, forearms , legs, feet including itching on the bottoms of my feet. Right eye itched for maybe 3 days. Palms of my hands also. Moved to the right side of my body down my side and under my bra line. This continued for all of December. Towards the end of the month the rash was in smaller areas on my body. it would just come up at any given point of the day. The egg shaped mass lasted 5 days and went down. I have documented some of the days with pictures on my cell phone. I contacted my Dr. was told to take allergy medication. I used Caladryl on the sites as well. This is January 1st and I still have small flair ups. Not as severe as the first 3 weeks after the booster. Going forward, my question is, if another booster is needed in the future should I get a booster? I have asthma and other upper respiratory issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: Asthma, Bronchiectasis, vocal cord disfunction
Andere Medikamente: Digoxin, Flecainide,Protonix,Singular,Claritan,MulitiVit,Calci
Allergien: Ceclor,Keflex,Sulfa,Demerol
Vorherige Impfungen: -

VAERS 1995613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 51,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Axillary pain Immunisation Swelling

Symptomtext

2 days after vaccine, my left under arm pit was sore and swollen when I woke up in the morning; 2 days after vaccine, my left under arm pit was sore and swollen when I woke up in the morning; Dose number: 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in left arm, administration date 20Dec2021 at 12:00 (Lot number: FH8027) at the age of 51 years as dose 3 (booster), single for COVID-19 immunisation. The patient did not have any relevant medical history. Concomitant medications included: PROTONIX, ADVIL and unspecified MULTIVITAMINS. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EP6955, Administration location: left arm, Route of administration: intramuscular), administration date: 16Mar2021, when the patient was 50 years old, for COVID-19 immunisation, reactions: "No adverse reaction" and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EP6955 ; Administration location: left arm; Route of administration: intramuscular, administration date: 08Apr2021, when the patient was 50 years old, for COVID-19 immunisation, reactions: "No adverse reaction". The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 at 12:00, outcome "unknown", described as "Dose number: 3"; AXILLARY PAIN (non-serious), LYMPHADENOPATHY (non-serious) both with onset 22Dec2021 at 05:00, outcome "recovered" (22Dec2021), and both described as "2 days after vaccine, my left under arm pit was sore and swollen when I woke up in the morning". Therapeutic measures were taken as a result of axillary pain and lymphadenopathy. Additional information: The patient had no known allergies. 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 prior to the COVID 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. Treatment for reported events included advil (patient reported to feel okay after approximately 3 hours after taking advil).

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: PROTONIX [PANTOPRAZOLE SODIUM SESQUIHYDRATE]; ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 1995602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 40,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Arthralgia Axillary pain Breast pain Hypoaesthesia Immunisation

Symptomtext

Pain in armpit, breast, and elbow; Pain in armpit, breast, and elbow; Pain in armpit, breast, and elbow; Numbness in fingers; Dose number: 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in left arm, administration date 20Dec2021 at 11:45 (Lot number: FH8027) at the age of 40 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing). Patient has taken unspecified concomitant medications. Past drug history included: Augmentin, reaction: "Drug allergy", notes: Known allergies: augmentin; Marcaine, reaction: "Drug allergy", notes: Known allergies: marcaine and Lidocaine, reaction: "Drug allergy", notes: Known allergies: lidocaine. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Lot number: EW0176, Route of administration: Intramuscular), administration date: 12May2021, when the patient was 40 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 1, SINGLE, Lot number: ER8731, Route of Administration: Intramuscular), administration date: 21Apr2021, when the patient was 40 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 at 11:45, outcome "unknown", described as "Dose number: 3"; AXILLARY PAIN (non-serious), BREAST PAIN (non-serious), ARTHRALGIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 21Dec2021, outcome "not recovered", and all described as "Pain in armpit, breast, and elbow". The events "Pain in armpit, breast, and elbow" and "Numbness in fingers" were evaluated at the physician office visit. Therapeutic measures taken as a result of pain in armpit, breast, and elbow, numbness in fingers increased was unknown. 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 prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events resulted in doctor or other healthcare professional office/clinic visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1995599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Arthralgia Immunisation Myalgia Vaccination site pain Vaccination site swelling

Symptomtext

Dose number 3; Pain at injection site; Swelling at injection site; Muscle aches; Joint aches; This is a spontaneous report from a contactable reporter (consumer or other non-hcp). An adult female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 15Dec2021 at 09:30 (Lot number: FH8027) 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, SINGLE; Lot number: EP6955; Anatomical site: left arm; Route of administration: intramuscular), administration date: 16Mar2021, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EP6955; Anatomical site: left arm; Route of administration: intramuscular), administration date: 06Apr2021, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021 at 09:30, outcome "unknown", described as "Dose number 3"; VACCINATION SITE PAIN (non-serious) with onset 15Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Pain at injection site"; VACCINATION SITE SWELLING (non-serious) with onset 15Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Swelling at injection site"; MYALGIA (non-serious) with onset 15Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Muscle aches"; ARTHRALGIA (non-serious) with onset 15Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Joint aches". Therapeutic measures were not taken as a result of vaccination site pain, vaccination site swelling, myalgia and arthralgia. 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. 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 1995537

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 17,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Body temperature Headache Immunisation Malaise Pain Pyrexia Vaccination site pain Vomiting

Symptomtext

Some glands under her left arm where she got the shot are sore; Headache; Fever; Sore on the left side of her breast is sore under her breast; started to feel pretty sick; she got her COVID Booster shot; Throw up; throwing up several more times since then; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 17 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 16Dec2021 (Lot number: FH8027) at the age of 17 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing); "Depression" (unspecified if ongoing). Concomitant medication(s) included: ZOLOFT taken for anxiety, depression. Vaccination history included: Bnt162b2 (LOT# of 1st shot: EP7534), administration date: 31Mar2021, when the patient was 17 years old, for COVID-19 immunization; Bnt162b2 (LOT# of 2nd shot: ER8729), administration date: 21Apr2021, when the patient was 17 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021, outcome "unknown", described as "she got her COVID Booster shot"; VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "Some glands under her left arm where she got the shot were sore"; VOMITING (non-serious) with onset 16Dec2021, outcome "unknown", described as "Throw up; throwing up several more times since then"; MALAISE (non-serious) with onset 17Dec2021, outcome "unknown", described as "started to feel pretty sick"; HEADACHE (non-serious), outcome "unknown", described as "Headache"; PYREXIA (non-serious), outcome "unknown", described as "Fever"; PAIN (non-serious), outcome "unknown", described as "Sore on the left side of her breast is sore under her breast". Relevant laboratory tests and procedures were available in the appropriate section. Therapeutic measures (Tylenol once) were taken as a result of vaccination site pain, vomiting, malaise, headache, pyrexia, pain. Additional information: Reporter stated, "So her daughter was 17 and she got her COVID Booster shot on Thursday afternoon and she throw up Thursday night and then yesterday she started to feel pretty sick. She has a headache a fever. Some glands under her left arm where she got the shot were sore. Sore on the left side of her breast was sore under her breast and she was throwing up several more times since then. She did not have any of this reaction with her first two shots. She just kind of report and wondering what we should do (voice distortion) advise of a doctor this morning. She just want to kind of report it. She just want to report her side effects because they seem like they were out of the normal side effects". Reporter further stated, "was there somebody on your staff like another phone number I can call to talk to like a doctor or nurse to find out what we should be doing. Was there a doctor or a nurse on your staff at Pfizer that I can call to talk to about this to find out what I should be doing for her".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Depression
Andere Medikamente: ZOLOFT
Allergien: -
Vorherige Impfungen: -

VAERS 1995357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 59,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Chills Fatigue Headache Immunisation Nausea Pain Rhinorrhoea Somnolence

Symptomtext

sleepiness; Nausea; headache; chills; body aches; runny nose; fatigue; Dose number 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 15Dec2021 11:30 (Lot number: FH8027) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Sjogren's Syndrome" (unspecified if ongoing); "Hashimoto's" (unspecified if ongoing); "Allergies: Iodine-based dyes" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE; MELOXICAM. Vaccination history included: Bnt162b2 (Dose 2, Dose product: COVID-19, Dose brand: Pfizer, Lot number: EP6955, Route of administration: Intramuscular), administration date: 08Apr2021, when the patient was 59 years old, for COVID-19 Immunization; Bnt162b2 (Dose 1, Dose product: COVID-19, Dose brand: Pfizer, Lot number: EP6955), administration date: 18Mar2021, when the patient was 59 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021 11:30, outcome "unknown", described as "Dose number=3"; SOMNOLENCE (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "sleepiness"; NAUSEA (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "Nausea"; HEADACHE (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "headache"; CHILLS (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "chills"; PAIN (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "body aches"; RHINORRHOEA (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "runny nose"; FATIGUE (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "fatigue". Therapeutic measures were taken as a result of somnolence, nausea, headache, chills, pain, rhinorrhoea, fatigue. Additional information: Patient was not received any other vaccines within 4 weeks. Patient was not diagnosed with covid prior vaccination and also not tested for covid-19 post vaccination. Treatment received for the adverse event was Tylenol. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's disease; Iodine allergy; Sjogren's syndrome
Andere Medikamente: LEVOTHYROXINE; MELOXICAM
Allergien: -
Vorherige Impfungen: -

VAERS 1995347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Pain Vaccination site pain

Symptomtext

Slight body acheyness; Arm pain at injection site in left arm; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 26 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 15Dec2021 (Lot number: FH8027) at the age of 26 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 Number: 1, Batch/Lot No: EL3247), administration date: 05Feb2021, when the patient was 25 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247), administration date: 25Feb2021, when the patient was 25 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021, outcome "unknown", described as "Booster"; PAIN (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "Slight body acheyness"; VACCINATION SITE PAIN (non-serious) with onset 15Dec2021 17:00, outcome "recovering", described as "Arm pain at injection site in left arm". Therapeutic measures were not taken as a result of pain, vaccination site pain. No follow-up attempts are possible. No further information is expected. Additional information: This is not serious case. It did not meet any of the seriousness criteria. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not diagnosed with COVID-19, prior to vaccination. Patient has not been tested positive since the vaccination. 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 1995318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 24,0
Geschlecht: F
Eingang: 31.12.2021
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: ja

Chills Fatigue Headache Immunisation Myalgia Nausea Pain in extremity Pyrexia

Symptomtext

arm pain; tiredness; headache; muscle aches; chills; fever; nausea; Booster Dose; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from a sales representative. The reporter is the patient. A 24 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Dec2021 10:45 (Lot number: FH8027) at the age of 24 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: 1, Batch/Lot No: EL3247), administration date: 04Feb2021, when the patient was 23 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247), administration date: 25Feb2021, when the patient was 23 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 13Dec2021, outcome "unknown", described as "Booster Dose"; PAIN IN EXTREMITY (non-serious) with onset 13Dec2021 15:00, outcome "recovered" (Dec2021), described as "arm pain"; FATIGUE (non-serious) with onset 13Dec2021 15:00, outcome "recovered" (Dec2021), described as "tiredness"; HEADACHE (non-serious) with onset 13Dec2021 15:00, outcome "recovered" (Dec2021), described as "headache"; MYALGIA (non-serious) with onset 13Dec2021 15:00, outcome "recovered" (Dec2021), described as "muscle aches"; CHILLS (non-serious) with onset 13Dec2021 15:00, outcome "recovered" (Dec2021), described as "chills"; PYREXIA (non-serious) with onset 13Dec2021 15:00, outcome "recovered" (Dec2021), described as "fever"; NAUSEA (non-serious) with onset 13Dec2021 15:00, outcome "recovered" (Dec2021), described as "nausea". Therapeutic measures were taken as a result of pain in extremity, fatigue, headache, myalgia, chills, pyrexia, nausea. Additional information: The patient had no known allergies. The patient received treatment with Tylenol. The patient had not received other vaccine in four weeks. The patient had no COVID prior vaccination and had not been tested for COVID post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
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 1995285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

mild

Staat: CT
Alter: 47,0
Geschlecht: F
Eingang: 31.12.2021
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

Fatigue Headache Immunisation Vaccination site pain

Symptomtext

sore arm at injection site; headache; fatigue; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Dec2021 13:15 (Lot number: fh8027) at the age of 47 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, Time of administration: 13:00, Anatomical location: Arm Left, Batch/Lot No: ep6955), administration date: 31Mar2021, when the patient was 46 years old, for COVID-19 Immunization, reaction(s): "muscle aches", "chills"; Bnt162b2 (Dose Number: 1, Batch/Lot No: el3247), administration date: 10Mar2021, when the patient was 46 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 13Dec2021 13:15, outcome "unknown", described as "booster"; VACCINATION SITE PAIN (non-serious) with onset 14Dec2021 06:30, outcome "recovering", described as "sore arm at injection site"; HEADACHE (non-serious) with onset 14Dec2021 06:30, outcome "recovering", described as "headache"; FATIGUE (non-serious) with onset 14Dec2021 06:30, outcome "recovering", described as "fatigue". Therapeutic measures were not taken as a result of vaccination site pain, headache, fatigue. Additional information: Facility where the most recent COVID-19 vaccine was administered was noted as workplace clinic. The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with covid-19 and 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 and list of any other medications, the patient received within 2 weeks of vaccination was noted as no. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
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: -
Allergien: -
Vorherige Impfungen: -

VAERS 1991910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: OH
Alter: 12,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Headache Injection site pain Vomiting

Symptomtext

Chills started at 0200 on 12/30/21. Left arm pain, headache, and vomiting at 0800 on 12/30/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: No e
Andere Medikamente: Mulit-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1984965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: OR
Alter: 71,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal distension Chills Decreased appetite Headache Nausea Pain

Symptomtext

Patient reported worse headache of life ("worse than pain of childbirth"), nausea, chills, bloating, body aches, and loss of appetite. Symptoms started morning following vaccine administration and lasted 4 days (Friday, Saturday, Sunday, Monday). Patient discussed event with PCP however did not go in to seek medical care at hospital, pcp, or ugent care.

Weitere VAERSDATA-Felder

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

VAERS 1981594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WI
Alter: 70,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 15.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Balance disorder Fall Headache Muscular weakness Pain in extremity

Symptomtext

Received vaccine on 12/15 at Clinic. Noted on 12/16 that she had a sore arm and a bit of a headache, this was an expected reaction as the pt had similar with the first two doses. Upon waking on 12/17 she noted significant weakness in bilateral lower extremities. Describes herself as "Bambi" when she tries to stand/walk as her legs are very weak and wobbly. Pt has continue with LE weakness and been unsteady on her feet since, little to no improvement noted. Pt did lose balance and lean into wall on 12/26, resulting in slide/fall to floor. Reports no injuries were sustained. Pt had went to see PCP on 12/20 related to LE weakness. Discussed recent vaccination and history of MS. Pt reports discussion with MD as possible vaccine adverse event vs MS flare up vs MS triggered flare up by vaccine. Received 3 day treatment of solumedrole with little to no improvement noted since.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Pt reports no testing or diagnostics completed at time of MD visit on 12/20.
Aktuelle Erkrankungen: none
Vorgeschichte: Arthritis, hypertension, MS
Andere Medikamente: Vitamin D, Celebrex, Lisinopril, Glucosamine Controd, Daily Vit, Calcium, Stool Softener, Lovastatin, Vitamin D, ASA.
Allergien: PCN's, Sulfaides
Vorherige Impfungen: -

VAERS 1980719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 25,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Chills Fatigue Immunisation Lymphadenopathy Malaise Myalgia Pyrexia Vaccination site pain Vaccination site swelling

Symptomtext

Fever; chills; swollen lymph nodes; pain and swelling at injection site; pain and swelling at injection site; tiredness; muscle and joint pain; muscle and joint pain; feeling unwell; booster; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 25 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 22Nov2021 12:00 (Lot number: FH8027) at the age of 25 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "IBS" (unspecified if ongoing), notes: Other medical history: IBS, asthma, allergies; "asthma" (unspecified if ongoing), notes: Other medical history: IBS, asthma, allergies; "allergies" (unspecified if ongoing), notes: Other medical history: IBS, asthma, allergies. Concomitant medication(s) included: SPIRONOLACTON; BUPROPION; SINGULAIR. Past drug history included: Ammoxicillin, reaction(s): "Known allergies: Ammoxicillin". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0171, Location of injection: Arm Left), administration date: 10Aug2021, when the patient was 25 years old, for COVID-19 immunization, reaction(s): "Dose 1: 01May2021, Dose 2: 10Aug2021"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0150, Location of injection: Arm Left), administration date: 01May2021, when the patient was 25 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 22Nov2021, outcome "unknown", described as "booster"; PYREXIA (non-serious) with onset 22Nov2021 20:00, outcome "recovered" (2021), described as "Fever"; CHILLS (non-serious) with onset 22Nov2021 20:00, outcome "recovered" (2021), described as "chills"; LYMPHADENOPATHY (non-serious) with onset 22Nov2021 20:00, outcome "recovered" (2021), described as "swollen lymph nodes"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE SWELLING (non-serious) all with onset 22Nov2021 20:00, outcome "recovered" (2021) and all described as "pain and swelling at injection site"; FATIGUE (non-serious) with onset 22Nov2021 20:00, outcome "recovered" (2021), described as "tiredness"; MYALGIA (non-serious), ARTHRALGIA (non-serious) all with onset 22Nov2021 20:00, outcome "recovered" (2021) and all described as "muscle and joint pain"; MALAISE (non-serious) with onset 22Nov2021 20:00, outcome "recovered" (2021), described as "feeling unwell". Therapeutic measures were not taken as a result of pyrexia, chills, lymphadenopathy, vaccination site pain, vaccination site swelling, fatigue, myalgia, arthralgia, malaise. Additional information: The patient was not pregnant at time of vaccination. 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, has the patient been tested for COVID-19 was reported as no. Hospitalization prolonged was reported as no. The device date was on 24Nov2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Other medical history: IBS, asthma, allergies); Asthma (Other medical history: IBS, asthma, allergies); Irritable bowel syndrome (Other medical history: IBS, asthma, allergies)
Andere Medikamente: SPIRONOLACTON; BUPROPION; SINGULAIR
Allergien: -
Vorherige Impfungen: -

VAERS 1978788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
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 Vaccination site pain

Symptomtext

Pain in the injection area; Swollen lymph nodes; dose number=3; This is a spontaneous report from a non-contactable reporter (consumer or other non-HCP). An adult female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 15Dec2021 at 14:30 (Lot number: FH8027) 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 2, SINGLE Lot Number: EP6955 Anatomical site: Left Arm Administration time: 10:15 Route of administration: Intramuscular), administration date: 30Mar2021, for COVID-19 immunisation and Bnt162b2 (DOSE 1, SINGLE Lot Number: EL3247 Anatomical site: Left Arm Administration time: 10:00 Route of administration: Intramuscular), administration date: 09Mar2021, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021 at 14:30, outcome "unknown", described as "dose number=3"; VACCINATION SITE PAIN (non-serious) with onset 16Dec2021, outcome "unknown", described as "Pain in the injection area"; LYMPHADENOPATHY (non-serious) with onset 16Dec2021, outcome "unknown", described as "Swollen lymph nodes". Therapeutic measures were not taken as a result of vaccination site pain and lymphadenopathy. Additional Information: The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to COVID 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1978713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 24.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain upper Arthropathy Chills Fatigue Head discomfort Headache Immunisation Malaise

Symptomtext

feel like every joint is twisting; Fatigue; Chills; cramps in my stomach; I cannot repeat, it just hurt my head even more; my head is so heavy; I cannot repeat, it just hurt my head even more; my head is so heavy; I can't speak right, just not feeling well; I had the booster yesterday; 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 08Dec2021 (Lot number: FH8027) 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, SINGLE), for Covid-19 immunization; Bnt162b2 (DOSE 2, SINGLE), for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 09Dec2021, outcome "unknown", described as "I had the booster yesterday"; ARTHROPATHY (non-serious), outcome "unknown", described as "feel like every joint is twisting"; FATIGUE (non-serious), outcome "unknown", described as "Fatigue"; CHILLS (non-serious), outcome "unknown", described as "Chills"; ABDOMINAL PAIN UPPER (non-serious), outcome "unknown", described as "cramps in my stomach"; HEADACHE (non-serious), HEAD DISCOMFORT (non-serious), outcome "unknown" and all described as "I cannot repeat, it just hurt my head even more; my head is so heavy"; MALAISE (non-serious), outcome "unknown", described as "I can't speak right, just not feeling well". Additional Information: Consumer stated, "Look if I have to report this I am calling to through 'rc' I will feel tomorrow better and call you back. I'm having like post the vaccine (voice not clear) like not feeling well and I cannot repeat, it just hurt my head even more. I had the booster yesterday before noon I should say. I feel a little bit fatigue and 'feel better' in the evening but it was tolerable. But during the night time I started feel chills, shivers and cramps in my stomach and I feel like every joint is twisting and my head is so heavy. I don't think I do have a fever. But I can't even get up from the bed. Paraphrased the concern, Consumer stated, I had them over night, I didn't had them right away. I want to know is there anything that I can do to feel better. Is there any ideal for, I don't know for care of me, 'to gather' anything I can take just to feel better. Right now I'm not feeling well. I'm almost falling, I can't get up." No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1978690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Axillary pain Chills Fatigue Headache Immunisation Lymph node pain Neck pain Vaccination site pain

Symptomtext

chills; Pain at injection site; pain neck and armpit (lymph nodes?); tired; headache; pain neck and armpit; pain neck and armpit (lymph nodes?); Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 06Dec2021 09:00 (Lot number: FH8027) at the age of 45 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included high blood pressure (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left, Vaccine Administration Time: 11:45 AM, Route of Administration: Intramuscular), administration date: 30Mar2021, when the patient was 44 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 12:45 PM, Route of Administration: Intramuscular), administration date: 09Mar2021, when the patient was 44 years old, for COVID-19 immunization. The following information was reported CHILLS (non-serious) with onset 06Dec2021 21:00, outcome recovering; VACCINATION SITE PAIN (non-serious) with onset 06Dec2021 21:00, outcome recovering; NECK PAIN (non-serious), LYMPH NODE PAIN (non-serious) all with onset 06Dec2021 21:00, outcome recovering; FATIGUE (non-serious) with onset 06Dec2021 21:00, outcome recovering; HEADACHE (non-serious) with onset 06Dec2021 21:00, outcome recovering; IMMUNISATION (non-serious) with onset 06Dec2021 09:00, outcome unknown; AXILLARY PAIN (non-serious) with onset 06Dec2021 21:00, outcome recovering. Therapeutic measures were not taken as a result of chills, vaccination site pain, neck pain, fatigue, headache, axillary pain, and lymph node pain. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient did not receive any medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. Patient had no known allergies. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Blood pressure high
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1978675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 59,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Headache Immunisation Malaise Myalgia Pain in extremity

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 03Dec2021 10:00 (Lot number: FH8027) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included VITAMIN D3; VITAMIN C; ATORVASTATIN. Vaccination history included Bnt162b2 (Dose Number: 2, Batch/Lot No: Pfizer EL3247, Location of injection: Arm Right, Vaccine Administration Time: 10:30 AM), administration date: 23Feb2021, when the patient was 58 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: Pfizer EL3247, Location of injection: Arm Right, Vaccine Administration Time: 10:30 AM), administration date: 02Feb2021, when the patient was 58 years old, for COVID-19 immunisation. The following information was reported IMMUNISATION (non-serious) with onset 03Dec2021 10:00, outcome unknown; PAIN IN EXTREMITY (non-serious) with onset 03Dec2021 20:00, outcome recovering; MYALGIA (non-serious) with onset 03Dec2021 20:00, outcome recovering; HEADACHE (non-serious) with onset 03Dec2021 20:00, outcome recovering; MALAISE (non-serious) with onset 03Dec2021 20:00, outcome recovering. Therapeutic measures were not taken as a result of pain in extremity, myalgia, headache, and malaise. No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination. Follow-up attempts are completed. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: VITAMIN D3; VITAMIN C; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1975042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

mild

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 14.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Breast pain Lymph node pain

Symptomtext

Extreme lymph pain under arm put on side of vaccine. Left. And breast area. For 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Quartet birth control pill
Allergien: -
Vorherige Impfungen: -

VAERS 1974973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Injection site erythema Injection site pain Injection site swelling Injection site warmth Lymph node pain Pain in extremity

Symptomtext

I got the three doses of the vaccine in the same arm. About 24 hours after the third dose of the vaccine my left arm was painful. Over the course of the day my arm became red and swollen all the way down to my elbow. It became hot, extremely painful swollen and painful to touch. I used Tylenol and Advil as well as an antihistamine and Triamcinolone cream. I used the cream and put cellophane over it. I consulted my doctor by Telehealth, and they prescribed the antihistamine and cream. It has been six days and my arm is still red but fading. The swollen area is about half the size. The Lymph nodes under my arm are still painful and my shoulder aches. The swelling remained below the injection site and not above. I have pictures of the arm over time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Dose 1: ER8729-04/09/2021, Dose 2: EW0167-04/29/2021-Medical Center
Aktuelle Erkrankungen: N/A
Vorgeschichte: Evaluation for Pre-Diabetes
Andere Medikamente: N/A
Allergien: Multiple Antibiotics, Latex, Multiple food allergies, Bananas, Mango and Avocado
Vorherige Impfungen: -

VAERS 1974264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Immunisation Pain

Symptomtext

body aches for 24 hrs; COVID19 Booster; This is a spontaneous report received from contactable reporter(s) (Other HCP) from a sales representative. The reporter is the patient. A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 06Dec2021 14:30 (Lot number: FH8027) at the age of 45 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: 1, Batch/Lot No: EL 3247, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM, Route of Administration: Intramuscular), administration date: 11Mar2021, when the patient was 44 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EP-6955, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM, Route of Administration: Intramuscular), administration date: 01Apr2021, when the patient was 44 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 06Dec2021 14:30, outcome "unknown", described as "COVID19 Booster"; PAIN (non-serious) with onset 06Dec2021 20:00, outcome "recovered" (07Dec2021 20:00), described as "body aches for 24 hrs". Therapeutic measures were not taken as a result of pain. Additional Information: The patient had no list of any other medications received within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. The patient had no known allergies No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
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 1974259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 63,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Immunisation Vaccination site pain Vaccination site swelling

Symptomtext

Pain and swelling at the injection site.; Pain and swelling at the injection site.; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 63 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 06Dec2021 10:45 (Lot number: FH8027) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Depression" (unspecified if ongoing); "Anxiety" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP-6955, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 24Mar2021, when the patient was 63 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 01Mar2021, when the patient was 63 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 06Dec2021 10:45, outcome "unknown", described as "booster"; VACCINATION SITE SWELLING (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 07Dec2021 05:30, outcome "recovering" and all described as "Pain and swelling at the injection site.". Therapeutic measures were not taken as a result of vaccination site swelling, vaccination site pain. Additional information: reported seriousness was reported as non-serious. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not diagnosed with covid-19 prior to vaccination. Since the vaccination patient was not tested for covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Depression
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 53,0
Geschlecht: U
Eingang: 23.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Injection site pain Nausea Pain in extremity

Symptomtext

booster; Pain at the injection site; Really very sore arm, it is still sore; Nausea; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old patient received bnt162b2 (BNT162B2), administered in arm left, administration date 06Dec2021 10:00 (Lot number: FH8027) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. 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 06Dec2021 10:00, outcome "unknown", described as "booster"; INJECTION SITE PAIN (non-serious) with onset 06Dec2021, outcome "not recovered", described as "Pain at the injection site"; PAIN IN EXTREMITY (non-serious) with onset 06Dec2021, outcome "not recovered", described as "Really very sore arm, it is still sore"; NAUSEA (non-serious) with onset 06Dec2021, outcome "recovered" (Dec2021), described as "Nausea". Therapeutic measures were not taken as a result of injection site pain, pain in extremity, nausea. Follow-Up (14Dec2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: RI
Alter: 37,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Choking sensation Dysphagia Headache Neck pain Oropharyngeal pain X-ray

Symptomtext

severe headache like a migraine; one side of my throat like the left side of my throat, I had severe severe pain; Neck pain; trouble swallowing; feeling like I was going to choke; 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 received bnt162b2 (BNT162B2, solution for injection), administration date 01Dec2021 15:00 (Lot number: FH8027, Expiration Date: Feb2022) at the age of 37 years as dose number unknown, single for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), administration date 01Dec2021 (Batch/Lot number: unknown) as dose number unknown, single for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: HEADACHE (non-serious) with onset 02Dec2021, outcome "recovering", described as "severe headache like a migraine"; OROPHARYNGEAL PAIN (non-serious) with onset 02Dec2021, outcome "recovering", described as "one side of my throat like the left side of my throat, I had severe severe pain"; NECK PAIN (non-serious) with onset Dec2021, outcome "recovering", described as "Neck pain"; DYSPHAGIA (non-serious) with onset Dec2021, outcome "not recovered", described as "trouble swallowing"; CHOKING SENSATION (non-serious) with onset Dec2021, outcome "unknown", described as "feeling like I was going to choke". The events "severe headache like a migraine", "one side of my throat like the left side of my throat, i had severe severe pain", "neck pain", "trouble swallowing" and "feeling like i was going to choke" 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 headache, oropharyngeal pain, neck pain, dysphagia, choking sensation. Additional information: Consumer stated, Patient woke up with a severe headache like a migraine then she develop something else which like was actually kind of rose strange which was on one side of her throat like the left side of her throat, she had severe pain and like trouble swallowing like feeling like she was going to choke so she went to the emergency room for it actually. They treated her, they gave her like some Ibuprofen and some pain medicine and take here there and monitored her and took x-rays, they didn't see anything with the x- rays but they sent her home. So she still have a little bit of like pain but it's definitely it's getting better but it's just like it's kind of weird it never had happened to her before. She still have some of this like neck pain actually, it's like difficulty swallowing. Consumer stated, No prior vaccination within 4 Weeks, just when she got her COVID vaccine on 02Dec, she also got my flu vaccine (Unspecified Vaccine). She was only taking like birth control (Further not clarified) that's the only other thing that she take. Treatment for Adverse Event received as Ibuprofen, Oral administration, 600 milligrams in every 6 hours. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: X-ray; Result Unstructured Data: Test Result:they didn't see anything
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: -
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Chills Headache Immunisation Malaise Pain Pain in extremity Pyrexia Sleep disorder

Symptomtext

had chills that night; couldn''t sleep well; she is not feeling well/she doesn't feel good; headache; Feverish; feeling a little achy; she got the shingles vaccine and the booster dose; arms are so sore; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 01Dec2021 11:35 (Lot number: FH8027) as dose 3 (booster), single for covid-19 immunisation; varicella zoster vaccine rge (cho) (SHINGRIX), administered in arm left, administration date 01Dec2021 11:35 (Batch/Lot number: unknown) as dose number unknown, single for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (1st dose), for Covid-19 Immunization; Bnt162b2 (2nd dose), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 01Dec2021, outcome "unknown", described as "she got the shingles vaccine and the booster dose"; PAIN IN EXTREMITY (non-serious) with onset 01Dec2021, outcome "unknown", described as "arms are so sore"; CHILLS (non-serious) with onset 01Dec2021 19:00, outcome "unknown", described as "had chills that night"; SLEEP DISORDER (non-serious) with onset 01Dec2021, outcome "unknown", described as "couldn''t sleep well"; MALAISE (non-serious) with onset 01Dec2021, outcome "unknown", described as "she is not feeling well/she doesn't feel good"; HEADACHE (non-serious) with onset 01Dec2021, outcome "unknown", described as "headache"; PYREXIA (non-serious) with onset 01Dec2021, outcome "unknown", described as "Feverish"; PAIN (non-serious) with onset 01Dec2021, outcome "unknown", described as "feeling a little achy". Therapeutic measures were taken as a result of chills, sleep disorder. Additional information: The reporter had said to the caller in a note that her arms are so sore, she had chills that night and she couldn't sleep well. Caller confirms that these began on 01Dec2021 when patient got the shingles vaccine and the booster dose and she said that her side effects were horrible. Inquired if caller is aware if these are ongoing and she states that the reporter had reported them in and then cancelled their meeting and had asked for them to meet on Monday so apparently she is not feeling well since the rationale for rescheduling the meeting was for the side effects and that she doesn't feel good. It was unknown if patient receive any other vaccines within four weeks prior to the first administration date of the suspect vaccine. Patient had received the shingrix vaccine on her left arm and the COVID Booster vaccine in her right arm on 01Dec2021 at 11:35am and later in the evening started feeling achy her arms were sore and getting more sore as the daylight went on. Patient started having the chills around 7: 00pm and took 2 Tylenol. Then went to bed and needed to take Tylenol every 4hours throughout the night because patient then had headache and felt feverish. patient was able to stop taking the Tylenol as often and only took it sporatically when feeling a little achy. No follow-up attempts are possible. No further information is expected. Follow-Up (13Dec2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1974204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 23.12.2021
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: unbekannt Erholt: nein

Hypoaesthesia Immunisation Lymph node pain SARS-CoV-2 test

Symptomtext

pain in my lymph nodes under my left arm pit.; Slight numbness in face and arm on side where shot was given; Booster; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 27Nov2021 16:00 (Lot number: FH8027) at the age of 33 years as dose 3 (booster), 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: 2, Batch/Lot No: Unknown. Not available/provided to reporter at the time of report completion, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 01Apr2021, when the patient was 33 years old, for COVID-19 immunization, reaction(s): "common side effects"; Bnt162b2 (Dose Number: 1, Batch/Lot No: Unknown. Unable to locate or read the details, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 11Mar2021, when the patient was 33 years old, for COVID-19 immunization, reaction(s): "common side effects". The following information was reported: IMMUNISATION (non-serious) with onset 27Nov2021 16:00, outcome "unknown", described as "Booster"; LYMPH NODE PAIN (non-serious) with onset 27Nov2021 18:00, outcome "not recovered", described as "pain in my lymph nodes under my left arm pit."; HYPOAESTHESIA (non-serious) with onset 27Nov2021 18:00, outcome "not recovered", described as "Slight numbness in face and arm on side where shot was given". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of lymph node pain, hypoaesthesia. Additional information: Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. The patient had no known allergies. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. No other medications the patient received within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19.Device Date :29Nov2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: Test Date: 20211102; Test Name: covid-19 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 : Na
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1970762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 81,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 02.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chills Dizziness Fatigue Head discomfort Immunisation Insomnia Nasopharyngitis Night sweats

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (005570). The reporter is the patient. A 81 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02Dec2021 10:00 (Lot number: FH8027) at the age of 81 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "borderline diabetes" (unspecified if ongoing), notes: Patient's Medical History: borderline diabetes. Concomitant medication(s) included: METFORMIN taken for glucose tolerance impaired (ongoing). Vaccination history included: Bnt162b2 (First Dose, Lot: EL9265, Expiration: unknown, Anatomical location: left arm, She did not have any problem with the first two shots of the covid vaccine.), administration date: 17Feb2021, when the patient was 80 years old, for Covid-19 Immunization, reaction(s): "She did not have any problem with the first two shots of the covid vaccine."; Bnt162b2 (Second dose, Lot: EL9269, Expiration: unknown, Anatomical location: left arm, She did not have any problem with the first two shots of the covid vaccine.), administration date: 10Mar2021, when the patient was 80 years old, for Covid-19 Immunization, reaction(s): "She did not have any problem with the first two shots of the covid vaccine."; Flu shot (She had no problems with flu shot.), for Immunization, reaction(s): "She had no problems with flu shot". The following information was reported: IMMUNISATION (non-serious) with onset 02Dec2021 10:00, outcome "unknown", described as "Covid booster shot"; CHILLS (non-serious) with onset 02Dec2021 09:00, outcome "recovered" (03Dec2021), described as "Chills/getting cold and got colder and colder/shivering"; NASOPHARYNGITIS (non-serious) with onset 02Dec2021 09:00, outcome "recovered" (03Dec2021), HEAD DISCOMFORT (non-serious) with onset Dec2021, outcome "recovered" (Dec2021) and all described as "pressure on left side of her head"; NIGHT SWEATS (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "woke up soaking wet"; DIZZINESS (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "Light-headed"; CHILLS (non-serious) with onset 02Dec2021, outcome "recovered" (03Dec2021), described as "so cold her teeth was chattering"; FATIGUE (non-serious) with onset 03Dec2021, outcome "not recovered", described as "extremely tired"; INSOMNIA (non-serious) with onset Dec2021, outcome "not recovered", described as "Took two naps". No follow-up attempts are possible. No further information is expected. Additional information: The patient had no other products, no investigation assessment and no family medical history relevant to AE. The patient was calling about the covid booster shot. She had a problem with it. She received the booster on Thursday. Thursday night she not only had, but she was also. She was in bed for a couple of hours and her teeth were still chattering. On day two she and was and she does not know if it is classified as a headache, but she had more like. Her naps were two hours in the morning and three hours in the afternoon. She went to bed at 21:00. At 02:00 she, even her hair was wet, like she just got out the shower. On Day three, she did the same thing with the naps and she felt the same way and. Come night at 04:00, she woke up and she was wet again, her night clothes and hair was wet. Not quite as wet as the day before on day 3. Last night was night 4, and she did not have any problem last night, however, she was still very tired. She just woke up from a three hour nap and she just feels that someone should not what happened to her. She did not have problems with the booster. She was still mowing her own lawn and is still active. Height: Used to be 5'3" and she is close to that unless she shrunk a little. Exactly 21:00 on Thursday was when she started getting cold and got colder and colder for 20 minutes. Started with her hands being cold at night and thought to put them in the pocket of her bath robe and did not get warmer and she was getting chills and was shivering. Treatment declines any. The only thing that remains today was being tired and taking three hour naps and she normally does not nap at all. Metformin dispensed in a pharmacy bottle: States it was a big tablet. She sees a S/N and GTIN. Manufacturer : Granules Pharmaceuticals Incorporated, NDC: thinks the fine print states NDC: 68645-584-59. Product strength and count size dispensed: 100mg tablet, 90 days. She had three bottles like this. She only had this bottle that she has opened. She had other bottles that has not been opened yet. She was not on insulin. She called first and was frustrated. Patient did not visit to emergency room and physician office. Patient did not take any prior vaccine within 4 weeks. Patient did not experience AE following prior vaccination. No relevant tests done. There was product complaint. Description of complaint: Metformin dispensed in a pharmacy bottle: States it is a big tablet. She sees a S/N and GTIN. Follow-up (08Dec2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Borderline diabetes (Patient's Medical History: borderline diabetes.)
Andere Medikamente: METFORMIN.
Allergien: -
Vorherige Impfungen: -

VAERS 1970759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Diarrhoea Dizziness Immunisation Peripheral swelling

Symptomtext

swollen under left arm pit; dizziness; diarrhea; Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 46-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 02Dec2021 15:15 (Lot number: FH8027) at the age of 46 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hashimotos thyroid" (unspecified if ongoing); "Sulpha allergy" (unspecified if ongoing); "soy allergy" (unspecified if ongoing); "eggs allergy" (unspecified if ongoing); "wheat allergy" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE SODIUM; PANTOPRAZOLE; PROZAC; LOSARTAN. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ew0161, Location of injection: Arm Left), administration date: 16Apr2021, when the patient was 46 years old, for COVID-19 immunisation; Bnt162b2 (Dose Number: 1, Batch/Lot No: er8727, Location of injection: Arm Left), administration date: 26Mar2021, when the patient was 46 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 02Dec2021 15:15, outcome "unknown", described as "Booster"; PERIPHERAL SWELLING (non-serious) with onset 04Dec2021 09:00, outcome "not recovered", described as "swollen under left arm pit"; DIZZINESS (non-serious) with onset 04Dec2021 09:00, outcome "not recovered", described as "dizziness"; DIARRHOEA (non-serious) with onset 04Dec2021 09:00, outcome "not recovered", described as "diarrhea". Therapeutic measures were not taken as a result of peripheral swelling, dizziness, diarrhoea. Additional information: The case assessed as non-serious by the reporter. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient not diagnosed with covid-19 prior to vaccination and since vaccination patient not tested for covid-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to grains; Egg allergy; Hashimoto's thyroiditis; Soy allergy; Sulfonamide allergy
Andere Medikamente: LEVOTHYROXINE SODIUM; PANTOPRAZOLE; PROZAC; LOSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1970729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 50,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Chills Fatigue Immunisation Myalgia

Symptomtext

Tiredness; muscle aches; chills; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 01Dec2021 13:45 (Lot number: FH8027) at the age of 50 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: CLARITIN; VITAMIN C; VITAMIN B12. Vaccination history included: Bnt162b2 (Dose 2, Lot No: EL3247, Route of Administration: Intramuscular), administration date: 11Feb2021, when the patient was 49 years old, for COVID-19 Immunization; Bnt162b2 (Dose 1, Lot No: EL3247, Route of Administration: Intramuscular), administration date: 21Jan2021, when the patient was 49 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 01Dec2021 13:45, outcome "unknown", described as "Booster"; FATIGUE (non-serious) with onset 02Dec2021, outcome "recovered" (Dec2021), described as "Tiredness"; MYALGIA (non-serious) with onset 02Dec2021, outcome "recovered" (Dec2021), described as "muscle aches"; CHILLS (non-serious) with onset 02Dec2021, outcome "recovered" (Dec2021), described as "chills". Therapeutic measures were not taken as a result of fatigue, myalgia, chills. Additional information: The patient did not receive other vaccine in four weeks. The patient did not have covid prior vaccination. The patient did not get covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CLARITIN; VITAMIN C; VITAMIN B12
Allergien: -
Vorherige Impfungen: -

VAERS 1970724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 31,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Chills Fatigue Headache Immunisation Myalgia Pyrexia Vaccination site pain

Symptomtext

Booster; Mild fever; Pain at injection site; Tiredness; Headache; Overall muscle aches; Chills; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 01Dec2021 09:45 (Lot number: FH8027) at the age of 31 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 (Prev dose Product: COVID 19, Prev dose Brand: Pfizer, Prev dose Lot number: EL3247, Prev dose Administrator route: Intramuscular, Prev dose Vaccine location: Left arm, Prev dose Dose number: 2), administration date: 19Feb2021, when the patient was 30 years old, for COVID-19 Immunization; Bnt162b2 (Prev dose Product: COVID 19, Prev dose Brand: Pfizer, Prev dose Lot number: EL3247, Prev dose Administrator route: Intramuscular, Prev dose Vaccine location: Left arm, Prev dose Dose number: 1), administration date: 29Jan2021, when the patient was 30 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 01Dec2021 20:00, outcome "recovering", described as "Booster"; PYREXIA (non-serious) with onset 01Dec2021 20:00, outcome "recovering", described as "Mild fever"; VACCINATION SITE PAIN (non-serious) with onset 01Dec2021 20:00, outcome "recovering", described as "Pain at injection site"; FATIGUE (non-serious) with onset 01Dec2021 20:00, outcome "recovering", described as "Tiredness"; HEADACHE (non-serious) with onset 01Dec2021 20:00, outcome "recovering", described as "Headache"; MYALGIA (non-serious) with onset 01Dec2021 20:00, outcome "recovering", described as "Overall muscle aches"; CHILLS (non-serious) with onset 01Dec2021 20:00, outcome "recovering", described as "Chills". Therapeutic measures were taken as a result of immunisation, pyrexia, vaccination site pain, fatigue, headache, myalgia, chills. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine.Treatment with Tylenol (OTC) received for the adverse event.Prior to vaccination, was the patient was not diagnosed with COVID-19.Since the vaccination, has the patient 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: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No Known allergies: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1970694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

mild

Staat: CT
Alter: 40,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Headache Immunisation Lymphadenopathy Nausea Pain in extremity

Symptomtext

Swollen lymph node near injection site; Head ache; Tired; Slightly nauseous; Sore arm; 3rd dose; 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 (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 22Nov2021 10:45 (Lot number: Fh8027) at the age of 40 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 Number: 2, Lot Number: Ep6955), for covid 19 immunization; Bnt162b2 (Dose Number: 1, Lot Number: El3247), for covid 19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 22Nov2021 10:45, outcome "unknown", described as "3rd dose"; LYMPHADENOPATHY (non-serious) with onset 22Nov2021 15:00, outcome "recovering", described as "Swollen lymph node near injection site"; HEADACHE (non-serious) with onset 22Nov2021 15:00, outcome "recovering", described as "Head ache"; FATIGUE (non-serious) with onset 22Nov2021 15:00, outcome "recovering", described as "Tired"; NAUSEA (non-serious) with onset 22Nov2021 15:00, outcome "recovering", described as "Slightly nauseous"; PAIN IN EXTREMITY (non-serious) with onset 22Nov2021 15:00, outcome "recovering", described as "Sore arm". Therapeutic measures were not taken as a result of lymphadenopathy, headache, fatigue, nausea, pain in extremity. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1970673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 54,0
Geschlecht: U
Eingang: 22.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Immunisation Vaccination site pain

Symptomtext

Pain at the injection site when arm moves on certain position.; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54 year-old patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 29Nov2021 11:00 (Lot number: FH8027) at the age of 54 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: EL 3247, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 16Feb2021, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: FL 3247, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 26Jan2021, for COVID-19 immunization. The following information was reported IMMUNISATION (non-serious) with onset 29Nov2021 11:00, outcome unknown; VACCINATION SITE PAIN (non-serious) with onset 29Nov2021 19:00, outcome unknown. Therapeutic measures were not taken as a result of vaccination site pain. Additional information: It was reported that the event started around After the 8 hours. Around 7pm that same day. The patient had no prior vaccinations within 4 weeks prior to the vaccination and had no 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. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1970642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 51,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Herpes zoster Immunisation Rash Rash pruritic

Symptomtext

a very itchy rash on my neck lasted all day; woke up the next morning the rash was over my; diagnosed it with shingles; dose number=3; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 51 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 23Nov2021 02:00 (Lot number: FH8027) at the age of 51 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Total mastectomy due to breast cancer" (unspecified if ongoing), notes: Total mastectomy due to breast cancer; "Shingles" (unspecified if ongoing), notes: I had shingles before that was mild like this about seven years prior; "breast cancer" (unspecified if ongoing). Concomitant medication(s) included: EFFEXOR; CONCERTA. Vaccination history included: Bnt162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose lot number= ER8729, Prev dose dose number=2, Prev dose vaccine location=Left arm), administration date: 10Apr2021, when the patient was 50 years old, for Covid-19 immunization; Bnt162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose lot number= ER8727, Prev dose dose number=1, Prev dose vaccine location=Left arm), administration date: 20Mar2021, when the patient was 50 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 23Nov2021 02:00, outcome "unknown", described as "dose number=3"; RASH PRURITIC (non-serious) with onset 24Nov2021, outcome "recovering", described as "a very itchy rash on my neck lasted all day"; RASH (non-serious) with onset 24Nov2021, outcome "recovering", described as "woke up the next morning the rash was over my"; HERPES ZOSTER (non-serious) with onset 24Nov2021, outcome "recovering", described as "diagnosed it with shingles". The events "a very itchy rash on my neck lasted all day", "woke up the next morning the rash was over my" and "diagnosed it with shingles" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of rash pruritic, rash, herpes zoster. Additional information: There were no other vaccine taken in four weeks. The patient took the antiviral Valtrex as the treatment. There were no allergies. 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: Breast cancer; Shingles (I had shingles before that was mild like this about seven years prior); Total mastectomy (Total mastectomy due to breast cancer)
Andere Medikamente: EFFEXOR; CONCERTA
Allergien: -
Vorherige Impfungen: -

VAERS 1970639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8027

mild

Staat: NJ
Alter: 43,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 18.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Exposure during pregnancy Immunisation Pain in extremity Vaccination site pain

Symptomtext

Booster only.; Booster only. Had side effects .Pain in left arm , sore left arm injection site pain. Felt better in 2 days; Pain in left arm; sore left arm injection site pain; This is a spontaneous report received from a non-contactable reporter(s) (Pharmacist). A 43 year-old female patient (pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 18Nov2021 (Lot number: Fh8027) at the age of 43 years as dose 3 (booster), single for covid-19 immunisation. The patient is expected to deliver a baby(s) on 03Jul2022. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (previous dose product=COVID 19, previous dose brand=Pfizer, previous dose lot number=En6208, previous dose administrator route=Intra muscular, previous dose administration date=19Mar2021, previous Dose Number: 2, Previous Dose vaccine location : Left Arm), administration date: 19Mar2021, when the patient was 42 years old, for COVID-19 Immunization; Bnt162b2 (previous dose product=COVID 19, previous dose brand=Pfizer, previous dose lot number= En6205, previous dose administrator route=Intra muscular, previous dose administration date=26Feb2021, previous Dose Number: 1, Previous Dose vaccine location : Arm Left), administration date: 26Feb2021, when the patient was 42 years old, for COVID-19 Immunization. The following information was reported: EXPOSURE DURING PREGNANCY (non-serious) with onset 18Nov2021, outcome "unknown", described as "Booster only. Had side effects .Pain in left arm , sore left arm injection site pain. Felt better in 2 days"; IMMUNISATION (non-serious) with onset 18Nov2021, outcome "unknown", described as "Booster only."; PAIN IN EXTREMITY (non-serious) with onset Nov2021, outcome "recovered" (Nov2021), described as "Pain in left arm"; VACCINATION SITE PAIN (non-serious) with onset Nov2021, outcome "recovered" (Nov2021), described as "sore left arm injection site pain". Therapeutic measures were taken as a result of pain in extremity, vaccination site pain. The was patient was treated with Tylenol. 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 1970638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NC
Alter: 47,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Axillary pain Body temperature abnormal Body temperature increased Feeling abnormal Headache Immunisation Influenza like illness Lymphadenopathy Tenderness

Symptomtext

elevated temperature maxing out at 102; general flu like symptoms; extreme headache; achy joints; generally miserable; lymph nodes in my arm pit are enlarged; My right armpit is also enlarged; Both are tender to the touch; Booster dose; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Nov2021 13:30 (Lot number: FH8027) at the age of 47 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin; "Known allergies: Sulfa drugs" (unspecified if ongoing), notes: Known allergies: Sulfa drug. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN0176, Location of injection: Arm Left), administration date: 05May2021, when the patient was 47 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN8729), administration date: 05Apr2021, when the patient was 47 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 22Nov2021, outcome "unknown", described as "Booster dose"; BODY TEMPERATURE INCREASED (non-serious) with onset 23Nov2021, outcome "recovered" (2021), described as "elevated temperature maxing out at 102"; INFLUENZA LIKE ILLNESS (non-serious) with onset 23Nov2021, outcome "recovered" (2021), described as "general flu like symptoms"; HEADACHE (non-serious) with onset 23Nov2021, outcome "recovered" (2021), described as "extreme headache"; ARTHRALGIA (non-serious) with onset 23Nov2021, outcome "recovered" (2021), described as "achy joints"; FEELING ABNORMAL (non-serious) with onset 23Nov2021, outcome "recovered" (2021), described as "generally miserable"; LYMPHADENOPATHY (non-serious) with onset 23Nov2021, outcome "recovering", described as "lymph nodes in my arm pit are enlarged"; AXILLARY PAIN (non-serious) with onset 23Nov2021, outcome "recovering", described as "My right armpit is also enlarged"; TENDERNESS (non-serious) with onset 23Nov2021, outcome "recovering", described as "Both are tender to the touch". The patient underwent the following laboratory tests and procedures: body temperature abnormal: 102, notes: Elevated temperature maxing out at 102,. It was unknown if therapeutic measures were taken as a result of body temperature increased, influenza like illness, headache, feeling abnormal, lymphadenopathy, axillary pain, tenderness. Therapeutic measures were taken as a result of arthralgia. Additional information: it was reported that the patient was not received any vaccine in four weeks and was not tested for covid post vaccination. The patient had not covid prior vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: Elevated temperature; Result Unstructured Data: Test Result:102; Comments: Elevated temperature maxing out at 102,
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: Penicillin); Sulfonamide allergy (Known allergies: Sulfa drug)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1967897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NC
Alter: 60,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Flushing Rash pruritic

Symptomtext

Approximately 2 hours after the injection she developed a generalized, pruritic rash and became flushed in the face. She took benadryl and "everything cleared up."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash pruritic
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Metabolic syndrome; HTN; sleep apnea
Andere Medikamente: Amlodipine, atorvastatin, doxepin,loratadine, losartan, magnesium, metformin, trintellix, trulicity, B12, Xyzal
Allergien: ACE inhibitors, bydureon, metrogel, phentermine, thimerosal
Vorherige Impfungen: -

VAERS 1967161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NV
Alter: 67,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 15.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Injection site swelling

Symptomtext

Site: Swelling at Injection Site-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site swelling
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1963293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AR
Alter: 42,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 08.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Axillary pain Headache Inappropriate schedule of product administration Pain in extremity

Symptomtext

Patient received his first Covid vaccine on 11/30/2021. He should of returned to the clinic on 12/21/2021. He was scheduled by the front desk to return on 11/8/2021. He was given the second dose. Tthe shot room nurse noticed when she was filling out his card. She notified the patient immediately and the nursing supervisor. Patient was stable and instructed to call the clinic if he has any adverse reaction to the vaccine. Front desk supervisor notified. Front desk lead is to check all appointment for patient returning for second dose. Shot Room nurse was given a reprimand and told to check card and chart before administering the Covid Shot. Patient reported reaction on 12/14/2021 and was seen same day. He states symptoms started on six day earlier. Symptoms included headache left arm pain, and pain in the arm pit area. OTC Advil was recommended.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: Tension Type Headache
Vorgeschichte: NONE
Andere Medikamente: No Medication
Allergien: No Drug or Food allergies
Vorherige Impfungen: -

VAERS 1963277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 7,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 01.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered Pain in extremity

Symptomtext

arm pain (reporting due to administration error of giving pediatric patient the adult concentration of Pfizer)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: esotropia, autism, asthma, obesity
Andere Medikamente: Flovent, albuterol, loratadine, acetaminophen
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1963191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NJ
Alter: 48,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 12.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Nausea Tinnitus

Symptomtext

Tinnitus, Nausea, Dizziness

Weitere VAERSDATA-Felder

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

VAERS 1962861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CO
Alter: 48,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Decreased appetite Headache Influenza like illness Nausea Pain Pyrexia Tinnitus

Symptomtext

Within 6 hours of receiving the COVID-19 Pfizer booster shot, I developed a fever reaching 105.2?F. I also developed other severe flu-like symptoms, including extreme body aches (especially in right elbow where I had recent surgery), shivering and chills, loss of appetite, nausea, and severe headache (non-migraine). At times of high fever, I could hear my pulse in my ear. I treated the fever with 1000mg acetaminophen every 6 hours for 48 hours. Symptoms began to resolve 54 hours after injection, except for a lingering, mild headache. The medication was effective in reducing the fever to the range of 102-103?F but fever returned to 104.8-105.2?F exactly 6 hours after taking the acetaminophen. My fever did not "break" until 50 hours after injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None; stayed home in bed
Aktuelle Erkrankungen: Recovering from elbow surgery - repairs of tears in the extensor and flexor tendons in the right elbow 11-09-2021; routine colonoscopy 12-14-2021.
Vorgeschichte: Thyroid removed in 2014 due to Hashimoto's.
Andere Medikamente: Synthroid, B-12, vitamin D, acetaminophen
Allergien: Penicillin, aspirin, cyclines, and ibuprofen
Vorherige Impfungen: Same effects after receiving each of the 1st and 2nd COVID-19 Pfizer shots earlier this year

VAERS 1962435

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IL
Alter: 23,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Dizziness Nausea Panic reaction

Symptomtext

Patient presented to the mobile vaccination clinic site at Fire Department in on 12/17/2021. She received her Adult Pfizer Covid-19 Booster shot, dose 0.3mL . After receiving the booster shot and proceeding to the 15-min waiting area, the patient complained of feeling light headed. The patient was seated in a chair and refused offer to lie down on yoga mats. She stated that she initially felt nauseous immediately after receiving the booster dose, which further caused her to start to panic. She was attended to by myself, Dr. ; Quality Assurance Officer; and an LPN . Patient's blood pressure was approximately 100/70, pulse was 64, and oxygenation was 97% SAO2 at the time of assessment. Patient was advised to lie down and given water and food to consume. Approximately 15 min later, she claimed her symptoms had resolved. Pulse rate at that time was 76+, BP also improved within normal limits. Vital signs were all within normal limits. Patient was reassured and advised to seek urgent medical attention if symptoms are present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1962034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WI
Alter: 45,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Oedema peripheral

Symptomtext

Heavy swelling and discomfort in the left armpit

Weitere VAERSDATA-Felder

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

VAERS 1961713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 22,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Back pain Pain Sleep disorder

Symptomtext

Woke up in the middle of the night with horrible joint pain. Couldn?t lay comfortably in any position. Every single joint in my body was aching, even the small joints in my fingers. It was especially horrible in my upper back and shoulders.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Endometriosis
Andere Medikamente: Ibuprofen, Senna, and Dulcolax
Allergien: Blueberries, Kale, Buspar
Vorherige Impfungen: -

VAERS 1959016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 10.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / UN

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

Dizziness Dyskinesia Headache Hypoacusis Malaise Movement disorder Muscle spasms Musculoskeletal stiffness Nausea Pain in extremity Retching Thirst Visual impairment

Symptomtext

The following day, about 16 hours later, after waking up she felt very thirsty and when she got out of bed started feeling dizzy, nauseous, with dry heaves and feeling like she was going to pass out, with vision and hearing diminishing. She sat on the toilet with her head between her knees for a while and it took a few minutes to feel better. When she went to the kitchen to fill her water bottle her arms got very stiff and painful from the elbows down to her fingers and she could not open her water bottle at the time because her hands were closed in a spasm. She got back to her bed and sat on her opened hands to stop them from involuntarily closing again. No color changes were noticed. The day before she did not have any activity that involved her neck or arms to move differently. She said she had a mild headache, but no other symptoms. The spasms resolved a few minutes later and everything was back to normal. She has been fine since then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: No.
Vorgeschichte: Asthma Chronic tonsillitis
Andere Medikamente: Mirena IUD
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 1943518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 52,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Feeling jittery Hyperventilation

Symptomtext

Pt stayed in the office for about 50 minutes. myself and the on call provider, AM were monitoring her. Pt had chills, jitters, and a bit of hyperventilation. States this happened last time as well. Pt states her body just needed time to adjust to it. After 50 minutes she was feeling much better. Checked her BP twice per AM request. It was lower the second time. No other concerns.

Weitere VAERSDATA-Felder

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

VAERS 1954504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site swelling Swelling

Symptomtext

Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: patient called to report swelling that got worse after administration of her vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1954237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 16.12.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Asthma Heart rate Heart rate increased Immunisation Interchange of vaccine products Off label use Pain

Symptomtext

fast heartbeat; asthma attack; Full body is aching; I had booster shot of Pfizer, and first two shots were of Moderna; first and second shot/Moderna; first and second shot/Moderna; 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 (PFIZER-BIONTECH COVID-19 VACCINE), administration date 17Nov2021 (Lot number: FH8027) as dose 3 (booster), single for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Moderna (First dose), for COVID-19 immunization; Moderna (Second dose), for COVID-19 immunization. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 2021, outcome "unknown" and all described as "first and second shot/Moderna"; IMMUNISATION (non-serious) with onset 17Nov2021, outcome "unknown", described as "I had booster shot of Pfizer, and first two shots were of Moderna"; HEART RATE INCREASED (non-serious) with onset 18Nov2021, outcome "not recovered", described as "fast heartbeat"; ASTHMA (non-serious) with onset 18Nov2021, outcome "not recovered", described as "asthma attack"; PAIN (non-serious) with onset 18Nov2021, outcome "not recovered", described as "Full body is aching". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of heart rate increased, asthma, pain. Additional information: For Taking the pain relief medicines (Unspecified medications) but after every two hour like I get relief for only two hour and again after two hours I experience all the same symptoms: Unspecified QR Comment: Reporter type could not be probed over the call as the consumer was unwilling to share any further information, hence captured by default as consumer or other non-health professional in tab. Since majority of the information was provided by the consumer itself, so 'is patient also the reporter?' checked as yes in tab. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20211118; Test Name: heartbeat; Result Unstructured Data: Test Result:fast heartbeat
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1952857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Breast pain Lymph node pain Lymphadenopathy

Symptomtext

Swollen and sore lymph nodes in left armpit; moderate-severe breast pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic idiopathic urticaria
Andere Medikamente: 3mg Melatonin/day
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 1952131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MD
Alter: 62,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain Joint range of motion decreased Needle issue Pain Pain in extremity Syringe issue Underdose

Symptomtext

Patient is describing difficulty with range of motion of left arm and experiences pain that radiates when lifting There is also sensitivity/pain at the site of injection Patient was given booster dose on 11/20/21, but there was a needle/syringe malfunction where the full dose was not administered - most of the vaccine had spilled from the syringe during administration. Patient was then given another dose to ensure that she had gotten the entire recommended dosage for the booster. After receiving the doses patient described above reactions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure, high cholesterol, persistent cough, acid reflux
Andere Medikamente: amlodipine, rosuvastatin, famotidine, amitriptyline, omeprazole, vitamin d
Allergien: morphine
Vorherige Impfungen: -

VAERS 1951394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: AZ
Alter: 55,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary mass Chills Feeling abnormal Headache Hyperhidrosis Lymphadenopathy Mass Pain Pyrexia Vaccine positive rechallenge

Symptomtext

Almost exactly 12 hours after receiving the booster the chills and body aches hit like a frieght train. I went to bed and was sweating, running a low grade fever. Woke the next morning still feeling horrible, but now had a very bad headache. For the next 2 days I had the headache and would run a low grade fever off and on. I had lump in my armpit on my left arm and a lump near my collar bone on my left side. My wife made me go to an urgent care on the 3rd day because of the lumps. By the time of my appointment I was feeling much better. The doctor at urgent care said he thought it was swollen lymph node or glands not sure which he said.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Influenza (Seasonal) Afluria Quadrivalent
Allergien: None
Vorherige Impfungen: Same issues with 2nd dose of Pfizer

VAERS 1951220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IL
Alter: 33,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Chills Pain in extremity

Symptomtext

Chills, joint pain in hips and knees, sharp pain shooting down legs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: sertraline, diltiazem,alprazolam
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1948407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CO
Alter: 14,0
Geschlecht: M
Eingang: 14.12.2021
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

Dizziness Lethargy Pallor Slow response to stimuli

Symptomtext

At 3:00 pm MST nurse called to waiting area/observation where patient was feeling lightheaded. Patient sitting up and slightly lethargic, lips and skin palor pale, and eyes closed. Parents and sisters at patient's side. Patient able to ingest a juice box while sitting up. Patient helped onto mat on carpeted floor with second nurse and legs elevated and put on chair. Smelling salt used to ilicit stronger response from patient. Patient able to open eyes, converse, and drink second juice box. Parents stated that patient often feels dizzy after receiving vaccinations, and asked to inform nurses/providers in advance of future vaccines. After 10 minutes lying on floor, legs lowered off chair. Patient more conversant and color in lips and face pink and normal. Patient able to sit up on own without dizziness, and drink a bottle of water and eat a snack (granola bar). After 5 minutes able to stand up and walk without dizziness and stated he felt 'normal'. Patient discharged to care of family (parents and 2 sisters) at 3:25 pm without incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKDA
Vorherige Impfungen: Was informed after event occurred that patient often gets dizzy after receiving vaccines

VAERS 1948385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NV
Alter: 43,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 14.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Feeding disorder Oral herpes Pyrexia Stomatitis

Symptomtext

I received my COVID Booster shot at Pharmacy on Sunday morning, 11/14/21. The next day, less than 24 hours after receiving the shot I had a fever that night and had fever blisters in my mouth, 2 at the time. I was not able to go to work on Monday. The next night I had a fever again and woke up with 2 more mouth sores/blisters. I had a total of about 6 mouth sores and was unable to eat for about 10 days. I did not have this reaction with the 2 doses of Moderna. The blisters were gone for about a week and reappeared and this is when I called my doctor to get an appointment to get seen. I thought this was normal until I started to read about the Pfizer shot and herpes simplex if dormant it will appear. I have a history of HSV 1 and 2. I have not had an outbreak of HSV 2 for about 10 years and my last outbreak of HSV 1 was in September 2018. I usually have a backup prescription of Acyclovir in case of an outbreak. Since I have not had one it never occurred that the COVID shot would have depressed my immune system and caused me to have an outbreak. I had to make an appointment to see my primary care provider and was seen on 12/9/21 and was prescribed Acyclovir 400mg 1 tab 2 times a day for 7 days. After being on the medication for 3 days I have improved and my sores are better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: I was given a lab slip to test again for HSV 1 and 2 but have not been able to go and get the test done at.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1947112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MD
Alter: 38,0
Geschlecht: F
Eingang: 14.12.2021
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: nein

Immunisation Insomnia Nausea

Symptomtext

Booster; Nausea; Sleeplessness; 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 26Nov2021 13:00 (Lot number: FH8027) at the age of 38 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "SLE" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: FLU, administration date 19Nov2021; METHOTREXATE; FOLIC ACID. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Unknown. Unable to locate or read the details, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 09May2021, when the patient was 37 years old, for COVID-19 immunization, reaction(s): "Dose number:1 02May2021 Dose number:2 09May2021"; Bnt162b2 (Dose Number: 1, Batch/Lot No: Unknown. Unable to locate or read the details, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 02May2021, when the patient was 37 years old, for COVID-19 immunization, reaction(s): "Dose number:1 02May2021 Dose number:2 09May2021". The following information was reported: IMMUNISATION (non-serious) with onset 26Nov2021 13:00, outcome "unknown", described as "Booster"; NAUSEA (non-serious) with onset 26Nov2021 01:00, outcome "not recovered", described as "Nausea"; INSOMNIA (non-serious) with onset 26Nov2021 01:00, outcome "not recovered", described as "Sleeplessness". Therapeutic measures were not taken as a result of nausea, insomnia. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; SLE.
Andere Medikamente: METHOTREXATE; FOLIC ACID.
Allergien: -
Vorherige Impfungen: -

VAERS 1947078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NH
Alter: 59,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Fatigue Headache Immunisation Pain Pyrexia

Symptomtext

fever; severe joints aching; severe headache day two; severe fatigue; Severe stinging down to my finger tip on left arm at time of injetion; Dose number: 3; 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), administered in arm left, administration date 15Nov2021 03:00 (Lot number: FH8027) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU VACCINE VII, administration date 06Oct2021. Past drug history included: Sulphur, reaction(s): "known allergies: Sulphur". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6202, Location of injection: Arm Left, Vaccine Administration Time: 12:00 AM), administration date: 06Mar2021, when the patient was 59 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6207, Location of injection: Arm Left), administration date: 30Mar2021, when the patient was 59 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Nov2021 03:00, outcome "unknown", described as "Dose number: 3"; PYREXIA (non-serious) with onset 16Nov2021 13:00, outcome "recovering", described as "fever"; ARTHRALGIA (non-serious) with onset 16Nov2021 13:00, outcome "recovering", described as "severe joints aching"; HEADACHE (non-serious) with onset 16Nov2021 13:00, outcome "recovering", described as "severe headache day two"; FATIGUE (non-serious) with onset 16Nov2021 13:00, outcome "recovering", described as "severe fatigue"; PAIN (non-serious) with onset 15Nov2021 03:00, outcome "recovering", described as "Severe stinging down to my finger tip on left arm at time of injetion". Therapeutic measures were not taken as a result of pyrexia, arthralgia, headache, fatigue, pain. Additional information: Facility where the most recent COVID-19 vaccine was administered in Pharmacy or Drug Store. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient not been tested for COVID-19. Follow-Up (22Nov2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1944414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Pain Pyrexia

Symptomtext

12a fever, chills, achy for 24hrs. Tylenol extra strength q6hrs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Previously Covid
Vorgeschichte: Palpitations, hi cholesterol
Andere Medikamente: Metroprolol, Hztz, zoloft, Zocor, Claritin
Allergien: Hot dogs
Vorherige Impfungen: 2nd covid vaccine

VAERS 1944294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 11,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered Injection site pain Product administration error

Symptomtext

Accidental Error of administration of vaccination- Pfizer adult dose accidently was given to 11 year old pt. This is his 1st dose. Pt does not have any side effects or adverse event except injection site pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None. Done continuous observation only. - It is an administration Error ONLY.
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Asthma
Andere Medikamente: None. He does have history of Asthma.
Allergien: None
Vorherige Impfungen: -

VAERS 1944081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: IL
Alter: 10,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 07.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Decreased appetite Incorrect dose administered Lacrimation increased Pain Pyrexia

Symptomtext

Adult dose of Pfizer given to 10 year old Pt. Called mom to inform once the problem was discovered and she states he was fine for 3 days then had body aches, fever, was eating less, and had watery eyes. everything resolved after 3 days except still has the watery eyes a little.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: eczema
Vorgeschichte: eczema
Andere Medikamente: hydrocortisone 2.5% cream
Allergien: none
Vorherige Impfungen: -

VAERS 1942026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

mild

Staat: UT
Alter: 47,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: 10.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Feeling cold Feeling hot Headache Heart rate increased Hyperhidrosis Interchange of vaccine products Peripheral coldness

Symptomtext

I did the mix and match with Moderna from February 2021 because I had a reaction to the second shot then too. My current reaction started with feeling really cold and shivers. I wasn't able to get warm. Hands and feet were very cold and I had to sit over a forced air heater to warm them up. Nothing was tingling, no discoloration. My heart rate is also elevated and still elevated as I write this. I normally hover in the 70-80's for heart rate but from about 3am on it's been between 110-126 according to my apple watch. Blood oxygenation is 93% according to the watch. At 6am I now feel hot all over, I have a headache (lap of sleep mostly) and I woke up sweating but my thermometer only says 98 degrees F. The pharmacist told me to try and eat and drink as much as possible to prevent a "starvation of resources" from the reaction the vaccine might cause. I ate all night till I was full and drank fluids until I was urinating frequently. I stopped eating and drinking around 9pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Moderna 2nd shot. 2/12/2021 lot 015m20a, age 46

VAERS 1941927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8027

mild

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Fatigue Immunisation Vaccination site pain

Symptomtext

moderate fatigue; mild injection site pain; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 16Nov2021 00:45 (Lot number: fh8027) at the age of 44 years as dose 3 (booster), single for covid-19 immunisation. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: en6203, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 23Mar2021, when the patient was 43 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: en6203, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 02Mar2021, when the patient was 43 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 16Nov2021 00:45, outcome "unknown", described as "Booster"; FATIGUE (non-serious) with onset 17Nov2021, outcome "recovered" (19Nov2021), described as "moderate fatigue"; VACCINATION SITE PAIN (non-serious) with onset 17Nov2021, outcome "recovered" (18Nov2021), described as "mild injection site pain". Therapeutic measures were not taken as a result of fatigue, vaccination site pain. Additional Information: The patient had moderate fatigue lasting 48 hours post vaccine mild injection site pain lasting 24hours post vaccine. The patient did not have covid prior to vaccination. The patient did not have known allergies. The patient did not tested covid post vaccination. No follow up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Obesity
Andere Medikamente: PROBIOTICS; MULTIVITAMIN [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1888316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NJ
Alter: 55,0
Geschlecht: F
Eingang: 11.12.2021
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

Headache Immunisation Swelling face Joint range of motion decreased Musculoskeletal stiffness Nodule Tenderness

Symptomtext

Booster; painful knots on my temple and it is like its still here. It feels like my, back side of my face is like so huge; back side of my face is like so huge.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 17Nov2021 (Lot number: FH8027) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU), administered in arm left, administration date 21Oct2021 (Batch/Lot number: unknown) as dose number unknown, single. Relevant medical history included: "Diabetes mellitus" (unspecified if ongoing), notes: Verbatim: Diabetes; "Allergy" (unspecified if ongoing). Concomitant medication(s) included: OZEMPIC taken for diabetes mellitus; ZYRTEC taken for hypersensitivity. Past drug history included: Tylenol, reaction(s): "headaches", notes: (Dose: 400mg) twice and only 2 tablets each time. . Vaccination history included: Bnt162b2 (Dose: 01), for COVID-19 Immunization; Bnt162b2 (Dose: 02), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 17Nov2021, outcome "unknown", described as "Booster"; HEADACHE (non-serious) with onset 17Nov2021, outcome "unknown", described as "painful knots on my temple and it is like its still here. It feels like my, back side of my face is like so huge"; SWELLING FACE (non-serious) with onset 17Nov2021, outcome "unknown", described as "back side of my face is like so huge.". Therapeutic measures were taken as a result of swelling face. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Diabetes (Verbatim: Diabetes)
Andere Medikamente: OZEMPIC; ZYRTEC
Allergien: -
Vorherige Impfungen: -

VAERS 1940496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 17.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Alanine aminotransferase Asthenia C-reactive protein Chest X-ray Differential white blood cell count Epstein-Barr virus antibody positive Epstein-Barr virus test positive Fatigue Full blood count Infectious mononucleosis Neck pain Pain Pyrexia Red blood cell sedimentation rate Urine analysis Viral load

Symptomtext

Weakness, fatigue, body aches, neck pain, daily fever beginning 48 hours after vaccine. Daily fever (triggers body aches) starting each morning with regular temperature increasing to 101.5 (max) every day around 4pm. Cross reactive antibody of epstein barr virus (mono). Positive EBV IVCA Igm 3 weeks and 2 days post vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: EBV, ALT, CBC, chest xray, Urine analysis, Urine culture, c reactive protein, ESR, white blood cell differential - all on12/9 & EBV viral load DNA on 12/10
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal allergies
Andere Medikamente: Tylenol, Junel (birth control pill), zyrtec, lexapro 10mg
Allergien: Demerol
Vorherige Impfungen: -

VAERS 1940483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: MA
Alter: 71,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 22.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / OT

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

Rash Rash erythematous Rash pruritic Urticaria

Symptomtext

Hives/rash red deep itch sacrum, upper hips, lower front abdomen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: acid reflux ( intermittent)
Vorgeschichte: fibromyalgia, migraine/TMJ/trigeminal neuralgia; gluten sensitivity; osteoporosis
Andere Medikamente: vit D3, calcium, magnesium, biotin
Allergien: gluten sensitivity; lactose intolerance
Vorherige Impfungen: Pfizer Covid 19 03/20/2021

VAERS 1938811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: PA
Alter: 40,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Body temperature Decreased appetite Feeling abnormal Headache Joint swelling Lethargy Lymphadenitis Pyrexia Vaccination site bruising

Symptomtext

Temperature of 100; Right shoulder swollen; Bruised on the injection spot; Inflammation on lymphatic nodules on the right side, from neck to hip.; Headache; No appetite; Brain fog; Lethargy; This is a spontaneous report from a non-contactable reporter (Consumer or other non HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in right arm, administration date 29Nov2021 at 11:45 (Lot number: FH8027) at the age of 40 years as dose 2, single for COVID-19 immunisation. The patient had no relevant medical history. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: FH8030, Anatomical location: Right arm, Administration time: 11:45), administration date: 08Nov2021, when the patient was 40 years old, for COVID-19 immunisation. The following information was reported: PYREXIA (non-serious) with onset 30Nov2021 at 01:00, outcome "recovered" (an unknown date in 2021), described as "Temperature of 100"; JOINT SWELLING (non-serious) with onset 30Nov2021 at 01:00, outcome "recovered" (an unknown date in 2021), described as "Right shoulder swollen"; VACCINATION SITE BRUISING (non-serious) with onset 30Nov2021 at 01:00, outcome "recovered" (an unknown date in 2021), described as "Bruised on the injection spot"; LYMPHADENITIS (non-serious) with onset 30Nov2021 at 01:00, outcome "recovered" (an unknown date in 2021), described as "Inflammation on lymphatic nodules on the right side, from neck to hip"; HEADACHE (non-serious) with onset 30Nov2021 at 01:00, outcome "recovered" (an unknown date in 2021), described as "Headache"; DECREASED APPETITE (non-serious) with onset 30Nov2021 at 01:00, outcome "recovered" (an unknown date in 2021), described as "No appetite"; FEELING ABNORMAL (non-serious) with onset 30Nov2021 at 01:00, outcome "recovered" (an unknown date in 2021), described as "Brain fog"; LETHARGY (non-serious) with onset 30Nov2021 at 01:00, outcome "recovered" (an unknown date in 2021), described as "Lethargy". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, joint swelling, vaccination site bruising, lymphadenitis, headache, decreased appetite, feeling abnormal and lethargy. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to the 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, emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20211130; Test Name: Body temperature; Result Unstructured Data: Test Result:100?; Comments: at 01:00
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: WI
Alter: 70,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Immunisation Urticaria

Symptomtext

Hives starting on upper body that appeared ~36-48 hours after vaccination and slowly spreading; Dose number=3; This is a spontaneous report from a contactable reporter (pharmacist). A 70-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 01Dec2021 (Lot number: FH8027) at the age of 70 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, SINGLE, Lot Number : EN6200, Route of Administration : Intramuscular, Anatomical Location : Right arm), administration date: 20Feb2021, when the patient was 69 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number : EN6202, Route of Administration : Intramuscular, Anatomical Location : Right arm), administration date: 13Mar2021, when the patient was 69 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 01Dec2021, outcome "unknown", described as "Dose number:3"; URTICARIA (non-serious) with onset 02Dec2021 at 22:00, outcome "unknown", described as "Hives starting on upper body that appeared approximately 36-48 hours after vaccination and slowly spreading". Therapeutic measures were not taken as a result of urticaria was unknown. Additional Information: The patient had no known drug allergies (NKDA). 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-19 vaccine. Since the vaccination, it was unknown if the patient had been tested for COVID-19. The events resulted in emergency room/department or urgent care.

Weitere VAERSDATA-Felder

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

VAERS 1938772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: NY
Alter: 32,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Dizziness Fatigue Headache Immunisation

Symptomtext

Fatigue; Headache; Dizziness; Dose number:3; This is a spontaneous report from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 32-year-old male patient received bnt162b2 (COMIRNATY), intramuscular, administered in right arm, administration date 28Nov2021 at 10:00 (Lot number: FH8027) at the age of 32 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. Concomitant medications were not reported. Vaccination history included: Comirnaty (DOSE 2, SINGLE, Lot Number: EL3247, Anatomical location: Left arm, Route of administration: Intramuscular), administration date: 09Feb2021, when the patient was 31 years old, and Comirnaty (DOSE 1, SINGLE, Lot Number: EL3247, Anatomical location: Right arm, Route of administration: Intramuscular), administration date: 19Jan2021, when the patient was 31 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 28Nov2021 at 10:00, outcome "unknown", described as "Dose received: 3"; FATIGUE (non-serious) with onset 29Nov2021, outcome "recovering", described as "Fatigue"; HEADACHE (non-serious) with onset 29Nov2021, outcome "recovering", described as "Headache"; DIZZINESS (non-serious) with onset 29Nov2021, outcome "recovering", described as "Dizziness". Therapeutic measures were not taken as a result of fatigue, headache and dizziness. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
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 1938743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CT
Alter: 64,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Vaccination site pain

Symptomtext

Soreness at injection site starting about 8 hours after vaccination; Dose Number: 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-years-old male patient received third dose of bnt162b2 (BNT162B2, Batch/Lot number: FH8027) administered in arm left, administration date 24Nov2021 (at 12:00) (age at the time of vaccination was 64-years-old) as DOSE 3 (booster), SINGLE for covid-19 immunization. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU VACCINE VII, administration date 10Nov2021; ATORVASTATIN; LISINOPRIL. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 24Mar2021, when the patient was 63 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM), administration date: 03Mar2021, when the patient was 63 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 24Nov2021 14:00, outcome "unknown", described as "Dose Number: 3"; VACCINATION SITE PAIN (non-serious) with onset 24Nov2021 22:00, outcome "recovering", described as "Soreness at injection site starting about 8 hours after vaccination". Therapeutic measures were not taken as a result of vaccination site pain. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ATORVASTATIN; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1936601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 29.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / LA

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

Impaired healing Injection site pain Lymphadenopathy Pruritus Tinnitus

Symptomtext

11/29/21 - Got Pfizer booster 11/30- Started getting sore left deltoid at injection site 12/1 - Lymph nodes in left armpit feel swollen 12/2 - Lymph nodes at left collarbone feel swollen, feel itchy around neck/chest for a few days 12/3-12/4 - Armpit feels better, itchiness resolves, collarbone lymph nodes still swollen 12/5 - MAIN ADVERSE EVENT: Woke up with muffled hearing in left ear, felt like cotton in ear. Towards evening, noticed rumbling/high-pitched whine/tinnitus in quiet rooms, hearing still poor. Right ear feels OK. Took 2 rounds of 2 pills of OTC ibuprofen throughout the day, no change 12/6 - No change, called for ENT appts. Took 1 Aleve around midday, no change 12/7 - Saw ENT, he looked in ears/nose/throat with otascope and said no sign of wax problem or infection, noted swollen lymph nodes at left collarbone. Got prescription for Prednisone: 2x20mg once a day for 4 days, 1x20mg once a day for 4 days after that (12 pills over 8 days total). Took first dose (2X20mg) around 11am. No change in hearing. Tried to sleep with head elevated and on right side per ENT suggestion. 12/8 - Took 2nd dose (2x20mg) at 8:45am. No change in hearing. 12/9 - Took 3rd dose (2x20mg) at 8:45am. No change in hearing thus far. Lymph nodes at left collarbone still seem swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: No tests performed besides visual inspection by ENT doctor
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity
Andere Medikamente: Kirkland multivitamin
Allergien: Cloth bandaid adhesive (causes rash)
Vorherige Impfungen: -

VAERS 1936540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8027

mild

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness Fatigue Headache Hypoaesthesia oral Nausea

Symptomtext

Patient felt lightheaded, nauseated and complained of numbness in tongue. Patient did not have any further symptoms of allergies. After a few minutes, she developed a headache and was tired. She was released after 30 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 3 pm BP 134/90. 3:05 pm 131/80.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -