VAERS Reports 320 30 BD

VAERS 2712436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 10.11.2023
Impfdatum: 13.11.2021
Beginn: 27.08.2023
Tage bis Beginn: 652,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Blood lactic acid Bronchial secretion retention C-reactive protein increased COVID-19 Computerised tomogram thorax abnormal Cough Dyspnoea Fibrin D dimer increased Hyperglycaemia Hypertension Hypoxia Immunosuppressant drug therapy Lactic acidosis Leukopenia Lung opacity Pyrexia SARS-CoV-2 test positive

Symptomtext

BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider at Discharge: DO Admission Date: 8/27/2023 Discharge Date: 8/28/2023 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute on chronic respiratory failure with hypoxia (HCC) [J96.21] Acute respiratory failure due to COVID-19 (HCC) [U07.1, J96.00] HOSPITAL COURSE: Patient is a 68 year old male with a history of COPD, OSA, DM2, recurrent non-small cell lung cancer with mass in RUL stage IV currently on immunotherapy that presented to the ED with increased shortness of breath, cough, and fever (reported 100.9) that started on 8/22 (last immunotherapy). He denies any pain, nausea, vomiting, diarrhea, edema, palpitations. Vital signs were significant for hypoxia to 84% on room air, stabilized with 2 liters O2 per NC, tachypnea in the low 20s, and hypertension. Lab work was significant for hyperglycemia, lactic acid 2.1, leukopenia 3.57, and covid positivity. CT of the chest showed RUL tumor with mass invading mediastinum unchanged, and stable mucous plugging and tree in bud opacities in the LUL (suspicious for metastasis. No PE, no new consolidation. He was given IV fluids and nebulized bronchodilators in ED. He was admitted observation for acute on chronic respiratory failure with hypoxia related to covid-19 for further supportive care and monitoring. The patients oxygenation and work of breathing improved overnight with supportive care including dexamethasone. Leukopenia and lactic acidosis resolved. CPR and D-dimer mildly elevated. It was noted that he had significant improvement in work of breathing with nebulized bronchodilators in the ED. The patient does not have a nebulizer at home, one will be ordered. He was discharged home in stable condition with home oxygen as prior, duoneb with nebulizer, tessalon short course as needed, and recommendations to pick up guaifenesin at pharmacy. Oncology follow up has been rescheduled for September.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Epigastric abdominal pain Gallstone AAA (abdominal aortic aneurysm) (HCC) Precordial pain Dyspnea on exertion Smoker Essential hypertension Diabetes mellitus type 2 in obese Abnormal nuclear stress test Coronary artery disease involving native coronary artery of native heart without angina pectoris Non-small cell cancer of right lung (HCC) Malignant neoplasm of upper lobe of right lung (HCC) Hypoxemic respiratory failure, chronic (HCC) COPD (chronic obstructive pulmonary disease) (HCC) Obstructive sleep apnea syndrome COVID-19
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) 108 (90 Base) MCG/ACT inhaler ALPRAZolam (XANAX) 0.5 mg tablet ALPRAZolam (XANAX) 1 MG tablet amoxicillin-clavulanate (AUGMENTIN) 875-125 mg per tablet (Expired) budeson-glycopyrrol-formoterol (BREZTR
Allergien: Chantix [Varenicline]Hallucinations PrednisoneOther
Vorherige Impfungen: -

VAERS 2710306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: OH
Alter: 65,0
Geschlecht: F
Eingang: 06.11.2023
Impfdatum: 28.10.2021
Beginn: 12.10.2023
Tage bis Beginn: 714,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute myocardial infarction Acute respiratory failure Arthralgia C-reactive protein increased COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Essential hypertension Fibrin D dimer increased Full blood count normal Gastrooesophageal reflux disease Hyperlipidaemia Hypothyroidism Lung infiltration Metabolic function test Nasal congestion

Symptomtext

Patient is a 67 y.o. female patient ofl, DO with history of arthritis, CKD, GERD, essential HN, HLD, hypothyroidism, COPD, and OSA presented to General Hospital with SOB and worsening breathing. Acute hypoxic respiratory failure d/t Sepsis was present on admission s/t COVID-19 pneumonia NSTEMI, suspected type 2 due to demand Suspected acute PE with elevated D-dimer -ruled out on VQ scan P/w 10 day history of cough, nasal congestion, and sore throat. Pt fully vaccinated with 1 booster shot Afebrile on arrival, HR 84, RR 18, BP 120/73, satting >92% on 2L by NC (no home O2 needs) CBC unremarkable. BMP with AKI as below CXR: Slight area of inflammation or small infiltrate in the lateral aspect in the right midlung field Cont supplemental O2 to maintain goal SpO2 >90%, wean off to room air as tolerated Decadron 6mg daily for 10 days CRP 16.9, Pro-Cal 0.07 Albuterol, robitussin-DM, tylenol PRN; encourage IS use Contact precautions PT/OT/SW VQ scan negative for PE. Lovenox changed to prophylactic dose Home O2 evaluation prior to discharge. Case management consulted for discharge needs Acute kidney injury Initial Cr 2.09 (baseline ~1). Likely pre-renal given poor PO intake secondary to above Improved with IVF Essential HTN HLD Normotensive on admission Continue home amlodipine and statin Hold hyzaar pending improvement of kidney function Hypothyroidism Continue home synthroid GERD Continue home protonix PRN tums Chronic arthritic pain Continue home tramadol and gabapentin Obesity OSA Body mass index is 37.12 kg/m?. Discussed dietary and lifestyle modifications Continue home CPAP Nicotine dependence Current 1 PPD smoker Discussed and encouraged smoking cessation, >3min total time spent Nicotine replacement ordered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2700953

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 32030BD

kritisch

Staat: MN
Alter: 86,0
Geschlecht: F
Eingang: 24.10.2023
Impfdatum: 27.10.2021
Beginn: 08.10.2023
Tage bis Beginn: 711,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Cough Decreased appetite Fatigue Myalgia Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient was seen in the ED on 10/8/23 with cough, fatigue, poor appetite, myalgias, and fever that began three days prior. A COVID PCR test done in the ED resulted positive. Ultimately, the patient was admitted to the hospital from 10/8/23 - 10/12/23, with discharge diagnoses including pneumonia due to COVID-19 virus and secondary acute hypoxic respiratory failure, among other diagnoses. During admission, the patient required supplemental O2, however was able to wean to room air by discharge. She was briefly on dexamethasone. Of note, the patient has received three doses of the Pfizer monovalent COVID vaccine (given 2/2/2021; 2/23/2021; 10/27/2021).

Weitere VAERSDATA-Felder

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

VAERS 2693402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 98,0
Geschlecht: F
Eingang: 10.10.2023
Impfdatum: 21.10.2021
Beginn: 23.09.2023
Tage bis Beginn: 702,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure COVID-19 Cachexia Chest X-ray normal Cough Cyanosis Death Dementia Electrocardiogram normal Hypophagia Hypoxia Lethargy Malnutrition Pyrexia Quadriplegia Respiratory arrest SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient is a 100 y.o. female with a history of dementia who presented to Hospital 9/23/2023 from her ALF with fever, poor p.o. intake and increased cough with ambulatory COVID test positive. She was found to be mildly hypoxic in the ER. She was admitted as a DNRCC. Patient was weaned from oxygen, but reportedly spontaneously turned blue and ceased to breathe. She ultimately passed on 9/24/23 at 1038 AM. 1. COVID 19, lethargic only no encephalopathy: Noted decreased p.o. intake, lethargy and worsening cough on 9/22. Ambulatory and ER testing +ive for COVID. Vaccinated x3. Mild hypoxia. CXR non acute. Inflammatory markers ordered. Initiated Decadron, gentle IVF for 1L as appeared dry on exam. 2. Acute hypoxic RF: Secondary to above. Admitted on 2 L. Weaned to RA. 3. Elevated troponin: Noted on admission high sensitive troponin of 37. Suspected demand ischemia in the setting of above. EKG without acute ST changes. No ischemic work-up per goals of care. 4. End stage dementia, functional quadriplegia: Per history, patient nonverbal at baseline, bedbound and did not perform any ADLs. Cargivers provide pureed diet and crushed meds. Admitted at baseline. 5. Severe malnutrition with cachexia POA: BMI 15.62. Due to end stage dementia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2674247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 21.08.2023
Impfdatum: 27.10.2021
Beginn: 29.04.2023
Tage bis Beginn: 549,0
Dosis: 2
Route/Site: IM / RA

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

Deep vein thrombosis Pulmonary embolism

Symptomtext

SADDLE PULMONARY EMBOLISM 4/28/2023 ACUTE PULMONARY EMBOLISM ACUTE PULMONARY EMBOLISM 4/29/2023 ACUTE PULMONARY EMBOLISM ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 4/29/2023 ACUTE PULMONARY EMBOLISM

Weitere VAERSDATA-Felder

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

VAERS 2671546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 15.08.2023
Impfdatum: 15.12.2021
Beginn: 21.12.2022
Tage bis Beginn: 371,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Hypoxia Pulmonary embolism

Symptomtext

MULTIPLE SUBSEGMENTAL PULMONARY EMBOLI WITHOUT ACUTE COR PULMONALE ACUTE HYPOXEMIC RESPIRATORY FAILURE ACUTE PULMONARY EMBOLISM HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2642351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 07.06.2023
Impfdatum: 05.11.2021
Beginn: 01.06.2022
Tage bis Beginn: 208,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Febrile neutropenia Lumbar vertebral fracture Pathological fracture

Symptomtext

ACUTE RESPIRATORY FAILURE 4/12/2023 LUMBAR VERTEBRAL PATHOLOGICAL FX, INIT ACUTE RESPIRATORY FAILURE 4/12/2023 NEUTROPENIC FEVER, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2627323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 05.05.2023
Impfdatum: 20.10.2021
Beginn: 19.01.2022
Tage bis Beginn: 91,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI

Weitere VAERSDATA-Felder

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

VAERS 2605938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: TX
Alter: 25,0
Geschlecht: F
Eingang: 29.03.2023
Impfdatum: 23.11.2021
Beginn: 08.05.2022
Tage bis Beginn: 166,0
Dosis: 1
Route/Site: IM / AR

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

Anticoagulant therapy Apraxia Cerebrovascular accident Computerised tomogram head Computerised tomogram neck Deep vein thrombosis Hemiparesis Laboratory test Magnetic resonance imaging head Magnetic resonance imaging neck Swelling Swelling face Ultrasound scan

Symptomtext

Swelling within 10 minutes. Face and body. Had to use Benadryl. Diagnosed with multiple deep vein blood clots Hemiparesis, apraxia, stroke, prescribed lifelong blood thinners

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Labs, ultrasound, CT of neck/head, MRI of head and neck
Aktuelle Erkrankungen: None
Vorgeschichte: Bipolar, ADHD, anxiety, factor V Leiden, history of DVT in 2018
Andere Medikamente: Abilify, Lexapro, Tylenol, Adderall
Allergien: Sulfa, Pencilline, Lamotragine , Adhesive, Cipro
Vorherige Impfungen: -

VAERS 2577338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: MN
Alter: 82,0
Geschlecht: M
Eingang: 07.02.2023
Impfdatum: 18.11.2021
Beginn: 30.11.2022
Tage bis Beginn: 377,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Asthenia COVID-19 Dyspnoea Hypoxia Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient with history of diabetes. Patient seen in the ED for shortness of breath on 11/30/22. Patient has had several weeks of shortness of breath and weakness which has worsened over the past few days. In the ED, he was found to be hypoxic with O2 sats in 80's, so was placed on 4L supplemental O2 via nasal cannula. COVID PCR test performed on 11/30 resulted positive. Ultimately patient admitted 11/30/22 - 12/13/22 for acute on chronic hypoxic respiratory failure and COVID infection, among other problems.

Weitere VAERSDATA-Felder

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

VAERS 2554626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: WI
Alter: 90,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 17.11.2021
Beginn: 18.12.2022
Tage bis Beginn: 396,0
Dosis: 3
Route/Site: IM / RA

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

Death

Symptomtext

Death on 12/18/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COVID-19; OSC: ESRD; DM2; CHF; a-fib; PVD; CAD; HTN; HLD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2539040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 25.03.2021
Beginn: 27.09.2022
Tage bis Beginn: 551,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain Acute respiratory failure Asthenia Blood loss anaemia COVID-19 Cardiac perfusion defect Cellulitis Confusion postoperative Constipation Coronary artery bypass Decreased appetite Depressed mood Depression Dysphagia Facetectomy Fall Feeding disorder Foraminotomy

Symptomtext

71y.o. male with multiple medical problems including BPH, chronic LBP with LLE radicular pain, DMII and PPN who was admitted to the hospital on 9/5/2022 for N/V and abdominal pain. Upon admission, lexiscan MPI showed a reversible perfusion defect. Cardiovascular surgery was consulted and performed CABG x3 on 9/13. Pts hospital course has been c/b acute hypoxic respiratory failure, post-op acute blood loss anemia, dysphagia and right forearm cellulitis with completion of abx courses. Corpak was pulled on 9/21 by the pt. SLP is following and have the pt on mechanical soft diet with thickened liquids. Psych was consulted for depression and started the pt on Wellbutrin. Pt with recent hx of (7/27/2022) lumbar laminectomy with medial facetectomy and foraminotomy with fusion at L4-5 on by Dr., post-op course complicated by lethargy and confusion. Patient with unwitnessed fall with RRT activated on 9/26- no head trauma and no head CT required. He was transferred to the med ward for a dx of COVID with fever and anorexia. He was treated with remdesivir - he did not have hypoxia. He had quite some anorexia and asthenia and some depressed mood. He has been recovering and is now showing signs of resolution of these problems and we anticipated return to HCF, but he was denied by insurance, including a peer to peer. Evaluation on Day of Discharge: Last night he had nausea and vomiting and could not eat dinner. Also did not eat lunch. This morning he felt good and ate the entire BKF. He has had multiple stools (constipation was an issue in the past days and received plenty of stool softners) - stool sfotners will be held now. Suspect component of gastroparesis - this should improve as he becomes more active.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 30,0
Labordaten: 10/7 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2506693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 91,0
Geschlecht: M
Eingang: 12.11.2022
Impfdatum: 08.11.2021
Beginn: 14.10.2022
Tage bis Beginn: 340,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Asthenia Atrial fibrillation Benign prostatic hyperplasia COVID-19 Cardiac failure congestive Chills Condition aggravated Death Essential hypertension Hyperglycaemia Hypokalaemia Malnutrition Sepsis Troponin increased

Symptomtext

The patient is a 92 y.o. male with history of BPH, hypertension, squamous cell carcinoma and dementia presented with generalized weakness and chills due to COVID 19 infection, acute hypoxic respiratory failure and in A fib with RVR. He was followed by pulmonary, cardiology and palliative team. While his management was in progress, patient expired on 10/17/22 at 1335. Discharge Diagnoses: Acute respiratory failure with hypoxia. Sepsis due to covid-19 infection, POA Acute CHF exacerbation, systolic, uncompensated Elevated troponin without chest pain. A fib with RVR Hypokalemia Steroid induced hyperglycemia Benign essential hypertension BPH Severe malnutrition, POA

Weitere VAERSDATA-Felder

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

VAERS 2480449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 17.11.2021
Beginn: 24.04.2022
Tage bis Beginn: 158,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory distress syndrome Acute respiratory failure Anticoagulant therapy Blood gases COVID-19 Cardiac failure Cardiomegaly Cerebral haemorrhage Chest X-ray abnormal Computerised tomogram abnormal Computerised tomogram head abnormal Computerised tomogram thorax abnormal Confusional state Crepitations Death Dysphagia Echocardiogram abnormal Endotracheal intubation

Symptomtext

4/24/2022-Presented to ED, unwitnessed fall states hit head large hematoma on L eye, admitted to drinking alcohol daily. Confused. CT Had, R parafalcine subdural and L frontal/parietal subdural hygroma. CT-sacral fracture and L subtrochanteric femur fx. Covid -test. Baseline 02 use 2L NC. Increased to 3L intermittently desat to mid 80's.Admit intraparenchymal hemorrhage with subdural hematoma s/t to fall. 4/25/2022-Left subtrochanteric hip fracture repair. R occiptal intraparenchymal hemorrhage inceased to 1.5cm L anterior frontal intraparenchymal hemorrhage increased to 5mm. No surgical intervention. BP controlled less then 140/80 currently 104/62, o2 sat 90's on 3L NC. Keppra 750mg BID. ST eval clear liquids, swallowing difficulties. 4/26/2022- R occipital intraparenchymal hemorrhage stable on f/u CT. 4/27/2022-On NRB, sat in mid 70's, o2 changed to 5L sata now 88-92%. 4/28/2022-AM-Mentation decline, desat 70-80 becoming more altered, fine wheezes bilateral and creptation on R side. Placed on NRB 15L. CXR-mod airpace disease/infiltrates LAsix IV and levaquin , CT no evidence of PE. IVC filter placed to prevent PEd/t recent surgery and immobility. PM-Sats in high 90's with NRB, but patient would not keep on, desatting to 70's. 5L NC was placed so suctioning could occur, sats would not maintain over 70%, thick yellow sputum obtained by suction. Became tachy and transfered to ICU and intubated. Acute on chronic hypoxemic resp failure s/t to ARDS d/t pneumonia vs pulm edema in setting of HFrEF and AMS. Current bilevel setting FiO2 60%. 4/29/2022-Bilevel 16 25/10 35%. WBC and h&h stable. On Vanco cefepime and flagyl. 4/30/2022- recent echo showed severe L ventricular dilatation with moderate miral regurg EF 20%. Continue entresto hold toresemide 5/2/2022- Exubated on 2L NC. Continue cefepime and flagyl. 5/3/2022- WBC 15.4 from 13.3 ABG 7.453/31.9/66/22.3/90 cxr-pulmonary vascular congestion and cardiomegaly. Cont digoxin and metoprolol 5/5/2022- Transfered to ICU. Wears bipap at HS. o2 sat on 2L stable. 5/13/2022- Rapid response called Acute RF, hypoxic 80's on sat , tachypneic using resp muscles. BP 154/104 RR 24 ABG 7.45/25/97/18/ on NRB worsening CT chest -pulmonary infiltrates and b/l pleural effusion. Bipap with PEEP 8. Continued distress, intubated and transfered to ICU. Chest Ct consisten with b/l diffuse groundglass opacities/ Covid + test. Ferritin 535.0. Started on steroids, barcitinib, remdesivir, vitamins and heparin. Cefepime and Vanco. 5/15/2022- Vent 12 22/6 60% 5/17/2022-Palliative orders placed d/t severe HF and mitral valve issues, fluid is in lungs and she is at high risk for reintubation if extubation is attempted. Terminally exubated. Morphine increased. WBC 15.5 5/19/2022- Time of death 1003.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ETOH abuse, COPED, Afib, CAD. HLD and post CABG ICD placement
Andere Medikamente: -
Allergien: Aspirin, PCN and adhesive
Vorherige Impfungen: -

VAERS 2473479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 25.10.2021
Beginn: 29.09.2022
Tage bis Beginn: 339,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure COVID-19 SARS-CoV-2 test positive

Symptomtext

Discharge Provider: DO Primary Care Provider: PA Admission Date: 9/29/2022 Discharge Date: Oct 2, 2022 PRESENTING PROBLEM: Acute respiratory failure with hypoxia (HCC) [J96.01] HOSPITAL COURSE: The patient is a 64 y.o. male with past medical history of HTN, HLD, obesity, OSA and venous insufficiency who presented to the ED with hypoxia. He was subsequently found to be COVID positive and initiated on treatment with remdesivir and decadron. He was also covered for CAP with ceftriaxone and azithromycin. He subsequently weaned to room air with no oxygen needs on pulm rehab consultation and was able to be discharged to home on 10/2/22. He was transitioned of oral Ceftin and Zmax to finish a 5 days course and continued on Decadron oral to finish 10 days. Wound care was consulted for his wound management, but was unable to see him prior to d/c. It was recommended he have close follow up with his PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia Hypertension Special screening for malignant neoplasms, colon Primary osteoarthritis of right knee OSA (obstructive sleep apnea) Class 3 obesity (HCC) CAP (community acquired pneumonia)
Andere Medikamente: atorvastatin (LIPITOR) 10 MG tablet dexamethasone (DECADRON) 6 MG tablet (Expired) diphenhydramine-acetaminophen (TYLENOL PM EXTRA STRENGTH) 25-500 MG TABS metoprolol Succinate-XL (TOPROL-XL) 200 MG 24 hr tablet nicotine (NICODERM CQ) 21 MG
Allergien: None
Vorherige Impfungen: -

VAERS 2456299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: SD
Alter: 66,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 02.12.2021
Beginn: 14.07.2022
Tage bis Beginn: 224,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal hernia Anastomotic leak COVID-19 Death General physical health deterioration SARS-CoV-2 test positive Small intestinal obstruction Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 04/05/2021, 04/26/2021, and 12/02/2021. They presented to hospital on 06/24/2022 with a strangulated ventral hernia and a small bowel obstruction. They were admitted same day. They experienced further complications of an anastomotic leak. They were transferred to a different hospital on 07/12/2022 for nursing care after their health continued to deteriorate. They transitioned to comfort care only. They tested positive for COVID-19 on 07/14/2022 and died on 07/15/2022. It is not well understood if the individual experienced COVID-19 symptoms since this was a medically complex situation and the individual had several underlying medical conditions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 22,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Kidney Disease, Osteoarthritis, Morbid Obesity with past gastric bypass; Hypothyroid (past thyroidectomy for non-follicular thyroid neoplasm), Hypertension, Likely Renal Cell Carcinoma (further work up not done); Lung Mass/nodule (further work up not done) At the time of the adverse event, they were experiencing complications related to a strangulated ventral hernia and a small bowel obstruction.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2446402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: OH
Alter: 90,0
Geschlecht: M
Eingang: 15.09.2022
Impfdatum: 19.10.2021
Beginn: 08.06.2022
Tage bis Beginn: 232,0
Dosis: 3
Route/Site: - / UN

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Tested COVID positive, died on 6/9/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Nasal swab collected 6/8/2022 detected SARS-CoV-2 Antigen on 6/08/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: MN
Alter: 45,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 17.11.2021
Beginn: 30.07.2022
Tage bis Beginn: 255,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 Pneumonia SARS-CoV-2 test positive

Symptomtext

Positive COVID, acute respiratory failure, pneumonia

Weitere VAERSDATA-Felder

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

VAERS 2395005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: TX
Alter: 82,0
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: 22.11.2021
Beginn: 18.07.2022
Tage bis Beginn: 238,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation COVID-19 Death Dyspnoea General physical health deterioration Malaise Renal injury SARS-CoV-2 test positive

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA Rec'd Pfizer COVID Vaccines on 4/29/2021, 5/20/2021 and 11/22/2021. Presented to ED on 7/3 with SOB and malaise 2/2 COVID in a-fib with RVR in 150s tx'd w/amiodarone gtt w/improvement. O2 saturation down to 82% req'd NC. During stay pt also experienced KI. Pt cont'd to decline. Rapid response called 7/14 for a-fib and increasing O2 requirements. Transitioned to comfort care and moved to inpatient hospice. Expired on 7/18/22. Pt was tx'd with cefepime, ceftriaxone, remdesivir, and decadron.

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Praegender Schweregrund: Death
Hospital-Tage: 15,0
Labordaten: COVID + 7/4/22.
Aktuelle Erkrankungen: -
Vorgeschichte: stage IV follicular lymphoma s/p R-CVP C1D1 6/21), involving bone (T6), spleen, axillary/cervical node mass C3/C4, CHF, chronic atrial fibrillation, CAD s/p CABG, HTN, HLD, PVD, AoS s/p TAVR, hypothyroidism
Andere Medikamente: Allopurinol, Vitamin C, Aspirin, Atorvastatin, Vitamin B-12, Gabapentin, Levothyroxine, Lidocaine, Lidocaine/Prilocaine, Losartan, Metoprolol, Prednisone, Prochlorperazine, Torsemide
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2364319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 29.01.2021
Beginn: 07.07.2022
Tage bis Beginn: 524,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Pt has a history of asthma, chronic diastolic CHF, and obesity. Pt presented for evaluation of nonproductive cough, rhinorrhea and hypoxia. Pt was noted to be COVID positive and was admitted with acute hypoxic respiratory failure and COVID pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2307096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: FL
Alter: 84,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 15.11.2021
Beginn: 26.05.2022
Tage bis Beginn: 192,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Cardio-respiratory arrest Cardiomyopathy Chest pain Computerised tomogram thorax abnormal Death Dyspnoea Echocardiogram abnormal Hypotension Inappropriate schedule of product administration Lung opacity Pulmonary septal thickening Rhinorrhoea Road traffic accident SARS-CoV-2 test positive Ventricular fibrillation

Symptomtext

He received Covid vaccines on 1/30/21, 2/27/21, and 11/15/21. On 5/25/22, he was brought to ER due to weakness, SOB, and runny nose. He was recently involved MVC and was released from the other hospital. He tested positive COVID requiring oxygen therapy, so he was admitted to the hospital. He received Remdesivir and Steroid. On 5/28/22, he complained of chest pain. Echo shoed cardiomyopathy with EF 35-40%. He went to ventricular fibrillation. He was coded twice. He was able to achieve return of spontaneous circulation but was still hypotensive with maximum support. His family decided DNR and pronounced death at 13:51 on 5/28.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 4,0
Labordaten: SARS CoV2 PCR COVID19 positive on 5/25/22. CT chest with multifocal patchy groundglass opacities with mild associated intralobular septal thickening.
Aktuelle Erkrankungen: -
Vorgeschichte: Atrial fibrillation, HTN, pacemaker, Type 2 DM
Andere Medikamente: -
Allergien: Neosporin, Polyspoin, Sulfadiazine
Vorherige Impfungen: -

VAERS 2261835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: NY
Alter: 60,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 12.10.2021
Beginn: 09.01.2022
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Anticoagulant therapy Atelectasis Atrial fibrillation Body temperature increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Echocardiogram normal Respiratory failure SARS-CoV-2 test positive Sepsis White blood cell count increased

Symptomtext

1/9/2022- Presented to ER, with complaint of SOB. Tested + for Covid 1 week ago. T-100.4, WBC-32, P-89. RR-22. O2 via nc 2L. Chest x ray-Mild bibasilar atelectasis. Admit with acute on chronic hypercapnic respiratory failure due to Covid-19 pneumonia with severe sepsis int he setting of home oxygen dependent at COPD 2L. Started on remdesivir, baricitinib, Zosyn, vancomysin and Decadron. 1/10/2022-WBC-21.Tolerating oxygen at 4L. New onset A fib, echo report-no evidence wall abnormality or valvular disease. On Lovenox and started eliquis. 1/13/2022- 3L o2 via NC, 96%. Covid -Test. 1/14/2022- Tolerating 3L o2, which is his home oxygen base. Afebrile. Discharged to sub acute rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHS, Type 2 Dm, COPD, Morbid obesity, Alcohlism, Bipolar disorder
Andere Medikamente: -
Allergien: Metformin
Vorherige Impfungen: -

VAERS 2216108

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 22.11.2021
Beginn: 29.12.2021
Tage bis Beginn: 37,0
Dosis: 3
Route/Site: IM / LA

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

Cerebral infarction Cerebrovascular accident Magnetic resonance imaging head abnormal

Symptomtext

Cerebrovascular accident -MRI showed multifocal areas of infarct involving the left cerebral hemisphere. Suggesting an embolic phenomenon, will need 30 days holter monitor on discharge. Other hospital problems treated and discharges to home. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2173309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 05.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation CHA2DS2-VASc-score Death General physical health deterioration Unresponsive to stimuli

Symptomtext

Found to be in A fib with RVR. On dilt gtt, converted to NSR, then able to go back on metoprolol. Elevated chadsvasc score so started on eliquis. Finally decisions was made to switch to hospice on discharge. Although the patient did show general decline day-to-day consistent with end of life, the did take longer than expected. Patient was made comfort measures on 12/8, but by 12/13, the patient had only recently become nonresponsive. ED visit, hospital admission and death within 6 weeks of receiving the COVID vaccine.

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Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 03.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Cerebrovascular accident Electrocardiogram ambulatory normal Hypertension Ischaemia Lacunar infarction Magnetic resonance imaging head abnormal

Symptomtext

Patient had just completed a hospitalization from 11/21/2021-11/23/2021 for acute stroke. This is a lacunar appearing infarct due to hypertension ischemia and MRI was done. She will have a Holter monitor 10 days set up, due to 1 episode of atrial fibrillation to make sure there is not any further. She had monitoring, both first hospitalization and this hospitalization, and no atrial fibrillation. Hypertension up titrated to Norvasc 10 mg total daily. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2114543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 02.11.2021
Beginn: 01.02.2022
Tage bis Beginn: 91,0
Dosis: 3
Route/Site: - / RA

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

Arteriogram coronary normal Chest pain Electrocardiogram normal Myocarditis Troponin increased Carditis Myocardial infarction

Symptomtext

Heart attack; Heart inflammation; 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 male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 02Nov2021 (Lot number: 32030BD) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Blood pressure high" (unspecified if ongoing); "Thyroid" (unspecified if ongoing), notes: Thyroid. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, LOT: EN6207), administration date: 17Mar2021, when the patient was 58 years old, for COVID-19 Immunization; Bnt162b2 (Dose: 2, LOT: EWO153), administration date: 08Apr2021, when the patient was 58 years old, for COVID-19 Immunization. The following information was reported: MYOCARDIAL INFARCTION (hospitalization, medically significant) with onset Feb2022, outcome "unknown", described as "Heart attack"; CARDITIS (hospitalization, medically significant) with onset Feb2022, outcome "unknown", described as "Heart inflammation". The patient was hospitalized for myocardial infarction, carditis (start date: 06Feb2022). The events "heart attack" and "heart inflammation" were evaluated at the physician office visit. Therapeutic measures were taken as a result of myocardial infarction, carditis. Reported that had a heart attack last week and my doctor said that it was due to me having a reaction to the COVID 19 vaccine because I had heart inflammation and he told me that I need to call and tell you guys this was what was going on. I went to the hospital. I had a heart attack and they gave me pills now. Prior vaccination before four weeks was none reported. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Thyroid disorder (Thyroid)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2096049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: MN
Alter: 66,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 02.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Ammonia normal Blood creatine phosphokinase increased Blood culture negative Blood pressure increased Blood sodium increased C-reactive protein increased COVID-19 COVID-19 pneumonia Cerebral small vessel ischaemic disease Cervical spinal stenosis Chest X-ray abnormal Chronic kidney disease Computerised tomogram head abnormal Computerised tomogram spine Condition aggravated Confusional state

Symptomtext

HOSPITAL COURSE: 66-year-old male with PMH of reversible posterior leukoencephalopathy syndrome, seizure disorder, hypertension, and diabetes mellitus who presented to the hospital after being found on the ground with acute confusion that resolved while in ED. Admitted to medicine for additional monitoring of acute toxic-metabolic encephalopathy and found to be COVID-19 positive with associated acute hypoxic respiratory failure. Acute toxic metabolic encephalopathy Reversible posterior leukoencephalopathy syndrome Seizure disorder, chronic Cervical Spine Stenosis, moderate to severe Elevated creatinine kinase Patient was found on the ground, unclear how long. He was confused and thought that it was 1950 at the time of initial assessment. Mentation had improved upon arrival to ED. Noted to have BP elevated to 180 systolic on presentation to ED. Unclear if encephalopathy is related to seizure with postictal state, hypertensive encephalopathy, or possible depakote toxicity, or other etiology. CT head was without acute abnormality, but notes chronic encephalomalacia of the right temporal occipatal and inferior parietal lobe, as well as mild chronic small vessel ischemic changes. CT C-spine was without fracture or malalignment however noted to have baseline developmentally narrow cervical spinal canal with superimposed degenerative changes resulting in moderate to severe spinal canal narrowing at C3-C4 and C4-C5. Ammonia normal at 12. Depakote level within range at 96.8. - Continue monitoring - Keppra level: wnl - Continue PTA Keppra BID - Blood culture: no growth at 48 hours - Continue PTA depakote daily - CK mildly elevated to 300s in the setting of being found down; continue gentle IVF given AKI as well - Continue PTA gabapentin - Acetaminophen PRN, Cepacol lozenge PRN, Tessalon TID PRN Constipation-resolved - Bowel regimen: bisacodyl PRN, miralax PRN, senna BID Acute hypoxic respiratory failure COVID-19 pneumonia Patient presenting with mildly elevated temp to 100F. Also reported URI symptoms for 4 to 5 days. Cough has been nonproductive. Chest x-ray with subtle interstitial infiltrates in both lungs which was reported as possible early or developing COVID pneumonia. Also with retrocardiac airspace opacity of LLL which may represent atelectasis or left basilar pneumonia. Procalcintonin negative. Has been vaccinated and boosted. D-dimer minimally elevated to 0.53. Noted to have LLE warm and slightly larger than RLE on initial evaluation. Bilat LE US to eval given elevated VTE risk in COVID-19 and mildly elevated d-dimer. US negative for DVT - With Decadron while on oxygen, weaned off oxygen before discharge - CRP peak to 6.7downtrending to 2 at discharge Hypertensive urgency - resolved Hypertension, chronic BP initially 180s systolic but improved. - Continue PTA amlodipine 10mg daily - Continue PTA lisinopril 20mg daily Diabetes mellitus type 2 Steroid-induced hyperglycemia A1c 7.6% as of 1/26/22. - continue home empagliflozin while in house Normocytic anemia, chronic Iron deficiency anemia Hb 12 on presentation, trending down. - Daily CBC to trend - Continue PTA ferrous sulfate BID -Hemoglobin on discharge 10.5 Hyperlipidemia - Continue PTA atorvastatin Mild thrombocytopenia Platelets 130 on presentation. Improving. - Continue to monitor - Trend daily CBC Hypomagnesemia Hypokalemia - Trend daily and replete daily Elevated creatinine, suspected mild CKD Hypernatremia, mild Creatinine 1.35 on presentation. Most recent prior was 1.18, however has ranged 1.1-1.4 on prior checks over past few years. Cr improved to 1.2 with IVF hydration. Does not meet criteria for AKI given baseline as noted above. Na minimally elevated to 146 in setting of reduced PO intake. Received IVFs. - Trend BMP daily; improved to 1. 25 as of 1/30

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: COVID PCR POSITIVE 1/28/2022
Aktuelle Erkrankungen: -
Vorgeschichte: 66-year-old male with a history of reversible posterior leukoencephalopathy syndrome, seizure disorder, hypertension, and diabetes Past Medical History: Diagnosis Date ? CHF (congestive heart failure) (HCC) ? Hospitalism as child 2nd burn-R side of face? ? Hypertensive urgency 10/7/2018 ? RPLS (reversible posterior leukoencephalopathy syndrome) 10/07/2018 hosp 2018 ? SBO (small bowel obstruction) (HCC) 6/11/2018 ? Severe malnutrition (HCC) 5/20/2018
Andere Medikamente: -
Allergien: NO KNOWN
Vorherige Impfungen: -

VAERS 2095983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: NY
Alter: 82,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 17.11.2021
Beginn: 09.12.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Alanine aminotransferase increased Anticoagulant therapy Aphasia Aspartate aminotransferase increased Atelectasis Atrial fibrillation Blood gases Bradycardia COVID-19 Cardiac pacemaker insertion Cerebellar infarction Chest X-ray abnormal Death Endotracheal intubation Fall Femur fracture

Symptomtext

12/9/21: Patient admitted post fall and left sided weakness. Found to have left cerebellar infarct and left intertrochanteric femur fracture. Covid negative on admission and no symptoms. 12/10/21: OR for nailing of femur fracture 12/11/21: developed aphasia and aspiration PNA 12/13-12/17: in and out of afib with RVR treated with IV Cardizem. Continues to have no Covid symptoms. NPO due to aspiration risk. For PEG tube. Improving lung imaging post IV abx for aspiration PNA. On 2L via NC sat >97%. 12/22/21: Symptomatic bradycardia events. Need for pacemacker 12/24/21: GI bleed with transfusion needed. Continues to have no Covid symptoms. 2L NC sat >95%. Ferritin 235 WBC 20.8 12/27/21: Continued leukocytosis WBC 18.2, GFR 34. Increased resp. rate 26-32, increased oxygen need 4L NC to sat >92%. Temp 98.6 F. Tested Covid positive and concerns for aspiration. CXR shows increased pulmonary infiltrates bilaterally with small left pleural effusion. Started IV Remdesivir, decadron, flagyl, cefepime, and vitamin cocktail. 12/28/21: Concern for PE, unable to do VQ scan due to AKI and allergies. Started on heparin gtt. GFR 30, temp 99.5 F, AST 39 ALT 32. Remdesivir stopped. Started on renal dose baricitinib. RR 30-32 sat >92% on 5L NC. 12/29/21: @0540 patient becoming unresponsive with desaturation. On NRBM sat 80% RR varied from 12 to 40. Rapid response called. ABG on NRBM 6.992 CO2 >100 unobtainable BE or HCO3. Rhonchi and rales throughout bilateral lungs with weak inspiratory effort in acute hypercapnic/hypoxic respiratory failure. Patient intubated and placed on Bilevel 28/20 PS 20 FiO2 100%. CXR shows increased bilateral atelectasis and infiltrates. GFR 29 Temp 100.0F. BP 82/41 started on Levophed. Two hour post intubation ABG 7.298/54.6/236/26.7/-0.2. 12/30/21: Off Levophed and sedation, minimal response to painful stimuli. Afebrile, breathing only with vent, Bilevel 28/8 PS 20 RR 18 FiO2 45% sat 97%. WBC 13.4, Ferritin 108, GFR 23, Ddimer 2576, AST 71, ALT 50. 12/31/21: GFR 18 continues to be minimal nonpurposeful movement to painful stimuli off sedation. Sputum cx negative. End of life family meeting decide to make comfort care. @2020 terminal extubation with rapid decline and expiration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 22,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN; Hypercholesteremia; NIDDM type 2; CKD; HFpEF; AAA with repair
Andere Medikamente: -
Allergien: IVP, contrast dye, Iodine
Vorherige Impfungen: -

VAERS 2079407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: WI
Alter: 75,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 17.11.2021
Beginn: 23.01.2022
Tage bis Beginn: 67,0
Dosis: 3
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: OSC: COPD; pulmonary fibrosis; DM; CAD; HTN; obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2051545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: IL
Alter: 88,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 29.10.2021
Beginn: 17.01.2022
Tage bis Beginn: 80,0
Dosis: 1
Route/Site: IM / LA

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

Amnesia Aortic arteriosclerosis Aortic stenosis Bacterial test positive Bladder wall calcification Blood pH decreased Blood potassium increased COVID-19 Cardiac failure congestive Cardiomegaly Chest X-ray abnormal Cholelithiasis Computerised tomogram thorax abnormal Condition aggravated Cystitis Death Haematemesis Hepatic lesion

Symptomtext

Received pfizer vaccine on 10/29/21 and 11/19/21. COVID positive on 1/17/22. Presented to ER on 1/17/22 and admitted. presented 01/17/22 with hematemesis . It is noted that she was alert and oriented to person and place , but has short term memory loss. She was a nursing home resident. She also has history of combined CHF . CXR in ED showed congestive heart failure , small right pleural effusion. CT scan of chest showed large right and smaller left pleural effusions , extensive consolidative changes , calcific changes of posterior wall of urinary bladder , 1.5 cm right hepatic lobe posterior medial lesion of uncertain etiology , cholelithiasis , extensive arthrosclerotic changes abdominal aorta with areas of severe stenosis at level of proper haptic artery . She tested positive for COVID 19 01/17/22. She was noted to have hyperkalemia 5.6, INR elevated 1.4 , many bacteria in urine . She was admitted for upper GI bleed , acute cystitis , and COVID 19 infection. Patient became unresponsive , ABG showed PH 7.08 , PCO2 117 , PO2 55 on 6 L NC . She was tried on BIPAP with no improvement. Per chart review, family decided for comfort measures only. Patient passed away 01/18/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: 1/17/22 COVID 19: positive 1/17/22 chest xray: Cardiomegaly. Congestive heart failure.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, hx of PE
Andere Medikamente: Apixaban, ascorbic acid, calcium carbonate, vitamin D3, ferrous sulfate, furosemide, gentamicin eye drops, guaifenesin, norco PRN, lorazepam PRN, nystatin powder, pantoprazole, potassium chloride, multivitamin, zinc sulfate
Allergien: codeine
Vorherige Impfungen: -

VAERS 2000413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Coma Condition aggravated Fatigue Feeding disorder Feeling abnormal General physical health deterioration Loss of consciousness Memory impairment Respiratory rate decreased Immunisation Off label use Product use issue Thinking abnormal

Symptomtext

more or less in a coma; unable to eat; Felt tired; felt a "fog" on her brain; difficult to think; it got worse / condition had deteriorated rapidly; Booster; Other vaccine same date vaccine date 08Nov2021; Other vaccine same date vaccine date 08Nov2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 08Nov2021 14:30 (Lot number: 32030BD) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine inact sag 4v (FLUAD QUAD), administered in arm left, administration date 08Nov2021 (Lot number: 312879) as dose 1, single for immunisation. Relevant medical history included: "allergies: egg" (unspecified if ongoing), notes: known allergies: maybe eggs. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8730, Location of injection: Arm Right, Vaccine Administration Time: 13:15), administration date: 10Mar2021, when the patient was 68 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6199, Location of injection: Arm Right, Vaccine Administration Time: 13:15), administration date: 31Mar2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: OFF LABEL USE (hospitalization, medically significant), PRODUCT USE ISSUE (hospitalization, medically significant) all with onset 08Nov2021, outcome "unknown" and all described as "Other vaccine same date vaccine date 08Nov2021"; IMMUNISATION (hospitalization, medically significant) with onset 08Nov2021 14:30, outcome "unknown", described as "Booster"; FATIGUE (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "Felt tired"; FEELING ABNORMAL (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "felt a "fog" on her brain"; THINKING ABNORMAL (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "difficult to think"; CONDITION AGGRAVATED (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "it got worse / condition had deteriorated rapidly"; COMA (hospitalization, medically significant) with onset 09Nov2021 14:30, outcome "not recovered", described as "more or less in a coma"; FEEDING DISORDER (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "unable to eat". The patient was hospitalized for off label use, product use issue, immunisation, fatigue, feeling abnormal, thinking abnormal, condition aggravated (start date: 17Dec2021, hospitalization duration: 9 day(s)); for coma, feeding disorder (start date: 28Dec2021). The events "other vaccine same date vaccine date 08nov2021", "other vaccine same date vaccine date 08nov2021", "booster", "felt tired", "felt a "fog" on her brain", "difficult to think", "it got worse / condition had deteriorated rapidly", "more or less in a coma" and "unable to eat" were evaluated at the physician office visit and emergency room visit. It was reported the patient felt tired for 2 days then within the next 3 days felt a "fog" on her brain. She started to find it difficult to think. Over the next 2 weeks it got worse and the reporter took her to the emergency room (ER) on 27Nov2021. They could not find an answer; then they went to her family doctor and he did not have an answer. She was admitted to the hospital on 17Dec2021 as her condition had deteriorated in the previous 3 weeks. She was released to another hospital on 28Dec2021 where she was "more or less" in a coma unable to eat. The patient had not been tested for COVID post-vaccination. It was unknown if therapeutic measures were taken as a result of fatigue, feeling abnormal, thinking abnormal, condition aggravated, coma, feeding disorder..

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coma
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Egg allergy (known allergies: maybe eggs)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2000413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Coma Condition aggravated Fatigue Feeding disorder Feeling abnormal General physical health deterioration Loss of consciousness Memory impairment Respiratory rate decreased Immunisation Off label use Product use issue Thinking abnormal

Symptomtext

more or less in a coma; unable to eat; Felt tired; felt a "fog" on her brain; difficult to think; it got worse / condition had deteriorated rapidly; Booster; Other vaccine same date vaccine date 08Nov2021; Other vaccine same date vaccine date 08Nov2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 08Nov2021 14:30 (Lot number: 32030BD) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine inact sag 4v (FLUAD QUAD), administered in arm left, administration date 08Nov2021 (Lot number: 312879) as dose 1, single for immunisation. Relevant medical history included: "allergies: egg" (unspecified if ongoing), notes: known allergies: maybe eggs. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8730, Location of injection: Arm Right, Vaccine Administration Time: 13:15), administration date: 10Mar2021, when the patient was 68 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6199, Location of injection: Arm Right, Vaccine Administration Time: 13:15), administration date: 31Mar2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: OFF LABEL USE (hospitalization, medically significant), PRODUCT USE ISSUE (hospitalization, medically significant) all with onset 08Nov2021, outcome "unknown" and all described as "Other vaccine same date vaccine date 08Nov2021"; IMMUNISATION (hospitalization, medically significant) with onset 08Nov2021 14:30, outcome "unknown", described as "Booster"; FATIGUE (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "Felt tired"; FEELING ABNORMAL (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "felt a "fog" on her brain"; THINKING ABNORMAL (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "difficult to think"; CONDITION AGGRAVATED (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "it got worse / condition had deteriorated rapidly"; COMA (hospitalization, medically significant) with onset 09Nov2021 14:30, outcome "not recovered", described as "more or less in a coma"; FEEDING DISORDER (hospitalization) with onset 09Nov2021 14:30, outcome "not recovered", described as "unable to eat". The patient was hospitalized for off label use, product use issue, immunisation, fatigue, feeling abnormal, thinking abnormal, condition aggravated (start date: 17Dec2021, hospitalization duration: 9 day(s)); for coma, feeding disorder (start date: 28Dec2021). The events "other vaccine same date vaccine date 08nov2021", "other vaccine same date vaccine date 08nov2021", "booster", "felt tired", "felt a "fog" on her brain", "difficult to think", "it got worse / condition had deteriorated rapidly", "more or less in a coma" and "unable to eat" were evaluated at the physician office visit and emergency room visit. It was reported the patient felt tired for 2 days then within the next 3 days felt a "fog" on her brain. She started to find it difficult to think. Over the next 2 weeks it got worse and the reporter took her to the emergency room (ER) on 27Nov2021. They could not find an answer; then they went to her family doctor and he did not have an answer. She was admitted to the hospital on 17Dec2021 as her condition had deteriorated in the previous 3 weeks. She was released to another hospital on 28Dec2021 where she was "more or less" in a coma unable to eat. The patient had not been tested for COVID post-vaccination. It was unknown if therapeutic measures were taken as a result of fatigue, feeling abnormal, thinking abnormal, condition aggravated, coma, feeding disorder..

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coma
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Egg allergy (known allergies: maybe eggs)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2034673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: CA
Alter: 73,0
Geschlecht: U
Eingang: 14.01.2022
Impfdatum: 02.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: - / RA

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

Blood creatinine Blood test Computerised tomogram thorax Dyspnoea Embolism Fibrin D dimer Full blood count Immunisation Investigation Liver function test Pain Pulmonary embolism Pulmonary infarction

Symptomtext

Booster; I am in the hospital with pulmonary embolism; clot; pulmonary infract which is going to affect my lungs; couldn't breathe; Pain; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 73 year-old patient received bnt162b2 (BNT162B2), administered in arm right, administration date 02Dec2021 (Lot number: 32030BD) at the age of 73 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1, Manufacturer- Unknown), for COVID-19 Immunization; Covid-19 vaccine (Dose 2, Manufacturer- Unknown), for COVID-19 Immunization. The following information was reported: IMMUNISATION (hospitalization, medically significant) with onset 16Dec2021, outcome "unknown", described as "Booster"; PULMONARY EMBOLISM (hospitalization, medically significant) with onset 16Dec2021, outcome "unknown", described as "I am in the hospital with pulmonary embolism"; EMBOLISM (medically significant), outcome "unknown", described as "clot"; PULMONARY INFARCTION (medically significant), outcome "unknown", described as "pulmonary infract which is going to affect my lungs"; DYSPNOEA (medically significant), outcome "unknown", described as "couldn't breathe"; PAIN (medically significant), outcome "unknown", described as "Pain". The patient was hospitalized for pulmonary embolism (start date: 16Dec2021). The events "i am in the hospital with pulmonary embolism", "clot", "pulmonary infract which is going to affect my lungs", "couldn't breathe" and "pain" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: blood creatinine: unknown results; blood test: unknown results; computerised tomogram thorax: unknown results, notes: Chest; unknown results; fibrin d dimer: unknown results, notes: For blood clot; full blood count: unknown results; investigation: unknown results, notes: various other test; liver function test: unknown results. Therapeutic measures were taken as a result of pulmonary embolism, embolism, pulmonary infarction, dyspnoea, pain. Clinical course: "I ended up in emergency department and I am in the hospital with pulmonary embolism (Further clarification unknown for duration and reason of hospitalization, hence Seriousness criteria was left unchecked). after I received the booster shot. Start date for Adverse event: Nurse stated, "I had the side effect probably (Incomplete Sentence) well the event that took me to the hospital was on 16Dec not this year last year 2021 (Further not clarified) that is where I ended up in the hospital in the emergency department then I was hospitalized now I am on anticoagulant (Intent Treatment).Anatomical site of adverse event: Nurse stated, "It was in my right arm. Causality: Nurse stated, "Yes, I believe it was related, I have never had pulmonary embolism before and I am generally very healthy and I know that the some of the vaccine can cause clot (Further clarification unknown, hence Ae captured conservatively) so right now I have pulmonary infract which is going to affect my lungs." "I wasn't on any medication at all until I received the vaccines after that I am on blood thinners or anticoagulant. I was in the emergency department I couldn't breathe I had been given morphine for the pain and I was fine and three people die (Further not clarified, hence split not made) from pulmonary embolism if not treated. I feel I am very fortunate I am still alive today." (Further clarification unknown). Treatment (Morphine): Nurse stated, "Yes and it was diluted with the other pain medication. They treated me initially with I.V heparin, after I received the I.V heparin they switched over to me lovenox which is injectable medicine. I was discharged with that and I had to give myself Lovenox injection twice a day for 5 days and now, I am on Pradaxa which is anticoagulant now put me on that for next six months."; Sender's Comments: Based on the available information and a possible contributory role of the suspect product BNT162B2 to the development of events cannot be totally 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 re-sponse, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Test Name: creatinine; Result Unstructured Data: Test Result:unknown results; Test Name: blood test; Result Unstructured Data: Test Result:unknown results; Test Name: CT of my chest; Result Unstructured Data: Test Result:unknown results; Comments: Chest; Test Name: CT pulmonary angiogram; Result Unstructured Data: Test Result:unknown results; Test Name: D-Dimer test; Result Unstructured Data: Test Result:unknown results; Comments: For blood clot; Test Name: cbc; Result Unstructured Data: Test Result:unknown results; Test Name: test; Result Unstructured Data: Test Result:unknown results; Comments: various other test; Test Name: liver function test; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: TX
Alter: 84,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 16.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 46,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Death Diarrhoea General physical health deterioration

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/19/2021, 2/9/2021, and 11/16/2021. Patient presented to ED on 1/1/2022 with complaints of diarrhea that has been progressively getting worse for the past two days. Patient had been previously diagnosed with COVID and had received bamlanivimab and etesevimab on 12/24/2021. On 1/5/2022 patient decompensated and expired on 1/7/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, Hyperlipidemia, BPH, Waldenstrom's, Anxiety
Andere Medikamente: Aspirin 81 mg QD, Desvenlafaxine 100 mg QD, Adderall 20 mg TID, Enalapril 10 mg QD, Hydrochlorothiazide 25 mg QD, Lorazepam 0.5 mg BID, Metoprolol 50 mg QD, Mirtazepine 30 mg QD, Olanzepine 7.5 mg QD, Simvastatin 40 mg QD, Tamsulosin 0.4 mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1989016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: WI
Alter: 72,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 14.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

fully vaccinated-covid related death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Complications of combined systolic and diastolic CHF,DM2; CAD; HTN; HLD; a-fib; Hx of TIA; obesity; psoriasis with immunosuppressant therapy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1961975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 30.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Pulmonary embolism Thrombosis

Symptomtext

PATIENT REPORTED TODAY THAT HE WAS ADMITTED TO HOSPITAL 12/10-12/12/21 FOR LEFT LEG BLOOD CLOT AND PULMONAY EMBOLISM POSSIBLY CONNECTED TO COVID VACCINE. HE PRESENTED VISIT VERIFICATION PAPERWORK STATING THAT. WORKUP IS CURRENTLY ONGOING FOR OTHER CAUSES OR RISK FACTORS FOR BLOOD CLOTS. UNTIL WORKUP IS COMPLETE AND REVIEWED BY OUTPATIENT PRIMARY CARE PHYSICIAN, WOULD RECOMMEND PATIENT DEFER FURTHER COVID VACCINATION UNTIL WORKUP IS COMPLETE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: DIVALPROEX DR 250MG
Allergien: NSAIDS
Vorherige Impfungen: -

VAERS 1932979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: IL
Alter: 44,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure Angiogram pulmonary abnormal COVID-19 Cough Dyspnoea Infection Lung opacity Pneumonia bacterial Pulmonary mass Pyrexia SARS-CoV-2 test positive Superinfection

Symptomtext

Came to ER on 11/27/21. Received 2nd dose of COVID vaccine on 11/17/21. Developed fever on next day Until yesterday. Developed dry cough and shortness of breath for last 3 days, She went to an urgent care, Saturation 86-88% on room air. Transfer to ED for further management. Found to be COVID positive. Was placed on HFNC @4L. Placed on remdesivir and dexamethasone. Also placed on ceftriaxone and doxycycline. Was admitted 11/27/21 for acute hypoxemic respiratory failure secondary to COVID 19 viral and suspected superimposed bacteria pneumonia , also have right middle lobe cavitary lesion . Was on room air on 12/3/21 which patient was discharged

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: 11/27/21 COVID19: positive 11/27/21 CTA chest: Extensive bilateral airspace disease and ground-glass opacities within both lungs most consistent with multifocal infection. COVID-19 pneumonia could have this appearance. However, in addition, there is cavitary nodular densities within the right middle lobe which are not common in COVID-19. Other atypical or fungal infection is a possibility. Metastatic disease could have this appearance. Septic emboli thought less likely. Recommend follow-up/further evaluation.
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes (HCC) and Obesity, Class II, BMI 35-39.9
Andere Medikamente: Metformin and tramadol PRN
Allergien: -
Vorherige Impfungen: -

VAERS 1903733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: NC
Alter: 38,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Breast pain Chest discomfort Dyspnoea Immunisation Myocardial infarction Pain SARS-CoV-2 test

Symptomtext

heart attack; Short breaths; My left side of my chest was being stabbed; My left breast I wanted to rip out; pain; the patient received third dose; This is a spontaneous report from a contactable consumer (patient). A 38-years-old non-pregnant female patient received third dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: 32030BD), via an unspecified route of administration, administered in arm left on 11Nov2021 at 18:00 (at the age of 38-years-old) as dose 3 (booster), single for covid-19 immunization. Medical history included allergy to mango and generic depo, endometriosis and autoimmune thyroiditis from an unknown date and unknown if ongoing. The patient previously received other vaccine in four weeks which included flu shot on 28Oct2021. Concomitant medications included unspecified other medications in two weeks. Prior to vaccination, the patient was not diagnosed with covid-19. The patient historical vaccines included first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number Er8729), via an unspecified route of administration, administered in arm left on 18Mar2021 as dose 1, single for covid-19 immunization and second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number Er8729), via an unspecified route of administration, administered in arm left on 08Apr2021 as dose 2, single for covid-19 immunization. On 11Nov2021 at 18:00, the patient received third dose of vaccine (coded to booster). On 11Nov2021 at 22:00, the patient thought she was having a heart attack, her left side of chest was being stabbed. She wanted to rip out her left breast. She had short breaths. Next day she could not say full sentences and was still in pain, but better. The patient underwent lab test and procedures which included sars-cov-2 test (nasal swab): negative on 05Sep2021. The patient did not receive any treatment. Device date was reported as 13Nov2021. The outcome of the event pain was recovering and for all other events was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Date: 20210905; Test Name: covid test; Test Result: Negative ; Comments: nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Endometriosis; Fruit allergy; Hashimoto's disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1868183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

kritisch

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 27.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

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

Atrial fibrillation Chest pain Hypertension Myocardial infarction Pericarditis

Symptomtext

Systemic: Heart Attack-Medium, Systemic: Hypertension-Medium, Additional Details: per patient she experienced chest pain and high blood pressure and went to urgent care & emergency room. She was admitted to the hospital and MD reported she had A.fib, pericarditis, heart attack, and high blood pressure. she got discharged with losartan, asa, pepcid, metoprolol, plavix, lipitor and nitroglycerin SL

Weitere VAERSDATA-Felder

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

VAERS 1829041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

kritisch

Staat: OH
Alter: 83,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 25.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac arrest

Symptomtext

Patient went into cardiac arrest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: COPD
Vorgeschichte: COPD, Cardiomegaly, CHF, Anemia, Sick Sinus Syndrome, Hypertension, A-Fib, Heart Valve Disease, Type 2 Diabeties
Andere Medikamente: Anoro, ellipta, Atorvastatin, B-12 Injection, Fenofibrate, Ipratropium albutarol, Juvan, Lasix, Lisinopril, Metformin, Metoprolol Tartrate Omepralzole, Spironolactone, multi vitamin, Tramadol, Vascepa, Vitamin D Sugar Free Med Pass
Allergien: NKA
Vorherige Impfungen: -

VAERS 2402960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 08.11.2021
Beginn: 31.07.2022
Tage bis Beginn: 265,0
Dosis: 1
Route/Site: - / -

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

Angiogram pulmonary normal Arteriogram coronary normal Arthralgia Back pain COVID-19 Chemotherapy Chest pain Constipation Decreased appetite Dyspnoea Echocardiogram normal Electrocardiogram ST segment elevation Lung adenocarcinoma Pericarditis Productive cough Radiotherapy Right ventricular ejection fraction decreased SARS-CoV-2 test positive

Symptomtext

7/31--8/3 48-year-old male with past medical history significant for COPD and newly diagnosed right sided adenocarcinoma of the lung. He presented on 7/31/2022 for complaint of chest pain. He initially presented to Facility on 7/30 for the same complaint and his EKG revealed ST elevation in leads II, III and aVF as well as V4 through V6. He was transferred here to Facility for higher level of care. He was taken to the Cath Lab emergently, but the angiogram revealed normal coronaries. He was also found to be COVID-positive. This is a new infection as he had a recent negative COVID test on 7/2/2022. Of note he was recently discharged from Facility after a long hospital stay from 7/6 until 7/19 for an acute SVC syndrome secondary to his lung carcinoma. At that time he was treated with chemotherapy and a few bouts of radiation with resolution of his symptoms. Given his COVID-positive status and the recent radiation, his chest pain was considered to be an acute pericarditis. He was requiring 2 L nasal cannula of oxygen during his stay, thus he was started on Decadron 6 mg daily to treat his COVID as well as treating his pericarditis until discharge. He was also started on Remdesivir 100mg IV once daily on 7/31 and Robitussin by ID for COVID. 7/31 he was no longer needing supplemental oxygen, saturating well on room air. Troponin wnl. CTA PE on 7/31 was negative for PE and 2D echo on 8/1 had no pericardial effusion visualized but was limited as patient could not turn; L ventricle normal size with EF 55% and R ventricle moderately decreased. During admission, WBC was up-trending, and he continued to have unchanged R back and R shoulder pain, some relief with leaning forward. IV morphine for breakthrough pain started on 8/1 was switched to Percocet on 8/2 every 6 hours for longer pain relief. Chest pain improved over the 3 day stay and he regained his appetite and was able to eat full meals starting 8/2. His constipation improved as well and he did not need bowel regiment on 8/2. He continued to have sputum production once a day with relief of SOB after coughing out sputum. He was continued on abluterol and breo during his stay. Hemeonc withheld chemo and radiation in the context of his current COVID + status. Prior to discharge, cardiology recommended discontinuing Decadron and beginning colchicine 0.6mg daily (weight adjusted) until followup with them in outpatient clinic. Patient has been saturating well on room air for over 3 days and he is stable for discharge home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 7/31-- SARS-CoV-2 by NAA, detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: CT
Alter: 65,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / UN

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

Anxiety Arthralgia Balance disorder Bruxism Cataract operation Chest discomfort Computerised tomogram Depression Dysphagia Electric shock sensation Fatigue Feeling hot Foot fracture Gait disturbance Headache Impaired work ability Limb discomfort Loss of personal independence in daily activities

Symptomtext

He got his vaccine and also got his high dose flu and pneumonia vaccine at the same time. He had no reaction except feeling warmth like stream down his arm. He went to work afterwards and stayed until 10:00 PM and had no issues. He woke up the next morning, the arm was aching like normal, was fatigued, in pain with his neck and head, which he thought was a sinus problem. He had some itching as well. Then other things started happening, he felt like there was electricity coming of them, tingling. He also felt like he had an ice pick stuck in the middle of his head between his eyes, and had difficulty swallowing, feeling like esophagus is tight, tightness in chest. Is shaking all of the time, he is unsteady and stumbled and broke his foot. He is also having pain in his joints, heavy leg syndrome, vision problems, had cataracts removed and now has worse vision than he ever had before. He suffers now from depression and anxiety since getting the vaccine. He now sees a psychiatrist and a neurologist. He was then diagnosed with possible TMJ problems, went to doctor, had a CAT scan and cone scan, and did not see problems with his jaw other than bruxism. He also has some other problems happening, and his neurologist said he did not have TMJ. His neurologist believes his problems could be related to the vaccine as he did not have those problems prior. He now takes Zoloft, Xanax, Divaleroex-ER 250 mg 2 every night at bedtime to sleep. She wants to some type of new therapy to help him, but there are a lot of side effects and will FU with her to see what the next step could be. He has now not worked since 10/25/2021, and he was slowly phased out of his position and having his title/computer and other company property changed. He is now on a leave of absence after being on short term disability. He does not see any improvement and is trying to get on disability due to this condition. He has worked for the company for 18 years. He was on short term disability, now on leave of absence and trying to get on permanent disability. He continues to have pain in his head, temples, and other parts of his body. Was put on medications by the doctor, students and they gave him muscle relaxers and anti-inflammatories which did help some. He has internal shaking all over his body, vibration like sensation all the time. His hands also shake if he tries to hold something. It is hard for him to do anything. His vision also seems to be worsening. He is now struggling and cannot work due to his current condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: 2 CT scans, MRI, Cone scan.
Aktuelle Erkrankungen: Persistent headaches after 2nd vaccine.
Vorgeschichte: None.
Andere Medikamente: Certirizine 10 mg.
Allergien: Penicillin, IV contrast dye.
Vorherige Impfungen: 2nd vaccine had headaches, which he thought was from a sinus infection, but then had the 3rd vaccine and symptoms have exacerbat

VAERS 2258527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: MD
Alter: 34,0
Geschlecht: M
Eingang: 29.04.2022
Impfdatum: 18.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Computerised tomogram Deep vein thrombosis Scan with contrast Ultrasound scan

Symptomtext

DVT OF 5 VEINS UPPER LEFT EXTREMITY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 1,0
Labordaten: ER RAN TESTS ON 11/30 (ULTRASOUND, CT SCAN W/ AND W/O CONTRAST, BLOOD TESTS...)
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: FENASTERIDE, MELATONIN, VIT B, VIT D, GERD MEDICATION
Allergien: NONE
Vorherige Impfungen: -

VAERS 2068112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

schwer

Staat: WV
Alter: 43,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 06.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: - / RA

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

Asthenia Chest pain Dizziness Dyspnoea Hot flush Impaired work ability Myalgia Pain in extremity SARS-CoV-2 test Syncope Vision blurred

Symptomtext

fainting; Chest pain; shortness of breath; blurred vision; dizzy; Haven't been able to work with all this; left arm pain; weakness; hot/flush; muscle pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 06Nov2021 11:00 (Lot number: 32030bd) at the age of 43 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Thyroid disease" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "Penicillin allergy" (unspecified if ongoing); "covid " (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL; LEVOTHYROXINE; OMEPRAZOLE; ASPIRIN [ACETYLSALICYLIC ACID] and anodizing. The following information was reported: SYNCOPE (medically significant) with onset 18Nov2021 17:30, outcome "not recovered", described as "fainting"; CHEST PAIN (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "Chest pain"; DYSPNOEA (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "shortness of breath"; PAIN IN EXTREMITY (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "left arm pain"; ASTHENIA (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "weakness"; HOT FLUSH (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "hot/flush"; DIZZINESS (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "dizzy"; VISION BLURRED (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "blurred vision"; MYALGIA (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "muscle pain"; IMPAIRED WORK ABILITY (non-serious) with onset 18Nov2021 17:30, outcome "not recovered", described as "Haven't been able to work with all this". The events "fainting", "chest pain", "shortness of breath", "left arm pain", "weakness", "hot/flush", "dizzy", "blurred vision", "muscle pain" and "haven't been able to work with all this" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: negative. Therapeutic measures were not taken as a result of syncope, chest pain, dyspnoea, pain in extremity, asthenia, hot flush, dizziness, vision blurred, myalgia, impaired work ability.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; COVID-19; Penicillin allergy; Thyroid disorder
Andere Medikamente: METOPROLOL; LEVOTHYROXINE; OMEPRAZOLE; ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2057436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 08.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: OT / -

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

General physical health deterioration Loss of consciousness Memory impairment Respiratory rate decreased

Symptomtext

Basically unconscious; Very slow breathing; Memory started to deteriorate; Condition continued to deteriorate / was deteriorating rapidly; This spontaneous case was retrieved on 20-Jan-2022 from Vaccine Adverse Event Reporting System (VAERS) (reference number: 2000413-1), reported by other non-healthcare professional and concerned a 69-year-old, female patient. The patient's concurrent condition included allergy to eggs (also reported as 'maybe eggs'). The patient's concomitant medications were not reported. On 08-Nov-2021, the patient was vaccinated with Fluad Quadrivalent (influenza vaccine, inactivated influenza virus surface antigen (subunit), egg-derived, mf59; dose: reported as 'one', route of administration: intramuscular (IM), anatomical location: reported as 'in 2 different arms' and indication: not reported. The batch number reported was 312879. On the same day, the patient was vaccinated with non-company co-suspect Pfizer BioNTech COVID-19 vaccine (tozinameran; dose: reported as 'third', route of administration: IM, anatomical location: reported as 'in 2 different arms' and indication: not reported. The batch number reported was 32030BD. On 10-Nov-2021, two days after receiving Fluad Quadrivalent and Pfizer BioNTech COVID-19 vaccine, the patient's memory started to deteriorate. On 27-Nov-2021, the patient was admitted to emergency room (ER) where they did a battery of test and could find nothing wrong. On an unspecified date in 2021, over the next three weeks, as reported, the patient's condition continued to deteriorate. On 17-Dec-2021, the patient was admitted to the hospital. Again they could find nothing wrong and she was deteriorating rapidly. On 27-Dec-2021, the patient was discharged from hospitala and moved to hospice care. On an unspecified date, the patient was basically unconscious with very slow breathing. At the time of initial reporting, the patient had not recovered from the events. The reporter did not provide a causality assessment. All events were assessed as serious due to seriousness criteria of life-threatening condition, disability and hospitalisation. Additionally, the event of 'unconscious' was considered to be medically significant by Physician within regulatory authority. Company comment: A 69-year-old patient experienced memory impairment on the same day after receiving the suspect product Fluad Quadrivalent and non-company co-suspect Pfizer BioNTech COVID-19 vaccine. The patient also developed loss of consciousness, general physical health deterioration, and decreased respiratory rate an unknown amount of time after vaccination. Advance age of patient contributed to the development of the events memory impairment and general physical health deterioration. Based on biological implausibility and confounding factor, causality for the event memory impairment is assessed as not related. For the rest of the events causality is unassessable, due to unclear time relationship.; Sender's Comments: A 69-year-old patient experienced memory impairment on the same day after receiving the suspect product Fluad Quadrivalent and non-company co-suspect Pfizer BioNTech COVID-19 vaccine. The patient also developed loss of consciousness, general physical health deterioration, and decreased respiratory rate an unknown amount of time after vaccination. Advance age of patient contributed to the development of the events memory impairment and general physical health deterioration. Based on biological implausibility and confounding factor, causality for the event memory impairment is assessed as not related. For the rest of the events causality is unassessable, due to unclear time relationship.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: Egg allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2019937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: PR
Alter: 22,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 09.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Exercise tolerance decreased Gastrooesophageal reflux disease Magnetic resonance imaging abnormal Myocardial necrosis marker increased Myocarditis

Symptomtext

Myocarditis, extreme chest pain on ocations, and acid reflux. 1 week of hospitalization on november 28th, 2021 Aspirin Ibuprofen 3 times a day and colchicine once a day Outcomes: while the chest pain has releived, I am now NOT able to lift heavy weights or do any exercise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 5,0
Labordaten: Heart enzymes were above 5,000 on day of hospitalization, gradually going down afterwards MRI Catheterism Studies showed potential myocardial infarction and pericardial effusion
Aktuelle Erkrankungen: Acute gastritis
Vorgeschichte: -
Andere Medikamente: Clonazepam 0.5 MG twice times a day Bupropion XL 300 MG once a day Tadafil 20 MG twice a week
Allergien: No
Vorherige Impfungen: -

VAERS 1982427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: WI
Alter: 91,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 28.10.2021
Beginn: 16.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

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

Blood test abnormal Brain natriuretic peptide increased Cardiac failure congestive Cardiac ventricular thrombosis Chest X-ray Echocardiogram abnormal Left ventricular dysfunction Troponin increased

Symptomtext

The patient developed symptoms of congestive heart failure about 1-2 weeks after receiving her COVID booster. She presented to the ED on 11/15/2021 with clinical evidence of congestive heart failure. An echocardiogram revealed severe global left ventricular systolic dysfunction with multiple mobile echodensities noted within the left ventricle suggestive of thrombi. Clinical picture and left ventricular thrombi were suggestive of possible underlying myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac ventricular thrombosis
Hospital-Tage: 8,0
Labordaten: 11/15/2021 Blood tests including elevated troponin and BNP, CXR 11/16/2021 Echocardiogram
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension, hyperlipidemia
Andere Medikamente: Quinapril
Allergien: None.
Vorherige Impfungen: -

VAERS 1963467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: WI
Alter: 90,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 12.03.2021
Beginn: 16.11.2021
Tage bis Beginn: 249,0
Dosis: 3
Route/Site: IM / UN

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

Cardiac ventricular thrombosis Chronic left ventricular failure Hypercoagulation

Symptomtext

1. Chronic systolic heart failure She is clinically stable at this time. Time course and clinical picture suggest possible vaccine associated myocarditis. Continue GDMT including furosemide, lisinopril, metoprolol and spironolactone. She will also be seen in heart failure clinic. 2. Left ventricular thrombi Possibly secondary to myocarditis with hypercoagulable state as noted above. Continue warfarin. Repeat echocardiogram in about 6-8 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac ventricular thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cardiovascular and Mediastinum Essential hypertension Nonischemic cardiomyopathy (HCC) Varicose veins of legs (Hx of varicose ulcer) Left ventricular thrombus Severe aortic stenosis Heart failure with reduced ejection fraction (HCC)
Vorgeschichte: Nervous and Auditory Benign positional vertigo Confusion Musculoskeletal and Integument Degenerative joint disease involving multiple joints Osteoporosis Other Hyperlipidemia History of allergic rhinitis Stress bladder incontinence, female Edema of extremities Glaucoma Chronic low back pain Memory loss Heart murmur, systolic Generalized weakness Hyponatremia Fall with generalized weakness Elevated troponin Elevated CK Warfarin anticoagulation
Andere Medikamente: unknown
Allergien: Duricef [cefadroxil
Vorherige Impfungen: -

VAERS 1943423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: PA
Alter: 16,0
Geschlecht: F
Eingang: 13.12.2021
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

Loss of consciousness Pallor

Symptomtext

Patient became pale and passed out 3 minutes after injection. BP; 86/60 Pulse: 53 RR: 20 O2 Sat: 98%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: history of fainting in the past with vaccine

VAERS 1888926

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: IN
Alter: 28,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Dizziness Feeling hot Headache Hyperhidrosis Pallor Paraesthesia Presyncope

Symptomtext

PATIENT RECEIVED A BOOSTER SHOT OF PFIZER AND HAD A VAGAL RESPONSE. SHE STARTED TO SWEAT AND TURN PALE. SHE FELT FAINT AND WEAK. BP WAS 127/83 P 77. SHE COMPLAINED OF HER FEET TINGLING. I KEPT HER TALKING SO SHE DIDN'T PASS OUT. SHE WAS HOT AND SWEATING AFTER 5MINS HER COLOR CAME BACK AND SHE WAS NO LONGER SEEING SPOTTY. SHE WAS NO LONGER FEELING WEAK AND FAINT BUT COMPLAINED OF A HEADACHE AND LEG TINGLING. SHE HAD SOME WATER AND WAS GIVEN SOME ORANGE JUICE. HER BP WAS 115/75 P 64. SHE FELT FINE AFTER A FEW MORE MINUTES AND THEN LEFT.

Weitere VAERSDATA-Felder

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

VAERS 1877730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: OH
Alter: 31,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Seizure

Symptomtext

patient's mother reported she experienced a seizure on 11/14/21 at 03:00 patient has not has a seizure since 5/20/2019

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: history of seizures - last recorded seizure 5/20/2019
Andere Medikamente: albuterol, iron, ibuprofen, famotidine, prednisone
Allergien: none known
Vorherige Impfungen: -

VAERS 1877653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: FL
Alter: 23,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Chest pain Electrocardiogram abnormal Myocarditis Pericarditis

Symptomtext

Pt reported chest pain at midnight on Friday, 11/5; presented to ER on Saturday, 11/6 after intermittent chest pain. Saturday?s chest pain was non-relenting; pt admitted to hospital. He received a NSAID on 11/6 in the am and 11/7 at approx 1am, with an asa in between. Pt received nitroglycerin between 1am-2am on 11/7, as well as oxygen due to non-reduction of chest pain with nsaid administration. Pt remained hospitalized until 11/9, and followed proper with his cardiologist, on 11/17. The pt was discharged without meds.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: Please contact facility, for detailed tests and results. The EKG showed acute pericarditis, leading to a diagnosis of myocarditis.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1877541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: NC
Alter: 16,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Dizziness Seizure

Symptomtext

Patient visibly upset before receiving vaccine but did go ahead and receive She then went to waiting area where she felt faint and other RPh said she had what looked to be a small seizure for a very brief moment but then she came to and was feeling ok--EMS came and checked her out and she left with her family without any assistance

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: has had seizures in the past but mother said it had been a few years since she had one
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1873457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: MO
Alter: 42,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Loss of consciousness

Symptomtext

PT FELT DIZZY AND LOST CONSCIOUSNESS FOR 1-2 SECONDS AFTER RECEIVING FIRST DOSE OF PFIZER VACCINE, ABOUT 5 MINUTES POST ADMINISTRATION. PT STATES HAS HAD VASOVAGAL REACTION IN THE PAST WITH BLOOD DRAW. PT RECOVERED AFTER LAYING DOWN WITH LEGS UP AND DRINKING SOME WATER AND ORANGE JUICE.

Weitere VAERSDATA-Felder

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

VAERS 1869854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Fall Humerus fracture Syncope X-ray limb abnormal

Symptomtext

13 hours after administration of vaccine, episode of syncope walking towards bathroom Fall resulted in fractured left humerus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 11/07/2021 X-rays showing at least 2 views of the shoulder
Aktuelle Erkrankungen: none
Vorgeschichte: Nephrolithiasis Hypertension Hypercholesterolemia Osteopenia Hypercalcemia Hyperparathyroidism Hypothyroidism Psoriasis Anemia Hair loss
Andere Medikamente: Atorvastatin (LIPITOR) Escitalopram oxalate (LEXAPRO) Spironolactone (ALDACTONE) Vitamin D3 Biotin
Allergien: Propofol Fentanyl Percocet Percodan Midazolam Hydromorphone Dexamethasone sodium phosphate
Vorherige Impfungen: -

VAERS 1867755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: CO
Alter: 37,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Dizziness Hyperhidrosis Pallor Presyncope Supine position Vital signs measurement

Symptomtext

Patient had a vasovagal response after shot given. Patient diaphoretic, pale and dizzy, never lost consciousness about 5 minutes after administration of vaccine. Patient was placed in supine position with knees bent, vital signs stable, water given. Patient made full recovery in 10 minutes after laying supine with with stable vital signs.

Weitere VAERSDATA-Felder

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

VAERS 1853773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: OH
Alter: 13,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 22.10.2021
Beginn: 07.11.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / RA

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

Electrocardiogram Loss of consciousness

Symptomtext

Passed out while taking a shower

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: ECG, possible left ventricular hypertrophy
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 1849085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: IN
Alter: 25,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cold sweat Feeling hot Hyperhidrosis Peripheral coldness Syncope Tinnitus Tremor Visual impairment

Symptomtext

PATIENT COLAPSED AFTER VACCINE BP 114/66 HAD RINGING OF EARS, COLD CLAMY HANDS, GRAINY/DARK VISION. HE HAD NO PAIN OR PHYSICAL INJURY. BP RETESTED 125/85 --PT WAS FEELING BETTER BUT WAS HOT SWEATING AND SLIGHTLY SHAKEN. HE WAS OBSERVED FOR 30 MINS THEN RELEASED IN HIS OWN CARE

Weitere VAERSDATA-Felder

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

VAERS 1848651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: IL
Alter: 33,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Flushing Hyperhidrosis Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Medium, Additional Details: Patient stated that his blood pressure does goes low frequently. We provided him with water. We checked his blood pressure 5min after receiving injection and it was 68/40mmHg (HR 47). His blood pressure 15min after receiving the vaccination was 107/65mmHg (HR 48). Patient was feeling much better 30min after receiving vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1847406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

schwer

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Cold sweat Dizziness Pallor Presyncope

Symptomtext

A couple of minutes after receiving the first dose of Pfizer, patient felt faint, was clammy and pale. BP 58/38 HR 62, SAO2 98%,. Appeared to be having a vaso vagal episode. Never lost consciousness. Patient taken by wheelchair to cot, laid supine, legs up. BP then 110/66 HR 83. Patient feeling better. Patient able to sit up and drink water, ?feeling normal?. BP 107/67 HR 82 and discharged in stable condition with mom. Patient and mom stated that pt was extremely nervous and anxious about vaccine and stated that he is scared of needles.

Weitere VAERSDATA-Felder

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

VAERS 1847181

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 32030BD

schwer

Staat: PA
Alter: 31,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Loss of consciousness Malaise Vomiting

Symptomtext

Patient said he did not feel well, As we were attending to him he started to lose consciousness. We laid him down, within a minute he regained consciousness and after throwing up, over the next hour pt gradually felt better, only complaint is that he felt tired. His parents came in and took him home.

Weitere VAERSDATA-Felder

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

VAERS 1836690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: TN
Alter: 77,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Deep vein thrombosis Pain in extremity Ultrasound scan

Symptomtext

PATIENT STARTED TO EXPERIENCE LOWER EXTREMITY LEG PAIN SHORTLY AFTER RECEIVING BOOSTER PFIZER DOSE. HE WENT TO THE ER 5 DAYS POST VACCINE AND WAS DIAGNOSED WITH LOWER LEFT LEFT DVT. PATIENT CONTINUED XARELTO THERAPY 20MG DAILY. PATIENT WAS ALREADY ON XARELTO 20MG DAILY FOR PREVIOUS DVTS (SINCE 2007).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: ULTRASOUND 11/1/2021
Aktuelle Erkrankungen: PREVIOUS BLOOD CLOT IN A SEPERATE AREA OF THE BODY
Vorgeschichte: BLOOD CLOT
Andere Medikamente: XARELTO 20MG
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 1834467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: WI
Alter: 56,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Paraesthesia Syncope

Symptomtext

about 10 minutes after vaccination, the patient reported tingling in the arms, feeling light headed, brief syncope, patient self recovered without intervention but was given water and watched for further reaction until EMS arrived. Patient ultimately walked out of the store with EMS and I (the pharmacist) am unaware of what happened to the patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EMS took blood pressure and reported it as 116/78 mmHg
Aktuelle Erkrankungen: None reported
Vorgeschichte: Stage 4 Non-hodgkins Lymphoma others are not known
Andere Medikamente: Unknown
Allergien: None reported on Vaccine administration Record
Vorherige Impfungen: -

VAERS 1832956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: NY
Alter: 38,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 31.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Amnesia Cold sweat Dizziness Loss of consciousness Nausea Retching Tremor

Symptomtext

I woke up around 5 am to go to the bathroom. On the way, I started feeling nauseous and a little lightheaded. I don't recall what happened next but I woke up with my head next to the toilet and my right hand in the toilet bowl. After coming to, I continued to feel nauseous and dry-heaved 3 or 4 times followed by intense trembling and cold sweat running down my face. After about 5 minutes, I felt better and have had no more adverse symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Type 1 diabetes
Vorgeschichte: Type 1 diabetes
Andere Medikamente: Insulin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1832238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: IN
Alter: 23,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

Patient fainted approximately 5 minutes after receiving the vaccine and was unconscious for about 30 seconds. To note, patient hadn't eaten before receiving the vaccine. We had her seat for 30 minutes and gave her orange juice and water.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: OMEPRAZOLE, SPRINTEC,SERTRALINE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1831693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: NY
Alter: 16,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Immediate post-injection reaction Seizure

Symptomtext

Patient experienced 2 seizure immediately following administration of vaccine, each less than 1 minute.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Seizure disorder
Andere Medikamente: Lamictal, birth control
Allergien: none
Vorherige Impfungen: -

VAERS 1831465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Flushing Hyperhidrosis Nausea Syncope Tremor Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Nausea-Medium, Systemic: Shakiness-Medium, Systemic: Vomiting-Medium

Weitere VAERSDATA-Felder

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

VAERS 1808528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

schwer

Staat: KY
Alter: 25,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Feeling abnormal Seizure Syncope

Symptomtext

The patient received the 3rd dose of pfizer COVID-19 on 10-22-21 at 4:51 pm. The patient was feeling ok and was in the store waiting the allotted 15 minutes. After about 10 minutes, she returned to the immunization room saying she did not feel ok. She started to faint and had a what appeared to be a small seizure. 911 was called, an Epi-pen was administered and her vitals were monitored. She began to respond immediately to the epi-pen and was directed to go to the emergency room by EMS and staff. The patient's mom picked her up and took her to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: lo loestrin
Allergien: slight allergy to latex (gets a rash if latex gloves are used)
Vorherige Impfungen: -

VAERS 1808119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: -
Alter: 35,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 19.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / -

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

Catheterisation cardiac abnormal Chest pain Electrocardiogram ST segment abnormal Intensive care Myocarditis Troponin increased

Symptomtext

ADVERSE EVENT: MYOPERICARDITIS Patient received 2nd dose of Pfizer Covid-19 vaccine on 10/19/21. On 10/21/21 at 8pm, patient experienced chest pain 7/10 that did not resolve with famotidine. He presented to the ED and was found to have ST changes in V2-V6 and elevated troponins. Patient was taken for an emergency diagnostic cath. The cath did not show any severe stenosis in major cardiac vessels, findings were consistent with probable myopericarditis. Patient was monitored in the ICU for monitoring post cath. He will be medically managed with aspirin and colchicine. Patient is hospitalized at the time of reporting this event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: GERD, chronic back pain secondary to L5 vertebral disc herniation & radiculopathy, fatty liver
Andere Medikamente: Omeprazole, tramadol, tizanidine
Allergien: NKA
Vorherige Impfungen: -

VAERS 1801250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

schwer

Staat: MA
Alter: 33,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood glucose normal Dizziness Flushing Hyperhidrosis Paraesthesia Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: EMS came and treated patient. was evaluated, blood pressure was normal, blood sugar normal. Patient did not go to hospital. Stayed for 10 minutes more and then left

Weitere VAERSDATA-Felder

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

VAERS 2679382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 05.09.2023
Impfdatum: 26.10.2021
Beginn: 31.07.2023
Tage bis Beginn: 643,0
Dosis: 3
Route/Site: - / -

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

Angiogram cerebral normal Arteriogram carotid normal Asthenia COVID-19 Cough Dyspnoea Neurological symptom SARS-CoV-2 test positive Viral infection

Symptomtext

Patient is a 71 y.o. female with a history of CAD,NSVTand OSA who presented to ED with subacute viral syndrome and generalized weakness with Left more than right found to have CTA H/N nonacute, COVID + thus transferred 7/31/2023 for further neuro eval. 1. Transient neurological symptoms: Suspect related to viral syndrome. CTA H/N without LVO, CVA. Initially planned MRI - however with rapid clinical improvement per discussion with neurology cancelled MRI. Neurology recommended PCP follow up. 2. COVID Infection: Present on admit, symptomatic 7/26/23 with dyspnea and cough. Initially required 2-3 L O2, but was weaned off and discontinued steroids and remdesevir 3. CAD: S/p LAD and PDA dissection in 2014. Followed w/ Dr. Previously on ASA. Myalgias with statin. 4. OSA: NPPV at bedtime.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2638444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: OH
Alter: 56,0
Geschlecht: F
Eingang: 30.05.2023
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

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

Dizziness Feeling hot Paraesthesia Tremor

Symptomtext

According to the patient, as soon as the needle went into her arm she felt a warm feeling go up her arm, into her neck and up into her head. She felt dizzy and like her hands had pins and needles, only worse. She stated that she has had tremors and some of the symptoms ever since. She has seen a physician who would like to refer her to a neurologist, but she does not see the sense in it. She stated she feels like the vaccine went into her blood stream.

Weitere VAERSDATA-Felder

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

VAERS 2629167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 11.04.2022
Beginn: 20.06.2022
Tage bis Beginn: 70,0
Dosis: 4
Route/Site: IM / RA

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

Hypotension

Symptomtext

HYPOTENSION.

Weitere VAERSDATA-Felder

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

VAERS 2628462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 08.05.2023
Impfdatum: 11.11.2021
Beginn: 13.07.2022
Tage bis Beginn: 244,0
Dosis: 3
Route/Site: IM / LA

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

Hypotension Symptom recurrence

Symptomtext

HYPOTENSION 2/24/2023 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2617561

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 19.04.2023
Impfdatum: 28.12.2020
Beginn: 17.04.2023
Tage bis Beginn: 840,0
Dosis: 3
Route/Site: - / -

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

Dyspnoea SARS-CoV-2 test SARS-CoV-2 test negative Secretion discharge

Symptomtext

Pt had been in inpatient rehab since 4/5 where she tested negative for COVID on admission. Pt was retested for COVID on 4/17 and had complaints of mild shortness of breath and increased secretions. She also had family with COVID.

Weitere VAERSDATA-Felder

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

VAERS 2587309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: IL
Alter: 52,0
Geschlecht: M
Eingang: 25.02.2023
Impfdatum: 01.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 61,0
Dosis: 2
Route/Site: IM / -

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

Anxiety Arthritis Condition aggravated Depression Epistaxis Irritable bowel syndrome Oral blood blister Pain

Symptomtext

Starting getting blood blisters on inside of my mouth on cheek & lip areas. Lasted for about a year. I started having nose bleeds off and on, lasted about a year. My IBS issues seemed to worsen & my methods of dealing with it sometimes did not help and I was left trying to discover new ways to help cope. My arthritis seemed to bother me more. Over the year my anxiety worsened and I got more and more depressed. I now take medicine to help with the pain, anxiety, and depression originally prescribed by my GP and now monitored by a psychiatrist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Irritable Bowel Syndrome, Small intestinal bacterial overgrowth (SIBO), Arthritis (not considered Auto-Immune type like Rheumatoid)
Vorgeschichte: Irritable Bowel Syndrome, SIBO, Arthritis
Andere Medikamente: Gabapentin, Hyocyamine Sulfate, Ibuprofen, SCD (specific carbohydrate diet) safe multi-vitamin, Vit-D, Pre-Pro biotic supplement.
Allergien: PCN, carbohydrates, sugars, starches, polysorbates, gums (guar, xantham), certain food dyes, certain cheeses, processed foods in general. The legal/illegal list of foods to avoid for IBS conditions.
Vorherige Impfungen: -

VAERS 2586340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 23.02.2023
Impfdatum: 22.10.2021
Beginn: 04.01.2023
Tage bis Beginn: 439,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain COVID-19 Computerised tomogram abdomen abnormal Condition aggravated Constipation Enema administration Explorative laparotomy Fluid intake reduced Internal hernia Intestinal strangulation Mental status changes Nausea Pain Physical deconditioning SARS-CoV-2 test positive Small intestinal anastomosis Small intestinal resection Urinary tract infection

Symptomtext

"Patient with history of COVID vaccines who was hospitalized and had a COVID detected PCR during stay. Provider d/c note: ""82 y/o female patient with PMH significant for HTN, hyperlipidemia, Sjogren's syndrome, malignant lung ca, CVA, pessary placement, recurrent UTI, who presents with complaint of moderate, constant, non-radiating, dull abdominal pain associated with nausea and vomiting which started this morning. She vomited once since the onset of pain. Patient denies any food triggers but admits to constipation since midnight last night. Patient's spouse at bedside who states that he tried to treat the pain with otc medications without relief. He also tried to use fleet enema for constipation with no relief either. Denies fever, chills, chest pain, shortness of breath, melena, dysuria, urinary urgency, low back pain, loss of appetite, weakness, dizziness, headaches. Admits to lack of fluid intake. Spouse also reports patient's recurrent UTI with no urinary symptoms but presence of altered mental status. Patient is a, a & o x 3, coherent, in no acute distress. Still complains of mild generalized abdominal pain but denies nausea or vomiting currently. CT showed suspicion for a possible strangulated hernia in addition to possible ischemic colitis and she was taken to the OR for exploratory laparotomy. She underwent an open small bowel resection with anastomosis secondary to internal hernia containing strangulated small bowel. She tolerated surgery and recovery well receiving antibiotics for both this and a UTI. She did well with rehab initially and gradual increase in food and was recommended to return home however at the time of discharge was incidentally found to be covid positive. Patient sustained deconditioning and therapy recommendations changed to Pine Ridge however patient consistently worked with PT/OT during isolation period and was ultimately strong enough to return home. She will follow up with Surgery in the outpatient setting. She will also receive PT/OT and home care at home."""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 19,0
Labordaten: Covid PCR detected on 01/13/2023.
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Mild mitral and aortic regurgitation Hypertension, essential, benign High cholesterol Respiratory Sleep apnea Dyspnea on exertion Malignant neoplasm of lower lobe of right lung (HCC) Urinary Urge incontinence Renal insufficiency Other Enlarged lymph nodes History of primary malignant neoplasm of lung Status post bilateral minimally invasive L3-4 decompressions of stenosis/Left L3-4 far lateral minimally invasive diskectomy on 11/2/15 Unsteady gait History of lung cancer Hemiplegia and hemiparesis following cerebral infarction affecting right dominant side (HCC) Insomnia Benign essential tremor Sjogren's syndrome (*) Hyperproteinemia Metabolic encephalopathy Weakness History of CVA (cerebrovascular accident
Andere Medikamente: artificial tears,hypromellose, (GENTEAL) 0.3 % drop Place 1 drop into both eyes 4 (four) times daily as needed (dry eyes). aspirin 81 mg EC tablet Take 1 tablet by mouth daily. atorvastatin (LIPITOR) 40 mg tablet Take 1 tablet by mouth da
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2557480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 90,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 24.02.2021
Beginn: 14.12.2022
Tage bis Beginn: 658,0
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

12/14/22 presents to ED for "shortness of breath". PMHx of "DM, HTN, CKD, hypothyroidism, CHF, AFib"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/14/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2520541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 16.11.2021
Beginn: 15.07.2022
Tage bis Beginn: 241,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure Dry mouth Palpitations Panic attack Thirst

Symptomtext

Nasal Swab: positive; Nasal Swab: positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 59-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Mar2021 at 08:30 as dose 1, single (Lot number: EN6199), in left arm, on 29Mar2021 at 08:00 as dose 2, single (Lot number: EP6955), in left arm and on 16Nov2021 at 12:15 as dose 3 (booster), single (Lot number: 32030BD) at the age of 58 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: VITAMIN D [VITAMIN D NOS]. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 15Jul2022, outcome "unknown" and all described as "Nasal Swab: positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (15Jul2022) Positive. Clinical course: No known allergies. Prior to vaccination, the patient did not have COVID.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201336176 same patient/drug, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20220715; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2513999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 19.11.2021
Beginn: 15.04.2022
Tage bis Beginn: 147,0
Dosis: 3
Route/Site: IM / LA

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

Asthma COVID-19 Condition aggravated Decreased appetite Diarrhoea Fatigue Gait disturbance Malaise Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive Vomiting

Symptomtext

I felt very tired after the vaccine for a day. On 08/02/2022, I tested positive with a home test for COVID-19. I had a sore throat, runny nose, body aches but no fever. I was sick for five days but by day seven I was feeling much better. I previously tested positive for COVID-19 on 04/15/2022. I had no appetite, diarrhea, vomiting and extreme fatigue. I contacted my doctor and was given the prescription PAXLOVID. It helped but my asthma was aggravated. For two months I took prednisone to manage my asthma. I was really sick up until the end of June 2022. Now, I can't walk as fast as I once did. COVID-19 really knocked me out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 02AUG2022 COVID-19 test positive; 15APR2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: SYMBICORT
Allergien: Penicillin; CT contrast dye; lidocaine
Vorherige Impfungen: -

VAERS 2490866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: GA
Alter: -
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 24.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Dyspnoea SARS-CoV-2 test

Symptomtext

shortness of breath; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 55-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 24Oct2021 as dose 2, single (Lot number: 32030BD), in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Past drug history included: 13 yrs ago took tetanus, reaction(s): "Allergy: tetanus", notes: 13 yrs ago took tetanus; Whooping cough shot mix. it reduced my mobility, reaction(s): "reduced my mobility", notes: whooping cough shot mix. It reduced my mobility; Whooping cough shot mix. it reduced my mobility, reaction(s): "Allergy", notes: whooping cough shot mix. It reduced my mobility. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: 30155BA, Location of injection: Arm Right), administration date: 03Oct2021, when the patient was 55-year-old, for COVID-19 immunization. The following information was reported: DYSPNOEA (disability), outcome "not recovered", described as "shortness of breath". The event "shortness of breath" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative, notes: Agency. Therapeutic measures were not taken as a result of dyspnoea. Additional information: No illness other than vaccine reactions. Dose #2 - Vaccine administered at Pharmacy or Drug Store. No other vaccine in four weeks. No other medications in two weeks, 5 different Irregular Breathing Issues - My cardiologist classifies it as shortness of breath. The issue started in my sleep the night of my first dose. Each week I experience the issue. It slowly spread throughout the day by Jan. I waited until Jan for the issues to resolve. Since it grew worse I went to visit with my doctor. Since then I've undergone a vast amount of tests with specialist on every level at least 2-3 times a month. Specialist visits includes, Cardiology, Sleep Specialist, Allergist, Neurologist, Pulmonary Medicine, etc. Cardiology/Neurology just confirmed it's vaccine related. No Covid prior vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Test Result: Negative ; Comments: Agency
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2072176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: GA
Alter: 55,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 03.10.2021
Beginn: 03.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Dyspnoea Nasopharyngeal swab Pain in extremity Vaccination site pain Head discomfort Injection site reaction Pain

Symptomtext

felt a pin sticking feeling on my right arm in there are the dose was administered.; Each month the spread grew worse and developed into a feeling like when my hands feel like their falling asleep of a scratchy feeling in patches over my entire body; shortness of breath; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 03Oct2021 as dose 1, single (Lot number: 30155BA) at the age of 55 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Tetanus (13 yrs ago took tetanus/whooping cough shot mix. It reduced my mobility), for Immunization, reaction(s): "It reduced my mobility"; Whooping cough shot (13 yrs ago took tetanus/whooping cough shot mix. It reduced my mobility), for Immunization, reaction(s): "It reduced my mobility". The following information was reported: PAIN IN EXTREMITY (disability) with onset 03Oct2021, outcome "not recovered", described as "Each month the spread grew worse and developed into a feeling like when my hands feel like their falling asleep of a scratchy feeling in patches over my entire body"; VACCINATION SITE PAIN (disability) with onset 03Oct2021, outcome "not recovered", described as "felt a pin sticking feeling on my right arm in there are the dose was administered."; DYSPNOEA (disability) with onset 03Oct2021, outcome "not recovered", described as "shortness of breath". The events "felt a pin sticking feeling on my right arm in there are the dose was administered.", "each month the spread grew worse and developed into a feeling like when my hands feel like their falling asleep of a scratchy feeling in patches over my entire body" and "shortness of breath" required physician office visit. The patient underwent the following laboratory tests and procedures: Nasopharyngeal swab: Negative, notes: Hospital. Therapeutic measures were not taken as a result of vaccination site pain, pain in extremity, dyspnoea. Clinical course: Patient Age group Adult (18-64 Years). After dose 1 patient Within 5 minutes she felt a pin Sticking feeling on her right arm in there are The dose was administered. By the end of The day it randomly spread to her toes and Other parts of her body. Each month the Spread grew worse and developed into a Feeling like when her hands feel like their Falling asleep of a scratchy feeling in Patches over her entire body. AE resulted in Doctor or other healthcare professional Office/clinic visit, Emergency Room/department or urgent care, Disability Or permanent damage]. No covid prior vaccination. No any other vaccine and other medication received in four weeks. Covid tested post vaccination as positive. No other medical history, no illness other than vaccine reactions. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Test Result: Negative ; Comments: Hospital
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2456485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: OH
Alter: 87,0
Geschlecht: M
Eingang: 13.10.2022
Impfdatum: 08.04.2022
Beginn: 05.09.2022
Tage bis Beginn: 150,0
Dosis: 3
Route/Site: IM / LA

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

Confusional state Dyspnoea Mental status changes SARS-CoV-2 RNA SARS-CoV-2 test COVID-19 SARS-CoV-2 test positive

Symptomtext

Symptoms include shortness of breath and confusion in mental status.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS-CoV-2 Antigen specimen collection 9/5/22 2019 Novel Coronavirus RNA specimen collection 9/9/22
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular disease, Hypertension, Chronic Renal Disease, and Cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 58,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 12.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

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

Migraine Oropharyngeal pain Secretion discharge

Symptomtext

24 hours after receiving vaccination started getting what was a start of migraines, which would come to a peak, and just stop. Over the past month still getting migraines at random times of the of the day, but symptoms have become worse. For the past three days have been experiencing soreness this in my throat, and Mucus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Have not yet seen my physician, video conference scheduled for this Friday afternoon.
Aktuelle Erkrankungen: none
Vorgeschichte: Don?t know if this question pertains to conditions prior to vaccination or after?
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2452027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 28.10.2021
Beginn: 27.01.2022
Tage bis Beginn: 91,0
Dosis: 3
Route/Site: IM / LA

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

Body temperature increased COVID-19 pneumonia Computerised tomogram thorax abnormal Dyspnoea Hypoxia Interstitial lung disease Lung opacity Sepsis

Symptomtext

1/27/2022- Presented to ER, complaint of SOB. Temp-101.5. p-90. Chest CT-Coarse interstitial disease with ground-glass opacities. Admit Sepsis/Acute hypoxia secondary to Covid 19 pneumonia. IV decadron, IV Remdesivir, baricitinib, vitamins, ceftriaxone and doxycycline. 1/29/2022-Spo2 stable on RA. Afebrile. 1/30/2022-VSS, discharged to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ANCA- associated vasculitis, GERD, Sicca and interstitial cystic.
Andere Medikamente: -
Allergien: Bee Venom
Vorherige Impfungen: -

VAERS 2433757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 02.03.2021
Beginn: 03.08.2022
Tage bis Beginn: 519,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

SOB, HYPOXIC

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: POSITIVE COVID TEST 8/3/22
Aktuelle Erkrankungen: -
Vorgeschichte: Aortic aneurysm Atrial fibrillation Aortic stenosis COPD Hashimoto's thyroiditis CHF Chronic pain -nerve pain from shingles Hypertension Hyperlipidemia Meningioma NSTEMI PAD SSS Rheumatoid arthritis Glaucoma Chronic sinusitis Constipation Difficulty waking up after anesthesia Postoperative nausea and vomiting Diverticulitis Heartburn CAD AKI Postherpetic neuralgia Peripheral arterial disease -monophasic waveforms below the knee Squamous cell vulvar cancer
Andere Medikamente: Acetaminophen (TYLENOL) 500 mg oral tablet Albuterol HFA 90mcg/puff (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl Atorvastatin (LIPITOR) 40 mg oral tablet B Complex with Vitamin C Calcium carbonate-vitamin D3 500 mg, 1250 mg,-200 units (OS
Allergien: Levaquin [Levofloxacin] Aldactone [Spironolactone] Amoxicillin Ciprofloxacin Doxycycline Fosamax [Alendronate] Imuran [Azathioprine] Lisinopril Plaquenil [Hydroxychloroquine] Sulfa (Sulfonamide Antibiotics) Thimerosal Vicodin [Hydrocodone-Acetaminophen]
Vorherige Impfungen: -

VAERS 2419339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 24.08.2022
Impfdatum: 06.11.2021
Beginn: 14.08.2022
Tage bis Beginn: 281,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Computerised tomogram thorax normal Condition aggravated Dyspnoea Haematuria Hypotension Hypoxia Lumbar vertebral fracture Spinal compression fracture Thoracic vertebral fracture

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 8/14/2022 Discharge Date: Aug 22, 2022 PRESENTING PROBLEM: Hypoxemia [R09.02] Hypotension [I95.9] Microscopic hematuria [R31.29] Compression fracture of body of thoracic vertebra (HCC) [S22.000A] Compression fracture of L2 vertebra, initial encounter (HCC) [S32.020A] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 90-year-old male with PMH significant for CVA and DM who presented with with generalized weakness and SOB. Patient was noted to have COVID-19 in ER, CT showed no PE and no infiltrate. Patient was hypoxic and was placed on supplemental oxygen. Patient was started on dexamethasone and admitted. Patient did not qualify for remdesivir as there were no infiltrates. Hypoxia quickly resolved and Decadron was stopped. Physical therapy recommended subacute rehab. This was much delayed due to COVID so family eventually decided to discharge to home with home health care despite continued weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Dysphagia Diabetes mellitus (HCC) Personal history of colonic polyps Gallstones with biliary obstruction Colitis Hypothyroid Essential hypertension Cerebrovascular accident (CVA) (HCC) History of prostate cancer Dementia without behavioral disturbance (HCC) Mixed hyperlipidemia Weakness of both lower extremities Generalized weakness Late effect of cerebrovascular accident (CVA) Parotid gland enlargement TIA (transient ischemic attack) TIA (transient ischemic attack) Aortic root dilation (HCC) Peripheral neuropathy Hypotension
Andere Medikamente: aspirin EC 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) tablet enzalutamide (XTANDI) 40 MG insulin glargine, 1 unit dial, (TOUJEO SOLOSTAR) 300 UNIT/ML pen-injector insulin li
Allergien: CortisoneItching Metformin PenicillinsRash
Vorherige Impfungen: -

VAERS 1897484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 27.09.2021
Beginn: 07.12.2021
Tage bis Beginn: 71,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dyspnoea Feeling abnormal Malaise SARS-CoV-2 test positive Productive cough

Symptomtext

12/07/21 presents to EC ED "malaise and feeling foggy" "shortness of breath". PMHx of " cirrhosis and MELD of 30 currently on the liver transplant list"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/07/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1897484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 27.09.2021
Beginn: 07.12.2021
Tage bis Beginn: 71,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea Feeling abnormal Malaise SARS-CoV-2 test positive Productive cough

Symptomtext

12/07/21 presents to EC ED "malaise and feeling foggy" "shortness of breath". PMHx of " cirrhosis and MELD of 30 currently on the liver transplant list"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/07/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2357799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MN
Alter: 90,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 27.10.2021
Beginn: 02.07.2022
Tage bis Beginn: 248,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Cough Hypophagia Pneumonia bacterial Pyrexia Respiratory failure SARS-CoV-2 test positive

Symptomtext

Cough, fever, and poor oral intake for a few days prior to ER visit on 7/4/22. Admitted to Medical unit 7/4/22 with hypoxic respiratory failure likely due to COVID 19 pneumonia with probable bacterial component (per admission).

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: COVID Positive PCR on 7/4/22
Aktuelle Erkrankungen: -
Vorgeschichte: Prediabetes
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1845958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: FL
Alter: -
Geschlecht: U
Eingang: 03.07.2022
Impfdatum: 04.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Cardiac failure Chest pain Expired product administered Chest X-ray normal Computerised tomogram normal Dizziness Dyspnoea Fibrin D dimer increased Monocyte count normal Monocyte percentage increased Product storage error

Symptomtext

heart failure; had mistakenly given me an expired dose that was in the throw away batch; severe chest pains; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP), Program ID: (005570). The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 04Nov2021 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization completed, Manufacturer unknown), for Covid-19 immunization. The following information was reported: CARDIAC FAILURE (medically significant), outcome "unknown", described as "heart failure"; EXPIRED PRODUCT ADMINISTERED (non-serious), outcome "unknown", described as "had mistakenly given me an expired dose that was in the throw away batch"; CHEST PAIN (non-serious), outcome "unknown", described as "severe chest pains". Clinical course: Hello, I was given a COVID booster shot on 04Nov2021. The pharmacist called me a couple of hours later to inform me the nurse had mistakenly given me an expired dose that was in the throw away batch. Twenty four hours later I started having severe chest pains. I have been under the doctors care since then and (8 months later) was recently diagnosed with heart failure. I was told by the company at fault to contact Pfizer because you all were at fault due to my adverse reaction. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

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

VAERS 2309301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: SC
Alter: 45,0
Geschlecht: M
Eingang: 04.06.2022
Impfdatum: 03.01.2022
Beginn: 01.04.2022
Tage bis Beginn: 88,0
Dosis: 2
Route/Site: IM / LA

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

Injected limb mobility decreased Injection site muscle weakness Magnetic resonance imaging head normal Magnetic resonance imaging neck Muscle atrophy Muscular weakness Pain in extremity Paraesthesia

Symptomtext

Left arm severe weakness from shoulder to hands and fingers . Unable to use left upper extremity as before covid vaccine. Left arm pain with muscle loss and tingling. Inset followed 2nd vaccine dosage given 012422.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: MRI OF BRSIN AND NECK 0N MAY 6 2022. MO CHANGES IN MRI RESULTS OF BRAIN FROM PRIOR MRI'S THERE ARE SIG ICICANT CONCERNS TEGARFING MRI OF THE NECK
Aktuelle Erkrankungen: MS
Vorgeschichte: MS
Andere Medikamente: Celebrex, baclophen, tylenol, cromolyn nasal inhl, lexapro, fluticasone prop nasal inhl, loratadine, melatonin, multivitamin. Miralax, senkot
Allergien: None
Vorherige Impfungen: -

VAERS 2293114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 24.05.2022
Impfdatum: 30.10.2021
Beginn: 10.12.2021
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: IM / LA

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

Injected limb mobility decreased Nerve injury

Symptomtext

patient got covid booster in 10/30/2021, and then more than 1 month later (December), he called and said the injection touched his nerve and that he can't barely move his arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Heart, stroke
Vorgeschichte: Heart, Stroke
Andere Medikamente: -
Allergien: no
Vorherige Impfungen: -

VAERS 2281085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: WI
Alter: 67,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 01.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Anxiety Back pain Pain Paraesthesia

Symptomtext

On 11/08, I began having mid and low back pain, the body sensations (twinges all over), tingling in my feet and legs and hands. After the second dose, I was prescribed Gabapentin. I started taking that then and took it again with the symptoms from the 3rd dose. The symptoms lasted until 11/22. After the second dose, the symptoms continued until 03/21, longer and more extensive than after the 3rd dose. I'm a bit anxious about taking the 4th dose, but think I will since the Covid cases are increasing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None. Since this was the second adverse reaction, I was disappointed, but knew what to do, take the Gabapentin.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pfizer Covid (see previous report)

VAERS 2270843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 12.01.2021
Beginn: 01.02.2022
Tage bis Beginn: 385,0
Dosis: UNK
Route/Site: - / -

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

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

Symptomtext

02/01/22 presents to ED for "Fatigue" "Shortness of Breath". PMHx of "non-hodgkin's lymphoma s/p radiation"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/01/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: IL
Alter: 83,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 05.11.2021
Beginn: 08.05.2022
Tage bis Beginn: 184,0
Dosis: 3
Route/Site: SYR / -

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

Cough Dyspnoea Oropharyngeal pain

Symptomtext

Patient presents to ER with SOB, cough, sore throat, and no relief after using cough medication.

Weitere VAERSDATA-Felder

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

VAERS 2243653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: OR
Alter: 46,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 01.11.2021
Beginn: 26.01.2022
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Pneumonia SARS-CoV-2 test positive Vomiting

Symptomtext

I got covid Jan 3rd, that progressed to pneumonia in my left lung by Jan 26

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: 3 Jan went to Urgent Care, tested positive for covid, got Tessalon pearls, cough medicine and inhaler. Isolated for 15 days, cough got better then returned and got worse, 26th Jan went back to Urgent Care, diagnosis pneumonia in my left lung, prescribed 1000mg amoxicillin 3x daily, doxycyclin 100mg 2xs daily, 27 Jan ended up in Emergency because of vomiting
Aktuelle Erkrankungen: None
Vorgeschichte: Anemia, migraines, allergies
Andere Medikamente: None
Allergien: Z-pack
Vorherige Impfungen: -

VAERS 2226085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MN
Alter: 61,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 17.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / RA

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

Acute kidney injury Cellulitis Dehydration Orthostatic hypotension

Symptomtext

Patient presented to the ED and was subsequently hospitalized for dehydration, acute kidney injury, orthostatic hypotension, cellulitis of right foot within 6 weeks of receiving covid vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2223142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MO
Alter: 74,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 02.04.2021
Beginn: 08.04.2022
Tage bis Beginn: 371,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 pneumonia Cough Fatigue Oropharyngeal pain Respiratory tract congestion

Symptomtext

Case's spouse reported that case has a sore throat, cough, fatigue, congestion. Hospitalized 04/08/2022 with COVID induced pneumonia.

Weitere VAERSDATA-Felder

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

VAERS 2209213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 05.11.2021
Beginn: 03.02.2022
Tage bis Beginn: 90,0
Dosis: 3
Route/Site: - / -

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

Atrial fibrillation COVID-19 Cardioversion Dyspnoea Echocardiogram abnormal Electrocardiogram normal Glomerular filtration rate decreased Hypoxia Pneumonia Polyuria Renal impairment SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient up to date on Pfizer COVID vaccinations who admitted to the hospital with positive COVID test and complications likely related to COVID. Provider discharge note below: "Patient developed increased shortness of breath, admitted with hypoxia though it should be noted that he was recently started on home oxygen @ 2 L/m and the hypoxia was noted on room air. The hypoxia may be due to several factors. He may have had some mild Pneumonia due to COVID-19 virus as he was found to be positive for COVID infection but with diuresis he was saturating well on room air. He had been started on steroids but since he was not truly hypoxic related to the COVID infection and was risk for fluid retention and exacerbation of his heart he was continued on steroids at discharge. He also has a history of Ischemic dilated cardiomyopathy (EF 20% Echo 12/2021) with AICD (automatic cardioverter/defibrillator) present and may have Acute on chronic systolic (congestive) heart failure though just recently had his diuretic dose increased at last hospitalization. He was started on intravenous FUROSEMIDE while monitoring CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min with solitary kidney. At admission patient noted to have a decreased GFR (21 to 13) likely due to recent increase in TORSEMIDE dose. Discussed with Dr of cardiology and at discharge his dose was reduced to previous regimen of 10 mg twice daily. Paroxysmal atrial fibrillation on APIXABAN, AMIODARONE and had cardioversion prior to admission. Note that the patient is nearly eighty and has renal dysfunction and likely should be on the lower dose of 2.5 mg twice daily. Elevated troponin values with negative delta, no acute findings on electrocardiogram. No chest pain. Likely demand phenomena. Hypertension Controlled. Pure hypercholesterolemia ROSUVUSTATIN Gout ALLOPURINOL Issues Requiring Follow Up: Recommend follow up basic metabolic panel to monitor renal function. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: COVID "detected" PCR on 02/03/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Pure hypercholesterolemia Ischemic dilated cardiomyopathy AICD (automatic cardioverter/defibrillator) present Paroxysmal atrial fibrillation Pulmonary hypertension (*) CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min Gout Benign prostatic hyperplasia Coronary artery disease with angina pectoris, unspecified vessel or lesion type, unspecified whether native or transplanted heart (*) DDD (degenerative disc disease), lumbar Primary osteoarthritis of right shoulder History of prostate cancer Degenerative disc disease, lumbar NYHA class 2 heart failure with reduced ejection fraction (*) History of renal cell carcinoma Left bundle branch block
Andere Medikamente: Zyloprim Pacerone Eliquis Zyrtec Farxiga Toprol XL Multivitamin Crestor Demadex Vitamin E
Allergien: Shellfish: swelling
Vorherige Impfungen: -

VAERS 2203983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: FL
Alter: 59,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 19.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Fear Illness Influenza like illness Injection site swelling Mobility decreased Nausea Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Severe swelling on upper left arm at injection point that lasted 5 days. Severe Flu-like symptoms (fever, aches, nausea)for nearly 6 days. On January 3, 2022 I tested positive for Covid-19. I was severely sick for 10 days. I was given steroids and antibiotics. I was bedridden for 9 days but did not go to the hospital because I was scared.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Covid-19 Nasal/Nasopharynx: Positive for 2019-nCoV. Speciman taken January 3, 2022 Test taken at Facility by Dr. T
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: estridiol
Allergien: none
Vorherige Impfungen: -

VAERS 2196246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: OH
Alter: 33,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal discomfort Asthenia Back pain Blood pressure systolic increased Chills Dehydration Diarrhoea Feeling of body temperature change Flatulence Headache Illness Mobility decreased Myalgia Nausea

Symptomtext

First, at about 3:30 p.m. on 3/23 I had my blood pressure taken and it was 130/77. This is the highest blood pressure reading that I have ever had in my entire life. I have never had a systolic number this high and rarely a diastolic that high. By about 5:00 p.m. I could bare lift my left arm. By 9:00 p.m. I began to feel sick to my stomach and had he chills - simultaneously feeling freezing cold and burning hot. I had to be covered in blankets even though the room was 71 Fahrenheit and I was too sick to move or get up from the couch. This continued until about 3:00 a.m. when I moved from the couch to the bed, feeling very weak and like I would throw up. I had severe gas during the night. By about 7:00 a.m. I could move again, and I had diarrhea. Today I feel dehydrated and have muscle soreness, lower back pain, a woozy stomach, and a headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: At about 3:30 p.m. on 3/23 I had my blood pressure taken and it was 130/77.
Aktuelle Erkrankungen: None
Vorgeschichte: Joint pain, muscle tension
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: I reported arm pain, chest soreness, and vertigo after first Pfizer COVID-19 vaccine dose on 2/23/2022

VAERS 2194902

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 32030BD

moderat

Staat: MO
Alter: 52,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 03.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Dyspnoea Fatigue Oedema peripheral Peripheral swelling Swelling

Symptomtext

Shortness of breath, severe edema and swelling in extremities, specially feet and legs. Extreme tiredness and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid-19 in November 2021
Vorgeschichte: Diabetic, congenital heart defect
Andere Medikamente: Lantas, Humalog, metropol, amplodine
Allergien: Azirthomycin
Vorherige Impfungen: -

VAERS 2194477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: VA
Alter: 73,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 09.11.2021
Beginn: 16.01.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Electrocardiogram abnormal Tachycardia Ultrasound scan

Symptomtext

I had severe chest pains at around noon and it was a consistent pain till around the evening so decided to go to the hospital. They kept me for a day in the hospital doing vital signs and EKG s, the results were tachycardia so they suggested that I continue a visit with a heart doctor with a complete EKG with a ultra sound now I am scheduled on 3/30/2022 with a stress test with a CAT scan and I will let you know how that goes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: EKGs, and Ultrasound.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2189701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: TN
Alter: 76,0
Geschlecht: M
Eingang: 21.03.2022
Impfdatum: 02.12.2021
Beginn: 31.01.2022
Tage bis Beginn: 60,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram head abnormal Dizziness Laboratory test Transient ischaemic attack

Symptomtext

1/31/22 ER visit- diagnosed with TIA, continued to have dizziness and weakness. Admitted to hospital 2/5/22 and diagnosed with COVID pneumonia, discharged to rehab facility 2/18/22 through 3/20/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 43,0
Labordaten: Numerous testing while admitted- CT Head to confirm the TIA 1/31/22 Numerous CXR with findings of covid pneumonia
Aktuelle Erkrankungen: no
Vorgeschichte: CAD, HTN, DM, COPD
Andere Medikamente: budensonide, aspirin, vitamin d3, buspirone, fluticasone, sertraline, omeprazole, citalopram, albuterol, symbicort, incruse, finasteride, tamsulosin, atorvastatin
Allergien: pcn, metformin
Vorherige Impfungen: -

VAERS 2179886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / UN

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

Chronic obstructive pulmonary disease Essential hypertension

Symptomtext

Patient presented to the ED and was subsequently hospitalized within 6 weeks of receiving covid booster. Patient hospitalized for COPD and essential hypertension.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Essential hypertension
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: PA
Alter: 45,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 24.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: - / LA

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

Blood test Paraesthesia

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 24Oct2021 (Lot number: 32030BD) at the age of 45 years as dose 1, single for Covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PARAESTHESIA (non-serious) with onset Nov2021, outcome "not recovered", described as "Pins and needles all through body". The event "pins and needles all through body" 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 not taken as a result of paraesthesia. Additional information included: The report was not related to a study or programme. Caller stated that, she was calling regarding the Pfizer shot, the first shot. She stated that it was mandatory for her job. Clarified that she was referring to the Pfizer Covid-19 vaccine. She was wondering why she had the shot 3 weeks ago and was put in the hospital because she was having pins and needles all through her body after the first shot. Pins and needles all through body: Caller states that it occurred 3 weeks after she got the first shot. She stated that, she was still experiencing it and it has stayed the same. Clarified that she was in the hospital for 4 hours on Saturday and it was clarified that she was referring to this past Saturday, 13Nov2021. Clarified that she was not admitted to the hospital overnight, that she was in the emergency room for 4 or 5 hours. Treatment: No, they did not give her anything in the hospital. She states that they did blood work. She stated that, she has had no other medications for treatment for the pins and needles. She visited to physician Office, right after the next day. Time of Vaccination Was Given: around 3:30 or 4:00 in the afternoon. History of all previous immunization with the Pfizer vaccine considered as suspect was reported as no. Additional Vaccines Administered on Same Date of the Pfizer Suspect was reported as no. The patient did not receive any vaccine prior to Covid-19 vaccine. Family Medical History Relevant to AE(s) was given as No. Relevant Tests: None. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20211113; Test Name: Blood work; Result Unstructured Data: Test Result: Unknown results.
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's Medical History (including any illness at time of vaccination) None.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: CT
Alter: 57,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Fatigue Paraesthesia Vaccination site pain

Symptomtext

Mild tingling at site of previous shingles; Sore arm at site of injection; Fatigue; This is a spontaneous report received from a contactable reporter(s) (Physician). A 57 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 27Oct2021 07:30 (Lot number: 32030BD) at the age of 57 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Shingles", start date: Apr2021, stop date: May2021; "Dyspepsia" (ongoing). Concomitant medication(s) included: OMEPRAZOLE taken for dyspepsia, start date: Oct2021 (ongoing). Vaccination history included: Bnt162b2 (dose 2 single, Batch/Lot No: ER8732, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM, Route of Administration: Intramuscular), administration date: 28Mar2021, when the patient was 57 years old, for covid 19 immunization, reaction(s): "Shingles"; Bnt162b2 (dose 1 single, Batch/Lot No: EN6206, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM, Route of Administration: Intramuscular), administration date: 03Mar2021, when the patient was 57 years old, for covid 19 immunization; Flu vaccine (anatomical location: arm left), administration date: 08Oct2021, when the patient was 57 years old. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 27Oct2021 22:00, outcome "recovered" (2021), described as "Sore arm at site of injection"; FATIGUE (non-serious) with onset 27Oct2021 22:00, outcome "recovered" (2021), described as "Fatigue"; PARAESTHESIA (non-serious) with onset 28Oct2021, outcome "recovered" (2021), described as "Mild tingling at site of previous shingles". Therapeutic measures were not taken as a result of vaccination site pain, fatigue, paraesthesia. Additional information included: On 08Oct2021, the patient received other Flu vaccine with in 4weeks (arm left). The patient was not diagnosed with covid prior vaccination. The patient was not tested for covid-19 post vaccination. Did the patient provide information to you regarding the reported adverse event(s) with the use of the product? Yes. If yes above, do you consider the Pfizer product had a causal effect to the adverse event? Yes. Complete only if a 3rd dose was administered, Check one option: Booster dose due to high risk of frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 complications). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Dyspepsia
Vorgeschichte: Medical History/Concurrent Conditions: Shingles
Andere Medikamente: OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2146466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Body temperature Burning sensation Decreased appetite Fatigue Headache Lymph node pain Lymphadenopathy Mobility decreased Nausea Pain Pruritus Pyrexia Rash Rash erythematous Vomiting

Symptomtext

sunburn rash; "burning sensation" including on her hands; a "pimple rash" mostly on her arms and legs and "one or two on my chest"; low-grade fever; body aches all over/achy; headache; lymph nodes on the "injection side" were hurting; extremely fatigued; nauseous; vomiting; couldn't lift my head off the pillow/couldnt move; left underarm lymph node swelling; The rash was severely itchy and her hair was itchy; appetite has been a little less; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 53 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 01Nov2021 13:30 (Lot number: 32030BD, Expiration Date: 31May2022) at the age of 53 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "allergic to PEG and other components of the vaccine" (unspecified if ongoing); "allergic to PEG and other components of the vaccine" (unspecified if ongoing), notes: She does have a history of allergies to medication and vaccines. She has several allergies; "COVID-19" (unspecified if ongoing), notes: Caller reports having had COVID twice, before vaccination. She recovered from COVID 3 months ago. The patient's concomitant medications were not reported. The following information was reported: HEADACHE (non-serious) with onset 01Nov2021, outcome "recovered" (2021), described as "headache"; PYREXIA (non-serious) with onset 02Nov2021, outcome "recovered" (2021), described as "low-grade fever"; PAIN (non-serious) with onset 02Nov2021, outcome "recovered" (2021), described as "body aches all over/achy"; LYMPH NODE PAIN (non-serious) with onset 2021, outcome "unknown", described as "lymph nodes on the "injection side" were hurting"; FATIGUE (non-serious) with onset 2021, outcome "unknown", described as "extremely fatigued"; RASH (non-serious) with onset 03Nov2021, outcome "recovering", described as "a "pimple rash" mostly on her arms and legs and "one or two on my chest""; RASH ERYTHEMATOUS (non-serious) with onset 04Nov2021, outcome "unknown", described as "sunburn rash"; BURNING SENSATION (non-serious) with onset 04Nov2021, outcome "unknown", described as ""burning sensation" including on her hands"; NAUSEA (non-serious) with onset 2021, outcome "unknown", described as "nauseous"; VOMITING (non-serious) with onset 2021, outcome "unknown", described as "vomiting"; MOBILITY DECREASED (non-serious) with onset 2021, outcome "unknown", described as "couldn't lift my head off the pillow/couldnt move"; LYMPHADENOPATHY (non-serious) with onset 2021, outcome "recovered" (2021), described as "left underarm lymph node swelling"; PRURITUS (non-serious) with onset 2021, outcome "unknown", described as "The rash was severely itchy and her hair was itchy"; DECREASED APPETITE (non-serious) with onset 2021, outcome "unknown", described as "appetite has been a little less". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache. Additional information: The patient received first dose of the vaccine on Monday, 01Nov2021 at 13:30 pm. The patient reported that she went through a desensitization process before receiving the vaccine with her allergist because she was allergic to PEG and other components of the vaccine. She stated she was desensitized before getting the vaccine since she was sensitive to certain components of the vaccine and other medications and vaccines in the past. She was given the vaccine in a hospital setting just in case something was to happen or she were to have an allergic reaction. She was fine and that she kept drinking water until five hours after the administration of the vaccine when she developed a headache and took two extra-strength Tylenol. She developed a low-grade fever at midnight. The day after the vaccine dose, Tuesday, she developed body aches all over and her fever subsided. She also reported her lymph nodes on the injection side were hurting, was extremely fatigued, and achy. Her aches subsided during the day. On Wednesday, she developed a pimple rash mostly on her arms and legs and one or two on her chest. The rash was severely itchy and her hair was itchy. She was unable to wear her CPAP and decided to not take Benadryl right away. On Thursday, she went to work and said she started developing sunburn rash, the other rash was subsiding. This rash lasted several hours, got worse before it got better, and there was a burning sensation including on her hands. She also said last night, she developed a red dot rash on legs and arms and was nauseas and had vomiting all night. She also reported she couldn't lift her head off the pillow, those effects seems like it was subsiding. She had COVID twice, before vaccination. She waited the recommended 90 days before getting the vaccine, as recommended by her primary doctor and allergist. She stated that for the first 8 hours was fine, after 8 hours she started to experience bad headache, then around midnight she got a low grade fever, the following day she then had really bad body aches and couldn't move. She recovered from COVID 3 months ago. On Wednesday she had a headache and stuff, states now seem like everything was okay, she went back to work yesterday, in the evening she started breaking out in a rash, she got a sunburn rash, and then last night got a red dot rash on her body, it was worse on her legs and has had nausea and vomiting. Now this morning she felt better, did not go to work. She took tylenol for headache, did not take more tylenol for the low grade fever, they subsided on its own in less than 12 hours, no exact times or dates known. The rash did get worse before it started getting better on Thursday. Rash got worse while she was at work and then when she left work yesterday at 13:00 pm her hands were beat red, by 16:00 pm it had subsided. and then in the evening she felt itchy again, and noticed she started developing a red dot rash, which was different than the sunburn rash. Looks like today everything had gone away. After she started developing the rash, after she ate, but she had eaten that before. Her appetite had been a little less. Nausea and vomiting all night, did not go to work today. Did drink lemon and hot water to calm down the nausea, a quarter teaspoon of baking soda and 8 oz of water to calm down the vomiting. She stated she did have a history of allergies to medication and vaccines. This was her first vaccine since she was 20 years old. On the second day the lymph node under left arm pit swelled but that had gone away. No redness or anything at injection site. She wanted to know if these side effects were normal during the week after the vaccine and how long she should expect these side effects. Now it's been five days. She asked if she should expect these same symptoms with the second shot. She wanted to know about treating her side effects or knowing if the symptoms she was experiencing were side effects or allergic reactions. She said she was "always leery about mixing medications" because she had several allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20211102; Test Name: Body temperature; Result Unstructured Data: Test Result:Low-grade fever
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Caller reports having had COVID twice, before vaccination. She recovered from COVID 3 months ago.); Drug allergy (She does have a history of allergies to medication and vaccines. She has several allergies.); PEG allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2146446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 26.02.2022
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: unbekannt Erholt: nein

Abdominal distension Arthralgia Balance disorder Blood pressure increased Blood pressure measurement Body temperature Body temperature increased Cough Diarrhoea Dizziness Ear pain Eye pain Fatigue Headache Jaw disorder Myalgia Nausea Palpitations

Symptomtext

loss of balance; Severe heart pounding; elevated blood pressure; Severe headache; sharp pains behind eyes; exaggerated tinnitus; exhaustion; muscle aches; nauseous; vomiting; dizziness; unable to focus; diarrhea; severe bloating and gas in chest and belly; muscle pain in shoulders; exaggerated tmj; lock jaw left jaw; pain in both ears; coughing; sneezing; 2 degrees elevated temperature; 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), administered in arm left, administration date 29Oct2021 13:00 (Lot number: 32030BD) at the age of 53 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Bilateral pulmonary embolism" (unspecified if ongoing); "Oleo anal pouch anastomoses" (unspecified if ongoing); "Hernia repair" (unspecified if ongoing); "Osteoporosis" (unspecified if ongoing); "Arthritis" (unspecified if ongoing); "Shell fish" (unspecified if ongoing); "propoxyphene" (unspecified if ongoing). Concomitant medication(s) included: XARELTO. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0202, Location of injection: Arm Left, Vaccine Administration Time: 04:45 PM), administration date: 08Oct2021, when the patient was 53 years old, for Covid-19 immunization, reaction(s): "Covid-19 immunization". The following information was reported: BALANCE DISORDER (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "loss of balance"; PALPITATIONS (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "Severe heart pounding"; BLOOD PRESSURE INCREASED (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "elevated blood pressure"; HEADACHE (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "Severe headache"; EYE PAIN (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "sharp pains behind eyes"; TINNITUS (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "exaggerated tinnitus"; FATIGUE (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "exhaustion"; MYALGIA (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "muscle aches"; NAUSEA (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "nauseous"; VOMITING (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "vomiting"; DIZZINESS (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "dizziness"; VISION BLURRED (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "unable to focus"; DIARRHOEA (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "diarrhea"; ABDOMINAL DISTENSION (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "severe bloating and gas in chest and belly"; ARTHRALGIA (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "muscle pain in shoulders"; TEMPOROMANDIBULAR JOINT SYNDROME (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "exaggerated tmj"; JAW DISORDER (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "lock jaw left jaw"; EAR PAIN (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "pain in both ears"; COUGH (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "coughing"; SNEEZING (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "sneezing"; BODY TEMPERATURE INCREASED (non-serious) with onset 29Oct2021 12:00, outcome "not recovered", described as "2 degrees elevated temperature". The events "loss of balance", "severe heart pounding", "elevated blood pressure", "severe headache", "sharp pains behind eyes", "exaggerated tinnitus", "exhaustion", "muscle aches", "nauseous", "vomiting", "dizziness", "unable to focus", "diarrhea", "severe bloating and gas in chest and belly", "muscle pain in shoulders", "exaggerated tmj", "lock jaw left jaw", "pain in both ears", "coughing", "sneezing" and "2 degrees elevated temperature" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. List of any other medications the patient received within 2 weeks of vaccination: Xarelto and others. Did the adverse event result in any of the following? Doctor or other healthcare professional office/clinic visit. Prior to vaccination, the patient was not diagnosed with COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20211029; Test Name: blood pressure; Result Unstructured Data: Test Result:Elevated; Test Date: 20211029; Test Name: temperature; Result Unstructured Data: Test Result:2 degrees elevated
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Drug allergy; Fish allergy; Hernia repair; Ileoanal anastomosis; Osteoporosis; Pulmonary embolism
Andere Medikamente: XARELTO
Allergien: -
Vorherige Impfungen: -

VAERS 2140245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: OH
Alter: 33,0
Geschlecht: M
Eingang: 25.02.2022
Impfdatum: 23.02.2022
Beginn: 25.02.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Vertigo

Symptomtext

Some chest soreness on left side around 1:15 p.m. and 4:15 p.m. on 2/23/2022 and vertigo at 10:00 a.m. on 2/25 and chest soreness at 3:10 p.m. on 2/25/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Called the immunization clinic and spoke to the immunization clinic nurse on 2/25/2022. Nurse went over symptoms with me by phone and advised me to complete VAERS. She did not want me to come back to the clinic.
Aktuelle Erkrankungen: None
Vorgeschichte: joint pain, headaches, traumatic brain injury
Andere Medikamente: None
Allergien: None - just seasonal allergies
Vorherige Impfungen: -

VAERS 2123186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 15.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

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

Dyspnoea Musculoskeletal chest pain

Symptomtext

Patient with PMH AML, s/p stem cell transplant x2, history of GVHD including lung - baseline oxygen supp of 3L at home, previous pulmonary embolism in past. Received Pfizer vaccine on 2/15 and presented to our emergency center with new onset chest pain across anterior chest wall, more severe than usual, and shortness of breath, not improved by inhalers. Admitted to hospital.

Weitere VAERSDATA-Felder

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

VAERS 2201210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 23.11.2021
Beginn: 25.12.2021
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Headache Myalgia Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 03/082, Pfizer, dose #1 03/27, Pfizer, dose #2 11/23, Pfizer, dose #3 12/27 COVID swab, result: detected 12/25 pt cc: cough, rhinorrhea, headache, myalgias, dyspnea, sore throat exposure: unknown

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/27 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2095609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 13.12.2021
Beginn: 27.01.2022
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Atrial fibrillation Bladder catheterisation Blood creatinine increased Blood immunoglobulin G normal Bradycardia COVID-19 COVID-19 pneumonia Cardiac telemetry Chest X-ray abnormal Chromaturia Chronic obstructive pulmonary disease Cough Dehydration Electrocardiogram abnormal Exposure to SARS-CoV-2 Fatigue Glomerular filtration rate

Symptomtext

PROGRESS NOTE 02/07/2021 The patient is an 82-year-old woman with complicated past medical history including chronic systolic heart failure (EF 40-45%), history of bilateral ureteral obstruction and bladder outlet obstruction s/p bilateral ureteral stent exchange 12/20/2021, stage I CLL taking ibrutinib, history of limited stage renal cancer s/p partial left nephrectomy in 2009, CKD stage IV (baseline creatinine around 1.7), essential hypertension, type 2 diabetes, mild dementia with agitation and behavioral disturbances, gout, neuropathy, and recent positive Covid test 1/23/2022 who was admitted to hospitalist medicine service from emergency department 2/3/2022 with mild to moderate COVID-19, Covid pneumonia. #. COVID pneumonia #. Moderate COVID 19: Recovering. The patient tested positive for COVID-19 1/23/2022 as a patient was screened due to recent Covid exposure. COVID symptoms began 1/27/2022 (harsh, nonproductive cough with associated fatigue). Portable chest x-ray on admission demonstrating vascular congestion with increased opacification to right lung field concerning for infection. The patient's resting room air SPO2 was transiently 89%, but acute hypoxemic respiratory failure not present. Procalcitonin 0.04; however white count more elevated and more focal opacity to right perihilar lung field concerning for superimposed bacterial pneumonia. -Empiric dexamethasone 6 mg p.o. daily, discontinue 2/7/2022 as patient appears to be recovering -Taking apixaban (also for atrial fibrillation - see below) -Continuing empiric IV ceftriaxone + oral doxycycline through 2/10/2022 -Trending inflammatory markers -As needed antitussives #. Acute kidney injury on CKD stage III-IV: Patient's baseline creatinine is 1.7, and the patient's creatinine was 2 on admission. The patient's acute kidney injury most likely prerenal due to dehydration; however, mild cardiorenal syndrome can't be ruled out. Cr of 2 might be patient's new baseline. Bladder outlet obstruction ruled out. Protein/Creatine ratio > 9, nephrotic range proteinuria. Less likely cardiorenal syndrome (acute CHF) but will continue to watch closely. -Ginger diuresis w/ IV lasix 2/7/2022 -Holding PTA oral lasix -Trending GFR #. Chronic systolic heart failure: Acute CHF less likely as lung findings thought to be mainly 2/2 viral and bacterial pneumonia. EDW 225 lbs, and admission weight 233 lbs. Would benefit from fluid de resuscitation since oral held since admission. -20 mg IV lasix every 6 hours x 3 doses -Daily weights -Strict Is and Os #. Asymptomatic bradycardia: The patient's daughter reported that the patient has had low heart rates for at least 3 weeks. Twelve-lead EKG demonstrating atrial fibrillation with slow response perhaps related to sick sinus syndrome. No immediate need for pacemaer -Cardiology following, recommendations much appreciated -Holding PTA metoprolol indefinitely -Telemetry #. Newly diagnosed atrial fibrillation: 2/3/2022 twelve-lead EKG demonstrating slow atrial fibrillation. The patient does not have a known history of atrial fibrillation. CHADS2VASC of at least 4. -Cardiology following -Apixaban 2.5 mg po bid (renally dosed), initiated 2/4/2022 #. Hx of bladder outlet obstruction and bilateral ureteral obstruction: S/P bilateral ureteral stent placement 12/20/2021 and patient's daughter was told that patient's left ureteral stent high risk for occluding. 2/4/2022 renal US only demonstrating mild hydronephrosis bilaterally, acute ureteral obstruction and bladder outlet obstruction ruled out. #. Gross hematuria: Starting 2/7/2022, more red urine observed in foley bag. Will re evaluate for UTI. Gross hematuria most likely exacerbated by taking apixaban. -Continue to monitor -Consider urology consult #. CLL: Diagnosed stage I 6/30/2021. Patient follows w/ Dr. through Health Center. Restarting PTA ibrutinib after discussing case w/ Dr. IgG level WNL, no IVIG needed. #. Complex lesion to left kidney, incidental finding: Was present on previous US 8/21/2020, actually decreased in size. Did not discuss findings with patient. #. Essential HTN: -PTA hydralazine and imdur -Holding PTA metoprolol XL due to bradycardia #. Leukocytosis: Hx of CLL further exacerbated by dexamethasone. -Dexamethasone discontinued 2/7/2022 #. Dementia w/ agitation and behavioral disturbances: -PRN seroquel, PRN haldol if not tolerating PO #. COPD: -PTA inhalers #. Gout: -PTA allopurinol #. Depression: -PTA cymbalta #. Morbid obesity: BMI 44.99

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: COVID POSITIVE HOME TEST 1/23/2021
Aktuelle Erkrankungen: -
Vorgeschichte: 82-year-old woman with complicated past medical history including chronic systolic heart failure (EF 40-45%), history of bilateral ureteral obstruction and bladder outlet obstruction s/p bilateral ureteral stent exchange 12/20/2021, stage I CLL taking ibrutinib, history of limited stage renal cancer s/p partial left nephrectomy in 2009, CKD stage IV (baseline creatinine around 1.7), essential hypertension, type 2 diabetes, mild dementia with agitation and behavioral disturbances, gout, neuropathy,
Andere Medikamente: -
Allergien: Dilaudid [hydromorphone (bulk)], Nsaids (non-steroidal anti-inflammatory drug), Penicillins, and Vicodin [hydrocodone-acetaminophen]
Vorherige Impfungen: -

VAERS 2075700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 18.03.2021
Beginn: 27.01.2022
Tage bis Beginn: 315,0
Dosis: 3
Route/Site: - / -

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

Atrial fibrillation COVID-19 Dyspnoea Heart rate increased SARS-CoV-2 test positive

Symptomtext

Pt came to ED due to rapid heart rate (pt has atrial fibrillation) and feeling short of breath. He was found to be COVID positive.

Weitere VAERSDATA-Felder

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

VAERS 2074723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: SC
Alter: 49,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Cough Dyspnoea Influenza like illness Laryngitis Wheezing

Symptomtext

Worsen cough than normal. Constant wheezing flu like symptoms hard time breathing laryngitis. Several rounds of antibiotics and steroid. Cough meds mucinex and tesslon pearls duo neb treatments

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sinus and post nasal drip. Severe allergies and asthma
Vorgeschichte: Asthma with slight cough since I was a child
Andere Medikamente: Met Formin 500 mg 2 tabs 2 x day Escitalopram 20 mg 1 x day Cetirizine 10 mg 1 x day Amplodipine besylate 10 mg 1 x day
Allergien: Allergic to shellfish
Vorherige Impfungen: TB skin test

VAERS 2068943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 29.11.2021
Beginn: 19.01.2022
Tage bis Beginn: 51,0
Dosis: 3
Route/Site: IM / LA

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

Cough Decreased appetite Diarrhoea Dyspnoea

Symptomtext

reported to the ER and later admitted with shortness of breath and cough X 1 week. decreased appetite, and diarrhea. fully vaccinated with booster. treated with supportive care, O2, steroids and remdesivir

Weitere VAERSDATA-Felder

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

VAERS 2065548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MN
Alter: 62,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 26.04.2021
Beginn: 25.01.2022
Tage bis Beginn: 274,0
Dosis: 3
Route/Site: UN / UN

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

Back pain Chills Decreased appetite Dyspnoea Exposure to SARS-CoV-2 Haemorrhage Headache Nausea Oropharyngeal pain Renal pain SARS-CoV-2 test negative SARS-CoV-2 test positive Ureteral stent insertion

Symptomtext

ED NOTES 1/25/22: Patient first noticed blood in L PNT 5 days ago on 1/20, which persisted for 2 days and then stopped. It restarted last night (1/24). Has not noticed clots. Also reporting chills, nausea with her pain (back/"kidney" pain), decreased appetite, shortness of breath, and headache. Regarding COVID, her son who lives her tested positive about 19 days ago. She had a sore throat 2 weeks ago, which has since resolved. She suspects that she got it from her son as she does not leave the house much beyond that, gets her groceries delivered. They had attempted to quarantine as much as possible with living on separate floors and masks in the house. She did also undergo a PNT exchange 1/5/2022. When her son tested positive, she did do a home test, which was negative at that time. She did not get another test after her sore throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Positive COVID-19 PCR 1/25/22
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety, depression, GERD, HTN, and anorectal CA c/b rectovaginal fistula s/p s/p colostomy and chemoradiation c/b radiation cystitis c/b cystectomy w/ transverse colon conduit (2017) c/b L ureterocolonic stenosis s/p colostomy, nephrostomy tube, and L PNT (last exchanged 1/5/2022).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: FL
Alter: 86,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 13.03.2021
Beginn: 19.01.2022
Tage bis Beginn: 312,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest X-ray normal Cough Dyspnoea Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 02/20/2021. 86 y/o PMH HTN, Vertigo, Neuropathy, Depression, Laminectomy presents to ED with c/o increasing SOB, intemittent fevers, cough and congestion. Room air sat 84%, O2 2L NC 97%. CXR-clear. Treated with IV Steroids, IV ABX and Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected 01/19/2022
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Vertigo, Neuropathy, Depression, chronic back pain s/p laminectomy
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1971600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 24.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Bacterial test negative Chlamydia test negative Dehydration Feeding disorder Fluid intake reduced Behcet's syndrome Investigation Mouth ulceration Oropharyngeal pain Pharyngeal ulceration HIV test negative Herpes simplex test negative Laboratory test normal Oral disorder SARS-CoV-2 test Symptom recurrence Tongue disorder Vaginal ulceration

Symptomtext

Behcet's disease; symptoms progressed to ulcerations in oral/throat/vaginal area; symptoms progressed to ulcerations in oral/throat/vaginal area; symptoms progressed to ulcerations in oral/throat/vaginal area; sore throat and tongue lesions/ symptoms reoccur with additional vaginal pain/burning; sore throat and tongue lesions/ symptoms reoccur with additional vaginal pain/burning; sore throat and tongue lesions/ symptoms reoccur with additional vaginal pain/burning; vaginal pain/burning; vaginal pain/burning; This is a spontaneous report received from a contactable reporter [other healthcare professional (HCP)] via company. A 39 year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), intramuscular, administered in arm left, administration date 24Nov2021 (Lot number: 32030BD) at the age of 39 years as dose 2, single for COVID-19 immunization. Relevant medical history included: "diagnosed with COVID-19" (unspecified if ongoing), notes: prior to vaccination. The patient had no known allergies (NKDA). The patient's concomitant medications were not reported. Vaccination history included: BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE (dose 1, single, Lot number: 301358A, administration route and location: intramuscular, left arm), administration date: 07Oct2021, when the patient was 39 years old, for COVID-19 immunization, reactions: "sore throat" and "tongue lesions." Since the vaccination, the patient had been tested for COVID-19 with COVID-19 test result of negative post vaccination on an unspecified date. The following information was reported: BEHCET'S SYNDROME (hospitalization, medically significant), outcome "unknown," described as "Behcet's disease;" OROPHARYNGEAL PAIN (hospitalization), TONGUE DISORDER (hospitalization), and SYMPTOM RECURRENCE (hospitalization) all with onset 26Nov2021, outcome "unknown" and all described as "sore throat and tongue lesions/ symptoms reoccured with additional vaginal pain/burning;" VULVOVAGINAL PAIN (hospitalization) and VULVOVAGINAL BURNING SENSATION (hospitalization) both with onset 26Nov2021, outcome "unknown" and both described as "vaginal pain/burning;" and MOUTH ULCERATION (hospitalization), PHARYNGEAL ULCERATION (hospitalization), and VAGINAL ULCERATION (hospitalization) all with onset Dec2021, outcome "unknown" and all described as "symptoms progressed to ulcerations in oral/throat/vaginal area." All the events were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: extensive work-up: (2021) negative for infection and COVID-19 test: (unspecified date) negative, notes: post vaccination. Therapeutic measures were taken as a result of all the events. It was further reported that on 24Nov2021, the patient received 2nd dose and on 26Nov2021, the symptoms that developed during 1st Pfizer dose (sore throat and tongue lesions) reoccurred with additional vaginal pain/burning. Over the next month, symptoms progressed to ulcerations in oral/throat/vaginal area, for which she had multiple visits and hospitalization and an extensive work-up negative for infection. Ultimately, the patient was diagnosed with Bechet's disease; symptoms responded to steroids.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events BEHCET'S SYNDROME, OROPHARYNGEAL PAIN, TONGUE DISORDER, SYMPTOM RECURRENCE, VULVOVAGINAL PAIN, VULVOVAGINAL BURNING SENSATION, MOUTH ULCERATION, PHARYNGEAL ULCERATION, VAGINAL ULCERATION 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: Dehydration
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Extensive work-up; Result Unstructured Data: Test Result:negative for infection; Test Name: COVID-19 test; Test Result: Negative ; Comments: post vaccination
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (prior to vaccination)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 24.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: OT / LA

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

Bacterial test negative Chlamydia test negative Dehydration Feeding disorder Fluid intake reduced Behcet's syndrome Investigation Mouth ulceration Oropharyngeal pain Pharyngeal ulceration HIV test negative Herpes simplex test negative Laboratory test normal Oral disorder SARS-CoV-2 test Symptom recurrence Tongue disorder Vaginal ulceration

Symptomtext

Behcet's disease; symptoms progressed to ulcerations in oral/throat/vaginal area; symptoms progressed to ulcerations in oral/throat/vaginal area; symptoms progressed to ulcerations in oral/throat/vaginal area; sore throat and tongue lesions/ symptoms reoccur with additional vaginal pain/burning; sore throat and tongue lesions/ symptoms reoccur with additional vaginal pain/burning; sore throat and tongue lesions/ symptoms reoccur with additional vaginal pain/burning; vaginal pain/burning; vaginal pain/burning; This is a spontaneous report received from a contactable reporter [other healthcare professional (HCP)] via company. A 39 year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), intramuscular, administered in arm left, administration date 24Nov2021 (Lot number: 32030BD) at the age of 39 years as dose 2, single for COVID-19 immunization. Relevant medical history included: "diagnosed with COVID-19" (unspecified if ongoing), notes: prior to vaccination. The patient had no known allergies (NKDA). The patient's concomitant medications were not reported. Vaccination history included: BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE (dose 1, single, Lot number: 301358A, administration route and location: intramuscular, left arm), administration date: 07Oct2021, when the patient was 39 years old, for COVID-19 immunization, reactions: "sore throat" and "tongue lesions." Since the vaccination, the patient had been tested for COVID-19 with COVID-19 test result of negative post vaccination on an unspecified date. The following information was reported: BEHCET'S SYNDROME (hospitalization, medically significant), outcome "unknown," described as "Behcet's disease;" OROPHARYNGEAL PAIN (hospitalization), TONGUE DISORDER (hospitalization), and SYMPTOM RECURRENCE (hospitalization) all with onset 26Nov2021, outcome "unknown" and all described as "sore throat and tongue lesions/ symptoms reoccured with additional vaginal pain/burning;" VULVOVAGINAL PAIN (hospitalization) and VULVOVAGINAL BURNING SENSATION (hospitalization) both with onset 26Nov2021, outcome "unknown" and both described as "vaginal pain/burning;" and MOUTH ULCERATION (hospitalization), PHARYNGEAL ULCERATION (hospitalization), and VAGINAL ULCERATION (hospitalization) all with onset Dec2021, outcome "unknown" and all described as "symptoms progressed to ulcerations in oral/throat/vaginal area." All the events were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: extensive work-up: (2021) negative for infection and COVID-19 test: (unspecified date) negative, notes: post vaccination. Therapeutic measures were taken as a result of all the events. It was further reported that on 24Nov2021, the patient received 2nd dose and on 26Nov2021, the symptoms that developed during 1st Pfizer dose (sore throat and tongue lesions) reoccurred with additional vaginal pain/burning. Over the next month, symptoms progressed to ulcerations in oral/throat/vaginal area, for which she had multiple visits and hospitalization and an extensive work-up negative for infection. Ultimately, the patient was diagnosed with Bechet's disease; symptoms responded to steroids.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events BEHCET'S SYNDROME, OROPHARYNGEAL PAIN, TONGUE DISORDER, SYMPTOM RECURRENCE, VULVOVAGINAL PAIN, VULVOVAGINAL BURNING SENSATION, MOUTH ULCERATION, PHARYNGEAL ULCERATION, VAGINAL ULCERATION 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: Dehydration
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Extensive work-up; Result Unstructured Data: Test Result:negative for infection; Test Name: COVID-19 test; Test Result: Negative ; Comments: post vaccination
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (prior to vaccination)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: PR
Alter: 47,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea

Symptomtext

Patient verbalizes that when he arrived home after the administration of the COVID-19 vaccine he presented respiratory difficulty and epinephrine of his own was administered and he did not have to go to the hospital.

Weitere VAERSDATA-Felder

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

VAERS 2025746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MT
Alter: 22,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 29.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / RA

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

Anxiety Blood test Cardiac monitoring Chest discomfort Chest pain Chills Dyspnoea Echocardiogram Fatigue Heart rate increased Magnetic resonance imaging heart Nausea Retching

Symptomtext

Rapid heart rate, extreme fatigue, chills, chest pain, shortness of breath, chest tightness, nausea, dry heaves, abnormal anxiety

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 8,0
Labordaten: Heart MRI, Heart Echocardiogram, Blood tests (unknown which ones exactly), heart monitor.
Aktuelle Erkrankungen: Covid on 11/10/21-11/20/21
Vorgeschichte: None
Andere Medikamente: Zyrtec allergy medicine every now and then. And FloNase
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2001409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: SC
Alter: 74,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Bundle branch block right Chest pain Electrocardiogram Laboratory test Troponin

Symptomtext

PATIENT DEVELOPED SHARP CHEST PAIN ON THE RIGHT SIDE WITHIN 15 MINUTES OF RECEIVING BOOSTER. NO SHORTNESS OF BREATH. PATIENT TRANSFERRED TO THE ED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ECG - NORMAL SINUS RHYTHM AT 60 BPM WITH A RIGHT BUNDLE BRANCH BLOCK. UNCHANGED FROM PREVIOUS ECG. LAB TESTS - NO ISSUES. TROPONIN <0.012
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: CODEINE
Vorherige Impfungen: -

VAERS 1995304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 31.12.2021
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

Arthralgia Dyspnoea Immunisation Muscle fatigue Myalgia

Symptomtext

achy joints/deep joint pain; achy joints/muscles; breathing issues/difficulty breathing heavily during exercise (lungs dont feel like they expand or breath in enough).; Normal muscle fatigue; booster; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 17Nov2021 18:30 (Lot number: 32030BD) at the age of 35 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: ER8780, Location of injection: Arm Right), administration date: 07Apr2021, when the patient was 35 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP6955, Location of injection: Arm Right), administration date: 23Mar2021, when the patient was 35 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 17Nov2021 18:30, outcome "unknown", described as "booster"; ARTHRALGIA (non-serious) with onset 18Nov2021, outcome "recovering", described as "achy joints/deep joint pain"; MYALGIA (non-serious) with onset 18Nov2021, outcome "recovering", described as "achy joints/muscles"; DYSPNOEA (non-serious) with onset 18Nov2021, outcome "recovering", described as "breathing issues/difficulty breathing heavily during exercise (lungs dont feel like they expand or breath in enough)."; MUSCLE FATIGUE (non-serious) with onset 18Nov2021, outcome "recovering", described as "Normal muscle fatigue". Therapeutic measures were not taken as a result of immunisation, arthralgia, myalgia, dyspnoea, muscle fatigue. Additional information: It was reported that beyond that 48 hour after the booster (3rd) shot, the patient continues to have achy joints, muscles plus some minor breathing issues. Normal muscle fatigue was normal with working out etc. However, the deep joint pain, difficulty breathing heavily during exercise (lungs don't feel like they expand or breath in enough). The patient reported that the events are nothing severe however it was persistent and not normal based on her body before the booster vaccine. No issues persisting after initial, or 2nd dose. 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 had not received any other vaccines within 4 weeks prior to the COVID vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: Penecillin); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1982085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: HI
Alter: 39,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 13.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test normal Hypertension

Symptomtext

At a routine visit with my gynecologist for an annual exam on 12/13/2021, my blood pressure was the highest it has ever been in my life. It was 125/100 at the time of my appt. My normal blood pressure is 100/70. My doctor was concerned and took it again 30 min later, and it was still 125/100. She told me to have it taken again later in the afternoon. Three hours later, my blood pressure was read to be 122/89. I had to make an appt with my primary care to have everything else checked out. At my appt with my PCP on 12/17/21, my blood pressure was read at 122/75. NP Butac suggested buying a blood pressure machine and to check it regularly. He also ordered a complete metabolic blood lab. Since then, my blood pressure has remained in the "hypertension - stage 1" level with my diastolic reading above 80.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Blood pressure readings listed above. Blood work/labs all were in normal ranges.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypoglycemia
Andere Medikamente: BCP
Allergien: Penicillin Amoxicillin
Vorherige Impfungen: -

VAERS 1933131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 23.12.2021
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: nein

Electrocardiogram Tachycardia Vaccine positive rechallenge Immunisation

Symptomtext

Tachycardia; Dose received:3/ dose number=3; This is a spontaneous report from a contactable reporter (Other HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 07Dec2021 at 11:45 (Lot number: 32030BD) at the age of 54 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Hashimoto's thyroiditis" (unspecified if ongoing); "Sulfonamide allergy" (unspecified if ongoing), notes: Known allergies: Sulfa Drugs and "Allergy to antibiotic" (unspecified if ongoing), notes: Known allergies: Tetracyclines. Concomitant medication(s) included: SYNTHROID. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: ER8732; Administration Time: 13:45: Anatomical location: Left Arm; Route of administration: Unspecified), administration date: 01Apr2021, when the patient was 53 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EW0171; Administration Time: 13:45: Anatomical location: Left Arm; Route of administration: Unspecified), administration date: 22Apr2021, when the patient was 53 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 07Dec2021 at 11:45, outcome "unknown", described as "Dose received:3/ dose number=3"; TACHYCARDIA (non-serious) with onset 08Dec2021 at 00:00, outcome "recovering", described as "Tachycardia". The event "Tachycardia" was evaluated at the physician office visit. Therapeutic measures were taken as a result of tachycardia. 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. Treatment for TACHYCARDIA included Bystolic (Beta Blocker).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic (Known allergies: Tetracyclines); Hashimoto's thyroiditis; Sulfonamide allergy (Known allergies: Sulfa Drugs)
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1967934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MD
Alter: 37,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 05.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Depression Headache Heavy menstrual bleeding Injection site discolouration Lymph node pain Lymphadenopathy Mood swings Weight increased

Symptomtext

I experienced excessive bleeding during my menstrual cycle, increased headache, weight gain and sadness & depression. My lymph nodes on the left side of my neck were swollen and lymph nodes under my left axillary tender to touch (difficult to apply deodorant). I contacted my GYN and was advised that these are common symptoms that people are experiencing. As of today, I still have skin discoloration at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Headaches (hormonal)
Andere Medikamente: Excedrin
Allergien: Pet litter, Dust, Mold, Seasonal allergies
Vorherige Impfungen: Flu vaccine (2020 tired, weakness).

VAERS 1962204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: GA
Alter: 39,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Injected limb mobility decreased Pain in extremity

Symptomtext

Arm and shoulder pain, loss of mobility on arm of injection site, still occurring

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin Liquid Gold
Allergien: None
Vorherige Impfungen: -

VAERS 1959143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 10.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Diarrhoea Dyspnoea Pyrexia SARS-CoV-2 test positive

Symptomtext

11/28/21 pt was admitted to hospital with SOB, diarrhea, and fevers - pt confirmed pos for COVID pt treated with O2, Decadron and remdesivir 12/7/21 pt discharged to home on O2 12/14/21 pt feels she has improved ox readings arounf 95%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: s/p renal transplant, CKD, HTN, chronic pain syndrome, hyperparathyroidism
Andere Medikamente: acetaminophen, cinacalcet, clonidine, doxazosin, famotidine, labatelol, lorazepam, Mg, mycophenolate, prednisone, tacrolimus
Allergien: Benadryl, Bactrim, Augmentin, morphine, sulfa, Coreg, spironolactone
Vorherige Impfungen: -

VAERS 1950750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 83,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Blood sodium Blood sodium decreased Body temperature Constipation Dehydration Immunisation Investigation Pyrexia Urine output decreased Weight increased

Symptomtext

Booster dose; Got a temperature of a 103; It caused me not to go to the bathroom and I just did not/ I wasn't peeing; My sodium had gone much too low; I was dehydrated/ High temperature was using up all the liquid in my body; I suddenly gained 10 pounds; Constipation; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 83-year-old female patient received bnt162b2 (BNT162B2), administration date 11Nov2021 (Lot number: 32030BD) at the age of 83 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Lupus" (unspecified if ongoing), notes: not taking any medication for that; "heart condition" (unspecified if ongoing), notes: have a heart condition and is taking 'Norpace'. Concomitant medication(s) included: NORPACE taken for cardiac disorder. Vaccination history included: Covid-19 vaccine (Dose:01, Unknown manufacturer, unknown lot number), for Covid-19 immunization; Covid-19 vaccine (Dose:02, Unknown manufacturer, unknown lot number), for Covid-19 immunization. No any prior vaccinations. The following information was reported: PYREXIA (hospitalization) with onset 2021, outcome "unknown", described as "Got a temperature of a 103"; URINE OUTPUT DECREASED (hospitalization) with onset 2021, outcome "unknown", described as "It caused me not to go to the bathroom and I just did not/ I wasn't peeing"; BLOOD SODIUM DECREASED with onset 2021, outcome "unknown", described as "My sodium had gone much too low"; DEHYDRATION with onset 2021, outcome "unknown", described as "I was dehydrated/ High temperature was using up all the liquid in my body"; WEIGHT INCREASED with onset 2021, outcome "unknown", described as "I suddenly gained 10 pounds"; CONSTIPATION with onset 2021, outcome "unknown", described as "Constipation". The patient was hospitalized for pyrexia, urine output decreased (start date: 17Nov2021, discharge date: 18Nov2021, hospitalization duration: 1 day(s)). The events "got a temperature of a 103" and "it caused me not to go to the bathroom and I just did not/ I wasn't peeing" were evaluated at the emergency room visit. Additional infomation: Consumer stated that she had an adverse reaction to the Pfizer booster shot and they sent her to the hospital twice and she wants to report it.". Vaccine name: Pfizer Covid-19 Vaccine. Weight: Consumer stated, her weight is 94 or 95 pounds. When further confirmed if discharged date is 18Nov2021, consumer stated that she think so. Treatment: Consumer stated, "The first time, they gave me, I was dehydrated, the high temperature was using up all the liquid in my body and so, they told me to take Tylenol. The patient underwent the following laboratory tests and procedures: blood sodium: (2021) too low, notes: sodium had gone much too low; body temperature: (2021) 103, notes: high; investigation: (2021) unknown results; weight increased: (2021) 10, notes: pounds. Therapeutic measures were taken as a result of pyrexia, treatment included Tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: Test Date: 2021; Test Name: Sodium; Result Unstructured Data: Test Result:Too low; Comments: sodium had gone much too low; Test Date: 2021; Test Name: Temperature; Result Unstructured Data: Test Result:103; Comments: high; Test Date: 2021; Test Name: bunch of lab tests; Result Unstructured Data: Test Result:Unknown results; Test Date: 2021; Test Name: gained 10 pounds; Result Unstructured Data: Test Result:10; Comments: pounds
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cardiac disorder (have a heart condition and is taking 'Norpace'); Lupus syndrome (not taking any medication for that)
Andere Medikamente: NORPACE
Allergien: -
Vorherige Impfungen: -

VAERS 1947833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: AZ
Alter: 34,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 08.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Echocardiogram Electrocardiogram Musculoskeletal chest pain

Symptomtext

First symptoms were chest tightness and pain. The following three days, the left side of chest was tender to the touch and I had tightness in chest anytime I tried to take a deep breath. Heavy feeling in chest and pain. The next few days the pain subsided slightly and to this day, still have little pings of pain in area where heart is located.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: November 24, 2021: visit to cardiologist, they did EKG and blood saturation check. Results were normal. December 6, 2021: second visit to cardiologist where they did an echocardiogram. Will not get results until Dec 21. December 15, 2021: will be going to 3rd visit for a treadmill stress test. Will get results on Dec 21.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1868275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Pain Pain in extremity Sciatica Condition aggravated Immunisation

Symptomtext

Severe sciatica pain on my left leg, starting at the hip level and radiating downwards; It is worse when I try to get up in the morning; booster shot we got; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 09Nov2021 17:00 (Lot number: 32030BD) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing), notes: other medical history: No. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6206, Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 22Mar2021, when the patient was 61 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6202, Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 01Mar2021, when the patient was 61 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 09Nov2021 17:00, outcome "unknown", described as "booster shot we got"; SCIATICA (non-serious) with onset 11Nov2021 08:00, outcome "not recovered", described as "Severe sciatica pain on my left leg, starting at the hip level and radiating downwards"; CONDITION AGGRAVATED (non-serious) with onset 11Nov2021 08:00, outcome "not recovered", described as "It is worse when I try to get up in the morning". Additional information: It started one and a half day after I got the vaccine. It is worse when I try to get up in the morning. The patient had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. At that point she didn't connect this to the vaccine. Now she thinks that this may be correlated to the booster shot she got. The patient was not diagnosed with COVID-19 prior to vaccination, nor was tested since vaccination. The device date was 14Nov2021. Follow-up attempts completed. No further information expected; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101578829 same reporter/drug, different patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No, Comment: other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1868275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Pain Pain in extremity Sciatica Condition aggravated Immunisation

Symptomtext

Severe sciatica pain on my left leg, starting at the hip level and radiating downwards; It is worse when I try to get up in the morning; booster shot we got; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 09Nov2021 17:00 (Lot number: 32030BD) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing), notes: other medical history: No. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6206, Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 22Mar2021, when the patient was 61 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6202, Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 01Mar2021, when the patient was 61 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 09Nov2021 17:00, outcome "unknown", described as "booster shot we got"; SCIATICA (non-serious) with onset 11Nov2021 08:00, outcome "not recovered", described as "Severe sciatica pain on my left leg, starting at the hip level and radiating downwards"; CONDITION AGGRAVATED (non-serious) with onset 11Nov2021 08:00, outcome "not recovered", described as "It is worse when I try to get up in the morning". Additional information: It started one and a half day after I got the vaccine. It is worse when I try to get up in the morning. The patient had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. At that point she didn't connect this to the vaccine. Now she thinks that this may be correlated to the booster shot she got. The patient was not diagnosed with COVID-19 prior to vaccination, nor was tested since vaccination. The device date was 14Nov2021. Follow-up attempts completed. No further information expected; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101578829 same reporter/drug, different patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No, Comment: other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1936702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: IL
Alter: 73,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 10.11.2021
Beginn: 09.12.2021
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / RA

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

Muscle spasms Pain in extremity Paraesthesia Tenderness

Symptomtext

Patient received his COVID booster 11/10/2021. Patient came in on 12/09/2021 to let me know that he has had intermittent right arm and right leg pain. Reports he believes related to vaccine as it started day after the vaccine and has been intermittent since receiving the vaccine. Described right arm pain as cramping and tender with movement. Described right leg pain as pins and needles. Reports right leg pain does not interfere with walking and not bothersome with walking

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Referred patient to his primary care doctor for further work up to see if related to vaccine or other chronic causes
Aktuelle Erkrankungen: HTN Diabetes
Vorgeschichte: HTN Diabetes
Andere Medikamente: Patient poor historian with medications Reported being on two blood pressure medications and two blood sugar medications (knows one was metformin)
Allergien: Aspirin Penicillin
Vorherige Impfungen: -

VAERS 1923929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: IL
Alter: 27,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 08.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal discomfort Anion gap Aspiration Basophil count increased Basophil percentage decreased Blood calcium decreased Blood chloride normal Blood creatinine decreased Blood culture negative Blood glucose normal Blood lactic acid Blood magnesium normal Blood potassium normal Blood sodium decreased Blood urea decreased Blood urea nitrogen/creatinine ratio Carbon dioxide normal Chest X-ray abnormal

Symptomtext

Vaccine was given on November 8th at approximately 12:30pm in my right upper arm. Upon leaving, my arm was sore and I had some fatigue, and cough The next morning November 9th at around 1:30am I was having chills. Around 08:30am I had woke up and had a slight fever of 100.5 , I drank water and it went away, Also during this time I had a bad cough and chest congestion November 10th I woke up around 7:30am extremely dizzy, my cough returned so I took two teaspoons of cough syrup and returned to my bed to lie down for an hour. 08:30am I woke up still remaining extremely dizzy and I also had an upset stomach, I felt nauseated so I continued to take my daily medication and made myself oatmeal for breakfast, I ate a few bites and vomited. I continued to vomit the next several hours, during this I aspirated and my oxygen level dropped to 68% on 3L of oxygen and I also had a 103.5 fever. Upon this time my Grandma and I decided to go to the ER, I was hospitalized for four days for Aspiration Pneumonia and a partly collapsed lung

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia aspiration
Hospital-Tage: 4,0
Labordaten: November 10th Covid test : Negative Portable Chest Xray: pneumonia CT with Contrast: Partly Collapsed Lung BLOOD CULTURE FOR BACTERIA: CULTURE RESULTS NO GROWTH WITHIN 5 DAYS, FINAL RESULT November 11th LACTIC ACID ASSAY - Component Your Value Standard Range Flag LACTIC ACID 1.0 mmol/L 0.7 - 2.0 mmol/L CBC WITH AUTO DIFFERENTIAL: Component Your Value Standard Range Flag WBC 25.47 10(3)/mcL 4.00 - 12.00 10(3)/mcL H RBC 4.40 10(6)/mcL 3.80 - 5.30 10(6)/mcL HEMOGLOBIN (HGB) 13.4 g/dL 12.0 - 15.8 g/dL HEMATOCRIT (HCT) 42.0 % 36.0 - 47.0 % MCV 95.5 fL 82.0 - 96.0 fL MCH 30.5 pg 26.0 - 34.0 pg MCHC 31.9 g/dL 31.0 - 36.0 g/dL PLATELET COUNT 133 10(3)/mcL 140 - 440 10(3)/mcL L RDW 13.6 % 11.8 - 15.5 % MPV 10.8 fL 9.7 - 12.4 fL NEUTROPHILS 84.3 % 47.0 - 73.0 % H LYMPHOCYTES 8.2 % 18.0 - 42.0 % L MONOCYTES 7.1 % 4.0 - 12.0 % EOSINOPHILS 0.2 % 0.0 - 5.0 % BASOPHILS 0.2 % 0.0 - 1.0 % ABSOLUTE NEUTROPHILS 21.45 10(3)/mcL 1.60 - 7.70 10(3)/mcL H ABSOLUTE LYMPHOCYTES 2.10 10(3)/mcL 1.30 - 3.20 10(3)/mcL ABSOLUTE MONOCYTES 1.80 10(3)/mcL 0.20 - 1.00 10(3)/mcL H ABSOLUTE EOSINOPHIL 0.06 10(3)/mcL 0.00 - 0.40 10(3)/mcL ABSOLUTE BASOPHILS 0.06 10(3)/mcL 0.00 - 0.10 10(3)/mcL NRBC PER 100 WBC 0 RESULTS ARE CONSISTENT WITH PERIPHERAL SMEAR REVIEW Yes BMP WITH CA,TOTAL Component Your Value Standard Range Flag SODIUM 133 mmol/L 136 - 145 mmol/L L POTASSIUM 3.7 mmol/L 3.5 - 5.1 mmol/L CHLORIDE 100 mmol/L 98 - 107 mmol/L CO2, VENOUS 23 mmol/L 22 - 30 mmol/L ANION GAP 10.0 mmol/L <18.0 mmol/L GLUCOSE 76 mg/dL 70 - 99 mg/dL BUN 9 mg/dL 5 - 18 mg/dL CREATININE, BLOOD 0.49 mg/dL 0.60 - 1.00 mg/dL L BUN/CREATININE RATIO 18 ratio 12 - 20 ratio CALCIUM 8.3 mg/dL 8.7 - 10.5 mg/dL L GFR, EST. NONAFRICAN >60 >=60 GFR, EST. AFRICAN >60 >=60 November 12th BMP WITH CA,TOTAL Component Results Component Your Value Standard Range Flag SODIUM 134 mmol/L 136 - 145 mmol/L L POTASSIUM 4.0 mmol/L 3.5 - 5.1 mmol/L CHLORIDE 97 mmol/L 98 - 107 mmol/L L CO2, VENOUS 28 mmol/L 22 - 30 mmol/L ANION GAP 9.0 mmol/L <18.0 mmol/L GLUCOSE 105 mg/dL 70 - 99 mg/dL H BUN 10 mg/dL 5 - 18 mg/dL CREATININE, BLOOD 0.45 mg/dL 0.60 - 1.00 mg/dL L BUN/CREATININE RATIO 22 ratio 12 - 20 ratio H CALCIUM 8.6 mg/dL 8.7 - 10.5 mg/dL L GFR, EST. NONAFRICAN >60 >=60 GFR, EST. AFRICAN >60 >=60 ASSAY MAGNESIUM MAGNESIUM 1.6 mg/dL CBC WITH AUTO DIFFERENTIAL WBC 13.44 10(3)/mcL 4.00 - 12.00 10(3)/mcL H RBC 4.25 10(6)/mcL 3.80 - 5.30 10(6)/mcL HEMOGLOBIN (HGB) 13.2 g/dL 12.0 - 15.8 g/dL HEMATOCRIT (HCT) 40.5 % 36.0 - 47.0 % MCV 95.3 fL 82.0 - 96.0 fL MCH 31.1 pg 26.0 - 34.0 pg MCHC 32.6 g/dL 31.0 - 36.0 g/dL PLATELET COUNT 144 10(3)/mcL 140 - 440 10(3)/mcL RDW 13.6 % 11.8 - 15.5 % MPV 10.7 fL 9.7 - 12.4 fL NEUTROPHILS 72.5 % 47.0 - 73.0 % LYMPHOCYTES 16.1 % 18.0 - 42.0 % L MONOCYTES 10.7 % 4.0 - 12.0 % EOSINOPHILS 0.6 % 0.0 - 5.0 % BASOPHILS 0.1 % 0.0 - 1.0 % ABSOLUTE NEUTROPHILS 9.74 10(3)/mcL 1.60 - 7.70 10(3)/mcL H ABSOLUTE LYMPHOCYTES 2.16 10(3)/mcL 1.30 - 3.20 10(3)/mcL ABSOLUTE MONOCYTES 1.44 10(3)/mcL 0.20 - 1.00 10(3)/mcL H ABSOLUTE EOSINOPHIL 0.08 10(3)/mcL 0.00 - 0.40 10(3)/mcL ABSOLUTE BASOPHILS 0.02 10(3)/mcL 0.00 - 0.10 10(3)/mcL NRBC PER 100 WBC 0 November 13th CBC WITH AUTO DIFFERENTIAL Component Your Value Standard Range Flag WBC 10.02 10(3)/mcL 4.00 - 12.00 10(3)/mcL RBC 4.18 10(6)/mcL 3.80 - 5.30 10(6)/mcL HEMOGLOBIN (HGB) 13.0 g/dL 12.0 - 15.8 g/dL HEMATOCRIT (HCT) 40.5 % 36.0 - 47.0 % MCV 96.9 fL 82.0 - 96.0 fL H MCH 31.1 pg 26.0 - 34.0 pg MCHC 32.1 g/dL 31.0 - 36.0 g/dL PLATELET COUNT 150 10(3)/mcL 140 - 440 10(3)/mcL RDW 13.1 % 11.8 - 15.5 % MPV 10.7 fL 9.7 - 12.4 fL NEUTROPHILS 74.7 % 47.0 - 73.0 % H LYMPHOCYTES 16.3 % 18.0 - 42.0 % L MONOCYTES 8.8 % 4.0 - 12.0 % EOSINOPHILS 0.0 % 0.0 - 5.0 % BASOPHILS 0.2 % 0.0 - 1.0 % ABSOLUTE NEUTROPHILS 7.49 10(3)/mcL 1.60 - 7.70 10(3)/mcL ABSOLUTE LYMPHOCYTES 1.63 10(3)/mcL 1.30 - 3.20 10(3)/mcL ABSOLUTE MONOCYTES 0.88 10(3)/mcL 0.20 - 1.00 10(3)/mcL ABSOLUTE EOSINOPHIL 0.00 10(3)/mcL 0.00 - 0.40 10(3)/mcL ABSOLUTE BASOPHILS 0.02 10(3)/mcL 0.00 - 0.10 10(3)/mcL NRBC PER 100 WBC 0 BMP WITH CA,TOTAL SODIUM 135 mmol/L 136 - 145 mmol/L L POTASSIUM 3.9 mmol/L 3.5 - 5.1 mmol/L CHLORIDE 96 mmol/L 98 - 107 mmol/L L CO2, VENOUS 32 mmol/L 22 - 30 mmol/L H ANION GAP 7.0 mmol/L <18.0 mmol/L GLUCOSE 134 mg/dL 70 - 99 mg/dL H BUN 9 mg/dL 5 - 18 mg/dL CREATININE, BLOOD 0.40 mg/dL 0.60 - 1.00 mg/dL L BUN/CREATININE RATIO 23 ratio 12 - 20 ratio H CALCIUM 8.4 mg/dL 8.7 - 10.5 mg/dL L GFR, EST. NONAFRICAN >60 >=60 GFR, EST. AFRICAN >60 >=60
Aktuelle Erkrankungen: No
Vorgeschichte: Congenital Heart Defects:Tetralogy Of Fallot(TOF)and Double Outlet RIght Ventricle(DORV) Right Bundle Branch Block (RBBB) Congestive Heart Failure Heart Murmur Stents BT Shunts x2 Chronic pulmonary disease Asthma GERD Scoliosis Omphalocele Obstructive Sleep Apnea Pacemaker with ICD Splenectomy Appendectomy
Andere Medikamente: Albuterol Sul 2.5mg/3ml soln (as needed via nebulizer ) Bipap (nightly) Clotrimazole-Betamethasone (as needed) Enalapril 5mg (twice a day) Ensure plus 8oz (twice a day) Flonase spray (as needed) Flovent HFA 110 MCG inhaler (twice a day) Fu
Allergien: Digoxin Bradycardia Fentanyl Unknown Silver nitrate Rash Around Gtube site Clindamycin Rash Amoxicillin Diarrhea Levaquin Ventricular tachycardia Adhesive Dressing rash
Vorherige Impfungen: -

VAERS 2565285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Ageusia Arthralgia Chills Dizziness Hypertension Nausea Pyrexia Vomiting

Symptomtext

Dizziness, Fever, NauseaVomiting, HYPERtension, loss of taste, chills, pain to left ankle and bilateral shoulders. Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1923555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: OH
Alter: 41,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 02.10.2021
Beginn: 18.11.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: IM / LA

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

Electrocardiogram normal Laboratory test normal Migraine Vertigo

Symptomtext

Vertigo daily since November 18th. I?ve never had vertigo issues before now. The vertigo is causing migraines more frequently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Hospital visit on November 18, 1st day of symptoms. Lab tests and ekg were all normal. Diagnosed with vertigo.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension
Andere Medikamente: Hydrochlorthiazide, potassium, ginger root, vitamin D, low dose aspirin, multivitamin, Zyrtec
Allergien: Macrobid and sulfa antibiotics
Vorherige Impfungen: -

VAERS 1922531

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 32030BD

moderat

Staat: NY
Alter: 57,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 04.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Herpes zoster Injection site pain

Symptomtext

Herpes Zoster outbreak, unusually severe. Sharp pains in the chest. As of the date of this report, some pain still at the injection site in the arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: slightly elevated blood pressure
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1914111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Dyspnoea Throat tightness

Symptomtext

Pt presented with signs shortness of breath. RN checked patients throat and saw that it was closing. Pt given epi 0.3mg on left thigh at 1617. Vitals taken, 96-98% O2 levels. Pt transferred to ED on first floor.

Weitere VAERSDATA-Felder

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

VAERS 1887818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: FL
Alter: 20,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Abdominal discomfort Chest pain Headache Pain in extremity

Symptomtext

Sore arm; Headache; Upset stomach; Chest pain; This is a spontaneous report from a contactable consumer, the patient. A 20-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the left arm on 12Nov2021 at 11:00 (at the age of 20-years-old) as a single dose for COVID-19 immunisation. Medical history included COVID-19. The patient had no known allergies. Prior to the vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient did not receive any concomitant medications. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF8841) via an unspecified route of administration in the left arm on 22Oct2021 at 11:00 (at the age of 20-years-old) as a single dose for COVID-19 immunisation. On 13Nov2021 at 09:00, the patient experienced sore arm, headache, upset stomach and chest pain. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events sore arm, headache, upset stomach and chest pain was resolved with sequelae on unknown date in Nov2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?: Yes.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1882908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Diarrhoea Dyspnoea Lymphadenopathy Muscle spasms Pain Palpitations

Symptomtext

Swollen lymph nodes, racing heart rate, diarrhea, muscle spasms, muscle cramps, body aches, shortness of breath.

Weitere VAERSDATA-Felder

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

VAERS 1880996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Dyspnoea

Symptomtext

Patient received her Pfizer booster on 11/18/21 at around 11:15 am. About 5 minutes after injection, patient began to experience 10/10 chest tightness across her entire chest, with trouble catching her breath. Patient was transported to the gurney and initial vital signs were 156/81, HR 91, 99% on RA. Patient was observed for an additional 30 minutes. At 11:55 VS: 116/74 HR 73 100% on RA. Patient states chest discomfort had improved but was still present at 4/10. She states she did not experience any issues or anxiety with previous doses of Pfizer. Patient was transported to ED via wheelchair for further evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1880801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: OR
Alter: 53,0
Geschlecht: M
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: unbekannt Erholt: ja

Dyspnoea Pruritus

Symptomtext

Vaccination provided at approximately 9:20am. 9:30am: Patient stated he was beginning to feel itchy and some trouble breathing, but only requested Diphenhydramine. Diphenhydramine 50mg given IM. Pulse was 76, respiration was 12. Emergency services initiated. 9:40am: Pulse 78, respiration 13. Ambulance arrived approximately 9:44am. Paramedics did not note any signs of urticaria, patient stated he was breathing ok. Patient was alert and responsive throughout. Denied further evaluation or transport to hospital for further assessment by paramedics. Requested patient have others also continue to keep an eye on him and seek emergency services if necessary.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None indicated
Vorgeschichte: None Indicated
Andere Medikamente: None indicated
Allergien: Shellfish and Bee Venom
Vorherige Impfungen: -

VAERS 1879636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MO
Alter: 46,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Paraesthesia

Symptomtext

Have feelings of tingling like needles in my hands and knees; This is a spontaneous report from a contactable consumer, the patient. A 46-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the right arm on 30Oct2021 at 22:30 (at the age of 46-years-old) as a single dose for COVID-19 immunisation. Medical history included high blood pressure and COVID-19. It was unknown whether the patient had any allergies. Prior to vaccination, the patient was diagnosed with COVID-19. The patient received the first dose of influenza vaccine (FLU VACCINE) in the left arm on 21Oct2021 for immunization. The patient received unspecified concomitant medications for unknown indication from an unknown date and unknown if ongoing. On 30Oct2021 at 23:30, the patient had feelings of tingling like needles in his hands and knees. It was not constant but it did happen a lot throughout the days (at the time of this report). The event did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event had feelings of tingling like needles in his hands and knees was not resolved at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (High blood pressure); COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1876933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: PA
Alter: 32,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chest pain Fear

Symptomtext

Pain in left side of chest, feels like my heart is sore. I also have less energy, and feel afraid to exercise or push myself to do much physical activity. I think it's maybe getting slightly better and will clear on it's own. I've not called my doctor or done anything to treat it other than take it easy. It hurts more if I cough, clear my throat, or take really deep breaths. I also remember having this type of pain for a week or two following my second COVID vaccine (also Pfizer, 3/12/21), beginning about a day after I got the vaccine. When I looked up these symptoms it appears to fit the description of myocarditis, so I wanted to report so it is documented and for my own safety.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: I also remember having pain in left side of chest, like my heart was sore or weak for a week or two following my second COVID va

VAERS 1875937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: FL
Alter: 31,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Migraine

Symptomtext

Bad migraine since 2nd shot; This is a spontaneous report from a contactable consumer, the patient. A 31-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030bd) via an unspecified route of administration in the left arm on 09Nov2021 at 16:30 (at the age of 31-years-old) as a single dose for COVID-19 immunisation. Medical history included known allergies to sulfa. 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 vaccination. The patient did not take any concomitant medications. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF8841) via an unspecified route of administration in the left arm on 19Oct2021 (at the age of 31-years-old) as a single dose for COVID-19 immunisation. On 09Nov2021 at 16:30, the patient experienced bad migraine since the 2nd shot. The event did not result in doctor or other healthcare professional office or clinic visit and emergency room or department or urgent care. Therapeutic measures were not taken as a result of the event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event bad migraine since the 2nd shot was not recovered at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy (Known allergies: sulfa)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 48,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Blister Chills Dizziness Herpes zoster Neuralgia Pain Paraesthesia Pyrexia Scab Urticaria

Symptomtext

Developed shingles within 24 hours of dose two of Pfizer vaccine. Within 9 hours of vaccine was bed ridden for 3 days with high fever, extreme pins and needles chills, dizziness and welts covering the back left side of my body. Most welts disappeared after the fever broke except a severe cluster of blisters that developed on my left back to buttocks that remain now and have been diagnosed by my primary doctor as shingles. I am still experiencing severe nerve pain and the shingles have crusted over and are incredibly sore. I have never had shingles ever before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Diagnosed by primary doctor and now taking Gabapentin for pain.
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: Botox for migraines, Zomig and Naratriptan
Allergien: Latex
Vorherige Impfungen: -

VAERS 1873020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: FL
Alter: 42,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 06.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / AR

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

Chest discomfort Electrocardiogram normal Heart rate increased Palpitations Tachycardia

Symptomtext

She has the vaccine on 11/6/21 and on 11/10/21 developed tachycardia, chest pressure and palpitations. Heart rate would increase to 110-115 with minimal activity and even at rest. Symptoms resolved, including heart rate normalizing, with ibuprofen. On 11/14 the symptoms suddenly resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG on 11/15 was normal but symptoms resolved by that point
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: aviane oral contraceptive pill
Allergien: bactrim-rash
Vorherige Impfungen: -

VAERS 1864984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: WI
Alter: 39,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Condition aggravated Erythema Eye discharge Eye swelling Pruritus Swelling face

Symptomtext

Pt received the first pfizer dose 11/10/2021. This reaction happened 2-3 hours later. Her eye was swollen with yellow discharge, and her chin was swollen/red/itchy. She has a history of this happening after receiving allergy shots (12years ago) She experienced the same symptoms, but did not have any throat swelling like she had with the allergy shots. Today: Eye swelling is down, still having discharge. Chin swelling down. Redness/itchiness is gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Allergic rhinitis, multiple allergies, acute atopic conjunctivitis, chronic migraine without aura, eczema, atopic dermatitis
Andere Medikamente: cetirizine-pseudoephedrine (ZYRTEC-D) 5-120 MG per tablet montelukast (SINGULAIR) 10 MG tablet azelastine (ASTELIN) 0.1 % nasal spray clobetasol (TEMOVATE) 0.05 % cream norethindrone-ethinyl estradiol and ferrous fumarate (MINASTRIN 24
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 1864864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: DE
Alter: 26,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 27.10.2021
Beginn: 11.11.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Back pain Dyspnoea Headache Paranasal sinus discomfort

Symptomtext

next day pt experienced back pain, headache with pressure in sinus cavitiy, pain in hip and trouble breathing. As of 11/11 he was still having adverse effects

Weitere VAERSDATA-Felder

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

VAERS 1864023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 05.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Arthralgia Chills Diarrhoea Dysstasia Fall Headache Hyperhidrosis Immunisation Insomnia Nausea Neck pain Nervousness Tremor Vaccination site pain

Symptomtext

Next morning, I got up for breakfast, felt shaky; Next morning, I got up for breakfast, felt shaky, suddenly started shaking/body shakes; sweating very heavily (dripping from my face); couldn't stand up, tried and fell to the floor, had to lay there, couldn't get up without help; couldn't stand up, tried and fell to the floor, had to lay there, couldn't get up without help; Spouse helped me to the bathroom, didn't vomit, but some diarrhea; About 8 hours after my shot, I started having intense pain at the shot area.; and it spread up behind my head/neck and down to my knees, left side; and it spread up behind my head/neck and down to my knees, left side; and it spread up behind my head/neck and down to my knees, left side; The patient received the third/booster dose of BNT162b2; Chills; Nausea; Too painful to sleep, chills, nausea; This is a spontaneous report from a contactable consumer, the patient. A 58-year-old non-pregnant female patient received the third dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the arm left on 05Nov2021 at 13:00 (at the age of 58-years-old) as a single dose for COVID-19 immunisation. The medical history included osteoarthritis, arthritis, allergy to diary and hay fever. 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 vaccination. The concomitant medications included paracetamol (TYLENOL) for arthritis and antihistamines (unspecified) for allergy, both from unknown dates and unknown if ongoing. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8727) via an unspecified route of administration in the arm left on 21Mar2021 at 10:30 (at the age of 58-years-old) and second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0153) via an unspecified route of administration in the arm left on 11Apr2021 at 10:45 (at the age of 58-years-old) as a single dose for COVID-19 immunisation. On 05Nov2021 at 21:00, about 8 hours after the shot, the patient started have intense pain at the shot area and it spread up behind her head/neck and down to her knees, left side. It was too painful to sleep, chills and nausea. On 06Nov2021, next morning, when the patient had got up for breakfast, she felt shaky and suddenly started shaking, sweating very heavily (dripping from her face) and couldn't stand up. She tried and fell to the floor and had to lay there and couldn't get up without help. Her spouse helped her to the bathroom, she didn't vomit but had some diarrhea, body shakes and after an hour or so of rest, it passed. The patient stated that she did not have this kind of a reaction to the first two shots. The adverse events did not result in doctor or other healthcare professional office or clinic visit and emergency room or department or urgent care. Therapeutic measures were not taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events intense pain at the shot area, and it spread up behind head/neck and down to knees, left side, too painful to sleep, chills and nausea were resolved on an unknown date in Nov2021, while the clinical outcome of the events felt shaky, shaking/body shakes, sweating very heavily, couldn't stand up, fell to the floor, couldn't get up without help and diarrhea were resolved on 06Nov2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Hay fever (Known allergies: Hayfever); Milk allergy (Known allergies: Dairy); Osteoarthritis
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1861499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NC
Alter: 40,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest pain Dizziness Dyspnoea Electrocardiogram abnormal Headache Inflammation Vaccination complication

Symptomtext

Chest pain, headache, dizziness, shortness of breath starting 24 hours after vaccine and chest pain continues a week later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG (abnormal), ER visit, blood tests. Cardiologist advised inflammation following vaccine. Echocardiogram scheduled by cardiologist.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin
Allergien: Codeine
Vorherige Impfungen: -

VAERS 1857386

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 32030BD

moderat

Staat: CO
Alter: 16,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Chest pain Heart rate increased

Symptomtext

Heart rate sustained between 125-132 for two days. Chest tightness. Chest pain day after injection for about four hours. Pain upon inhalation during morning of chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Back pain, pectus carinatum
Andere Medikamente: ibuprofen
Allergien: Azithromycin
Vorherige Impfungen: -

VAERS 1851016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 08.11.2021
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

Differential white blood cell count Dizziness Electrocardiogram Flushing Full blood count Heart rate increased Hypertension Immunodeficiency Metabolic function test Tachycardia Troponin

Symptomtext

Within 15 minutes of receiving the vaccine, I became tachycardic to the 150's (documented with Fitness Watch), with facial flushing and lightheadedness. No shortness of breath or difficulty swallowing. Pulse corroborated by vaccine nurse. walked over to Emergency Dept where at triage, my heart rate was 120s and I was hypertensive to 150's/100's. Labs sent- CBC/diff, metabolic panel, and troponin (all WNL) EKG X 2 (first with tachycardia to 120's, otherwise WNL, 2nd with HR 80's, otherwise WNL. 1 Liter of LR given IV and I was observed for about 2 hours before being discharged home. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Labs sent- CBC/diff, metabolic panel, and troponin (all WNL) EKG X 2 (first with tachycardia to 120's, otherwise WNL, 2nd with HR 80's, otherwise WNL. 1 Liter of LR given IV and I was observed for about 2 hours before being discharged home.
Aktuelle Erkrankungen: none
Vorgeschichte: High cholesterol
Andere Medikamente: Liptor 10 mg daily
Allergien: sulfa, topical neomycin, kiwi, cats
Vorherige Impfungen: -

VAERS 1850824

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 32030BD

moderat

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 29.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Mobility decreased Pain Pain in extremity

Symptomtext

I received the PFIZER Booster Shot on 10/29/21. I had NO symptoms until 11/03/21. My prior to Pfizer shots were on 03/14/21 and 04/06/21. I had NO symptoms after ANY of those 2 shots. I should also note that I received the 2021 Flu shot in my right shoulder. My right arm has had no adverser symptoms from the 2021 Flu shot. On 11/03/21, right after I woke up for the day, I noticed that that my upper left arm/shoulder was causing some pain. I figured that was a normal symptom after receiving a shot. However, since 11/03/21, the level of pain in my upper left arm/shoulder has increased to the point to where it is very painful to raise my left arm up just a few inches. I also can not use my left to bear any amount of weight (such as if I am trying to use my left arm to push off the ground to move from sitting position to a standing position.) It feels like my left arm is just hanging there without much strength within it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None so far. I have not seen any doctor about this.
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Metformin Pravastatin
Allergien: n/a
Vorherige Impfungen: -

VAERS 1850182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MI
Alter: 43,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

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

Chest pain Dyspnoea Electrocardiogram Injection site erythema Myalgia Productive cough

Symptomtext

yesterday pfizer covid-19 vaccine. Lot 32030BD. he and wife got vaccine from the same lot. last night developed severe myalgia, chest pain - intermittent stabbing left chest reproducible worse with lying flat especially with the shortness of breath, cough is productive - phlegm - clear, some shortness of breath no leg swelling arm where got the vaccine minimally red not taking meds for the cough

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG 11-2-21
Aktuelle Erkrankungen: Acute combined systolic and diastolic heart failure
Vorgeschichte: Cardiomyopathy Back pain
Andere Medikamente: furosemide (Lasix 20 mg oral tablet) 20 mg = 1 tab(s), PO (oral), qDay, Taking as prescribed; dose verified metoprolol (metoprolol succinate 25 mg oral tablet, extended release) 50 mg = 2 tab(s), PO (oral), qDay, Taking as prescribed; dose
Allergien: enalapril
Vorherige Impfungen: -

VAERS 1849721

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 32030BD

moderat

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 29.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Headache Hypoaesthesia oral Pain in extremity

Symptomtext

There is consistent pain on the left side of my chest right above my breast. I have random pains that shoot up my left and my right arm. I constantly have headaches throughout the day. I?m also experiencing numbness on my tongue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1846789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
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 Dizziness

Symptomtext

At 1135 client described feeling dizzy as she was waiting in observation. Clinicians layed client down in supine position on top of a foam matt. At 1140, vital signs were taken. At 1145 client stated she was feeling better and sat up. At 1147 client stated she was ?feeling okay now? and stood up. Pt ambulated away at 1149.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Vital signs on 11/5/2021 at 1140: BP 104/61, HR 65, SpO2 98%, and RR 16
Aktuelle Erkrankungen: Mast Cell Activation
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: Red and orange food dye and coloring
Vorherige Impfungen: Patient consistently feels dizzy with any vaccine administration

VAERS 1843350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: MO
Alter: 66,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Feeling abnormal Immunodeficiency Paraesthesia oral

Symptomtext

pt states she started to feel weird shortly after receiving vaccine. She also reported tingling in lip. We closely monitored. Checked bp which was normal. Lip tingling subsided shortly after showing. Pt felt tired and "brain fog". RPh sat w her for 15 minutes. Symptoms subsided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: tizanidine hallucinations, sulfa hives
Vorherige Impfungen: pt stated she had brain fog after 2nd pfizer vaccine but did not notify rph today before receiving booster.

VAERS 1842258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MD
Alter: 63,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anxiety Chills Dizziness Eye pain Headache Hyperhidrosis Nausea Pain Palpitations

Symptomtext

Headache; Chills; Sweatiness; Body aches; Dizziness; Nausea; Eye pain; Anxiety; Racing heart; This is a spontaneous report from a contactable consumer, the patient. A 63-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the left arm on 31Oct2021 at 14:45 (at the age of 63-years-old) as a single dose for COVID-19 immunisation. Medical history included diabetes and mast cell activation syndrome (MCAS) and the patient was allergic to eggs. 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 vaccination. Concomitant medications included cetirizine hydrochloride (ZYRTEC), lisinopril (MANUFACTURER UNKNOWN), metformin (MANUFACTURER UNKNOWN) and acetylsalicylic acid (ASPIRIN), all taken for unknown indications from an unknown date and unknown if ongoing. The patient previously received influenza vaccine (flu vaccine) (MANUFACTURER UNKNOWN) for immunisation and experienced allergy to vaccine. On 31Oct2021 at 14:45, the patient experienced headache, chills, sweatiness, body aches, dizziness, nausea, eye pain, anxiety and racing heart. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events headache, chills, sweatiness, body aches, dizziness, nausea, eye pain, anxiety and racing heart were not resolved at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Egg allergy (Known allergies: Eggs); Mast cell activation syndrome (MCAS)
Andere Medikamente: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; LISINOPRIL; METFORMIN; ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2598380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Headache Hot flush

Symptomtext

Headache HOT FLASHES,SHORT OF BREATH Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1835828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: OR
Alter: 43,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Chest X-ray Electrocardiogram Palpitations

Symptomtext

45 minutes after shot heart start to race and atrial fibrillation took place for the next five hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Two EKG?s done in ER and a chest xRay
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1832925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 29.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Dyspnoea Fatigue Glossodynia Hypoaesthesia oral Immunodeficiency Pyrexia Tongue discolouration Tongue eruption

Symptomtext

This was a booster after a J&J first dose in March. I had what looked like strawberry tongue? The edges of my tongue very suddenly went numb and were covered with small very painful bumps (blisters? swollen taste buds? no idea...), my tongue looked gray, and I felt like I was having a little bit of trouble breathing because my mouth and throat felt swollen, but they didn't look swollen other than the bumps. I also started getting feverish. I drank a lot of water and went to sleep and felt fine by morning other than fatigue and a bit of RA joint pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Did not seek medical treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid Arthritis, Celiac Disease
Andere Medikamente: Methotrexate, Hydroxychloroquine, Leucovorin, Birth Control
Allergien: Gluten
Vorherige Impfungen: -

VAERS 1991923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Palpitations Paraesthesia Paraesthesia oral Urticaria

Symptomtext

patient felt tingling on her face, mouth, palpitation gave 2 capsules of benadryl (total 50mg) Call 911 and went to emergency room

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No
Vorgeschichte: Had hives on second Covid (Pfizer) shot
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Hives~COVID19 (COVID19 (Unknown))~2~0.00~Patient

VAERS 1832360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Chills Dyspnoea Erythema Tachycardia

Symptomtext

Shortness of breath, erythema of the face, abdominal cramping, chills, tachycardia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Not applicable
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1829134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: NY
Alter: 24,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Hypoaesthesia Muscular weakness Paraesthesia

Symptomtext

Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: 10 MINS AFTER SHOT, PT REPORTED WEAKNESS IN ARM THAT RECEIVED SHOT AND NUMBNESS. PT SAID THEY WOULD FOLLOW UP IF IT CONTINUED.

Weitere VAERSDATA-Felder

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

VAERS 1826652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: AZ
Alter: 48,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Dyspnoea

Symptomtext

Chest pain, Difficulty breathing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Pain
Vorgeschichte: Hypercholesterolemia, Pain, Anxiety, Prediabetic
Andere Medikamente: Tamsulosin 0.4mg, Percocet 5/325, Amitriptyline 10mg, Duloxetine 30mg, duloxetine 60mg, Prazosin 5mg, Metformin ER 750mg, Pravastatin 40mg, Lidocaine/Prilocaine2.5/2.5% cream
Allergien: Codeine
Vorherige Impfungen: -

VAERS 1825531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Mobility decreased Nausea Pain in extremity Peripheral swelling Skin warm

Symptomtext

Woke up next morning after shot and arm couldn't move . Arm is hot red swollen and painful even 3 days later. Pt feels nauseous continuously.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: diabetes,
Andere Medikamente: aspirin, metformin, januvia, lisinopril, sertraline, b-12
Allergien: None
Vorherige Impfungen: -

VAERS 1825116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

moderat

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 28.10.2021
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: ja Erholt: nein

Hypoaesthesia Paraesthesia

Symptomtext

Pt with numbness, tingling in right arm and leg within an hour of the vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None noted
Vorgeschichte: Asthma
Andere Medikamente: ALbuterolHFA Vitamin d , Fish oil Nasacort Turmeric
Allergien: Asmanex
Vorherige Impfungen: -

VAERS 1823910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: VA
Alter: 47,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Gait disturbance Hypoaesthesia Muscle spasms Muscle tightness Pain in jaw Paraesthesia Poor peripheral circulation Sleep disorder

Symptomtext

I am having a serious continuous tingling Sensation in my legs and arms. The tingling sensation has caused my legs to go numb, making it difficult to walk. Feels like poor circulation. And tighten. Nerve pain in my jaw . It?s causing me to lose sleep. Neck cramping

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Not Applicable
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: Lamotrigine 100 mg D-Amphetrimine Salt 20mg Advil 220 mg
Allergien: No
Vorherige Impfungen: -

VAERS 1818678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: PR
Alter: 61,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood glucose normal Dizziness Dyspnoea

Symptomtext

Patient refers feeling dizzy and need of air. Patient oriented in time place and person. Vitals are taken BP 120/80, R 18, P 96, Sat 98, Dextro 95. Patient was laid down and given juice to elevate sugar. Doctor was consulted and recommended keeping patient in observation and to retake vitals and if patient was feeling better to discharge. After 30 minutes vitals were retaken BP 120/80, R 18, P 96, Sat 98, Dextro 104. Patient reports feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Migraine; Fibromyalgia; Hypertension; Asthma; Pre-diabetes; Melena
Vorgeschichte: Migraine; Fibromyalgia; Hypertension; Asthma
Andere Medikamente: Irbesartan; SYNTHROID; Clobetasol; SINGULAR; SYMBICORT; Albuterol
Allergien: Tramadol; Penicillin; Morphine; NUBAIN
Vorherige Impfungen: -

VAERS 1813525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

moderat

Staat: PR
Alter: 40,0
Geschlecht: F
Eingang: 23.10.2021
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: ja Erholt: nein

Asthenia Blood glucose normal Feeling hot Somnolence Tremor

Symptomtext

Patient 40 years old started to experience weakness, drowsiness, feeling hot and shaky. Vitals were taken BP 120/80, P66, R12, Sat 96%. dexto 96 patient was lyed and kept oriented in time, place and person, lower limbs were elevated and patch was removed from lumbar area. Vitals were retaken P72, BP 120/80, R12, Sat 96% dextro 96. Doctor was called and recommended transferring patient to emergency room for evaluation. Patient was transferred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Low pressure; Anemia; Back pain; Under review for Fibromyalgia
Vorgeschichte: -
Andere Medikamente: NORFLEX; Arthritis pain; PARCHO MEDICATED HEAT PATCH (VICODIN)
Allergien: ASPIRIN; SEAFOOD; IODINE
Vorherige Impfungen: -

VAERS 2723544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 58,0
Geschlecht: M
Eingang: 13.12.2023
Impfdatum: 20.10.2021
Beginn: 23.02.2022
Tage bis Beginn: 126,0
Dosis: 2
Route/Site: IM / UN

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

Asthenia COVID-19 Chest X-ray normal Chills Cough Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Started having chest congestion, cough, chills, fever, and weakness. CXR was negative, but covid test was positive. Received antibiotics.

Weitere VAERSDATA-Felder

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

VAERS 2513031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WA
Alter: 52,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Affect lability Arthralgia Blood test Fatigue Fibromyalgia Loss of personal independence in daily activities Magnetic resonance imaging Impaired self-care Impaired work ability Laboratory test abnormal Loss of employment Malaise Osteoarthritis Rheumatoid arthritis X-ray limb

Symptomtext

Within hours of first vaccine symptoms started feel unwell, hand joint pain, fatigue, not taking care of self due to body changes happening so fast. 11/19/2021 primary tested for RA after 6 months of hand joint pain, fatigue, unable to handle daily life well. 10/07/2022 got diagnosis of RA. That was third dr as first two miss diagnosed me, never having read my medical records.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 9/2022 MRI, 11/2021, 3/2022, 9/2022 Blood work and physical exam.
Aktuelle Erkrankungen: Was just going off diabetic medication after losing weight, was healthy.
Vorgeschichte: minor depression, restless legs high cholesterol
Andere Medikamente: Lexapro, meloxicam for shoulder, garlic, vitamin B, vitaminD
Allergien: none
Vorherige Impfungen: -

VAERS 2513031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WA
Alter: 52,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Affect lability Arthralgia Blood test Fatigue Fibromyalgia Loss of personal independence in daily activities Magnetic resonance imaging Impaired self-care Impaired work ability Laboratory test abnormal Loss of employment Malaise Osteoarthritis Rheumatoid arthritis X-ray limb

Symptomtext

Within hours of first vaccine symptoms started feel unwell, hand joint pain, fatigue, not taking care of self due to body changes happening so fast. 11/19/2021 primary tested for RA after 6 months of hand joint pain, fatigue, unable to handle daily life well. 10/07/2022 got diagnosis of RA. That was third dr as first two miss diagnosed me, never having read my medical records.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 9/2022 MRI, 11/2021, 3/2022, 9/2022 Blood work and physical exam.
Aktuelle Erkrankungen: Was just going off diabetic medication after losing weight, was healthy.
Vorgeschichte: minor depression, restless legs high cholesterol
Andere Medikamente: Lexapro, meloxicam for shoulder, garlic, vitamin B, vitaminD
Allergien: none
Vorherige Impfungen: -

VAERS 2618386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TN
Alter: 69,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 07.12.2021
Beginn: 01.07.2022
Tage bis Beginn: 206,0
Dosis: 4
Route/Site: SYR / LA

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

Back pain Chills Computerised tomogram normal Dysphonia Feeling cold Headache SARS-CoV-2 test positive

Symptomtext

1st week July 2022 your voice started horse and it goes worst in the evening and went to the urgent care and had chills. I was quarantined I was freezing. I test positive and I cant remember the date. Then I had headaches sometime in fall of 2022. I went to my doctor and did a CT scan and it came back negative and it gets worse in the night. I have pain in my back and it feels like arthritis and the doctor will order a sleep apnea test and sleep study.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Jul2022 COVID-19 positive; 7NOV2022 CT scan negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levothyroxine; COLON HEALTH; vitamin multivitamin; atorvastatin
Allergien: Pollen allergies
Vorherige Impfungen: -

VAERS 2611211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: SC
Alter: -
Geschlecht: U
Eingang: 07.04.2023
Impfdatum: 01.12.2021
Beginn: 09.01.2022
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: - / RA

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

Arthralgia Musculoskeletal disorder Musculoskeletal stiffness Periarthritis Vaccination site pain

Symptomtext

Right Shoulder completely frozen; No right arm function/ loss of arm function; Started with stiff neck on right side; Pain in area of right arm where vaccine was given; Pain in shoulder/ pain in the front & back of shoulder; 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 patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 01Dec2021 as dose 3 (booster), single (Lot number: 32030BD), in right arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN, Anatomical location: Left Arm), for COVID-19 immunisation; Covid-19 vaccine (DOSE 2; MANUFACTURER UNKNOWN, Anatomical location: Left Arm), for COVID-19 immunisation. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 09Jan2022, outcome "unknown", described as "Pain in area of right arm where vaccine was given"; ARTHRALGIA (non-serious) with onset 09Jan2022, outcome "unknown", described as "Pain in shoulder/ pain in the front & back of shoulder "; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 09Jan2022, outcome "unknown", described as "Started with stiff neck on right side"; MUSCULOSKELETAL DISORDER (non-serious) with onset 12Jan2022, outcome "unknown", described as "No right arm function/ loss of arm function"; PERIARTHRITIS (non-serious) with onset 12Jan2022, outcome "unknown", described as "Right Shoulder completely frozen". Additional information: On 09Jan2022, started with stiff neck on right side with pain in arm & shoulder. Right Shoulder completely frozen on 12Jan2022. No right arm function on 12Jan2022 with severe pain in Right arm & shoulder. Majority of pain has been in the area of right arm where vaccine was given with pain in the front & back of shoulder too.

Weitere VAERSDATA-Felder

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

VAERS 2584849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 89,0
Geschlecht: M
Eingang: 21.02.2023
Impfdatum: 06.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / -

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

Asthenia COVID-19 Oedema peripheral Pyrexia SARS-CoV-2 test positive Sepsis

Symptomtext

Hospitalization: 1/20/2023 - 1/24/2023 (4 days) Presentation to the ED: fevers, bilateral lower extremity edema, and weakness. admitted for sepsis. COVID + date: 1/24/2023 Treatment: none. patient was found positive on a transfer screen to hospital. Discharge to: EN6200 2/19/2021 EN6206 3/13/2021 32030BD 11/12/2021 010H22A 1/6/2023

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Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, insulin-dependent diabetes mellitus type 2, CKD stage 2, BPH, GERD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2584320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 21.11.2021
Beginn: 09.07.2022
Tage bis Beginn: 230,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Fatigue Headache Nasopharyngitis SARS-CoV-2 test positive Sneezing

Symptomtext

I started having a headache, fatigue, sneezing. I felt like I had a cold for another 10 days after. I tested positive for COVID-19 for about a week following. I still felt pretty tired and fatigue a week following. I wasn't prescribed anything, but I took acetaminophen for my headache and rested until I recovered.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: JULY2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2561480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: LA
Alter: 58,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 13.01.2021
Beginn: 03.01.2023
Tage bis Beginn: 720,0
Dosis: 3
Route/Site: SYR / -

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

Asthenia COVID-19 Dizziness Fatigue Feeling abnormal Illness Malaise Nasopharyngitis Nausea Pyrexia SARS-CoV-2 antibody test positive SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Break thru covid infection between Dose 2 and 3 of covid vaccine. Had antibodies IV. illness lasted 2 weeks. several weeks before I felt myself again. mild covid infection after dose 3 of covid vaccine. did not feel ill, only had cold symptoms. had antibody therapy. 1/3/2023 very sick, dizzy, fever, severe fatigue, nausea and generalized weakness for 10 days. took 2 weeks to recover. self medicated with OTC Tylenol, advil, fluids and rest.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: positive CUE test and PCR, positive Binax, positive Binax.
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure, hypothyroidism, arthritis, depression-anxiety, obesity
Andere Medikamente: thyroid, toprol, mobic, cymbalta, aldactone, estrogen
Allergien: none
Vorherige Impfungen: -

VAERS 2544529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MN
Alter: 95,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 26.10.2021
Beginn: 26.12.2021
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

Fever and generalized weakness on 12/26/22 with a positive home COVID test.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: PCR positive 12/27/22
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic anticoagulation, heart murmur, hiatal hernia, IBS
Andere Medikamente: -
Allergien: Nitrofurantoin, Opiods-Morphine, Augmentin, Codeine, Linzess, Trees
Vorherige Impfungen: -

VAERS 2543595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 65,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 24.06.2022
Beginn: 27.07.2022
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: IM / RA

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

Balance disorder COVID-19 Exposure to SARS-CoV-2 Fall Fatigue Nasopharyngitis SARS-CoV-2 test positive Sinusitis

Symptomtext

I did not have problems with vaccine, but I got COVID-19 in July. I had a home test, and it was positive. My husband had it first and I was required to take the test within 5 days before I returned to work. The doctor put me on PAXLOVID. It was like a bad cold; I had a rebound after the PAXLOVID. Then, I got a sinus infection, I went to ear, nose & throat specialist, and then I was start having balance problem (I was falling) I was put with antibiotics, the sinus infection resolved, I was still having balance issues and I am doing therapy, and I also had fatigue.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: July2022 COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Hyperthyroidism; High Cholesterol
Andere Medikamente: SYNTHROID; amlodipine; estrogen patch; multivitamins; BENADRYL
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2535154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 29.10.2021
Beginn: 25.11.2022
Tage bis Beginn: 392,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Cardiac pacemaker insertion Malaise Positive airway pressure therapy SARS-CoV-2 test positive Ventricular asystole

Symptomtext

"Patient with 4 COVID vaccines with esophageal cancer admitted to acute care for ventricular asystole and had pacemaker placed. Patient then admitted to Rehab unit and tested detected for COVID prior to discharge. Provider d/c note re COVID: ""1. Symptomatic Covid 19 detected the evening before planned discharge. He was given 3 days of iv remdesivir and had an oncology appt rescheduled. He will be seen next 12/21 by oncology and has f/u with cardiology and sleep medicine. He has remained afebrile and on room air (except for evening cpap/bipap - which is baseline) for over 48 hours. 2. He feels safe and ready to dc home today. He has been room independent for over 48 hours and has done well."" "

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Praegender Schweregrund: Malaise
Hospital-Tage: 14,0
Labordaten: COVID Detected PCR on 12/6/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Hypertension Hyperlipidemia CAD (coronary artery disease) Orthostatic hypotension Digestive Colon cancer (HCC) Esophageal dysphagia Cancer of distal third of esophagus (HCC) Chemotherapy induced nausea and vomiting Endocrine Diabetes mellitus type II Integumentary PYOGENIC GRANULOMA (686.1) Respiratory Obstructive sleep apnea DOE (dyspnea on exertion) Urinary AKI (acute kidney injury) (HCC) Other Chronic back pain History of TIA (transient ischemic attack) Arthritis Morbid obesity (HCC) Blood in the stool Morbid obesity with BMI of 45.0-49.9, adult (HCC) History of colon cancer History of colon polyps History of diabetes mellitus History of coronary artery stent placement Esophageal mass Anxiety Dehydration Syncope and collapse Chemotherapy-induced thrombocytopenia
Andere Medikamente: -
Allergien: Ketorolac Tromethamine
Vorherige Impfungen: -

VAERS 2512162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: IL
Alter: 57,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 03.11.2021
Beginn: 05.05.2022
Tage bis Beginn: 183,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Confusional state Cough Exposure to SARS-CoV-2 Fatigue Feeling abnormal Headache Pain Respiratory tract congestion SARS-CoV-2 test positive Taste disorder

Symptomtext

I received my first Pfizer booster for COVID-19 on 11/3/2021. On 5/5/2022, I had a cough, body aches, and a severe headache. On 5/6/2022, a coworker informed me that she had tested positive for COVID-19. On 5/7/2022, I took a home test and got a positive result. I then isolated. My symptoms continued, plus I developed chest congestion, fatigue, mental confusion, and a loss of taste and smell. At the time of this writing, I still have coughing, chest congestion, and brain fog. I still have difficulty tasting food, because food usually doesn't taste right. I think I also probably still have trouble with my sense of smell, but it's not as noticeable as the issue I'm having with my sense of taste. I had a telehealth visit with my doctor on 5/12/2022. He did not prescribe me Paxlovid, because he said that it was too late, since more than 5 days had already passed since the onset of symptoms. I treated myself with hot tea, Robitussin, Tylenol for body aches, and ibuprofen. I began to finally feel better around a month and a half after the onset of the symptoms. However, I did return to work around 5/23/2022. With regard to the symptoms I still have, I try to treat them with Robitussin, Tylenol, ibuprofen, and hot tea. They help me feel better temporarily, but the symptoms always return.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 5/7/2022--Home COVID-19 Test--Positive Result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Arthritis (Mostly in Lower Back).
Andere Medikamente: Multivitamin; Possibly Vitamin E.
Allergien: Gadolinium Contrast Media.
Vorherige Impfungen: I had body aches for a few days after I received the first Pfizer vaccination for COVID-19.

VAERS 2481197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: DE
Alter: 63,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Body temperature Pyrexia

Symptomtext

earlier Pfizer COVID vaccines, I had fevers the next day/she had a fever of 100-101 degrees; 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 63-year-old female patient received BNT162b2 (BNT162B2), on 02Nov2021 as dose 3 (booster), single (Lot number: 32030BD) at the age of 63 years for covid-19 immunisation. The patient's relevant medical history included: "thyroid" (unspecified if ongoing), notes: Caller states that she just takes an unspecified thyroid medication; does not think it is relevant. The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose:01, EP6955; Anatomical Location: Unknown.), administration date: 18Mar2021, when the patient was 63-year-old, for Covid-19 immunization, reaction(s): "Fever"; BNT162b2 (Dose:02, Lot Number: Reported by the caller as being either CRM29 or LRM29; Anatomical Location: Unknown.), administration date: 15Apr2021, when the patient was 63-year-old, for Covid-19 immunization, reaction(s): "Fever"; flu shot, administration date: 06Oct2022, when the patient was 64-year-old, for immunisation; tetanus shot, administration date: 29Sep2022, when the patient was 64-year-old, for immunisation. The following information was reported: PYREXIA (non-serious) with onset 03Nov2021, outcome "unknown", described as "earlier Pfizer COVID vaccines, I had fevers the next day/she had a fever of 100-101 degrees". Relevant laboratory tests and procedures are available in the appropriate section. Follow-Up (17Oct2022): Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201224743 same pateint/event/drug, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20211103; Test Name: Body temparature; Result Unstructured Data: Test Result:100-101 degrees; Comments: she had a fever of 100-101 degrees; Test Date: 20211103; Test Name: Body temparature; Result Unstructured Data: Test Result:100-101.5 degrees; Comments: her fevers actually ranged from 100-101.5 degrees
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Thyroid disorder (Caller states that she just takes an unspecified thyroid medication; does not think it is relevant)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2453122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 22.09.2022
Impfdatum: 13.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Alopecia Headache Menstruation irregular COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Nurse) from product quality group. The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Nov2021 as dose 2, single (Lot number: 32030BD) at the age of 41 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Multiple sclerosis" (unspecified if ongoing). Concomitant medication(s) included: AUBAGIO, start date: 07Mar2015. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Vaccine was received. Other medication in 2weeks was Yes. Anti-viral details: Product: COVID 19 Treatment. Brand: Paxlovid. Treatment start date: 17Sep2022. Stop date: 17Sep2022. Lot number: 2692144. Indication: Treatment of COVID- 19. Other medication in 2weeks product was Aubagio on 07Mar2015. Adverse event: within 45 minutes of taking her first dose, she had an awful metallic taste in her mouth and left ear started ringing. It was about 24 hours later and she still have a very loud ringing in her left ear. Her oxygen level also decreased her heart rate went up and she actually felt worse after taking just one dose of Paxlovid. No Known allergies. Other medical history was Multiple sclerosis.; Sender's Comments: Based on the available information in the case, the causal association between the events Drug ineffective, COVID-19 and the suspect drug BNT162B2 cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: Treatment of COVID-19.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Multiple sclerosis
Andere Medikamente: AUBAGIO
Allergien: -
Vorherige Impfungen: -

VAERS 2429620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 04.02.2021
Beginn: 01.09.2022
Tage bis Beginn: 574,0
Dosis: 2
Route/Site: - / -

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

Blood lactic acid increased COVID-19 Encephalopathy Immunosuppression Lymphopenia Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient admitted on 8/30 with a PMH of multiple myeloma s/p bone marrow transplant, type 2 DM, and CKD stage IV. He was admitted with concern for acute encephalopathy, febrility in immunosuppressed state with lymphopenia and elevated lactic acid. COVID swab was done on 9/1 and patient was found to be positive.

Weitere VAERSDATA-Felder

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

VAERS 2422478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: UN / UN

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

Rash

Symptomtext

Rash on chest and back.

Weitere VAERSDATA-Felder

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

VAERS 2374697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: VA
Alter: 58,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 29.10.2021
Beginn: 05.03.2022
Tage bis Beginn: 127,0
Dosis: 3
Route/Site: IM / LA

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

Antinuclear antibody negative Balance disorder Basophil percentage Blood uric acid normal C-reactive protein increased Eosinophil percentage Erythema Full blood count normal Gait disturbance Gout Loss of personal independence in daily activities Lymphocyte percentage Metabolic function test normal Monocyte percentage Neutrophil percentage Osteoarthritis Osteopenia Pain in extremity

Symptomtext

In March I started with left big toe swelling and redness which quickly progressed to the entire foot. This was thought to be gout (although I have never had gout before) and was treated with a course of Augmentin and steroids. There was no improvement. Labs were done that were ALL normal and I was given a double prednisone taper. There was some minimal improvement and as soon as I started to taper down, the swelling and redness returned. I am now seeing a podiatrist who repeated labs and does not show gout or any inflammatory process going on. All my labs are normal again. He started me on Colchicine which did not help and he took me off of it. My foot actually got worse. I am now on Celebrex. He does not know what is going on. He is treating me for gout but my labs do not indicate this. My foot continues to be extremely painful, red and swollen. The big toe and over into the 2nd and 3rd toe are red, swollen and hot to touch. There are days I can not wear shoes due to swelling. My balance is off because it hurts to bear weight on the foot. I have almost fallen several times. I have great difficulty walking which inhibits me from doing my daily activities. I have not had any insect bites or any trauma to the foot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Augmentin, Prednisone, Colchicine, Celebrex. Labs: Basic Metabolic Panel--all normal ANA with Reflex--negative Antistreptolysin O Antibodies--<20.0 C Reactive Protein--0.4 RA Factor--<20 Uric Acid--3.1 Sed Rate--9 CBC with Diff--all normal WBC- 10.8, lymphocytes-22%, Monocytes-7%, Eosinophils-3%, Basophils-1%, segmented neutrophils-68% Xray left foot, 5/5/22: There is mild osteopenia. No acute fracture or dislocation is seen. Degenerative joint space narrowing is seen involving the interphalangeal joints.
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, high cholesterol, type 2 diabetes, asthma, sleep apnea
Andere Medikamente: Verapamil, Claritin, Neurontin, Losartan, Crestor, MVI, B Complex, Collagen supplement, tylenol prn, Probiotic
Allergien: Biaxin, Diclofenac, Coreg, Dapiprazole, uncooked Egg whites, Lisinopril, Motrin, Tessalon,
Vorherige Impfungen: allergic reaction to flu shot due to egg white base

VAERS 2325502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MN
Alter: 10,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered Pain in extremity

Symptomtext

Pharmacy had date of birth wrong, so he was administered the adult vaccine dose instead of the child vaccine dose. Only birth month and day were confirmed at the appointment. There were no unusual reactions, just a sore arm. He was also given the adult dose for his second dose on 11/27/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2322873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: GA
Alter: 79,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 02.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 180,0
Dosis: 3
Route/Site: - / LA

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

Abdominal discomfort Asthenia COVID-19 Headache Illness SARS-CoV-2 test Vaccination failure Weight Weight decreased

Symptomtext

tested positive for COVID after COVID-19 Vaccinations; tested positive for COVID after COVID-19 Vaccinations; got sick; headache; sick to her stomach; felt weak; Lost some pounds; This is a spontaneous report received from contactable reporter(s) (Nurse) from product quality group. The reporter is the patient. A 79-year-old female patient received BNT162b2 (BNT162B2), on 28Jan2021 as dose 1, single (Lot number: EL8982, Expiration Date: 31May2021), on 18Feb2021 as dose 2, single (Lot number: EL9264, Expiration Date: May2021) and on 02Nov2021 as dose 3 (booster), single (Lot number: 32030BD) at the age of 79 years, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "cataracts removed", start date: 2004 (unspecified if ongoing), notes: had her cataracts removed; "Cholesterol" (unspecified if ongoing); "reflux" (unspecified if ongoing), notes: reflux; "Anemia" (unspecified if ongoing). Concomitant medication(s) included: ZETIA taken for blood cholesterol increased (ongoing); NEXIUM 24HR taken for gastrooesophageal reflux disease (ongoing); VITAMIN B12 [CYANOCOBALAMIN] (ongoing); VITAMIN C [ASCORBIC ACID] (ongoing); GERITOL [VITAMINS NOS] taken for anaemia (ongoing). Vaccination history included: First shingles shot (got her first shingles shot before her COVID-19 Vaccinations); Pneumonia (gets her Pneumonia and Flu Shot in October every year, got the Pneumonia and Flu Shot last year in October), administration date: Oct2021; Flu shot (Flu Shot, gets her Pneumonia and Flu Shot in October every year, got the Pneumonia and Flu Shot last year in October), administration date: Oct2021. The following information was reported: VACCINATION FAILURE (medically significant) with onset 14May2022 at 01:30, outcome "unknown", COVID-19 (medically significant) with onset 14May2022 at 01:30, outcome "recovered" (2022) and all described as "tested positive for COVID after COVID-19 Vaccinations"; ASTHENIA (non-serious) with onset May2022, outcome "recovered" (2022), described as "felt weak"; ILLNESS (non-serious) with onset May2022, outcome "recovered" (May2022), described as "got sick"; HEADACHE (non-serious) with onset May2022, outcome "recovered" (2022); ABDOMINAL DISCOMFORT (non-serious) with onset May2022, outcome "recovered" (2022), described as "sick to her stomach"; WEIGHT DECREASED (non-serious) with onset 2022, outcome "unknown", described as "Lost some pounds". The events "tested positive for covid after covid-19 vaccinations", "got sick", "headache", "sick to her stomach" and "felt weak" required emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14May2022) Positive, notes: Unit: Not Provided at 01:30 Am; (2022) Negative, notes: Thursday evening; Weight: (unspecified date) lost some pounds. Therapeutic measures were taken as a result of covid-19, illness, headache, abdominal discomfort, asthenia, weight decreased. Tested positive for COVID after COVID-19 Vaccinations. Her teeth in the root of her gums felt like something was in the root of her teeth. Additional Information for Other medicines Zetia: She has been taking Zetia for a long time for her elevated cholesterol and can't take statin drugs. Additional Information for Other medicines Nexium: This is over the counter and has been taking 4-6 years. Additional Information for Other medicines Geritol: This is over the counter and is a multivitamin, multi mineral supplement. Dosage and Relevant Information for Preser Vision: : in morning and at night. Dosage text for Areds 2: 1 in the morning and 1 at night. Additional Information for Other medicines Hydroxine: She takes this as needed and knows she didn't take any last week or this week. Additional information: Caller was calling about the antiviral medication that she took for COVID. She asked how long after she finished the 5 day treatment and after COVID can she get her second booster shot. Caller stated the medication was Paxlovid. She stated she was fully vaccinated and had one booster of the COVID-19 Vaccine and wants to go ahead and get the second booster. Caller turned 80 years old last Monday. She stated over a month ago was when she got COVID and went to the Emergency Room and tested positive and was given the antiviral for 5 days. Tested positive for COVID after COVID-19 Vaccinations: Caller stated Mother's day was 08May and she tested positive on Saturday morning, 14May2022, at 1:30am in the emergency room. She was not admitted to the hospital. She really thinks she got sick was because she didn't have the second COVID-19 Vaccine booster dose. She didn't have a high fever just a headache, sick to her stomach and felt weak and this is why she went to the emergency room. She knows she was exposed to COVID because she went to a neighbor's house after a passing of a neighbor and everyone in that house tested positive. She and her son tested Thursday evening but was negative but she got sick on Friday morning with a terrible headache. She went to the emergency room. Seriousness: She states her pre vaccination and booster was what kept her from being admitted to the hospital. Outcome: She recovered completely. She stated she wasn't sick after the first day and felt good after 2 or 3 days. Her teeth in the root of her gums felt like something was in the root of her teeth: She had a side effect from the Paxlovid which was her teeth in the root of her gums felt like something was in the root of her teeth. She knows nothing was there because she brushes her teeth everyday and flosses after every meal. She had this feeling well after she stopped taking the Paxlovid. She also mentioned her 2 front teeth are a little loose and her teeth weren't like that before the Paxlovid. Product Details: She put the Paxlovid in the trash after she finished the Paxlovid. Dose: 6 pills a day; She doesn't know the milligrams but took 3 in the morning and 3 at night. She took the Paxlovid at 9am and 9pm because she is a retired Registered nurse. Received her 1st and 2nd dose of the COVID-19 Vaccine at withheld. Received at withheld.She mainly takes vitamins and cholesterol medication every day. She takes over the counter eye drops too as a lubricant for her dry eyes. She had intraocular lens as she had her cataracts removed in 2004. The eye drops are daily for dry eyes. She was not taking any blood pressure medication and hasn't taken any blood pressure medication in over a year. She lost some pounds when she was sick with COVID and is hoping to keep the pounds off. She exercises daily and turned 80 years old Monday. Anatomical Location of Administration of Pfizer vaccine considered as suspect: In her arm; Left deltoid usually as that is her non-dominant arm. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): No; She needs her next shingles shot because she got her first shingles shot before her COVID-19 Vaccinations. She gets her Pneumonia and Flu Shot in October every year and got the Pneumonia and Flu Shot last year in October. AE(s) following prior vaccinations: None. Patient's Medical History (including any illness at time of vaccination): None. Family Medical History Relevant to AE(s): No. Relevant Tests: None. Is there a product complaint to report: Yes. Description of Product Complaint: Description of complaint: She is fully vaccinated and had one booster of the COVID-19 Vaccine. She tested positive on Saturday morning, 14May2022, at 1:30am in the emergency room. Packaging sealed and intact: For her booster dose the technician or pharmacist had already drawn up the vaccine in the syringe.; Sender's Comments: As there is limited information in the case provided, the causal association be-tween the event and the suspect drug cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20220514; Test Name: COVID test; Test Result: Positive ; Comments: Unit: Not Provided at 01:30 Am; Test Date: 2022; Test Name: COVID test; Test Result: Negative ; Comments: Thursday evening; Test Name: weight; Result Unstructured Data: Test Result:lost some pounds
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anemia; Cataract operation (had her cataracts removed); Cholesterol; Reflux esophagitis (reflux)
Andere Medikamente: ZETIA; NEXIUM 24HR; VITAMIN B12 [CYANOCOBALAMIN]; VITAMIN C [ASCORBIC ACID]; GERITOL [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2314073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PA
Alter: 51,0
Geschlecht: F
Eingang: 09.06.2022
Impfdatum: 04.12.2021
Beginn: 24.04.2022
Tage bis Beginn: 141,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Fatigue Feeling abnormal Headache Pyrexia SARS-CoV-2 test positive

Symptomtext

I got the shingles vaccine, and I had slight reaction to it with a fever. After about 5 days of feeling terrible, I called my doctor and said if the symptoms progressed, I should test for COVID-19. On day 9, I decided to test and came back positive for COVID-19. I lost my taste and sense of smell, higher fever, and terrible fatigue. The fever altered through the days, from low-grade to high-grade. I developed a terrible headache that lasted for 10 days. Currently, I still haven't regained my taste and smell back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test: 04/24/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: Metoprolol 25mg; VERMAPIL 120mg; LIPITOR 10mg; COPAXONE 40mg; REXALL
Allergien: Soy; Seasonal Allergies
Vorherige Impfungen: -

VAERS 2311631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: GA
Alter: 63,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Blood test normal Headache Magnetic resonance imaging normal Myalgia Pain Pyrexia Rash SARS-CoV-2 test negative Vision blurred

Symptomtext

I received my vaccine on 12/6/2021 and that evening I had a fever and muscle aches. I had a rash all over my body too not just at the injection. I took Motrin to help with the fever and muscle aches for a couple of days. I have had flare ups since the vaccine in February, April and June with high fever, headache, blurry vision and body/joint/muscle aches. I have been to the doctor and they have prescribed (unknown) medicine but it didn't help. I have alternated Tylenol and Motrin which helps with the fever and headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I have tested for Covid 19 at home and it was negative. At clinic I had an MRI and bloodwork. For the rash, the dermatologist took bloodwork. All resulted in within normal range.
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD
Andere Medikamente: N/A
Allergien: Bactrim and antibiotics
Vorherige Impfungen: -

VAERS 2278518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 66,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 08.04.2022
Beginn: 09.05.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Exposure to SARS-CoV-2 Exposure via direct contact Malaise SARS-CoV-2 test positive Throat irritation

Symptomtext

I woke up with a scratchy throat on 05/09/2022. I was informed by a close contact that they tested positive for COVID-19. So the next morning on 05/10/2022, my symptoms worsened, and I went to the clinic to get tested. The PCR COVID-19 test came back positive and was prescribed Paxlovid. I completed the course of the medication and tested negative on 05/15/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 test: 05/10/2022
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: N/A
Allergien: Onions
Vorherige Impfungen: -

VAERS 2278490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 89,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 21.10.2021
Beginn: 17.04.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 Chest X-ray normal Fatigue Inappropriate schedule of product administration SARS-CoV-2 test positive Urinary tract infection

Symptomtext

COVID-related hospitalization after receiving Pfizer series + booster (10/21/2021, 2/12/2021, 1/21/2021) Pfizer Vaccines: 10/21/2021 Right arm, lot 32030BD 2/12/2021 left deltoid, lot EL9264 1/21/2021 Right deltoid, lot EL3249 Admitted 4/17/2022 Discharged 4/28/2022 Per hospital notes: Admitted to the hospital for generalized weakness and fatigue. Symptoms chronic, ongoing for 2 months, but worsening due to covid-19. Tested positive for covid 4/17/22 Chest x-ray: no acute findings Received monoclonal antibody (bebtelovimab) on 4/18 Patient found to have a UTI during admission and Rocephin started 4/23/22, de-escalated to Keflex. Symptoms improved prior to discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CKD Hypertension Atrial fibrillation History of CVA HF
Andere Medikamente: Atorvastatin Metoprolol succinate Eliquis Ferrous sulfate Lisinopril Pantoprazole Tamsulosin
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2273837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OR
Alter: 46,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 10.11.2021
Beginn: 04.05.2022
Tage bis Beginn: 175,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Cough Diarrhoea Exposure to SARS-CoV-2 Fatigue Feeling abnormal Malaise Oropharyngeal pain Paranasal sinus discomfort Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sick relative

Symptomtext

My child's teacher had covid. Then my kid got sick, and then I got sick as well. I took a covid test that day, and it was positive. I had a runny nose, sinus pressure, congestion, mild coughing, fatigue, an extreme sore throat, diarrhea, and I lost my taste and smell. My symptoms progressively got worse so I called my doctor. I got a prescription for Paxlovid. I had horrible side effects from it, and it didn't seem to help any of my covid symptoms. When I finished the medication I felt terrible, but today I feel much better. I got my smell back last night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: At Home Covid Test- positive (5/4/2022)
Aktuelle Erkrankungen: none
Vorgeschichte: ADHD PTSD Depression Reactive Airway Disease
Andere Medikamente: Bupropion Adderall Amitriptyline Vitamin B
Allergien: none
Vorherige Impfungen: -

VAERS 2271161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 10.03.2021
Beginn: 20.01.2022
Tage bis Beginn: 316,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Decreased appetite Dizziness SARS-CoV-2 test positive

Symptomtext

01/20/22 presents to EC for "weakness, lightheadedness and decreased appetite". PMHx of "aflutter (s/p ablation, off Eliquis due to GI bleed ) , polymyalgia rheumatica on prednisone , HTN , recently diagnosed colon adenocarcinoma"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 01/10/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2269314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 17.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Joint range of motion decreased Magnetic resonance imaging abnormal Pain in extremity Periarthritis

Symptomtext

Pt reports "frozen shoulder" about 2 weeks about vaccination on 10/17/21. Saw MD, had an MRI, which showed no damage per pt. Pt says arm still hurts and has limited range of motion. Submitting for documentation purposes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: MRI (reported, date unknown)
Aktuelle Erkrankungen: none mentioned
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2264541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NC
Alter: 63,0
Geschlecht: M
Eingang: 05.05.2022
Impfdatum: 03.11.2021
Beginn: 27.12.2021
Tage bis Beginn: 54,0
Dosis: 2
Route/Site: IM / AR

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

COVID-19 Headache Malaise Nasopharyngitis Pain Paranasal sinus discomfort Rhinorrhoea SARS-CoV-2 test positive Tinnitus

Symptomtext

COVID-19 symptoms started 12/27/2021, tested positive 3-4 days after that. Symptoms included cold-like symptoms such like runny nose, sinus pressure, no coughing, achiness, and headache. Symptoms were very mild. I had ear ringing that started within a week after the other symptoms and it is still ongoing. The other symptoms lasted 3 days. I have an appointment with PCP for the ear ringing on 05/24/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 12/30/21 Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: One a Day Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2263765

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: SC
Alter: 57,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Gait disturbance Headache Inflammation Influenza like illness Pain

Symptomtext

Flu-like symptoms, which include chills & headache; Extremely painful body aches; Inflammation from my hips down to my leg; I could hardly walk.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia Autoimmune unspecified disorder Alpha-1 deficient Multiple myeloma Back issues
Andere Medikamente: Atenolol Protonix Synthroid Nasal steroid Advil Singulair Multivitamin mineral supplement Mucinex
Allergien: Sulfa Shrimp Chocolate Morphine
Vorherige Impfungen: 1st & 2nd dose of Pfizer - body aches, inflammation, chills, headache.

VAERS 2263748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 02.11.2021
Beginn: 12.01.2022
Tage bis Beginn: 71,0
Dosis: 2
Route/Site: IM / LA

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

Ageusia Asthenia COVID-19 Fatigue Hypersomnia Hypoaesthesia Hypoaesthesia oral Magnetic resonance imaging head normal Nasopharyngitis Pyrexia Sinus disorder

Symptomtext

Got COVID -I felt extremely fatigue, with sinus, I developed a cold and a fever. I was weak. I slept 16 hours a day. The day before I lost my sense of taste. I developed numbness on my mouth. On my feet, hand and my face. And inside my mouth. I had to see a Neurologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: MRI of the brain - normal.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Rheumatoid arthritis; gastro reflex decease
Andere Medikamente: Q nasal spray daily, Cortrosyn 10 mg daily, 600 mg Calcium daily, Pantoprazole 40 mg daily, 0.5 mg of Estradiol
Allergien: NONO
Vorherige Impfungen: Sept 2021 Shingrix - extremely fatigue

VAERS 2263458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 02.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Psoriasis Rash Rash erythematous Streptococcus test

Symptomtext

I started with a red rash on my thigh then it went up to my buttocks and my back my doctor diagnosed me with plaque psoriasis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Bloodwork Strep Test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Valsartan/HCTZ Levoxyl Zyrtec Metoprolol Montelukast Pravastatin Esomeprazole Liquid Gaviscon Flonase
Allergien: Tree nuts Sesame seeds; penicillin; erythromycin
Vorherige Impfungen: -

VAERS 2256474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 58,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Body temperature Malaise

Symptomtext

feeling lousy about noon the next day; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old male patient received BNT162b2 (BNT162B2), on 18Nov2021 at 17:00 as dose 3 (booster), single (Lot number: 32030BD) at the age of 58 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "GERD" (unspecified if ongoing), notes: GERD; "airborne allergies" (unspecified if ongoing), notes: airborne allergies Caller says this was diagnosed when he was a very tiny child. Concomitant medication(s) included: FEXOFENADINE oral taken for rhinitis allergic; LANSOPRAZOLE oral taken for gastrooesophageal reflux disease. Vaccination history included: BNT162b2 (He says his first dose was 20Mar2021 with NDC: not provided on the card, EXP: 31Jul2021, and LOT: EN6207., first dose, injected in his right arm), administration date: 20Mar2021, when the patient was 58-year-old, for COVID-19 Immunization; BNT162b2 (He says his second dose was on 10Apr2021 with NDC: not provided on the card, LOT: EW0158, and EXP: July2021.), administration date: 10Apr2021, when the patient was 58-year-old, for COVID-19 Immunization, reaction(s): "felt feverish with no measurable fever", "Fatigue". The following information was reported: MALAISE (non-serious) with onset 19Nov2021, outcome "not recovered", described as "feeling lousy about noon the next day". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: He says his feeling lousy did not get better until two days of sleep afterwards. He says for his second booster of the COVID-19 vaccine, which he is in the middle of that now, he took the shot about 5 o'clock yesterday and today he felt woozy before about 10 or so. He says he took two Tylenol last night and two this morning, the 500mg caplets. He says he took it to make his wife happy, they have been married 34 years, and it seemed to make her happy. He says that his wooziness has stayed about the same, and he slept from 11:30 for almost two hours today and will go back to sleep soon. Investigations: Caller says he took his temperature with an infrared thermometer when he was first out of bed this morning and it was 101.7 degrees Fahrenheit, then he took it again and the second temperature was 100.2 degrees Fahrenheit, then his third was 97.3 degrees Fahrenheit, all within 15 minutes down to the last reading, so it might have been elevated from being just out of the bed. He clarifies that it was 101.7 degrees Fahrenheit and then ten minutes later it was 97.3 degrees Fahrenheit.

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Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Test Date: 20220422; Test Name: Body temperature; Result Unstructured Data: Test Result:101.7 Fahrenheit; Comments: Result: 101.7 degrees Fahrenheit; Unit: Not Provided; Test Date: 20220422; Test Name: Body temperature; Result Unstructured Data: Test Result:100.2 Fahrenheit; Comments: Result: 100.2 degrees Fahrenheit; Unit: Not Provided; Test Date: 20220422; Test Name: Body temperature; Result Unstructured Data: Test Result:97.3 Fahrenheit; Comments: Result: 97.3 degrees Fahrenheit; Unit: Not Provided.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic rhinitis (airborne allergies Caller says this was diagnosed when he was a very tiny child.); GERD.
Andere Medikamente: FEXOFENADINE; LANSOPRAZOLE.
Allergien: -
Vorherige Impfungen: -

VAERS 2254829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CO
Alter: 55,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Blood test normal Bone pain Cough Dysstasia Feeling abnormal Frustration tolerance decreased Gait disturbance Grip strength decreased Headache Irritability Loss of personal independence in daily activities Pain Pain in extremity Urine analysis normal X-ray limb normal

Symptomtext

11/29/2021 Vaccination. 11/30/2021 I started to feel bad the following day; HA, body aches, dry cough, unsure of fever, joint pain all over. Brain fog. Irritability due to the pain. Difficulty holding a pen and I am an artist. My whole body, my leg, my arm. I will get stuck going to grocery store as it will just hit me. Hurts to take that first step. Hurts my pelvic bone to sit at computer. I can't take the laundry to the laundry room; my sons have to. Aches when I lift up. I have to use the banisters for assistance which I never had to use. Sometimes I even have to crawl up the stairs. It hurts when I stretch, nearly killed me doing some of the yard work; my hands hurt if I do too much. I am also a write but the pain medication is not helping and makes me fall asleep. My lower back, when I sit more for a certain amount of time, its hard to pull myself up. It is hard now to step into the bathtub which was never an issue. I feel anything I do, not in a good way. No diagnosis as of yet. Appt 05/05/2022. I feel frustrated but they are trying.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: blood panel; neg, Urinalysis; neg, x-ray of hands; neg
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism
Andere Medikamente: Vitamins, Thyroid Medication
Allergien: Red Dye, Hypertension Medication
Vorherige Impfungen: -

VAERS 2237673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 18.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Diarrhoea Inappropriate schedule of product administration Investigation Systemic infection Urinary tract infection

Symptomtext

2nd dose it spread to systemic infection.; Dose: 2nd Date: 18Nov2021; severe diarrhea for 5-6 days after that I developed UTI'S; Diarrhea; 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 18Nov2021 as dose 2, single (Lot number: 32030BD) at the age of 72 years intramuscular, in arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes", start date: 1980 (unspecified if ongoing); "heart disease", start date: 1980 (unspecified if ongoing); "allergies: food related since birth" (unspecified if ongoing), notes: food releated since birth. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1,SINGLE, Date: 12May2021, Site and route of injection, Anatomical Site of injection: arm, Route of administration: Intramuscular [checked], Batch/Lot number: EW0176), administration date: 12May2021, when the patient was 72-year-old, for COVID-19 immunization, reaction(s): "I developed UTI's", "Feels really awful", "She is achy/achy all over", "Her arm hurt/arm hurts", "Nausea", "Diarrhea", "I threw up. Not only that, it was brown", "feel lazy", "I threw up; I threw up it was brown and my stomach hurt too". The following information was reported: DIARRHOEA (non-serious) with onset Nov2021, outcome "unknown", described as "Diarrhea"; URINARY TRACT INFECTION (non-serious) with onset Nov2021, outcome "unknown", described as "severe diarrhea for 5-6 days after that I developed UTI'S"; INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 18Nov2021, outcome "unknown", described as "Dose: 2nd Date: 18Nov2021"; SYSTEMIC INFECTION (medically significant), outcome "unknown", described as "2nd dose it spread to systemic infection.". The events "severe diarrhea for 5-6 days after that i developed uti's" and "diarrhea" required emergency room visit. The patient underwent the following laboratory tests and procedures: ER evaluation: (Nov2021) Diarrhea, notes: 6 days diarrhea followed by UTI put on antibiotics. Therapeutic measures were taken as a result of urinary tract infection. Clinical Courses: Vaccination Facility Type was Hospital. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: ER evaluation; Result Unstructured Data: Test Result:Diarrhea; Comments: 6 days diarrhea followed by UTI put on antibiotics
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Food allergy (food releated since birth); Heart disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2236011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MO
Alter: 65,0
Geschlecht: F
Eingang: 15.04.2022
Impfdatum: 12.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: SYR / LA

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

Bacterial infection Chest X-ray Computerised tomogram Fatigue Secretion discharge Throat irritation

Symptomtext

On 11/17/2021 I started getting an itchy throat. I felt like a cold was coming on. I had a lot of mucus build up and fatigue. It continued for a week before I went urgent care for the first time. Over the course of a month I would go to urgent and my doctor and they would prescribe me antibiotics and prednisone. I would get better for 7-14 days and then the symptoms would come back. Since November I had 3 urgent care, 1 emergency room, and 2 doctor visits. Then I was sent to a pulmonologist and was provided another antibiotic that as of today, after two weeks from finishing antibiotic seems to have killed the bacteria that was causing the issues.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Chest x-ray, CT scan.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lisinopril; Hydrochlorothiazide; Rosuvastatin; Magnesium; Multivitamin; Vitamin E; Vitamin D3; Probiotic; Super B complex; Super collagen w/ Vitamin C and Biotin; Zinc; Melatonin; Stool softener; Fish oil w/ Omega 3; Happy Camper natural ba
Allergien: Compazine; Hyoscyamine
Vorherige Impfungen: -

VAERS 2204935

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 29.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Blood immunoglobulin A Blood immunoglobulin G Blood immunoglobulin M Chills Chlamydia test Culture negative Epstein-Barr virus antibody Full blood count Hepatitis C antibody Herpes simplex test negative Interchange of vaccine products Neisseria test Pain Pyrexia Smear test Urine analysis Vulval ulceration Vulvovaginal pain

Symptomtext

I received my second shot on Monday, April 5. 12 hours after my second shot I began to have body aches, fevers and chills, which were all to be expected. Those symptoms continued to get worse and my fever did not break until 48 hours later. On Wednesday, three days after my second shot, two or three bumps appeared on my posterior vulva. On Thursday, I was in terrible pain and the bumps got larger and turned white. I called NP and asked to be seen that day because something was very wrong. I was seen by NP and the gynecologist she worked with. Both mistakenly thought I had herpes and ran multiple tests and cultured the ulcers but they all came back negative. They prescribed me antivirals, which I stopped taking once the test results came back negative for herpes and they prescribed a lidocaine gel which made things worse. I came back a few days later for a follow up exam. I was still in excruciating pain. I told them about acute genital ulcers related to Epstein-Barr and they ran those tests also. After two weeks things progressively got better and I followed up with my gynecologist and all doctors/nurses I saw or spoke to had no idea what happened. It was absolutely related to the vaccine. I have received a third dose and switched to Pfizer and had no adverse reactions to it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: CBC (COMPLETE BLOOD COUNT) WITH DIFFERENTIAL CHLAMYDIA TRACHOMATIS ANTIBODY PANEL (IMMUNOGLOBULINS G, A AND M) WHITE BLOOD CELL DIFFERENTIAL EPSTEIN BARR VIRUS ANTIBODY PANEL GENITAL CULTURE WET SMEAR FOR TRICHOMONAS, YEAST, AND CLUE CELLS URINE CHLAMYDIA TRACHOMATIS AND NEISSERIA GONORRHOEAE DETECTION TREPONEMA PALLIDUM ANTIBODY SCREEN HEPATITIS C ANTIBODY HERPES SIMPLEX VIRUS 1 AND 2 DETECTION
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2197355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NC
Alter: 65,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / RA

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

Lymph node pain Lymphadenopathy

Symptomtext

Approximately 2 days after injection #2 in the right arm, swelling of the right IB or IIA lymph node was noticeable. Swelling lasted about 1 hour and shank rapidly. Approximately 5 days after injection #3 in the right arm, swelling of the right IB or IIA lymph node was noticeable and painful. The swelling persisted for two (2) days and I went to my Dr's office on the second day. The office PA examined me and my neck and asked me to apply compresses and monitor the swelling for another day . If it did not reduce within a day or two I should return and they would run further testing. Within that day the pain subsided and the swelling started to reduce after applying a compress. The swelling subsided.

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Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes,hypertension,high celestrol
Andere Medikamente: Metformin,glipizide,losartan,Victoza,atorvastatin
Allergien: Sudafed/Actifed at high doses
Vorherige Impfungen: -

VAERS 2179256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: SC
Alter: 42,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 06.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Abdominal pain upper Investigation Malaise Nausea

Symptomtext

Nausea like he wants to throw up but nothing comes up, like a pump is sucking water out but the water isn''t coming up; Cramps in Stomach; Not feeling well; 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 male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 06Nov2021 15:20 (Lot number: 32030BD) at the age of 42 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: ABDOMINAL PAIN UPPER (non-serious) with onset 08Nov2021, outcome "recovered" (15Nov2021), described as "Cramps in Stomach"; NAUSEA (non-serious) with onset 09Nov2021 12:00, outcome "recovered" (15Nov2021), described as "Nausea like he wants to throw up but nothing comes up, like a pump is sucking water out but the water isn''t coming up"; MALAISE (non-serious) with onset Nov2021, outcome "unknown", described as "Not feeling well". The events "cramps in stomach", "nausea like he wants to throw up but nothing comes up, like a pump is sucking water out but the water isn''t coming up" and "not feeling well" 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 nausea. Additional information: Caller states the Doctor at the Urgent Care couldn't find anything wrong and all of the tests were normal so he gave him something for nausea, Omeprazole. It is unknown for history of all previous immunization with the Pfizer vaccine considered as suspect. It is unknown if any Additional Vaccines Administered on Same Date of the Pfizer Suspect and no prior vaccinations within 4 weeks. It is unknown for patient medical history including any illness at time of vaccination. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: Tests; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 14.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Gait inability Pain

Symptomtext

After 2nd dose I will let you know as time continues but 24 hours later I have chronic pain all over my body, joints the worse, can't walk.; After 2nd dose I will let you know as time continues but 24 hours later I have chronic pain all over my body, joints the worse, can't walk. This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Nov2021 16:30 (Lot number: 32030BD) at the age of 56 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 number: 1, Product: COVID 19, Brand: Pfizer, lot number: 30125BA, dose Administration date: 24Oct2021, Administration time: 01:00 PM, Vaccine location: Right arm), administration date: 24Oct2021, when the patient was 56 years old, for Covid-19 Immunization, reaction(s): "Severe joint pain starting in elbow, moved to lower back, then hips, and knees by between date of 1st and 2nd dose.", "Severe joint pain starting in elbow, moved to lower back, then hips, and knees by between date of 1st and 2nd dose.", "Severe joint pain starting in elbow, moved to lower back, then hips, and knees by between date of 1st and 2nd dose.", "Severe joint pain starting in elbow, moved to lower back, then hips, and knees by between date of 1st and 2nd dose.". The following information was reported: GAIT INABILITY (non-serious), PAIN (non-serious) all with onset 15Nov2021, outcome "unknown" and all described as "After 2nd dose, she will let you know as time continues but 24 hours later she had chronic pain all over her body, joints the worse, can't walk.". Additional Information: After 2nd dose, the patient will let you know as time continues but 24 hours later she had chronic pain all over her body, joints the worse, can't walk. The patient has not had Covid prior to vaccination and post-vaccination. No other vaccines were administered in four weeks. She has not received treatment for events, she did not test with the Covid test post-vaccination. She had no Covid vaccination prior. No follow-up attempts are possible. No further information is expected.

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

VAERS 2179111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: IL
Alter: 49,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chills Disturbance in sexual arousal Dizziness Insomnia Muscle spasms Musculoskeletal discomfort Nightmare Pain

Symptomtext

Body aches; chills and shivering at night but no fever; Dizziness; Back and neck muscle spasms; Back and neck muscle spasms; Sleeplessness and nightmares; Sleeplessness and nightmares; Sexual arousal at night; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 01Nov2021 09:30 (Lot number: 32030bd) at the age of 49 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: LIPITOR. Vaccination history included: Bnt162b2 (Dose Number: 1, prev dose lot number: fc3182, prev dose vaccine location: Left Arm), administration date: Sep2021, when the patient was 49 years old, for Covid-19 immunization. The following information was reported: PAIN (non-serious) with onset 01Nov2021 23:30, outcome "unknown", described as "Body aches"; CHILLS (non-serious) with onset 01Nov2021 23:30, outcome "unknown", described as "chills and shivering at night but no fever"; DIZZINESS (non-serious) with onset 01Nov2021 23:30, outcome "unknown", described as "Dizziness"; MUSCLE SPASMS (non-serious), MUSCULOSKELETAL DISCOMFORT (non-serious) all with onset 01Nov2021 23:30, outcome "unknown" and all described as "Back and neck muscle spasms"; INSOMNIA (non-serious), NIGHTMARE (non-serious) all with onset 01Nov2021 23:30, outcome "unknown" and all described as "Sleeplessness and nightmares"; DISTURBANCE IN SEXUAL AROUSAL (non-serious) with onset 01Nov2021 23:30, outcome "unknown", described as "Sexual arousal at night". Therapeutic measures were not taken as a result of pain, chills, dizziness, muscle spasms, musculoskeletal discomfort, insomnia, nightmare, disturbance in sexual arousal. Additional information: Adverse event: Body aches, chills and shivering at night but no fever.Dizziness.Back and neck muscle spasms. Sleeplessness and nightmares Sexual arousal at night. Patient did not receive any other vaccine within four weeks. Patient did not test prior to COVID vaccination and post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2177719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 14.03.2022
Impfdatum: 10.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Hip fracture Hip surgery Laboratory test normal Pain

Symptomtext

Closed right hip fracture - Pt was admitted following surgery. Pt post-op course was uncomplicated. Pt continued to progress with physical therapy. Pt pain was controlled on oral medications. Pt was on antibiotic prophylaxis for 24hrs post-operatively. Pt was continued on lovenox for DVT prophylaxis throughout the hospitalization. Labs and vitals were stable at time of discharge. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2176371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Inappropriate schedule of product administration Off label use Vaccination site pain

Symptomtext

pain in the spot the vaccine was given; 1st dose was 22MAR2021 and 2nd dose was 31OCT2021; 1st dose was 22MAR2021 and 2nd dose was 31OCT2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 61 year-old female patient received bnt162b2 (BNT162B2), administration date 31Oct2021 (Lot number: 32030BD, Expiration Date: 28Feb2022) at the age of 61 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "autoimmune disease", start date: 11Jan1960 (ongoing), notes: Caller states she has an autoimmune disease and asthma.; "asthma", start date: 2017 (ongoing), notes: Caller states she has an autoimmune disease and asthma.; "Arthritis", start date: 1980 (ongoing); "Allergies", start date: 11Jan1960 (ongoing). Concomitant medication(s) included: ADVILCAPS taken for inflammation; CLARITIN [LORATADINE]. Vaccination history included: Bnt162b2 (dose 1, expiry date: Jun2021, Caller states after the first dose, within 4 hours she couldn't breathe and had to do inhalers every 4 hours), administration date: 22Mar2021, when the patient was 61 years old, for COVID-19 immunization, reaction(s): "she couldn't breathe and had to do inhalers every 4 hours", "she has never had a vaccine without a fever", "couldn't drive for 3 weeks", "Fuzzy", "Floating", "Floating", "Sore throat", "swollen glands", "Headache", "Tender arm", "Vertigo", "Double vision", "Taste", "Smell", "nauseated", "Diarrhoea", "Hot flashes", "Chills"; Bnt162b2 (dose 1, expiry date: Jun2021), administration date: 22Mar2021, when the patient was 61 years old, for COVID-19 Immunization, reaction(s): "Body aches"; Tetanus shots (Caller states she has always had severe reactions even to the tetanus shots it took her 3 weeks to recover), reaction(s): "she has always had severe reactions". The following information was reported: VACCINATION SITE PAIN (non-serious s) with onset 31Oct2021, outcome "recovered" (2021), described as "pain in the spot the vaccine was given"; INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious), OFF LABEL USE (non-serious) all with onset 31Oct2021, outcome "unknown" and all described as "1st dose was 22MAR2021 and 2nd dose was 31OCT2021". Additional Information: The caller was calling because she had her 2nd dose yesterday and said that she is not having side effects and she is concerned because with her 1st dose of the vaccine she had so many side effects that went on for months. She has an autoimmune disease and asthma. She has previously had severe reactions even to a tetanus shot that took her 3 weeks to recover from. With the first dose of the COVID vaccine it took her 5 months to recover. Within 5 minutes of the first dose she experienced symptoms. She couldn't drive for 3 weeks. After the 2nd dose, within 4 hours she couldn't breathe and was using her inhalers every 4 hours and the doctor put her on steroids. With the 2nd dose she had no side effects but had pain in the spot where she had the vaccine. The lot number is 32030BD. Caller clarifies and confirms that it was after the 1st dose that she couldn't breathe and was using her inhalers every 4 hours, not after the 2nd dose as provided by transfer agent. With her 2nd dose she had nothing and she has never had that happen in her life because of her autoimmune disease that she was born with. She usually will at least get a fever and this time she had nothing so she was wondering if she had an expired vaccine or one that was not stored properly. The doctor wanted to make sure that she had everything, including steroids at home. The doctor gave her a 6 day pack of the steroids in advance even though normally they would only give those afterwards but previously the caller couldn't drive and once she got home the symptoms had kicked in so she needed to have that on hand. She also had to make sure that she had her inhalers on hand since she was using both every 4 hours after the 1st dose. They make you sit there for 15 minutes after the vaccine and she just thought, uh oh here we go, it is all expected when she has a vaccine. Mentally she was very conscious and aware of what was going on but she can only describe it like she felt like she was floating and then sounds became amplified and light became so bright and everything was getting fuzzy and she thought that she better get home where she has her medications. When she stood up and looked down she thought, okay she is standing now, and when she was trying to make herself walk it was weird. She only had to drive 2.5 miles to get home and when she did she had started with a sore throat, fever, swollen glands and then she felt like she had ran a mile and she only walked from her car into the house. She laid down and took a nap and she woke up 4 hours later. She also had body aches, chills, and she was sweating and then freezing which was like hot flashes she had when she was going through menopause. The reason that she woke up at 4 hours was because she was having problems with her breathing and her asthma has been under control for 2 months before this. She began using her inhalers and when she was getting off of the sofa she was out of breath. She thought well her asthma has just flared and that's possible. She also was nauseated and had diarrhea and thought good Lord. The next day she couldn't taste or smell anything and then that lasted the whole day but she still had all the other symptoms too. When she woke up from her nap the lights were still really bright and sounds were still amplified and then she was starting to have double vision and that was kicking up her vertigo. She has suffered from vertigo her whole life. Eventually, later that week, she figured out that if she covers her right eye, then she could see everything normal out of her left eye, but out of her right eye everything was at a 45 degree angle. It was brutal and she couldn't drive for 3 weeks. When she was able to get to the doctor's office they had prescribed her steroids to see if a dose of steroids for a week would get it under control and it didn't. The doctor said that she was surprised with the vison issues. The caller also had severe headaches. Finally after all of this the fever broke after 5 days and then the headache went away but the double vison continued and the other side effects were starting to dissipate. The sound and light sensitivity, nausea and weakness had all continued. Then the doctor had gave her the prescription for steroids and after a week, finally, the double vison started getting better but the steroids didn't resolve it. The doctor sent the caller to an ophthalmologist who said that there was no medical reason for her double vision and referred her to a neurologist and when she was eventually able to go to see the neurologist, months later since she was a new patient, he diagnosed it an as BPPV migraine that was triggered. He asked the caller why she didn't recognize her own migraine and she said that she had never had one in her life. After 5 months she had the okay to get the 2nd dose but she decided to get her flu shot first since she knew she would recover faster from that. Now she was wondering when she should get her booster. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy multiple; Arthritis; Asthma (Caller states she has an autoimmune disease and asthma.); Autoimmune disorder (Caller states she has an autoimmune disease and asthma.)
Vorgeschichte: -
Andere Medikamente: ADVILCAPS; CLARITIN [LORATADINE]
Allergien: -
Vorherige Impfungen: -

VAERS 2176189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 31,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Headache Lymphadenopathy Malaise Myalgia Vaccination site pain

Symptomtext

Fatigue; headache; muscle pain; injection site pain; feeling unwell; swollen lymph nodes; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). The reporter is the patient. A 31 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Oct2021 (Lot number: 32030BD) at the age of 31 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE; ESCITALOPRAM. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL0140, Location of vaccine: Arm Left), administration date: 06Jan2021, when the patient was 31 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3302, Location of Vaccine: Arm Left), administration date: 27Jan2021, when the patient was 31 years old, for COVID-19 Immunization. The following information was reported: FATIGUE (non-serious) with onset 22Oct2021, outcome "recovering", described as "Fatigue"; HEADACHE (non-serious) with onset 22Oct2021, outcome "recovering", described as "headache"; MYALGIA (non-serious) with onset 22Oct2021, outcome "recovering", described as "muscle pain"; VACCINATION SITE PAIN (non-serious) with onset 22Oct2021, outcome "recovering", described as "injection site pain"; MALAISE (non-serious) with onset 22Oct2021, outcome "recovering", described as "feeling unwell"; LYMPHADENOPATHY (non-serious) with onset 22Oct2021, outcome "recovering", described as "swollen lymph nodes". Therapeutic measures were not taken as a result of fatigue, headache, myalgia, vaccination site pain, malaise, lymphadenopathy. Additional Information: The patient had no known allergies. The patient did not received any other vaccines within 4 weeks prior to the covid 19 vaccine. The patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: LEVOTHYROXINE; ESCITALOPRAM
Allergien: -
Vorherige Impfungen: -

VAERS 2161903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 72,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 19.11.2021
Beginn: 23.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient was admitted to Hospital on 12/23/2021. The only symptom charted in system is high fever. Patient tested at same facility on 12/31/2021 for covid: positive. No underlying health conditions listed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 2019 Novel Coronavirus RNA -Detected 12/31/2021
Aktuelle Erkrankungen: -
Vorgeschichte: None charted in system
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2161525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 03.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Abdominal discomfort Balance disorder Dizziness Fall Illness Vomiting

Symptomtext

throwing up; off balance; dizzy; falling; he got really sick; feeling sick to stomach; 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 66 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Nov2021 (Lot number: 32030BD) at the age of 66 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "sick to his stomach" (unspecified if ongoing), notes: Stated that he has been getting sick to his stomach for the last 40 years.; "lost some weight" (unspecified if ongoing), notes: Stated that he lost some weight. Stated that he gradually lost weight before the Covid vaccine. There were no concomitant medications. The following information was reported: ILLNESS (non-serious) with onset Nov2021, outcome "recovered" (2021), described as "he got really sick"; ABDOMINAL DISCOMFORT (non-serious) with onset Nov2021, outcome "recovered" (Nov2021), described as "feeling sick to stomach"; VOMITING (non-serious) with onset 05Nov2021, outcome "recovered" (Nov2021), described as "throwing up"; BALANCE DISORDER (non-serious) with onset 05Nov2021, outcome "recovered" (2021), described as "off balance"; DIZZINESS (non-serious) with onset 05Nov2021, outcome "recovered" (Nov2021), described as "dizzy"; FALL (non-serious) with onset 05Nov2021, outcome "unknown", described as "falling". Therapeutic measures were not taken as a result of illness, abdominal discomfort, vomiting, balance disorder, dizziness, fall. Additional information: Patient was Stated he had the first dose of the pfizer covid vaccine on 03Nov. Reports 1-2 days after his first shot, he got really sick. Reports feeling sick to stomach; throwing up; dizzy ; off balance. He was scheduled for his 2nd shot on 24Nov but cancelled as he did not want to be sick for holiday. wanting to reschedule his appt/find out where he can. Stated that he cancelled it because it was the day before holiday and he did not know if he would get sick or not. Stated that some of his friends got sick off the first and second shots. Stated that they got sick to their stomach and nauseated. Declined to complete reports at this time. Stated that he lost some weight. Stated that he gradually lost weight before the Covid vaccine. Wanted to know if it would be safe to get the second shot. Patient was stated that 1-2 days after the shot that he got sick to his stomach for about two days. Recovered completely. Stated that he has been getting sick to his stomach for the last 40 years. Stated that two days after the shot that he was throwing up for about 2-3 days. Recovered completely. Stated that he was dizzy and off balance two days after the shot. Stated that every now and then that he will raise out of bed and like he was falling. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Stomach discomfort (Stated that he has been getting sick to his stomach for the last 40 years.); Weight loss (Stated that he lost some weight. Stated that he gradually lost weight before the Covid vaccine.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1833233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 27.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Blood test Joint swelling Muscular weakness Nodule Rash Extra dose administered Grip strength decreased Injection site erythema Injection site pain Injection site pruritus Injection site rash Injection site warmth Rash erythematous Rash pruritic Thermal burn

Symptomtext

I was very weak in my right hand (same side as vaccination).; My wrist was even swollen.; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 49 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 27Oct2021 14:30 (Lot number: 32030BD) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing); "COVID-19" (unspecified if ongoing). Concomitant medication(s) included: ESTRADIOL; PROMETRIUM [PROGESTERONE]. Past drug history included: No. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL1283, Location of injection: Arm Right, Vaccine Administration Time: 11:30 AM), administration date: 15Jan2021, when the patient was 49 years old, for COVID-19 Immunization, reaction(s): "I had zero side effects"; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL9265, Location of injection: Arm Left, Vaccine Administration Time: 11:30 AM), administration date: 03Feb2021, when the patient was 49 years old, for COVID-19 immunization, reaction(s): "I developed a full blown sickness", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days"; Flu shot (Flu shot 6 weeks prior on 15Sep2021 flu shot), administration date: 15Sep2021, when the patient was 49 years old. The following information was reported: MUSCULAR WEAKNESS (non-serious) with onset 30Oct2021 07:15, outcome "not recovered", described as "I was very weak in my right hand (same side as vaccination)."; JOINT SWELLING (non-serious) with onset 30Oct2021 07:15, outcome "not recovered", described as "My wrist was even swollen."; RASH ERYTHEMATOUS (non-serious), NODULE (non-serious), THERMAL BURN (non-serious), RASH PRURITIC (non-serious), RASH (non-serious) all with onset 30Oct2021 07:15, outcome "not recovered" and all described as "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful". The events "i was very weak in my right hand (same side as vaccination).", "my wrist was even swollen.", "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful", "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful", "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful", "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful" and "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful" 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 muscular weakness, joint swelling, rash erythematous, nodule, thermal burn, rash pruritic, rash. Additional information: It was reported by reporter that "Dose 1, I had zero side effects. Dose 2, I developed a full-blown sickness like the flu. Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days. This dose 3 was even more different. Nothing flu or cold like, but 24 hours later, I was very weak in my right hand (same side as vaccination). i kept dropping things i was trying to hold all day. My wrist was even swollen. Possibly they hit a nerve. But, then 4 days later, I developed covid arm. I have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful. It's not responding to benadryl cream or pills and wakes me up at night. I'm 6 days out and still have it and it's waking me up at night with pain and i have to ice it". Facility where the most recent COVID-19 vaccine was administered was hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Patient provided information regarding the AE with the use of the product by herself. Patient considered that the Pfizer product had a causal effect to the AE. Patient willing to be contacted again by Pfizer on the reported AE. Patient had not required medical intervention. Patient was not seen in the emergency department. Patient was not hospitalized. Patient was not admitted to an intensive care unit. Device Date was reported as 01Nov2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: Test Date: 20211029; Test Name: Blood test; Result Unstructured Data: Test Result:Negative; Comments: Physcian did blood test for guillan bank since I had
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: ESTRADIOL; PROMETRIUM [PROGESTERONE]
Allergien: -
Vorherige Impfungen: -

VAERS 1833233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 27.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: OT / RA

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

Blood test Joint swelling Muscular weakness Nodule Rash Extra dose administered Grip strength decreased Injection site erythema Injection site pain Injection site pruritus Injection site rash Injection site warmth Rash erythematous Rash pruritic Thermal burn

Symptomtext

I was very weak in my right hand (same side as vaccination).; My wrist was even swollen.; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 49 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 27Oct2021 14:30 (Lot number: 32030BD) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing); "COVID-19" (unspecified if ongoing). Concomitant medication(s) included: ESTRADIOL; PROMETRIUM [PROGESTERONE]. Past drug history included: No. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL1283, Location of injection: Arm Right, Vaccine Administration Time: 11:30 AM), administration date: 15Jan2021, when the patient was 49 years old, for COVID-19 Immunization, reaction(s): "I had zero side effects"; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL9265, Location of injection: Arm Left, Vaccine Administration Time: 11:30 AM), administration date: 03Feb2021, when the patient was 49 years old, for COVID-19 immunization, reaction(s): "I developed a full blown sickness", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days", "Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days"; Flu shot (Flu shot 6 weeks prior on 15Sep2021 flu shot), administration date: 15Sep2021, when the patient was 49 years old. The following information was reported: MUSCULAR WEAKNESS (non-serious) with onset 30Oct2021 07:15, outcome "not recovered", described as "I was very weak in my right hand (same side as vaccination)."; JOINT SWELLING (non-serious) with onset 30Oct2021 07:15, outcome "not recovered", described as "My wrist was even swollen."; RASH ERYTHEMATOUS (non-serious), NODULE (non-serious), THERMAL BURN (non-serious), RASH PRURITIC (non-serious), RASH (non-serious) all with onset 30Oct2021 07:15, outcome "not recovered" and all described as "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful". The events "i was very weak in my right hand (same side as vaccination).", "my wrist was even swollen.", "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful", "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful", "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful", "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful" and "have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful" 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 muscular weakness, joint swelling, rash erythematous, nodule, thermal burn, rash pruritic, rash. Additional information: It was reported by reporter that "Dose 1, I had zero side effects. Dose 2, I developed a full-blown sickness like the flu. Not just aches, pains and chills, but sore throat, running nose and cough that all last 3-4 days. This dose 3 was even more different. Nothing flu or cold like, but 24 hours later, I was very weak in my right hand (same side as vaccination). i kept dropping things i was trying to hold all day. My wrist was even swollen. Possibly they hit a nerve. But, then 4 days later, I developed covid arm. I have a hard lump with a very large red rash that is hot to the touch that hurts, burns, itches, and is painful. It's not responding to benadryl cream or pills and wakes me up at night. I'm 6 days out and still have it and it's waking me up at night with pain and i have to ice it". Facility where the most recent COVID-19 vaccine was administered was hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Patient provided information regarding the AE with the use of the product by herself. Patient considered that the Pfizer product had a causal effect to the AE. Patient willing to be contacted again by Pfizer on the reported AE. Patient had not required medical intervention. Patient was not seen in the emergency department. Patient was not hospitalized. Patient was not admitted to an intensive care unit. Device Date was reported as 01Nov2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: Test Date: 20211029; Test Name: Blood test; Result Unstructured Data: Test Result:Negative; Comments: Physcian did blood test for guillan bank since I had
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: ESTRADIOL; PROMETRIUM [PROGESTERONE]
Allergien: -
Vorherige Impfungen: -

VAERS 2146478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 02.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / LA

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

Erythema Lip pain Lip swelling Pain in extremity

Symptomtext

lip swelling; inside of the mouth lip area it was sore and bright red; inside of the mouth lip area it was sore and bright red; sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP) from medical information team. The reporter is the patient. A 67-year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 02Nov2021 (Lot number: 32030BD) at the age of 67 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Allergy: Penicillin" (unspecified if ongoing), notes: she is a 67 year-old female with a medical history of allergic reactions to penicillin, azithromycin, and cephalosporin; "Allergy: cephalosporin" (unspecified if ongoing), notes: Caller is a 67 year-old female with a medical history of allergic reactions to penicillin, azithromycin, and cephalosporin; "Asthma" (unspecified if ongoing); "High Blood Pressure" (unspecified if ongoing); "Allergy" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID; METOPROLOL. Past drug history included: Azithromycin, reaction(s): "Allergy: azithromycin", notes: reporter is a 67 year-old female with a medical history of allergic reactions to penicillin, azithromycin, and cephalosporin; Erythromycin, reaction(s): "Allergy: Erythromycin", notes: Allergies: Penicillin, Erythromycin, cephalosporines, Keflex, and she is allergic to Dramamine which she found out on a trip.; Keflex, reaction(s): "Allergy: Keflex", notes: Allergies: Penicillin, Erythromycin, cephalosporines, Keflex, and she is allergic to Dramamine which she found out on a trip.; Dramamine, reaction(s): "Allergy: Dramamine", notes: Allergies: Penicillin, Erythromycin, cephalosporines, Keflex, and she is allergic to Dramamine which she found out on a trip. The following information was reported: LIP SWELLING (non-serious) with onset 04Nov2021, outcome "recovered" (06Nov2021), described as "lip swelling"; LIP PAIN (non-serious), ERYTHEMA (non-serious) all with onset 04Nov2021, outcome "recovered" (06Nov2021) and all described as "inside of the mouth lip area it was sore and bright red"; PAIN IN EXTREMITY (non-serious) with onset Nov2021, outcome "unknown", described as "sore arm". The event "lip swelling" was evaluated at the physician office visit. Additional Information: she is a 67-year-old female with a medical history of allergic reactions to penicillin, azithromycin, and cephalosporin and mentioned that her daughter is allergic to penicillin as well. she received the first dose of the Pfizer Covid-19 vaccine on 02Nov2021 and afterwards had complaints of lip swelling which has since resolved per reporter. she denies having dermal fillers in her lips and states that she read somewhere that study participants for the Pfizer Covid-19 vaccine had dermal fillers and complaints of lip swelling. she is asking if lip swelling is an allergic reaction symptom of the Pfizer Covid-19 vaccine. she is asking if its okay to get the second dose of the Pfizer Covid-19 vaccine if she did have an allergic reaction to the first dose. Adverse Reactions: Severe allergic reactions, including anaphylaxis, and other hypersensitivity reactions (e.g., rash, pruritus, urticaria, angioedema), diarrhea, vomiting, pain in extremity (arm), and syncope have been reported following administration of the Pfizer-BioNTech COVID-19 Vaccine outside of clinical trials. Follow-up (09Nov2021): New information received. Additional Context: she states that she is calling about the Pfizer Covid Vaccine, she has a concern. She is fine now but this happened last week. She had the covid vaccine on Tuesday and was fine no problem but then on Thursday, her bottom lip was swollen, it was 2 times the normal size. She has been googling, and she has no fillers or cosmetic work done on the lip. The swelling took 2 days to go away. She also noticed that the inside of the lip was really sore, and this has never happened to her. She checked with the doctor's office but then since she got better, she never checked back in with them. This happened with the first dose, should she still get the second, she doesn't know what to do next. Should she see an allergist. she states that she knows about allergies but this was not an anaphylactic reaction, something that she is aware of since her daughter gets them but she still thinks it was some sort of reaction. Her First Dose was on 02Nov2021, and the first thing in the morning on Thursday 04Nov2021 is when she noticed the lip swelling. HCP: She has talked to the doctor but has not seen them. Her Primary Care was not around last week. She doesnt have an allergist anymore, she might have to get a new one since they retired. Lip Swelling: The lip swelling was totally gone on Saturday the 06Nov2021. She would like to add that the inside of the mouth it was really sore, specifically the other side of lip but inside, it was bright red, she also noticed Thursday morning, she first noticed her mouth felt weird, then she went and looked and the inside of the mouth was sore and red. It subsided the same time as the lip swelling. She is due for the second dose on 23Nov2021. Concomitant medications: She doesn't think any medications she takes has anything to do with this, she takes Synthroid and metoprolol all the time daily, but she does not think it has anything to do with the lip swelling, she also x weird either. Medical Conditions: She has Asthma but does not take any medications for it when it comes its like a cold or something. She has High Blood Pressure. She is an allergic person, she is allergic to penicillin erythromycin. She has never had a reaction to a vaccine other then a sore arm. Follow-Up (17Nov2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lip pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Asthma; Blood pressure high; Drug allergy (allergic reactions to penicillin, azithromycin, and cephalosporin); Penicillin allergy (allergic reactions to penicillin, azithromycin, and cephalosporin)
Andere Medikamente: SYNTHROID; METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2146459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TN
Alter: 54,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Dyskinesia Muscle twitching Pain

Symptomtext

jerky feelings/ jerk in my hands and my legs; my whole body just hurts all over; I was good and turned over this like I was hurting so bad so I could not turn over hardly; soreness; Twitching; severe pain; 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 54 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Nov2021 (Lot number: 32030BD) at the age of 54 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Fibromyalgia" (unspecified if ongoing); "Osteoarthritis" (unspecified if ongoing); "back problems" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (MANUFACTURER UNKNOWN 1st dose, She notes not having any reactions to the 1st 2 doses of the vaccine, Date of first vaccine: 24Mar2021), administration date: 24Mar2021, for COVID-19 immunization; Covid-19 vaccine (MANUFACTURER UNKNOWN 2nd dose, She notes not having any reactions to the 1st 2 doses of the vaccine, Date of second shot: 14Apr2021), administration date: 14Apr2021, for COVID-19 immunization. The following information was reported: PAIN (non-serious) with onset 04Nov2021 04:30, outcome "unknown", described as "severe pain"; DYSKINESIA (non-serious), outcome "unknown", described as "jerky feelings/ jerk in my hands and my legs "; PAIN (non-serious), outcome "unknown", described as "my whole body just hurts all over; I was good and turned over this like I was hurting so bad so I could not turn over hardly"; ARTHRALGIA (non-serious), outcome "unknown", described as "soreness"; MUSCLE TWITCHING (non-serious), outcome "unknown", described as "Twitching". Additional Information: She got up at 04:30 today and turned over in bed and had "severe pain." She notes not having any reactions to the 1st 2 doses of the vaccine and didn't know if the vaccine could be causing her symptoms. The reporter states that she was not upset she just wanted to know if this could be the cause of her having "jerky" feelings and "pain and stuff." The reporter believes that she filed a report with the DSU as she spoke with them this AM and they gave MI phone number for her to call back once they opened. Booster may have accelerated the side effects she had with that because she was having lot of jerk in her hands and her legs and she had that with fibromyalgia. Her whole body just hurts all over; she was good and turned over this like she was hurting so bad so she could not turn over hardly. Concern: Consumer stated, "Yes she got the booster vaccine, yesterday and she don't know if she was having a reaction, the first two vaccines she didn't have a problem but she also had fibromyalgia (Intent: Medical History) and osteoarthritis (Intent: Medical History) and she had issues with that kind of what she was having now and she don't know whether the booster may have accelerated the side effects she had with that because she was having lot of jerk in her hands and her legs and she had that with fibromyalgia (Event captured as per verbatim) and she was having like 'musky' and 'hurt' and her whole body just hurts all over because she was good and turned over this like she was hurting so bad so she could not turn over hardly." 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: Back discomfort; Fibromyalgia; Osteoarthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 15.10.2021
Beginn: 08.02.2022
Tage bis Beginn: 116,0
Dosis: 3
Route/Site: SYR / AR

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

Aphonia COVID-19 Cough Dizziness Exposure to SARS-CoV-2 Fatigue Headache Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

My husband tested positive for covid on Sunday. Then I caught it on Tuesday. I had a headache, congestion, exhaustion, dizziness, and I lost my voice. Thursday and Friday were the really bad days. Then it started to get better. I just took some Zinc, and I was drinking Vitamin C shots. When I had went to see my doctor they prescribed me with Ibuprofen 600mg, Fluticasone, Loratadine, Azithromycin 500mg, and Benzonatate as needed. I didn't take the Benzonatate though because my cough never got that bad. A few days after getting well I still had a little bit of dizziness. It also took a while for my voice to come back to normal for a couple of weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Covid test- positive (2/8/2022) Covid test- negative (2/19/2022)
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Multivitamin
Allergien: none
Vorherige Impfungen: -

VAERS 2128147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NJ
Alter: 59,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 05.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Bursitis Magnetic resonance imaging Rotator cuff syndrome SARS-CoV-2 test Vaccination site erythema Vaccination site pruritus

Symptomtext

3 weeks after receiving the 3rd dose, I began having severe pain in both my shoulders that were never like that before; Both shoulders and have severe tendinitis and bursitis; Both shoulders and have severe tendinitis and bursitis; I did have redness around injection site and area was itchy for 4 days; I did have redness around injection site and area was itchy for 4 days; This is a spontaneous report from a contactable reporter (nurse). The reporter is the patient. A 59-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Nov2021 at 09:00 (Lot number: 32030BD) at the age of 59 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Penicillin allergy" (unspecified if ongoing), notes: Known allergies: Penicillin. There were no concomitant medications. Past drug history included: Fentanyl, reaction: "Drug allergy", notes: Known allergies: Fentanyl and Morphine, reaction: "Drug allergy", notes: Known allergies: Morphine. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EL8982; Anatomical Location: Left arm; Administration time: 13:30), administration date: 04Feb2021, when the patient was 58 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EL9264; Anatomical Location: Left arm; Administration time: 10:30), administration date: 25Feb2021, when the patient was 58 years old, for COVID-19 immunisation. The following information was reported: ARTHRALGIA (non-serious) with onset 24Nov2021 at 10:00, outcome "not recovered", described as "3 weeks after receiving the 3rd dose, I began having severe pain in both my shoulders that were never like that before"; ROTATOR CUFF SYNDROME (non-serious), BURSITIS (non-serious) all with onset 24Nov2021 at 10:00, outcome "not recovered", and all described as "Both shoulders and have severe tendinitis and bursitis"; VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 24Nov2021 at 10:00, outcome "not recovered", and all described as "I did have redness around injection site and area was itchy for 4 days". The events "3 weeks after receiving the 3rd dose, I began having severe pain in both my shoulders that were never like that before", "Both shoulders and have severe tendinitis and bursitis" and "I did have redness around injection site and area was itchy for 4 days" 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 arthralgia, rotator cuff syndrome and bursitis. 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. The patient had magnetic resonance imaging (MRI) of both shoulders as had severe tendinitis and bursitis in both and it continued until 13Feb2022 (at the time of this report) and physical therapy (PT) was barely helping so far. The patient had redness around injection site and area was itchy for 4 days after the 3rd dose, which she also had a picture of. Treatment for the events arthralgia, rotator cuff syndrome and bursitis included MRI and was receiving PT (at the time of this report). Since the vaccination, the patient had been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20211124; Test Name: MRI; Result Unstructured Data: Test Result:Severe tendinitis and bursitis in both the shou...; Comments: Severe tendinitis and bursitis in both the shoulders. at 10:00; Test Date: 20211206; Test Name: Covid 19 swab; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2118784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 42,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 15.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / RA

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

Depression Discomfort Erythema Inflammation Loss of personal independence in daily activities Mechanical urticaria Pruritus Swelling Urticaria

Symptomtext

Starting (11/2021) one week after the second dose of Pfizer/BioNTech (Covid 19) shot I began having substantial disruption of the ability to conduct normal life functions. Everyday I would break out into hives and dermatographia, from head to toe, multiple times throughout the day. This includes my scalp, face, ears, arms, chest, legs, feet, hands and encompasses raised red lines, swelling and inflammation, along with severe itching. This has persisted for over 90 days and still continues to this day. This condition, caused by the Pfizer/BioNTech (Covid 19) shot has caused not only physical distress and massive discomfort but has also caused depression.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: First appointment to my general practitioner was on 1/19/2022, where I was diagnosed with chronic dermatographia/hives/urticaria. Second appointment scheduled for 3/9/2022 with a immunologist specialist
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Birth control
Allergien: azithromycin
Vorherige Impfungen: -

VAERS 2107416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 18,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Overdose Product preparation error Pyrexia

Symptomtext

reported slight fever x 24hrs only; The dose the patient received however was of an undiluted product; The dose the patient received however was of an undiluted product; This is a spontaneous report from a contactable registered nurse.(Other HCP) from medical information team. A 18-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA Vaccine, Solution for injection, Batch/Lot number was not reported), intramuscular, administered in deltoid right, administration on 11Nov2021 as Dose 2, Single (at the age of 18-year-old) for covid-19 immunization. Relevant medical history included: "Prosthetic valve functioning normally", start date: 24Nov2015 (ongoing), notes: Patient Medical History (including any illness at time of vaccination):, Illness/AE: Prosthetic valve functioning normally, Onset date: placed 24Nov2015 , 18Oct2021, stop date: Ongoing. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, Pfizer/BioNtech COVID-19 Vaccine Details:, Dose: 1st, Date: 18Oct2021, Time (24hr): Approx. 16:40 , Anatomical site of Location: Right deltoid, Batch/Lot number: 30145BA, Route of administration: Intramuscular, Illness/AE: Tetralogy of Fallot, Onset date: 18Oct2021, stop date: Ongoing checked), administration date: 18Oct2021, when the patient was 18 years old, for Covid-19 immunization, reaction(s): "Tetralogy of Fallot", "Prosthetic valve functioning normally". The reported stated that the patient that received his 2nd dose of the Pfizer COVID 19 Vaccine yesterday (11Nov2021) and was of an undiluted dose of the vaccine and they wanted to know what to do next or what guidance Pfizer may have pertaining to this situation. The patient was monitored in clinic for 30 minutes post administration and no adverse reactions were reported that the reporter was aware of at this time. They haven't reached out to the patient yet, but he was fine that they knew of, but they're in the process of reporting this and they need to know what they need to do and when they need to do it if anything should be done differently. She said that she needs to know how much she should freak out right now. No investigation assessment was reported. The events that are reported as OVERDOSE (non-serious), PRODUCT PREPARATION ERROR (non-serious) all with onset 11Nov2021 16:42, outcome "unknown" and all described as "The dose the patient received however was of an undiluted product"; PYREXIA (non-serious), outcome "recovered", described as "reported slight fever x 24hrs only". Follow up(18Nov2021): Additional Information:Patient provided information regarding the adverse event(s) with the use of the product: Yes, There is no causal effect to the adverse effect. Patient did not take any vaccine prior vaccination (within 4 weeks). Patient concomitant drug therapy was none. Patient Family medical history relevant to AE was none. Specific Relevant Test for thromboembolic events with thrombocytopenia was None Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Prosthetic valve dehiscence
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2089001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 68,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 27.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / LA

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

Axillary mass Body temperature Pyrexia SARS-CoV-2 test Blood culture Blood test Computerised tomogram Ultrasound scan X-ray

Symptomtext

9 days after getting my booster, I had a lump under my armpit the size of an egg. Still there; I also have been running a fever of 100-103 since Nov 6th , little over a week after my booster.This is a spontaneous report received from a contactable consumer. The reporter is the patient. A 68-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 27Oct2021 at 10:30 (Lot number: 32030BD)at the age of 68 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Emphysema" (unspecified if ongoing); "Achalashia" (unspecified if ongoing), notes: Achalashia Type3; "Complex regional pain syndrome" (unspecified if ongoing), notes: CRPS; "Chronic kidney disease" (unspecified if ongoing), notes: CKD Stage 3; "Penicillin allergy" (unspecified if ongoing), notes: Known allergies: Penicillin and "Seafood allergy" (unspecified if ongoing), notes: Known allergies: Tuna. Concomitant medications included: OXYCONTIN ER; FLOMAX; NORVASC and ALBUTEROL. Past drug history included: Dermabond, reactions: "Drug allergy" and Vicodin, reactions: "Drug allergy". Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EL9264; Anatomical site: Left arm; Administration time: 10:30), administration date: 08Feb2021, when the patient was 67 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EN6203; Anatomical site: Right arm; Administration time: 10:30), administration date: 01Mar2021, when the patient was 67 years old, for COVID-19 immunisation. The following information was reported: AXILLARY MASS (non-serious) with onset 06Nov2021 at 15:00, outcome "not recovered", described as "9 days after getting my booster, I had a lump under my armpit the size of an egg. Still there"; PYREXIA (non-serious) with onset 06Nov2021 at 15:00, outcome "not recovered", described as "I also have been running a fever of 100-103 since Nov 6th , little over a week after my booster". The events "9 days after getting my booster, I had a lump under my armpit the size of an egg. Still there" and "I also have been running a fever of 100-103 since Nov 6th , little over a week after my booster." 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 axillary mass and pyrexia. 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. It was reported that the patient's doctors have had done endless tests and could not find the cause. The patient stated whether this might be due to injection. Since the vaccination, the patient had been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20211106; Test Name: Body temperature; Result Unstructured Data: Test Result:100-103; Comments: Fever of 100-103 Time: 15:00; Test Date: 20211112; Test Name: PCR; Test Result: Negative; Comments: Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Achalasia (Achalashia Type3); Chronic kidney disease (CKD Stage 3); Complex regional pain syndrome (CRPS); Emphysema; Penicillin allergy (Known allergies: Penicillin); Seafood allergy (Known allergies: Tuna.)
Andere Medikamente: OXYCONTIN; FLOMAX [TAMSULOSIN HYDROCHLORIDE]; NORVASC; ALBUTEROL [SALBUTAMOL].
Allergien: -
Vorherige Impfungen: -

VAERS 2091556

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WI
Alter: 68,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 03.11.2001
Beginn: 15.01.2022
Tage bis Beginn: 7.378,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Feeling abnormal Laboratory test Poor quality sleep Pruritus

Symptomtext

Starting around Jan. 15, 2022, started experiencing itching all over my body especially at night and from unknown cause. I also was feeling poorly with feeling extra tired. Four nights of poor sleep contributed to this. Seen in clinic on 1/20/22 and prescribed Hydroxyzine HCL 25mg tabs: take 1-2 every 6 hours as needed for itching. The itching resolved within about 4-5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Several lab tests were ordered to be done after 1/24/22 including blood and urinalysis
Aktuelle Erkrankungen: B 12 deficiency
Vorgeschichte: Hypothyroidism (Hashimoto's Disease), Autoimmune Metaplastic Atrophic Gastritis, Irritable Bowel Disease
Andere Medikamente: Levothyroxine, Lisinopril, Vit D, Calcium Sup., Nortriptaline, Famotidine, Gas and Bloating Prevention Food Enzyme Sup., Miralax
Allergien: Watermelon Radish
Vorherige Impfungen: -

VAERS 2206326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 23.11.2021
Beginn: 23.12.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Headache Myalgia Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/10, Pfizer, dose #1 11/23, Pfizer, dose #2 12/07 COVID swab, result: not detected 12/23/21 COVID swab, result: detected 12/23 SARS-COV-2 Variant Sequencing: pending 1/4/22 COVID swab, result: detected 12/23 pt cc: cough, fatigue, fever, headache, myalgias, rhinorrhea, sore throat exposure: unknown 12/26/21 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 12/07 COVID swab, result: not detected 12/23/21 COVID swab, result: detected 12/23 SARS-COV-2 Variant Sequencing: pending 1/4/22 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: AR
Alter: 81,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 04.11.2021
Beginn: 31.01.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Chills Cough Headache Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had cough, congestive, fever, chills, and headache. These lasted for about a week or so. On Jan 31, I tested positive for Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid-19 test
Aktuelle Erkrankungen: n/a
Vorgeschichte: COPD, sleep apnea
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2074423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: NY
Alter: 24,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 22.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: - / LA

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

COVID-19 Drug ineffective Fatigue Headache SARS-CoV-2 test Vertigo

Symptomtext

covid test result= Positive; covid test result= Positive; headaches; vertigo; extreme fatigue; 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 24 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 22Oct2021 (Lot number: 32030bd) at the age of 24 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Auto immune disease" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant) with onset 20Dec2021, outcome "unknown", COVID-19 (medically significant) with onset 20Dec2021, outcome "recovered with sequelae" and all described as "covid test result= Positive"; HEADACHE (non-serious) with onset 05Nov2021, outcome "recovered with sequelae", described as "headaches"; VERTIGO (non-serious) with onset 05Nov2021, outcome "recovered with sequelae", described as "vertigo"; FATIGUE (non-serious) with onset 05Nov2021, outcome "recovered with sequelae", described as "extreme fatigue". The events "covid test result= positive", "headaches", "vertigo" and "extreme fatigue" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (20Dec2021) positive. Therapeutic measures were not taken as a result of covid-19, headache, vertigo, fatigue. The patient not received other vaccine in four weeks. Other medications in two weeks were reported as Autoimmune disease medication. 2 weeks after vaccine the patient developed headaches, vertigo and extreme fatigue. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient had been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20211220; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2072122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NE
Alter: 31,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Fatigue Feeling abnormal Lymphadenopathy Pyrexia

Symptomtext

Starting at 4am the following day I had a fever of 101.5 f that I struggled to keep from rising for the next 24 hours. I took the maximum amount of tylenol on the label, ate lots of ice cream, and took a lot of lukewarm showers. I could not get up the stairs to the shower without assistance. I was very weak. My left lymphnode was quite swollen for the following week. Had the fever gone up higher I would have gone to the er. I was exhausted and spacey for a week. I am afraid what will happen the next time I need a covid booster as each shot in the sequence has had a more extreme reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none. We kept the fever between 101 and 101.5 for the day, which was below the threshold at which we were going to seek medical assistance.
Aktuelle Erkrankungen: none
Vorgeschichte: possible asthma, seasonal and food allergies
Andere Medikamente: zyrtec, mirena,
Allergien: cashews, alcohol, spinach, poppy seeds, cyclobenzaprine
Vorherige Impfungen: The second shot gave me a fever of 101 briefly and generally made me spacey and fatigued, but for a shorter period. The fever w

VAERS 1861053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: NE
Alter: 64,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Antinuclear antibody negative Deafness neurosensory Ear discomfort Hypoacusis Rash Chills Headache Pain Pyrexia Red blood cell sedimentation rate normal

Symptomtext

Just after the administration of the Pfizer vaccine he started to experience symptoms. A fullness sensation and decreased hearing in his right ear. Sensorineural hearing loss, worse in the right ear. Intermittent butterfly rash across his cheeks. This continues to the present and patient has now seen ENT's and is having bloodwork of an ana sed rate and c reactive protein.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Sed rate is at 4. ANA is negative,
Aktuelle Erkrankungen: He had Covid Oct 25, 21 prior to the vaccination, 11/09/21
Vorgeschichte: Hypercholesterolemia, Hypertension, Hypothyroidism
Andere Medikamente: Sildenafil 25 mg tab, One tab by mouth daily, prn erectile dysfunction
Allergien: NKMA
Vorherige Impfungen: -

VAERS 2054085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NJ
Alter: 69,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Bedridden Injection site bruising Injection site haemorrhage Injection site pain Nausea Vomiting

Symptomtext

Blood pooling on arm at injection entry point. Pooling had a radius of 2 inches around the injection entry point with pain. Next day additional symptoms began and include severe nausea and vomiting. All symptoms cleared after 14 days with little bruising remaining at injection entry point. During symptoms, patient was bedridden.

Weitere VAERSDATA-Felder

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

VAERS 2028785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TN
Alter: 56,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 22.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia

Symptomtext

Patient complained of shoulder pain on morning of 12/30, first thought to be from "sleeping wrong". Continued having nagging shoulder pain, and 1/12 diagnosed with possible Parsonage-Turner Syndrome of right upper extremity

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Diagnosis based on patient's complaints and physical exam per Doctor. Too early to do EMG for definitive diagnosis.
Aktuelle Erkrankungen: diabetic foot ulcer, osteomyelitis with MRSA, Enterococcus, and Proteus.
Vorgeschichte: Type 2 diabetes, GERD, depression, chronic low back pain, hypertension, morbid obesity, vitamin D deficiency, chronic venous stasis,
Andere Medikamente: Acetaminophen PO 1000mg TID; ammonium lactate topical 1 app daily; Amoxicillin-clavulanate 875-125mg PO BID; Ascorbic acid 500mg PO BID; Bumetanide 2mg PO BID; buspirone 15mg PO Q8HR; cetirizine 10mg PO daily; cholecalciferol 125mcg PO dail
Allergien: Levemir- rash, itchiness morphine- altered mental status, vomiting ziconotide- rash, itchiness
Vorherige Impfungen: -

VAERS 2014084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: NJ
Alter: 39,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 27.10.2021
Beginn: 16.11.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Blood test Colon operation Intestinal obstruction Ultrasound abdomen

Symptomtext

Started with abdominal pain on 11/16/2021 admitted to hospital 11/17/2021 with bowel obstruction had to have colon resection on 11/23/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: T scan of abdomen admission blood work
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birt control pills
Allergien: Penicillin
Vorherige Impfungen: Heart palpitations after 1st injection

VAERS 1996974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NC
Alter: 30,0
Geschlecht: M
Eingang: 01.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Chills Fatigue Immunisation

Symptomtext

In the day after the booster shot was received, patient experienced chills and fatigue; In the day after the booster shot was received, patient experienced chills and fatigue; Dose number: 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). A 30-year-old male patient received bnt162b2 (BNT162B2), intramuscular, administration date 23Dec2021 (Lot number: 32030BD) at the age of 30 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: EL3247; Route of administration: Intramuscular), administration date: 28Jan2021, when the patient was 29 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EL3247; Route of administration: Intramuscular), administration date: 18Feb2021, when the patient was 30 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 23Dec2021, outcome "unknown", described as "Dose number: 3"; CHILLS (non-serious) with onset 24Dec2021, outcome "recovered" (24Dec2021), described as "In the day after the booster shot was received, patient experienced chills and fatigue"; FATIGUE (non-serious) with onset 24Dec2021, outcome "recovered" (24Dec2021), described as "In the day after the booster shot was received, patient experienced chills and fatigue". Therapeutic measures were not taken as a result of chills and fatigue. Additional information: The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

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

VAERS 1985179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: HI
Alter: 61,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 10.02.2021
Beginn: 23.12.2021
Tage bis Beginn: 316,0
Dosis: 3
Route/Site: - / -

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

Activated partial thromboplastin time Anti-cyclic citrullinated peptide antibody Antinuclear antibody Arthralgia Blood creatine phosphokinase Blood uric acid C-reactive protein Contusion Full blood count International normalised ratio Liver function test Metabolic function test Prothrombin time Red blood cell sedimentation rate Rheumatoid factor

Symptomtext

bruising of b/l forearms and finger joint pain of b/l hands since 12/23/2021 after the 3rd booster shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: labs ordered ((BMP, CBC with diff, LFTs, uric acid, rheumatoid factor, PT, PTT, INR, CRP, ESR, ANA, anti-CCP, CK) on 12/28/2021
Aktuelle Erkrankungen: pls see #12
Vorgeschichte: HTN, proteinuria, prediabetes, CKD2,
Andere Medikamente: Losartan and PRN Zyrtec
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1984629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 30,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

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

Malaise Product preparation issue

Symptomtext

NURSE DIDN'T RECONSTITUTE PFIZER VIAL AND 0.3ML OF CONCENTRATED SOLUTION WAS GIVEN TO THE PATIENT. FACILITY HAS FOLLOWED THE RESIDENT-ONE DAY THE PATIENT DIDN'T FEEL WELL BUT OTHER WISE THE PATIENT HAS BEEN FINE. NO FURTHER MEDICAL CARE HAS BEEN NEEDED

Weitere VAERSDATA-Felder

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

VAERS 1980787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: SC
Alter: 31,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 09.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Abdominal pain upper Appendicitis Constipation Myalgia SARS-CoV-2 test Vomiting

Symptomtext

Appendicitis; stomach pains; muscle aches; vomiting; constipation; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 09Dec2021 17:00 (Lot number: 32030BD) 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 (Dose Number: 2, Pfizer, lot number=EW0158, on 27May2021 at 03:30PM, Left arm), administration date: 27May2021, when the patient was 30 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Pfizer on 06May2021 at 03:30PM, Right arm), administration date: 06May2021, when the patient was 30 years old, for COVID-19 Immunization. The following information was reported: APPENDICITIS (hospitalization, disability, medically significant) with onset 11Dec2021 04:00, outcome "recovering", described as "Appendicitis"; ABDOMINAL PAIN UPPER (hospitalization, disability) with onset 11Dec2021 04:00, outcome "recovering", described as "stomach pains"; MYALGIA (hospitalization, disability) with onset 11Dec2021 04:00, outcome "recovering", described as "muscle aches"; VOMITING (hospitalization, disability) with onset 11Dec2021 04:00, outcome "recovering", described as "vomiting"; CONSTIPATION (hospitalization, disability) with onset 11Dec2021 04:00, outcome "recovering", described as "constipation". The patient was hospitalized for appendicitis, abdominal pain upper, myalgia, vomiting, constipation (hospitalization duration: 1 day(s)). The events "appendicitis", "stomach pains", "muscle aches", "vomiting" and "constipation" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (11Dec2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of appendicitis, abdominal pain upper, myalgia, vomiting, constipation and included treatment with Appendix Removal. Clinical course: Patient did not have covid prior vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: 1,0
Labordaten: Test Date: 20211211; Test Name: Nasal Swab; 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: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1978682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PA
Alter: 58,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 02.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Immunisation Pruritus Rash

Symptomtext

Pfizer booster; I had a rash starting all over my body and its still here; it itches, its a crazy, crazy itch; my neck, side of my face, my back, my stomach, my arms and my legs; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 02Dec2021 17:45 (Lot number: 32030BD) at the age of 58 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing), notes: Patient History: No. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Manufacturer unknown), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 02Dec2021 17:45, outcome "unknown", described as "Pfizer booster"; RASH (non-serious) with onset Dec2021, outcome "not recovered", described as "I had a rash starting all over my body and its still here"; PRURITUS (non-serious) with onset Dec2021, outcome "unknown", described as "it itches, its a crazy, crazy itch; my neck, side of my face, my back, my stomach, my arms and my legs". Therapeutic measures were taken as a result of rash, pruritus. Additional Information: It was reported that I am gonna call my doctor now because I have to I thought it would go away you know I have been putting lotion on and taking a Zyrtec (Treatment) everyday but this is now that's the fourth day and so I don't know I mean I hope it goes away I just need something for the itching so I am gonna call my doctor but I wanted you guys to know because that's really the only thing that happen with can be attributed to it.". Prior vaccinations (Within 4 weeks) was reported as none. Treatment: Consumer stated, "Yes I took Zyrtec, I have been taking a Zyrtec everyday and just I am putting cream Cetaphil moisturizer, Cetaphil moisturizing cream." And then so I am gonna call my doctor just to see if she can give something to stop the itching and then I will just tell her, I had already reported this so she doesn't have to do it again right?" Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 23.12.2021
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

Dizziness Immunisation

Symptomtext

dizziness/dizzy spells; Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 41 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 15Nov2021 (Lot number: 32030BD) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetic" (unspecified if ongoing), notes: Illness/AE: Diabetic on Metformin and not insulin. Concomitant medication(s) included: METFORMIN taken for diabetes mellitus. Vaccination history included: Bnt162b2 (1st dose , Lot EN5318, Expiration unknown. , Injected in right arm in the muscle.), administration date: 13Feb2021, when the patient was 41 years old, for COVID-19 immunization; Bnt162b2 (2nd dose , Lot EN5318, expiration is unknown., injected in left arm in the muscle.), administration date: 08Mar2021, when the patient was 41 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Nov2021, outcome "unknown", described as "Booster"; DIZZINESS (non-serious) with onset 18Nov2021, outcome "not recovered", described as "dizziness/dizzy spells". Additional Information: It was reported that, received call from consumer regarding the Pfizer COVID vaccine booster. She got the booster on 15Nov2021, and 3 days later started having dizzy spells. If she sits down or up or lays down too fast, she gets really, really dizzy. She got vaccinated with booster on 15Nov2021, and about 18Nov2021, is when she started having dizzy spells and lasted until now. Caller also added that she was on a diet pill that she was taking for a month now and she was not sure if this is associated to her reaction that she was experiencing. They was still here. It seemed like today is worse. She wanted to know if there are others who have reported these symptoms. She called the pharmacy. and they suggested she call Pfizer. Vaccination Facility Type: Pharmacy. Time the Vaccination was Given: 12:45-13:00. Additional vaccines administered on same date of the Pfizer suspect: None. Dizzy Spells - third night around 12:30-01:00 and noticed she was dizzy when she sat up. The patient did not require visit to Emergency Room/ Physician Office for adverse events. Prior Vaccinations, the patient did not receive any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. AE(s) following prior vaccinations: None. Patient's Medical History included: Diabetic on Metformin and not insulin. Onset Date: She was pre-diabetic but diagnosed as being full diabetic for a year or year and a half. Family Medical History Relevant to AE(s): None. Relevant Tests: None Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetic (Illness/AE: Diabetic on Metformin and not insulin.)
Andere Medikamente: METFORMIN
Allergien: -
Vorherige Impfungen: -

VAERS 1974129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MN
Alter: 41,0
Geschlecht: F
Eingang: 23.12.2021
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

Immediate post-injection reaction Injection site pain Loss of personal independence in daily activities Musculoskeletal pain Neck pain Pain Sleep disorder

Symptomtext

immediate burning pain at site of insertion, radiates down arm, into neck and shoulder blade. has persisted X 3 weeks. interferes with daily activities, sleep. no improvement with heat, tylenol, ibuprofen. no previous reaction like this to first 2 covid shots or any other immunization. no rash, swelling , bruising.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: amoxicillin prednisone
Vorherige Impfungen: -

VAERS 1972056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CO
Alter: 36,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 04.01.2021
Beginn: 15.02.2021
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: IM / RA

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

Blood test normal Cardiac flutter Electrocardiogram Electrocardiogram ambulatory Fatigue Headache Supraventricular extrasystoles Ventricular extrasystoles

Symptomtext

For about a month in Feb into March 2021, after my initial 2 doses of the COVID vaccine I had pretty consistent heart fluttering feelings I've never had before. There were intense the first few weeks, would wake me up at times and I would feel headaches and tiredness. Then they started spreading out and eventually after a couple months went away. My tests ruled everything out and was just found to have some PAC's or PVC's, but this resolved, everything else was normal. I did seek a health visit on 2/22/21 and my PCP on 3/5/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Blood work, EKG, holter monitor test
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: Vit D 5000 iu daily Baby Aspirin 81mg daily DHEA 50mg daily COQ10 50mg daily
Allergien: PCN
Vorherige Impfungen: -

VAERS 1971590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

Pt reported hives to the COVID vaccine. Unknown time course or which dose pt had hives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Recent medical issues prior to booster vaccine dose: uricaria
Vorgeschichte: PMH: MEDIASTINAL LYMPHADENOPATHY, IFP, Vitamin D deficiency
Andere Medikamente: Medications: Betamethasone Dipropionate Aug (DIPROLENE AF) 0.05 % Top Crea Indications: URTICARIA Apply to affected area(s) 2 times a day Cetirizine 10mg PO Daily Vitamin D3 1000units Po daily
Allergien: Allergies: Crab (rash), Iodine (Rash)
Vorherige Impfungen: -

VAERS 1968014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 75,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Brain natriuretic peptide Differential white blood cell count Electrocardiogram Full blood count Injection site bruising Metabolic function test Oedema Peripheral swelling Prothrombin level Prothrombin time

Symptomtext

Patient received a booster dose of Pfizer COVID vaccine on 12/8/21. The next day, she said she started with a large bruise on her left upper arm. The bruise on exam did not blanch and covered the anterior part of her left upper arm. She also developed bilateral lower leg swelling, and exam showed pitting 3+ edema. Labs and ECG were grossly normal. Spoke to her today, and she said the large bruise is slowly fading. Edema is slowly resolving with furosemide 20mg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: ECG, CMP, CBC with diff, PT/PTT, BNP
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia
Andere Medikamente: omeprazole 20mg, potassium 20 mEq, loratadine 10mg, simvastatin 10mg, ca + vit D, ASA 81mg, metoprolol 50mg, hctz 50mg, benazepril 20mg, gabapentin 300mg tid
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1962152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: IN
Alter: 45,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Nausea Night sweats Pain Pyrexia

Symptomtext

103 degree fever for 14 hours, severe body aches, nausea, night sweats

Weitere VAERSDATA-Felder

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

VAERS 1962015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: HI
Alter: 45,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Headache Impaired work ability Lymph node pain Lymphadenopathy Nausea Pain Pain in extremity Pyrexia Rash Rash erythematous Rash pruritic Urticaria

Symptomtext

12/4 10:00pm start 102 fever all night, extreme chills, body aches, nausea,very bad headache in the back of head 12/5 same symptoms except chills.Fever was 99-100.Very bad headache .Arm still sore and lymph node under arm swollen sore 12/6 no fever. Bad body aches and very bad headache.Rash all over back of my head.This started at night.down my neck, on chest, itchy.lymph node still swollen,sore 12/7 Body aches, headache, rash wasn?t as bad but still there and itchy, especially on chest.I went to the doctor to just check to make sure it was ok.Lymph node still a bit sore but not as swollen 12/8 still light rash, got a couple hive looking bumps on right arm. One by my elbow was itchy and red lump.This lump lasted a couple days and then disappeared. 12/9 I was able to go to work.Still had the lump on elbow but not as red and swollen By 12/10 symptoms gone

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: No tests were given at the doctors office on 12/7 visit
Aktuelle Erkrankungen: None
Vorgeschichte: None known
Andere Medikamente: Centrum womens one a day multi vitamin
Allergien: Sudophed, codeine
Vorherige Impfungen: 1981. Age 5 I passed out right after getting required shots for school. Unsure of shot type

VAERS 1952838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: UT
Alter: 57,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Arthralgia Blood test Chills Confusional state Diarrhoea Fatigue Feeling cold Hallucination Homicidal ideation Myalgia Psychiatric investigation Pyrexia Rhinorrhoea Suicidal ideation Vomiting

Symptomtext

Fever over 101 for 2 days, Cold Chills, hallucinations, Muscle and Joint pain. Vomiting and Diarrhea (6 weeks and counting), Suicidal and Homicidal ( thoughts(4 weeks), Extreme fatigue (6 weeks and counting), Confusion and runny nose (6 weeks and counting)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: 4,0
Labordaten: Blood test and mental exam Nov 14th
Aktuelle Erkrankungen: Covid
Vorgeschichte: Hypothyroidism, Type 2 Diabetes, GERD, Migraines, High Cholesterol and sleep apnea .
Andere Medikamente: Vitamin D and B-12
Allergien: Balsam of Peru
Vorherige Impfungen: -

VAERS 1952086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: DC
Alter: 24,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 15.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain lower Back pain Herpes zoster Pruritus Rash Scab

Symptomtext

Initially pain on right lower abdomen and back, then rash developed in linear band across abdomen and one spot on back. Bumps clustered, although did not blister. Began scabbing 4-5 days after onset. Itching began after 1.5 weeks. Pain subsided following full course of valacyclovir after diagnosis with shingles. Had chickenpox sometime between ages 3-6.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: Cold symptoms mid November (not COVID-19) confirmed by 2 PCR tests.
Vorgeschichte: Viral-induced asthma.
Andere Medikamente: N/A.
Allergien: N/A.
Vorherige Impfungen: -

VAERS 1941868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NJ
Alter: 53,0
Geschlecht: U
Eingang: 11.12.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Feeling abnormal Immunisation Lymphadenopathy Lymphoedema Pruritus

Symptomtext

lymphoedema; arm in which I got the shot, the lymph nodes under my arm became very swollen/then big swelling in my glands; fatigue/being just tried; feeling funky; itching under the arm; Booster shot; 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 07Nov2021 (Lot number: 32030BD, Expiration Date: 28Feb2022) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Allergy" (unspecified if ongoing), notes: Verbatim: Allergy. Concomitant medication(s) included: FLONASE ALLERGY RELIEF taken for hypersensitivity; FLUMAX [AMBROXOL HYDROCHLORIDE], start date: 09Oct2021. Vaccination history included: Flu vaccine (Fluvax vaccine by secure and the LOT# is 309613 and I have no issues with that., little tired and feeling under the weather), administration date: 09Oct2021, for Immunization, reaction(s): "little tired", "feeling under the weather"; Covid-19 vaccine (Dose:1, MANUFACTURER UNKNOWN), for COVID-19 Immunization, reaction(s): "did not get this effect"; Covid-19 vaccine (Dose:2, MANUFACTURER UNKNOWN), for COVID-19 Immunization, reaction(s): "did not get this effect". The following information was reported: IMMUNISATION (non-serious) with onset 07Nov2021, outcome "unknown", described as "Booster shot"; LYMPHOEDEMA (non-serious) with onset 08Nov2021, outcome "recovering", described as "lymphoedema"; LYMPHADENOPATHY (non-serious) with onset 08Nov2021, outcome "recovering", described as "arm in which I got the shot, the lymph nodes under my arm became very swollen/then big swelling in my glands"; PRURITUS (non-serious) with onset 07Nov2021, outcome "recovered" (2021), described as "itching under the arm"; FATIGUE (non-serious) with onset 08Nov2021, outcome "recovering", described as "fatigue/being just tried"; FEELING ABNORMAL (non-serious) with onset 08Nov2021, outcome "recovering", described as "feeling funky". Therapeutic measures were not taken as a result of lymphoedema, lymphadenopathy, pruritus, fatigue, feeling abnormal. Additional information: When probed for adverse event, consumer stated, so, patient was fine now but it was important to report it. It was a lymphoedema, so the arm in which patient got the shot, the lymph nodes under patient arm became very swollen. It might still be a little bit but that became itching under the arm then big swelling in patient glands. Itching had gone away but it was on 07Nov. while patient had fatigue and the usual stuff but about 24 hours afterward so on November 8th. Yes, like patient got the shot on 7th and patient had the additional reactions on 8th beyond the normal side effect you know of being just tried and feeling funky. That was patient booster dose. So, patient did not get this effect on the first two. LOT#: Consumer stated, 32030BD (Captured as provided.). Consumer stated patient had not gone to doctor about it. Patient thought it was still there a little bit but had not had a chance to follow up with the doctor. Patient yet had no treatment. Patient would rush to my doctor by chance if its urgent. Consumer further stated, just in progress to that, patient had gotten the flu vaccine on 09Oct2021. Patient was not taking any other medications probably one of the questions patient was lined anyway patient thought was if you have had any other vaccines for 09Oct, a month prior, which had no side effect with? Patient never had any side effects from any vaccine except for the normal you know getting a little tired and feeling under the weather. This was for the first time patient had a swollen lymph gland. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Verbatim: Allergy)
Andere Medikamente: FLONASE ALLERGY RELIEF; FLUMAX [AMBROXOL HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1939323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: GA
Alter: 51,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Injection site erythema Injection site warmth

Symptomtext

Client states that the injection site became red and warm to touch after receiving vaccine. He states that is has progressively gotten worse over the course of 4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: UT
Alter: 87,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 02.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / AR

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

Oedema peripheral Urticaria

Symptomtext

Hives that started on trunk and moved to legs and arms. He also experienced edema in feet and ankles. Hives increased in size and lasted from 12/4 to 12/8/2021, for a total of 5 days. On 12/8/21 he began taking Benedryl, and now symptoms are decreasing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Was diagnosed with a tumor in the bladder about two weeks prior to booster. Further testing on the tumor is necessary. A biopsy is scheduled for 12/15/21.
Vorgeschichte: Patient does not have any chronic health conditions.
Andere Medikamente: Does not take any prescriptions. Had not taken any over the counter medications at the time of vaccination.
Allergien: No known allergies to anything.
Vorherige Impfungen: -

VAERS 1935166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Abdominal pain upper Back pain Chills Dyspepsia Gastrooesophageal reflux disease Immunisation Nausea Night sweats Pain SARS-CoV-2 test Vomiting

Symptomtext

Nausea; Vomiting/constant vomiting; Severe stomach and back pain; Severe stomach and back pain; Chills; Severe acid reflux; Night sweats; That feels like shooting pain and a knot; Severe ingestion; Dose received 3/ dose number=3; This is a spontaneous report received from a contactable reporter (nurse). The reporter is the patient. A 46 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in right arm, administration date 19Nov2021 at 18:00 (Lot number: 32030BD) at the age of 46 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was not reported. Concomitant medications included: SYNTHROID and LISINOPRIL. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: EL9261, Anatomical site: left arm), administration date: 23Jan2021, when the patient was 45 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot number: EL9266, Anatomical site: right arm), administration date: 19Feb2021, when the patient was 45 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021 at 18:00, outcome "unknown", described as "Dose received 3/ dose number=3"; NAUSEA (non-serious) described as "Nausea"; VOMITING (non-serious) described as "Vomiting/constant vomiting"; ABDOMINAL PAIN UPPER (non-serious) and BACK PAIN (non-serious); both described as "Severe stomach and back pain"; CHILLS (non-serious) described as "Chills"; GASTROOESOPHAGEAL REFLUX DISEASE (non-serious) described as "Severe acid reflux"; NIGHT SWEATS (non-serious) described as "Night sweats"; PAIN (non-serious) described as "That feels like shooting pain and a knot"; DYSPEPSIA (non-serious) described as "Severe ingestion"; all with onset 27Nov2021, outcome "recovering''. The events "Nausea", "Vomiting/constant vomiting", "Severe stomach and back pain", "Chills", "Severe acid reflux", "Night sweats", "That feels like shooting pain and a knot" and "Severe ingestion" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. 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 vaccine. Since the vaccination, the patient had been tested for COVID-19. On 02Nov2021, the patient underwent SARS-COV-2 test by test type nasal swab and the result was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Test Date: 20211102; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: SYNTHROID; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1935104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Pain Swelling

Symptomtext

Swelling; Extreme pain in left under arm.; Booster; 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 female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 18Nov2021 09:00 (Lot number: 32030BD) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergy: Penicillin" (unspecified if ongoing), notes: Known allergy: Penicillin. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8727, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM), administration date: 04Mar2021, when the patient was 55 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6205, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM), administration date: 25Mar2021, when the patient was 55 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021 09:00, outcome "unknown", described as "Booster"; SWELLING (non-serious) with onset 19Nov2021 09:30, outcome "not recovered", described as "Swelling"; PAIN (non-serious) with onset 19Nov2021 09:30, outcome "not recovered", described as "Extreme pain in left under arm.". Therapeutic measures were not taken as a result of swelling, pain. Clinical course: Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination, has the patient has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No other medications were received within 2 weeks of vaccination Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Known allergy: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: -
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Immunisation Pain Pyrexia Somnolence Vaccination site pain

Symptomtext

Entire body aches; exhaustion; low grade fever; pain at injection site; unable to stay awake; Dose Number 3; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 71 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 09Nov2021 11:00 (Lot number: 32030BD) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "COPD" (unspecified if ongoing), notes: verbatim: Long hauler, COPD; "Allergy: bee stings" (unspecified if ongoing), notes: Relevant past drug history, Name of Drug as Reported: Imitrex, bee stings , Reaction: Allergy; "if_covid_prior_vaccination: Yes" (unspecified if ongoing), notes: if_covid_prior_vaccination: Yes. The patient took concomitant medications. Past drug history included: Imitrex, reaction(s): "allergy: Imitrex", notes: Relevant past drug history, Name of Drug as Reported: Imitrex, bee stings , Reaction: Allergy. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8731), administration date: 18Apr2021, when the patient was 70 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: OEJ1685), administration date: 22Dec2020, when the patient was 70 years old, for COVID-19 immunization. The following information was reported: PAIN (non-serious) with onset 10Nov2021 00:30, outcome "recovered" (Nov2021), described as "Entire body aches"; FATIGUE (non-serious) with onset 10Nov2021 00:30, outcome "recovered" (Nov2021), described as "exhaustion"; PYREXIA (non-serious) with onset 10Nov2021 00:30, outcome "recovered" (Nov2021), described as "low grade fever"; VACCINATION SITE PAIN (non-serious) with onset 10Nov2021 00:30, outcome "recovered" (Nov2021), described as "pain at injection site"; SOMNOLENCE (non-serious) with onset 10Nov2021 00:30, outcome "recovered" (Nov2021), described as "unable to stay awake"; IMMUNISATION (non-serious) with onset 09Nov2021 11:00, outcome "unknown", described as "Dose Number 3". Therapeutic measures were not taken as a result of pain, fatigue, pyrexia, vaccination site pain, somnolence, immunisation. Additional information: Patient was not pregnant at the time of vaccination. Patient didn't receive other vaccines within 4 weeks prior to vaccination. Patient had received other medications within 2 weeks of vaccination. Patient was diagnosed with covid-19 prior to vaccination. Patient was not tested with covid to post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bee sting hypersensitivity (Relevant past drug history Name of Drug as Reported: Imitrex, bee stings Reaction: Allergy); COPD (verbatim: Long hauler, COPD); COVID-19 (if_covid_prior_vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 79,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Chills Cough Immunisation Off label use Oxygen saturation Oxygen saturation decreased Product use issue Pyrexia SARS-CoV-2 test

Symptomtext

Chills; Fever 103.9; Pulseox92; Cough; DOSE 3 on 01Nov2021 and Flu vaccine on 01Nov2021; DOSE 3 on 01Nov2021 and Flu vaccine on 01Nov2021; dose received 3; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 79 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 01Nov2021 12:00 (Lot number: 32030BD) at the age of 79 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU), administered in arm left, administration date 01Nov2021 (Batch/Lot number: unknown) as dose 1 for immunisation. Relevant medical history included: "Arthritis" (unspecified if ongoing); "Secondary hypogonadis" (unspecified if ongoing), notes: Secondary hypogonadis; "Hyperthyroid" (unspecified if ongoing), notes: Hyperthyroid. Concomitant medication(s) included: ANDROGEL; TAPAZOLE; MAXZIDE. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE,Lot number: E29261, Anatomical location: Left arm, Administration time: 11:00.), administration date: 22Jan2021, when the patient was 79 years old, for COVID-19 immunisation; Bnt162b2 (DOSE 2, SINGLE,Lot number: BN6201, Anatomical location: Left arm, Administration time: 10:45.), administration date: 12Feb2021, when the patient was 79 years old, for COVID-19 immunisation. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 01Nov2021 12:00, outcome "unknown" and all described as "DOSE 3 on 01Nov2021 and Flu vaccine on 01Nov2021"; IMMUNISATION (non-serious) with onset 01Nov2021 12:00, outcome "unknown", described as "dose received 3"; CHILLS (non-serious) with onset 03Nov2021 01:00, outcome "recovered" (Nov2021), described as "Chills"; PYREXIA (non-serious) with onset 03Nov2021 01:00, outcome "recovered" (Nov2021), described as "Fever 103.9"; OXYGEN SATURATION DECREASED (non-serious) with onset 03Nov2021 01:00, outcome "recovered" (Nov2021), described as "Pulseox92"; COUGH (non-serious) with onset 03Nov2021 01:00, outcome "recovered" (Nov2021), described as "Cough". Relevant laboratory tests and procedures included Body temperature was 103.9, Pulse oximetry was 92, PCR Nasal swab was Negative are available in the appropriate section. Therapeutic measures were not taken as a result of chills, pyrexia, oxygen saturation decreased, cough. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211103; Test Name: Body temperature; Result Unstructured Data: Test Result:103.9; Comments: Fever 103.9; Test Date: 20211103; Test Name: Pulse oximetry; Result Unstructured Data: Test Result:92; Comments: pulseox92; Test Date: 20211103; Test Name: PCR; Test Result: Negative ; Comments: Nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Hyperthyroidism (Hyperthyroid); Secondary hypogonadism (Secondary hypogonadis)
Andere Medikamente: ANDROGEL; TAPAZOLE; MAXZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1917190

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 12,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Injection site erythema Injection site pain Vaccination site erythema Vaccination site pain

Symptomtext

Dizziness at 3:30am 12/2; Redness/Pain at injection site 12/2; Redness/Pain at injection site 12/2; This is a spontaneous report from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 12-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), administered in left arm, administration date 01Dec2021 at 09:00 (Lot number: FJ1611) at the age of 12 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: "None" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: 32030BD, Route of administration: unknown, Anatomical site: Left arm, Administration time: 09:45), administration date: 10Nov2021, when the patient was 12 years old, for COVID-19 immunisation. The following information was reported: DIZZINESS (non-serious) with onset 02Dec2021 at 03:30, outcome "recovering", described as "Dizziness at 3:30am 12/2"; VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 02Dec2021, outcome "recovering", and all described as "Redness/Pain at injection site 12/2". Therapeutic measures were not taken as a result of dizziness, vaccination site erythema and vaccination site pain. Additional Information: The patient's known allergies were reported as not applicable. 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 events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.

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 1932976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: GA
Alter: 48,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect route of product administration Lymph node pain Lymphadenopathy

Symptomtext

The patient reported pain and swelling in the lymph node under her left armpit approximately 2 days after administration. She reported that she visited the doctor on the third day. She stated that the Dr said the vaccine was given in the wrong spot of the deltoid and should have been given more centrally in the deltoid. The Dr prescribed unknown antiobiotics, steroids and pain medication and asked to see the patient in a week or two.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1931492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NC
Alter: 83,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Chills Dizziness Feeding disorder Immunisation Malaise Nausea Poor quality sleep

Symptomtext

nauseated on and off/ was a little nauseated; chills; not feeling any better; a little dizzy; she was not eating much today because she was nauseated; Booster; did not sleep well for the rest of the night; This is a spontaneous report from a contactable consumer (patient herself). A 83 year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection), via unspecified route of administration on 31Oct2021 16:00 (Lot number: 32030BD) at the age of 83 years as dose 3 (booster), single for COVID-19 immunization. Relevant medical history included: "Afib" (ongoing) (diagnosed 6 years ago. Medication is working); "CKD" (ongoing); "Osteoporosis" (ongoing); "Hypertension" (ongoing) and "Increase Cholesterol". Concomitant medications included: LOVASTATIN, XARELTO, DILTIAZEM, FLECAINIDE and TIMOLOL. Vaccination history included: Bnt162b2 (Dose: 1, Lot/Batch number: EL9263), administration date: 23Jan2021, when the patient was 83 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2, Lot/Batch number: EN6201), administration date: 15Feb2021, when the patient was 83 years old, for COVID-19 immunization, reaction(s): "headache". On 31Oct2021 16:00, the patient had booster and on the same day, did not sleep well for the rest of the night. On 01Nov2021 11:30, the patient experienced nauseated on and off/ was a little nauseated, chills, not feeling any better, a little dizzy and she was not eating much today because she was nauseated. The clinical outcome of the events nauseated on and off/ was a little nauseated, chills, not feeling any better, a little dizzy and she was not eating much today because she was nauseated was recovering and for remaining was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: AFib (diagnosed 6 years ago. Medication is working); Chronic kidney disease (Verbatim: CKD); Hypertension; Osteoporosis
Vorgeschichte: Medical History/Concurrent Conditions: Cholesterol high (Verbatim: Increase Cholesterol)
Andere Medikamente: LOVASTATIN; XARELTO; DILTIAZEM; FLECAINIDE; TIMOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1928550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PA
Alter: 57,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site erythema Injection site induration Injection site pain Injection site pruritus Injection site reaction Urticaria

Symptomtext

Large red welt adjacent to the injection site that is 4? long x 3? wide and is sore and hard and itches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tramadol ER 100mg Vitamin B12 500mg Vitamin D3 1000 IU
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1925074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MN
Alter: 55,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 27.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Pain Pain in extremity

Symptomtext

Patient received vaccine a week ago Saturday. Patient said her arm started hurting on Sunday. Her arm still hurts to move it a week later.

Weitere VAERSDATA-Felder

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

VAERS 1923917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Pain

Symptomtext

body aches (mainly upper body) that have not gone away since the booster shot was received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: diabetes type 2, vitamin d deficiency, high cholesterol
Andere Medikamente: trulicity, synjardy, montelukast, linzess, rovastatin
Allergien: none
Vorherige Impfungen: -

VAERS 1923785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chills Dizziness Headache Nausea Pain Pain in extremity Pyrexia Tinnitus Vertigo

Symptomtext

I began developing symptoms about 10 minutes after my third dose. I developed a headache, dizziness, and nausea. By the evening of 12/3/2021, my right arm began hurting intensely and I began getting body aches. All throughout the night I had body aches and headaches. By that evening, I had also chills and a low-grade fever. Today on 12/5/2021, the body aches, fever, and chills resolved themselves, but I continue to have a headache and nausea, plus I have developed tinnitus and the vertigo has worsened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma, atrial fibrillation, atrial flutter, premature ventricular contractions, premature atrial contractions, junctional rhythm, left bundle branch blockage, sinus node dysfunction, mitral valve prolapse, GERD, iron deficiency anemia.
Andere Medikamente: Flecainide, Verapamil, Potassium CLER, Magnesium Oxide, Ferrous Sulfate, Atorvastatin, Omeprazole, Cetirizine, Montelukast, Alvesco inhaler, Xopenex inhaler, Centrum women's Multivitamin, vegan B complex, standardized cranberry capsules.
Allergien: Most antibiotics, codeine, Vicodin, Darvocet, Dilauded, fentanyl, ketamine, morphine, Lanoxin, Norpace, Pendolol, Procalnamide, quinidine, Rythmol, sotalol, Tenormin, Toprol, Bystolic, metoprolol, electrode tape, thimerosal, chickpeas, coconut, eggs.
Vorherige Impfungen: I had an adverse reaction after my first and second doses of Pfizer.

VAERS 1923020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NC
Alter: 43,0
Geschlecht: F
Eingang: 04.12.2021
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

Chills Dizziness Fatigue Immunisation Pain Pyrexia

Symptomtext

Received third dose; Extreme fatigue; Body aches; Chills; Dizzy; Feverish; This is a spontaneous report received from a contactable reporter (consumer). The reporter is the patient. A 43-year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in left arm, administration date 27Nov2021 at 15:00 (Batch/Lot number: 32030BD) at the age of 43 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "colitis ulcerative" (unspecified if ongoing), notes: ulcerative colitis; "bronchiolitis obliterans with organizing pneumonia" (unspecified if ongoing), notes: BOOP; "raynaud's syndrome" (unspecified if ongoing); "gallbladder removal" (unspecified if ongoing), notes: no gall bladder and "colectomy" (unspecified if ongoing), notes: no large intestine. Concomitant medications included: VITAMIN D and unspecified multivitamins. Vaccination history included: BNT162b2(PFIZER-BIONTECH COVID-19 mRNA VACCINE, DOSE 1, SINGLE, Lot Number: ER8727, Route of administration: Unspecified), administration date: on an unknown date in Mar2021, when the patient was 42 years old, for COVID-19 immunisation and BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, DOSE 2, SINGLE, Lot Number: ER8729, Route of administration: Unspecified), administration date: on an unknown date in Apr2021, when the patient was 42 years old, for COVID-19 immunisation. The following information was reported: FATIGUE (non-serious), PAIN (non-serious), CHILLS (non-serious), DIZZINESS (non-serious), PYREXIA (non-serious); all with onset 27Nov2021, outcome "recovering" and described as ''extreme fatigue, body aches, chills, dizzy and feverish''. Therapeutic measures were not taken as a result of fatigue, pain, chills, dizziness and pyrexia. 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, and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bronchiolitis obliterans with organizing pneumonia (BOOP); Colectomy (No large intestine); Colitis ulcerative (Ulcerative Colitis); Gallbladder removal (No gall bladder); Raynaud's syndrome
Andere Medikamente: VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1913402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: ID
Alter: 63,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Swelling face Urticaria

Symptomtext

Facial Swelling/Urticaria developed the night of 11/20/21. Pt lives in city and did not go to Medical Center ER until 11/22/21. Was attempting to treat sx's with OTC Benadryl with not much relief. Staff administered IV diphenhydramine, methylprednisolone, and famotidine. Advised to take OTC Claritin x5 days after discharge. Phone call f/u made.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Upper Respiratory Infection 11/10/21 - Given Augmentin 875-125 mg tab x 10 days - Prednisone 20 mg 2 tabs PO x 5 days
Vorgeschichte: Type 2 DM Dyslipidemia Dysthymia GERD Anxiety D/o
Andere Medikamente: Received TDAP on 10/29/2021 Gabapentin 300 mg cap 1 cap PO TID Glipizide 10 mg tab 1 PO BID Jardiance 10 mg tab 1 PO QD Metformin 1000 mg tab 1 PO BID Omeprazole 20 mg cap 2 caps PO QD Pravastatin 10 mg tab 1 PO QHS Sertraline 100 mg tab 2
Allergien: Lantus Sulfa
Vorherige Impfungen: -

VAERS 1912275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anxiety Chills Dizziness Hypokinesia Vaccination site pain

Symptomtext

Injection site pain; Inability to lift arm; Dizzy; Anxiety; Chills; This is a spontaneous report from a non-contactable other healthcare professional, the patient. A 38-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the left arm on 23Nov2021 at 14:30 (at the age of 38-years-old) as a single dose for COVID-19 immunisation. The patient had no medical history and no known allergies. Concomitant medications included levothyroxine sodium (SYNTHROID), metformin (MANUFACTURER UNKNOWN) and norethisterone acetate/ ethinylestradiol (AUROVELA); all for unknown indications from unknown dates and unknown if ongoing. 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. On 23Nov2021 at 21:00, the patient experienced injection site pain, inability to lift arm, dizzy, anxiety and chills. Therapeutic measures were not taken as a result of events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events injection site pain, inability to lift arm, dizzy, anxiety and chills was not resolved at the time of the report. 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.
Andere Medikamente: SYNTHROID; METFORMIN; ETHINYLESTRADIOL;NORETHISTERONE ACETATE.
Allergien: -
Vorherige Impfungen: -

VAERS 1909257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: VA
Alter: 44,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Breast discomfort Breast swelling Breast tenderness Chills Pain Pain in extremity Pyrexia

Symptomtext

Pain in left arm lasted longer than 48 hours. Left breast was extremely swollen, heavy and tender by day 3 after my shot. I had chills, low grade fever, and aches for two days. My left breast is still swollen, however not tender or pain. I take Ibuprofen occasionally. No major issues /concerns from my previous vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none.
Vorgeschichte: Graves Disease-hyperthyroidism
Andere Medikamente: I take methimazole 5mg twice a week and GNC women's multivitamin
Allergien: n/a
Vorherige Impfungen: -

VAERS 1908581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: FL
Alter: -
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: -
Beginn: 13.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chest discomfort Chills Immunisation

Symptomtext

as dose 3 (booster), single; Severe chest discomfort; cold chills; This is a spontaneous report from a contactable consumer (patient). A 50-year-old male patient third dose of received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: 32030bd, Expiry date: unknown), via an unspecified route of administration, administered in left arm on an unspecified date as dose 3 (booster), single for covid-19 immunisation at Pharmacy or Drug store. Medical history included heart bypass, diabetes mellitus, cholesterol, blood pressure. The concomitant medications were not reported. No other vaccine received in four weeks. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: Er8727, Expiry date: unknown), via an unspecified route of administration, administered in arm left on 17Mar2021 at 17:00 as dose 1, single and second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: Er8727, Expiry date: unknown), via an unspecified route of administration, administered in arm left on 07Apr2021 at 17:00 as dose 2, single both for covid-19 immunisation at Pharmacy or Drug store. Known allergies to Vancomycin was reported. Prior to vaccination, the patient was not diagnosed with COVID-19; Since the vaccination. The patient had not been tested for COVID-19 post vaccination. On an unspecified date the patient received DOSE 3 (booster) and experienced severe chest discomfort on 13Nov2021 at 14:00 and cold chills on 13Nov2021 approximately at 21:00. Patient took nitro to relieve some discomfort. No treatment was taken for cold chills. The outcome of the event severe chest discomfort and cold chills was resolving. 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: Blood pressure abnormal; Cholesterol; Coronary bypass; Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1906215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 30.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / AR

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

Arthralgia Blood test normal Gait disturbance Neck pain Pain

Symptomtext

Extreme pain in joints, shoulders, hips, and neck, mainly. No swelling. Could barely walk. Blood work was done (normal) Doctor prescribed prednisone and advised continuing OTC pain regimen. Ongoing issue with pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Blood work done and found to be normal (11/5, 11/18)
Aktuelle Erkrankungen: None
Vorgeschichte: Environmental Allergies Grave's Disease
Andere Medikamente: Zyrtec Methimazole
Allergien: Bee Pollen
Vorherige Impfungen: -

VAERS 1905968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Immediate post-injection reaction Injection site erythema Injection site pain Injection site swelling

Symptomtext

Dose 1: immediate swelling, redness and pain at injection site. Resolved approx 1 week. Pharmacist concerned about allergic reaction. Dose 2: swelling, redness and pain at injection site approx 2 hrs later. Pharmacist recommended watching for allergic reaction, take Benadryl as needed, and report if necessary.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None, COVID vaccine dose 1 11/6/2021 with same affect.
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin, pertussis, pine nuts (seeds)
Vorherige Impfungen: Pertussis early childhood Tdap series. Same reaction at injection site on thigh. Unknown date and brand name.

VAERS 1903746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: -
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Back pain Immunisation Sciatica

Symptomtext

Booster; severe back and sciatica pain; severe back and sciatica pain; This is a spontaneous report from a contactable consumer (patient's wife). A male patient of an unspecified age received third dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: 32030BD), via an unspecified route of administration on an unspecified date in 2021 as dose 3 (booster), single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/ lot number was not reported), via an unspecified route of administration as dose 1, single and received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/ lot number was not reported), via an unspecified route of administration as dose 2, single both for covid-19 immunization. On an unspecified date in 2021, a couple days after the vaccine, the patient experienced back and sciatica pain. The patient received steroids as therapeutic measure to relieve the pain. The outcome of the event was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101578115 same reporter/drug, different patients.

Weitere VAERSDATA-Felder

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

VAERS 1902344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: FL
Alter: 67,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Immediate post-injection reaction Pain Pain in extremity

Symptomtext

Radiating pain in left arm since time of injection.

Weitere VAERSDATA-Felder

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

VAERS 1902069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 20.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Fatigue Myalgia Oxidative stress Tendonitis Vaccination complication

Symptomtext

I am writing because I was fine before I took the 2nd dose of Vaccine. I believe any people who have had adverse reactions to antibiotics such as Ciprofloxacin should not have a to take a 2nd shot and be be medically excused to take a 2nd shot. So they can fulfill the requirements to go back to work and travel and everything else. All they need is one shot. I believe after taking the 2nd dose of the vaccine it begins to bring back symptoms and adverse reactions similar to what Ciprofloxacin did to me. I had an adverse reactions to Ciprofoxacin. It's a term called being floxed. I believe the Vaccine brings back those symptoms and the same damage that happens when you get an adverse reaction to an antibiotic. It makes people who got bad reactions from an antibiotic like Cipro, the symptoms come back. The immune system can not handle the new MRNA TECHNOLOGY. IT IS RE-TRIGGERING THE symptoms. Joint Pain, Tendonosis. With me it's my right knee. Fatigue, and legs. but not just any type of fatigue. OXIDATIVE STRESS TO THE JOINTS AND MUSCLES. Once you cause too much OXIDATIVE STRESS on the cells they die, or you damage may be irreversible for some people who have been floxed. A person who has not been floxed it just seems like they are tired after taking the vaccine. A person who has been floxed. Times it at about 50 times worst. People who have been floxed should have a medical excuse or have to take a lower dosage of the Vaccine and only need to take one shot depending how severe their reactions where to the antibiotic they took years back before taking a the COVID 19 Vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None. I am writing because I was fine before I took the 2nd shot. I believe any people who have had adverse reactions to antibiotics and Cipro should not have a to take a 2nd shot or should be medically excused or take a lower dosage of the shot. For example, take the dosage of what a kid has to take(PFIZER). I believe after taking the vaccine it begins to bring back symptoms and adverse reactions similar to what Ciprofloxacin did to me. It's a term called being floxed. I believe the Vaccine brings back those symptoms and same damage that happens when you get an adverse reaction to an antibiotic. It makes people who got bad reactions from an antibiotic like Cipro, the symptoms come back. The immune system can not handle the new MRNA TECHNOLOGY. IT IS RE-TRIGGERING THE symptoms. Joint Pain, Tendonosis. With me it's my right knee. Fatigue, but not just any type of fatigue. OXIDATIVE STRESS TO THE JOINTS AND MUSCLES. A person who has not been floxed it just seems like they are tired. A person who has been floxed. Times it at about 100 times worst. People who have been floxed should have a medical excuse or have to take a lower dosage of the Vaccine.
Vorgeschichte: NA
Andere Medikamente: Asthma Pump (Albuterol Sulfate)
Allergien: Adverse reactions to Ciproflloxacin Antibiotic and any Quinolone antibiotic.
Vorherige Impfungen: -

VAERS 1897982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NC
Alter: 49,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 19.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Breast swelling Breast tenderness Lymph node pain Postmenopausal haemorrhage Ultrasound scan normal Uterine spasm

Symptomtext

That evening my lymph nodes in my left armpit started hurting and this lasted a couple of days. When that pain went away both of my breasts became tender and slightly swollen and continued for several days when slight uterine cramping started. Both continued when I had menstrual bleeding on the 4th and 5th of November. The cramps stopped by the 18th but my breasts are still tender. Because I have been in menopause for two years, my gynecologist required me to have an ultrasound on the 17th at which time he stated everything appeared to be healthy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: Ultrasound
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Asthma
Andere Medikamente: Estrogen, progesterone, Advil, liothyronine, levothyroxine, Vitamin D, Multivitamin, Vitamin B-12,
Allergien: Mango, amoxicillin, topimax, pristique, Zyrtec
Vorherige Impfungen: -

VAERS 1897813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: GA
Alter: 69,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Injection site erythema Injection site warmth

Symptomtext

Spoke with client 11/24/2021 he states he has a "palm sized area under injection site that is red and warm to the touch." He states Friday night 11/19/2021 is when he discovered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1895365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 23.11.2021
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

Abdominal pain Cough Vomiting Wheezing

Symptomtext

Pt developed coughing , vomiting one time , abdominal pain and wheezing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, allergic rhinitis
Andere Medikamente: albuterol inhaler, azelastine 0.05% nasal spray, spiriva inhaler, wixela inhaler, montelukast, cetirizine
Allergien: none known
Vorherige Impfungen: -

VAERS 1894669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 23.11.2021
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: nein

Dizziness Headache Nausea Pain Pyrexia Urticaria Vomiting

Symptomtext

Patient received booster dose of Pfizer Covid vaccine on 11/16. Same day of vaccine, she developed nausea, vomiting, body aches, hives, and fever. On 11/18, she developed intermittent headache and dizziness. She notified her PCP regarding symptoms and was informed that the symptoms were normal and most likely an immune response to the vaccine. She managed her symptoms with Tylenol, Motrin, and Zofran. She reports that her headache resolved on 11/22.

Weitere VAERSDATA-Felder

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

VAERS 1894410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NH
Alter: 33,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Feeling abnormal Mental impairment

Symptomtext

Fatigue approx 3 days, brain fog/inability to experience normal thought processing approx 10 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Raynaud's phenomenon
Andere Medikamente: Zyrtec, Levonorgestrel-ethyl estradiol contraceptive
Allergien: Shellfish, penicilins, clindamycin (oral)
Vorherige Impfungen: -

VAERS 1893108

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TN
Alter: 33,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / LA

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

Chills Headache Immunisation Interchange of vaccine products Off label use

Symptomtext

originally received the J&J vaccine in June went to get the Pfizer booster 10/30/2021; originally received the J&J vaccine in June went to get the Pfizer booster 10/30/2021; headache; originally received the J&J vaccine in June went to get the Pfizer booster 10/30/2021; chills; This is a spontaneous report from a Non contactable Pharmacist (Healthcare Professional). This Pharmacist reported for a 33-Years-Old male patient received the third dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/lot number: 32030BD and expiration date not reported), via an Intramuscular route of administration in arm Left anatomical location on 30Oct2021 at 05:30 AM (at the age 33-year-old) as a DOSE 3, (BOOSTER DOSE) SINGLE for covid-19 immunisation. Patient historical vaccine included received the first dose and second of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/lot number and expiration date not reported), via an unspecified route of administration on an unspecified anatomical location on unspecified date as a dose 1 single and dose 2 single for covid-19 immunisation. The patient medical history included asthma start from unspecified date and unknown if ongoing. The patient's concomitant medications were not reported. Patient had Off label use, Interchange of vaccine products, Booster. Patient who originally received the J&J (COVID-19 VACCINE JANSSEN) vaccine in June went to get the Pfizer booster at the local pharmacy The next evening, on 31Oct2021 developed chills and a headache adverse event start time was 08:00 PM. Patient took treatment of Excedrin. The outcome of the event chills and a headache was recovering. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1890524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PA
Alter: 83,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 19.02.2021
Beginn: 20.06.2021
Tage bis Beginn: 121,0
Dosis: UNK
Route/Site: SYR / LA

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

Erythema Herpes zoster Injection site pain Injection site swelling Periorbital pain Periorbital swelling Symptom recurrence

Symptomtext

2/19/21 Second COVID Pfizer shot. 6/20/21 Severe shingles develops over and around right eye and forehead. Patient hospitalized for a week to receive antiviral medication via vein. After hospital release, five months later, patient has severe swelling/pain at the site and continues receive physical therapy massage. 11/12/2021 Third COVID Pfizer shot given. One day later: The area around patients right eye where the shingles area occurred previously shows renewed redness, swelling and pain. This continues without relief as of the date of this report 11/22/2021. The patients physical therapist has noted the recurrence as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid removed, osteoarthritis
Andere Medikamente: Advil
Allergien: None
Vorherige Impfungen: -

VAERS 1890059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 40,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Headache

Symptomtext

Daily headaches since receiving the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Migraines that were under control with preventative medication
Andere Medikamente: Aimovig, topiramate
Allergien: none
Vorherige Impfungen: -

VAERS 1888376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 13,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Immediate post-injection reaction Injection site rash

Symptomtext

Immediately after administration of both vaccines, patient developed a local rash at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: asthma
Andere Medikamente: unknown
Allergien: None
Vorherige Impfungen: -

VAERS 1887962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WI
Alter: 32,0
Geschlecht: F
Eingang: 20.11.2021
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

Headache Injection site pain Malaise Pyrexia

Symptomtext

Woke up at 4 am the day after with severe headache, low-grade fever of 100?, moderate injection site pain. (I am still glad I got the vaccine and would do so again if a 4th is ever needed. I feel icky but I know that means my body is making antibodies to protect me.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No illnesses. Just a LOT of stress that manifested in some physical symptoms.
Vorgeschichte: Anxiety, depression, obesity, knee osteoarthritis, high blood pressure
Andere Medikamente: Birth control, hydrochlorothiazide, sertraline, vitamin D, prenatal vitamins, fish oil.
Allergien: Shrimp.
Vorherige Impfungen: -

VAERS 1886888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MD
Alter: 27,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Lymph node pain Lymph node palpable Lymphadenopathy

Symptomtext

Palpable left supraclavicular lymph node swelling and tenderness. Pain with cervical rotation bilaterally.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Claritin; Prilosec
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1886475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Contusion Erythema Peripheral swelling Pruritus

Symptomtext

Arm got very itchy, swelling and redness about the size of a baseball, and a severe bruise

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: No illness
Vorgeschichte: None stated
Andere Medikamente: Patient states she takes multiple OTC supliments
Allergien: Penicillin and all derivitives, Sulfa
Vorherige Impfungen: -

VAERS 1885559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: IL
Alter: 13,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Asthenopia Deafness Dizziness Immediate post-injection reaction Lethargy Malaise Nasal congestion Nausea Vision blurred

Symptomtext

Patient immediately felt ill after administration of the second dose of Pfizer. Patient felt dizzy, nauseous, had blurry vision and could not hear for a few moments. Patient complained that her nose got congested and that her eyes felt extremely heavy and she felt extremely lethargic. Patient did not lose conscientiousness at any time. We immediately put her to sit next to her father in the waiting area, applied an ice pack to her neck and gave her some water. We continued to talk to her to keep her awake and alert. Father asked that we call the paramedics which we did and in the meantime prior to their arrival we continued to engage the patient in conversation. She had no difficulty breathing at any time. Paramedics came, we informed them of the event and they offered to take the patient in for medical attention. The father and daughter both declined transport via ambulance to the hospital. After about 30 minutes, the patient was better, the symptoms for the most part had subsided and she was able to stand up and walk out with her father.

Weitere VAERSDATA-Felder

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

VAERS 1885117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Lymph node pain Lymphadenopathy

Symptomtext

Large, painful swollen lymph nodes on the side of my body that got the injection beginning the evening of the vaccine and continuing. Noticeably large in the area of my collar bone and armpit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin D 5,000 iu Levothyroxine 75mcg
Allergien: dust
Vorherige Impfungen: -

VAERS 1881035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: OH
Alter: 85,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 08.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain

Symptomtext

"Severe" pain in shoulder where vaccine was administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Tramadol
Allergien: None known
Vorherige Impfungen: -

VAERS 1880402

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 32030BD

mild

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Rash

Symptomtext

Severe rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: B12, D3, fish oil
Allergien: none
Vorherige Impfungen: -

VAERS 1880293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PA
Alter: 33,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Asthenia Fatigue Headache Injection site erythema Injection site pain Injection site swelling Myalgia Pyrexia

Symptomtext

Injection site pain, swelling, and redness Fatigue and weakness Muscle and joint pain Fever Headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Velivet (oral contraceptive), Restasis (dry eyes)
Allergien: None
Vorherige Impfungen: -

VAERS 1879625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: KS
Alter: 12,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Body temperature Fatigue Pyrexia SARS-CoV-2 test

Symptomtext

Felt exhausted the next day (10Nov2021).; Had a fever of 100.7.; This is a spontaneous report from a contactable consumer. A 12-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via intramuscular route of administration in the right arm on 09Nov2021(at the age of 12-years-old) as a single dose for COVID-19 immunisation. Medical history included COVID-19, the patient was diagnosed with COVID-19 prior to the vaccination. The patient had no other medical history and no known allergies. The patient did not receive other vaccines within four weeks prior to the COVID vaccine. Concomitant medications were not reported. The reporter was a Pfizer colleague and was on a phone call on 11Nov2021 with a friend of his. Reporter's friend stated that his 12-year-old son received the Pfizer COVID-19 vaccine on 09Nov2021 and had a fever of 100.7 and felt exhausted the next day on 10Nov2021. On 10Nov2021, his father stated that the patient went to the school nurse and they treated him with Tylenol and sent him home from school on 10Nov2021. The patient did not go to school on 11Nov2021 also and now at the time of reporting the patient felt back to normal per his father. The events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of events and included treatment with paracetamol (TYNELOL). On 09Nov2021, the patient underwent body temperature test and the result was 100.7 (units unspecified). Since the vaccination, the patient had been tested for COVID-19. On 10Nov2021, the patient underwent SARS-CoV-2 test via nasal swab and the result was pending. The clinical outcome of the events fever of 100.7 and felt exhausted the next day were resolved on an unknown date in Nov2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20211109; Test Name: Body temperature; Result Unstructured Data: Test Result:100.7; Comments: Fever of 100.7; Test Date: 20211110; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Pending
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1876080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CT
Alter: 69,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 02.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Balance disorder Dizziness Inflammation Middle ear effusion Vertigo

Symptomtext

Healthy athletic male with no history of ear/vestibular issues. Received Pfizer booster and flu vaccine together. Typical inflammatory symptoms occured and resolved after 24-36 hrs, as is typical for pt. However, 5 days post-vaccination he had onset of dizziness, disequilibrium, and vertigo. These continued and when seen by physician on day 14 post-vaccination, prominent bilateral middle ear effusions were seen. Medical treatment plan initiated.

Weitere VAERSDATA-Felder

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

VAERS 1875944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CT
Alter: 47,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Back pain Muscle strain Neck pain

Symptomtext

I have had constant back pain starting the day after my shot. The pain is across my upper back between my shoulders and up to my neck. I can't even carry my purse for more then 5 minutes without pain and strain across my back.; I can't even carry my purse for more then 5 minutes without pain and strain across my back; The pain is across my upper back between my shoulders and up to my neck. I can't even carry my purse for more then 5 minutes without pain and strain across my back.; This is a spontaneous report from a contactable consumer, the patient. A 47-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the left arm on 21Oct2021 at 17:00 (at the age of 47-years-old) as a single dose for COVID-19 immunisation. The patient did not have any medical history. The patient had no known allergies. 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 vaccination. The patient did not receive any medication within two weeks of vaccination. On 22Oct2021 at 07:00, the day after her shot, the patient had constant back pain. The pain was across her upper back between her shoulders and up to her neck. She could not even carry her purse for more than 5 minutes without pain and strain across her back. The adverse events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events constant back pain/ pain across upper back between shoulders and up to neck and could not even carry purse for more than 5 minutes without pain and strain across back were not resolved at the time of this report.

Weitere VAERSDATA-Felder

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

VAERS 1875939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Asthenia Chills Headache Nausea Pain Polyuria Pyrexia SARS-CoV-2 test Sleep disorder Suffocation feeling Vaccination site pain Vaccination site swelling Vaccination site warmth

Symptomtext

Fully body pains; Fever; Chills; Feeling of suffocation; Feeling weak/ very weak; Slight headache/ excruciating headaches/ headache was bearable; Nausea; Shortly after the shot my arm swell and was hot in the region of the shot; Shortly after the shot my arm swell and was hot in the region of the shot; I took some allergy pills which helped with the feeling of suffocation and helped me to sleep; Urinating a lot; The only part of my body that still ached was the injection site; This is a spontaneous report from a contactable consumer, the patient. A 51-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the left arm on 05Nov2021 at 18:00 (at the age of 51-years-old) as a single dose for COVID-19 immunisation. Medical history included obesity and known allergies to shell food. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications were not reported. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF8841) via an unspecified route of administration in left arm on 12Oct2021 (at the age of 51-years-old) as a single dose for COVID-19 immunisation. On 05Nov2021 at 19:00, shortly after the shot, the patient had arm swelling and was hot in the region of the shot. On 06Nov2021, by 12:00 the next day, she was feeling weak with slight headache and nausea. On the same day by 15:00, she was very weak, excruciating headaches and fully body pains, fever and chills, with the feeling of suffocation. She took some unspecified allergy pills which helped with the feeling of suffocation and helped her to sleep and she was also urinating a lot on an unknown date in Nov2021. On an unknown date in Nov2021, at about 04:00, when she got up to go to the bathroom the headache was bearable, she no longer felt like she was suffocating and her body was not as painful. She was nauseas for 07Nov2021 and 08Nov2021 and by evening on 08Nov2021, the only part of the body that still ached was the injection site. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were taken as a result of shortly after the shot her arm swell and was hot in the region of the shot, fever, chills, feeling of suffocation and the only part of her body that still ached was the injection site which include unspecified allergy pills on an unknown date in Nov2021. On 07Nov2021, the patient underwent SARS-COV-2 test (polymerase chain reaction (PCR)) by test type nasal swab and the result was negative. Since the vaccination, the patient had been tested for COVID-19. The clinical outcome of the events nausea and fully body pains was resolved on 08Nov2021. The clinical outcome of the events shortly after the shot her arm swell and was hot in the region of the shot, urinating a lot, feeling weak/ very weak, slight headache/excruciating headaches/ headache was bearable, fever, chills, feeling of suffocation and she took some allergy pills which helped with the feeling of suffocation and helped her to sleep was resolved on an unknown date in Nov2021. The clinical outcome of the event the only part of her body that still ached was the injection site was not resolved at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211107; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy (Known allergies: Shell Food); Obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1875879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CT
Alter: 62,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Interchange of vaccine products Off label use Pain in extremity SARS-CoV-2 test

Symptomtext

soreness in arm; received the J and J vaccine on 08Mar2021. Pfizer vaccine was administered as a booster dose; received the J and J vaccine on 08Mar2021. Pfizer vaccine was administered as a booster dose; This is a spontaneous report from a contactable consumer. This consumer reported for a 62-year-old female patient that: A 62-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: 32030BD), dose 2 intramuscular, administered left arm on 22Oct2021 (at the age of 62-year-old) as DOSE 2 (BOOSTER), SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. 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 and no other medications the patient received within 2 weeks of vaccination. Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. The patient had previously received first of COVID-19 VACCINE NRVV AD26 (JNJ 78436735), (Batch/lot number: unknown), via an unspecified route of administration on 08Mar2021. On 22Oct2021 the patient received the J and J vaccine on 08mar2021. Pfizer vaccine was administered as a booster dose. On 23Oct2021 the patient experienced the only side effect was soreness in arm the next day after vaccination. It was currently subsiding. The patient underwent lab tests and procedures which included COVID-19 test unknown results (Nasal Swab) on an unspecified date in 2021. Prior to vaccination, was the patient not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. The patient was not received any treatment. The outcome of soreness in arm was recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Covid-19 test; Result Unstructured Data: Test Result:Unknown results; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 17,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Headache

Symptomtext

Patient was waiting in waiting area for 15 minute post immunization period. Mother came to get nurses and noted son was already experiencing a headache in the middle of his forehead. Vital signs were obtained. Pulse 60, respiratory rate 16, blood pressure 106/64. Patient was given water and goldfish. Patient and mother then self administered Tylenol 500mg. Mother noted patient has not had anything to eat prior to vaccination. After ten minutes, patient noted he felt better and wanted to go home. Released to mothers care and advised to call hematology and neurology if anything worsens.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Epilepsy and known blood clotting disorder.
Andere Medikamente: Tylenol 500mg self administered by patient and mother.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1873123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 12,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 13.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Chills Diaphragmalgia Fatigue Painful respiration Pulmonary pain Pyrexia

Symptomtext

Pain in lower lungs, diaphragm, and/or abdomen when breathing; fever; chills; fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: pediatrician evaluation and referral to pediatric cardiologist.
Aktuelle Erkrankungen: none
Vorgeschichte: asthma and seasonal allergies.
Andere Medikamente: daily zyrtec for allergies; Qvar 40mg (1 puff daily); Nasacort nasal spray (1 spray/nostril daily); Olopatadine nasal spray as needed.
Allergien: allergy to pistachios and cashews.
Vorherige Impfungen: -

VAERS 1870924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CO
Alter: 43,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness

Symptomtext

Patient walked into the grocery store where the clinic is located. He was shopping for produce and started to feel very dizzy and like he would pass out. He came back to the clinic. Lay him down, put legs up. He started to feel better. BP measured 100/64. He sat up and drank some water. Ate a lollipop. After another 15 minutes felt 90% better and wished to leave, son to drive him home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: 1st dose Pfizer 21 days prior with no ill effects
Vorgeschichte: Hx of chronic pancreatitis and gastritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1869526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: UT
Alter: 52,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / RA

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

Axillary pain Pain Pain in extremity Respiratory tract congestion Rhinorrhoea

Symptomtext

days 1 and 2- arm and extreme armpit pain. Armpit pain continued for 7 days. day 3 - congestion, runny nose, all over aches and pain began. Day 14 congestion/runny nose continue. No fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: No tests
Aktuelle Erkrankungen: -
Vorgeschichte: hypothyroidism, fatty liver
Andere Medikamente: armour thyroid, omeprazole, imitrex, vitamin k2 & d3, magnesium, calcium, biotin, fish oil
Allergien: -
Vorherige Impfungen: -

VAERS 1869365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 08.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

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

Chills Pain Pyrexia

Symptomtext

Fever, Body aches, chills that last 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure,
Andere Medikamente: Atenenoyl, Lipitor, Paxil
Allergien: None
Vorherige Impfungen: -

VAERS 1869310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PR
Alter: 52,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Blood glucose normal Dizziness

Symptomtext

Patient sitting in observation are makes signs to go to him. Refers feeling dizzy, was moved to a wheelchair BP 1401/90, 18 resp, dext 105, 96 RA. Clear lungs to auscultation, no edema no rash patient denies another symptom. He was given a candy and waited 20 min. Patient refers feeling better reevaluated, was offered transportation but indicates he wishes to go home.

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 1869286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WA
Alter: 69,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 07.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / -

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

Blister Facial paresis Herpes zoster oticus Hypoacusis Pain in jaw Rash

Symptomtext

Onset of R mandibular pain on 11/9/21. Developed varicella zooster rash in the mandibular division of the R facial nerve as well as Ramsay Hunt Syndrome (R facial weakness, diminished hearing R ear, vesicles in R auditory canal)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in jaw
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Hypertension, Gout, Chronic Renal failure (stage 3B), Dyslipidemia
Vorgeschichte: Hypertension, Gout, Chronic Renal failure (stage 3B), Dyslipidemia
Andere Medikamente: Allopurinol, Atorvastatin, Diltiazem, Losartan, Probenicid-Colchicine, Triamcinolone ointment
Allergien: None
Vorherige Impfungen: -

VAERS 1868509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: FL
Alter: 14,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness

Symptomtext

Patient was feeling with dizziness after the vaccine administration. 911 was called but the father said to cancel the call because patient was feeling fine.

Weitere VAERSDATA-Felder

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

VAERS 1867956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NJ
Alter: 38,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 29.10.2021
Beginn: 13.11.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: SYR / LA

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

Balance disorder Dizziness Nausea Vertigo

Symptomtext

Onset of severe dizziness and vertigo, experiencing it all day from onset at 10:30am this morning and experiencing nausea from dizziness and vertigo. My balance is off and deep unstable on my feet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None. Will call and make an appt with my doctor on Monday November 15th.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1867915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 42,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Chills Discomfort Herpes zoster Pain Pyrexia Rash

Symptomtext

Shingles. Had burning pain and discomfort night of vaccination 11/9/21. Low fever and chills next day. Continued discomfort until rash developed on right side 11/12/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Shingles confined by medical observation at urgent care on 11//13/21. Valacyclovir prescribed.
Aktuelle Erkrankungen: None
Vorgeschichte: Borderline diabetes (elevated sugar): high cholesterol
Andere Medikamente: Vitamin D supplement
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1864826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: KS
Alter: 62,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Pain Pyrexia

Symptomtext

Body aches and feel feverish

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Back pain
Andere Medikamente: Oxycodone, levothyroxine, furosemide, potassium, ropinirole and pregabalin
Allergien: No
Vorherige Impfungen: 04/06/2021

VAERS 1859045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Blood pressure increased Fatigue Headache Injection site pain Nausea Pain Pyrexia

Symptomtext

Right arm pain Fever 102 Aches in legs, back, and neck Headache Increased blood pressure 150/120 Nausea Severe Fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None at this time, symptoms appear to be consistent with booster vaccine adverse effects for older patients.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension (controlled) Autoimmune Condition - Hashimoto Hearing loss (left auditory nerve damage)
Andere Medikamente: Verapamil 240mg x 2 daily Trandolapril 4mg x 2 daily Metformin 500mg x 3 daily Aspirin 80mg x daily Atorvastatin 20mg daily Vitamin C, D3, B12 Zinc Tumeric
Allergien: None
Vorherige Impfungen: -

VAERS 1858783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MN
Alter: 69,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Lymphadenopathy Pain in extremity Product preparation issue

Symptomtext

Given 0.3 ml of UNDILUTED pfizer vaccine. Reported sore arm and a swollen lymph node

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1858449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chills Cough Paranasal sinus discomfort Pyrexia Rhinorrhoea SARS-CoV-2 test negative Sneezing

Symptomtext

Around 3 hours after the vaccine I started having sinus pressure, running nose, coughing and sneezing, chills, 102 f fever

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid rapid test at 11/08 ( negative)
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto?s disease
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1857874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NJ
Alter: 42,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypersensitivity Pruritus

Symptomtext

Ears started itching, itchy body and allergic reaction.

Weitere VAERSDATA-Felder

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

VAERS 1857664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 42,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Erythema Feeling abnormal Injection site nodule Injection site swelling Pain Pruritus Pyrexia Skin warm Vaccination complication

Symptomtext

I had a fever of 101.8 degrees. I had really bad body aches. I felt like I was run over by a bus. The right arm was hot, red, itching, and the knot at injection site was very swollen like a golf ball size. I couldn't break the fever for 3 or 4 days with Tylenol. The redness spread down my arm a little bit. On 11/5/2021 I went to local urgent care. They told me I had a reaction from the vaccine. They prescribed me with azithromycin 250mg 1 tablet for 5 days and Claritin 10mg 1x day. I also took Tylenol for fever and pain. My arm still feel itchy, a little hot, and a little bit red, but my fever finally broke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site nodule
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Heart Condition Asthma Migraines
Andere Medikamente: Metformin Abilify Aspirin Propranolol ER Lisinopril Lasix Albuterol
Allergien: Penicillin Codeine Cephalexin Monohydrate Sulfa Sulfonamide Antibiotic Divalproex Sodium Iron Ferric Sulfate Sulfamethoxazole-Trimethoprim
Vorherige Impfungen: -

VAERS 1856838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Immunisation Vaccination site pain

Symptomtext

Experiencing sore right arm near injection site.; The patient received the third/booster dose of BNT162b2; This is a spontaneous report from a contactable consumer, the patient. A 57-year-old male patient received third (booster) dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the right arm on 03Nov2021 at 18:30 (at the age of 57-years-old), as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient did not receive any other vaccine within four weeks prior to the COVID-19 vaccine. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL3247) via an unspecified route of administration on 03Feb2021 (at the age of 56-years-old) and second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL3247) via an unspecified route of administration on 24Feb2021 (at the age of 56-years-old), as single doses for COVID-19 immunisation. On 04Nov2021, the patient woke up at 01:37 and noticed experiencing sore right arm near injection site. Soreness was minor and did not interfere with his daily tasks. The event did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. No therapeutic measures were taken as a result of event. The clinical outcome of the event experiencing sore right arm near injection site was resolving at the time of this report. 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: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1856833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MD
Alter: 66,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chills Fatigue Immunisation Myalgia Vaccination site pain

Symptomtext

Muscle ache at injection sight; Muscle ache at injection sight; Fatigue; Short term chills; The patient received third/booster dose of BNT162b2; This is a spontaneous report from a contactable consumer, the patient. A 66-year-old male patient received the third (booster) dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the left arm on 03Nov2021 at 09:45 (at the age of 66-years-old) as a single dose for COVID-19 immunisation. Medical history included diabetes and high blood pressure. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient received other medications within two weeks of vaccination which were not specified, for unknown indication from unknown date and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER2613) via an unspecified route of administration in the left arm on 21Mar2021 at 11:15 (at the age of 65-years-old) as single dose for COVID-19 immunisation and also second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8731) via an unspecified route of administration in the right arm on 17Apr2021 at 10:00 (at the age of 65-years-old) as single dose for COVID-19 immunisation. On 03Nov2021 at 22:00, the patient experienced muscle ache at injection site, fatigue and short term chills. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events muscle ache at injection site, fatigue and short term chills was resolving at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (High Blood Pressure); Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1856832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: KS
Alter: 37,0
Geschlecht: F
Eingang: 10.11.2021
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

Derealisation Disorientation Dizziness Headache Interchange of vaccine products

Symptomtext

A sudden feeling of extreme disorientation, time distortion; Dizziness/ a general feeling of wooziness; Sense of unreality that lasted about 3-4 hours; I still have a slight headache; The patient received JANSSEN on 12Mar2021 and BNT162B2 on 29Oct2021; The patient received JANSSEN on 12Mar2021 and BNT162B2 on 29Oct2021; The patient received the booster dose of BNT162b2; This is a spontaneous report from a contactable consumer, the patient. A 37-year-old non-pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the left arm on 29Oct2021 (at the age of 37-year-old), as a single dose for COVID-19 immunisation. Medical history included COVID-19 and known allergy to cane sugar. Prior to the vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Concomitant medications included cyanocobalamin (B12), iron (MANUFACTURER UNKNOWN), hyaluronic acid (MANUFACTURER UNKNOWN), probiotics nos (MANUFACTURER UNKNOWN) and fish oil (OMEGA 3); all for an unknown indication from an unknown date and unknown if ongoing. The patient previously received sulfamethoxazole/trimethoprim (BACTRIM) for an unknown indication from an unknown date and experienced drug allergy and received first dose of jnj 78436735(JANSSEN COVID-19 VACCINE, Lot Number: 1805025) via an unspecified route of administration on 12Mar2021 (at the age of 37-year-old), as a single dose for COVID-19 immunisation. On 03Nov2021 at 16:15, the patient experienced a sudden feeling of extreme disorientation, time distortion, dizziness, sense of unreality that lasted about 3-4 hours. The patient still had a slight headache and a general feeling of wooziness. The events resulted in emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events sense of unreality was resolved on 03Nov2021 (lasted about 3-4 hours) and of the sudden feeling of extreme disorientation, time distortion, dizziness, and still have a slight headache, general feeling of wooziness was resolved with lasting effects on unknown date of Nov2021 at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes); Food allergy (Known allergies: Cane sugar)
Andere Medikamente: B12 [CYANOCOBALAMIN]; IRON; PROBIOTICS NOS; OMEGA 3 [FISH OIL]; HYALURONIC ACID
Allergien: -
Vorherige Impfungen: -

VAERS 1855525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MI
Alter: 56,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 18.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Autoimmune disorder Chills Fatigue Feeling abnormal Gait disturbance Headache Nausea Neck pain

Symptomtext

extreme fatigue, head ache, chills, left knee pain could hardly bend it, rt hip pain, extreme neck pain, difficulty walking. nausea, symptoms were much worse than the first dose, the symptoms have continued now for 3 weeks a few good days and walking is often difficult. I still get days of nausea, foggy head feeling. neck pain it will come in waves some times during the day it will be hard to walk and other times it eases up. it has been 21 days since 2nd dose. These doses were mandated by my employer not voluntary, it has triggered a auto immune response.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Still feeling side effects from the first dose of the vaccine, foggy head, muscle aches, knee pain and neck pain
Vorgeschichte: Diabetes
Andere Medikamente: metformin, novolog, tresbia, synthroid, losartan
Allergien: demerol, lisinopril, demerol
Vorherige Impfungen: covid vaccine 1st dose

VAERS 1854577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CA
Alter: 38,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 22.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Chest discomfort Cough Headache Injection site pain Myalgia Oropharyngeal pain Pain in extremity Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had absolutely no symptoms related to vaccine except soreness in the arm tenderness at site of actual injection. I went to a very large concert event for three days and wasn't wearing a mask and was around people. Wednesday the 3rd I had symptoms onset. Initially I had headache, runny nose, and sore throat. Within 24 hours after that I started developing a cough, and muscle aches and in my head. Fever came on after that. A little tightness in the chest, chest pressure, muscle aches, headaches and runny nose. Drinking a lot of tea, sleeping a lot and isolating. I have been having trouble sleeping, and so he prescribed a cough suppressant which will get delivered today. Because I have a history of bronchitis and asthma. He would reach out to see if I could get the monoclonal antibodies. I can't smell or taste anything. That started Friday morning the 5th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test - nose swab at Kaiser November 5th results were received on Sunday November 7th, and those results were positive for COVID-19.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Chronic bronchitis - tend to get it every year if I get a cold
Andere Medikamente: Acyclovir Smoke weed herbal
Allergien: Allergies to Penicillin
Vorherige Impfungen: -

VAERS 1854519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Nausea Peripheral coldness

Symptomtext

Dizziness after about 5 minutes of the booster (3rd dose), Cold extremities, wanting to vomit (DID NOT VOMIT), Blood pressure 93/67 HR 58 at 10:15a. Patient lie flat on the floor and got better after 15 minutes. EMS came and checked patient blood pressure and blood sugar.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Latex, Milk, sulfa, shrimp
Vorherige Impfungen: Per patient, flu shot: dizziness

VAERS 1853907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WV
Alter: 32,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Peripheral swelling Rash Rash papular

Symptomtext

Patient reports raised bumps on thighs and abdomen on Friday (day after vaccine), both hands swollen on Saturday. She took Benadryl to help. She reports rash persisted and she had a new rash on leg a few days later. Her primary care doctor attributed it to anxiety.

Weitere VAERSDATA-Felder

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

VAERS 1852060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: GA
Alter: 50,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SC / LA

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

Fatigue Headache Influenza like illness Pyrexia

Symptomtext

72 hours of flu like symptoms, low grade fever. Dull headaches and fatigue continue 12 days after injection.

Weitere VAERSDATA-Felder

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

VAERS 1851793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MA
Alter: 91,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Fatigue Pain in extremity

Symptomtext

patient felt a little tired and a little sore arm after received the covid Pfizer shot. No major complains after an hour observational period.

Weitere VAERSDATA-Felder

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

VAERS 1850743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NC
Alter: 50,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Lymphadenopathy

Symptomtext

Painful, lime-sized lump in left armpit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Sinus infection
Vorgeschichte: Rheumatoid Arthritis, Asthma, Fibromuscular Dysplasia with renal stenosis, PFO, Chronic Migraine
Andere Medikamente: Xhance 1 Spray Each Nostril Amlodipine 5 mg X 2 Atenolol 25 mg Hydroxychloroquine 200 mg X 2 Aspirin 81 mg Fish Oil 1200 mg X 2 Super B with C Sertraline 50 mg Citracal 1300 mg Zyrtec 10 mg Humira 40 mg a week
Allergien: Latex, penicillin, codeine, pneumonia vaccine, phenergan
Vorherige Impfungen: Pneumonia Vaccine, Age 40ish

VAERS 1849593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: VA
Alter: 56,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Headache Oropharyngeal pain Pain Respiratory tract congestion

Symptomtext

Headache, severe congestion, sore throat, body aches, fatigue, joint aches.

Weitere VAERSDATA-Felder

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

VAERS 1849569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 74,0
Geschlecht: M
Eingang: 07.11.2021
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

Axillary pain Lymphadenopathy

Symptomtext

The day if my vaccination, no adverse reaction. The morning after, I woke up with a large and painful lump just under the left arm pit, I had received the shot in! It is painful and seems to be getting larger. It is APX. 4" WIDE 6" LONG AND 1 PLUS ".S HIGH!!!

Weitere VAERSDATA-Felder

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

VAERS 1849074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: TX
Alter: 32,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Nausea

Symptomtext

The patient began to experience lightheadedness and nausea within a few minutes of the vaccine administration. She did not experience this with either of the other two doses. She noted she had not eaten in over 12 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Allergic to eggs
Vorherige Impfungen: -

VAERS 1848930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: SC
Alter: 12,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness

Symptomtext

Patient complained of dizziness, felt like she was going to faint. I checked her blood pressure and monitored her symptoms, and called the ambulance. The ambulance checked her vitals, and monitored her for approximately 10 minutes until her and the parent felt comfortable leaving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1847168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: NC
Alter: 39,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling hot Inappropriate schedule of product administration

Symptomtext

after receiving the vaccines, pt felt hot and dizzy. symptoms started about 10 mins later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: pt is affraid to get blood drawn and needles injected.
Vorgeschichte: n/a
Andere Medikamente: just gave ice packs
Allergien: none
Vorherige Impfungen: -

VAERS 1846934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MA
Alter: 30,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Flushing Rash

Symptomtext

Given 1st dose of Pfizer-hx of allergic reaction/anaphalaxis to flu vaccine 6-7 yrs prior. Covid Vaccine ok'd by PCP. after 15 min of observation (being observed for 30) face became extremely flushed, given water, no difficulty breathing, no SOB. Rash contained to face, slight pink area to chest wall that subsided. given 50mg of Benadryl po-observed x 30 more, symptoms lessened, no new sx's.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Hx of allergic reaction to Flu vaccine 6-7 yrs ago-no epi given (was see in ER given iv meds)
Vorherige Impfungen: -

VAERS 1846920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: IL
Alter: 58,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Anxiety Erythema Pruritus Somnolence

Symptomtext

When filling out the consent, pt verbalized that she had some itching with the first dose that started when she got home about 30 minutes after she left the office. She had spoken with rheumatologist who had urged her to get the 2nd dose and her PCP, who had told her to take Benadryl 25mg prior to the second injection. Nurse had been observing pt and all seemed to be going well. Had no complaints until she was about to be released from the office at 3PM and then she stated that the itching had started. Was scratching on her thighs and then started itching on her arms. A little anxious and skin was turning red. Dr, collaborator for NP was in the office and asked to check pt. No complaints of breathing difficulties and no uvula swelling. Staff was instructed to administer 50 mg of IM Diphenhydramine in the left deltoid. Itching started to ease within a few minutes and resolved in 8 minutes. Pt was well enough to leave the office and was contacted at home at 3:45 and was resting quietly at home and a little drowsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: nothing acute.
Vorgeschichte: Type 2 DM, HTN, HPV, Hyperlipidemia, Lupus, Neuropathy, Vitamin D deficiency, Obesity, Nonuclear dyspepsia
Andere Medikamente: Acetaminophen, Zyrtec, Vitamin D, Hydroxychloroquine, Hydroxyzine, Linzess, Lorazepam, Losartan, Metformin, Pravastatin, Lyrica, Tramadol, Trazadone, Tretinoin Cream, Victoza
Allergien: Red Dye- Severe hives/ edema, NSAIDS -severe hives and edema
Vorherige Impfungen: milder itching with the first Pfizer dose, relieved with oral Benadryl

VAERS 1846722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NM
Alter: 26,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered Rash Rash pruritic Skin warm

Symptomtext

Patient received the Pfizer booster vaccine on 11-4-21, patient called on 11-5-2021 at 1030 and reported she developed a rash 1700 on her body except her face, stated rash was itchy and felt warm, patient denied any respiratory distress. Patient states went to the Urgent Care, but was taking long to be seen, she went home and took a benadryl at 1830, patient states rash, itching and and warmth was relieved with the benadryl, patient states the itchy and warmth returned at 0830, took benadryl at 0930 and was relieved again. At 1330 Called patient, patient states going to the Urgent Care now to be seen, patient states does not have the rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None reported
Aktuelle Erkrankungen: None stated
Vorgeschichte: None stated
Andere Medikamente: Vitamins
Allergien: KNDA
Vorherige Impfungen: -

VAERS 1844354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WI
Alter: 35,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Fatigue Headache Hot flush Myalgia Night sweats Pyrexia

Symptomtext

Fever 101.4, chills, headache, fatigue, muscle aches 10.5 hours after injection; peaking 20 hours after injection and resolved 36 hours after injection. Hot flashes and night sweats 72 hours after injection, lasting >1 week after injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin; Sulfa
Vorherige Impfungen: Pfizer COVID-19 vaccine 1/8/2021, fever 101, chills, hot flashes, night sweats and muscle aches.

VAERS 1843888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: CT
Alter: 67,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site erythema Injection site swelling Injection site warmth

Symptomtext

Redness, swelling at the site, warmth to touch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia, Allergic rhinitis
Andere Medikamente: cetirizine, synthroid, simvastatin, immodium, solifenacin
Allergien: None
Vorherige Impfungen: -

VAERS 1843150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Fatigue Headache Muscle spasms

Symptomtext

Fatigue, headache, muscle spasm lasted about 48 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Major depression and anxiety disorder
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Moderna dose 2, fever chills fatigue headache rigors 4/6/21 age 29

VAERS 1842658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: FL
Alter: 84,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Injection site erythema Lethargy Pain Pyrexia

Symptomtext

Site: Redness at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium

Weitere VAERSDATA-Felder

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

VAERS 1840039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MA
Alter: 53,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Oedema peripheral

Symptomtext

evening of day two (Nov 2nd) noticed soreness under left arm with armpit swelling .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no other illnesses
Vorgeschichte: colitis
Andere Medikamente: ativan
Allergien: zero
Vorherige Impfungen: Ist Pfizer covid vaccine. tingling of middle bottom lip 45 min after first injection into left arm. Lasted 5 min. Pfizer 3/30/2

VAERS 1839234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: OR
Alter: 34,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness

Symptomtext

Pt felt lightheadedness, requested some water, gave him water, and asked him to lay down. After about 5 minutes, he felt better.

Weitere VAERSDATA-Felder

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

VAERS 1837673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: TX
Alter: 69,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site haemorrhage Injection site inflammation Injection site pain Injection site swelling

Symptomtext

Administered patient her Pfizer booster Vaccine and noticed a large amount of blood into her inject safe bandage. I placed another regular bandage over it to help with additional blood but then patient alerted me while she was waiting her 15 minutes that the blood started flowing out down her arm. I proceeded to help her clean the area and blood that had dripped down her arm. When I felt the area it was tender, inflamed, and had a small bump. I placed another bandage on her arm and proceeded to have her lift her arm above chest level and place an icepack to help with inflammation. After a few more minutes the blood was no longer flowing and her arm was less inflamed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1836584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MD
Alter: 59,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / -

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

Chills Fatigue Muscle spasms

Symptomtext

chills, tired. toes cramped up several days in a row after shot. Very hard to get the cramp out of toe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: acid reflux
Allergien: none
Vorherige Impfungen: chills and headache

VAERS 1834254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WA
Alter: 30,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Eustachian tube obstruction Fatigue Impaired work ability Injection site erythema Injection site reaction Injection site warmth Lymph node pain Malaise Pain Rash macular Sinus disorder

Symptomtext

Left arm near injection site about 4 inches diameter there was a hot red hard splotch that had a ridge around it. I felt fatigued, malaise for 3 days, resolved as of the 4th day. Lymphnodes in left armpit were so painful I couldn?t get out of bed without significant pain. When I did get out of bed I held the lymphnode up with my arm. I had to cancel work today. I could see the size difference in my armpits. The left one looked like it had a halved orange under the skin. It is still visible as of day 4 and painful but I have more mobility and it?s the size of a halved lemon. I?m unsure if this is related but I am having sinus issues and my Eustachian tubes are blocked.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Ear infection - finished antibiotic drops 1 week prior
Vorgeschichte: Long QT syndrome, obesity, have pacemaker/defibrillator for the Long QT syndrome
Andere Medikamente: Atenolol 25 mg, lamotrigine 100 mg, buspirone 60 mg, clonodine .2 mg, Wellbutrin 300 mg, magnesium, venlafaxine 37.5, ashwagandha, probiotic, vitamin c,d,e, multivitamin, butterbur
Allergien: Acetaminophen
Vorherige Impfungen: -

VAERS 1833800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: VA
Alter: 70,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Headache Myalgia Nasal congestion Oropharyngeal pain Pyrexia

Symptomtext

Saturday early morning began with fever over 100, severe headache, every joint and muscle in body ached, sore throat, stuffy sinuses, very tired - fever finally broke around 3 PM on same day, headache and body aches continued until late evening. Everything better by 6 AM following morning (Sunday) except for still being tired. Back to normal Monday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: Cholesterol
Andere Medikamente: none
Allergien: mold, dust mites, seasonal allergies
Vorherige Impfungen: 69 years old, Pfizer Lot EW0153 injection on 04/13/2021

VAERS 1833723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: AZ
Alter: 68,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / LA

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

Chills Headache Nausea

Symptomtext

Headache, nausea, chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Heart surgery-Quadruple bypass 2018
Andere Medikamente: Aspirin 81 MG 1x day Atorvastatin 40 G 1x day Metoprolol Tartrate 25 MG 1/2 2 x day Levothyroxine 25 MCG 1 x day
Allergien: None
Vorherige Impfungen: -

VAERS 1832207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 53,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Malaise

Symptomtext

Patient is feeling tired and under the weather for the past day

Weitere VAERSDATA-Felder

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

VAERS 1832207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: OH
Alter: 53,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Malaise

Symptomtext

Patient is feeling tired and under the weather for the past day

Weitere VAERSDATA-Felder

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

VAERS 1831631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

mild

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Headache Injection site pain Lymph node pain Lymphadenopathy Malaise Musculoskeletal pain

Symptomtext

Pain/soreness at injection site, left armpit swollen and sensitive, slight headache, tired, general feeling unwell, left shoulder/scapula area sore/tired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Afib, hypertension, prediabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1828886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site pruritus Injection site swelling Injection site warmth

Symptomtext

injection site on arm became red, swollen, hot and itchy few hours after administration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: patient went to ER for treatment and started on antibiotic, Benadryl, cool compress
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: clonidine patch, birth control pills, multivitamin, omega 3 supplement, topiramate, vyvanse
Allergien: Compazine, ginger, ginger root, latex
Vorherige Impfungen: -

VAERS 1823907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PR
Alter: 53,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Injection site inflammation Injection site pain Interchange of vaccine products Myalgia Myositis

Symptomtext

First dose was Janssen on 03/31/2021. This is the second dose. Noted Right under arm, pectoral muscle inflammation and pain. Still have some inflammation and pain in the injection spot. Will consult with Doctor if it get worse or other symptoms appear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site inflammation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Shrimp and lobster
Vorherige Impfungen: -

VAERS 1815910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysphagia Rash

Symptomtext

Patient presented to the pharmacy counter about 5 minutes after injection with a rash on chest and left arm. At first I gave her 50mg of oral Benadryl. She started to mention she was having a hard time swallowing. I grabbed the Epipen and administer it into left thigh. At that time I also called emergency and EMS came. They evaluated her and took her to the emergency room. When she left she was able to breath and talk.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown, Patient was traveling
Vorgeschichte: Unknown, Patient was traveling
Andere Medikamente: Unknow, patient was traveling
Allergien: NKDA per form
Vorherige Impfungen: -

VAERS 1809011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: MA
Alter: 24,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Dizziness Hyperhidrosis Malaise Pallor Visual impairment

Symptomtext

On 10/20/21 patient received first dose of Pfizer COVID-19 vaccine. 5 minutes after administration, patient informed pharmacy team that he "did not feel good, felt light-headed" and that his vision seemed dim and obscured. He looked pale and was sweating. We asked him to sit down on the floor and to keep his back against the wall. We called 911 and his family member also arrived at the store. Patient claimed to have felt anxious prior to the vaccine. We gave him water to sip on. Ambulatory services arrived and checked his vitals. He started feeling better and a trip to the ER was deemed unnecessary . After 35 minutes his family member took him home. I called him the next day and he reported feeling fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1808562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Head discomfort Headache Neck pain

Symptomtext

Quality 7/10 pain in every joint of body, specifically joints and bones on top of foot, toes, wrists, which resolved in 3 days. Left should joint pain still lingering 8 days later. Back of head down patient's neck has pressure and soreness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis (unspecified etiology)
Andere Medikamente: not known
Allergien: Penicillin, sulfa antibiotics, NSAIDs
Vorherige Impfungen: -

VAERS 1804325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

mild

Staat: PR
Alter: 40,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blister Erythema Headache Hyperhidrosis Pain Pyrexia

Symptomtext

Excessive sweating, fever, body ache, headache, blisters on the scalp and redness of the armpits

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None reported
Vorgeschichte: Hypoglycemic, migraine
Andere Medikamente: Protonix
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2666428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 04.08.2023
Impfdatum: 12.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 03Mar2021 as dose 1, single (Lot number: EN6206), in right arm, on 25Mar2021 as dose 2, single (Lot number: EP7533), in left arm and on 12Nov2021 as dose 3 (booster), single (Lot number: 32030BD) at the age of 60 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Double pneumonia from a respiratory virus" (unspecified if ongoing), notes: 7 years ago. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (2023) Negative, notes: after 5 days; (2023) Positive, notes: again on day 11. Therapeutic measures were taken as a result of drug ineffective, covid-19. Additional information: No known allergies. Patient received anti-viral treatment for Covid 19 with Paxlovod from 24Jul2023 to 29Jul2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 2023; Test Name: Covid 19; Test Result: Negative ; Comments: after 5 days; Test Date: 2023; Test Name: Covid 19; Test Result: Positive ; Comments: again on day 11
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pneumonia due to respiratory syncytial virus (7 years ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2665615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 03.08.2023
Impfdatum: 29.10.2021
Beginn: 10.01.2022
Tage bis Beginn: 73,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Caesarean section SARS-CoV-2 test positive

Symptomtext

Admitted for labor & LTCS; incidental finding of COVID+, asymptomatic

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2647363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 20.06.2023
Impfdatum: 22.09.2021
Beginn: 23.09.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / AR

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

Anticoagulant therapy Atrial fibrillation Cardiac monitoring Electrocardiogram

Symptomtext

Developed AFIB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anticoagulant therapy
Hospital-Tage: -
Labordaten: EKG, Heart Monitor, ongoing medication including blood thinner
Aktuelle Erkrankungen: -
Vorgeschichte: COPD
Andere Medikamente: Losartan, Cymbalta
Allergien: None
Vorherige Impfungen: -

VAERS 2640627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: CO
Alter: 81,0
Geschlecht: M
Eingang: 02.06.2023
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

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

Expired product administered

Symptomtext

EXPIRED VACCINE GIVEN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2593236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 21.10.2021
Beginn: 06.06.2022
Tage bis Beginn: 228,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 3/12/21 Lot# EN6206; Pfizer 4/5/21 Lot# Ew0150; Pfizer 10/21/21 Lot# 32030BD

Weitere VAERSDATA-Felder

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

VAERS 2590346

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 32030BD

gering

Staat: MI
Alter: 46,0
Geschlecht: M
Eingang: 02.03.2023
Impfdatum: 05.12.2021
Beginn: 03.02.2023
Tage bis Beginn: 425,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 4/14/21 Lot# 043B21A; Moderna 5/12/21 Lot# 044B21A; Pfizer 12/15/21 Lot# 32030BD

Weitere VAERSDATA-Felder

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

VAERS 2584852

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 32030BD

gering

Staat: FL
Alter: 83,0
Geschlecht: M
Eingang: 21.02.2023
Impfdatum: 01.11.2021
Beginn: 22.01.2023
Tage bis Beginn: 447,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Transient ischaemic attack

Symptomtext

Hospitalization: 1/20/2023 - 1/24/2023 (4 days) Presentation to the ED: Admitted for transient ischemic attack COVID + date: 1/22/2023 Treatment: No indication for antiviral or steroids therapy. Discharge to: SNF EN5318 1/29/2021 EN6200 2/20/2021 32030BD 11/1/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, Parkinson's disease, chronic GERD, BPH, dementia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

gering

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 11.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / UN

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

Unevaluable event

Symptomtext

none

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: asthma
Andere Medikamente: Fulticasone Propionaten Nasal Spray, Advair inhaler 115 mcg/21 mcg, , albuterol inhaler, claritlin 24 hr, omerprazole caps 40 mg, rapaflo capsules 8 mg. multi vitimin , calicium, atrovastalin ca 10 mg montskukast sodium 10 mg
Allergien: sulfa and flomax
Vorherige Impfungen: -

VAERS 2531267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: MN
Alter: 36,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 16.12.2021
Beginn: 13.09.2022
Tage bis Beginn: 271,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19

Symptomtext

Contracted Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: ALLEGRA-D
Allergien: No
Vorherige Impfungen: -

VAERS 2521049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: FL
Alter: 46,0
Geschlecht: F
Eingang: 01.12.2022
Impfdatum: 22.10.2021
Beginn: 30.11.2022
Tage bis Beginn: 404,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

patient hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2519864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: AR
Alter: 65,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 09.11.2021
Beginn: 26.11.2022
Tage bis Beginn: 382,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

hospitalized with covid; fully vaccinated

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 1,0
Labordaten: positive covid pcr 11/26/22
Aktuelle Erkrankungen: unknown
Vorgeschichte: Atrial fibrillation GAD HFrEF Hypothyroidism ESRD
Andere Medikamente: unknown
Allergien: codeine, morphine
Vorherige Impfungen: -

VAERS 2515363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 18.11.2021
Beginn: 28.08.2022
Tage bis Beginn: 283,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 Cough SARS-CoV-2 test positive

Symptomtext

I had the vaccination on 11/18/2021. On 08/28/2022 I had a cough at night. During the day of 08/29/2022 the cough continued and the following days. I tested COVID-19 positive on 08/28/2022. I was prescribed an antibiotic for 5 days. I presently feel fine on 11/23/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 positive 08/28/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin D3; levothyroxine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2500677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: MI
Alter: 91,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 08.03.2021
Beginn: 09.09.2022
Tage bis Beginn: 550,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Muscular weakness SARS-CoV-2 test positive

Symptomtext

09/09/22 presents to ED for "extremity weakness". PMHx of "dementia, hypertension, hypothyroidism, skin cancer"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 09/09/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2496444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 20.10.2021
Beginn: 01.04.2022
Tage bis Beginn: 163,0
Dosis: 3
Route/Site: SYR / LA

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

Bacterial test Blood test Blood urine present Culture urine negative Laboratory test normal SARS-CoV-2 test negative Urine abnormality Urine analysis abnormal

Symptomtext

On 04 /28/2022 I went to the hospital to get urine and blood test which was referred by my doctor. The results were given around 10:20AM. They found blood, mucus, and bacteria in my urine. They even did urine culture it was negative. They did it again after couple of weeks later it was negative again. My doctor referred me to a Urologist. I went to the Urologist yesterday on 11/01/2022 and they did few more tests this time everything was normal even though I still have little blood present in my urine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bacterial test
Hospital-Tage: -
Labordaten: 02NOV22- COVID-19 Test- Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Pancreatitis
Andere Medikamente: None
Allergien: Anti-inflammatory; Codeine; Lovenox
Vorherige Impfungen: -

VAERS 2490846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

gering

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 07.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 07Nov2021 as dose number unknown (booster), single (Lot number: 32030bd) at the age of 65 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Treatment of COVID-19; (16Oct2022) Negative; (18Oct2022) Negative; (20Oct2022) Negative; (22Oct2022) Negative; (24Oct2022) Positive, notes: Tested Positive 24Oct2022. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: It was reported that no other medication in 2 weeks. Patient took Paxlovid for 5 days -11Oct2022 through 16Oct2022. Patient covid-19 test was negative on 16Oct, 18Oct, 20Oct and 22Oct. Patient symptoms returned on 22Oct evening and tested positive on 24Oct2022. No other medical history. Patient had known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20221016; Test Name: Covid-19 test; Test Result: Negative ; Test Date: 20221018; Test Name: Covid-19 test; Test Result: Negative ; Test Date: 20221020; Test Name: Covid-19 test; Test Result: Negative ; Test Date: 20221022; Test Name: Covid-19 test; Test Result: Negative ; Test Date: 20221024; Test Name: Covid-19 test; Test Result: Positive ; Comments: Tested Positive 24Oct2022
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 2474436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 02.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Interchange of vaccine products; Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient received BNT162b2 (BNT162B2), on 02Nov2021 as dose 3 (booster), single (Lot number: 32030BD) at the age of 66 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 18Mar2021 as dose 1, single (Lot number: 006B21A), in left arm and on 15Apr2021 as dose 2, single (Lot number: 040B21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Chronic Lymphocytic Luekemia" (unspecified if ongoing), notes: Other medical history: Chronic Lymphocytic Luekemia; "Known allergies: sulpha drugs" (unspecified if ongoing), notes: Known allergies: sulpha drugs. There were no concomitant medications.The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results, notes: Indication: Treatment of COVID-19; Positive, notes: tested positive with a strongly marked line. Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid from 22Sep2022 to 27Sep2022. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Result Unstructured Data: Test Result:Unknown results; Comments: Indication: Treatment of COVID-19; Test Name: Covid-19 Test; Test Result: Positive ; Comments: tested positive with a strongly marked line
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic lymphocytic leukaemia (Other medical history: Chronic Lymphocytic Luekemia); Sulfonamide allergy (Known allergies: sulpha drugs)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2471367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NC
Alter: 49,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Interchange of vaccine products SARS-CoV-2 test Vaccination failure

Symptomtext

Covid-19; Covid-19; interchange of vaccine products; This is a spontaneous report received from contactable reporter(s) (Physician) from product quality group. The reporter is the patient. A 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Nov2021 as dose 3 (booster), single (Lot number: 32030BD) at the age of 49 years for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 07Jan2021 as dose 1, single (Lot number: 025J20A), on 04Feb2021 as dose 2, single (Lot number: 016M20A) and on 22Apr2022 as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Sleep apnea" (unspecified if ongoing); "Depression" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "GERD" (unspecified if ongoing); "insomnia" (unspecified if ongoing). Concomitant medication(s) included: VENLAFAXINE; SUVOREXANT; VITAMIN D3; RYBELSUS; VITAMIN B12 [CYANOCOBALAMIN]. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 26Nov2021, outcome "unknown"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Covid-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: Patient received other medication in two weeks. Patient received anti viral treatment for COVID 19 with Paxlovid from 19Sep2022 till 24Sep2022. Patient taken multivitamin as concomitant. There were no known allergies.; 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.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Depression; GERD; Insomnia; Sleep apnea
Andere Medikamente: VENLAFAXINE; SUVOREXANT; VITAMIN D3; RYBELSUS; VITAMIN B12 [CYANOCOBALAMIN]
Allergien: -
Vorherige Impfungen: -

VAERS 2468229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 22.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / -

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

Computerised tomogram neck Dysphagia Hypoaesthesia Laboratory test Magnetic resonance imaging head Ultrasound scan Ultrasound thyroid Vitamin B12 Vitamin D

Symptomtext

Facial numbness, dysphagia.

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Praegender Schweregrund: Computerised tomogram neck
Hospital-Tage: -
Labordaten: Brain MRI, labs (vitamin d, vitamin b12, tick borne illnesses), thyroid, neck, CT soft tissue of neck pending.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism; Diabetes
Andere Medikamente: Ozempic; Calcium Citrate; Iron; Citalopram.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2461110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 01.12.2021
Beginn: 01.03.2022
Tage bis Beginn: 90,0
Dosis: 3
Route/Site: IM / LA

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

Colitis ulcerative

Symptomtext

New onset ulcerative colitis.

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

VAERS 2450156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: TN
Alter: 52,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 28.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; 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 (not pregnant) received BNT162b2 (BNT162B2), on 28Feb2022 as dose 3 (booster), single (Lot number: 32030BD) at the age of 52 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Recent weight loss revision surgery" (unspecified if ongoing). Patient had no known allergies. There were no concomitant medications, also reported as patient not received any other medication in 2weeks. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid started from 06Sep2022 and stopped on 09Sep2022. Clinical course was reported as, on 08Sep2022 at 20:00, patient experienced symptoms of Throat had restriction or tightening. Patient not received any treatment for the symptoms and was recovering from symptoms.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19 Treatment; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Surgery
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2439792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: VT
Alter: 52,0
Geschlecht: M
Eingang: 10.09.2022
Impfdatum: 23.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

General physical health deterioration

Symptomtext

Overall declined in health since he was forced to get these shots; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 52-year-old male patient received BNT162b2 (BNT162B2), on 23Oct2021 as dose 1, single (Lot number: 32030BD) at the age of 52 years, in right deltoid for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), in 2021 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Had COVID 6 weeks before being forced into getting first shot. There were no concomitant medications. The following information was reported: GENERAL PHYSICAL HEALTH DETERIORATION (non-serious) with onset 2021, outcome "not recovered", described as "Overall declined in health since he was forced to get these shots". Additional information: The patient did not have any family medical history relevant to the adverse event. The patient received first shot at mass medical event through battalion. The patient had COVID 6 weeks before being forced into getting first shot. Sense of taste and smell came back after that and was pretty good and everything was normal. Everything was pretty good after being forced to take first shot. The patient had overall declined in health since he was forced to get these shots. The patient wanted to know how long the side effects would last. The patient stated that he was wondering about the longevity of the side effects. No investigations were done. The case was reported as non-serious.

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Praegender Schweregrund: General physical health deterioration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Had COVID 6 weeks before being forced into getting first shot)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2426328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 25.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19; COVID 19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Jan2021 as dose 1, single (Batch/Lot number: unknown), in right arm, on 17Feb2021 as dose 2, single (Lot number: EN9581), in right arm and on 25Oct2021 as dose 3 (booster), single (Lot number: 32030BD) at the age of 69 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Diverticulitis" (unspecified if ongoing); "Known allergies: sulfa" (unspecified if ongoing). Concomitant medication(s) included: ZOVIRAX [ACICLOVIR]; LEVOTHYROXINE; VITAMIN D3; ALLERCLEAR; ROBITUSSIN DM; FLUTICASONE PROPIONATE; ACETAMINOPHEN. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Anti viral details COVID 19 Treatment, brand Paxlovid. treatment start date was 24Aug2022 treatment stop date was 25Aug2022 . The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diverticulitis; Sulfonamide allergy
Andere Medikamente: ZOVIRAX [ACICLOVIR]; LEVOTHYROXINE; VITAMIN D3; ALLERCLEAR; ROBITUSSIN DM; FLUTICASONE PROPIONATE; ACETAMINOPHEN
Allergien: -
Vorherige Impfungen: -

VAERS 2416720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 23.08.2022
Impfdatum: 11.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 51,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure Warm autoimmune haemolytic anaemia

Symptomtext

covid test date 01Jan2022; covid test result Positive; covid test date 01Jan2022; covid test result Positive; 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 (BNT162B2), on 09Apr2021 as dose 1, single (Lot number: EW0158), on 05May2021 as dose 2, single (Lot number: EW0173) and on 11Nov2021 at 16:30 as dose 3 (booster), single (Lot number: 32030BD) at the age of 36 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 01Jan2022, outcome "unknown" and all described as "covid test date 01Jan2022; covid test result Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (01Jan2022) Positive, notes: COVID test type post vaccination: Nasal Swab. Clinical course:The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications the patient received within 2 weeks of vaccination. Prior to vaccination, 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 information is necessary.

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Praegender Schweregrund: Warm autoimmune haemolytic anaemia
Hospital-Tage: -
Labordaten: Test Date: 20220101; Test Name: Abbott BinaxNOW; Test Result: Positive ; Comments: COVID test type post vaccination: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No Known allergies: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2410754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: MA
Alter: 61,0
Geschlecht: M
Eingang: 13.08.2022
Impfdatum: 16.10.2021
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

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 62-year-old male patient received BNT162b2 (BNT162B2), on 26Dec2020 at 10:30 as dose 1, single (Lot number: EH9899), in left arm, on 16Jan2021 at 11:00 as dose 2, single (Lot number: EK9231), in left arm and on 16Oct2021 at 09:00 as dose 3 (booster), single (Lot number: 32030BD) at the age of 61 years, in left arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 14May2022 at 11:00 as dose 4 (booster), single (Lot number: 002M21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "seasonal allergies" (unspecified if ongoing), notes: seasonal allergies. Concomitant medication(s) included: ASPIRIN [ACETYLSALICYLIC ACID] oral, start date: 19Nov2017. Past drug history included: Finasteride, reaction(s): "Known allergies: Finasteride", notes: Known allergies: Finasteride. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19 included COVID-19 Treatment included PAXLOVID from 26Jul2022 to 01Aug2022.; Sender's Comments: Based on available information, a possible contributory role of Comirnaty vaccine cannot be excluded for the reported events.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seasonal allergy (seasonal allergies)
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2403891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 06.08.2022
Impfdatum: 08.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: - / LA

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

COVID-19 Drug ineffective Polymerase chain reaction SARS-CoV-2 test

Symptomtext

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 (not pregnant) received BNT162b2 (BNT162B2), on 08Dec2021 as dose 1, single (Lot number: 32030BD) at the age of 26 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). Concomitant medication(s) included: FLOVENT HFA, start date: Jul2022, stop date: Jul2022. The following information was reported: COVID-19 (medically significant) with onset 17Dec2021, outcome "unknown", described as "COVID 19"; DRUG INEFFECTIVE (medically significant) with onset 17Dec2021, outcome "unknown". The patient underwent the following laboratory tests and procedures: Polymerase chain reaction: Positive, notes: Day 3: Positive rapid and PCR tests; SARS-CoV-2 test: Negative, notes: Day 1: Negative rapid result; Positive, notes: Day 8: Last Paxlovid dose in morning. Prominent positive band for rapid test; Positive, notes: Day 10: Slight positive band for positive result on rapid test; Negative, notes: Day 12:Negative rapid test result; Positive, notes: but had a clear/dark band for positive rapid test 9 days after dose; rebound, notes: Confirmed Covid-19 rebound via rapid test on August 3. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient receive Paxlovid as therapeutic measure.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: PCR tests; Test Result: Positive; Comments: Day 3: Positive rapid and PCR tests.; Test Name: COVID-19 test; Test Result: Negative ; Comments: Day 1: Negative rapid result.; Test Name: COVID-19 test; Test Result: Positive ; Comments: Day 8: Last Paxlovid dose in morning. Prominent positive band for rapid test.; Test Name: COVID-19 test; Test Result: Positive ; Comments: Day 10: Slight positive band for positive result on rapid test.; Test Name: COVID-19 test; Test Result: Negative ; Comments: Day 12:Negative rapid test result.; Test Name: COVID-19 test; Test Result: Positive ; Comments: but had a clear/dark band for positive rapid test 9 days after dose.; Test Name: COVID-19 test; Result Unstructured Data: Test Result:rebound; Comments: Confirmed Covid-19 rebound via rapid test on August 3.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: Flovent HFA
Allergien: -
Vorherige Impfungen: -

VAERS 2399252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 21.10.2021
Beginn: 30.07.2022
Tage bis Beginn: 282,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Vaccine breakthrough infection

Symptomtext

Fully vaccinated and one booster. COVID infection breakthrough

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

VAERS 2398000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: MI
Alter: 23,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 23.11.2021
Beginn: 01.08.2022
Tage bis Beginn: 251,0
Dosis: 3
Route/Site: IM / -

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

Asymptomatic COVID-19 Delivery Exposure during pregnancy SARS-CoV-2 test positive

Symptomtext

apparently asymptomatic, tested covid positive on 7/18 per pt, tested positive by PCR at hospital on 8/1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: SARS-COV-2 (COVID-19) by NAA, Micro Detected on 8/1/22
Aktuelle Erkrankungen: -
Vorgeschichte: gave birth on 8/1/22
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

gering

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 30.07.2022
Impfdatum: 16.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; 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), on 16Nov2021 as dose 3 (booster), single (Lot number: 32030bd) at the age of 37 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Breast cancer survivor (Nov2020)", start date: Nov2020 (unspecified if ongoing); "asthma" (unspecified if ongoing); "Known allergies: Tree nuts" (unspecified if ongoing); "Known allergies: soy" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient was treated with Paxlovid for COVID-19. Treatment start date was 16Jul2022. Treatment stop date was 20Jul2022. Patient received no other medications in two weeks. Paxlovid rebound after 11 days from starting the medicine. Adverse event start date was 26Jul2022. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19/PCR; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts; Asthma; Breast cancer; Soy allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: MA
Alter: 59,0
Geschlecht: F
Eingang: 30.07.2022
Impfdatum: 09.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Nov2021 as dose 3 (booster), single (Lot number: 32030BD) at the age of 59 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Bladder Cancer" (unspecified if ongoing); "High Blood Pressure" (unspecified if ongoing); "Thrombocytosis" (unspecified if ongoing); "Known allergies: Shellfish" (unspecified if ongoing), notes: Known allergies: Shellfish, Levaquin. The patient took concomitant medications. Patient received other medication in 2 weeks. Past drug history included: Levaquin, reaction(s): "Known allergies: Levaquin", notes: Known allergies: Shellfish, Levaquin. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: positive, notes: Treatment of COVID-19; negative, notes: positive Covid test after testing negative; positive, notes: positive Covid test after testing negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient received treatment from 11Jul2022 to 15Jul2022. Adverse event: Experiencing Rebound Covid and positive Covid test after testing negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Name: Covid-19 Test; Test Result: Negative ; Comments: positive Covid test after testing negative; Test Name: Covid-19 Test; Test Result: Positive ; Comments: positive Covid test after testing negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Bladder cancer; Blood pressure high; Shellfish allergy (Known allergies: Shellfish, Levaquin); Thrombocytosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2395778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: CA
Alter: 48,0
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: 02.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old male patient received BNT162b2 (BNT162B2), on 02Nov2021 as dose 2 (booster), single (Lot number: 32030BD) at the age of 48 years, in left arm for covid-19 immunisation; janssen coviD-19 vaccine (JANSSEN COVID-19 VACCINE), on 22Mar2021 as dose 1, single (Lot number: 1805020), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Pre-diabetes" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Known allergies: aspirin, reaction(s): "Known allergies: Aspirin", notes: Known allergies: Aspirin. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown Results, notes: Treatment of COVID-19; (Jul2022) positive, notes: Rebound infection. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient had not received any other medication in 2 weeks. Patient took Paxlovid from 12Jul2022 to 16Jul2022 as a treatment of COVID-19. Patient had Rebound infection on 20Jul2022 09:00 PM. Symptoms and positive test approx. 5 days after last dose. The patient also had known allergies of Aspirin and other medical history was pre-diabetes. Symptoms and positive test approx. 5 days after last dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19; Result Unstructured Data: Test Result:Unknown Results; Comments: Treatment of COVID-19; Test Date: 202207; Test Name: COVID 19; Test Result: Positive ; Comments: Rebound infection. Symptoms and positive test approx. 5 days after last dose.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pre-diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2395778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: CA
Alter: 48,0
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: 02.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old male patient received BNT162b2 (BNT162B2), on 02Nov2021 as dose 2 (booster), single (Lot number: 32030BD) at the age of 48 years, in left arm for covid-19 immunisation; janssen coviD-19 vaccine (JANSSEN COVID-19 VACCINE), on 22Mar2021 as dose 1, single (Lot number: 1805020), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Pre-diabetes" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Known allergies: aspirin, reaction(s): "Known allergies: Aspirin", notes: Known allergies: Aspirin. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown Results, notes: Treatment of COVID-19; (Jul2022) positive, notes: Rebound infection. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient had not received any other medication in 2 weeks. Patient took Paxlovid from 12Jul2022 to 16Jul2022 as a treatment of COVID-19. Patient had Rebound infection on 20Jul2022 09:00 PM. Symptoms and positive test approx. 5 days after last dose. The patient also had known allergies of Aspirin and other medical history was pre-diabetes. Symptoms and positive test approx. 5 days after last dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19; Result Unstructured Data: Test Result:Unknown Results; Comments: Treatment of COVID-19; Test Date: 202207; Test Name: COVID 19; Test Result: Positive ; Comments: Rebound infection. Symptoms and positive test approx. 5 days after last dose.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pre-diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2395009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: MI
Alter: 22,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 20.11.2021
Beginn: 25.07.2022
Tage bis Beginn: 247,0
Dosis: 2
Route/Site: UN / UN

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

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

Symptomtext

Breakthrough asymptomatic COVID infection. Tested positive 07/25/2022 as part of routine screening prior to admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: Positive SARS-COV-2 (COVID-19) collected 07/25/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2387446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 24.07.2022
Impfdatum: 30.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment.; COVID 19 Treatment; 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 male patient received BNT162b2 (BNT162B2), on 05Feb2021 as dose 1, single (Lot number: EL3247), on 26Feb2021 as dose 2, single (Lot number: EM9810) and on 30Oct2021 as dose 3 (booster), single (Lot number: 32030BD) for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ESCITALOPRAM; TRAZODONE. The following information was reported: VACCINATION FAILURE (medically significant), outcome "not recovered", described as "COVID 19 Treatment."; COVID-19 (medically significant), outcome "not recovered", described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Tested positive for COVID using at-home antigen tests on Day 5; Positive, notes: Tested positive for COVID using at-home antigen tests on Day10. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient had taken anti-viral treatment of drug Paxlovid from 05Jul2022 to 10July2022 for the treatment of covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: home antigen test; Test Result: Positive ; Comments: Tested positive for COVID using at-home antigen tests on Day 5; Test Name: home antigen test; Test Result: Positive ; Comments: Tested positive for COVID using at-home antigen tests on Day10
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ESCITALOPRAM; TRAZODONE
Allergien: -
Vorherige Impfungen: -

VAERS 2387399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 24.07.2022
Impfdatum: 27.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old male patient received BNT162b2 (BNT162B2), on 27Oct2021 at 12:00 as dose 3 (booster), single (Lot number: 32030BD) at the age of 48 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Diabetes Type 2" (unspecified if ongoing), notes: Other medical history: Diabetes Type 2. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown results, notes: 4 days after final dose of Paxlovid; (14Jul2022) Negative, notes: negative antigen test; (16Jul2022) Positive, notes: Positive test result 2 days after negative antigen test. Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: antigen test; Result Unstructured Data: Test Result:Unknown results; Comments: 4 days after final dose of Paxlovid; Test Date: 20220714; Test Name: antigen test; Test Result: Negative ; Comments: negative antigen test; Test Date: 20220716; Test Name: antigen test; Test Result: Positive ; Comments: Positive test result 2 days after negative antigen test
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type 2 diabetes mellitus (Other medical history: Diabetes Type 2)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2387207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030bd

gering

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 19.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 Vaccination failure

Symptomtext

COVID-19; COVID-19; 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 47-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Apr2021 as dose 1, single (Lot number: er8734), on 27Apr2021 as dose 2, single (Lot number: er8735) and on 19Nov2021 as dose 3 (booster), single (Lot number: 32030bd) at the age of 45 years for covid-19 immunisation. The patient's relevant medical history included: "Crohn's" (unspecified if ongoing), notes: other medical history: Crohn's. Concomitant medication(s) included: VITAMIN B12 [CYANOCOBALAMIN]; IRON; QVAR REDIHALER. Past drug history included: Flagyl, reaction(s): "known allergies: Flagyl", notes: known allergies: Flagyl. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information includes the patient received other medication in 2weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Crohn's (other medical history: Crohn's)
Andere Medikamente: VITAMIN B12 [CYANOCOBALAMIN]; IRON; QVAR REDIHALER
Allergien: -
Vorherige Impfungen: -

VAERS 2373851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 12,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 28.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 161,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 12,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 04.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 154,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: IM / LL

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 12,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 06.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 152,0
Dosis: 1
Route/Site: IM / RA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 04.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 154,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 13,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 13,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 04.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 154,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 15,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 15,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 16,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 06.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 152,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 16,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 04.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 154,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 16,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 04.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 154,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 16,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 04.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 154,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 17,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 17,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 28.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 161,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 18,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 04.01.2022
Beginn: 07.06.2022
Tage bis Beginn: 154,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 18,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: - / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 18,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 1
Route/Site: IM / RA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 19,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 28.12.2021
Beginn: 19.07.2022
Tage bis Beginn: 203,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 20,0
Geschlecht: U
Eingang: 19.07.2022
Impfdatum: 28.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 161,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

storage and handling error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2373767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 29.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 160,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

STORAGE+HANDLING ERROE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2356444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 03.07.2022
Impfdatum: 08.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old male patient received BNT162b2 (BNT162B2), on 08Nov2021 as dose 3 (booster), single (Lot number: 32030BD) at the age of 62 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Psoriatic arthropathy" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown result, notes: Covid rebound after Paxlovid treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown result; Comments: Covid rebound after Paxlovid treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Psoriatic arthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 22,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 37,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 55,0
Geschlecht: U
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 56,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327190

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 23,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327177

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 75,0
Geschlecht: U
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 41,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327148

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 45,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 34,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 55,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 29,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 63,0
Geschlecht: U
Eingang: 22.06.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 22,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 19,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 23,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 22.06.2022
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: unbekannt

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 30,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer >2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32030BD

gering

Staat: -
Alter: 23,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Stored in freezer > 2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -