VAERS Reports #EL3247

VAERS 2679453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: CO
Alter: 83,0
Geschlecht: F
Eingang: 05.09.2023
Impfdatum: 10.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 80,0
Dosis: UNK
Route/Site: IM / LA

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

Anticoagulant therapy Cerebral venous sinus thrombosis Cerebrovascular accident Death Haemorrhage intracranial Thrombectomy

Symptomtext

She developed signs of a CVA on or about May 6 following her vaccination series. In the hospital she was found to have a Cerebral Venous sinus thrombosis. She underwent intralumenal clot removal and was put on anti-coagulants. Her post operative course was complicated by further intracranial bleeding or clotting depending on how her coagulation status went. She slowly succumbed to these and was put on hospice after a week and sent home and passed away soon after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: rheumatoid arthritis seizure disorder
Andere Medikamente: Dilantin 300 mg/day
Allergien: none
Vorherige Impfungen: -

VAERS 2659318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 21.07.2023
Impfdatum: 25.02.2021
Beginn: 13.02.2023
Tage bis Beginn: 718,0
Dosis: 2
Route/Site: - / -

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

Death

Symptomtext

Patient deceased

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, Hyperlipidemia, atherosclerosis, Paroxysmal A-Fib and conduction system abnormality, Status post DDR with permanent pacemaker, herpetic neuralgia
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2651420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: SD
Alter: 57,0
Geschlecht: F
Eingang: 30.06.2023
Impfdatum: 29.04.2021
Beginn: 16.05.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / AR

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

Cardiac arrest Fatigue Laboratory test Sudden death Syncope

Symptomtext

She got tired the day before and on the 16th of May 2021 she suddenly collapsed and died immediately. She did not complain of chest pain her heart just stopped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: I don?t have them with me
Aktuelle Erkrankungen: Passed yearly physical exam
Vorgeschichte: -
Andere Medikamente: Omega oil Vitamin D3
Allergien: No
Vorherige Impfungen: -

VAERS 2616832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 51,0
Geschlecht: M
Eingang: 18.04.2023
Impfdatum: 10.02.2021
Beginn: 01.08.2022
Tage bis Beginn: 537,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Death Hypophagia Hypotension Metastatic neoplasm Sepsis Slow speech Treatment noncompliance

Symptomtext

pt had a positive COVID test on 8/10/22, 8/31/22, and 9/12/22; pt was brought from Center with low BP, slow speech, poor oral intake; pt has been missing HD due to weakness; at Center they did administer dexamethasone; at hospital, pt given inhalers, O2 supplementation; pt septic; CT of chest/abdomen/pelvis showed signs consistent with metastatic disease; did give empirical ABX; transitioned to hospice and pt passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: multiple myeloma, systolic CHF, atrial fibrillation-on anticoagulant, HTN, ESRD on HD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2612972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 80,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 24.09.2022
Beginn: 11.12.2022
Tage bis Beginn: 78,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Alanine aminotransferase increased Aspartate aminotransferase increased Blood creatinine increased Blood gases Blood urea increased C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Glomerular filtration rate decreased Hypertransaminasaemia Liver function test increased

Symptomtext

12/11/2022- Presents to ED, worsening SOB and cough. Afebrile. 02 mid 90's on 6L NCL (4L and cpap at HS baseline). Covid + test. CXR-b/l infiltrates . ABG 7.47/38/63/27 6L 02 via NC. Dexamethasone, hold remdesivir d/t elevated LFT's-AST 63 and ALT 66, transaminases 60's trending down. IV vanco and cefepime. Admit Acute on chronic hypoxemic respiratory failure b/l covid pna causing copd exacerbation. eGFR 27. WBC 15.8. AKI creat 2.4. BUN 87 . recently d/c 12/9 after 5 weeks stay COPD exacerbation and CAP. 12/12/-2022- cefepime d/c start meropenem. Pseudomonas. 12/19/2022-On 8L o2 via NC sat above 90's. IV decadron and meropenem. procalcitonin 0.10 and crp 1.3 d/c vanco. 12/27/2022- Transaminitis resolving, WBC 1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD on chronic 02 4L, CAD s/p CABG, AS s/p TAVR, OSA and CHF
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2563423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: KY
Alter: 76,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 02.02.2021
Beginn: 15.11.2022
Tage bis Beginn: 651,0
Dosis: UNK
Route/Site: IM / RA

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

Aspiration Atrial fibrillation COVID-19 Death Dyspnoea Pneumonia SARS-CoV-2 test positive

Symptomtext

Patient tested + for covid on 9-6-2022 and passed away 11-15-22. The medical records from hospital report he was admitted 11-12-22 with AFIB RVR and shortness of breath and suspected aspiration. Had pneumonia. This was two months after the covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: AFIB DIABETES DEMENTIA HYPERLIPIDEMIA, ANXIETY AND ANEMIA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2561965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: AZ
Alter: 79,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 27.09.2022
Beginn: 14.10.2022
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: SYR / LA

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

Amnesia Bradycardia Cerebral ischaemia Confusional state Dizziness Electrocardiogram abnormal Electroencephalogram Magnetic resonance imaging head abnormal Metamorphopsia Myocardial infarction Thalamic infarction Transient ischaemic attack Vision blurred

Symptomtext

Bivalent shot given on 9/27/2022. Suffered TIA on 10/14/2022 with Vision blurred and distorted, dizzy, confused, short term memory loss. Seen at Hospital the night of 10/14/2022 for Stroke protocol. EEG, MR without contrast. Seen by Dr on 11/21/2022 with slight light headed and short term memory loss. Vision appears to have returned to normal. MRI, EEG, Labs performed and reviewed by Dr. MRI impression: Moderate to severe chronic microvascular ischemic disease with small chronic infarct in the left thalamus. No preferential hippocampal volume loss. Symptoms of short term memory loss persists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: 10/14/22 EKG SINUS BRADYCARDIA WITH SINUS ARRHYTHMIA INFERIOR MYOCARDIAL INFARCTION, PROBABLY OLD WITH POSTERIOR EXTENSION Abnormal ECG Compared to ECG 09/02/2011 23:39:43 Myocardial at Neurology Care 11/21/22 EEG Awake and Drowsy MR - BRAIN WITHOUT CONTRAST W/NEUROQUANT W/3D RENDERING, At Diagnostic Radiology 12/2/22 MRI Brain without contrast and volumetric analysys (neuroguant/icobrain) Impression: Moderate to severe chronic microvascular ischemic disease with a small chromic infarct in the left thalamus. No preferential hippocampal volume loss. Doctor review finds short term memory loss remains.
Aktuelle Erkrankungen: no illiness
Vorgeschichte: High Blood Presssure, Anxiety, high coloresterol, over weight
Andere Medikamente: Alprazolam, Atenolol, Amlodipine, Benzapril, B12, Omega3, D3
Allergien: Sulfa, Loriditine, Zyrtec
Vorherige Impfungen: -

VAERS 2560828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: VA
Alter: 73,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 21.02.2021
Beginn: 05.04.2021
Tage bis Beginn: 43,0
Dosis: UNK
Route/Site: SYR / LA

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

Asthenia Cerebrovascular accident Magnetic resonance imaging Sensory loss

Symptomtext

A month after the injection I suffered a from a stoke. I woke up one morning and didn't have any feeling on my left side of my body. Until today I still feel weakness in my body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: MRI's
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2465440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MN
Alter: 70,0
Geschlecht: M
Eingang: 30.09.2022
Impfdatum: 29.10.2021
Beginn: 25.09.2022
Tage bis Beginn: 331,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy COVID-19 Chest pain Cough Deep vein thrombosis Pain in extremity Peripheral vein occlusion Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

Patient tested positive for COVID on 9/14 - he was experiencing some coughs but overall felt symptomatically improved. However on 9/24 he was seen in the ED for right leg pain and some chest pain. He tested positive again for COVID while in the ED. He was found to have an occlusive right femoral DVT with scattered pulmonary emboli. Patient was admitted from 9/24-9/25 for vascular consultation due to acute DVT. Per vascular surgery consult, the provider felt the right femoral DVT was likely secondary to COVID-19 infection. Patient was started on Eliquis at discharge. Additionally, he has received the COVID vaccine and one booster.

Weitere VAERSDATA-Felder

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

VAERS 2420179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: GA
Alter: 24,0
Geschlecht: F
Eingang: 25.08.2022
Impfdatum: 05.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

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

Arrhythmia Immunisation reaction Myocardial infarction

Symptomtext

I received my covid booster on 1/5/22, and on 1/14/22, I was in the hospital with symptoms of a heart attack. Since that time, I have been in and out of the hospital on several occasions with heart attack like symptoms, arrhythmias, and several cardiology visits. While during my first visit to the hospital, I had taken a CBD gummy to help me sleep which I later found out was not a CBD gumdid contain levels of THC in it. However, after talking with multiple cardiologists and other healthcare providers regarding the situation, they state that the heart issues I was experiencing would have to be stemming from the booster due to the timeline of symptoms and length of sympotomolgy ?continuation page

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: see continuation page.
Aktuelle Erkrankungen: none.
Vorgeschichte: PCOS, insulin resistance, endometriosis, pre-diabetes
Andere Medikamente: fiber pills, women's one a day multivitamin, yazmin .3m
Allergien: sulfa drugs, amoxicillon
Vorherige Impfungen: -

VAERS 2398039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: TX
Alter: 77,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 29.01.2021
Beginn: 22.07.2021
Tage bis Beginn: 174,0
Dosis: 2
Route/Site: SYR / -

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

Bradycardia COVID-19 Death Dyspnoea Endotracheal intubation Intensive care Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

Patient presented to the emergency room at the hospital the day of admission with complaints of shortness of breath. The patient was discovered to have an oxygen sat of 82% air. Initially the patient had improvement with supplemental oxygen in the ER. The patient did test positive for COVID-19.He was admitted to the critical care unit and initiated on IV antibiotics, dexamethasone, Remdesivir, the convalescent plasma as well as supplemental vitamin therapy. The patient was noted to be bradycardic and Cardiology was consulted and followed along. The patient was initially stabilized on 100% non-rebreather and subsequently placed on Vapotherm at 85% Fi02. He was then placed on continuous BiPAP. He subsequently had to be intubated on the night of 08/06. Patient expired on 09/02/2021.

Weitere VAERSDATA-Felder

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

VAERS 2359522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 18.12.2021
Beginn: 29.06.2022
Tage bis Beginn: 193,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure Atrial fibrillation COVID-19 COVID-19 pneumonia Fall Rib fracture SARS-CoV-2 test positive Thoracic vertebral fracture

Symptomtext

Provider summary "84 YO male with history of hypertension, Alzheimer's, BPH, recent diagnosis of atrial fibrillation presented to the hospital after fall from stairs Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) found to have COVID pneumonia, acute respiratory failure overnight, has acute T2 fracture and nondisplaced left rib 5th and 7th fractures, had AFib with RVR"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: Positive COVID PCR 6/29/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Closed wedge compression fracture of T2 vertebra 6/29/2022 HYPERTENSION, BENIGN ESSENTIAL (401.1) Unknown INJURY NOS, CHEST WALL (959.11) Unknown Sensorineural hearing loss, asymmetrical (Chronic) 10/19/2012 Closed fracture of multiple ribs of left side 6/29/2022 Alzheimer's dementia 6/30/2022 COVID-19 6/29/2022
Andere Medikamente: amoxicillin/potassium clav 875-125 mg 875 mg Oral 2 times daily benzonatate 100 mg Oral 3 TIMES DAILY PRN calcium carbonate 1,000 mg Oral EVERY 8 HOURS PRN dexamethasone 4 mg Oral DAILY WITH BREAKFAST diltiazem HCl 60 mg Oral 2 times da
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1454673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NC
Alter: -
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Anaphylactic shock Balance disorder Dizziness Dysstasia Electrocardiogram Rash Rash pruritic Speech disorder Urine analysis Urticaria

Symptomtext

This is a spontaneous report received from a contactable reporter (Consumer or other non HCP) from medical information team. The reporter is the patient. A 78-year-old female patient received BNT162b2 (Pfizer-BioNTech COVID-19), as dose 1, single (Batch/Lot number: unknown) for Covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Glycol, reaction(s): "she is allergic to "something something glycol", notes: Caller says she learned she is allergic to "something something glycol". The following information was reported: ANAPHYLACTIC SHOCK (hospitalization, medically significant), outcome "unknown", described as "hospitalized for anaphylaxis shock". Patient reports having anaphylaxis shock after the first dose of the Pfizer Covid-19 vaccine, hospitalized 42 hours after administration. 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: Anaphylactic shock
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2189979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 03.02.2021
Beginn: 12.03.2022
Tage bis Beginn: 402,0
Dosis: 2
Route/Site: - / -

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

Angiogram Angiogram pulmonary abnormal Back pain COVID-19 Cardio-respiratory arrest Catheterisation cardiac abnormal Chest discomfort Chest pain Computerised tomogram abdomen Coronary arterial stent insertion Death Dyspnoea Echocardiogram abnormal Ejection fraction decreased Electrocardiogram normal Full blood count abnormal Hyperchloraemia Hyperglycaemia

Symptomtext

Patient who completed initial course of Pfizer COVID vaccines, last dose 02/03/21, who tested detected for COVID upon admission for chest pain. Provider discharge note below: "79 year-old female with past medical history of anemia, PMR, and hypertension who presented to emergency department via EMS on 3/4 for chest pain. Her symptoms started hours prior to arrival. Her pain was described as pressure-like substernal pain with radiation to her back. Associated symptoms included shortness of breath and diaphoresis. Palliating factors included nitro and ASA. Initial vitals notable for hypertension, otherwise normal. She received Zofran for nausea and fentanyl for pain. CBC demonstrated leukocytosis with left shift. She had mild hyperglycemia and hyperchloremia on CMP. Troponin was elevated at 111, with significant positive delta troponin of 334. EKG demonstrated no acute changes. Echo demonstrated EF: 45%, apical hypokinesis and RVSP: 32 mmHg. CTA C/A/P demonstrated small pericardial effusion. Cardiology was consulted and the patient subsequently underwent left heart cath with placement of DES. On 3/12, code blue was called on the patient. CPR was performed. Contacted family and they arrived at bedside, they requested to discontinue CPR and pt did not have pulse at the end of CPR. Pt passed away on 3/12/22."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: COVID detected PCR on 03/04/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Normocytic normochromic anemia Primary hypertension PMR (polymyalgia rheumatica) (*) GERD (gastroesophageal reflux disease) Ascending aortic aneurysm (*) Atrial fibrillation with rapid ventricular response (*)
Andere Medikamente: Fosamax Excedrin B12 Vasotec Xalatan
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2161718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 03.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: - / LA

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

Cerebrovascular accident Computerised tomogram Echocardiogram Investigation Magnetic resonance imaging head

Symptomtext

Right thalamic stroke; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 57 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Feb2021 (Lot number: EL3247) at the age of 57 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Heart murmur" (unspecified if ongoing); "Environmental allergies" (unspecified if ongoing); "Allergic to Penicillin" (unspecified if ongoing); "dyslipidemia" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "Bronchial asthma" (unspecified if ongoing); "COVID 19" (unspecified if ongoing), notes: recently recovered. There were no concomitant medications. Vaccination history included: Bnt162b2 (Vaccine Name: First dose, Lot Number / Expiry Date: EL0140/ Unknown , ), administration date: 13Jan2021, when the patient was 57 years old, for COVID-19 immunization. The following information was reported: CEREBROVASCULAR ACCIDENT (hospitalization) with onset 11Feb2021, outcome "unknown", described as "Right thalamic stroke". The patient was hospitalized for cerebrovascular accident (start date: 11Feb2021, discharge date: 15Feb2021, hospitalization duration: 5 days). The event "right thalamic stroke" was evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: computerised tomogram: (11Feb2021) unknown result; echocardiogram: (11Feb2021) unknown result; (11Feb2021) unknown result; investigation: (11Feb2021) unknown results; magnetic resonance imaging head: (11Feb2021) unknown result. Therapeutic measures were taken as a result of cerebrovascular accident. The caller found the note the Cardiologist had written and it said "female with a past medical history of dyslipidemia and hypertension presented with a right thalamic stroke with symptoms of gait instability and slurred speech thought to be related to small vessel disease. Follow up information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 5,0
Labordaten: Test Date: 20210211; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210211; Test Name: TEE; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210211; Test Name: TTE with bubble study; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210211; Test Name: H/N; Result Unstructured Data: Test Result:unknown results; Test Date: 20210211; Test Name: MRI brain; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bronchial asthma; COVID-19 (recently recovered.); Dyslipidemia; Environmental allergy; Heart murmur; Hypertension; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2157877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: TN
Alter: 92,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 30.01.2021
Beginn: 22.02.2022
Tage bis Beginn: 388,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Fully vaccinated with Pfizer x 2. Tested positive for COVID 19 on 2/22/2022. Admitted to Hospital on 02/17/2022. Expired on 03/02/2022 while still hospitalized.

Weitere VAERSDATA-Felder

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

VAERS 2098641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: TX
Alter: 83,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 04.02.2021
Beginn: 30.01.2022
Tage bis Beginn: 360,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Cough Death Dyspnoea Fatigue Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/14/2021 and 2/4/2021. Telehealth visit 1/21/2022 c/o sore throat and persistent cough, declined COVID testing, given prescriptions for azithromycin and guaifenesin AC syrup. Presented to ED 1/30/2022 c/o of SOB, fatigue, fever and positive home COVID test on 1/24/2022. On presentation respiratory rate of 24 with an SpO2 of 81%. Admitted for acute hypoxic resp failure 2/2 Covid PNA. Treated with methylprednisolone, tocilizumab, and Max HF of 60L 95% FiO2 with O2 sat down to 86%. 2/4/2022 expressed desire to cease all Covid treatment, remove HFNC, w/comfort measures only. Expired 2/5/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Positive COVID-19 on 1/30/2022 using the BioFire FilmArray
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Myasthenia gravis in remission after thymectomy, hx of right hemidiaphragm paralysis due to phrenic nerve damage from previous right lower lobectomy, Sleep Apnea, BPH.
Andere Medikamente: Atorvastatin, Colestipol, Guaifenesin with codeine, Tamsulosin, Trazodone.
Allergien: Ciprofloxacin, Penicillin, Grass Pollen
Vorherige Impfungen: -

VAERS 2095737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: CO
Alter: 70,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 25.02.2021
Beginn: 29.01.2022
Tage bis Beginn: 338,0
Dosis: 1
Route/Site: IM / UN

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chills Cough Death Diarrhoea Dyspnoea Fatigue Oxygen saturation decreased Pain SARS-CoV-2 test positive

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 2/4/2021 and 2/25/2021. Presented to ED 1/29/2022 with complaints of increased shortness of breath, cough, chills, fatigue, aches, and diarrhea. Home O2 @2-3L NC. Provided IVF and increased prednisone dose, patient stated feeling better and agrees to discharge. Returned to ED on 1/30/2022 with increased SOB. Admitted for acute hypoxemic resp failure 2/2 Covid PNA. Increasing O2 requirement while on HFNC, and despite aggressive measures she began to desat even while maxed out on O2. She did not wish to be intubated. Expired 2/4/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: COVID-19 positive on 1/29/2022 using the Biofire Torch system
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, Severe Pulmonary fibrosis, Rheumatoid arthritis, hypothyroidism
Andere Medikamente: Atorvastatin, Cholecalciferol, Coenzyme Q-10, Levothyroxine, Loratidine, Metformin, Mycophenolate, Omeprazole, Prednisone.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2091252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 32,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 25.02.2021
Beginn: 17.01.2022
Tage bis Beginn: 326,0
Dosis: 2
Route/Site: - / -

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

Cerebrovascular accident Fatigue Hyperammonaemia Retinal neovascularisation SARS-CoV-2 test SARS-CoV-2 test positive Vaccination failure

Symptomtext

PCR test next day positive; PCR test next day positive; thought I was having a stroke; NVD; HA; Killer fatigue; A 32 year-old male patient received bnt162b2 (BNT162B2), administration date 25Feb2021 (Lot number: EL3247) at the age of 32 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 (Lot number: EL3247, dose number=1), administration date: 05Feb2021, when the patient was 31 years old, for Covid-19 Immunization. The following information was reported: VACCINATION FAILURE (medically significant) with onset 18Jan2022, outcome "unknown", SARS-COV-2 TEST POSITIVE (medically significant) with onset 18Jan2022, outcome "recovering" and all described as "PCR test next day positive"; CEREBROVASCULAR ACCIDENT (medically significant) with onset 17Jan2022, outcome "recovering", described as "thought I was having a stroke"; RETINAL NEOVASCULARISATION (medically significant) with onset 17Jan2022, outcome "recovering", described as "NVD"; HYPERAMMONAEMIA (non-serious) with onset 17Jan2022, outcome "recovering", described as "HA"; FATIGUE (non-serious) with onset 17Jan2022, outcome "recovering", described as "Killer fatigue". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (18Jan2022) positive, notes: Nasal Swab. It was unknown if therapeutic measures were taken as a result of sars-cov-2 test positive, cerebrovascular accident, retinal neovascularisation, hyperammonaemia, fatigue. It was reported that severe symptoms 17Jan2022 after work NVD and "killer fatigue and HA". Patient thought was having a stroke" had a PCR test next day positive. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the known safety profile and Limited information in the case report a casual association between the LOE events, Cerebrovascular accident, Retinal neovascularization, Hyperammonemia, Fatigue the suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Test Date: 20220118; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1390953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MD
Alter: 72,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 25.02.2021
Beginn: 05.03.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: - / -

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

Activated partial thromboplastin time Alanine aminotransferase Anion gap decreased Aspartate aminotransferase Bilirubin conjugated Back pain Brain death Cerebral haemorrhage Computerised tomogram abdomen Computerised tomogram head Blood albumin Blood alkaline phosphatase Blood bilirubin Blood calcium Blood chloride Blood creatinine Blood fibrinogen Blood glucose

Symptomtext

TTP; brain hemorrhage; This is a spontaneous report received from a contactable reporter (Physician). A 72-year-old male patient received bnt162b2 (BNT162B2), administration date 25Feb2021 (Batch/Lot number: unknown) at the age of 72 years as dose 1, single for COVID-19 immunization. Relevant medical history included: "CAD" (unspecified if ongoing), notes: ICD CABG; "Vitamin D deficiency" (unspecified if ongoing), notes: Vitamin D deficiency; "BPH" (unspecified if ongoing), notes: BPH; "hyperlipidemia" (unspecified if ongoing), notes: hyperlipidemia; "Allergies" (unspecified if ongoing), notes: Allergies; "ICD", start date: 2013 (unspecified if ongoing), notes: ICD; "CABG", start date: 2013 (unspecified if ongoing), notes: CABG; "Former smoker" (unspecified if ongoing). Concomitant medications included: ASPIRIN [ACETYLSALICYLIC ACID] taken for coronary artery disease (ongoing); ATORVASTATIN taken for coronary artery disease, hyperlipidaemia (ongoing); METOPROLOL taken for coronary artery disease (ongoing); CHOLECALCIFEROL taken for vitamin D deficiency (ongoing). Vaccination history included: Tdap (Tdap> 7 years, 12:00:00 AM), administration date: 22Feb2021, for Immunization; Influenza (Influenza, seasonal, high dose, 12:00:00 AM), administration date: 26Nov2014, for Immunization; Fluzone high dose (Fluzone High Dose, 04:56:22 PM), administration date: 13Dec2018, for Immunization; Fluzone high dose (Fluzone High Dose, 04:31:22 PM), administration date: 08Nov2017, for Immunization; Pneumo (Pneumo (3 years older) 12:00:00 AM), administration date: 01Jan2015, for Immunization. The following information was reported: THROMBOTIC THROMBOCYTOPENIC PURPURA (death, hospitalization, life threatening, medically significant) with onset 05Mar2021, outcome "fatal", described as "TTP"; CEREBRAL HAEMORRHAGE (death, hospitalization, life threatening, medically significant) with onset 05Mar2021, outcome "fatal", described as "brain hemorrhage". The events "TTP" and "brain hemorrhage" were evaluated at the physician office visit and emergency room visit. Patient was a 72-year-old man with a history of a CABG and ICD who administered to the ICU for possible TTP. He presented to the ED because of dark stools. HC recently had back pain for which he took NSAIDS. He then noted bruising over his arms and legs and had an episode of dark stool. In the ED, he had a temperature of 38.2, hemoglobin of 9.0 and a platelet count of 11000. Hematology reviewed his smear and saw a few schistocytes, and is concerned about TTP. They have recommended plasmapheresis. Per patient, he had intermittent low back pain for which he took 1 dose of Motrin and 5 doses of Aleve over 1 week with some relief. Upon stopping pain medication, the patient had noted scattered bruises over his arms and legs. He also reportedly had one episode of black stools on 03May2021, He visited his PCP who performed focal occult and was reportedly positive. No prior history of endoscopy or peptic ulcer disease. Had a colonoscopy more than 10 years ago that was reportedly negative. He had cold-like symptoms with rhinorrhea 1 month ago but without cough, fever or chills, or diarrhea. No other new medications or changes to diet. No recent nosebleed, hematuria or mouth bleeding. On arrival in the ED, patient was noted to be febrile T-max 38.2, tachycardia, saturating at 97% on room air. Labs were significant for anemia hemoglobin 9.0, hematocrit 25.6 [baseline hemoglobin 14.3, HCT 43.9 in Nov2020] and thrombocytopenia PLT 11K [81K in Nov2020) Low fibrinogen 174 and low haptoglobin Hematology was consulted by ED, suggested further lab work-up, no acute indication for platelet transfusion. CT Gl bleed Was negative but did show moderate to large stool burden consistent with constipation. He was given 1 dose of ceftriaxone and 1 dose of IV pantoprazole. No passage of black stools in ED. Plan for CV: Continue beta-blocker. Hold aspirin. For GI: Continue PPI twice daily. Follow hemoglobin, LFTs. For ID: Fever likely from TTP, doubt acute infection-follow. Hemo: per hematology, will start plasmapheresis and prednisone. Check Adam 13 antibody. This patient is critical with a high probability of imminent or life threatening deterioration. Critical Care Time was 40 minutes. The patient underwent the following laboratory tests and procedures: activated partial thromboplastin time: (03May2021) 37.4 seconds, notes: HI; alanine aminotransferase: (03May2021) 36, notes: Unit/L; anion gap decreased: (03May2021) 6 mmol/L, notes: LOW; aspartate aminotransferase: (03May2021) 108, notes: Unit/L, HI; bilirubin conjugated: (03May2021) 0.40 mg/dl, notes: HI; blood albumin: (03May2021) 3.7 g/dl; blood alkaline phosphatase: (03May2021) 230, notes: unit/L, HI; blood bilirubin: (03May2021) 2.30 mg/dl, notes: HI; blood calcium: (03May2021) 8 .4 mg/dl, notes: LOW; blood chloride: (03May2021) 104 mmol/L; blood creatinine: (03May2021) 0.67 mg/dl; blood fibrinogen: (03May2021) 174 mg/dl, notes: LOW; blood glucose: (03May2021) 104 mg/dl, notes: HI; blood lactate dehydrogenase: (03May2021) 1062 uL, notes: HI; blood potassium: (03May2021) 3.8 mmol/L; blood pressure diastolic: (03May2021) 68 mmHg; blood pressure systolic: (03May2021) 134 mmHg; blood urea: (03May2021) 21 mg/dl, notes: HI; carbon dioxide: (03May2021) 25.4 mmol/L; chest x-ray: (03May2021) lungs clear; computerised tomogram: (03May2021) negative; fibrin d dimer: (03May2021) 20.00 mg/l, notes: FEU; haematocrit: (03May2021) 21.2 %, notes: low; haemoglobin: (03May2021) 7.5 g/dl, notes: LOW; haptoglobin: (03May2021) 20 mg/dl, notes: Low; heart rate: (03May2021) 98, notes: Bpm; investigation: (03May2021) 3.0/100 wbc, notes: HI; (03May2021) negative; mean cell haemoglobin: (03May2021) 30.9, notes: PG; mean cell haemoglobin concentration: (03May2021) 35.4 g/dl; mean cell volume: (03May2021) 87.2, notes: FL; oxygen saturation: (03May2021) unknown results; platelet count: (03May2021) 10, notes: K/MM3; protein total decreased: (03May2021) 5.8 g/dl, notes: LOW; prothrombin time: (03May2021) 18.1 seconds, notes: HI; red blood cell count: (03May2021) 2.43, notes: M/MM3, Low; (03May2021) 2.43, notes: M/MM3, LOW; red cell distribution width increased: (03May2021) 13.9 %; sars-cov-2 test: (03May2021) negative; (03May2021) negative; smear test: (03May2021) clumps absent; white blood cell count: (03May2021) 9.74; haemoglobin: (unspecified date) 9.0; (unspecified date) 11000; body temperature: (unspecified date) 38.2; (unspecified date) concerned about ttp, notes: saw a few schistocytes, and is concerned about TTP. Therapeutic measures were taken as a result of thrombotic thrombocytopenic purpura, cerebral haemorrhage. The patient date of death was 05May2021. The reported cause of death was thrombotic thrombocytopenic purpura, cerebral haemorrhage. It was not reported if an autopsy was performed. The lot number for bnt162b2 was not provided and will be requested during follow up.; 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 thrombotic thrombocytopenic purpura, cerebral haemorrhage 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; Reported Cause(s) of Death: TTP; brain hemorrhage

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain death
Hospital-Tage: -
Labordaten: Test Date: 20210503; Test Name: APTT; Test Result: 37.4 s; Comments: HI; Test Date: 20210503; Test Name: ALT; Result Unstructured Data: Test Result:36; Comments: Unit/L; Test Date: 20210503; Test Name: Anion Gap; Result Unstructured Data: Test Result:6 mmol/L; Comments: LOW; Test Date: 20210503; Test Name: AST; Result Unstructured Data: Test Result:108; Comments: Unit/L, HI; Test Date: 20210503; Test Name: Direct Bilirubin; Test Result: 0.40 mg/dl; Comments: HI; Test Date: 20210503; Test Name: Albumin; Result Unstructured Data: Test Result:3.7 g/dl; Test Date: 20210503; Test Name: Alk Phos; Result Unstructured Data: Test Result:230; Comments: unit/L, HI; Test Date: 20210503; Test Name: Total bilirubin; Test Result: 2.30 mg/dl; Comments: HI; Test Date: 20210503; Test Name: Calcium; Test Result: 8.4 mg/dl; Comments: LOW; Test Date: 20210503; Test Name: Chloride; Result Unstructured Data: Test Result:104 mmol/L; Test Date: 20210503; Test Name: CREATININE; Test Result: 0.67 mg/dl; Test Date: 20210503; Test Name: Fibrinogen; Test Result: 174 mg/dl; Comments: LOW; Test Date: 20210503; Test Name: Glucose; Test Result: 104 mg/dl; Comments: HI; Test Date: 20210503; Test Name: LDH; Test Result: 1062 uL; Comments: HI; Test Date: 20210503; Test Name: Potassium; Result Unstructured Data: Test Result:3.8 mmol/L; Test Date: 20210503; Test Name: Automatic Cuff diastolic; Result Unstructured Data: Test Result:68 mmHg; Test Date: 20210503; Test Name: Automatic Cuff Systolic; Result Unstructured Data: Test Result:134 mmHg; Test Date: 20210503; Test Name: Blood urea Nitrogen; Test Result: 21 mg/dl; Comments: HI; Test Name: temperature; Result Unstructured Data: Test Result:38.2; Test Date: 20210503; Test Name: carbon dioxide; Result Unstructured Data: Test Result:25.4 mmol/L; Test Date: 20210503; Test Name: Chest x-ray; Result Unstructured Data: Test Result:Lungs clear; Test Date: 20210503; Test Name: CT; Test Result: Negative ; Test Date: 20210503; Test Name: D-Dimer; Result Unstructured Data: Test Result:20.00 mg/l; Comments: FEU; Test Date: 20210503; Test Name: Hematocrit; Test Result: 21.2 %; Comments: low; Test Name: hemoglobin; Result Unstructured Data: Test Result:9.0; Test Date: 20210503; Test Name: Hemoglobin; Result Unstructured Data: Test Result:7.5 g/dl; Comments: LOW; Test Date: 20210503; Test Name: Haptoglobin; Test Result: 20 mg/dl; Comments: Low; Test Date: 20210503; Test Name: Peripheral Pulse Rate; Result Unstructured Data: Test Result:98; Comments: Bpm; Test Date: 20210503; Test Name: Auto "NRBC; Result Unstructured Data: Test Result:3.0/100 WBC; Comments: HI; Test Date: 20210503; Test Name: GI bleed; Test Result: Negative ; Test Date: 20210503; Test Name: MCH; Result Unstructured Data: Test Result:30.9; Comments: PG; Test Date: 20210503; Test Name: MCHC; Result Unstructured Data: Test Result:35.4 g/dl; Test Date: 20210503; Test Name: MCV; Result Unstructured Data: Test Result:87.2; Comments: FL; Test Date: 20210503; Test Name: Oxygen Saturation; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210503; Test Name: Platelet; Result Unstructured Data: Test Result:10; Comments: K/MM3; Test Name: platelet count; Result Unstructured Data: Test Result:11000; Test Date: 20210503; Test Name: Total protein; Result Unstructured Data: Test Result:5.8 g/dl; Comments: LOW; Test Date: 20210503; Test Name: Prothrombin time; Test Result: 18.1 s; Comments: HI; Test Date: 20210503; Test Name: RBC; Result Unstructured Data: Test Result:2.43; Comments: M/MM3, Low; Test Date: 20210503; Test Name: Red blood cell; Result Unstructured Data: Test Result:2.43; Comments: M/MM3, LOW; Test Date: 20210503; Test Name: RDW; Test Result: 13.9 %; Test Date: 20210503; Test Name: COVID-19 antigen; Test Result: Negative ; Test Date: 20210503; Test Name: COVID-19 Antigen; Test Result: Negative ; Test Date: 20210503; Test Name: Platelet Citrate Smear Review Pit; Result Unstructured Data: Test Result:clumps absent; Test Name: smear; Result Unstructured Data: Test Result:concerned about TTP; Comments: saw a few schistocytes, and is concerned about TTP; Test Date: 20210503; Test Name: WBC; Result Unstructured Data: Test Result:9.74
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Allergies); BPH; CABG; Coronary artery disease (ICD CABG); Hyperlipidemia; Implantable cardioverter defibrillator insertion (ICD); Smoker; Vitamin D deficiency
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]; ATORVASTATIN; METOPROLOL; CHOLECALCIFEROL
Allergien: -
Vorherige Impfungen: -

VAERS 2068790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MN
Alter: 86,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 01.10.2021
Beginn: 26.01.2022
Tage bis Beginn: 117,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure COVID-19 pneumonia

Symptomtext

Patient admitted to Hospital on 1/26/22 with COVID pneumoia and acute respiratory failure after 3 doses of Pfizer COVID vaccine on 10/1/21, 2/22/21, and 2/1/21

Weitere VAERSDATA-Felder

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

VAERS 2024674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: TN
Alter: 92,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 04.02.2021
Beginn: 20.08.2021
Tage bis Beginn: 197,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Fully vaccinated with covid vaccine (pfizer). Tested positive for Covid 19 on 8/20/2021 and expired on 8/26/2021.

Weitere VAERSDATA-Felder

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

VAERS 2021455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MN
Alter: 86,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 15.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 82,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 1/27, 2/17, 10/15/21 Tested positive for COVID by PCR on 1/5/22 Hospitalized 1/5-1/10 for multiple subsegmental pulmonary embolism, COVID 19 infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 02.02.2021
Beginn: 12.08.2021
Tage bis Beginn: 191,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Confusional state Death Hypoxia Pyrexia SARS-CoV-2 test positive Sepsis

Symptomtext

pt was seen at PCP's office and was positive for COVID; came to ED with c/o fever and confusion; diagnosed with acute hypoxia, and sepsis secondary to COVID; was treated with supplemental O2, antibiotics, remdesivir, decadron, and vitamin supplementation; pt's status improved and he was dc'd to home; pt's condition worsened at home and he was brought back to ER; per death certificate, pt died in the ER

Weitere VAERSDATA-Felder

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

VAERS 2010477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 01.02.2021
Beginn: 13.10.2021
Tage bis Beginn: 254,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cardiomegaly Chronic kidney disease Condition aggravated Death Dyspnoea Endotracheal intubation Mechanical ventilation Multiple organ dysfunction syndrome Pneumonia Productive cough Respiratory disorder SARS-CoV-2 test positive Sputum discoloured Urinary tract infection

Symptomtext

diagnosed positive for COVID on 10/13/21; to hosp with increasing SOB and O2 sats in the 70s on 2L O2 via NC; coughing up yellow sputum; placed on NRB mask; cardiomegaly, chronic renal failure, UTI, suspected pneumonia; started on antibiotics; required intubation with mechanical ventilation due to worsening respiratory status; multiorgan failure; DNR; family withdrew care; comfort measure; pt extubated and died in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: obesity, OSA, chronic HRF, COPD, chronic renal failure
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2496127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 21.01.2021
Beginn: 16.02.2021
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: IM / RA

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

Death Fall Haematoma Rhabdomyolysis

Symptomtext

Narrative: Patient was not previously Covid positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. Patient was admitted on 2/4/21 with rhabdomyolysis and a hematoma after a a fall. Details surrounding his death on 2/16/21 uncertain due to admission at non-facility. Comorbidities include CHF, anemia, history of stroke, traumatic brain injury, and aortic aneurysm.

Weitere VAERSDATA-Felder

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

VAERS 1981343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 26.12.2021
Impfdatum: 24.02.2021
Beginn: 28.07.2021
Tage bis Beginn: 154,0
Dosis: 1
Route/Site: SYR / RA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Numbness, lathargic, Tingling
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1933021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: IL
Alter: 87,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 01.03.2021
Beginn: 04.11.2021
Tage bis Beginn: 248,0
Dosis: 1
Route/Site: IM / -

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

Anticoagulant therapy Pulmonary embolism Respiratory tract congestion

Symptomtext

Congestion for 2 weeks, came to ER, Dx with bilateral PE's, started on Heparin drip, discharged home 11/20/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN Dementia Complete heart block
Andere Medikamente: -
Allergien: Diclofenac, HMG-CoA-R inhibitors, Metronidazole, Rofecoxib, statins, Tizanidine, Tramadol
Vorherige Impfungen: -

VAERS 2567412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 12.01.2021
Beginn: 16.08.2021
Tage bis Beginn: 216,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Death Hypoxia Pyrexia Respiratory failure SARS-CoV-2 test positive Sepsis Urinary tract infection

Symptomtext

Narrative: Patient received the two doses of COVID 19 Vaccine in Jan/Feb 2021. The patient tested positive on 15 August 2021 and was admitted to the hospital with fever, hypoxia, and COVID 19 pneumonia. The patient died due complications of covid 19 (sepsis, respiratory failure, and urinary tract infection, and COVID pneumonia). The EUA for the vaccine requires that all patients testing positive for COVID 19 and requiring hospitalization or death is reported.

Weitere VAERSDATA-Felder

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

VAERS 2570403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 02.02.2021
Beginn: 16.10.2021
Tage bis Beginn: 256,0
Dosis: 2
Route/Site: IM / RA

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

Cardiac arrest Death

Symptomtext

Narrative: Not reporting a reaction to the vaccine. Reporting VAER as required for pt who received COVID vaccine and passed away some time after receiving the vaccine. Pt passed away months after receiving COVID vaccine d/t other causes (likely cardiac arrest per report).

Weitere VAERSDATA-Felder

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

VAERS 1850346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 91,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 17.02.2021
Beginn: 11.10.2021
Tage bis Beginn: 236,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Acute myocardial infarction Death

Symptomtext

death I21.4 - Non-ST elevation (NSTEMI) myocardial infarction N17.9 - Acute kidney failure, unspecified

Weitere VAERSDATA-Felder

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

VAERS 2599942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 29.01.2021
Beginn: 08.08.2021
Tage bis Beginn: 191,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Blood bicarbonate decreased Blood fibrinogen Blood gases abnormal Blood pH normal Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiac failure congestive Chest X-ray abnormal Dyspnoea Exposure to SARS-CoV-2 Fibrin D dimer International normalised ratio increased PCO2 decreased PO2 decreased Pneumonia Procalcitonin

Symptomtext

Narrative: COVID infection following COVID vaccine serious 01/08, Pfizer, dose #1 01/29 Pfizer, dose #2 08/08 pt cc: fever, rhinorrhea, dyspnea exposure: GOLFING PARTNER 08/09 -- 0902 pt symptoms continue 08/16 COVID swab, result: detected 08/16 CXR impression: CHF versus hazy infiltrates most prominent in the LEFT lower lung. Correlate with clinical scenario. Follow-up recommended. 08/16 pt admit to ED, admit to medicine Cc: SOB dx: ACUTE HYPOIX RESPIRATOR FAILURE 2/2 COVID PNEUMONIA LOS: 14 days 08/16 Troponin I result: <0.016 08/16 PROCALCITONIN result <0.11 08/16 ESR result: 26 08/16 BNP Result: 672 08/16 ABG: I-[H 7.42, iPCO2 28.3, i-PO2 62, i-HCO3 18.2 08/16 DDIMER results: 0.97 08/21 ESR result: 24 08/21 Fibrinogen result: 308 08/21 DDIMER result: 30.29 08/23 PT result: 47.1 08/23 INR Result: 4.21 08/23 DDIMER result: 17.82 08/23 FIBRINOGEN result: 245 08/23 ESR Result: 16 08/24 PT result: 38.1 08/24 INR Result: 3.40 08/24 DDIMER Result: 15.52 08/25 PT Result: 25.2 08/25 DIIMER result: 7.59 08/26 PT Result 24.0 08/26 INR Result 2.14 08/26 DDIMER result 14.096

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 08/16 troponin I result: <0.016 08/16 PROCLACITONIN result <0.11 08/16 ESR result: 26 08/16 BNP result: 67.2 08/16 ABG: I-pH 7.42, i-PCO2 28.3, i-PC2 62, i-HCO3 18.2 08/16 DDIMER result; 0.97 08/21 ESR result: 0.97 08/21 ESR result: 24 08/21 Fibrinogen result: 308 08/21 DDIMER result: 30.29 08/23 PT Result: 47.1 08/23 INR result: 4.21 08/23 DDIMER result: 17.82 08/23 FIBRINOGEN result: 245 08/23 ESR result: 16 08/24 PT Result: 38.1 08/24 INR result: 3.40 08/24 DDIMER result: 15.52 08/25 PT result: 25.2 08/25 INR result: 2.25 08/25 DDIMER result: 7.59 08/26 PT result: 24.0 08/26 INR result: 2.14 08/26 DDIMER result: 14.096
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2601552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 01.02.2021
Beginn: 28.07.2021
Tage bis Beginn: 177,0
Dosis: 2
Route/Site: IM / LA

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

Alanine aminotransferase increased Aortic dilatation Aspartate aminotransferase increased Asthenia Atypical pneumonia Blood bicarbonate normal Blood fibrinogen normal Blood gases abnormal Blood pH normal Brain natriuretic peptide increased C-reactive protein normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest pain Computerised tomogram thorax abnormal Cough Death

Symptomtext

Narrative: COVID infection following COVID vaccine series 01/16, Pfizer, dose #1 02/06, Pfizer, dose #2 07/28 pt wife called cc: chest pain, cough, dyspnea, weakness. SOB, headache 08/04 COVID swab, result: detected 08/04 hospitalized dx. PNA 08/04 CXR impression: Bilateral pneumonia. 08/05 CXR impression: Persistent mixed interstitial and patchy airspace opacities in the mid and lower lungs bilaterally not significantly changed. Findings with patient's known history of COVID pneumonia. 08/09 Fungitell result <31 08/09 CXR impression: Stable chest radiograph since 4 days ago as above. 08/10 Tacrolimus result: 7.4 08/10 ESR 12 8/10 Fibrinogen/ DDIMER results: 261/ 1.11 8/10 CXR impression: Similar groundglass and interstitial opacities in the lungs, consistent with atypical pneumonia. 08/11 ESR 8 08/11 Fibrinogen/ DDIMER result: 230/ 0.99 08/11 CXR impression: Similar appearance of bilateral lung opacities. 08/12 ESR result: 6 08/12 Fibrinogen/ DDIMER result: 203/ 1.11 08/13 ESR result: 7 08/13 Fibrinogen/ DDIMER result: 216/ 1.16 08/14 Fungitel result: <31 08/14 ESR result: 12 08/14 Fibrinogen/ DDIMER result: 207/ 1.37 08/14 Procalcitonin result: 0.07 08/14 CXR impression: Underinflated lungs. Interval increase in bilateral opacities accentuated by differences in technique. 08/15 ESR result: 13 08/15 Fibrinogen/ DDIMER result: 212/ 1.08 08/15 CT Chest impressions: Multifocal bilateral groundglass opacities throughout both lungs with more confluent involvement at the posterior lung bases. This may reflect a nonspecific infectious/inflammatory process, including the possibility of viral pneumonia in the setting of known COVID positivity. Interlobular septal thickening is also present component of pulmonary edema may also be considered. Clinical correlation and attention on short-term follow-up is recommended to assess for clearance. 2. Oval nodular opacity at the posterior left upper lobe which may reflect nonspecific infection/inflammation with neoplasia not excluded. Attention on short-term follow-up is recommended. 3. Ectasia of the ascending thoracic measurement of 4.1 cm in diameter. 08/16 ESR result: 5 0816 Fibrinogen/ DDIMER result: 226/ 0.87 08/17 Fibrinogen/ DDIMER result: 230/ 0.98 08/17 ESR 11 08/17 Tacrolimus result: 2.1 08/18 ALT/AST result: 27/38 08/18 ESR result: 11 08/18 Fibrinogen/ DDIMER result: 226/ 1.22 8/18 ABG result: i-pH 7.41, i-PCO2 34.9, i-Po2 65, i-HCO3 22.1 8/18 C-Reactive result: 0.114 8/19 ESR result: 10 8/19 Fibrinogen/ DDIMER result: 216/ 1.87 8/20 BNP result: 136.3 8/20 ESR result: 14 8/20 Fibrinogen/ DDIMER result: 258/ 1.53 8/21 CXR Impression: Essentially stable chest radiography since 6 days ago with imaging findings most in keeping with ongoing COVID pneumonitis 8/21 Fibrinogen/ DDIMER result: 271/ 1.66 8/21 ALT/AST Result: 35/ 44 8/21 ferritin result: 2211 8/21 C-Reactive Protein result: 0.272 8/21 ESR 12 8/21 CXR Impression: Diffuse bilateral airspace opacities, mildly worsened. Low lung volumes. 8/22 Fibrinogen/ DDIMER Result: 296/ 2.08 8/22 ALT/AST result: 41/43 8/22 C-Reactive Protein result: 0.240 8/22 ESR 30 8/24 pt decease

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 08/04 CXR impression: Bilateral pneumonia. 08/05 CXR impression: Persistent mixed interstitial and patchy airspace opacities in the mid and lower lungs bilaterally not significantly changed. Findings with patient's known history of COVID pneumonia. 08/09 Fungitell result <31 08/09 CXR impression: Stable chest radiograph since 4 days ago as above. 08/10 Tacrolimus result: 7.4 08/10 ESR 12 8/10 Fibrinogen/ DDIMER results: 261/ 1.11 8/10 CXR impression: Similar groundglass and interstitial opacities in the lungs, consistent with atypical pneumonia. 08/11 ESR 8 08/11 Fibrinogen/ DDIMER result: 230/ 0.99 08/11 CXR impression: Similar appearance of bilateral lung opacities. 08/12 ESR result: 6 08/12 Fibrinogen/ DDIMER result: 203/ 1.11 08/13 ESR result: 7 08/13 Fibrinogen/ DDIMER result: 216/ 1.16 08/14 Fungitel result: <31 08/14 ESR result: 12 08/14 Fibrinogen/ DDIMER result: 207/ 1.37 08/14 Procalcitonin result: 0.07 08/14 CXR impression: Underinflated lungs. Interval increase in bilateral opacities accentuated by differences in technique. 08/15 ESR result: 13 08/15 Fibrinogen/ DDIMER result: 212/ 1.08 08/15 CT Chest impressions: Multifocal bilateral groundglass opacities throughout both lungs with more confluent involvement at the posterior lung bases. This may reflect a nonspecific infectious/inflammatory process, including the possibility of viral pneumonia in the setting of known COVID positivity. Interlobular septal thickening is also present component of pulmonary edema may also be considered. Clinical correlation and attention on short-term follow-up is recommended to assess for clearance. 2. Oval nodular opacity at the posterior left upper lobe which may reflect nonspecific infection/inflammation with neoplasia not excluded. Attention on short-term follow-up is recommended. 3. Ectasia of the ascending thoracic measurement of 4.1 cm in diameter. 08/16 ESR result: 5 0816 Fibrinogen/ DDIMER result: 226/ 0.87 08/17 Fibrinogen/ DDIMER result: 230/ 0.98 08/17 ESR 11 08/17 Tacrolimus result: 2.1 08/18 ALT/AST result: 27/38 08/18 ESR result: 11 08/18 Fibrinogen/ DDIMER result: 226/ 1.22 8/18 ABG result: i-pH 7.41, i-PCO2 34.9, i-Po2 65, i-HCO3 22.1 8/18 C-Reactive result: 0.114 8/19 ESR result: 10 8/19 Fibrinogen/ DDIMER result: 216/ 1.87 8/20 BNP result: 136.3 8/20 ESR result: 14 8/20 Fibrinogen/ DDIMER result: 258/ 1.53 8/21 CXR Impression: Essentially stable chest radiography since 6 days ago with imaging findings most in keeping with ongoing COVID pneumonitis 8/21 Fibrinogen/ DDIMER result: 271/ 1.66 8/21 ALT/AST Result: 35/ 44 8/21 ferritin result: 2211 8/21 C-Reactive Protein result: 0.272 8/21 ESR 12 8/21 CXR Impression: Diffuse bilateral airspace opacities, mildly worsened. Low lung volumes. 8/22 Fibrinogen/ DDIMER Result: 296/ 2.08 8/22 ALT/AST result: 41/43 8/22 C-Reactive Protein result: 0.240 8/22 ESR 30
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1797961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

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

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

Death Gastrointestinal haemorrhage Syncope

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 1749953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: GA
Alter: 56,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 23.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 37,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test Catheterisation cardiac abnormal Chest X-ray Chest discomfort Chest pain Coronary artery occlusion Dyspnoea Echocardiogram Fatigue Inappropriate schedule of product administration Insomnia Laboratory test Myocardial infarction Pericarditis

Symptomtext

I received the Pizer Covid-19 Vaccine on February 23, 2021 and March 23, 2021. Shortly thereafter, in April of 2021, I started experiencing fatigue, chest tightness, breathing issues and sleeplessness. I thought these symptoms were indications of acid reflux and stress, and took Tylenol and over-the-counter acid reflux medication, Omeprazole. On July 31, 2021, I went to Hospital due to shortness of breath and chest pain. I was then transferred to another hospital, where they ran blood work and tests. I stayed in the hospital until August 3, 2021 and was told that I had inflammation around my heart. Later, I followed-up with Dr., a Cardiologist, on August 18, 2021 and was told that I had in fact, suffered a Heart Attack! Hence, I have been on seven (7) different medications (Omeprazole 20 mg, Aspirin 81 mg, Colchicine 0.6 mg, Isosorbide Mononitrate 30 mg, Atorvastatin 80 mg, Lisinopril 2.5 mg, and Metoprolol ER Succinate 25 mg) for my conditions in order for the inflammation to subside and have a stent placed in a blocked artery. On September 27, 2021, I was informed by Dr. that a stent would be too risky to perform, since the artery is blocked 100%. Therefore, I will have to live with this "permanent injury" for the rest of my life. Consequently, I have been told I have a rare case of inflammation. Therefore, I certainly believe it is Covid-19 vaccine related, and have filed a VAERS report (Vaccine Adverse Event Reporting System) with the CDC. Thus, I do not have a family history of Heart Disease and never have been on ANY prescription medications other than for very brief illnesses. These are some of the symptoms and/or side effects that I have experienced from my medications, since August 5, 2021 to date: 1.) Sore throat/cold 2.) Headaches/migraines 3.) Diarrhea 4.) Chills/hot and cold 5.) Stomach aches 6.) Light-headedness 7.) Low energy 8.) Unstable on feet; fell on September 15, 2021 around 12:30 p.m. 9.) Sleeplessness 10.) Loss of appetite 11.) Tightness in left calf area 12.) Cramping in both legs 13.) Fever 14,) Feeling depressed 15.) Woozy and dizzy 16.) Constipation 17.) Excessive coughing 18.) Body aches, specifically, back, arms and legs 19.) Nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: Blood work, Heart X-rays, MKGs, Heart Ultrasound, and Heart Cather from July 31, 2021 through August 3, 2021.
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1731686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 47,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 06.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Death Endotracheal intubation Mechanical ventilation SARS-CoV-2 test positive

Symptomtext

Patient is a 47 year old female with a multiple co morbidties including asthma, bipolar disorder, primary hypothyroidism, oxygen dependent possible chronic obstructive lung disease ( 3 liters nasal cannula), liver cirrhosis(Non alcoholic serohepatitis), depression, history of tobacco use, diabetes mellitus type 2, gastroesophageal reflux and obesity (BMI 60). Tested COVID positive 8/31. Patient required intubated. Patient completed 10 days of Decadron and 5 days of Remdesivir. Patient was not able to be weaned from the vent and was made comfort care 9/23 and expired shortly after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 23,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1689378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 28.02.2021
Beginn: 10.08.2021
Tage bis Beginn: 163,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Death Endotracheal intubation Exposure to SARS-CoV-2 Extubation SARS-CoV-2 test positive

Symptomtext

Patient admitted on 8/10/2021 with acute respiratory failure secondary to COVID pneumonia. She was COVID positive on 7/22/2021 following a family gathering. She had been hospitalized for 3 days previously (8/4 - 8/7/2021) and seen in the ED on 8/8/2021. This current admission, she was intubated and required high dose dexamethasone. After 20 days, she was converted to comfort care and compassionate extubation was performed. She passed away comfortably soon after this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 20,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple sclerosis
Andere Medikamente: Ocrelizumab
Allergien: -
Vorherige Impfungen: -

VAERS 1678836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 23.01.2021
Beginn: 01.09.2021
Tage bis Beginn: 221,0
Dosis: 2
Route/Site: IM / -

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

Angiogram pulmonary abnormal COVID-19 Chest pain Chills Computerised tomogram abdomen abnormal Diverticulum Dyspnoea Lung infiltration Malaise Oxygen saturation decreased Pain Pneumonia Pulmonary embolism Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient is a pleasant 66-year-old female, has been sick for the last week or 10 days. She was recently tested positive for COVID. She was given antiparasitic medication. Patient's symptomatology has not improved. She continued to have shortness of breath. Three days ago, she also developed chest pain. Patient's family was quite concerned about her. Oxygenation has been also dropping. Her shortness of breath got worse. Now she is running fever and chills as well as body aches. Her daughter got concerned, brought her to the emergency department. Patient was again tested positive for COVID. She underwent a CT scan of the abdomen, which was found to be negative except for diverticulosis. CT angiography of the chest shows pulmonary embolism as well as patchy infiltrates consistent with multifocal pneumonia

Weitere VAERSDATA-Felder

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

VAERS 1663794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 01.09.2021
Impfdatum: 11.02.2021
Beginn: 25.08.2021
Tage bis Beginn: 195,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Angiogram Anticoagulant therapy Aphasia Atrioventricular block Blood creatine increased COVID-19 Cellulitis Cerebral atrophy Cerebrovascular accident Computerised tomogram head normal Confusional state Delirium Dysphagia Echocardiogram Ejection fraction Electrocardiogram normal Encephalopathy

Symptomtext

Hospitalized; COVID-19 positive 8.25.21 (fully vaccinated) Admission Date: 8/25/2021 Discharge Date: 9/1/2021 PRESENTING PROBLEM: Patient is a 87 y.o. male with history coronary artery disease, hypertension, hyperlipidemia, hypothyroidism, insulin-dependent diabetes, obesity, and recent subdural hematoma status post burr hole as well as recent MCA stroke with seizures who presented to the ER from his rehab facility with concern for aphasia/confusion. It is reported that there is a COVID outbreak on the floor he resides on at the nursing home. His wife spoke with him around 9 am the morning of presentation and he reported feeling ill and had a fever. He tested positive for COVID and shortly after he was brought to the hospital with concern for abnormal speech/confusion. The patient was evaluated by Neurology in the ER, loaded with Keppra 20 milligrams/kilogram. In the ER, vitals remained stable, afebrile, normotensive, O2 sat 98% on room air. Labs showed mild AKI with creatinine 1.23, stable hemoglobin 11.1, no leukocytosis. EKG showed normal sinus rhythm, 63 ppm, first-degree AV block. Confirmed COVID positive. CT head, CTA head/neck, and CT brain perfusion did not show acute pathology, fairly stable interval imaging. Neurology recommended admission to Medicine for MRI brain, EEG monitoring, and workup for stroke. The patient was admitted to Internal Medicine for further evaluation and treatment. HOSPITAL COURSE: Multiple small embolic subacute ischemic CVAs of both hemisphere CTA head/neck: multiple areas of narrowing/stenosis without large vessel occlusion CT brain perfusion: large, chronic left holohemispheric cerebral convexity subdural hematoma, and a small, resolving, chronic right PCA territory. There is apparent ischemia within the bilateral cerebellar hemispheres, which is favored to be artifactual. No acute core infarction is apparent. -MRI brain w/o contrast: 1. Stable bilateral subdural hematomas and stable associated mass effect. 2. 6 mm focus of early subacute ischemic infarction in the right putamen without hemorrhagic transformation. 3. Small noncontiguous foci of subacute ischemic infarctions in the right PCA distribution without hemorrhagic transformation. 4. Stable late subacute/early chronic infarction in the right temporal occipital region. There is stable petechial hemorrhagic transformation without space-occupying mass effect of this infarction. 5. There are numerous tiny chronic infarctions throughout the cerebellum. 6. Focal and more confluent areas of hyperintense T2 signal are noted in the periventricular and in the subcortical white matter. This is nonspecific. Statistically however it is most consistent with mild chronic small vessel ischemic change of the white matter. 7. Age-appropriate brain atrophy. -Echo: left ventricular ejection fraction is 65%. No clear evidence for regional wall motion abnormalities noted but not all walls are seen well in all views. The mid and distal right ventricular free wall appear to contract well. The base is not well visualized. Today's study was compared to one performed on 7/28/21. The LVEF was 63% on the prior report. -LINQ implanted on 8/30, if having A. fib than he can be started on Amiodarone per EP -continue statin -aspirin 81 mg started on 8/31 after discussion with patient and wife, who are in agreement to start it [Neurosurgery: Recommend holding ASA indefinitely if able, but if pt must continue ok to restart] -PT/OT recommended subacute rehab, and he was transferred on 9/1/2021 -he should follow up with neurosurgery in 2 weeks and with neurology clinic Seizure - cEEG: The inpatient video EEG reveals epileptiform abnormalities involving the right temporal and left frontocentrotemporal head regions, consistent with an increased risk of focal seizures. There is a severe degree of multifocal bihemispheric slowing, consistent with a focal cerebral dysfunction involving the indicated regions. There is also a mild degree of generalized slowing, consistent with a diffuse cerebral dysfunction or encephalopathy - continue Keppra 750 mg bid, when taking 1000 mg bid, he was too sedated -follow-up with epilepsy clinic in few weeks Recent bilateral SDH (L>R) with MMA embolization (7/21/21) SDH stable on interval imaging Continue daily Provigil Asa 81 mg daily started on 8/31, watch closely Neurosurgery recommending to hold ASA indefinitely if able, but if patient must continue okay to restart. Plan to repeat imaging in 6-8 weeks (First week Oct). Patient to follow-up in neurosurgery clinic in 2 weeks. Has absorbable sutures at forehead, wound healing well Dysphagia SLP: thin liquids, regular solid (cracker/cookie), liquids via cup and no straws Asymptomatic COVID-19 positive Tested positive at rehab facility 8/25, confirmed in hospital s/p Pfizzer COVID-19 vaccine Jan/Feb OK to transfer

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: Hospitalization 7.27.21 - 8.5.21: HOSPITAL COURSE: Patient is an 87 y.o. man with PMh: CAD, s/p PCI, Dm2, HTN, hypothyroidism who recently had bilateral SDH s/p left Burrnhole on 7/22/21 and Right MMA embolization on 7/23/21 who was admitted from 07/20 02/07/2020 7/21 to neurosurgery and discharged to a rehabilitation specialists presented back on same day for change in mental status and left-sided weakness consult for acute CVA. Patient was initially admitted to neurosurgery with neurology consult. He was found to have a cryptogenic right MCA territory stroke with seizures. Aspirin was not given, due to his recent subdural hematoma and risk for re-bleeding. He was started on Lipitor 40 mg daily. He was placed on Keppra for epilepsia partialist continua. Neurosurgery added Provigil due to daytime somnolence, and dose was titrated up to 200 mg daily during admission. Neurology recommended 14-day ZIO patch at discharge, and clinic follow-up in 3 months. Care was transferred to Internal Medicine service. Patient's course was complicated by encephalopathy, likely multifactorial due to left hand cellulitis and hospital delirium. He was treated with cefazolin, and left hand cellulitis resolved. Due to his encephalopathy, patient was not eating so a Corpak was placed. Once patient received nutrition, his mental status gradually improved. His appetite and oral intake improved, such that Corpak was able to removed on 8/5. Both SLP and nutrition followed, and he was tolerating mechanical soft diet with nectar-thickened liquids. He will need to be followed by PT, OT and SLP following discharge. He was felt stable for discharge to subacute rehabilitation on 8/5/21. He will require outpatient Neurosurgery follow-up in 2 weeks. He will continue on Lipitor 40 mg daily and Provigil 200 mg daily. No antiplatelet agents/Aspirin due to recent brain bleed. He should follow-up with stroke clinic in 3 months and PCP in 1 week.
Vorgeschichte: CAD (coronary artery disease) Old MI 3/2009, 11/2009 S/P PTCA RCA 3/2009 Hypertension Hypercholesterolemia Diabetes mellitus, type II (HCC) Arthritis Statin intolerance Trigeminal neuralgia Abscess, gall bladder fosxxa, post cholecystectomy 5/1/19 Chronic diastolic CHF (congestive heart failure) (HCC) Hypothyroidism, unspecified type Subdural hematoma (HCC) Epilepsia partialis continua (HCC) Left homonymous hemianopsia Acute right MCA stroke (HCC) Counseling regarding advance care planning and goals of care Aphasia Multiple small embolic subacute ischemic CVAs of both hemisphere Seizure disorder (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet allopurinol (ZYLOPRIM) 100 MG tablet amlodipine (NORVASC) 2.5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 MG tablet blood glucose test strips brimonidine (ALPHAGAN) 0.2 % ophthalmi
Allergien: Ace Inhibitors Cough Statins Other
Vorherige Impfungen: -

VAERS 1641253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NC
Alter: 65,0
Geschlecht: M
Eingang: 27.08.2021
Impfdatum: 19.02.2021
Beginn: 07.05.2021
Tage bis Beginn: 77,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Cardiac imaging procedure Computerised tomogram thorax abnormal Cough Dyspnoea exertional Haemoptysis Pulmonary embolism Ultrasound Doppler

Symptomtext

In May of 2021 I started experience shortness of breath upon exertion (walking up one flight of stairs; walking up hills; bicycling) that was unusual. I have fairly extensive seasonal allergies and, thinking the shortness of breath was due to allergies, treated them with medicine prescribed by my doctor. In late May I developed a dry cough and, again, thought it was due to seasonal allergies. In early June I went to see Doctor B. when I couldn't get rid of the cough. He prescribed an inhaler (Albuterol Sulfate 90 mcg) and suggested that, if it did not help, I should see an ENT. In late June I met with Doctor M., an ENT, who prescribed Singluair 10 mg tablet, believing I was experiencing allergy-induced asthma. I was on the Singulair for 2 weeks, and then I started coughing up blood. Doctor B. ordered a CT scan for July 15th. The scan showed an extensive PE, and I was directed to the emergency room Medical Center that same day. I was treated at Medical Center first with Heparin drip and later with Eliquis. I was observed for 24 hours and then released. I have been put on Eliquis (5 mg 2X/day) and am told I will be on it for life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: July 15, 2021 - CAT Scan - Radiology July 15, 2021 - Heart Scan - Medical Center July 15, 2021 - Scan for DVTs in both legs - Medical Center
Aktuelle Erkrankungen: None
Vorgeschichte: History of DVT (right calf in 2018); superficial blood clot (right calf 2020)
Andere Medikamente: Allegra 180 mg 1X/Day; Flonase 20 mcg 1X/Day; Centrum Silver Multivitamin 1X/Day
Allergien: No allergies to medications or foods; seasonal allergies (grass, mold, trees)
Vorherige Impfungen: -

VAERS 1641127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: GA
Alter: 80,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 09.03.2021
Beginn: 04.08.2021
Tage bis Beginn: 148,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death

Symptomtext

Patient was hospitalized due to COVID-19 and died. Patient is fully vaccinated.

Weitere VAERSDATA-Felder

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

VAERS 1637169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: TN
Alter: 90,0
Geschlecht: M
Eingang: 26.08.2021
Impfdatum: 01.02.2021
Beginn: 16.08.2021
Tage bis Beginn: 196,0
Dosis: 2
Route/Site: IM / -

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

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

Symptomtext

Patient was fully vaccinated with Pfizer with last dose given on 02/01/2021. Case developed covid symptoms on and tested positive for COVID 8/14/2021. He was admitted to Hospital on 8/16/2021. Case expired on 8/21/2021.

Weitere VAERSDATA-Felder

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

VAERS 1586737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 19.08.2021
Impfdatum: 11.02.2021
Beginn: 17.07.2021
Tage bis Beginn: 156,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram abnormal Asthenia COVID-19 Chest X-ray abnormal Computerised tomogram thorax abnormal Death Diarrhoea Dizziness Dyspnoea Endotracheal intubation Hypophagia Hypoxia Intensive care Leukocytosis Lung opacity Oxygen saturation decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient tested positive for COVID-19 on 7/24. She felt well for the first week following the test but then started to have symptoms including dizziness, SOB, weakness, diarrhea, and decreased PO intake. She was started on prednisone 5 mg PO on 8/5 and presented to urgent care on 8/10 because her symptoms continued to worsen. She went to an outside hospital ED and was hypoxic to 91% requiring NC. CXR and CTA chest at that time showed diffuse ground glass opacities. She was administered dexamethasone 6 mg IV and 1 L of normal saline. She arrived to the hospital on 8/11 satting well on 4L of nasal cannula. She continued on dexamethasone. Thereafter, her oxygen requirements escalated to max high flow nasal cannula on 8/13 and 8/14. She received tocilizumab 8 mg/kg IV x 1 on 8/14 and transferred to the medical intensive care unit. On 8/15, she was having oxygen desaturations to the 70s and 80s and was intubated. Over the next 24 hours, she developed increasing pressor requirements, was spiking fevers, and started on iNO. She was started on vancomycin and cefepime and her leukocytosis progressed to >200. The patient was made DNR and passed on 8/17.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: CLL
Vorgeschichte: CLL Rheumatoid arthritis Hypogammaglobulinemia R foot stress fracture of R 2nd metatarsal Osteopenia Iron deficiency anemia GERD
Andere Medikamente: Rituximab 1600 mg subcut every 8 weeks Tretinoin 0.025% topical cream at bedtime 3 times per week Ventolin HFA 2 puffs by mouth every 4 hours PRN SOB/wheezing Acyclovir 400 mg PO BID Estradiol 10 mcg tablet vaginally 1-2 times per week Famo
Allergien: Cheese (anaphylaxis) Sulfa (anaphylaxis) Carrageenan, corn-containing products, cor syrope, dextrose, geltain, ketchup, lecithin, mayonnaise, molasses, mustard, rennet, sulfites, wine spirit (swelling)
Vorherige Impfungen: -

VAERS 1058152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 01.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Cerebrovascular accident Injection site pain Lymphadenopathy

Symptomtext

Swollen lymph nodes, pain at injection site, suffered a stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Iron overload- secondary hemochromatosis.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 1541629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

kritisch

Staat: NV
Alter: 77,0
Geschlecht: F
Eingang: 10.08.2021
Impfdatum: 09.02.2021
Beginn: 16.03.2021
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac arrest Chest discomfort Electrocardiogram normal Sudden death

Symptomtext

DEATH. My wife was in excellent health with no heart issues when she awoke five weeks after her second Pfizer shot feeling "like a load of bricks was on her chest". She was transported by ambulance to the Hospital Emergency Room around 11 am on March 16, 2021. She was monitored closely and after a couple of hours, the attending folks said they didn't think it was a heart issue per fine blood work and full time EKG hook up. They were looking at GI possibilities and wanted to keep her overnight, do a couple more tests in the morning and then send her home. She stayed in an ER bay because there were no regular beds available. We made plans for the next morning and I left her around 8 pm and drove home. Around 2:50 am on the 17th, I received a phone call that she had a massive coronary event. The were able to bring her back one time momentarily, but then she passed away within a few minutes. I'm submitting this report because of the general belief that older women have heart attacks all the time. However, though she felt a heavy chest pressure, twelve plus hours in an ER bay couldn't find any issues. She may have had some coronary inflammation that may have been exacerbated by the vaccine but I and we will never know. Nevertheless, this was sudden and unexpected and five weeks after her second vaccine dose and it seemed appropriate to toss it in your data pile. Thanks.

Weitere VAERSDATA-Felder

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

VAERS 1523481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 03.08.2021
Impfdatum: 20.01.2021
Beginn: 01.08.2021
Tage bis Beginn: 193,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram Blindness Cerebrovascular accident Diagnostic aspiration Injury Retinal artery occlusion

Symptomtext

I had an eye stroke and lost 50% vision in my right eye

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Went to ER on 8/1 with vision loss. Had CT angio scan, several radiograph injection tests that looked at blood flow to eye and found ?retinal artery occlusion?. They couldn?t believe I had this because I was so young and perfectly healthy. All follow-up tests to determine a cause came up negative. They do not know why this happened to me and I wondered if it had anything to do with the vaccine. My vision loss is permanent. :(
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, mild depression
Andere Medikamente: Synthroid 137 mcg, Sertraline 50mg
Allergien: None
Vorherige Impfungen: -

VAERS 1509479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: PA
Alter: 45,0
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 23.01.2021
Beginn: 01.03.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: - / RA

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

Dysphagia Laryngospasm Pneumonia Respiratory arrest

Symptomtext

I couldn't breathe or swallow. This started about 2 months after vaccination. I went to the ED and they admitted me for 2 days. I went to hospital. They finally came up with laryngeal spasmatic pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Lisinopril; cimetidine; vitamin
Allergien: Bees; losartan
Vorherige Impfungen: -

VAERS 1463450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: CT
Alter: 63,0
Geschlecht: M
Eingang: 11.07.2021
Impfdatum: 19.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: SYR / LA

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

Pulmonary embolism

Symptomtext

13 days after receiving first dose I had a Pulmonary Emoblism in my left lung

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Pulmonary Embolism
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: Allopurinol 300 mg - 1 daily Anastrozole 1 mg - 1 daily Atorvastatin 20 mg - 1 daily Finasteride 5 mg - 1 daily Olmesartan Medoxomil 20 mg - 1 daily Potassium Citrate 1620 mg (15 MEQ) - 1 daily Tamsulosin 0.4 mg - 2 daily Testosterone CYP 2
Allergien: Altace
Vorherige Impfungen: -

VAERS 1460207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: IL
Alter: 81,0
Geschlecht: M
Eingang: 09.07.2021
Impfdatum: 14.02.2021
Beginn: 07.07.2021
Tage bis Beginn: 143,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Anticoagulant therapy Asymptomatic COVID-19 Bladder catheterisation Chest X-ray normal Deep vein thrombosis Haematuria Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

Patient presented to the ER on 7/7/21 with hematuria and was found to have acute kidney injury. Patient was recently diagnosed with a PE and bilateral DVT 4 weeks PTA and was on Eliquis for these. Patient also has a history of lung cancer and COPD and is chronically on 4L O2 at home. A foley was placed by Urology in the ER and Eliquis was held due hematuria and changed to heparin drip upon admission. In the ER, patient was tested for COVID per policy, and was found to be positive on 7/7/21 despite being fully vaccinated (1/24/21 and 2/14/21). Patient was admitted for further work-up and has not been started on COVID treatment due to patient being asymptomatic for COVID. Pt's chest X-ray was negative for pneumonia.

Weitere VAERSDATA-Felder

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

VAERS 1454790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: SD
Alter: 73,0
Geschlecht: F
Eingang: 07.07.2021
Impfdatum: 26.01.2021
Beginn: 23.03.2021
Tage bis Beginn: 56,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Death Multiple organ dysfunction syndrome Pyrexia Respiratory distress SARS-CoV-2 test positive

Symptomtext

Patient tested positive for COVID-19 on 03/29/2021 via both antigen and PCR despite being fully vaccinated. She was subsequently hospitalized and then died on 03/30/2021. Symptom onset for COVID-19 was 03/23/2021, with symptoms of fever (101.8) and respiratory distress which required an increase in oxygen. Per the death certificate, causes of death are as follows: Part 1: Cause of Death: A. Multi organ failure B. COVID-19 infection Part 2: Other Significant Conditions: Congestive Heart Failure, Diastolic Heart Failure with Preserved Ejection, history of cerebrovascular accident, diabetes mellitus type 2, and morbid obesity

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: Patient tested positive for COVID-19 on 03/29/2021 (both antigen and PCR) despite being fully vaccinated.
Aktuelle Erkrankungen: Patient in overall poor health and was in care at time of hospitalization and subsequent death; she was in a facility.
Vorgeschichte: Patient in care at time of hospitalization and subsequent death; she was in a facility. Patient has history of congestive heart failure, Type 2 diabetes, morbid obesity, diastolic heart failure with preserved ejection fraction, previous Cerebrovascular Accident.
Andere Medikamente: -
Allergien: HMG-COA-R Inhibitors; adhesives; Morphine Sulfate
Vorherige Impfungen: -

VAERS 986901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NC
Alter: 33,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anal incontinence Death Drug screen negative Toxicologic test normal Autopsy Hyponatraemia Immunomodulatory therapy Laboratory test Myocardial fibrosis Myocardial ischaemia Obesity Pericardial effusion Sudden death Syncope

Symptomtext

Sudden unexpected death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Autopsy (2/1/2021) Death contemporaneous w/ vaccine (same day); however, she gave herself a SQ injection of glatiramer acetate and it appears she collapsed and died immediately after that SQ injection; the Pfizer vaccine was earlier in the day; she had unspecified chronic myocardial ischemia (interstitial fibrosis), a pericardial effusion (50 mL), hyponatremia (vitreous Na: 123 mmol/L), and obesity (BMI: 39).
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity Optic neuritis (2019), resolved with steroids
Andere Medikamente: Sertraline (100 mg); 1 tab PO daily Glatiramer acetate (40 mg/mL pre-filled syringe); 40 mg SQ 3X/week Lorazepam (0.5 mg), PO PRN Junel FE 1/20 (1-20 mg-mcg) 1 tab PO daily
Allergien: Penicillin (rash) Sulfa drugs (rash)
Vorherige Impfungen: -

VAERS 986901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NC
Alter: 33,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Anal incontinence Death Drug screen negative Toxicologic test normal Autopsy Hyponatraemia Immunomodulatory therapy Laboratory test Myocardial fibrosis Myocardial ischaemia Obesity Pericardial effusion Sudden death Syncope

Symptomtext

Sudden unexpected death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Autopsy (2/1/2021) Death contemporaneous w/ vaccine (same day); however, she gave herself a SQ injection of glatiramer acetate and it appears she collapsed and died immediately after that SQ injection; the Pfizer vaccine was earlier in the day; she had unspecified chronic myocardial ischemia (interstitial fibrosis), a pericardial effusion (50 mL), hyponatremia (vitreous Na: 123 mmol/L), and obesity (BMI: 39).
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity Optic neuritis (2019), resolved with steroids
Andere Medikamente: Sertraline (100 mg); 1 tab PO daily Glatiramer acetate (40 mg/mL pre-filled syringe); 40 mg SQ 3X/week Lorazepam (0.5 mg), PO PRN Junel FE 1/20 (1-20 mg-mcg) 1 tab PO daily
Allergien: Penicillin (rash) Sulfa drugs (rash)
Vorherige Impfungen: -

VAERS 986901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NC
Alter: 33,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Anal incontinence Death Drug screen negative Toxicologic test normal Autopsy Hyponatraemia Immunomodulatory therapy Laboratory test Myocardial fibrosis Myocardial ischaemia Obesity Pericardial effusion Sudden death Syncope

Symptomtext

Sudden unexpected death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Autopsy (2/1/2021) Death contemporaneous w/ vaccine (same day); however, she gave herself a SQ injection of glatiramer acetate and it appears she collapsed and died immediately after that SQ injection; the Pfizer vaccine was earlier in the day; she had unspecified chronic myocardial ischemia (interstitial fibrosis), a pericardial effusion (50 mL), hyponatremia (vitreous Na: 123 mmol/L), and obesity (BMI: 39).
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity Optic neuritis (2019), resolved with steroids
Andere Medikamente: Sertraline (100 mg); 1 tab PO daily Glatiramer acetate (40 mg/mL pre-filled syringe); 40 mg SQ 3X/week Lorazepam (0.5 mg), PO PRN Junel FE 1/20 (1-20 mg-mcg) 1 tab PO daily
Allergien: Penicillin (rash) Sulfa drugs (rash)
Vorherige Impfungen: -

VAERS 986901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NC
Alter: 33,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anal incontinence Death Drug screen negative Toxicologic test normal Autopsy Hyponatraemia Immunomodulatory therapy Laboratory test Myocardial fibrosis Myocardial ischaemia Obesity Pericardial effusion Sudden death Syncope

Symptomtext

Sudden unexpected death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Autopsy (2/1/2021) Death contemporaneous w/ vaccine (same day); however, she gave herself a SQ injection of glatiramer acetate and it appears she collapsed and died immediately after that SQ injection; the Pfizer vaccine was earlier in the day; she had unspecified chronic myocardial ischemia (interstitial fibrosis), a pericardial effusion (50 mL), hyponatremia (vitreous Na: 123 mmol/L), and obesity (BMI: 39).
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity Optic neuritis (2019), resolved with steroids
Andere Medikamente: Sertraline (100 mg); 1 tab PO daily Glatiramer acetate (40 mg/mL pre-filled syringe); 40 mg SQ 3X/week Lorazepam (0.5 mg), PO PRN Junel FE 1/20 (1-20 mg-mcg) 1 tab PO daily
Allergien: Penicillin (rash) Sulfa drugs (rash)
Vorherige Impfungen: -

VAERS 1446875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: AR
Alter: 83,0
Geschlecht: M
Eingang: 05.07.2021
Impfdatum: 18.01.2021
Beginn: 13.06.2021
Tage bis Beginn: 146,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Chronic obstructive pulmonary disease Condition aggravated Death General physical health deterioration Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient is an 83 year old male admitted with COVID respiratory failure who has end stage COPD. His condition declined throughout hospitalization and expired 7/2/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 16,0
Labordaten: 6/30/2021 Delta variant
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Resp Failure with home oxygen COPD DM 2 Atrial Fibrillation with Watchman Procedure
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1446041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: CT
Alter: 33,0
Geschlecht: F
Eingang: 03.07.2021
Impfdatum: 25.02.2021
Beginn: 24.05.2021
Tage bis Beginn: 88,0
Dosis: UNK
Route/Site: - / LA

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

Pulmonary embolism SARS-CoV-2 test

Symptomtext

I was diagnosed with a pulmonary embolism in each lobe of my right lung on 24May2021; This is a spontaneous report from a contactable consumer (patient). A 33-year-old female patient (not pregnant at the time of vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL3247), via an unspecified route of administration in left arm on 25Feb2021 (at the age of 33 years old) as single for covid-19 immunisation. Medical history included brain tumor, chronic migraine, premature ovarian failure. The patient had known allergies to codene, dust, tree pollen. The patient received other concomitant medications in the past two weeks. The patient did not receive any other vaccines within four weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient underwent lab tests and procedures which included nasal swab sars-cov-2 test: negative on 24May2021. On 24May2021, patient was diagnosed with a pulmonary embolism in each lobe of right lung. The event resulted in: Emergency room/department or urgent care, hospitalization. The patient was hospitalized for 9 days. The patient received treatment due to the event with placed on heprin, evaluated for additional clots. The reporter considered events as serious. Since the vaccination, the patient tested for COVID-19. The outcome of event was resolving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 9,0
Labordaten: Test Date: 20210524; Test Name: COVID test type post vaccination: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Brain tumor; Chronic migraine; Dust allergy; Pollen allergy; Premature ovarian failure
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1440579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 01.07.2021
Impfdatum: 18.02.2021
Beginn: 24.06.2021
Tage bis Beginn: 126,0
Dosis: UNK
Route/Site: - / -

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

Cerebrovascular accident

Symptomtext

I63.9 - Cerebrovascular accident (CVA), unspecified mechanism

Weitere VAERSDATA-Felder

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

VAERS 1434080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: ND
Alter: 78,0
Geschlecht: M
Eingang: 29.06.2021
Impfdatum: 29.01.2021
Beginn: 30.04.2021
Tage bis Beginn: 91,0
Dosis: 1
Route/Site: UN / UN

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

Death

Symptomtext

2nd vaccine given 2/19/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 24,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown exactly
Vorgeschichte: History of Deep vein thrombosis Anemia Abdominal aortic aneurysm 3.4 cm infrarenal - Repair Arthritis Chronic kidney disease stage 3 Cerebrovascular accident Gastroesophageal reflux disease History of GI Bleed Hypertensive disorder History of myocardial infarction History of TIA Degenerative disorder of macula Multiple myeloma Coronary atherosclerosis stenting Proteinuria Diverticular disease Polyp of colon Tubular adenoma Hemorrhoids Benign hypertension Hyperlipidemia Monoclonal paraproteinemia
Andere Medikamente: unknown
Allergien: CAPSAICIN ZOSTER VACCINE LIVE
Vorherige Impfungen: -

VAERS 1423438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: GA
Alter: 97,0
Geschlecht: F
Eingang: 24.06.2021
Impfdatum: 15.02.2021
Beginn: 21.04.2021
Tage bis Beginn: 65,0
Dosis: 1
Route/Site: SYR / UN

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

COVID-19 Chest X-ray abnormal Death Hypopnoea Hyporesponsive to stimuli Mydriasis Pulse absent Pupil fixed Respiratory arrest SARS-CoV-2 test positive Vomiting

Symptomtext

PMH Afib, BiV PPM, HTN, pHTN, hypothyroidism, hemorrhoids, hearing loss, macular degeneration, squamous cell carcinoma, Parkinsons brought to ED after her caregiver found her in bed in AM w/a "dark substance in her bed" and minimally responsive. On admission vomiting x1, no cough, no SOB, abnormal CXR, covid+ Admission originally planned by IMS, but CCM asked to take over due to rapid decline.Pt w/ shallow breathing, guarded prognosis.In the morning on May 1, 2021 around 830 in the morning patient found to be without any pulse or breathing. DNR DNI with pupils fixed and dilated without any spontaneous breathing. No pulse palpated.pronounced dead at 8:30 a.m.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular disease Chronic Lung Disease ( Asthma or COPD) Hypertension Former Smoker
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1415978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: CA
Alter: 79,0
Geschlecht: F
Eingang: 21.06.2021
Impfdatum: 26.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: SYR / AR

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

Cerebral haemorrhage Death Lower limb fracture Magnetic resonance imaging head abnormal

Symptomtext

Brain bleed, broken leg, death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 5,0
Labordaten: MRI taken at Hospital 4/1/2021
Aktuelle Erkrankungen: -
Vorgeschichte: bi-polar, crohns, fibromyalgia, psoriatic arthritis
Andere Medikamente: depakote, quetipaine, lithium, buprenorphine, atorvastatin, methotrexate
Allergien: tetanus, arithamacian, morphine,
Vorherige Impfungen: -

VAERS 1375673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: ND
Alter: 88,0
Geschlecht: M
Eingang: 04.06.2021
Impfdatum: 29.01.2021
Beginn: 02.04.2021
Tage bis Beginn: 63,0
Dosis: 1
Route/Site: SYR / UN

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

Death

Symptomtext

Patient passed away 4/14/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 12,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown. Former smoker
Andere Medikamente: unknown
Allergien: Pet Dander, Hay fever, possibly more
Vorherige Impfungen: -

VAERS 1368397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 23.02.2021
Beginn: 28.05.2021
Tage bis Beginn: 94,0
Dosis: UNK
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

I21.4 - NSTEMI (non-ST elevated myocardial infarction)

Weitere VAERSDATA-Felder

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

VAERS 1358186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

kritisch

Staat: NY
Alter: 59,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 20.03.2021
Beginn: 20.04.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram coronary artery abnormal Pulmonary embolism

Symptomtext

Unprovoked bilateral pulmonary embolism Impression: multiple bilateral pulmonary emboli and proximol of which are in the right interlobar right middle lobar, right lower lobar and left lobar arteries. there is also multiple bilateral segmental pulmonary emboli. there is no CT evidence of pulmonary arterial hypertension or right sided heart strain however recommend echocardiogram

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: CT FindingPulmonary artery: the pulmonary arterial system is adequately opacified. there are bilateral filling defects within the right interlobar artery extending into the right middle and lower lobe are arteries the left lower lobar artery extending into multiple segment arteries, there are additional segment filling defects in the upper right, middle and lower lobes the main pulmonary artery is normal in caliber there is no CT findings of right sided heart strain
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1340939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

kritisch

Staat: AZ
Alter: 91,0
Geschlecht: U
Eingang: 22.05.2021
Impfdatum: 21.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Chills Death Dysstasia Fatigue Gait disturbance Visual impairment

Symptomtext

Approximately two days after first shot, he was unable to stand in the Am. He had to crawl to the bathroom. The following day he expressed vision problems. He also experienced fatigue. He was very active for his age, but his loss of energy kept him in his room most of the time (very unlike him.) After the second shot, he expressed chill in his body and stated he was unable to feel warm. The fatigue and chills continued. At approximately four weeks after the second shot, he felt it necessary to try to go outside and do some mild yardwork. His symptoms continued, so he returned to his room. On April the 3rd he passed away in the AM after I had a brief conversation with him on the phone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: neuropathy/legs
Vorgeschichte: none
Andere Medikamente: Blood pressure, heart medication
Allergien: none
Vorherige Impfungen: -

VAERS 1337366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 81,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Body temperature increased Death Respiratory rate increased

Symptomtext

Resident received vaccine at 10am and was observed for 15 minutes post vaccine with no reaction noted. Pre and post vitals were at baseline. Upon rounds at 12pm, nurse noted resident with increased respirations and an elevated temperature (Resp 40, Temp 103.5). Nurse notified nursing supervisor and MD called. Patient was transferred via 911 to Hospital at 12:25pm.

Weitere VAERSDATA-Felder

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

VAERS 1307713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 11.05.2021
Impfdatum: 28.01.2021
Beginn: 15.02.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: IM / LA

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

Pulmonary embolism

Symptomtext

Pulmonary embolism

Weitere VAERSDATA-Felder

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

VAERS 1296454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 07.05.2021
Impfdatum: 05.02.2021
Beginn: 02.05.2021
Tage bis Beginn: 86,0
Dosis: 2
Route/Site: IM / RA

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

Acute myocardial infarction Asthenia Dizziness Speech disorder Vision blurred

Symptomtext

dizzy, weakness, blurry vision, abnormal speech; non-STEMI

Weitere VAERSDATA-Felder

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

VAERS 1294116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MN
Alter: 55,0
Geschlecht: M
Eingang: 06.05.2021
Impfdatum: 19.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / AR

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

Cerebral haemorrhage Death

Symptomtext

Five days post vaccine patient had a massive cerebral hemorrhage resulting in death.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: heart valve replaced due to bicuspid insufficiency, high blood pressure, high cholesterol. chronic anticoagulation
Andere Medikamente: Coumadin, metoprolol, crestor, lisinopril
Allergien: none
Vorherige Impfungen: -

VAERS 1238360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 48,0
Geschlecht: U
Eingang: 01.05.2021
Impfdatum: 21.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: - / RA

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

Blood test Dyspnoea Loss of consciousness Near death experience Pulmonary thrombosis Pulmonary embolism

Symptomtext

Passed out; Blood clots in lungs; almost died from the vaccine; Problem in breathing; This is a spontaneous report from a contactable consumer (patient) reported that a 48-year-old patient of an unspecified gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration, administered in arm right on 21Jan2021 (at the age of 48-years-old) as a single dose for covid-19 immunisation. The patient was healthy and had no suffering from any medical condition. Concomitant medication included sertraline hydrochloride (ZOLOFT) taken for an unspecified indication, start and stop date were not reported. The patient had his/her shot on 21Jan2021 and about 10 days later he/she was having problem in breathing. When the patient went to work, he/she passed out at work and they sent him/her to the hospital and he/she wound up in the hospital on 12Feb2021 and they found out that he/she have blood clots in his/her lungs. The patient added that the matter of concern was he/she almost died from the vaccine. The patient was discharged on 14Feb2021 and he/she went in on 12Feb2021 and they did the catheter to remove the blood clot. The patient was hospitalized due to blood clots in his/her lungs and prior to going to the hospital, a week, and a half before that he/she was having breathing issues. The patient underwent lab tests and procedures which included blood test with unknown results on Feb2021. The patient was supposed to get the 2nd dose on 11Feb2021, but he/she never went because he/she wound up in hospital. The patient right now was taking blood thinner named Eliquis after he/she wind up with clot. The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Test Date: 202102; Test Name: blood test; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ZOLOFT
Allergien: -
Vorherige Impfungen: -

VAERS 1238360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

kritisch

Staat: NY
Alter: 48,0
Geschlecht: U
Eingang: 01.05.2021
Impfdatum: 21.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Dyspnoea Loss of consciousness Near death experience Pulmonary thrombosis Pulmonary embolism

Symptomtext

Passed out; Blood clots in lungs; almost died from the vaccine; Problem in breathing; This is a spontaneous report from a contactable consumer (patient) reported that a 48-year-old patient of an unspecified gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration, administered in arm right on 21Jan2021 (at the age of 48-years-old) as a single dose for covid-19 immunisation. The patient was healthy and had no suffering from any medical condition. Concomitant medication included sertraline hydrochloride (ZOLOFT) taken for an unspecified indication, start and stop date were not reported. The patient had his/her shot on 21Jan2021 and about 10 days later he/she was having problem in breathing. When the patient went to work, he/she passed out at work and they sent him/her to the hospital and he/she wound up in the hospital on 12Feb2021 and they found out that he/she have blood clots in his/her lungs. The patient added that the matter of concern was he/she almost died from the vaccine. The patient was discharged on 14Feb2021 and he/she went in on 12Feb2021 and they did the catheter to remove the blood clot. The patient was hospitalized due to blood clots in his/her lungs and prior to going to the hospital, a week, and a half before that he/she was having breathing issues. The patient underwent lab tests and procedures which included blood test with unknown results on Feb2021. The patient was supposed to get the 2nd dose on 11Feb2021, but he/she never went because he/she wound up in hospital. The patient right now was taking blood thinner named Eliquis after he/she wind up with clot. The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Test Date: 202102; Test Name: blood test; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ZOLOFT
Allergien: -
Vorherige Impfungen: -

VAERS 1271746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 05.02.2021
Beginn: 29.04.2021
Tage bis Beginn: 83,0
Dosis: 2
Route/Site: IM / RA

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

Acute myocardial infarction Asthenia Dizziness

Symptomtext

weakness, dizziness, NSTEMI heparin given

Weitere VAERSDATA-Felder

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

VAERS 1201475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 88,0
Geschlecht: F
Eingang: 25.04.2021
Impfdatum: 26.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Cardiac arrest Death Unresponsive to stimuli

Symptomtext

cause of death as cardiac arrest; This is a spontaneous report from a contactable consumer. This consumer reported for a 88-year-old female patient (mother) that she received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on 26Jan2021 10:45 (Lot Number: EL3247) as SINGLE DOSE for covid-19 immunisation. Medical history included Parkinsons, known allergies: Macadamia Nuts. No pregnant. No covid prior vaccination. The patient's concomitant medications were not reported. Historical vaccine included the first dose of BNT162B2 on 05Jan2021 (88-year-old) at 11:00 AM, Vaccine location: Right arm for covid-19 immunisation. The patient experienced cardiac arrest on 27Jan2021 16:45 with outcome of fatal. Patient passed away 30 hours after receiving the second dose of the Pfizer vaccine. The Facility put on her death certificate - cause of death as cardiac arrest. Treatment included CPR. The patient died on 27Jan2021. An autopsy was not performed.; Reported Cause(s) of Death: cause of death as cardiac arrest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts; Parkinson's disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1201475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 88,0
Geschlecht: F
Eingang: 25.04.2021
Impfdatum: 26.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / AR

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

Cardiac arrest Death Unresponsive to stimuli

Symptomtext

cause of death as cardiac arrest; This is a spontaneous report from a contactable consumer. This consumer reported for a 88-year-old female patient (mother) that she received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on 26Jan2021 10:45 (Lot Number: EL3247) as SINGLE DOSE for covid-19 immunisation. Medical history included Parkinsons, known allergies: Macadamia Nuts. No pregnant. No covid prior vaccination. The patient's concomitant medications were not reported. Historical vaccine included the first dose of BNT162B2 on 05Jan2021 (88-year-old) at 11:00 AM, Vaccine location: Right arm for covid-19 immunisation. The patient experienced cardiac arrest on 27Jan2021 16:45 with outcome of fatal. Patient passed away 30 hours after receiving the second dose of the Pfizer vaccine. The Facility put on her death certificate - cause of death as cardiac arrest. Treatment included CPR. The patient died on 27Jan2021. An autopsy was not performed.; Reported Cause(s) of Death: cause of death as cardiac arrest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts; Parkinson's disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1229686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MS
Alter: 72,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 30.01.2021
Beginn: 11.02.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Adrenal mass Chest X-ray Dyspnoea Myocardial strain Pneumonia Pulmonary embolism

Symptomtext

Presented to the ER with dyspnea. Brought by ambulance from where he lives. Please note-this chart is entered after a review of all patients presenting to the hospital with diagnosis of DVT, PE or stroke since we started vaccinating for Covid-19 on 12/23/2020. He got a pfizer vaccine on 1/30/2021. We pulled all charts of theses diagnosis if it occurred within 14 days of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: All tests done 2/11/2021. WBC-7.8, RBC-4.16, HGB- 12.8, HCT-39.4, Platelets-128, Sodium-147, Chloride -108, CO2-33, Albumin 3.0, BUN- 27, Covid 17-negative, U/A- 1+ blood with 3-5 RBCs, Magnesium 2.1, Lactic Acid-1.0, Troponin- 0.03,CPK- 30, CKMB- 1.0, Myoglobin- 34, CXR: No acute radiographic abnormality, Chest CT with PE protocol: Acute extensive pulmonary emboli bilaterally with evidence of right heart strain. Patchy pneumonia in the upper lobes. Left adrenal gland mass which is enlarging.
Aktuelle Erkrankungen: subdural hemorrhage, coronary atherosclerosis, atrial fibrillation,
Vorgeschichte: Parkinsons, epilepsy, noninsulin dependent diabetes, chronic pain, anemia, depression, chronic airway obstruction, hypertension, COPD, GERD, HTN, Hemiplegia
Andere Medikamente: Bacid, Lisinopril, Dilantin, Sinemet, Lasix, Duoneb, Lipitor, Symbicort, Multivitamin, Nitrostat, Zyrtec, Lanoxin, Fenofibrate, Prozac, Melatonin, Flomax, Depakote, Isosorbide, Risperdal, Ventolin, Pepcid, Aspirin, Amlodipine, Metoprolol, N
Allergien: acetominophen, codeine
Vorherige Impfungen: -

VAERS 1225703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NC
Alter: 68,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 13.02.2021
Beginn: 18.03.2021
Tage bis Beginn: 33,0
Dosis: 1
Route/Site: SYR / RA

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

Carotid artery thrombosis Cerebral thrombosis Cerebrovascular accident

Symptomtext

ON 3/18/2021 I had a massive stroke due to several blood clots in the caratid artery and in the brain. I survived and am now in the process of rehab to regain full mobility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Medical Center 3/18/2021 - 3/22/2021
Aktuelle Erkrankungen: -
Vorgeschichte: mild asthma (seasonal)
Andere Medikamente: diabetis prilosec statin losartan
Allergien: no
Vorherige Impfungen: -

VAERS 1207228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 92,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 24.02.2021
Beginn: 07.04.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

death

Weitere VAERSDATA-Felder

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

VAERS 1180107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 24.02.2021
Beginn: 24.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: IM / AR

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

Death SARS-CoV-2 test negative

Symptomtext

Death within 30 days of vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 2/12/21 positive for diarrhea tested for COVID-19 and found to be negative.
Aktuelle Erkrankungen: COPD exacerbation and CT revealed lung mass concerning for malignancy w/ mets causing a hospitalization in January.
Vorgeschichte: COPD, current smoker, chronic hypoxemic and hypercapnic respiratory failure, OSA on CPap, HFpEF, CKD3, gout, anxiety /depression and remote history of renal carcinoma s/p right nephrectomy.
Andere Medikamente: Advair, albuterol-ipratropium, alllopurinol, ativan, azithromycin, carvedilol, citalopram, cyanocobalamin, flonase, furosemide, gabapentin, magnesium, olmesartan, potassium chloride, prednisone, sennosides-docusate, spironolactone, sucralfa
Allergien: Augmentin, ciprofloxacin, codeine, doxycycline, Iodine containing IV Dye, Penicillins, protonix, sulfa
Vorherige Impfungen: -

VAERS 1143581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NC
Alter: 60,0
Geschlecht: M
Eingang: 29.03.2021
Impfdatum: 19.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Cerebrovascular accident Computerised tomogram abnormal Echocardiogram normal Hypoaesthesia Hypoaesthesia oral Injection site hypoaesthesia Magnetic resonance imaging abnormal Scan with contrast

Symptomtext

numbing of right hand side of face/mouth and right arm. symptoms subsided after about 10-15 minutes but continued to present every few days. I advised when i presented for my 2nd shot and they told me they had other reports of that and that is was fine/safe for me to take the 2nd shot, but to wait in a holding area for 30 minutes after the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: symptoms continued and on March 23rd at 10:58pm i suffered a stroke. My wife put 2 baby aspirin under my tounge and symptoms subsided by the time I was seen in the ER. CTscan with contrast and MRI revealed I had 4 other minor strokes or TIAs within the last 6 weeks. Echo heart test shows heart is healthy and strong. I will be seeing on March 31st.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish Oil - GNC Omega-3 EPA/DHA (half dose per day).
Allergien: None
Vorherige Impfungen: -

VAERS 1139677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

kritisch

Staat: NM
Alter: 68,0
Geschlecht: M
Eingang: 27.03.2021
Impfdatum: 27.01.2021
Beginn: 23.03.2021
Tage bis Beginn: 55,0
Dosis: 1
Route/Site: IM / LA

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

Death Escherichia bacteraemia Hepatic cirrhosis Hepatic failure Jaundice Laboratory test abnormal Renal failure Somnolence Weight increased

Symptomtext

Per family pt became more somnolent, gaining weight, jaundiced after 2nd covid vaccine dose. Pt was admitted to the hospital on 3/23 with decompensated cirrhosis and ecoli bacteremia and died on 3/25.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 2,0
Labordaten: Labs done on hospitalization confirm Ecoli bacteremia, liver, renal failure
Aktuelle Erkrankungen: Liver cirrhosis, with Hepatocellular carcinoma
Vorgeschichte: Alcoholic cirrhosis, Hepatocellular carcinoma, HTN, spinal stenosis
Andere Medikamente: -
Allergien: Sulfa, gabapentin
Vorherige Impfungen: -

VAERS 1130109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 24.03.2021
Impfdatum: 20.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Patient passed away unrelated to covid vaccination Narrative: The patient received his first dose of Pfizer vaccine on 1/20. Patient was on hospice and passed away at his home with family on 1/26. Cause of death not documented. No indication that death was related to COVID 19 vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1130052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: ID
Alter: 49,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 05.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Pulmonary embolism

Symptomtext

She reports having a surgery on 1/4/2021. Received vaccine on 3/5/2021 and went to ED on 3/7/2021 and diagnosed with bilateral PE's.

Weitere VAERSDATA-Felder

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

VAERS 1129413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: AK
Alter: 91,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 19.01.2021
Beginn: 19.03.2021
Tage bis Beginn: 59,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: UTI HX, GERD, Pericarditis, Anxiety,
Vorgeschichte: UTI HX, GERD, Pericarditis, Anxiety,
Andere Medikamente: Morphine, Lorazepam, Oxycodone, Cyclosporine Emulsion, Haloperidol
Allergien: Codeine, NSAIDS
Vorherige Impfungen: -

VAERS 1118968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 19.03.2021
Impfdatum: 21.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / RA

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

Cardiac arrest Death

Symptomtext

Patient passed away due to cardiac arrest Narrative: The patient had with PMH of CAD and multiple PCI, HFpEF, HTN. DM2, ESRD on HD, COPD and home O2 and other co-morbidities. Patient received his first dose of Pfizer vaccine on 1/21 and no adverse reaction was reported. Patient had a cardiac arrest on 2/1 and he was admitted to hospital. Patient passed away naturally on 2/1. Cause of death is not related to COVID 19 vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1110673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 28.01.2021
Beginn: 11.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / RA

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

Death Limb injury

Symptomtext

shoulder injury death

Weitere VAERSDATA-Felder

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

VAERS 1095392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: GA
Alter: 66,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 04.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / AR

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

Cardiac arrest

Symptomtext

Received shot 02/04/2021, sudden Cardiac Arrest 2/8/2021, found 2/10/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Heart stent June 2020
Andere Medikamente: Brilinta 90mg 2/day Valsartan 80mg 1/day Rosuvastatin 20ms 1/day Bupropion SL 150mg 1/day Asprin 81mg 1/day
Allergien: none known
Vorherige Impfungen: -

VAERS 1094421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 28.01.2021
Beginn: 09.02.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac death

Symptomtext

cardiac arrest death

Weitere VAERSDATA-Felder

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

VAERS 1069026

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge EL3247

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 03.03.2021
Impfdatum: 05.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death Endotracheal intubation Mechanical ventilation

Symptomtext

Death Narrative: Family was able to be present at bedside shortly after patient was extubated. Fentanyl bolus given 10-15 minutes prior. Patient passed away soon after endotracheal tube removed. Time of death 10:14am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Patient admitted with severe COVID on 2/12. Prolonged hospital course requiring intubation. Treated with mechanical ventilation, proning therapy, as well as medical therapy to no avail. Other "significant conditions contributing to death" but not resulting in the underlying cause given in PART I: HTN, T2DM, ESRD, CAD
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1066322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 02.03.2021
Impfdatum: 15.02.2021
Beginn: 15.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Aortic aneurysm rupture Death Dyspnoea

Symptomtext

Patient was vaccinated approx 9a. Later that evening, patient was having trouble breathing so they called son who lives down the road to come, 20 mins after the call the patient has passed. Per medical examiner, pt died due to possible PE, MI, or his aortic aneurysm ruptured.

Weitere VAERSDATA-Felder

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

VAERS 1057369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MD
Alter: 68,0
Geschlecht: M
Eingang: 26.02.2021
Impfdatum: 01.01.2021
Beginn: 09.02.2021
Tage bis Beginn: 39,0
Dosis: 2
Route/Site: SYR / RA

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

Chest X-ray Echocardiogram Electrocardiogram Laboratory test Pulmonary embolism Ultrasound scan

Symptomtext

Admitted to ER on 2/19/21. CT scan showed two pulmonary embolisms one in each lung. I'm currently on blood thinners.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Chest X-ray, blood tests, echocardiogram, ekg, sonogram of both legs. Completed on 2/19/21.
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: Lipitor 10 mg daily; Gabapentin 900mg twice a day
Allergien: None
Vorherige Impfungen: -

VAERS 1059622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: MA
Alter: 85,0
Geschlecht: M
Eingang: 25.02.2021
Impfdatum: 02.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / AR

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

Death Metabolic encephalopathy Resuscitation Unresponsive to stimuli Urinary tract infection Vomiting

Symptomtext

Resident rec'd COVID vaccine #2 on 02/02/2021 and was hospitalized on 02/03/2021. Diagnosed with UTI & Metabolic Encephalopathy. He was re-admitted to facility on 02/05/2021. On 02/08/2021 resident was found to be unresponsive with small amount of tan emesis in mouth and on bed. CPR initiated and resident was transferred to ER. ER MD notified facility that resident had died.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UTI & metabolic encephalopathy
Vorgeschichte: Chronic Kidney Di Stage 5 with Renal Dialysis Diabetes Type 2, CHF, H/o Bladder CA, HTN
Andere Medikamente: Lipitor Renvela caps, Pantoprazole, Humalog, Midodrine, Neptro caps, Metoprolol, Levemir, Levothyroxine
Allergien: Ace Inhibitors
Vorherige Impfungen: -

VAERS 1055027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: IL
Alter: 81,0
Geschlecht: M
Eingang: 25.02.2021
Impfdatum: 29.01.2021
Beginn: 15.02.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

patient deceased no show to 2nd appointment notified by family

Weitere VAERSDATA-Felder

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

VAERS 1035553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 17.02.2021
Impfdatum: 19.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: OT / -

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

Abdominal wall haematoma Abdominal wall haemorrhage Acute respiratory failure COVID-19 pneumonia Death Hypotension

Symptomtext

Pt passed soon after; shortly after progressed with other covid symptoms and was admitted / acute resp failure, COVID pneumonia; acute resp failure, COVID pneumonia; Became hypotensive due to massive hamatoma 2' bleeding into abd rectus muscle.; Became hypotensive due to massive hamatoma 2' bleeding into abd rectus muscle.; Became hypotensive due to massive hamatoma 2' bleeding into abd rectus muscle.; This is a spontaneous report from a non-contactable Pharmacist. A 76-years-old non-pregnant female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE lot number EL3247), intramuscular on 19Jan2021 at single dose for COVID-19 immunisation. The patient medical history included COVID symptoms from 16Jan2021 and ongoing. Concomitant medications were not reported. The patient with acute resp failure, COVID pneumonia, that developed symptoms 9 days prior to admit and ultimately received first vaccine 6 days prior to a admit, then shortly after progressed with other covid symptoms and was admitted on 25Jan2021. She decompensated while intp and was transferred to ICU for rising O2 needs, ultimately had to be intubated. Became hypotensive due to massive hamatoma 2' bleeding into abd rectus muscle. Sx and IR consulted and did beside exploration of hematoma. Initially blood pressure responded but overnight continued with refractory hypotension. Maxed out vasopressin and levophed, hemodynamics deteriorated. The patient died on 02Feb2021. It was not reported if an autopsy was performed. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on temporal association, the causal relationship between bnt162b2 and the events death, COVID-19 pneumonia, acute respiratory failure, hypotension, abdominal wall haematoma and abdominal wall haemorrhage cannot be excluded. The information available in this report is limited and does not allow a medically meaningful assessment. This case will be reassessed once additional information becomes available. 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.; Reported Cause(s) of Death: Pt passed soon after

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: Suspected COVID-19
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1024817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: GU
Alter: 68,0
Geschlecht: M
Eingang: 11.02.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Aspiration Blood pressure systolic decreased Cardio-respiratory arrest Death Dialysis Endotracheal intubation Gastrointestinal haemorrhage Mechanical ventilation Pulse absent Pulseless electrical activity Respiratory arrest Resuscitation Seizure like phenomena Unresponsive to stimuli Ventricular fibrillation

Symptomtext

Patient was coded and expired Code Blue: Patient was in dialysis, after 30 minutes his sbp dropped to 60s he was given 4 albumin. Patient who was responsive before that became unresponsive, had seizure like activity, lost pulse and spontaneous breathing. HD stopped. Code called. Cpr started. A few minutes into cpr patient started to profusely bleed - gi bleed and ventilation became very hard., intubation was very difficult and ventilation hard as we suctioned large amounts of aspirated blood. Patient was eventually intubated. More than 8 doses of epi ws given, sodium bicarbonate * 2 given with continuous cpr. It was mostly PEA with one shockable rhythym. And shock delivered for vfib. patient continued to profusely bleed, og insertion was not successful and effective ventilation was very tough due to massive aspiration,. Possible variceal rupture with cpr from his cirrhosis is likely scenario. After 30 minutes of unsuccessful ventilation and acls protocol. Code was stopped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: NIDDM, HTN, CAD s/p CABG x4v, liver cirrhosis, ESRD on HD, cataracts, dysarthria, PAD s/p angioplasty 2020 bilateral lower extremity
Vorgeschichte: social history of alcohol abuse
Andere Medikamente: Meds Prior to hospitalization: Propanolol, cilostazol, duloxetine HCL DR 30
Allergien: Ampicillin sodium
Vorherige Impfungen: -

VAERS 1024013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 81,0
Geschlecht: M
Eingang: 11.02.2021
Impfdatum: 18.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: SYR / LA

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

Brain operation Cerebrovascular accident Thrombectomy

Symptomtext

Had a stroke, blood clot removed from brain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Kidney transplant, Diabetes, Heart, Aortic valve replacement, High blood pressure
Andere Medikamente: Metoprolol, Eliquis, Allopurinal, Atorvastatin, Procardia, Prograf, Cellcept, Furosemude, Tujeo, Humalog
Allergien: None
Vorherige Impfungen: -

VAERS 1020816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 19.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: IM / AR

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

Abdominal wall haematoma Acute respiratory failure COVID-19 pneumonia Death Endotracheal intubation Haemodynamic instability Hypotension Intensive care Oxygen saturation abnormal

Symptomtext

Pt with acute resp failure, COVID PNA, that developed symptoms 9 days prior to admit and ultimately received first vaccine 6 days prior toa admit, then shortly after progressed with other covid symptoms and was admitted. She decompensated while intp and was transferred to ICU for rising O2 needs, ultimately had to be intubated. Became hypotensive due to massive hamatoma 2' bleeding into abd rectus muscle. Sx and IR consulted and did beside exploration of hematoma. Initially blood pressure responded but overnight continued with refractory hypotension. Maxed out vasopressin and levophed, hemodynamics deteriorated. Pt passed soon after(2/2).

Weitere VAERSDATA-Felder

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

VAERS 1006641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: IA
Alter: 90,0
Geschlecht: M
Eingang: 09.02.2021
Impfdatum: 30.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cardiovascular symptom Dehydration Myocardial infarction

Symptomtext

symptoms resembled a heart attack - doctor feels that it was a reaction to second shot, he was very dehydrated.

Weitere VAERSDATA-Felder

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

VAERS 992759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: AZ
Alter: 48,0
Geschlecht: F
Eingang: 01.02.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Axillary pain Chills Coma Headache Lymphadenopathy Nausea Pyrexia Vaccination site pain

Symptomtext

Fever chills, headache, nausea , vomiting , a large amount of pain from vaccination. The first one no pain . The second one really hurt maybe due to the person giving it . I had a fever low grade till noon 1/31/21. The scariest was pain and swelling in my lower armpit on my left arm where vaccinated. I found a study that it can happen but I freaked out . 48 after I experienced the lymphnodes swelling the pain went away but still swollen . I think this should be listed as people with a cancer history will freak out if they think their cancer is back . Lymphoma or breast . I aldd also read that vaccinated women need to alert their radiologists before a mammogram as the swollen lymphnodes could mimic Breast cancer and lymphnodes involvement, which would scare women to death . Physicians should be made aware and the public should be iNformed of the above to reduce panic and unnecessary testing .

Weitere VAERSDATA-Felder

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

VAERS 991213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: VA
Alter: 32,0
Geschlecht: M
Eingang: 01.02.2021
Impfdatum: 19.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / -

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

Acute myocardial infarction Alanine aminotransferase increased Aspartate aminotransferase increased Blood creatine phosphokinase increased Electrocardiogram abnormal Full blood count normal Pericarditis Troponin increased White blood cell count normal

Symptomtext

Heart swelling (pericarditis) , abnormal EKG showing STEMI initially on Saturday approximately 3 days after 2nd vaccine dose administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: EKG (STEMI) next 3 EKGs NORMAL Troponin- Saturday 0.63, then 1.84 then 1.87 finally 3.3 next day. WBC count normal none out of range CBC normal. CK elevated ALT elevated, AST slight elevation.
Aktuelle Erkrankungen: none
Vorgeschichte: None
Andere Medikamente: Prozac Adderall (I have since discontinued)
Allergien: NONE NKDA
Vorherige Impfungen: -

VAERS 960714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 28.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Angiogram Cerebrovascular accident Computerised tomogram head normal Headache Hemianopia Computerised tomogram neck Conversion disorder Dizziness Hemiparesis Hemiplegic migraine Magnetic resonance imaging brain normal Migraine Magnetic resonance imaging Muscular weakness Pain Sensory loss

Symptomtext

Left sided headache described as "shooting pain" and light headedness 1hr and 15 min after vaccination. Evaluation in urgent care - acute left sided weakness and sensory loss, stroke protocol, admitted for advanced work up and monitoring due to working diagnosis on presention of hemiplegic migraine headache in setting of COVID vaccination vs. acute stroke. All imaging negative for acute stroke. Chronic abnormalities present. Neurology at Weill Cornell diagnosis: COMPLEX MIGRAINE vs. CONVERSION DISORDER. Discharged with neurology and PCP follow up and PT as patient c/o persistent weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Head/neck CT, CTAngio 1/20, MRI brain, MRA head, MRA neck 1/20: No evidence of stroke, no significant stenosis, no suggeston of acute ischemia, bleed or disecction. Chronic findings
Aktuelle Erkrankungen: -
Vorgeschichte: CVST in 2011, GI bleed, hep b with cirrosissudden cardiac arrest ? stroke 2000, L eye trauma, ptosis, hypothyroidism
Andere Medikamente: -
Allergien: none known
Vorherige Impfungen: -

VAERS 976011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

kritisch

Staat: AK
Alter: 71,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 19.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Cerebrovascular accident Hemiparesis

Symptomtext

Began experiencing left sided weakness, Evaluated in ER, Medivac'd to other facility for stroke

Weitere VAERSDATA-Felder

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

VAERS 2315484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: GA
Alter: 64,0
Geschlecht: M
Eingang: 10.06.2022
Impfdatum: 02.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Atrial fibrillation Cardiac failure Cardiac function test abnormal Cardiac stress test Computerised tomogram abnormal Congestive cardiomyopathy Dilatation atrial Dyspnoea Echocardiogram Ejection fraction decreased Electrocardiogram ambulatory abnormal Magnetic resonance imaging heart Myocardial fibrosis Myocarditis Scan with contrast abnormal Ventricular arrhythmia

Symptomtext

Shortness of breath weakness- within 2 weeks of 2nd dose of the vaccine New onset multifocal ventricular arrhythmia- Note 3 weeks after the vaccine seen on Holter Monitor 5/20/21, Trans thoracic Echo 5/20/21 LV low end of normal then Nuclear stress treadmill 5/20/21 VEF 33% with low probability of coronary stenosis or ischemia New onset atrial dilation- Noted on cardiac tests CT CCTA w Contrast showed LV ejection fraction 26% Cardiac MRI -9/28/21 dilated cardiomyopathy with basal septal and inferior scarring of mid to lower myocardium due to myocarditis. Heart Failure Myocarditis Heart Failure New Onset Atrial Fibrillation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: New onset multifocal ventricular arrhythmia- Note 3 weeks after the vaccine seen on Holter Monitor 5/20/21, Trans thoracic Echo 5/20/21 LV low end of normal then Nuclear stress treadmill 5/20/21 VEF 33% with low probability of coronary stenosis or ischemia New onset atrial dilation- Noted on cardiac tests CT CCTA w Contrast showed LV ejection fraction 26% Cardiac MRI -9/28/21 dilated cardiomyopathy with basal septal and inferior scarring of mid to lower myocardium due to myocarditis. Heart Failure Myocarditis Heart Failure New Onset Atrial Fibrillation 5/25/2022- ECG
Aktuelle Erkrankungen: -
Vorgeschichte: Benign essential Hypertension Osteoarthritis shoulder Lynch Syndrome
Andere Medikamente: Losartan 50 mg po q day, Hydrochlorothiazide 12.5 mg Po Q day, Resveratrol 500mg PO q day, Niacinamide 500 mg PO q day, Celecoxib 200 mg PQ q day, Myrbetriq 25 mg PO day, Aspirin 325 mg PO day
Allergien: NONE
Vorherige Impfungen: -

VAERS 2314111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 09.06.2022
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Adrenal disorder Angiotensin converting enzyme increased Anti-HLA antibody test positive Antiacetylcholine receptor antibody positive Antibody test positive Arrhythmia Atrial fibrillation Audiogram normal Autonomic nervous system imbalance Back pain Biopsy skin abnormal Blood pressure fluctuation Burning sensation Cardiac dysfunction Chest discomfort Computerised tomogram abnormal Cytokine test

Symptomtext

Dose 1: Paresthesias developed almost immediately after injection into right delotoid along right arm with warm/cold/tingling sensations. By day 2, I had paraesthesias radiating into axilla with a sensation of sweat without actual sweating. The paraesthesias continued into my right face with tingling, right eye with irritation, and right ear with flushing. I consulted with a neurologist at my place of employment. He conducted basic blood work and EMG on right arm which were normal. I was instructed to proceed with the second dose against my better medical judgement. On January 19, 2021, I received the second dose in my left deltoid. For the following 3 days, I had severe pain at the injection site radiating into my neck and upper back. On day 4, I awoke with intense itching in right ear canal and tinnitus. I also developed extreme abdominal pain, nausea, intense headache. By January 30, 2021, I was having tachycardic episodes that sometimes lasted through the night, chest discomfort, and blood pressure swings with elevations as high as 200s/120s. I went to the ER on January 30, 2021 and suggested I was having a severe reaction. A CT showed mesenteric panniculitis. My suggestion was dismissed, and I was sent home with ibuprofen and instructions to follow up with GI and ENT. No explanation for the wide variety of my symptoms was given. Through February I continued with tachycardia and blood pressure issues. Follow up with GI included upper and lower endoscopies that were unrevealing. Medrol dose pack was given which improved mesenteric panniculitis. Audiogram was performed by ENT and was normal. One ENT attributed the tinnitus to post vaccine inflammation. Others dismissed it without further investigation (this was before tinnitus as side effect was known). Symptoms continued to progress to include autonomic dysfunction: positional tachycardia, temperature dysregulation, intractable insomnia, adrenal dumps, brain fog. Muscle fasciculations, tremors, and skin ?zaps? continued. The right eye irritation progressed to blurry vision and problems adjusting to light changes. The electrical paraesthesias progressed to full blown body wide neuropathies with stinging, stabbing, burning, prickling sensations. The cardiac dysfunction progressed to atrial fibrillation, symptomatic PVCs and NSVT. In Sept a skin biopsy was indicative of small fiber neuropathy and tilt table was positive for POTs. After clinic gave a presentation to Neuromuscular Department in October 2021, my neurologist (who suspected sudomotor, small fiber) decided on a trial of IVIg. This improved the neuropathy symptom, but due to side effect of hemolysis, it was halted. After reaching out to Dr., I was directed to Neurology for evaluation. SCIg trial was initiated. This continued to improve symptoms but exacerbated the tinnitus and cardiac symptoms and was halted. As the medical profession was not actively investigating reactions and I could obtain no response from Pfizer, I took it upon myself to research my affliction. The only labs that were revealing were autoantibody labs from overseas. I was positive for numerous antibodies including ACE2, MAS1, AT1R, beta and muscarinic cholinergic receptors. The validity of these results is questioned. However, based on these findings, a trial of plasmapheresis was undertaken in March 2021. Neuropathies resolved and POTs symptoms improved. Tinnitus was only marginally improved. Muscle fasciculations were reduced. Repeat autoantibody testing post plex showed elimination and/or reduction in antibodies. At 8 weeks, symptoms slowly returned and post plex labs were repeated showing an marked increase in autoantibodies. Persisting symptoms include cardiac arrythmias, muscle fasciculations, paraesthesia, severe tinnitus, muscle weakness, brain fog, headache/head pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: 10,0
Labordaten: Tilt Table 7/2021 - Positive Skin Biopsy - Small Fiber Neuropathy 9/2021 Labs - positive autoantibodies Cytokine Panel - SCD40L and CCR5 (Rantes) elevated
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2243202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: FL
Alter: 78,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 02.02.2021
Beginn: 19.04.2022
Tage bis Beginn: 441,0
Dosis: UNK
Route/Site: - / -

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

Body temperature increased COVID-19 Chest X-ray normal Hypoxia Mental status changes Respiratory distress SARS-CoV-2 test positive Sepsis Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 01/12/2021. 79 y/o female with PMHx of hypothyroidism, dementia, HTN, GERD, and hx of right breast cancer with possible mets presents to ED from nursing home after testing Covid + on 4/18. Pt with AMS and hypoxia per NH. Upon arrival to ED, pt with temp of 102.7, room air sat 95% but placed on 5L NC for resp distress. Sepsis alert in ED. CXR with no focal consolidation. Pt started on IV ABX, Steroids and Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected on 04/19/2022, pt also tested positive at NH on 04/18/2022 but those records unavailable.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism, Dementia, HTN, GERD, Right breast cancer with possible mets
Andere Medikamente: -
Allergien: Neomycin, Neosporin Opthalamic
Vorherige Impfungen: -

VAERS 2027318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: GA
Alter: 28,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 19.02.2021
Beginn: 29.04.2021
Tage bis Beginn: 69,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac stress test normal Dizziness Dyspnoea Echocardiogram abnormal Ejection fraction decreased Heart rate increased Myocarditis

Symptomtext

Myocarditis-fast heart rate , shortness of breath and dizziness. Was prescribed coreg for 6 months after my echo came back a little reduced.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Echocardiogram showed heart was a little reduced Stress test was normal
Aktuelle Erkrankungen: Asthma attack
Vorgeschichte: -
Andere Medikamente: Singular Black seed oil Zinc
Allergien: -
Vorherige Impfungen: -

VAERS 2006455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: GA
Alter: 63,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 25.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Computerised tomogram Facial paralysis Neurological symptom

Symptomtext

Right side of face was drooping, Bells Palsy Symptoms like a stroke. Prednisone and Anti Viral Medicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: CT scan
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Deltizin 180 MG, Omothyroid 2 60 MG & 1 30 MG. Protonix
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1997204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 15.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / AR

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

Bell's palsy Hypoaesthesia

Symptomtext

Bells Palsy on side of face; facial numbness x 7 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: Emergency C, ambien as needed
Allergien: None
Vorherige Impfungen: -

VAERS 1995289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 23.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Anaemia Arthralgia Atrioventricular block Atrioventricular block first degree Cerebral venous sinus thrombosis Chillblains Dural arteriovenous fistula Investigation Magnetic resonance imaging Palindromic rheumatism Polyarthritis SARS-CoV-2 antibody test SARS-CoV-2 test Tinnitus

Symptomtext

right shoulder pain; inflammatory polyarthritis; suspected palindromic rheumatism; pulsatile tinnitus; left cerebral venous sinus narrowing with dural AV fistula; left cerebral venous sinus narrowing with dural AV fistula; developed anemia; pernio; first degree heart block; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 37 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 23Jan2021 (Lot number: EL3247) at the age of 37 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Prediabetes" (unspecified if ongoing); "borderline hyperlipidemia" (unspecified if ongoing); "mild macular degeneration" (unspecified if ongoing). Concomitant medication(s) included: LO LOESTRIN FE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; TYLENOL. Vaccination history included: Bnt162b2 (Dose Number: 1, prev dose product=COVID 19, prev dose brand=Pfizer, prev dose brand unknown=False, prev dose lot number=EL0140, prev dose lot unknown=False, prev dose administrator route=Intramuscular, prev dose administration date=26Dec2020 , prev dose dose number=1 , prev dose vaccine location=Left arm), administration date: 26Dec2020, when the patient was 36 years old, for COVID-19 immunization, reaction(s): "headache", "prominent veins in right arm". No other vaccine in four weeks. No COVID prior vaccination. COVID tested post vaccination. No known allergies. The following information was reported: ARTHRALGIA (disability) with onset 2021, outcome "not recovered", described as "right shoulder pain"; POLYARTHRITIS (disability, medically significant) with onset 2021, outcome "not recovered", described as "inflammatory polyarthritis"; PALINDROMIC RHEUMATISM (disability, medically significant) with onset 2021, outcome "not recovered", described as "suspected palindromic rheumatism"; TINNITUS (disability) with onset 2021, outcome "not recovered", described as "pulsatile tinnitus"; CEREBRAL VENOUS SINUS THROMBOSIS (disability, medically significant), DURAL ARTERIOVENOUS FISTULA (disability, medically significant) all with onset 2021, outcome "not recovered" and all described as "left cerebral venous sinus narrowing with dural AV fistula"; ANAEMIA (disability) with onset 2021, outcome "not recovered", described as "developed anemia"; CHILLBLAINS (disability) with onset 2021, outcome "not recovered", described as "pernio"; ATRIOVENTRICULAR BLOCK FIRST DEGREE (disability) with onset 2021, outcome "not recovered", described as "first degree heart block". The events "right shoulder pain", "inflammatory polyarthritis", "suspected palindromic rheumatism", "pulsatile tinnitus", "left cerebral venous sinus narrowing with dural av fistula", "left cerebral venous sinus narrowing with dural av fistula", "developed anemia", "pernio" and "first degree heart block" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: anaemia: (unspecified date) anaemia; atrioventricular block: (unspecified date) first degree heart block, notes: first degree heart block; investigation: (unspecified date) sle, notes: labwork was consistent with new-onset SLE; magnetic resonance imaging: (unspecified date) dural av fistula, notes: MRI of brain showed left cerebral venous sinus narrowing with dural AV fistula; sars-cov-2 antibody test: (22Aug2021) negative, notes: Blood test; sars-cov-2 test: (01Sep2021) negative, notes: Blood test; (09Jan2021) negative, notes: Nasal Swab; (21Jan2021) negative, notes: Nasal Swab; (13Sep2021) negative, notes: Nasal Swab; (28Sep2021) negative, notes: Nasal Swab; (07Oct2021) negative, notes: Nasal Swab; (07Oct2021) negative, notes: Nasal Swab; (23Nov2021) negative, notes: Nasal Swab; (30Nov2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of arthralgia, polyarthritis, palindromic rheumatism, tinnitus, cerebral venous sinus thrombosis, dural arteriovenous fistula, anaemia, chillblains, atrioventricular block first degree. Patient was treated with Prednisone, hydroxychloroquine. Clinical course: Autoimmune disease: had headache, then prominent veins in right arm after 1st dose, suspected to have thoracic outlet syndrome. After 2nd dose, right shoulder pain then inflammatory polyarthritis, suspected palindromic rheumatism. Also pulsatile tinnitus, MRI of brain showed left cerebral venous sinus narrowing with dural AV fistula. Later also developed anemia, pernio and first degree heart block, labwork was consistent with new-onset SLE.; Sender's Comments: Based on possible temporal association the causal role of BNT162B2 Vaccine cannot be excluded for reported events. Case will be reviewed further on receipt of FU information 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: Cerebral venous sinus thrombosis
Hospital-Tage: -
Labordaten: Test Name: Anaemia; Result Unstructured Data: Test Result:Anaemia; Test Name: Heart block; Result Unstructured Data: Test Result:first degree heart block; Comments: first degree heart block; Test Name: labwork; Result Unstructured Data: Test Result:SLE; Comments: labwork was consistent with new-onset SLE; Test Name: MRI; Result Unstructured Data: Test Result:dural AV fistula; Comments: MRI of brain showed left cerebral venous sinus narrowing with dural AV fistula; Test Date: 20210822; Test Name: SARS-CoV-2 Antibodies, Nucleocapsid; Result Unstructured Data: Test Result:Negative; Comments: Blood test; Test Date: 20210901; Test Name: Adaptive T-Detect COVID; Result Unstructured Data: Test Result:Negative; Comments: Blood test; Test Date: 20210109; Test Name: COVID-19 NAAT (PCR,TMA); Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 20210121; Test Name: COVID-19 NAAT (PCR,TMA); Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 20210913; Test Name: COVID-19 NAAT (PCR,TMA); Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 20210928; Test Name: COVID-19 NAAT (PCR,TMA); Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 20211007; Test Name: COVID-19 NAAT (PCR,TMA); Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 20211007; Test Name: COVID-19 NAAT (PCR,TMA); Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 20211123; Test Name: COVID-19 NAAT (PCR,TMA); Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 20211130; Test Name: COVID-19 NAAT (PCR,TMA); Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hyperlipidemia; Macular degeneration; Prediabetes
Andere Medikamente: LO LOESTRIN FE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1898173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: SD
Alter: 30,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 31.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hepatic fibrosis Hepatitis alcoholic Jaundice cholestatic Loss of consciousness

Symptomtext

passed out unknowingly for hours, 2 and a half weeks later hospitalized with jaundice

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: Hepatic fibrosis, advanced fibrosis Alcoholic hepatitis, unspecified whether ascites present Obstructive Jaundice
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Alprazolam, Alcohol
Allergien: Amoxicillin, Neosporin, Tramadol, Clindamycin
Vorherige Impfungen: -

VAERS 1897744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 20,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 17.01.2021
Beginn: 14.07.2021
Tage bis Beginn: 178,0
Dosis: UNK
Route/Site: IM / LA

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

Myocarditis

Symptomtext

Myocarditis

Weitere VAERSDATA-Felder

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

VAERS 1870651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: UT
Alter: 25,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 14.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / -

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

Dyspnoea Loss of consciousness Palpitations

Symptomtext

Symptomatic palpitation, shortness of breath, passing out at 5:05 am in the morning. Heart continues to race and then slowdown all today, current time is 6:05 pm.

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

VAERS 1829463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: IL
Alter: 26,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 06.02.2021
Beginn: 28.10.2021
Tage bis Beginn: 264,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Cough Dehydration Diarrhoea Malaise SARS-CoV-2 test positive Syncope

Symptomtext

10/27/21 in ED with Covid symptoms: diarrhea, cough, syncope, dehydration.

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Praegender Schweregrund: Syncope
Hospital-Tage: 1,0
Labordaten: 10/27/21 Covid +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1749873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 83,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 15.02.2021
Beginn: 17.04.2021
Tage bis Beginn: 61,0
Dosis: 2
Route/Site: IM / RA

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

Acupuncture Bell's palsy Facial paralysis Magnetic resonance imaging

Symptomtext

Developed sudden onset of Bell's Palsy, with paralysis of left side of face, affecting left eye and mouth Received Prednisone - 60 mgm QD for 10 days with no improvement Acupuncture 3 sessions a week for 3 weeks with some improvement Physical Therapy - ongoing, with some improvement

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: MRI - April 22, 2021
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis Glaucoma Hypothyroidism
Andere Medikamente: Levothyroxin 25 mg QD, Combigan eye drops OU BID Vit C 1000mgm QD, Turmeric 500 mg QD, Vit B 1000 mg QD, Vit. D 2000 mg QD
Allergien: Bacitracin, Neomycin, Lumigan eye drops
Vorherige Impfungen: -

VAERS 1737439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 27.09.2021
Impfdatum: 04.01.2021
Beginn: 25.09.2021
Tage bis Beginn: 264,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction COVID-19 SARS-CoV-2 test positive

Symptomtext

Hospitalization being treated for anaphylaxis and covid screening positive.

Weitere VAERSDATA-Felder

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

VAERS 1689543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

schwer

Staat: NY
Alter: 86,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 21.01.2021
Beginn: 11.02.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Dyspnoea exertional Fatigue Loss of consciousness Oxygen saturation decreased

Symptomtext

87-year-old female with history of hypertension, hyperlipidemia, diabetes presents to emergency department complaining of worsening fatigue, shortness of breath, cough as well as 2 episodes when she passed out at home. Patient mentions that she was recently diagnosed with COVID-19 infection on 8/25/2021 at which time she was evaluated in this emergency department but was feeling well and was discharged home as she was not hypoxic. Her oxygen saturations ranging high 80s to low 90s on room air. When she exerts her oxygen saturation drops down further.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1685570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 71,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 25.02.2021
Beginn: 18.05.2021
Tage bis Beginn: 82,0
Dosis: 2
Route/Site: IM / LA

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

Hypotension Thrombosis Ultrasound Doppler

Symptomtext

Three months after taking the 2nd dose, I developed a blood clot on my left leg. I was prescribed with Eliquis, a blood thinner. Also, my blood pressure decreased to a very low state. Recently my blood pressure has improved, but I am still dealing with the blood clot.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type II Diabetes; Hypothyroid ; Hypertension; High cholesterol; PMR - Polymyositis; Rheumatica; Gastric reflux disease
Andere Medikamente: Olmesartan 40 mg; Indapamide 2.5 mcg; Jentadueto 2.5 mg; Atorvastatin 20 mg; Levothroid 125 mcg; Dexilant 60 mg; Cialis 5 mg; Prednisone 7.5 mg; Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 973928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 13.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Anaphylactic reaction Bronchospasm Dysphonia Dyspnoea Hypoaesthesia Lip swelling Oral discomfort Respiratory distress Respiratory failure Stridor Tachypnoea Throat tightness Urticaria Wheezing

Symptomtext

severe allergic reaction (anaphylaxis) after the 2nd dose; her lips felt like they were on fire; lips started swell; bronchospasm; wheezing; stridor; respiratory failure; Both arms were completely numb; respiratory distress; tachypnea; hoarse voice; difficulty breathing; sensation of throat closure; a little bit of hives, mostly on chest and abdomen; This is a spontaneous report from a contactable nurse (patient). This 39-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration administered in right arm on 13Jan2021 (at the age of 39 years) (Batch/Lot Number: EL3247; Expiration Date: May2021) as a single dose for COVID-19 immunization. Medical history included immunodeficiency common variable diagnosed about 4 years ago or a little longer and allergy to sulfa antibiotics as a child. Concomitant medications included famotidine (PEPCID), diphenhydramine hydrochloride (BENADRYL), and montelukast sodium (SINGULAIR) all taken a week prior to getting both doses of the COVID vaccine. With her immunodeficiency, she gets weekly IGg infusions and has been getting these infusions for at least 4 years or more. The patient previously received the first dose of bnt162b2 administered in right arm on 23Dec2020 (lot number: EL1284) for COVID-19 immunization. Patient also previously took Demerol and experienced anaphylactic reaction. Patient is a part of the immunocompromised population but experienced a severe allergic reaction (anaphylaxis) on 13Jan2021, after the second dose of the Pfizer BioNTech Covid-19 Vaccine. The signs and symptoms of the anaphylactic reaction were reported as follows: First thing she noticed was that her lips felt like they were on fire, then lips started swell, she went into a bronchospasm with wheezing and stridor, then started to go into respiratory failure. Code team was called. Both arms were completely numb. They thought she was going to need a breathing tube put in but they did not "bronc" her. Patient was not hospitalized and was not admitted to an Intensive Care Unit. Information on organ involvement/multiorgan involvement were reported as follows: Respiratory: wheezing/bronchospasm; stridor; respiratory distress (details: tachypnea; hoarse voice; difficulty breathing, sensation of throat closure), Cardiovascular: tachycardia due to Epi, no shock or blood pressure issues, and Dermatological: she thought she got a little bit of hives, mostly on chest and abdomen, no gastrointestinal symptoms, no any other symptoms/signs. AEs did not require visit to the physician office (also reported as "she called her doctors"). No relevant tests were performed. These started within 7 minutes of receiving the second dose. Treatment received included epinephrine (Recemic Epi, may have received an epinephrine nebulizer), steroids, Benadryl, and was in the ER for 6 hours. Patient did not receive any recent vaccines for any other conditions or for SARS-CoV2 other than Pfizer- BioNTech COVID-19 Vaccine prior to the event being reported. Patient did not receive any other vaccines around the time of Pfizer-BioNTech COVID-19 Vaccine vaccination and within 4 weeks prior to the COVID vaccine. Outcome of the events was recovered on 13Jan2021. Reporter's seriousness assessment for anaphylactic reaction was life threatening. The patient wanted to know if we have information on tests being done involving alteration of doses of the Pfizer BioNTech COVID-19 Vaccine for people who experienced severe allergic reaction after the dose of the vaccine. The patient to know the Pfizer BioNTech Covid-19 Vaccine booster dose recommendations for a patient who is part of the immunocompromised population who is exposed to COVID-19 patients, but had an anaphylactic reaction after the second dose of the vaccine. She is interested in getting the booster dose of the vaccine. She might be potentially contraindicated to get the booster dose since she had a severe reaction to the second dose of the COVID vaccine, she had an anaphylactic reaction.; Sender's Comments: Based on the available information, there is a reasonable possibility of a causal relationship between the suspect vaccine BNT162B2 (COMIRNATY) and reported events Anaphylactic reaction, oral discomfort, lip swelling, bronchospasm, wheezing, stridor, Respiratory failure, Hypoesthesia, respiratory distress, tachypnoea, Dysphonia, dyspnea, Throat tightness and urticaria which cannot be fully assessed/excluded. The case will be reassessed if additional information becomes available. 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: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Common variable immunodeficiency; Sulfonamide allergy (allergy to sulfa antibiotics as a child)
Andere Medikamente: PEPCID [FAMOTIDINE]; BENADRYL; SINGULAIR; IGG
Allergien: -
Vorherige Impfungen: -

VAERS 1667554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CO
Alter: 53,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 05.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / LA

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

Back pain Disturbance in attention Electric shock sensation Insomnia Memory impairment Pain in extremity

Symptomtext

Not long after the vaccine I began to develop sharp, electrical, stabbing pains all over my body in random places; arms, legs, back, feet. The foot pain is getting worse so I felt I should report it. It feels like someone is driving hot, electrified needles in to my skin. It is not chronic, but it happens sporadically throughout the week and is very painful. I am also having memory issues. My concentration and focus is worse and I am not sleeping as well as I used to.

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None. I already tested positive for COVID in November 2020
Vorgeschichte: LBBB, asthma, history of heart failure (caused by Lyrica)
Andere Medikamente: Tylenol, Advil, vitamin D, C
Allergien: Flagyl, Lyrica
Vorherige Impfungen: -

VAERS 1624526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CT
Alter: 60,0
Geschlecht: F
Eingang: 23.08.2021
Impfdatum: 23.01.2021
Beginn: 17.08.2021
Tage bis Beginn: 206,0
Dosis: 2
Route/Site: IM / UN

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

Abdominal abscess Abdominal infection Abdominal pain Abscess drainage COVID-19 Cough Dyspnoea Explorative laparotomy Gastrointestinal tube insertion Incisional hernia repair Intensive care Intestinal adhesion lysis Intra-abdominal fluid collection Listeria test positive Nasal congestion Neutropenia Oedema peripheral Oropharyngeal pain

Symptomtext

Patient tested for COVID-19 on 8/17: 61yo physician with h/o MM s/p ASCT on daratumumab/pomalidomide, HCV cirrhosis / HCC s/p OLT 5/2019 c/b incisional hernia s/p hernia repair with mesh 6/4/20, c/b infected mesh and abdominal abscess s/p ex-lap, washout and mesh removal on 8/5 with OR cx +listeria monocytogenes, now with fever and shortness of breath. He was discharged on 8/11 on augmentin, then over the weekend developed fever to 102 on 8/13 and progressive shortness of breath. Reports nonproductive cough as well and has been using nebulizer with partial improvement. No chest pain. No significant change in abdominal pain - mainly feels sore with using the incentive spirometer. Also reports nasal congestion and sore throat intermittently since having NG tube recently. No known sick contacts. He had recent parainfluenza virus infection prior to his last admission. He also complains of asymmetric RLE edema. Tested positive for COVID-19 on 8/17 and received compassionate use casirivimab-imdevimab, remdesivir, dexamethasone. Tocilizumab not given due to neutropenia. Received zosyn then unasyn for intra-abdominal infection. Patient remains in ICU on HFNC 100% Fio2 and 40 L.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 8,0
Labordaten: 8/17: COVID-19 PCR - positive 8/17: Antibody- negative IGG Anti-spike assay - negative
Aktuelle Erkrankungen: -
Vorgeschichte: 60 yo male s/p OLT 5/7/2019 for HCV cirrhosis, PVT, HCC, hx of multiple myeloma follows at MSK. S/p exlap / LOA and incisional hernia repair 6/4/21 after sx has been growing fluid collection presents to ED on 8/4/21 with abd pain and wound erythema over mercedes scar.
Andere Medikamente: Tacrolimus, Tamsulosin, pantoprazole, aspirin, bortezomib
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1591676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

schwer

Staat: NC
Alter: 34,0
Geschlecht: F
Eingang: 20.08.2021
Impfdatum: 29.01.2021
Beginn: 02.08.2021
Tage bis Beginn: 185,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Bell's palsy Blood test normal Ear pain Facial paralysis Headache Heart rate irregular Muscle tightness Nausea

Symptomtext

Starting in spring of 2021 I noticed I would have an irregular heart rate when running, something I had not experienced prior. I also started having severe abdominal pain to the point I went to my PCP to inquire. It was not stated what the cause of this was, blood work was done everything looked OK and ultrasound was offered. I declined as I knew I would be told ?I don?t know what it is.? Sunday, August 1, 2021 I went to bed with ear pain in my right ear, a headache and a tightness in my neck. I woke up Monday, August 2, 2021 to the right side of my face being paralyzed. After going to the ER that day they diagnosed me with Bell?s palsy. Monday will be three weeks I have had it. I?m experiencing constant dizziness, nausea, pain in my ear & neck.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1574630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: OR
Alter: 63,0
Geschlecht: M
Eingang: 16.08.2021
Impfdatum: 07.02.2021
Beginn: 20.06.2021
Tage bis Beginn: 133,0
Dosis: 2
Route/Site: IM / LA

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

Allergy to arthropod sting Anaphylactic reaction Asthma Condition aggravated Hypotension Urticaria Wheezing

Symptomtext

First time ever anaphylactic reaction to insect sting (later determined to be bald faced hornet. Symptoms included wheezing/asthma exacerbation, diffuse hives and hypotension to BP 66/42 sitting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: HTN; Asthma; elevated fasting glucose
Vorgeschichte: As above
Andere Medikamente: Amlodipine; irbesartan; QD Advair; albuterol; ASA; Saw Palmetto; MVI
Allergien: NEW: Anaphylactic reaction to bald-faced hornet sting
Vorherige Impfungen: -

VAERS 1550442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MS
Alter: 37,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 22.01.2021
Beginn: 19.07.2021
Tage bis Beginn: 178,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Seizure

Symptomtext

Seizures have worsened in the last 3 weeks. I was having about 7-10/day. Now I?m having up to 22/day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None so far.
Aktuelle Erkrankungen: Brain tumor, seizures
Vorgeschichte: Brain tumor. Seizures
Andere Medikamente: Lexapro, triliptal, Ativan, briviact
Allergien: None
Vorherige Impfungen: -

VAERS 1531881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: AZ
Alter: 55,0
Geschlecht: M
Eingang: 06.08.2021
Impfdatum: 02.02.2021
Beginn: 12.04.2021
Tage bis Beginn: 69,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Computerised tomogram spine Magnetic resonance imaging spinal Pain Pain in extremity Paraesthesia Peripheral swelling Scan with contrast Thrombosis Ultrasound Doppler abnormal

Symptomtext

Around 4/12/2021 I began I started realizing my left leg was throbbing, but I was linking it to my torn hip muscle, my doctor stated it could have been from my back. The pain was unbearable so I went to the ER on 4/30/2021, they did an ultra sound and found that I had a blood clot in my leg which was causing the pain. I was admitted over night at the Hospital and went home on 5/1/2021. I went to my PCP for follow up and again I went for a follow up ultra sound last week and it showed that I still have the blood clot. I was given Eliquis. The pain that was in my leg is gone, but I continue to have swelling and a tingling sensation in my leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 1,0
Labordaten: Ultra sound - showed a blood clot. CT Scan and contrast MRI on my back.
Aktuelle Erkrankungen: torn hip muscle
Vorgeschichte: none
Andere Medikamente: Multi-vitamin, probiotic
Allergien: codeine
Vorherige Impfungen: -

VAERS 1513106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: TX
Alter: 29,0
Geschlecht: F
Eingang: 29.07.2021
Impfdatum: 01.01.2021
Beginn: 01.06.2021
Tage bis Beginn: 151,0
Dosis: 1
Route/Site: UN / LA

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

Dehydration Electroencephalogram Magnetic resonance imaging Muscle twitching Seizure

Symptomtext

Twitching, dehydration, seizures

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: EEG, MRI
Aktuelle Erkrankungen: none
Vorgeschichte: thyroid issues
Andere Medikamente: None
Allergien: sulfur
Vorherige Impfungen: -

VAERS 1500798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: AZ
Alter: 38,0
Geschlecht: F
Eingang: 24.07.2021
Impfdatum: 18.01.2021
Beginn: 18.02.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: SYR / LA

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

Abnormal behaviour Amnesia Blood test normal Computerised tomogram Condition aggravated Loss of consciousness Magnetic resonance imaging head normal Migraine Nausea Nephrolithiasis Pain

Symptomtext

I have been getting severe migraines. I was getting them once or twice a month after the vaccine but in the last month, I have had four or five a week (prior to vaccine I would get light sensitivity and bad headache but that was once every three-five months). When I'm having the migraines, I have no recollection of what I am doing or where I am. I have full conversations with people but they don't make sense, I ask "Did you remember the spaghetti for Thanksgiving?" To me, the sentence makes sense. I can be in the middle of the sentence and I pass out. Medication for the migraines, I was put on Fioricet and Phenalgin for nausea and Ubrelvy (migraine preventative pill, can take it when I start to feel one coming on). Doctor just put me on a monthly shot. Aimovig, that's a one-time monthly injection. At the time of the event, they help but overall no they are not stopping it. I've had ER visits, two, both were at the same hospital and they did bloodwork and imaging. One was in January and the other one was April 15th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Hospital ER, January, CAT Scan and bloodwork - Medication while I was there to help with the pain and the migraine affects. Hospital ER, April 15, they thought I had a kidney stone, and I did have one, I have had kidney stones prior. Doctor, follow up appts, bloodwork each time, came back okay. Imaging, MRI, Brain, that came back okay. Two weeks ago.
Aktuelle Erkrankungen: No.
Vorgeschichte: Gout.
Andere Medikamente: Estradiol.
Allergien: Wheat; Cow's Milk; Eggs; Bananas.
Vorherige Impfungen: Flu shot, I usually get a low grade fever and headache and had last year's 2020.

VAERS 1478107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: AR
Alter: 83,0
Geschlecht: M
Eingang: 16.07.2021
Impfdatum: 12.02.2021
Beginn: 12.07.2021
Tage bis Beginn: 150,0
Dosis: 2
Route/Site: IM / UN

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

Asthenia COVID-19 Chest X-ray abnormal Dyspnoea Fibrin D dimer increased Hypoxia Intensive care Pneumonia Pulmonary oedema SARS-CoV-2 test positive Serum ferritin increased White blood cell count increased

Symptomtext

Presented to hospital for increased SoB and weakness. Diagnosed with COVID-19 on 7/8. Discharged home on 2L O2 and dexamethasone. On 7/12 presented again with hypoxia, elevated WBC/ D-dimer. O2 titrated to 5 L NC and transferred to our facility on 7/12. Oxygen requirement continued to increase and patient admitted to ICU on 7/14. Currently receiving dexamethasone and received tocilizumab 7/13. Received remdesivir initially but was discontinued on transition to HFNC> Currently on HFNC w/NRB 50 L at 90%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: 7/8 COVID test positive (per report) 7/12 CXR persistent/worsening multifocal PNA vs edema 7/14 Ferritin 1255
Aktuelle Erkrankungen: -
Vorgeschichte: Arteriosclerotic heart disease, BPH, GERD, HLD, HTN, PUD, osteoarthritis
Andere Medikamente: Medications at time of admission: Apixaban, clopidogrel, finasteride, folic acid, losartan, montelukast, pantoprazole, pravastatin, tamsulosin
Allergien: -
Vorherige Impfungen: -

VAERS 1469712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NE
Alter: 19,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 04.03.2021
Beginn: 04.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Dysarthria Headache Heart rate increased Presyncope Tremor

Symptomtext

shakiness; increased heart rate; horrible headache; i have almost passed out multiple times; slurred speech; This is a spontaneous report from a contactable other HCP. A 19-years-old non pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for Injection, Batch/Lot number: EL3247) via an unspecified route of administration, administered in arm left on 04Mar2021 at 11:00 for COVID-19 immunisation. The patient medical history not reported. The patient concomitant medications included alprazolam (XANAX), ascorbic acid, beta vulgaris root, iron amino acid chelate, rosa canina fruit, rubus idaeus leaf (IRON SUPPLEMENT). The patient historical vaccine included first dose on 09Feb2021 at 07:00 PM (lot number: EL3241) as single dose for COVID-19 immunisation. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received birth control, xanax, iron supplement medications within 2 weeks of vaccination. On 04Mar2021 at 11:00 AM, the patient experienced the same reaction that get anemic, shakiness, increased heart rate, horrible headache and patient had almost passed out multiple times, had slurred speech. These happened directing after the vaccine. No treatment was received. The outcome of the event was resolving. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Weitere VAERSDATA-Felder

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

VAERS 1467092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: HI
Alter: 32,0
Geschlecht: F
Eingang: 13.07.2021
Impfdatum: 05.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: IM / LA

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

Alanine aminotransferase normal Anion gap Aspartate aminotransferase Blood albumin normal Blood alkaline phosphatase normal Blood bicarbonate normal Blood bilirubin increased Blood calcium increased Blood chloride increased Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood urea increased Chest pain Differential white blood cell count Dyspnoea Echocardiogram abnormal

Symptomtext

Patient with pericarditis starting 14 days after 2nd covid vaccine with small but detectable tropI responding to nsaids however continue chest pain and SOB and failure to taper without discomfort while on Colchicine 0.6mg once a day for 2 months resulted in transitioning therapy to steroids currently on 15mg to taper to 10mg , 7.5mg, 5mg, 2.5 mg. Her taper extends by 2.5mg q30 days until complete with plan to wean off by mid fall then start return to exercise as tolerated and eventual duty. A CMR was performed without evidence of overt myocarditis however her etiology at this point is suggesting of covid19 vaccine induced perimyocarditis although idiopathic cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Echocardiogram MAR21 ? mildly dilated LV and LA with normal right ventricular size. Normal valves LVEF 60-65% ziopatch every 20 21?14 days a monitoring no symptoms reported multiple brief episodes of supraventricular tachycardia up to 10 beats suggestive of atrial tachycardia or flutter no AV block or significant positives no triggered events CMR MAR21 ? dilated RV and LV LVEF 62%, no LGE normal wall motion omprehensive Metabolic Panel Site / Specimen 08 Jan 2021 0912 Units Ref Range Glucose SERUM 93 mg/dL (70-105) Creatinine SERUM 0.82 mg/dL (.57-1.25) Urea Nitrogen SERUM 9 mg/dL (7-23) Sodium SERUM 141 mmol/L (136-145) Potassium SERUM 4.6 mmol/L (3.7-5.3) Chloride SERUM 108 (H) mmol/L (98-107) Bicarbonate SERUM 27 mmol/L (22-29) Anion Gap SERUM 6 (L) mmol/L (8-16) Calcium SERUM 8.8 mg/dL (8.4-10.2) Alanine Aminotransferase SERUM 8 (L) U/L (10-55) Albumin SERUM 4.4 g/dL (3.5-5.0) Alkaline Phosphatase SERUM 47 U/L (40-150) Aspartate Aminotransferase SERUM 14 U/L (5-34) Bilirubin SERUM 2.5 (H) mg/dL (0.2-1.2) Protein SERUM 6.8 g/dL (6.4-8.3) GFR Non-Black SERUM 95.0 mL/min GFR Black SERUM 109.5 <i> mL/min Triiodothyronine Site / Specimen 08 Jan 2021 0912 Units Ref Range Triiodothyronine SERUM 1.28 ng/mL (.5-1.6) Thyroxine Free Site / Specimen 08 Jan 2021 0912 Units Ref Range Thyroxine Free SERUM 1.00 ng/dL (.8-1.6) hCG Quant Site / Specimen 08 Jan 2021 0912 Units Ref Range hCG SERUM <1.20 <i> mIU/mL CBC W/Auto Diff Site / Specimen 08 Jan 2021 0912 Units Ref Range WBC BLOOD 5.8 x10(9)/L (3.5-11.0) RBC BLOOD 5.49 (H) x10(12)/L (4.1-5.1) Hemoglobin BLOOD 14.2 g/dL (11.7-15.7) Hematocrit BLOOD 46.4 % (35.1-47.1) Platelets BLOOD 187 x10(9)/L (150-440) Troponin I Cardiac PLASMA 0.446 (H*) <i> <r>
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism (Surgical).
Andere Medikamente: Levothyroxine 112mcg daily; Liothyronine 10mcg daily.
Allergien: NKA, NKDA.
Vorherige Impfungen: -

VAERS 1442573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MO
Alter: 65,0
Geschlecht: F
Eingang: 02.07.2021
Impfdatum: 29.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Arteriosclerosis coronary artery Atelectasis Atrial fibrillation Cardiac failure Cardiomegaly Computerised tomogram Dyspnoea Echocardiogram Electrocardiogram Fatigue Influenza like illness Mitral valve calcification Pain Pain in extremity Pleural effusion Pulmonary function test Pulmonary oedema Pyrexia

Symptomtext

stridal wheezing; Ache; Arm was sore/Soreness left arm at site of injection; Low grade fever like a 100 or below/Mild fever 99.9; A-fib 40s was diagnosed, it started on Jan2021& echocardiogram: a-fib 140s, moderate mitral regurgitation a-fib on 23Mar2021; Heart failure; mild interstitial pulmonary edema; shortness of breath; I felt like I had the flu; computerised tomogram: pleural effusion; partial atelectasis; computerised tomogram: pleural effusion; partial atelectasis; Cardiomegaly; Heavy mitral calcifications; Mild coronary artery calcifications. Moderate Atherosclerotic disease; fatigue; This is a spontaneous report from a contactable other hcp. A 65-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCIN, Solution for injection,Batch/Lot Number: EL3247), intramuscular, administered in Arm Left on 29Jan2021 10:30 (AM) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included hodgkin's disease, alopecia, asthma, back pain, dyspepsia, heartburn, pulmonary embolism (patient had a 2 time history of pulmonary emboli, she was having pulmonary emboli starting 15Jan2021), oral surgery - 2 teeth extracted on 13Jan2021, low thyroid due to mantle radiation, constipation. Concomitant medication(s) included levothyroxine taken for hypothyroidism; biotin taken for alopecia; finasteride taken for alopecia areata; colecalciferol (VITAMIN D3) taken for supplementation therapy; calcium taken for supplementation therapy; ascorbic acid (VIT C) taken for supplementation therapy; salbutamol sulfate (ALBUTEROL) taken for asthma, clobetasol propionate taken for alopecia areata; paracetamol, tramadol hydrochloride (ULTRAM) taken for back pain; lorazepam taken for an sleep, amoxicillin trihydrate, clarithromycin, esomeprazole magnesium (NEXIUM 1-2-3) taken for dyspepsia, rivaroxaban (XARELTO) taken for pulmonary embolism, calcium, colecalciferol (CALCIUM +D3) taken for supplementation therapy, docusate sodium, sennoside a+b (DOCUSATE SODIUM AND SENNA) taken for constipation; triamcinolone acetonide taken for rash pruritic and steroid Injections to scalp for alopecia areata. Previously she took bnt162b2 (Lot Number: EJ1686), intramuscular, administered in Arm Left on 09Jan2021 3:30 pm as dose 1, single for covid-19 immunisation and had experienced malaise, tachy irregular pulse, fatigue, shortness of breath (SOB), atrial fibrillation. The patient experienced heart failure, mild interstitial pulmonary edema, shortness of breath, patient felt like he had the flu, computerised tomogram: pleural effusion; partial atelectasis, cardiomegaly, heavy mitral calcifications, mild coronary artery calcifications. moderate atherosclerotic disease, fatigue on an unspecified date in 2021, A-fib (atrial fibrillation) 40s was diagnosed, it started on Jan2021& echocardiogram: a-fib 140s, moderate mitral regurgitation a-fib (on 23Mar2021) in Jan2021, low grade fever like a 100 or below/mild fever 99.9, arm was sore/soreness in left arm at site, ache on 30Jan2021, stridal wheezing on 18Mar2021. Reporter stated, "she received the COVID-19 Vaccine on January 9 and the second one on January 29 and about two weeks, she had an appointment with the cardiologist on (DATE). They said she was in A-fib and they put her on cardiac medications she knows to try and to get her medically to convert back into sinus rhythm and that was in February. In March she had an allergic reaction to Diltiazem they switched her to Metoprolol and then two and half months later she was still in A-fib, they sent her to electrophysiologist and Monday she had a cardioversion done. she was in sinus rhythm now but she had still having symptoms shortness of breath and fatigue. Reporter further stated, "When she did have the second vaccine which was on (DATE), she did have a few side effect that are normal. she had like a low grade fever like a 100 or below, you know the arm was sore she felt like she had the flu you know, when your body was reacting from having the vaccine so she mean in less than two days it was gone but those things are kind of normal." She took Metoprolol (treatment) because she was in A-fib they are trying to medically convert her and right now her dose had been tapered because she awasm back in sinus rhythm (Clarification unknown). So in a month she would be off of it. Dermatologist strong encouraged her to saw a Dr for symptoms of shortness of breath and fatigue and to report her symptoms to Pfizer. Diagnosed with A-Fib by cardiologist. Medications started to treat A-Fib none worked. Cardioversion 05May2021 not successful long term. Still do shortness of breath and fatigue. AV Node ablation with micra leadless pacemaker inserted into 26Apr2021 heart ventricle. Pacing. Still do shortness of breath and fatigue. CT scan with contrast done. Pleural effusion with partial bilateral atelectasis and heart failure. diuretics started and shortness of breath and fatigue improved. The patient underwent lab tests which included computerised tomogram: pleural effusion; partial atelectasis; on 05May2021 heart failure; negative for pulmonary emboli, Cardiomegaly with mild interstitial pulmonary edema and greater than left pleural effusions suggesting heart failure with atelectasis. Heavy mitral calcifications. Mild coronary artery calcifications. Moderate atherosclerotic disease. neg. PEs, echocardiogram: unknown, echocardiogram: a-fibration 140 on 18Mar2021 Lots of stridal wheezing when laying down, echocardiogram: moderate mitral regurgitation a-fib on 23Mar2021, electrocardiogram: a-fib 140's, pulmonary function test: unknown results on 01Jun2021. Therapeutic measures were taken as a result of a-fib (atrial fibrillation), shortness of breath and fatigue. Adverse event atrial fibrillation resulted in physician visit. The outcome of event stridal wheezing was not resolved, dyspnoea, fatigue was resolving, ache, pain in arm, pyrexia was resolved with 1 days duration, whereas unknown for all other events.; Sender's Comments: Based on the available information in the case, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events Afib,Cardiac failure and pulmonary edema.,Linked Report(s) : US-PFIZER INC-2021411065 same patient/drug, different vaccine dose/event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: Test Date: 20210505; Test Name: CT scan with contrast; Result Unstructured Data: Test Result:Pleural effusion; Partial atelectasis;; Comments: Heart failure; Neg for pulmonary emboli Cardiomegaly with mild interstitial pulmonary edema and greater than left pleural effusions suggesting heart failure with atelectasis. Heavy mitral calcifications. Mild coronary artery calcifications. Mod. Atherosclerotic disease. Neg. PEs; Test Name: ECHOCARDIOGRAM; Result Unstructured Data: Test Result:UNKNOWN; Test Date: 20210318; Test Name: ECHOCARDIOGRAM; Result Unstructured Data: Test Result:A-Fib 140s; Comments: Lots of stridal wheezing when laying down; Test Date: 20210323; Test Name: ECHOCARDIOGRAM; Result Unstructured Data: Test Result:Moderate Mitral Regurgitation A-Fib; Test Name: ELECTROCARDIOGRAM; Result Unstructured Data: Test Result:UNKNOWN; Test Name: ELECTROCARDIOGRAM; Result Unstructured Data: Test Result:A-Fib 140's; Test Date: 20210601; Test Name: PFT; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Alopecia (Verbatim: Alopecia); Alopecia areata (Verbatim: Alopecia areata); Asthma (Verbatim: Asthma); Back pain (Verbatim: Back pain); Constipation; Heartburn (Verbatim: Heartburn); Hodgkin's disease (Verbatim: Hodgkin's disease); Hypothyroidism; Pulmonary embolism (I have a 2 time history of pulmonary emboli); Tooth extraction
Andere Medikamente: LEVOTHYROXINE; BIOTIN; FINASTERIDE; VITAMIN D3; CALCIUM; VIT C; ALBUTEROL [SALBUTAMOL SULFATE]; CLOBETASOL PROPIONATE; ULTRAM [PARACETAMOL;TRAMADOL HYDROCHLORIDE]; LORAZEPAM; NEXIUM 1-2-3; XARELTO; CALCIUM +D3; DOCUSATE SODIUM AND SENNA; TR
Allergien: -
Vorherige Impfungen: -

VAERS 1020241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: SD
Alter: 49,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Echocardiogram Electrocardiogram Dizziness Dyspnoea Nausea Paraesthesia oral Throat tightness

Symptomtext

anaphylaxis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Electrocardiogram 02/11/2021 Echocardiogram 02/15/2021 Electrocardiogram 02/26/2021
Aktuelle Erkrankungen: no
Vorgeschichte: Hx breast cancer
Andere Medikamente: aremidex 1mg celebrex 60mg
Allergien: Doxitaxil Paxitaxil CT dye shellfish
Vorherige Impfungen: -

VAERS 1430184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: OR
Alter: 51,0
Geschlecht: F
Eingang: 27.06.2021
Impfdatum: 26.01.2021
Beginn: 06.02.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / LA

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

Deep vein thrombosis Ultrasound Doppler

Symptomtext

DVT in right leg in popliteal and axial and muscular calf veins

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: duplex ultrasound done on 3/9/2021
Aktuelle Erkrankungen: none
Vorgeschichte: depression, obesity
Andere Medikamente: calcium, cetirizine, cranberry, fish oil, nuvaring, lysine, tumeric, venlafaxine
Allergien: none
Vorherige Impfungen: -

VAERS 1418140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MN
Alter: 92,0
Geschlecht: M
Eingang: 22.06.2021
Impfdatum: 19.02.2021
Beginn: 22.06.2021
Tage bis Beginn: 123,0
Dosis: 2
Route/Site: IM / LA

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

Electrocardiogram ambulatory Fall Syncope

Symptomtext

near fall, was helped down by family; "syncope"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: holter monitor placed on patient.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1395550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: IL
Alter: 57,0
Geschlecht: M
Eingang: 14.06.2021
Impfdatum: 01.12.2020
Beginn: 25.01.2021
Tage bis Beginn: 55,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram Cough Electrocardiogram Hypertension Pericarditis

Symptomtext

1st dose Pfizer 12/26/2020 Lot# EL0140, 2nd dose 01/20/2021 Lot# EL3247 Sever coughing, pericarditis, high blood pressure medication on now 50mg Metoprolol twice daily

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: EKG, Cat scan
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol, Trouble sleeping
Andere Medikamente: TRICOR, Crestor, Doxepin, O mega 3 fish oil, multi vitamin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1271052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: ID
Alter: 49,0
Geschlecht: M
Eingang: 10.06.2021
Impfdatum: 19.02.2021
Beginn: 23.04.2021
Tage bis Beginn: 63,0
Dosis: 2
Route/Site: IM / LA

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

Dysarthria Facial paralysis Hypoaesthesia oral

Symptomtext

Eye, cheek, and mouth droopy; Slurred speech; Lip numbness; This is a spontaneous report from a contactable nurse. A 49-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EK9231), intramuscular in left arm, on 19Feb2021 (at the age of 49 years), as second dose, single dose, for COVID-19 immunization. The patient's medical history included rosacea. There were no concomitant medications. The patient previously took the first dose of BNT162B2 (Lot Number: EK9231) on 29Jan2021 (at the age of 49 years) for COVID-19 immunization (intramuscular in left arm). The patient had no known allergies. The patient was not diagnosed with COVID-19 prior vaccination. No other vaccine was administered in four weeks. The vaccine was administered in a hospital facility. On 23Apr2021, the patient experienced lip numbness. On 24Apr2021, the patient experienced eye, cheek, and mouth droopy, and slurred speech. The adverse events resulted in emergency room or department or urgent care. The patient received treatment for the events including steroids and antivirals. The patient has not been tested for COVID-19 post-vaccination. The patient had not recovered from the events.; Sender's Comments: A possible contribution role of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) to the onset of the reported events cannot be excluded considering temporal relationship. This case will be reassessed should additional information become available. 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: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Rosacea
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1374676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 04.06.2021
Impfdatum: 28.01.2021
Beginn: 08.02.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: - / RA

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

Bell's palsy Facial paralysis Hypoaesthesia

Symptomtext

Patient developed Bell's Palsy 2-3 weeks after receiving the 2nd vaccine. Patient reported symptoms that worsened on 4/17/2021. Patient was currently at work and could not feel her legs. She was able to walk but could not sense her legs. She presented to the ED on 4/17/2021 with bilateral leg numbness and left facial droop. After ED observation she had resolution of left facial droop and left leg weakness. Patient did leave against medical advice but stated she would follow up with her doctor.

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

VAERS 1368781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 71,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Angina pectoris Arthralgia Blood test Chest X-ray Dehydration Feeling abnormal Headache Hospitalisation Nausea Palpitations

Symptomtext

I ended up at the hospital because of dehydration and my heart was racing because of HL Fib. I also have severe nausea and headaches. The joint pain made me feel really bad. My Doctor became concerned because of my sever heart pains and he was the reasons that I went to the hospital.

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Praegender Schweregrund: Hospitalisation
Hospital-Tage: -
Labordaten: Chest x-rays and blood work performed. I was under supervision all day long and released that evening when my husband came to pick me up.
Aktuelle Erkrankungen: No
Vorgeschichte: I have chronic HL Fib.
Andere Medikamente: I take my daily medications and they are as follows: Eliquis 5mg Chlordane 250mg Wellbutrin Estrogen patch for hormone therapy Donepezil HCL 10mg Progesterone Chlorthalidone 25mg Magnesium Oxide 400 mg Multi-vitamins
Allergien: I am allergic to Anesthesia and Antibiotics, and Sulphur. I am also allergic to eggs and gluten..
Vorherige Impfungen: -

VAERS 1293051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

schwer

Staat: NY
Alter: 74,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 05.02.2021
Beginn: 15.04.2021
Tage bis Beginn: 69,0
Dosis: 2
Route/Site: IM / LA

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

Blood potassium decreased Cardiac stress test Chest X-ray Dyspnoea Echocardiogram Fibrin D dimer Heart rate increased Herpes zoster Malaise Migraine Mitral valve incompetence Palpitations Thrombosis Ultrasound scan

Symptomtext

she did not feel good; Migraine after second dose; her heart was pounding; felt palpitations in her chest; potassium was low; dimer test that showed 0.30 clot; slight mitral regurgitation; breathing problems; shingles; This is a spontaneous report received from Pfizer sponsored program. A 74-year old contactable female consumer (patient) reported for herself that she received the second dose of BNT162B2 (Lot No. unknown) at single dose for Covid-19 immunization on 05Feb2021 at 17:30. Relevant history included Shingles when she was 42, Chicken pox. Relevant concomitant drug was unknown. The patient received the first dose of BNT162B2 (Lot No. EL3247) at 0.3 ML single dose for Covid-19 immunization on 15Jan2021, experienced Left arm Pain at injection site. Prior Vaccinations (within 4 weeks): none. The patient went to Urgent care and was diagnosed with Shingles on 15Apr2021, which was started with pain in her side, and on 30Apr2021, she was having breathing problems/ breathing was not well at 15:30-16:00. She said shingles were from the shot. The patient started shrinking before she got the vaccine. It was years before. There was no prescriber. She did not have the pain from the Shingles any longer. The pain was gone for a couple of days now. She had it for 2 1/2 weeks. She was cooking and the next day, she said she did not feel good, her heart was pounding and breathing was difficult. She went to ER and they did dimer test. They took 12 vials of blood. They told her she had .30 clot. She later stated the Dimer result was 0.30. They did chest x-ray and nothing showed. They looked at her legs too. That is why they did the sonogram. They wanted her to stay, but he gave her a sonogram of her heart. It is not enlarged and there is no fluid around it. She thought he gave referral for outpatient. She has been calling ER for an appointment. She then found that the doctor was not able to refer to an Echo cardiogram. She needs to go to the one in her home state and she is still in a different state visiting her daughter. She goes home next week and will get it then. She went for stress test Apr 2019 and emailed results said she had slight mitral regurgitation, so maybe that is where the blood is coming from. Her sister called and she told her she did not feel well. Breathing problem only lasted a day. She was cooking again and was not doing anything strenuous and felt palpitations in her chest and felt breathing issues again. It is better, but every now and then she gets palpitations. She had a migraine after second dose at 16:00 (unknown date). She went to bed at 4pm and woke up at 1am. She thought she took an Ibuprofen and did not know if it would affect vaccine or not. When she woke up, she was fine. She had shingles prior. She assumes she must have had COVID and did not know. he had the antibodies present in May 2020, when she was tested. When she googled, the people in another country were getting Shingles. She had the chicken pox when she was young. If you get the Chicken pox and the COVID, you are susceptible to shingles. She does not have any information on those people in other country to report. Her brother and sister both received the Moderna COVID vaccine. Her brother did not have any issues an her sister already reported her issues to them. No further details provided. Separate report completed for her sister. When looking up an address, she stated she needs a magnifying glass. She needed this before the vaccine. She always has her glasses to read with. ER visited on 15Apr2001 and 01May2021. On 15 They gave her ketorolac and ondansetron, potassium chloride. because her potassium was low. The outcome of event shingles, breathing problems was resolving, the outcome of other events was unknown. Follow-up attempts are needed. Information about batch/lot number is expected.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Name: stress test; Result Unstructured Data: Test Result:slight mitral regurgitation; Test Name: Chest x-ray; Result Unstructured Data: Test Result:Showed nothing; Test Name: sonogram of heart; Result Unstructured Data: Test Result:no enlarged, no fluid around it; Test Name: dimer test; Result Unstructured Data: Test Result:0.30; Test Name: Sonogram; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chickenpox; Shingles (when she was 42)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1336785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

schwer

Staat: MS
Alter: 70,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Respiratory distress

Symptomtext

Respiratory distress.

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Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Rosuvastatin, hydrochlorothiazide, losartin, bystic, vitamins E B12 D3 , and saw palmetto
Allergien: Aspirin; Sulfur; Cat scan dye (contrast material); Peppers (jalapeno); Dark leafy greens
Vorherige Impfungen: -

VAERS 1278757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 89,0
Geschlecht: F
Eingang: 01.05.2021
Impfdatum: 23.01.2021
Beginn: 09.02.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: OT / -

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

Bell's palsy

Symptomtext

Bell's Palsy 09Feb2021 dx 12Feb2021; This is a spontaneous report from a contactable Physician. An 89-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 1, intramuscular on 23Jan2021 at 13:15 (Batch/Lot Number: EL3247) as single dose (at the age of 89 years-old) for COVID-19 immunisation. Medical history included high blood pressure, spinal stenosis, kyphosis and known allergy to sulfa-hives. The patient was not pregnant. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included donepezil, methadone, sertraline, hydrocodone, metoprolol, alprazolam (XANAX), nifedipine, mirtazapine, hydralazine, and spironolactone; all taken from unknown dates for unspecified indications. On 09Feb2021 the patient experienced Bell's palsy (diagnosed on 12Feb2021). The event resulted in emergency room visit. Therapeutic measures were taken as a result of Bell's palsy and included steroids and acyclovir. The patient was recovered from Bell's palsy on an unknown date. The patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), intramuscular on 28Feb2021 at 14:15 (Lot number EN6203) for COVID-19 immunisation. It was also reported that since the vaccination, the patient had not been tested for COVID-19.; Sender's Comments: Based on the available information and known product profile, the causal relationship between the reported Bell's palsy and the use of BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic urticaria; Blood pressure high; Kyphosis; Spinal stenosis; Sulfonamide allergy
Andere Medikamente: DONEPEZIL; METHADONE; SERTRALINE; HYDROCODONE; METOPROLOL; XANAX; NIFEDIPINE; MIRTAZAPINE; HYDRALAZINE; SPIRONOLACTONE
Allergien: -
Vorherige Impfungen: -

VAERS 1274512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NE
Alter: 21,0
Geschlecht: F
Eingang: 30.04.2021
Impfdatum: 21.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chills Gaze palsy Heart rate increased Loss of consciousness Nasopharyngitis

Symptomtext

She was waiting the advised 15 minutes and passed out. Rapid heart rate with fluttering eyes - unsure if it was seizure. after about 5 minutes she came to and started complaining of being cold with chills .

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

VAERS 1269542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 20.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Muscle spasms SARS-CoV-2 test Seizure

Symptomtext

Spasms in left arm; Went to ER bc I thought it was a seizure; This is a spontaneous report from a contactable consumer. A 65-year-old non-pregnant female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) at the age of 65 years, via an unspecified route of administration, administered in Arm Left on 20Jan2021 (Batch/Lot Number: EL3247) as a single dose for covid-19 immunization. Medical history included cancer from an unknown date and unknown if ongoing. Concomitant medications included levetiracetam (KEPPRA); mesalamine; prednisone; and folic acid, all taken for an unspecified indication, start and stop date were not reported. In Jan2021, the patient experienced spasms in left arm and went to ER because she thought it was a seizure. The patient was hospitalized due to the events for 2 days. The patient underwent lab tests and procedures which included negative test for Covid-19 on 26Mar2021. The outcome of the events was recovered with sequelae

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Praegender Schweregrund: Seizure
Hospital-Tage: 2,0
Labordaten: Test Date: 20210326; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer
Andere Medikamente: KEPPRA; MESALAMINE; PREDNISONE; FOLIC ACID
Allergien: -
Vorherige Impfungen: -

VAERS 1265977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: GA
Alter: 69,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 17.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: - / LA

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

Blood pressure decreased Blood pressure fluctuation Blood pressure measurement Dyspnoea Pulmonary thrombosis

Symptomtext

blood clot in her lung; Shortness of breath; blood pressure dropped extremely low; blood pressure fluctuates; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EL3247), via an unspecified route of administration, administered in the left arm on 17Mar2021 at the age of 69-years-old as single dose for COVID-19 immunization. The patient had no medical history. There were no concomitant medications. The patient previously received the first dose of BNT162B2 on 24Feb2021 (Batch/Lot number was not reported) at the age of 69-years-old for COVID-19 immunization. On 07Apr2021, the patient experienced shortness of breath and blood dropped extremely low. On 08Apr2021, the patient experienced blood clot in her lung. And on Apr2021, the patient experienced blood pressure fluctuates. The patient had her final Pfizer Covid vaccine on 17Mar2021. The patient reported that she had to go to the hospital for shortness of breath and her blood pressure dropped extremely low. She stated that they did tests and found out she had a blood clot in her lung. The patient reported that she came home Sunday evening and took the drip thing out and started her on blood thinner that started with an E (as reported). The patient stated that she was told her cardiologist told her to report this. The patient wanted to know if there have been any other reports called in about people calling in with blood clots. The patient was hospitalized due to events shortness of breath, blood dropped extremely low, and blood clot in her lung from 08Apr2021 to 11Apr2021. The patient reported that her blood pressure fluctuates. She stated that it was better than when she was in the hospital. They gave her the drip. The patient reported that her values did come down and this was the only thing they could go by. The outcome of the events shortness of breath and blood pressure dropped extremely low was recovering. The outcome of the events blood clot in her lung and blood pressure fluctuates was unknown.

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Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 3,0
Labordaten: Test Date: 20210407; Test Name: blood pressure; Result Unstructured Data: Test Result:Dropped; Test Date: 202104; Test Name: blood pressure; Result Unstructured Data: Test Result:Fluctuates
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1259458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

schwer

Staat: TX
Alter: 19,0
Geschlecht: M
Eingang: 26.04.2021
Impfdatum: 26.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Head injury Loss of consciousness

Symptomtext

During the 15 minutes of the after vaccination waiting time , patient passed out and hit his head on the floor, we called 911 and provided the patient the first aid until EMS arrived and took over patient care, patient was awake after the fall. Mother was present with patient at all time during the event.

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

VAERS 1015657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 21.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / LA

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

Blood pressure abnormal Dizziness Feeling abnormal Heart rate irregular Shock symptom

Symptomtext

she was having a feeling like she was in shock; woke up last night not feeling right and this morning; irregular heart beat/Pulse 112/Pulse 108/went to 112; checked her blood pressure on 25Jan2021, the lower number was high, upper number lower than what it usually was, it was exactly: 130/96; then 110/78; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (batch/lot number EL3247 and expiry date not reported) via an unspecified route of administration on 21Jan2021 10:00 am at 71 years of age as single dose in left arm for COVID-19 immunization. Medical history included ongoing high blood pressure. Concomitant medication included atenolol, amlodipine, lisinopril; all ongoing for high blood pressure. The patient received the Pfizer COVID-19 vaccine at 10 am yesterday, her symptoms started last night and came on suddenly. She went and checked her blood pressure on 25Jan2021, the lower number was high, upper number lower than what it usually was, it was exactly: 130/96, pulse 112, then 110/78, pulse 108, after taking her medication. Her pulse went to 112, it does that when it gets irregular, it did get better after blood pressure medication atenolol. She woke up last night not feeling right and this morning, she was having a feeling like she was in shock. She developed an irregular heart beat last night on 25Jan2021. It was still bothering her. She had her first shot on Thursday of this past week. She was unsure if this was a side effect. Received the vaccine on 21Jan2021. She says it felt like it was right before you pass out. No treatment received. She was supposed to take blood pressure medication but she was being cautious right now. Her blood pressure medications were: atenolol, amlodipine, lisinopril. She did not take them this morning; all have taken for years. At the time of this report, the outcome of the event irregular heart beat/pulse 112/pulse 108/went to 112 was not recovered, while unknown for the rest of the events. Follow-up (25Mar2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Shock symptom
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:110/78; Comments: lower number was high, upper number lower than what it usually was; Test Date: 20210125; Test Name: Blood pressure; Result Unstructured Data: Test Result:130/96; Comments: lower number was high, upper number lower than what it usually was; Test Name: Pulse; Result Unstructured Data: Test Result:112; Test Name: Pulse; Result Unstructured Data: Test Result:108; Test Name: Pulse; Result Unstructured Data: Test Result:better; Test Date: 20210125; Test Name: Pulse; Result Unstructured Data: Test Result:112; Comments: irregular
Aktuelle Erkrankungen: Blood pressure high
Vorgeschichte: -
Andere Medikamente: ATENOLOL; AMLODIPINE; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1228712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: AR
Alter: 70,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 10.02.2021
Beginn: 24.03.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram thorax abnormal Pulmonary thrombosis Thrombosis Ultrasound scan abnormal

Symptomtext

Patient had blood clots in right leg and in each lung.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 1,0
Labordaten: Ultrasound, CT scan
Aktuelle Erkrankungen: none
Vorgeschichte: Restless leg syndrome
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1227978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 23,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 25.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Deep vein thrombosis Nodule Peripheral venous disease Thrombophlebitis superficial Vascular pain

Symptomtext

Nodule on both forearm; swelling along veins and they became painful; swelling along veins and they became painful; 2 superficial venous thromboses, one in my arm and another in my leg; 2 superficial venous thromboses, one in my arm and another in my leg; Deep vein thrombosis leg; This is a spontaneous report from a contactable consumer (patient). A 23-year-old male patient received the 2nd dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration in arm left on 25Jan2021 (Lot Number: EL3247), as single dose, for COVID-19 immunisation. Patient was vaccinated in the hospital. Medical history and concomitant medications were none. Patient did not have known allergies. Patient did not have COVID-19 prior to vaccination. Previously the patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech, lot# EL0142) on 04Jan2021 at 11:30 AM in left arm and experienced nodule on extremity and vaccination site nodule. The patient experienced deep vein thrombosis leg (medically significant, life threatening) in 2021 with outcome of not recovered, nodule on both forearm (life threatening) on 25Jan2021 with outcome of not recovered, swelling along veins and they became painful (life threatening) in 2021 with outcome of not recovered, swelling along veins and they became painful (life threatening) in 2021 with outcome of not recovered, 2 superficial venous thromboses, one in arm and another in leg (life threatening) in 2021 with outcome of not recovered. It was reported that within hours from second dose the nodules reappeared. At this time, patient was told to take Allegra and did so for 4 weeks. A month later, patient began to see some swelling along his veins and they became painful. This developed into a DVT, deep venous thrombosis, in leg and 2 superficial venous thromboses, one in arm and another in leg. all the events required physician office visit. None of the events occurred at vaccination site, but physician believed they were triggered by receiving the vaccine. Treatment of Eliquis was initiated the day before report. Patient was not tested for COVID-19 post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
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 1205919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 23,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 04.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / LA

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

Antinuclear antibody Blood thyroid stimulating hormone normal C-reactive protein increased Coagulation test Deep vein thrombosis Fibrin D dimer Full blood count normal Injection site nodule Injection site rash Metabolic function test normal Nodule Pain in extremity Rash Rash erythematous Red blood cell sedimentation rate normal Thrombophlebitis superficial Thrombosis Ultrasound Doppler abnormal

Symptomtext

approximately 1 week after the first dose I began to have red, painful nodules of both forearms; approximately 1 week after the first dose I began to have red, painful nodules of both forearms; This is a spontaneous report from a contactable consumer (patient). A 23-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: EL0142), first dose via an unspecified route of administration, administered in Arm Left on 04Jan2021 11:30, single dose covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Approximately 1 week after the first dose (12Jan2021) at 12:30 patient began to have red, painful nodules of both forearms not just the left arm, he received the vaccine in. At this time, he was advised and took Benadryl for around 10 days. This appeared to alleviate the symptoms as the nodules went away. The adverse events resulted in visit to doctor. The events were assessed as life threatening. The outcome of the events was not recovered. Treatment of Eliquis was initiated yesterday. No COVID prior vaccination. Not COVID tested post vaccination. No Known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
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 1224636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 14.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Laboratory test Pulmonary thrombosis Thrombosis Ultrasound Doppler

Symptomtext

Blood clots after the 2nd dose; Blood clot split and some went into side of lung; This is a spontaneous report from a contactable consumer (patient). A 73-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration in the right arm, on 14Feb2021 at 15:45 (Lot Number: EL3247) (at the age of 73-years-old) as a single dose for COVID-19 immunisation. The patient had no medical history, family history, or concomitant medications. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot number: E10142 (as reported)), in the right arm, on 24Jan2021 at 15:45 (at the age of 73-years-old) for COVID-19 immunisation. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient experienced blood clots after the 2nd dose and blood clot split and some went into side of lung in Feb2021, which required hospitalization from 27Feb2021 to 28Feb2021. The clinical course was reported as follows: The patient stated he did not know what date the blood clots occurred and can't tell when that happened, but it was maybe a few weeks after the second dose of the vaccine. He stated that one blood clot is in the right leg near the calves and the blood clot broke and split some and went up into the side of his lung as it was detected in a doppler on 27Feb2021. The patient was hospitalized from 27Feb2021 to 28Feb2021. The doppler was performed as soon as he went into the emergency room and they went through a series of tests with unknown results on 27Feb2021 and 28Feb2021. The patient stated that the right leg is bigger than the other leg and they told him it might stay that size and may not go down. The patient is now on apixaban (ELIQUIS) 5 mg for the rest of his life. In the beginning, they gave him an unspecified shot in his stomach, then after that he began taking apixaban at two pills in the morning and two pills at night, then they cut him down to 1 pill in the morning and 1 pill in the evening, and he started it right when he went into the hospital immediately. Therapeutic measures were taken as a result of the event as aforementioned. The clinical outcome of blood clots after the 2nd dose and blood clot split and some went into side of lung was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 1,0
Labordaten: Test Date: 20210227; Test Name: tests; Result Unstructured Data: Test Result:unknown results; Test Date: 20210228; Test Name: tests; Result Unstructured Data: Test Result:unknown results; Test Date: 20210227; Test Name: doppler; Result Unstructured Data: Test Result:the blood clot broke and split some and went up; Comments: into the side of his lung
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1192138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: KS
Alter: 85,0
Geschlecht: M
Eingang: 10.04.2021
Impfdatum: 01.02.2021
Beginn: 08.04.2021
Tage bis Beginn: 66,0
Dosis: 2
Route/Site: IM / RA

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

Bell's palsy Computerised tomogram head

Symptomtext

When I smile, only the right side of my face reacts. The left side of my face does not react at all. I thought I had a stroke, so I went to the emergency room after two days of being unable to move the left side of my face. They diagnosed it as Bell's palsy and prescribed prednisone (deltasone), 10 Mg tablets for 9 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: The hospital conducted a CT scan just on my head to determine whether I had a stroke. They did tests where I had to squeeze the doctor's hands and other tests to assess whether I had a stroke. They looked in my eyes and at my tongue. They determined that I did not have a stroke.
Aktuelle Erkrankungen: n/a
Vorgeschichte: glaucoma
Andere Medikamente: Atorvastatin, vitamin D, 81 mg baby aspirin, latanoprost eye drops
Allergien: n/a
Vorherige Impfungen: -

VAERS 1190974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MA
Alter: -
Geschlecht: U
Eingang: 10.04.2021
Impfdatum: -
Beginn: 24.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Body temperature Chills Dizziness postural Dyspnoea Fatigue Headache Heart rate Heart rate increased Malaise Myalgia Nasal congestion Neck pain Pain in extremity Presyncope Pyrexia Rhinorrhoea Swelling face Vaccination site erythema

Symptomtext

I thought I was going to pass out.; Fatigue; congestion and runny nose; congestion and runny nose; arm pain; head and neck pain/head started throbbing/headache; head and neck pain; chills; I had a puffy face post-vaccine; I wasn't feeling well; I had difficulty breathing; I felt dizzy when bending over and standing up; My heart rate also increased to 100-120 bpm; Arm injection site is very itchy; Arm injection site is very itchy, and now around 2 inches in size; Arm injection site swelling; Arm injection site swelling and redness; muscle aches; Fever maximum 100.5F; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 2 via an unspecified route of administration in the arm on an unspecified date (Lot Number: EL3247; Expiration Date: May2021) as SINGLE DOSE for COVI-19 immunization. Medical history included allergy/contact dermatitis from latex, allergy/sensitivity to dairy, eczema in teens and IBS in 2018. The patient's concomitant medications were not reported. The patient previously took steroids and experienced allergies to steroids. The patient previously had first dose of BNT162B2 on unspecified date for COVID-19 immunisation and experienced site injection and shoulder pain in left arm, left hand pinky finger and ring finger tingling and ache and pain all day in left hand. The patient experienced fatigue, congestion and runny nose, arm pain, head and neck pain and chills on unspecified date. On 24Mar2021, the patient had arm injection site swelling and redness, headache, muscle aches, severe chills and fever maximum 100.5F and kept stable with Tylenol taken every 6 hours. The patient had a puffy face post-vaccine. This started 3 hours after vaccination dose 2, and resolved by evening of 24Mar2021. The patient wasn't feeling well on unspecified date. On 25Mar2021, the patient was still severely fatigued. The patient went downstairs to get takeout/delivery, and after coming up half a flight of stairs which would consider as minor exertion by the patient. The patient had difficulty breathing, stated, "my head started throbbing, and I thought I was going to pass out. This happened again when I was trying to load/unload the dishwasher and I felt dizzy when bending over and standing up. I developed a headache for around 1 hour. My heart rate also increased to 100-120 bpm." The patient had arm injection site was very itchy, and now around 2 inches in size. The events took place after use of product. Therapeutic measures were taken as a result of , arm injection site swelling and redness, muscle aches and fever maximum 100.5f. The outcome of the event fatigue was not recovered. The outcome of the event puffy face was recovered on 24Mar2021. The outcome of the rest of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Name: temperature; Result Unstructured Data: Test Result:100.5 Fahrenheit; Comments: Fever maximum; Test Name: heart rate; Result Unstructured Data: Test Result:increased to 100-120; Comments: bpm
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Contact dermatitis; Dairy intolerance; Eczema; Irritable bowel syndrome; Latex allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1148784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NJ
Alter: 46,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Chills Cold sweat Lethargy Syncope

Symptomtext

felt very faint and weak; chills/shivers; cold sweating; felt very faint and weak; extreme lethargy; This is a spontaneous report from a contactable consumer (patient). A 46-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 2 via an unspecified route of administration, in Arm Left on 17Mar2021 10:45 (Lot Number: EL3247) as SINGLE DOSE for COVID-19 immunization. Medical history and concomitant medication was reported as none. The patient previously had BNT162B2 first dose lot number: EL3247 on 24Feb2021 10:00 AM, in left arm for COVID-19 immunization. The patient was not pregnant at time of vaccination. The facility where the most recent COVID-19 vaccine was administered was in the clinic. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 17Mar2021 20:30, the patient experienced chills, shivers, cold sweating, felt very faint and weak and extreme lethargy. No treatment was given to the patient for the events. The outcome of the events was recovered on unspecified date.

Weitere VAERSDATA-Felder

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

VAERS 1103867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 88,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 18.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / UN

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

Blood test normal Chest X-ray normal Chorea Cognitive disorder Computerised tomogram head normal Dysphemia Loss of control of legs SARS-CoV-2 test Seizure Full blood count normal Mental status changes Metabolic function test SARS-CoV-2 test negative Troponin normal Tic Urine analysis normal Walking aid user

Symptomtext

admitted to our hospital with concerns for possible seizure; sudden stuttering of his voice; Pt began to experience sudden choreiform movements; experiencing changes in meditation and facial tics; inability to control his limbs.; This is a spontaneous report from a contactable other healthcare professional. An 88-year-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL3247), intramuscular on 18Feb2021 10:00 as a single dose for covid-19 immunization. The patient's medical history included hypothyroidism, parkinson's disease and benign prostatic hyperplasia from an unknown date and unknown if ongoing. The patient has no known allergies. Concomitant medications included carbidopa, levodopa (SINEMET); metoprolol (METOPROLOL); finasteride (FINASTERIDE); ergocalciferol (VIT D); and levothyroxine (LEVOTHYROXINE). The patient received the first dose of bnt162b2 on 28Jan2021 (lot: EL3249), intramuscularly for covid-19 immunization. On 28Feb2021, the patient began to experience sudden choreaform movements 10 days post 2nd dose of vaccine. Symptoms continued to progress and he was admitted in a hospital with concerns for possible seizures. Patient was displaying severe choreaform movement and inability to control his limbs. He was also experiencing changes in meditation and facial tics and sudden stuttering of his voice. The patient was treated for the events (not specified). The patient tested negative for Covid-19 on 14Mar2021 (via nasal swab). The outcome of the events was not recovered and patient remains hospitalized as of 15Mar2021.; Sender's Comments: Considering the plausible temporal association, (reportedly, the events occurred 10 days post 2nd dose of vaccine), a causative role of BNT162B2 for all reported events cannot be completely excluded. The contributory role of known Parkinsons disease 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: Seizure
Hospital-Tage: -
Labordaten: Test Date: 20210314; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: BPH; Hypothyroidism; Parkinson's disease
Andere Medikamente: SINEMET; METOPROLOL; FINASTERIDE; VIT D; LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1103867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 88,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 18.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: OT / -

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

Blood test normal Chest X-ray normal Chorea Cognitive disorder Computerised tomogram head normal Dysphemia Loss of control of legs SARS-CoV-2 test Seizure Full blood count normal Mental status changes Metabolic function test SARS-CoV-2 test negative Troponin normal Tic Urine analysis normal Walking aid user

Symptomtext

admitted to our hospital with concerns for possible seizure; sudden stuttering of his voice; Pt began to experience sudden choreiform movements; experiencing changes in meditation and facial tics; inability to control his limbs.; This is a spontaneous report from a contactable other healthcare professional. An 88-year-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL3247), intramuscular on 18Feb2021 10:00 as a single dose for covid-19 immunization. The patient's medical history included hypothyroidism, parkinson's disease and benign prostatic hyperplasia from an unknown date and unknown if ongoing. The patient has no known allergies. Concomitant medications included carbidopa, levodopa (SINEMET); metoprolol (METOPROLOL); finasteride (FINASTERIDE); ergocalciferol (VIT D); and levothyroxine (LEVOTHYROXINE). The patient received the first dose of bnt162b2 on 28Jan2021 (lot: EL3249), intramuscularly for covid-19 immunization. On 28Feb2021, the patient began to experience sudden choreaform movements 10 days post 2nd dose of vaccine. Symptoms continued to progress and he was admitted in a hospital with concerns for possible seizures. Patient was displaying severe choreaform movement and inability to control his limbs. He was also experiencing changes in meditation and facial tics and sudden stuttering of his voice. The patient was treated for the events (not specified). The patient tested negative for Covid-19 on 14Mar2021 (via nasal swab). The outcome of the events was not recovered and patient remains hospitalized as of 15Mar2021.; Sender's Comments: Considering the plausible temporal association, (reportedly, the events occurred 10 days post 2nd dose of vaccine), a causative role of BNT162B2 for all reported events cannot be completely excluded. The contributory role of known Parkinsons disease 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: Seizure
Hospital-Tage: -
Labordaten: Test Date: 20210314; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: BPH; Hypothyroidism; Parkinson's disease
Andere Medikamente: SINEMET; METOPROLOL; FINASTERIDE; VIT D; LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 980191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CO
Alter: 52,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Burning sensation Exercise tolerance decreased Hypoaesthesia Laboratory test Facial paresis Muscle contractions involuntary Paraesthesia Limb discomfort Magnetic resonance imaging Pain in extremity Tongue paralysis

Symptomtext

Paresthesias in upper and lower extremities; left facial numbness and paresthesias; left facial weakness; fasciculations in abdomen and face; This is a spontaneous report from a contactable physician. A 52-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at the age of 52-year-old intramuscular on 21Jan2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. There were no covid prior vaccination and covid tested post vaccination. The patient experienced Paresthesias in upper and lower extremities, left facial numbness and paresthesias, left facial weakness, fasciculations in abdomen and face on 21Jan2021, resulted in: Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. Treatment was received including Prednisone. The outcome of events was recovering. Information on batch/lot number was requested.

Weitere VAERSDATA-Felder

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

VAERS 1143474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: -
Geschlecht: M
Eingang: 29.03.2021
Impfdatum: 24.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: - / LA

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

Peripheral swelling Thrombosis

Symptomtext

blood clots in couple of toes near nails; observed swollen; This is a spontaneous report from a non-contactable consumer. A 55-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL3247), via an unspecified route of administration, administered in arm left on 24Feb2021 15:15 as a single dose for covid-19 immunisation . The patent has no medical history. The patient has no known allergies. The patient's concomitant medications were not reported. In Mar2021, the patient was observed with swollen and blood clots in couple of toes near nails. The events was not treated. The outcome of the events was not recovered. The patient has not had covid prior to vaccination and was not testes for Covid post vaccination. No follow-up attempts are possible. Information about Lot/Batch cannot be obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
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 1142932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 29.03.2021
Impfdatum: 28.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Facial paralysis Headache Neck pain

Symptomtext

Facial Paralysis of the left side, including the forehead of acute onset that occurred two days after receiving the vaccine; moderate to severe pain on the left side of the back of the neck and head.; moderate to severe pain on the left side of the back of the neck and head.; This is a spontaneous report from a contactable consumer (patient). This 66-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot Number: EL3247) at the age of 66 years via an unspecified route of administration at single dose in the left arm on 28Jan2021 05:30 for COVID-19 immunisation. Medical history included appendicectomy, prediabetes, aortic valve calcification, allergy to Sulfa. Concomitant medication included pantoprazole. The vaccine was administered at Clinic. 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 previously took codeine and experienced allergy. On 30Jan2021 07:00, the patient experienced facial paralysis of the left side, including the forehead of acute onset that occurred two days after receiving the vaccine (medically significant), moderate to severe pain on the left side of the back of the neck and head. Primary Care physician prescribed Prednisone 20 mg BID (twice a day) for 5 days with improvement of neck pain but no improvement on facial paralysis. Facial paralysis has improved in 60%, still with some degree of compromise. The outcome of the events was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Aortic valve calcification; Appendectomy; Drug allergy; Prediabetes
Andere Medikamente: PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1142638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

schwer

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 28.03.2021
Impfdatum: 23.02.2021
Beginn: 17.03.2021
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: SYR / LA

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

Bell's palsy Magnetic resonance imaging

Symptomtext

Developed Bells Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 2,0
Labordaten: MRI
Aktuelle Erkrankungen: Diabetes type 2
Vorgeschichte: -
Andere Medikamente: Glimepiride - 2mg once daily Novolin 70/30. - 60 units twice daily Losartan - 50mg once daily Ascitalopram - 20mg once daily Metforman - 500mg once daily Buspirone - 30mg once daily Euthyrox - 25 mcg once daily
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1127202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 23.03.2021
Impfdatum: 08.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Ischaemic stroke

Symptomtext

Patient was found in the bathroom , urinating , walked to the wheelchair complaining of numbness over his whole right side denies any chest pain no tingling no trauma no incontinenc

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 5,0
Labordaten: Hospital evaluation identified an internal capsule ischemic stroke
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1112472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 76,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 09.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Blood test Computerised tomogram Magnetic resonance imaging

Symptomtext

Bells Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 3/17/2021 taken to Emergency Room with symptoms of either stroke or bells palsy. Cat Scan, MRI and blood tests performed immediately. Stroke was ruled out and diagnosis was Bells Palsy.
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, High BP, AcidReflux,
Andere Medikamente: Avalide, Trulicity, Rabeprazole Sodium, Vitamin D3, Zinc, Vitamin B12, Calcium
Allergien: Seashell, Dairy
Vorherige Impfungen: -

VAERS 1107549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Dizziness Nausea Presyncope

Symptomtext

Patient complained of dizziness, abdominal pain, nausea, and near syncope.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Patient was transferred to the ED.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1029052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 10.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Back pain Balance disorder Blood test Body temperature Chills Contusion Decreased appetite Computerised tomogram Concussion Dizziness Fall Hand fracture Fatigue Headache Loss of consciousness Impaired driving ability Impaired quality of life

Symptomtext

I was lethargic; had no energy; appetite was gone; nauseous; head was a little dizzy, especially when I lay down/dizzy spells; I also felt unbalanced; I was shaky; I was unable to sit or stand up by myself. I was so weak.; Whiplash; fainted or passed out; fallen down the whole flight of stairs; I had no recollection on how I got there.; acromioclavicular joint separation; right thumb fracture; thumb was very sore; back was sore; felt so sick; My right thumb was very sore and I could not move my left shoulder or arm.; temperature was high; felt terrible; pale; pain; I had bruises all over my shins, knees, right elbowand 2 bumps on my head; headache; chills; no idea when I will fully heal, or when I will be able to get back to normal activities; Concussion; imbalance in my inner ear from the fall and from the bangs I received on my head; This is a spontaneous report from a contactable consumer, the patient. A female patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number unknown), via an unspecified route of administration on 10Feb2021 at 09:30 as a single dose for COVID-19 immunization. The patient's medical history included an unspecified immune system disorder from an unknown date and unknown if ongoing. The patient's historical vaccinations included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) on 20Jan2021 after her Remicaide infusion. The patient's concomitant medications were not reported. The patient experienced loss of consciousness on 11Feb2021, fall on 11Feb2021, joint dislocation on 11Feb2021, thumb fracture on 11Feb2021, concussion on an unspecified date in Feb2021, dizzy spells beginning on 13Feb2021, headache on 10Feb2021, chills on an unspecified date in Feb2021, fever on 11Feb2021, being unwell on 11Feb2021, being pale on 11Feb2021, pain beginning on 11Feb2021, contusions on 11Feb2021, decreased appetite on 14Feb2021, nausea on 14Feb2021, back pain on an 11Fev2021, sickness on 11Feb2021, pain in arm on 11Feb2021, memory deficit on 11Feb2021, weakness on 11Feb2021, balance difficulty on 13Feb2021, had no energy on 14Feb2021, being shaky beginning on 12Feb2021, whiplash injury on 11Feb2021, lethargic on 17Feb2021, inner ear disorder in Feb2021 and ADL impaired in Feb2021. Event descriptions were provided in the following first person account which was provided by reporter (the patient): "This is a chronological record of my experience after the Pfizer Vaccine 20Jan2021, I received my first shot of the Pfizer vaccine after my Remicade infusion in (hospital name) Wednesday, 10Feb2021, I received my second shot of the Pfizer vaccine at 9:30am at (hospital name). I started getting a headache before I went to bed at around 8pm. During the night, I got a severe headache and very bad chills. So bad my teeth were rattling and I had to pull an extra blanket over me. Thursday, 11Feb2021, I got up at 7.08am. I went into the bathroom and washed my face. I was very pale and I felt terrible. I went downstairs to the kitchen. I put the kettle on and took my temperature. I had three doctor appointments that morning in and I was worried I would not be able to get into them if my temperature was high. It was 100.1. I went into the ground floor bathroom. I left the bathroom when I heard the kettle was fully boiled. The next thing I remember was the feel of carpet on my left cheek. I knew the only floor in my house that had carpet, was the basement floor. I opened my eyes and to my horror, I was able to see the basement storage room. I had no recollection on how I got there. I knew straight away, that I had fainted or passed out, on the stairs landing and had fallen down the whole flight of stairs. I was afraid to move because I didn't know if I had broken my back or my neck. I was home alone. After laying there for a few minutes, I knew I had to try to get back up the stairs so I could get to a phone. If I didn't, I knew my husband would not find me there, until after 2:30pm. I tried to get up. I struggled but I got to my knees. The next thing I recall is waking up again on the carpeted floor. This time I was sprawled out in the opposite direction, this time my head was near the thread mill. I had obviously passed out again. Now this really frightened me, I was terrified to stand up in case I fell back down again. I literally crawled up the stairs on my hands and knees. I grabbed my cell phone and called my husband to come home from work. I made that call at 7.34am. I didn't move from the sofa until he came home. He made me a cup of tea. He then brought me into the bathroom to wash my teeth. When I was finished washing my teeth, I passed out again. I woke up this time to my husband tapping my face and calling my name. I had fainted again; he had caught me and had carried me into the sofa. I was unable to sit or stand up by myself. I was so weak. I felt so sick, I couldn't even drink the tea. My husband brought me up to bed. He checked on me every hour. I came back downstairs at 4pm. I hurt all over. I had bruises all over my shins, knees, right elbow and 2 bumps on my head. My back was sore. My right thumb was very sore and I couldn't move my left shoulder or arm. I put ice on my shoulder and thumb all night. I took Tylenol pm to help me sleep. Friday, 12Feb2021, my husband helped me to get dressed. I came down the stairs with him. I was very weak. I was shaky and did not trust myself to walk down the stairs. He was having knee surgery that morning. His friend took him to the hospital as I was not fit to drive. I did not move from the sofa until he came home at around 2pm. We talked about going to the ER but I really didn't want to go because of Covid. I was not steady on my feet and I would have to be dropped outside the hospital on my own. I took pain killers all day and iced down my left shoulder and right thumb. Saturday, 13Feb2021: I was still in a lot of pain and my head was a little dizzy, especially when I lay down. I went to Urgent care at 9am. I was seen by Dr. (Name provided). She sent me for 4 x rays and took my blood. My back and right shin were x rayed, I had no broken bones. My shins and knees were badly bruised. The other 2 x rays showed I had a fracture on my right thumb and there was something wrong with my left shoulder. She suggested I go to see an orthopedic doctor on Monday. I forgot to tell her about the dizzy spells and my neck been sore. She did not examine my head or neck. She found no other reason for my fainting, except that I got the Pfizer vaccine the day before. Sunday, 14Feb2021, I continued with the pain killers and ice on my shoulder and thumb. I continued to have dizzy spells. I also felt unbalanced. My appetite was gone and I felt nauseous sometimes when I was eating. I had no energy and I hurt all over. Monday, 15Feb2021, I got an appointment with an Orthopedist at 4.30pm. My husband dropped me off. Nurse and his assistant looked after me before I saw the doctor. I was told I have a separated bone in my left shoulder. It's called acromioclavicular joint separation. AC (collar bone) separates from the scapula (shoulder blade). So, I will have to wear a sling for a few weeks. I will also have to wear a temporary cast on my right hand for a few weeks to heal the fracture on my right thumb. No surgery is needed for either. They also put me on steroids for 2 weeks, Prednisone. Tuesday 16Feb2021, I rested all day. I was still having dizzy spells and I felt off balanced & very shaky. My husband, a close friend and a coworker thought I may have a concussion and advised me to get it checked out. I spent all day on the phone trying to get an appointment with a neurologist. I did get an appointment for the next day. Wednesday 17Feb2021, I still felt the same dizziness and I was lethargic. I had an appointment with the neurologist, Dr. (Name provided) at 2pm. I had a CAT scan and it was normal, no bleeding. The doctor said I had whiplash and a concussion. He did not find any other reason for my fainting, except for the side effects of the Pfizer vaccine. He told me, I just have to rest and the symptom from the concussion should subside in a few weeks. Wednesday 24Feb2021. The Dr.'s nurse called to see how I was. I told her there was not much improvement and that I was still having dizzy spells. She called me back after she related everything to the doctor He is concerned and wants to see me again on Monday 01Mar2021. He may do an MRI to see if there is anything else going on, other than the concussion. Friday 26Feb2021. I am still having dizzy spells. Monday 01Mar2021. I had another appointment with the neurologist at 9:30 am. I need to stay off work for another week and he will re-access me again next Monday. He says I have an imbalance in my inner ear from the fall and from the bangs I received on my head. He demonstrated some EPLEY exercise, that he wants me to do. The dizzy spells have not improved. I don't feel well at all. I cannot complete house hold tasks. I still cannot drive. I can'' go to work. I have used over 40 hours of sick leave already. Now I have to be off work for another week and probably longer. I am worried and I have no idea when I will fully heal, or when I will be able to get back to normal activities. Prior to getting the vaccine, I was an ardent runner. I exercised every day and exercise is very important to me. I don't know how long it will be before I can go back to work or back to my exercise routine. I would never be in this situation, if I had not taken the Pfizer vaccine. I feel I was overdosed. I think one shot of the Pfizer vaccine would have been sufficient. I just went through 12 months without getting Covid. My immune system is suppressed so I am seriously careful about picking up germs. I have been using sanitizer wipes and hand gel for years because of my immune system being suppressed. Long before the whole world heard about Covid, I was acutely aware of germs & viruses in public places. I am so sorry now that I got this Pfizer vaccine. I think I could have gone on living for the rest of my life, without catching Covid, because I am so careful. If I had to do it all again, I would not get this vaccine. The research was not completed. The trials were not long enough. The trails were conducted in a controlled setting. They do not know all the side effects. They do not know the extent of the adverse effect on anybody, never mind somebody with my suppressed immune system. They said the side effects could be chills, fever, flu symptoms, tiredness, joint pain, muscle pain and headache. Nobody told me I might pass out or faint. Nobody warned me. If I had known fainting was a possibility, I would not have been home on my own. The word needs to get out about this side effect. The media needs to know. The public needs to know. I do not want this to happen to anybody else. Since this happened to me, I heard or someone else, that also fainted. These vaccines need more research period." The patient underwent lab tests and procedures which included unspecified blood test on 13Feb2021 with unknown results, body temperature of 100.1 on 11Feb2021, computerised tomogram: normal on 17Feb2021, X-ray on 13Feb2021 had no broken bones but otherwise with unknown results. The clinical outcome of loss of consciousness, fall, joint dislocation, thumb fracture, concussion, dizzy spells, headache, chills, fever, being unwell, being pale, pain, contusions, decreased appetite, nausea, back pain, sickness, pain in arm, memory deficit, weakness, balance difficulty, fatigue, shaky, whiplash injury, lethargic, inner ear disorder and ADL impaired were unknown. Information on Lot/Batch number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210213; Test Name: blood; Result Unstructured Data: Test Result:Unknown Results; Test Date: 20210211; Test Name: temperature; Result Unstructured Data: Test Result:100.1; Test Date: 20210217; Test Name: CAT scan; Result Unstructured Data: Test Result:Normal; Test Date: 20210213; Test Name: x-rays; Result Unstructured Data: Test Result:Unknown Results; Comments: had no broken bones. My shins and knees were badly bruised. fracture on my right thumb and there was something wrong with my left shoulder
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Immune system disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1103235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CO
Alter: 67,0
Geschlecht: M
Eingang: 15.03.2021
Impfdatum: 11.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / AR

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

Bell's palsy Blood test Computerised tomogram Eye disorder Facial paresis Mania

Symptomtext

His left eye started looking funny on Thursday night, 2/25/21. Friday morning the left side of his face wasn?t able to smile. Took him to medical center where, after CT scan and blood work, he was diagnosed with Bell?s palsy. Unfortunately the treatment for this is a steroid and antiviral medication. By Sunday night he was exhibiting signs of mania.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CT scan, bloodwork 2/26
Aktuelle Erkrankungen: -
Vorgeschichte: Bipolar 1 disorder, chronic kidney disease, traduce dyskinesia
Andere Medikamente: Allopurinol, tamsulosin, Depakote, amiloride, la, finasteride, lithium, vitamin D3, vitamin B12, ginkgo biloba
Allergien: Niacin
Vorherige Impfungen: -

VAERS 1086895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 45,0
Geschlecht: M
Eingang: 10.03.2021
Impfdatum: 02.02.2021
Beginn: 14.02.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: - / LA

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

Bell's palsy

Symptomtext

Bell's palsy; This is a spontaneous report from a contactable consumer (patient's wife). A 45-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration on 02Feb2021 at 11:00 at a single dose on left arm for COVID-19 immunisation. Medical history included ongoing systemic lupus erythematosus (Lupus), ongoing hypertension (High Blood Pressure), ongoing gout and hip arthroplasty from Dec2020 to an unknown date; all diagnosed about 20 years ago. Concomitant medications included allopurinol, atorvastatin, benzonatate, chlorthalidone, apixaban (ELIQUIS), hydrocodone bitartrate, paracetamol (HYDROCODONE/ACETAMINOPHEN), hydroxychloroquine, iron, loratadine, losartan potassium, mycophenolate mofetil, omeprazole, paricalcitol, prednisone, spironolactone and valacyclovir [valaciclovir] and vitamin D NOS. The reporter's husband had a reaction to the vaccine. She was wondering if it is ok to have the second dose. He got paralysis, Bell's Palsy on 14Feb2021. She clarified vaccine as COVID19 Vaccine. She would like any information available about second dose after having Bell's Palsy with the first dose. The outcome of the event was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Gout (Verbatim: Gout/diagnosed about 20 years ago); Hypertension (Verbatim: High Blood Pressure/diagnosed about 20 years ago); Lupus syndrome (Verbatim: Lupus/diagnosed about 20 years ago)
Vorgeschichte: Medical History/Concurrent Conditions: Hip replacement (Verbatim: Hip replacement/diagnosed about 20 years ago)
Andere Medikamente: ALLOPURINOL; ATORVASTATIN; BENZONATATE; CHLORTHALIDONE; ELIQUIS; HYDROCODONE/ACETAMINOPHEN; HYDROXYCHLOROQUINE; IRON; LORATADINE; LOSARTAN POTASSIUM; MYCOPHENOLATE; OMEPRAZOLE; PARICALCITOL; PREDNISONE; SPIRONOLACTONE; VALACYCLOVIR [VALACIC
Allergien: -
Vorherige Impfungen: -

VAERS 2620401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Hypoaesthesia oral Paraesthesia Paraesthesia oral Seizure

Symptomtext

Seizures NOTE this is typical of symptoms this patient has d/t seizure disorder already known, Episode occurred after vaccine. Numbness and tingling of tongue and tingling of L arm Narrative: has history of seizures. PCP does not believe it to be related. States typical of her seizure disorder. Other Relevant History:

Weitere VAERSDATA-Felder

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

VAERS 2518440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 05.03.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Fatigue Headache Hypoaesthesia oral Seizure

Symptomtext

Narrative: Pt with history of right parietal AVM s/p multiple embolizations (last 1/2011), simple partial seizures s/p VNS 4/2015 on keppra, gabapentin and lamictal, and migraines. Also with history of asthma, GERD, fatty liver disease, obstructive sleep apnea, and obesity. Patient states she felt numbness of her mouth and left side 5 minutes after receiving the second dose. This is typical of her seizure disorder. The following day she felt tired and had a headache.

Weitere VAERSDATA-Felder

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

VAERS 1070729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: -
Geschlecht: F
Eingang: 03.03.2021
Impfdatum: 20.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Balance disorder Diarrhoea Fatigue Hallucination, auditory Loss of consciousness

Symptomtext

heard a loud bang in my brain; blacked out for an instant; tired and wobbly; Did not get my balance/wobbly; 1,Day after the vaccine, I had violent projectile diarrhea; This is a spontaneous report from a contactable consumer (patient). An 83 year-old elderly female patient received first dose of BNT162B2 (lot number: EL3247), via an unspecified route of administration from 20Jan2021 20:30 at single dose in the right arm for COVID-19 immunisation. Medical history included small cell lung, 2cm, no follow -up treatment necessary. No known allergies. Concomitant medication included levothyroxine sodium (SYNTHROID), and losartan potassium. One day after the vaccine administration on 21Jan2021 10:00, the patient had violent projectile diarrhea. Two days after the vaccine, she blacked out for an instant and heard a loud bang in her brain. She was tired and wobbly for over one week. She did not get her balance back for nearly 3 weeks. The events resulted in Disability or permanent damage. Treatment for the events was unknown. The patient was not pregnant at the time of vaccination. 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 outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Small cell lung cancer (Small cell lung cancer, 2cm, no follow up treatment necessary)
Andere Medikamente: SYNTHROID; LOSARTAN POTASSIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1070675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MO
Alter: 69,0
Geschlecht: F
Eingang: 03.03.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Blood pressure increased Blood pressure measurement Chills Dizziness Fatigue Headache Hot flush Illness Malaise Presyncope Tinnitus Vomiting Weight

Symptomtext

she was sick for about 8 hours; Throwing up; Unable to keep anything down; Headache; Chills; Ringing in the ears; Hot flashes; Blood pressure went up; Was so dizzy if she moved her eyes she would nearly pass out; Was so dizzy if she moved her eyes she would nearly pass out; Very weak and tired; Very weak and tired; not feeling well; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received her first dose of bnt162b2 (BNT162B2 reported as PFIZER COVID VACCINE; lot number: EL3247; expiration date: unknown) at vaccination age of 69-year-old via an unspecified route of administration left arm on 28Jan2021 10:00 at a single dose for To keep from getting COVID (covid-19 immunization). The patient medical history was none. The patient's concomitant medications were not reported. The patient stated that she got the first vaccine the other day and within 12 hours (28Jan2021 22:00), she was not feeling well. At 8:30 the next morning (29Jan2021), she was sick for about 8 hours. She was throwing up, had a headache, chills, ringing in the ears, hot flashes, her blood pressure went up, she was unable to get anything down, not even medication [pending clarification]. She was so dizzy if she moved her eyes, she would nearly pass out. She could not move out of the chair for about 6-8 hours. The dizziness was severe and awful. She added only one ear is ringing really bad, the right ear. It is off and on and persisting. Her very weak and tired which was persistent. One hour it may be bad and the next she will be drained. The patient inquired if it is true since she heard the second dose is worse. She also wants to know if she should get the second dose or not. The received treatment for the adverse events was reported as none [pending clarification]. The patient underwent lab tests and procedures which included blood pressure (blood pressure measurement) was reported that her blood pressure went up and recovered on 29Jan2021, and weight was 175-180 pounds on an unspecified date. The outcome of the event feeling unwell was unknown, as for the events weakness, tiredness and ringing in ears were not recovered, while the outcome of the other events was recovered on 29Jan2021. Information about Lot/Batch number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20210129; Test Name: blood pressure; Result Unstructured Data: Test Result:her blood pressure went up; Test Date: 20210129; Test Name: blood pressure; Result Unstructured Data: Test Result:recovered; Test Name: Weight; Result Unstructured Data: Test Result:175-180 pounds
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1059220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 35,0
Geschlecht: F
Eingang: 27.02.2021
Impfdatum: 26.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Computerised tomogram head normal Differential white blood cell count normal Dizziness Full blood count normal Generalised tonic-clonic seizure Headache Metabolic function test Pregnancy test Urine analysis

Symptomtext

??I had a SEIZURE?? -only symptoms I had right before it happened were: 1-headache and 2-Dizziness -lasted almost 4 minutes, it was tonic clinic -911 was called and I went by ambulance to ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: -CBC AND DIFFERENTIAL -Comprehensive Metabolic panel -pregnancy, urine -urinalysis with microscopic -urine drug screen (it happened at work) -CT Head WO contrast ALL TESTS were NEGATIVE /OF NORMAL results (drug test did test positive for amphetamines because of my Adderall) ALL OF ABOVE WERE COMPLETED ON 2/4/2021 @ hospital
Aktuelle Erkrankungen: NONE
Vorgeschichte: These conditions aren?t Chronic; but I am Diagnosed with ADD & I have suffered from a few Vertigo Episodes over the past 2 years
Andere Medikamente: **DAILY MEDS** ?30 mg Adderall 2x a day ?20 mg Adderall 1x a day ?2 Women?s Multivitamin 1x a day ?2 Vitamin C Gummies 1x a day ?2 Vitamin D (2000 MG) Gummies 1x a day ?2 Chewable Magnesium= (400mg) 1x a day ?Skyla IUD (new as of 1/23/20) -
Allergien: NONE
Vorherige Impfungen: -

VAERS 1007864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 52,0
Geschlecht: M
Eingang: 27.02.2021
Impfdatum: 18.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Computerised tomogram Facial paralysis Magnetic resonance imaging

Symptomtext

Pt states he developed Bell's palsy two weeks after his first Covid vaccine. He states he saw his PCP. His PCP recommended he still get the second injection-but to put it off as long as possible. Pt said the symptoms from Bell's Palsy have entirely resolved.

Weitere VAERSDATA-Felder

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

VAERS 1007864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 52,0
Geschlecht: M
Eingang: 27.02.2021
Impfdatum: 18.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy Computerised tomogram Facial paralysis Magnetic resonance imaging

Symptomtext

Pt states he developed Bell's palsy two weeks after his first Covid vaccine. He states he saw his PCP. His PCP recommended he still get the second injection-but to put it off as long as possible. Pt said the symptoms from Bell's Palsy have entirely resolved.

Weitere VAERSDATA-Felder

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

VAERS 1058366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 56,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram cerebral normal Aphasia Blood pressure management Chest X-ray normal Computerised tomogram head normal Computerised tomogram normal Facial paralysis Fatigue Hemiparesis Magnetic resonance imaging brain normal Neurological examination Perfusion brain scan abnormal Vision blurred

Symptomtext

15 minutes after receiving shot, extreme fatigue, blurry vision, bp 250/200. ON the medic transport to ER, Left side weakness, loss of speech. Er evaluated for sudden onset left sided weakness, facial droop.Code stroke was called CT angiography was unremarkable and patient admitted for bp control. Bp normalized with Clonidine , neurological exam is stable. Md felt that thus was a combination adverse reaction to vaccine in combination with Wellbutrin. Discharge after 24 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 1,0
Labordaten: CT Stroke with perfusion ; negative. MRI brain normal ,Xray chest : no acute cardiac pulmonary disease
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension
Andere Medikamente: Chlorthalidone 25 mg, Losartan 100 mg, vitamin D, MVI, Potassium Chloride 10 meQ, Wellbutrin150 mg
Allergien: Ethanol, Wasps, bees
Vorherige Impfungen: -

VAERS 1048887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 23.02.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Presyncope Unresponsive to stimuli

Symptomtext

Near syncope, dizziness, unresponsive to sternal rub. RRT called and transported to ER where she regained adequate mentation without intervention.

Weitere VAERSDATA-Felder

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

VAERS 1048846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 23.02.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Allergy test Anaphylactic reaction Dyspnoea Palpitations Pruritus Tachycardia

Symptomtext

Anaphylaxis - tachycardia, palpitations, shortness of breath, skin itching. Received epi pen and ER transport. Now undergoing allergy testing.

Weitere VAERSDATA-Felder

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

VAERS 2674724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Hot flush Hyperhidrosis

Symptomtext

Anaphylaxis Hot flash, sweats, Narrative: Other Relevant History:

Weitere VAERSDATA-Felder

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

VAERS 1039939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 87,0
Geschlecht: M
Eingang: 18.02.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Dizziness Fatigue Headache Nausea Syncope Vomiting

Symptomtext

fainted; nauseated; vomited 4 times; dizzy; bad headache; extremely tired; This is a spontaneous report from a contactable consumer. An 87-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in Right arm (at age of 87-year-old) on 21Jan2021 at 12:00 PM as a single dose for COVID-19 immunisation, lot number: EL3247. Medical history was none. Patient had no allergies to medications, food, or other products. Concomitant medications within 2 weeks of vaccination included ibuprofen (ADVIL) and melatonin (minimal usage). Patient did not receive other vaccine in four weeks prior to the COVID vaccine. Prior to vaccination the patient was not diagnosed with COVID-19. It was reported that on 21Jan2021 at 02:45 PM (also reported as 2 1/2 hours after vaccine) patient became nauseated, he vomited four times, was dizzy, fainted, had bad headache and was extremely tired. Events resulted in Doctor or other healthcare professional office/clinic visit. Patient was treated for the events with nausea medications and ibuprofen (ADVIL). Since the vaccination patient had not been tested for COVID-19. Patient recovered with lasting effects from the events.

Weitere VAERSDATA-Felder

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

VAERS 1037950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 60,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 01.02.2021
Beginn: 01.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Arthralgia Body temperature Dizziness Inappropriate schedule of product administration Myalgia Presyncope Pyrexia

Symptomtext

This is a spontaneous report from a contactable nurse reported for herself. A 60-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE;lot EL3247) intramuscular in right arm on 01Feb2021 at 11:30 am (at 60 years) at single dose for covid-19 immunisation . Medical history included hypertension (HTN) , hypergammaglobulinaemia benign monoclonal (MGUS) , mononucleosis (recent mononucleosis one year before). Patient was not pregnant. Concomitant medication included venlafaxine hydrochloride (EFFEXOR), hydrochlorothiazide/ losartan potassium (HYZAAR), amfepramone hydrochloride (TENUATE). The patient previously took IV dramamine, tetanus and ceclor and experienced allergy. Previously, on 18Jan2021 at 10:30 am (at 60 years) she took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE;lot EL3248) intramuscular in right arm for covid-19 immunisation. Patient took the 1st dose of the vaccine on 18Jan2021 and 2nd dose on 01Feb2021 (inappropriate schedule of vaccine administered). Events were described as follows: next day, on 02Feb2021 at 06:00 temperature of 100.6, arthralgias and myalgias, dizziness. Second day (Feb2021), temp lower but still around 99.8 (normal for her 97.2), vasovagal, dizziness, arthralgias and myalgias. Events were non serious. Patient (a nurse) treated herself with dramamine for the dizziness, Nyquil and Advil. The final outcome of pyrexia, vasovagal, dizziness, arthralgias and myalgias was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20210202; Test Name: temp; Result Unstructured Data: Test Result:100.6; Test Date: 202102; Test Name: temp; Result Unstructured Data: Test Result:around 99.8; Comments: temp lower but still around 99.8 (normal for me 97.2)
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension (HTN); MGUS; Mononucleosis (recent mononucleosis one year ago)
Andere Medikamente: EFFEXOR; HYZAAR; TENUATE
Allergien: -
Vorherige Impfungen: -

VAERS 1037917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NH
Alter: 45,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 01.02.2021
Beginn: 01.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood pressure measurement Presyncope

Symptomtext

Vasovagal response; This is a spontaneous report from a contactable consumer. A 45-year-old female patient reported that she received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number EL3247) into the left arm on 01Feb2021 08:15 AM at single dose for COVID-19 immunization. Age at vaccination 45 years. Concomitant drugs included multi-vitamin, D3, AERids eye vitamins. The patient had not history of allergies to medications, food, or other products. On 01Feb2021 at 08:30 AM the patient experienced a vasovagal response.Occupational Health/Wellness nurse checked blood pressure and had her lay down with legs up. After 10 minutes she went away and felt back to normal. No treatment was received. The outcome was recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20210201; Test Name: blood pressure; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: D3
Allergien: -
Vorherige Impfungen: -

VAERS 1036262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CO
Alter: 76,0
Geschlecht: M
Eingang: 17.02.2021
Impfdatum: 28.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Blood urea Body temperature increased Cardiac failure congestive Chest X-ray abnormal Condition aggravated Encephalopathy Full blood count Lethargy Lung infiltration Mental status changes Metabolic encephalopathy Nausea Respiratory distress Systemic inflammatory response syndrome

Symptomtext

Following day after vac. resident had increased lethargy, nausea, altered mental stats, temp 100.1 bp 96./52, hr 107. Sent to er 1/29, returned 1/31 diagnosis systemic inflammatory response syndrome. On 2/1 resident had temp and respiratory distress. Sent to er again. Returned 2/3 with diagnosis CHF. On 2/7 resident sent out again after stat labs and xray. xray showed infiltrates. Returned from er on 2/10 diagnosis acute encephalopathy and metabolic encephalopathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 8,0
Labordaten: BUN, CBC, Chest Xray.
Aktuelle Erkrankungen: -
Vorgeschichte: Dementia, DM, CKD, HTN, metabolic encephalopathy, anemia, urinary retention, hematuria.
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1023484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 43,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Hypoaesthesia oral Paraesthesia Presyncope Vital signs measurement

Symptomtext

felt like she was going to pass out; face started to tingle/tingling returned but this time it was down her chest; lips started going numb; This is a spontaneous report from a contactable nurse (patient). A 43-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3247, expiry date: unknown), via an unspecified route of administration, in the right arm, on 27Jan2021 12:00 at a single dose for covid-19 immunization. The patient's medical history was not reported. There were no concomitant medications. The patient previously took amoxicillin and experienced allergies. The patient is not pregnant. The patient had no other vaccine in four weeks and no other medications in two weeks. The patient was not diagnosed with covid-19 prior to vaccination and was not tested for covid-19 post vaccination. On 27Jan2021, after getting the vaccine, the patient experienced face started to tingle and felt like she was going to pass out. On 27Jan2021, vitals were taken and showed normal. The patient reported that on her way home on 27Jan2021, lips started going numb and the tingling returned but this time it was down her chest. Therapeutic measures were taken as a result of all the events which included diphenhydramine (BENADRYL). Outcome of all the events was recovered on unspecified date in Jan2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20210127; Test Name: Vitals; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 972439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MD
Alter: 34,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 21.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: OT / RA

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

Facial paralysis Facial paresis Headache Hemiplegia Migraine Pain

Symptomtext

right sided facial paralysis; headache/migraine from base of R skull radiating to R Ear and top of head; This is a spontaneous report from a contactable nurse. This 34-Year-Old female nurse (patient) received 2nd dose of BNT162B2 (lot number=EL3247) Intramuscular on 21Jan2021 00: 00 AM (reported as 20Jan2021 12:00 PM) on Right arm for covid-19 immunization. Medical history and concomitant drug were not reported. Past drug was Known allergies to doxycycline. Historical Vaccine was 1st dose of BNT162B2 (lot number=EL1284, on 31Dec2020, 12:15 PM, administrator route=Intramuscular, vaccine location=Right arm). No other vaccine in four weeks. Patient received vaccine on Wednesday 20Jan2021, went to ER on Sunday 24Jan2021 with right sided facial paralysis and headache/migraine from base of R skull radiating to R Ear and top of head from 23Jan2021 10:00 AM with outcome was Recovering. Treatment was medications prednisone and antiviral. No covid prior vaccination. No covid tested post vaccination. No follow-up attempts possible. No further information expected.; Sender's Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the reported events of facial paralysis due to temporal relationship and current drug safety profile. This case will be reassessed once additional information is available. 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 RAs, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 1017138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 87,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 08.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Systemic: Other- Fainting only

Weitere VAERSDATA-Felder

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

VAERS 995462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 71,0
Geschlecht: M
Eingang: 09.02.2021
Impfdatum: 27.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / LA

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

Blood sodium decreased Confusional state Feeling abnormal SARS-CoV-2 test negative Seizure

Symptomtext

Confusion; General "Don't feel right"; Seizure; Low Sodium level; This is a spontaneous report from a contactable consumer (reported for himself). A 71-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL3247), via an unspecified route of administration on 27Jan2021 11:15 at single dose in left arm for COVID-19 immunization. Medical history included High Cholesterol; No known allergies. Concomitant medication in two weeks included atorvastatin. Facility type vaccine was Hospital. No other vaccine in four weeks. On 30Jan2021 23:00, the patient experienced Seizure, Low Sodium level, Confusion, General "Don't feel right". The events resulted in Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event). The number of days hospitalization was 3 (from unspecified date in 2021 to an unspecified date in 2021). It was unknown if treatment received. No covid prior vaccination. Covid tested post vaccination: Nasal Swab tested on 01Feb2021 with the result of Negative. The outcome of the events was recovered on an unspecified date in 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 3,0
Labordaten: Test Date: 20210130; Test Name: Sodium level; Result Unstructured Data: Test Result:Low; Test Date: 20210201; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol
Andere Medikamente: ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 995462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 71,0
Geschlecht: M
Eingang: 09.02.2021
Impfdatum: 27.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Blood sodium decreased Confusional state Feeling abnormal SARS-CoV-2 test negative Seizure

Symptomtext

Confusion; General "Don't feel right"; Seizure; Low Sodium level; This is a spontaneous report from a contactable consumer (reported for himself). A 71-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL3247), via an unspecified route of administration on 27Jan2021 11:15 at single dose in left arm for COVID-19 immunization. Medical history included High Cholesterol; No known allergies. Concomitant medication in two weeks included atorvastatin. Facility type vaccine was Hospital. No other vaccine in four weeks. On 30Jan2021 23:00, the patient experienced Seizure, Low Sodium level, Confusion, General "Don't feel right". The events resulted in Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event). The number of days hospitalization was 3 (from unspecified date in 2021 to an unspecified date in 2021). It was unknown if treatment received. No covid prior vaccination. Covid tested post vaccination: Nasal Swab tested on 01Feb2021 with the result of Negative. The outcome of the events was recovered on an unspecified date in 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 3,0
Labordaten: Test Date: 20210130; Test Name: Sodium level; Result Unstructured Data: Test Result:Low; Test Date: 20210201; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol
Andere Medikamente: ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1014508

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 08.02.2021
Impfdatum: 02.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

Resident received second dose of C0VID -19 ON 2/2/21 on 2/3/21 resident had a fall after an episode of syncope

Weitere VAERSDATA-Felder

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

VAERS 1013296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

schwer

Staat: OK
Alter: 75,0
Geschlecht: M
Eingang: 08.02.2021
Impfdatum: 22.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: SYR / RA

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

Bell's palsy Computerised tomogram abnormal Dyskinesia Eyelid function disorder Facial paralysis

Symptomtext

Paralysis of left side of face; left eye won?t blink: left side of mouth doesn?t move. Went to facility on 2/6/2021 and diagnosed with Bells Palsy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 2/6/2021 had CT scan to rule out a strike. Confirmed no stroke. Saw Dr on call doctor at facility and he diagnosed Bells Palsy?s.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure High cholesterol Had a triple bypass in 1999 Bladder cancer (polyps removed)
Andere Medikamente: Carvedilol Ezetimbe Enalapril Rosuvastatin Aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 1009685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: SD
Alter: 67,0
Geschlecht: M
Eingang: 07.02.2021
Impfdatum: 18.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / UN

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

Dysarthria Facial paralysis

Symptomtext

Right facial droop with slurred speech

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Depression, Cerebellar ataxia, anemia, RA, EtOH abuse, COPD, EtOH encephalopathy, Bilateral pseudophakia
Vorgeschichte: Depression, Cerebellar ataxia, anemia, RA, EtOH abuse, COPD, EtOH encephalopathy, Bilateral pseudophakia
Andere Medikamente: Latanoprost 0.0005% OPHTH SOLN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1008847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: LA
Alter: 69,0
Geschlecht: M
Eingang: 06.02.2021
Impfdatum: 29.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy Physical examination

Symptomtext

Diagnosed with bell's palsy 8 days after shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Doctor examination Feb 6,2021.
Aktuelle Erkrankungen: No
Vorgeschichte: NO
Andere Medikamente: I have Ramipril and Rosuvastn, Centrium, Zinc, Vitamin E and also Vitamin D3. I also takes Bayer 81 mg. Omeprazole 20mg.
Allergien: No
Vorherige Impfungen: -

VAERS 1007113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MN
Alter: 57,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SC / RA

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

Asthenia Headache Loss of consciousness Pain

Symptomtext

I woke up in the middle of the night with a headache and body aches. I got up to take ibuprofen and when I was in my bathroom, I collapsed. I do not remember actually falling but I heard the thud when I hit the floor. I tried to get up and had absolutely no strength in any part of body. My husband came to help me up but I could not even lift up my head. He was finally able to help me up and I took a few steps and collapsed/fainted again. This has never happened to me in my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Mild insomnia
Andere Medikamente: Trazadone 50 mg
Allergien: None
Vorherige Impfungen: -

VAERS 1005049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MO
Alter: 45,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 14.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Headache Syncope

Symptomtext

Patient states that her physician advised against second dose. She states she had a severe headache for days following vaccine, she collapsed at work and was hospitalized for a few days. She also reports ongoing dizziness. All information was left in a private message sent to the health departments social media page. Further requests for information have been unsuccessful thus far.

Weitere VAERSDATA-Felder

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

VAERS 1004369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MD
Alter: 36,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anaphylactic reaction Dizziness Dysphagia Dyspnoea Feeling hot Flushing Full blood count normal Injection site pain Nausea Swollen tongue Urticaria Wheezing

Symptomtext

hives started to appear on her body/hives on her neck; nauseous/ was going to throw up; dizzy; difficulty breathing (wheezing); difficulty breathing (wheezing); injection site soreness; She was hot, flush; difficulty swallowing; the tongue started swelling/Swollen tongue; Anaphylactic reaction/anaphylaxis; This is a spontaneous report from a contactable consumer reported for self. This 36-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 20Jan2021 12:52 left arm at single dose (Lot: EL3247) for covid-19 immunisation. Medical history included ongoing Anaphylaxis to Walnuts, Oranges, and morphine, ongoing allergy to a steroid cream Kenalog, and a steroid powder which she broke out immediately and ongoing Colitis. Concomitant therapy was none. She received the first dose of the vaccine yesterday on 20Jan2021 12:52 and 10 minutes later (20Jan2021 13:02) the tongue started swelling/Swollen tongue so they gave her Benadryl to try to stop it but it didn't help enough, hives started to appear on her body so they gave her a dose of epinephrine in the right arm and put on an IV, because she was feeling nauseous and dizzy. She started to feel better and was transferred to the hospital, when she was in the hall of the hospital she started having difficulty breathing (wheezing) and difficulty swallowing so she received another dose of Epinephrine (EpiPen) and also Benadryl, Prednisone and Pepcid. She went home and was taking Prednisone (1 daily), Benadryl and salbutamol (twice daily). She went into anaphylaxis within 15 minutes of receiving it on 20Jan2021. She brought 2 Epi injections with her. They monitored at the hospital for a few hours. She knows exactly how it happened. She was sitting in the observation room. She had told them multiple times that she had allergies before. She came in with two Epi pens and Benadryl. She let them know that as well. She was very verbal that she has history of anaphylaxis. They gave it to her. They said they were going to monitor her for 30 minutes. Her tongue started to swell 10 minutes after. She was sent to the paramedic tent. She took liquid children's Benadryl to try to stop the reaction. It did not help. She clarified it just didn't work enough to delay it. She doesn't have UPC, but provided the following information from the bottle: PLD-H242C LB004314 Lot WJ00896 Expiration Feb2023. She then started getting hives on her neck. She was hot, flush, and dizzy. She felt like she was going to throw up. That passed. They then gave her Epi in the opposite arm, her right arm. She got the COVID vaccine in her left arm. Then, they got her ready to go to the hospital. The transfer was smooth. She was waiting for intake when she started to not be able to swallow. She complained quickly. The nurses ran to get Epi, but the paramedic grabbed the patient's Epi pen and injected it in her thigh. She was IVed up at the vaccine center before transfer. They gave her Benadryl, Pepcid, and methyl prednisone. The Epi pen they gave her was her own shot. They monitored her a few hours. Then sent her home with Pepcid, more Epi pens, and Prednisone for 4 days. She has had normal soreness in her arm at the injection site. It has been status quo, it feels like a tetanus shot. She still has swelling in tongue, but they told her that might take a day or two to go away. She is supposed to also take Benadryl for the next 2 days. She was given the vaccine at the (Place name). Events visit to Emergency Room. They did a CBC and she was in normal range for everything. Lab data included on 20Jan2021: CBC normal. Outcome of the event Swollen tongue was recovering. Outcome of the event Anaphylactic reaction/anaphylaxis was recovered. Outcome of the event injection site soreness was not recovered. Outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 20210120; Test Name: CBC; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: Anaphylaxis (to Walnuts, Oranges, and morphine); Colitis (Verbatim: Colitis)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 996329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 23,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 18.01.2021
Beginn: 18.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Electric shock sensation Head discomfort Heart rate increased Hypoaesthesia Pain Tension headache

Symptomtext

symptoms occurred at home with following symptoms dizziness, fast heart beat (120-125) all day, generalized body aches, pressures and tightness/numbness on the back of head. Took Tylenol 48hrs. HR still occasionally goes up. Both arms and hands occasionally goes numb with a shock feeling and drops things. PCP follow up appt 2/2. 2nd dose was in 2nd arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Hep B carrier and asthma
Andere Medikamente: none
Allergien: Shrimp and crawfish
Vorherige Impfungen: -

VAERS 995563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: TX
Alter: 85,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose increased Cyanosis Eye movement disorder Metabolic function test Myoclonus Seizure

Symptomtext

Seizure - onset approximately 1 hour after vaccination administration. No medical history of seizures. Duration estimated 3 min - myoclonic head jerking, eyes rolled back, cyanosis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Blood glucose - 228 directly after episode BMP pending
Aktuelle Erkrankungen: NA
Vorgeschichte: DM2, HTN, anemia, Vit D deficiency, R PCA stenosis, HLD, hypothyroidism, aortic sclerosis, dysphagia - s/p PEG, depression, CKD, OA, Hx of CVA
Andere Medikamente: Lisinopril Metoprolol oxyCODONE Melatonin Famotidine Sertraline amLODIPine Levothyroxine Lantus Acetaminophen Cholecalciferol Lactobacillus Sennosides-Docusate
Allergien: NKDA
Vorherige Impfungen: -

VAERS 995255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: TX
Alter: 16,0
Geschlecht: M
Eingang: 02.02.2021
Impfdatum: 17.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Blood glucose normal Heart rate Loss of consciousness

Symptomtext

He passed out; His blood sugar was 143; This is a spontaneous report from a contactable consumer (patient's parent). A 16-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Batch/lot number: EL3247) via an unspecified route of administration on the right arm on 17Jan2021 at single dose for COVID-19 immunisation. Medical history included hypopituitarism. Concomitant medication included somatropin (NORDITROPIN) taken for hypopituitarism. He passed out (emergency room visit needed) on 17Jan2021, his blood sugar was 143 in Jan2021. Caller stated that her son received his first dose of the Pfizer COVID vaccine on 17Jan2021, stated he passed out. Caller stated they had to drive 3 hours away to get the vaccine and wanted to know that if because he experienced this after the first dose if it would be possible to find somewhere closer to home to get the second vaccine. Caller stated she is in the trial as an adult, that she reached out to her trial coordinator and they told her that they can only administer to persons in the trial. Son feels like maybe there is a drug interaction, caller stated she was not sure about this. Stated after her son passed out, they called an ambulance, states the Medic watched him for about 45 minutes, stated they ran some tests in Jan2021, he did go home that day. His blood sugar was 143 in Jan2021. Heart Rate monitor in Jan2021 she couldn't see so is unsure of the readings. The outcome of the event passed out was recovered on 17Jan2021, of other remain event was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 202101; Test Name: blood sugar; Result Unstructured Data: Test Result:143; Test Date: 202101; Test Name: Heart Rate; Result Unstructured Data: Test Result:unsure of the readings; Test Date: 202101; Test Name: ran some tests; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypopituitarism
Andere Medikamente: NORDITROPIN
Allergien: -
Vorherige Impfungen: -

VAERS 994675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: IL
Alter: 31,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 16.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Asthenia Hypoaesthesia Influenza like illness Injection site pain Mobility decreased Neck pain Paralysis Vomiting

Symptomtext

numbness has moved up her neck; she touches her neck, it hurts a little; maintains numbness and "no control of her arm"/can barely move her right arm; paralyzed at the shoulder from the elbow up;it's numb; can barely move her right arm; paralyzed at the shoulder from the elbow up; flu like symptoms; Threw up a couple times; mild pain at the injection site; This is a spontaneous report from a contactable nurse reporting for herself. A 31-years-old female patient received the first dose of BNT162B2 Pfizer-BioNTech COVID-19 Vaccine, Batch/lot number: EL3247, Expiry date 31May2021, via an unspecified route of administration in right arm on 16Jan2021 at 07:30 at single dose for COVID-19 immunization as frontline worker. The patient had no relevant medical history. There were no concomitant medications. The patient received BNT162B2 Pfizer-BioNTech COVID-19 Vaccine in Hospital. The patient reported that she was fine all day Saturday (16Jan2021), she just had some very mild pain at the injection site started a couple hours after getting injection. She developed flu like symptoms on the following day (17Jan2021) at 18:00PM and threw up a couple times. On 18Jan2021 at noon she noticed that she could barely move her arm: anything above her elbow on her right arm was not moving; it was paralyzed at the shoulder from the elbow up. If someone were to pick it up and let go, she couldn't control it at all. She also stated that she had no pain at all in that arm; she couldn't feel anything at all; it was numb. When she woke up on 19Jan2021 the numbness had moved up her neck, instead of being localized to her arm. She stated that when she touched her neck, it hurt a little, but it was not super significant. She stated that it was debilitating at that point as she was maintaining numbness and "no control of her arm". The nurse reported that this event had not required yet a visit to physician, but she has a feeling it will. She will probably have to go somewhere due to her paralyzed arm, but she had not yet. At the time of the report the event "No control of her arm"/can barely move her right arm; paralyzed at the shoulder from the elbow up; it's numb" had not resolved yet; the event "mild pain at the injection site" resolved on 17Jan2021, the events "Flu like symptoms" and "Threw up a couple times" were recovering and outcome of the events "Numbness has moved up her neck" and "She touches her neck, it hurts a little" was unknown. The reporter assessed the events "Pain injection site" and "Flu like symptoms" as non-serious and assessed the event "Can barely move her right arm; paralyzed at the shoulder from the elbow up; it's numb" as disabling. She assessed all the reported events as related to BNT162B2 Pfizer-BioNTech COVID-19 Vaccine (method of assessment: Global Introspection).; Sender's Comments: Based on the temporal relationship, the association between the events numbness of upper extremity and arm paralysis with BNT162b2 use can not be fully 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: Paralysis
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 955141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

schwer

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 15.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Bell's palsy Blood test Computerised tomogram Electrocardiogram Facial paralysis

Symptomtext

Bell's Palsy; This is a spontaneous report from a contactable other HCP (patient). A 53-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL 3247), via an unspecified route of administration at Left arm on 15Jan2021 11:00 AM at SINGLE DOSE for covid-19 vaccination. The patient was not pregnant. Concomitant medications in two weeks included lithium, levothyroxine sodium (LEVOTHROID), omeprazole. Historical Vaccine included first dose of bnt162b2 (lot number EL 1284) on 29Dec2020 11:00 AM at Left arm for covid-19 vaccination. The patient previously took ziprasidone hydrochloride (GEODON) and experienced drug allergies. It was reported no other medical history. On 17Jan2021 the patient woke up with left side of her face dropping. She went to the ER. She was diagnoses with Bell's Palsy. The event onset date was 17Jan2021 04:00 AM. AE resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. Treatment drugs predizone and Acyclovir received for the event. The outcome of the event was not recovered. No covid prior vaccination, no covid tested post vaccination.; Sender's Comments: Based on the close temporal relationship, the association between the event Bell's palsy with BNT162b2 can not be fully excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 955141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

schwer

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 15.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Bell's palsy Blood test Computerised tomogram Electrocardiogram Facial paralysis

Symptomtext

Bell's Palsy; This is a spontaneous report from a contactable other HCP (patient). A 53-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL 3247), via an unspecified route of administration at Left arm on 15Jan2021 11:00 AM at SINGLE DOSE for covid-19 vaccination. The patient was not pregnant. Concomitant medications in two weeks included lithium, levothyroxine sodium (LEVOTHROID), omeprazole. Historical Vaccine included first dose of bnt162b2 (lot number EL 1284) on 29Dec2020 11:00 AM at Left arm for covid-19 vaccination. The patient previously took ziprasidone hydrochloride (GEODON) and experienced drug allergies. It was reported no other medical history. On 17Jan2021 the patient woke up with left side of her face dropping. She went to the ER. She was diagnoses with Bell's Palsy. The event onset date was 17Jan2021 04:00 AM. AE resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. Treatment drugs predizone and Acyclovir received for the event. The outcome of the event was not recovered. No covid prior vaccination, no covid tested post vaccination.; Sender's Comments: Based on the close temporal relationship, the association between the event Bell's palsy with BNT162b2 can not be fully excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 989770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: OR
Alter: 57,0
Geschlecht: M
Eingang: 31.01.2021
Impfdatum: 26.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram Chest X-ray Computerised tomogram thorax Endoscopy upper gastrointestinal tract Hiccups Impaired gastric emptying Laboratory test Nausea Retching SARS-CoV-2 test Syncope Ultrasound abdomen Vomiting

Symptomtext

On 12/31/20, patient started to develop nausea and vomiting. Progressed to recurrent nausea/retching/intractable hiccups on 1/1/20. Presented for evaluation/iv rehydration on 1/3/21, 1/5/21 and 1/6/21. Multiple vasovagally-mediated syncopal spells on 1/5/21 - 1/6/21. Suspected to have gastroparesis on 1/8/21. Symptoms improved with Reglan 10 mg po qid by 1/15/21. Received dose 2 of COVID-19 vaccine on 1/18/21. Symptoms of gastroparesis redeveloped a few hours later, symptoms improved with domperidone 10 mg po qid by 1/23/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Labs, COVID-19 PCR, CXR, CT chest on 1/3/21. Labs, RUQ ultrasound 1/6/21. CTA abdomen/pelvis 1/18/21. EGD 1/19/21.
Aktuelle Erkrankungen: None
Vorgeschichte: Paroxysmal atrial fibrillation, gout
Andere Medikamente: ASA, Sotalol, atorvastatin, probenecid, vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 989322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

schwer

Staat: AZ
Alter: 85,0
Geschlecht: M
Eingang: 31.01.2021
Impfdatum: 28.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Dysphagia Nausea Pyrexia Syncope Vomiting

Symptomtext

Trouble swallowing: 30 hours after shot, continuing though current time of 70 hours Nausea, vomiting, dizzy, fainting 65 hours after shot. 2 episodes Fever - 72 hours after shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Mulitple Myeloma
Andere Medikamente: Velcade Acyclovir Simvistatin Tamsulosin Plavix
Allergien: -
Vorherige Impfungen: -

VAERS 989113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

schwer

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 31.01.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Chest discomfort Chills Discomfort Fatigue Headache Injection site pain Injection site swelling Lymphadenopathy Malaise Myalgia Nausea Pain Seizure

Symptomtext

Injection site pain, tiredness, headache, severe aches and pains throughout body joints and muscles, chills so bad that I was convulsing, injection site swelling, nausea, feeling sick for more than 2 days, swollen lymph nodes in left arm pit, chest feeling tight and lungs feeling heavy

Weitere VAERSDATA-Felder

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

VAERS 988249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MO
Alter: 34,0
Geschlecht: F
Eingang: 30.01.2021
Impfdatum: 19.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood pressure measurement Cardiac monitoring Fatigue Febrile convulsion Myalgia Oxygen saturation Paraesthesia oral Pyrexia Throat tightness Vital signs measurement

Symptomtext

About 5 minutes after the vaccine, my tongue began tingling. I drank water but didn't tell anyone at the vaccine clinic. I did wait 17 minutes before leaving. I went to the car to look in the mirror and assess my oral airway. My tongue and pharynx were not swollen. I kept drinking water and proceeded to go home. About 10 minutes into my drive my throat became tight, so I went back and checked into the ER. My vitals were stable, and you couldn't see any swelling. My throat felt tight and my tongue tingly. I had already taken pepcid and zyrtec that morning, so they gave me Solumedrol and Benadryl IV. The tingling and tightness improved and went away by about 0930. It did return around 2300 that night (not as bad, just tongue tingly and slight tightening of my throat), and I took another pepcid and benadryl. I also had myalgias, felt febrile and fatigued for about 48 hours. ++See previous VAERS report I did about vaccine #1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Febrile convulsion
Hospital-Tage: -
Labordaten: Vital sign monitoring-BP, SPO2, Heart monitor
Aktuelle Erkrankungen: Strained back; LUQ abdominal pain-constipation
Vorgeschichte: -
Andere Medikamente: Multi vitamin, pepcid, protonix, carafate, magnesium, vitamin D
Allergien: Amoxicillin-hives
Vorherige Impfungen: -

VAERS 987687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 30.01.2021
Impfdatum: 23.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Hyperhidrosis Laboratory test Loss of consciousness Pain in extremity Vomiting

Symptomtext

Severe pain in injection arm, profuse sweating on second day. A lot of vomiting causing me pass out out and be taken to the hospital via ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 3,0
Labordaten: all test were inconclusive for other conditions
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 983252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 34,0
Geschlecht: M
Eingang: 28.01.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Hyperhidrosis Loss of consciousness Pallor Unresponsive to stimuli

Symptomtext

Client became unresponsive for about 15 seconds after sitting in the observation area. He was pale and diaphoretic but came to almost immediately and was AO x4. BP was 128/74. Client reported having a history of "passing out" with needles prior but it had been years since that had happened. He was observed until 4:14pm and EMT observer on site took a final BP: 120/84 and walked him to his car. He had a steady gait walking to the car and ate a muffin before driving away.

Weitere VAERSDATA-Felder

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

VAERS 982529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MO
Alter: 52,0
Geschlecht: F
Eingang: 28.01.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypokinesia Petit mal epilepsy Seizure

Symptomtext

Petite mal seizure blank stare with poor respond to staff. Has not experienced this effect under current med regimen in 3 years according to caregiver.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Caregivers called 911 and patient was transported to Hospital for evaluation
Aktuelle Erkrankungen: None
Vorgeschichte: Seizure disorder (last episode 3 years ago)) CP herpes Zoster Mood disorder Constipation Areata Alopecia Urinary retention Hypotension Sleep disorder
Andere Medikamente: Bisacodyl 5mg daily Carbamezepine susp 15 ml TID Clonazepam 0.5mg BID Colace 100 BID Levetiracetam 10ml q 12hours Lisinopril 10mg daily Neudexta 20mg q12hours Oxybutynin 5mg BID Calcium 500mg BID Phenytoin 200mg HS Simvastatin 20mg HS Vitam
Allergien: NKDA
Vorherige Impfungen: -

VAERS 982414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 28.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Dyskinesia Fatigue Nausea Seizure Urinary incontinence Vomiting

Symptomtext

Approximately 10 mins post Pfizer vaccine patient notified EMT she was going to have a seizure. She was placed in a safe position, seizure lasted about 30 seconds. Mild body movement, patient urinated, no physical injury. Mother was present, primary historian. Described course of seizure as regular and last seizure 6months ago. As EMT began taking vitals, she expressed feeling nauseous, and vomited. Afterwards patient stated feeling very tired and wanted to leave. Refused paramedics to be called. Patient wanted to rest, left at 3:00PM. Alert and oriented, no complaints besides feeling tired, able to walk with steady gate. Counseled patient to follow up with provider as soon as possible.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: History of seizures. Regularly follows up with provider.
Andere Medikamente: Daily seizure medication.
Allergien: -
Vorherige Impfungen: -

VAERS 981821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NE
Alter: 23,0
Geschlecht: F
Eingang: 28.01.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chills Dizziness Fall Feeling cold Hyperhidrosis Loss of consciousness Myalgia Nausea Pain Pain in extremity Sleep disorder Tinnitus Vision blurred

Symptomtext

The evening after I got the first dose I experienced painful muscle aches starting in my legs and progressing to the rest of my body, around 7pm. My left shoulder was a little achy, but no different than any other shot. About 30 minutes later I felt chills and felt really cold. I went to bed and tried to sleep. I woke up several times in pain. I did not take any pain meds. At 1am I went to the bathroom and felt nauseous and lightheaded. My vision got blurry and it felt like I was going to pass out, so I grabbed the towel rack and closed my eyes. I must have blacked out for a second and lowered myself down to the floor. I came to, and I was sitting on the ground, sweating a lot. I stayed on the floor for at least 10 minutes cooling down. (I had dressed warmly and turned on my heater after the chills started). I heard ringing in my ears while I was sitting on the floor. It went away after 5 minutes. I got up and went back to bed. I woke up at 9am and felt a lot better. Some minimal soreness. No more chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Possibly exposed to someone who had Covid symptoms about 5 days prior to getting first dose. I had no signs of sickness or any illness one month before the first dose of vaccine.
Vorgeschichte: Eczema on my hands.
Andere Medikamente: A Women's Multivitamin. Supplemental vitamin C, vitamin D. Quercetin. Selenium.
Allergien: None
Vorherige Impfungen: -

VAERS 981762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MA
Alter: 17,0
Geschlecht: F
Eingang: 28.01.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Anaphylactic reaction Cough Dyspnoea Rash Wheezing

Symptomtext

Systemic: Anaphylaxis-Medium, Systemic: Rash (other than injection site)-Mild, Systemic: Other- wheezing, shortness of breath, coughing-Medium

Weitere VAERSDATA-Felder

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

VAERS 974457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NE
Alter: 21,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 25.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood pressure increased Dyspnoea Nausea Ocular hyperaemia Syncope Tachycardia

Symptomtext

DEVELOPED ELEVATED BLOOD PRESSURE (181/106) AND TACHYCARDIA (125), SOB, FAINTNESS, NAUSEA, RED EYES. GAVE BENADRYL 25MG PO AT 0940. BP DECREASED TO 143/88 AND PULSE 99.

Weitere VAERSDATA-Felder

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

VAERS 974398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NE
Alter: 38,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Dyspnoea Neck pain Pain in extremity Pruritus Pyrexia Seizure Tremor

Symptomtext

AT 2130 ON 1/20/21 DEVELOPED SHAKES, THAT PROGRESSED TO 'CONVULSING. DEVELOPED FEVER OF 104.3. SEVERE ARM, NECK, AND CHEST PAIN. SHORTNESS OF BREATH THAT IMPROVED OVER TIME. ON 1/23/21 COMPLAINED OF SEVERE ITCHING OVER ENTIRE BODY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: PFIZER-COVID-19 VACCINE 1ST DOSE

VAERS 974130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: AZ
Alter: 48,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 25.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Diarrhoea Dyspnoea Nausea Presyncope Tremor Vital signs measurement Vomiting

Symptomtext

Sudden onset of nausea, vomiting, diarrhea, shortness of breath, uncontrolled shaking and vasovagal response with near syncope episode. Gave Diphenhydramine approximately 25 minutes after onset.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Call paramedics, BP normal, HR normal, refused transport to hospital.
Aktuelle Erkrankungen: None
Vorgeschichte: Exercised Induced Asthma
Andere Medikamente: None
Allergien: Sulfa, IVP Dye
Vorherige Impfungen: -

VAERS 973939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: WV
Alter: 40,0
Geschlecht: M
Eingang: 26.01.2021
Impfdatum: 21.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Corneal reflex decreased Dysphagia Ear pain Facial pain Facial paralysis Lagophthalmos Oral pain

Symptomtext

Inmate seen in health services with complaint of left ear pain extending into left cheek and around his mouth. He has some drooping of the left side of his mouth and he is not able to blink or close his left eye. He noticed symptoms on 1-23-2021, the Saturday after getting the COVID 19 vaccine on 1-21-2021 (Thursday). Had some trouble swallowing liquids without having them dribble out the left side of his mouth and he says that he is not able to chew on the left side without biting his tongue. Says that his left ear is causing him a great deal of pain.

Weitere VAERSDATA-Felder

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

VAERS 970709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MD
Alter: 27,0
Geschlecht: M
Eingang: 25.01.2021
Impfdatum: 23.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Loss of consciousness

Symptomtext

5 mins after injection, loss consciousness, was lowered to floor, complained of dizziness and look confused prior to passing out. Hx of passing out after vaccine. When regaining consciousness, appeared confused. Unconscious for approx 1 min; Evaluated by MD. 835: 129/63, O2: 98% 8:37: Transferred to stretcher; BP: 97/50, O2: 98% 8:43: BP: 122/75, O2: 98%, awake, alert, monitoring continued; denied SOB 8:53: 120/80, O2: 98%, patient reports feeling beter Observation ended at 8:54

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: Hx of passing out after vaccines
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 968165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 87,0
Geschlecht: M
Eingang: 23.01.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Headache Syncope Vomiting

Symptomtext

- vomiting multiple times 2-3 hours after the vaccine - severe headache 2-3 hours after the vaccine- given tylenol - severe dizziness 2-3 hours after the vaccine - fainting 2-3 hours after the vaccine - extremely tired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none
Vorgeschichte: dementia
Andere Medikamente: advil
Allergien: none
Vorherige Impfungen: -

VAERS 967460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: -
Alter: 24,0
Geschlecht: F
Eingang: 23.01.2021
Impfdatum: 23.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blindness Cold sweat Feeling cold Pallor Presyncope

Symptomtext

Patient received 1st dose of Pfizer vaccine. Patient likely vasovagal, blood pressure 56/33 initially. Patient stated that she almost completely lost her vision. Patient extremely pale and cold and clammy. Patient stated she did eat breakfast this morning and had not had a reaction like this in the past. Patient provided with a sugar source and was placed supine. Blood pressure 105/63. Patient monitored for 30 minutes and sent home.

Weitere VAERSDATA-Felder

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

VAERS 966826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MO
Alter: 72,0
Geschlecht: F
Eingang: 22.01.2021
Impfdatum: 19.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Blood chloride normal Blood creatinine normal Blood glucose normal Blood pH normal Blood potassium normal Blood sodium normal Blood urea normal Calcium ionised decreased Carbon dioxide normal Electrocardiogram abnormal Haematocrit normal Haemoglobin normal Headache Influenza virus test negative Metabolic function test Presyncope SARS-CoV-2 test negative Sinus bradycardia

Symptomtext

Patient had an increase in chronic headache frequency and had a near-syncopal episode on 1/21/21. She stated that the near-syncopal episode lasted for about 10 minutes. She has had one prior episode that was caused by hypotension and dehydration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: EKG: Sinus bradycardia, No ST or T changes. BMP: Na 139, K 3.8, Cl 106, iCa 1.21, Co2 25, Glu 98, BUN 16, Creat 0.6, HGB 12.9, HCT 38%. UA: Clean, PH 6.0, SG 1.020, Urobilinogen 0.2 E.U/dL. Covid molecular PCR negative. Flu negative.
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary artery disease, hypercholesterolemia, hypertension
Andere Medikamente: metoprolol succinate, zetia, lipitor, isosorbide mononitrate, HCTZ
Allergien: NKA
Vorherige Impfungen: -

VAERS 966769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: GA
Alter: 68,0
Geschlecht: F
Eingang: 22.01.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Dry throat

Symptomtext

Dry throat with onset of anaphylaxis

Weitere VAERSDATA-Felder

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

VAERS 966768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 39,0
Geschlecht: M
Eingang: 22.01.2021
Impfdatum: 21.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

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

Chills Dizziness Feeling hot Syncope

Symptomtext

Woke up at 6:00am, felt hot, had to use the bathroom. Got up, went to the bathroom felt dizzy, I was able to get to the floor before passing out/fainted. Felt chills when I finally went back, but could have been from how long I was laying on the floor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: vasovagal syncope
Andere Medikamente: None
Allergien: Lactose intolerant
Vorherige Impfungen: -

VAERS 966057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 80,0
Geschlecht: F
Eingang: 22.01.2021
Impfdatum: 19.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Cardiac monitoring Computerised tomogram head Electrocardiogram Muscle spasms Syncope

Symptomtext

Extreme cramping in both legs, fainting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG, blood drawn, head CT, heart monitor
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Amlodapin, klonapin, raloxifen, vitamin D, multi vitamin, baby aspirin
Allergien: None
Vorherige Impfungen: Shingrax age 78

VAERS 965837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NY
Alter: 69,0
Geschlecht: M
Eingang: 22.01.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Post-traumatic epilepsy Seizure Slow response to stimuli Vital signs measurement

Symptomtext

Received vaccine without complication. Has a known seizure disorder secondary to brain injury. Seizures often triggered by stress. During observation period, RN was made aware that patient had decreased responsiveness. States this is common activity for absent seizures which he has several per week. First set of vitals: HR 70, RR 20, SpO2 95% on RA. He was taken to tent where he became more alert and was A&O x 3 and recovered quickly. Second vital set taken 10 mins after first: HR 70, RR 16, BP 140/96, 97% on RA. Evaluated by provider: clear lung sounds, no signs of stridor or difficulty breathing denied any rash, SOB, CP, swelling of mouth or throat. Returned to baseline within 10 mins. Recommended to be evaluated at the ER though left AMA.

Weitere VAERSDATA-Felder

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

VAERS 965215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: AL
Alter: 58,0
Geschlecht: F
Eingang: 22.01.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Paralysis

Symptomtext

Systemic: Patient experienced temporary paralysis from the shoulders down lasting approximately 20 minutes-Severe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Patients is allergic to bee stings and Benadryl.
Vorherige Impfungen: -

VAERS 964489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: WV
Alter: -
Geschlecht: F
Eingang: 22.01.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Dyspnoea Nausea Retching Syncope

Symptomtext

SOB - Shortness of Breat requiring O2, Nausea, Syncopy, Dry Heaving Transported to the ER

Weitere VAERSDATA-Felder

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

VAERS 964127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: OK
Alter: 57,0
Geschlecht: F
Eingang: 22.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / AR

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

Bell's palsy

Symptomtext

Bell's palsy - left

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, peripheral neuropathy
Andere Medikamente: -
Allergien: TB test
Vorherige Impfungen: -

VAERS 962900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

schwer

Staat: CO
Alter: 64,0
Geschlecht: F
Eingang: 21.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Movement disorder Pallor Presyncope

Symptomtext

Vaccine recipient c/o near syncope to RN monitor in the vaccination clinic. Cool, pale, dry skin. She placed her head on the table and asked for help. RN monitor requested assistance. Patient had strong pulse, no respiratory difficulties, no hives noted but was unable to stand. ED Charge nurse notified and ED RN transported patient to the ED via gurney without incident.

Weitere VAERSDATA-Felder

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

VAERS 961731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: IL
Alter: 55,0
Geschlecht: M
Eingang: 21.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction

Symptomtext

Systemic: Anaphylaxis-Medium; symptoms lasted 1 day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: aspirin, egg, peanuts, bee venom, tramadol, penicillin
Vorherige Impfungen: -

VAERS 960934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MD
Alter: 38,0
Geschlecht: M
Eingang: 21.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
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 Headache Hypotension Pallor Presyncope

Symptomtext

Near syncopal a few minutes after receiving the vaccine. Was pale and hypotensive. Also c/o mild headache and LUQ abd pain. Laid down and given PO fluids and crackers. He felt better and went home.

Weitere VAERSDATA-Felder

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

VAERS 959600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: IA
Alter: 53,0
Geschlecht: F
Eingang: 20.01.2021
Impfdatum: 19.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Facial paralysis Nausea Pain Vomiting

Symptomtext

ON 1/20/21 DEVELOPED EYE/MOUTH DROOPING, VOMITING, NAUEA, CHILLS AND BODY ACHES. HAS CALL OUT TO PCP

Weitere VAERSDATA-Felder

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

VAERS 958576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

schwer

Staat: VA
Alter: 44,0
Geschlecht: F
Eingang: 20.01.2021
Impfdatum: 19.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Anaphylactic reaction Hypersensitivity Seizure

Symptomtext

Systemic: Anaphylaxis, Systemic: Seizure-Severe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No
Vorherige Impfungen: -

VAERS 956078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: MD
Alter: 29,0
Geschlecht: F
Eingang: 19.01.2021
Impfdatum: 19.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Syncope

Symptomtext

Syncope minutes after vaccination

Weitere VAERSDATA-Felder

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

VAERS 955649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: NC
Alter: 37,0
Geschlecht: M
Eingang: 19.01.2021
Impfdatum: 18.01.2021
Beginn: 18.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Blood pressure decreased Syncope

Symptomtext

Pt. had a Syncope episode within 20 min. of getting immunization. BP dropped to 80's - Systolic. , and HR dropped to the 40's. Pt. placed on Ground-Legs elevated. Provided PO H2O, Rest, Cool packs and recovered well within 30 min. Left Hospital without incident.

Weitere VAERSDATA-Felder

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

VAERS 953681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

schwer

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 18.01.2021
Impfdatum: 18.01.2021
Beginn: 18.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Loss of consciousness Palpitations Petit mal epilepsy Syncope Tachycardia

Symptomtext

20-30 min post injection, patient experienced tachycardia, palpitations, shortness of breath, syncope, loss of consciousness. 911 contacted by nursing home staff. Patient was placed in nursing home bed, 1 EpiPen dose administered by clinic nurse (RN. Nursing home staff began supportive care, supplemental oxygen given. patient experienced petit mal seizure and was non-responsive for a few minutes. Eventually came to but was still unstable. Paramedics took over at this point and patient was evaluated and transferred to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP 160/80, HR 120, Oxygen Sat 98%
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes type II,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2683542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: WA
Alter: 39,0
Geschlecht: F
Eingang: 19.09.2023
Impfdatum: 27.01.2021
Beginn: 01.05.2021
Tage bis Beginn: 94,0
Dosis: 2
Route/Site: IM / UN

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

Aortic disorder Arrhythmia Blood pressure increased Cardiac valve disease Echocardiogram abnormal Electrocardiogram ambulatory Laboratory test normal Palpitations Sinus tachycardia Tricuspid valve incompetence Ventricular extrasystoles

Symptomtext

After my 2nd dose of PFIZER COVID Vaccine on 1/27/2021, I started developing heart palpitations approximately 3-4 weeks after the vaccine. On 5/14/2021 I suffered a cardiac event at my place of work that entailed elevated blood pressure and heart arrhythmias. Since this time, I have developed chronic heart palpitations, elevated blood pressure and diagnosed with heart valve disease with aortic dilation, I have no history of cardiac issues and have been a healthy woman prior to this vaccine. After doing some research, I felt it was best to report my case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: 1/3/2021 1st COVID Vaccine 1/27/21 2nd COVD Vaccine 2/14/21-5/14/21 Developed unprovoked heart palpitations 5/14/2021 EKG revealed Sinus tachycardia at 114 with occ PVC's. Lab tests were within normal limits. 6/2021 Holter Monitor did not capture any abnormalities during the 2 weeks of wearing it. 3/2022 Primary Care appointment and reported increased heart palpitations, referred to obtain echocardiogram 5/2022 Echocardiogram revealed Tricuspid Valve with trace-mild regurgitation with dilated aorta measuring 4.0cm at the sinus and 4.2cm at the Valsava
Aktuelle Erkrankungen: None
Vorgeschichte: Since the 2nd COVID vaccine, I developed heart palpitations, heart arrhythmias.
Andere Medikamente: Daily multi-vitamin
Allergien: Codeine- nausea, vomiting
Vorherige Impfungen: -

VAERS 2683348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MS
Alter: 70,0
Geschlecht: M
Eingang: 18.09.2023
Impfdatum: 21.01.2021
Beginn: 01.02.2023
Tage bis Beginn: 741,0
Dosis: 2
Route/Site: - / AR

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

Atrial fibrillation Feeling abnormal Hypotension Influenza virus test negative Magnetic resonance imaging thoracic Malaise Pyrexia SARS-CoV-2 test negative

Symptomtext

In Feb of 2023, the afternoon of the 13th I started to feel something coming on. By the next afternoon I felt feverish and taking my temp confirmed it. I called to reschedule an ENT appt for the next day and to schedule an appt with Dr. At the appt I tested negative for Covid and the flu. They did an MRI of my chest to make sure it wasn't pneumonia and listened to my heart and did my blood pressure and then Rx'd a z-pac and cough syrup. Monday (a holiday) I still felt terrible and decided to check my bp. It was 90/53! Time for the ER! Feb 19: Not only was my bp low, I was in atrial fibrillation. Lots of things done for me to stabilize me. They kept me overnight for observation and released me the next morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: heart attack with stent, after affects of radiation & chem for cancer of the tongue (10 years in remission at time of the jab)
Andere Medikamente: Plavix, Crestor, Synthroid,Prilosec,ipratropium, krill oil
Allergien: Celebrex
Vorherige Impfungen: -

VAERS 2652954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 05.07.2023
Impfdatum: 13.01.2021
Beginn: 05.11.2022
Tage bis Beginn: 661,0
Dosis: UNK
Route/Site: IM / -

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

Atrial fibrillation COVID-19 pneumonia Chills Cough Dyspnoea Palpitations Pyrexia Respiratory depression Respiratory failure Sepsis Tachypnoea

Symptomtext

Reported Symptoms: 10033556:PALPITATION; 10038678:RESPIRATORY DEPRESSION; 10040047:SEPSIS; 10043088:TACHYPNEA; 10084380:COVID-19 PNEUMONIA; Narrative: Patient has received two Pfizer COVID 19 Vaccines (Jan/Feb 2021). The patient presented to the ED on 5 Nov 2022 with fever, chills, cough, and shortness of breath. The patient was admitted to the hospital with sepsis, covid pneumonia, respiratory failure, and afib. The patient was treated with remdesivir and dexamethasone. The patient was discharged on 9 November 2022 in stable condition. Reported per EUA. Other Relevant HX: Other: COVID Pneumonia, sepsis

Weitere VAERSDATA-Felder

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

VAERS 1261793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 23.05.2023
Impfdatum: 17.02.2021
Beginn: 01.12.2021
Tage bis Beginn: 287,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain upper Back pain Blood pressure orthostatic increased Bowel movement irregularity Deafness COVID-19 Disease recurrence SARS-CoV-2 test Vaccination failure Dizziness Gait disturbance Gastric disorder Headache Herpes zoster Lumbar puncture Magnetic resonance imaging Meningitis Migraine

Symptomtext

SARS-CoV-2 test: (Dec2021) Positive; (Jan2023) Positive; covid test result: Positive; 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 73-year-old male patient received BNT162b2 (BNT162B2), on 26Jan2021 as dose 1, single (Lot number: EL9262), in left arm and on 17Feb2021 as dose 2, single (Lot number: EL03247) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hemochromatosis" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing). Concomitant medication(s) included: B VITAMIN COMP [CALCIUM PANTOTHENATE;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Dec2021, outcome "unknown" and all described as "covid test result: Positive"; DISEASE RECURRENCE (medically significant) with onset Jan2023, outcome "unknown", described as "SARS-CoV-2 test: (Dec2021) Positive; (Jan2023) Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Dec2021) Positive; (Jan2023) Positive. Additional information: Facility type vaccine was Regulatory Authority facility. No other vaccine in four week. Other medications in two weeks was reported as B vitamins. No covid prior vaccination. covid tested post vaccination. Covid test type post vaccination was Nasal Swab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: Nasal Swab; Test Result: Positive ; Test Date: 202301; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hemochromatosis; Sulfonamide allergy
Andere Medikamente: B VITAMIN COMP [CALCIUM PANTOTHENATE;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RIBOFLAVIN;THIAMINE HYDRO
Allergien: -
Vorherige Impfungen: -

VAERS 2633536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MS
Alter: 73,0
Geschlecht: F
Eingang: 18.05.2023
Impfdatum: 01.11.2022
Beginn: 04.03.2023
Tage bis Beginn: 123,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia COVID-19 Cough Loss of personal independence in daily activities Malaise Mobility decreased Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

woke up on last day of a 7 night cruise with a sore throat. Drove home for 2 days with running nose and coughing. Treated with over the counter medicine and finally called the doctor on 6 after not getting any better. He told me to continue what I was doing as it was too late to treat for COVID. After another day or two went to a walk in clinic. Received a shot, and perscription for a steroid and cough medicine. Continued to take my medicine but was still sick with horrible cough and bad congestion. Was in bed about 2 1/2 weeks not able to do anything. After I was able to be up I continued to have no energy for about 2 months. I now feel back to normal and able to do the things I enjoy. I am NEVER sick and I think that is the reason it hit me so hard.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: at home covid test on March 6, 2023 - tested positive Went to walk in clinic and took another Covid test on March 10, 2023 - tested positive
Aktuelle Erkrankungen: none
Vorgeschichte: High blood pressure controlled with medicine High cholesterol controlled with medicine High pressure in eyes controlled with medicine
Andere Medikamente: Bupropion HCL XL 300 mg Lisinopril 40 mg tablet Estradiol 2 mg tablet Latanoprost 0.005% eye drops Atorvastatin 20 mg tablet Multi vitamin Calcium twice daily 800mg/800 vitamin D3 Glucosamine chondroitin 1500/1200 stool softener zinc 50 mg
Allergien: none
Vorherige Impfungen: -

VAERS 2565655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 23.01.2023
Impfdatum: 21.01.2021
Beginn: 28.04.2021
Tage bis Beginn: 97,0
Dosis: 2
Route/Site: IM / AR

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

Blood glucose increased Blood test normal Cardiac monitoring abnormal Chest X-ray normal Heart rate increased Implantable cardiac monitor insertion Stress echocardiogram normal Supraventricular tachycardia Tachycardia Ventricular tachycardia

Symptomtext

I went to donate blood and my heart rate was at 220 beats per minute. We waited it out and I eventually ended up donating blood. I followed up with my physician on 04/28/2021. She referred me to a cardiologist. I saw the cardiologist on 06/16/2021. They set me up with an event recorder, which I wore for 28 days. I went for a stress echocardiogram which was negative. The event recorder showed tachycardia, SCT, and ventricular tachycardia. They advised that I repeat the event recorder in another year, which indicated that I was still having episodes of SCT and ventricular tachycardia. I had a loop recorder implanted for further monitoring. During this time, they also noticed that my blood sugar was elevated, and I am now taking a medication to lower that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: -
Labordaten: APR2021 blood work, nothing abnormal found; 23JUN2021 Stress Echocardiogram, no vascular disease noted; Chest X-ray, nothing abnormal found
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: EMGALITY; IMITREX; TYLENOL P.M.
Allergien: ROBAXIN; RITALIN; CIPRO; MACROBID; flu vaccine
Vorherige Impfungen: Date unknown, Flu vaccine, generalized muscle weakness.

VAERS 2604527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 10.01.2023
Impfdatum: 27.04.2022
Beginn: 19.05.2022
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / RA

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

Acute kidney injury Anaemia Asthenia COVID-19 Condition aggravated Cough Failure to thrive Fall Hypophagia Malaise Parkinson's disease SARS-CoV-2 test positive Tremor

Symptomtext

Narrative: 79 y/o male w/ PMH significant for HTN, Anemia, PAD, HLD, BPH, T2DM, CKD, PAF, seizures and recent diagnosis of Parkinson's Disease. Pt presented to ED on 05/19/22 w/ decreased oral intake, weakness, cough and multiple falls. Pt admitted to hospital for failure to thrive, COVID 19 positive, anemia and AKI. Failure to thrive with increasing tremors in association with worsening Parkinson's Disease and possibly secondary to COVID. Pt with mild symptoms of COVID during hospital stay, mild cough. Pt received supplements of zinc and MVI during hospital stay. Pt improved and discharged to home on 5/31.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 05/19/22- COVID 19 positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1424317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 01.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: OT / LA

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

Blood creatine phosphokinase increased Burning sensation Condition aggravated Electromyogram normal Muscle contractions involuntary Loss of personal independence in daily activities Neuropathy peripheral Rash vesicular Paraesthesia

Symptomtext

unable to wear shoes and has difficulty wearing pants; I've had neuropathy since 1994, but it was made much worse by the vaccine.; I've had neuropathy since 1994, but it was made much worse by the vaccine.; Lower Extremity Vesiculation Increased; Lower Extremity Vesiculation Increased; 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 51-year-old male patient received BNT162b2 (BNT162B2), on 01Feb2021 at 14:30 as dose 2, single (Lot number: EL3247) at the age of 51 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Neuropathy", start date: 1994 (ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (dose 1, Time: 2:30pm, Anatomical Site of injection: Left Arm (right below shoulder), Route of Administration: intramuscular, Batch/Lot number: EL0142, No reaction after first dose.), administration date: 11Jan2021, when the patient was 51-year-old, for COVID-19 Immunization. The following information was reported: NEUROPATHY PERIPHERAL (disability, medically significant), CONDITION AGGRAVATED (disability) all with onset 22Feb2021, outcome "not recovered" and all described as "I've had neuropathy since 1994, but it was made much worse by the vaccine."; RASH VESICULAR (non-serious), CONDITION AGGRAVATED (non-serious) all with onset 22Feb2021, outcome "not recovered" and all described as "Lower Extremity Vesiculation Increased"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "not recovered", described as "unable to wear shoes and has difficulty wearing pants". The events "i've had neuropathy since 1994, but it was made much worse by the vaccine.", "lower extremity vesiculation increased" and "unable to wear shoes and has difficulty wearing pants" required physician office visit. Therapeutic measures were taken as a result of neuropathy peripheral, condition aggravated, rash vesicular, condition aggravated, loss of personal independence in daily activities. Patient received your COVID vaccine first dose in Jan2021 and second dose was 01Feb2021. Route of Administration: intramuscular right below shoulder. No reaction after first dose. 3 weeks after the second dose, his neuropathy got markedly worse, he woke up and his neuropathy was worse. He thought it was a flare up, but it has gotten so much worse. Neuropathy Worsened: Ebbs and flows, progressed to where it was worse. Virtually disabled and has to work from home. Has erythema in his feet, they are swollen and red. The muscle vesiculation was increased and markedly worse. Dramatic increase in pain and burning. Hot and swollen feet. Increase in visible vesiculation in lower extremities. Wants to know, he presumes Pfizer is aware, but have there been people complaining of neurological complications? Treatment: Neurologist tried on different medications, high dose IV steroids to no effect nothing has worked. He had neuropathy since 1994, but it was made much worse by the vaccine. While anecdotal, there are thousands of others like himself who either developed neuropathy from the vaccine or had a pre-existing neuropathy made markedly worse by the vaccine. Patient was asking was Pfizer aware of this? If so, what are you doing about them? Why are there no warnings about this potential adverse event in your advertising? He was nearly disabled now due to your vaccine." He "tolerated the first dose fine, but three weeks from his second dose (01Feb2021) on 22Feb2021, awoke to a massive increase in neuropathic burning pain." He was evaluated by a neurologist. States there have been times over the past 18 months where "it seems to get a little better for periods of time, but it was now markedly worse than pre-COVID." He was unable to wear shoes and has difficulty wearing pants. "It's a shame that his entire life he have gotten all his vaccines, including this one, in order to do his good duty as a citizen, and now this vaccine has irreparably damaged his health. He has been reading about "an inordinate number of people that claim they either experienced new or worsened neuropathy after vaccination with Comirnaty. Does have preexisting vesicular peripheral neuropathy diagnosis since 1994 but the administration of the COVID vaccine made his symptoms markedly worse. May have to potential retire early because he has so much pain. Vaccination Facility Type: Senior Living Facility. Prior Vaccinations (within 4 weeks): None. Family Medical History Relevant to Adverse Events (AEs): Potentially one of his children has similar symptoms genetically.

Weitere VAERSDATA-Felder

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

VAERS 1424317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 01.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: SYR / AR

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

Blood creatine phosphokinase increased Burning sensation Condition aggravated Electromyogram normal Muscle contractions involuntary Loss of personal independence in daily activities Neuropathy peripheral Rash vesicular Paraesthesia

Symptomtext

unable to wear shoes and has difficulty wearing pants; I've had neuropathy since 1994, but it was made much worse by the vaccine.; I've had neuropathy since 1994, but it was made much worse by the vaccine.; Lower Extremity Vesiculation Increased; Lower Extremity Vesiculation Increased; 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 51-year-old male patient received BNT162b2 (BNT162B2), on 01Feb2021 at 14:30 as dose 2, single (Lot number: EL3247) at the age of 51 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Neuropathy", start date: 1994 (ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (dose 1, Time: 2:30pm, Anatomical Site of injection: Left Arm (right below shoulder), Route of Administration: intramuscular, Batch/Lot number: EL0142, No reaction after first dose.), administration date: 11Jan2021, when the patient was 51-year-old, for COVID-19 Immunization. The following information was reported: NEUROPATHY PERIPHERAL (disability, medically significant), CONDITION AGGRAVATED (disability) all with onset 22Feb2021, outcome "not recovered" and all described as "I've had neuropathy since 1994, but it was made much worse by the vaccine."; RASH VESICULAR (non-serious), CONDITION AGGRAVATED (non-serious) all with onset 22Feb2021, outcome "not recovered" and all described as "Lower Extremity Vesiculation Increased"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "not recovered", described as "unable to wear shoes and has difficulty wearing pants". The events "i've had neuropathy since 1994, but it was made much worse by the vaccine.", "lower extremity vesiculation increased" and "unable to wear shoes and has difficulty wearing pants" required physician office visit. Therapeutic measures were taken as a result of neuropathy peripheral, condition aggravated, rash vesicular, condition aggravated, loss of personal independence in daily activities. Patient received your COVID vaccine first dose in Jan2021 and second dose was 01Feb2021. Route of Administration: intramuscular right below shoulder. No reaction after first dose. 3 weeks after the second dose, his neuropathy got markedly worse, he woke up and his neuropathy was worse. He thought it was a flare up, but it has gotten so much worse. Neuropathy Worsened: Ebbs and flows, progressed to where it was worse. Virtually disabled and has to work from home. Has erythema in his feet, they are swollen and red. The muscle vesiculation was increased and markedly worse. Dramatic increase in pain and burning. Hot and swollen feet. Increase in visible vesiculation in lower extremities. Wants to know, he presumes Pfizer is aware, but have there been people complaining of neurological complications? Treatment: Neurologist tried on different medications, high dose IV steroids to no effect nothing has worked. He had neuropathy since 1994, but it was made much worse by the vaccine. While anecdotal, there are thousands of others like himself who either developed neuropathy from the vaccine or had a pre-existing neuropathy made markedly worse by the vaccine. Patient was asking was Pfizer aware of this? If so, what are you doing about them? Why are there no warnings about this potential adverse event in your advertising? He was nearly disabled now due to your vaccine." He "tolerated the first dose fine, but three weeks from his second dose (01Feb2021) on 22Feb2021, awoke to a massive increase in neuropathic burning pain." He was evaluated by a neurologist. States there have been times over the past 18 months where "it seems to get a little better for periods of time, but it was now markedly worse than pre-COVID." He was unable to wear shoes and has difficulty wearing pants. "It's a shame that his entire life he have gotten all his vaccines, including this one, in order to do his good duty as a citizen, and now this vaccine has irreparably damaged his health. He has been reading about "an inordinate number of people that claim they either experienced new or worsened neuropathy after vaccination with Comirnaty. Does have preexisting vesicular peripheral neuropathy diagnosis since 1994 but the administration of the COVID vaccine made his symptoms markedly worse. May have to potential retire early because he has so much pain. Vaccination Facility Type: Senior Living Facility. Prior Vaccinations (within 4 weeks): None. Family Medical History Relevant to Adverse Events (AEs): Potentially one of his children has similar symptoms genetically.

Weitere VAERSDATA-Felder

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

VAERS 2493803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge EL3247

moderat

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: -
Beginn: 09.06.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury COVID-19 pneumonia Hypotension Hypoxia Respiratory depression

Symptomtext

Narrative: The patient received three doses of Pfizer COVID 19 in Jan/Feb/Sep 2021. The patient presented to the ED with hypoxemia and hypotension on 9 Jun 2022. The patient was admitted with covid 19 pneumonia, Acute kidney injury, and respiratory depression. The patient was treated with steroids, inhalers, antibiotics, and remdesivir. The patient was discharged on oxygen on 18 June 2022. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2485485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

moderat

Staat: OK
Alter: 63,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 13.01.2021
Beginn: 16.11.2021
Tage bis Beginn: 307,0
Dosis: 1
Route/Site: IM / AR

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

Borrelia test Condition aggravated Lyme disease

Symptomtext

symptoms of lyme disease after taking the covid vaccines. Not sure if it was from the vaccines but had been in remission for 6 years.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Igenex Lyme Testing
Aktuelle Erkrankungen: Lyme Disease in remission from 2014 to 2021. Symptoms started again after Covid Vaccines????? was it due to vaccines???
Vorgeschichte: Lyme Disease
Andere Medikamente: malarone, azithomicin, probiotics, enlyte, multiple vitamin, ,
Allergien: none
Vorherige Impfungen: -

VAERS 2481810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AK
Alter: 35,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 19.01.2021
Beginn: 22.11.2021
Tage bis Beginn: 307,0
Dosis: 2
Route/Site: IM / UN

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

Angiogram Blood pressure increased Cardiac telemetry Chest pain Dyspnoea Echocardiogram Electrocardiogram Full blood count Heart rate increased Magnetic resonance imaging heart Metabolic function test Stress cardiomyopathy Troponin increased

Symptomtext

Chest pain, SOB, increase HR, increased BP, increased troponin levels. Takotsuba Cardiomyopathy confirmed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: 11/22/21: EKG x2, Troponin, CBC, CMP 11/22/21: EKG, Angiogram, Cardiac MRI, CBC, CMP, Telemetry, Echocardiogram
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Norethindrone
Allergien: None
Vorherige Impfungen: -

VAERS 2450140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 29.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Heart rate increased Investigation Palpitations Tachycardia

Symptomtext

Palpitations; Tachycardia; Increased heart rate; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 53-year-old female patient received BNT162b2 (BNT162B2), on 29Jan2021 as dose 2, single (Lot number: EL3247), in left deltoid 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. The following information was reported: HEART RATE INCREASED (non-serious) with onset 2021, outcome "unknown", described as "Increased heart rate"; PALPITATIONS (non-serious) with onset 2021, outcome "unknown"; TACHYCARDIA (non-serious) with onset 2021, outcome "unknown". The events "palpitations", "tachycardia" and "increased heart rate" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. The action taken for BNT162b2 was unknown. Therapeutic measures were not taken as a result of palpitations, tachycardia, heart rate increased. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Increased heart rate; Result Unstructured Data: Test Result:increased
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2431322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 77,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 20.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Abnormal loss of weight Blood test Computerised tomogram thorax Discomfort Dyspnoea Ear pain Head discomfort Hypoaesthesia Paraesthesia Swelling Tinnitus Tremor Ultrasound abdomen Vision blurred

Symptomtext

Right ear pain, tinnitus, head pressure tremors, paresthesias , numbness on right side of body from toes to hands.Abdomial pain, waves of constriction and swelling across diaphragm. periods of shortness of breath, unintended wt loss periodic blurred vision PCP visits 2/23/21, 6/21/21 and others rec short steroid course, Neurology, MD rec steroids and Gabapentin MD ENT Ophthalmologist

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood tests 3/3/21,Abdominal Ultra sound3/17/21, CT of lung
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, high blood pressure, high cholesterol, fleeting nerve pain, osteoporosis
Andere Medikamente: Crestor, Avapro, vit D, symbocort
Allergien: aspirin, nsaids amoxicillin,penicillin,sulfur
Vorherige Impfungen: -

VAERS 2431103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 21.01.2021
Beginn: 21.07.2022
Tage bis Beginn: 546,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: POSITIVE COVID TEST 7/28/22
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Malignant neoplasm of right lung
Andere Medikamente: amLODIPine (NORVASC) 5 mg tablet clobetasoL (TEMOVATE) 0.05 % cream Dupixent Syringe 300 mg/2 mL injection ibuprofen (ADVIL,MOTRIN) 600 mg tablet lisinopriL (PRINIVIL,ZESTRIL) 40 mg tablet metoprolol succinate (TOPROL-XL) 100 mg 24 hr
Allergien: Cat Dander
Vorherige Impfungen: -

VAERS 2427593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 93,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 08.04.2022
Beginn: 08.08.2022
Tage bis Beginn: 122,0
Dosis: 2
Route/Site: - / -

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

Angiogram pulmonary normal Asthenia COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Patient up to date on COVID vaccines who admitted with complications r/t COVID and COVID detected PCR. Provider d/c note: "94 F with PMH HLD, Anemia, HTN, OA, Mild Cognitive impairment with memory loss, Chronic Insomnia, Depression who is presenting to the ED for evaluation of worsening weakness, cough, and SOB. Patient is on chronic O2 nasal cannula at home. Was found outpatient to be COVID positive and started on Paxlovid Initial workup included a CTA that was negative for PE. Patient was found to be COVID positive. Patient was started on Decadron as well as remdesivir and monitored overnight. Patient maintained on her home O2 nasal cannula and her strength improved. Patient was discharged home to resume Paxlovid therapy and follow-up with primary care provider for continued care."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: COVID detected PCR on 08/08/22
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic obstructive pulmonary disease with acute exacerbation (*) HYPERLIPIDEMIA, MIXED (272.2) HYPERTENSION, BENIGN ESSENTIAL (401.1) Macular degeneration of both eyes Anxiety Osteoarthritis of right hip Mild cognitive impairment with memory loss Iron deficiency anemia Panlobular emphysema (*) Depression, major, in remission (*) Aortic valve stenosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 12.01.2021
Beginn: 26.04.2022
Tage bis Beginn: 469,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Chest pain Cough Dyspnoea Pneumothorax Respiratory failure SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received three doses of Pfizer COVID 19 Vaccine. The patient tested positive for COVID 19 on 26 April 2022. The patient presented to the ED with chest pain, shortness of breath, and cough. The patient was admitted to the hospital with respiratory failure with hypoxia, and chest pain. The patient was treated with IV antibiotics, steroids, and bronchodilators. The patient was discharged from the hospital on 27 April 2022 and then re-admitted to another hospital on 7 May 2022 with continued respiratory failure and pneumothorax. The patient was still in the hospital as of 17 May 2022. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2435983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 94,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 12.01.2021
Beginn: 23.04.2022
Tage bis Beginn: 466,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury COVID-19 COVID-19 pneumonia Cough Decreased appetite Hyperglycaemia Malaise SARS-CoV-2 test positive Wheezing

Symptomtext

Narrative: Patient received three doses of Pfizer COVID 19 Vaccine. The patient tested positive for COVID 19 on 23 April 2022. The patient presented to the ED with cough, malaise, wheezing and decreased appetite. The patient was admitted to the hospital with acute kidney injury, covid pneumonia, and hyperglycemia. The patient was treated with supportive care, antitussives, and bronchodilators. The patient was discharged on 2 May 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2308310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 91,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 12.01.2021
Beginn: 10.03.2022
Tage bis Beginn: 422,0
Dosis: 2
Route/Site: IM / UN

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

Anxiety Asymptomatic COVID-19 Blood pressure increased COVID-19 Fall Headache Pain Pain in extremity Paraesthesia Rhinalgia SARS-CoV-2 test positive

Symptomtext

Pt brought to the emergency department by EMS status post fall 3/8. Pt is on Pradaxa and complains of pain in her forehead and nose. Reports tingling sensation in her arms. No chest pain. No abdominal pain. On 3/9 pt having pain in right arm, but has improved with pain medications. Pt is asymptomatic but has tested positive for COVID 3/10, patient A&Ox4 from the 3rd floor with no complaints of pain and no signs of respiratory distress. On 3/11 pt with elevated blood pressure. Patient was anxious and complaining of generalized pain. Xanax and Norco given. Pt discharged 3/12 in stable condition. No c/o any pain or shortness of breath. Iv removed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: 5,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Syncope
Andere Medikamente: amLODIPine (NORVASC) 5 MG PO Tab, amLODIPine (NORVASC) 5 MG PO Tab atorvastatin (LIPITOR) 10 MG PO Tab busPIRone (BUSPAR) 5 MG PO Tab busPIRone (BUSPAR) 5 MG PO Tab Cyanocobalamin 1000 MCG PO Tab Ferrous Sulfate 28 MG PO Tab losartan (COZAA
Allergien: None
Vorherige Impfungen: -

VAERS 2306897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

moderat

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 31.01.2021
Beginn: 06.03.2021
Tage bis Beginn: 34,0
Dosis: 2
Route/Site: SYR / AR

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

Asthenia Blood pressure increased Blood test Cardiac stress test Computerised tomogram Dizziness Echocardiogram Electrocardiogram ambulatory Fatigue Heart rate increased Impaired work ability Laboratory test Magnetic resonance imaging Oesophagogastroduodenoscopy Postural orthostatic tachycardia syndrome Ultrasound scan

Symptomtext

Fast Heart beat- Light Headed,Fatique and weakness, extreme Blood pressure Spikes Unable to work 1 year now Still in treatment- over 20 ER Visits 3 Hospital Admissions Cardiologist test and exams Neurologist- Test and exams Endocrinologist Test and Exams Waiting for referral approval for high level of care Hospital- End Results- ( POTS)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Postural orthostatic tachycardia syndrome
Hospital-Tage: 5,0
Labordaten: Stress Test- Holtier Monitors Echos Cat Scans MRI Ultrasounds Blood Test EGD
Aktuelle Erkrankungen: NONE
Vorgeschichte: Diabetic
Andere Medikamente: Humalog Insulin
Allergien: PHENOGREN
Vorherige Impfungen: -

VAERS 2328539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 13.01.2021
Beginn: 20.01.2022
Tage bis Beginn: 372,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Cough Dyspnoea Respiratory failure SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received three doses of Pfizer COVID 19 Vaccine. The patient tested positive for COVID 19 on 20 Jan 2022. The patient presented to the ED with shortness of breath, cough, and wad admitted in another hospital for COVID pneumonia. The patient was treated with remdesivir and dexamethasone. The patient was discharged, but the patient was readmitted to the hospital on 6 February 2022 with cough and shortness of breath. The patient was admitted with COVID pneumonia and respiratory failure. The patient was treated with antibiotics. The patient was discharged 10 Feb 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2216032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Back pain Condition aggravated Decreased appetite Headache Heart rate increased Mobility decreased Nausea Pain Vaccine positive rechallenge

Symptomtext

I suffer from an unknown abdominal pain but since the vaccine my symptoms have worsening. Within 12-14 hours after the vaccine I had severe body aches, headaches that was all over without any concentrated pain locations and backaches. I also experience nausea which caused me to not have an appetite and I only could drink cold drinks. I was experiencing an increased heart rate of over 100 BPM which is not normal for me. The next morning I contacted my doctor the next morning to let her know about my symptoms. She advised it could be a side effect of the vaccine. She advised me to take Tylenol for pain and Zofran for my nausea. After 3 days I was okay. I stayed home for almost a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown Abdominal Pain; Migraines; Gout; Tendinitis of left foot
Andere Medikamente: Namenda 10mg twice daily; Protonix 20mg once daily; Probiotic Supplement 250mg once daily; Multivitamins once daily.
Allergien: Ketorolac; Morphine Sulfate; Vicodin; Docusate Sodium; Latex
Vorherige Impfungen: Same symptoms with 1st dose of Pfizer 01/30/2021.

VAERS 2209310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

moderat

Staat: IL
Alter: 83,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 01.05.1938
Beginn: 27.03.2022
Tage bis Beginn: 30.646,0
Dosis: 1
Route/Site: SYR / -

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

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

Symptomtext

Patient admitted to hospital 3/28/22 with SOB and cough. Some diarrhea is reported but no chest pain, vomiting, fever or chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: SARS COV2 COVID19 NAAT positive 3/27/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2180077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CO
Alter: 84,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 08.10.2021
Beginn: 11.01.2022
Tage bis Beginn: 95,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dizziness Fall Fluid intake reduced Hypophagia Pneumonia

Symptomtext

Patient fully vaccinated and boosted with Pfizer on 2/4/21, 2/25/21, and 10/8/21. Previously diagnosed with COVID on 12/30/21. Patient presented to ED with a fall on 1/13/22. Previously was seen in the ED on 1/11/22 for pneumonia, however sent home on doxycycline. Patient was not eating or drinking, felt light headed, and fell. Patient admitted on 1/13/22 and discharged 1/16/22.

Weitere VAERSDATA-Felder

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

VAERS 1574102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 39,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 19.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / -

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

Blood test Chest X-ray Electrocardiogram Electrolyte imbalance Feeling abnormal Heart rate irregular SARS-CoV-2 antibody test Heart rate increased Hypertension

Symptomtext

Developed erratic heart rate and irregular heart rate; Developed severe electrolyte imbalance; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Feb2021 09:00 (Lot number: EL9263) at the age of 39 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Penicillin. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Batch/lot number: EL3247, Administration time: 09:00 AM.), administration date: 29Jan2021, when the patient was 39 years old, for Covid-19 immunisation. The following information was reported: HEART RATE IRREGULAR (non-serious) with onset 20Feb2021 18:00, outcome "recovered" (2021), described as "Developed erratic heart rate and irregular heart rate"; ELECTROLYTE IMBALANCE (non-serious) with onset 20Feb2021 18:00, outcome "recovered" (2021), described as "Developed severe electrolyte imbalance". The events "developed erratic heart rate and irregular heart rate" and "developed severe electrolyte imbalance" 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 heart rate irregular, electrolyte imbalance. Additional information: Patient developed erratic heart rate and irregular heart rate with 48 hours. No history of rate problems. Developed severe electrolyte imbalance within 48 hours of vaccine. Patient evaluated by Emergency Room staff at hospital, primary care physician and cardiologist. Patient received numerous medications for adverse events. Patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was diagnosed with COVID-19 and since the vaccination, patient was tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210313; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AL
Alter: 58,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 22.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Gait disturbance Mobility decreased Muscle spasms X-ray

Symptomtext

I started having severe muscle spasms in my lower back pain to the point where I was unable to get off the couch. I could hardly walk. This lasted for about a month getting better on a week by week basis, I went to the chiropractor and he did not see anything wrong. The chiropractic still did an adjustment and that helped. It took about a full month to get better. I also had an xray at a different providers office to see if my hip was causing the issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Trazadone, Estradiol, Progesterone
Allergien: Celebrex
Vorherige Impfungen: -

VAERS 2162606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 66,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 19.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

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

Blood test Cardiac monitoring abnormal Chest scan Chills Decreased appetite Echocardiogram Electrocardiogram Extrasystoles Fatigue Headache Heart rate increased Lung disorder Pain in extremity Pneumonia Pulmonary function test Pyrexia SARS-CoV-2 test negative Supraventricular tachycardia

Symptomtext

Extreme fatigue, sore arm, fever, chills, headache, lack of appetite. Took Tylenol. Everything went away except for the fatigue. Fatigue continued through the second dose, and got worse during the following months. I had a fever and a rapid heartbeat event in April 2021. Tested negative for COVID. Went to the ER in May thinking I was having a heart attack. They sent me home saying it was pneumonia. Fatigue got worse. I asked to be referred to a cardiologist in June. Dr., cardiologist, diagnosed me with SVT (supra ventricular tachycardia) in September. I later found out from other family members that my mother (deceased in 2017) was also diagnosed with SVT two years before she died. I didn't think the vaccine was responsible, but V-safe wanted me to report it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: May 17-18, 2021: Chest scan, EKG, blood work, done at the ER in May. Lungs were "hazy", so antibiotics given for pneumonia. July 2-July 4, 2021: Heart monitor worn for 48 hours. Showed premature heartbeat. SVT diagnosed July 21, 2021: Echocardiogram of the heart. October 26, 2021: Pulmonary testing
Aktuelle Erkrankungen: None
Vorgeschichte: Slightly high blood pressure
Andere Medikamente: Lisinopril--5mg
Allergien: None
Vorherige Impfungen: -

VAERS 2118717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 29.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Fatigue Joint swelling Lymphadenopathy Pain Rash SARS-CoV-2 test Tremor

Symptomtext

Uncontrol able shaking all over; Tired; rash on arms & legs; swollen lymph node under left arm; swollen joints and pain x 2 weeks; swollen joints and pain x 2 weeks; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 58 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 29Jan2021 08:45 (Lot number: EL3247) at the age of 57 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "hypothyroid" (unspecified if ongoing); "migraines" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: TREMOR (non-serious) with onset Jan2021, outcome "recovered" (2021), described as "Uncontrol able shaking all over"; FATIGUE (non-serious) with onset Jan2021, outcome "recovered" (2021), described as "Tired"; RASH (non-serious) with onset Jan2021, outcome "recovered" (2021), described as "rash on arms & legs"; LYMPHADENOPATHY (non-serious) with onset Jan2021, outcome "recovered" (2021), described as "swollen lymph node under left arm"; JOINT SWELLING (non-serious), PAIN (non-serious) all with onset Jan2021, outcome "recovered" (2021) and all described as "swollen joints and pain x 2 weeks". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of tremor, fatigue, rash, lymphadenopathy, joint swelling, pain. Additional information: patient had no known allergies. Adverse events (Uncontrol able shaking all over, Tired, rash on arms & legs, swollen lymph node under left arm, swollen joints and pain x 2 weeks) start time: 09:30 PM. Facility where the most recent COVID-19 vaccine administered was Hospital. the patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient received other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since vaccination the patient tested for COVID-19. Patient had also received second dose on 09Feb2021 at 09:00, lot number:EL9267 via Intramuscular route in the left arm. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20210916; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism; Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2116383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: FL
Alter: 93,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 01.02.2021
Beginn: 12.02.2022
Tage bis Beginn: 376,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Chest X-ray abnormal Dyspnoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 01/11/2021. 94 y/o with PMHx of DM type 2, HTN, HLD, CAD s/p CABGx4, GERD, BPH with LUTS presents to ED via EMS for c/o SOB and generalized weakness. EMS found pt with O2 sats in the 80's, placed on 4L NC. CXR with possible atypical viral PNA. Afebrile. Pt started on Steroids and then Remdesivir added.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected on 02/12/2022
Aktuelle Erkrankungen: -
Vorgeschichte: DM2,HLD, HTN, CAD/CABG, GERD,BPH,OA
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2111083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 15.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea exertional Electrocardiogram Gait disturbance Laboratory test normal Oxygen saturation decreased Palpitations Sinus rhythm

Symptomtext

1-2 weeks after receiving my second dose of Pfizer, I started having heart palpitations, and dyspnea on exertion. I didnt think much of it at first, but it continues for over a month and it became difficult to climb stairs. I got the first available doctors appointment at the end of March, and the doctor noted that my saturations were dropping as we walked around the clinic. The symptoms continued for another month, but resolved around May. I was in good health previously. I was referred to pulmonology and cardiology, but wasnt able to get an appointment with cardiology given scheduling issues. At the time, the association between vaccine side effects like myocarditis weren't well known, so my PCP was more concerned with asthma, though as a doctor myself, I keep articulating that I think its heart related and having been so close to when I received the vaccine, there was a causation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: An ekg was obtained which showed sinus rhythm, no cardiac enzymes obtained, all other basic labs normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control
Allergien: Cephalosporins, vicodin
Vorherige Impfungen: -

VAERS 2090302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 28,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chills Headache Tremor Vaccination site pain

Symptomtext

Injection site soreness (mild); headache (severe); chills/shakes (moderate); chills/shakes (moderate); This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 28 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 25Mar2021 09:00 (Lot number: EL3247) at the age of 28 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Bipolar II" (unspecified if ongoing). Concomitant medication(s) included: LAMOTRIGINE. Vaccination history included: Bnt162b2 (lot number=EL3247,, lot unknown=False,, administration time=10:00 AM,, vaccine location=Left arm,, dose number=1), administration date: 03Mar2021, when the patient was 28 years old, for COVID-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 25Mar2021 18:00, outcome "recovering", described as "Injection site soreness (mild)"; HEADACHE (non-serious) with onset 25Mar2021 18:00, outcome "recovering", described as "headache (severe)"; CHILLS (non-serious), TREMOR (non-serious) all with onset 25Mar2021 18:00, outcome "recovering" and all described as "chills/shakes (moderate)". Therapeutic measures were not taken as a result of vaccination site pain, headache, chills, tremor. Additional information: Facility where the most recent COVID-19 vaccine was administered was workplace clinic. The patient didnot receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not been tested for COVID-19. Allergies to medications, food, or other products were none. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bipolar II disorder
Andere Medikamente: LAMOTRIGINE
Allergien: -
Vorherige Impfungen: -

VAERS 2215744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 05.02.2021
Beginn: 31.07.2021
Tage bis Beginn: 176,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Leukopenia Pneumonia bacterial SARS-CoV-2 test positive

Symptomtext

Narrative: Patient hospitalized 7/31/21 after completion of COVID-19 vaccination series in Feb 2021. Did not need steroids or oxygen for COVID but did develop bacterial pneumonia and leukopenia which was treated during stay. Discharged to rehab facility 8/10/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia bacterial
Hospital-Tage: -
Labordaten: 7/31/21 Test positive for COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 72,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 26.01.2021
Beginn: 15.06.2021
Tage bis Beginn: 140,0
Dosis: 2
Route/Site: - / -

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

Anticoagulant therapy Blood creatinine increased Dyspnoea Fibrin D dimer increased Full blood count normal Glomerular filtration rate normal Immobile Ventilation/perfusion scan abnormal

Symptomtext

covid vax 2 given 2/16/21, and #3 ? mfg or lot # given 8/21/21 Sudden onset shortness of breath, called EMS, D-dimer was noted to be elevated at 32,072 on 15 June 2021 and a VQ scan showed high risk for bilateral pulmonary emboli, he was started on a heparin drip and transitioned to Eliquis, aspirin was continued that he was on prior to admission, and symptoms of shortness of breath continue to improve on anticoagulation He has not had Covid but has had his Covid vaccines completed 16 February 2021, CBC normal, creatinine 1.37, GFR greater than 60, no travel or hormone use or recent surgeries though he is immobile on a regular basis, weight is just over 120 kg December 2021 will transition to Eliquis 2.5 mg twice daily plus baby aspirin

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: see above
Aktuelle Erkrankungen: n/a
Vorgeschichte: h/o stroke and kidney transplant
Andere Medikamente: n/a
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2074595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 87,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 06.02.2021
Beginn: 28.01.2022
Tage bis Beginn: 356,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Confusional state Hypoxia Lung infiltration Mental status changes SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID . Pt is a 88 yo F brought to ED on 1/27 for hypoxia and AMS. Pt had tested COVID+ at prior to admission, date unknown, and again tested + in ED on 1/28. Pt vaccinated on 1/16/21 and 2/6/21, pt did not receive a booster. Pt confused and unable to endorse other symptoms besides the hypoxia and AMS noted by staff. ED workup showed Chest XR with right lung infiltrates, started on IV abx and steroids. Admitted for covid pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: COVID + ED test on 1/28
Aktuelle Erkrankungen: -
Vorgeschichte: Dementia, CHF, recurrent UTI, hypertension, GERD, CVA
Andere Medikamente: -
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2071983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LL

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

Chest pain Electrocardiogram

Symptomtext

Prior Covid patient prior to getting the vaccination Dose 1, anaphylaxis situation, vomiting for six hours, off work for few days; then recommended to have second dose by workplace. Three days after the Dose 2, chest pains, called primary care right away advised to wait, then she made office appointment appointment was not able to be seen until one month later and scheduled currently still waiting for ECHOcardiogram due to community COVID this delayed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Observation and EKG was complete at Dr. visit.
Aktuelle Erkrankungen: No
Vorgeschichte: IBSD
Andere Medikamente: Lomotil; Pepcid; Omeprazole; Bentyl; Levsin; Zofran
Allergien: Hydrochlorothiazide; Gadolinium; Latex; Eggs; Pet Allergies; Cat Dander; Lactose
Vorherige Impfungen: Pfizer-BioNTech Dose 1 vomiting; Special Flu vac, egg allergy.

VAERS 2065575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

moderat

Staat: MD
Alter: 48,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 09.10.2021
Beginn: 06.12.2021
Tage bis Beginn: 58,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dizziness Dyspnoea Headache Pain SARS-CoV-2 test positive

Symptomtext

Headache short breath dizzy body aches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Positive Covid test
Aktuelle Erkrankungen: None
Vorgeschichte: PTSD hypothyroidism depression anxiety allergies
Andere Medikamente: Claritin, synthesis, topamax, magnesium, potassium, calcium, vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2059527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 55,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 12.02.2021
Beginn: 23.01.2022
Tage bis Beginn: 345,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

respiratory difficulty

Weitere VAERSDATA-Felder

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

VAERS 2057111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 70,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 12.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Blood iron decreased Blood pressure measurement Condition aggravated Dizziness Fall Investigation Tardive dyskinesia

Symptomtext

dizziness; increased dizziness; falling; dyskinesia; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. A 70 year-old male patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 12Feb2021 08:30 (Lot number: EL3247) at the age of 70 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Parkinson's disease", start date: 2017 (ongoing), notes: Verbatim: Parkinson's disease. Concomitant medication(s) included: REGLAN [METOCLOPRAMIDE HYDROCHLORIDE] taken for parkinson's disease, start date: 2017. Vaccination history included: Bnt162b2 (Dose: 1, lot: EL3248, expiry date Apr2021), administration date: 22Jan2021, when the patient was 70 years old, for Covid-19 Immunization. The following information was reported: CONDITION AGGRAVATED (disability) with onset 2021, outcome "recovered" (2021), described as "increased dizziness"; FALL (disability) with onset 2021, outcome "recovered" (2021), described as "falling";TARDIVE DYSKINESIA (disability) with onset 2021, outcome "recovered" (2021), described as "dyskinesia"; DIZZINESS (non-serious) with onset Feb2021, outcome "recovered" (2021), described as "dizziness". The events "increased dizziness", "falling", "tardive dyskinesia" and "dizziness" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood iron decreased: very low; blood pressure measurement: very very low; investigation: normal, notes: More information available (Y/N): No; fine. Therapeutic measures were taken as a result of condition aggravated, fall, dyskinesia, dizziness. Clinical course: Prior Vaccinations (within 4 weeks): None. Relevant Tests: cardiac workup normal. States the tardive dyskinesia was diagnosed and was really increased and is terrible since the patient had the Pfizer covid vaccine 2nd and 3rd doses; states the tardive dyskinesia is ongoing and now is the same; despite further attempts at clarification, information captured as stated by the caller. Caller states for seriousness criteria, she would say it is disabling and the patient also went to the hospital a few times and clarified to state it was not an overnight admission to the hospital but emergency room visits. Caller states the cardiac workup and he saw the neurologists and had everything done trying to figure out why he was getting dizzy and falling and they adjusted his medications and then said he seems to have resolved and then the symptoms began again with the Pfizer booster vaccine and that is why she herself is not getting the vaccine; states the patient had the booster and then all this started up all over again. Caller states for the patient's medications that were adjusted, it was his Rytary dose and the patient puts his medicine in and the dosage is 36.25mg /145mg which he takes every 3-4 hours and he began taking it for a while prior to the vaccine and takes it for Parkinsons; states the Rytary is carviopa and levodopa and the lot is 30000054, expiry date Mar2024, states she is looking for the manufacturer and does not see the manufacturer and it is a white bottle and label and states it does not have the NDC but has the GTIN; states the Rytary label has his name and Rx number and there is nothing underneath when she peels the label away; instructed not to peel the label and states the manufacturer is (withheld) and the patient takes Rytary up to five times per day; states the Rytary is the only medication that was adjusted. Caller states the patient also takes 1mg once per day of Razaglan and has been taking that for a long time since he was diagnosed with Parkinson's disease in 2017. Caller states for the cardiac workup and everything was normal and the only thing the patient did was have his iron level was very low and he had the iron infusions and everything else was fine and the holter monitor was fine and the other workup was fine and he had low very very low blood pressure and that blood pressure is not really ongoing and his pressure came up. Caller states she has no name, dosage or lot number to provide for the patient's Iron infusion. Reporter assesses all the events related to vaccine. No follow-up attempts are possible. No further information is expected.; Sender's Comments: There is not a reasonable possibility that reported event of Tardive dyskinesia is related to BNT162B2, this events are most likely intercurrent medical conditions of and concomitant medication for this elderly patient with underlying Parkinsonism. However a possible contributory role of the suspect vaccine to the reported events of Fall, dizziness and condition aggravated a possible contributory role of the suspect vaccine. 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: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: iron level; Result Unstructured Data: Test Result:very low; Test Name: blood pressure; Result Unstructured Data: Test Result:very very low; Test Name: cardiac workup; Result Unstructured Data: Test Result:Normal; Comments: More information available (Y/N): No; Test Name: other workup; Result Unstructured Data: Test Result:fine
Aktuelle Erkrankungen: Parkinson's disease (Verbatim: Parkinson's disease)
Vorgeschichte: -
Andere Medikamente: REGLAN [METOCLOPRAMIDE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2039646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el3247

moderat

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 09.02.2021
Beginn: 11.01.2022
Tage bis Beginn: 336,0
Dosis: UNK
Route/Site: IM / -

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

COVID-19 Dyspnoea

Symptomtext

presents today with shortness of breath at the context of being on day five of COVID-19 infection

Weitere VAERSDATA-Felder

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

VAERS 2034395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MA
Alter: 58,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 15.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Mobility decreased Vaccination site pain

Symptomtext

Unable to move shoulder much; Injection site very sore; 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 male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 15Mar2021 11:45 (Lot number: EL3247) at the age of 58 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Allergy to cats and rabbits" (unspecified if ongoing). Concomitant medication(s) included: ACETAMINOPHEN, start date: 2021. Vaccination history included: Bnt162b2 (Batch/lot number: EL3247, Date of start of drug/ time: 22Feb2021 11:00 AM, Anatomical Location: Arm Left, Dose Number: 1), administration date: 22Feb2021, when the patient was 58 years old, for Covid-19 immunization, reaction(s): "Sore throat", "Cough increased", "Upper respiratory infection". The following information was reported: MOBILITY DECREASED (non-serious) with onset 15Mar2021 16:00, outcome "recovering", described as "Unable to move shoulder much"; VACCINATION SITE PAIN (non-serious) with onset 15Mar2021 16:00, outcome "recovering", described as "Injection site very sore". Therapeutic measures were not taken as a result of mobility decreased, vaccination site pain. Additional information included: Events started about 4 hours after injection. Peaked at about 12 hours after injection. It was slowly improving at 30 hours post injection and was still unable to raise arm. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to animals
Andere Medikamente: ACETAMINOPHEN
Allergien: -
Vorherige Impfungen: -

VAERS 2028202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 01.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Herpes zoster

Symptomtext

Background info: about 25 years ago I had a classic case of shingles. I subsequently received two courses of shingles vaccines, the single vaccine and the more recent double vaccine. About a week after I received the booster COVID vaccine, I broke out on my upper back shoulder and around the top of my right shoulder. At first I thought it was an allergic reaction to something else but didn't know what it could be. Over the next week, the rash traveled across my back in a straight line. I took one leftover Valtrex pill that calmed the breakout and it was then I thought it could be a Shingles breakout. I scheduled a visit with my PCP. She had not seen any research on a relationship between the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Atorvastatin; Finasteride; Spironotactone; mirabegron; Flonase.
Allergien: Penicillin.
Vorherige Impfungen: -

VAERS 2028102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Blood test COVID-19 COVID-19 pneumonia Computerised tomogram Exposure to SARS-CoV-2 Fatigue Full blood count Metabolic function test Myocardial necrosis marker Procalcitonin Pulmonary haemorrhage Rhinorrhoea SARS-CoV-2 test positive Tracheal haemorrhage Ultrasound scan

Symptomtext

About 24 hours after the vaccine, I got very very tired which lasted about a day and subsided on its own. Then on 12/30 my nose got really runny. My husband had tested positive for Covid so I took a test as well an on 12/31 I tested positive to Covid myself. On 1/3 I got Monoclonal Antibiotics but on 1/5 I begin experiencing blood in my trach and lungs, so my PCP advised I go to the ER. At ER a CT scan, ultrasound, and blood work was performed and it was discovered I had Covid Pneumonia in my lower left lobe of my lung. My O2 sat level has been running in the mid-90s.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 1,0
Labordaten: CT scan; Ultrasound; COVID-19 test; CBC/CMB; Cardiac Enzyme Test; Procalcitonin Test
Aktuelle Erkrankungen: No
Vorgeschichte: Cancer; Hypertension
Andere Medikamente: Atenolol, Neurontin, Synthroid, Prilosec, Tylenol, Norco, Ambien
Allergien: Any Antibiotic; AC inhibitors; Antihistamines
Vorherige Impfungen: -

VAERS 2027525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 37,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 08.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Fatigue Headache Migraine Photophobia

Symptomtext

Throbbing headache almost like a migraine; Throbbing headache almost like a migraine; light sensitivity; tiredness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Mar2021 (Lot number: EL3247) at the age of 37 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: HEADACHE (non-serious), MIGRAINE (non-serious), outcome "not recovered" and all described as "Throbbing headache almost like a migraine"; PHOTOPHOBIA (non-serious), outcome "not recovered", described as "light sensitivity"; FATIGUE (non-serious), outcome "not recovered", described as "tiredness". Additional information: The patient did not receive other vaccine in four weeks. The patient did not covid prior vaccination. The patient did not have covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2027499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

moderat

Staat: CT
Alter: 53,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 09.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Fatigue Migraine Sinus headache Vaccination site pain

Symptomtext

sinus pressure headache; right side migraine; soreness at inject site; Slight fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 09Mar2021 11:45 (Lot number: EL 3247) at the age of 53 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Migraine" (unspecified if ongoing). There were no concomitant medications. The following information was reported: SINUS HEADACHE (non-serious) with onset 10Mar2021 06:00, outcome "recovered" (Mar2021), described as "sinus pressure headache"; MIGRAINE (non-serious) with onset 10Mar2021 06:00, outcome "recovered" (Mar2021), described as "right side migraine"; VACCINATION SITE PAIN (non-serious) with onset 10Mar2021 06:00, outcome "recovered" (Mar2021), described as "soreness at inject site"; FATIGUE (non-serious) with onset 10Mar2021 06:00, outcome "recovered" (Mar2021), described as "Slight fatigue". Therapeutic measures were not taken as a result of sinus headache, vaccination site pain, fatigue. Therapeutic measures were taken as a result of migraine. Additional information: It was reported that 20 hours after injection, began as sinus pressure headache that turned into a right-side migraine. Patient do have migraines but this one was unaffected by Advil which was typically very effective. Headache remained until 10pm 10Mar2021 at which time it ceased rather abruptly. Also had soreness at inject site for approximately the same amount of time. Slight fatigue which subsided once headache ended. No other vaccine in four weeks and no other medications in two weeks. No covid prior vaccination and no covid tested post vaccination. No known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2025245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 68,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 27.08.2021
Beginn: 06.01.2022
Tage bis Beginn: 132,0
Dosis: 1
Route/Site: SYR / UN

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

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

Symptomtext

Received Pfizer vaccines on 1/18, 2/8, 8/27 COVID-19 positive by PCR on 1/6/22 admitted to hospital on 1/6 d/t pneumonia d/t COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1117047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MA
Alter: 29,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 16.02.2021
Beginn: 28.12.2021
Tage bis Beginn: 315,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Migraine Nausea COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Breakthrough case / covid test result=Positive; Breakthrough case / covid test result=Positive; 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. An 30 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Feb2021 (Lot number: EL3247) at the age of 29 years as dose 2, single, and administration date 26Jan2021 (Lot number: El3247) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 28Dec2021, outcome recovering. The patient underwent the following laboratory tests and procedures sars-cov-2 test (28Dec2021) positive, Nasal Swab. Therapeutic measures were not taken as a result of vaccination failure, covid-19. No, covid prior vaccination. No known allergies. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20211228; Test Name: Rapid Test; Test Result: Positive; Comments: Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 17.11.2021
Beginn: 02.01.2022
Tage bis Beginn: 46,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Asthenia COVID-19 Chronic obstructive pulmonary disease Condition aggravated Cough Malaise Oxygen saturation decreased Pneumonia SARS-CoV-2 test positive Sputum discoloured

Symptomtext

Hospitalized 1/2/2022; COVID-19 positive 1/2/2022; fully vaccinated plus booster BRIEF OVERVIEW: Discharge Provider:, MD Primary Care Provider: MD Admission Date: 1/2/2022 Discharge Date: Jan 6, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: COPD with acute exacerbation (HCC) Community acquired pneumonia of right lower lobe of lung COVID-19 HOSPITAL COURSE: Patient is a 85 y.o. female who presented with cough, weakness. Patient has a history of COPD, chronic respiratory failure on 3L NC at baseline, Hx pseudomonas pneumonia, chronic diastolic CHF, hypothyroid. Patient's symptoms started on 12/31 with a cough and malaise. Per patient, she was having severe coughing up a greenish sputum so she called her pulmonologist who started the patient on Levaquin 2 days ago, she was able to take 2 doses, but then began having pain in both her ankles, and called her pulmonologist again who recommended she come to the emergency department for IV antibiotics. Patient took a COVID test at home which was positive. She was admitted to HCF and maintained on cefepime/azithromycin. Oxygen weaned to baseline 4L. Patient continued to improve though would desaturate to low 80's with activity. Local rehab consult was placed who recommended patient remain on 4 L nasal cannula at rest, with activity she will need to increase to 5-6 L.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD (Chronic Obstructive Pulmonary Disease), Very severe. Chronic obstructive pulmonary disease, unspecified COPD type (HCC) Bronchiectasis with acute exacerbation (HCC) Hypoxemia requiring supplemental oxygen, since 2007 Chronic sinusitis of both maxillary sinuses Pneumonia Acute on chronic respiratory failure with hypoxia (HCC) Chronic deep vein thrombosis (DVT) of femoral vein of right lower extremity (HCC) Paroxysmal atrial fibrillation (HCC) Pulmonary hypertension due to lung diseases and hypoxia (HCC) Chronic diastolic congestive heart failure (HCC) Obesity, BMI 33. Diverticulosis GERD (gastroesophageal reflux disease) COVID-19 Tobacco abuse, in remission. 30 pack years. Hyperlipidemia Hypoxemia, chronic Dyslipidemia Hypothyroidism Immunoglobulin deficiency, noted 9/2010. Osteoarthritis Osteoarthritis of lumbar spine Cyst of finger Insomnia Mild cognitive impairment
Andere Medikamente: albuterol HFA (PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet B Complex Vitamins (VITAMIN B COMPLEX) tablet budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler busPIRone (BUSPAR) 7.5 MG tablet cetirizine (ZYR
Allergien: Oxycodone
Vorherige Impfungen: -

VAERS 2010494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 51,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 05.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / LA

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

Ear discomfort Mobility decreased Tinnitus Vertigo

Symptomtext

Tinnitus, vertigo and pressure in ears on multiple occasion after 2nd dose. Requiring me to stop and wait for symptoms to lessen to be able to continue with my day. I have seen my primary care doctor and an Audiologist. Symptoms still remain but less frequently occurring about 4 times a month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 11/2021 Audiologist- hearing test and exam
Aktuelle Erkrankungen: none
Vorgeschichte: Hashimotos
Andere Medikamente: Synthroid. hormones, vitamins
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2529722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 05.02.2021
Beginn: 16.04.2021
Tage bis Beginn: 70,0
Dosis: 2
Route/Site: IM / LA

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

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

Symptomtext

Narrative: admitted to hosptal for COVID pneumonia, after being fully vaccinated

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: covid positive 4-16-2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1999382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: TX
Alter: 64,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 16.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / AR

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

Arrhythmia

Symptomtext

On March 19, 2021, I had a 2+ hour episode of a heart arrhythmia. I put on my apple watch and catalogued the heart rate which was between 100 and 162 for most of the time period. I had once before (in 2019 had a very short episode of a-flutter-- under 10 minutes long). This was different.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Since then, I have worn a 30 day event monitor, and in June 2021, I received an implantable heart monitor (Reveal LNQ11). To date, I have had no irregular heartbeats of note since the monitor was implanted.
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: atorvastatin, 10mg baby aspirin (81 mg)
Allergien: none
Vorherige Impfungen: -

VAERS 1983159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 40,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SC / LA

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

Asthenia Crying Feeling abnormal Grip strength decreased Headache Impaired work ability Inflammation Lethargy Loss of personal independence in daily activities Musculoskeletal stiffness Paraesthesia Peripheral swelling Thinking abnormal

Symptomtext

Within a day or two of getting the injection, I experienced an intense increase in inflammation all over my body. Most notably, my hands were stiff and swollen every morning. I was very foggy, and hard a hard time doing my job due to body stiffness. I tried to chalk it up to the past surgeries, but I had been healing very well until the vaccination. I had an awful 48 hours after the vaccination as well, my body clearly was in a state of fighting something. After the second shot, my reaction was even more profound. The day I had the second shot of the series, within a few hours I had the worst headache of my life. I had to leave work and went home and cried. It felt like an ice pick was being bored into my head. Within a few hours of the shot, I also started feeling intense tingling all over my body. It lasted for MONTHS. My hands became even more stiff, and I struggled to do even small things. I also became lethargic, and I felt weak all of the time. My hands and feet in particular tingled so much I dropped things constantly. I couldn't think of anything else for months. It wasn't until just a couple of months ago that I have started to feel better. My mentor and I talked about it constantly, as it effected my work so badly. My income was impacted, I could only work about 70% of the hours I did previously. While I feel mostly better, I still have frequent tingling in my hands. It is not carpal tunnel or other related conditions. Prior to receiving the vaccine I had been a presumed positive case of COVID in March 2020 after being exposed to several members of the association who tested positive while working as their flight attendant. I believe that I all ready had antibodies and that my body was reacting strongly to something it all ready knew how to fight, at deep personal cost to me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: I have mentioned it to all medical professionals I have seen but no tests were recommended.
Aktuelle Erkrankungen: None
Vorgeschichte: Several auto-immune and inflammatory conditions, including lichen sclerosis, arthritis and IBS, frozen shoulder in the past. Past anorexia nervosa, gall bladder disease (removed), frozen shoulder, had tonsils removed one year prior, had surgery six months prior (hysterectomy and breast reduction), had abdominal surgery two months prior
Andere Medikamente: Adderall, ibuprofen, sinex
Allergien: Penicillin, Amoxicillin, eggs, dairy, gluten, soy
Vorherige Impfungen: I have very strong reactions to every vaccine I get

VAERS 1971217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 37,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 27.01.2021
Beginn: 19.12.2021
Tage bis Beginn: 326,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

fever, cough, shortness of breath, chest pain, diarrhea, arthralgias

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: covid-19 pcr positive
Aktuelle Erkrankungen: -
Vorgeschichte: autism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2564302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 29.01.2021
Beginn: 16.07.2021
Tage bis Beginn: 168,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Ageusia Asthenia Chest pain Chills Cough Decreased appetite Dehydration Diarrhoea Dizziness Ex-tobacco user Heart rate increased Myalgia Nausea SARS-CoV-2 test positive Tachycardia Transfusion Vomiting

Symptomtext

Narrative: COVID infection after completion of COVID vaccine series: 01/07/2021 COVID vaccine dose #1 01/29/2021 COVID vaccine dose #2 07/02/2021 Pt reported onset of CP and cough coinciding with quitting smoking. Also reported loss of sense of taste. 07/16/2021 Pt presented to ED c/o 2-week h/o CP and cough. Also reported N/V, diarrhea, abd pain associated with N/V/D, myalgia, and chills 07/16/2021 COVID positive per nasopharyngeal swab 07/16/2021 Pt admitted to facility due to tachycardia and dehydration and atypical CP 07/17/2021 MD attending note reported increased HR, but otherwise pt was stable. Continued loss of appetite. Continuation of supportive care. 07/18/2021 MD attending note reported pt became tachycardic with ambulation. No other issues, but mild non-productive cough at times. Continuation of supportive care. 07/19/2021 Med IP note reported pt looked comfortable with no cough/CP. DDimer rising. 07/20/2021 Med IP note reported pt doing well. No CP/SOB/cough/fever. 07/21/2021 Pt discharged home 07/23/2021 Pt reported feeling better 07/24/2021 Pt reported continued cough 07/25/2021 Pt reported ongoing "dry hacking cough that makes him dizzy." Advised to use alb inh given at discharge. 07/26/2021 Pt's spouse reported visit to non-agency ED for c/o severe abd pain and weakness 07/26/2021 Pt admitted to non-agency facility 07/29/2021 Pt's spouse requested transfer to agency facility due to extensive tx/procedure being performed (blood transfusion)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 07/16/2021 COVID positive (nasopharyngeal swab)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2563055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 01.02.2021
Beginn: 23.07.2021
Tage bis Beginn: 172,0
Dosis: 2
Route/Site: IM / LA

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

Blood test COVID-19 Chest X-ray Chest discomfort Computerised tomogram Cough Dyspnoea Fatigue Infusion Nasopharyngitis Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sinusitis

Symptomtext

Narrative: COVID infections following completion of COVID vaccine series 01/07/21 COVID vaccine dose #1 02/01/21 COVID vaccine dose #2 07/23/21 Pt reports sinus infection/head cold, congestion, worsening cough, low grade fever earlier in the week, temp 97.6; COVID POSITIVE 07/26/21 Pt reports cough, fatigue, fever, runny nose, shortness of breath, chest tightness; states he was seen at medical facility where CT scan, CXR, blood work, antibody infusion performed 07/27/21 Pt reports no symptoms and is improving 07/28/21 Clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 07/23/21 COVID POSITIVE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2569145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 01.02.2021
Beginn: 17.07.2021
Tage bis Beginn: 166,0
Dosis: 2
Route/Site: IM / LA

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

Anal incontinence Asthenia COVID-19 Cardiac hypertrophy Chest X-ray abnormal Chest pain Computerised tomogram head normal Cough Diarrhoea Dyspnoea Echocardiogram abnormal Ejection fraction decreased Fatigue Headache Hypophagia Hypotension Lung adenocarcinoma recurrent Lung opacity

Symptomtext

Narrative: COVID infections following completion of COVID vaccine series 01/07/21 COVID vaccine dose #1 02/01/21 COVID vaccine dose #2 06/11/21 Suspected recurrence of adenocarcinoma RUL; pt prefers to wait 3 months and re-evaluate 07/24/21 Pt presents to ED reporting cough, general weakness x7 days, dry cough, shortness of breath, occasional headache; COVID POSITIVE, chronic elevated troponin with no chest pain, CXR and CT head wnl; admitted inpatient 07/25/21 Pt reports congestion, dry cough, and intermittent left sided chest pain; CT brain wnl 07/26/21 Pt reports cough improved and overall feeling better; ECHO revealed normal left ventricle size with severe concentric hypertrophy, LVEF 35-40% 07/27/21 Pt discharged with rx for DM/guiafenesin, lisinopril, polyethylene glycol, albuterol/ipratropium 07/30/21 Pt reported to not be eating or drinking and has diarrhea; reports extremely fatigued; advised to stop miralax 08/01/21 Pt remains weak but stable, reports BP is low; diarrhea has lessened but has bowel/bladder incontinence 08/02/21 Pt is improving, reports fatigue 08/04/21 Daughter calls into CCC reporting low BP 83/49; presents to ED reporting weakness and fatigue with shortness of breath and decrease PO intake; CT head wnl, CXR indicative of pneumonia; treated with IV fluids and discharged with rx for azithromycin, thiamine; advised to decrease dose of lisinopril to 10mg 08/05/21 Daughter reports difficulty in splitting tablet and has held BP medication due to low BP readings in the 70-80s/40-50s

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 07/27/21 CT Head wnl, CXR wnl, 08/04/21 CXR New patchy parenchymal opacity within the left mid and lower lung zone concerning for pneumonia given history
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2565490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 24.02.2021
Beginn: 18.07.2021
Tage bis Beginn: 144,0
Dosis: 1
Route/Site: IM / RA

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

Atrial fibrillation COVID-19 COVID-19 pneumonia Cough Dizziness Feeling abnormal Myalgia Oxygen saturation decreased Pyrexia SARS-CoV-2 test positive Troponin increased

Symptomtext

Narrative: Completed Pfizer 2 dose COVID19 vaccination on 2/25/21. Presented to ER on 7/18/21 with one day of lightheadedness and cough. New onset afib and COVID + test. Patient declined hospital admission and was d/c the same day. Patient presented to ER again on 7/24/21 due to continued fever, myalgias, and "generally feeling bad". O2 saturation dropped to 88% and troponins were slightly elevated. Diagnosed with COVID pneumonia Admitted with supplemental O2 and dexamethasone 6mg daily initiated. COVID supportive care and oxygen provided during hospitalization. Discharged 8/2/21 with guaifenesin, benzonatate, and methylprednisolone dose pack. Multiple comorbidities including CHF, cardiac defibrillator/pacemaker placement DM, PVD, CAD, MI, ESRD on hemodialysis, obesity, COPD, and microvascular DM complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: COVID + 7/18/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2572876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 81,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 13.01.2021
Beginn: 07.09.2021
Tage bis Beginn: 237,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Respiratory failure SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received two doses of Pfizer COVID 19 vaccine in Jan/Feb 21. The patient tested positive for COVID 19 on 7 September 2021 and was hospitalized with respiratory failure and COVID pneumonia. The patient was treated and was discharged still requiring oxygen on 20 Sep 21. The EUA requires that any patients that tested positive for COVID 19 and required hospitalization after receiving the vaccine must be reported.

Weitere VAERSDATA-Felder

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

VAERS 2571817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 29.01.2021
Beginn: 01.11.2021
Tage bis Beginn: 276,0
Dosis: 2
Route/Site: IM / LA

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

Ageusia Anosmia Asthenia COVID-19 Chest X-ray normal Cough Dyspnoea Exposure to SARS-CoV-2 Fatigue Pain SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 01/08, Pfizer, dose#1 01/29, Pfizer, dose #2 11/02 COVID swab, result: detected 11/02 Pt admit ED cc: Generalized weakness and bodyaches dx: COVID 19 LOS: 1 day 11/02 CXR impression: No evidence of acute cardiopulmonary process. 11/01 pt cc: cough, fatigue, myalgias, loss of taste or smell, dyspnea, exposure: son/recent travel 11/15 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/02 COVID swab, result: detected 11/02 CXR impression: No evidence of acute cardiopulmonary process.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576148

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 12.01.2021
Beginn: 16.09.2021
Tage bis Beginn: 247,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Respiratory failure SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received two covid 19 vaccine doses (Jan/Feb 2021). The patient tested positive for COVID 19 on 16 September 2021 and hospitalized with respiratory failure and COVID pneumonia. The patient was treated and discharged on oxygen on 29 September 2021. The EUA requires that any patients that tested positive for COVID 19 and required hospitalization after receiving the vaccine must be reported.

Weitere VAERSDATA-Felder

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

VAERS 2574810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 01.02.2021
Beginn: 02.10.2021
Tage bis Beginn: 243,0
Dosis: 2
Route/Site: IM / RA

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

Arrhythmia Atrioventricular block first degree Atrioventricular block second degree Blood electrolytes normal Blood thyroid stimulating hormone normal Bradycardia COVID-19 COVID-19 pneumonia Cough SARS-CoV-2 test positive

Symptomtext

Narrative: Patient admitted to Medicine team for COVID pneumonia, off supplemental O2. concern for cardiac instability, confirmed 1st degree AV block with intermittent 2nd degree Mobitz I AV block which was new for the patient, transferred to medical step down unit. In the MSDU the patient was comfortable on room air with his only symptom being a cough. He did not have any chest pain/pressure, shortness of breath, lightheadedness/presyncope, or other concerning symptoms. Patient had intermittent bradycardia with baseline 1st degree AV block and intermittent 2nd degree Mobitz I AV block. Checked TSH given cardiac arrhythmia in patient with hypothyroidism however this was normal. Medication list reviewed, not on AV nodal agents, no electrolyte abnormalities. Patient not on supplemental O2 so did not use dexamethasone, remdesivir. Given no signs of high-grade block, patient discharged to home. After discussion patient noted he would prefer to come back tomorrow to have Holter/event. Will follow-up with Cardiology as outpatient. Will also follow with PCP and have both skilled & non-skilled home health services.

Weitere VAERSDATA-Felder

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

VAERS 1852055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: OH
Alter: 74,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 01.02.2021
Beginn: 14.07.2021
Tage bis Beginn: 163,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Cardiac monitoring Dyspnoea Fatigue Palpitations

Symptomtext

Palpitations and general fatigue weakness shortness of breath on exercise

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Heart monitor and eval in progress
Aktuelle Erkrankungen: High blood pressure
Vorgeschichte: Hypertension
Andere Medikamente: Carvidalol thyroid supplements dyazide
Allergien: Latex
Vorherige Impfungen: -

VAERS 1851293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: TX
Alter: 76,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 15.01.2021
Beginn: 27.03.2021
Tage bis Beginn: 71,0
Dosis: 2
Route/Site: - / RA

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

Chest pain Coronary arterial stent insertion Coronary artery occlusion Intracardiac thrombus

Symptomtext

With the first COVID vaccine, I had fatigue and chills for four days. I had no symptoms with the second vaccine on Feb. 9,2021. Then a few weeks later, I had chest pain when I exercised. This went on for weeks until I went to emergency on March 27th, 2021. I had a clot in a small diagnol heart vessel. The cardiologist stented the small vessel. All my major heart arteries had 50 percent and lower blockage. Although it can never be proved, I believe my clot was due to the Pfizer covid vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: On file at the local Hospital
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: lyrica, Estrace,
Allergien: -
Vorherige Impfungen: -

VAERS 2576229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 18.02.2021
Beginn: 28.08.2021
Tage bis Beginn: 191,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort COVID-19 Cough Dyspnoea Flatulence Illness Nausea SARS-CoV-2 test positive Tachypnoea

Symptomtext

Narrative: 8-year-old male with comorbidities of hepatitis C s/p treatment in 2/2019, ulcerative colitis, seropositive non-erosive rheumatoid arthritis, high risk medication use (tofacitinib and hydroxychloroquine) who presents to the ED with a chief complaint of dyspnea. Symptoms started, 8/28/2021. Dyspnea started yesterday and is progressively worsening. It is associated with a non-productive cough. He had an outpatient Covid test done that was positive. He was vaccinated with Moderna x2 in 1/2021 and 2/2021. No fevers or chills. Diarrhea started Thursday but seems to have slowed down. He is passing flatus. He has generalized abdominal discomfort with eating or drinking, as well as nausea. He is unsure how he contracted Covid. Wife also has Covid but is doing well. He has been taking tofacitibin and hydroxychloroquine throughout illness, up until ED visit. He was placed on 2 L NC due to tachypnea.

Weitere VAERSDATA-Felder

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

VAERS 2576966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 30.01.2021
Beginn: 26.08.2021
Tage bis Beginn: 208,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia COVID-19 Chest pain Fibrin D dimer Injection site pain Neck pain Pain SARS-CoV-2 test positive Troponin I normal

Symptomtext

Narrative: COVID infection following COVID vaccine series 01/09, Pfizer, dose #1 01/30, Pfizer, dose #2 08/28 COVID swab, result: detected 08/28 SARS-COV-2 Variant Sequencing result: pending 08/31 TROPONIN I<0.016 08/31 ddimer <0.22 08/31 pt admit ED cc: neck pain radiated to shoulders since he started presenting Covid Virus symptoms. dx: Nonspecific chest pain Acute Covid positive status LOS: 1 day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 08/28 COVID swab, result: detected 08/28 SARS-COV-2 Variant Sequencing result: pending 08/31 TROPONIN I <0.016 08/31 ddimer <0.22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1843072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 30,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 26.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Blood test Hyperhidrosis Palpitations Sleep disorder

Symptomtext

Had heart palpitations after 12+ hours of receiving the 2nd dose of Pfizer COVID-19 vaccine. I was sleeping and it woke me up in the middle of the night at around 215am, where my heart rate was in the 200s (I was in SVT). I then drank a liter of water and then urinate which helped me calm down. I also took Tylenol to help alleviate my pain. I was also sweating profusely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Since the adverse event, I went to get a check up and requested from my PCP to get blood works on my thyroid function levels because I had a speculation that my hyperthyroid/ Graves' Disease might relapse. I was treated with Graves' Disease 6 years ago and was on medication for under a year and then my TSH levels were back to normal and my endocrinologist at the time had me stop my medication and since then I've been fine. I believed my 2nd COVID-19 vaccine might have triggered my autoimmune/ Graves' Disease.
Aktuelle Erkrankungen: History of hyperthyroidism (Graves' Disease)
Vorgeschichte: History of hyperthyroidism (Graves' Disease)
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 1828940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 50,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Pneumonia SARS-CoV-2 test negative Sinusitis

Symptomtext

Pneumonia, sinusitis, persistent Covid symptoms, however PCR negative

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: PCR 10/27/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, sinus disease
Andere Medikamente: Zyrtec, adviair, truvada, Celebrex, topical clindamycin, singular
Allergien: None
Vorherige Impfungen: -

VAERS 1826671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 17.01.2021
Beginn: 12.10.2021
Tage bis Beginn: 268,0
Dosis: 1
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Chills Cough Diarrhoea Dyspnoea Dyspnoea exertional Fatigue Headache Myalgia Nausea Oropharyngeal pain Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Fever or Chills Cough Shortness of Breath Difficulty breathing Fatigue Muscle or body aches Headache New loss of taste or smell Sore throat Congestion or running nose Nausea or vomiting Diarrhea oTelephone Visit 10/20/2021 Internal Medicine - MD Internal Medicine COVID-19 Dx HPI: Patient is 68 y.o. female for whom I am doing a telephone visit discuss her current Covid infection. She started with symptoms last Tuesday which is October 12 with chills and headaches and body ache followed by temperature ranging up to 100.4 ?F. This was followed by cough with clear to brownish phlegm along with nausea vomiting and diarrhea which has now resolved but she continues to have some cough and some shortness of breath on exertion. She does not have any shortness of breath on rest. She is overall feeling better compared to last week. She has not checked her temperature this week at all. She has not been checking her oxygen level because she does not have a pulse oximetry. I discussed in length about the risk benefits of monoclonal antibody infusion and that she would be a candidate although she is nearly on day 9 of the 10-day window for the infusion. She would not like to get that and would like to monitor and treat conservatively. Did recommend to drink lots of fluids rest and monitoring the temperature and oxygen level.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 10/19/2021 1142 COVID-19 (SARS CoV-2,RNA Molecular Amplification) Collected: 10/19/21 1142 | Final result | Specimen: Swab from Nasopharynx COVID-19 SARS-CoV-2 Overall Result Detected Critical 10/19/2021 1142 COVID-19 PCR Collected: 10/19/21 1142 | Final result | Specimen: Swab from Nasopharynx
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Other chronic pain Respiratory OSA treated with BiPAP Circulatory Paroxysmal atrial fibrillation Hypertension PAC (premature atrial contraction) Hypertension associated with type 2 diabetes mellitus Digestive Class 3 severe obesity with serious comorbidity in adult Genitourinary Stage 3a chronic kidney disease Musculoskeletal Arthritis Hallux rigidus Primary localized osteoarthritis of left knee Primary localized osteoarthritis of right knee Endocrine/Metabolic Type 2 diabetes mellitus Hyperlipidemia, unspecified hyperlipidemia type Hematologic Anemia, iron deficiency Other Long-term (current) use of anticoagulants
Andere Medikamente: acetaminophen (TYLENOL ARTHRITIS PAIN) 650 mg 8 hr tablet atorvastatin (LIPITOR) 10 mg tablet cholecalciferol, vitamin D3, (VITAMIN D3) 10 mcg (400 unit) capsule diclofenac sodium (VOLTAREN GEL) 1 % gel ELIQUIS 5 mg tablet flecainide (
Allergien: NKA
Vorherige Impfungen: -

VAERS 1825789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Urinary incontinence

Symptomtext

One episode of urinary incontinence that has never happpened before

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: BP Depression Seasonal allergies Acid reflux High Cholesterol
Andere Medikamente: Zyrtec. Rouvastin Valtrex. Carvedilol Omega 3. Hyzaar Psyllium. Prilosec Multi Vit Glucosamine. Calcium Vit. K Folate Probiotic Vit C L-Lysine Selenium Magnesium Zinc Prozac
Allergien: Sulfa Tetracycline Artificial sweetners
Vorherige Impfungen: One episode of Urinary Incontinence with each shot

VAERS 1823865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MA
Alter: 42,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Pain in extremity Paraesthesia Vaccination site pain

Symptomtext

left hand pinky finger and ring finger tingling and ache/pain all day; left hand pinky finger and ring finger tingling and ache/pain all day; site injection and shoulder pain in left arm; This is a spontaneous case received from a contactable consumer (patient herself). A 42-year-old female patient received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EL3247, Expiration date: May2021), via an unspecified route of administration, administered on 02Mar2021 as DOSE 1, SINGLE (age at vaccination 42-year-old) for COVID-19 immunization. The patient medical history included allergies to steroids, allergy/contact dermatitis from latex, allergy/sensitivity to dairy, diagnosed with eczema in teens and with IBS (irritable bowel syndrome) in 2018. Concomitant medications were reported as none. On 02Mar2021, the patient experienced site injection and shoulder pain in left arm. On 03Mar2021, the patient experienced left hand pinky finger and ring finger tingling and ache/pain all day. The outcome of the event on was recovering (04Mar2021 symptoms subsiding). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Dairy intolerance; Eczema; Irritable bowel syndrome; Latex allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1820972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 27.01.2021
Beginn: 21.10.2021
Tage bis Beginn: 267,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Dyspnoea

Symptomtext

SOB and weakness

Weitere VAERSDATA-Felder

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

VAERS 1808772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: OR
Alter: 49,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 13.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal discomfort Abdominal pain upper Appendicectomy Appendicitis Blood test Flank pain Gastrointestinal disorder Colitis Computerised tomogram abnormal Condition aggravated Impaired work ability Irritable bowel syndrome Stool analysis Ultrasound abdomen abnormal X-ray

Symptomtext

Had my first Pfizer vaccine on 1/13/21 started feeling pain and burning within 48 hours of the injection that went into the right flank and stomach area. An ultrasound was performed and later had a appendicitis, appendectomy and later a CT scan showed Colits. All stemmed from or happened after a very short time window of receiving my first vaccine. I am still experiencing colits, spastic colon with IBD, IBS-C and have not worked since February.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: I am not sure of the exact dates of tests: CT Scan, Ultra sound, blood tests, stool tests xray
Aktuelle Erkrankungen: none
Vorgeschichte: ibs, spastic colon, thyroid
Andere Medikamente: multi vitamin, levothyroxine, birth control , zanax
Allergien: ampicillin
Vorherige Impfungen: -

VAERS 1812149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 28.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: OT / -

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

Body temperature Body temperature increased Cough Dyspnoea Insomnia Lip blister Lip pain Loss of personal independence in daily activities Pain SARS-CoV-2 test Wheezing

Symptomtext

Temp went up to 101; hardly slept; she was unable to work; Whole body aches; Small blister on lower lip; lip soreness; coughing; wheezing; having difficulty breathing; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 62-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 2 intramuscular on 28Apr2021 09:00 (at the age of 62-Years-old) (Batch/Lot Number: EL3247) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included Epicondylitis of arms and knees. Concomitant medication included losartan taken for unspecified indication and folic acid taken for an unspecified indication and Oxtrexup within 2 weeks of vaccination. The patient received first dose of BNT162B2 PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1, intramuscular administered in left arm on 07Apr2021 09:00 (at the age of 62-Years-old) (Batch/Lot Number: EL3247) as DOSE 1, SINGLE for covid-19 immunisation. On 29Apr2021, the patient temperature went up to 101, temperature went up to 101 around 3am this morning, down to 100 at 7:46am, for 2 days and body aches, hardly slept and low-grade fever from 99-100 for 5 days. Small blister on lower lip appeared on 2d day after vaccine, coughing and wheezing started on 2nd day after vaccine and still as of today have needed to use nebulizer every day as patient had difficulty breathing. She used Neosporin on lips for blisters on lower lip - not visible now but can still feel lip soreness. As of today, Thursday, May 6, Still coughing and having difficulty breathing and needing to nebulize. Patient took Tylenol and drank fluids, etc. The patient underwent lab tests and procedures which included body temperature and showed 101 Fahrenheit on Mar2021, sars-cov-2 test was negative on Mar2021. Patient did not receive any other vaccines within 4 weeks prior to the COVID. Patient was diagnosed with COVID-19 Prior to vaccination. Patient was not tested for COVID-19, since the vaccination. Therapeutic measures were taken as a result of events. At the time of this report, the outcome of event was not recovered. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 202103; Test Name: body temperature; Result Unstructured Data: Test Result:101 Fahrenheit; Test Date: 202103; Test Name: covid-19 test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Epicondylitis
Andere Medikamente: LOSARTAN; FOLIC ACID
Allergien: -
Vorherige Impfungen: -

VAERS 1205162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: OR
Alter: 79,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 05.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Blood pressure measurement Heart rate Heart rate increased Herpes zoster Hypertension Pneumonia Rash

Symptomtext

shingles on the right upper side of my torso (front and back); This is a spontaneous report from a contactable consumer (patient). An 80-year-old non pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: EL3247, expiration date was not reported), via an unspecified route of administration administered in right arm on 05Feb2021 (at the age of 79-years-old) as dose 1, single for covid-19 immunization at public health clinic/veterans administration facility. The patient medical history was not reported. Concomitant medication included levothyroxine taken for an unspecified indication from an unknown date. List of any other medications the patient received within 2 weeks of vaccination included levothyroxine. The patient previously took polyethylene glycol compound and experienced allergies: poly-ethylene glycol. Patient was not pregnant at time of vaccination. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. It was reported that 2 weeks after the first vaccine on Feb2021 she came down with shingles on the right upper side of her torso (front and back). Was treated by a physician for symptoms. Therapeutic measures were taken as a result of shingles on the right upper side of my torso (front and back). The reporter assessed the seriousness as non-serious. The outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1791441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: -
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 19.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Dizziness Headache Paraesthesia Vision blurred

Symptomtext

Bad headache; Blurred vision; Tingling in the arm where the vaccine was administered (not at injection site but down the arm).; felt dizzy; This is a spontaneous report from a contactable pharmacist. An adult male patient of unknown age received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL3247) via an unspecified route of administration on 19Jan2021 as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on an unknown date, as a single dose for COVID-19 immunisation. On 19Jan2021, within 15 minutes of vaccination, the patient experienced a bad headache, blurred vision, and tingling in the arm where the vaccine was administered (not at injection site but down the arm). The patient was asked to sit and rest for continued monitoring. After 20-30 minutes, the patient attempted to stand but felt dizzy. The events resulted in emergency room/department or urgent care for further evaluation. The clinical outcome of the events bad headache, blurred vision, tingling in the arm where the vaccine was administered (not at injection site but down the arm) and felt dizzy was unknown at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1791350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 27,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 18.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Fatigue Migraine Pain

Symptomtext

Migraines; general body achiness; exhaustion 12 hours after receiving the shot; This is a spontaneous report from a contactable consumer (patient). A 27-year-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247) via an unspecified route of administration, administered in left arm on 18Feb2021 13:45 (at the age of 27-year-old) as dose 2, single for COVID-19 immunization at clinic. Medical history was reported as none. Patient had no known allergies. Concomitant medications included Escitalopram via an unspecified route of administration from an unknown date and unknown if ongoing for an unspecified indication. The patient had not received any other vaccine within 4 weeks. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Historical vaccine included the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247) via an unspecified route of administration, administered in right arm on 28Jan2021 13:45 (at the age of 27-Year-old) as dose 1, single for COVID-19 immunization at clinic. It was reported that on 19Feb2021 01:00, the patient experienced migraines, general body achiness, and exhaustion 12 hours after receiving the shot. Patient did not receive any treatment for the events. The outcome of all events was resolving. No follow up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1278474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AL
Alter: 60,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Back pain Body temperature Chest discomfort Chest pain Chills Dyspnoea Erythema Limb discomfort Migraine Nausea Feeling abnormal Joint range of motion decreased Malaise Palpitations Pyrexia Swelling face Tinnitus

Symptomtext

Arms really heavy, can hardly lift them; Chest pain; Heart palpitations; Difficulty breathing; Migraine headache; Ears ringing; Pressure in chest; Really red face, cheeks; Chills; Nausea; Very high fever; Back pain a lot worse; This is a spontaneous report from a contactable consumer (patient). A 60-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/lot number: EL3247, Expiration date unknown), first dose via an unspecified route of administration, administered in right arm deltoid on 08Apr2021 at 14:30 to 15:00 (at the age of 60-year-old) as dose 1, single for COVID-19 immunisation at pharmacy/drug store. Medical history included intervertebral disc protrusion from 2003 and ongoing Verbatim: herniated disc and chronic back pain patient medical continuing : yes, back pain from 2003 and ongoing Verbatim: herniated disc and chronic back pain patient medical continuing : yes, ongoing epilepsy Verbatim: Epilepsy Patient medical continuing : yes, started at 16-year-old. Concomitant medications included carbamazepine (CARBAMAZEPINE) taken for seizure, start and stop date were not reported; phenytoin (DILANTIN [PHENYTOIN]) taken for an unspecified indication, start and stop date were not reported. No additional vaccines were administered on same date of the Pfizer suspect. The patient did not receive any vaccination within 4 weeks. The patient reported that on the Pfizer COVID-19 vaccine and Patient had very, very bad side effects. She was running a fever and had every side effect on the template from the pharmacy. She was not doing good and should probably be in the hospital. She could not drive her-self. On 08Apr2021, the patient had very high fever and back pain a lot worse. On 09Apr2021, she had chills, red face, cheeks, and nausea. On 10Apr2021, the patient experienced migraine headache, heart palpitations, difficulty breathing, pressure in chest, and ears ringing. On 14Apr2021, she had chest pain. On 15Apr2021, the patient experienced arms heavy, can hardly lift them. Adverse events did not require to visit emergency room or physician office. The reporter assessed arms heavy, can hardly lift them as medically significant. Upon follow-up received on 29Mar2021, it was reported that caller stated she went to the place where they said who we share information, and it was a lot of people. Caller stated she wanted all personal information, age, doctor, Carbamazepine and Dilantin use. Caller stated she wants all personal information retracted except for her name and address. Caller wanted to make sure that this agent had she wanted to cancel her personal information, age, and seizure medication information. No product quality complaint was reported. No medical information was requested. The outcome of very high fever, migraine headache and chills, ears ringing was recovering on an unspecified date in 2021, while outcome of back pain a lot worse, heart palpitations, pressure in chest, red face, cheeks, arms heavy, can hardly lift them and nausea was not recovered and outcome for other events was unknown. Follow-up (29Mar2021): new information report was received from a consumer. This consumer (patient) reported in response to non-HCP telephonic follow-up activity which included that: Concomitant medication DILANTIN was added. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210408; Test Name: Very high fever; Result Unstructured Data: Test Result:Very high
Aktuelle Erkrankungen: Chronic back pain (Verbatim: herniated disc and chronic back pain patient medical continuing : yes); Epilepsy (Verbatim: Epilepsy Patient medical continuing : yes started at 16 years old); Herniated disc (Verbatim: herniated disc and chronic back pain patient medical continuing : yes)
Vorgeschichte: -
Andere Medikamente: CARBAMAZEPINE; DILANTIN [PHENYTOIN]
Allergien: -
Vorherige Impfungen: -

VAERS 1784817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 23.01.2021
Beginn: 03.09.2021
Tage bis Beginn: 223,0
Dosis: 1
Route/Site: IM / UN

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

Atypical pneumonia Blood glucose decreased Chest X-ray abnormal Decreased appetite Hypoglycaemia Hypotension Lung opacity Pneumonia viral Pyrexia

Symptomtext

70 y/o female with pmhx CVA w/ right-sided deficit, htn, dm and glaucoma present to Hospital for fevers, decreased appetite and hypoglycemia. Chest XR demonstrated scattered bilateral interstitial opacities likely typical/atypical viral pneumonia. Patient was found to have BG 30's and hypotensive prior to coming to ED. EMS given glucagon en route to hospital. Oxygen sat 88 on room air, put on 2L nasal cnnula, sat mid 90's.

Weitere VAERSDATA-Felder

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

VAERS 1782839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 88,0
Geschlecht: M
Eingang: 13.10.2021
Impfdatum: 09.02.2021
Beginn: 12.10.2021
Tage bis Beginn: 245,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Cough Dyspnoea exertional Hypoxia

Symptomtext

Patient diagnosed with covid-19 on 9/30/2021 and sent by PCP's office with hypoxia. Patient had cough and received monoclonal antibody infusion on 10/8/2021. Patient completed steroids on 10/9/2021 and had worsening SOB on exertion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: chronic kidney disease hypertension
Andere Medikamente: amlodipine, triamterene/hydrochlorothiazide
Allergien: none
Vorherige Impfungen: -

VAERS 1776731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

moderat

Staat: MO
Alter: 81,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 27.03.2021
Beginn: 29.08.2021
Tage bis Beginn: 155,0
Dosis: 1
Route/Site: IM / AR

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

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

Symptomtext

developed Shortness of breath although exact date of onset is unknown. He was admitted to local Hospital on 8/29/2021 and tested (+) that day. Diagnosed with COVID Pneumonia and hospitalized 8/29 until 9/3. Was on up to 7 liters of oxygen while at hospital. Went home on room air.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: hypertension, asthma
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1774632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: OH
Alter: 78,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Blood test Condition aggravated Erythema Pruritus Rash

Symptomtext

itchy when they appear; Rash; little red spots; his symptoms are worsening; This is a spontaneous report from a contactable consumer (patient). A 78-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration in left arm on 10Feb2021 at 11:00 (at the age of 78-years) as dose 2, single for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had not received any other vaccine within 4 weeks. The patient did not experience any event prior vaccination. The patient had previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EK4174), via an unspecified route of administration in left arm on 20Jan2021 (at the age of 78-years) as dose 1, single for covid-19 immunization. The patient had no additional vaccines administered on same date of the Pfizer suspect. Following second dose of vaccination, on 10Feb2021 the patient had rash; little red spots, itchy when they appear, all over body and worse on arms. The patient stated that his symptoms had worsened from 10Feb2021, spots were not that noticeable, but they looked like mosquito bites. They were mostly on his arms and looked almost like they were under the skin. Other locations on his body, like his shoulders, they looked like they were on top of the skin. Patient also stated that the bumps are not raised, just a red blotch on his skin which were maybe 1/16th of an inch or less in size. This resulted in physician office visit and the patient was advised to put lotion and hydrocortisone cream on it by this doctor. The patient underwent lab tests and procedures in between the first and second dose on an unspecified date in 2021 at his 6-month check-up and included blood test resulted normal. The outcome of the events was not recovered at the time of report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood work; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1771583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 20,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 25.01.2021
Beginn: 31.08.2021
Tage bis Beginn: 218,0
Dosis: 1
Route/Site: IM / -

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

Body temperature increased COVID-19 Cough Dyspnoea Malaise Nasal congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

C/O Shortness of breath, difficulty breathing, cough, elevated temperature, runny nose and/or congestion, and malaise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Positive Covid-19 PCR test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1374459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 77,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 18.02.2021
Beginn: 18.05.2021
Tage bis Beginn: 89,0
Dosis: 2
Route/Site: SYR / LA

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

Hypoaesthesia Laboratory test normal Lumbar puncture normal Mobility decreased Nerve injury Lumbar puncture Myelitis transverse Walking aid user Wheelchair user

Symptomtext

Pfizer two shot first 1/28/21 second 2/18/21. Total numbness left leg on May 18, 2021. One week in hospital with steroid treatment. No change in leg mobility. PT for a week, wheelchair, walker, cane now walking without but not good muscle control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 7,0
Labordaten: Tests all normal including spinal tap. Just nerve damage no feeling upper theigh, left abdominal area.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1764970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CO
Alter: 80,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 05.02.2021
Beginn: 02.10.2021
Tage bis Beginn: 239,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Influenza A virus test negative Influenza virus test negative Oropharyngeal pain Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

Patient required inpatient admission to hospital with COVID-19 on 10/2/2021 (presented with cough, shortness of breath, and sore throat for the past week per provider notes). As of 10/6/2021, the patient remains admitted to the hospital for treatment of COVID-19 infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: FLUVID test: Positive for COVID-19 on 10/3/2021 (negative for influenza A, influenza B, and RSV on test panel).
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Diabetes mellitus, hyperlipidemia, spinal stenosis, thyroid disease, hypertension.
Andere Medikamente: Unknown
Allergien: Patient has an allergy to iodinated contrast media (reports throat swelling).
Vorherige Impfungen: -

VAERS 1762040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Blood pressure increased Heart rate increased Palpitations

Symptomtext

Within seconds, I could start feeling my heart race and they told me to sit down for 15 minutes. I sat there for 20 minutes hoping it would go away. It didn't. I started walking away but went back in and reported it and they brought people to evaluate me. My heart rate and blood pressure were elevated. They brought in someone from the St Joseph Medical Center ER dept and that person decided I needed to go over and be admitted to ER. I stayed there for 3-4 hours before it finally came down and they let me go home. No treatment at that time - just observed me. I did not experience re-occurrence of symptoms. I went to see my doctor to follow up and she said everything was okay. I had different medical tests related to my asthma.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Vitals only.
Aktuelle Erkrankungen: no
Vorgeschichte: asthma
Andere Medikamente: Singular; Tramadol; Vit D3; Probiotic; I was using an allergy medicine: Fexofenadine Hydrochloride tablet.
Allergien: Allergy to Atenolol - blood pressure medicine; allergy to all NSAIDs (like ibuprofen, etc); Mucinex - can't use it
Vorherige Impfungen: -

VAERS 1761995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 63,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 03.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Back pain Mobility decreased Musculoskeletal pain Pain in extremity Spinal X-ray normal

Symptomtext

The day after receiving the second dose, I experienced a very sore arm. I could hardly lift it for the day. About two weeks later, I started experiencing pain around my upper back/ shoulder blade. I had been playing badminton and I thought I may have been sore from that. The pain did not go away and continued for weeks. I went to the doctor and he did an x-ray. Everything came back okay with the x-ray. I still have the shoulder pain, at times, but I just live with it. We do not know the cause.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: I had an x-ray performed on my back.
Aktuelle Erkrankungen: I was not experiencing any illness.
Vorgeschichte: I have degenerative disc disease in my lower back and scoliosis.
Andere Medikamente: Celebrex; Levothyroxine; Calcium; Magnesium; Vitamin B; Vitamin C; Fish Oil.
Allergien: I do not have any allergies.
Vorherige Impfungen: -

VAERS 1750231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

moderat

Staat: MO
Alter: 81,0
Geschlecht: M
Eingang: 30.09.2021
Impfdatum: 16.02.2021
Beginn: 20.09.2021
Tage bis Beginn: 216,0
Dosis: 1
Route/Site: IM / AR

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

Ageusia Anosmia Decreased appetite Diarrhoea Dyspnoea

Symptomtext

diarrhea, SOB, decreased appetite, loss of smell tast

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1745552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 29.09.2021
Impfdatum: 12.03.2021
Beginn: 24.09.2021
Tage bis Beginn: 196,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Chest X-ray Computerised tomogram thorax Computerised tomogram thorax abnormal Cough Diarrhoea Dyspnoea Hypoxia Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

Hospitalized 09/24/2021; COVID-19 positive 09/24/2021; fully vaccinated HOSPITAL COURSE: Patient is a 43 y.o. female Comes from an AFC home Mother is guardian History is obtained from supervisor of AFC Home who is at bedside It appears on the 19th, patient had onset of symptoms of fever, shortness of breath, cough Also recalls some diarrhea but denies any loss of taste or smell Self-medicated with Tylenol and Robitussin At that point, she was tested, results of which came back positive 9/21 She presented on 09/24 due to shortness of breath Was 92% on room air in the emergency department Chest x-ray obtained, patient was discharged on doxycycline She was referred to the monoclonal antibody clinic A she received monoclonal antibody 9/24 Upon returning to facility, patient appeared to be more short of breath Was found to be hypoxic, 87 on room air and febrile She was brought in for repeat evaluation. CT angiogram thorax obtained. CT angiogram thorax negative for PE but did show a pneumonia In addition, she was requiring supplemental oxygen, received dexamethasone, ceftriaxone, doxycycline Subsequently admitted to Medicine. She was treated with Remdesevir and Decadron , and empirically with IV ceftriaxone and Doxycyline, her procal was low and there was no evidence of Secondary bacterial infection, antibiotics discontinued and she was successfully weaned of O2 , she remain afebrile while she is in the hospital . She was discharged in stable condition .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diagnosis Date ? Cardiac arrest Anesthesia to dental procedure ? Cognitive impairment ? Constipation ? GERD (gastroesophageal reflux disease) ? Hemorrhoid ? Hypothyroid ? Intermittent explosive disorder ? Morbid obesity with BMI of 45.0-49.9, adult ? Multiple drug allergies ? Stress incontinence
Andere Medikamente: acetaminophen (TYLENOL 8 HOUR) 650 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Alum & Mag Hydroxide-Simeth 200-200-20 MG/5ML SUSP ARTIFICIAL TEAR OINTMENT OP benzonatate (TESSALON) 100 MG
Allergien: Macrobid [nitrofurantoin] Aspirin Caffeine Chocolate Erythrocin Grapefruit Ibuprofen Oranges Penicillins Sulfa Drugs Tomato Astelin [azelastine] Citrus [cholecalciferol] Zithromax [azithromycin]
Vorherige Impfungen: -

VAERS 1745552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 29.09.2021
Impfdatum: 12.03.2021
Beginn: 24.09.2021
Tage bis Beginn: 196,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest X-ray Computerised tomogram thorax Computerised tomogram thorax abnormal Cough Diarrhoea Dyspnoea Hypoxia Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

Hospitalized 09/24/2021; COVID-19 positive 09/24/2021; fully vaccinated HOSPITAL COURSE: Patient is a 43 y.o. female Comes from an AFC home Mother is guardian History is obtained from supervisor of AFC Home who is at bedside It appears on the 19th, patient had onset of symptoms of fever, shortness of breath, cough Also recalls some diarrhea but denies any loss of taste or smell Self-medicated with Tylenol and Robitussin At that point, she was tested, results of which came back positive 9/21 She presented on 09/24 due to shortness of breath Was 92% on room air in the emergency department Chest x-ray obtained, patient was discharged on doxycycline She was referred to the monoclonal antibody clinic A she received monoclonal antibody 9/24 Upon returning to facility, patient appeared to be more short of breath Was found to be hypoxic, 87 on room air and febrile She was brought in for repeat evaluation. CT angiogram thorax obtained. CT angiogram thorax negative for PE but did show a pneumonia In addition, she was requiring supplemental oxygen, received dexamethasone, ceftriaxone, doxycycline Subsequently admitted to Medicine. She was treated with Remdesevir and Decadron , and empirically with IV ceftriaxone and Doxycyline, her procal was low and there was no evidence of Secondary bacterial infection, antibiotics discontinued and she was successfully weaned of O2 , she remain afebrile while she is in the hospital . She was discharged in stable condition .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diagnosis Date ? Cardiac arrest Anesthesia to dental procedure ? Cognitive impairment ? Constipation ? GERD (gastroesophageal reflux disease) ? Hemorrhoid ? Hypothyroid ? Intermittent explosive disorder ? Morbid obesity with BMI of 45.0-49.9, adult ? Multiple drug allergies ? Stress incontinence
Andere Medikamente: acetaminophen (TYLENOL 8 HOUR) 650 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Alum & Mag Hydroxide-Simeth 200-200-20 MG/5ML SUSP ARTIFICIAL TEAR OINTMENT OP benzonatate (TESSALON) 100 MG
Allergien: Macrobid [nitrofurantoin] Aspirin Caffeine Chocolate Erythrocin Grapefruit Ibuprofen Oranges Penicillins Sulfa Drugs Tomato Astelin [azelastine] Citrus [cholecalciferol] Zithromax [azithromycin]
Vorherige Impfungen: -

VAERS 1731242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AL
Alter: 69,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 26.02.2021
Beginn: 25.08.2021
Tage bis Beginn: 180,0
Dosis: 2
Route/Site: SYR / LA

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

Adenocarcinoma Condition aggravated Non-small cell lung cancer Positron emission tomogram abnormal

Symptomtext

I am in active treatment for NSCLC adenocarcinoma with an oral targeted therapy drug Alecensa (alectinib). After 4 years of being stable I had progression within months of receiving the second dose of the COVID vaccine. I do not know if the two are in any way connected but felt it important enough to report

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: PET scan 08/25/2021 showed progression of disease NSCLC adenocarcinoma up until that time the disease had been stable
Aktuelle Erkrankungen: NSCLC adenocarcinoma
Vorgeschichte: NSCLC adenocarcinoma
Andere Medikamente: Alecensa (alectinib), Lexapro, multi vitamin and Glucosamin/Chondrotin tablet
Allergien: None Known
Vorherige Impfungen: -

VAERS 1716323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 18.02.2021
Beginn: 12.09.2021
Tage bis Beginn: 206,0
Dosis: 2
Route/Site: UN / UN

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

Aortic arteriosclerosis Asthenia Bacterial test positive COVID-19 Cerebral small vessel ischaemic disease Chest X-ray abnormal Computerised tomogram abnormal Computerised tomogram head abnormal Condition aggravated Cough Culture urine positive Dystrophic calcification Fall Fatigue Haemorrhage intracranial Head injury Klebsiella test Lung opacity

Symptomtext

Patient is an 84-year-old female who presented for evaluation due to fatigue and weakness. The patient was found to be COVID positive in the ER (she is fully vaccinated). She was found to have a UTI as well. She did not have any leukocytosis or hypoxia. She was admitted for PT/OT evaluation. On the day of discharge, the patient was feeling much better. The patient continued to maintain her saturations on room air. She was given monoclonal antibodies for COVID and treated with keflex for her UTI. OT evaluated the patient and recommended that she have home health PT. Care management helped arrange for this. The patient was given a prescription for keflex at discharge to complete her course of antibiotics. She was encouraged to follow up with her PCP for continued monitoring after discharge

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: DR CHEST SINGLE VIEW [340531708] Resulted: 09/12/21 1556 Order Status: Completed Updated: 09/12/21 1558 Narrative: EXAMINATION: Single View Chest EXAM DATE: 9/12/2021 2:21 PM TECHNIQUE: Single view chest INDICATION: cough, covid+ COMPARISON: Chest radiograph 4/19/2017 ENCOUNTER: Not applicable _________________________ FINDINGS: Multiple overlying leads. Heart is normal in size for technique. Atherosclerotic calcification of the aorta. Perihilar opacities are similar to prior study likely related to chronic change. Hazy medial left upper lobe opacity. No large pleural effusion or pneumothorax. Degenerative changes of the glenohumeral joints, progressed from prior study. Ovoid hyperdensity projecting over the right scapula, stable and related to dystrophic calcification when compared to prior CT. Degenerative changes of the spine with upper thoracic dextroscoliosis. _________________________ Impression: Hazy left upper lobe opacity may relate to summation artifact or consolidation. CT HEAD WITHOUT IV CONTRAST [340531711] Resulted: 09/12/21 1508 Order Status: Completed Updated: 09/12/21 1510 Narrative: EXAMINATION: CT Head without Contrast EXAM DATE: 9/12/2021 2:20 PM TECHNIQUE: Multiple axial noncontrast images of the brain were obtained and reformatted according to the standard protocol. QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: fall, head injury COMPARISON: None HAND DOMINANCE: Unknown ENCOUNTER: Not applicable ____________________ FINDINGS: Intracranial hemorrhage: None. Infarct/Vascular: No CT evidence of acute infarct. A few small areas of hypoattenuation are noted within the periventricular and subcortical white matter, nonspecific but consistent with mild chronic small vessel ischemic changes. Intracranial Mass: No evidence of intracranial mass. CSF Spaces: The ventricles, sulci, and cisterns are normal. Calvarium and Scalp: Unremarkable. Paranasal Sinuses and Orbits: Visualized paranasal sinuses are clear. Orbits are unremarkable. ____________________ Impression: 1. No acute intracranial abnormality. Procedure Component Value Ref Range Date/Time Urine Culture [340531718] (Abnormal) Collected: 09/12/21 1616 Order Status: Completed Specimen: Urine, clean catch Updated: 09/14/21 0831 Bacterial culture, urine >=100,000 CFU/mL Klebsiella pneumoniae Abnormal Susceptibility Klebsiella pneumoniae Not Specified Ampicillin Resistant Ampicillin/sulbactam Resistant Cefazolin Susceptible 1 Ceftriaxone Susceptible Ciprofloxacin Susceptible Gentamicin Susceptible Nitrofurantoin Susceptible Tobramycin Susceptible Trimethoprim/Sulfamethoxazole Susceptible 1 For uncomplicated UTIs due to E. coli, K. pneumoniae, and P. mirabilis, cefazolin predicts susceptibility to oral cephalosporins including cephalexin, cefpodoxime, cefprozil, cefdinir, and cefuroxime. Linear View COVID-19 PCR, Rapid [339140887] (Abnormal) Collected: 09/12/21 1258 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 09/12/21 1310 COVID-19 PCR Detected Abnormal Not Detected Comment: COVID-19 (SARS-CoV-2) test is positive. Clinical correlation with patient history and other diagnostic information is necessary to determine infection status. This test has received Emergency Use Authorization (EUA) by the FDA, but performance has not been evaluated for asymptomatic patients. Testing was performed using a nucleic acid amplification method. The specimen source may have been changed from the original order per patient situation or symptoms. Covid 19 Result Comment See Comment Comment: COVID-19 results reported as "detected" means COVID-19 positive. Positive patients should self-isolate for 10 days or 24 hours after fever resolves and other symptoms are improving, whichever is longer: - Stay home except to get medical care and wear a facemask if you must leave - Separate yourself from other people in your home, known as home isolation - Cover your coughs and sneezes - Wash your hands often - Avoid sharing household items - Clean high-touch surfaces everyday - If you have a medical emergency and need to call 911, notify dispatch personnel that you may have COVID-19 and put on a facemask before emergency medical services arrive. If the result is "inconclusive" or "invalid" and you have not been contacted by a medical professional from us about your result or if you have questions about COVID-19, your symptoms, or need a return to work/school note, please contact your primary care provider (PCP).
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory Nasal congestion Circulatory HTN (hypertension) Digestive GERD (gastroesophageal reflux disease) Diarrhea Infectious/Inflammatory UTI (urinary tract infection) COVID-19 Nervous Neuropathy Post-polio syndrome Essential tremor Genitourinary CKD (chronic kidney disease) Endocrine/Metabolic Hyperlipidemia Other Osteoarthritis Risk and functional assessment Edema Weakness
Andere Medikamente: Alpha-Lipoic Acid 200 MG TABS apoaequorin (PREVAGEN) 10 MG CAPS capsule atenolol (TENORMIN) 25 MG tablet B Complex Vitamins (VITAMIN B COMPLEX) TABS celecoxib (CELEBREX) 200 MG capsule Cholecalciferol (VITAMIN D3) 2000 UNITS TABS gabapentin
Allergien: Lisinopril [Ace Inhibitors]Cough Hydrocodone-acetaminophenGI Upset LisinoprilCough Meperidine Morphine Propoxyphene N-apapGI Upset Statins
Vorherige Impfungen: -

VAERS 1714949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 68,0
Geschlecht: M
Eingang: 20.09.2021
Impfdatum: 01.02.2021
Beginn: 01.06.2021
Tage bis Beginn: 120,0
Dosis: 1
Route/Site: - / -

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

Back pain Dyspnoea Fatigue Headache Palpitations

Symptomtext

Shortness of breath, heart palpitations, lower back pain, a feeling of exhaustion, and headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Suffered from a stroke - 2010 and 2018.
Andere Medikamente: -
Allergien: None.
Vorherige Impfungen: -

VAERS 1357956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 73,0
Geschlecht: F
Eingang: 18.09.2021
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Blood test Cardiac monitoring Echocardiogram Facial pain Fatigue Face oedema Facial discomfort Limb discomfort Mammogram Gait disturbance Mobility decreased Neck pain Pain Pain in extremity Muscle twitching Pain in jaw Peripheral swelling Swelling face

Symptomtext

quiver in her lip on the left side; soreness and swelling in my arm; Her right upper arm is swollen after getting her second COVID-19 Vaccine shot; her said her right upper arm is sore & swollen & feels like someone had fist bumped her; The right side of her face became swollen later in the day on 22Feb2021/Puffiness face; right sided facial edema going under her ear, where she reports a knot the size of a penny was noted; lobe and patient couldn't open her mouth without feeling pain; face was sore where the swelling is; if she tries to open her mouth, her mouth doesn't open as wide as it should. Her face has a TMJ like feeling; This is spontaneous report from a contactable consumer (patient). A 73-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; lot number: EL3247; expiration date: 31May2021) via an unknown route of administration in right arm on 22Feb2021 (Monday afternoon) between 15:30-16:00 (at the age of 73-year-old) as single dose for COVID-19 immunization at Hospital. Medical history of the patient included kidney stones from Nov2019, nosebleed in Jan2021. She said she woke up at 5:00 to go to the bathroom. She said when she stood up from the side of her bed, her nose wouldn't stop bleeding. She stated she doesn't remember exactly when she had gone to the Emergency Room for her nose bleed in Jan2021. No further details provided. Concomitant medications included Potassium Citrate started in Dec2020 taken for Kidney stones. Patient did not receive any Prior Vaccinations (within 4 weeks) of covid vaccine. Patient previously received Shingle vaccine in 2020 and received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; lot number: EN5318; expiration date: 31May2021) Intramuscular in right arm on 01Feb2021 as single dose for COVID-19 immunization. On 22Feb2021, later at night patient developed soreness and swelling in arm where she received the vaccine. She had swelling on the right side of face that she noticed later in the day on Monday and experienced right sided facial edema going under her ear, where she reports a knot the size of a penny was noted. The swelling was under eye to the cheek to right ear lobe and patient couldn't open her mouth without feeling pain. Patient have heard that some people have developed bells palsy after getting the vaccine. Patient spoke with her doctor and the doctor told to visit ER. The right side of her face was sore where the swelling is & if she tries to open her mouth, her mouth doesn't open as wide as it should. Her face has a TMJ like feeling. She clarified her right upper arm was sore and swollen and feels like someone had fist bumped her. On an unspecified date, not often but at times caller notices a quiver in her lip on the left side. She clarified she received the COVID-19 Vaccine in her right arm, and the swelling and soreness started on Monday night (22Feb2021). She said her right arm has improved, and her right arm now feels like it would if she were to get a regular flu shot in it. She said prior to today, her arm soreness felt like it was 5 times that of a flu shot. She said her right arm soreness and swelling didn't concern her. Reportedly, the right side of her face became swollen later in the day on Monday (22Feb2021). She clarified that the swelling started under her right eye and continued down her right cheek. She said the swelling continued from her right cheek to under the front of her right earlobe (where an earring would hang). She said the right side of her face was sore where the swelling was. She said if she tries to open her mouth, her mouth doesn't open as wide as it should. She said it is like a TMJ feeling. She said if she puts her finger in front of her right ear, and then opens her mouth, she can feel something. She said the right sided facial swelling and soreness has improved a little bit, but the right side of her face continues to be puffy with some swelling on 24Feb2021. She said she heard some people have a problem with Bells Palsy after getting the COVID-19 Vaccine. She said she called her doctor, and he told her to go the Emergency Room. She said she called the facility that administered both doses of the COVID-19 Vaccine to her, and the facility told her to go to the Emergency Room. She said it appeared that nobody wanted to get involved with helping her, so she figured she would call Pfizer. She said she was wondering if Pfizer had some type of treatment for her to try. She said the Emergency Room is very busy and she would probably have to wait 2-6 hours to get in to see a doctor, and she didn't want to wait around with a bunch of people who haven't been vaccinated for the COVID-19 Virus. Reported she has only had a mammogram in the last couple of weeks, and no other testing. Caller was advised by HCP to be seen in the ER. She was prescribed Prednisone for 3 days at ER but was advised by nurse with HCP to hold off on taking. Caller has been taking Tylenol. Edema has improved, continues to have a little facial puffiness. Outcome of the event quiver in her lip on the left side was unknown and for all other events was resolving. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Name: mammogram; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kidney stones; Nose bleed (she went to the Emergency Room for a nose bleed Jan2021.)
Andere Medikamente: POTASSIUM CITRATE
Allergien: -
Vorherige Impfungen: -

VAERS 1700633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 77,0
Geschlecht: F
Eingang: 15.09.2021
Impfdatum: 24.03.2021
Beginn: 12.08.2021
Tage bis Beginn: 141,0
Dosis: 2
Route/Site: - / -

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

Dyspnoea Mechanical ventilation

Symptomtext

Patient is currently in the hospital and is on a ventilator since yesterday. She stated she has no idea where she was exposed. Patient was brought to the hospital because she was having difficulty breathing. Patient is fully vaccinated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Lung Disease, Diabetes, Cardiovascular Disease, Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1696862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 04.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: IM / RA

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

Anxiety Arthralgia Asthenia Balance disorder Computerised tomogram Constipation Depression Diarrhoea Disturbance in attention Dizziness Ear discomfort Feeling abnormal Head discomfort Illusion Impaired work ability Insomnia Laboratory test Magnetic resonance imaging

Symptomtext

Continuous migraine with severe nausea, vomiting, imbalance, vertigo, unable to bend over, ear fullness, pressure in head and ears, jaw pain, ringing in ears, constipation & diarrhea (chronic), weakness, photophobia, increased neck/shoulder pain, perception, ocular migraines, dizziness, insomnia, unretractable pain, anxiety, increased depression, brain fog, inability to work, inability to concentrate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: 3,0
Labordaten: MRI 4/21, 6/21. 7/21. 8/21, MRV 4/21, CT 7/21, visual tests 3/21, 7/21, labs 4/21 6/21, 7/21, 8/21
Aktuelle Erkrankungen: headaches, body aches, stress
Vorgeschichte: OA, thoracic outlet syndrome, diarrhea, GERD, sleep apnea, hypothyroid, IIH, psoriasis, depression, insomnia,
Andere Medikamente: Synthroid 100mcg dly Calcium 500mg dly Prilosec 20mg dly Xiidra 1 gtt each eye BID Vit D3 10000 unit dly Biotin 5000mg dly Glucosamine 2100mg dly
Allergien: Sulfa (not sure true allergy told was as kid, had 2nd & 3rd generation without problem) Morphine (not sure problem was after surgery could be that or in combo with anesetha) Plaquenil
Vorherige Impfungen: -

VAERS 1692518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 17.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Mobility decreased Pain in extremity

Symptomtext

Severe arm pain with limited mobility; Severe arm pain with limited mobility; This is a spontaneous report from a non-contactable consumer(patient) or other non hcp. A 62-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3247) via an unspecified route of administration on 17Feb2021 (at the age of 62-year-old) as dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient did not receive COVID prior vaccination and was not tested for COVID-19. The patient experienced severe arm pain with limited mobility on 17Feb2021. Therapeutic measures were taken as a result of severe arm pain with limited mobility with Acetaminophen 650mg. Outcome of the events was unknown. No follow up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1689316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NM
Alter: 59,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 28.01.2021
Beginn: 01.09.2021
Tage bis Beginn: 216,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Cough Dyspnoea Influenza A virus test negative Influenza B virus test Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

some cough, congestion and shortness of brath; no other symptoms or concerns; high risk for complications

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Sept 2, 2021@13:38 FLU A (CEPHEID) NEGATIVE, FLU B (CEPHEID) NEGATIVE, RSV (CEPHEID) NEGATIVE _COVID-19 (CEPHEID) POSITIVEA
Aktuelle Erkrankungen: None
Vorgeschichte: Asynnetrical hearing loss, DM type 2, Hypercholesterolemia, HTN, Cardiomyopathy, Hx of stent for coronary Artery disease, chronic periodontitis, Acoustic neuroma, Vitamin D deficiency,
Andere Medikamente: Ascorbic Acid, Atorvastatin, guaifenesin, lisinopril, Metformin, Metoprolol, phenylephrine, Ticagrelor, Vitamin D3, Zinc
Allergien: None
Vorherige Impfungen: -

VAERS 1685613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 85,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 21.01.2021
Beginn: 31.08.2021
Tage bis Beginn: 222,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dyspnoea Oxygen saturation decreased Pneumonia SARS-CoV-2 test positive

Symptomtext

Presented to Emergency Room with shortness of breath and decreased O2 sats on pulse oximetry. Recently treated at Hospital twice over the past month. Received Ceftriaxone and Azithromycin at Hospital from 8/31-9/7/2021 for Pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID -19 rapid result positive 9/8/2021
Aktuelle Erkrankungen: -
Vorgeschichte: AFib, NSVT, COPD, Bronchiectasis, Prostate CA treated with XRT and ADT, Radiation Therapy, Squamous cell CA tongue, HCV treated in 2014,
Andere Medikamente: Abiraterone Acetate, Apixaban, Clonazepan, Ditiazem, Advair, Lopressor, Remeron, Pravastatin, Prednisone, Ramelteon
Allergien: Penicillin, Ragweed
Vorherige Impfungen: -

VAERS 1685473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 63,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 28.01.2021
Beginn: 27.08.2021
Tage bis Beginn: 211,0
Dosis: 1
Route/Site: IM / RA

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

Ageusia Anosmia Chills Cough Decreased appetite Diarrhoea Dyspnoea Fatigue Headache Myalgia Nausea Pyrexia

Symptomtext

fever, cough, SOB, loss of taste and smell, poor appetite, nausea, diarrhea, headache, fatigue, muscle aches and chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: idiopathic pulmonary fibrosis diabetes cardiac disease
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1684166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 09.09.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Dysgeusia Pain in extremity Paraesthesia

Symptomtext

Soar arm; taste of iron or metal in my mouth; tingling in arm/fingers; This is a spontaneous report from a contactable consumer (patient) who is a Pfizer colleague. A 39-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot number: EL3247, Expiration Date: not reported), via an unspecified route of administration, administered in left arm on 02Mar2021 at 13:15 (at the age of 39 years old) as dose number unknown, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient was not pregnant at the time of vaccination and prior to vaccination was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and has no list of any other medications received within 2 weeks of vaccination. On 02Mar2021 at 14:00, the patient experienced "Soar arm" (as reported), taste of iron or metal in her mouth and tingling in arm/fingers. No treatment was received for the adverse events. Since vaccination, the patient has not been tested for COVID-19. Outcome of all events was not recovered. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1683782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CT
Alter: 48,0
Geschlecht: M
Eingang: 08.09.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Chills Migraine Vaccination site pain

Symptomtext

Chills; Soreness at injection site; Headache (migraine like); This is a spontaneous report from a contactable consumer (Patient). A 48-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: EL3247), via an unspecified route of administration on 11Feb2021 10:30 AM (at the age of 48-year-old) as a dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medication were not reported. The patient did not receive any other vaccines within four weeks. Patient does not have COVID prior vaccination and was not tested to COVID post vaccination. Patient had no known allergies. On 12Feb2021 12:00 AM the patient experienced chills, Soreness at injection site, Headache (migraine like). Patient had not received any treatment for the events reported. The outcome of the events was recovered on unspecified date in 2021. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1676806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AR
Alter: 34,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Blindness C-reactive protein increased Chills Diarrhoea Dry eye Dry mouth Fatigue Feeling abnormal Fibromyalgia Haemorrhoids thrombosed Headache Migraine Nausea Pain Pyrexia Vaginal haemorrhage

Symptomtext

1/28/21, 2 hrs post vaccine: vaginal bleeding started, ended 3/12/21 despite continuing dura apri birth control daily. Last menstrual period was 6 days in June 2019. Birth control placebos are skipped to deter menstruation d/t endometriosis. 12 hrs post vaccine: nausea, diarrhea, migraine, low-grade fever (99.8), body aches and chills. Lasted 36 hrs post vaccine. On 2/3/21, I developed thrombosed hemorrhoids that didn't resolve until 2/26/21. Mild headaches daily until 3/12/21. Headaches continue to occur 4-7 days/wk to date. Other effects post vaccine continuing to date: constant mild-moderate aching in right wrist and elbow, daily severe fatigue, brain fog, dry eyes/mouth, eyesight deterioration (I have to get a revision on my lasik surgery)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Elevated CRP on 7/13/21 by PCP referred to rheumatologist. Elevated CRP by rheumatologist Dr. diagnosed me with fibromyalgia on 8/30/21
Aktuelle Erkrankungen: None
Vorgeschichte: Epilepsy, ADHD, PTSD, endometriosis, GERD, hx of migraines, seizures, neurocardiogenic syncope, malignant melanoma
Andere Medikamente: spironolactone, Adderall, lamotrigine, omeprazole, dura apri, multivitamin gummies, hair skin and nails gummies
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1675315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 47,0
Geschlecht: F
Eingang: 05.09.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Disturbance in attention Dizziness Echocardiogram Electrocardiogram Fatigue Feeling hot Heart rate increased Memory impairment Nausea

Symptomtext

Rapid heart rate. My heart heart rate goes as up as 202. I have chest pain, I feel very tired all the time. I feel dizzy, nauseous. I have a hard time remembering things. I have a hard time focusing. I feel hot at times. This has been happening since 1/27/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I have been to the emergency room several times. I seen three cardiologists and two electrophysiologists. I have EKGs, echo. I am taking taking beta blocker and Corlanor (ivabradine). I can't rememeber my appointment dates, but I can provide all my medical records.
Aktuelle Erkrankungen: COVID
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1674988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

moderat

Staat: CO
Alter: 74,0
Geschlecht: F
Eingang: 05.09.2021
Impfdatum: 18.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / RA

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

Anxiety Arthralgia Back pain Cough Dyspnoea Fatigue Feeling abnormal Herpes virus infection Immune system disorder Malaise Memory impairment Pain SARS-CoV-2 test negative Spirometry Vaginal infection Wound infection

Symptomtext

Long covid symptoms recurred--fatigue, cough, joint aches, body aches, herpes outbreak, back pain, anxiety, shortness of breath. Brain fog, forgetfulness, paper cuts became very infected for 2 weeks each, vaginal infections, I felt like my immune system had shut down, or become so overly active, it couldn't protect me against very minor infections. I did not have brain fog, brain inflammation before the vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid PCR test - negative Spirometry for asthma - breathing at 94%
Aktuelle Erkrankungen: Long Covid after Covid-19 in 3/9/2020 - improving
Vorgeschichte: Asthma - mild
Andere Medikamente: Famciclovir Omeprazole Famotadine Livalo
Allergien: Codeine
Vorherige Impfungen: -

VAERS 1670778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: WA
Alter: 71,0
Geschlecht: M
Eingang: 03.09.2021
Impfdatum: 25.02.2021
Beginn: 16.08.2021
Tage bis Beginn: 172,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Chest discomfort Dyspnoea Fatigue Headache Heart rate decreased Immediate post-injection reaction Musculoskeletal discomfort Oxygen saturation decreased

Symptomtext

Immediately after vaccine, no significant ones other than I reported on v-safe permanent a fib - my heart rate/vitals changed dramatically; usually I'm stable 115/75 BP normal to 100-110 - Pulse rate; dropped to as low as 39 pulse rates. Average heart rate was 78 and BP 124/74. The lowest being as low as 39 for heart rate. I had a little shortness of breath and my O2 saturation dropped to 90 a nd that happened over a couple of day period. Normally I can't even force it down to 94. I had general fatigue. Persistent headache - slight pulse rate is coming back up. At the beginning of the episode periodic discomfort at my left pec and shoulder. Increased anxiety levels with this - didn't trust me to go out to get the mail. Spoke with a doctor - did not see a doctor - the facility is two hours away; did it via message service. They decreased the Metoprolol to 50 mg, and they are monitoring it now. And then we'll examine it again. I am free to message them at any time. I have confirmed that I am feeling better as I am compliant with the decrease, and I will be getting back to them on Tuesday of next week. So, it's an ongoing monitoring process. The average on the Pulse rate is 64 now. Anxiety has come down - but I do still have some recognized fatigue - I'm easily fatigued. We're still maintaining self-quarantining - over this last year and a half. Not being very social at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: A Fib; Idiopathic Peripheral Neuropathy; Episodic Gout; Chronic low back pain
Andere Medikamente: Eliquis (Apixaban); Omeprazole; Atorvastatin; Diltiazem; Alopurinol; Metoprolol Succinate; Hydrocodone; Supplements: Iron; Vitamin D3; Daily Multi-Vitamin; Chromium; Ubiquinol; Glucosamine/Chondroitin; Tart cherry extract - natural anti-inf
Allergien: Augmentin - ankle rash
Vorherige Impfungen: -

VAERS 1662986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 48,0
Geschlecht: M
Eingang: 01.09.2021
Impfdatum: 26.01.2021
Beginn: 10.08.2021
Tage bis Beginn: 196,0
Dosis: 1
Route/Site: SYR / UN

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

COVID-19 pneumonia Diarrhoea Malaise Nausea Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

patient was admitted to the hospital on 8/10 @4am. His diagnosis is COVID Pneumonia. She stated his symptoms began on 8/4 with fever and body aches and diarrhea and nausea. She said he went to be tested on 8/6 and tested negative but was very sick with symptoms. then tested again and was positive on 8/10. She stated he has a history of Diabetes and hypertension and has Obesity

Weitere VAERSDATA-Felder

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

VAERS 1662750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 02.02.2021
Beginn: 27.08.2021
Tage bis Beginn: 206,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Fatigue Hypotension Infection SARS-CoV-2 test positive

Symptomtext

COVID breadthrough first vax 1/12/2021 . 87-year-old female admitted from rehab seen by MD at the Health Center for hypotension and generalized fatigue and tiredness. Initially the plan was to have her go to the emergency room and be placed in outpatient observation for IV regeneron infusion however, she started having hypoxia in the emergency room and therefore she was placed in inpatient unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: COVID + 8/27/2021
Aktuelle Erkrankungen: -
Vorgeschichte: coronary artery disease, hypertension, esophagitis, madular degeneration, a fib, hip replacement
Andere Medikamente: -
Allergien: ceclor, ceftin, dilaudid, hydrocodone
Vorherige Impfungen: -

VAERS 1661430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CT
Alter: -
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 24.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Headache Lethargy Migraine Myalgia Nausea Thirst

Symptomtext

lethargy; Joint pain/aches; muscle pain; headache/migraine; nausea; headache/migraine; persistent thirst; This is a spontaneous report from a contactable consumer (patient). A 31 years old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EL3247), via an unspecified route of administration in Left Arm on 24Feb2021 at 13:15 as a Dose 2, single for COVID-19 immunization. The patient's medical history included Heart murmur, history of lyme disease, kenyan tick typhus, known allergies to Sulfa drugs, red dye. The patient's concomitant medication(s) included biotin supplement, melatonin, Multivitamin (unspecified) within two weeks after vaccination. Facility type vaccine was reported as Other. The patient had no Covid infection prior vaccination. The patient was not tested to Covid post vaccination. The patient had not received any other vaccine four weeks prior to Covid-19 vaccination. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247) via an unspecified route of administration in Left arm on 04Feb2021 at 09:00 AM, as a Dose 1, Single for COVID-19 immunization. On 25Feb2021 at 11:00, the patient had experienced lethargy, joint pain/aches, muscle pain, headache/migraine, nausea, persistent thirst. No treatment received for resulted events. The outcome of the events was recovered on an unknown date in 2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Red dye allergy); Heart murmur; Lyme disease; Sulfonamide allergy; Typhus
Andere Medikamente: BIOTIN; MELATONIN
Allergien: -
Vorherige Impfungen: -

VAERS 1658871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: FL
Alter: 93,0
Geschlecht: M
Eingang: 31.08.2021
Impfdatum: 25.01.2021
Beginn: 13.08.2021
Tage bis Beginn: 200,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 COVID-19 pneumonia Hypoglycaemia Hypoxia Malaise SARS-CoV-2 test positive

Symptomtext

8/14/2021 Admitted. Sick at home x 7-10 days. He was found to have severe hypoglycemia by ambulance. He was screened with COVID testing, which turned out to be positive. Hypoxic, Admitted to COVID unit. Diagnosed with: Coronavirus pneumonitis Note: previously received COVID-19 Pfizer Vaccine: First dose: 01/04/21 Lot Number EL1284; Second dose: 01/25/21 Lot Number EL3247 8/17/21: patient discharged

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: 8/14/2021 SARS CoV 2 PCR COVID19 detected
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, HTN, DM 2, GERD, Pacemaker, COPD, hypothyroidism
Andere Medikamente: Doxycycline, hydrocortisone, synthroid, metoprolol, prilosec,
Allergien: Avandia, Januvia
Vorherige Impfungen: -

VAERS 1653590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

moderat

Staat: IL
Alter: 24,0
Geschlecht: F
Eingang: 29.08.2021
Impfdatum: 28.08.2021
Beginn: 28.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Nausea Pallor Pyrexia Tremor

Symptomtext

Shivering, trembling 101.2 degrees Fahrenheit fever Pale lips and face Temporary spots on right hand Nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Possibly fibromyalgia or similar illness (still testing with rheumatologist) that started developing recently. Experiences flair-ups of pain at random times and after strenuous labor.
Vorgeschichte: Hashimoto?s hypothermia Eczema Low blood pressure
Andere Medikamente: Levothyroxine 88 mcg Duloxetine 60 mg Methylprednisolone 4 mg
Allergien: Penicillin Some fruits Tree nuts Peanuts Cinnamon Silicone Soy Chocolate
Vorherige Impfungen: -

VAERS 1652776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CT
Alter: 60,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 05.03.2021
Beginn: 22.04.2021
Tage bis Beginn: 48,0
Dosis: 1
Route/Site: - / LA

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

Palpitations

Symptomtext

palpitations, heart racing only at night; This is a spontaneous report from a contactable consumer reporting for herself. A 60-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EL3247; Expiration date was not reported), via an unspecified route of administration, administered in Arm Left on 05Mar2021 15:00 (at the age of 60-years-old) as dose 1, single for covid-19 immunization at other facility. The patient was not pregnant at the time of vaccination. Medical history included gastrooesophageal reflux disease (severe acid reflux disease, GERD) from an unknown date and unknown if ongoing. Concomitant medications in 2 weeks included esomeprazole sodium (NEXIUM) and levothyroxine taken for an unspecified indication, start and stop date were not reported. Known allergies, other vaccine in four weeks, covid prior vaccination included none. The patient experienced palpitations, heart racing only at night on 22Apr2021 00:30 (12:30 AM). The patient did not receive any treatment for the event. The patient underwent lab tests and procedures which included SARS-COV-2 test: negative on 03May2021 (covid test post vaccination). Clinical outcome was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210503; Test Name: COVID 19; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD
Andere Medikamente: NEXIUM [ESOMEPRAZOLE SODIUM]; LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1648497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MA
Alter: 25,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 25.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Body temperature Fatigue Migraine Pain Pyrexia

Symptomtext

heavy migraine; full body soreness; a fever over 100 F; fatigue; loss of strength; This is a spontaneous report from a contactable 25-year-old male consumer reported for himself that received second dose of bnt162b2 (BNT162B2, Formulation was Solution for injection, Lot Number EL3247), dose 2 via unspecified route in left Arm on 25Feb2021 10:00, as dose 2, single for COVID-19 immunization (age at time of vaccination 25 years). The patient medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (BNT162B2, Formulation was Solution for injection, Lot Number EL3247), dose 1 via unspecified route in left Arm on 04Feb2021 10:00, as dose 1, single for COVID-19 immunization. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed COVID-19. Since the vaccination, the patient was not tested for COVID-19. On 26Feb2021 02:45 AM the patient experienced a heavy migraine, full body soreness, a fever over 100 F, fatigue, and loss of strength. The patient was did not received treatment for the adverse event. On 26Feb2021 he had lab test Body temperature result was fever over 100 F. The outcome of all events was unknown. No follow up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20210226; Test Name: body temperature; Result Unstructured Data: Test Result:over 100 Fahrenheit; Comments: fever over 100 F
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1648060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 08.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Chills Feeling cold Nausea Tremor

Symptomtext

Real bad chills; Nausea; Weakness; shaking; get real cold; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247), via an unspecified route of administration in left arm on 08Feb2021 (at the age of 69-year) as dose 1, single for COVID-19 immunisation (didn't want to catch it. Was up in age thought she needed it). Medical history included eye surgery three weeks ago from "yesterday" to an unknown date. There were no concomitant medications. The vaccine was not administered at facility. Investigation assessment was not provided. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient had first COVID-19 Vaccine on Monday (08Feb2021). Did alright until early "this" morning. Wanted to know if it was natural for this to happen. Was having real bad chills, nausea, and feeling weak. She was started to experience nausea, real bad chills, and weakness around 09:00-10:00 this morning. She was started get real cold and put a heating pad in her bed. She was shaking. Was alright until she took the shot. Assuming it was side effects of the shot. The outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Surgery (have eye surgery three weeks ago from yesterday)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1647611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 28,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 09.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Body temperature Chills Cold sweat Fatigue Pyrexia Tremor

Symptomtext

Chills; shakes; Slight fever (99.6 F); moderate fatigue; cold sweating; This is a spontaneous report from a contactable consumer (patient). A 28-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EL3247, and Expiration date: Unknown), via an unspecified route of administration, administered in left arm on 09Feb2021 11:00 (at the age of 28-year-old) as dose 2, single for COVID-19 immunization. The patient medical history included one Kidney (his kidneys fused pre birth, fully funcitonal) and shellfish allergy. The concomitant medications for the patient were not reported. Previously the patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EL3247, and Expiration date: Unknown), via an unspecified route of administration, administered in left arm on 19Jan2021 09:00 AM (at the age of 28-year-old) for COVID-19 immunization. The patient did not receive other vaccine in four weeks. The patient did not receive other medication in two weeks. The patient did not have COVID prior vaccination. The patient was not tested for COVID post vaccination. On 09Feb2021 23:00, the patient experienced chills, shakes, slight fever (99.6 F), moderate fatigue, and cold sweating. No treatment was given for the events. The outcome of the events was reported as resolving. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20210209; Test Name: Body temperature; Result Unstructured Data: Test Result:99.6 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kidney disorder; Shellfish allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1647565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MA
Alter: 36,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 09.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Migraine Pain

Symptomtext

Severe migraine; Body aches; This is a spontaneous report from a contactable consumer (patient). A 36-year-old male patient received BNT162B2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247), via an unspecified route of administration, administered in left arm on 09Feb2021 (at the age of 36-year-old) as dose 1, single for COVID-19 immunisation. Medical history included tested positive for COVID on 30Dec2020. concomitant medication was not reported.There were no other products. On 10Feb2021 at about 11-12 patient had developed body aches and a severe migraine. The body aches were off and on, sometimes he felt them and sometimes he did not, but they were persisting. The migraine was constant (at the time of report). Outcome of the events were not resolved. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 virus test positive (Suspect product: Indication: He had tested positive for COVID back on 30Dec2020)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1632390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 61,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 03.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: SYR / LA

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

Arthritis Condition aggravated Joint warmth Pain Swelling

Symptomtext

Beginning in March began having more severe arthritis flare ups than usual (pain, swelling, hot joints) may have no connection to vaccine. Maybe it's an age thing. Usually have minor flareups that do not affect working however have had 3+ since March. I plan to get the booster as soon as possible

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: arthritis
Andere Medikamente: Tylenol, ibuprofen, vitamin d, aspirin, Allegra
Allergien: Cipro, codeine
Vorherige Impfungen: -

VAERS 1624029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 82,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 20.01.2021
Beginn: 16.08.2021
Tage bis Beginn: 208,0
Dosis: 2
Route/Site: IM / -

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

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

Symptomtext

Received Postive Covid-19 test results. Admission to Hospital for diagnosis that included cough, shortness of breath, pneumonia. Per notification, patient has not been admitted to an intensive care unit and has not required any mechanical ventilation during hospitalization to date. It is unknown if he has been discharged from the hospital at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: 8/16/21 RT PCR Positive at clinic 8/23/21 RT PCR Positive at hospital (upper respiratory sample)
Aktuelle Erkrankungen: Not specified
Vorgeschichte: none reported
Andere Medikamente: Not specified
Allergien: Not specified
Vorherige Impfungen: -

VAERS 1617420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 24.02.2021
Beginn: 28.07.2021
Tage bis Beginn: 154,0
Dosis: 2
Route/Site: IM / LA

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

Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Echocardiogram Extra dose administered Fatigue Lung consolidation Oedema peripheral Oxygen saturation decreased SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient required hospitalization due to breakthrough infection. She received Pfizer vaccine (third dose in series) on 02/24/2021. Hospitalized from 07/28/21 - 07/30/21. Below is copied from discharge summary: Patient is a 79 y.o. female with a pmh of sigmoidal colon cancer (s/p colostomy 2019, chemoradiation 2020, currently on IV 5-FU and Avastin), multiple myeloma (on Revlimid), CKD, HTN and hx of PE (2020, Eliquis 5 BID) presents to ED for several days of fatigue. She was found to be COVID + in ED with desaturations to the mid 70's and was started on 3L NC. She was admitted to medicine for management and evaluation of COVID-19 pneumonia. Patient was started on antibiotics since she had a questionable R sided consolidation on CXR, as well as methylprednisolone and Lipitor. Patient also presented with bilateral LEx edema of unknown etiology. BNP was elevated from previous 547 (2020) to 800, TTE was unchanged from prior. Patient was started on Lasix 40 qd. PT was consulted and worked with patient, noting desats to 85, recommending patient be discharged with full time assistance (daughter), home health care and home O2. Patient was stable for d/c on 7/30.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: SARS-COV-2, NAA, Detected on 07/28/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia Hypertension Malignant neoplasm of sigmoid colon 10/3/2019 Multiple myeloma
Andere Medikamente: ACETAMINOPHEN (TYLENOL) 325 MG PO TABLET Take 3 tablets by mouth every 6 hours for 14 days. APIXABAN (ELIQUIS) 5 MG ORAL TABLET Take 1 tablet by mouth 2 times daily. ATORVASTATIN (LIPITOR) 40 MG PO TABLET CARVEDILOL (COREG)
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1602558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 51,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 14.01.2021
Beginn: 18.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Blood test normal Electrocardiogram normal Fluid retention Full blood count normal Heart rate increased Metabolic function test Palpitations Swelling

Symptomtext

4 days after receiving the first dose of COVID 19 vaccination, I experienced rapid heart beat and elevated blood pressure and noted swelling/fluid retention. After 2 days I took hydrochlorathiazide 25 mg for 2 days and then 12.5 mg for 2 days. My blood pressure came back down but my heart pounded in my chest for about 8 weeks. I finally went to my doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 03/24/2021 EKG, CBC, CMP, Thyroid bloodwork - All WNL
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid, B12, Vit D
Allergien: Zithromax, Naprosen
Vorherige Impfungen: -

VAERS 1587124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NM
Alter: 57,0
Geschlecht: F
Eingang: 19.08.2021
Impfdatum: 29.01.2021
Beginn: 14.08.2021
Tage bis Beginn: 197,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Chest X-ray abnormal Dyspnoea Fatigue Lung infiltration Lung opacity Pain SARS-CoV-2 test positive Total lung capacity decreased

Symptomtext

8/13/2021 Complaining of shortness of breath, fatigue and body aches x 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 8.14.2021 Cov19 Fluab RSV PCR- abnormal; notable for the componets, Covid-19 result Detected. 8/14/21: XR: impression: low lung volumes with minimal linear opacities in the rt. midlung which could represent bronchovascular crowding versus early infiltrate.
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, hypothyroidism, Asthma, Rheumatoid arthritis, Lupus erythematosus, GERDs,
Andere Medikamente: Acetaminophen/Oxycodone, Albuterol inhaler, Aspirin 81 mg, calcium, cyclobenzaprine, folic acid, hydroxychloroquine sulfate tabs, ibuprofen, levothyroxine, loratadine, losartan, montelukast, omeprazole, pilocarpine, predisone, sodium bicarb
Allergien: Leflunomide metrotrexate
Vorherige Impfungen: -

VAERS 1586895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 35,0
Geschlecht: F
Eingang: 19.08.2021
Impfdatum: 30.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Blood oestrogen Chest pain Computerised tomogram Computerised tomogram head Erythema Hemiparesis Impaired work ability Laboratory test Magnetic resonance imaging head Magnetic resonance imaging neck Migraine Nerve conduction studies Skin burning sensation Tinnitus Ultrasound Doppler Urine organic acid test Urticaria

Symptomtext

5 days after 2nd vaccine I developed my first migraine ever. They then went on to persist until this day 4-5x a week around 2am and I developed pulsatile tinnitus. I also started reacting to foods I?ve never reacted to with red burning skin and hives. I have photos. These symptoms prompted visit to ER, neurologist, cardiologist for testing including head MRI, neck MRI, carotid ultrasound, ct scan of head and a slew of medications to help control my migraines that did not work. I?ve had to cut out all histamine foods and histamine releasing foods, gluten, eggs, dairy and I stopped working my full time job as an RN May 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 2/22/2021- ct scan and a lot of labs at the ER for chest pain and 1 R sides weakness I?ve been getting since migraines. Head CT to r/o MS or other causes 3/30/2021- head mri w contract looking for cause of new onset migraines and pulsatile tinnitus 4/13/2021- nerve conduction test for right sided weakness and tingling or arm and face 4/20/2021- carotid u/s to look for cause of pulsatile tinnitus 5/18/2021- neck mri to see if neck was causing migraines 5/2021- oats test, hair tissue mineral analysis, hormone panel, food sensitivity test to try and find cause of migraines
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid arthritis since 2019
Andere Medikamente: Humira and methotrexate which I stopped the week before and after each vaccine per my rheumatologist
Allergien: None at the time, a lot food sensitivities post vaccine
Vorherige Impfungen: -

VAERS 1583136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 72,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 01.02.2021
Beginn: 12.07.2021
Tage bis Beginn: 161,0
Dosis: 2
Route/Site: SYR / UN

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

COVID-19 Cough Dyspnoea Pyrexia

Symptomtext

Pt was hospitalized at for COVID-19 from 07/13/2021-08/05/2021. Updated symptoms and pre-existing medical conditions per medical records. Pt experienced shortness of breath, fever and cough. Pt has hypertension, dyslipidemia, COPD, hypothyroidism, and dementia. Per medical records, family found out that one of the pt's visiting granddaughters was found to be positive for COVID-19, so the family brought the pt to the hospital for further management. Per medical records, pt was seen and examined on day of discharge in stable condition and transferred to Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 24,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Dementia, Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1582332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 78,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 23.01.2021
Beginn: 16.08.2021
Tage bis Beginn: 205,0
Dosis: 1
Route/Site: IM / -

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

Asthenia COVID-19 Chills Dehydration Fatigue SARS-CoV-2 test positive

Symptomtext

Received notification that patient was admitted to the hospital for weakness, fatigue, and chills. Positive COVID 19 test result at the Hospital. Reported that patient was admitted for 1 day d/t dehydration and has been discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: 8/16/21 RT-PCR positive via upper respiratory sample
Aktuelle Erkrankungen: Not specified
Vorgeschichte: Diabetes Mellitus
Andere Medikamente: Not specified
Allergien: Not specified
Vorherige Impfungen: -

VAERS 1578068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 72,0
Geschlecht: M
Eingang: 17.08.2021
Impfdatum: 23.02.2021
Beginn: 12.07.2021
Tage bis Beginn: 139,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cough Dyspnoea Pyrexia

Symptomtext

Patient hospitalized due to COVID-19. Patient is fully vaccinated. Patient had fever, cough, shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 23,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, dyslipidemia, COPD, hypothyroidism, dementia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1574012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NE
Alter: 60,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 19.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Chest pain Dysphagia Fatigue Feeling abnormal Hyperhidrosis Lymphadenopathy Mobility decreased Muscle tightness Speech disorder

Symptomtext

Swollen lymph nodes under right arm and into right side of neck within a few days of vaccine. 2 weeks after 2nd vaccine - had episode of chest pain, severe diaphoresis, then severe weakness and inability to speak or move but still aware of surroundings. Lasted about 10-15 mins. Had fatigue and mental fog for at least 24 hrs after. Have had a total of 4 of these episodes with the last 2 including additional symptoms of muscle tightness in jaw and neck, difficulty swallowing. Have had multiple tests including cardiac work up. Cleared by cardiologist. Then started Neuro work up - EEG was abnormal so referred to Doctor. After last episode on 08/15 went to ER per Doctor to have Prolactin level drawn. Waiting on results that should confirm if these are new onset seizures. Being referred to an Epileptologist also for further testing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, Stress/Echo, Cardiac labs done in March/April EEG, Brain MRI, labs done in July
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pro-biotic, low dose ASA, Claritin, Vit D, Calcium, Biotin, B-Complex
Allergien: Vistaril, amlodipine
Vorherige Impfungen: -

VAERS 1536206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 59,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 12.01.2021
Beginn: 02.04.2021
Tage bis Beginn: 80,0
Dosis: 2
Route/Site: SYR / LA

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

Bursitis Computerised tomogram Injected limb mobility decreased Injection site pain Magnetic resonance imaging Neck pain Rotator cuff syndrome

Symptomtext

Had reaction in left arm? shoulder to neck?. Shoulder BLEW UP on me on APRIL 02 ?. 2021. Say Dr TORN or RIPPED ROTARY CUP and ligaments?. .. Had mri or catscan .. Sent me to ORTH SURGERY? told bursitis ?. Here we are 6 months later and I care BARELY USE my left arm. CONSTANTLY IN PAIN FROM NECK THRU SHOULDER INTO ARM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: MRI or CT on 04/23/2021
Aktuelle Erkrankungen: HIV+. 40 years
Vorgeschichte: HIV+ 40 years
Andere Medikamente: Genvoya ?. Bactrim?. Aspirin Atorvastatin Calcium? Sea Kelp ? C OMEGA -3. Vitamin D ? medical cannabis
Allergien: NOT APPLICABLE
Vorherige Impfungen: -

VAERS 1536008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 74,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 26.01.2021
Beginn: 05.08.2021
Tage bis Beginn: 191,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Cough Dizziness Dyspnoea Fall SARS-CoV-2 test positive Sepsis

Symptomtext

Admitted to Hospital on 8/5/2021 for cough/dizzy/fall/SOB and sepsis. COVID-19 test was positive upon admission. RT-PCR was performed. Hospital reported that he was not admitted to the ICU, did not require mechanical ventilation and did not expire from the illness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: Nasopharyngeal swab RT-PCR postive for COVID-19 8/5/2021. No other tests/laboratory results were reported.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Diabetes Mellitus
Andere Medikamente: Information not available
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1530624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 06.08.2021
Impfdatum: 09.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Dyspnoea Feeling hot Hyperhidrosis Maternal exposure during pregnancy Tachycardia

Symptomtext

Feeling of shortness of breath; Tachycardia; Sweating; Hot; Pregnant/ Gestational period: 16; This is a spontaneous report from a contactable nurse (patient). This is a maternal report. A 34-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EL3247), via intramuscular, administered in left arm on 09Feb2021 14:15 (at the age of 34-year-old) as dose 1, single dose for COVID-19 immunisation. Medical history included pregnant and COVID-19 from an unknown date. Patient had no known allergies. Other vaccine included in two weeks doxylamine succinate, pyridoxine hydrochloride (DICLEGIS). The patient did not receive other vaccine in four weeks. Post vaccination, the patient had not been tested for COVID. On 11Feb2021 at 08:00, patient experienced feeling of shortness of breath, tachycardia, sweating, hot. Treatment was not received in response to the events. The mother reported she became pregnant while taking bnt162b2. The mother was 16 Weeks pregnant at the onset of the event. The mother was due to deliver on 24Aug2021. Outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Pregnant
Andere Medikamente: DICLEGIS
Allergien: -
Vorherige Impfungen: -

VAERS 1528731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 31,0
Geschlecht: M
Eingang: 05.08.2021
Impfdatum: 09.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain

Symptomtext

After the first dose of the Pfizer vaccine I noticed some mild chest pain that mostly resolved with 325mg acetaminophen and 200mg ibuprofen. However, after the second dose, the chest pain was severe two to three days following the vaccination dose, so much so that it did not adequately resolve with acetaminophen or even with 800mg ibuprofen TID. At the point when I decided the pain was severe I determined that if it worsened, I would seek medical care. However the next morning, the pain was improving and I did not seek immediate care. By the next day the pain had resolved entirely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None - I did not seek medical care at the time.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypoglycemia
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1528260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 01.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Arrhythmia

Symptomtext

Prolonged arrhythmia episodes starting after 1st dose; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), intramuscular, administered in arm left in Feb2021 12:00 (Batch/Lot Number: EL3247) (at the age of 67-years-old) as dose 1, single for covid-19 immunisation. The patient was not pregnant at the time of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Facility where the most recent COVID-19 vaccine was administered in a hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and did not receive any other medications within 2 weeks of vaccination. Medical history included thyroiditis, non-specified atopic dermatitis and allergies: fragrances used in cosmetics/cleaning products. There were no concomitant medications. The patient previously took melaleuca alternifolia oil (TEA TREE OIL) and experienced allergies: tea tree oil. The patient experienced prolonged arrhythmia episodes starting after first dose on 12Mar2021. It was unknown if this will be permanent. The patient considered the report as serious. Did not results in death, not medically significant, not life threatening, did not cause/prolong hospitalization, not disabling/incapacitating, no intervention required and no congenital anomaly/birth defect. There was no treatment for the event. The outcome of the event was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atopic dermatitis; Fragrance sensitivity; Thyroiditis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1522861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: PA
Alter: 60,0
Geschlecht: M
Eingang: 03.08.2021
Impfdatum: 15.01.2021
Beginn: 28.07.2021
Tage bis Beginn: 194,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea paroxysmal nocturnal Facial pain Lacrimation increased Nasal congestion Non-tobacco user Paranasal sinus discomfort Rhinorrhoea SARS-CoV-2 test positive Sinus disorder Sinus pain

Symptomtext

Chief Complaint Patient presents with ? Cough ? Sinus Problem facial pain, PND, sneezing, watery eyes x 3 days. OTC Tylenol and Benadryl. HPI Patient is a 61 y.o. M presenting today for evaluation of sinus symptoms x 3-4 days. He states that he is having nasal congestion, sinus pain/pressure, rhinorrhea, cough, watery eyes. No fevers, V/D, ear pain, sore throat. He has been taking Tylenol and benadryl. No sick contacts. No hx of COVID-19, but he is fully vaccinated. No hx of asthma or COPD. Nonsmoker.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea paroxysmal nocturnal
Hospital-Tage: -
Labordaten: 07/31/21 1244 POCT COVID-19 PCR Collected: 07/31/21 1243 | Final result | Specimen: Swab from Nares POC COVID-19 PCR DetectedAbnormal Lot # 1000271669 Point of Care COVID-19 PCR Testing Method Cepheid Lot Expiration Date 06/05/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Right lower quadrant abdominal pain Endocrine/Metabolic Lactic acidosis Hematologic Leukocytosis Other S/P colonoscopic polypectomy Anxiety
Andere Medikamente: albuterol HFA (PROVENTIL;VENTOLIN) 90 mcg/actuation inhaler ALPRAZolam (XANAX) 0.5 mg tablet amoxicillin-pot clavulanate (AUGMENTIN) 875-125 mg per tablet BYSTOLIC 5 mg tablet desvenlafaxine (PRISTIQ) 100 mg 24 hr tablet diphenoxylate-atrop
Allergien: Contrast [Iodinated Contrast Media]Rash
Vorherige Impfungen: -

VAERS 1518202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Fatigue Pain in extremity Paraesthesia

Symptomtext

On 3/16/21: Sore left arm; body tingling (hard to describe); tired; This is a spontaneous report from a contactable consumer. This 45-year-old Female consumer (patient) reported for herself patient received second dose of BNT162B2 (Pfizer, Formulation: Solution for injection, Lot number: EL3247, Expiry date: unknown), via an unspecified route of administration in the left arm on 16Mar2021 at 10:45 AM as dose 2, single for COVID-19 immunization. Patient historical vaccine included received second dose of BNT162B2 (Pfizer, Formulation: Solution for injection, Lot number: EL3247, Expiry date: unknown), via an unspecified route of administration in the left arm on 23Feb2021at 10:00 AM as dose 1, single for COVID-19 immunization. Patient medical history included pre-diabetes, glucose tolerance impaired. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient did not receive other vaccine in four weeks and other medications in two weeks. The patient had no known allergies. patient was not tested for Covid post vaccination. Patient had not covid prior vaccination. On 16Mar2021 at 11:45 AM patient experienced sore left arm, body tingling (hard to describe), tired. Patient did not receive any treatment during or after event. The outcome of the event was recovered in Mar 2021. Follow-up (22Mar2021) This is a follow up spontaneous report in response to mail trail sent regarding the confirmation of below mentioned query. This reported included that. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1487259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: -
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / RA

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

Abdominal pain upper Condition aggravated Diarrhoea Nausea Salivary hypersecretion

Symptomtext

Began experiencing persistent nausea; This is a spontaneous report from a contactable consumer. A 41-year-old female patient received bnt162b2 (BNT162B2 PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number: UNKNOWN), via an unspecified route of administration on an unspecified date as dose 2, single for COVID-19 immunisation. The patient medical history was not reported. The concomitant medications of the patient included lithium taken for an unspecified indication. The patient historical vaccine includes first dose of BNT162B2 on an unspecified date as single dose for COVID-19 immunisation and experienced nausea, a big loss of appetite for a few days and indigestion/stomach bug. The patient reported that 3 weeks after second COVID vaccine dose, she experienced persistent nausea. She had the nausea for 24 days. She stated this was exactly what happened after her first vaccine dose (which she also reported on 22 days of nausea). The outcome of the event was reported as unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Weitere VAERSDATA-Felder

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

VAERS 1500617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CO
Alter: 26,0
Geschlecht: M
Eingang: 24.07.2021
Impfdatum: 19.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Anosmia COVID-19 Drug ineffective Dyspnoea Nasal congestion Pyrexia

Symptomtext

Contracted COVID-19 symptomatically; contracted the COVID-19 virus and its symptomatic with the virus now; Contracted COVID-19 symptomatically; contracted the COVID-19 virus and its symptomatic with the virus now; Fever; Congestion; Shortness of breath; Lost sense of smell; This is a spontaneous report from a contactable consumer. A 27-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 19Jan2021 (Lot Number: EL3247, Expiration date: 31May2021) at the age of 26 years as single dose, and dose 1 via an unspecified route of administration, administered in Arm Left on 29Dec2020 (Lot Number: EH9899, Expiration date: 31Mar2021) at the age of 26 years as single dose, for covid-19 immunisation. The patient medical history was not reported. Concomitant medications included multivitamin like is generic multivitamin of men, a chewable Vitamin D3, and L-Lysine. On unspecified date the patient contracted covid-19 symptomatically; contracted the covid-19 virus and its symptomatic with the virus now, experienced fever, congestion, shortness of breath, lost sense of smell. Therapeutic measures taken as a result of the event contracted covid-19 symptomatically, included Sudafed 120 mg once a day and Ibuprofen 400 mg twice a day first 3 days. The outcome of the events was unknown. Subsequently Product Quality Complaint Group provided the following conclusions: Conclusion: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot EH9899 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EH9899, fill lot EH9783, and the formulated drug product lot EH9782. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Conclusion: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot EL3247 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EL3247, fill lot EL3230, and the formulated drug product lot EL3223. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: VITAMIN D3; L-LYSINE [LYSINE]
Allergien: -
Vorherige Impfungen: -

VAERS 1493754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 95,0
Geschlecht: M
Eingang: 22.07.2021
Impfdatum: 04.02.2021
Beginn: 20.07.2021
Tage bis Beginn: 166,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cardiac failure congestive Dyspnoea Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

Direct exposure to Covid positive resident during dining. He is on Hospice due to CHF and sob

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Tested Covid positive 7/20/21
Aktuelle Erkrankungen: No acute illness
Vorgeschichte: Atrial fib, CAD, chronic diastolic heart failure
Andere Medikamente: Acetaminophen, apixaban, clopidogrel, atrovastatin, colace, Esomeprazole magnesium, Fomasterode, gabapentin, isosorbide mononitrate, levothyroxine, lisinopril, lorazepam, metoclopramide hydrochloride, metoprolol succinate, polyethelene glyc
Allergien: N/K
Vorherige Impfungen: -

VAERS 1482096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 42,0
Geschlecht: M
Eingang: 18.07.2021
Impfdatum: 24.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Myalgia Tremor

Symptomtext

Muscle pain; tremor; This is a spontaneous report received from a contactable consumer, the patient. A 42-year-old male patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: EL3247) via an unspecified route of administration on the left arm on 24Mar2021 at 10:00 (at the age of 42-year-old) as a single dose for COVID-19 immunisation. Medical history was not reported. The patient was not allergic to medications, food or other products. Concomitant medications were not reported. The patient did not receive any other vaccine within four weeks of receiving the second dose COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: Unknown) via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunisation. The patient experienced muscle pain and tremor on 24Mar2021 at 22:00. The patient did not receive any treatment for the reported events. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The clinical outcome of the event muscle pain and tremor was resolving at the time of reporting. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1481896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL-3247

moderat

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 18.07.2021
Impfdatum: 23.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Hypoaesthesia Paraesthesia Paraesthesia oral

Symptomtext

Development of right index finger tingling; left leg numbness; left great toe tingling/Faint tingling right great toe; Developed lower lip and tip of tongue tingling post vaccination; Developed lower lip and tip of tongue tingling post vaccination; This is a spontaneous report from a contactable Nurse (patient). A 39-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection; Batch/Lot Number: EL-3247), via an unspecified route of administration, administered in Arm Left on 23Jan2021 09:30 (age the age of 39-year-old) as single dose, for covid-19 immunization in hospital. The patient medical history was not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient had no known allergies. The patient sis did not receive any other vaccine in four weeks. Concomitant medications included ethinylestradiol, ferrous fumarate, norethisterone acetate (MICROGESTIN FE); cyanocobalamin (VITAMIN B12 [CYANOCOBALAMIN]), and multivitamin. On 23Jan2021 10:00 (after receiving vaccine at 09:33 am), the patient experienced developed lower lip and tip of tongue tingling post vaccination. On 25Jan2021 20:30, the patient experienced left leg numbness and left great toe tingling/faint tingling right great toe while development of right index finger tingling on 26Jan2021. At 10:00 am, Developed lower lip and tip of tongue tingling post vaccination. Lower lip tingling resolved 5 minutes later, and tip of tongue tingling continued. Tip of tongue tingling resolved on 24Jan2021. On 25Jan2021 at 20:30 pm; developed sudden left leg numbness and left great toe tingling but at 21:00 pm left leg numbness decreased and left great toe continued to have tingling sensation. She also had faint tingling right great toe. 26Jan2021 08:00 am; left leg numbness improved but left great toe continued to tingle and Right great toe tingling was intermittent. On 26Jan2021, she had new development of right index finger intermittent tingling but at 10:00; Left leg numbness was resolved. As of 27Jan2021, she remained with intermittent left and right great toe tingling and right index finger tingling. In week of 08Feb, the above remaining symptoms were resolved. The adverse events resulted into doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. The patient did not receive any treatment for the reported events. The outcome of the event Tingling lips was resolved on an unspecified date in 2021, Tingling tongue resolved on 24Jan2021, numbness in leg resolved on 26Jan2021; and left great toe tingling/Faint tingling right great toe and development of right index finger tingling resolved on 08Feb2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: MICROGESTIN FE; VITAMIN B12 [CYANOCOBALAMIN]
Allergien: -
Vorherige Impfungen: -

VAERS 1481879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 32,0
Geschlecht: F
Eingang: 18.07.2021
Impfdatum: 23.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / -

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

Paraesthesia

Symptomtext

Recurring tingling sensation in muscle at the back of the shoulder; This is a spontaneous report from a contactable consumer (patient). A 32-years-old non-pregnant female patient received first dose of bnt162b2 (BNT162B2, solution for injection, Lot Number: EL3247), via an unspecified route of administration on 23Feb2021 (age at the vaccination 32-year-old) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history was not reported. The patient received Multivitamins as other medications within 2 weeks of vaccination. Concomitant medication(s) included betacarotene, bioflavonoids nos, biotin, calcium ascorbate, calcium pantothenate, calcium phosphate, choline bitartrate, chromic chloride, colecalciferol, copper sulfate, cyanocobalamin, folic acid, hesperidin, inositol, iron amino acid chelate, lycopene, lysine hydrochloride, magnesium oxide, manganese sulfate, molybdenum trioxide, nicotinamide, phytomenadione, potassium iodide, potassium sulfate, pyridoxine hydrochloride, retinol acetate, riboflavin, selenomethionine, silicon dioxide, colloidal, sodium borate decahydrate, thiamine mononitrate, tocopheryl acid succinate, ubidecarenone, zinc oxide (MULTIVITAMIN & MINERAL) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. Since vaccination patient was not tested for covid-19. The patient experienced recurring tingling sensation in muscle at the back of the shoulder on 25Feb2021. Treatment was not received for the adverse event. The outcome was not recovered. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: MULTIVITAMIN & MINERAL
Allergien: -
Vorherige Impfungen: -

VAERS 1478276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL - 3247

moderat

Staat: LA
Alter: 30,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 01.01.2021
Beginn: 01.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / -

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

Injected limb mobility decreased Injection site pain Pain

Symptomtext

Arm soreness at injection sight for seven months. Inability to twist shoulder in certain directions and severe pain with some motions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: PCOS
Andere Medikamente: Metformin
Allergien: None.
Vorherige Impfungen: -

VAERS 1478044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 40,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chills Dizziness Fatigue Feeling abnormal Headache Hyperhidrosis Malaise Migraine Nausea Pyrexia SARS-CoV-2 test negative

Symptomtext

I started with a fever and a headache about 3 hours after receiving the vaccine. I took Tylenol and felt better. About 10 am that evening I had chills, I jumped in the shower to warm up my body which helped and I went to bed. Wednesday about mid day I became quite nauseated, dizziness and just did not feel well. I took benedryl that evening and went to bed. Thursday around mid- day again I continued to have nausea and dizziness, then I also started having chest tightness, I used my albuterol inhaler which is new to me for allergy induced asthma, which helped. Overnight Thursday into Friday I woke up in the night and had sweat through my clothes. I had the same symptoms carry on into Friday. Saturday I was beginning to feel better until mid afternoon I had a different chest discomfort and nausea and I reported to the emergency room they ruled out a cardiac event, gave me 2 baby aspirin and zofran and sent me home. Sunday I woke up with a terrible migraine I treated with alternating tylenol and ibuprofen for about 24 hours. Monday- Tuesday- Wednesday I just felt worn out, fatigued over all not well. Thursday I finally started feeling better and contiue dto feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: I had a COVID test 4 days (Saturday) before my vaccine and 3 days (Friday) following the COVID vaccine which also came back negative. Saturday (January 30) I went into the emergency room because it was the 3rd day of chest tightness and a I had a new chest discomfort.
Aktuelle Erkrankungen: none
Vorgeschichte: Leiden Factor5, pulmonary sarcoidosis
Andere Medikamente: Pepcid and Omeprazole Norplanon implant
Allergien: sulfa, clomid, latex
Vorherige Impfungen: -

VAERS 1470327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NM
Alter: 62,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 28.01.2021
Beginn: 13.07.2021
Tage bis Beginn: 166,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain upper Arthralgia Chills Dyspnoea Ear pain Influenza A virus test negative Influenza B virus test Oropharyngeal pain Productive cough Respiratory syncytial virus test positive SARS-CoV-2 test positive

Symptomtext

complains of sore throat, left ear ache, chills, painful knees, stomach ache, productive cough, and shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Jul 13, 2021@14:10:07 FLU A NEGATIVE, FLU B NEGATIVE, RSV NEGATIVE _COVID-19 POSITIVE*
Aktuelle Erkrankungen: None
Vorgeschichte: Smoker, Obesity, hearing loss, DM type 2, Arthritis of knee, tricompartmental degeneration
Andere Medikamente: Tylenol, Aspirin, Atorvastatin, CalciumCyclobenzaprine HCL, Estrogens cream, Guaifenesin/DM, Ibuprofen, Lisinopril, Loratadine, Metformin hcl, mULTIVITAMIN, Naproxen,Semaglutide ,
Allergien: Vancomycin
Vorherige Impfungen: -

VAERS 1077652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

moderat

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 22.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: - / LA

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

Blood immunoglobulin A Blood immunoglobulin G Diarrhoea Dyspnoea Fatigue Dysphagia Eye swelling Lip swelling Laboratory test Mobility decreased Pruritus Skin test Swelling face

Symptomtext

swelling of face (lips, eyes, cheeks); swelling of face (lips, eyes, cheeks); swelling of face (lips, eyes, cheeks); severe itching of both hands; difficulty swallowing; massive diarrhea; Extreme tiredness; This is a spontaneous report from a contactable consumer (patient). This is the 1st of 2 reports, for the 1st dose. A 69-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration and administered in left arm at 69-years, on 22Jan2021 11:30 (Lot Number: El3247) as single dose for covid-19 immunisation. The patient was not pregnant. Medical history included RA/4 back surgeries; allergic sinusitis; sulfa allergy. Concomitant medications included prednisone; indomethacin [indometacin]; tolterodine l-tartrate (DETROL); metoprolol succinate (TOPROL); famotidine (FAMOTIDIN). The patient previously took ibuprofen and morphine and experienced drug allergy. There was no other vaccine in four weeks. Exactly one week after the first vaccine, the patient had swelling of face (lips, eyes, cheeks), severe itching of both hands, difficulty swallowing, massive diarrhea, all within 30 minutes of each other. Extreme tiredness for several days after this response and continued to have swelling of eyes and lips. The adverse events start date provided as 29Jan2021 10:00. Events resulted in Doctor or other healthcare professional office/clinic visit. Treatment received included prednisone & benadryl, Allegra & prednisone inject. Patient had no covid prior vaccination or no covid tested post vaccination. Events outcome was recovering. 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: Allergic sinusitis; Back surgery; Sulfonamide allergy
Andere Medikamente: PREDNISONE; INDOMETHACIN [INDOMETACIN]; DETROL; TOPROL; FAMOTIDIN
Allergien: -
Vorherige Impfungen: -

VAERS 1077652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 22.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Blood immunoglobulin A Blood immunoglobulin G Diarrhoea Dyspnoea Fatigue Dysphagia Eye swelling Lip swelling Laboratory test Mobility decreased Pruritus Skin test Swelling face

Symptomtext

swelling of face (lips, eyes, cheeks); swelling of face (lips, eyes, cheeks); swelling of face (lips, eyes, cheeks); severe itching of both hands; difficulty swallowing; massive diarrhea; Extreme tiredness; This is a spontaneous report from a contactable consumer (patient). This is the 1st of 2 reports, for the 1st dose. A 69-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration and administered in left arm at 69-years, on 22Jan2021 11:30 (Lot Number: El3247) as single dose for covid-19 immunisation. The patient was not pregnant. Medical history included RA/4 back surgeries; allergic sinusitis; sulfa allergy. Concomitant medications included prednisone; indomethacin [indometacin]; tolterodine l-tartrate (DETROL); metoprolol succinate (TOPROL); famotidine (FAMOTIDIN). The patient previously took ibuprofen and morphine and experienced drug allergy. There was no other vaccine in four weeks. Exactly one week after the first vaccine, the patient had swelling of face (lips, eyes, cheeks), severe itching of both hands, difficulty swallowing, massive diarrhea, all within 30 minutes of each other. Extreme tiredness for several days after this response and continued to have swelling of eyes and lips. The adverse events start date provided as 29Jan2021 10:00. Events resulted in Doctor or other healthcare professional office/clinic visit. Treatment received included prednisone & benadryl, Allegra & prednisone inject. Patient had no covid prior vaccination or no covid tested post vaccination. Events outcome was recovering. 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: Allergic sinusitis; Back surgery; Sulfonamide allergy
Andere Medikamente: PREDNISONE; INDOMETHACIN [INDOMETACIN]; DETROL; TOPROL; FAMOTIDIN
Allergien: -
Vorherige Impfungen: -

VAERS 1463104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 51,0
Geschlecht: M
Eingang: 11.07.2021
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Headache Malaise Myalgia Paraesthesia

Symptomtext

right hand finger tingling; Headache, Right sided.; body muscle aches; overall feeling of being sick; This is a spontaneous report from a contactable other healthcare professional. A 52-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration, administered in Arm Right on 25Feb2021 09:00 am (at the age of 51-year-old) as dose 2, single for covid-19 immunisation. Medical history included high cholesterol, heart disease, diabetes from an unknown date and unknown if ongoing. Concomitant medications included atorvastatin calcium (LIPITOR) taken for an unspecified indication, start and stop date were not reported; carvedilol (COREG) taken for an unspecified indication, start and stop date were not reported; olmesartan medoxomil (BENICAR) taken for an unspecified indication, start and stop date were not reported. The patient had no allergies to medications, food, or other products. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The Patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration, administered in Arm Right on 04Feb2021 09:00 am (at the age of 51-year-old) as dose 1, single for covid-19 immunisation. On 25Feb2021 16:00, the patient experienced right hand finger tingling, headache, right sided, body muscle aches, overall feeling of being sick. No treatment was taken as a result of events. The outcome of the events were recovered on an unknown date in 2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Heart disease, unspecified; High cholesterol
Andere Medikamente: LIPITOR [ATORVASTATIN CALCIUM]; COREG; BENICAR
Allergien: -
Vorherige Impfungen: -

VAERS 1458838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 33,0
Geschlecht: F
Eingang: 09.07.2021
Impfdatum: 08.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Chest pain Dyspnoea Headache Pain in extremity Pyrexia

Symptomtext

chest pain, heart so heavy can hardly breathe; chest pain, heart so heavy can hardly breathe; Fever; serious headaches, which whole body hurts and in pain; body aches; This is a spontaneous report from a contactable consumer (Patient) reporting herself. A 33-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL3247), dose 2 via an unspecified route of administration, administered in Arm Left on 08Feb2021 (14:00-15:00, as reported), (at the age of 33-years-old) as dose 2, single for covid-19 immunization. The patient medical history and concomitant medications was not reported. Patient took first done of bnt162b2 (Lot Number/Expiry Date: EL1283, unable to provide expiry) in Arm Left on 23Jan2021 for covid-19 immunization. On 09Feb2021 03:00, the patient experienced chest pain, heart so heavy can hardly breathe, fever, serious headaches, which whole body hurts and in pain and body aches. No emergency room and physician office visit. Outcome of the events was not recovered. Additional Context: Caller reports, the second shot yesterday and has come down with side effects so bad and she can't go to the emergency room due to no insurance. Received the second shot 08Feb. Has had fever, chest pain with heart so heavy she can barely breathe, body so hot, serious headaches, which whole body hurting and in pain, body aches that all started at 3am this morning. No further details provided. Unable to provide NDC, expiry, or dose for second Covid vaccine. No other vaccines given the same day. 4 weeks prior did get the first Covid vaccine, 23Jan and provides a lot number of EL1283. Mentions with that one it was in same arm and she had side effects, but not as much as this second one. Had light headache, nausea, pain in left hand. Again, mentions second vaccine much worse. No history of problems with vaccines in past. No further details provided. Mentions she has already missed work and looking to see what Pfizer can do to help her with side effects, looking for medical advice. Talks about a form she saw with help for medical care. Recommended caller for further medical advice to seek medical care, Pfizer is unable to provide medical advice. No further details provided. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1446154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NE
Alter: 67,0
Geschlecht: M
Eingang: 03.07.2021
Impfdatum: 11.02.2021
Beginn: 18.05.2021
Tage bis Beginn: 96,0
Dosis: 2
Route/Site: - / -

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

Arthralgia Bone pain Condition aggravated Fatigue Muscular weakness Neuropathy peripheral Sleep disorder

Symptomtext

Fatigue, Weakness in legs, Leg Muscles, Pain in Bones, Neuropathy 3 times worse, .Knees very Painful, hard to sleep

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: I have Colon Rectal Cancer in Nov. 2008....Had all Radiation and Chemo (3 types). Chemo has had effects on legs...Nueorathy...also had Heart Disease 5 years later from chemo....# stents in 2015....
Andere Medikamente: Lansoprazole 30mg , Aspirin 81mg , Losartan 100mg , Atorvastatin Calcium 80mg , NatureMade Multi For Him 50+, Cranberry Extract 400mg, Calcium 650mg, Vitamin D 3 2,000 IU
Allergien: Claritin
Vorherige Impfungen: -

VAERS 1445928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 03.07.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia Chills Cough Dyspnoea Ear pain Headache Lymph node pain Nasal congestion Nausea Pain Pyrexia Vaccination site pain

Symptomtext

congestion intermittently through the night; Headcahe; Earache; Nausea; Lymph node pain; General body pain; Pain from injection site; Joint pain /pain radiating to elbow; Chills; Fever; Cough; hard time breathing; This is a spontaneous report received from a contactable consumer, the patient . A 42-year-old female patient received an unknown dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EL3247) via an unspecified route of administration in an unspecified arm on 22Mar2021 (at the age of 49-years-old) as a single dose for COVID-19 immunisation. The patients medical history and concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19 and has not been tested for COVID-19 since the vaccination. On 22Mar2021, the patient experienced pain from injection site (vaccination site pain) which radiated to elbow, chills and fever, cough developed, hard time breathing (breathing difficulty), congestion intermittently through the night (nasal congestion) headache developed, ear ache developed, nausea, pain in lymph nodes (lymph node pain), body aches (general body pain) and join pain especially along the back (joint pain). No treatment was received for the adverse events. The clinical outcome of the events vaccination site pain, chills, fever, cough, breathing difficulty, headache, ear ache, nausea, nasal congestion lymph node pain, general body pain and joint pain was recovering at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1445840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 03.07.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Body temperature Chills Headache Heart rate Pain Palpitations Pyrexia

Symptomtext

103 F fever; racing heartbeat with rates between 120-150 bpm; Rigors; headache; body aches; This is a spontaneous report from a contactable consumer, the patient. A 41-year-old non-pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EL3247) via an unspecified route of administration in the left arm on 22Mar2021 at 10:15 (at the age of 41-years-old), as a single dose for COVID-19 immunisation. The patient had no medical history and no known allergies. Concomitant medications were not reported. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EL3247) via an unspecified route of administration in the left arm on 01Mar2021 at 10:30, as single dose for COVID-19 immunisation. 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 patient experienced 103 F fever 8 hours post-dose and it continued for 24 hours, racing heartbeat with rates between 120-150 bpm (palpitation), headache, body aches and rigors on 22Mar2021 at 19:30. The patient did not received treatment for the reported events. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The clinical outcome of fever and rigors was resolved on 23Mar2021 while that of palpitation, headache, body ache was resolved on an unknown date in Mar2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210322; Test Name: Heart rate measurement; Result Unstructured Data: Test Result:120-150 bpm; Test Date: 20210322; Test Name: Body temperature measurement; Result Unstructured Data: Test Result:103 Units:[degF]
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1445823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 56,0
Geschlecht: F
Eingang: 03.07.2021
Impfdatum: 17.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Agitation Blood pressure measurement Chills Diarrhoea Dizziness Heart rate Heart rate increased Hypertension Palpitations

Symptomtext

felt very agitated; diarrhea; chills; blood pressure and it was like 170over 90; racing heart; pulse rate of 110; dizzy; This is a spontaneous report from a contactable non-healthcare professional. A 56-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: EL3247), via an unspecified route of administration on the left arm on 17Mar2021 at 10:00 (at the age of 56-year-old), as a first single dose for COVID-19 immunisation. Medical history included bad back and knee. Concomitant medications included vit C (MANUFACTURER UNKNOWN), magnesium (MANUFACTURER UNKNOWN), calcium (MANUFACTURER UNKNOWN), zinc (MANUFACTURER UNKNOWN) all drugs started on an unknown date for unknown indications. The patient also reported that back was pulled out the week before and was in bed a few days and took a few unspecified muscle relaxers. The patient had no known allergies. The patient did not receive any other vaccines within 4 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 tested positive for COVID-19. On 18Mar2021 at 00:30, after the shot, the patient experienced that night when sleeping woke up witha racing heart and felt very agitated. The blood pressure and pulse rate were measured and recorded as 170 over 90 with a pulse rate of 110. The patient got up because felt dizzy. The patient walked around kitchen for an hour until it passed. It happened again two days later. On 21Mar2021, three days after the shot, the patient experienced diarrhea and chills. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The patient did not receive any treatment for the events. The clinical outcome of the events racing heart, felt very agitated, dizzy, diarrhea and chills were resolving at the time of the report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210318; Test Name: Pulse rate; Result Unstructured Data: Test Result:110; Test Date: 20210318; Test Name: Blood Pressure; Result Unstructured Data: Test Result:170/90
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back pain (Just a bad back); Knee pain (Just a bad knee)
Andere Medikamente: Vitamin c; MAGNESIUM; CALCIUM; ZINC
Allergien: -
Vorherige Impfungen: -

VAERS 1438286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

moderat

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 30.06.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chills Delirium Dyspnoea Fatigue Hyperhidrosis Impaired work ability Pain Pyrexia SARS-CoV-2 test negative

Symptomtext

104.7 fever, shortness of breath, delirious, fatigue, body aches, sweats and chills. Fever, body ache, delirious, sweats and chills lasted several days. Shortness of breath, body ache, fatigue was more than 2 weeks and I had to miss work and go out on FMLA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: I had to have 3 covid tests (all negative)
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia, asthma, anxiety
Andere Medikamente: Magnesium vitamin 500mg, topiramate 25mg 2x a day, escitalopram 10mg, pantoprazole 20mg
Allergien: Almost antibiotics
Vorherige Impfungen: -

VAERS 1436009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 45,0
Geschlecht: M
Eingang: 30.06.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Muscular weakness Paraesthesia

Symptomtext

Having tingling sensation in fingertips, fingernails; general weakness in the arms; This is a spontaneous report from a contactable other healthcare professional (patient). A 45-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247), via an unspecified route of administration in the left arm on 27Jan2021 (at the age of 45-year-old) as single dose for COVID-19 immunisation. Medical history included COVID-19 from an unknown date and unknown if ongoing. Prior to the vaccination, the patient was diagnosed with COVID-19. The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient's concomitant medications were not reported. On 28Jan2021, the patient experienced having tingling sensation in fingertips, fingernails and general weakness in the arms starting second day of initial dose. It has been almost 2 weeks since and symptoms not going away. The patient did not receive any treatment for the events. Since the vaccination, the patient had not been tested for COVID-19. The outcome of the events was reported as not resolved. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1427930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 74,0
Geschlecht: M
Eingang: 25.06.2021
Impfdatum: 19.01.2021
Beginn: 15.02.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / AR

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

Bursa removal Condition aggravated Hydrocele operation

Symptomtext

NOTE: Date of 2nd dose -- 2/10/2021 at 10:50 AM (1) Around 2014, I developed a hydrocele. Cause is unknown. An ultrasound on the scrotum was performed Sept 2015. No action was required and I resolved to live with it. However, sometime in February 2021, the hydrocele grew substantially to the point where treatment was required. I had a hydrocelectomy on 4/27/2021. (2) In November 2019, I fell on a concrete sidewalk, landing mainly on my right wrist and elbow. Bruises developed but eventually cleared up. A slight lump ? a swollen bursa ? soon appeared on my elbow but remained stable and small. However, sometime in February or early March, the bursa expanded dramatically. My primary care physician aspirated the bursa on April 12 and again on April 19. The bursa fully reinflated within a day of each aspiration. On June 10, the bursa was surgically removed. Summary ? Following my Covid vaccinations in January and February, two preexisting conditions ? a hydrocele and a swollen bursa ? worsened to an extent that surgeries were required ? in April and June respectively. Both surgeries were outpatient surgeries.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Kappa light chain MGUS
Andere Medikamente: Multivitamins, Beano
Allergien: -
Vorherige Impfungen: -

VAERS 1426345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MD
Alter: 61,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Hypoaesthesia Hypoaesthesia oral Paraesthesia oral Swollen tongue

Symptomtext

Tingling tongue; Numbness of circle all over my mouth; Numbness is medically up my jaw line/Numbness went like from my chin to top of my head; My tongue like swelling; Tingling back in the tongue; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 61-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL3247 and expiration date was reported) second dose via an unspecified route of administration on 27Jan2021 as 2ND DOSE, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number was not reported and expiration date was30Apr2021) first dose via an unspecified route of administration on unspecified date as 1ST DOSE, SINGLE for covid-19 immunisation. On 27Jan2021 evening Patient got a tingling in the tongue, numbness of circle all over my mouth which then it went up my jawline. Patient took a Benadryl but it subsides still there and ended up going to urgent care because of tongue like swelling. And doctor advised to continue with the Benadryl. And that was on Saturday. Further patient added Now yesterday continue Benadryl last Saturday to Monday of this week through February first. And side effects subside, yesterday all sudden I got a tingling back in the tongue. And numbness went like from my chin to top of my head. While patient further questioned what he was supposed to do with side effects. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1426281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CO
Alter: 75,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 24.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Body temperature Body temperature increased Chills Condition aggravated Feeling abnormal Illness Pain Pain in extremity Sensitive skin Somnolence

Symptomtext

had a slight temperature; chills; achy; felt awful; slept most of the day; She got sick on the second day and stayed in bed; arm was sore; Three to five days after the shot she started to have sensitivity on the skin; Three to five days after the shot she started to have sensitivity on the skin, it is progressing and getting worse; This is a spontaneous report from a contactable consumer (patient). A 75-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration, administered in right arm on 24Jan2021 (at the age of 75-year-old) as a single dose for covid-19 immunisation at a new medical centre (Clinic). The patient medical history included ongoing chronic pain because of spine surgeries, allergies (unspecified) and allergy to dust, mold, mildew, trees and grass (her allergies are environmental, and she was taking a daily allergy pill for years and kind of dropped off with that recently to take one less drug), sleep disorder and night terrors. Concomitant medications included naltrexone (4.5 mg) for chronic pain ongoing from on an unspecified date in 2020 (low dose Naltrexone, it was an opioid antagonist and works for pain. It was working on the pain really well until this started in Mar or Apr2020) and was ongoing. LDN gives her night terrors so she was taking half a zolpidem tartrate (AMBIEN). She is trying not to take it more than every third day. When they were really bad, she took Ambien every night. She takes it maybe two or three times a week for sleep. Fluoxetine hydrochloride (PROZAC) at a lowest dose 10mg, omeprazole (PRILOSEC), losartan (6.25 mg daily) (she takes a quarter of the smallest dose), fish oil and colecalciferol (VITAMIN D) and an unspecified vitamin. Patient takes allergy shots (It was an injection for her allergies. She didn't have it for ten days before the vaccine and didn't get it for seven days after. She doesn't have lot number for allergy shots. This last time it was a new vial and it was just a test injection. She hadn't had a real injection since 10 days before vaccine. The patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EK9231), via an unspecified route of administration on 03Jan2021 at 13:20 as a single dose for covid-19 immunisation and did not experienced any adverse effect. The patient previously received flu shot in 1996 and got sick once and she thinks as flu. She thinks it was a live virus and she didn't get it for a while. She started to get the flu shot again as she got older. She had two doses of the Pfizer vaccine. She only had the reaction after the second dose. On 24Jan2021, the patient was fine on the first day except her arm was sore. Her arm is bothering her, but it is not from the shot. She may have done something to it. On 25Jan2021, on the second day the patient got sick and stayed in bed, she had slight temperature, chills, achy, felt awful and slept most of the day. On an unspecified date in Jan2021, three to five days after the shot she started to have sensitivity on the skin, it was progressing and getting worse. It is sensitive to touch and to cold. It is at the level of the belly button to the left of the rib cage and goes around to her back. There was no rash or anything like that. It hurts all the time. It sometimes is ok at night. It is a large area and is very sensitive. It was getting worse. On 30Jan2021 when she googled Pfizer and area on stomach skin sore to touch. She was not sure if that is a reaction to the vaccine or not. She takes LDN which is low dose naltrexone. It was working on the pain really well until this started. She was thinking maybe it could be symptoms of the vaccine since it has to do with COVID symptoms. The events did not result in emergency room and physician office (she reported that she was trying to get in to see the physician). The outcome of the event arm was sore was resolved in three or four days (Jan2021) and the rest of the events was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20210125; Test Name: Temperature; Result Unstructured Data: Test Result:a slight temperature
Aktuelle Erkrankungen: Chronic pain
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Allergy to molds; Dust allergy; Environmental allergy; Grass allergy; Night terrors; Sleep disorder; Spinal cord operation
Andere Medikamente: NALTREXONE; PROZAC; PRILOSEC [OMEPRAZOLE]; LOSARTAN; AMBIEN; FISH OIL; VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 1426197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CT
Alter: 48,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 01.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: - / LA

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

Chills Cough Fatigue Migraine Oropharyngeal pain Pain

Symptomtext

Slight cough; Chills; body aches; fatigue; migraine; Sore throat; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EL3247) via an unspecified route of administration in left arm on 01Feb2021 at 12:30 as 1st dose, single for COVID-19 immunization. Medical history included recurring sinusitis, recurring migraines, hypothyroid, anxiety. Patient had allergies with Codiene, Dillauded. Concomitant medications included thyroid (ARMOUR THYROID), guaifenesin, pseudoephedrine hydrochloride (MUCINEX D), levocetirizine dihydrochloride (XYZAL), ibuprofen, ergocalciferol (VIT D). Patient did not receive any other vaccine in four weeks. Patient was not diagnosed with covid prior to vaccination. Patient was not pregnant. On 06Feb2021 at 04:30 PM, patient experienced slight cough, chills, body aches, fatigue, migraine, sore throat. No treatment was received for the adverse events. Patient had not been tested covid post vaccination. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Drug allergy; Hypothyroidism; Migraine; Sinusitis
Andere Medikamente: ARMOUR THYROID; MUCINEX D; XYZAL; IBUPROFEN; VIT D
Allergien: -
Vorherige Impfungen: -

VAERS 1426028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Arthralgia Asthenia Chills Condition aggravated Feeling of body temperature change Hyperhidrosis Lethargy Musculoskeletal discomfort Pain Pain in extremity Somnolence

Symptomtext

Joints hurting/joint ache; Her left shoulder received the shot but the right is feeling worse; Feeling warm and cold; Knees are killing her with so much pain; Cold and hot sweats; Chills; She got very lethargic; She was very weak; She was falling asleep, she actually fell asleep for about 20-25 minutes; Body ache; Her fingers and feel like pain; Right is feeling worse as well/it was horrendously worse, like 10 times worse than her normal arthritis pain/her arthritis just worsened; This is a spontaneous report from a Contactable Consumer. A 54-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for Injection, Batch/Lot number: EL3247) via an unspecified route of administration on 04Feb2021 10:00 (at the age of 54-year-old) as single dose for covid-19 immunisation. The patient's medical history included arthritis, (She has arthritis and she took 2 tylenol last night which made her able to sleep). Patient's concomitant medications were not reported. The patient had her 1st dose of the Pfizer Covid vaccine yesterday(04Feb2021) at 10 AM and started experiencing cold and hot sweats, chills, and joints hurting like body aches. The patient also complained that her left shoulder received the shot but the right is feeling worse as well. She is also reporting a body ache, joint ache, feeling warm and cold. She has arthritis and she took 2 tylenol last night which made her able to sleep. but today, all the symptoms came back and her knees are killing her with so much pain. The thing was she took it yesterday and she was fine with in a half hour she stayed, they had her stay 15 minutes and she stayed and stayed a little more because it was through her work, she works at a facility, an assisted living facility. The thing was that she came home and ate some eggs, she ate breakfast and she got very lethargic and was very weak and she was falling asleep, she actually fell asleep for about 20-25 minutes and she woke up and could not get up, she was very weak and had chills and went to get blanket she had some paperwork and it said she could experience this but she then after that she went upstairs and laid down and fell asleep and her joints started hurting like body aches, she has arthritis in her knees, she put on lotion and the thing was it was horrendously worse, like 10 times worse than her normal arthritis pain she was wondering kind of like what was going on was this side effects going on. Then it was hard for her to fall asleep she was kind of uppity and she did not fall asleep until 3 am, she got up she was hurting so bad and it was like the same locations that she usually gets pain from her arthritis just worsened, her fingers and feel like pain. She was wondering how long does it last. She did read the paper and it was part of it and she wanted to see does this last or does it go way or repeat itself. She reported that It started happening probably when she was 39 or 40. She clarifies that is when she first ever had joint arthritis pain. She clarifies the experience with the vaccine happened right now when she is 54. She confirms this was her first COVID 19 vaccine she did not previously received a different manufacturers COVID 19 vaccine. The outcome of the events reported was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis (She has arthritis and she took 2 tylenol last night which made her able to sleep.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1419979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 21,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 26.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac stress test Chest pain Computerised tomogram Echocardiogram Tachycardia X-ray

Symptomtext

Tachycardia, chest pain for several hours. Outcomes: resolved on its own. Cardiac stress test, X-ray, echo and CT with contrast revealed no abnormalities.

Weitere VAERSDATA-Felder

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

VAERS 1419875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 37,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 08.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / LA

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

Palpitations

Symptomtext

Heart palpitations; This is a spontaneous report received from a contactable consumer, the patient. A 37 years old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3247) first dose via an unknown route in left arm on 08Mar2021 at 08:30 AM as a single dose (at the age of 37 years) for COVID-19 vaccination. The patient was not allergic to the medications, food or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested positive for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no COVID prior immunisation. Medical history reported as none. Concomitant medication includes ibuprofen (ADVIL) and congestion medicine occasionally. On 12Mar2021, the patient experienced heart palpitations. No therapeutic measures were taken as a result of these events. The clinical outcome of palpitation's was reported as not resolved. No follow-up attempts are needed. No further information is expected. Amendment: This follow-up report is being submitted to amend previously reported information: reporter/patient details updated, patient's age added, medical history details updated, lab data corrected("COVID-19 virus test" deleted), stop date of vaccine added, concomitant drugs details updated, vaccine facility information added and treatment information added(no).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 1406629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 52,0
Geschlecht: F
Eingang: 17.06.2021
Impfdatum: 19.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: SYR / LA

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

Cardiac monitoring Cardiac stress test Catheterisation cardiac Echocardiogram Electrocardiogram Full blood count Human chorionic gonadotropin N-terminal prohormone brain natriuretic peptide Palpitations Troponin

Symptomtext

I woke up the morning of January 30, 2021 and it felt like my heart was racing. I checked my vitals with a wrist cuff BP monitor and my pulse was over 100. This lasted for several minutes before going away. I experinced the same thing at least 2 to 3 more times on separate occasions which prompted me to seek medical attention on Friday, February 5th. I scheduled a visit to see my PCP for 2/9/21 and messaged my oncologist. My oncologist ordered a STAT echocardiogram. That was not completed until after my PCP office visit. After the results of the echocardiogram were received I was referred to a cardiolgist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: ECG 12 lead 2/9/2021 POCT CBC w/ DIFF 02/09/2021 Echocardiogram 02/11/2021 ECG 12 lead 02/22/2021 Troponin Labs 02/23/2021 NT- PROBNP Labs 02/23/2021 Heart Monitor 03/12/2021 NM Heart SPECT PH Stress 04/22/2021 ECG 12 Lead 04/27/2021 Basic Metabolic Panel 04/27/2021 CBC 04/27/2021 POCT HCG 04/27/2021 Cardiac Catheterization 04/27/2021
Aktuelle Erkrankungen: none
Vorgeschichte: Diagnosed with breast cancer Dec 2017; surgery chemotherapy and radiation 2018
Andere Medikamente: Femara, Saxenda, phentermine, multi vitamin, vitamin d 2000 units, biotin 10,000 units, Claratin, low dose asprin, Alieve,
Allergien: succinylcholine
Vorherige Impfungen: -

VAERS 1399029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 15.06.2021
Impfdatum: 19.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Eosinophilia Headache Magnetic resonance imaging normal Muscle spasms Nausea Paraesthesia Pyrexia Sleep disorder Tinnitus Vertigo White blood cell count decreased

Symptomtext

After 1st shot I developed strong unvolunteer spasms in both my legs down the knees. After 10 hours getting 2nd shot there was 101 F fever, strong headache, sleep disorder, nausea, tingling ( needles) in my both legs down knees, dizziness, vertigo, tinnitus. Fever and strong headache were gone in a few days but all the other symptoms are still here and I am suffering so much.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI ( head) came negative, blood work came OK but with WHITE BLOOD Count low , EOS LOW
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: CoQ10, Vitamins C, D, Collagen, Move Free
Allergien: none
Vorherige Impfungen: -

VAERS 1384727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 09.06.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Fatigue Hypokinesia Migraine Pain in extremity Peripheral swelling

Symptomtext

This is a spontaneous report form the contactable consumer (patient). A 59-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Solution for injection, Lot Number: EL3247, NDC number and Expiry Date: Unknown) via an unspecified route of administration in left arm on 16Apr2021 (at the age of 59-years-old) as a single dose for COVID-19 immunization. Medical history included autoimmune disorder (diagnosed 35 years ago) and has not been experiencing any symptoms from that just some very minor symptoms very recently. Concomitant medication was not reported. No additional vaccines administered on same date of the Pfizer suspect. No prior vaccinations within 4 weeks. Patient had previously received first dose of vaccine (Lot no: EP7534) on 26Mar2021 and had left arm swelling (injection arm) and pain, along with migraines and fatigue which resolved after a week. Immediately the same day as the 2nd dose of the vaccine, the patient had pain in her left (injection) arm/hurting and restricted movement in her left arm. On an unspecified date (after the second dose), patient was extremely tired, very fatigued and had migraines along with pain and swelling in her left (injection) arm. The pain in her arm continued for about 6 weeks. Patient did not remember what got better and what got worse and forgot about it, but the pain never went away. The swelling got better but was not as bad. No treatment was received for the events. Events did not require visit to emergency room or physician office. The outcome of events pain in her left (injection) arm was swelling and hurting and restricted movement in this arm was not resolved while for other events fatigue and migraine was unknown. Additional information has been requested.; Sender's Comments: Agent, caller is a consumer that reported her side effects after receipt of both doses of Pfizer COVID vaccine, however her question is if she can get further clarification if possible, regarding if she should go have quantitative antibody testing that will tell her if she is protected or not? caller was warm transferred by Agent and caller stated "I got information that I did not understand", caller asked: "How do I know if my second dose worked if I had this side effects?. E-transmitted duplicate AE, caller did not provide additional AE details Response: Responded per documents attached and referred for discussion. Offered to send PRD by email, but caller declined and stated her HCP will have that information. Product: PFIZER-BIONTECH COVID-19 VACCINE Question: Caller stated from prior INT: "I got information that I did not understand" Caller stated she also did not understand information provided by Agent during this follow-up INT. Response: Referred back to her HCP for specific recommendations and medical advice regarding antibody testing, and offered to email the PRD from response provided in prior Request and Interaction, but caller declined and stated her HCP will have that information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder (Diagnosed 35 years ago.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1384476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 09.06.2021
Impfdatum: 09.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Chills Fatigue Pain Paraesthesia Pyrexia Swelling

Symptomtext

tingling in finger tips; pain; swelling; fever; chills; tiredness; This is a spontaneous report from a contactable consumer (patient). A 51-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in left arm on 09Mar2021 at 10:00 (Batch/Lot Number: EL3247) (at the age of 51-years-old) as first dose, single dose for COVID-19 immunisation. Medical history included high blood pressure and Covid-19 prior to vaccination. Concomitant medications included amlodipine and carvedilol; both taken for an unspecified indication, start and stop date were not reported. On 10Mar2021 at 08:00, patient experienced tingling in finger tips, pain, swelling, fever, chills, tiredness. Patient did not received any treatment for the events. Patient had not tested for Covid post vaccination. Outcome of the events was recovering. No follow-up attempts needed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes); Hypertension
Andere Medikamente: AMLODIPINE; CARVEDILOL
Allergien: -
Vorherige Impfungen: -

VAERS 1382261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
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 upper Anxiety Dyspnoea Hypertension Rash Tachycardia

Symptomtext

Patient reports 10 days of high BP, tachycardia, anxiety, stomach ache, difficulty breathing following first dose of Pfizer vaccine. Per patient, the patient's doctor stated this reaction was likely anxiety-induced. Patient reports also having a rash a week later, which was resolved by Benadryl. Patient's doctor recommended second dose of Pfizer and patient requested to receive second dose despite reaction.

Weitere VAERSDATA-Felder

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

VAERS 1380970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 31,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 05.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Condition aggravated Discomfort Mass

Symptomtext

a palpable supraclavicular mass on my left collarbone; got worse a few days after 2nd injection (bigger and moreuncomfortable); got worse a few days after 2nd injection (bigger and moreuncomfortable); This is a spontaneous report from a contactable female consumer (Patient). A 31-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3247) via an unspecified route of administration in arm left on 05Feb2021 14:15 (at the age of 31-years-old) as second dose, single for COVID-19 immunization. The patient medical history included polycystic ovarian syndrome, shortness of breath, heart palpitations, vitamin D deficiency, seasonal allergies, allergy to horse serum and cats. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot number: EL8982) via an unspecified route of administration in arm left on 15Jan2021 as first single, dose for COVID-19 immunization. The patient received unspecified medications with 2 weeks of vaccination. The patient received COVID-19 vaccine Pfizer/BioNtech (dose 1) prior to the COVID second dose within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient had not tested for COVID-19 post vaccination. On an unspecified date in Jan2021 (10-days after receiving first dose COVID-19 vaccine), patient experienced a palpable supraclavicular mass on my left collarbone. Patient had reported to PCP, he ordered ultrasound and LDH/CBC/CMP labs. Then followed up with ENT Head/Neck Specialist for further follow-up. Mass varied in prominence over about 6 weeks and got worse a few days after 2nd injection (bigger and more uncomfortable). Now much smaller and less prominent but still noticeable upon examination. The patient did not receive any treatment for the events. Patient had doctor or other healthcare professional office/clinic visit for the event. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic to cats; Allergic to horses; Palpitations; Polycystic ovarian syndrome; Seasonal allergy; Shortness of breath; Vitamin D deficiency
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1371223

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge EL3247

moderat

Staat: NC
Alter: 25,0
Geschlecht: F
Eingang: 03.06.2021
Impfdatum: 05.02.2021
Beginn: 05.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: SYR / LA

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

Dry mouth Ear discomfort Eustachian tube dysfunction Hyperacusis Loss of personal independence in daily activities Migraine Sinus disorder Tinnitus

Symptomtext

Moderate tinnitus symptoms and Eustachian tube has unequalized pressure. Severe symptoms aggravated by excess noise, and travel by plane. Impacts daily life constantly and increases frequency and severity of migraines, leading to an ER visit for severe migraine in March25. unequal pressure has also effected sinus cavity and resulted in constant dry mouth. Symptoms seem to be chronic and ultimately leading to expensive alternative medical solutions.

Weitere VAERSDATA-Felder

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

VAERS 1360446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 71,0
Geschlecht: M
Eingang: 29.05.2021
Impfdatum: 18.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Arthritis Asthenia Back pain Fatigue Hypersomnia Lethargy Middle insomnia Mobility decreased Muscle spasms Musculoskeletal discomfort Myalgia Neck pain Pain Pain in extremity Poor quality sleep Weight Weight decreased

Symptomtext

severe fatigue; achy shoulder; neck not sleeping well; body pain; he can't even lift his arms up due to the pain; when he lays down at 10:00 PM at night to go to sleep, he is up at 12:00 in pain; arthritis; had no energy; sleeping from 12 to 16 hours a day, very lethargic; sleeping from 12 to 16 hours a day; lost four to five pounds; muscles and joints started to ache; pain in his hands; pain in his neck; bottom of his feet will start to grab and cramp up and hurt; pain in his back; doesn't get good sleep; This is a spontaneous report from a contactable consumer (patient). This patient reported similar events for 5 patients. This is the 1st of 5 reports. A 71-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in the left arm on 18Feb2021 (Lot Number: EL3247) as a single dose for COVID-19 immunisation; age at time of vaccination: 71 years. Medical history included open heart surgery (8 to 10 years ago since they found a blockage and fixed it, there was no damage, it was a double bypass), blood cholesterol abnormal, blood pressure abnormal. Concomitant medications included atorvastatin taken for cholesterol from an unspecified start date and ongoing; amlodipine taken for blood pressure from an unspecified start date and ongoing; acetylsalicylic acid (BABY ASPIRIN) taken for an unspecified indication from an unspecified start date and ongoing; and ongoing unspecified multivitamin. The patient previously received 1st dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) as a single dose on 27Jan2021 10:00 (lot: EK4176) in the left arm for COVID-19 immunisation. The patient reported severe fatigue, achy shoulder, neck not sleeping well and body pain. The patient went to hospital in April and was referred to Chiropractor, he has been going for two weeks. He cant even lift his arms up due to the pain. This patient also reports that four other people he has talked to are telling him they are having the same side effects. Events very fatigued, tired, had no energy started Apr2021 with outcome of recovering. Events sleeping from 12 to 16 hours a day, very lethargic, lost four to five pounds in the last couple of months, started Apr2021 with outcome of unknown. Events muscles and joints started to ache like crazy, pain in his shoulders, pain in muscles from his groin to his thigh, pain in his hands when he wakes up in the morning, pain in his neck, bottom of his feet will start to grab and cramp up and hurt, pain in the ankles, pain in his back started Apr2021 with outcome of not recovered and reported as worsened. Event doesnt get good sleep at night started Apr2021 with outcome of not recovered. Events neck not sleeping well, body pain, he can't even lift his arms up due to the pain started Apr2021 with outcome of unknown. The patient underwent shoulder and neck x-ray in May2021 result arthritis. It was also reported as January and early February, he was out walking 4 to 6 miles a day, not having any real problems. He had the Pfizer vaccine both shots and he did not have any problem at the time of the shot, his arm didnt get sore, he didnt have any problems at all. Fast forward a couple of months, he was very fatigued, tired, had no energy, sleeping from 12 to 16 hours a day and very lethargic and then his muscles and joints started to ache like crazy, pain in his shoulders, and now if he walks a mile thats a long walk for him, hes very tired. He has lost 4 to 5 pounds in the last couple of months, he just wonders if this Pfizer vaccine is causing his antibodies to kick against itself. He went to the emergency room about 2 to 3 weeks ago, they did x-rays of the neck and shoulders because it was bad. He had some arthritis and sent him to physical therapy because he cant lift his arms up above his chest. His muscles are starting to hurt and as long as he is up and moving, he is not as bad. When he lays down at 10:00 PM at night to go to sleep, he is up at 12:00 in pain. He got his shots in February, and in April it started, so it was like a couple of months after the shot because he went online and they said side effects usually last one to two weeks right after it, but he didn't have anything right after, but then 2 months after, he started getting really tired and aching and then the pain came. The pain in his shoulders, muscles from his groin to his thigh, it's in his hands when he wakes up in the morning. Once he starts moving things, it's okay. The pain also began in the first two weeks of April. He's tired still and aching but could be due to the fact that he doesn't get good sleep at night, if he was sleeping all night then maybe he wouldn't be as tired. Fatigue, tiredness has gotten better, its improved. But the pain is getting worse; sometimes he will be lying in bed at night and the bottom of his feet will start to grab and cramp up and hurt. The events required a visit to Emergency Room; he doesnt really remember when he went, he knows its been over two weeks ago. The first part of MAY 2021, they did an x-ray on the shoulder and neck, that's where the greatest pain was, and all they saw was arthritis. They scheduled physical therapy and he started physical therapy and did that for two weeks but that has not done anything. He has continued with physical therapy while doctors start doing other checks. The patient called physician today and he is having blood work done this week and they are having a CT scan done next week. Outcome of the events arthritis and when he lays down at 10:00 PM at night to go to sleep, he is up at 12:00 in pain was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021542938 Same reporter/drug/event, different patients;US-PFIZER INC-2021542943 Same reporter/drug/event, different patients;US-PFIZER INC-2021542944 Same reporter/drug/event, different patients;US-PFIZER INC-2021542945 Same reporter/drug/event, different patients

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 202104; Test Name: Weight; Result Unstructured Data: Test Result:lost 4 to 5 pounds; Test Date: 202105; Test Name: x-ray on the shoulder and neck; Result Unstructured Data: Test Result:arthritis
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood cholesterol abnormal; Blood pressure abnormal; Coronary occlusion; Double vessel bypass graft (8 to 10 years ago. they found a blockage and fixed it, there was no damage, it was a double bypass.)
Andere Medikamente: ATORVASTATIN; AMLODIPINE; BABY ASPIRIN
Allergien: -
Vorherige Impfungen: -

VAERS 1360209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 35,0
Geschlecht: M
Eingang: 29.05.2021
Impfdatum: 18.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Dyspnoea Headache

Symptomtext

Very mild headache; shortness of breath; This is a spontaneous report from a non-contactable consumer or other non hcp. A 35-years-old male patient received bnt162b2, (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL3247), via an unspecified route of administration on 18Feb2021 as 1st dose, single for COVID-19 immunization (at the age of 35 years). The patient medical history and concomitant medications were not reported. Patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. On 19Feb2021, the patient experienced very mild headache and shortness of breath for about 1-2 hours. Patient did not receive any treatment for adverse events. The outcome of event was recovered on an unspecified date. No follow up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1360189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NH
Alter: 23,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 25.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Chest discomfort Dyspnoea Vomiting

Symptomtext

Chest tightness; hard to breathe; Vomiting; This is a spontaneous report from a contactable consumer. A 23-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, in Arm Left on 25Feb2021 11:00 (Batch/Lot Number: EL3247) as single dose, for covid-19 immunisation. The patient medical history was not reported. Concomitant medication(s) included sertraline hydrochloride (ZOLOFT) taken for an unspecified indication, start and stop date were not reported. The patient previously took codeine and experienced drug hypersensitivity. Patient received first dose of bnt162b2 for covid-19 immunisation on 04Feb2021 01:00 PM (Lot number: EL3247) in left arm. On 26Feb2021 01:45 AM, patient experienced chest tightness to the point it was hard to breathe and vomiting also occurred. Outcome of events was recovering. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1359713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 42,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 06.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Dizziness Migraine Nausea Pyrexia Vertigo Vomiting

Symptomtext

vertigo, nausea, fever, vomiting, chills, migraine, dizziness for 17 hours

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

VAERS 1357182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 33,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 10.02.2021
Beginn: 08.04.2021
Tage bis Beginn: 57,0
Dosis: UNK
Route/Site: - / LA

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

Idiopathic intracranial hypertension

Symptomtext

bilateral paplliodema and idiopathic increased intracranial pressure; This is a spontaneous report from a contactable consumer (nurse). A 33-year-old female patient received BNT162B2, via an unspecified route of administration, administered in the left arm on 10Feb2021 (Lot Number: EL3247) as unknown, single for COVID-19 immunization. Medical history included depression and Polycystic ovarian syndrome (PCOS), both from an unknown date and unknown if ongoing. No known allergies. Concomitant medications included ziprasidone hydrochloride (GEODON [ZIPRASIDONE HYDROCHLORIDE]) taken for an unspecified indication, start and stop date were not reported; ethinylestradiol, norgestimate (SPRINTEC) taken for an unspecified indication, start and stop date were not reported. On 08Apr2021 12:00, the patient experienced bilateral paplliodema and idiopathic increased intracranial pressure. Therapeutic measures were taken as a result of bilateral paplliodema and idiopathic increased intracranial pressure which included lumbar puncture and acetazolamide. The patient was not pregnant at the time of vaccination. 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 adverse event result in Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. The outcome of the event was not recovered.

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Praegender Schweregrund: Idiopathic intracranial hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Polycystic ovarian syndrome
Andere Medikamente: GEODON [ZIPRASIDONE HYDROCHLORIDE]; SPRINTEC
Allergien: -
Vorherige Impfungen: -

VAERS 1354121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NM
Alter: 61,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 29.01.2021
Beginn: 21.05.2021
Tage bis Beginn: 112,0
Dosis: 2
Route/Site: IM / LA

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

Asymptomatic COVID-19 Body temperature increased Cough Dyspnoea Influenza A virus test negative Influenza B virus test Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

Routine screening. for Covid-19. Asymptomatic. Date 2 developed shortness of breath with exertion, dry cough and afebrile. Day 5 same symptoms, plus temperature of 100 to 101.1 F

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 05/21/2021 Patient tested positivea for Covid 19 by Cepheid method. Influenza A & B, and RSV tested negative
Aktuelle Erkrankungen: Spina Bifida, Degeneration of LS intervertebral Disc, DM type 2, GERD, Obesity, Spondylolisthesis, Diabetic preipheral neuropathy, Tobacco user, Hyperlipidemia, Osteoporosis, Diverticulosis of colon
Vorgeschichte: Spina Bifida, Degeneration of LS intervertebral Disc, DM type 2, GERD, Obesity, Spondylolisthesis, Diabetic preipheral neuropathy, Tobacco user, Hyperlipidemia, Osteoporosis, Diverticulosis of colon
Andere Medikamente: Alendronate, Metformin HCL, Nicotine gum, Omeprazole, Pioglitazone, Calcium, Omega-3 Fish Oil
Allergien: Silk tape, Motrin, Promethazine, Toradol, Augmentin and Glyburide
Vorherige Impfungen: -

VAERS 1353241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 35,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Burning sensation Nausea Paraesthesia Peripheral coldness Urticaria Vaccination site pain

Symptomtext

This is a spontaneous report from a contactable other HCP (Pfizer colleague). This other HCP (patient) reported the following: A 35-years-old female patient received the first dose of BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, Batch/Lot Number: Not reported), via an unspecified route of administration in left arm on 22Feb2021 at 03:30 PM as a single dose for COVID-19 immunization. The patient medical history allergies to bee/wasp and to medication including Naprosyn/Naproxen. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccine within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, has the patient had not been tested for COVID-19. Concomitant medications were not reported. The patient stated that on 22Feb2021, within 30 minutes after vaccination, she was aware of hives and within 1 hour after vaccination, her had epidermis had a burning sensation all over body. The patient reported that an hour after her COVID-19 injection, she began to experience itching all over her body from head to toe, hives, a burning sensation under her skin, nausea, and a tingling sensation in her extremities. Also, they became cold to the touch. Also, the pain at the injection site was more severe the 2nd day than the 1st. The events resulted in doctor or other healthcare professional office/clinic visit. The patient received treatment for the events including Benadryl (antihistamine). The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to analgesics (Verbatim : known allergies: naproxen); Allergic reaction to bee sting; Allergic reaction to wasp sting
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1353165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 27.05.2021
Impfdatum: 28.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Blood pressure measurement Erythema Feeling abnormal Head discomfort Headache Hypertension Vaccination site bruising

Symptomtext

Headache; head felt like it was going to explode/head seemed full; blood pressure was higher; feel like I am racing and I can't relax, like I drank a bunch of caffeine drinks; a red area the size of the band aid/impression of the bandaid was all reddish; still black and blue from vaccine shot/arm was still bruised; This is a spontaneous report from a contactable Consumer or other non health professional (patient). A 69-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number was EL3247 and expiration date were not reported), via an unspecified route of administration, administered in arm left on 28Jan2021 at 09:25 as 1st dose, single for COVID-19 immunisation. The patient medical history included prostate cancer from 02Dec2020 to an unknown date, diabetes from an unknown date and unknown if ongoing , blood pressure from an unknown date and unknown if ongoing (blood pressure was higher), blood thinner (anticoagulant therapy) from an unknown date and unknown if ongoing , neuropathy from an unknown date and unknown if ongoing, cholesterol from an unknown date and unknown if ongoing, allergy: trees grass and pollen mold, from an unknown date and unknown if ongoing. Family history included stroke from an unknown date and unknown if ongoing (dad had a stroke 20 years ago). Concomitant medications included insulin aspart (FIASP) at an unknown dose, daily (sliding scale dose; take with meals by injection daily) for diabetes (taking 8 years) from an unspecified start date and ongoing; insulin glargine (LANTUS, injection) at 14 mL once daily by injection for diabetes (taking 8 years) from an unspecified start date and ongoing; hydrochlorothiazide, losartan potassium (LOSARTAN HCTZ) at 100mg/12.5mg once daily by mouth (orally) for blood pressure (taking for 8 years; added the HCTZ 3 years ago; no product to provide information for the old product, added the HCTZ to his Losartan product about three years ago. He has none of his old Losartan product to provide NDC, lot or expiration date) from an unspecified start date and ongoing; pentoxifylline at 400mg three times daily by mouth (orally) as blood thinner (taking 4 or 5 years) from an unspecified start date and ongoing; gabapentin at 400mg three times daily by mouth for neuropathy (taking for 5 years) from an unspecified start date and ongoing; atorvastatin at 10mg once daily by mouth for cholesterol (taking for 5 years) from an unspecified start date and ongoing; Align Daily Probiotic Supplement at an unknown dose once daily by mouth for an unspecified indication from an unspecified start date and ongoing; calcium at 500mg twice daily by mouth for an unspecified indication from an unspecified start date and ongoing; aspirin (acetylsalicylic acid) at 81mg once daily by mouth for an unspecified indication from an unspecified start date and ongoing; fish oil at an unknown dose for an unspecified indication from an unspecified start date and ongoing; vitamin D3 at an unknown dose for an unspecified indication from an unspecified start date and ongoing, multivitamins at an unknown dose once daily by mouth for an unspecified indication from an unspecified start date and ongoing, and products allergy shots at an unknown dose by injection monthly for allergy: trees grass, pollen mold from 1994 and ongoing. On an unspecified date in Jan2021, the patient experienced headache, head felt like it was going to explode, blood pressure was higher, feel like I am racing and I can not relax, like I drank a bunch of caffeine drinks, a red area the size of the band aid/impression of the bandaid was all reddish, and still black and blue from vaccine shot/arm was still bruised. The clinical course of the event was reported as follow: the patient received 1st dose of the COVID vaccine last Thursday, 8 days ago (as reported), he got headaches, and he inquired how long do they last. Headache started a couple days after, his head felt like it was going to explode, his blood pressure was higher, base line was 120/70 - 130/75, it went to 150/. The doctor turned off the light and it went to 130/. He had not had it that high in a long time, his dad had a stroke 20 years ago and inquired if all of this related to the vaccine. He felt like he was racing and he could not relax, like he drank a bunch of caffeine drinks. This started just after getting the vaccine, could be a coincidence, but could be something else. He got an allergy shot today at 10:00 am eastern time, in the arm where they did the vaccine. It was still black and blue from vaccine shot, the band aid the person put over it, he asked if he was allergic to latex. He reported that where the band aid was, it was a red area the size of the band aid. He questioned that there was latex in his vaccine or was this due to the band aid, making a red mark after he had taken off the band aid for 7 days. Going to healthcare professional on Monday (as reported), he talked with his medical assistant and set up an appointment. He also inquired if increased blood pressure was side effect and how long did it last. The patient mentioned he asked his son who was a pharmacist and he did not know the answer to his question about his headache. Patient stated his head seemed full and now after a week he still had a headache. He added it felt like his head was going to explode. It was still there but better now but it came and went. His blood pressure was up too. Usually, it was only 130 at the top but now it was 130 to 150 on the top. Added he felt like he was racing all the time and could not relax. He was unsure how long after the vaccine he noticed these effects but stated it had been going on for several days. He was scheduled to get the second dose 18Feb2021. Patient went to get his allergy shot today (as reported) and when the nurse went to do the shot, his arm was still bruised and where they put the bandaid over there was an impression of the bandaid was all reddish. No events required a visit to physician or ER (emergency room). No prior vaccinations (within 4 weeks) were reported. History of all previous immunization with the Pfizer vaccine considered as suspect was none. Additional Vaccines Administered on Same Date of the Pfizer Suspect was none.The outcome of the event headache was recovering, outcome of the event head felt like it was going to explode was unknown, and outcome of the other events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 202101; Test Name: blood pressure; Result Unstructured Data: Test Result:higher; Comments: base line is 120/70 - 130/75, it went to 150/. The doctor turned off the light and it went to 130/.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anticoagulant therapy; Blood pressure abnormal (blood pressure was higher.); Cholesterol; Diabetes; Grass allergy (trees grass); Neuropathy; Pollen allergy (pollen mold); Prostate cancer (Patient Medical start date: 02Dec2020); Stroke (family history: my dad had a stroke 20 years ago.)
Andere Medikamente: FIASP; LANTUS; LOSARTAN HCTZ; PENTOXIFYLLINE; GABAPENTIN; ATORVASTATIN; PROBIOTICS; CALCIUM; ASPIRIN [ACETYLSALICYLIC ACID]; FISH OIL; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 1349141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 31,0
Geschlecht: M
Eingang: 26.05.2021
Impfdatum: 18.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Arthralgia Chills Headache Nausea Oropharyngeal pain Pyrexia Tremor

Symptomtext

achy joints; mild sore throat; nausea; Fever; chills; shaking; Headache; This is a spontaneous report from a contactable consumer (patient). A 31-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 2 via an unspecified route of administration, administered in Arm Right on 18Feb2021 11:45 (Batch/Lot Number: EL3247) as age at vaccination of 31-years-old, as single dose, for covid-19 immunisation. Medical history was none; the patient had no allergy. Patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Right on 28Jan2021 03:00 PM (Batch/Lot Number: EL3247) for covid-19 immunisation. There were no concomitant medications. The patient did not receive other vaccine in four weeks and did not receive other medications in two weeks. Starting at 2 AM on 19Feb2021, the patient experienced achy joints then fever, chills, shaking, headache, nausea and mild sore throat were all experienced. Therapeutic measures were taken as a result of the events and included administration of ibuprofen. The patient had not covid prior vaccination and was not covid tested post vaccination. The patient was recovering from the events. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
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 1347763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 42,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / -

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

Electrocardiogram Heart rate increased Hypoaesthesia Palpitations

Symptomtext

1/29 Vaccination at 1022. Three minutes later, I sat down and then started feeling numbness. My HR was increasing at rest. I told the nurse. She monitored. I hadn't ate anything, she directed me to take something and check vitals. 144 HR. 160/100 BP. I do not have high BP. They gave me some oranges. They were monitoring me for 15 minutes. 136,150. HR kept fluctuating between and I was just sitting for an hour. They asked if I wanted to tx to ER. In the ER, same heart questions, EKG, HR still not going down, gave Ativan. I have never taken before. After an hour, eventually I was very sleepy. The doctor never explained what happened but said to take the second dose. I do not know what had happened, if this happened before, I just wanted to go home. I have never had anxiety before, I am not an anxious person. I was ready physically and mentally for the vaccine. I think related to vaccine not to me being anxious. *COVID+; 10/2021 *PCM; recommended Ativan for 2nd dose. I decided not to receive. My BP was never that high. I don't know what would happen the second time. *Have had a couple more episodes of heart palpitations since. Woke me up at night. 2-3 more times out of no where. 115 and stayed like that for 30 minutes. It has been 3 months since last episode. It can just 'happen' at rest.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: COVID +; 10/29/2021
Vorgeschichte: chronic allergies/post nasal drip
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1346892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: PA
Alter: 37,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 24.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chills Condition aggravated Eye pain Facial pain Headache Muscle tightness Pain Temporomandibular joint syndrome

Symptomtext

Like 5-10 mins after receiving the vaccine I began to have right temporal pain. This stayed for 2-3 hours. The pain then started to creep over my right eye and then my entire right face. Within the next 4-5 hours I was having pain over both eyes. By midnight I woke up with pain at the right backside of my head along with chills and body aches. The headache lasted for 2 weeks. I called my Dr. after 1 week. He prescribed prednizone 40mg which did not work. He then prescribed 600mg Advil every 4-6 hours which also did not work. Then imotrex which also didn't help. Also, the last 3/4 days, I had increased jaw tightness. I usually have TMJ issues but this was extraordinary. Eventually the symptoms resolved themselves.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Chronic headaches
Andere Medikamente: None
Allergien: Dexilant
Vorherige Impfungen: -

VAERS 1346856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CO
Alter: 70,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Hypoaesthesia Hypoaesthesia oral Paraesthesia oral Pruritus Urticaria

Symptomtext

It started 8 minutes after, numbness nd tingling in lower lip and spread to tongue and to scalp and then to neck and arms. I started feeling my tongue was tingling. I notified them and they brought me to EMT and he checked my O2 stats - 88 - When I took a deep breath they dropped to 86. My blood pressure was raised. Hives on chest. They gave me Benadryl - I think it was 25 mg and Oxygen and kept monitoring me. They decided to transfer me ER at. - I had three doses of Benadryl before I got to the hospital - one dose in the ambulance. The Benadryl was IM and IV. I was transported to the local hospital that has an ER. It took about three days for the itching to stop. It got better with the 60 total that first night but for it to totally stop it took three days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: At ER that day - blood pressure - IV Benadryl; IV cortico-steroids; Checked my oxygen. They discharged be with an epi-pen and steroids. I was still itching. I took the 40 of Prednisone - but was still itching and I called me doctor after I left the ER and my doctor had me take another 20 of prednisone (to make it a total of 60 that day) and then the itching was helped. My doctor had me do a taper of the Prednisone after that - two 60, two 40, and tapered with two days of each of these doses down to 5 and then done.
Aktuelle Erkrankungen: no
Vorgeschichte: asthma; mild CHF; type 2 diabetes; hypertension ; and hypothryoid; obstructive sleep apnea; and I developed afib recently
Andere Medikamente: Servent - 50 mcg (one inhalation twice a day); Flovent HFA 220 mcg - 2 puffs twice a day; Oxygen at night with CPAP; potassium chloride SR - 20 meqs once a day; Metformin 1000 mg - 1 tab twice a day; Furosemide - 40 meqs once a day; Furos
Allergien: Amoxicillin - itching and a rash; Darvon - nausea and vomiting; Percocet - nausea, vomiting and itching; Morphine and Vicodin - itching, rash, and swelling in my throat and my tongue and I require Oxygen as O2 starts dropping; Shrimp and Iodine - same thing as the Morphine; Adhesive tape - skin breaks out red and blistered; Latex - itching and blisters; and they said with COVID shot I may have reacted to Polyethylene Glycol - but that's a question
Vorherige Impfungen: -

VAERS 1346023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MD
Alter: 82,0
Geschlecht: M
Eingang: 25.05.2021
Impfdatum: 22.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / LA

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

Dyspnoea SARS-CoV-2 antibody test

Symptomtext

never had difficulty breathing like he did 3 days after the vaccine; This is a spontaneous report from a contactable consumer or other non-Health Care Professional. An 82-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 22Jan2021 01:45 AM (Batch/Lot Number: EL3247) as 1ST DOSE, SINGLE for covid-19 immunization. The patient's medical history included High Blood Pressure (hypertension); COPD (chronic obstructive pulmonary disease) and drug hypersensitivity from an unknown date and it was unknown if ongoing. Concomitant medications included lisinopril; felodipime; XARELTO (rivaroxaban); hydrochlorothiazide; zinc; folic acid; Vitamin C; pravastatin sodium; ALLEGRA (fexofenadine hydrochloride); VITRN C (ascorbic acid, ferrous fumarate); atropin; TIMOPTIC (timolol maleate); REFRESH PLUS (carmellose sodium); REFRESH PM (paraffin, liquid, white soft paraffin); BREO ELLIPTA (fluticasone furoate, vilanterol trifenatate ); FLONASE SENSIMIST ALLERGY RELIEF (fluticasone furoate) taken for an unspecified indication, start and stop date were not reported. The patient's allergic conditions included Penicillin, Tetracycline, NSAID eye meds (drug hypersensitivity). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with covid 19 and was not tested for COVID-19 prior vaccination. On 25Jan2021 at 12:00, the patient reported that he "never had difficulty breathing like he did 3 days after the vaccine". The patient was treated with Prednisone 10 mg, Azithromycin 250 mg, Clonidine HCL .2 mg, Albuterol Sulfate 4 mg. On 04Feb2021, the patient underwent lab test for sars-cov-2 antibody test with nasal Swab which was revealed to be negative. The outcome of event was not recovered. No follow-up attempts are possible. Information about batch number cannot be obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210204; Test Name: COVID-19 Test; Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LISINOPRIL; FELODIPINE; XARELTO; HYDROCHLOROTHIAZIDE; ZINC; FOLIC ACID; PRAVASTATIN SODIUM; VITAMIN C [ASCORBIC ACID]; ALLEGRA; VITRON C; ATROPINE; TIMOPTIC; REFRESH PLUS; REFRESH PM [PARAFFIN, LIQUID;WHITE SOFT PARAFFIN]; BREO ELLIPTA; FLO
Allergien: -
Vorherige Impfungen: -

VAERS 1332563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 32,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Chest pain Dysgeusia Fatigue Feeling hot Heart rate Heart rate increased Hypoaesthesia Hypoaesthesia oral Menstruation delayed Oral pruritus Oxygen saturation Palpitations Throat irritation Tongue pruritus

Symptomtext

her period is now 11 days late; tired; stabbing shocks in her chest (chest pain) that lasted for 3 hours; heart started to pound; she had a metallic taste in her mouth; face was numb and warm; face was numb and warm; heart rate at 160 bpm; her mouth/tongue felt itchy; her mouth/tongue felt itchy; throat felt itchy; lips numb; This is a spontaneous report from a contactable consumer (patient) from a Pfizer Sponsored Program. A 32-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in left arm on 28Jan2021 16:00 (lot number: EL3247) at the age of 32 years old, as 1ST DOSE, SINGLE for COVID-19 immunisation. Medical history included asthma from 3 years, allergies (all her life), Chiari malformation from 10 years, vocal cord dysfunction from 3 years, Vitamin D low, constipation and Ferritin low. Concomitant medications included albuterol [salbutamol] (ALBUTEROL) taken for asthma; clarithromycin (CLARITIN) taken for allergies; iron taken for ferritin low; magnesium taken for constipation; and vitamin d [vitamin d nos] (VITAMIN D) taken for Vitamin D low; all taken from an unspecified start date and ongoing. The patient reported she had the first dose of the Pfizer COVID 19 vaccine on 28Jan2021 at 16:00PM in the left arm. About 10 minutes into her wait period (28Jan2021), her heart started to pound; her lips numb and face went numb and warm; she had metallic taste in her mouth; and her mouth/tongue and throat felt itchy. She went up to the nurse to tell her about her symptoms and they hooked her up to an O2 monitor that showed her heart rate at 160 beats per minute but her 02 was okay, it was not under 97%. She was given a generic form of Zyrtec. They monitored her for an hour and her heart pounding stopped. The metallic taste was very brief, and lips and face numbness, and mouth and throat felt itchy all resolved that same day. The next day (29Jan2021), she was tired. Then about 50 hours after the shot, in the night on the 29Jan2021 to 30Jan2021 she started getting weird stabbing shocks in her chest (chest pain) that lasted 3 hours. She would wake up with the pain and then fall back to sleep. It happened several times for a few hours then went away. Lastly, she added that she never ever misses her period but now she is two weeks late (also reported as 11 days late) and she is not pregnant. She expected her period to start on 02Feb2021. She did visit her allergist before getting the vaccine and he said none of her allergies were related to any of the ingredients in the shot. Then she saw the allergist again after the shot and the allergist didn't think she needed to be concerned as the allergist said her symptoms are not in line with an anaphylactic reaction. She is planning to receive the second dose of the vaccine on 18Feb2021. Outcome of the event 'stabbing shocks in her chest (chest pain)' was recovered on 30Jan2021. Outcome of 'her period is now 11 days late' was recovered on unspecified date. Outcome of tired was recovered on 29Jan2021, while outcome of the remaining events was recovered on 28Jan2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210128; Test Name: heart rate; Result Unstructured Data: Test Result:160 beats per minute; Test Date: 20210128; Test Name: O2; Result Unstructured Data: Test Result:not under 97%
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (all her life); Asthma (from 3 years); Chiari malformation (from 10 years); Constipation; Ferritin low; Vitamin D low; Vocal cord dysfunction (from 3 years)
Andere Medikamente: ALBUTEROL [SALBUTAMOL]; CLARITIN [CLARITHROMYCIN]; IRON; MAGNESIUM; VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1332522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Body temperature Burning sensation Dizziness Oral pruritus Paraesthesia Pruritus Pyrexia Rash pruritic Thirst Tremor

Symptomtext

10 minutes post-administration, patient developed itchy rash on right cheek.; Symptoms include itching, burning, and tingling at rash site/ Itching worsened and spread throughout body; Symptoms include itching, burning, and tingling at rash site.; Symptoms include itching, burning, and tingling at rash site.; Patient was also thirsty (was given water).; feverish; dizzy; Itching started in mouth; began to feel shaky and still feeling dizzy; This is a spontaneous report from a contactable Pharmacist. This Pharmacist reported for a 67-year-old (non-pregnant) female patient who received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: EL3247) intramuscularly into the left arm on 28Jan2021 (at the age of 67-year-old) as first dose single for COVID-19 immunization. The patient medical history included hypertension, hypothyroid and known allergies to Aspirin, Codeine, Tolyn, Compazine, Nubain, Reglan, Toradol, Vicodin, morphine and Dilaudid at an unspecified date. Concomitant medications included Lisinopril, gabapentin, Ambien, Synthroid on an unspecified date. On an unspecified date, the patient had COVID prior vaccination and not tested post vaccination. On 28Jan2021, ten minutes post-administration, the patient developed itchy rash on right cheek. Symptoms included itching, burning and tingling at rash site. Patient was also thirsty (was given water). Benadryl oral was given. Symptoms were not resolving and patient began to feel feverish and dizzy. Itching worsened and spread throughout body. Dexamethasone oral was given. Itching started in mouth. EpiPen was administered intramuscularly to left vastus lateralis. Hypertension was seen. Itching in mouth subsided 15 minutes post EpiPen, but patient began to feel shaky and still feeling dizzy. The patient underwent lab tests which included body temperature as feverish on 28Jan2021. Monitored for additional 20 minutes. After, patient was stable and walked out via wheelchair enroute home. No other vaccines in four weeks. Treatment was received with Benadryl, dexamethasone, EpiPen. The outcome of the events were recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210128; Test Name: Feverish; Result Unstructured Data: Test Result:Feverish
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If COVID prior vaccination: Yes); Hypertension; Hypothyroidism
Andere Medikamente: LISINOPRIL; GABAPENTIN; AMBIEN; SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1329340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CT
Alter: 52,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Joint range of motion decreased Mobility decreased Pain in extremity Vaccination site bruising Vaccination site pain

Symptomtext

This is a spontaneous report from a contactable consumer. A 52-years-old female Non pregnant patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Solution for injection; Lot Number: EL3247) dose1, via an unspecified route of administration in Arm Right on 27Jan2021 11:00 as 1ST DOSE, SINGLE for covid-19 immunization. No prior vaccination and did not tested after post vaccination. Medical history included drug hypersensitivity, known allergies penicillin. The patient's concomitant medications were not reported. On an unspecified date, the patient experienced continue chronic pain in right upper arm where 1st dose vaccine was administered, limited range of motion a large bruise at injection site, a large bruise at injection site, Upon follow-up on 18Mar2021, it was reported that arm pain, lack of mobility occurred about 6 hours after the vaccine was administered on 27Jan2021. Therapeutic measures were taken as a result of continue chronic pain in right upper arm where 1st dose vaccine was administered, limited range of motion, a large bruise at injection site. The clinical outcome of the events were not recovered and arm pain, lack of mobility of the outcome was unknown. Follow-up (18Mar2021): This is a follow-up spontaneous report received in response to the mail trail sent regarding the confirmation below mentioned query. The response included: Additional events were updated (arm pain, lack of mobility) and updated event onset date. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (known allergies penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1329288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 01.01.2021
Beginn: 01.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Condition aggravated Rash

Symptomtext

This is a spontaneous report from a contactable consumer (patient). A 72-years-old male patient received BNT162B2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EL3247; Expiration Date: unknown), dose 1 via an unspecified route of administration, administered in Arm Left on 14Jan2021 at 17:45 (age at the time of vaccination was 72 years), as single for COVID-19 immunization. The patient's medical history included fungal infection on his body. He said he does not know the name of the fungus, but he was diagnosed with the fungal condition about 7-10 years ago. On Oct 2020, (about 3 weeks ago at the time of report), the patient had shingles vaccine about 3 weeks ago. He said he was scheduled to receive a second Shingles Vaccine dose in Jan2021. He said he cancelled his appointment for his second Shingles Vaccine dose in Jan2021 because he wanted to take the COVID-19 Vaccine instead. "The patient height: 5'9-1/2" as provided as, who said he used to be 5'10" and was sure his height had gone down". The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On an unknown date in Jan 2021, (after 2 to 3 days of getting his first COVID-19 vaccine), the patient saw something on his feet that looked like a rash and spread to the lower part of his body, especially in his groin area. The patient said, he wears boots, so he did not notice anything sooner than that. The patient did not visit emergency room and physician Office. The patient reported, he had his Shingles Vaccine about 3 weeks ago. The patient did not visit emergency Room and physician Office. No lab tests and procedures were reported. The outcome of events was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fungal infection (diagnosed with the fungal condition about 7-10 years ago.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1329285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CO
Alter: 84,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 21.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Chills Fatigue Freezing phenomenon Headache Illness Influenza like illness Lip injury Musculoskeletal stiffness Nasopharyngitis Nausea Productive cough Rhinorrhoea Tremor

Symptomtext

she seems to have a cold with a runny nose; full of phlegm; Adds now she seems to have a cold with a runny nose; feeling tired/she is tired; extreme chills and freezing; she cut her lip in two places from her teeth chattering; Uncontrollable shaking/worst part was the chills, almost like a seizure'; she had extreme chills and freezing for 3 hours starting when she went to bed.; She started to feel nausea later on Monday; stiff neck on the right side of the back of her neck the day after the vaccine; headachy; Adds hers were like a fast flu; she was so sick she had to get back in bed yesterday; This is a spontaneous report from a contactable consumer (Patient). A 84-year-old female patient re-ceived first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot Number: EL3247; Expiration Date: unknown), via an unspecified route of administration, administered in arm left on 21Jan2021 16:00 (at the age of 84-year-old) at a 1st dose, single for COVID-19 immuniza-tion. Medical history included thyroid disorder. No medical history (including any illness at time of vac-cination) was reported. None of the patient family medical history was reported. The patient did not receive any other vaccines prior to the COVID vaccine within 4 weeks. Concomitant medication includ-ed levothyroxine sodium (SYNTHROID) at a dose of 0.88 mg 1x/day (.088 mg; take once daily by mouth) via oral route of administration taken for thyroid disorder. Consumer states she received the Pfizer COVID 19 vaccine 21Jan2021 at 1600PM in the left arm. The effects didn't come until Tuesday night when she went to bed. The patient experienced worst part was the chills, almost like a seizure, headachy, she was so sick she had to get back in bed yesterday, hers were like a fast flu on an unspeci-fied date in Jan2021, she seemed to have a stiff neck on the right side of the back of her neck the day after the vaccine on 21Jan2021, she started to feel nausea later on Monday on 25Jan2021 and she had extreme chills and freezing for 3 hours starting when she went to bed on 26Jan2021. Adds she took two Advil, put on sweats and took a heating pad into bed then she was able to fall asleep. She cut her lip in two places from her teeth chattering and uncontrollable shaking Tuesday night on 26Jan2021. When she put the heavy clothes on and took that Advil the chills stopped, and she slept for four hours. she is tired on 27Jan2021, she seems to have a cold with a runny nose and full of phlegm on 28Jan2021. The patient received Advil as a treatment medication to the events extreme chills and freezing. The events were reported as non-serious. Outcome of the events she seems to have a cold with a runny nose, full of phlegm was not recovered; headachy, adds hers were like a fast flu, she seems to have a cold with a runny nose, worst part was the chills, almost like a seizure, she was so sick she had to get back in bed yesterday was unknown; she started to feel nausea later Monday, she cut her lip in two places from her teeth chattering, feeling tired/she is tired was recovering; stiff neck on the right side of the back of her neck the day after the vaccine was recovered on 25Jan2021, and re-maining other events extreme chills and freezing, she had extreme chills and freezing for 3 hours start-ing when she went to bed, uncontrollable shaking recovered on 26Jan2021. She was asking about getting the second dose considering her chills, Mentioned she talked to a few people who had the chills and were tired after the second dose but they were not as bad and every-thing was over in a day or so. Caller declined to report on anyone she knows who had chills and was tired after the vaccine. Adds she is scheduled to receive the next dose of the vaccine 10Feb2021. Adds it scares her a little bit because of the extreme chills. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Thyroid disorder
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1280290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 56,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Drug ineffective Muscular weakness SARS-CoV-2 test Suspected COVID-19 Vaccination site hypoaesthesia Hypoaesthesia Immediate post-injection reaction Injection site hypoaesthesia Injection site pain Injection site paraesthesia Pain Paraesthesia Vaccination site pain Vaccination site paraesthesia

Symptomtext

VAULT - Saliva, covid test positive on 22Feb2021; VAULT - Saliva, covid test positive on 22Feb2021; shooting tingling/numbness/pain that went from the injection site down my arm to my fingers; shooting tingling/numbness/pain that went from the injection site down my arm to my fingers; shooting tingling/numbness/pain that went from the injection site down my arm to my fingers; Weakness in my right arm; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 vaccine), dose 1 via an unspecified route of administration, administered in Arm Right on 22Jan2021 18:30 (Batch/Lot Number: EL3247) as 1st dose, single for covid-19 immunisation. The patient medical history was not reported. The patient is not pregnant at the time of vaccination. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. On 22Jan2021 18:30, immediately after administration, the patient experienced shooting tingling/numbness/pain that went from the injection site down my arm to my fingers. The sensation worsened and became more painful accompanied by a weakness in her right arm. The patient went my primary care physician to have this looked at. Her injection was nearly 3.5 months ago and she still continue to experience the same symptoms. The events were considered serious, disability. The patient did not receive treatment for the events. The patient underwent lab tests and procedures which included VAULT - Saliva, covid test on 08Feb2021, 24Feb2021 and 01Mar2021 with negative result and positive on 22Feb2021. The outcome of events VAULT - Saliva, covid test positive on 22Feb2021 was unknown; all other events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210208; Test Name: VAULT - Saliva; Test Result: Negative ; Test Date: 20210222; Test Name: VAULT - Saliva; Test Result: Positive ; Test Date: 20210224; Test Name: VAULT - Saliva; Test Result: Negative ; Test Date: 20210301; Test Name: VAULT - Saliva; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1280290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 56,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Drug ineffective Muscular weakness SARS-CoV-2 test Suspected COVID-19 Vaccination site hypoaesthesia Hypoaesthesia Immediate post-injection reaction Injection site hypoaesthesia Injection site pain Injection site paraesthesia Pain Paraesthesia Vaccination site pain Vaccination site paraesthesia

Symptomtext

VAULT - Saliva, covid test positive on 22Feb2021; VAULT - Saliva, covid test positive on 22Feb2021; shooting tingling/numbness/pain that went from the injection site down my arm to my fingers; shooting tingling/numbness/pain that went from the injection site down my arm to my fingers; shooting tingling/numbness/pain that went from the injection site down my arm to my fingers; Weakness in my right arm; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 vaccine), dose 1 via an unspecified route of administration, administered in Arm Right on 22Jan2021 18:30 (Batch/Lot Number: EL3247) as 1st dose, single for covid-19 immunisation. The patient medical history was not reported. The patient is not pregnant at the time of vaccination. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. On 22Jan2021 18:30, immediately after administration, the patient experienced shooting tingling/numbness/pain that went from the injection site down my arm to my fingers. The sensation worsened and became more painful accompanied by a weakness in her right arm. The patient went my primary care physician to have this looked at. Her injection was nearly 3.5 months ago and she still continue to experience the same symptoms. The events were considered serious, disability. The patient did not receive treatment for the events. The patient underwent lab tests and procedures which included VAULT - Saliva, covid test on 08Feb2021, 24Feb2021 and 01Mar2021 with negative result and positive on 22Feb2021. The outcome of events VAULT - Saliva, covid test positive on 22Feb2021 was unknown; all other events was not recovered.

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Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210208; Test Name: VAULT - Saliva; Test Result: Negative ; Test Date: 20210222; Test Name: VAULT - Saliva; Test Result: Positive ; Test Date: 20210224; Test Name: VAULT - Saliva; Test Result: Negative ; Test Date: 20210301; Test Name: VAULT - Saliva; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1315916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 25.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Asthenia Body temperature Body temperature increased Chills Dizziness Fatigue Feeling abnormal Headache Nausea Pain Pyrexia SARS-CoV-2 test Tremor

Symptomtext

low-grade fever; headache; body ache; dizzy; weak; queasy; chills; shaky; fatigue/tired another 24 hours/Third day still tired.; mild brain fog; higher fever 101.5+/couldn't get fever below 100.; This is a spontaneous report from a contactable other health care professional. A 48-year-old non pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL3247) via an unspecified route of administration in right arm on 25Jan2021 11:30 as second dose, single for COVID-19 immunization. The patient previously received first dose on 04Jan2021 11:00, (lot number: EL0142) via an unspecified route of administration in right arm as first dose, single for COVID-19 immunization. Medical history included non-Hodgkins lymphoma from 1995, invasive ductal carcinoma 2009 with breast reconstruction; phrenic nerve paralysis left side; cardiomyopathy. Concomitant medications included metoprolol 100 mg, vitamin D [COLECALCIFEROL], beclometasone dipropionate (QVAR) 80 ug. No known allergies reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was tested for COVID-19 (nasal swab, rapid test) post vaccination on 21Jan2021 test result was pending. On 25Jan2021 24:00, the patient experienced mild brain fog at 3pm; fatigue at 7pm; 11pm low-grade fever, headache, body aches; 4 am higher fever 101.5+, headache, body ache, dizzy, weak, queasy, chills, fatigue. Started ibuprofen and took every 4 hours and could not get fever below 100. Fever broke early hours the next day, but still was queasy, shaky, dizzy, achy and tired another 24 hours. Third day still tired. The patient received treatment for the events as OTC non-steroidal anti-inflammatory drugs. The events were non serious. The outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021007634 same patient/drug, different vaccine dose/event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20210125; Test Name: fever; Result Unstructured Data: Test Result:low-grade fever/higher fever 101.5+; Comments: Started ibuprofen and took every 4 hours and couldn't get fever below 100; Test Date: 20210125; Test Name: fever; Result Unstructured Data: Test Result:101.5+,; Comments: 4 am higher fever 101.5+; Test Date: 20210125; Test Name: fever; Result Unstructured Data: Test Result:low-grade fever; Comments: 11pm low-grade fever; Test Date: 20210126; Test Name: fever; Result Unstructured Data: Test Result:Fever broke early hours the next day; Comments: Fever broke early hours the next day; Test Date: 20210121; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Result Unknown; Comments: result: Pending
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast reconstruction; Cardiomyopathy; Invasive ductal breast carcinoma; Non-Hodgkin's lymphoma; Phrenic nerve paralysis
Andere Medikamente: METOPROLOL; QVAR; VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 1314832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Chills Diarrhoea Feeling abnormal Nausea Palpitations Pyrexia

Symptomtext

They started at 08:00PM, I got a high fever - 102 and 103 - which lasted 24 hours and it caused me to have heart palpitations (lasted about 12 hours). I was getting chills and nausea and diarrhea - lasted about 24 hours. I was in a mental fog. I couldn't think clearly. I was having stomach pain. I was too out of it to really treat my symptoms - it was all I could do to go to the bathroom and take my temperature. At 36 hours, I called nurse advice line and I was feeling better - fever had gone down after 24 hours. The diarrhea though didn't stop and so I went to URGENT CARE - and they referred me to my to doctor and doctor gave me Vancomycin - for ten days. That helped it to stop.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: sinus infection - had finished antibiotic
Vorgeschichte: Myascinia Gravis; Asthma; Migraines; PCOS; Bio-Acid Diarrhea
Andere Medikamente: Mestinon - 60 mg - 5 times a day; Adair - 2 times a day; Singulair - 10 mg one time a day; Ventolin - as needed; Topamax - 100 mg - two times a day; Sumatriptan 50 mg as needed. Spironolactone - 200 mg - 1 time of day; Metformin XR - 750 mg
Allergien: maybe alcohol
Vorherige Impfungen: annual flu shot: makes me feel weak after each flu shot; Dose 1 of Pfizer COVID vaccine 1/13/2021

VAERS 1314757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 23.02.2021
Beginn: 20.04.2021
Tage bis Beginn: 56,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Chest pain Dyspnoea

Symptomtext

N17.9 - Acute kidney failure, unspecified Chest pain shortness of breath

Weitere VAERSDATA-Felder

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

VAERS 1312901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MA
Alter: 35,0
Geschlecht: M
Eingang: 13.05.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Blood pressure measurement Hypotension Vaccination site hypoaesthesia Vaccination site pain

Symptomtext

This is a spontaneous report from a contactable consumer (patient). A 35-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection), via an unspecified route of administration, administered in Arm Left on 27Jan2021 (Batch/Lot Number: EL3247, expiration date:unknown) as 1st dose, single for COVID-19 immunization. Medical history include allergy to amoxicillin. The concomitant medications were not reported.The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. On 28Jan2021 at 11:00 AM, the patient experienced pain and numbness at injection site and low blood pressure 88/60. The events were not treated. The outcome of these events was recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Date: 20210128; Test Name: Blood Pressure; Result Unstructured Data: Test Result:88/60; Comments: Low
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1420230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 88,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 12.01.2021
Beginn: 02.02.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / AR

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

Biopsy bone marrow Condition aggravated Myelodysplastic syndrome Platelet count decreased Thrombocytopenia

Symptomtext

History of Thrombocytopenia (low normal). Please see attached record of platlets. It appears platelets decreased below 100,000 in 8/19. Nine days after receiving immunization #2, Platelets decreased to 44, 37, 33... Although, the immunization did not cause the thrombocytopenia, I ' m wondering if it accelerated the decline. Bone Marrow Biopsy done 4/26/21 = MDS. Staging pending. My father ' s brother is 10 years younger. He has a history of normal platlets/normal hematology. He received both COVID immunizations. After routine visit to PCP, he learns his platlets are 40,000 and sent to hematologist for f/u.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: See attached
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Diastolic heartfailure; COPD, Sleep Apnea, colon cancer x2, bladder ca x1, Anemia, Thrombocytopenia
Andere Medikamente: Torsemide, Multivitamin, Escitalopram, Ferrous Sulfate, Pantoprazole, Spironolactone, Vitamin D
Allergien: Iodine median, Betablockers
Vorherige Impfungen: -

VAERS 1311181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 18.02.2021
Beginn: 10.04.2021
Tage bis Beginn: 51,0
Dosis: 1
Route/Site: IM / LA

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

Haemoptysis Pneumonia

Symptomtext

J18.9 - Pneumonia, unspecified organism COUGING UP BLOOD

Weitere VAERSDATA-Felder

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

VAERS 1300552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

moderat

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 08.05.2021
Impfdatum: 28.01.2021
Beginn: 13.02.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / RA

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

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

Symptomtext

This 74 year old white male received the Covid shot on 1/28/21 and went to the ED on 2/13 /21 with the following diagnoses listed below. U07.1 - COVID-19 chest pain

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

VAERS 1046184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: FL
Alter: 27,0
Geschlecht: F
Eingang: 08.05.2021
Impfdatum: 01.02.2021
Beginn: 01.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Herpes zoster Hypersensitivity Migraine with aura Pain in jaw Physical examination abnormal Rash Rash vesicular Skin weeping Toothache

Symptomtext

got shingles; This is a spontaneous report from a Pfizer sponsored program received from a contactable consumer (patient). A 27-year-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration on Feb2021 (Batch/Lot number was not reported) as a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient reported that she received the second dose last Tuesday (Feb2021) and she got shingles yesterday (Feb2021). The outcome of the event was unknown. Information about lot/ batch number has been requested

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine with aura
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1294340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MA
Alter: 45,0
Geschlecht: M
Eingang: 06.05.2021
Impfdatum: 17.04.2021
Beginn: 04.05.2021
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: - / -

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

Herpes zoster Pain Paraesthesia Rash

Symptomtext

Was diagnosed today with shingles- rash on chest, back and under arm on one side. Stabbing pains and tingling. Have had chicken pox but this is first time with shingles

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

VAERS 1288245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 65,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Blood pressure measurement Hypertension

Symptomtext

lower HTN (160/98); This is a spontaneous report from a contactable other healthcare professional. A contactable other healthcare professional reported in response to HCP Letter sent in cross-referenced case. A 65-years-old female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EL3247), via an intramuscular route of administration, in deltoid right on 28Jan2021 (at the age of 65-year-old) as single dose for COVID-19 immunization. The patient medical history included, first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, frequency (0.3cc) solution for injection, Batch/Lot Number: EH-9899), via an intramuscular route of administration in Lt Deltoid (Arm Left) on 23Dec2020; 15:48 as single dose for COVID-19 immunization. Patient's Medical History (including any illness at time of vaccination): None. Family Medical History Relevant to AE (s) includes, Father, HTN died ago 80 Lung cancer (Fire fighter), Sister: HTN. Concomitant medications included Losartan (MANUFACTURER UNKNOWN) taken for indication, suspected underlying HTN from 07Jan2021 and Continues. Most recent dose (daily dose and regimen including Formulation, Route, Frequency): 50mg PO (per oral) Daily; clonidine (MANUFACTURER UNKNOWN) taken for an unspecified indication from 28Jan2021 to an unspecified stop date. On 28Jan2021 at 12:48 (15 min after admin), patient had low HTN (160/98) resolved with Clonidine at site. Adverse event required visit to the physician office, visit to Emergency Room was not required. Relevant Tests were None. The outcome of event was recovered. Causal Relationship, a reasonable possibility that the event is related to suspect product/s was reported as Yes.; 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 event Hypertension cannot be excluded. The case will be reassessed if additional information becomes available. 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: Hypertension
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:low HTN (160/98); Comments: resolved with Clonidine
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blurred vision (reduced spontaneously approx. 45 min); COVID-19 vaccination (Dose 1 Time Vaccination was given: 15:28 Anatomical location : Arm Left (Lt Deltoid) Lot Number/Expiry Date: EH-9899); Hypertension (Father, HTN died ago 80 Lung cancer (Fire fighter), Sister: HTN); Hypertension; Lung cancer (Father, HTN died ago 80 Lung cancer (Fire fighter), Sister: HTN); Tachycardia; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: CLONIDINE; LOSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1288143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 53,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 21.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Body temperature Headache Lethargy Paraesthesia Pyrexia

Symptomtext

Headache; tingling in arms and hand; severe lethargy; fever 101.8; This is a spontaneous report from a contactable consumer (patient). A 53-years-old non pregnant female patient received first dose of BNT162B2 (Solution for injection, PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL3247),via unspecified route of administration, administered in left arm on 21Jan2021 at 13:00 (at the age of 53 years) as single dose for COVID-19 immunization. The patient medical history included vertigo, migraine, asthma. The patient had an unknown allergy to medications, food, or other. The concomitant medication that the patient received within 2 weeks of vaccination included pseudoephedrine hydrochloride (SUDAFED) and ibuprofen (ADVIL). Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 22Jan2021 the patient experienced headache, tingling in arms and hand, severe lethargy and fever 101.8. The patient did not receive treatment for the events. On 22Jan2021 the patient underwent lab tests and procedures which included body temperature was 101.8. fever. The outcome of event was recovered in 2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210122; Test Name: temperature; Result Unstructured Data: Test Result:101.8; Comments: fever 101.8
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Asthma; Migraine; Vertigo
Andere Medikamente: SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]; ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 1278836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 83,0
Geschlecht: F
Eingang: 01.05.2021
Impfdatum: 24.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Aphasia Blood lactic acid Blood lactic acid increased Blood potassium Blood potassium decreased Blood test Blood urine present Cellulitis Chest X-ray Chromaturia Computerised tomogram Confusional state Culture urine Decreased appetite Dehydration Dementia Dysuria Gait inability

Symptomtext

lactic acid was high; dementia had suddenly progressed; spot where her lung was starting to collapse; potassium, Vitamin D and Vitamin B12 were low; potassium, Vitamin D and Vitamin B12 were low; potassium, Vitamin D and Vitamin B12 were low; stopped talking; Cellulitis in her arm/ cellulitis was further down her arm, around her wrist hand area (Her wrist was huge, hot, red, and her hand was swollen); it burned when she peed; blood in her urine; wanted to sleep/getting worse with sleeping; was shutting down; she was dehydrated because her urine was dark; urine was dark; began just feeling bad/having like a terrible time/having a hard time/really not feeling good; more confused; lethargic; had trouble her getting up/was having to do everything for her, feed her, bathe her; couldn't walk; lost her appetite; arm was sore; This is a spontaneous report from a contactable consumer (patient's daughter). An 83-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration, administered in the left arm, on 24Feb2021, as single dose, for COVID-19 immunisation. Medical history included mild asthma, dementia (moments like putting things in the wrong place and being forgetful) and was confused. There were no concomitant medications. Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231) received at age 83 years, on 03Feb2021, for COVID-19 immunisation. On 24Feb2021, after the second vaccinations, the patient's arm was sore. On 06Mar2021, the patient began just feeling bad, was having like a terrible time, having a hard time, was really not feeling good; was more confused; lethargic; had trouble getting her up, was having to do everything for her, feed her, bathe her; couldn't walk and lost her appetite. On 09Mar2021, the patient was shutting down. On the same day at 18:30, the patient had gone in the bathroom and said it burned when she peed. So, the patient was taken to urgent care so it would not get out of hand. At the urgent care, they said she has a UTI, there was blood in her urine so they gave her Cipro but they cultured her urine and it grew no bacteria but there was still blood in her urine and she was getting worse with sleeping and she didn't even get up to eat. The patient was also dehydrated and her urine was dark. The events dehydrated, urine was dark, it burned when she peed, blood in her urine required emergency visit on 16Mar2021. The reporter thought the patient was going to die. On 16Mar2021, in the ER, they did blood work (unknown result), chest xray which showed she had a spot where her lung was starting to collapse (they said it was a tiny place, from not getting up and moving around, they said it would correct itself) and the patient's potassium, Vitamin D and Vitamin B12 were low. They did a CT scan of the head and chest to look for stroke or seizure and there was nothing. They blamed it on her dementia that had suddenly progressed. The patient was hospitalized from 16Mar2021 to 18Mar2021. On 12Mar2021, the patient experienced cellulitis in her arm. The reporter clarified that the cellulitis was further down her arm, around her wrist hand area. Her wrist was huge, hot, red, and her hand was swollen. On 24Mar2021, the patient followed up with the family doctor because the hospital wanted her to follow up with a GYN because they didn't feel it was urinary at all. When the reporter took the patient in to see the doctor, she couldn't walk in, she had to roll her in a wheelchair, she had stopped talking again. On 26Mar2021, the doctor sent the patient to the emergency room (unspecified reason) and they kept her. They said her said lactic acid was high. She was admitted on 26Mar2021 and discharged on 29Mar2021. On 29Mar2021, the patient's potassium was 3.3 and her lactic acid level was back to 2. The patient was recovering from lactic acid was high; potassium, Vitamin D and Vitamin B12 were low; began just feeling bad/having like a terrible time/having a hard time/really not feeling good; more confused; lethargic; had trouble her getting up/was having to do everything for her, feed her, bathe her; couldn't walk; lost her appetite; was shutting down; stopped talking. The patient recovered from cellulitis in her arm/ cellulitis was further down her arm, around her wrist hand area (Her wrist was huge, hot, red, and her hand was swollen) in Mar2021; and arm was sore on 29Mar2021. The outcome of events spot where her lung was starting to collapse, dementia had suddenly progressed; she was dehydrated because her urine was dark; it burned when she peed; blood in her urine; and wanted to sleep/getting worse with sleeping was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 3,0
Labordaten: Test Date: 20210326; Test Name: Lactic acid; Result Unstructured Data: Test Result:high; Test Date: 20210329; Test Name: Lactic acid; Result Unstructured Data: Test Result:2; Test Date: 20210316; Test Name: Potassium; Result Unstructured Data: Test Result:low; Test Date: 20210329; Test Name: Potassium; Result Unstructured Data: Test Result:3.3; Test Date: 20210316; Test Name: blood work; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210316; Test Name: chest xray; Result Unstructured Data: Test Result:spot where her lung was starting to collapse; Comments: spot where her lung was starting to collapse (it was a tiny place, from not getting up and moving around, they said it would correct itself); Test Date: 20210316; Test Name: CT Scan of the head and chest; Result Unstructured Data: Test Result:there was nothing; Test Date: 20210309; Test Name: urine culture; Result Unstructured Data: Test Result:grew no bacteria; Test Date: 20210316; Test Name: Vitamin B12; Result Unstructured Data: Test Result:low; Test Date: 20210316; Test Name: Vitamin D; Result Unstructured Data: Test Result:low
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Confused; Dementia (She had moments like putting things in the wrong place and being forgetful before all this)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1271219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 72,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 26.01.2021
Beginn: 17.04.2021
Tage bis Beginn: 81,0
Dosis: 1
Route/Site: SYR / UN

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

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

Symptomtext

Developed COVID-19 and was hospitalized. Symptoms were cough and shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Tested positive for COVID-19 by PCR on 4/17/2021.
Aktuelle Erkrankungen: -
Vorgeschichte: Renal Disease and Diabetes. and Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1269326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 72,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 27.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Burning sensation Condition aggravated Pain in extremity Paraesthesia

Symptomtext

increased neuropathic symptoms; trouble in her arms.; tingling and burning sensation from shoulder to wrist; tingling and burning sensation from shoulder to wrist; This is a spontaneous report from a contactable consumer (patient) to a Pfizer-sponsored program. This 72-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3247and expiry date unknown, Solution for injection), via an unknown route on 27Jan2021 at 14:15 (at the age of 72-years-old) at single dose arm for COVID-19 immunization. The patient had relevant history of neuropathy prior to receiving vaccine. Concomitant medications was nor reported. On an unspecified date, the patient mentioned that she experienced increased neuropathic symptoms and fair amount of tingling and burning sensation from shoulder to wrist after receiving the first dose. Especially having trouble in her arms between her wrists and shoulder. The patient also felt like burning, stinging, and pins and needles. The patient was scheduled to receive the second dose. Outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Neuropathy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1269297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: LA
Alter: 74,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 18.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Condition aggravated Malaise Memory impairment Myalgia Pain in extremity

Symptomtext

Aching legs; Gradually getting worse; Her memory is affected; Muscle aches and pains; Felt out of sorts; Arm was sore; This is a spontaneous report from a contactable other hcp (nurse). A 74-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in arm right on 18Jan2021 at 09:00 (Lot Number: EL3247, Expiration Date: Apr2021) as single dose for COVID-19 immunization. The patient's medical history included spinal fusion surgery from 2019 to an unknown date. The patient previously received 1st Shingrix injection and experienced her arm turned really red and swelled up (so her doctor told her not to take the 2nd injection). There were no concomitant medications. On 19Jan2021, the patient experienced arm was sore. On 21Jan2021, the patient felt out of sorts. On 22Jan2021, the patient experienced muscle aches and pains. She is not sure if the muscle aches are due to her just getting old or from the vaccine. The muscle aches are especially in her legs. On an unspecified date, the patient experienced aching legs, gradually getting worse and her memory is affected. She is gradually getting worse, but doesn't know if it's the weather, or is it a possibility that it's the vaccine. The patient's memory is affected, then clarified that it has nothing to do with the vaccine, she is just getting old. She asked if people have reported muscle aches and pains for weeks after. She is due to have the second injection on 08Feb2021. No family medical history relevant to events. The events did not result in emergency room visit or physician office visit. The outcome of the muscle aches and pains was not recovered and was unknown for the rest of the events. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Spinal fusion
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1267353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Paraesthesia

Symptomtext

within 10 minutes fingers and hand on left side got extremely tingly and I felt a tad lightheaded

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: heart disease (CAD, abnormal valve), diabetes, neuropathy, hypertention, abnormal growing lung nodules
Andere Medikamente: metformin, insulin, metoprolol succ er, aspirin
Allergien: wellbutrin
Vorherige Impfungen: 1984 adenovirus (flu shot)when eggs were used in vaccines

VAERS 1254186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NV
Alter: 77,0
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: 09.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Pain Paraesthesia Vaccination site paraesthesia

Symptomtext

severe throbbing pain in my left arm; Tingling in my left hand for 3-days til present time; This is a spontaneous report from a contactable other health care professional. A 77-years-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number: EL3247, Expiry date: Unknown), via an unspecified route of administration, administered in Arm Left on 09Feb2021 17:30 at SINGLE DOSE for covid-19 immunization. The patient had a previous history of allergy to amoxicillin therapy. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not test Covid post vaccination. Concomitant medication includes Vitamins taken in two weeks. The patient experienced tingling in my left hand for 3-days til present time, severe throbbing pain in my left arm on 11Feb2021 12:00. The treatment included Tylenol-MAPP 650 Mg every 8 hrs and Ibuprofen 400MG 4-hrs after taking Tylenol. The outcome of the events was not recovered. Information about lot/batch number has been requested.

Weitere VAERSDATA-Felder

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

VAERS 1255089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AL
Alter: 57,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 06.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Biopsy skin Blood pressure measurement Headache Heart rate Hypertension Memory impairment Night sweats Pain Pain in extremity

Symptomtext

This is a spontaneous report from a contactable consumer (patient). A 57-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247 and expiration date not provided), via an unspecified route of administration, on 06Apr2021 10:30 (at the age of 57-year-old), at single dose, for COVID-19 immunization. Medical history included chronic obstructive pulmonary disease (COPD) from 2018 and ongoing, and had a shot, a steroid for COPD; high blood pressure from 2016 and ongoing, and patient took medication for it; 7 heart attacks; 8 stents in his heart; patient was a smoker (ongoing, had been smoking for a long time. He was a walking post card for don't smoke. He stated that he can only walk twenty feet before he was out of breath); and patient was allergic to penicillin and Lortab. Family history included patient had a family member die of cancer and lupus. Patient had two biopsies for skin cancer (unknown date) within 4 weeks prior vaccinations. Concomitant medications were not reported. On 07Apr2021, the patient experienced extremely high blood pressure, arm aching, body aches, night sweats, and headaches. The patient stated since receiving the vaccine, that his blood pressure was very high and his medications were not bring it down. He stated that one of his blood pressures was 197/121 and this morning it was 181/130, which was extremely high for him. He stated that he went through the aches and his arm was hurting. He even had sweats last night. Patient stated that his blood pressure still hadn't come down and he could feel headache from the pressure. He stated he already called the doctor, and the doctor told him that if it persisted to go to the emergency room. He stated that he took a couple of medications for his blood pressure and he declined giving medication information. He said that one started with an R and he took another one twice a day. He said that all the names of them, remembering them at his age was hard. He stated that he could read that small writing he had to get a magnifying glasses. Patient was scheduled for next vaccine on 04May2021. He stated that his blood pressure was not so unbearable but it was pretty high, he checked his blood pressure twice a day for everyday. He stated whatever he was lucky if he remembers if he had breakfast in the morning, until he remembered that he hadn't had breakfast. He stated that his arm started aching on 07Apr2021, it had improved but was still ongoing. He stated that it felt pretty good. Patient's blood pressure had been constant since today was the 8th it's only been a little over 24 hours now. On 07Apr2021 he had night sweats. He woke up pillow was soaking wet. He stated that his body aches still ongoing started about the same time. His headache started at the same time and was still going on. Patient stated he had a heart attack in 2016 and he hadn't had a normal blood pressure since. He hadn't been able to keep it all in check since the vaccine. His blood pressure medicine had been changed from 20 mgs to 40 mgs. He was under constant doctor care. The patient underwent lab tests and procedures, which included blood pressure was 197/121 (unknown date), 181/130 (08Apr2021), and 165/116 (08Apr2021). Patient's heart rate was 85 (unknown date). Patient stated his normal blood pressure was 135/85, his normal heart rate was 75. The outcome of the events "extremely high blood pressure", "body aches", "headaches" was not recovered; of event "arm aching" was recovering; of other events was unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: biopsies; Result Unstructured Data: Test Result:unknown results; Test Name: blood pressure; Result Unstructured Data: Test Result:197/121; Test Name: blood pressure; Result Unstructured Data: Test Result:135/85; Comments: patient's normal blood pressure; Test Date: 20210408; Test Name: blood pressure; Result Unstructured Data: Test Result:181/130; Test Date: 20210408; Test Name: blood pressure; Result Unstructured Data: Test Result:165/116; Test Name: heart rate; Result Unstructured Data: Test Result:85; Test Name: heart rate; Result Unstructured Data: Test Result:75; Comments: patient's normal heart rate
Aktuelle Erkrankungen: Blood pressure high; COPD (had a shot, a steroid for COPD); Smoker (had been smoking for a long time)
Vorgeschichte: Medical History/Concurrent Conditions: Angioplasty (8 stents in his heart); Cancer (patient had a family member die of cancer and lupus); Drug allergy; Heart attack (7 heart attacks); Lupus erythematosus (patient had a family member die of cancer and lupus)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1254152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 25.04.2021
Impfdatum: 31.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Alanine aminotransferase Alanine aminotransferase increased Aspartate aminotransferase Aspartate aminotransferase increased Asthenia Blood test Chest discomfort Chest pain Dizziness Dyspnoea Electrocardiogram Electrocardiogram T wave abnormal Enzyme level test Exercise electrocardiogram Hyperventilation Liver function test

Symptomtext

This is a spontaneous report from a contactable consumer (patient). A 74-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 31Jan2021 (Batch/Lot Number: EL3247; Expiration Date: May 2021) (at the age of 74-years-old) as single dose for COVID-19 immunization/COVID-19 protection. Medical history included low thyroid, blood pressure high and cholesterol (abnormal), and drinks 2-3 Oz of Vodka per night before immediately falling asleep. The patent did not have COVID-19 prior to vaccination. The patient had no known allergies. The patient was not pregnant. The patient did not receive other vaccine in four weeks. Concomitant medications included hydrochlorothiazide, lisinopril taken for blood pressure from an unspecified start date and ongoing; atorvastatin taken for cholesterol from an unspecified start date and ongoing; liothyronine sodium taken for thyroid in the 1970's and ongoing; liothyronine sodium (CYTOMEL) taken for thyroid from an unspecified start date and ongoing, unspecified sleeping pill (from Costco) at night. It was reported that the day after the first vaccine, patient had tightness of chest pain, heavy breathing and started having severe weakness. If she walked from one room to another, she was dizzy and lightheaded and felt like she was going to pass out. She didn't call her doctor because she had an appointment already scheduled for 09Feb2021. The patient also experienced shortness of breath on Feb 2021. Patient didn't put that to the vaccine but 7 days later, she started feel better and went to see a doctor. He did an EKG on 09Feb2021. The EKG came back abnormal/irregular with elongated T waves. Ten days later (Feb 2021), patient had treadmill test, it was normal. She was feeling normal. Patient was curious if there is possibility that it might have been caused by the vaccine. The treadmill test was normal but first EKG about 9 days after getting the vaccine was irregular that is why he sent patient to get treadmill. Patient also stated she had normal liver function test. Patient got the first vaccine on 31Jan2021 and the liver enzymes were part of the panel test doctor gave but the liver enzymes were way high. Patient was curious because that might be result of Pfizer vaccine. She had some blood test on 09Feb2021 and some things were abnormal. Her liver enzymes jumped significantly compared to the results 27Oct2020. The ALT on 27Oct2020 was 43. On 09Feb2021 the ALT was 84. Her AST increased from 37 on 27Oct2020 to 94 on 09Feb2021. Patient further stated her main concern is the elevated liver enzyme because vaccine has caused that because she never had elevated liver enzymes before. The last laboratory (whole panel blood test: unknown results) patient had was on 09Feb2021. Her doctor is convinced that she is an alcoholic. She is not an alcoholic. She takes a Costco brand sleeping pill at night and drinks 2-3 Oz of Vodka. She falls asleep immediately. She has since had some lab work done, which indicated elevated LFTs. Patient says her LFTs "doubled in a 3 month period". They were in the 30's in November (2020) and 09Feb2021 was 84. The events resulted to a visit to the physician's office. No treatment was provided for the elevated liver enzymes and irregular EKG result. The patient visited the physician office due to the severe weakness, dizzy, Tightness in her chest and heavy breathing, elevated liver enzymes. The patient recovered from severe weakness, dizzy/lightheaded on 07Feb2021, from heavy breathing on 08Feb2021, from the tightness in chest pain on 10Feb2021. The outcome of dyspnea was recovering, event EKG T wave abnormal was recovered on unspecified date, event while for other events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20201027; Test Name: ALT; Result Unstructured Data: Test Result:43; Test Date: 20210209; Test Name: ALT; Result Unstructured Data: Test Result:84; Test Date: 20201027; Test Name: AST; Result Unstructured Data: Test Result:37; Test Date: 20210209; Test Name: AST; Result Unstructured Data: Test Result:94; Test Date: 20210209; Test Name: whole panel blood test; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210209; Test Name: EKG; Result Unstructured Data: Test Result:abnormal/irregular with elongated T waves; Test Name: Liver enzymes; Result Unstructured Data: Test Result:previously always normal; Test Date: 20210209; Test Name: Liver enzymes; Result Unstructured Data: Test Result:high/jumped significantly; Test Date: 202102; Test Name: treadmill test; Result Unstructured Data: Test Result:normal; Test Date: 202011; Test Name: LFTs; Result Unstructured Data: Test Result:30s; Test Date: 20210209; Test Name: LFTs; Result Unstructured Data: Test Result:84; Test Date: 202102; Test Name: LFTs; Result Unstructured Data: Test Result:elevated/doubled
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Alcohol use; Blood cholesterol abnormal; Blood pressure high; Thyroid function decreased (take medications for high blood pressure and cholesterol)
Andere Medikamente: LISINOPRIL AND HYDROCHLOROTHIAZIDE; ATORVASTATIN; LIOTHYRONINE SODIUM; CYTOMEL
Allergien: -
Vorherige Impfungen: -

VAERS 1247884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 44,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 26.01.2021
Beginn: 22.04.2021
Tage bis Beginn: 86,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Chills Cough Dyspnoea Headache Myalgia Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 1/5/21, 1/26/21 Tested positive for COVID by PCR on 4/22/21 Onset date of symptoms 4/21/21 w/ mild SOB, cough, chills, myalgias, sore throat, H/A, rhinorrhea/congestion Possible household exposure to COVID

Weitere VAERSDATA-Felder

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

VAERS 1224925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: -
Geschlecht: U
Eingang: 18.04.2021
Impfdatum: 26.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Ageusia Anosmia Arrhythmia Arthralgia Asthenia Condition aggravated Discomfort Dizziness Encephalopathy Fall Infection Loss of personal independence in daily activities Memory impairment Muscle spasms Myalgia Pain in extremity SARS-CoV-2 antibody test SARS-CoV-2 test

Symptomtext

brain dysfunction; dysrhythmia; literally had to quit working because could not function; I got my second vaccine and my symptoms became much worse; weak; dizzy; Forgetful; I had quite severe cramps with muscle pains; I had quite severe cramps with muscle pains; Loss of taste and smell; Loss of taste and smell; I am having dizziness to the point where I am literally tripping over and specially; I can't see that is my eyes are closed or lights are off; a loop problem which was small irritation on finger tips; specially can't see that is eyes are closed or lights are off; joint pain; now had turned into a very pain full and persisting what appeared to be kind of infection; uncomfortable; was having all of the pain in my limbs, arms and thighs.; This is a spontaneous report from a contactable physician (patient). This 77-Year-old patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 26Jan2021 (Lot: EL3247) as single dose for COVID-19 immunisation and unspecified medication. Medical history included Myopathy, Sleep apnea diagnosed from 2006 (reported for 15 years ago, as of 02Apr2021), High cholesterol, Blood pressure high, first heart attack in 2010 and second heart attack in 2017, Trauma, Prostate enlargement from 2016, prostate enlargement that was biopsy that didn't have any cancer and some changes in PSA levels and then stating so on. But it was diagnosed about 5 years ago, acoustic neuroma. Concomitant drugs included tocotrienols nos at 200 mg, 1x/day, ascorbic acid (VIT C) at 2000 mg, 1x/day, pramipexole dihydrochloride (MIRAPEX) at 5 mg, ASPIRIN [ACETYLSALICYLIC ACID], lisinopril (NEOPRIL [LISINOPRIL]), Metoprolol at 50 mg, and aluminium sulfate, calcium acetate (BUROFIX) at 2.5mg. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 07Jan2021 at age of 77-year-old lot number: EK9231 for COVID-19 immunisation and experienced fatigue, not feeling well, muscle aches, dizziness. The patient got second vaccine on Jan 26th and symptoms became much worse. The patient literally had to quit working because could not function was weak, dizzy, forgetful, had quite severe cramps with muscle pains, had puzzling symptoms similar to long hour Covid patient, loss of taste and smell. The patient thought may have Covid. The patient got tested again for Covid the test result of the active disease came negative. And then got Covid antibody test to see if any way that even the test was negative, so the patient had the infection and now the patient was having side effects and that came negative. The patient saw the neurologist and brain specialist, had the Brain scan saw the cardiologist as was having dysrhythmia. The patient saw back and bone expert the orthopedic doctor because was having all of the pain in limbs, arms and thighs. The patient saw rheumatologist as it was causing a lot of muscle pain, joint pain and things. Now, all of them basically said that the organ they were checking had minor problems. The patient had prior heart attack but there was no sign to do in the way of heart attack and heart failure had previous acoustic neuroma radiated in brain and that used to cause a little bit of dizziness but it was pretty much gone away and now was having dizziness to the point where was literally tripping over and specially can't see that is eyes are closed or lights are off. The patient further stated, this is more disturbing. Since the patient had the symptoms, did returned to work briefly at the end of Feb and after 3 days of work had to quit. The patient was not up to functioning so it's about a month now still feel a very, very strong presence of this function brain dysfunction and muscle pain. The patient had a course of steroids during this time to see if that would help had number of things pain medications (Unspecified Medications) and so on but nothing really is demonstrating any real help. The patient was having a loop problem which was small irritation on finger tips and now had turned into a very pain full and persisting what appeared to be kind of infection. And that still since the second shot. Outcome of the events was unknown. Causality included the patient believed they are. And would say that because a lot of people have the similar but less side effects.; Sender's Comments: Based on the information provided, known drug safety profile and plausible temporal association, the causality between the suspect drug and the events cannot be completely excluded. The impact of this report on the benefit-risk profile of the Pfizer product and on the conduct of the study 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: Arrhythmia
Hospital-Tage: -
Labordaten: Test Name: Covid antibody test; Test Result: Negative ; Test Name: tested; Result Unstructured Data: Test Result:active disease came negative; Test Name: Brain scan; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acoustic neuroma; Blood pressure high; Dizziness (previous acoustic neuroma radiated in brain and that used to cause a little bit of dizziness but it was pretty much gone away); Heart attack (Verbatim: Heart attack/First heart attack in 2010 and and second heart attack in 2017.); High cholesterol; Myopathy; Prostate examination (that was biopsy that didn't have any cancer and some changes in PSA levels and then stating so on. But it was diagnosed about 5 years ago); Sleep apnea; Trauma
Andere Medikamente: TOCOTRIENOLS NOS; VIT C; MIRAPEX; ASPIRIN [ACETYLSALICYLIC ACID]; NEOPRIL [LISINOPRIL]; METOPROLOL; BUROFIX
Allergien: -
Vorherige Impfungen: -

VAERS 1222707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: WI
Alter: 70,0
Geschlecht: M
Eingang: 17.04.2021
Impfdatum: 21.01.2021
Beginn: 09.03.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: - / LA

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

Blood test Dysstasia Fatigue Mobility decreased Musculoskeletal pain Pain in extremity White blood cell count increased

Symptomtext

26 DAYS AFTER 2ND SHOT - PAIN in upper arm/thigh/buttocks. SEVERE in the morning/lesser in evening. Difficult to raise arms/stand up/sit down/roll over in bed. Has gotten much worse. Also FATIGUE. Been working with the clinic. Still waiting for any relief.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: BLOOD PANEL done on 3/12/21. All was good except elevated white count. Being referred to a Rheumatologist. It's been a WAITING GAME with the clinic.
Aktuelle Erkrankungen: NONE
Vorgeschichte: CONGESTIVE HEART FAILURE/GOUT/HIGH BLOOD PRESSURE/STROKE
Andere Medikamente: SACUBITRIL/SPIRONOLACTONE/METROPOLOL/SOTALOL/FINASTERIDE/FUROSEMIDE/MIN=CHEX/CATAPLEX-G
Allergien: NONE
Vorherige Impfungen: -

VAERS 999445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

moderat

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Chest X-ray Computerised tomogram Dizziness Dysphagia Electrocardiogram Heart rate Heart rate increased Paraesthesia Swollen tongue Hypertension Laboratory test Skin warm

Symptomtext

Dizzy; lightheaded; warm tingly arm; tongue swelling; fast heart rate; This is a spontaneous report from a contactable Other HCP.A 47-years-old female patient received the first dose of the bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot noEL3247, Expiration date: unknown), via an unspecified route of administration anatomical location Right arm on 28Jan2021 12:30PM at single dose for COVID-19 immunization. Patient medical history included Hypothyroid, depression,add, Known allergies: Diflucan. Concomitant medication included Levothyroxine, Valacyclovir, Bupropion, Pepcid. On 28Jan2021 at 12:30 PM patient experienced Dizzy, lightheaded, warm tingly arm, tongue swelling, fast heart rate.resulted in: [Emergency room/department or urgent care] patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. the patient was not diagnosed with COVID-19; Since and prior to the vaccination. The outcome of the events was Recovering

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: heart rate; Result Unstructured Data: Test Result:fast
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADD; Depression; Hypothyroidism
Andere Medikamente: LEVOTHYROXINE; VALACYCLOVIR [VALACICLOVIR]; BUPROPION; PEPCID [FAMOTIDINE]
Allergien: -
Vorherige Impfungen: -

VAERS 999445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest X-ray Computerised tomogram Dizziness Dysphagia Electrocardiogram Heart rate Heart rate increased Paraesthesia Swollen tongue Hypertension Laboratory test Skin warm

Symptomtext

Dizzy; lightheaded; warm tingly arm; tongue swelling; fast heart rate; This is a spontaneous report from a contactable Other HCP.A 47-years-old female patient received the first dose of the bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot noEL3247, Expiration date: unknown), via an unspecified route of administration anatomical location Right arm on 28Jan2021 12:30PM at single dose for COVID-19 immunization. Patient medical history included Hypothyroid, depression,add, Known allergies: Diflucan. Concomitant medication included Levothyroxine, Valacyclovir, Bupropion, Pepcid. On 28Jan2021 at 12:30 PM patient experienced Dizzy, lightheaded, warm tingly arm, tongue swelling, fast heart rate.resulted in: [Emergency room/department or urgent care] patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. the patient was not diagnosed with COVID-19; Since and prior to the vaccination. The outcome of the events was Recovering

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: heart rate; Result Unstructured Data: Test Result:fast
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADD; Depression; Hypothyroidism
Andere Medikamente: LEVOTHYROXINE; VALACYCLOVIR [VALACICLOVIR]; BUPROPION; PEPCID [FAMOTIDINE]
Allergien: -
Vorherige Impfungen: -

VAERS 1204827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 81,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 21.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood thyroid stimulating hormone C-reactive protein Chest X-ray Decreased appetite Fatigue Full blood count Loss of personal independence in daily activities Metabolic function test Red blood cell sedimentation rate Tremor Vitamin B12 Vitamin D

Symptomtext

3rd or 4th day after shot: Extreme fatigue, severe weakness, shakiness, especially in lower extremities. Often trembly with complete lack of appetite (lost 6 pound in 2 weeks). Only wanted to sit or lie down- unable to go for daily walk (no strength). No fever or respiratory symptoms. This extreme condition lasted for approx. 10 weeks, during which time I saw my doctors five times for diagnosis or assistance. They could find no reason for my sudden symptoms except for adverse reaction to the vaccine, and were unable to assist. I mostly sat and laid around for 10/11 weeks , after which my symptoms improved gradually, and I am feeling better at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Labs Feb.01, 2021 : CBC, Metabolic, TSH chest Xray Feb17, 2021 CBC, Metabolic, Vitamin B12, D3, Creactive protein, Sed Rate
Aktuelle Erkrankungen: None
Vorgeschichte: Insomnia, borderline HBP and cholesterol
Andere Medikamente: Montelukast 10mg - 1 per day (Singulair)
Allergien: None
Vorherige Impfungen: -

VAERS 1190787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: OK
Alter: 65,0
Geschlecht: M
Eingang: 10.04.2021
Impfdatum: 05.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Ageusia Back disorder Condition aggravated

Symptomtext

No sense of taste in my mouth; It is like 75% has gone/no taste, no taste buds/after Covid-19 Vaccine it got worsened; No sense of taste in my mouth; It is like 75% has gone/no taste, no taste buds/after Covid-19 Vaccine it got worsened; chronic back problem, they seem to worsening, in his spine, in his joint, his back in lower back area and in his shoulder part; chronic back problem, they seem to worsening, in his spine, in his joint, his back in lower back area and in his shoulder part; This is a spontaneous report from a contactable consumer (patient). A 65-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot Number: EL3247, expiration date unknown), via an unspecified route of administration on 05Feb2021 at the age of 65 years old at a single dose for COVID-19 immunization. The patient's medical history included ongoing arthritis, started experiencing this problem with my taste in Aug2020. Concomitant medications included acetaminophen for arthritis, cetirizine (tablet) at 1 DF, once a day, vitamin D1, vitamins and multivitamins. Patient stated on 05Feb2021, got first Pfizer shot. Patient noticed that they told him to come back in about three weeks. From 05Feb2021, they told him to come back on 26Feb2021. He said okay. First of 15 minutes they told him to stay there to see if he had any reactions. He was okay. He noticed in probably the last week and half though that he had a sense like no taste, no taste buds, and no sense of taste in his mouth. It is like 75% has gone on an unspecified date in 2021. Other symptoms are, patient got some chronic back problem, they seem to worsening, in his spine, in his joint, his back in lower back area and in his shoulder part area also on an unspecified date in 2021. Should he get his second shot coming up 26Feb2021, go ahead and get it?" was his question. Patient stated, "I am disabled vet (not clarified). I am like kind of regarded like 100% disabled vet. I am on 'test' in hospital where I got my shot. "Patient stated, "I just wanted to know if other people called in, told you about they start losing taste buds too, the sense of smell and taste." Patient stated, "I started experiencing this problem with my taste. It seems like around, probably Aug2020, I had like a some taste that I was losing but it seems like after I got this shot about when 4 months later, after I got the shot (Covid-19 Vaccine) I noticed it got worsened. But I am not running, no fever. I haven't had fever, cold or cough or chills or anything." The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Arthritis
Vorgeschichte: Medical History/Concurrent Conditions: Taste absent
Andere Medikamente: ACETAMINOPHEN; CETIRIZINE; VITAMIN D1
Allergien: -
Vorherige Impfungen: -

VAERS 1183012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 14.02.2021
Beginn: 11.03.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Abdominal pain upper Acute kidney injury Alanine aminotransferase increased Alpha 1 foetoprotein Analgesic drug level Aspartate aminotransferase increased Biliary dilatation Biopsy Bladder neck operation Blood bilirubin Blood phosphorus increased Computerised tomogram abdomen Condition aggravated Dyspepsia Endoscopic retrograde cholangiopancreatography normal Haemoglobin decreased Hepatitis viral test negative

Symptomtext

Pt admitted on 4/5/2021 c/o roughly 4 weeks of just general dyspepsia and feeling like she had acid reflux. She reports that then progressed to some nausea and then vomiting and then some generalized right upper quadrant midepigastric abdominal pain. She also noticed that her skin was becoming yellow. She reports no changes in any of her medications recently she had her second COVID-19 vaccination on 2/14 and blood work on 2/ 8 consisting of liver enzymes/CMP was normal. she arrived severely jaundiced with severe transaminitis, hyperbilirubinemia and acute renal failure. ERCP revealed no gross obstruction and free flowing bile and sphincterotomy was done with no improvement in her blood work. she remains hospitalized and is being transferred for HLOC due to worsening condition REVIEW OF SYSTEMS:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 6,0
Labordaten: CT abd/pelvis and MRI abd Significant intrahepatic and extrahepatic bile duct dilatation ERCP unrevealing and biopsies done and pending wbc 13.3, hgb 11.4, platelets 216 UA normal bilirubin 13.2, ast 2277, alt 1746, alk phos 1863, AFP neg, hepatitis and acetaminophen levels neg, autoimmune hepatitis work up pending
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, DM-2, obesity, past hx R sided breast cancer
Andere Medikamente: asa, Victoza, spironolactone, tradjenta, metoprolol, losartan, vit d, multivitamin
Allergien: codeine
Vorherige Impfungen: -

VAERS 1181550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 34,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Feeling hot Hyperventilation Malaise Nausea Respiratory rate increased Throat tightness Unresponsive to stimuli

Symptomtext

On Tuesday April 6th at around 4pm patient came in for her second vaccine dose with her co-worker. I asked them the questions surrounding the protocol for the vaccination and proceeded to take temperatures. One thing that did stand out before the injection was she mentioned that she was out of work for about 3 days after getting the shot because she fell ill. I asked her how long it lasted and she replied about 3 days. I then asked her if she wanted me to proceed with her second injection. that day and she said yes, and added it's one of those things that unfortunately happen. Some people have a reaction and I happen to be one of them:end quote. I gave her co-worker their injection first, then I gave her injection. About 5 mins in she started saying she was hot. I offered her some water and she said she was getting hot. About 10 mins in she started saying that she feels nauseous and hot still. We put a wet paper towel on the back of her neck. By that Time I has staff were up front assisting me with patient. That is when I asked someone to grab the Epinephrine injection for stand by and proceeded to call 911. I gave them all the information about the patient, but noticed that she was telling the ladies that her throat was tightening up and it was becoming hard to breathe. Her breathing was becoming deep and fast as I watched her from the phone. That is when I told one of them to give her the injections, because the patient was becoming unresponsive to our questions except for nodding of the head when asked can we inject her with the pen. After the injection was given, EMT was right at the door and started to triage the patient. I informed them that the patient had just received the epinephrine shot not even 5 mins before they walked through the door and she was given the wet paper towels to keep her cool because she was saying she was hot. After that another vehicle arrived and asked if she wanted to go to the Hospital and she said yes. They got her on the gurney and I gave them the information about what happened before they arrived along with her Injection card.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: illness for 3 days after 1st COVID-19 shot 3 weeks ago
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: illness for 3 days after first COVID-19, 03/16/2021, COVID 19, Pfizer-BioNTech vaccine

VAERS 1179217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NH
Alter: 28,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 15.02.2021
Beginn: 15.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Dizziness Dyspnoea Nausea Vomiting

Symptomtext

This is a spontaneous report from a contactable consumer. A 28-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration, administered in Arm Left on 15Feb2021 to 15Feb2021 (Lot Number: EL3247, at the age of 28-years-old) as single dose for covid-19 immunization. The patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 25Jan2021 (Lot Number: EL3247) as single dose for COVID-19 immunization. The patient did not have known allergies. There were no concomitant medications. The patient experienced shortness of breath, nausea, vomiting, dizziness when going from a sitting to standing on 15Feb2021. The outcome of the events was not recovered.

Weitere VAERSDATA-Felder

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

VAERS 1004413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 68,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 19.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / RA

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

Blood count Computerised tomogram Dizziness Dyspnoea Pulmonary mass Skin discolouration Weight decreased

Symptomtext

About 3 days I noticed the palm of my hands were like my veins, or arteries were very green and red I could see them through the palm of my hands, it was very obvious on the palm of my hands, both hands. It was not a lot, it was going towards my thumb and my little finger. I decided to go to the hospital the next day. I noticed the coloration would come and go several times a day. I also felt dizzy but I was already having the dizziness before the vaccine. I don't feel it now. I also have been experiencing weight loss. Unexplained. I have lost about 10-12 lbs. I have been about that they recommended a colonoscopy and an endoscopy. My PCP did a Cat scan and they saw some granules/nodules in my right lung and they want to monitor it. They said very little, about 6 of them. In the morning I also have been experiencing shortness of breath. I am very active, I do Zumba and I do not know why I have this shortness of breath. My hands have recovered, they never came back the coloration but I am concerned about your weight loss.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood work done at the ER. Dr. (PCP) ordered the Cat Scans
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure, arthritis, supraventricular tachycardia
Andere Medikamente: Amlodipine 10 mg, Metoprolol, Vitamin D, Zinc liquid, Flax Seed, Omega 3, Aspirin 81mg, Calcium, Chromium, multivitamin, drinking a lot of ginger tea and lemon tea.
Allergien: No
Vorherige Impfungen: -

VAERS 1175442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IN
Alter: 48,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 20.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Dyspnoea Injection site pain Lymphadenopathy Pain

Symptomtext

Pain at injection site; swelling under arm in lymph node area and left side of left breast; tenderness under arm, achiness, pain when sneezing/coughing or taking deep breaths in under arm/side breast area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Going to see doctor for exam 4/8/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lisinoprol 5m g; Claritin; Flonase
Allergien: None
Vorherige Impfungen: -

VAERS 1173638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: ME
Alter: 74,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 26.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Tremor

Symptomtext

violent shaking of all limbs / shaking so hard; This is a spontaneous report from a contactable consumer. A 74-year-old female patient (non-pregnant) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration on the left arm on 26Jan2021 at 12:30 PM at the age of 74 years old at a single dose for COVID-19 immunisation at nursing home. Medical history included hypertension, osteoporosis and spinal stenosis. Concomitant medications included hydrocodone bitartrate, paracetamol (HYDROCODONE/ACETAMINOPHEN) 5/325 mg, clonidine hcl. The patient previously took fluconazole, sulfamethoxazole, clindamycin and experienced allergies. Patient reported that patient fell asleep in chair after dinner 2-3 nights after vaccination was awakened by violent shaking of all limbs / shaking so hard on 28Jan2021 at 21:00 (09:00 PM) that her head and arm banged hard against the table almost fell out of the chair. She was awake but could not stop the shaking as though dreaming yet saw herself violently shaking as if in an earthquake lasted a full minute before completely waking no problems only being weirded out was told to report this incident by staff administering her second dose of vaccine. Patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient had not been tested for COVID-19. No treatment received for the event. The patient recovered from the event on an unspecified date in 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Osteoporosis; Spinal stenosis
Andere Medikamente: HYDROCODONE/ACETAMINOPHEN; CLONIDINE HCL
Allergien: -
Vorherige Impfungen: -

VAERS 1171912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: TX
Alter: 23,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 22.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Cough Fatigue Mobility decreased Oropharyngeal pain Respiratory tract congestion

Symptomtext

I experienced extreme fatigue, congestion, slight cough, sore throat after my vaccination. I had a virtual telemedicine. I was instructed to take a decongestion that had a anti-decongestion and Tylenol for pain. I was down for quite a bit for few days.

Weitere VAERSDATA-Felder

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

VAERS 1170875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: VA
Alter: 47,0
Geschlecht: M
Eingang: 06.04.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Urticaria chronic

Symptomtext

Acute exacerbation of Chronic Urticaria intractable to steroid taper and antihistamines. Sent to Immunologist. No Improvement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Sent to Immunologist for Testing/Work up on 3/15/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia, Chronic Urticaria
Andere Medikamente: Unknown
Allergien: History of Chronic Urticaria to unknown substances. KNDA, KNA
Vorherige Impfungen: -

VAERS 1162041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CT
Alter: 51,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 19.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Cardiac flutter Palpitations

Symptomtext

have been experiencing heart palpitations/flutter on and off for about 6-7 hours; have been experiencing heart palpitations/flutter on and off for about 6-7 hours; This is a spontaneous report from a contactable consumer (patient). A 51-years-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) (Batch/Lot Number: EL3247), via an unspecified route of administration administered in left arm on 19Feb2021 13:15 at single dose for COVID-19 immunisation. Medical history included migraines from an unknown date and unknown if ongoing. No known allergies. Concomitant medications included clarithromycin (CLARITIN), omeprazole (PRILOSEC), sertraline hydrochloride (ZOLOFT), and statin for cholesterol. The patient previously took the first dose of bnt162b2 (Batch/Lot Number: EL3247), administered in left arm on 27Jan2021 09:15 for COVID-19 immunisation. Patient was not pregnant. Facility type vaccine was clinic. No other vaccine received in four weeks. The patient has been experiencing heart palpitations/flutter on and off for about 6-7 hours on 23Feb2021 04:00. No treatment received. No COVID prior vaccination. No COVID tested post vaccination. Outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine
Andere Medikamente: CLARITIN [CLARITHROMYCIN]; PRILOSEC [OMEPRAZOLE]; ZOLOFT
Allergien: -
Vorherige Impfungen: -

VAERS 1058853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain upper Computerised tomogram Eye irritation Headache Hypertension Abdominal pain Acoustic stimulation tests normal Blood pressure increased Colonoscopy normal Computerised tomogram abdomen abnormal Ear discomfort Endoscopy normal Magnetic resonance imaging brain normal Mesenteritis Inflammation Insomnia Pain in extremity Pharyngeal paraesthesia

Symptomtext

has a constant severe headache; tinnitus in right ear/Tinnitus continues to persist/Right Ear ringing; stomach pain; high BP; sore arm; tinging in in throat and right side of face,; irritated right eye; Right Ear ringing worsened culminated in 8 days of insomnia from severe ringing; mesenteric inflammation; This is a spontaneous report from a contactable nurse (patient) and a consumer. A 51-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, administered in arm left on 29Jan2021 (Batch/Lot Number: EL3247) at single dose for COVID-19 immunization. Medical history included sciatica (resolved), and the patient took the first dose of BNT162B2 (lot/batch number: EL0142) at 15:00 on 29Dec2020 administered in arm right for COVID-19 immunization and developed paresthesias in right arm, into axilla, nex and right side of face and burning irritation of right eye, both on 24Jan2021. The patient's concomitant medications were not reported. Clinical course: 3 days after vaccination, patient developed sore arm, tinging in in throat and right side of face, irritated right eye. 6 days after vaccination, patient woke up with tinnitus in right ear, stomach pain and high BP. On 30Jan2021 (as reported), patient went to Emergency Room. CT scan showed mesenteric inflammation. Right Ear ringing worsened which culminated in 8 days of insomnia from severe ringing. Tinnitus continues to persist. He also had a constant severe headache. All events were reported as serious and seriousness criteria were disability. No allergies to medications, food, or other products. The adverse event result in Doctor or other healthcare professional office/clinic visit. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of events was not recovered.; Sender's Comments: Based on the information provided, known drug safety profile and plausible temporal association, the causality between BNT162B2 and the events cannot be completely excluded. The impact of this report on the benefit-risk profile of the Pfizer product and on the conduct of the study 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: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210130; Test Name: CT Scan; Result Unstructured Data: Test Result:mesenteric inflammation
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Conjunctivitis; Paresthesia; Sciatica (resolved)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac flutter Impaired work ability Injection site pain Injection site warmth Nausea Pain Palpitations Vomiting

Symptomtext

NauseaVomiting, Palpitations, pain and heat at injection site Narrative: Arrived to vaccine clinic observation area after receiving second COVID vaccine dose. Per vaccination RN needed to be 30 min observation due to anaphylaxis history and had strong reaction after 1st COVID dose of left sided pain, weakness (unable to walk fully 24 hours post dose #1). After dose #2 had initial complaints of nausea and sensation of heart fluttering, pain and heat at injection site on left deltoid. She was given water and white flower smelling oil/balm. Vitals were 140/71, HR 97, Tem; 96.8, 99% on RA, RR 24. At 2:30pm She was given zyrtec 10mg tab and ice pack to left arm and neck. At 2:40pm nausea and heart flutter resolved and she was was able to return to work. Employee was contacted on 1/30 and she had complaints of sore arm and body aches on 1/28 as well and had to call off work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: yes; PCN, flu and TB vaccine--anaphylaxis. Unknown, age, vaccine date and type and brand name.

VAERS 1151329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Body temperature Chills Erythema Pain in extremity Peripheral swelling Pruritus Pyrexia Tremor

Symptomtext

Approximately 18 hours after shot, woke up with extreme chills; body shaking head to toe; fever of 100.5; Left arm very sore; it was swollen and very red; it was swollen and very red; it feels itchy; This is a spontaneous report from a contactable consumer. This 57-year-old female consumer(patient) reported that:A 57-years-old female patient received bnt162b2 ((PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EL3247)dose 2 via an unspecified route of administration, administered in Arm Left on 11Feb2021 07:45 asfor covid-19 immunisation .The patient medical history was not reported. The patient experienced approximately 18 hours after shot, woke up with extreme chills on 12Feb2021 01:00, body shaking head to toe on 12Feb2021 01:00 and, fever of 100.5 on 12Feb2021 01:00 and, left arm very sore and on 12Feb2021 01:00 and it was swollen and very red on 12Feb2021 01:00 and , it was swollen and very red on 12Feb2021 01:00 and, it feels itchy on 12Feb2021 01:00 and.The patient underwent lab tests and procedures which included body temperature: 100.5 on , body temperature: 101.9 and Approximately 18 hours after shot, woke up with extreme chills, body shaking head to toe and fever of 100.5 Took 600mg Ibuprofen, an hour later fever was 101.9, took 400mg Ibuprofen. Left arm very sore noticed that it was swollen and very red on Saturday. Swelling continued to get worse & redder & is still present today (Monday) & it feels itchy. Fever finally stopped Sunday evening. Every time the fever returned it took 1000 mg Ibuprofen and about 2 - 2-1/2 hours to go down and outcome of the events was not recovered. No follow-up attempts are possible; information about lot number cannot be obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: fever; Result Unstructured Data: Test Result:100.5; Test Name: fever; Result Unstructured Data: Test Result:101.9
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1150818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: TN
Alter: 86,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 19.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Chest X-ray Dehydration Erythema Periorbital swelling Peripheral swelling Pruritus Swelling Swelling face

Symptomtext

After vaccination began to experience itching and swelling of hands, arms, chest, back, and face which continued for almost two weeks; After vaccination began to experience itching and swelling of hands, arms, chest, back, and face which continued for almost two weeks; After vaccination began to experience itching and swelling of hands, arms, chest, back, and face which continued for almost two weeks; The symptoms progressed to redness swelling of the face, including swelling around the eyes; After vaccination began to experience itching and swelling of hands, arms, chest, back, and face which continued for almost two weeks; The symptoms progressed to redness swelling of the face, including swelling around the eyes; slight dehydration.; This is a spontaneous report from a contactable 86-year-old female non-pregnant patient (nurse) received first dose BNT162B2 (Solution for injection, lot number: EL3247, COVID 19, brand: Pfizer) on 19Jan2021 12:30 PM on Arm Left for COVID-19 Immunization. Patient medical history included Hypetension, mitral valve prolapse, cornea transplants both eyes, Allergies: sulfa. Concomitant medications included metoprolol, furosemide (LASIX), KCL, losartan, apixaban (ELIQUIS), cefalexin (KEFLEX). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. After vaccination began to experience itching and swelling of hands, arms, chest, back, and face which continued for almost two weeks even after taking an antihistamine, Allegra after the 3rd day of onset of symptoms on 21Jan2021. The symptoms progressed to redness swelling of the face, including swelling around the eyes on 21Jan2021. No shortness of breath. Went to physician on 05Feb2021 who prescribed lab work and chest X-ray to rule out SVC syndrome; chest X-ray was normal. Lab work was normal. With exception of slight dehydration on 21Jan2021. He gave her a shot of steroids and a prednisone dosing pack as well as ointment for the arms and hands which were still red and itching on that day. Redness of face was much improved within 24 hours and most facial swelling resolved by 08Feb2021. The physician did advise her not to take the second COVID shot. He do have photographs of the reaction on her face, arms and hands. No Seriousness criteria reported. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Outcome of events was recovering.; Sender's Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the reported events due to temporal relationship. Clinical presentation is suggestive of allergic reaction. There is limited information provided in this report. This case will be reassessed upon receipt of follow-up information. 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 Name: chest X-ray; Result Unstructured Data: Test Result:normal; Comments: chest X-ray was normal.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Corneal disorder (cornea transplants both eyes); Hypertension; Mitral valve prolapse; Sulfonamide allergy (Allergies: sulfa)
Andere Medikamente: METOPROLOL; LASIX [FUROSEMIDE]; KCL; LOSARTAN; ELIQUIS; KEFLEX [CEFALEXIN]
Allergien: -
Vorherige Impfungen: -

VAERS 1150504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MN
Alter: 68,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain upper Chills Headache Nausea Tremor Vomiting

Symptomtext

Nausea; Vomiting; Chills; Stomach pain; Slight headache; Uncontrollable shaking; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 68-year-old female patient (patient was not pregnant at the time of vaccination) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EL3247, Expiry date: unknown) via an unspecified route of administration, administered in Left arm on 28Jan2021 at 14:00 (at the age of 68-years-old) at a single dose for covid-19 immunisation. Medical history included bronchiectasis and dysthymia. Allergies to medications, food, or other products included Rash with amoxicillin. Concomitant medication patient received within 2 weeks of vaccination included sertraline hydrochloride (ZOLOFT) and ovata (METAMUCIL [PLANTAGO OVATA]). The patient previously took amoxicillin and experienced rash. The patient experienced nausea, vomiting, chills, stomach pain, slight headache and uncontrollable shaking on 28Jan2021 at 21:30 PM. The event was considered as non-serious. The most recent COVID-19 vaccine was administered in hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. No treatment was received for the adverse event. The patient was recovering form all the events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bronchiectasis; Dysthymia
Andere Medikamente: ZOLOFT; METAMUCIL [PLANTAGO OVATA]
Allergien: -
Vorherige Impfungen: -

VAERS 1149356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 63,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 05.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Electrocardiogram Heart rate increased Hypertensive crisis Lymphadenopathy Metabolic function test Palpitations Troponin Ultrasound scan

Symptomtext

Enlarged left sided supra clavicular lymph nodes noted 2/6/2021. Hypertensive crisis on 2/11/2021 with blood pressure 202/101 and palpitations with heart rate 113.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 12 lead EKG, troponin levels, BMP, Left upper neck ultrasound all on 2/11/2021,
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Penicillin, Morphine
Vorherige Impfungen: -

VAERS 1096425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 58,0
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 18.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: - / LA

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

Cardiac stress test abnormal Chest pain Computerised tomogram abnormal Electrocardiogram abnormal Prinzmetal angina Scan with contrast abnormal Ultrasound scan normal

Symptomtext

5 days after I started to have chest pain. It was variable and now I have been diagnosed with Prinzmetal angina; This is a spontaneous report from a contactable other healthcare professional (patient). A 58-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3247) via an unspecified route of administration, administered on the left arm on 18Jan2021 11:00 at a single dose for COVID-19 immunisation. Medical history included high BP that was under control and allergy: glue on tape used in hospitals. Concomitant medications included losartan, levothyroxine and hydrochlorothiazide. On 23Jan2021 02:00 PM (5 days after), the patient started to have chest pain. It was variable and now I have been diagnosed with Prinzmetal angina. Treatment was received for the events. The events resulted to a doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient is in the process of stabilizing the angina. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient has not been tested for COVID-19. Patient was not pregnant. The facility where the vaccine was administered was in a hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Outcome of the events was not recovered.; Sender's Comments: Based on temporal association, the causal relationship between BNT162B2 and the event Prinzmetal angina cannot be excluded. The information available in this report is limited and does not allow a medically meaningful assessment. This case will be reassessed once additional information becomes available. 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: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adhesive tape allergy; Blood pressure high
Andere Medikamente: LOSARTAN; LEVOTHYROXINE; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1096425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 58,0
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 18.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac stress test abnormal Chest pain Computerised tomogram abnormal Electrocardiogram abnormal Prinzmetal angina Scan with contrast abnormal Ultrasound scan normal

Symptomtext

5 days after I started to have chest pain. It was variable and now I have been diagnosed with Prinzmetal angina; This is a spontaneous report from a contactable other healthcare professional (patient). A 58-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3247) via an unspecified route of administration, administered on the left arm on 18Jan2021 11:00 at a single dose for COVID-19 immunisation. Medical history included high BP that was under control and allergy: glue on tape used in hospitals. Concomitant medications included losartan, levothyroxine and hydrochlorothiazide. On 23Jan2021 02:00 PM (5 days after), the patient started to have chest pain. It was variable and now I have been diagnosed with Prinzmetal angina. Treatment was received for the events. The events resulted to a doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient is in the process of stabilizing the angina. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient has not been tested for COVID-19. Patient was not pregnant. The facility where the vaccine was administered was in a hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Outcome of the events was not recovered.; Sender's Comments: Based on temporal association, the causal relationship between BNT162B2 and the event Prinzmetal angina cannot be excluded. The information available in this report is limited and does not allow a medically meaningful assessment. This case will be reassessed once additional information becomes available. 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: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adhesive tape allergy; Blood pressure high
Andere Medikamente: LOSARTAN; LEVOTHYROXINE; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 975692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 29.03.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Antinuclear antibody Electromyogram normal Eye irritation Feeling cold Feeling hot Paraesthesia Flushing Muscle twitching Ocular discomfort Pain in extremity Skin warm Throat tightness

Symptomtext

Developed paresthesias in right arm, into axilla, nex and right side of face; burning irritation of right eye; This is a spontaneous report from a contactable nurse (the patient). A 51-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot#: EL0142), via an unspecified route of administration, in the right arm on 29Dec2020 at 15:00 PM (at the age of 51 years) as a single dose for COVID-19 immunization. Medical history included sciatica. There was no known allergies. There were no concomitant medications. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 29Dec2020, within 4 hours of vaccination, the patient developed paresthesia's in right arm, into axilla, neck and right side of face, burning irritation of right eye. The patient was evaluated by neurologist. No treatment given. Symptoms resolved in 10 days. The clinical outcome of the events paresthesia's in right arm, into axilla, neck and right side of face, burning irritation of right eye was recovered on 08Jan2021. It was also reported that since the vaccination, the patient had not been tested for COVID-19.; 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 cannot be excluded. The case will be reassessed if additional information becomes available. 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.

Weitere VAERSDATA-Felder

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

VAERS 1142294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: LA
Alter: 63,0
Geschlecht: F
Eingang: 28.03.2021
Impfdatum: 06.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Fatigue Impaired work ability Tinnitus

Symptomtext

Fatigue: I had Covid last summer and experienced fatigue for several months. I felt better by the Fall but fatigue returned after my 2nd dose of the vaccine. Unable to work for normal 8-9 hours/day. This has been for the past two months. Symptoms seem to be getting better slowly. Tinnitus: I had mild tinnitus prior to the vaccine but it has increased. No change in the past two months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None. I contacted my doctor who recommended that I rest, sleep, walk 45 minutes per day, good nutrition, multi vitamin.
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia Migraine Headaches
Andere Medikamente: Duloxetine Lunesta clonazepam Multi Vitamin Benadryl
Allergien: None
Vorherige Impfungen: -

VAERS 1136083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 25,0
Geschlecht: F
Eingang: 25.03.2021
Impfdatum: 27.01.2021
Beginn: 20.03.2021
Tage bis Beginn: 52,0
Dosis: 1
Route/Site: SYR / LA

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

Headache Hypertension Tinnitus

Symptomtext

I have been experiencing high blood pressure between about 140/90 and 130/85 with headaches and tinnitus. Blood pressure remains high throughout the day and was first noticed on 03/20/2021. I first took my blood pressure after noticing a mild headache that was not alleviated with hydration or OTC pain medication. Headaches have returned intermittently since 03/20/2021 but now only lasts 1-2 hours. Tinnitus was noticed several weeks ago (specific date is unknown) and is a mild and quiet but constant high frequency ringing. Unsure if any of these are related but I have never had tinnitus and my blood pressure is not this high nor do I have headaches often or back-to-back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Pfizer COVID-19 vaccine first dose on 01/27/2021 and second dose on 02/23/2021.
Aktuelle Erkrankungen: Asymptomatic COVID diagnosis on 12/24/2020. No others.
Vorgeschichte: None.
Andere Medikamente: Yaz hormonal birth control. Ibuprofen or Naproxen occasionally (about x1 tablet/month) for pain.
Allergien: None.
Vorherige Impfungen: -

VAERS 1129949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: OR
Alter: 62,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Electrocardiogram abnormal Heart rate increased Hot flush Lethargy Throat irritation Tongue pruritus Tremor Troponin increased Vaccination complication

Symptomtext

Within 30 min of shot, starting feeling itchy tongue and throat. Drank water and within a few minutes got a full body heat flush and starting shaking all over. Heart beating fast and having some pain in chest. Drove to her work place and was assessed by MD and RN on staff. BP was 220/120, pulse over 100. She took a Claritin and was monitored in the work place. She became lethargic and chest pain continued so she went to the closest Emergency Room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 2/2/2021- In ER had abnormal EKG, elevated troponin levels. 5ng/L and second one 17ng/L. Diagnosis at discharge: Adverse effect to vaccine.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma, Hypothyroid
Andere Medikamente: Levothyroxine, Estradiol, Women's multivitamin, Albuterol
Allergien: None
Vorherige Impfungen: -

VAERS 1123128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 28.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Burning sensation Dizziness Erythema Feeling hot Paraesthesia Pruritus Rash

Symptomtext

right cheek redness; right cheek redness and rash with burning; right cheek redness and rash with burning; itching; tingling sensations; felt hot; dizzy; This is a spontaneous report from a contactable consumer. A 67-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, lot EL3247, expiry date not reported), via an unspecified route of administration, administered in the left arm on 28Jan2021 as a single dose for COVID-19 immunisation. Medical history included hypertension and hypothyroidism, both from an unknown date and unknown if ongoing. The patient had COVID prior vaccination (dates unspecified). The patient was not pregnant at the time of the vaccination and report. The patient's concomitant medications were not reported. The patient had known allergies to aspirin, codeine, metoclopramide, morphine, hydromorphone, tramadol, hydrocodone, and prochloperazine maleate (COMPAZINE). The vaccination was done in the hospital. In Jan2021 (also reported as 18Jan2021), patient experienced right cheek redness and rash with burning, itching, tingling sensations. The patient also felt hot and dizzy. The events caused hospitalization from an unspecified date in 2021. The patient was not tested for COVID post vaccination. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If COVID prior vaccination: Yes); Hypertension; Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1121149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 21.03.2021
Impfdatum: 20.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Electrocardiogram Electrocardiogram ambulatory Fatigue Headache Postural orthostatic tachycardia syndrome Pyrexia

Symptomtext

24 hours after receiving the second vaccine, I developed fevers, headaches, chills, exhaustion and tachycardia. All symptoms improved within 4 days. However, the tachycardia has persisted. I am experiencing postural tachycardia. When sitting my HR is 80s to 90s, upon standing my heart rate increases to 120s-130s. Currently I am under the care of a cardiologist. She is unsure if the tachycardia is due to the vaccine or if it triggered something that was underlying. Plan to increase my fluids, wear compression stockings, and follow up in 3 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Postural orthostatic tachycardia syndrome
Hospital-Tage: -
Labordaten: I had a ECG, Echocardiogram, 24 hour holter monitor and 1 week holter monitor.
Aktuelle Erkrankungen: -
Vorgeschichte: Constipation
Andere Medikamente: BCP pill, Linzess
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1114277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 83,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 22.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain lower Asthenia Back pain Body temperature Body temperature increased Computerised tomogram Dyspnoea Lung opacity Nausea Pain SARS-CoV-2 test

Symptomtext

Ground Glass Opaque lung problem; Weak; nausea; diff.breathing; pain on rt.side waist around to back,down to lower belly; slight temp almost 100; pain on rt.side waist around to back,down to lower belly; pain on rt.side waist around to back,down to lower belly; This is a spontaneous report from a contactable consumer. A 83-year-old female patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL3247), via an unspecified route of administration, administered in Left Arm on 22Jan2021 10:45 am as SINGLE DOSE for covid-19 immunisation. Medical history included overweight, sleep apnoea syndrome and ongoing shortness of breath. Concomitant medication included levothyroxine strength 125 mcg; triamterene; colecalciferol (VIT.D3) and thiamine (VITAMIN B1). The patient previously took tylenol and experienced drug intolerance (Known allergies: Cannot tolerate anything but Tylenol). No other vaccine in four weeks. Facility type vaccine was Workplace clinic. The patient experienced weak (asthenia) on 23Jan2021 15:00, nausea on 23Jan2021 15:00, diff. breathing (dyspnoea) on 23Jan2021 15:00, pain on rt.side waist around to back, down to lower belly (pain) on an unspecified date in 2021, ground glass opaque lung problem (lung opacity) on an unspecified date, slight temp almost 100 (body temperature increased) on an unspecified date in 2021 and pain on rt.side waist around to back, down to lower belly both on an unspecified date in 2021. AE resulted in [Emergency room/department or urgent care]. Treatment was received for these events (Levofloxacin 500mg). It was reported that Weak, nausea, diff. breathing, urgent care on Fri. 05Feb2021, with pain on rt. side waist around to back, down to lower belly. Contrast Cat Scan showed no signs where pain was, but found Ground Glass Opaque lung problem. Is it safe to take #2 vaccine I'm on oxygen now, slight temp almost 100, usually 97. There was no covid prior vaccination. Patient has covid tested post vaccination as SARS-COV-2 test: negative (Nasopharyngeal) on 05Feb2021. The outcome of events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: temp; Result Unstructured Data: Test Result:slight temp almost 100; Comments: usually 97; Test Date: 2021; Test Name: Contrast Cat Scan; Result Unstructured Data: Test Result:Ground Glass Opaque lung problem; Comments: Contrast Cat Scan showed no signs where pain was, but found Ground Glass Opaque lung problem.; Test Date: 20210205; Test Name: Nasal Swab; Test Result: Negative ; Comments: Nasopharyngeal
Aktuelle Erkrankungen: Shortness of breath
Vorgeschichte: Medical History/Concurrent Conditions: Overweight; Sleep apnea
Andere Medikamente: LEVOTHYROXINE; TRIAMTERENE; VIT.D3; VITAMIN B1 [THIAMINE]
Allergien: -
Vorherige Impfungen: -

VAERS 1112016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 27.01.2021
Beginn: 11.02.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / LA

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

Hypersensitivity Paraesthesia

Symptomtext

allergic reaction Paresthesia of skin

Weitere VAERSDATA-Felder

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

VAERS 1108510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Balance disorder Chest discomfort Dizziness Ear disorder Immediate post-injection reaction Muscular weakness Tachycardia

Symptomtext

Received vaccine stood up immediately felt light headed, off balance, tachycardia, weak in the knees. Sat for 15 minute taking deep breaths and symptoms resolve. 8-10 hour late at bedtime felt all above symptoms again plus heighten hearing and tunnel vision. Again took deep breaths and symptoms resolved For the week after was having chest tightness, frequently but has become intermittent. PCP thinks may be anxiety.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multi Vitamins
Allergien: Sulfa - eye drops
Vorherige Impfungen: -

VAERS 1108169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 27,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Paraesthesia Pruritus

Symptomtext

Pt with hx of anaphylactic reaction to several medications. After 30 minutes, pt feels tingling and itchy skin on entire torso. No hives noted. No other symptoms. Actions Taken: Vitals taken at 1722 as follows: 135/82, HR 86, Respirations 14. O2 sats on RA 95%. No c/o shortness of breath, throat closing, itchy throat, SOB or stridor. After 15 minutes, Pt feels the same and no changes for the worse. Vitals at 1738 as follows 119/68, HR 85. O2 sat 96% on RA. Pt requests to head home and will take Benadryl upon arrival. Disposition: PT d/c to home per pt request @ 1820

Weitere VAERSDATA-Felder

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

VAERS 2620461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea exertional Headache Myalgia Pyrexia

Symptomtext

Headache, Myalgia, Fever, slight shortness of breath after walking a flight of stair on day 4 post vaccine Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2554161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 15.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Chills Headache Pyrexia Tremor

Symptomtext

Headache, Arthralgia, Fever, Shaking chills Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1104777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 24.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood thyroid stimulating hormone Breast tenderness Dizziness Feeling abnormal Headache Menstrual disorder Mood swings Paraesthesia Pharyngeal swelling

Symptomtext

Within an hour of receving the vaccine, I became dizzy, had face tingling and arm tingling and felt mentally foggy. As the day progressed, I felt a fullness in my throat and fatigue. Over the next week, the dizziness became worse, I experienced intense headaches and shortness of breath for several days. I had difficulty sleeping and vivid dreams. I have had thyroiditis twice in my life after giving birth to my 2 children with similar dizziness and throat fullness. I decided to contact my doctors and had my thyroid levels checked. My TSH was abnormal and my doctor thinks I could be having another episode of thyroiditis. My menstrual cycle arrived a week early. Following this, I continued to have dizziness, throat fullness, and intense headaches. I developed sore breasts and breast discharge as well as in increase in frequency of urination. I decided to postpone the second shot until I was feeling better as past episodes of thryoiditis took about 2 months to resolve. My next menstrual period was a week late, also accompanied by mood swings, breast tenderness and intense headaches. SIx weeks later, I continue to experience occasional dizziness and throat fullness and increased urination. Prior to the vaccine, I was feeling fine and it seems like the vaccine triggered some kind of hormone/endocrine response in my body. I have not had reactions to any vaccines prior to this. I am quite hesitant to receive the second vaccine and am wondering if I should wait a period of time and try something different such as the Johnson and Johnson one. I? not quite sure what in the Pfizer vaccine ( perhaps the mRNA?) could have triggered this reaction in my thyroid and endocrine system. and would appreciate guidance on what to do next as I would like to be fully protected from COVID-19 but do not want to endure these unusual side effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: TSH .31 on 2/3/21
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma VonWillebrands Disease GERD Thyroid Goiter
Andere Medikamente: Protonix
Allergien: Erythromyocin Ceftin Almonds
Vorherige Impfungen: -

VAERS 984471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Chest pain Dizziness Feeling hot Musculoskeletal stiffness Blood pressure increased Blood test Breast pain Echocardiogram Electrocardiogram Flushing Hepatic enzyme increased Immediate post-injection reaction Mammogram Neck pain Palpitations Panic reaction Troponin

Symptomtext

Within 2-3 mins I felt immediate flush light headed. Then shortly felt achy chest neck area for 20-25 mis. I left to go to my car while driving continue to feel light headed, heart racing and in panic. For 5 straight weeks exp burung left upper chest (breast area )occurring 10-15 times a day. I now have elevated high blood pressure have had appts with PCP, Allergist, Urgent Care don't know if this is vaccine related dint have these heart concerns before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: (4 )EKG, (1)Echocardiogram, Bloodwork, Troponin level(possible heart attack), Liver enzymes was elevated then took second it was normal. Mammogram
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Penicillin, Arrothromycine
Vorherige Impfungen: -

VAERS 984471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chest pain Dizziness Feeling hot Musculoskeletal stiffness Blood pressure increased Blood test Breast pain Echocardiogram Electrocardiogram Flushing Hepatic enzyme increased Immediate post-injection reaction Mammogram Neck pain Palpitations Panic reaction Troponin

Symptomtext

Within 2-3 mins I felt immediate flush light headed. Then shortly felt achy chest neck area for 20-25 mis. I left to go to my car while driving continue to feel light headed, heart racing and in panic. For 5 straight weeks exp burung left upper chest (breast area )occurring 10-15 times a day. I now have elevated high blood pressure have had appts with PCP, Allergist, Urgent Care don't know if this is vaccine related dint have these heart concerns before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: (4 )EKG, (1)Echocardiogram, Bloodwork, Troponin level(possible heart attack), Liver enzymes was elevated then took second it was normal. Mammogram
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Penicillin, Arrothromycine
Vorherige Impfungen: -

VAERS 1100529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Asthenia Contusion Diarrhoea Dizziness Fatigue Headache Hypoaesthesia Hypotension Nausea Pain in extremity Pallor SARS-CoV-2 test

Symptomtext

unexplained bruising; hypotension; pale face; diarrhea; facial numbness; nausea; general weakness/Low energy; dizzy; mild headache/severe headache; Sore arm; tired/Fatigue; This is a spontaneous report from a non-contactable Pharmacist reporting for herself. A 42-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3247), via an unspecified route of administration at right arm on 29Jan2021 13:45 at single dose for covid-19 immunisation. The COVID-19 vaccine was administered at Hospital. The patient's medical history included allergies to Sulfa, PCN, Ceph. Concomitant medications included calcium, colecalciferol (VITAMIN D) and Multivitamin. Patient was not pregnant. On 29Jan2021 07:00 PM: Sore arm, tired at night, 30Jan2021: Sore arm, fatigue, mild headache, 31Jan2021: Fatigue, severe headache, hypotension, pale face, diarrhea, facial numbness, nausea, general weakness, dizzy, 01Feb2021: Fatigue, severe headache, unexplained bruising, facial numbness, nausea, general weakness, dizzy. Employee Health sent patient for COVID testing at 13:20 (result: Negative). 02Feb2021: Fatigue, severe headache, facial numbness, nausea, general weakness, dizzy. 03Feb2021- 12Feb2021: Fatigue, severe headache, facial numbness, nausea, general weakness, dizzy. 11Jan2021: Fatigue, facial numbness. 12Feb2021: Fatigue, severe headache, facial numbness, general weakness. 23Feb2021 - Present: Low energy, intermittent mild-medium headaches. Adverse events resulted in: Doctor or other healthcare professional office/clinic visit, Disability or permanent damage. Therapeutic measures were taken as a result of sore arm and headache included Pain relievers. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient was not been tested for COVID-19. The outcome of the events was not recovered.; Sender's Comments: Considering temporal association and lacking of alternative explanation, a possible contributory role of BNT162B2 to all reported events cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Date: 20210201; Test Name: Covid-19; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Sulfonamide allergy
Andere Medikamente: CALCIUM; VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 1100412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MD
Alter: 77,0
Geschlecht: M
Eingang: 15.03.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Body temperature Body temperature decreased Chills Tremor Vaccination site pain

Symptomtext

low temperature (96.5); Chills; slight tremors; soreness at injection site; This is a spontaneous report from a non-contactable consumer (patient). A 77-years-old male patient received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3247), via an unspecified route of administration on 10Feb2021 08:15 at age of 77-years-old at arm left at single dose for COVID-19 immunisation. Medical history included bladder cancer, high blood pressure and no known allergies. Concomitant medication included allopurinol, amlodipine, valsartan, indapamide, atorvastatin (LIPITOR), pregabalin (LYRICA), metformin hydrochloride (MEDFORMIN), metoprolol succinate (TOPROL) and vitamin supplements. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The historical vaccine included the 1st dose of BNT162B2 on 18Jan2021 at age of 77-years-old for COVID-19 immunisation. The patient experienced chills, low temperature (96.5) and slight tremors, soreness at injection site on 10Feb2021 06:00 (as reported). No treatment was received for the adverse events. The events outcome was recovered on an unspecified date in Feb2021. No COVID prior vaccination, since the vaccination the patient hadn't been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20210210; Test Name: temperature; Result Unstructured Data: Test Result:96.5
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bladder cancer; Blood pressure high
Andere Medikamente: ALLOPURINOL; AMLODIPINE; VALSARTAN; INDAPAMIDE; LIPITOR [ATORVASTATIN]; LYRICA; MEDFORMIN; TOPROL
Allergien: -
Vorherige Impfungen: -

VAERS 1099086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 83,0
Geschlecht: F
Eingang: 14.03.2021
Impfdatum: 18.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Arthralgia Mobility decreased Pain

Symptomtext

Soreness in joints and pain in arm from shoulder to elbow. Soreness is going into upper portion of back and neck on right side. Very hard to lift arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None to date
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ibuprofen, Centrum silver, Hydrochlorot, pantoprazole
Allergien: None
Vorherige Impfungen: -

VAERS 1090267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: -
Geschlecht: M
Eingang: 11.03.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Muscular weakness Paraesthesia

Symptomtext

he has experienced tingling sensation in his fingertips and his nails; weakness in his arms; This is a spontaneous report from a Contactable consumer. A male consumer (patient) of an unspecified age received dose one of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EL3247 and Expiry date: Unknown), via an unspecified route of administration from 27Jan2021 as a SINGLE DOSE for covid-19 immunisation. Medical history included covid-19 from Nov2020. By 02Dec2020 he was fine and back to work. The patient's concomitant medications were not reported. The patient experienced tingling sensation in his fingertips and his nails on 28Jan2021 with outcome of unknown and, weakness in his arms on 28Jan2021 with outcome of unknown. He says it takes extra effort to move his arms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 992076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MD
Alter: 40,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 27.01.2021
Beginn: 11.03.2021
Tage bis Beginn: 43,0
Dosis: 2
Route/Site: IM / AR

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

Arthralgia Fatigue Hypoaesthesia Hypoaesthesia oral Laboratory test Pain Paraesthesia oral Myalgia

Symptomtext

20 minutes post injection developed numbness of the mouth and tongue that lasted for 48 hours then resolved. Myalgias, fatigue and athralgias lasted a week and improved in 1 week in severity but intermittent athrlagias continue to occur. Over 1 month post 2 nd injection developed numbness of bilateral hands and feet and numbness of the mouth had recurred and is persistent for 6 days now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: Labs are pending
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril 20 mg daily
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1086991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 10.03.2021
Impfdatum: 17.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Paraesthesia Vaccination site paraesthesia

Symptomtext

Started as localized tingling/pins and needle sensation by injection site approximately 4 hours after initial injection.; the sensation spread to all extremities (arms, hands, legs, and feet).; This is a spontaneous report from a contactable consumer (patient). This 27-year-old female patient received dose 1 of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL3247) via an unspecified route of administration on 17Jan2021 at 15:00 (at the age of 27-years-old) as a single dose in the left arm for COVID-19 immunization. Medical history was not reported. The patient was not pregnant at the time of vaccination. It was unknown if the patient had COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the vaccine. The patient did not receive any concomitant medications. The patient previously received cefprozil (CEFZIL) and vancomycin from unknown dates and experienced allergy. On 17Jan2021 at 19:00, the patient experienced localized tingling/pins and needle sensation by the injection site approximately 4 hours after initial injection. Over the course of the next day the sensation spread to all extremities (arms, hands, legs, and feet). It was three weeks since first dose and sensation had lessened but still felt at times. The patient did not receive any treatment for the events. The outcome of tingling by the injection site and sensation spread to all extremities was not recovered. It was also reported the patient had not been tested for COVID-19 since the vaccine. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1083513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: VA
Alter: 47,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Blood culture negative Blood test normal Chest X-ray normal Computerised tomogram abnormal Dyspnoea Impaired work ability Lethargy Malaise Pleuritic pain Pneumonia

Symptomtext

That same evening I began to be more short of breath and just didn't feel good. I had lethargy and general malaise. I had pleuritic pain in my right upper back that was a sharp pain with inspiration. All of this continued to get worse over time and I developed pneumonia. I wasn't able to go back to work from 1/27/21 to 3/6/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 1/29/21 - Dr visit with chest x-ray and D-dimer normal. Prednisone and Mobic prescribed. 2/3/21 - CT Scan ordered with contrast showing inflammation and pneumonia. 2/9/21 - ER visit with chest x-ray showing worsening pneumonia. Tons of labs obtained. Blood cultures negative. IV fluids and IV antibiotics given. Sent home with new po antibiotic. 2/16/21 - Dr's appointment
Aktuelle Erkrankungen: COVID positive 12/28/2020
Vorgeschichte: Hypertension diagnosis within 6 months prior
Andere Medikamente: Losartan 10 mg, HCTZ 12.5mg, Sertraline 200mg, Singulair, Vitamin B12, Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1083076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 10.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / -

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

Chest pain Electrocardiogram Headache Hypertensive crisis Laboratory test Palpitations Paraesthesia

Symptomtext

Severe hypertension. Following the second dose I was having severe headaches. I checked my blood pressure on 2/17/21 and it was 212/116. I was having palpitations and parathesia in my right foot. I immediately contacted my provider and he confirmed my hypertension and I was prescribed two separate anti hypertensive medications. I began these medications however they have been ineffective at treating the high blood pressure. I began to have chest pains, headaches continued, and due to the hypertensive crisis I presented to the ER on 3/3/21 which required IVP BP medications, EKG, cardiac labs, etc. Prior to the COVID vaccination I have always had a normal blood pressure at all of my physical appointments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 2/18/21 BP at doctors appointment was 160/100. On 3/2/21 an ER visit at MC was a high of 200/111 requiring IVP BP meds (PO did not work) and multiple lab work up.
Aktuelle Erkrankungen: Hypothyroidism , hypersomnia
Vorgeschichte: None
Andere Medikamente: Levothyroxine, methylphenidate, buprenorphine/naloxone, sertraline.
Allergien: Know known diagnosed allergies
Vorherige Impfungen: -

VAERS 1082972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: GA
Alter: 85,0
Geschlecht: M
Eingang: 08.03.2021
Impfdatum: 27.01.2021
Beginn: 10.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: OT / RA

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

COVID-19 pneumonia Drug ineffective SARS-CoV-2 test

Symptomtext

Developed Covid pneumonia and admitted to hospital; Developed Covid pneumonia and admitted to hospital; This is a spontaneous report from a contactable physician. An 85-year-old male patient received first dose of bnt162b2 (brand: Pfizer, lot number: EL3247), intramuscularly in right arm on 27Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced developed covid pneumonia and admitted to hospital on 10Feb2021, the event was reported as serious per hospitalization. The patient underwent lab tests and procedures which included nasal swab: positive on 15Feb2021. Therapeutic measures were taken as a result of developed covid pneumonia and admitted to hospital. The outcome of event was unknown. Facility type vaccine: Doctor's office/urgent care. The event resulted in hospitalization. No covid prior vaccination. Covid test post vaccination: nasal swab on 15Feb2021 showed positive.; Sender's Comments: Considering the plausible temporal association, the possibility that the reported COVID-19 pneumonia in a setting of drug ineffective is related BNT162B2 vaccine cannot be completely excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Test Date: 20210215; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1082915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El3247

moderat

Staat: AZ
Alter: 37,0
Geschlecht: M
Eingang: 08.03.2021
Impfdatum: 31.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain upper Chills Diarrhoea Fatigue Insomnia Migraine Myalgia Pain Pyrexia SARS-CoV-2 test Vomiting

Symptomtext

Insomnia; 103 Fever; Chills; Muscle and Total body pain; Muscle and Total body pain; Profuse vomiting; Migraine; Tiredness; Stomach pain; Diarrhea; This 37- year-old male patient contactable consumer (reported for himself) received the first dose BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE lot El3247), via an unspecified route of administration, on 31Jan2021 at 10:00 AM (at the age of 37-years-old) as a single dose for COVID-19 immunization, in left arm. The facility where COVID-19 vaccine was administered was at a Hospital. She has had no other vaccines on the same day or in the past 4 weeks. The patient has allergy to Ceclor and Cephalosporin. The patient has no relevant medical history and is not taking any concomitant medications. On 04Feb2021 at 5:00PM, the patient experienced 103 Fever, Chills, Muscle and Total body pain, Profuse vomiting, Migraine, Tiredness, Stomach pain and Diarrhea, Insomnia. The patient did not receive treatment for the events. The clinical outcome of the events 103 Fever, Chills, Muscle and Total body pain, Profuse vomiting, Migraine, Tiredness, Stomach pain and Diarrhea, Insomnia was not recovered. It was reported that since the vaccination, the patient had been tested for COVID-19 via nasal swab on 05Feb2021 with a negative result.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result:103; Test Date: 20210205; Test Name: Nasal Swab/ Rapid Test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1080209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NM
Alter: 73,0
Geschlecht: M
Eingang: 08.03.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dyspepsia Erythema Flatulence Lip swelling Paraesthesia oral Pruritus

Symptomtext

feeling in tongue had changed; skin turned rosy on face; lip swollen; digestive issues; gas; Itchy skin; This is a spontaneous report from a contactable consumer. A 73-year-old male patient received the first dose of the bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: EL3247), via an unspecified route of administration in the left arm on 26Jan2021 at 11:00 at 73-years-old at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 26Jan2021, the patient experienced events and outcomes: feeling in tongue had changed (non-serious) with outcome of recovering, skin turned rosy on face (non-serious) with outcome of recovering, lip swollen (non-serious) with outcome of not recovered, digestive issues (non-serious) with outcome of not recovered, gas (non-serious) with outcome of not recovered, itchy skin (non-serious) with outcome of not recovered; all of which required an emergency room (ER) visit. The patient stated that immediately after the vaccination, he came down with a mild reaction. The patient stated the feeling in his tongue felt off, skin turned rosy, lower lip was swollen, and he has had some gas and digestive issues. The patient stated that he spent an hour and a half in the emergency room (ER), and everything calmed down there, and he was able to go home. The patient stated that he may not take the second dose.

Weitere VAERSDATA-Felder

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

VAERS 1078948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CO
Alter: 71,0
Geschlecht: F
Eingang: 07.03.2021
Impfdatum: 11.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / LA

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

Paraesthesia Thyroid function test normal Vitamin B12 normal

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine: During clinic visit eleven days after vaccination patient reports they started to experience diffuse paresthesias including tingling into face, arms bilaterally, hands, legs bilaterally, and feet. Started five days after getting vaccine. No other associated symptoms. No loss of muscle strength, slurred speech, shortness of breath, throat tightening, skin reaction such as rash or hives, or visual changes. No history of multiple sclerosis, diabetes, or thyroid disorder. Based on lab values patient advised to start vitamin B12 supplementation. Two days after clinic visit reported symptom improvement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: During clinic visit: vitamin B 12: 325 pg/mL; thyroid stimulating hormone within normal range
Aktuelle Erkrankungen: None reported
Vorgeschichte: hypertension, hyperlipidemia, Menierie's disease, tinnitus, colon adenoma, colon polyps, osteopenia, osteoporosis, chronic fatigue
Andere Medikamente: atorvastatin
Allergien: None reported
Vorherige Impfungen: -

VAERS 1073221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: OK
Alter: 55,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Paraesthesia oral Pruritus Rash Throat irritation

Symptomtext

C/o throat feeling tickly or itchy, Denied SOB, felt like her lips were tingling as well. Later had itching in her arm. After second co-vid vaccine had a headache for 2 weeks, now has a rash that comes and goes on her antecubital area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: history of breast cancer 6 yrs ago, had a lumpectomy and radiation
Andere Medikamente: Valproic Acid, Effexor XR
Allergien: Allergic to raw parsley,
Vorherige Impfungen: -

VAERS 1068835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 54,0
Geschlecht: M
Eingang: 03.03.2021
Impfdatum: 16.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Paraesthesia

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA Tingling on Left side of body, in the area between the top of shoulder to left side neck area. Tingling occurs 4 to 5 times daily. No pain to report or server discomfort. Reported to my primary physician

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Diagnosed with Multiple Myeloma (2018), Stem cell transplant (2018) 2 years remissions
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1068056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: OR
Alter: 40,0
Geschlecht: F
Eingang: 03.03.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Chills Dizziness Fatigue Loss of personal independence in daily activities Migraine Nausea

Symptomtext

chills; fatigue; migraine-like headaches; dizziness; nausea; migraine-like headache and fatigue severe enough to prevent normal activity; This is a spontaneous report from a contactable nurse (patient). A 40-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3247), intramuscularly into the left arm on 28Jan2021 14:15 at a single dose for COVID-19 immunisation. Medical history included Polycystic ovarian syndrome (PCOS), depression, obesity and allergies to latex. Patient was not pregnant. Concomitant medication included duloxetine hydrochloride (CYMBALTA), bupropion hydrochloride (WELLBUTRIN), colecalciferol (VITAMIN D) and cyanocobalamin (VITAMIN B12). The patient previously took tetracycline and experienced drug allergy. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EJ1685), intramuscularly into the right arm on 06Jan2021 03:15 PM at a single dose for COVID-19 immunisation. On 28Jan2021 20:00, patient experienced chills, fatigue, migraine-like headaches, dizziness, nausea and migraine-like headache and fatigue severe enough to prevent normal activity. The events were reported as non-serious. The patient did not receive any treatment for the events reported. Outcome of events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Latex allergy; Obesity; Polycystic ovarian syndrome
Andere Medikamente: CYMBALTA; WELLBUTRIN; VITAMIN D; VITAMIN B12
Allergien: -
Vorherige Impfungen: -

VAERS 1067992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MO
Alter: 32,0
Geschlecht: F
Eingang: 03.03.2021
Impfdatum: 27.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: OT / LA

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

Migraine Nausea Pyrexia Vomiting

Symptomtext

Fever; Migraine; Nausea; Throwing up; This is a spontaneous report from a contactable healthcare professional (patient). A 32-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot: EL3247), intramuscular on the left arm (at the age of 32years) on 27Jan2021 at 14:00 at single dose for covid-19 immunisation. The patient was not pregnant at the time of vaccination. Medical history included migraines, kidney stones and high cholesterol. The patient had no allergies to medications, food, or other products. Concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient was not tested for COVID-19. The reported adverse events were fever, migraine, nausea, and throwing up on 31Jan2021 with no treatment received on all events. The patient considered the events as non-serious. Did not results in death, non- life threatening, did not cause/prolong hospitalization, non-disabling/incapacitating and no congenital anomaly/birth defect. The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol; Kidney stones; Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1065400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 02.03.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia Back pain Joint swelling Muscular weakness Myalgia Neck pain Pain in extremity Peripheral swelling Vaccination site pain Vaccination site paraesthesia

Symptomtext

swelling in the wrist, hand, fingers; swelling in the wrist, hand, fingers; muscle soreness in the left arm and difficulty in the lifting; muscle soreness in the left arm and difficulty in the lifting; soreness in shoulder, upper left quadrant, back, neck; soreness in shoulder, upper left quadrant, back, neck; achy injection site/throbbing in left arm where she got the vaccine; soreness in the upper arm, in the forearm; throbbing and tingling in left arm where she got the vaccine; achy elbow 3 hours after the injection.; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age (Age: 40; Unit: Unknown) received BNT162B2 (Pfizer-Biontech covid-19 vaccine, Solution for injection, Lot number: EL3247, exp date not reported), via an unspecified route of administration on 28Jan2021 08:25 for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient wanted to report a reaction that she had after receiving the Pfizer covid vaccine. She said she received the vaccine on site (not specified). On 28Jan2021, after receiving the vaccine she had achy injection site, soreness in the upper arm, in the forearm; throbbing and tingling in left arm where she got the vaccine; and achy elbow 3 hours after the injection. She said around 3 PM, she had swelling in the wrist, hand, and fingers; she had to remove the ring she was wearing. She also experienced muscle soreness in the left arm and difficulty in the lifting; soreness in shoulder, upper left quadrant, back, neck. Patient took ibuprofen for the events. The events improved over night and she just have some soreness the day of reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1065116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 02.03.2021
Impfdatum: 21.01.2021
Beginn: 11.02.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: - / LA

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

Chills Dyspnoea Nausea Pneumonia Pyrexia SARS-CoV-2 test

Symptomtext

pneumonia; Fever; chills; nausea; difficulty breathing; This is a spontaneous report from a contactable other HCP (patient). A 33-year-old non-pregnant female patient received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EL3247), via an unspecified route of administration in the left arm on 21Jan2021 11:00 at a single dose for COVID-19 immunisation. There were no medical history and concomitant medications. The patient experienced fever, chills, nausea, pneumonia, and difficulty breathing on 11Feb2021 23:00 with outcome of recovering. The events resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient was not diagnosed of covid prior vaccination. The patient underwent lab tests and procedures which included Nasal Swab test post vaccination: negative on 13Feb2021. Therapeutic measures were taken as a result of events (antibiotics, IV fluids, Tylenol). The patient received second dose (Lot Number: EN6201) on 12Feb2021 12:00 PM in the left arm.; Sender's Comments: There is a reasonable possibility that the events fever, chills, and nausea were related to BNT162b2 based on known drug safety profile. Based on the temporal relationship, the association between the events pneumonia and difficulty breathing with Bnt162b2 can not be fully 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: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210213; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1063923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: MD
Alter: 74,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 13.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: - / LA

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

Back pain Chills Computerised tomogram normal Pain Procalcitonin normal Pyrexia SARS-CoV-2 test negative Tremor

Symptomtext

At 10am on Thursday February 25, I SUDDENLY experienced the onset of violent chills, shaking so hard I couldn't initially place a thermomenter in my mouth. Moments later, this was accompanied by throbbing pain in my lower back. Eventually I was able to take my temperature and I had fever. My daughter contacted my primry care physician who told us to go the emergency room. By the time we went to hospital, the chills had stopped as well as the lower back pain. I was quarantined (though they knew I had been vaccinated for COVID) until they tested me for COVID, the test came back negative in an hour. They did a number of tests and I was discharged around 6:00 pm that evening

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Normal WBC, Undetectable CRP, Low-risk procalcitonin, CT to check for kidney stones-negative
Aktuelle Erkrankungen: -
Vorgeschichte: Waldenstrom's Macroglobulenemia diag. 2010 Cardiac stent, Nov 2020
Andere Medikamente: Levthyroxine, Lipitor, Metoprolol, Brilinta, Eliquis
Allergien: penicillin, sulfa
Vorherige Impfungen: -

VAERS 1063490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 75,0
Geschlecht: M
Eingang: 01.03.2021
Impfdatum: 20.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Fall Muscular weakness

Symptomtext

7 a.m. the morning following the 2nd vaccination, pt. got out of bed, walked a few steps to the master bathroom. He was having some difficulty breathing so reached for his BREO & his legs wouldn't hold him up. He collapsed to the floor. His wife got him to bed where he stayed for a few minutes. He got up again & walked a few steps to the master bathroom, started brushing his teeth & his legs collapsed again where his wife caught him & helped with controlled descent. He could not remember some of the first collapse & none of the second collapse. He crawled to bed & stayed for 1/2 hour. Got up & felt fine the rest of the day & since then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: BREO Ellipta, Ipratropium Bromide Nasal Solution, Acetaminophen, Cilostazol, NifedipineER, Vision Formula 50+, Vitamin D3
Allergien: none
Vorherige Impfungen: -

VAERS 1062230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NJ
Alter: 30,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Back pain Blood pressure decreased Blood pressure measurement Chest pain Dizziness Fatigue Influenza Nasopharyngitis Pain Pain in extremity Pyrexia Somnolence

Symptomtext

whole body felt sore and exhausted; whole body felt sore and exhausted; bad cold/flu; bad cold/flu; little chest pain; minor fever; blood pressure dropped; dizziness; backpain; left arm felt sore; sleepy/light drowsiness; This is a spontaneous report from a contactable consumer (patient). A 30-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration on the left arm on 11Feb2021 15:30 at a single dose (at the age of 30-years-old) for COVID-19 immunization. Medical history included >13 years ago: diagnosed TB with no symptom, completed TB treatment 1 year-plan and has issue no since then; >16 years ago: Hepatitis-b positive but received treatment and cleared out on diagnostics afterward. The patient was not pregnant. Concomitant medications were not reported. The patient had no COVID prior to vaccination. The patient has no known allergies. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247) on 21Jan2021 at 13:15 on the left arm at a single dose (at the age of 30-years-old) for COVID-19 immunization. After about 4.5h post-vaccination (20:00), her left arm felt sore and within the next 3h, she felt sleepy and experienced random light drowsiness. She woke up around 06:30 the next day (12Feb2021) only felt continued sore arm. However, at 08:30 to 09:30, her whole body felt sore and exhausted, especially back pain, as if she having a bad cold/flu. She also felt a little chest pain, had a minor fever and went sleeping from 12:00, woke up around 18:00-19:00. The whole body ache was almost gone but her back was still in pain and her blood pressure dropped with random dizziness when she was walking or standing up. The next morning (13Feb2021), the back pain was gone and she felt it back to normal except for a little random dizziness in movement. She did not take any medication to alleviate the adverse effects during the timeline. The patient was not COVID tested post vaccination. The patient recovered from back pain in 13Feb2021, the patient recovered from the remaining events in Feb2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210211; Test Name: Blood pressure; Result Unstructured Data: Test Result:dropped
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hepatitis B antibody positive (>16 years ago: Hepatitis-b positive but received treatment and cleared out on diagnostics afterward.); TB (>13 years ago: completed TB treatment 1 year-plan and has issue no since then)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1062002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 23,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 25.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

fingers were numb and tingling; 12 hours post 2nd dose the left side of patient face and left ear were numb as well as both arms and both legs/fingers were numb and tingling; This is a spontaneous report from a contactable consumer. A 23-year-old female patient (not pregnant) received the second dose of bnt162b2 (BNT162B2 also reported as BIONTECH Covid vaccine, lot EL3247), via an unspecified route of administration in the left arm on 25Jan2021 at SINGLE DOSE for Covid-19 immunisation. The patient's medical history was not reported. There were no concomitant medications. She received her first dose of bnt162b2 (lot EK9231) on 05Jan2021 in the left arm. On 26Jan2021, the left side of patient's face and left ear were numb as well as both arms and both legs and 800mg of ibuprofen was taken. Next morning (27Jan2021), the numbness in legs gone but the left arm from shoulder to fingers were numb and tingling. The outcome of events was recovered.

Weitere VAERSDATA-Felder

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

VAERS 1061996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 26.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Dizziness Dry mouth Dysphagia Hypoaesthesia Lip swelling Muscle tightness Nervousness Pain in extremity Paraesthesia oral Peripheral swelling Sensation of foreign body Taste disorder

Symptomtext

nervousness; slight swelling/tingling in lips; slight swelling/tingling in lips; dizziness; like she has a cough in her throat; swelling and soreness of her arm; swelling and soreness of her arm; Tightness in her jaw; Numbness in hand; difficulty swallowing; taste in her mouth; dry mouth; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, lot number: EL3247, unknown expiration), via an unspecified route of administration in left arm on 26Jan2021 at 08:30 AM at a single dose for COVID-19 immunization in a clinic. Medical history included ongoing underactive thyroid, cataract surgery on 14Oct2020 and on 28Oct2020, and cholesterol (abnormal). Concomitant medications included ongoing levothyroxine for underactive thyroid and ongoing rosuvastatin calcium for cholesterol. The patient experienced nervousness, slight swelling/tingling in lips, dizziness, like she has a cough in her throat, swelling and soreness of her arm, tightness in her jaw, numbness in hand on 26Jan2021. The patient also had difficulty swallowing, had taste in her mouth, and dry mouth in Jan2021. The patient on the line calling about the COVID-19 vaccine. She got the shot yesterday (26Jan2021) and was calling to report on the reaction that occurred. She initially stated she had slight swelling/tingling in lips, difficulty swallowing, numbness in hands, jaws became tight, and nervousness which she is still experiencing. She mentioned she took benadryl. She was wondering if she should go and get the second shot. The patient first experienced dizziness which lasted for a second and this occurred while waiting in the lobby for observation after getting the vaccine. Slight swelling and tingling in lips were noticed two minutes after the dizziness. It felt like a tingle sensation. She clarified she does not necessarily have difficulty swallowing. It was not so much she could not swallow, but it was like she has a cough in her throat. It feels like she could cough but would need to keep swallowing and drinking water. Once she got the shot it caused her to get a taste in her mouth. The feeling like a cough in her throat has gone away, but now she feels nervousness, dry mouth, and she still has that taste in her mouth from getting the shot. She had swelling and soreness of her arm, but she knew that was to be expected which started an hour after getting the vaccine. Tightness in her jaw was noticed an hour after getting the vaccine. The numbness in hand started at the same time as the tightness of her jaw. Her left hand is what went numb, and she had the vaccine administered in her left arm. The nervousness is getting better, but she felt very nervous. She also mentioned she has thyroid problems and is not sure if this has anything to do with it. She had this nervousness feeling 2 hours after getting the shot. Patient is scheduled to get the second vaccine on 18Feb2021. Benadryl has helped a lot. The patient has no additional vaccines administered on the same date and has no prior vaccination within four weeks. The events did not require emergency room and physician office visit. Vaccine was not administered in a military facility. The patient was recovering from events nervousness, slight swelling/tingling in lips, swelling and soreness of her arm, tightness in her jaw, and numbness in hand; recovered from dizziness on 26Jan2021; recovered from event "like she has a cough in her throat" on unspecified date; not yet recovered from event "taste in her mouth"; while unknown outcome for the remaining events. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Thyroid function decreased
Vorgeschichte: Medical History/Concurrent Conditions: Blood cholesterol abnormal; Cataract operation
Andere Medikamente: LEVOTHYROXINE; ROSUVASTATIN CALCIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1061981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 3247

moderat

Staat: CT
Alter: 40,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Blood pressure measurement Dizziness Feeling hot Heart rate Heart rate increased Hypertension

Symptomtext

felt a little dizzy; felt a wave of heat from my head to my feet; my heartrate elevated; blood pressure as 132/90; This is a spontaneous report from a contactable other healthcare professional (patient). A 40-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL 3247 and expiration date not provided), intramuscular in the right arm on 27Jan2021 09:30 at a single dose for COVID-19 immunization. Medical history included asthma and Seasonal Allergies. The patient is not pregnant. The patient had no known allergies. The patient did not receive any other vaccine in 4 weeks. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included sertraline hydrochloride (ZOLOFT), fexofenadine hydrochloride (ALLEGRA), and budesonide, formoterol fumarate (SIMBICORT TURBUHALER). After receiving the vaccine on 27Jan2021 09:30, the patient walked to the waiting room, sat down and felt a little dizzy, then felt a wave of heat from her head to her feet and her heart rate elevated. This lasted for the first ~5 minutes immediately receiving the vaccine, then completely subsided. From the firefighter's report: blood pressure as 132/90 and pulse of 76. Treatment was not provided in response to the events. The outcome of the events was recovered on 27Jan2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210127; Test Name: blood pressure; Result Unstructured Data: Test Result:132/90; Test Date: 20210127; Test Name: heartrate; Result Unstructured Data: Test Result:elevated; Test Date: 20210127; Test Name: pulse; Result Unstructured Data: Test Result:76
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Seasonal allergy
Andere Medikamente: ZOLOFT; ALLEGRA; SIMBICORT TURBUHALER
Allergien: -
Vorherige Impfungen: -

VAERS 1059461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 74,0
Geschlecht: F
Eingang: 27.02.2021
Impfdatum: 08.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Feeling cold Hyperhidrosis Palpitations Paraesthesia

Symptomtext

PALPATATIONS, SWEATY HANDS, BODY TINGLING. PALPATATIONS RESOLVED PATIENT STILL FELT COLD AND CHILLS STARTED. SHE WAS SENT TO THE ED FOR EVAULATION.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, HYPOTHYROIDISM
Andere Medikamente: SYNTHROID, AMLODIPINE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1059410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: NC
Alter: 75,0
Geschlecht: M
Eingang: 27.02.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dysphagia Dyspnoea Swelling

Symptomtext

PATIENT REPORTED FEELING AS IF LIPS WERE SWOLLEN. SHORTNESS OF BREATH AND DIFFICULTY SWALLOWING. RN ASSESSED AND GAVE 50 MG BENEDRYL AND EMS ALERTED.

Weitere VAERSDATA-Felder

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

VAERS 1058674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: CO
Alter: 81,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 05.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Dyspnoea Hypoaesthesia Hypoaesthesia oral Paraesthesia Tremor

Symptomtext

Patient received second dose of Pfizer vaccine. Both patient and her daughter went to the car to wait. Was approached by security as daughter returned to the center stating her mother was having a reaction. I went to the car & assessed patient. Patient c/o numbness/tingling along the left side of her face and head. Significant tremors and shortness of breath noted at the time. Daughter went and secured wheelchair & we brought the patient back into the vaccine clinic. VS at 1340: BP: 164/65, PO2: 88% on 3L, HR: 60 Patient reported anxiety prior to coming in for vaccine. VS at 1347: BP: 184/82, PO2: 94% on 3L, HR: 60. Patient states numbness/tingling increasing; reporting circumoral tingling/numbness. 25mg Benadryl given. VS at 1355: BP: 233/102, PO2: 92% on 3L, HR: 60 Discussed with Pharmacist. EMTs called for transport to ED per patient's request. Observed in ED and d/c home with no further treatment in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: alcohol swabs, meclizine, Librium, flagyl, gabapentin, losartan, nitrofurantoin, catelope, Phenergan, Prozac, strawberry, watermelon, zoloft
Vorherige Impfungen: -

VAERS 1058632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: AZ
Alter: 75,0
Geschlecht: M
Eingang: 26.02.2021
Impfdatum: 25.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Nervousness Pain Tremor

Symptomtext

Relatively severe body aches & chills, but body temperature is averaging 95F. Feels like getting a bad dose of the flue. No runny nose, no unusual body functions other than the body feels very nervous and shaky.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None to date
Aktuelle Erkrankungen: No other illnesses suspected at time of vaccination. All appeared normal at that time.
Vorgeschichte: Have a Pacemaker and Watchman installed and history of irregular heartbeat.
Andere Medikamente: Metoprolol Tartrate 25MG /day, Atorvastatin Calcium 40MG/day, Baby Aspirin 81MG/Day, Vitamin B-12 2500Mcg/Day, Centrum Multi vitamin/Day, Vitamin D3 125Mcg/Day.
Allergien: None
Vorherige Impfungen: -

VAERS 1057880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL-3247

moderat

Staat: CT
Alter: 37,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Chills Dyspnoea Fatigue Headache

Symptomtext

tiredness; chills; headache; achiness of joints; congestion(hard to breathe); This is a spontaneous report from a contactable consumer (patient). A 37-years-old female patient received the second dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine, Lot # EL-3247, in Workplace clinic, via an unspecified route of administration on 11Feb2021 at 23:30 (at 37 years of age) at single dose in left arm for COVID-19 immunization. The patient's medical history was not reported. The patient didn't receive any concomitant medication. The patient was not pregnant at the time of vaccination. She had received the first dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine, Lot # EL-3247, via an unspecified route of administration on 21Jan2021 at 23:30 (at 37 years of age) at single dose in left arm for COVID-19 immunization. She was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. On 11Feb2021 at 20:00 (to be clarified) the patient experienced tiredness, chills, headache, achiness of joints and congestion (hard to breathe). The patient didn't receive any treatment. The reported events were resolving at the time of the report.

Weitere VAERSDATA-Felder

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

VAERS 1057553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL3247

moderat

Staat: IL
Alter: 24,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Anxiety Asthenia Chills Confusional state Disorientation Dizziness Fatigue Hallucination Headache Myalgia SARS-CoV-2 test Tachycardia

Symptomtext

hallucination; severe confusion; dizziness/light headedness; disorientation; fatigue; tachycardia; anxiety; full body weakness; full body muscle aches; chills; headache; This is a spontaneous report from a contactable healthcare professional (patient). A 24-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL3247), intramuscular in left arm on 22Jan2021 at a single dose for COVID-19 immunisation. Medical history included generalised anxiety and allergies: Sulfa sensitive. Patient was not pregnant at the time of vaccination. Prior to vaccination, the patient has not been diagnosed with COVID-19. The patient's concomitant medications were not reported. On 22Jan2021, 45-60 minutes after vaccination, patient experienced hallucination, severe confusion, dizziness/light headedness, disorientation, fatigue, tachycardia, anxiety, full body weakness, then on 22Jan2021, 8 hours after, patient had full body muscle aches, headache, chills, fatigue, confusion, hallucination, anxiety, tachycardia, 16 hours after, experienced confusion, full body muscle aches, headache, chills, fatigue, confusion, hallucination, tachycardia, anxiety, then 48 hours after, had confusion, full body muscle aches (TYLENOL helped), headache, fatigue, confusion, hallucination, tachycardia, anxiety, then 1 week after vaccination, patient was experiencing confusion, anxiety, and hallucinations throughout the entire week. Patient was unsure if she ever had a fever, as she did not check her temperature. The events were reported as non-serious. The patient underwent lab tests and procedures which included COVID saliva test: negative on 27Jan2021 and negative on 10Feb2021. Therapeutic measures were taken as a result of full body muscle aches. No treatment was received for the other adverse events. The outcome of the events was recovered with sequelae.; Sender's Comments: Based on the limited information currently available, a possible contributory role of the suspect drug in the reported event hallucination cannot be completely excluded given the known suspect drug profile and/or implied temporal association. 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 Regul atory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Date: 20210127; Test Name: covid test (saliva); Test Result: Negative ; Test Date: 20210210; Test Name: covid test (saliva); Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Generalized anxiety disorder (Generalized Anxiety); Sulfonamide allergy (allergies: Sulfa sensitive)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -