VAERS Reports FH8030

VAERS 2727299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 26.12.2023
Impfdatum: 02.12.2021
Beginn: 13.08.2023
Tage bis Beginn: 619,0
Dosis: 3
Route/Site: - / -

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

Acute chest syndrome Acute kidney injury Acute respiratory failure Anaemia Aortic stenosis Asthenia Blood creatinine increased Blood culture negative Blood lactate dehydrogenase increased COVID-19 Cardiac arrest Chest tube insertion Computerised tomogram thorax abnormal Condition aggravated Culture negative Decubitus ulcer Deep vein thrombosis Echocardiogram

Symptomtext

Patient is a 56 y.o. female patient of MD with history of SCD, HTN, CKD 4, presented to Medical Center with sickle cell pain, admitted for pain crisis and hypoxia. Course prolonged by sepsis due to PNA requiring chest tubes; AKI. Now improved and awaiting further improvement in Hb. Severe anemia Acute sickle cell crisis 2/2 sickle crisis 2/2 COVID; severe pain, refractory to multiple interventions Hgb 2-3 on admission (no blood products) LDH>2500, low Haptoglobin, consistent w/ hemolysis Was following OSU Hematology, baseline Hg ~6 s/p Procrit, IV iron (x >2wk course) PO B12, folic acid Dc'd oral Fe as causes pt constipation, pt adamantly refusing Heme/onc consulted, restarted EPO on 9/22 Family states that pt is usually discharged when Hb is 5. Currently 5 and patient requesting discharge home. Patient accepted by Dr, Heme Onc, will follow outpatient on discharge 10/21 Heme recs suggested for EPO Monday Wednesday Friday for 1 week with repeat CBC and then further EPO based on blood counts Acute on chronic pain Generalized weakness 2/2 critical care myopathy, deconditioning, protracted inpatient hospitalization, B/L chest tube insertion s/p removal, intermittent hypoxia from severe anemia with in setting of SCD Was prev on Oxy 10mg q4h scheduled and PRN since end of 09/25 -> weaned inpatient Oxycodone to 5mg q4h prn, Will discharge on Oxycodone with further doses to be arranged outpatient via PCP and/or Heme Cardiac arrest- resolved Acute hypoxic respiratory failure - stable B/L exudative pleural effusion Acute chest syndrome - resolved COVID-19 - resolved Brief loss of pulse 8/21, ROSC after 1 round ACLS Arrest 2/2 hyperkalemia, severe anemia Resp failure 2/2 COVID, cardiac arrest, CAP COVID-19+ (8/12) on admission, completed isolation 8/24, completed steroids, Remdesevir held d/t AKI ETT 8/21-9/4, in setting of cardiac arrest TTE 8/13 with EF 61%, Initial CT w/ RUL infiltrate, worsened on f/u CT, completed Rocephin/Doxy, steroids course ARF, prerenal - resolved Cr 0.8-0.9 at baseline, peak 2.5, now 1.01 on discharge Multifocal PNA - resolved 9/24: fevers -> WBC 17K CT 9/25 showed significant worsening of B/L effusions and MF PNA BCx 9/25 -ve; Ur Ag, sputum Cx and Resp PCR panel -ve Pleural fluid cx 9/27 -ve Completed Cefepime 10/2 S/p B/L chest tubes 9/2: exudative; -ve for malignancy Repeat CT 10/1: significant improvement in effusions R chest tube dced 10/3 L chest tube dced 10/6 CM consulted to arrange for home o2 on discharge Acute VTE USG duplex 9/26: acute L gastrocnemius DVT, chronic R DVT Heme with recs for no AC and also risk of bleed with IVCF D/t AKI, V/Q scan 09/25 - intermed prob of PE suspected PE -> troponin leak, no RV strain. On RA since 10/6 with periodic need for nc CM consulted to arrange for home o2 on discharge Thrombocytopenia - resolved 2/2 sepsis Sacral pressure ulcer, stage 3 Wound care was consulted, recs appreciated. Outpatient monitoring and ongoing wound care follow up with referral if needed AS TTE: mild AS, recommended TEE to better assess AV structure given patient's age Cards recs for outpatient follow up Essential HTN Continue Norvasc Anxiety Continue Lexapro Goals of Care Palliative consulted Full code with goals rehabilitative (husband - estranged) LNOK, mother visiting frequently Family aware of limitations given her wishes. Hyperkalemia - Resolved Shock-POA - Resolved Acute Metabolic Encephalopathy - resolved

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 71,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2715364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 18.11.2023
Impfdatum: 24.11.2021
Beginn: 01.04.2022
Tage bis Beginn: 128,0
Dosis: 3
Route/Site: - / LA

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

Ageusia Anosmia Blood cholesterol Blood cholesterol decreased Blood cholesterol increased Cerebrovascular accident Feeling abnormal Investigation Laboratory test Memory impairment Pain Thrombosis Ultrasound scan

Symptomtext

Stroke; Blood clot; she had sharp burning pains; cholesterol went way high; Her cholesterol had dropped really low; Lost all taste; Lost all smell; cant remember things and has short term memory; Fuzzy brain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 57-year-old female patient received bnt162b2 (BNT162B2), on 24Nov2021 as dose 3 (booster), single (Lot number: FH8030) at the age of 57 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Anxiety" (ongoing). Concomitant medication(s) included: CLONAZEPAM oral taken for anxiety (ongoing). Vaccination history included: bnt162b2 (DOSE 1, SINGLE, Batch\lot number: ER8735, Time: In the morning, between 8-10am), administration date: 31Mar2021, for COVID-19 immunisation; bnt162b2 (DOSE 2, SINGLE, Batch\lot number: ER8735, Time: In the morning, between 8-10am), administration date: 21Apr2021, for COVID-19 immunisation, reaction(s): "Stents installed. One was in May2021". The following information was reported: FEELING ABNORMAL (non-serious) with onset 2021, outcome "not recovered", described as "Fuzzy brain"; MEMORY IMPAIRMENT (non-serious) with onset 2021, outcome "not recovered", described as "cant remember things and has short term memory"; CEREBROVASCULAR ACCIDENT (hospitalization) with onset Apr2022, outcome "unknown", described as "Stroke"; ANOSMIA (non-serious) with onset 2022, outcome "not recovered", described as "Lost all smell"; AGEUSIA (non-serious) with onset 2022, outcome "not recovered", described as "Lost all taste"; THROMBOSIS (medically significant), outcome "unknown", described as "Blood clot"; PAIN (non-serious), outcome "unknown", described as "she had sharp burning pains"; BLOOD CHOLESTEROL INCREASED (non-serious), outcome "unknown", described as "cholesterol went way high"; BLOOD CHOLESTEROL DECREASED (non-serious), outcome "unknown", described as "Her cholesterol had dropped really low". The patient was hospitalized for cerebrovascular accident (start date: Apr2022, discharge date: Apr2022, hospitalization duration: 7 day(s)). The events "stroke", "blood clot", "lost all taste", "lost all smell", "cant remember things and has short term memory", "fuzzy brain", "she had sharp burning pains", "cholesterol went way high" and "her cholesterol had dropped really low" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood cholesterol: went way high; dropped really low; brain test: Unknown results; Unknown results, notes: he did shock wave test on legs on what nerves were responding; Some test: Unknown results; Ultrasound scan: Unknown results; everything was free and clear, notes: recently for the yearly follow-up. Therapeutic measures were taken as a result of cerebrovascular accident, thrombosis, ageusia, anosmia, memory impairment, feeling abnormal, pain, blood cholesterol increased, blood cholesterol decreased. Clinical course: She had three COVID shots over period of time; its been 2 years. She lost all taste and smell and has not been able to get it back. She was calling to ask if Pfizer has come up with anything to help with the lost of taste and smell from the shot. She confirmed she never had COVID, but after the vaccines she lost sense of smell and taste. This was after the three Pfizer COVID Shots. She states that she has been experiencing this for 2.5 years along with a fuzzy brain, could not remember things, and has short term memory and also states that she turns around and forgets why she turned around. She then added she has had three strokes, 2 blood clots remove, and 2 stents installed through all this period and after the shots had lost in taste and smell. She also still has brain fuzziness. Confirmed this was after the COVID shots. The nurse practitioner was located at the neurologist doctors office. She sees the nurse practitioner as well as the doctor, Dr. PRIVACY. This was the doctor who went to check the stent that was placed in. Lost all taste and smell- Started to away around Jan2022 or Feb2022. It started slowly to go away then went to nothing over period of 4-5 months. Once it was nothing, it continued to be nothing. No smell or taste, nothing period. She tried bite of lime and does not effect her or anything. First Stroke occurred as clarified Apr2022. Reporter was in as clarified (PRIVACY) located (PRIVACY). Was there three days without any surgical procedure happening and sent home. Then went home for one day and was having another stroke. She could not move or get to phone, could not get to anything. She was stuck there. They went through the right side of her groin up to right side of brain and removed 1-2 clots and put a stent in carotid artery. During this occasion she was in the hospital for seven days. The third stroke occurred during this hospitalization in Apr2022. Does not remember all details for treatment/intervention after the third stroke. Does not remember that time. When she got out of the hospital she had to go through rehabilitation. She had to learn how to talk, walk, write, brush teeth, etc. The main thing at this was at this time was her right leg in the groin if took 15-20 steps she had sharp burning pains and had to sit down. She was referred to Dr. PRIVACY and he did shock wave test on legs on what nerves were responding. He was befound and did not know what to do. Then was sent Dr. PRIVACY he was back over (PRIVACY) in (PRIVACY) and he was a vascular vein treatment doctor. He put hand on ankle of left leg and then right leg. Doctor then said she had blood clot. They did a sonogram and some test before was placed under for removal. They went down right side of groin area and removed clot. After four hours she could walk again. She had a sonogram recently for the yearly follow-up and everything was free and clear. Everything was operating correctly. The blood clot was removed Sep2022. Stents installed. One was in May2021 and other 2022. Reporter then stated her dates were messed up and she has fuzzy brain. It started within this year. She can have lunch and its like she does not remember what had for lunch. She had brain test done. Treatment- Neuriva an over-the-counter brain health for memory and focus. While probing for details mentioned cholesterol went way high. She does not remember the number. She was placed on cholesterol medication, Atorvastatin 40mg while in the hospital. It was then later knocked down to 5mg. Her cholesterol had dropped really low. She was no longer on the Atorvastatin. She was also placed on a blood thinner, Plavix, 75mg tablet once every morning. She will be on rest of life.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300369406 Same patient/product, different event/dose;

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 7,0
Labordaten: Test Name: Cholesterol; Result Unstructured Data: Test Result:went way high; Test Name: Cholesterol; Result Unstructured Data: Test Result:dropped really low; Test Name: brain test; Result Unstructured Data: Test Result:Unknown results; Test Name: shock wave test; Result Unstructured Data: Test Result:Unknown results; Comments: he did shock wave test on legs on what nerves were responding; Test Name: Some test; Result Unstructured Data: Test Result:Unknown results; Test Name: sonogram; Result Unstructured Data: Test Result:Unknown results; Test Name: sonogram; Result Unstructured Data: Test Result:everything was free and clear; Comments: recently for the yearly follow-up
Aktuelle Erkrankungen: Anxiety
Vorgeschichte: -
Andere Medikamente: CLONAZEPAM
Allergien: -
Vorherige Impfungen: -

VAERS 2712467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 10.11.2023
Impfdatum: 20.12.2021
Beginn: 04.09.2023
Tage bis Beginn: 623,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute myocardial infarction Anxiety Atrial fibrillation COVID-19 Cardiac stress test Chest pain Cough Decreased appetite Dizziness Dyspnoea Feeling abnormal Hyperglycaemia Hypotension Inflammatory marker test Infusion Liver function test increased Orthostatic hypotension

Symptomtext

Discharge Provider: DO Primary Care Provider at Discharge: MD Admission Date: 9/4/2023 Discharge Date: 9/6/2023 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Orthostatic hypotension [I95.1] COVID [U07.1] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 84 year old male with a history of HLD, DM 2, CKD stage 3. He was admitted for chest pain, NSTEMI, on 8/31, had a dobutamine stress test and post infusion developed atrial fib with RVR, alternated with NSR, SVT. Rhythm management took several days and he was discharged with the addition of metoprolol succinate and apixaban on 9/3. History of hypotension with metoprolol in past. He returned to the ED on 9/4 with increased cough overnight, feeling of low blood pressure with dizziness and feeling "out of it". He reports a decreased appetite, shortness of breath, palpitations, and rhinorrhea as well. He denies chest pain, sore throat, nausea, vomiting, diarrhea. Vital signs significant for orthostatic hypotension in ED, heart rate controlled and NSR, afebrile, oxygen sat stable on room air. Lab work significant for AKI, hyperglycemia, elevated LFTs, trop 38, 31 indeterminate. He was Covid positive. He was given a 1 liter bolus in ED. He was admitted with Covid-19 and orthostatic hypotension for further monitoring and treatment as needed. Patient was admitted remained stable throughout his stay he never had significant physical symptoms from the COVID-19. His inflammatory markers did not require acute intervention. He remained stable and was seen on the day of discharge anxious to go home. He was evaluated by Physical and Occupational therapy who recommended home with no skilled services. He could return to his regular medications as previously ordered. He could return to diet and activity as tolerated. He was cautioned that given his COVID-19 infection he was to make sure he was getting plenty of rest for the next 2-4 weeks. He understood all these instructions and was discharged home in stable condition. 32 minutes were spent discharging this patient over 50% of this was spent in face-to-face counseling and coordination of care

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis Nodule of right kidney Essential hypertension Type 2 diabetes mellitus with stage 3a chronic kidney disease, without long-term current use of insulin DM type 2 with diabetic dyslipidemia Hypervitaminosis D Sensorineural hearing loss (SNHL) of both ears Coronary artery disease of native artery of native heart with stable angina pectoris Age-related osteoporosis without current pathological fracture History of non-ST elevation myocardial infarction (NSTEMI) Bee sting allergy Dyslipidemia Constipation DOE (dyspnea on exertion) Atrial flutter Age-related physical debility COVID-19 virus infection Transaminitis
Andere Medikamente: apixaban (ELIQUIS) 5 mg tablet atorvastatin (LIPITOR) 40 mg tablet Calcium Carbonate Antacid (TUMS PO) Calcium Carbonate Antacid (TUMS ULTRA 1000 PO) cetirizine (ZYRTEC) 10 MG tablet cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) CAPS EPINE
Allergien: BeeNausea and Vomiting, Dizziness Forteo [Teriparatide, Recombinant] Grass Pollen PenicillinsRash
Vorherige Impfungen: -

VAERS 2710858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: KY
Alter: 77,0
Geschlecht: M
Eingang: 07.11.2023
Impfdatum: 04.11.2021
Beginn: 03.11.2023
Tage bis Beginn: 729,0
Dosis: UNK
Route/Site: IM / LA

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

Acute kidney injury Ageusia Anosmia Asthenia COVID-19 Chronic obstructive pulmonary disease Condition aggravated Death Dyspnoea Left ventricular failure SARS-CoV-2 test positive

Symptomtext

TESTED + FOR COVID 9-26, WENT TO er 10-08 FOR DYSPNEA, LOSS OF SENSE OF TASTE AND SMELL, WEAKNESS AND WAS ADMITTED 10-9 WITH COPD EXACERBATION, DIASTOLIC HEART FAILURE, COVID, ACUTE KIDNEY INJURY , DECEASED 11-3-23 IN THE HOSPITAL

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: TESTED + FOR COVID 9-26-23
Aktuelle Erkrankungen: -
Vorgeschichte: COPD CHRONIC KIDNEY DISEASE HTN OBSTRUCTIVE SLEEP APNEA CHRONIC DIASTOLIC HEART FAILURE
Andere Medikamente: -
Allergien: NKDA PER H AND P 10-9-23
Vorherige Impfungen: -

VAERS 2686782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: MD
Alter: 61,0
Geschlecht: F
Eingang: 26.09.2023
Impfdatum: 22.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: - / -

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

Alopecia Diarrhoea Dyspnoea Fall Headache Illness Malaise Oxygen saturation abnormal Pulmonary embolism Pyrexia Syncope Vomiting

Symptomtext

pulmonary embolism; fainted; violently ill/violently sick; violently not feeling well; throwing up; fever; headache; diarrhea; couldn't breathe; oxygen level was 40; fell; falling hair; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 61-year-old female patient received bnt162b2 (BNT162B2), on 22Dec2021 as dose 3 (booster), single (Lot number: FH8030) at the age of 61 years for covid-19 immunisation, as the patient has COPD, asthma, and everyone said to get it. The patient's relevant medical history included: "COPD", start date: 2000 (unspecified if ongoing); "Adult onset asthma", start date: 2000 (unspecified if ongoing), notes: She never had a problem until she turned 40. There were no concomitant medications. Vaccination history included: bnt162b2 (DOSE 1;, Manufacturer: Pfizer, EXP: 21Jul2021, LOT: EP7534, NDC: Unknown, Anatomical Site of injection: dose unknown; given in the arm , Route: Unknown), administration date: 18Mar2021, for COVID-19 Immunization; bnt162b2 (DOSE 2;, Manufacturer: Pfizer , EXP: 21Jul2021, LOT: ER8729, NDC: Unknown, Anatomical Site of injection: Unknown , Route: Unknown), administration date: 08Apr2021, for COVID-19 Immunization. The following information was reported: ALOPECIA (non-serious) with onset Feb2022, outcome "unknown", described as "falling hair"; PULMONARY EMBOLISM (hospitalization, medically significant) with onset Aug2022, outcome "unknown"; SYNCOPE (medically significant), outcome "unknown", described as "fainted"; ILLNESS (non-serious), outcome "unknown", described as "violently ill/violently sick"; MALAISE (non-serious), outcome "unknown", described as "violently not feeling well"; VOMITING (non-serious), outcome "unknown", described as "throwing up"; PYREXIA (non-serious), outcome "unknown", described as "fever"; HEADACHE (non-serious), outcome "unknown"; DIARRHOEA (non-serious), outcome "unknown", described as "diarrhea"; DYSPNOEA (non-serious), outcome "unknown", described as "couldn't breathe"; OXYGEN SATURATION ABNORMAL (non-serious), outcome "unknown", described as "oxygen level was 40"; FALL (non-serious), outcome "unknown", described as "fell". Therapeutic measures were taken as a result of pulmonary embolism. Clinical courses: Caller stated that she had a terrible reaction to the covid vaccine (Not confirmed if the Pfizer brand) where she received 3 shots. The patient got violently ill when she had her third Pfizer COVID vaccine. She had pulmonary embolism, falling hair and got really sick when she got her third Pfizer COVID vaccine. Confirms all of her COVID-19 Vaccines were manufactured by Pfizer. She had 3 doses and is not getting any more. She was violently ill and sick for 10 days with the last COVID-19 Vaccine shot. It was right after got the third shot, the day after. States she got the third shot on a Thursday. She was throwing up, had a fever, had a headache, diarrhea, it was awful. States she probably would have rather had COVID than got the shot. She had long hair. She would play with her hair, it didn't come out in chunks, but more and more was coming out in the tub and towel. Wanted to know what was causing this. Can't say for sure that losing her hair and the pulmonary embolism was from the COVID shots, but she knows they are side effects and has no other history of that. She doesn't know. Her pharmacist just told her to report it. Investigations: For the pulmonary embolism, she went to their local hospital, but they couldn't handle it so the ambulance took her to Trauma in (Withheld address). With regards to her Pulmonary Embolism, she was admitted for almost a week, it was pretty serious. If her granddaughter hadn't been there, caller wouldn't be here. Caller passed out. She had no pain or anything. She stood up, thought she had to throw up, thought she was going to pass out. She fell, fainted, and woke up enough to holler her granddaughter's name. By the time the ambulance got there, caller couldn't breathe, her oxygen level was 40. Caller was begging for oxygen. They took her to the local hospital and guesses a lady was trained at Trauma and knew their local hospital would not be able to handle her lung without doing surgery so they took caller to Trauma, which is more advanced. They were wonderful, gave her all the medicines and put her on machine that took care of it. She wanted Pfizer to be aware of the reaction she was having.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adult onset asthma (She never had a problem until she turned 40); COPD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2682064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 14.09.2023
Impfdatum: 16.11.2021
Beginn: 10.09.2023
Tage bis Beginn: 663,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Anticholinergic syndrome Bradycardia COVID-19 Mental status changes SARS-CoV-2 test positive Toxic encephalopathy Urinary retention

Symptomtext

Patient with history of COVID-19 vaccination admitted to hospital with COVID-19 detected test. Per provider discharge note, "Hospital Course: Patient was admitted for toxic metabolic encephalopathy suspected secondary to polypharmacy and acute hypoxic respiratory insufficiency secondary to COVID Infection. He also presented with bradycardia, for which beta blocker was placed on hold. He complained of urinary retention, likely secondary to anticholinergic syndrome, possibly secondary to patient's home atarax. Patient was weaned off oxygen. His mental status returned to baseline. He was medically optimized and stable for discharge home with appropriate follow up. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: COVID-19 detected PCR 9/10/2023
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2674891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

kritisch

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 22.08.2023
Impfdatum: 30.11.2021
Beginn: 19.08.2023
Tage bis Beginn: 627,0
Dosis: 3
Route/Site: SYR / -

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

Activated partial thromboplastin time normal Acute respiratory failure Anion gap Asthenia Basophil count decreased Basophil percentage Blood calcium normal Blood chloride decreased Blood creatinine normal Blood glucose increased Blood lactic acid Blood magnesium Blood potassium normal Blood pressure increased Blood sodium decreased Blood urea decreased Brain natriuretic peptide normal Carbon dioxide normal

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on August 19, 2023 18:40 Verified By: MD on August 19, 2023 18:40 Encounter Info: Hospital, Inpatient, 08/19/23 - * Final Report * History of Present Illness/Subjective This is a 72-year-old female with past medical history of lymphedema and obesity presents to the emergency department with complaints of cough weakness sore throat since past 1 week. The patient's phlegm has now turned yellow and has been feeling febrile. She also complains of facial swelling on the right side and neck pain. Denies any chest pain or chest tightness. Denies any history of smoking, COPD, asthma. She has never been vaccinated of COVID neither influenza. She sees a naturopath yearly. Patient is saturating 97% on 2 L of oxygen meets sepsis criteria, sepsis tachycardic. Last blood pressures charted at 1447 are elevated. 186/96. Labs showed normal WBC count, troponins are 6 BNP is 31, lactate is 1.2. She is influenza positive. X-ray is suggestive of cardiac enlargement with vascular congestion and central edema. Her last echo in the system is from 2017 and at that time her ejection fraction was 56 with no obvious valvular abnormality Review of Systems 13 point review of systems negative except for what is mentioned above Physical Exam/Objective Vitals & Measurements most recent past 24 hours Hemodynamics Neurologic Patient Weight Patient Height None Reported Constitutional: No acute distress, Eyes: PERRLA, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: wheezing Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Acute hypoxemic respiratory failure J96.01 - Combination of pulmonary edema and influenza -The patient is symptoms are 10 days old, no utility of Tamiflu -Concern for bacterial super infection considering the age group I will start ceftriaxone and doxycycline -Follow pneumonia work-up -We will start gentle diuresis, she is Lasix na?ve, likely trigger was her elevated blood pressures 2. Influenza A J10.1 - Outside therapeutic window for influenza, -Symptomatic management -Respiratory eval -DuoNebs 3. Pulmonary edema J81.1 - There is congestion secondary to elevated blood pressures likely -Echocardiogram -Lasix IV twice daily 5. Uncontrolled hypertension I10 - I do not see her to be on any blood pressure medications at home - awaiting order reconciliation . Code Status None Recorded Chronic Problem List Fatigue Lymphedema Obesity Procedure/Surgical History ?Dilation and Curettage (12/2015) ?Cholecystectomy Open (1951) ?appendectomy ?Hysterectomy Surgical History Internal 03/03/2017 Hysteroscopy W Polypectomy MD Medications Active Scheduled Inpatient Medications None Reported One-Time Medications Given 08/18/23 00:00:00 TO 08/19/23 18:40:33 None Reported PRN Medications (0600 - 0559) from 08/18 - 08/19 None Reported Allergies NKA Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School Retired Home/Environment Lives with Spouse. Nutrition/Health Diet: Regular. Substance Abuse Denies Tobacco Tobacco Use: Former smoker, quit more than 30 days ago. Family History Family history is negative Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 8.1 k/cumm (08/19/23 16:42:00) RBC: 4.85 million/cumm (08/19/23 16:42:00) Hgb: 13.8 GM/dL (08/19/23 16:42:00) Hct: 41.4 % (08/19/23 16:42:00) MCV: 85 fL (08/19/23 16:42:00) MCH: 28.5 pg (08/19/23 16:42:00) MCHC: 33.4 GM/dL (08/19/23 16:42:00) RDW: 14.4 % (08/19/23 16:42:00) Platelet: 251 k/cumm (08/19/23 16:42:00) MPV: 7.9 fL (08/19/23 16:42:00) Neutrophils %: 71 % (08/19/23 16:42:00) Lymphocytes %: 15 % (08/19/23 16:42:00) Monocytes %: 13 % (08/19/23 16:42:00) Eosinophils %: 0 % (08/19/23 16:42:00) Basophils %: 1 % (08/19/23 16:42:00) Absolute Neutrophil: 5.7 k/cumm (08/19/23 16:42:00) Absolute Lymphocyte: 1.2 k/cumm (08/19/23 16:42:00) Absolute Monocyte: 1 k/cumm (08/19/23 16:42:00) Absolute Eosinophil: 0 k/cumm (08/19/23 16:42:00) Absolute Basophil: 0 k/cumm (08/19/23 16:42:00) Chemistry: Sodium SerPl QN: 132 mmol/L Low (08/19/23 16:42:00) Potassium SerPl QN: 3.9 mmol/L (08/19/23 16:42:00) Chloride SerPl QN: 94 mmol/L Low (08/19/23 16:42:00) Carbon Dioxide SerPl QN: 30 mmol/L High (08/19/23 16:42:00) Anion Gap: 8 mmol/L (08/19/23 16:42:00) BUN SerPl QN: 9 mg/dL (08/19/23 16:42:00) Creatinine SerPl QN: 0.63 mg/dL (08/19/23 16:42:00) Estimated GFR (CKD-EPI, no race): >90 (08/19/23 16:42:00) Estimated CRCL (CG): >120 (08/19/23 16:42:00) Glucose SerPl QN: 286 mg/dL High (08/19/23 16:42:00) Calcium Total SerPl QN: 9 mg/dL (08/19/23 16:42:00) Magnesium SerPl QN: 1.9 mg/dL (08/19/23 16:42:00) Troponin-I High Sensitivity: 6 ng/L (08/19/23 17:20:00) BNP Pl QN: 31 pg/mL (08/19/23 17:20:00) Lactate Venous Pl QN: 1.2 mmol/L (08/19/23 16:42:00) Influenza A, POC: Positive Abnormal (08/19/23 14:34:00) Influenza B, POC: Negative (08/19/23 14:34:00) Coagulation: PT: 13 seconds (08/19/23 17:20:00) INR: 1.13 (08/19/23 17:20:00) aPTT: 33.8 seconds (08/19/23 17:20:00) Micro - Last 7 days Coronavirus SARS Ag FIA, POC: Negat (08/19/23 14:33:00) Diagnostics Radiology Results - Last 24 hours Across Visits 08/19/2023 16:21 - XR Chest PA or AP Portable IMPRESSION:1. Severe cardiac enlargement with vascular congestion and centraledema.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us with any questions. Signature Line Electronically Signed on 08/19/23 18:40 ________________________________________________________ MD

Weitere VAERSDATA-Felder

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

VAERS 2672976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 17.08.2023
Impfdatum: 18.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Angioedema Hypoxia

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA ANGIOEDEMA, SUBSEQ

Weitere VAERSDATA-Felder

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

VAERS 2638382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 30.05.2023
Impfdatum: 10.11.2021
Beginn: 10.05.2022
Tage bis Beginn: 181,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure Hypoxia Neuropathy peripheral Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE NEUROPATHY ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXEMIA 6/14/2022, 8/23/2022, 8/29/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2635478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 23.05.2023
Impfdatum: 04.11.2021
Beginn: 14.04.2022
Tage bis Beginn: 161,0
Dosis: 2
Route/Site: - / -

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

Cerebral artery occlusion Cerebrovascular accident Ischaemic stroke

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE STROKE DUE TO OCCLUSION OF LEFT MIDDLE CEREBRAL ARTERY ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2634835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 19.11.2021
Beginn: 27.09.2022
Tage bis Beginn: 312,0
Dosis: 2
Route/Site: IM / RA

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

Acute myocardial infarction

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI

Weitere VAERSDATA-Felder

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

VAERS 2633087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 17.05.2023
Impfdatum: 19.11.2021
Beginn: 28.06.2022
Tage bis Beginn: 221,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Anaemia Hypoxia Metastases to lung Metastases to lymph nodes Neoplasm Neoplasm malignant Respiratory failure Thoracic vertebral fracture

Symptomtext

J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/8/2022 CANCER METASTATIC TO UNSPECIFIED LN J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 11/26/2022 CANCER METASTATIC TO UNSPECIFIED LN J96.90 RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/25/2022 CANCER METASTATIC TO UNSPECIFIED LN R09.02 HYPOXIA 6/28/2022 CANCER METASTATIC TO UNSPECIFIED LN J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/8/2022 ANEMIA J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 11/26/2022 ANEMIA J96.90 RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/25/2022 ANEMIA R09.02 HYPOXIA 6/28/2022 ANEMIA J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/8/2022 THORACIC VERTEBRA PATHOLOGICAL FX DUE TO NEOPLASM, INIT J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 11/26/2022 THORACIC VERTEBRA PATHOLOGICAL FX DUE TO NEOPLASM, INIT J96.90 RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/25/2022 THORACIC VERTEBRA PATHOLOGICAL FX DUE TO NEOPLASM, INIT R09.02 HYPOXIA 6/28/2022 THORACIC VERTEBRA PATHOLOGICAL FX DUE TO NEOPLASM, INIT J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/8/2022 CANCER METASTATIC TO UNSPECIFIED LUNG J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 11/26/2022 CANCER METASTATIC TO UNSPECIFIED LUNG J96.90 RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/25/2022 CANCER METASTATIC TO UNSPECIFIED LUNG R09.02 HYPOXIA 6/28/2022 CANCER METASTATIC TO UNSPECIFIED LUNG

Weitere VAERSDATA-Felder

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

VAERS 2629223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 26.05.2022
Beginn: 09.06.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: IM / LA

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

Acute respiratory failure Hypotension Symptom recurrence

Symptomtext

HYPOTENSION ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE 6/17/2022, 6/28/2022, 8/8/2022, 8/9/2022, 8/10/2022, 8/22/2022, 9/20/2022, 10/14/2022, 10/24/2022, 12/28/2022, 11/1/1/2022, 12/30/2022, 3/9/2023, 2/1/2023, 1/17/2023 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2627379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 05.05.2023
Impfdatum: 06.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / RA

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

Acute myocardial infarction Angina pectoris Hypersensitivity

Symptomtext

STABLE ANGINA ACUTE NON ST ELEVATION MI ALLERGIC REACTION, INIT

Weitere VAERSDATA-Felder

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

VAERS 2624672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 14.11.2021
Beginn: 22.03.2022
Tage bis Beginn: 128,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Hypoxia

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2621507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 26.04.2023
Impfdatum: 15.07.2022
Beginn: 13.02.2023
Tage bis Beginn: 213,0
Dosis: 4
Route/Site: IM / LA

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

Acute myocardial infarction Acute respiratory failure Deep vein thrombosis Epilepsy Hypersensitivity Status epilepticus Symptom recurrence

Symptomtext

STATUS EPILEPTICUS EPILEPSY, UNSPECIFIED ACUTE NON ST ELEVATION MI ACUTE DVT OF LEFT FEMORAL VEIN ACUTE RESPIRATORY FAILURE ALLERGIC DISORDER, SUBSEQ 1/9/2023 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2620632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 14.11.2021
Beginn: 16.12.2021
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Hypoxia

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2616083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 23.11.2021
Beginn: 11.04.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Hypotension Hypoxia Imaging procedure abnormal Organ failure Pyrexia Sepsis

Symptomtext

I95.9 HYPOTENSION 4/16/2022 FEVER J96.00 ACUTE RESPIRATORY FAILURE 4/23/2022 FEVER R09.02 HYPOXIA 4/23/2022 FEVER I95.9 HYPOTENSION 4/16/2022 ABNL GENITOURINARY SYSTEM IMAGING R09.02 HYPOXIA 4/23/2022 ABNL GENITOURINARY SYSTEM IMAGING I95.9 HYPOTENSION 4/16/2022 SEVERE SEPSIS W ACUTE ORGAN DYSFUNCTION J96.00 ACUTE RESPIRATORY FAILURE 4/23/2022 SEVERE SEPSIS W ACUTE ORGAN DYSFUNCTION R09.02 HYPOXIA 4/23/2022 SEVERE SEPSIS W ACUTE ORGAN DYSFUNCTION

Weitere VAERSDATA-Felder

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

VAERS 2607561

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 14.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Neuropathy peripheral

Symptomtext

G62.9 NEUROPATHY 12/13/2021 J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/13/2021 G62.9 NEUROPATHY 12/13/2021 J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/13/2021

Weitere VAERSDATA-Felder

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

VAERS 2582326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 15.02.2023
Impfdatum: 18.11.2021
Beginn: 04.01.2023
Tage bis Beginn: 412,0
Dosis: 3
Route/Site: - / -

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

Abdominal X-ray Acute kidney injury Acute respiratory failure Atelectasis Blood lactate dehydrogenase Bronchial disorder C-reactive protein increased COVID-19 pneumonia Chest X-ray abnormal Cough Culture negative Dyspnoea Echocardiogram normal Ejection fraction normal Increased upper airway secretion Laboratory test normal Lung disorder Lung opacity

Symptomtext

Patient is a 64 y.o. male patient of CNP with history of MRDD, CKD, seizure disorder, hypertension, tracheostomy/GJ tube placement, who resides at nursing facility, presented with cough, shortness of breath and increased tracheal secretions, found to have acute hypoxemic respiratory failure. Patient unable to provide history due to MRDD, I met with one of her caregivers at bedside, noted 2 days of cough, increased secretions/suctioning requirements, and shortness of breath in addition to hypoxia. Acute hypoxemic respiratory failure Concern for pneumonia, multidrug-resistant S/p tracheostomy but no oxygen at baseline History of prolonged hospitalization secondary to pneumonia Chest x-ray 1/4 reviewed low lung volumes. Some atelectasis versus opacities within the lower lobe bilaterally. Chest x-ray 1/11 personally reviewed?low lung volumes with some bronchovascular crowding. Echocardiogram in August reviewed?normal EF normal diastolic function. Some pulmonary congestion due to IV fluids. Status post 10 days of IV Zosyn. Tracheal cultures and antigen negative. Now down to room air just using T-piece oxygenation for humidification. Okay to discharge back to group home. Covid-19 Virus Infection Pneumonia secondary to COVID Date of onset of symptoms: 1/3/23 Symptoms present on admission: Shortness of breath Date of covid positive test: 1/4/2023 Vaccination status: vaccinated status post 3 doses of Pfizer Imaging: Chest x-ray, past reviewed, lower lobe airspace disease Oxygen requirements on admission: Trach mask, 10 L Current oxygen requirements: RA Medical therapy: steroids Consultants following: Infectious disease starting remdesivir Anticipated special isolation end date: January 14 LDH ESR and CRP 23.5 S/p remdesivir and dexamethasone. AKI resolved Resolved with IV fluids. GJ feeding tube Status ISOSOURCE HN at 20ml/hr w/ 100ml free water flush q 4 hours; ADVCANCE 10ml/hr q 4 hours to GOAL: ISOSOURCE HN at 70ml/hr w/ 100ml free water flush q 4 hours(HOLD 1 hour before and after synthroid) Abdominal x-ray reviewed satisfactory position of jejunal feeding tube

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2561877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 04.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Cerebrovascular accident Failure to thrive Gastrointestinal haemorrhage Headache Inappropriate schedule of product administration COVID-19 Drug ineffective Nasopharyngeal swab Overdose SARS-CoV-2 test Sinus node dysfunction Syncope

Symptomtext

if covid tested post vaccination: Yes; if covid tested post vaccination: Yes; This is a spontaneous report received from contactable reporter(s) (Nurse). A 75-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 04Nov2021 as dose 1, single (Lot number: FF2590) intramuscular, in right arm and on 04Nov2021 as dose 2, single (Lot number: FH8030) at the age of 74 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Breast cancer" (unspecified if ongoing); "heart disease" (unspecified if ongoing); "hypothyroid" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "bradycardia" (unspecified if ongoing); "Known allergies: Shellfish" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Known allergies: penicillin, reaction(s): "allergy". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "if covid tested post vaccination: Yes". The patient underwent the following laboratory tests and procedures: Nasopharyngeal swab: If covid tested post vaccination: Yes.; Sender's Comments: The efficacy of a drug varies from patient to patient and can be affected by different factors; however, a contributory role of the suspect product bnt162b2 to the reported drug ineffective / COVID-19 cannot be ruled out

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Test Name: Covid test type post vaccination=Nasal Swab; Result Unstructured Data: Test Result:If covid tested post vaccination: Yes
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bradycardia; Breast cancer; Heart disorder; Hypertension; Hypothyroidism; Shellfish allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555135

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: IA
Alter: 49,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 03.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / LA

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

Death Gastrointestinal haemorrhage Renal failure Shock

Symptomtext

Gastrointestinal bleeding / circulatory shock/ kidney failure leading to death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: shoulder injury back injury
Andere Medikamente: metformin
Allergien: -
Vorherige Impfungen: -

VAERS 2525365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 04.12.2021
Beginn: 28.11.2022
Tage bis Beginn: 359,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Asthenia Atrial fibrillation Bronchial obstruction COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax abnormal Confusional state Cough Dyspnoea Electrolyte depletion Electrolyte substitution therapy Hyponatraemia Hypotension Intensive care Mental status changes Oxygen saturation decreased

Symptomtext

Discharge Physician: MD Primary Care Physician: MD Date of Admission: 11/28/2022 Discharge Date: 12/6/2022 COVID positive Date 11/28/2022 PRESENTING PROBLEM: Lung mass Acute respiratory failure with hypoxia (HCC) COVID Pneumonia due to COVID-19 virus Acute hypoxemic respiratory failure (HCC) HOSPITAL COURSE: Patient is an 87-year-old male with a past medical history of coronary artery disease status post CABG, melanoma, squamous cell cancer of the head neck, paroxysmal atrial fibrillation not anticoagulated presenting for weakness and shortness of breath. He has had a 10 lb weight loss, cough, decreased energy. He was found to be positive for COVID. CT scan was performed on his chest which revealed a right hilar mass encasing the right main bronchus with partial occlusion of the proximal right lower lobe bronchus and significant narrowing of the right upper lobe bronchus which was suspicious for a primary bronchogenic malignancy like small cell lung cancer. Patient was started on Decadron remdesivir for COVID 19 infection. Overnight and into the early morning patient had an episode of desaturation requiring initially high-flow nasal cannula with non-rebreather over top. With this intervention he was still only saturating in the mid to high 80s and was confused. Patient was brought to the intensive care unit and placed on BiPAP. Repeat chest x-ray showed developing pneumonia in the right lower lobe, so he was placed on broad-spectrum antibiotics and MRSA nasal PCR was performed which ended up being negative. Extensive discussion was had with the daughter who then called the family meeting. At that point patient had improved in his mentation and was able to participate in the meeting. Patient decided that he wanted to speak with Hematology Oncology about the possibilities of the cancer. Dr. consulted and recommended the patient improved from his current infections before discussing intervention and biopsy. He also discussed with patient the unlikely could you be able to tolerate chemotherapy. Dr. stated that hospice would be appropriate and any time. Patient did improve during the day on 11/30/2022 and was weaned from BiPAP to high-flow nasal cannula with improving mentation and acceptable saturations. During the course of the day on 11/30/2022 patient was given a dose of IV Lopressor x1 for atrial fibrillation with rapid ventricular response. That did improve his rate but caused some hypotension. Over the course next several days the patient did improve significantly. He was able to be weaned down to room air during the day, he did still require 2 L at night. Patient was found to be significantly orthostatic and had a near syncopal event while working with therapy. He has also noted to initially have an improvement in his hyponatremia and then also worsened again. Discussions with family were ongoing in regards to discharge planning. They have opting to take him home with hired caregivers. There were also multiple ongoing discussions with family regarding the patient's underlying cancer. They are aware that he likely will not tolerate treatment. Patient himself is hesitant to make himself hospice without a known diagnosis. Family discussion with hospice on 12/6/2022. Family and patient decided to go home with home hospice. Electrolytes were monitored and repleted throughout the admission. Patient clinically improved and hemodynamically stable for discharge. Discussed plan of care discharge with patient including outpatient follow-up PCP within 7 days. Patient voiced understanding was agreeable with plan of care discharge.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic cough Chronic rhinitis Pulmonary mass Near syncope Coronary artery disease involving native coronary artery of native heart with other form of angina pectoris (HCC) Paroxysmal atrial fibrillation (HCC) Hypotension, unspecified hypotension type AF (paroxysmal atrial fibrillation) (HCC) Aortic valve sclerosis Diastolic dysfunction Heart murmur NSVT (nonsustained ventricular tachycardia) White coat syndrome without diagnosis of hypertension Hypertension Dysphagia Constipation Protein-calorie malnutrition, moderate (HCC) Arthritis Syncope Chronic low back pain Early dry stage nonexudative age-related macular degeneration of both eyes Optic neuropathy of both eyes Regular astigmatism, right eye Benign non-nodular prostatic hyperplasia with lower urinary tract symptoms Urinary retention Hypercholesteremia Hyponatremia Lymphadenopathy of head and neck S/P AVR (aortic valve replacement) Ventral hernia Left inguinal hernia Osteoarthritis of left knee S/P CABG x 4, AVR, PVI, LAA Squamous cell carcinoma of skin of scalp and neck Central scotoma, bilateral Insomnia Myopia with presbyopia of both eyes
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet Ascorbic Acid (VITAMIN C PO) aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 20 MG tablet Docusate Sodium (COLACE PO) levothyroxine (SYNTHROID) 75 MCG tablet LORazepam (ATIVAN) 2 MG/ML concentrated
Allergien: Pollen Codeine
Vorherige Impfungen: -

VAERS 2518704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: VA
Alter: 40,0
Geschlecht: F
Eingang: 29.11.2022
Impfdatum: 28.11.2021
Beginn: 16.09.2022
Tage bis Beginn: 292,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy COVID-19 Computerised tomogram thorax abnormal Conjunctivitis Cough Dizziness Dyspnoea Ear infection Fatigue Headache Influenza virus test positive Myalgia Nasal congestion Oropharyngeal pain Pain Pulmonary embolism Pulmonary thrombosis Pyrexia

Symptomtext

I had COVID-19 twice. The first I was in Sept. 16th coughing, had stuffy nose, fever, fatigue, shortness of breath, muscle ache, sore throat. They were moderate, not that bad. They lasted about 2 weeks. I got a Pulmonary embolism from this where I started feeling really dizzy and shortness of breath. I went to the ER and they found a blood clot in my lung from a CT scan. I was put on a blood thinner. My home Nov 7th I got COVID-19 again. This time I also had a Flu and double ear infection, and sinus infection. I had body ache, cough, headache, runny nose, sore throat and had these for a week and it was getting worse. I went to urgent care and was tested. And my home tests of COVID-19 the previous week was negative. I was put on antibiotics and eye drops because I was starting to get pink, and I got cough medication with codeine.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT scan blood clot in my lung; COVID-19 test positive; Flu positive
Aktuelle Erkrankungen: No
Vorgeschichte: Obesity; Asthma; Acid reflux
Andere Medikamente: Omeprazole
Allergien: No
Vorherige Impfungen: -

VAERS 2470633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: KY
Alter: 81,0
Geschlecht: M
Eingang: 06.10.2022
Impfdatum: 02.12.2021
Beginn: 19.02.2022
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Patient had a positive COVID test on 2/07/2022 and expired on 2/19/2022.

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Praegender Schweregrund: Death
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CVA Dementia Atrial fibrillation CAD HTN Hyperlipidemia MI DM type 2 Rheumatoid arthritis
Andere Medikamente: Duloxetine Metoprolol tartrate Furosemide Methocarbamol
Allergien: Niacin Penicillins
Vorherige Impfungen: -

VAERS 2461626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: NY
Alter: 76,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Computerised tomogram Constipation Epigastric discomfort Gastric polyps Joint swelling Peripheral swelling Pneumonia Pulmonary embolism SARS-CoV-2 test Uterine leiomyoma

Symptomtext

huge blood clot covering both lungs against her heart; had pain on her side and belching; fibroids (colon); feet swollen tremendously; ankle swollen tremendously; Constipation; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76-year-old female patient received BNT162b2 (BNT162B2), on 30Nov2021 as dose 3 (booster), single (Lot number: FH8030) at the age of 76 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Second Covid vaccine was on 03Mar2021 with a lot number of EN6203), administration date: 03Mar2021, when the patient was 75-year-old, for COVID-19 immunization; BNT162b2 (Dose 1), administration date: 15Feb2021, when the patient was 75-year-old, for COVID-19 immunization. The following information was reported: CONSTIPATION (non-serious) with onset Dec2021, outcome "recovered" (Dec2021); JOINT SWELLING (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "ankle swollen tremendously"; PERIPHERAL SWELLING (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "feet swollen tremendously"; GASTRIC POLYPS (medically significant) with onset Dec2021, outcome "recovered" (Dec2021), described as "fibroids (colon)"; PULMONARY EMBOLISM (hospitalization, medically significant, life threatening) with onset 20Jan2022, outcome "recovered" (20Jan2022), described as "huge blood clot covering both lungs against her heart"; EPIGASTRIC DISCOMFORT (non-serious), outcome "unknown", described as "had pain on her side and belching". Caller stated that she had gotten the booster on 30Nov2021. About 1.5 weeks after that her feet and ankles swollen tremendously. Called her cardiologist and was told to take a diuretic once a day for week. Swelling went down. Did not call her cardiologist and he did not call her. Two weeks after that she had constipation. Had herself checked. Had fibroids which were removed and were not cancerous. Flew to (state withheld) 1.5 weeks later and had pain on her side and belching so she took Gas-X but it did not help. Went to a walk in clinic and was tested for Covid and there was none. Was tested for pneumonia and there was none. Tested for Covid and pneumonia on 20Jan2022. Had a CAT scan on 20Jan2022 and there was a huge blood clot on her lungs. Was sent to the hospital by ambulance immediately. Called her family because they were unsure if she would make it. Used on 20Jan2022 which was two catheters from the groin to the blood clot which broke it up. Was put on blood thinners and today is on still on blood thinners. Unsure if this is related to but thinks so. Is for the first booster after the first two vaccines. Later clarified that it was for the Covid vaccine. Wanted to know do they now tell you how much the dosage is since the question was asked. Later clarified fibroids were on her colon. Later clarified that the huge blood clot was covering both lungs against her heart. All vaccines were Pfizer. Feet and ankles swollen tremendously: Resolved week after taking diuretic. Constipation: Resolved at the end of Dec2021. Took over the counter enemas and things to relieve gas and whatever doctor suggested over the counter. Fibroids (colon). Had six taken out from her colon that were tested and were negative in Dec2021. The events "huge blood clot covering both lungs against her heart", "fibroids (colon)", "feet swollen tremendously", "ankle swollen tremendously", "constipation" and "had pain on her side and belching" required physician office visit. The patient underwent the following laboratory tests and procedures: Computerized tomogram: (20Jan2022) there was a huge blood clot on her lungs; Pneumonia: (20Jan2022) there was none; SARS-CoV-2 test: (20Jan2022) there was none; Uterine leiomyoma: (Dec2021) Negative, notes: Had six taken out from her colon that were tested and were negative in Dec2021. Therapeutic measures were taken as a result of pulmonary embolism, gastric polyps, peripheral swelling, joint swelling, constipation, epigastric discomfort. Follow-up (26Sep2022): Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Test Date: 20220120; Test Name: CAT scan; Result Unstructured Data: Test Result:there was a huge blood clot on her lungs; Test Date: 20220120; Test Name: pneumonia; Result Unstructured Data: Test Result:there was none; Test Date: 20220120; Test Name: COVID-19 Test; Result Unstructured Data: Test Result:there was none; Test Date: 202112; Test Name: Fibroids (colon); Test Result: Negative ; Comments: Had six taken out from her colon that were tested and were negative in Dec2021.
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 87,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 03.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 60,0
Dosis: 3
Route/Site: IM / RA

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

Death Dementia

Symptomtext

Narrative: hospice consulted for severe dementia- death few days later

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

VAERS 2433343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 23.08.2022
Impfdatum: -
Beginn: 22.02.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Death Neurodegenerative disorder

Symptomtext

Narrative: hospice consulted for Senile degeneration of brain tissue. pt died a few days later

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

VAERS 2237849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8030

kritisch

Staat: MO
Alter: 59,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chills Fatigue Hyperhidrosis Illness Near death experience Pulmonary pain SARS-CoV-2 test Somnolence

Symptomtext

Thought I was going to die; sick; Sweating; Chills; serious fatigue/fatigue; Lungs hurt 24/7; have to take several naps everyday; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE), on 20Nov2021 as dose 3 (booster), single (Lot number: FH 8030) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Gallstones" (unspecified if ongoing); "Fatty liver" (unspecified if ongoing). None of Known allergies. The patient did not receive any other vaccine in four weeks. The patient did not receive any other medications in two weeks. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Batch/Lot number: EO7533, Location of injection: Arm Right), administration date: 26Mar2021, when the patient was 58-year-old, for Covid-19 Immunization; BNT162b2 (Dose 2, Batch/Lot number: EWO151, Location of injection: Arm Left), administration date: 16Apr2021, when the patient was 58-year-old, for Covid-19 Immunization. The following information was reported: CHILLS (life threatening) with onset 20Nov2021, outcome "not recovered"; PULMONARY PAIN (life threatening) with onset 20Nov2021, outcome "not recovered", described as "Lungs hurt 24/7"; HYPERHIDROSIS (life threatening) with onset 20Nov2021, outcome "not recovered", described as "Sweating"; NEAR DEATH EXPERIENCE (medically significant, life threatening) with onset 20Nov2021, outcome "not recovered", described as "Thought I was going to die"; SOMNOLENCE (life threatening) with onset 20Nov2021, outcome "not recovered", described as "have to take several naps everyday"; FATIGUE (life threatening) with onset 20Nov2021, outcome "not recovered", described as "serious fatigue/fatigue"; ILLNESS (life threatening) with onset 20Nov2021, outcome "not recovered", described as "sick". Nothing had been the same since getting booster. The patient did not have covid prior vaccination. The patient had been covid tested post vaccination. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (26Mar2022) Negative, notes: Nasal Swab. Therapeutic measures were not taken as a result of near death experience, illness, hyperhidrosis, chills, fatigue, pulmonary pain, somnolence.

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Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: Test Date: 20220326; Test Name: COVID-19; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fatty liver; Gallstones
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2062188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 29.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 33,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Blood creatinine increased Blood lactic acid increased COVID-19 Cardio-respiratory arrest Death Dehydration Hypophagia Cyanosis Electrocardiogram normal Fibrin D dimer Malaise Pyrexia Unresponsive to stimuli SARS-CoV-2 test positive Sepsis

Symptomtext

pt to ED with c/o fever, poor oral intake; dehydrated; treated with fluids, steroids, O2 supplementation, cefepime; AKI; staff found pt unresponsive in ED room, CODE BLUE called; pt expired in ED room at local hospital.

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

VAERS 2148632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: MI
Alter: 49,0
Geschlecht: M
Eingang: 28.02.2022
Impfdatum: 12.12.2021
Beginn: 13.01.2022
Tage bis Beginn: 32,0
Dosis: UNK
Route/Site: IM / -

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

Abdominal distension Acute kidney injury Acute respiratory failure Anticoagulant therapy Atrial fibrillation Base excess increased Blood bicarbonate increased Blood bilirubin decreased Blood culture positive Blood gases abnormal Blood pH decreased Blood pressure decreased Bronchiectasis Bronchoalveolar lavage abnormal Bronchoscopy abnormal Computerised tomogram thorax abnormal Condition aggravated Culture positive

Symptomtext

Deceased (2.20.22); Hospitalized (1.13.22 at hospital for 36 days / transferred to privacy on 2/18/22-2/20/22); COVID-19 positive (1.5.22); Fully vaccinated - unknown # of doses as pt has >4 doses documented. HOSPITAL Discharged as Deceased Summary BRIEF OVERVIEW: Discharge Provider: (privacy) Primary Care Physician at Discharge: (privacy) Admission Date: 2/18/2022 Active Hospital Problems Diagnosis Date Noted POA ? Acute respiratory failure 02/18/2022 Unknown ? COVID-19 02/18/2022 Unknown ? AKI (acute kidney injury) 02/18/2022 Unknown ? DVT of lower limb, acute 02/18/2022 Unknown ? PAF (paroxysmal atrial fibrillation) 02/18/2022 Unknown Date of Death: 2/20/22 Time of Death: 1:24 AM Preliminary Cause of Death: Acute respiratory failure due to COVID-19 Discharge Disposition: Deceased DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute respiratory failure HOSPITAL COURSE: Patient is a 49 year old with history of ESRD secondary to interstitial nephritis (h/o LUE AV fistula). He had renal transplant from his father 1/'03 with eventual allograft failure. First transplant was complicated by histoplasmosis in '07. He received a second renal transplant 1/'19 with persistent CKD3. Second transplant was complicated by ganciclovir-resistant CMV infection as well as PE (1/'19). He also has a history of pAfib (OP Coumadin), HFrEF, HTN, obesity. He tested (+) for COVID-19 1/5 (fully vaccinated). He received mAb 1/7 and was admitted to hospital 1/13 with hypoxemia. He received Tocilizumab 1/15 and started on steriods. On 1/24, he was noted to have a RLE peroneal DVT (while on Coumadin) and was transitioned to Eliquis. He developed escalating oxygen needs, up to intermittent BiPAP / HFNC 1/25. He was started on increased steroids and was empiric Cefepime / Vori. CT 2/5 showed an increase in GGO and bronchiectasis. Bronchoscopy was done 2/7 with cultures (+) for CMV for which Foscarnet was started 2/11. He had already showed improvement as was weaned to 4L NC by 2/11. He, however, again developed increased oxygen needs and again was briefly placed on BiPAP 2/13 followed by increasing HFNC requirement. He was diuresed and treated with 3 days pulse Solumedrol 2/13-2/15. Followup CT 2/16 showed increased bilateral ASD. Empiric Zosyn and IV Vanco were added 2/16. Reportedly 1:2 blood cultures were (+) in anaerobic bottle. On 2/17, he required intubation for type 2 respiratory failure - requiring 70% FiO2. He was transferred to hospital 2/18 for lung transplant evaluation. Despite aggressive measures, he has been persistently hypercapnic with worsening ABGs. After multiple discussion with his family and the progressive decline, the decision to pursue comfort care was made. His paralytic was stopped and he started to initiate his own breaths. His family remained at his bedside. Before he was extubated and pressors stopped his BP dropped significantly to 44/20. He was extubated and was found without spontaneous pulses or respiraiotns at 0124. His pupils were fixed and dilated. He was pronounced deceased at that time. Dr. was notified and will sign the death certificate 2/18/22 Med Critical Care H&P: CHIEF COMPLAINT: Acute respiratory failure ASSESSMENT / PLAN: 49 y.o. male admitted to the ICU for COVID-19 pneumonia Assessment and Plan PAF (paroxysmal atrial fibrillation) Assessment & Plan PAF on coumadin at home Now on eliquis --given developing aki will transition to heparin gtt. DVT of lower limb, acute Assessment & Plan DVT -right peroneal DVT on 1/24 On eliquis AKI (acute kidney injury) Assessment & Plan AKI S/p renal transplant x2 most recently a Deceased donor in 2019 Baseline cr 1.3 Suspect over diuresis Hold lasix Consult nephrology Was on MMF and tacrolimus: while clarify infection status would prefer to hold MMF COVID-19 Assessment & Plan Positive on 1/13 Hospitalized from 1/13-2/17 BAL with CMV, no bacteria or fungus on 2/15 Worsened and intubated on 2/16--at this stage active covid infection is still possible given his immunosuppressed status but organizing pneumonia, acquired and opportunistic infections are more likely the culprit * Acute respiratory failure Assessment & Plan Covid-19 pneumonia Admitted to hospital on 1/13 and transferred to another hospital on 2/17 with request to be evaluated for a lung transplant. During course at hospital was treated with decadron, Tocilizumab, Monoclonal abs and the an extended solumedrol course. He worsened acutely an required intubation on 2/16. Suspected HCAP, also BAL on 2/15 was positive for CMV and he was treated for CMV viremia and presumed CMV pneumonitis with foscarnet Most recently he started on Vancomycin and zosyn on 2/16 after being intubated. Plan: On propofol only for sedation, will add fentanyl and target RASS -5 for brief paralytic period to measure lung compliance and get a CT chest to assess parenchymal disease pattern At this point it is not clear if he has hospital acquired bacterial pneumonia, CMV pneumonitis and post-acute sequelae of COVID-19 including organizing pneumonia which a CT may be helpful to assess. Solumedrol: had been off steroids entirely since 2/15. Will decide on steroid regimen after CT chest. Consult ID Discussion Deepen sedation, get CT Notified by hospital that 1/2 blood cultures from 2/16 are positive for GPCs in pairs and clusters. Continue vancomycin and zosyn, MRSA swab x2 negative at hospital. Reason for transfer was consideration of lung transplant evaluation however there is a lot of diagnostic uncertainty and likely acute infection present. Will get CT chest, rest of plan above. Subjective HISTORIES: HPI: 49 y.o. male 49 year old with history of ESRD secondary to interstitial nephritis. He had renal transplant from his father 1/'03 with eventual allograft failure. First transplant was complicated by histoplasmosis in '07. He received a second renal transplant 1/'19 with persistent CKD3. Second transplant was complicated by ganciclovir-resistant CMV infection as well as PE (1/'19). He also has a history of pAfib (OP Coumadin), HFrEF, HTN, obesity. He tested (+) for COVID-19 1/5 (fully vaccinated). He received mAb 1/7 and was admitted to hospital 1/13 with hypoxemia. He received Tocilizumab 1/15 and started on steriods. On 1/24, he was noted to have a RLE peroneal DVT (while on Coumadin) and was transitioned to Eliquis. He developed escalating oxygen needs, up to intermittent BiPAP / HFNC 1/25. He was started on increased steroids and was empiric Cefepime / Vori. CT 2/5 showed an increase in GGO and bronchiectasis. Bronchoscopy was done 2/7 with cultures (+) for CMV for which Foscarnet was started 2/11. He had already showed improvement as was weaned to 4L NC by 2/11. He, however, again developed increased oxygen needs and again was briefly placed on BiPAP 2/13 followed by increasing HFNC requirement. He was diuresed and treated with 3 days pulse Solumedrol 2/13-2/15. Followup CT 2/16 showed increased bilateral ASD. Empiric Zosyn and IV Vanco were added 2/16. On 2/17, he required intubation for type 2 respiratory failure - requiring 70% FiO2. He was transferred to hospital 2/18 for lung transplant evaluation OBJECTIVE: Pulse 69 | Temp 37.4 ?C | Resp 27 | Ht 1.8 m | Wt 88.7 kg | SpO2 93% | BMI 27.38 kg/m? FIO2 (%): 70 % Score 9.5 SOFA RESPIRATORY: 3.1 SOFA COAGULATION: 2.1 SOFA LIVER (BILIRUBIN): 0.1 SOFA CARDIOVASCULAR: 0.1 SOFA CENTRAL NERVOUS SYSTEM: 0 SOFA RENAL: Physical Exam Constitutional: Appearance: He is ill-appearing. Pulmonary: Breath sounds: Rales present. Abdominal: General: There is distension. Tenderness: There is no abdominal tenderness. Skin: General: Skin is warm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: Complete Blood Count without Differential [370250788] (Abnormal) Collected: 02/19/22 2205 Order Status: Completed Specimen: Blood, Venous Updated: 02/19/22 2230 White Blood Cell 4.78 4.00 - 10.80 x10*3/uL Red Blood Cell 3.31 Low 4.60 - 6.00 x10*6/uL Hemoglobin 9.7 Low 14.0 - 18.0 g/dL Hematocrit 32.9 Low 42.0 - 52.0 % Mean Cell Volume 99.4 80.0 - 100.0 fL Mean Cell Hemoglobin 29.3 27.0 - 33.0 pg NRBC Absolute Count 0.02 High 0.00 - 0.01 x10*3/uL NRBC Automated 0.4 High 0.0 - 0.1 %WBC Mean Cell Hemoglobin Concentration 29.5 Low 32.0 - 37.0 g/dL Red Cell Diameter Width 13.2 11.0 - 16.0 % Platelet 184 140 - 400 x10*3/uL Mean Platelet Volume 10.9 7.4 - 11 fL CritCare Arterial Blood Gas [370250789] (Abnormal) Collected: 02/19/22 2205 Order Status: Completed Specimen: Blood, Arterial Updated: 02/19/22 2224 O2 Percent 100.0 Oxygen Device VENT pH Arterial 6.98 Low Panic 7.35 - 7.45 PCO2 Art >150.0 High Panic 35.0 - 45.0 mm Hg PO2 Art 62.1 Low 75.0 - 100.0 mm Hg Bicarbonate Arterial 36.7 High 20.0 - 28.0 mmol/L Base Excess Art 5.0 High -2.0 - 2.0 mmol/L Measured O2 Sat Art 76.8 Low 92.0 - 100.0 % Aa O2 Difference 476.8 mm Hg a/A O2 Ratio 12.00 % pO2 / FiO2 Ratio 62.1 Low >=200.0 CritCare Arterial Blood Gas [370250783] (Abnormal) Collected: 02/19/22 1645 Order Status: Completed Specimen: Blood, Arterial Updated: 02/19/22 1655 O2 Percent 100.0 Oxygen Device VENT pH Arterial 7.00 Low Panic 7.35 - 7.45 PCO2 Art >150.0 High Panic 35.0 - 45.0 mm Hg PO2 Art 62.6 Low 75.0 - 100.0 mm Hg Bicarbonate Arterial 36.4 High 20.0 - 28.0 mmol/L Base Excess Art 5.1 High -2.0 - 2.0 mmol/L Measured O2 Sat Art 78.2 Low 92.0 - 100.0 % pO2 / FiO2 Ratio 62.6 Low >=200.0
Aktuelle Erkrankungen: -
Vorgeschichte: ADHD (attention deficit hyperactivity disorder) ? Anemia - of CKD ? Anxiety ? Arrhythmia 03/15/2018 - paroysmal Atrial fibrillation ? CHF (congestive heart failure) - combined systolic/diastolic ? Chronic combined systolic and diastolic congestive heart failure -combined systolic/diastolic ? Chronic interstitial nephritis 4/23/2020 ? Chronic kidney disease - stage 5, living donor 2003, failed 2015 on HD ? CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min ? COVID-19 1/13/2022 ? Cytomegalovirus infection 12/10/2019 - From Kidney Transplant 1/2019 ? Deceased-donor kidney transplant recipient 1/7/2019 49 y.o. white male with original history of ESRD secondary to interstitial nephritis. S/P haploidentical living related renal transplant from his father 1/2003, with eventual allograft failure and return to hemodialysis 5/2015. The course of first transplant was complicated by histoplasmosis in 2007. He received a second renal transplant from nonheartbeating deceased donor 1/7/2019. HLA-2A,2B, ? Depression ? Diverticulitis ? Dyspnea on exertion 10/24/2019 ? ESRD (end stage renal disease) 11/16/2016 no longer in need of Dialysis.Last documented Bun 21,Creatinine 1.4 GFR 54 on 11/08/19Kidney transplant 01/07/19currently dialysis m,w,f thru permacath on left chest, follows with Dr. on the transplant list at u of m currently dialysis m,w,f thru permacath on left chest, follows with Dr. on the transplant list at privacy ? Generalized anxiety disorder ? GERD (gastroesophageal reflux disease) ? H/O histoplasmosis 2007 - h/o disseminated histoplasmosis ? History of anemia 4/23/2020 ? History of blood clots - RLL PE ? History of histoplasmosis 12/10/2019 ? History of pulmonary embolism 1/14/2019 ? Hyperlipidemia ? Hyperparathyroidism - Secondary ? Hypertension ? Hypomagnesemia ? Infection due to antimicrobial resistant virus 12/10/2019 ? Insomnia ? Internal hemorrhoids ? Kidney transplant status, living related donor 01/2003 - Returned to hemodialysis 5/2015 ? Major depressive disorder 9/30/2014 ? Mixed hyperlipidemia ? Obstructive sleep apnea 11/15/2018 -uses c-pap No longer uses C Pap can't tolerate itcpap ? Paroxysmal atrial fibrillation 1/26/2020 ? Post-transplant erythrocytosis ? Primary hypertension 9/30/2014 ? Pulmonary embolism 01/14/2019 ? Restless leg syndrome - only when was on hemodialysis ? S/P partial colectomy 7/20/2016, 10/2015 10/2015 ? Secondary hyperparathyroidism ? Sleep apnea - CPAP
Andere Medikamente: acetaminophen (Tylenol Arthritis Pain) 650 mg 8 hr tablet, Take 650 mg by mouth. Take two tabs by mouth daily as needed, ? amphetamine-dextroamphetamine (ADDERALL) 30 mg tablet, Take 1 tablet (30 mg total) by mouth 2 (two) times a day., ?
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2129356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 06.11.2021
Beginn: 17.02.2022
Tage bis Beginn: 103,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Patient was fully vaccinated, developed COVID, and passed away on 02/17/2022. Patient is currently being investigated by the COVID mortality review team to determine if death was COVID related.

Weitere VAERSDATA-Felder

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

VAERS 2119289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 27.02.2021
Beginn: 20.01.2022
Tage bis Beginn: 327,0
Dosis: 3
Route/Site: IM / UN

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

Death

Symptomtext

ADMITTED TO HOSPITAL, EXPIRED

Weitere VAERSDATA-Felder

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

VAERS 2101893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: PA
Alter: 89,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 18.11.2021
Beginn: 14.12.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: SYR / -

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

Blood test Chest X-ray Computerised tomogram Electrocardiogram Myocardial infarction

Symptomtext

Mild heart attack, has contributed to progression in dementia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Chest x-ray, CAT scan of head, blood tests, EKG, assay thyroid
Aktuelle Erkrankungen: none
Vorgeschichte: One heart attack 4 years ago
Andere Medikamente: Levothyroxin, amiodarone, finasteride, olanzapine, tamsulosin
Allergien: none known
Vorherige Impfungen: -

VAERS 2215735

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 14.12.2021
Beginn: 11.01.2022
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / RA

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

Death

Symptomtext

Narrative: 88 year-old patient with multiple comorbidities expired under care of hospice service after receiving COVID vaccine

Weitere VAERSDATA-Felder

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

VAERS 2206325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 100,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 10.11.2021
Beginn: 09.01.2022
Tage bis Beginn: 60,0
Dosis: 3
Route/Site: IM / RA

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

Death

Symptomtext

Narrative: death

Weitere VAERSDATA-Felder

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

VAERS 2206316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 18.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Death

Symptomtext

Narrative: Patient expired in hospice house

Weitere VAERSDATA-Felder

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

VAERS 2206309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 98,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 10.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Narrative: Hospice part of the facility.

Weitere VAERSDATA-Felder

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

VAERS 2037883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: PA
Alter: 64,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 09.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / AR

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

Angiogram cerebral abnormal Anticoagulant therapy Atrial septal defect Cerebral artery occlusion Cerebral haemorrhage Cerebrovascular accident Confusional state Echocardiogram normal Headache Magnetic resonance imaging head abnormal Road traffic accident

Symptomtext

confusion, headache on 12-22, then hospitalized on 12-23 after an auto accident. Diagnosed with stroke, initially received aspirin, which was then stopped b/o small hemorrhages on CT. Discharged on 12-24, slow improvement in symptoms after that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 2,0
Labordaten: CT angiogram and brain MRI showing right sided ischemic CVA with occlusion of branch of right middle cerebral artery. Also had an echocardiogram showing a patent foramen ovale.
Aktuelle Erkrankungen: polymyalgia rheumatica
Vorgeschichte: -
Andere Medikamente: prednisone
Allergien: NKA
Vorherige Impfungen: -

VAERS 1989298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 17.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: ID / LA

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

Aphasia Blood culture Chest X-ray Chest pain Computerised tomogram head Confusional state Culture urine Death Decreased appetite Disturbance in attention Dyspnoea Electrocardiogram Laboratory test Lumbar puncture normal Magnetic resonance imaging head Mental status changes Mobility decreased Troponin

Symptomtext

Patient received 3rd Covid Pfizer vaccine on 11/17. On 11/19, patient complained of chest pain, shortness of breath, and lack of appetite. On 11/20, patient remained in bed with multiple blankets and did not eat. When daughter visited patient on 11/21, patient was found still in bed, confused, incontinent of urine, with intermittent word-finding difficulties. Patient was brought to the emergency department on 11/22 and had difficulty concentrating (unable to count backwards from 30) and general confusion. Throughout hospital admission, patient continued to have waxing/waning of mental status which never recovered. Patient ultimately passed on 12/28.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 37,0
Labordaten: 11/22: labs, EKG, troponin, CXR, urine analysis/culture, blood culture, CT of the head, MRI of the brain (possible subacute infarct involving right splenium of corpus callosum with associated punctate focus of enhancement) 11/24: LP (negative for infections) 12/2: repeat CT head 12/8, 12/26: repeat MRI brain
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, hyperlipidemia, diabetes, peripheral artery disease, gout; history of leukemia and allogeneic stem cell transplant
Andere Medikamente: Aspirin, lisinopril, repaglinide, hydrochlorothiazide, sirolimus, atorvastatin, allopurinol, rivaroxaban, atenolol, folic acid, acyclovir, voriconazole, cholecalciferol, magnesium oxide, fluticasone/salmeterol inhaler, fluticasone nasal spr
Allergien: Sulfamethoxazole/trimethoprim
Vorherige Impfungen: -

VAERS 1951545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 22.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 10,0
Dosis: UNK
Route/Site: IM / LA

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 1951531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 22.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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 1951521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 22.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

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 1951509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

kritisch

Staat: VA
Alter: 74,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 22.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / 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: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1951507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: -
Alter: 92,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 22.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 15,0
Dosis: 3
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 1942545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: DC
Alter: 79,0
Geschlecht: M
Eingang: 12.12.2021
Impfdatum: 22.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / AR

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

Coma Dyspnoea Mechanical ventilation

Symptomtext

Two days after the vaccination, and one day after he was brought home, my husband could not breathe. A nurse measured his oxygen saturation at 75%. He was taken by ambulance to the local Emergency Room. He went into a coma and was put on a ventilator.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coma
Hospital-Tage: 18,0
Labordaten: -
Aktuelle Erkrankungen: acute tubal necrosis
Vorgeschichte: diabetes, high blood pressure
Andere Medikamente: -
Allergien: Atorvastatin, Rosuvastatin
Vorherige Impfungen: -

VAERS 1920373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

kritisch

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Anaphylactic shock

Symptomtext

Anaphylaxis shock. Epipen administered by pharmacist within 10 minutes of receiving vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal Vitamins, vitamin B12, B complex, calcium
Allergien: Peanut and Strawberries
Vorherige Impfungen: Covid 19 vaccine 1st shot

VAERS 2641436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 06.06.2023
Impfdatum: 30.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 13,0
Dosis: UNK
Route/Site: - / -

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

Angiogram cerebral abnormal Cerebral venous sinus thrombosis Computerised tomogram head abnormal Heavy menstrual bleeding Intensive care Intracranial contrast-enhanced magnetic resonance venography Thrombosis Transverse sinus thrombosis

Symptomtext

Cerebral Venous Sinus Thrombosis Covid vaccine on 12/17/2020, 1/7/2021 and 11/30/2021. After first two I had worsening Menorrhagia So started loestrin in 2/2021. exactly two weeks after my Covid booster I was admitted to the Neuro ICU with the thrombus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous sinus thrombosis
Hospital-Tage: -
Labordaten: CT HEAD BRAIN, 13-Dec-2021, acute thrombosis within the right transverse venous; CTA, 13-Dec-2021, There is a filling defect within the right transve; MRV, 14-Dec-2021, There is lack of opacification of the right transv
Aktuelle Erkrankungen: No other issues. Physician
Vorgeschichte: Asthma
Andere Medikamente: Loestrin, Albuterol, iron; Magnesium
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2513096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: OH
Alter: 48,0
Geschlecht: M
Eingang: 21.11.2022
Impfdatum: 17.11.2021
Beginn: 23.09.2022
Tage bis Beginn: 310,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy COVID-19 Chills Coagulation factor V level normal Compression garment application Cough Deep vein thrombosis Headache Inflammation Laboratory test Pain in extremity Pyrexia SARS-CoV-2 test positive Scar Superficial vein thrombosis

Symptomtext

I had a fever that lasted for about 3 days until I went on PAXLOVID. I had headaches, chills, and some slight coughing. The symptoms dissipated after 5 days. On October 8, I drove 13 hours and didn't get out much. Less than a week after testing positive for COVID-19. I had some foot pain later that week. I noticed scarring or inflammation on my right foot on a vein. Shortly after that, I started having pain in my left calf. Superficial clot on the right foot and a DVT in the left calf a week later. This was all diagnosed by the clinic on October 27. This was roughly 20 days after that drive. I'm fairly certain I got it on my first road trip after I was no longer testing positive. I was taking baby aspirin and using compression socks because I've had DVTs in the past. The healthcare providers are relating it to the COVID-19 infection itself. They're treating the clots with ELIQUIS/blood thinners. The recommended treatment is 6 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Factor V family genetics for clotting negative; other tests from clinic
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 2511930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: IN
Alter: 67,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 19.11.2021
Beginn: 11.11.2022
Tage bis Beginn: 357,0
Dosis: 3
Route/Site: SYR / -

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

Abdominal mass Abdominal pain Adrenomegaly Anticoagulant therapy Aortic arteriosclerosis Ascites Biliary dilatation Computerised tomogram abdomen abnormal Decreased appetite Intervertebral disc degeneration Liver opacity Lymphadenopathy Metastases to liver Metastatic neoplasm Pancreatic enlargement Portal vein cavernous transformation Portal vein thrombosis Renal cyst

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on November 11, 2022 08:14 EST Verified By: MD on November 11, 2022 08:14 EST Encounter Info: Hospital, Outpatient in a Bed, 11/11/22 - 11/11/22 * Final Report * Chief Complaint liver mets History of Present Illness/Subjective abnormal ct scan with liver mets, needs endoscopic evaluation of gi tract as possible source Review of Systems Constitutional: No fever, No chills, No sweats, No weakness, No fatigue, No decreased activity, wt loss Eyes: No Icterus ENMT: No nasal congestion, No sore throat Respiratory: No SOB, No cough Cardiovascular: No Chest pain, No palpitations, No peripheral edema Gastrointestinal: No nausea, vomiting, No diarrhea, No constipation, No Heartburn, Abdominal pain, No hematemesis Genitourinary: No dysuria, No hematuria, No change in urine stream Hema/Lymph: No bruising tendency, No bleeding tendency, No swollen lymph glands Endocrine: No excessive thirst, No polyuria, No cold intolerance, No heat intolerance, No excessive hunger Immunologic: No immunocompromised, No recurrent fevers, No recurrent infections, No malaise Lymphatics: No lymphadenopathy neck, Axilla, Groin Musculoskeletal: Normal gait Integumentary: Warm, Dry, Pink, No pallor, No rash, No Pruritus, No Abrasions, No Breakdown, No Burns, No Dryness, No Petechiae, No Skin Lesion, No Hypertrophic scar, No Keloid Neurologic: Alert, Oriented, No Abnormal balance, No Confusion, No Numbness, No Tingling, No Headache Psychiatric: No Anxiety, No Depression, No Mania, Non-Suicidal, Non-Delusional, No Halluciations Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 36.5 (36.5-36.5) Temp (FAHR) 97.7 (97.7-97.7), BP 201/98 (178-201)/(91-98), HR 83 (83-86), RR 16 (16-16), O2Sat 98 (98-98) Patient Weight Current Daily Weight: 55 kg 11/11/22 BMI: 19.5 11/11/22 Normal Weight (BMI 18.5-24.9) Patient Height Current Height: 168 cm 11/11/22 General: Alert and oriented, No acute distress Eye: PERRL, EOMI, Normal conjunctiva HENT: Normocephalic Neck: Supple, Non-tender, No JVD, No lymphadenopathy, No thyromegaly Cardiovascular: Regular rate, Normal rhythm, No murmur, S1, S2 Breast: No mass, No tenderness, No discharge Respiratory: Lungs CTA, Non-labored, BS equal Gastrointestinal: Soft,-tender, Non-distended, Normal bowel sounds, No organomegaly Lymphatics: No lymphadenopathy neck, Axilla, Groin Musculoskeletal: Normal gait Integumentary: Warm, Dry, Pink, No pallor, No rash Neurologic: Alert, Oriented, No focal defects, CN II-XII intact Psychiatric: Cooperative, Appropriate & affect, Normal judgement Assessment/Plan 1. Metastasis to liver C78.7 Needs endoscopic evaluation of GI tract will schedule EGD and Colonoscopy. Surgical risks and benefits explained to patient. Included but not limited to infection, hemmorage, and perforation. Patient understands and wished to comply. patient verbalize understanding and compliance with the plan will proceed as scheduled Orders: Lactated Ringers 1,000 mL, Total Volume (mL) = 1,000, IV, 11/11/22 7:14:00 EST, 100 mL/hr Message to Nursing Message to Nursing Procedure/Test Scheduled Date/Time Verify per Nursing (Specify) Verify per Nursing (Specify) Code Status None Recorded Chronic Problem List No qualifying data Medications Home Medications (1) Active Lovenox Active Scheduled Inpatient Medications Lactated Ringers 1,000 mL IV 100 mL/hr One-Time Medications Given 11/10/22 00:00:00 TO 11/11/22 08:13:19 None Reported PRN Medications (0600 - 0559) from 11/10 - 11/11 None Reported Allergies NKA Diagnostics Radiology Results - Last 24 hours Across Visits No radiology results found in the last 24 hours. Signature Line Electronically Signed on 11/11/22 08:14 EST ________________________________________________________ MD

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Praegender Schweregrund: Portal vein thrombosis
Hospital-Tage: -
Labordaten: ocument Type: CT Abdomen W/ IV Contrast Document Subject: CT Abdomen W/IV Contrast Performed By: MD on October 24, 2022 17:28 EDT Verified By: MD on October 25, 2022 10:05 EDT Encounter Info: Hospital, Outpatient, 10/24/22 - 10/24/22 * Final Report * Reason For Exam epi mass Addendum ADDENDUM BEGINS Addendum Date: 10/25/2022 10:03 AM This radiology interpretation contains an amendment and/or addendum. The information in this addendum supersedes any previous report. I discussed these findings personally with Dr. at 2012 hours. ADDENDUM ENDS Electronically Signed by: Dictated on: 10/25/2022 10:03 AM Signature Line This examination and reported findings have been reviewed and confirmed by the undersigned. Read By: MD I authorize my name to be Electronically affixed by using my unique signature access code. Report EXAMINATION: CT Abdomen W/IV Contrast, 10/24/2022 HISTORY: Epigastric mass. Decreased appetite. A pound weight loss over 3 weeks. COMPARISON: None available. TECHNIQUE: Multislice axial imaging was obtained through the abdomen utilizing 100 mL of Isovue-370 intravenous contrast and oral contrast. Contrast waste 0 mL. INTERPRETATION: Liver: There are extensive areas of decreased attenuation within the liver, predominantly the right lobe, consistent with widespread metastatic disease. There is thrombosis beginning at the portal confluence and extending into the right portal venous branches. There is opacification of the left portal vein. There is cavernous transformation of the portal vein with numerous collateral vessels noted in the porta hepatis. Spleen: Spleen is prominent in size. The splenic vein is patent. Pancreas: The head of the pancreas appears somewhat prominent in size but enhances normally. Gallbladder/Bile Ducts: Gallbladder is distended. No obvious stones. Multiple collateral vessels around the periphery of the gallbladder. No obvious biliary ductal dilatation. Adrenals: There is mild diffuse enlargement of the left adrenal gland. Unremarkable right adrenal gland. Kidneys/Ureters: No stones or hydronephrosis. Subcapsular hypodensity in the posterior right kidney is probably a cyst. Lymph Nodes/Mesentery/Peritoneum: 10 mm lymph node in the gastrohepatic ligament on image 37. Portacaval lymph node on image 55 measures at least 17 x 13 mm. A small to moderate amount of ascites is present in the abdomen. No free air is noted. Vascular Structures: There is thrombosis of the portal vein from its origin through the right portal venous branches. The left portal vein opacifies normally. A small portion of the superior mesenteric vein may be thrombosed. Atherosclerosis of the aorta and proximal iliac vessels. The superior mesenteric artery opacifies normally. GI Tract: The visualized bowel loops are unremarkable. Many of the bowel loops are not included on this study. Abdominal Wall: Small umbilical hernia containing only fat. Lung Bases: No significant abnormality. Lower Chest: Normal heart size. Musculoskeletal: Degenerative disc disease. No lytic or blastic bone lesions are identified. Other: No other significant abnormality. IMPRESSION: 1. Extensive liver metastases. Most likely, this is due to a GI primary, such as a colon primary. The most direct route to a diagnosis would likely be a CT-guided biopsy of the liver. 2. Portal vein thrombosis. The portal vein is distended with thrombus. The right portal venous branches are thrombosed. The left portal vein is patent. The thrombus may include a small portion of the superior mesenteric vein near the portal confluence. 3. Ascites. Enlarged gastrohepatic lymph node. Enlarged portacaval lymph node. 4. Medical oncology consultation recommended. Message left with the answering service at 1750 hours. Electronically Signed by: Dictated on: 10/24/2022 5:31 PM Signature Line This examination and reported findings have been reviewed and confirmed by the undersigned. Read By: MD I authorize my name to be Electronically affixed by using my unique signature access code.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2504107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: IN
Alter: 26,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 03.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chest discomfort Chills Dizziness Electrocardiogram Fall Full blood count Hyperhidrosis Irregular breathing Loss of consciousness Metabolic function test Nervousness Oxygen saturation decreased Pallor Skin discolouration Tachycardia Tremor

Symptomtext

At work(Nurse), I started feeling nervous, lightheaded, weak, sweating and my chest was pounding. I sat down and the symptoms did not subside. I stood up and stumbled to the door to get help, blacked out and fell into a wall. Was told I was unconscious for ~20 minutes, very pale/grey, very sweaty, irregular breathing, very tachycardic. A respiratory therapist put a pulse oximeter on me and my oxygen saturation was in the low to mid-80s, they applied an oxygen cannula. Taken to ED by hospital's code team, IVs placed, fluids given, CT scan, EKG, labs drawn. While recovering, I had uncontrollable shaking and shivers. Start of event to time of ED discharge ~3.5 hours.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG 12/13/21 CBC 12/13/21 BMP 12/13/21 EKG 1/12/21
Aktuelle Erkrankungen: -
Vorgeschichte: Recurrent UTIs
Andere Medikamente: Acycolvir Ceterizine
Allergien: Sulfa products
Vorherige Impfungen: -

VAERS 2460498

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FH8030

schwer

Staat: NY
Alter: 76,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 30.12.2021
Beginn: 13.02.2022
Tage bis Beginn: 45,0
Dosis: 1
Route/Site: - / -

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

Abdominal distension Acute kidney injury Adrenal insufficiency Anticoagulant therapy Atelectasis Atrial fibrillation Azotaemia Blood creatinine increased Blood gases Blood urea increased Body temperature decreased C-reactive protein increased COVID-19 Cardiac failure Cardiac failure congestive Chest X-ray abnormal Computerised tomogram thorax abnormal Decubitus ulcer

Symptomtext

2/13/2022-Transfer from LTC, report of AMC, SOB and distended abdomen. Afebrile HR-97. WBC-21.3 CRP-5.5 Covid +. Start baricitinib, IV Decadron, IV azithromycin and cefepime. 2.5 L via NC 02 sat 98%, Admit- Acute encephalopathy metabolic due to uremia in the setting of dehydration and poor oral intake. AKIBUN 77 CReatnine-1.7 EGFR-31 Chest CT-Bibasilar atelectactic change. 2/15/2022-Titrated down to 2L . Given 2 units PRBC due to excessive bleeding for RLE wound bleeding. H/H 6.6/19.1. 2/16/2022-Baricitinib,decadron and cefepime d/c, pt asymptomatic. 2/18/2022- Tachy HR 150-170. HFpEF exacerbation A fib with RVR: Lasix IV and lopressor once, carvedilol increased to 12.5mg. Placed on bipap, after sat 93% on 5L. 2/18/2022- CXR: possible pluer effusion. ABg: 7.460/38.1/77/27.1/96. Started on Zosyn for older sacral decub with exposed bone concerning for osteo. Am:rapid called. HR in 160's Sob and lethargic. Bipap. PM: Rapid called, BP in the 70's systolic, pt intubated and transfered to ICU. Pt on neo-synephrine 100 mcg, Levo at 36 mcg. Levo weaned down to 15 mcg and Neo weaned down to 50 mcg to maintain sbp >90. Cm NSR and Temp 99. Hydrocortisone for Cushings. 2/19/2022- Shock st to acute adrenal insufficiency recent systemic corticosteroid taper for large sacral ulcer with osteo. MSSA and chronic hypoxemic resp failure. AKI. Continue IV piperacillian/tazobactam and IV vanco, for ID coverage. On levo at 40 mcg off IV phenylephrine 100mcg. BP 79/45 and hr 68. Intubated BiLevel 14/PEEP 8/PS 24cm h20/FIO@ 50%. 2/21/2022-sputum cuture. Continue Zosyn D/C vanco Extubated. 2L via NC and Bipap at HS . CR is 1.2 H &H stable. A fib rate controlled, on eliquis. 2/23/2022- ICU downgrade. 2L via NC stable. 2/26/2022- Hgb down to 6.3 tranfused 2 units PRBC. repeat hgb 8.0. 2/28/2022-Low temp 95.6, D5LR IV. 3/8/2022- Stable on RA, CHFpEF better on LAsix 40 mg. Continue Zosyn for osteo. A fib rate is controlled. 3/15/2022-Stable on RA, BP-117/67 P-86. EFGR 36, WBC 9.8, H &H 7.63/23.1 1 unit PRBC given amd continue Zosyn for osteo. Discharged.

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Praegender Schweregrund: Intensive care
Hospital-Tage: 37,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, GERD, Hyperthyroidism, Pulmonary Emphysema, CAD, ETOH abuse, Obesity and hyponatremia
Andere Medikamente: -
Allergien: Levofloxacin and Moxifloxacin
Vorherige Impfungen: -

VAERS 2431218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 01.12.2021
Beginn: 22.08.2022
Tage bis Beginn: 264,0
Dosis: 3
Route/Site: - / -

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

Anticoagulant therapy COVID-19 Computerised tomogram abdomen abnormal Infusion International normalised ratio decreased Pain in extremity Peripheral swelling SARS-CoV-2 test positive Thrombectomy Vascular stent occlusion Vascular stent thrombosis Venogram abnormal

Symptomtext

Patient is a 60 y.o. male who presents today with RLE swelling and pain. Pt. has a PMH of factor V Leiden mutation with recurrent DVTs, chronic back pain, essential HTN. Pt. was recently admitted from 7/10/22 to 7/16/22 with recurrent RLE DVT despite compliance with pradaxa. He was started on a heparin qtt and hematology and IR were consulted. He underwent a thrombectomy with right common iliac stneting. Hematology recommended changing oral anticoagulant to coumadin with 30 days of plavix. Since discharge patient was doing well until about one to two weeks ago he started to have RLE swelling and now worsening pain. Found to be COVID positive. CT abdomen and pelvis with thrombotic occlusion of the right iliofemoral stent. He underwent Right lower extremity venography with catheter directed mechanical thrombectomy8/25.Hematology following since patient has multiple anticoagulation regimen failure, recommend warfarin with INR goal 2.5 to 3.5 and Plavix. In the meantime, patient was anticoagulated on IV heparin drip. Pharmacy dosed patient's Coumadin while in the hospital. Eventually over an extended period, patient's INR began to climb and on the day of discharge was at 2.1. Patient was comfortable with Lovenox bridging at home and following up with his PCP at discharge. An appointment was made for him prior to discharge. Patient already had prescriptions for Lovenox at home and was trained on its use. Patient was medically stable for discharge.

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Praegender Schweregrund: Vascular stent thrombosis
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: Admission Date: 11/20/2021 Discharge Date: 11/24/2021 Leg DVT (deep venous thromboembolism), acute, right (HCC)
Vorgeschichte: Seasonal affective disorder (HCC) Chronic back pain Arthritis Factor V Leiden (HCC) Contracture, neck S/P split thickness skin graft Deep vein thrombosis (DVT) of popliteal vein of right lower extremity (HCC) Leg DVT (deep venous thromboembolism), acute, right (HCC) DVT of deep femoral vein, right (HCC) DVT (deep vein thrombosis) in pregnancy
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet amLODIPine (NORVASC) 5 MG tablet carvedilol (COREG) 6.25 MG tablet clopidogrel (PLAVIX) 75 MG tablet cyclobenzaprine (FLEXERIL) 10 MG tablet enoxaparin sodium (LOVENOX) 100 MG/ML SOSY gabapentin (NEURON
Allergien: Nsaids
Vorherige Impfungen: -

VAERS 2162756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MI
Alter: -
Geschlecht: U
Eingang: 30.08.2022
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Chest pain Computerised tomogram Dyspnoea Echocardiogram Cardiac disorder Myocarditis Electrocardiogram Heart rate increased Magnetic resonance imaging Pain in extremity X-ray

Symptomtext

I was admitted in to the hospital because your shot made my heart inflamed; heart hurt; chest pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 14Dec2021 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series completed and Manufacturer unknown), for COVID-19 immunization. The following information was reported: MYOCARDITIS (hospitalization, medically significant) with onset 14Dec2021, outcome "unknown", described as "I was admitted in to the hospital because your shot made my heart inflamed"; CHEST PAIN (non-serious) with onset 14Dec2021, outcome "not recovered"; CARDIAC DISORDER (non-serious) with onset 14Dec2021, outcome "unknown", described as "heart hurt". Clinical Course: We have received an Adverse event letter from (withheld) to Pfizer Inc.in the (withheld) Mail Room on Thursday, 25Aug2022. Shared scan as attachment. The patient was given a booster shot on 14Dec2021 and that night was admitted in to the hospital because the shot made patient's heart inflamed, and as of 17Aug2022, still getting chest pains. For compensation for the shot making the heart hurt which could be a lifetime of pain Patient states, "You guys can decide whether you give me money, you can decrease it increase it or give me nothing. But i'd like to give my thanks for the vaccine and for making it come out quickly. And I would like to say ever since I got your vaccine I haven't gotten covid since." The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

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

VAERS 2402960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 08.11.2021
Beginn: 31.07.2022
Tage bis Beginn: 265,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

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

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

VAERS 2370692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MO
Alter: 49,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 03.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / -

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

Blood prolactin increased Electroencephalogram normal Hemiparesis Hypoaesthesia Loss of consciousness Magnetic resonance imaging head normal Paraesthesia Seizure Syncope

Symptomtext

Patient was administered Pfizer booster (3rd dosage) on 12/3/21. Previous Pfizer dosages were received on 12/23/20 and 1/11/21 as mandated. I collapsed at home with loss of consciousness on 12/17/22 and was taken to Hospital by EMS, admitted overnight for suspected Seizure. EEG completed and negative. Prolactin levels were elevated, Neurology was consulted and suspected seizure activity. I was given Keppra in the hospital setting. I was not discharged home on Keppra due to being first seizure. Follow up MRI head ordered and follow up with Neurology planned. I then had another episode at home on 12/23/21 with total weakness to left side of body with numbness and tingling to bilateral lower extremities. I was seen in hospital ER on 12/23/21, MRI head completed and negative. Neurology again consulted in ER due to symptoms and elevated prolactin levels. Determined seizure activity and diagnosis of Seizure disorder given by Neurologist. I was given IV Keppra in ER and discharged home with Keppra prescription and follow up with Neurology. No etiology given for new-onset of seizures. I did discuss with Neurologist that Pfizer vaccine was received on 12/3/21.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Hx scoliosis
Vorgeschichte: Scoliosis
Andere Medikamente: Trazodone 50mg at bedtime
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2336513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: VA
Alter: 59,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Balance disorder Bell's palsy Computerised tomogram head Dizziness Fall Fatigue Gait disturbance Headache Herpes zoster Laboratory test Ophthalmological examination

Symptomtext

Pfizer Vaccines: 1/14/2021--Headaches, fatigue; 1/25/2021--Headaches; 12/1/2021(booster); started having unexplained headaches with increase fatigue and balance issues. End of February 2022 diagnosed with Shingles. Beginning in March 2022 noticed frequent headaches, altered gait, unexplained dizzy spells which continued into April 2022. May 2022 increase dizziness and unsteady gait, fell on right side. June diagnosed with Bell's Palsy.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: February 2022-Urgent Care Clinic for Shingles and follow up with Primary Care March-April-Follow up with Primary Care for Chronic Pain and other symptoms mentioned but did not relate it to the vaccines at that time June 17, 2022-Labs, Head CT. Eye Exam, Primary Care, Physical Therapy for Bell's Palsy
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic back and hip pain
Andere Medikamente: amlodipine 10mg
Allergien: latex, sulfa meds, lisinopril
Vorherige Impfungen: -

VAERS 2280458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 22.05.2022
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Angina pectoris Arthralgia Blindness Blood test Cardiac disorder Balance disorder Chest pain Cognitive disorder Diastolic dysfunction Disorientation Dizziness Dyspnoea Dyspnoea exertional Echocardiogram abnormal Electric shock sensation Fatigue Feeding disorder Headache

Symptomtext

Woke up that night in excruciating pain, body aches, rigid muscles, swollen joints (could not form a fist). Extreme fatigue and disorientation; headache, slight fever; shortness of breath; painful chest and heart; high blood pressure, then disregulated blood pressure after that; smell and taste off; significant weight loss from 132 to 120 lbs in two weeks; could not eat; shortness of breath on exertion is still bad at 6 months post-booster. Neuropathy (shooting electric shocks). Temperature not regulated (over-heat). Cognitive impairment; dizziness and balance problems; had either a TIA or ocular migraine April 2022 when I lost vision, and impaired vision; vision regained; ECHO ultrasound (May 2022) shows left v left ventricle diastolic dysfunction, Stage II. I had no prior heart condition or heart damage before the booster shot last November. At 6 months or so post-booster I am essentially disabled. Cannot perform normal living duties (home or garden). Shortness of breath, chest discomfort. I cannot sustain mental work - get fatigued and cognition is not good. PULS blood test for unstable cardiac lesions showed a 27% risk of ACS (5-yr). I am recovering some functions (smell, taste).

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: ECHO ultrasound April 2022 PULS blood tests March and May 2022
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, arthritis, electrosensitive
Andere Medikamente: Hydrochlorothiazide 12.5 mG; Wixeka (Advair)
Allergien: caynne pepper (red)
Vorherige Impfungen: -

VAERS 2280458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 22.05.2022
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Angina pectoris Arthralgia Blindness Blood test Cardiac disorder Balance disorder Chest pain Cognitive disorder Diastolic dysfunction Disorientation Dizziness Dyspnoea Dyspnoea exertional Echocardiogram abnormal Electric shock sensation Fatigue Feeding disorder Headache

Symptomtext

Woke up that night in excruciating pain, body aches, rigid muscles, swollen joints (could not form a fist). Extreme fatigue and disorientation; headache, slight fever; shortness of breath; painful chest and heart; high blood pressure, then disregulated blood pressure after that; smell and taste off; significant weight loss from 132 to 120 lbs in two weeks; could not eat; shortness of breath on exertion is still bad at 6 months post-booster. Neuropathy (shooting electric shocks). Temperature not regulated (over-heat). Cognitive impairment; dizziness and balance problems; had either a TIA or ocular migraine April 2022 when I lost vision, and impaired vision; vision regained; ECHO ultrasound (May 2022) shows left v left ventricle diastolic dysfunction, Stage II. I had no prior heart condition or heart damage before the booster shot last November. At 6 months or so post-booster I am essentially disabled. Cannot perform normal living duties (home or garden). Shortness of breath, chest discomfort. I cannot sustain mental work - get fatigued and cognition is not good. PULS blood test for unstable cardiac lesions showed a 27% risk of ACS (5-yr). I am recovering some functions (smell, taste).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: ECHO ultrasound April 2022 PULS blood tests March and May 2022
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, arthritis, electrosensitive
Andere Medikamente: Hydrochlorothiazide 12.5 mG; Wixeka (Advair)
Allergien: caynne pepper (red)
Vorherige Impfungen: -

VAERS 2271899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 09.11.2021
Beginn: 05.03.2022
Tage bis Beginn: 116,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Chest pain Echocardiogram Electrocardiogram Hypoaesthesia Magnetic resonance imaging heart Myocarditis

Symptomtext

On March 5 at 8:30 pm (4 months after my third covid vaccine), I experienced heart attack like symptoms - chest pain and numbness in my left arm down to my left hand. I went to the emergency room and admitted to the hospital later that night. I was released Tuesday night with a diagnosis of myocarditis. After tests run through cardiology and infectious disease in search of a cause all came back normal, my cardiologist concluded that the myocarditis was most likely caused by my last covid vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: During my hospital stay (3/5-3/8), I had many blood tests, ekgs, an echocardiogram, and a cardiac MRI.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2246305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MD
Alter: 37,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 19.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Eczema Pruritus Rash Skin discharge Syncope

Symptomtext

It still going on. It started a couple days after the booster and progressively got worse. I kind of ignored it for a while but I started to get these little bumps all over my arms and legs. The ones on my legs progressively got worse and worse and they started leaking and got very very itchy. I tried over the counter cream and it didn't work. On 12/13/2021, I went to urgent care and they said it looked like a rash. They gave me prednisone. I took it for a couple days and that put me in the ER due to an adverse side event from it. In that time I've seen a dermatologist, rheumatologist, ENT specialist and this week I started fainting so I now have an appointment with a neurologist. The dermatologist said that I basically have eczema now which I have never had before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Blood work
Aktuelle Erkrankungen: No
Vorgeschichte: Acid Reflux, HSV II, HPV
Andere Medikamente: Lansoprazole, Birth control, Flonase, Procerv HP- Thera Logix
Allergien: Prednisone
Vorherige Impfungen: -

VAERS 2225981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: SC
Alter: 38,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test abnormal Chest pain Computerised tomogram normal Dyspnoea Electrocardiogram normal Influenza Loss of consciousness Palpitations Ultrasound scan normal White blood cell count increased

Symptomtext

I got flu symptoms after the vaccine. Then, my start heart started racing and then I passed out. Then, I started having chest pain. I went to an ER about this. They did an EKG, normal results. They did blood work, showed evaluated WBC. The CT scan to make sure there was not blood clot, normal results. They did an ultra sound of the heart, normal results. I then followed up with my doctor. They was worried about my SOB and my evaluated heart rate. They started me on some medicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG; Blood work; CT scan; Ultrasound.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin; Latex; Wellbutrin.
Vorherige Impfungen: -

VAERS 2194322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Cold sweat Concussion Feeling of body temperature change Head injury Headache Hyperhidrosis Interchange of vaccine products Joint injury Ligament sprain Loss of consciousness Magnetic resonance imaging head abnormal Pain X-ray abnormal

Symptomtext

The day after receiving my vaccines I was hot and cold with some body aches. I went to the restroom and passed out. I hit my head and twisted my ankle. I went to the ER department and they stated my ankle was sprung and I had a concussion. They did not give me any treatment but did advised me the reaction was from the vaccine. My ankle was sore for a few weeks, my head was sore for only 24 hours, and hot and cold sweats went on for about 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: X-ray of the ankle; MRI of the brain.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bipolar disorder; Obesity; Migraines
Andere Medikamente: Escitalopram; Lamictal; Risperdal; Buspar; Multivitamins; Actigall
Allergien: Minocycline
Vorherige Impfungen: Covid-19 Moderna-Shaking, shivering, and body aches.

VAERS 2162861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: IN
Alter: 77,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 16.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Borrelia test negative Choking Computerised tomogram head normal Computerised tomogram neck Dysphagia Facial paralysis Fatigue Feeding disorder Hemiparesis Laboratory test normal Magnetic resonance imaging head normal Magnetic resonance imaging spinal normal Mobility decreased Muscular weakness Neurological symptom Scan with contrast normal Throat clearing

Symptomtext

Patient received a Pfizer Covid booster on 12/19/21. She had received a two dose Moderna vaccine prior, so this was her 3rd covid vaccine but the 1st Pfizer shot. Symptoms were visible to family members around 12/25/21, however may have started earlier. Symptoms started as neurological in nature (mimicking stroke symptoms) weakness in hands especially the left hand, overall body weakness and fatigue, trouble seeing, trouble swallowing and clearing throat. By 2/14/22, her symptoms continued to become more extreme in nature when she returned to the doctor's office. Her left arm had lost almost 100% function, her left side weakness had increased leaving her unable to get up by herself, her right eye was drooping, her throat and swallowing disfunction was causing her to choke even on water and she was unable to eat solid food. She went to her primary care, who then sent her to the neurologist and they ran an initial CT thinking she had a full stroke. After CT, MRI with and without contrast, and extensive medical testing there was no evidence of stroke found and no other underlying diseases that would cause these symptoms other than the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 11,0
Labordaten: CT of head. CT of neck. MRI of head, spine and back. Blood work to rule out autoimmune conditions such as MS, MG, and lyme disease. Tests to rule out cancer.
Aktuelle Erkrankungen: None.
Vorgeschichte: Slight high blood pressure managed by medications.
Andere Medikamente: lisinopril 10mg amlodipine 5 mg hydrochlorot 12.5 mg baby aspirin 81 mg (although this was advised to stop at the same 12/16/21 appointment)
Allergien: None
Vorherige Impfungen: -

VAERS 2123001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MI
Alter: 93,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 12.01.2021
Beginn: 06.01.2022
Tage bis Beginn: 359,0
Dosis: 4
Route/Site: IM / -

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

Aggression Blood creatinine increased Blood culture Blood gases Blood pH decreased Brain natriuretic peptide increased C-reactive protein COVID-19 COVID-19 pneumonia Chest X-ray abnormal Condition aggravated Cough Dyspnoea Electrocardiogram ST segment depression Electrocardiogram abnormal Extra dose administered Fatigue Haemoglobin decreased

Symptomtext

Pt to ED for respiratory distress and cough. Oxygen saturation on room air was less than 50%, improving to 81% on 12 L of non-rebreather and 100% on 15 L non-rebreather. In severe respiratory distress with rhonchi and had some peripheral edema. Labs showed a creatinine of 1.25. WBC count of 19.0, hemoglobin 9.1. ABG showed a pH of 7.28, PO2 264. BNP level was 406. Chest x-ray showed pleural and parenchymal opacity in the right lung base suggesting a combination of a small pleural effusion and right lower lobe infiltrate. A 12-lead EKG was reviewed showing sinus tachycardia with diffuse ST-segment depressions. Admitted for management of pneumonia COVID + 1/6/21. Found to have troponin elevation. Discharged.

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Praegender Schweregrund: Respiratory distress
Hospital-Tage: 12,0
Labordaten: see above
Aktuelle Erkrankungen: 2/21/21 to 3/31/21 ED for increasing SOB associated with 2 cough and fatigue. Evaluation in the emergency room included a COVID screen which was negative. A subsequent chest x-ray revealed chronic parenchymal changes and she was noted to have chronic nonhealing ulcer of the heel, which was suspected to have osteomyelitis. So, she was admitted for further care and Infectious Disease and Podiatry were consulted. She was placed on broad-spectrum antibiotic therapy. Subsequently, Podiatry evaluated the patient and find no evidence of osteomyelitis and they recommended continuing wound care and obtained blood cultures, sedimentation rate and CRP to evaluate further. Infectious Disease also evaluated the patient. Subsequent imaging failed to reveal any signs of osteomyelitis and she was symptomatically treated. During the course of the hospitalization, she also was seen to have aggressive behavior as part of her vascular dementia, which were treated with initiation of risperidone. she was discharged home via ambulance.
Vorgeschichte: Acute encephalopathy,Bilateral pneumonia Chest pain,CVA (cerebral vascular accident); Essential hypertension Hypokalemia Hypomagnesemia Hypoxia Ischemic cardiomyopathy Normochromic normocytic anemia Obesity (BMI 30-39.9) Osteomyelitis Sepsis SIRS (systemic inflammatory response syndrome) UTI (urinary tract infection)
Andere Medikamente: amLODIPine (NORVASC) , atorvastatin (LIPITOR); Cholecalciferol (VITAMIN D-1000 MAX ST PO) ferrous sulfate 325 (65 Fe) MG PO Tab furosemide (LASIX) 20 MG PO Tab lisinopril (PRINIVIL, ZESTRIL) 10 MG PO Tab magnesium oxide (MAG-OXIDE) 400 MG P
Allergien: No
Vorherige Impfungen: -

VAERS 2105068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 01.12.2021
Beginn: 23.01.2022
Tage bis Beginn: 53,0
Dosis: 3
Route/Site: - / -

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

Back pain Blood test abnormal Chest pain Thrombosis

Symptomtext

Blood clot in arm, severe back pain that spreads to chest area, blood work shows high inflammation markers, has been referred to see a rheumatologist.

Weitere VAERSDATA-Felder

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

VAERS 2098507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 01.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

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

Dysarthria Facial paralysis General physical health deterioration Inflammation Lumbar puncture Magnetic resonance imaging

Symptomtext

On day 6, 12/7/21, client said face was slightly drooping. Called hospital, advised to come in. ER told client she may have Bells Palsy. Client was admitted to hospital for ten days. Client states she had two MRI's and two lumbar punctures. Client was told she had inflammation. During the time in the hospital, her condition worsened to slurred speech and right sided face droop.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 10,0
Labordaten: unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Cancer survivor, rheumatic fever at 5 y/o
Andere Medikamente: -
Allergien: Sulfa allergy, food sensitivity to tomatoes and lemons
Vorherige Impfungen: -

VAERS 2092835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: PA
Alter: 34,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 14.12.2021
Beginn: 21.01.2022
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy Blood test Condition aggravated Eyelid ptosis Facial paralysis Magnetic resonance imaging

Symptomtext

Bell's Palsy/facial paralysis on left side had occurred approximately 1.5 months after second Pfizer-BioNTech COVID19 vaccine. Facial movement was recovering from full paralysis to nearly full movement in left half of face prior to date of adverse event (~1.5 months after "booster"/third Pfizer-BioNTech COVID19 vaccine). Patient experienced degradation of facial movement, notably the eye/eyebrow area became much less mobile, and left eye droop. The Bell's Palsy seemed to "relapse" in some areas that were previously recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Blood test, MRI conducted on Feb 2. Inconclusive results.
Aktuelle Erkrankungen: Recovering from Bell's Palsy
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: 05/03/2021, COVID19 Vaccine, Pfizer-BioNTech

VAERS 2074687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NJ
Alter: 28,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Hyperhidrosis Pain in extremity Syncope

Symptomtext

5 minutes after shots: vasovagal syncope. Laid down, felt better after 10 minutes. ~12 hours after shots: chills, sweating (resolved on its own after a couple of hours) for a few days after shots: sore arms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroidism, Anxiety, Depression, Eating disorder
Andere Medikamente: Levothyroxine, 0.50 mg Venlafaxine, 187.5 mg Natazia
Allergien: No
Vorherige Impfungen: sore arm(s)

VAERS 2038358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 09.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / RA

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

Deep vein thrombosis Dyspnoea Erythema Gait disturbance Peripheral swelling Laboratory test Pulmonary thrombosis SARS-CoV-2 test Sensory loss Tenderness Walking aid user

Symptomtext

Deep vein thrombosis; Blood clotting throughout lungs; my shot arm starring swelling, red and tender with in a week; my shot arm starring swelling, red and tender with in a week; my shot arm starring swelling, red and tender with in a week; I could not catch my breath; stumbled walking down the hall way/I have no felling in my right leg can not walk without a walker; I have no felling in my right leg can not walk without a walker.; I have no felling in my right leg can not walk without a walker.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 09Nov2021 10:15 (Lot number: FH8030) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Known allergies was reported as none. There were no concomitant medications. Other vaccine in four weeks was reported as no. Covid prior vaccination was reported as no. Covid tested post vaccination was reported as yes. Vaccination history included: Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: ER8734,, Previous dose lot unknown: False,, Previous dose administration date: 09Apr2021, Previous dose number: 2, Previous dose Vaccine location: Right arm), administration date: 09Apr2021, when the patient was 64 years old, for Covid-19 immunization; Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: ER8727,, Previous dose lot unknown: False,, Previous dose administration date: 10Mar2021, Previous dose administration time: 10:30 AM, Previous dose number: 1, Previous dose Vaccine location: Right arm), administration date: 10Mar2021, when the patient was 64 years old, for Covid-19 immunization. The following information was reported: DEEP VEIN THROMBOSIS (hospitalization, medically significant) with onset 12Nov2021 06:15, outcome "recovering", described as "Deep vein thrombosis"; PULMONARY THROMBOSIS (hospitalization, medically significant) with onset 12Nov2021 06:15, outcome "recovering", described as "Blood clotting throughout lungs"; PERIPHERAL SWELLING (hospitalization), ERYTHEMA (hospitalization), TENDERNESS (hospitalization) all with onset 12Nov2021 06:15, outcome "recovering" and all described as "my shot arm starring swelling, red and tender with in a week"; DYSPNOEA (hospitalization) with onset 12Nov2021 06:15, outcome "recovering", described as "I could not catch my breath"; GAIT DISTURBANCE (hospitalization) with onset 12Nov2021 06:15, outcome "recovering", described as "stumbled walking down the hall way/I have no felling in my right leg can not walk without a walker"; SENSORY LOSS (hospitalization), WALKING AID USER (hospitalization) all with onset 12Nov2021 06:15, outcome "recovering" and all described as "I have no felling in my right leg can not walk without a walker.". The patient was hospitalized for deep vein thrombosis, pulmonary thrombosis, peripheral swelling, erythema, tenderness, dyspnoea, gait disturbance, sensory loss, walking aid user (hospitalization duration: 42 day(s)). The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (03Jan2022) negative, notes: Other. Therapeutic measures were taken as a result of deep vein thrombosis, pulmonary thrombosis, peripheral swelling, erythema, tenderness, dyspnoea, gait disturbance, sensory loss, walking aid user. It was reported that Deep vein thrombosis, Blood clotting throughout lungs. just a few days after receiving the booster her shot arm starring swelling, red and tender with in a week her husband called 911 because she could not catch her breath and stumbled walking down the hall way with in the next week he took her to the hospital. she been in 3 hospitals in the last 42 days. prior to this she was on no medicine no doctors care able to walk talk and enjoy life now she have no felling in her right leg can not walk without a walker. she hope she get better. blood clot and operation for deep vein thrombosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 42,0
Labordaten: Test Date: 20220103; Test Name: prc covid test; Test Result: Negative ; Comments: Other
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2038358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 09.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

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

Deep vein thrombosis Dyspnoea Erythema Gait disturbance Peripheral swelling Laboratory test Pulmonary thrombosis SARS-CoV-2 test Sensory loss Tenderness Walking aid user

Symptomtext

Deep vein thrombosis; Blood clotting throughout lungs; my shot arm starring swelling, red and tender with in a week; my shot arm starring swelling, red and tender with in a week; my shot arm starring swelling, red and tender with in a week; I could not catch my breath; stumbled walking down the hall way/I have no felling in my right leg can not walk without a walker; I have no felling in my right leg can not walk without a walker.; I have no felling in my right leg can not walk without a walker.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 09Nov2021 10:15 (Lot number: FH8030) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Known allergies was reported as none. There were no concomitant medications. Other vaccine in four weeks was reported as no. Covid prior vaccination was reported as no. Covid tested post vaccination was reported as yes. Vaccination history included: Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: ER8734,, Previous dose lot unknown: False,, Previous dose administration date: 09Apr2021, Previous dose number: 2, Previous dose Vaccine location: Right arm), administration date: 09Apr2021, when the patient was 64 years old, for Covid-19 immunization; Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: ER8727,, Previous dose lot unknown: False,, Previous dose administration date: 10Mar2021, Previous dose administration time: 10:30 AM, Previous dose number: 1, Previous dose Vaccine location: Right arm), administration date: 10Mar2021, when the patient was 64 years old, for Covid-19 immunization. The following information was reported: DEEP VEIN THROMBOSIS (hospitalization, medically significant) with onset 12Nov2021 06:15, outcome "recovering", described as "Deep vein thrombosis"; PULMONARY THROMBOSIS (hospitalization, medically significant) with onset 12Nov2021 06:15, outcome "recovering", described as "Blood clotting throughout lungs"; PERIPHERAL SWELLING (hospitalization), ERYTHEMA (hospitalization), TENDERNESS (hospitalization) all with onset 12Nov2021 06:15, outcome "recovering" and all described as "my shot arm starring swelling, red and tender with in a week"; DYSPNOEA (hospitalization) with onset 12Nov2021 06:15, outcome "recovering", described as "I could not catch my breath"; GAIT DISTURBANCE (hospitalization) with onset 12Nov2021 06:15, outcome "recovering", described as "stumbled walking down the hall way/I have no felling in my right leg can not walk without a walker"; SENSORY LOSS (hospitalization), WALKING AID USER (hospitalization) all with onset 12Nov2021 06:15, outcome "recovering" and all described as "I have no felling in my right leg can not walk without a walker.". The patient was hospitalized for deep vein thrombosis, pulmonary thrombosis, peripheral swelling, erythema, tenderness, dyspnoea, gait disturbance, sensory loss, walking aid user (hospitalization duration: 42 day(s)). The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (03Jan2022) negative, notes: Other. Therapeutic measures were taken as a result of deep vein thrombosis, pulmonary thrombosis, peripheral swelling, erythema, tenderness, dyspnoea, gait disturbance, sensory loss, walking aid user. It was reported that Deep vein thrombosis, Blood clotting throughout lungs. just a few days after receiving the booster her shot arm starring swelling, red and tender with in a week her husband called 911 because she could not catch her breath and stumbled walking down the hall way with in the next week he took her to the hospital. she been in 3 hospitals in the last 42 days. prior to this she was on no medicine no doctors care able to walk talk and enjoy life now she have no felling in her right leg can not walk without a walker. she hope she get better. blood clot and operation for deep vein thrombosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 42,0
Labordaten: Test Date: 20220103; Test Name: prc covid test; Test Result: Negative ; Comments: Other
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2058899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 20.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Nausea Syncope

Symptomtext

~12 hours after administration patient woke up from sleeping, felt dizzy/nauseous, then fainted. They then waited until symptoms passed, and then went back to bed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Moderna, Nauseous/dizzy; no fainting

VAERS 2047730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MO
Alter: 81,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 18.12.2021
Beginn: 16.01.2022
Tage bis Beginn: 29,0
Dosis: UNK
Route/Site: IM / -

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

Angiogram cerebral Bell's palsy Magnetic resonance imaging

Symptomtext

1 mo later admitted with Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 2,0
Labordaten: MRI MRA ruled out CVA
Aktuelle Erkrankungen: none
Vorgeschichte: DM 2 with CKD
Andere Medikamente: ? amLODIPine (NORVASC) 10 mg tablet TAKE ONE TABLET BY MOUTH DAILY ? Aspirin 81 mg Tab Take 1 tablet by mouth daily. ? atorvastatin (LIPITOR) 80 mg tablet TAKE ONE TABLET BY MOUTH DAILY ? blood sugar diagnostic (ONETOUCH ULTRA TEST) test st
Allergien: bactrim and ciprofloxacin
Vorherige Impfungen: -

VAERS 2035060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MS
Alter: 53,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 08.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy Blood test Cellulitis Compression garment application Contusion Deep vein thrombosis Differential white blood cell count Full blood count Inflammation Injection site bruising Pallor Peripheral swelling Tenderness Ultrasound Doppler abnormal Vein disorder

Symptomtext

Swelling of the left arm, pale skin color, bruising on are and injection site Inflamed veins in left chest, breast, and under arm tenderness Went to the PA on 12/22/2021, blood work and was treated for cellulitis Returned to doctor on 12/28/21 after symptoms worsened and was sent to hospital for tests and was treated for blood clot (DVT) Prescribed Eliquis blood thinner, two weeks of medication and will continue for three months Wearing a compression sleeve on left arm Follow up and recheck for clot around mid-march

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: CBC w/differential Venous Duplex Exam
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity
Andere Medikamente: Zyrtec, 10mg/day at night Vitamin D3, 1,000 IU/day at night
Allergien: Allergies below are usually found in cosmetic and hair products: Formaldehyde Methylchloroisothiazolinone-Methylisothiazolinone Methyldibromo Glutaronitrile Methylisothiazolinone P-Phenylenediamine Propylene Glycol Quaternium-15
Vorherige Impfungen: -

VAERS 2034515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Menstruation delayed Thrombosis

Symptomtext

More clots noted; Menstrual period was eight days late.; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 23 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left (Lot number: Flg1611) as dose 2, single and administered in arm left (Lot number: FH8030) as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: THROMBOSIS (medically significant), outcome "unknown", described as "More clots noted"; MENSTRUATION DELAYED (non-serious), outcome "unknown", described as "Menstrual period was eight days late.". Therapeutic measures were not taken as a result of thrombosis, menstruation delayed. Clinical course: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not have any other medications received within 2 weeks of vaccination. The patient was not diagnosed with COVID-19 prior vaccination and the patient had not been tested for COVID-19 since the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2034497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 45,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 06.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Asthenia Bell's palsy Hypoaesthesia Paraesthesia

Symptomtext

diagnosed with Bell's Palsy; Extreme pain in my right elbow; loss of strength; Numbing and tingling in my left arm; Numbing and tingling in my left arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 06Nov2021 (Lot number: FH8030) at the age of 45 years as dose 1, single and administered in arm right, administration date 01Dec2021 (Lot number: FY8762) as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: BELL'S PALSY (medically significant) with onset 31Dec2021, outcome "recovered with sequelae", described as "diagnosed with Bell's Palsy"; ARTHRALGIA (non-serious) with onset 11Nov2021, outcome "recovered with sequelae", described as "Extreme pain in my right elbow"; ASTHENIA (non-serious) with onset 11Nov2021, outcome "recovered with sequelae", described as "loss of strength"; HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 11Nov2021, outcome "recovered with sequelae" and all described as "Numbing and tingling in my left arm". The events "diagnosed with bell's palsy", "extreme pain in my right elbow", "loss of strength", "numbing and tingling in my left arm" and "numbing and tingling in my left arm" were evaluated at the physician office visit. The patient did not receive any other vaccines within four weeks prior to the vaccination. covid prior vaccination was no. covid tested post vaccination was no. The patient did not have any known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2027663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Product administered to patient of inappropriate age Syncope

Symptomtext

fainted; patient received a vaccine that was from the purple cap formula for the COVID-19 vaccine (approved for 12-years and older); This is a spontaneous report received from a contactable consumer from Medical information team. The reporter is the parent. A 6 year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number: FH8030) 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: SYNCOPE (medically significant), outcome "unknown", described as "fainted"; PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), outcome "unknown", described as "patient received a vaccine that was from the purple cap formula for the COVID-19 vaccine (approved for 12-years and older)". Additional information: The patient fainted at the pharmacy after the injection The patient had her 2nd dose. When the patient received her 2nd dose the pharmacy staff looked at the first dose lot number and told that this was an adult dose, not the 5-11 orange cap formula. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1997206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MA
Alter: 38,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 14.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Angiogram Arrhythmia Chest X-ray Chest pain Computerised tomogram thorax Dyspnoea Dyspnoea exertional Echocardiogram Electrocardiogram Electrocardiogram ambulatory Heart rate irregular Pulmonary function test Syncope

Symptomtext

AFTER TWO DAYS, I STARTED HAVING CHEST PAIN, SHORTNESS OF BREATH, SEVERE DYSPNEA ON EXERTION, IRREGULAR HEART RATES, HEART ARRYTHMIAS AND SYNCOPE. I WENT TO THE EMERGENCY ROOM ON 11/24. I HAD EKGS, CTA OF CHEST, CHEST XRAY AND CARDIAC/BLOOD PRESSURE MONITORING . I FOLLOWED UP WITH MY PCP. FOLLOWED UP WITH CARDIOLOGIST AND HAD ECHOCARDIOGRAM, CT OF CHEST, PULMONARY FUNCTION TESTS AND A 24 HOUR HOLTER MONITOR. FOLLOWED UP WITH PULMONOLOGIST AND WILL HAVING REPEAT CATSCAN WITHIN THREE MONTHS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG- 11/24/21; CTA OF CHEST- 11/24/21, CHEST XRAY 11/24/21, 24 HOUR HOLTER MONITOR 12/7/21, ECHOCARDIOGRAM 12/15/21, CT OF CHEST 12/21/21, PULMONARY FUNCTION TESTS 12/21/21.
Aktuelle Erkrankungen: NONE
Vorgeschichte: SEIZURES, NARCOLEPSY, DEPRESSION
Andere Medikamente: LAMOTRIGINE, CYMBALTA, ADDERALL
Allergien: NONE
Vorherige Impfungen: -

VAERS 1989481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: FL
Alter: 81,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Loss of consciousness Speech disorder

Symptomtext

PT HUSBAND REPORTS "COMATOSE-LIKE" STATE - EYES CLOSED, NON-VERBAL

Weitere VAERSDATA-Felder

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

VAERS 1984141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8030

schwer

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 19.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: - / RA

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

Bell's palsy

Symptomtext

Diagnosed with bells palsy.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32 year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm right, administration date 19Nov2021 16:00 (Lot number: FH 8030) at the age of 31 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Anemia" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FH8020, Location of injection: Arm Right, Vaccine Administration Time: 04:00 PM), administration date: 29Oct2021, when the patient was 31 years old, for COVID-19 immunization. The following information was reported: BELL'S PALSY (medically significant) with onset 07Dec2021, outcome "recovering", described as "Diagnosed with bells palsy.". The event "diagnosed with bells palsy." was evaluated at the emergency room visit. Therapeutic measures were taken as a result of bell's palsy (Steriod and antiviral). 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 has not been tested for COVID-19

Weitere VAERSDATA-Felder

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

VAERS 1981883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Guillain-Barre syndrome Hypoaesthesia Laboratory test abnormal Muscular weakness Pain Paraesthesia

Symptomtext

Numbness, tingling and weakness of my lower extremities. Legs feel as if they will give out. Severe throbbing/pulsating sensation. Symptoms worsened after second dose on 11/26/2021 tingling and weakness moved up towards my hands and upper body. Diagnosed with Guillain Barre Syndrome on 12/15/2021 and currently receiving 30 grams of IVIG daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Labs 12/10/21 12/15/2021 Diagnosed with GBS
Aktuelle Erkrankungen: Thrombocytosis
Vorgeschichte: Thrombocytosis
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1974323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Immunisation Pericarditis

Symptomtext

pericarditis/ Tightness/heaviness in chest/ shallow breathing; booster; This is a spontaneous report received from a non-contactable reporter (Consumer). The reporter is the patient. A 65-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 06Dec2021 12:00 (Lot number: FH8030) at the age of 65 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Sjogren's syndrome" (unspecified if ongoing). The patient had not had COVID-19 and she was not diagnosed with COVID-19 prior vaccination. There were no concomitant medications received within two weeks of vaccination. Past drug history included: Amoxicillin, reaction: "Allergy", notes: Known allergies: Amoxicillin. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8734, Location of injection: Arm Left, Vaccine Administration Time: 12:30 PM), administration date: 03Apr2021, when the patient was 64 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6204, Location of injection: Arm Left, Vaccine Administration Time: 12:30 PM), administration date: 13Mar2021, when the patient was 64 years old, for COVID-19 Immunization. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The following information was reported: IMMUNISATION (medically significant) with onset 06Dec2021 12:00, outcome "unknown", described as "booster"; PERICARDITIS (medically significant) with onset 09Dec2021 02:00, outcome "recovering", described as "pericarditis/ Tightness/heaviness in chest/ shallow breathing". The event "pericarditis/ tightness/heaviness in chest/ shallow breathing" was evaluated at the physician office visit. Therapeutic measures were taken as a result of pericarditis and included prescription of indomethacin and colchicine. The patient had not been tested for COVID-19 since the vaccination. Clinical course: Tightness/heaviness in chest; shallow breathing. Diagnosed as pericarditis. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sjogren's syndrome
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1970955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: NM
Alter: 37,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Chills Confusional state Dyspnoea Fatigue Flushing Heart rate increased Hyperhidrosis Hypotension Lethargy Syncope Unresponsive to stimuli

Symptomtext

Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Chills-Severe, Systemic: Confusion-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Severe, Additional Details: After 15 minutes patient began to sweat profusely and began to come in and out of consiousness, blood pressure was very, pulse was elevated

Weitere VAERSDATA-Felder

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

VAERS 1970692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: -
Alter: -
Geschlecht: U
Eingang: 22.12.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Chills Immunisation Presyncope

Symptomtext

3rd dose; presyncopal episode along with 36hr of chills; presyncopal episode along with 36hr of chills; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administration date 10Nov2021 (Lot number: fh8030) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU VACCINE VII, administration date 20Oct2021. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: fh1950), administration date: 22Apr2021, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: er2613), administration date: 01Apr2021, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 10Nov2021, outcome "unknown", described as "3rd dose"; PRESYNCOPE (non-serious), CHILLS (non-serious) all with onset 2021, outcome "unknown" and all described as "presyncopal episode along with 36hr of chills". Therapeutic measures were not taken as a result of presyncope, chills. Additional information: Patient took the other vaccine in four weeks. Patient did not have covid prior to vaccination. Patient did not tested covid positive post vaccination. Facility type was Public Health Clinic. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1963303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NC
Alter: 51,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 28.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

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

Adverse event Amenorrhoea Blepharospasm Breast scan abnormal Cardiac disorder Inguinal mass Mammogram normal Menstrual disorder Menstruation irregular Pericarditis Ultrasound breast normal

Symptomtext

Four adverse events: 1.) Menstrual cycle started (11/1/21) one week early after first shot and then ceased after the second shot. My menstrual cycle was normal up until I had my first covid vaccination shot. 2.) Heart feels abnormal, labored on daily basis since covid vaccine, more so after second shot. Annual Breast Thermascan on 11/12/21 showed inflammation near heart. With abnormal breast thermascan, referred by gynecologist for diagnostic mammogram and breast ultrasound which was performed on 12/14/21 and indicated no breast cancer. Appointment made with Cardiologist which is delayed due to doctor availability until 1/20/22. 3.) Right upper eyelid spasms/twitches periodically. 4.) Small mass in right groin/upper inner thigh area that may be a blood clot just under skin. Need to schedule dermatologist appointment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: diagnostic mammogram and breast ultrasound which was performed on 12/14/21 expect additional tests to be done during Cardiologist appointment in January
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vit D, Vit C, Vit B, Magnesium, zinc
Allergien: None
Vorherige Impfungen: -

VAERS 1962991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NJ
Alter: 18,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 24.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 8,0
Dosis: UNK
Route/Site: - / -

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

C-reactive protein Electrocardiogram Enterovirus test positive Full blood count Human rhinovirus test positive Influenza A virus test positive Metabolic function test Respiratory viral panel Syncope

Symptomtext

About 1 week after the covid 19 vaccine, he had 4 episodes of syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 12/3/21 ER EKG Respiretory viral panel- possitive influenza A CBC CRP CMP positive rhinovirus/enterovirus
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1959164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: FL
Alter: 24,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Confusional state Dizziness Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Hypotension-Mild, Additional Details: Patient almost passed out after getting Covid vaccine and Boostrix, emergency number was called. EMS reviewed and patient was ok to go after about 40mins

Weitere VAERSDATA-Felder

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

VAERS 1959103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: FL
Alter: 33,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Additional Details: Pt had an episode of syncope and fell after vaccine administration, 911 was called to evaluate the fall. pt was good and left feeling fine.

Weitere VAERSDATA-Felder

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

VAERS 1955842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NY
Alter: 37,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered Fall Syncope

Symptomtext

Patient received booster dose of Pfizer Covid 19 vaccine. He fell from his seat while at his 15 minute observation. He had a syncope episode which lasted less than 2 minutes. VS WNL. RRT arrived in 3 minutes of being called. Patient was assessed by MD. Patient declined to go to the ER for further evaluation. He remained in the clinic for another 30 minutes and was escorted to his ride home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Patient declined to go to the ER for further evaluation.
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: Denies any
Allergien: Denies any
Vorherige Impfungen: -

VAERS 1952302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NY
Alter: 21,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram Fall Loss of consciousness Syncope

Symptomtext

patient had a syncope episode 8 minutes after taking the 1st dose of Pfizer covid 19 vaccine. He fell from his chair while seated in the observation area. He passed out for less than two minutes and regained mild consciousness. he was aware of his environment. His vitals were stable. RRT was called while vitals were being taken. RRT arrived within 3 minutes of being called. Patient was assessed by MD ad taken to ED for further assessment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: patient was transferred to ED. CT scan was taken.
Aktuelle Erkrankungen: DENIED ANY
Vorgeschichte: DENIED ANY
Andere Medikamente: DENIED TAKING ANY MEDICATIONS
Allergien: SHRIMP
Vorherige Impfungen: -

VAERS 1948408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CO
Alter: 39,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Electric shock sensation Feeling abnormal Pain

Symptomtext

Starting when I woke up around 5:30 the morning after the shot, it felt like my skin was a giant balloon and when I breathed in, I breathed in electricity, shooting it all over my body, expanding the balloon with lightning, and threatening to break it into a million tiny pieces. I was also sore. Sore all over. Like I ran a marathon. Managed to get out of bed at noon and eat and take 800mg ibuprofen, which helped along with sleep. By 4pm have less pain and electricity, but still some soreness. It?s not as bad as after shot 2, but the same type of symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal multivitamin, rhodiola, vitamin D, ashwarganda
Allergien: Na
Vorherige Impfungen: 2nd dose of Pfizer has similar and more severe symptoms next day. More painful, more debilitating. 4/15/21 lotER8737

VAERS 1947711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: IN
Alter: 22,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 10.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Feeling hot Headache Loss of consciousness Panic reaction

Symptomtext

Pt reports she passed out at home for about 10 seconds (witnessed by boyfriend). Upon awakening, pt felt panic, scared, but was hot. After recovering from passing out, pt reports headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Seen in clinic by writer today, 12/14/2021. Pt has normal vital signs, referred to PCP for further evaluation. Discussed if passes out again, go to the ER or have someone call 911. Today, patient reports she feels much better and normal.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Birth control daily, zofran PRN.
Allergien: None.
Vorherige Impfungen: -

VAERS 1944376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: AL
Alter: 58,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 06.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / -

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

Bell's palsy Facial paralysis

Symptomtext

Bells Palsy - Right sided facial paralysis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Stroke Rule out at ER
Aktuelle Erkrankungen: Slight Upper Respiratory Symptoms
Vorgeschichte: Allergic Rhinitis; Bipolar 1 disorder; GERD; Hyperlipidemia, Mixed; Hypertension, Primary Essential; Hypothyroidism; Long term use of drug; Major Depression (Recurrent); Mitral valve prolapse; Morbid obesity; OAB (overactive bladder); OSA on CPAP; Parkinsonism, Secondary; Rhinitis, Allergic; Schizophrenia; Tremor; Type 2 diabetes mellitus with other specified complication, with long-term current use of insulin
Andere Medikamente: alendronate 70 mg tablet; Aristada 662 mg/2.4 mL intramuscular suspension,extended rel syring; atorvastatin 40 mg tablet; benztropine 2 mg oral tablet; ezetimibe oral tablet 10 mg; fluphenazine HCl 1 mg oral tablet; fluticasone propionate 5
Allergien: Adhesive Tape; Staticin; SULFA (SULFONAMIDES)
Vorherige Impfungen: -

VAERS 1929097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MO
Alter: 30,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Seizure

Symptomtext

PATIENT HAD SEIZURE ACTIVITY LASTING APPROXIMATELY 20 MINUTES WITH TWO DIFFERENT EPISODES OF SEIZURES WITHIN THAT TIME FRAME LASTING APPROXIMATELY 5 MINUTES

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: SEIZURES
Vorgeschichte: SEIZURES
Andere Medikamente: KEPPRA 1000 MG CLOBAZAM 20 MG VIMPAT 200 MG
Allergien: NONE
Vorherige Impfungen: -

VAERS 1925893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NH
Alter: 32,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 10.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Dry eye Facial paralysis Feeling abnormal Hypoaesthesia Hypoaesthesia oral Pain in extremity Skin tightness

Symptomtext

At first, just the right arm pain for the rest of the day and into the next day. On Friday morning woke up and my right side of my face was droopy. Felt like I had gotten dentist work done my right side of my face was numb. I had to drink water from a straw on the other side of my mouth. when eating my tongue was number and I could only taste food around my tongue. My right eye was very dry had to keep rubbing it. Right side of my face felt so different and tight too. I also experienced a lot of brain fog too. The following week I could tell my brain was definitely not as sharp I could barely keep up with my work as I have a lot of multitasking to do.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Visited the doctors on 11/15 and on 12/6
Aktuelle Erkrankungen: -
Vorgeschichte: osteopenia, back pain from prior vehicle accident years ago
Andere Medikamente: vitamins (B, and D) anti-inflammatory type vitamin called (OPC-3), Prime Feminene (female support formula for balancing female hormones) , TLS ACTS which is a adrenal, Cortisol, Thyroid and Stress support formula, probiotics
Allergien: Betadine, minocycline, amoxicillin
Vorherige Impfungen: -

VAERS 1925224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MI
Alter: 28,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test abnormal Catheterisation cardiac Chest pain Computerised tomogram thorax Electrocardiogram Magnetic resonance imaging heart Myocarditis Pain in extremity Pyrexia Sleep disorder Troponin increased

Symptomtext

Chest pains that woke me up on during a weekend night (either Saturday or Sunday). Pain went away about an hour later. Occasional chest pains continued. Went to ER on Tuesday, and was admitted. Primary diagnosis was acute myocarditis. Also had a fever (around 101 degrees, but varied) for 2 days following the vaccine, but no fever after those 2 days. I also had arm soreness for about 2 days following the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: ECG (2x); Cardiac Catheterization; Chest CT; Various Blood Tests (troponin levels were high) all occurred on 11/30/2021. Cardiac MRI occurred on 12/1/2021.
Aktuelle Erkrankungen: Meniscectomy at the end of October 2021.
Vorgeschichte: Childhood asthma; potential high-blood pressure (no medications at the time, but identified as a possible problem during my physical in summer 2021); obesity.
Andere Medikamente: Occasionally a one-a-day vitamin.
Allergien: Azithromycin (as a kid, not confirmed as an adult).
Vorherige Impfungen: No Serious Adverse Events. With second dose of Pfizer COVID-19 vaccine, I had a fever (102 degrees) for one day following the va

VAERS 1924999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MA
Alter: 72,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 11.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Diplopia VIth nerve paralysis Visual impairment

Symptomtext

Systemic: 6th Cranial Palsy-Severe, Systemic: Visual Changes/Disturbances-Severe, Additional Details: Double vision starting 11/14/21 and progressively worsened 11/15/21 and 11/16/21. Diagnosed with 6th cranial palsy on 11/15/21.

Weitere VAERSDATA-Felder

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

VAERS 1921154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

Ear discomfort Feeling hot Flushing Headache Hyperhidrosis Loss of consciousness Tinnitus

Symptomtext

Woke up morning after vaccination went to use bathroom and start usual routine. Suddenly felt very hot, flush, and sweaty (while sitting bathroom). Decided to go lay down in bed again. Passed out walking back to bed. Recovered within a few minutes, but with headache persisting throughout day. Day 2 post, woke up with fullness in left ear (same side as shot) and mild tinnitus. Headache was still present but alleviated with analgesic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid, Liothyronine, Duloxetine, Magnesium Complex, Zyrtec, Pepsid
Allergien: NKA
Vorherige Impfungen: -

VAERS 1920266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: FL
Alter: 23,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anaphylactic reaction Pruritus

Symptomtext

itching, anaphlaxis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthm,anemia
Andere Medikamente: -
Allergien: flu vaccine, contrast dye from shellfish, orisella, penicillin
Vorherige Impfungen: influenza

VAERS 1919628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: IL
Alter: 50,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dizziness Electric shock sensation Heavy menstrual bleeding Lymphadenopathy Nausea

Symptomtext

Menstrual bleeding; large golf ball size swollen gland under left arm; dizziness; nausea; electric shock feeling in head.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Nov2021 15:30 (Lot number: FH8030) at the age of 50 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: HEAVY MENSTRUAL BLEEDING (non-serious) with onset 06Nov2021 23:00, outcome "not recovered", described as "Menstrual bleeding"; LYMPHADENOPATHY (non-serious) with onset 06Nov2021 23:00, outcome "not recovered", described as "large golf ball size swollen gland under left arm"; DIZZINESS (non-serious) with onset 06Nov2021 23:00, outcome "not recovered", described as "dizziness"; NAUSEA (non-serious) with onset 06Nov2021 23:00, outcome "not recovered", described as "nausea"; ELECTRIC SHOCK SENSATION (non-serious) with onset 06Nov2021 23:00, outcome "not recovered", described as "electric shock feeling in head.". Therapeutic measures were not taken as a result of heavy menstrual bleeding, lymphadenopathy, dizziness, nausea, electric shock sensation. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. Post the vaccination, the patient has not been tested for COVID-19. Known allergy was reported as none. Patient did not receive any other medication within 2 weeks of vaccination. It was unknown if the patient received any other vaccine in four weeks. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
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 1917197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

After 10-13 minutes, patient began walking towards the front of the store. Mother reports that patient fainted in the aisle. Mom caught patient to and prevents her from hitting her head. Mom escorted patient back to the pharmacy area where sh remained seated and monitored for an additional 15 minutes. Patient was given water and her blood pressure was later taken and found to be within normal range. When she was feeling well, patient left with her mother.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Blood pressure within normal range
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: Not Known
Allergien: No known allergy
Vorherige Impfungen: -

VAERS 1915842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Eye movement disorder Syncope Tremor

Symptomtext

Pt experience vasovagal syncope. Seconds after recieving the vaccine, the patient fainted, her eyes rolled back and she closed her eyes, tilted her head back, and started shaking. i assisted her to the floor so she can lay flat on the floor and she recovered consciousness. I remained with the patient for an additional 15 minutes. the patient stated she was feeling better and i assisted her to a chair where she sat for an additional 5 minutes. I assisted the patient to the car and followed up with them 30 minutes later over the phone to make sure they were feeling fine.

Weitere VAERSDATA-Felder

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

VAERS 1910049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: IL
Alter: 25,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Blood glucose increased Confusional state Eye movement disorder Hyperhidrosis Loss of consciousness Muscle twitching Nausea Skin warm

Symptomtext

Patient felt nauseated and then passed out very briefly. He seemed confused for a couple minutes and at one point looked like he might have been having a seizure. His eyes rolled and arm started twitch. It only last a few seconds. He was sweating and very warm. His blood pressure before EMTs arrived was 75/41 with a pulse of 55. EMTs came and checked him out. His blood sugar was 130. His blood pressure returned to normal after a few minutes and he started feeling better. He declined going to the hospital and the EMTs walked out with him when he was ready to go to make sure he was ok.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP 75/41 pulse 55 Blood sugar 130
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1906446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: GA
Alter: 48,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Blood test Chest pain Computerised tomogram normal Dyspnoea Electrocardiogram normal Fibrin D dimer increased Pain Pain in extremity Painful respiration Pericarditis

Symptomtext

24 hours after receiving vaccine, I began getting severe chest pain and shortness of breath. At 48 hours post vaccine, I called my PCP who advised me to go the the ER. I had pain in my arm (where the shot was given) and pain in my chest on the left side. It radiated to my back. It hurt to take a breath in. At the ER, I was put on the EKG machine, blood word done, chest xray. My d-dimmer was 660. That was the only number that was not within normal limits. They did a CT scan with and without contrast of my chest to look for a possible blood clot. Nothing was found. I was sent home with Naproxen and told to follow up with a cardiologist 3-5 days after. I went to the cardiologist 4 days after the ER, he diagnosed pericarditis most likely due to the covid booster vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 11/26 - tons of blood work at ER, d-dimmer, several ekg's, chest xray, ct scan with and without contrast. all negative except for the d-dimmer number was 660. 11/29 - Follow up with cardiologist who diagnosed pericarditis most likely due to covid vaccine.
Aktuelle Erkrankungen: None
Vorgeschichte: diabetes
Andere Medikamente: Metformin 500 mg 2x day, cymbalta 120mg, trazodone 100mg, tradjenta 5mg, klonipin .5mg, incassa (birth control) 1 pill per day progesterone only.
Allergien: None
Vorherige Impfungen: -

VAERS 1903892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Flushing Hyperhidrosis Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Shakiness-Mild, Additional Details: 10 minutes after vaccination, patient began to sweat then passed out and unresponsive for about 30 seconds or so (shook a few times) & then came to with continued sweating. EMS was called who checked him out but he did refuse transport and left later on his own after about 45 to 60 minutes .

Weitere VAERSDATA-Felder

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

VAERS 1902197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: WA
Alter: 69,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Alanine aminotransferase normal Albumin globulin ratio decreased Anion gap decreased Aspartate aminotransferase normal Basophil count normal Blood albumin normal Blood alkaline phosphatase normal Blood bicarbonate decreased Blood bilirubin normal Blood calcium normal Blood chloride increased Blood creatine phosphokinase increased Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood urea normal Brain natriuretic peptide normal

Symptomtext

Patient received his COVID-19 mRNA vaccine #3 (booster) on 11/16/2021. The following day (11/17/2021), he noticed weakness of both legs, such that he had difficulty lifting his legs to get into his work truck. The weakness progressed over the next few days to the point that even walking was difficult, necessitating use of a walking cane. When standing, he feels a cramping discomfort in the posterior pelvis. MRI of the entire spine was performed, demonstrating multilevel degenerative disc disease. There are no imaging findings to account for his presentation. Cerebrospinal fluid shows albuminocytologic dissociation. He was seen in consultation by neurology. He has reflexes on exam, and it is felt that we are seeing him early in the course of Guillain-Barre Syndrome secondary to the COVID-19 mRNA vaccine, with progressive bilateral lower extremity weakness starting 1 day after administration. He was treated with IVIG.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 3,0
Labordaten: Results for Patient as of 11/26/2021 13:40 11/24/2021 11:51 Color: Colorless Appearance: Clear Volume received: 5 Tube counted: 2 RBC: 90 WBC: 7 PMNs: 5 Lymphs: 75 Monocytes: 20 Glucose CSF: 63 Protein CSF: 68 (H) Results for PT (MRN 1408532) as of 11/26/2021 13:40 11/23/2021 09:37 WBC: 6.16 RBC: 4.81 Hgb: 14.8 Hct: 44.8 MCV: 93.1 MCH: 30.8 MCHC: 33.0 RDW: 13.3 Plt: 219 Differential type: Automated Abs neuts: 3.61 Abs immature grans: 0.02 Abs lymphs: 1.65 Abs monos: 0.66 Abs eos: 0.17 Abs basos: 0.05 Neuts: 58.6 Immature grans: 0.3 Lymphs: 26.8 Monos: 10.7 Eos: 2.8 Basos: 0.8 NRBCs: 0.0 Abs NRBCs: 0.00 Sed rate (ESR): 11 11/24/2021 06:20 WBC: 5.39 RBC: 4.70 Hgb: 14.4 Hct: 43.2 MCV: 91.9 MCH: 30.6 MCHC: 33.3 RDW: 13.2 Plt: 213 11/25/2021 19:16 WBC: 3.38 (L) RBC: 4.34 (L) Hgb: 13.3 (L) Hct: 40.0 MCV: 92.2 MCH: 30.6 MCHC: 33.3 RDW: 13.2 Plt: 195 Differential type: Automated Abs neuts: 2.31 Abs immature grans: 0.01 Abs lymphs: 0.50 (L) Abs monos: 0.43 Abs eos: 0.09 Abs basos: 0.04 Neuts: 68.3 Immature grans: 0.3 Lymphs: 14.8 Monos: 12.7 Eos: 2.7 Basos: 1.2 NRBCs: 0.0 Abs NRBCs: 0.00 Results for PT as of 11/26/2021 13:40 11/23/2021 09:37 BNP: 23 Troponin I: <0.010 Na: 138 K: 4.4 Cl: 107 CO2: 20 (L) Anion gap w/o K: 11 BUN: 19 Creatinine: 0.78 Glucose: 117 CK: 271 (H) SGOT/AST: 25 SGPT/ALT: 19 Alk Phos: 81 Bilirubin total: 0.5 Protein: 7.9 (H) Albumin: 4.2 Globulin (calc): 3.7 A:G Ratio: 1.1 Calcium: 10.1 11/24/2021 06:20 Na: 135 K: 4.5 Cl: 107 CO2: 21 Anion gap w/o K: 7 BUN: 15 Creatinine: 0.72 Glucose: 105 Calcium: 9.4 11/25/2021 19:16 Na: 135 K: 4.6 Cl: 108 CO2: 18 (L) Anion gap w/o K: 9 BUN: 23 Creatinine: 0.99 Glucose: 114 SGOT/AST: 30 SGPT/ALT: 20 Alk Phos: 54 Bilirubin total: 0.4 Protein: 10.5 (H) Albumin: 3.3 Globulin (calc): 7.2 (H) A:G Ratio: 0.5 (L) Calcium: 8.9 O XR CHEST 1 VIEW - PA OR AP Result Date: 11/23/2021 EXAM: Chest AP one view; lumbar spine 3 views; pelvis frontal one view; left hip 2 views 11/23/2021 10:05 AM HISTORY: SOB. Weakness TECHNIQUE: Chest frontal one view; lumbar spine 3 views; pelvis frontal one view; left hip 2 views COMPARISON: None FINDINGS: Mild bilateral interstitial prominence. No focal lung opacity. No large pleural effusion or pneumothorax. Cardiomediastinal contour is unremarkable. Grade 1 retrolisthesis of L1 on L2. Grade 1 anterolisthesis of L5 on S1. Remaining lumbar alignment is within normal limits. Vertebral body heights are preserved with no evidence for acute fracture. Mild to moderate multilevel degenerative disease worse at L1 and L2 and L5-S1. Moderate to advanced facet arthropathy of the lower lumbar spine. Pelvis is intact. 2 views left hip demonstrate left total hip arthroplasty in near-anatomic alignment with no evidence for hardware failure or complications. IMPRESSION: Mild diffuse interstitial prominence, nonspecific however can be seen with mild interstitial edema and nonspecific bronchitis. No acute bony findings. ....... Providers: To speak with a radiologist. O XR LSPINE 2-3 VIEW - AP, LAT Result Date: 11/23/2021 EXAM: Chest AP one view; lumbar spine 3 views; pelvis frontal one view; left hip 2 views 11/23/2021 10:05 AM HISTORY: SOB. Weakness TECHNIQUE: Chest frontal one view; lumbar spine 3 views; pelvis frontal one view; left hip 2 views COMPARISON: None FINDINGS: Mild bilateral interstitial prominence. No focal lung opacity. No large pleural effusion or pneumothorax. Cardiomediastinal contour is unremarkable. Grade 1 retrolisthesis of L1 on L2. Grade 1 anterolisthesis of L5 on S1. Remaining lumbar alignment is within normal limits. Vertebral body heights are preserved with no evidence for acute fracture. Mild to moderate multilevel degenerative disease worse at L1 and L2 and L5-S1. Moderate to advanced facet arthropathy of the lower lumbar spine. Pelvis is intact. 2 views left hip demonstrate left total hip arthroplasty in near-anatomic alignment with no evidence for hardware failure or complications. IMPRESSION: Mild diffuse interstitial prominence, nonspecific however can be seen with mild interstitial edema and nonspecific bronchitis. No acute bony findings. ....... Providers: To speak with a TRA radiologist, call. O MRI CSPINE W/&W/O CONTRAST Result Date: 11/25/2021 EXAM: MRI CSPINE W/ AND W/O CONTRAST, MRI TSPINE W/ AND W/O CONTRAST, 11/25/2021 6:00 AM HISTORY: 69 years Male Myelopathy, acute or progressive;progressive BLE weakness, ++DTRs, eval for cord pathology TECHNIQUE: MRI cervical spine: Sagittal T1, sagittal T2, sagittal STIR, axial T1, axial T2 and axial 3D T2 sequences were obtained of the cervical spine. Following the intravenous administration of 20 ml of ProHance, sagittal and axial T1 weighted sequences were acquired. MRI thoracic spine: Sagittal T1, sagittal T2, sagittal STIR, axial T1, and axial T2 sequences were obtained of the thoracic without contrast. Following the intravenous administration of gadolinium, sagittal and axial T1 sequences were acquired. COMPARISON: None available at the time of dictation. FINDINGS: MRI cervical spine: Sagittal images extend from skull base through upper T3. Axial images were obtained from C2 through T1. There is straightening of the normal cervical lordosis. Vertebral bodies are normal in height. Marrow signal is normal. The spinal cord shows no intrinsic signal abnormality. There is no abnormal enhancement. There is no epidural or paraspinal fluid collection. Visible posterior fossa structures are unremarkable, with no cerebellar tonsillar ectopia. The paraspinal soft tissues are unremarkable. Findings at individual disc levels are as follows: C2-C3: The disc height and signal are normal. There is mild bilateral facet arthropathy. There is no significant disc herniation, central canal stenosis or neural foraminal narrowing. C3-C4: There is moderate disc height loss and desiccation. There is moderate bilateral facet arthropathy. Disc osteophyte complex. No spinal canal stenosis. UVJ hypertrophy projected. Moderate left and mild right foraminal stenosis. C4-C5: There is moderate disc height loss and desiccation. There is mild bilateral facet arthropathy. Disc osteophyte complex and ligamentum flavum infolding. Mild spinal canal stenosis. UVJ hypertrophy. Moderate bilateral foraminal stenosis C5-C6: There is severe disc height loss and desiccation. There is mild bilateral facet arthropathy. Disc osteophyte complex and ligamentum flavum infolding. Mild-moderate spinal canal stenosis. UVJ hypertrophy. Moderate bilateral foraminal stenosis. C6-C7: There is severe disc height loss and desiccation. There is mild bilateral facet arthropathy. Disc osteophyte complex. Ligamentum flavum enfolding. Moderate spinal canal stenosis with flattening of the cord. UVJ hypertrophy. Moderate bilateral foraminal stenosis. C7-T1: The disc height and signal are normal. There is mild bilateral facet arthropathy. There is no significant disc herniation, central canal stenosis or neural foraminal narrowing. MRI thoracic spine: Sagittal images extend from C7 through L1. Axial images were obtained from C7 through L1. Spinal alignment is normal. There are no acute fractures. Vertebral bodies are normal in height. Marrow signal is normal. The spinal cord shows no intrinsic signal abnormality. There is no abnormal enhancement. There is no epidural or paraspinal fluid collection. The paraspinal soft tissues are unremarkable. There is mild thoracic spine disc and facet degeneration. There is no significant disc herniation, central canal stenosis or neural foraminal narrowing. IMPRESSION: MRI cervical spine: 1.No cervical cord signal abnormality or enhancement. 2.Multilevel cervical disc and facet degeneration, greatest at C6-7 with moderate spinal canal stenosis. 3.Multilevel moderate neural foraminal stenosis as detailed above. MRI thoracic spine: No cord signal abnormality, enhancement or significant spinal canal stenosis. ....... Providers: To speak with a radiologist O MRI TSPINE W/&W/O CONTRAST Result Date: 11/25/2021 EXAM: MRI CSPINE W/ AND W/O CONTRAST, MRI TSPINE W/ AND W/O CONTRAST, 11/25/2021 6:00 AM HISTORY: 69 years Male Myelopathy, acute or progressive;progressive BLE weakness, ++DTRs, eval for cord pathology TECHNIQUE: MRI cervical spine: Sagittal T1, sagittal T2, sagittal STIR, axial T1, axial T2 and axial 3D T2 sequences were obtained of the cervical spine. Following the intravenous administration of 20 ml of ProHance, sagittal and axial T1 weighted sequences were acquired. MRI thoracic spine: Sagittal T1, sagittal T2, sagittal STIR, axial T1, and axial T2 sequences were obtained of the thoracic without contrast. Following the intravenous administration of gadolinium, sagittal and axial T1 sequences were acquired. COMPARISON: None available at the time of dictation. FINDINGS: MRI cervical spine: Sagittal images extend from skull base through upper T3. Axial images were obtained from C2 through T1. There is straightening of the normal cervical lordosis. Vertebral bodies are normal in height. Marrow signal is normal. The spinal cord shows no intrinsic signal abnormality. There is no abnormal enhancement. There is no epidural or paraspinal fluid collection. Visible posterior fossa structures are unremarkable, with no cerebellar tonsillar ectopia. The paraspinal soft tissues are unremarkable. Findings at individual disc levels are as follows: C2-C3: The disc height and signal are normal. There is mild bilateral facet arthropathy. There is no significant disc herniation, central canal stenosis or neural foraminal narrowing. C3-C4: There is moderate disc height loss and desiccation. There is moderate bilateral facet arthropathy. Disc osteophyte complex. No spinal canal stenosis. UVJ hypertrophy projected. Moderate left and mild right foraminal stenosis. C4-C5: There is moderate disc height loss and desiccation. There is mild bilateral facet arthropathy. Disc osteophyte complex and ligamentum flavum infolding. Mild spinal canal stenosis. UVJ hypertrophy. Moderate bilateral foraminal stenosis C5-C6: There is severe disc height loss and desiccation. There is mild bilateral facet arthropathy. Disc osteophyte complex and ligamentum flavum infolding. Mild-moderate spinal canal stenosis. UVJ hypertrophy. Moderate bilateral foraminal stenosis. C6-C7: There is severe disc height loss and desiccation. There is mild bilateral facet arthropathy. Disc osteophyte complex. Ligamentum flavum enfolding. Moderate spinal canal stenosis with flattening of the cord. UVJ hypertrophy. Moderate bilateral foraminal stenosis. C7-T1: The disc height and signal are normal. There is mild bilateral facet arthropathy. There is no significant disc herniation, central canal stenosis or neural foraminal narrowing. MRI thoracic spine: Sagittal images extend from C7 through L1. Axial images were obtained from C7 through L1. Spinal alignment is normal. There are no acute fractures. Vertebral bodies are normal in height. Marrow signal is normal. The spinal cord shows no intrinsic signal abnormality. There is no abnormal enhancement. There is no epidural or paraspinal fluid collection. The paraspinal soft tissues are unremarkable. There is mild thoracic spine disc and facet degeneration. There is no significant disc herniation, central canal stenosis or neural foraminal narrowing. IMPRESSION: MRI cervical spine: 1.No cervical cord signal abnormality or enhancement. 2.Multilevel cervical disc and facet degeneration, greatest at C6-7 with moderate spinal canal stenosis. 3.Multilevel moderate neural foraminal stenosis as detailed above. MRI thoracic spine: No cord signal abnormality, enhancement or significant spinal canal stenosis. ....... Providers: To speak with a radiologist, O MRI LSPINE W/&W/O CONTRAST Result Date: 11/23/2021 EXAM: MRI LSPINE W/ AND W/O CONTRAST , 11/23/2021 3:39 PM HISTORY: Low back pain with progressive neurologic deficit. TECHNIQUE: The following sequences were performed on a 1.5 tesla magnet: Sagittal and axial T1 and T2 images. Sagittal STIR and coronal T2 images were also performed. COMPARISON: Lumbar spine radiograph 11/23/2021. FINDINGS: The vertebral bodies demonstrate normal alignment and bone marrow signal, similar to the 11/23/2021 study. Mild disc desiccation is present throughout the lumbar spine with diffuse disc bulge at each level. The conus is normal terminating at the inferior L1 level. The paraspinous muscles demonstrate mild diffuse atrophy.. Axial levels follow: T12/L1: Mild diffuse posterior disc bulge results in mild canal stenosis and bilateral neuroforaminal narrowing. L1/L2: Mild diffuse posterior disc bulge results in mild/moderate canal stenosis with slightly prominent dorsal epidural fat contributing to the stenosis. Lateral disc bulge also results in mild/moderate neuroforaminal narrowing, left worse than right with likely contact of the exiting left L1 nerve root. L2/L3: Mild diffuse posterior disc bulge with slightly prominent dorsal epidural fat results in mild/moderate canal stenosis along with mild bilateral neuroforaminal narrowing. Mild facet arthropathy is suggested bilaterally. L3/L4: Mild diffuse posterior disc bulge combined with facet arthropathy and ligamentum flavum thickening results in mild spinal canal stenosis and bilateral neuroforaminal narrowing. L4/L5: Mild diffuse posterior disc bulge combined with moderate facet arthropathy and ligamentum flavum thickening results in moderate canal stenosis with a tiny amount of CSF surrounding the descending nerve root. Lateral disc bulge results in mild/moderate neuroforaminal narrowing with superior deviation of the exiting L4 nerve roots. L5/S1: Mild diffuse posterior disc bulge results in mild spinal canal stenosis with moderate left and mild/moderate right neuroforaminal narrowing due to in part to severe facet arthropathy worse on the right. IMPRESSION: 1. Multilevel degenerative disc disease is worst at the L1/L2 level with moderate canal stenosis and mild/moderate neuroforaminal narrowing, left worst in right. Stenosis is doing part to mild epidural lipomatosis at this level. 2. Severe facet arthropathy from the L4-S1 levels, similar to the 11/23/2021 radiographs, also contributes to mild/moderate canal stenosis at L4/L5 along with mild/moderate neuroforaminal narrowing with superior deviation of the exiting L4 nerve roots. 3. Mild spinal canal stenosis and neuroforaminal narrowing is also noted from the L2-L4 levels. Mild diffuse paraspinous muscle atrophy. ....... Providers: To speak with a radiologist, call O VAS DUPLEX VENOUS LWR EXT BILATERAL IMPRESSION: There is no evidence of deep venous thrombosis, deep venous reflux, or outflow obstruction of the lower extremities. O XR HIP 2-3 VIEWS LEFT W/ PELVIS Result Date: 11/23/2021 EXAM: Chest AP one view; lumbar spine 3 views; pelvis frontal one view; left hip 2 views 11/23/2021 10:05 AM HISTORY: SOB. Weakness TECHNIQUE: Chest frontal one view; lumbar spine 3 views; pelvis frontal one view; left hip 2 views COMPARISON: None FINDINGS: Mild bilateral interstitial prominence. No focal lung opacity. No large pleural effusion or pneumothorax. Cardiomediastinal contour is unremarkable. Grade 1 retrolisthesis of L1 on L2. Grade 1 anterolisthesis of L5 on S1. Remaining lumbar alignment is within normal limits. Vertebral body heights are preserved with no evidence for acute fracture. Mild to moderate multilevel degenerative disease worse at L1 and L2 and L5-S1. Moderate to advanced facet arthropathy of the lower lumbar spine. Pelvis is intact. 2 views left hip demonstrate left total hip arthroplasty in near-anatomic alignment with no evidence for hardware failure or complications. IMPRESSION: Mild diffuse interstitial prominence, nonspecific however can be seen with mild interstitial edema and nonspecific bronchitis. No acute bony findings. ....... Providers: To speak with a radiologist. O IR LUMBAR PUNCTURE DIAGNOSTIC Result Date: 11/24/2021 EXAM: FLUOROSCOPIC-GUIDED LUMBAR PUNCTURE DATE: 11/24/2021 3:01 PM HISTORY: Lower extremity weakness. TECHNIQUE: Consent was obtained from the patient. In the prone position, fluoroscopy was utilized to mark the skin site a over the interspinous space of L4-L5. Skin site was prepped with Betadine in a sterile fashion. The procedure was completed using maximal sterile barrier technique. This includes wearing of a cap, a mask, sterile gloves, and a large sterile drape. Hand washing is completed prior to the procedure. 1% lidocaine was infiltrated as a local anesthetic. Under fluoroscopic guidance a 22-gauge x 3 1/2 inch spinal needle was advanced into the thecal sac. Approximately 5 ccs of clear, normal-appearing CSF was collected and sent to the lab for analysis. Fluoroscopic hard copy image was obtained for documentation purposes. No immediate complications. Patient left the department in stable condition. This procedure was performed by PA-C under the direct supervision of Dr. : None. FLUOROSCOPY TIME: 0.2 minutes. ACCUMULATED INCIDENT DOSE (Air Reference Kerma): 1 mGy. FLUOROSCOPIC IMAGES: 5 fluoroscopic images saved. CONCLUSION: Status post fluoroscopic-guided lumbar puncture via the L4-L5 interspinous space. This yielded approximately 5 cc of thin, clear normal-appearing CSF. ....... Providers: To speak with a radiologist.
Aktuelle Erkrankungen: none
Vorgeschichte: obesity hypertension
Andere Medikamente: amlodipine olmesartan paroxetine rosuvastatin tamsulosin
Allergien: None
Vorherige Impfungen: -

VAERS 1896968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: MN
Alter: 31,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 1894425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Syncope

Symptomtext

Patient had syncopal episode while waiting in the post-vaccination area. Patient recovered and was released to home.

Weitere VAERSDATA-Felder

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

VAERS 1894231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Chest X-ray Chest discomfort Cold sweat Cyanosis Injection site rash Pyrexia Syncope Disorientation Dysarthria Electrocardiogram Eye movement disorder Feeling abnormal Loss of consciousness Pallor Paraesthesia Seizure Tremor

Symptomtext

THE PATIENT'S MOTHER CALLED ON 11/23/21 TO REPORT THAT HER SON HAD A REACTION TO THE PFIZER VACCINE HE RECEIVED. HE FAINTED OUTSIDE THE PHARMACY IN THE PARKING LOT MINUTES AFTER RECEIVING THE VACCINE. THE PATIENT DID NOT WAIT FOR 15 MINUTES OBSERVATION AS REQUESTED BY THE VACCINATING PHARMACIST. PATIENT WAS TAKING TO THE EMERGENCY ROOM AND THEN DISCHARGED AFTER SERIES OF TEST AND OBSERVATION PER MOTHER. PATIENT ALSO COMPLAINED OF CHEST TIGHTNESS, DROWNING SENSATION, RASH AT THE INJECTION SITE AND FEVER FOR 5 DAYS.

Weitere VAERSDATA-Felder

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

VAERS 1894231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest discomfort Cold sweat Cyanosis Injection site rash Pyrexia Syncope Disorientation Dysarthria Electrocardiogram Eye movement disorder Feeling abnormal Loss of consciousness Pallor Paraesthesia Seizure Tremor

Symptomtext

THE PATIENT'S MOTHER CALLED ON 11/23/21 TO REPORT THAT HER SON HAD A REACTION TO THE PFIZER VACCINE HE RECEIVED. HE FAINTED OUTSIDE THE PHARMACY IN THE PARKING LOT MINUTES AFTER RECEIVING THE VACCINE. THE PATIENT DID NOT WAIT FOR 15 MINUTES OBSERVATION AS REQUESTED BY THE VACCINATING PHARMACIST. PATIENT WAS TAKING TO THE EMERGENCY ROOM AND THEN DISCHARGED AFTER SERIES OF TEST AND OBSERVATION PER MOTHER. PATIENT ALSO COMPLAINED OF CHEST TIGHTNESS, DROWNING SENSATION, RASH AT THE INJECTION SITE AND FEVER FOR 5 DAYS.

Weitere VAERSDATA-Felder

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

VAERS 1893781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: VA
Alter: 23,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

On 11/19/21 Patient came in for her first Pfizer vaccine appointment. Consent form was completed without questionable concerns for administration. Patient was administered the Pfizer vaccine while seated in the pharmacy waiting area. After the shot was given, I asked discussed reminder date for second shot, common side effects of vaccine, and asked her to remain seated in the pharmacy area for a little bit to make sure she was feeling alright. While administering the next patient's vaccine in the pharmacy waiting area just a few minutes (2-3 mins) later, my back was facing Patient across the room and as I was speaking to the other patient, I heard a loud clunk hit the floor. I immediately turned around to see Patient collapsed on the floor in front of her chair. We immediately call 911 and the floor manager and I rush over to her and place her on her side and call her name to elicit a response. She is responsive within about 15 seconds of calling her name. She begins to talk normally while remaining on the floor with me on the floor beside her. I asked if she had ever had a reaction like this to a vaccine to which she said no but she has had fainting episodes in the past. A few minutes go by and she has called her father to come pick her up and shes seated in a chair. The paramedics arrived and discussed with Patient her medical history, took vitals, and asked if she would like to go to the hospital. Patient said no and I confirmed that her father would come to pick her up from the pharmacy. As the paramedics are walking to the exit of the building, Patient fainted again and was quickly responsive again. The paramedics came back over and got her buckled into the stretcher for transport to the ED.

Weitere VAERSDATA-Felder

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

VAERS 1893458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: MN
Alter: 81,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe

Weitere VAERSDATA-Felder

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

VAERS 1892845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Face injury Hypotension Injection site pain Nausea Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Mild, Systemic: Nausea-Mild, Additional Details: pt insisted to get up to go to bathroom and got dizzy and fell on her way to bathroom hit the chin face down on the floor

Weitere VAERSDATA-Felder

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

VAERS 1890050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Dizziness Fall Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Weakness-Mild, Additional Details: PATIENT FELT DIZZY AND LIGHTHEADED SO I HAD HER STAY SEATED AND GAVE HER WATER TO DRINK. SHE ATTEMPTED TO STAND UP AT A FAST RATE AND FAINTED/FELL VERY BRIEFLY. I HAD HER STAY SEATED AFTERWARDS. AFTER SOME TIME SHE STATED SHE WAS FEELING BETTER

Weitere VAERSDATA-Felder

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

VAERS 1889601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 14,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 18.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / -

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

Haemoglobin normal Nausea Syncope Vomiting

Symptomtext

syncope multiple episodes nausea and vomiting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: coincidentally has sick contacts with viral syndrome at home. also started menses on 11/17/21 Hemoglobin 14.1 Urinalysis pending
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1888759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NC
Alter: 44,0
Geschlecht: M
Eingang: 21.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient has pas history of fainting during a blood draw years ago.

Weitere VAERSDATA-Felder

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

VAERS 1888757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: CA
Alter: 22,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 1888220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NY
Alter: 16,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Dizziness Dysphagia Throat tightness

Symptomtext

Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Dizziness / Lightheadness-Severe

Weitere VAERSDATA-Felder

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

VAERS 1887943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Injection site pain Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: PATIENT STATES SHE HAS A REGULAR HISTORY OF PASSING OUT AFTER RECEIVING VACCINATIONS - THIS IS NOT A NEW REACTION FOR HER. SHE IMMEDIATELY REGAINED CONSCIOUSNESS AFTER ABOUT 10 SECONDS. SHE STATED SHE FELT FINE RIGHT BEFORE LEAVING

Weitere VAERSDATA-Felder

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

VAERS 1849264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NJ
Alter: 55,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Hyperhidrosis Loss of consciousness Syncope Peripheral circulatory failure

Symptomtext

I lost my consciousness and collapsed; collapsed; This is a spontaneous report from a contactable consumer (patient). A 55-year-old male patient received bnt162b2 (BNT162B2), dose 3 via an unspecified route of administration on 05Nov2021 (at the age of 55-year-old) (Batch/Lot Number: FH8030) as dose 3 (booster), single for COVID-19 immunisation, administered at Pharmacy or Drug Store. Medical history included diabetes mellitus. No known allergies. The patient's concomitant medications were not reported. Historical vaccina included: MODERNA COVID-19 VACCINE (MODERNA COVID-19 VACCINE), dose 1 on an unknown date (Batch/Lot Number: 038AZ1A), dose 1 on an unknown date (Batch/Lot Number: 004MZ0A) for COVID-19 immunisation. No other vaccine in four weeks. No Covid prior vaccination. The patient lost his consciousness (medically significant) on 06Nov2021 13:00 with outcome of recovering, collapsed (medically significant) on 06Nov2021 13:00 with outcome of recovering. No treatment received. Covid was not tested post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1849264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NJ
Alter: 55,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: UN / LA

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

Hyperhidrosis Loss of consciousness Syncope Peripheral circulatory failure

Symptomtext

I lost my consciousness and collapsed; collapsed; This is a spontaneous report from a contactable consumer (patient). A 55-year-old male patient received bnt162b2 (BNT162B2), dose 3 via an unspecified route of administration on 05Nov2021 (at the age of 55-year-old) (Batch/Lot Number: FH8030) as dose 3 (booster), single for COVID-19 immunisation, administered at Pharmacy or Drug Store. Medical history included diabetes mellitus. No known allergies. The patient's concomitant medications were not reported. Historical vaccina included: MODERNA COVID-19 VACCINE (MODERNA COVID-19 VACCINE), dose 1 on an unknown date (Batch/Lot Number: 038AZ1A), dose 1 on an unknown date (Batch/Lot Number: 004MZ0A) for COVID-19 immunisation. No other vaccine in four weeks. No Covid prior vaccination. The patient lost his consciousness (medically significant) on 06Nov2021 13:00 with outcome of recovering, collapsed (medically significant) on 06Nov2021 13:00 with outcome of recovering. No treatment received. Covid was not tested post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1886902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 78,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient collapsed to the floor in the waiting area

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN, NEW PATIENT
Allergien: PENICILLIN, HEPARIN
Vorherige Impfungen: -

VAERS 1884997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: NV
Alter: 24,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Dysphagia Flushing Hyperhidrosis Hypotension Nausea Seizure Syncope Throat tightness Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Nausea-Medium, Systemic: Seizure-Mild, Systemic: Vomiting-Mild

Weitere VAERSDATA-Felder

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

VAERS 1884685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Balance disorder Bradycardia Dizziness Flushing Hyperhidrosis Hypotension Pallor Pupil fixed Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Seizure-Medium, Systemic: Weakness-Medium, Additional Details: 5 MINUTES AFTER ADMINISTRATION, PATIENT EXPERIENCES SEIZURE FOR ABOUT 5 SECONDS, PUPIL FIXED, PALE SKIN, SWEATING, LOSS OF BALANCE. HYPOTENSION (BP 104/61) . BRADYCARDIA (HR 49). PT RECOVERED FROM BRADYCARDIA IN ABOUT 15 MINS, AND HIS LIPS COLOR RETURNED BACK TO RED/PINK. PT WAS ABLE TO COMMUNICATE HE'S FEELING BETTER. AFTER 30 MINS HIS BP 115/87 THEN 123/88. HR 70 THEN 76. OXYGEN LEVEL 99. FOLLOWED UP WITH PATIENT. HE IS HOME AND FEELING FINE.

Weitere VAERSDATA-Felder

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

VAERS 1880079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: OR
Alter: 12,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling abnormal Loss of consciousness Pallor Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: Pt said she "felt weird" and fainted/passed out on floor for 5-10 seconds. Mom declined EMS. After laying on floor for a few seconds, pt said she felt better and stood up and was able to walk to chair to continue to lie down. Looked pale, but she said she felt fine. BP was 100/83mmHg, HR was 75 bpm. Patient said she felt completely fine and left with her mom after ~45 mins without issue. No further follow up needed.

Weitere VAERSDATA-Felder

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

VAERS 1873731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Diarrhoea Dysstasia Feeling abnormal Loss of consciousness Vomiting

Symptomtext

Vomiting, Diarrhea, Passed out, Had to crawl to the couch, Could not stand or get up. Fuzzy memories.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: 03/03/2021

VAERS 1872677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: MN
Alter: 19,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Presyncope

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Nausea-Mild, Additional Details: Vasovagal response

Weitere VAERSDATA-Felder

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

VAERS 1870107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Malaise Syncope

Symptomtext

Patient received first Pfizer vaccine and was sitting down for observation for about 3-5 mins before she reported not feeling well and very dizzy. She said she feels like fainting so I support her arm and upper shoulder and she fainted in her chair for about 30-40 seconds. We called emergency number to report the incident. She came back on her own and was conscious when the ambulance came. They came and gave her IV and transported her to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: no
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 1868209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Flushing Hyperhidrosis Syncope Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Fainting/Unresponsive-Severe, Systemic: Flushed/Sweating-Severe, Systemic: Vomiting-Medium, Additional Details: Patient fainted after receiving COVID-19 vaccine and Fluzone Quadrivalent vaccine (batch/lot#UT7411LA) concurrently. Paramedics called. Patient vitals checked in the store. Patient left unassisted approximately 30 minutes after the incident.

Weitere VAERSDATA-Felder

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

VAERS 1848701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

schwer

Staat: KS
Alter: 38,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anaphylactic reaction Cough Dysphagia Dyspnoea Eye swelling Hypersensitivity Pharyngeal swelling Throat irritation Mouth swelling Pruritus Swelling face Swollen tongue Throat tightness

Symptomtext

Patient received 2nd dose of pfizer-BNT COVID vaccine and 20 minutes after the injection developed "itching and throat swelling" EMS was called. Patient was given 50mg PO diphenhydramine and 0.3 mg IM epinephrine. Patient was still symptomatic upon arrival to the ECC. Patient was given IV 20 mg famotidine and 125 mg of methylprednisolone and observed for 3 hours. Symptoms had improved at that time, and sent home with PO prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: No labwork, per provider documentation, physical exam consistent with allergic reaction
Aktuelle Erkrankungen: -
Vorgeschichte: allergic rhinitis, endometriosis, fibromyalgia,
Andere Medikamente: Flonase, loratadine, buspirone, Bijuva, xarelto, hydroxyzine
Allergien: Contrast dye, Demerol, Phenergan, shellfish, wasp stings
Vorherige Impfungen: -

VAERS 1853970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

schwer

Staat: FL
Alter: 38,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Anaphylactic reaction Dysphagia Injection site pain Throat tightness

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild

Weitere VAERSDATA-Felder

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

VAERS 2724378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 90,0
Geschlecht: F
Eingang: 15.12.2023
Impfdatum: 19.11.2021
Beginn: 04.12.2023
Tage bis Beginn: 745,0
Dosis: 1
Route/Site: UN / UN

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

Arthralgia Asthenia Back pain COVID-19 Chest pain Chills Cough Dyspnoea Headache Mobility decreased Myalgia Nasal congestion Nausea Oxygen saturation decreased Pain Palpitations Pyrexia SARS-CoV-2 test positive

Symptomtext

Admit date: 12/4/2023 Discharge date: 12/5/2023 Admitting Physician: Reason for Admission: Acute respiratory insufficiency Brief Summary of Hospital Stay: Per HPI, a 93 year old female with a history of PE, CAD, Aortic stenosis, CHF, CKD stage III, RA, PMR, and osteoarthritis who presents to the ED with weakness, dyspnea, and myalgias. Patient reports her symptoms began yesterday. They include fever, chills, myalgias, chest pain, palpitations, headache, nausea, dyspnea, cough, and nasal congestion. She went to bed last evening and she was barely able to move. She reports she had pain everywhere including her shoulders, lower back, and chest. States she had Covid two years ago but she is in more pain this time around. Does admit to having a PE when she had covid. Did not get vaccinated because "a vaccine almost killed me."She denies urinary symptoms, sore throat, diarrhea, constipation, lower extremity edema, or vomiting. In the ED, patient was hemodynamically stable though febrile. Covid positive. She did desaturate when asleep and was placed on 2 liters nasal cannula. She was treated symptomatically. Due to her weakness, patient will be admitted under observation for further management. Discharged to Home.

Weitere VAERSDATA-Felder

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

VAERS 2713269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 13.11.2023
Impfdatum: 03.12.2021
Beginn: 05.09.2023
Tage bis Beginn: 641,0
Dosis: 3
Route/Site: - / -

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

Blood glucose normal Blood pressure increased COVID-19 Chest X-ray normal Cough Dyspnoea Full blood count normal Hypoxia Metabolic function test normal Oxygen saturation decreased Pyrexia Respiratory rate increased SARS-CoV-2 test positive

Symptomtext

BRIEF OVERVIEW: Admission Date: 9/5/2023 Discharge Date: Sep 7, 2023 Discharge Disposition: home or self care DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] COVID-19 virus infection [U07.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 72-year-old male with a past medical history of morbid obesity, type 2 diabetes, coronary artery disease, hypertension, hyperlipidemia, cardiomyopathy, OSA who presents to the emergency department with 24 hours of shortness of breath, cough, fever. Symptoms developed day prior to admission. Temperature in the emergency department was 101.7, blood pressure elevated, respiratory rate elevated. Oxygen saturation was low when he was placed on 2 L nasal cannula. She was found to test positive for COVID-19 in the emergency department. Chest x-ray was unremarkable. Complete blood count and CMP were unremarkable. He was started on oral dexamethasone and IV remdesivir. His oxygenation quickly improved to room air. He was discharged home on 09/07/2023 with the hospital at home service to follow. He was seen due to diabetes in the setting of steroids. He had stable blood sugars. He was discharged on his home dose of medicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Essential hypertension Coronary artery disease of native artery of native heart with stable angina pectoris (HCC) Dyslipidemia Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) Cardiomyopathy, nonischemic (HCC) Right bundle branch block BiPAP (biphasic positive airway pressure) dependence OSA (obstructive sleep apnea) Morbid obesity with body mass index of 50.0-59.9 in adult (HCC) History of stroke COVID-19 virus infection
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG tablet aspirin 81 MG tablet atorvastatin (LIPITOR) 80 mg tablet BD INSULIN SYRINGE ULTRAFINE 31G X 15/64" 1 ML MISC cyanocobalamin 1000 MCG tablet dapagliflozin (FARXIGA) 10 mg tablet FLUoxetine (PROZAC) 20 MG
Allergien: None
Vorherige Impfungen: -

VAERS 2711528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 08.11.2023
Impfdatum: 13.12.2021
Beginn: 23.07.2023
Tage bis Beginn: 587,0
Dosis: 2
Route/Site: - / -

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

Chronic obstructive pulmonary disease Dyspnoea

Symptomtext

Admission Date: 7/23/2023 Discharge Date: 7/26/2023 DETAILS OF HOSPITAL STAY: Clinical Narrative: The patient is a 70-year-old gentleman with a Gold-stage IV disease/mMRC functional status presented for a recurrent hospital admission. He has been offered hospice and palliative care on multiple previous occasions, given his appropriateness, but had deferred secondary to concerns regarding his disabled son. On this occasion you does desire to enter hospice in the home in an effort to stay in the home and avoid a return to the hospital. He hopes to die in his own home. We discussed his son circumstance in some detail including the 13 months of bereavement services available to his son after his death. We discussed the Social Work and Case Management availability with a hospice company and that this may facilitate better care coordination and reaching out to community resources to hopefully provide alternatives for his son. He will be discharged home to home hospice today at his request.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Simple chronic bronchitis (HCC) Anxiety Osteoporosis Compression fracture of thoracic vertebra (HCC) Type 2 MI (myocardial infarction) (HCC) Other gastritis with bleeding Primary hypertension PAOD (peripheral arterial occlusive disease) (HCC) Osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow syndrome Macrocytosis Unspecified severe protein-calorie malnutrition (HCC) Goals of care, counseling/discussion
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG chewable tablet budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler ipratropium (ATROVENT) 0.02
Allergien: None
Vorherige Impfungen: -

VAERS 2646597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NJ
Alter: 63,0
Geschlecht: F
Eingang: 16.06.2023
Impfdatum: 21.04.2023
Beginn: 24.04.2023
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Condition aggravated Cough Dry eye Dry mouth Laboratory test abnormal Nasal discomfort Pain Pyrexia Respiratory tract congestion Sjogren's syndrome Sneezing Urine analysis

Symptomtext

After I received the bivalent booster on 4/22/23, I experienced the normal side effects I had gotten from the four previous Covid vaccines (low-grade fever, body aches, and chills for 48 hours). Then on day 3 following the vaccine, I experienced burning in my nose, congestion, coughing, sneezing until day 8. Those symptoms resolved on their own. But since receiving the bivalent vaccine, I have expeienced a worsening of my Sjogren's symptoms - my dry eyes have gotten much worse, and my mouth dryness has gotten much worse. It has continued over the past two months (to the present). I made an appointment with the rheumatologist and opthamologist. The rheumatologist had me complete blood work and urinalysis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood work and urinalysis done on 5/11//23 and again on 5/15/23 for the rheumatologist when my Sjogren's symptoms worsened. Some of the lab results were abnormal and will repeat them
Aktuelle Erkrankungen: none
Vorgeschichte: Sjogren's Syndrome, Crohn's
Andere Medikamente: Crestor, Actonel, Tyrvaya, blood serum eye drops, vitamin D3
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2641064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 05.06.2023
Impfdatum: 03.12.2021
Beginn: 21.05.2022
Tage bis Beginn: 169,0
Dosis: 3
Route/Site: IM / LA

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

Hypotension Myocardial ischaemia Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE DEMAND ISCHEMIA HYPOTENSION 12/28/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2639185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 31.05.2023
Impfdatum: 13.11.2021
Beginn: 11.02.2022
Tage bis Beginn: 90,0
Dosis: 3
Route/Site: IM / RA

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

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2637050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 26.05.2023
Impfdatum: 30.03.2022
Beginn: 14.05.2022
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: - / -

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

Hypersensitivity Hypotension

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION ALLERGIC REACTION, SUBSEQ

Weitere VAERSDATA-Felder

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

VAERS 2555778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 24.02.2021
Beginn: 24.11.2022
Tage bis Beginn: 638,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

11/24/22 presents to ED for "shortness of breath". PMHx of "COPD, myelodysplastic disease"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/24/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2554744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 15.01.2021
Beginn: 21.11.2022
Tage bis Beginn: 675,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

11/21/22 presents to ED for "shortness of breath". PMHx of "RLD , HFpEF, HTN, HLD,mild OSA not on CPAP, and depression/GAD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/21/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2550244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 30.11.2021
Beginn: 31.12.2022
Tage bis Beginn: 396,0
Dosis: 3
Route/Site: IM / -

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

Brain natriuretic peptide increased COVID-19 Chest X-ray abnormal Dyspnoea Emphysema Hypoxia Oxygen saturation decreased Procalcitonin Pulmonary toxicity SARS-CoV-2 test positive White blood cell count normal

Symptomtext

COVID+ 12/31/2022. Vaccination status - Moderna x2 + Pfizer x1 Discharge Physician: PRIVATE MD, MPH Primary Care Physician: PRIVATE, MD Date of Admission: 12/31/2022 Discharge Date: 1/1/2023 Room Number: 2021/2021-1 BRIEF OVERVIEW: Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 01/01/2023 Yes ? Pulmonary emphysema (HCC) 01/01/2023 Yes ? Chronic systolic heart failure (HCC) 10/26/2022 Yes ? Amiodarone pulmonary toxicity 10/07/2022 Yes ? Hypertension Yes ? Biventricular automatic implantable cardioverter defibrillator in situ 01/15/2014 Yes ? Cardiomyopathy (HCC) DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 80 y.o. male who presents today with shortness of breath. He has a history of dilated cardiomyopathy with an EF of 29%, ICD, chronic systolic heart failure, HTN, CAD, and pulmonary toxicity from amiodarone. In the ER the patient was initially 93% on room air, but oxygen desaturation to 87% occurred with ambulation with prolonged recovery. He was placed on 2 Liters NC. He tested positive for COVID. Labs included BNP 3,540, procalcitonin 0.08, normal WBC of 8.49. CXR showed emphysema. Hospitalist service consulted for admission further evaluation. He was initiated on dexamethasone and was outside window therapeutic benefit for Remdesivir. He was quickly weaned to room air with stable oxygenation. Patient was advised to follow-up outpatient pulmonology and obtain PFTs which are currently scheduled for 1/27 with local Medical Group pulmonology. Patient clinically improved and hemodynamically stable for discharge. Discussed plan of care discharge with patient including outpatient follow-up PCP within 7 days. Patient voiced understanding was agreeable with plan of care discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary artery disease involving native coronary artery of native heart without angina pectoris Biventricular automatic implantable cardioverter defibrillator in situ Claudication (HCC) Cardiomyopathy (HCC) Hyperlipidemia Hypertension ICD (implantable cardioverter-defibrillator) discharge Paroxysmal ventricular tachycardia Long term current use of antiarrhythmic drug- Amiodarone Amiodarone pulmonary toxicity Acute respiratory failure with hypoxia (HCC) Chronic systolic heart failure (HCC) Elevated serum creatinine
Andere Medikamente: Amiodarone HCl 200 mg Oral Daily Aspirin 81 mg Oral Daily Calcium Carbonate Antacid 500 MG 1 tablet Oral Daily, As needed Carvedilol 12.5 mg Oral 2 times daily Losartan Potassium 50 MG Take 50 mg by mouth daily. Nitroglycerin 0.4 mg Subling
Allergien: AmiodaroneOther
Vorherige Impfungen: -

VAERS 2550179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

moderat

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 14.12.2021
Beginn: 13.12.2022
Tage bis Beginn: 364,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Blood creatinine increased COVID-19 Chest X-ray abnormal Chronic respiratory failure Cough Dyspnoea SARS-CoV-2 test positive Sepsis

Symptomtext

Patient is a 78 y.o. female patient of DO with history of COPD presented to a local Hospital with cough and dyspnea Covid-19 Virus Infection Sepsis resolved Date of onset of symptoms: ~ 12/12/22 Date of covid positive test: 12/13/22 Vaccination status: unknown Imaging: CXR Prominence of the bronchovascular markings Oxygen requirements on admission: home 2L O2 Current oxygen requirements: Home 2L O2 Medical therapy: Remdesivir and Steroids started on admission but given rapid improvement can stop at discharge Consultants following: none Anticipated special isolation end date: 12/22/22 DNR CC COPD, with chronic resp failure On 2L at home On chronic prednisone, advair, incruse and albuterol Resume home ARB in coming days AKI Creat on admission 1.22, was 0.8 several months ago Improved with IV fluids Dementia Moderate per history, stable Supportive care, delirium prevention measures (at high risk) Afib HTN On crestor, labetolol, cozaar, amiodarone, eliquis

Weitere VAERSDATA-Felder

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

VAERS 2537294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OR
Alter: 70,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 11.09.2021
Beginn: 11.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac monitoring normal Dyspnoea Echocardiogram normal Heart rate increased Laboratory test normal Tachycardia

Symptomtext

Date of booster 11/28/21 not 9/11/21 (correction) Increased heart rate and sob within hours of booster, still present but less frequently over a yr later-getting less and less frequent and shorter duration than previously-occurs randomly Resting heart rate 104-112 (normal 74-85) Occurs sporadically now and last few hours rather than days like before Increased heart rate not present after first and second vaccine but was present for 6 months after having covid 3/2020 and echo was normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: echo 6/2020 wnl Zio patch 11/2022 for a week but tachycardia did not occur during the week I wore it so was wnl labs wnl
Aktuelle Erkrankungen: none
Vorgeschichte: HTN XLH Ocular HTN
Andere Medikamente: 3 anti-hypertensive: Lisinopril Hydrazaline Metoprolol Succinate Rocaltrol and Phosphorous Timolol eye drops mulit-vitamin fish oil
Allergien: tetnus morphine Thimerosal
Vorherige Impfungen: -

VAERS 2528321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 19,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 28.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / LA

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

Antinuclear antibody Asthenia Blood triglycerides decreased Chest discomfort Chest pain Dyspnoea exertional Exercise tolerance decreased Fatigue Fibrin D dimer increased Haemoglobin normal Impaired work ability Laboratory test normal Loss of personal independence in daily activities Metabolic function test normal Tachycardia White blood cell count normal

Symptomtext

Weakness, disproportionate fatigue, chest pain and tightness with exertion, shortness of breath with exertion. Unable to continue working retail job, dance for college dance classes, and photography due to symptom onset and worsening. Unable to participate in desired social activities due to weakness and fatigue. Can only walk short distances and not stand for long, because of symptoms. Tachycardia with minimal exertion such as walking and activities of daily living. Difficulty washing hair, folding clothes due to weakness and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: D-Dimer, Quantitative - 0.87 mcg/mL FEU (November 9, 2022) Ana Titer - 1:160 titer (November 9, 2022) White Blood Count: normal (November 22, 2022) Comprehensive Metabolic Panel: normal (November 22, 2022) Hemoglobin pre diabetic: normal (November 22, 2022) Triglycerides: low (November 22, 2022) De Dimer: negative (November 22, 2022)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: sertraline 50 mg tablet (ZOLOFT) 1 (one) time each day. cetirizine 10 mg tablet (ZyrTEC) 10 mg by mouth 1 (one) time each day.
Allergien: Amoxicillin: Rash
Vorherige Impfungen: -

VAERS 2527784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CT
Alter: 75,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 03.12.2021
Beginn: 30.07.2022
Tage bis Beginn: 239,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Dyspnoea Magnetic resonance imaging abnormal Pericardial effusion

Symptomtext

I was admitted for fluid around my heart or Pericardial Infusion towards the end of July 2022. I was having pain in the upper part of my back and difficulty breathing, shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 7,0
Labordaten: MRI found fluid around my heart.
Aktuelle Erkrankungen: None
Vorgeschichte: Scoliosis
Andere Medikamente: CARDIZEM; calcium; magnesium
Allergien: Penicillin; MOTRIN
Vorherige Impfungen: -

VAERS 2520883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MD
Alter: 41,0
Geschlecht: F
Eingang: 01.12.2022
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chills Discomfort Dysstasia Emotional distress Feeling of body temperature change Impaired work ability Nausea Pain Pain in extremity Pyrexia Tremor

Symptomtext

I had a fever, felt nausea, hot and cold body chills, shakes, ache pain in body and a shooting pain in my legs. I could not stand for long period of time. I had to immediately lie down and struggle to drink water to help alleviate my pain and discomfort. As a result of this I called out of work as a worker working from home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: I was suffering at home trying to get better. Could not get blood work done. My husband took care of me. I'm a Cancer Survivor who took Booster shot.
Aktuelle Erkrankungen: No
Vorgeschichte: I'm a Cancer Survivor. I was diagnosed in June 2019 and completed Chemo in November 2019. As autoimmune compromised I was advised to get Booster Shot.
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: -

VAERS 2515237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: VA
Alter: 55,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 22.11.2021
Beginn: 08.06.2022
Tage bis Beginn: 198,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Dyspnoea Ear infection Pain Pyrexia SARS-CoV-2 test positive Sinus congestion Sinusitis

Symptomtext

On 06/08/2022 in the morning around 8:00AM . I had fever, body aches, sinus congestion, and difficulty breathing. On 06/09/2022 I contacted my doctor he advised me to take over the counter medications and if symptoms got worse to call him . On 06/29/2022 I went to the urgent care for an ear infection and sinus infection due to COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 23NOV2022 COVID-19 Test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep Apnea; High Cholesterol
Andere Medikamente: Crestor; Multi Vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 2505813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 10.11.2021
Beginn: 01.03.2022
Tage bis Beginn: 111,0
Dosis: 3
Route/Site: IM / LA

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

Arrhythmia Atrial septal defect Cardiac monitoring abnormal Echocardiogram Electrocardiogram Palpitations Stress echocardiogram Valsalva maneuver

Symptomtext

I received my third dose of the Pfizer COVID-19 vaccine on 11/10/2021. For about 2 years now, I have been having premature ventricular contractions. I have a family history of heart ailments, so I make it a point to stay on top of any health changes that could be related to my cardiovascular system. In March 2022, I was wearing a heart monitor for about 4 weeks. At one point, the cardiologist noticed that my heart rhythm had become irregular at one point, so he arranged to see me in April 2022. In April, I went to see the cardiologist, and he suggested that I undergo a stress echocardiogram to ensure my heart structures were normal. When I underwent the stress echocardiogram, the cardiologist noticed that there was a hole in the atrial septum. He decided that I also needed to undergo a transesophageal echocardiogram to determine whether I had a patent foramen ovale or an atrial septal defect. It was determined that I had a small patent foramen ovale, but no septal atrial defect. In September 2022, I was cleared and the cardiologist just told me that if there were any changes that I should contact him. On 10/24/2022, shortly after I had finished showering, my heart started racing. I put on my smart watch to measure my heartrate and record an EKG, and it indicated that my heart was beating 183 beats per minute. This lasted about 4 minutes until I did the Valsalva maneuver to attain a normal heartrate again. I called the cardiology clinic and saw my doctor's PA on 10/28/2022. I showed the PA the reading. He told me that the situation wasn't urgent, but should it recur, I was to do the Valsalva maneuver again. He also prescribed me metoprolol to take in case the Valsalva maneuver didn't work. On 11/1/2022, I had another episode, in which my heartrate was 197 beats per minute. It only lasted for about 20 seconds, though, since I immediately did the Valsalva maneuver. My cardiologist believes that I was likely born with the patent foramen ovale, but for some reason, something had recently triggered the events I just described. The PFO may or may not be related to the events; it's also possible that the events were triggered by another congenital abnormality. I plan to move out of state very soon. When I move to the new location, I plan to see another cardiologist, with whom my present cardiologist will be communicating. If my new cardiologist agrees with the current one about the etiology of my symptoms, I will likely undergo a heart ablation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Wearable heart monitor March 2022 irregular heart rhythm detected; Stress Echocardiogram April 2022 hole in Atrial Septum detected; Transesophageal Echocardiogram April 2022 Patent Foramen Ovale detected; smart watch EKG heartrate 183 beats per minute; smart watch EKG 11/1/2022 197 beats per minute.
Aktuelle Erkrankungen: Unknown.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Green peas; cefaclor.
Vorherige Impfungen: -

VAERS 2500653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 03.12.2021
Beginn: 27.10.2022
Tage bis Beginn: 328,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Cough Dizziness Dyspnoea exertional Fatigue SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID infection. Symptoms of fatigue, dizziness, with mild cough and shortness of breath on exertion. Unsure when symptoms started. Positive test collected 10/27/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: Positive SARS-CoV-2 -COVID-19 collected 10/27/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Essential hypertension, hyperlipidemia, chronic kidney disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2492514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 01.11.2021
Beginn: 15.10.2022
Tage bis Beginn: 348,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Asthenia Bladder catheterisation Bladder dilatation Bladder wall calcification Blood urine present COVID-19 Computerised tomogram abdomen abnormal Condition aggravated Culture urine positive Dehydration Diarrhoea Enterococcus test positive Fatigue Hypoxia Laboratory test abnormal Leukocytosis Respiratory disorder

Symptomtext

Discharge Provider: PRIVATE MD Primary Care Provider at Discharge: PRIVATE DO Admission Date: 10/15/2022 Discharge Date: 10/25/2022 PRESENTING PROBLEM: Dehydration [E86.0] Severe sepsis (HCC) [A41.9, R65.20] Sepsis due to urinary tract infection (HCC) [A41.9, N39.0] Diarrhea, unspecified type [R19.7] HOSPITAL COURSE: "84-year-old past medical history significant for type 2 diabetes, hypertension, chronic obstructive pulmonary disease, coronary artery disease, hyperlipidemia, history of MI who came to the ER complains of generalized weakness, fatigue. At baseline patient is oriented x2. After arrival, patient was found to be tachycardic, lab work showed leukocytosis of 24, AKI. CT abdomen/pelvis showed distended urinary bladder with tiny calcifications left ureterovesical junction which could reflect a recently passed calculus. Urine looked infected showing large leukocytes small blood. Urine culture collected. He was placed on 2 g Rocephin and given 3 L fluid resuscitation per sepsis protocol and admitted to Medicine. After admission, patient did improve with IV antibiotics. AKI quickly resolved. Urology was consulted for urinary retention which is felt to be acute on chronic, despite treatment with Flomax and Proscar. Urology recommended placement of Foley, commenting that it should NOT be removed at discharge, as the patient would have difficulty with intermittent straight cathing. Plan is for the patient to follow up with Urology as an outpatient for definitive plan. Urine culture finalized as Enterococcus Faecalis. ID was consulted and IV antibiotics switched to IV ampicillin. ID recommended treatment with IV ampicillin through 10/21. Patient was originally seen by PT/OT who recommended discharge to home. Patient was re-evaluated by therapy on 10/19, and at that time it was felt he would be better suited for discharge to subacute rehab. Referrals were made by care management, and the patient was set for discharge on 10/21/22 but the patient became hypoxic and was tachypenic and the discharge was cancelled. The patient was found to be COVID positive and he qualified for Dexamethasone and Remdisivir. Once the patient respiratory status improved, he was discharged to the facility in a stable condition

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Dysphagia Urinary retention Essential hypertension Hyperlipidemia COPD (chronic obstructive pulmonary disease) (HCC) Bladder outlet obstruction Unspecified severe protein-calorie malnutrition (HCC) Benign prostatic hyperplasia with urinary retention Coronary artery disease, unspecified vessel or lesion type, unspecified whether angina present, unspecified whether native or transplanted heart Hx of myocardial infarction PVD (peripheral vascular disease) (HCC) TIA (transient ischemic attack
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 5 MG tablet aspirin 325 MG tablet bisacodyl (DULCOLAX) 10 MG suppository budesonide/formoterol
Allergien: Atorvastatin Nebivolol Simvastatin
Vorherige Impfungen: -

VAERS 2492485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MA
Alter: 33,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / AR

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

Pyrexia Tachycardia

Symptomtext

Tachycardia- 150bpm at rest for 36 hours after vaccination. Spontaneously resolved after 48 hours. Slight fever of 100 F. degrees.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None. Resolved before I could be seen.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, unexplained orthostatic hypotension after mystery illness in March 2020, hormonal imbalance, GERD, anxiety disorders
Andere Medikamente: Zyrtec, Qvar, Aciphex
Allergien: Cipro, Septra, sulfa drugs, levoquin, macrobid, omnicef
Vorherige Impfungen: Quadrivalent flu vaccine and Pneumonia 23 vaccine. Both had large red spot and swelling that increased in size to a baseball and

VAERS 2491241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 10.04.2021
Beginn: 04.09.2022
Tage bis Beginn: 512,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain COVID-19 Fistula of small intestine Hypertension Intestinal perforation Osteoporosis Ovarian mass Pneumonia SARS-CoV-2 test positive Small intestinal obstruction Transfusion Vaginal fistula

Symptomtext

09/04/22 presents to ED for "abdominal pain". PMHx of "Anemia, Fistula of vagina to small intestine (03/2022), History of blood transfusion (03/2022), Hypertension, Osteoporosis, Ovarian mass, Pneumonia (03/2022), SBO (small bowel obstruction) (CMS/HCC), and Small bowel perforation (CMS/HCC) (03/2022)"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 09/05/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: ME
Alter: 65,0
Geschlecht: F
Eingang: 24.09.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Cardiac disorder Chest discomfort Chills Ear discomfort Fatigue COVID-19 immunisation Discomfort Head discomfort Headache Immunisation Interchange of vaccine products Lymphadenopathy Immunisation reaction Musculoskeletal stiffness Tension headache Migraine Neck pain Off label use

Symptomtext

Stiff neck; She had reaction with both the Moderna shots; Revaccination with different COVID-19 vaccine; Interchange of vaccine products; Headaches are all in the back of her head; Second Moderna shots which were not pleasant; Splitting headache; Felt really tired; Chills; Felt Iike a funny thing right around her chest, like her heart; This spontaneous case was reported by a patient and describes the occurrence of CHEST DISCOMFORT (Felt Iike a funny thing right around her chest, like her heart), MUSCULOSKELETAL STIFFNESS (Stiff neck), IMMUNISATION REACTION (She had reaction with both the Moderna shots), COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. The patient's past medical history included Migraine. On 16-Nov-2021, the patient received third dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 16-Nov-2021, the patient experienced CHEST DISCOMFORT (Felt Iike a funny thing right around her chest, like her heart) and CHILLS (Chills). On 17-Nov-2021, the patient experienced FATIGUE (Felt really tired). On 19-Nov-2021, the patient experienced HEADACHE (Splitting headache). On an unknown date, the patient experienced MUSCULOSKELETAL STIFFNESS (Stiff neck), IMMUNISATION REACTION (She had reaction with both the Moderna shots), COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine), INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products), TENSION HEADACHE (Headaches are all in the back of her head) and DISCOMFORT (Second Moderna shots which were not pleasant). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency and RIZATRIPTAN at an unspecified dose and frequency. At the time of the report, CHEST DISCOMFORT (Felt Iike a funny thing right around her chest, like her heart), MUSCULOSKELETAL STIFFNESS (Stiff neck), IMMUNISATION REACTION (She had reaction with both the Moderna shots), COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine), INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products), TENSION HEADACHE (Headaches are all in the back of her head), DISCOMFORT (Second Moderna shots which were not pleasant), FATIGUE (Felt really tired), HEADACHE (Splitting headache) and CHILLS (Chills) outcome was unknown. Patient was on the couch and felt really tired so kept pumping Tylenol. In Oct-2021 patient thinks she might have had a mild case of COVID, even though she was vaccinated. Patient could not get tested to verify if actually had COVID because she was taking care of her ill father. No concomitant medication information was reported. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in.

Weitere VAERSDATA-Felder

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

VAERS 2431184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 27.11.2021
Beginn: 25.08.2022
Tage bis Beginn: 271,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest X-ray normal Cough Dyspnoea Fatigue Hypoxia SARS-CoV-2 test positive

Symptomtext

Admission Date: 8/25/2022 Discharge Date: Aug 26, 2022 PRESENTING PROBLEM: Hypoxia [R09.02] COVID-19 [U07.1] HOSPITAL COURSE: 59-year-old female with past medical history significant for atrial fibrillation, hypothyroidism, hypertension. She presents emergency department 8/25 with several days of cough, shortness of breath and fatigue. She tested positive for COVID. She is hemodynamically stable initially however placed on 2 L of oxygen for support. Chest x-ray was unremarkable. She was started on Decadron. By the following morning patient is feeling much better and is on room air. Her symptoms were improved. Discharged home in improved primary care condition to complete a course of Decadron and follow-up with primary care as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HTN (hypertension) Fibromyalgia Raynaud's disease Thyroid cancer (HCC) IC (intermittent claudication) (HCC) Gastroesophageal reflux disease without esophagitis Paroxysmal atrial fibrillation (HCC) Postoperative hypothyroidism LVH (left ventricular hypertrophy) Hypocalcemia Primary localized osteoarthritis of right knee Major depressive disorder, recurrent episode, mild (HCC) Prediabetes COVID-19 Statin started by Vascular Surgery with Rx to be taken over by patient's PCP
Andere Medikamente: amLODIPine (NORVASC) 5 MG tablet apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG chewable tablet benzonatate (TESSALON) 100 MG capsule escitalopram (LEXAPRO) 5 MG tablet fluconazole (DIFLUCAN) 150 MG tablet guaifenesin (ROBITUSSIN) 100 MG/5ML
Allergien: CodeineHives MorphineNausea and Vomiting Neomycin-bacitracin-polymyxinOther Sulfa DrugsSwelling ZincItching
Vorherige Impfungen: -

VAERS 2429713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 03.11.2021
Beginn: 31.08.2022
Tage bis Beginn: 301,0
Dosis: 3
Route/Site: - / -

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

Dyspnoea

Symptomtext

SOB.

Weitere VAERSDATA-Felder

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

VAERS 2427595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: PA
Alter: 59,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 19.05.2022
Beginn: 14.06.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Barium swallow normal Blood culture negative Blood lactic acid increased Chills Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Cough Dyspnoea Dyspnoea exertional Emotional disorder Extra dose administered Hypoxia Impaired work ability Infusion Lactic acidosis Leukocytosis Lung disorder

Symptomtext

Before June 14,2022 I was perfectly healthy. Woke up in the middle of the night with acute symptoms of shortness of breath, shaking chills, Fever to 102, spastic coughing, hypoxia. Admitted to hospital 6/15/22-6/24/2022 with diagnosis of acute Bilateral lower lobe pneumonia, and small PE could not be excluded in LLL so MD aired on the side of caution and started Eliquis for 3 months. . Had 7 day course of IV Unasyn, and IV Zithromax. During this hospitalization was treated also with IV steroids, Nebulizer treatments, supplemental O2. Discharged on 6/24/2022 not feeling that great. Discharged on Prednisone taper. ON 7/1/2022 again developed acute sudden symptoms of spastic coughing, fever, chill, shortness of breath On 7/1/2022 Developed sudden acute symptoms again of spastic coughing, shortness of breath, fever, chills, O2 saturations down to 83% and vomiting. Admitted to hospital again 7/1/2022-7/7/2022. In ER had Lactic Acidosis, Procalcitonin level 0.38. Diagnosed with recurrent pneumonia, Leukocytosis, and shortness of breath. O2 saturation 87%. Treated with IV Vancomycin, IV Cefepime. Discharged 7/7/2022 on Ceftin 500mg, 1 tablet my mouth twice a day for 1 day to complete my 7 day course of antibiotic therapy. Presented to ER on 8/4/22 again with same presenting symptoms same as before. Since there was only mild leukocytos and no elevation in Lactic Acid or Procalitonin was discharged from ER and sent home Oral Zithromax and Ceftin. I had office visit with Dr., pulmonologist who feels that I have COP- Cryptogenic Organizing Pneumonia. Treatment for this is long course of steroids for 3 months. Before starting steroids, he wanted me to have a bronchoscopy. Washing were completely negative, no abnormal fungal findings. A few days later started Prednisone 40mg Daily for 3 months. On 8/15/2022 presented with same symptoms as previously mentioned above. Admitted 8/15/2022-8/19/2022 with pneumonia, Acute hypoxemia, and Respiratory Failure. O2 saturations in ER 85-88%. Required supplemental oxygen. Procalcitonin initially 0.09 in ER, but when rechecked on 8/16/2022, it was elevated at 1.21.WBC was 20.68 in the ER. Lactic acid was 2.3. Fever of 101.4. While still in the ER on 8/15 a recheck Lactic acid level was 3.0, Chest CT showed confirmed multilobar airspace disease, demostrating significant progression when compared to previous study, ID was consulted. Started on IV Vancomycin, IV Doxycyclien, and IV Cefepime. The IV vancomycin was discontinued a couple of days later as a repeat MRSA screen was now negative. I had modified barium swallow done that did not show any signs of aspiration. I had an EGD that showed esophagitis, no strictures. I do have a history of Barretts esophagus. Protonix was increased to 40mg BID. Also treated with IV steroids Supplemental O2. Discharged on 8/19/2022 on Levofloxacin 750 mg for 7 days. Then on day 8 started on single strength Bactrim Daily for the next 4 months. I was also discharged on O2 2 liters at night. (never wore Oxygen before) nebulizer treatments QIDPulmonologist increased the length of time on prednisone.. I am now to be treated with Prednisone 40mg Daily for a total of 4 months, I saw the hematologist on 9/1/2022 to get set up for an Iron infusion for known history of Iron deficient anemia. That morning, I woke up again with severe spastic coughing, Shortness of breath, Fever, Shaking chills, pain in lungs, and sore throat. My hematologist agrees with the diagnosis of Cryptogenic Organizing Pneumonia, and he strongly feels all this is related to the 2nd COVID vaccine I received on May 19, 2022. I was sent to ER from Hematology office. WBC-22.90, Lactic acid 2.6. Chest CT showed Improvement in the previously seen nodular and ground-glass opacities in both lungs likely resolving pneumonia or Alveo hemorrhage. Dr., pulmonologist, was pleasantly surprised that the Chest CT showed improvement. He feels the steroids for treatment of COP starting to work. No need for any further antibiotics as gold standard treatment for COP is Long term steroids. I was given 3 liters of IV fluids in the ER and was discharged home that day. I am a type 2 diabetic, and my blood sugar has been in the 400s from the steroids. I see endocrinology now. I am on a lot of insulins, but that is okay because I absolutely have to be on the steroids for 4 months to treat COP. It is important to note that before June 14, 2022 I was perfectly healthy. Every single time I was COVID negative, and I have never had COVID. I work for the agency in Home-based primary care. I am a Nurse. My life has been turned upside down. FMLA was approved, but I had no further Sick Leave, Annual leave left. Absolutely nothing to use as time to get paid. Entire medical work was negative. Negative blood cultures every single time, no findings on bronch. washings, COVID PCR test negative everytime. THrough work I get PCR tested twice a week, and has never come back positive. To be chronicly sick like this with no real medical findings since June 14, 2022 as effected my emotional well being. I have been off work. Based on my symptoms being treated for COP. I still get short of breath with exertion. I still have to wear supplemental O2 at night, Still on nebulizers treatments. I just want to be healthy again. Will be on Prednisone 40mg Daily for 4 months along with single strength Bactrim daily for the next 4 months. After the 4 months, whenever they start the steroid weaning, I can come off the Bactrim when Prednisone dose is under 20mg daily. Then to have a small PE as well. All of this min boggling. The only thing that makes since it is from the 2nd COVID Booster shot I received on May, 19, 2022. My Phycians strongly feel that it is related to this as well. Also I will be starting pulmonary rehab on 9/8/2022. Below is a list of my treating MDs: MD, Pulmonary and Critical Care MD, ( Hematologist) MD, for diabetes and Endocrine Health Hospital, All of my hospital admissions have been here. MD infectious disease

Weitere VAERSDATA-Felder

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

VAERS 2425302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: VA
Alter: 63,0
Geschlecht: M
Eingang: 31.08.2022
Impfdatum: 25.05.2022
Beginn: 01.05.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / UN

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

Blood test normal Electrocardiogram normal Extrasystoles Palpitations

Symptomtext

I seemed to be having intermittent heart palpitations mostly at night and sometimes during the day. Also my heart skips a beat dozens of time during the day. My PCP sent me to a Cardiologist. I'm now scheduled for a monitor to be placed on the 23rd.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG - normal; Blood pressure - normal; blood work - work.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Gabapentin; temocillin; finasteride
Allergien: No
Vorherige Impfungen: -

VAERS 2422607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 29.08.2022
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: UN / LA

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

Anxiety Axillary pain Chest discomfort Dyspnoea Extrasystoles Feeling hot Lymphadenopathy Palpitations

Symptomtext

After 8 minutes, I got a warm feeling and felt tight and short of breath in my chest area. My heart felt like it was was skipping and flipping. It lasted about 10 seconds but then of course it created anxiety and my heart started racing. I waited another 20 minutes before I left. I also had swollen lymph nodes the next morning and sporadic pain in the armpit which gradually got better over the next 3 to 4 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Sinusitis, arrhythmia (PVC and PAC) ,high cholesterol Hypothyroidism, sleep apnea
Andere Medikamente: Rosuvastatin, levothyroxine, calcium, women's one a day vitamin
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2393574

NOVAVAX · COVID19 (COVID19 (NOVAVAX)) · Charge FH8030

moderat

Staat: MD
Alter: 56,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 20.04.2022
Beginn: 20.05.2022
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

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

Hypotonia Injected limb mobility decreased Mobility decreased Swelling Tenderness

Symptomtext

Severe swelling for 3 weeks, limited arm movement, pain to touch and when arm is extended, arm feels limp due to limited mobility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: No evidence of a focal mass lesion. No fluid collection. Questionable mild subcutaneous edema.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Claritin-D
Allergien: N/A
Vorherige Impfungen: -

VAERS 2433514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 93,0
Geschlecht: M
Eingang: 22.07.2022
Impfdatum: 22.11.2021
Beginn: 05.07.2022
Tage bis Beginn: 225,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Failure to thrive Hypotension SARS-CoV-2 test positive

Symptomtext

Narrative: Fully vaccinated, admitted for failure to thrive and hypotension, incidentally COVID positive

Weitere VAERSDATA-Felder

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

VAERS 2370668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 10.12.2021
Beginn: 14.07.2022
Tage bis Beginn: 216,0
Dosis: 3
Route/Site: - / -

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

Cough Diarrhoea Dyspnoea Nausea Vomiting COVID-19

Symptomtext

covid

Weitere VAERSDATA-Felder

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

VAERS 2370668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 10.12.2021
Beginn: 14.07.2022
Tage bis Beginn: 216,0
Dosis: 3
Route/Site: UN / UN

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

Cough Diarrhoea Dyspnoea Nausea Vomiting COVID-19

Symptomtext

covid

Weitere VAERSDATA-Felder

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

VAERS 2329013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: TN
Alter: 59,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 07.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / LA

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

Injected limb mobility decreased Lymphadenopathy X-ray

Symptomtext

My lymph nodes were swollen under my arms. I went to physical therapy for 6 weeks. I am not able to lift my arm and I can't move my arm around to my back. I am supposed to start back in a couple of weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: I had an x-ray to see if it was arthritis.
Aktuelle Erkrankungen: No illnesses at the time of vaccination
Vorgeschichte: I have Fibromyalgia; PTSD; Degenerative Disc Disease
Andere Medikamente: No medications at the time of vaccination
Allergien: I am allergic to latex
Vorherige Impfungen: -

VAERS 2323391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 62,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 04.12.2021
Beginn: 19.04.2022
Tage bis Beginn: 136,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort COVID-19 Condition aggravated Cough Dysphagia Fatigue Feeding disorder Feeling abnormal Fibromyalgia Fluid intake reduced Gastrointestinal disorder Gastrointestinal pain Gastrooesophageal reflux disease Impaired work ability Influenza like illness Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

I started to feeling a little run down and a little flu like, my stomach was uneasy. On Monday I was coughing severely, fever of 101F, GI pain, severe flu symptoms, I took a home COVID 19 test that came up negative. On Tuesday it came up positive, I could not swallow so I could not eat or drink anything. I called my doctor on Wednesday, she prescribed me PAXLOVID, after my first dose I started feeling better. By the following Wednesday I was able to go back to work but it took a month before I felt 100 percent myself. I felt fatigue that whole month. While I had COVID 19 all my underlying conditions got worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Home COVID 19 test.
Aktuelle Erkrankungen: No
Vorgeschichte: GERD; Fibromyalgia; Gastro Issues
Andere Medikamente: LYRICA; omeprazole; vitamin D; vitamin B12; IBGARD
Allergien: No
Vorherige Impfungen: -

VAERS 2321537

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CO
Alter: 63,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 13.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Blood pressure measurement Blood test Body temperature Chest X-ray Computerised tomogram thorax Condition aggravated Costochondritis Electrocardiogram Pain Pyrexia

Symptomtext

With the first one she didn't feel good, low grade fever and aches and pains; With the first one she didn't feel good, low grade fever and aches and pains; States that with each dose the symptoms were worse than the one before and this last one she was in the ER; diagnosed with costochondritis; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), on 11Feb2021 at 15:00 as dose 1, single (Lot number: EN9581), in right arm, on 04Mar2021 at 15:00 as dose 2, single (Lot number: EN6199), in right arm and on 13Nov2021 at 19:00 as dose 3 (booster), single (Lot number: FH8030) at the age of 63 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "breast cancer" (unspecified if ongoing), notes: Breast cancer diagnosed 12 years ago; "High cholesterol" (unspecified if ongoing); "High blood pressure" (unspecified if ongoing); "Allergy" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL taken for hypertension (ongoing); SINGULAIR taken for hypersensitivity; ROSUVASTATIN taken for blood cholesterol (ongoing); MONTELUKAST taken for hypersensitivity (ongoing); DYMISTA taken for hypersensitivity; AZELASTINE taken for hypersensitivity. The following information was reported: PYREXIA (non-serious), PAIN (non-serious), outcome "not recovered" and all described as "With the first one she didn't feel good, low grade fever and aches and pains"; CONDITION AGGRAVATED (non-serious), outcome "not recovered", described as "States that with each dose the symptoms were worse than the one before and this last one she was in the ER"; COSTOCHONDRITIS (non-serious), outcome "unknown", described as "diagnosed with costochondritis". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of condition aggravated, costochondritis. Follow-up attempts are completed. No further information is expected. Amendment: This follow-up report is being submitted to amend previous information: Amended the made case as valid. updated narrative information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20220505; Test Name: Blood pressure; Result Unstructured Data: Test Result:152/75 mmHg; Comments: Norm Low- 100/60, Comments- 152/75; Test Date: 20220505; Test Name: Bloodwork; Result Unstructured Data: Test Result:RWD CT; Comments: Norm Low- 12, Comments- Low; Test Date: 20220505; Test Name: temperature; Result Unstructured Data: Test Result:101.5-96.5; Comments: Norm Low- 96.5, Comments- 99; Test Date: 20220505; Test Name: chest x-ray; Result Unstructured Data: Test Result: pleuritic and Costochondritis; Comments: Comments- Showed pleuritic and Costochondritis; Test Date: 20220505; Test Name: chest CT; Result Unstructured Data: Test Result: pleuritic and Costochondritis; Comments: Comments- Showed pleuritic and Costochondritis; Test Date: 20220505; Test Name: EKG; Result Unstructured Data: Test Result: Normal; Comments: Comments- Ok.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Blood pressure high; Breast cancer (Breast cancer diagnosed 12 years ago); High cholesterol.
Andere Medikamente: LISINOPRIL; SINGULAIR; ROSUVASTATIN; MONTELUKAST; DYMISTA; AZELASTINE.
Allergien: -
Vorherige Impfungen: -

VAERS 2318899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 75,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 22.11.2021
Beginn: 26.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Angiogram cerebral normal Anticoagulant therapy Asthenia C-reactive protein increased COVID-19 Cerebral infarction Condition aggravated Cough Glomerular filtration rate decreased Magnetic resonance imaging head abnormal Malaise Metabolic encephalopathy SARS-CoV-2 test positive

Symptomtext

12/26/2021 - In ED with c/o sudden weakness/stroke possibility. BP 138/70, HR 101, Temp 97.8, RR 24. Tested Covid positive. Admitted metabolic encephalopathy/r/o stroke. Received MAB in ED. Does have Cough. CRP-1.1. GFR-57. Mild AKI. CTA-no acute intracranial abnormality. 12/27/2022-MRI Brain-Probable small subacute infarct left centrum semiovale. Start Eliquis. 12/28 - started on Decadron/Lovenox therapeutic. O2 stable on rm air. Continuing to monitor. Vitals WNL. 12/30 - EGFR decrease-33, Covid symptoms improved.Discharged to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: AKI, Stroke, HTN, A-fib, DM, HF, TIA
Andere Medikamente: -
Allergien: Cephalexin
Vorherige Impfungen: -

VAERS 2317325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IL
Alter: 81,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 17.11.2021
Beginn: 03.06.2022
Tage bis Beginn: 198,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Chest X-ray abnormal Inappropriate schedule of product administration Osteoarthritis Pneumonia SARS-CoV-2 test positive

Symptomtext

Patient received pfizer vaccine on 2/11/21, 3/11/21 and 11/17/21. Admitted on 5/26/22 for osteoarthritis of knee. Was to be transferred to another hospital and found to be COVID positive on 6/3/22. From here, she was placed on isolation. Follow up chest x-ray showed right sided pneumonia. The hospitalist followed the patient for medical management and had her on Doxycycline and Rocephin. She was breathing okay and did not require increased respiratory support. She was eating and voiding without difficulty. She had an additional 5 day stay after her positive COVID confirmed test and was ultimately accepted to other facility swing bed for continued rehab on 6/9/22. She was transferred in stable condition on 6/9/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 14,0
Labordaten: 6/3/22 COVID19: positive
Aktuelle Erkrankungen: -
Vorgeschichte: Breast cancer, arthritis, low back pain.
Andere Medikamente: furosemide 20 MG Tabs Commonly known as: LASIX Take 10 mg by mouth daily. lactulose 10 GM/15ML Soln Commonly known as: CHRONULAC Take 30 mL by mouth daily. levothyroxine 50 MCG Tabs Commonly known as: SYNTHROID Take 50 mcg by mouth dail
Allergien: none
Vorherige Impfungen: -

VAERS 2317309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 93,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 18.02.2021
Beginn: 20.02.2022
Tage bis Beginn: 367,0
Dosis: 3
Route/Site: IM / UN

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

Agonal respiration COVID-19 Cardiac monitoring Confusional state Dyspnoea Hyporesponsive to stimuli Mental status changes Nausea Oxygen saturation decreased Positive airway pressure therapy SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

Pt to ED by EMS with shortness of breath and nausea upon arrival on 2/20. Pt COVID positive upon admission, respirations are even, unlabored, pt maintained on 2L NC. 2/23 pt continues to be confused and pull at Cardiac monitor, oxygen and IV. 2/25 pt is a&ox2 with delayed responses. 2/26 pt placed on Bipap unit due to desaturation and change in mental status. Pt unresponsive, agonal breathing and sating at 70% on 6lnc, placed on 15 l high flow and NR sating at 95%. 2/27 pt alert and oriented x2, on Cold air at 10 liters nasal cannula SPO2 95%. 3/2 pt denied any pain or discomfort. 3/4 No c/o any pain. Oxygen bumped down to 2L . 3/6 Pt alert and oriented x 2 denies any distress. Pt discharged 3/8.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 17,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Pneumonia ... Pneumonia HCAP (healthcare-associated pneumonia) Acute respiratory failure with hypoxia (CMS/HCC) Pleural effusion on right Hypoxia Acute respiratory failure with hypoxia (CMS/HCC) Acute respiratory failure (CMS/HCC) Bilateral pneumonia Respiratory failure (CMS/HCC) Chest pain UTI (urinary tract infection) Acute encephalopathy CVA (cerebral vascular accident) (CMS/HCC) Obesity (BMI 30-39.9) SOB (shortness of breath) SIRS (systemic inflammatory response syndrome) (CMS/HCC) Essential hypertension Normochromic normocytic anemia Sepsis (CMS/HCC) Severe sepsis with acute organ dysfunction (CMS/HCC) Ischemic cardiomyopathy Sepsis with encephalopathy, due to unspecified organism, unspecified whether septic shock present (CMS/HCC) UTI due to extended-spectrum beta lactamase (ESBL) producing Escherichia coli Hypokalemia Hypomagnesemia Osteomyelitis (CMS/HCC)
Andere Medikamente: amLODIPine (NORVASC) 10 MG PO Tab aspirin ... Additional information for Item 9: amLODIPine (NORVASC) 10 MG PO Tab aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 40 MG PO Tab Cholecalciferol (VITAMIN D-1000 MAX ST PO) ferrous sulfate 32
Allergien: None
Vorherige Impfungen: -

VAERS 2307046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 46,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 01.12.2021
Beginn: 01.05.2022
Tage bis Beginn: 151,0
Dosis: 3
Route/Site: SYR / LA

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

Asthma Bronchitis COVID-19 Cough Dyspnoea Exposure to SARS-CoV-2 Fatigue Feeling abnormal Headache Oropharyngeal pain Pain Pain in extremity SARS-CoV-2 test positive

Symptomtext

It started with shortness of breath, coughing, very mild sore throat and body aches. Little headache but not too bad. The cough got to where it would be when I have bronchitis. I called the doctor and they gave me the prednisone and it knocked the cough to manageable. I'm still dealing with coughing and had to up my asthma medicine. I don't feel sick but have a cough if I don't up my Symbicort dose. I do still experience extra fatigue. In the beginning it was a lot of brain fog, now it's just a mild brain fog. I also had leg aches that went away as well. My son had been positive and he had the PCR test so we did a home test.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid test at home-positive.
Aktuelle Erkrankungen: No
Vorgeschichte: High cholesterol; high blood pressure; asthma; acid reflux; hypothyroidism; migraines
Andere Medikamente: Pantoprazole, Levothyroxine, Amlodipine, Liothyronine, Metoprolol, generic for Crestor, Symbicort 2xday, birth control, Pepcid 20mg, Flonase, Claritin, Vit D3, Albuterol
Allergien: Iodine; sulfur
Vorherige Impfungen: -

VAERS 2303443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IN
Alter: 54,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

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

Aortic arteriosclerosis Blood test normal Blood urine present Computerised tomogram abdomen abnormal Fatigue Feeling abnormal Headache Malaise Mobility decreased Muscle fatigue Pain Tenderness

Symptomtext

With dose #2 Pfizer I previously reported: Since I woke from an afternoon nap, I can hardly hear and there is intense ringing in my ears (right worse than left). My injection was at 11:23AM and I woke up with this at 5:20PM. I have no cold or sinus symptoms and never have ear problems. These issues are currently still happening. Dose #3 Within 24 hours would have been the start of fatigue, feeling just wiped out, I feel like I never bounced back. Within the week or 2 weeks after vaccine I had a tenderness in my body aches, throat, headaches, extreme fatigue and brain fogginess, I could not do anything but go to bed, I felt so sick, but not sick. By week 2 I was able to get up but had to go lay down and a month later when I went to see my doctor, I was still the same. I saw my doctor on 12/20/2021. She was concerned with a possible thyroiditis or autoimmune condition. Extreme fatigue, headaches, brain fog, it has continued to get better though today, but I am just not well. Body aches have subsided. Headaches are daily nonstop. I have had to take Tylenol every 6 hours, I still have muscle fatigue, it's hard to lift arms and legs, it feels like I went on a hike or lifted weights, but I have not done anything. I have had blood in my urine detected 05/27/2022. We thought I may have had a UTI, but there was no infection, going to recheck in a month. Currently, I am down to trace amounts of blood in my urine. Abdominal CT scan, negative other than visible cholesterol on my aorta. Blood work came back normal. Both PCP, and ENT suggested holding off on the 2nd booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Abdominal CT scan negative other than visible cholesterol on my aorta. Blood work negative.
Aktuelle Erkrankungen: No
Vorgeschichte: High cholesterol; nerve pain
Andere Medikamente: Meloxicam; cimetidine; DILT XR; flecainide; simvastatin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2290438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 42,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Computerised tomogram Cough Pain in extremity Pneumonia Pyrexia Sneezing Vomiting

Symptomtext

Pain left arm and shoulder, high fever for one week, cough, sneezing, vomiting, pneumonia (3/11/22)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Antibiotics 3/11/22 for pneumonia, CT scan 3/18/22
Aktuelle Erkrankungen: seasonal allergies
Vorgeschichte: seasonal allergies
Andere Medikamente: Benadryl, Montelukast
Allergien: none
Vorherige Impfungen: -

VAERS 2284837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OH
Alter: 64,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 17.11.2021
Beginn: 06.04.2022
Tage bis Beginn: 140,0
Dosis: 3
Route/Site: SYR / RA

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

Bronchitis COVID-19 Chest discomfort Chills Dyspnoea Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

On the 11/17/2021 i received the Covid vaccine. On the 04/06/2022 around 5:30 I had a fever, sore throat and heavy chest. I took Tylenol and felt a little better. As the day went on I started to get worse and decided to get tested. I was positive. I had sore throat short of breath and chills. This lasted about 4 weeks. After I developed bronchitis and was put on antibiotics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sarcoidosis
Vorgeschichte: Sarcoidosis; obesity
Andere Medikamente: pretisome / Flovent/ multivitamin/ Pepcid/ albuterol/ dyazide/
Allergien: Penicillin; perc; red dye
Vorherige Impfungen: -

VAERS 2328560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Injected limb mobility decreased Injection site erythema Injection site pain Injection site warmth Pain

Symptomtext

Redness, pain, warm to touch at injection site. Limit range of motion on left arm due to pain. Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2267532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.12.2021
Beginn: 11.03.2022
Tage bis Beginn: 95,0
Dosis: 3
Route/Site: IM / LA

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

Anosmia Blood test Electrocardiogram Fatigue Hypoaesthesia Laboratory test Loss of personal independence in daily activities Magnetic resonance imaging Paraesthesia Pyrexia Ultrasound scan Vertigo

Symptomtext

I started getting symptoms of loss of smell, fever, and tiredness. After one week, my smell came back. Then I had tingling and numbness on the left side of my body from the arms and up to my face with vertigo. I went to the ER and had tests done and had an EKG and ultrasound. This lasted in episodes for 5-6 weeks. I could not do my normal activities during this time. I went to my doctor and had an MRI and blood. My doctor thinks it could be an inflammation of the nerves. I am waiting for the results. This still happens to this day but more mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI Bloodwork Ultrasound
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Iron
Allergien: None
Vorherige Impfungen: -

VAERS 2263503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MA
Alter: 63,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 10.11.2021
Beginn: 30.12.2021
Tage bis Beginn: 50,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia COVID-19 Cough Dyspnoea Fatigue Headache Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On 12/30/2021, I started getting symptoms of breathing issues and coughing. I also experienced tiredness. I got a positive COVID-19 at home test. I called my doctor and did a telehealth visit and was prescribed 2 round of steroids, cough medication, and inhaler. I also lost my of sense of taste which is not back all the way. I also got a positive COVID-19 on 5/3/2022. I have symptoms of congestion, mild headache, mild cough that feels like allergies. I contacted my doctor and was prescribed Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test - positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Simvastatin, Losartan, Oxybutynin, Vitamin C, D, E, Fish oil
Allergien: Sulfa, Codeine
Vorherige Impfungen: -

VAERS 2259943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MN
Alter: 42,0
Geschlecht: F
Eingang: 01.05.2022
Impfdatum: 02.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / RA

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

Atrial enlargement Chest pain Differential white blood cell count Dyspnoea Electrocardiogram ST segment abnormal Electrocardiogram abnormal Electrocardiogram ambulatory Fatigue Full blood count Heart rate irregular Metabolic function test Palpitations Platelet count Sinus tachycardia Troponin I Ventricular extrasystoles

Symptomtext

Sinus tachycardia with frequent premature ventricular complexes in a pattern of bigeminy, biatrial enlargement, nonspecific ST abnormality, abnormal ECG Symptoms include shortness of breath, feeling of burning in chest, feeling of pounding and irregular heartbeat (skipping beats), fatigue No treatments recommended Frequency of symptoms was greatest between 12/10/2021 and 12/26/2021, symptoms have continued since then but less frequently Note: This occurred after the booster dose of Covid-19 Vaccine, which was by Phizer/BioNTech, the first two doses were by Moderna

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Basic metabolic panel, Troponin I, CBC with platelets and differential, EKG 12-lead, tracing only, all completed on 12/21/2021 in Emergency Department at a local Hospital Holter Monitor completed on 12/23/2021 through 12/25/2021 by a local Clinic
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2252017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Computerised tomogram Hemiparesis Hypoaesthesia Intervertebral disc protrusion Intervertebral disc space narrowing Ligament disorder Magnetic resonance imaging head normal Magnetic resonance imaging spinal abnormal Muscular weakness Paraesthesia Scan with contrast abnormal Spinal disorder Spinal stenosis

Symptomtext

or if it worsens. Patient notified PCP office 7 days after vaccination and was seen via telemedicine on 12/28/2021. She was prescribed Gabapentin for symptoms and given ER precautions. Patient stated symptoms worsened to left arm weakness along with numbness/tingling. Patient went to Medical Center ER on 01/04/2022. She was discharged after 1 day to the care of her husband with recommendation to be evaluated by PCP as soon as possible. She was evaluated by PCP in person on 01/06/2022. Patient reported at the time that the symptoms haven't improved and the neurologist at the hospital wanted her to have MRI brain with and without contrast. PCP ordered MRI brain as well as MRI cervical spine with and without contrast. MRI brain was completed on 01/07/2022 and it was normal; patient was recommended to follow up with neurology per PCP. MRI cervical spine was completed on 01/12/2022 and showed "C6/C7 level: 3 mm broad-based disc bulge with ligamentum flavum buckling is noted. Mild canal stenosis. Bilateral uncovertebral hypertrophy is noted. There is mild bilateral neuroforaminal narrowing. Facets are normal." Patient was recommended to follow up with spine specialist. She saw spine specialist on 01/20/2022 and he ordered an EMG as well as prescribed Ibuprofen 600 mg, Gabapentin 300 mg, and Baclofen 10 mg to take as prescribed. Patient was advised to return for follow up in 6 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: 1,0
Labordaten: CT scan on 01/04/2022 at ER, MRI brain with and without contrast on 01/07/2022, MRI cervical spine with and without contrast on 01/12/2022.
Aktuelle Erkrankungen: n/a
Vorgeschichte: Hyperlipidemia
Andere Medikamente: Patient wasn't taking any medications at time of vaccination.
Allergien: NKA
Vorherige Impfungen: -

VAERS 2244069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 24,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Chest pain Full blood count Magnetic resonance imaging Ultrasound scan Urine analysis X-ray

Symptomtext

I had chest pain. I was given Maalox with lidocaine as treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood work; CBC; Urine test; X-ray; Ultrasound; MRI
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Daily Birth Control
Allergien: None
Vorherige Impfungen: 1st & 2nd dose Pfizer - fatigue & lethargy.

VAERS 2238715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 13.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / -

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

Dyspnoea

Symptomtext

Pt presented 2 days later with SOB but was stable and discharged stable without oxygen requirement.

Weitere VAERSDATA-Felder

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

VAERS 2231847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MS
Alter: 21,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Dizziness Dyspnoea Insomnia Palpitations SARS-CoV-2 antibody test positive SARS-CoV-2 test negative

Symptomtext

An hour after the vaccine I was a little bit dizzy but it went away pretty quickly. A week later I went to the emergency room with racing heart palpitations was told I did not have myocarditis. I did not have a positive PCR test but I did have a nucleocapsid test and it was positive for COVID, I have insomnia, trouble breathing, heart palpitations, chest pains. Currently on medications for those.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Probiotic; Allergy medication
Allergien: PCN; Amoxicillin; Minocycline; Bactrim; Augmentin
Vorherige Impfungen: TB

VAERS 2228535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 05.11.2021
Beginn: 11.01.2022
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: IM / UN

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

Anaemia Blood test abnormal Bronchoscopy abnormal Computerised tomogram abnormal Condition aggravated Microscopic polyangiitis Mycobacterium avium complex infection Pulmonary function test normal Pulmonary mass Renal impairment

Symptomtext

On 10/25/2021, I noticed a drop in kidney function and anemia in my lab results. Then on 01/11/2022, I had a more dramatic drop in kidney function, and on 01/14/2022, even more dramatic drop. The on 02/02/2022, I had a kidney biopsy and was diagnosed with Microscopic Polyangiitis. I am still having these issues at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood Panels (Abnormal), CT scan of lungs (Showed nodules), Bronchoscopy (Showed MAC), Pulmonary Function Test (Normal)
Aktuelle Erkrankungen: None
Vorgeschichte: Glaucoma, Osteoporosis, Osteoarthritis, Microscopic Polyangiitis, Wegeners
Andere Medikamente: Atorvastatin, Celebrex, Ambien, Valium, Calcium, Vitamin D3, Fosamax, Amoxicillin
Allergien: None
Vorherige Impfungen: -

VAERS 2228413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 78,0
Geschlecht: M
Eingang: 12.04.2022
Impfdatum: 13.11.2021
Beginn: 18.02.2022
Tage bis Beginn: 97,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Anticoagulant therapy Blood creatinine increased C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax abnormal Cough Dyspnoea Dyspnoea exertional Emphysema Fatigue Glomerular filtration rate decreased Lung infiltration Pain Pneumonia Pulmonary fibrosis

Symptomtext

2/8/2022- Patient called for Covid test: cough, congested and body aches. Covid + test. 2/9/2022- Monoclonals ordered ( Sotrovimab) Benzonatate ordered for cough. Received infusion. Rheumatology advised of Covid status, hold Imuran for at least once a week or until asymptomatic. 2/14/2022-Patient notes having body aches and SOB upon exertion, O2 sat at home 95% on RA. Advised to treat symptoms, seek immediate medical attention is SOB increases. 2/18/2022- Office visit for increased difficulty breathing on exertion and fatigue. Agreed to to hospital admission. Chest xray and labs were ordered,transfered to Medical Center. 2/18/2022-Presentated to ED, with complaints of SOB upon exertion and fatigue. 2/18/2022 Additional information for Item 18: Admitted with Acute Covid multilobar pneumonia without hypoxemic respiratory failure and mild AKI. Afebrile, HR-93, RR-18 o2 sat 97% on RA. CXR -Bilateral pulmonary infiltrates not visualized previously. Chest Ct w/o contrast- bilateral multi lobar multifocal pulmonary infiltrates , emphysema with underlying fibrosis. IV Ceftriaxone, IV Azithromycin and IV Vancomycin ordered (given in ED) . WBC -13, CRP 21.3, creatnine 1.7 and EGFR 45. On Bactrim for PCP prophylaxis, Lovenox, IV Cefepime , inhaled tobryamycin and IV doxycycline ordered. Remdesivir held due to AKI. 2/19/2022- CT chest pulmonary embolism w IV contrast patient is high risk: No evidence of PE. EGFR now >60, WBC trending down-Pulmonary added Solu-medrol. 2/20/2022- CRP-16.7. Continue with Lovenox for another 24 hours and then transition to Eliquis. Vitals WNL no supplemental oxygen needed. 2/21/2022- WBC 7.5 and Creatnine 1.0.Vitals WNL. Start Prednisone and d/c Solu-medrol. Continue current medications. Discharged to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, Granulomatosis with polyangiitis, macrocytosis , Chronic immunosuppressive medications
Andere Medikamente: -
Allergien: Albuterol
Vorherige Impfungen: -

VAERS 2204072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: MO
Alter: 70,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 10.03.2022
Beginn: 25.03.2022
Tage bis Beginn: 15,0
Dosis: UNK
Route/Site: IM / RA

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

Dyspnoea Laboratory test

Symptomtext

patient had shortness of breath and difficulty breathing and went to hospital and was tested and admitted

Weitere VAERSDATA-Felder

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

VAERS 2192241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 06.12.2021
Beginn: 05.03.2022
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: SYR / LA

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

Headache Impaired work ability Migraine Mobility decreased Musculoskeletal stiffness Neck pain Swelling

Symptomtext

03/05/2022, I woke up and started feeling kind of a crick in my neck but it was more painful than that but I didn't think much of it. I went the whole day as if nothing happened, and the next morning it was significantly more painful and I could feel swelling on the left side of my neck and I wasn't able to tilt my head and the pain started getting worse so I took Ibuprofen which didn't help. The next day 03/07/2022, I woke up and my neck was very swollen and stiff on the left side and I tried working but if I was in a position other than lying down I had a headache that started at the base of my neck into the left side of my head, like a migraine. I ended up taking 600 mg Ibuprofen and that didn't help so I tried Naproxen and Aleve and that didn't help either. 03/08/2022 the pain wasn't getting better and I couldn't tilt or rotate my head so I did a virtual doctor's appointment and the Doctor said to keep taking Ibuprofen and wait it out. I was in a state of pain for a week, and on Monday and Tuesday I couldn't work but half of a day because of the pain. Saturday 03/12/2022 it started to hurt less and I was able to tilt my head again, and on 03/13/2022 it was better and I was able to do things as normal but still got a headache if I sat up too long.

Weitere VAERSDATA-Felder

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

VAERS 2176709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: OT / LA

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

Dyspnoea Heart rate Heart rate increased Tachycardia Vaccination site pain

Symptomtext

heart was beating really fast; breathing kind of hard; tachycardia; pain at injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 52 year-old female patient received bnt162b2 (COMIRNATY), intramuscular, administered in arm left, administration date 09Dec2021 14:15 (Lot number: FH8030) at the age of 52 years as dose 2, 0.3 ml single for Covid-19 immunization. Relevant medical history included: "Chemotherapy" (unspecified if ongoing), notes: Received chemotherapy 5 years ago for a duration of 1 year. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, Route, Anatomical Location: Intramuscular; left arm, Lot Number / Expiry Date: FH8027), administration date: 18Nov2021, when the patient was 52 years old, for Covid-19 Immunization, reaction(s): "pain at the injection site". The following information was reported: TACHYCARDIA (non-serious) with onset 11Dec2021, outcome "recovered" (11Dec2021), described as "tachycardia"; DYSPNOEA (non-serious) with onset 11Dec2021 11:30, outcome "recovered" (11Dec2021), described as "breathing kind of hard"; VACCINATION SITE PAIN (non-serious) with onset 10Dec2021, outcome "recovered" (10Dec2021), described as "pain at injection site"; HEART RATE INCREASED (non-serious) with onset 11Dec2021 16:30, outcome "recovered" (11Dec2021), described as "heart was beating really fast". Relevant laboratory tests and procedures are available in the appropriate section. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211211; Test Name: heart was beating; Result Unstructured Data: Test Result:fast
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chemotherapy (Received chemotherapy 5 years ago for a duration of 1 year)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2173333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 27.11.2021
Beginn: 04.03.2022
Tage bis Beginn: 97,0
Dosis: 3
Route/Site: IM / -

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

Acquired diaphragmatic eventration Alanine aminotransferase normal Anion gap Anticoagulant therapy Aortic arteriosclerosis Aortic disorder Aspartate aminotransferase increased Asthenia Blood albumin normal Blood alkaline phosphatase normal Blood bicarbonate normal Blood bilirubin normal Blood calcium normal Blood chloride decreased Blood creatinine normal Blood glucose normal Blood lactic acid Blood lactic acid increased

Symptomtext

Hospitalized (3.4.22 - 3.5.22); COVID-19 positive (3.4.22); fully vaccinated PLUS Booster - pfizer x3 d/c summary:Attestation with edits by DO at 3/5/2022 3:59 PM I personally examined this patient on the day of discharge. The case was discussed with the Resident. I have reviewed the DC Summary; it accurately reflects the hospital course and dc recommendations. Came to ER early morning on 3/5 with fever, chills and weakness. Temp 38.6 on arrival. WBC 12.2. Lactic 4.2. Tested positive for Covid. Received 1L NS. Pts symptoms improved. She was admitted by our service at 5am. I saw pt at 11:00am and she was feeling much better, had eating a good breakfast. We observed a few more hous and she continue to feel wall at 2:00. She desired discharge. Resident discussed w/ family. Pt discharged home. DISCHARGE SUMMARY BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider at Discharge: DO Admission Date: 3/4/2022 Discharge Date: 3/5/2022 HOSPITAL PROBLEMS 1. COVID-19 2. Sepsis, resolved 3. Generalized Weakness 4. Type 2 Diabetes Mellitus 5. History of DVT 6. Hypertension 7. History of CAD No changes to home medication regimen PROCEDURES/IMAING Chest X-Ray DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: Patient is a 83 y.o. female presenting with chills, generalized weakness. Sepsis 2/2 COVID-19: SIRS Criteria, febrile, leukocytosis, lactic acidosis with source of infection. Tested positive for COVID-19. Chest x-ray negative for acute cardiopulmonary process. Urinalysis negative for UTI. With positive COVID test, no antibiotics were initiated for sepsis. Admitted for further evaluation and management. Patient was not hypoxic and did not require supplemental oxygen, steroids, or antivirals (remdesevir) during hospitalization for treatment of COVID-19. Timeline of symptoms unclear. Did discuss with patient and family that symptoms could potential worsen over the next few days, possibly requiring return to hospital. Patient medically stable, patient desired to discharge with plan to monitor symptoms at home over next few days. Chronic conditions: Stable throughout hospitalization. No change to home medication regimen. BP 119/88 | Pulse 66 | Temp 37.1 ?C (Oral) | Resp 18 | Ht 1.626 m | Wt 62 kg | SpO2 94% | BMI 23.46 kg/m? Physical Exam General: Alert, NAD Cardiac: RRR, no murmur Pulmonary: CTA bilaterally Abdomen: Soft, NTND MSK: No peripheral edema DISCHARGE RECOMMENDATIONS: Follow up after 10 days of quarantine (ending approximately 3/14) DISCHARGE DISPOSITION: Home without services CONDITION ON DISCHARGE: Stable and improved H&P: History and Physical HOSPITALIST Chief complaint Chills and weakness. Problem List Principal Problem: COVID-19 Active Problems: Generalized weakness DM (diabetes mellitus) (HCC) HTN (hypertension) History of DVT (deep vein thrombosis) left Popliteal vein - Unprovoked - Assessment and Plan Medical Decision Making This is an 83 years old lady who was presented to the emergency department because of generalized weakness, chills, and fever. Her COVID-19 PCR came back positive and the patient has elevated lactic acid and leukocytosis. She does not have hypoxia and her chest x-ray did not show any acute cardiopulmonary process. 1. COVID-19 infection. Present admission. Associated with fever, chills, and generalized weakness. The patient denied difficulty breathing, coughing, diarrhea, and vomiting. She does not have hypoxia. The patient is not qualified for dexamethasone or other COVID-19 treatment. Will give symptomatic treatment including Tylenol for fever and pain. Will give Lovenox for DVT prophylaxis. 2. Sepsis with fever, leukocytosis, and elevated lactic acid. Present admission. Associated with COVID-19 infection. The patient urinalysis did not show any evidence of urine tract infection and her chest x-ray did not show any evidence of acute cardiopulmonary process. Will follow the trend of white blood cell count and will give Tylenol for fever as needed. Will check lactic acid there is morning. Because of the patient COVID-19 infection, will avoid giving more IV fluid boluses. 3. Generalized weakness and physical deconditioning. Will ask PT OT to evaluate the patient and the need for potential placement or home therapy PT/OT. 4. Diabetes mellitus type 2. Will hold all oral hypoglycemic medications. We will put the patient on 24 hour corrective insulin. Latest blood sugar 161. 5. History of DVT in the past. The patient is going to be on Lovenox 40 mg subcutaneous daily. 6. Code status. Full code. I discussed with the patient her clinical presentation, as well as my assessment plan. All her questions were answered. This is a telemedicine admission, history and physical, observation status. History of Present Illness History and physical obtained using telehealth technology with the assistance of the bedside nurse. Patient is a 83 y.o. female who presents to hospital with chills and weakness. The patient is known to have history of diabetes mellitus type 2, DVT, hypertension, and mitral regurgitation. She lives alone at home and her daughter visits her between 2 and 3 times a day and check on her. The patient is a poor historian and most of the informations about her were taken from the emergency department documentations, and bedside nursing staff. The patient's daughter on noticed that the patient has been getting chills with generalized weakness but without documented fever at home. No reports of abdominal pain, vomiting, diarrhea, dysuria, chest pain, no difficulty breathing. She brought her to the emergency department for evaluation where the patient was found to have fever 38.6? C. The patient initial workup showed lactic acid 4.2, leukocytosis 12.2, and COVID-19 PCR rapid test positive. However the patient chest x-ray did not show any acute cardiopulmonary process. After initial IV fluid 1 L bolus in the emergency department, lactic acid decreased from 4.2 down to 2.4. Despite the patient lack of hypoxia, as well as dyspnea and coughing, she was very weak to be discharged home which she lives by herself. The patient is going to be admitted to the hospital for treatment, as well as potential placement. Review of Systems Review of Systems Constitutional: Positive for activity change (Decreased tolerance to activities.), chills, fatigue and fever. HENT: Positive for hearing loss ( baseline of hard of hearing.) and congestion. Negative for hoarse voice. Respiratory: Negative for cough, wheezing and shortness of breath. Cardiovascular: Positive for leg swelling ( chronic bilateral lower extremity edema. More on the left side.). Negative for chest pain. Gastrointestinal: Negative for vomiting, abdominal pain and diarrhea. Genitourinary: Negative for dysuria. Neurological: Negative for headaches. Psychiatric/Behavioral: Negative for hallucinations, hyperactivity, behavioral problems and decreased concentration. Objective BP 157/81 | Pulse 87 | Temp 37.1 ?C (Oral) | Resp 20 | Ht 1.626 m | Wt 62 kg | SpO2 93% | BMI 23.46 kg/m? Physical Exam Vitals and nursing note reviewed. Constitutional: General: She is in acute distress. Appearance: She is not ill-appearing or toxic-appearing. HENT: Head: Normocephalic. Cardiovascular: Rate and Rhythm: Regular rhythm. Heart sounds: No murmur heard. Pulmonary: Effort: No respiratory distress. Breath sounds: Rhonchi present. No wheezing. Abdominal: Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: Right lower leg: Edema present. Left lower leg: Edema present. Skin: Coloration: Skin is not jaundiced. Neurological: Mental Status: She is alert and oriented to person, place, and time. Motor: Weakness (Generalized weakness.) present. Comments: Slow mentation. Psychiatric: Behavior: Behavior normal. Behavior is not aggressive, hyperactive or combative. Thought Content: Thought content normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: DR CHEST 2 VIEWS FRONTAL AND LATERAL Resulted: 03/04/22 2345 Order Status: Completed Updated: 03/04/22 2347 Narrative: EXAMINATION: Frontal and Lateral View Chest EXAM DATE: 3/4/2022 11:36 PM TECHNIQUE: Frontal and lateral views INDICATION: Fever chills. COMPARISON: 7/22/2021 and 1/21/2021. ENCOUNTER: Not applicable _________________________ FINDINGS: No change in mild cardiomegaly. Coronary artery stent. Stable tortuous descending thoracic aorta. Aortic atherosclerotic disease. Normal pulmonary vasculature. Chronic elevation of the left diaphragm accentuated by gas in the stomach. Clear lungs. No pleural effusions or pneumothorax. Osteopenia. Mild hyperkyphotic curvature of the thoracic spine. Severe left glenohumeral joint osteoarthritis. _________________________ Impression: No acute cardiopulmonary process. Comprehensive Metabolic Panel (CMP) (Abnormal) Collected: 03/04/22 2254 Order Status: Completed Specimen: Blood, Venous Updated: 03/04/22 2325 Sodium Level 139 134 - 146 mmol/L Potassium Level 4.3 3.4 - 5.0 mmol/L Chloride 95 Low 98 - 112 mmol/L HCO3 27 21 - 29 mmol/L Anion Gap 17 9 - 18 mmol/L Glucose Level 161 High 70 - 99 mg/dL Blood Urea Nitrogen 23 High 8 - 20 mg/dL Creatinine 0.93 0.50 - 1.10 mg/dL MDRD eGFR 58 Low >=60 mL/min/1.73 CG eCrCl 38 mL/min/1.73 m2 Calcium Level Total 9.9 8.6 - 10.4 mg/dL Protein Total 8.7 High 6.0 - 8.0 g/dL Albumin Level 4.0 3.5 - 5.0 g/dL Bilirubin Total 0.4 0.2 - 1.0 mg/dL Alkaline Phosphatase 114 High 35 - 104 IU/L ALT w/ P5P 36 High 0 - 35 IU/L AST w/ P5P 36 High 0 - 35 IU/
Aktuelle Erkrankungen: -
Vorgeschichte: Past Medical History: Diagnosis Date ? ACE inhibitor induced angioedema ? DM (diabetes mellitus) (HCC) ? History of DVT (deep vein thrombosis) left Popliteal vein - Unprovoked - 9/3/2021 ? HTN (hypertension) ? Hypercholesterolemia ? Menopause age 45 with full hysterectomy ? Mitral regurgitation - moderate Echo 2013 ? Osteoporosis ? Venous insufficiency
Andere Medikamente: amLODIPine Besylate 5 mg Oral Daily Calcium-Magnesium-Zinc 1 tablet Oral Daily cloNIDine HCl 0.1 mg Oral 2 times daily Clopidogrel Bisulfate 75 mg Oral Nightly Dulaglutide 3 MG/0.5ML INJECT 3 MG UNDER THE SKIN ONCE PER WEEK Empagliflozin 10
Allergien: losartan - angioedema
Vorherige Impfungen: -

VAERS 2161672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 17.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / AR

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

Burning sensation Cardiac stress test Computerised tomogram Cough Discomfort Dizziness Dyspnoea Electrocardiogram Fluid retention Pain Pulmonary function test Respiratory syncytial virus infection Respiratory tract congestion Swelling X-ray

Symptomtext

Dec 20, 2021, I called ambulance. I went to the ER. I was extremely dizzy, difficulty breathing, acute congestion, swelling and soreness. I had a burning sensation in chest around heart, left/right and behind heart. Lots of fluid in lungs; difficulty with coughing to expel phlegm. I was released after testing, although I was still in acute discomfort and having difficulties breathing. Dec 21, 2021, I drove myself to the hospital emergency room with same symptoms. I was released in acute discomfort, distress and having difficulties breathing. Both times, I tested negative for COVID-19. I was told I had RSV, but I believe I had a reaction to my 3rd dose of Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Temperature, EKG, blood pressure/pulse rate, blood oxygen and x-rays done at ER. Pulmonary function testing, stress test and CAT scan. COPD (found out after pulmonary testing at hospital after reaction to 3rd dose of Pfizer).
Aktuelle Erkrankungen: -
Vorgeschichte: COPD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2151818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MO
Alter: 65,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 26.03.2021
Beginn: 18.02.2022
Tage bis Beginn: 329,0
Dosis: 3
Route/Site: SYR / -

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

Ageusia Anosmia COVID-19 Chills Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Fatigue Gastric disorder Headache Pyrexia Rectal haemorrhage Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Fever, chills, congestion, cough, SOB, fatigue, headache, loss of smell/taste, gastric sxs, (+) COVID, worsening COPD, rectal bleeding after mAb treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 6,0
Labordaten: 2/22: Reatl-Time Reverse Transcriptase PCR (+) COVID 2/25: Polymerase Chain reaction (PCR), (+) COVID
Aktuelle Erkrankungen: COPD
Vorgeschichte: COPD
Andere Medikamente: None reported
Allergien: NKA
Vorherige Impfungen: -

VAERS 1867779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NC
Alter: 26,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / RA

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

Dyspnoea Malaise Movement disorder Muscle contracture Muscle spasms

Symptomtext

Intense, painful muscle cramping; contraction in abdomen, sides, and back; Painful to move; Difficulty breathing; I felt sick; It was the most intense pain /I was not and currently am not pregnant, but I imagine that is what birthing contractions feel like".; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 26 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 10Nov2021 14:30 (Lot number: FH8030) at the age of 26 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA), intramuscular, administered in arm left, administration date 10Nov2021 (Batch/Lot number: unknown). The patient had no relevant medical history. Concomitant medication(s) included: TRI-ESTARYLLA taken for contraception, start date: Sep2014 (ongoing). Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8729, Location of injection: Arm Left, Vaccine Administration Time: 07:30 PM), administration date: 06Apr2021, when the patient was 25 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6206, Location of injection: Arm Right, Vaccine Administration Time: 07:15 PM), administration date: 13Mar2021, when the patient was 25 years old, for Covid-19 immunization. The following information was reported: MUSCLE SPASMS (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (11Nov2021), described as "Intense, painful muscle cramping"; MUSCLE CONTRACTURE (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (11Nov2021), described as "contraction in abdomen, sides, and back"; MOVEMENT DISORDER (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (11Nov2021), described as "Painful to move"; DYSPNOEA (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (Nov2021), described as "Difficulty breathing"; MALAISE (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (Nov2021), described as "I felt sick"; ABDOMINAL PAIN (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (11Nov2021), described as "It was the most intense pain /I was not and currently am not pregnant, but I imagine that is what birthing contractions feel like".". Therapeutic measures were taken as a result of muscle spasms, muscle contracture, movement disorder, malaise, abdominal pain. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There was no relevant past drug history. There were no known allergies. 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's family medical history relevant to AE(s) was none. Relevant tests performed were none. There were no specific relevant tests. The patient got the general influenza vaccine at the same time as the booster of the Pfizer covid-19 vaccine. This was advertised as safe to do by Pharmacy. Early the following morning (4:30 AM), she felt sick and got at of bed to go to the bathroom. After getting back into bed, she experienced these muscular contractions in her abdomen, side and back. It became painful and difficult to breathe. Her muscles would not relax. She took some ibuprofen. It was not until her fiancee giving her a heating pad, that her muscles relaxed at all. It was extremely painful and lasted for about 1 hour. She was then able to fall asleep and no longer had any muscle pain & contraction. It was most intense pain she had ever had in her life. She was not and currently was not pregnant, but she imagined that what birthing contraction feel like. Booster dose due to high risk of frequent institutional and occupational exposure to corona virus (and at risk of serious covid-19 complications were checked. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1867779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NC
Alter: 26,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Dyspnoea Malaise Movement disorder Muscle contracture Muscle spasms

Symptomtext

Intense, painful muscle cramping; contraction in abdomen, sides, and back; Painful to move; Difficulty breathing; I felt sick; It was the most intense pain /I was not and currently am not pregnant, but I imagine that is what birthing contractions feel like".; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 26 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 10Nov2021 14:30 (Lot number: FH8030) at the age of 26 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA), intramuscular, administered in arm left, administration date 10Nov2021 (Batch/Lot number: unknown). The patient had no relevant medical history. Concomitant medication(s) included: TRI-ESTARYLLA taken for contraception, start date: Sep2014 (ongoing). Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8729, Location of injection: Arm Left, Vaccine Administration Time: 07:30 PM), administration date: 06Apr2021, when the patient was 25 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6206, Location of injection: Arm Right, Vaccine Administration Time: 07:15 PM), administration date: 13Mar2021, when the patient was 25 years old, for Covid-19 immunization. The following information was reported: MUSCLE SPASMS (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (11Nov2021), described as "Intense, painful muscle cramping"; MUSCLE CONTRACTURE (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (11Nov2021), described as "contraction in abdomen, sides, and back"; MOVEMENT DISORDER (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (11Nov2021), described as "Painful to move"; DYSPNOEA (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (Nov2021), described as "Difficulty breathing"; MALAISE (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (Nov2021), described as "I felt sick"; ABDOMINAL PAIN (non-serious) with onset 11Nov2021 04:30, outcome "recovered" (11Nov2021), described as "It was the most intense pain /I was not and currently am not pregnant, but I imagine that is what birthing contractions feel like".". Therapeutic measures were taken as a result of muscle spasms, muscle contracture, movement disorder, malaise, abdominal pain. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There was no relevant past drug history. There were no known allergies. 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's family medical history relevant to AE(s) was none. Relevant tests performed were none. There were no specific relevant tests. The patient got the general influenza vaccine at the same time as the booster of the Pfizer covid-19 vaccine. This was advertised as safe to do by Pharmacy. Early the following morning (4:30 AM), she felt sick and got at of bed to go to the bathroom. After getting back into bed, she experienced these muscular contractions in her abdomen, side and back. It became painful and difficult to breathe. Her muscles would not relax. She took some ibuprofen. It was not until her fiancee giving her a heating pad, that her muscles relaxed at all. It was extremely painful and lasted for about 1 hour. She was then able to fall asleep and no longer had any muscle pain & contraction. It was most intense pain she had ever had in her life. She was not and currently was not pregnant, but she imagined that what birthing contraction feel like. Booster dose due to high risk of frequent institutional and occupational exposure to corona virus (and at risk of serious covid-19 complications were checked. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2128298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NC
Alter: 66,0
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: 21.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Tinnitus

Symptomtext

Have had tinnitus (constant, both ears) for a number of years. Perceived noise levels (constant) increased significantly to a level which is sometimes sufficiently distracting that I feel the need to depart discussions, work meetings, presentations, church services, etc for an environment with lower ambient noise levels.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: To date, I have not sought examination for this issue.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Dutasteride-Tamulosin 0.5-0.4MG
Allergien: NKA
Vorherige Impfungen: -

VAERS 2113099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 01.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: UN / LA

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

Blood thyroid stimulating hormone Cardiac stress test Dyspnoea Electrocardiogram abnormal Full blood count Glycosylated haemoglobin Lipids Low density lipoprotein Palpitations Thyroxine Tri-iodothyronine Ventricular extrasystoles

Symptomtext

A month after getting the shots I started experiencing heart palpitations, heart racing rapidly and shortness of breath around January 9 or 10th of 2022. The shortness of breath had been ongoing before due to lingering effects from covid that I got in January of 2021 but now the heart was racing and palpitating. Saw my family doctor January 11th. She discovered on the stethoscope pvc's were happening and sent me to a cardiologist immediately. Saw Dr. and had a heart monitor for a week, ectocardiogram and stress test. I have pvc's randomly due to the covid shots was the probable cause. I still have the problem currently at random times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CBC, Hemoglobin A1C, Lipid panel with reflex to direct LDL, Stress test, T4 free, TSH, T3, CV Trans-thoracic Electrocardiogram. Seeing PVC's in heart beat 2, pauses, beats 3,4.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Levothyroxine 200 mg
Allergien: Penicillin, Codeine, Latex
Vorherige Impfungen: -

VAERS 2201080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 30.11.2021
Beginn: 26.12.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cardiac imaging procedure normal Chest X-ray normal Cough Dyspnoea Fatigue Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 11/09/21, Pfizer, dose#1 11/30/21, Pfizer, dose #2 01/03 COVID swab, result: detected 12/26/21 pt cc: cough, congestion, fatigue, shortness of breath, exposure: unknown 01/03 CXR impression: 2 views of the chest. No coalescent lung consolidation. No pneumothorax. No pleural effusion. Cardiac silhouette within normal limits. No acute osseous abnormality seen 01/03/22 pt admit ED cc: cough, congestion, fatigue, shortness of breath, dx: Covid-10 LOS:1 day 01/06 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/03 COVI 01/03 CXR impression: 2 views of the chest. No coalescent lung consolidation. No pneumothorax. No pleural effusion. Cardiac silhouette within normal limits. No acute osseous abnormality seen.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2101789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 05.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Neck pain

Symptomtext

Chest pain and left neck pain while jogging. Sharp chest pain when laying down.

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

VAERS 2099906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: SC
Alter: 30,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 19.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: SYR / RA

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

Blood potassium decreased Cardiac discomfort Cardiac flutter Dyspnoea Electrocardiogram normal Headache Immediate post-injection reaction Injection site pain Nausea Palpitations Paraesthesia

Symptomtext

Immediately after getting the shot I felt a little nausea, had a headache and soreness in the area that I received the shot. The soreness remained for about 3 days and I was fine after. At about January 25, is when I started noticing heart palpitations. My heart felt like it was constantly fluttering unevenly and every now and then I could feel a "squeezing" sensation on my heart that would result in a "tingling" in my left hand. It occurred on and off for days. Before scheduling my appointment to see the doctor, my significant other mentioned that I seemed a lot more of of breath lately when speaking and doing regular tasks. When I went to the doctor and explaining the situation, they ran an Ekg/ECG to monitor my heart and everything came out normal. Several other blood work tests were ran to look at my levels and all of them came back good. My Potassium was .1 below what was considered the norm so I was given a small dose of Potassium to take over the next few days. At this time, I am currently not having any palpitations. The last I had them was on 2/5/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood work came out fine other than my Potassium being 0.1 below the norm. EKG/ECG came out fine.
Aktuelle Erkrankungen: N./A
Vorgeschichte: N/A, has asthma and bronchitis years ago. No inhaler needed now.
Andere Medikamente: Junel Fe - Generic
Allergien: N/A, allergic to dust
Vorherige Impfungen: -

VAERS 2098597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain upper Blood pressure increased COVID-19 Chills Diarrhoea Dyspnoea exertional Eye haemorrhage Fatigue Malaise Oropharyngeal pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Later that night after the vaccine I developed a little fatigue which lasted about 24hrs. On 1/4 I developed a broken blood vessel in my eye so I went to see my PCP and my BP was elevated at that time so I was prescribed Metoprolol. On 1/20 I developed a runny nose and a little sore throat. Chills developed as well and the next day I developed a fever so I went to the local Urgent Care where 2 COVID test were performed and both were positive for COVID-19. I was given a shot of prednisone and a B12 shot, Zithromax. I still didn't feel well and was extremely fatigue, a stomach ache followed by diarrhea so I took the pills that were prescribed at the urgent care. The sore throat finally went away, but to date I am still dealing with the congestion, a little fatigue, and I still have a little SOB with exertion but it has lessened significantly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: 2 COVID-19-positive.
Aktuelle Erkrankungen: no
Vorgeschichte: Hypothyroid, Hypo cholesterol, Hypertension
Andere Medikamente: Lipitor 40mg, Hydrochloride 12.5, Levothyroxine, Metoprolol 25mg, baby aspirin
Allergien: no
Vorherige Impfungen: -

VAERS 2095733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: DE
Alter: 44,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 27.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Asthenia Cold sweat Dyspnoea Hyperhidrosis Influenza Pallor Palpitations

Symptomtext

The day after (Sunday, November 28th) the second vaccine (Saturday, November 27th), while I was resting (watching a movie), I had one hour were my heart was racing uncontrollably and I had difficulty breathing/shortness of breath. I also was sweating and clammy, felt like I was going to pass out, and I was very pale in color in my face. On (Wednesday, December 1st this same situation occurred again when I was teaching; this time it lasted 30-40 minutes. I felt very weak after each episode. In addition to these two episodes I also felt flu-ish for 7-10 days. *NOTE: after my first vaccine I felt very sick (flu-ish symptoms) for 7-10 days; more than the typical 3-5 days that is noted.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Celiac's Disease Hashimoto's Disease Interstitial Cystitis Chronic Migraines
Andere Medikamente: I take Levoxyl (for thyroid and Hashimoto's disease), Amitriptyline (for migraines), and multivitamins. None were taken within an hour of the vaccine.
Allergien: Allergic to gluten (Celiac's Disease), latex, and morphine.
Vorherige Impfungen: -

VAERS 2095519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 31,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Dyspnoea Headache Hypoaesthesia Illness Myalgia Oropharyngeal pain Pain Palpitations Paranasal sinus discomfort Respiratory tract congestion Rhinorrhoea

Symptomtext

Sore throat, runny nose, congested, sinus pressure, headache, body/muscle aches, trouble breathing at night, and heart palpitations. Woke up from half my face being numb- lasted ~20 min. Was sick up until 2nd dose then sick again for another 2 weeks. Body aches still have not gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Seroquel, Lamotrigine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2092792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OH
Alter: 74,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 14.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Alopecia COVID-19 Cardiac monitoring Palpitations

Symptomtext

After my 2nd shot on 2/1, I had extreme hair loss, it came back over the summer On 9/12, I was diagnosed with Covid 19. On December 14 I got my Phizer booster In December I started loosing my hair again and it came out in handfuI In January I was put on a heart monitor for 30 day for heart palpitations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Heart monitor on 1/8/2022 and removed today 2/8/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Have asthma since I was 10 years old
Andere Medikamente: omperazole 40mg, Linsopril 20 mg, Montelukast 10 mg, Diltiazem 180 mg/24 hr, Pravastatin 40 mg, Vitamin B12, Probiotic, Biotin
Allergien: -
Vorherige Impfungen: -

VAERS 2091848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: VA
Alter: 46,0
Geschlecht: M
Eingang: 06.02.2022
Impfdatum: 01.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: SYR / LA

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

Headache Hypoaesthesia Laboratory test Migraine Vaccination complication Vision blurred

Symptomtext

Started with a sharp headache in the back left of my head about two hours after shot. Headache got worse over two days. On afternoon of second day, Monday Nov 29 Nov 2021 my left side of my face went numb and my left eye became blurry. The following morning the entire left half of my body went numb. I went to the ER on 30 Nov 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: 2,0
Labordaten: Numerous tests were taken at the ER. Suspicion was a vaccine induced migraine. I recovered 1 December 2021 from all symptoms with the exception of lingering numbness in my left cheek.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Alegra
Allergien: None
Vorherige Impfungen: -

VAERS 2086169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: KY
Alter: 13,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 04.12.2021
Beginn: 08.01.2022
Tage bis Beginn: 35,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain Abdominal pain upper Abdominal tenderness Acidosis Acidosis hyperchloraemic Activated partial thromboplastin time shortened Alanine aminotransferase increased Amylase normal Anticoagulant therapy Anticoagulation drug level Antithrombin III Aspartate aminotransferase increased Bacterial test positive Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate decreased Blood bilirubin normal Blood calcium normal

Symptomtext

ICC visit 1/8/22 patient has been sick since yesterday, with vomiting,diarrhoea , chills ( no fever ) headache, sore throat.ea ache bodyaches, clear runny nose, dry cough, SOB, has asthma Mom states she is exposed to COVID-19 and patient wants to get tested for COVID -19 1/14/22 ED note:Presented due to tender nodules on bilateral arms. Patient developed COVID symptoms 1/7 and tested positive the next day. She received sotrovimav 1/9 with improvement in symptoms two days later; however, two days ago, she developed a sharp pain in the right AC and realized there was a nodule there. She also developed nausea, vomiting, decreased PO intake, abdominal pain, and orange urine. She has been treating with zofran, tylenol, and motrin at home. She then developed a second nodule on her L forearm yesterday and a third nodule on her L AC this AM. ID and pharmacy were contacted yesterday but have not heard of nodules occurring with sotrovimav infusions. Of note, IV for infusion was in the right hand. No hx of blood clots but patient on birth control. On exam, nodules are tender to palpation (clinical photography in chart). She complains of right sided abdominal pain but abdomen soft. No lymphadenopathy. No fever since initial COVID symptoms began prior to infusion. Acetaminophen (TYLENOL PO) Take by mouth. albuterol HFA 108 (90 Base) MCG/ACT inhaler Inhale 4 puffs into the lungs every 4 (four) hours as needed for Wheezing or Shortness of Air cetirizine (ZYRTEC) 10 MG tablet Take 40 mg by mouth 20 mg AM 20 MG PM. Cholecalciferol 250 MCG (10000 UT) CAPS Take 250 mcg by mouth daily. clindamycin (CLINDAGEL) 1 % gel APPLY TO AFFECTED AREA TWICE DAILY cyclobenzaprine (FLEXERIL) 5 MG tablet Take 1 tablet by mouth 2 (two) times daily as needed for Muscle spasms. EPINEPHrine (EPIPEN) 0.3 MG/0.3ML SOL A-IJ use as directed by prescriber for ALLERGIC REACTION famotidine (PEPCID) 20 MG tablet Take 20 mg by mouth 2 (two) times daily. ferrous gluconate (FERGON) 324 MG tablet Take 1 tablet by mouth 2 (two) times daily. levonorgestrel-ethinyl estradiol (SEASONALE) 0.15-0.03 MG Take 1 tablet by mouth daily Take in a continuous manner, skipping placebo week and moving directly to next new pack meloxicam (MOBIC) 7.5 MG tablet Take 1 tablet by mouth daily. midodrine (PROAMATINE) 5 MG tablet Take 1 tablet by mouth Twice a Day for 7 days, THEN 2 tablets Twice a Day. Afternoon dose no later than 4 :00 pm. (Patient taking differently: THEN 2 tablets Twice a Day. Afternoon dose no later than 4 :00 pm.) montelukast (SINGULAIR) 5 MG chewable tablet Chew 5 mg by mouth nightly . polyethylene glycol (GLYCOLAX) powder Take 17 g by mouth as needed for Constipation : Mix in 4 oz of water/juice/milk. rizatriptan (MAXALT) 10 MG tablet Take 1 tablet by mouth as needed for Migraine, may repeat once in 2 hrs - max 30 mg/24 hrs. Spacer/Aero-Holding Chambers DEVICE Use 1 each as needed (For use with albuterol inhaler) tiotropium (SPIRIVA RESPIMAT) 1.25 MCG/ACT AERS inhalation Inhale 1 puff into the lungs nightly . topiramate (TOPAMAX) 25 MG tablet Take 1 tablet by mouth 2 (two) times daily for 7 days, THEN 2 tablets 2 (two) times daily. traZODone (DESYREL) 50 MG tablet Take 1 tablet by mouth nightly triamcinolone (KENALOG) 0.1 % ointment Apply topically 2 (two) times daily to affected area(s) of bilateral axilla twice a day for up to 2 weeks as needed. triamcinolone (NASACORT ALLERGY 24HR) 55 MCG/ACT nasal inhaler Instill 2 sprays into nose 2 (two) times daily 2 spray every day and she can use 4 spray PRN. WIXELA INHUB 250-50 MCG/DOSE AEPB inhaler INL 1 PUFF PO Q 12 HOURS. RM AFTER U 1/17/22-dischaHospital Course (by problem): Thrombophlebitis On admission, she had a exquisitely tender nodules without overlying erythema or rash in the superior aspect of the right antecubital fossa, left antecubital fossa, and anterior aspect of left forearm. The left forearm nodule had a hyperpigmented streak starting at the nodule and extending toward the hand. Her differential included nodular lymphangitis felt less likely due to lack of exposures and BL findings, new viral infection such as EBV, CMV, complications of the COVID itself or a reaction to her Sotrovimab. A Hepatitis panel was negative and EBV and CMV titers were sent and serial CMPs were ordered. She was initially just admitted on motrin prn with her home medications, PO ad lib and MIVFs. Infectious Disease and Heme Onc were consulted. By the next morning, her physical exam was notable for an "L" shaped hyperpigmented, painful lesion on the left forearm and this and her other lesions seemed more hard and cord like more so than mobile nodules or lymph nodes. Given this and the fact that she had multiple risk factors for increase risk of clotting (lupus anticoagulant, obesity, birth control, acute COVID-19 infection, and venous stasis), physical exam findings were felt to be most consistent with superficial thrombophlebitis. Pediatric ID and Heme/Onc agreed. A hypercoagulable work-up was initiated and she was started on Lovenox 40mg BID (prophylactic dose) for at least 2 weeks, stopping her estrogen-containing birth control during this time. She did develop some posterior calf and BL foot pain with a cord over her R foot and BL foot hyperpigmented streaking but these rapidly resolved and her UE lesions greatly improved. She'd also remained afebrile in house and repeat BL LE doppler was also again negative. By the day of discharge she had only some improving L forearm pain with improved TTP and discoloration and only mild BL AC TTP with minimal remaining masses with superficial changes. Heme Onc thus did not feel she needed increased to therapeutic dosing or Anti-Xa levels. Her mother, pharmacy, ID and Heme Onc were all okay with discharge to home. Her mother, already familiar with giving her sister injections for eczema, was easily able to take over her Lovenox injection in house and voiced comfort with doing so at home. She was then sent home in good condition. Her d-dimer was only mildly elevated at 612 and her homocyteine and ATIII had resulted as nml with Prothrombin, Factor V Leiden, Lipoprotein A, Pro C and Pro S as well as her EBV and CMV titers all still pending at the time of discharge. She will be followed up in 2 weeks at Hematology and ID. The length of her Lovenox and hold on OCPs will be readdressed at that time. Transaminitis with hyperbili and mild hypoalbuminemia on RUQ Pain, N/V, poor PO On admission, Hepatitis panel was normal and EBV/CMV testing were still in process at the time of discharge. Transaminitis was felt to be secondary to viral infection versus regular tylenol use during her COVID-19 infection versus COVID-19 itself. Throughout admission, CMP were trended. Her bili normlized, her alb dipped to 3.3 but was back up to 3.7 and AST and ALT downtrended to 82 and 526 respectively. Her RUQ tenderness improved some and then stabilized, her N/V resolved and her oral intake improved. She will continue to avoid tylenol (and motrin given her Lovenox) and needs another repeat CMP on 1/19/22 to continue to follow. Mild Hyperchloremic Acidosis on Dehydration Her Cl- bumped to 115 likely from her IVFs with a likely related mild acidosis to 19. Ketosis and her dehydration may have played roles as well. Her UOP normalized and her PO intake improved as above. She was off IVFs by HD#2. Her Cl and HCO3 improved to stable at 110 and 18 on last checks. Abnormal urine Her nurse noted some possible urine sediment on the night prior to d/c. Her UA was abnormal with moderate LE, 4 WBCs and trace bacteria but as she was not having any symptoms of a UTI this was not cultured. Repeat UA by her PMD is recommended. Of note her urobili was negative and her orange urine color change had resolved however as expect as her her hyperbili resolved and with hydration. Significant Hospital Labs: 1/14/2022 09:31 1/15/2022 04:49 1/15/2022 16:19 1/16/2022 05:37 1/17/2022 04:44 C-Reactive Protein <0.1 <0.1 Sodium 142 143 143 140 142 Potassium 3.6 3.7 4.2 4.1 4.0 Chloride 109 (H) 113 (H) 115 (H) 112 (H) 110 (H) CO2 22 22 19 (L) 22 18 (L) Glucose 111 (H) 88 101 (H) 103 (H) 107 (H) BUN 7 6 (L) 7 11 10 Creatinine 0.59 0.57 0.60 0.57 0.58 Total Protein 7.0 6.1 (L) 6.1 (L) 6.7 (L) Albumin 3.9 (L) 3.3 (L) 3.5 (L) 3.3 (L) 3.7 (L) Globulin 3.1 2.8 2.8 3.0 Calcium 9.8 8.8 8.8 9.0 9.5 Bilirubin-Total 0.9 (H) 0.8 (H) 0.4 0.4 ALT/SGPT 1,020 (H) 967 (H) 723 (H) 526 (H) AST/SGOT 442 (H) 431 (H) 173 (H) 82 (H) Alkaline Phosphatase 89 76 73 77 Phosphorus 3.5 Homocysteine 7.0 Amylase 24 (L) Lipase 15 1/14/2022 11:00 1/15/2022 17:34 1/16/2022 11:16 PT 11.9 INR 1.0 PTT 31.7 D-Dimer Quantitative 612 (H) AntiThromb III Func 114 Heparin LMW 0.29 1/15/2022 04:49 Hepatitis A IgM Ab Nonreactive Hepatitis B Surface Ag Nonreactive Hepatitis B Core Ab(IgM) Nonreactive Hepatitis C Ab Nonreactive 1/14/2022 09:31 WBC 5.00 RBC 4.88 HGB 13.1 HCT 39.4 MCV 80.7 MCH 26.8 MCHC 33.2 Platelet Count 403 Significant Hospital Imaging/Diagnostic Tests: Duplex US Venous Bilateral LE (1/14) Impression: No evidence of deep veinous thrombosis involving either lower extremity. Duplex US Venous Bilateral UE (1/14) IMPRESSION: No evidence of upper extremity deep venous thrombosis. Duplex US Venous Bilateral LE (1/16) IMPRESSION: No obvious evidence of thrombosis noted in the imaged part of bilateral lower extremities veins as described above. Abdominal US (1/14) FINDINGS: The liver demonstrates normal echotexture without focal defect or mass evident. Common duct is normal measuring 2 mm. Gallbladder is within normal limits for appearance. Visualized pancreas is unremarkable. Tail of pancreas is obscured by bowel gas. Kidneys are normal size measuring 9.6 cm on the right and 10.6 cm in length on the left. No renal mass lesion is visible. No hydronephrosis seen. Spleen demonstrate normal echotexture measuring 9.6 cm . Doppler evaluation demonstrates that the hepatic veins are patent. The portal vein is also patent and demonstrates normal direction of flow. Normal resistive index and waveform of the hepatic artery. IVC and aorta are grossly patent. Bladder demonstrates normal contour. IMPRESSION: No significant abnormality is identified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 3,0
Labordaten: 1/8/22 COVID Result IPOC PCR Not Detected Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Fibromyalgia, complex regional pain syndrome, potts disease
Andere Medikamente: Acetaminophen (TYLENOL PO) Take by mouth. o albuterol HFA
Allergien: Seasonal, Lyrica
Vorherige Impfungen: -

VAERS 2079578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8030

moderat

Staat: VA
Alter: 68,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 14.12.2021
Beginn: 19.01.2022
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: SYR / LA

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

Anxiety Dyspnoea Erythema Pain Palpitations

Symptomtext

Initial effects were soreness and redness. However, a couple of weeks later I experienced shortness of breath, anxiety, and a racing heart. This lasted for about an hour after which things calmed down. I have not had a repeated incident.

Weitere VAERSDATA-Felder

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

VAERS 2075918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 78,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 19.11.2021
Beginn: 23.01.2022
Tage bis Beginn: 65,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Patient presented to the hospital 1/24/2022 with progressive increasing dyspnea, COVID pneumonia and possible sepsis. Patient tested positive on 1/24/22. Onset of symptoms was 1/23/22. Patient was started on remdesivir and dexamethasone. Discharged 1/29/22. Previously vaccinated Pfizer 3/1/21, 3/23/21, 11/19/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: COVID19 PCR + 1/24/22
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, hyperlipidemia, COPD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 23.11.2021
Beginn: 09.01.2022
Tage bis Beginn: 47,0
Dosis: 3
Route/Site: IM / LA

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

Angioplasty Chest discomfort Chest pain Dyspnoea

Symptomtext

January 2022- started experiencing shortness of breath, pain/ pressure on chest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Hospitalized on 1/10. Angioplasties performed 1/11/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia
Andere Medikamente: Omeprazole, aspirin, amlodipine, atorvastatin, brilinta
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2074621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NH
Alter: 61,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 03.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain Abdominal pain upper Back pain Barium swallow normal Blood test normal Bowel movement irregularity Colonoscopy normal Computerised tomogram normal Culture stool Echocardiogram normal Electrocardiogram normal Endoscopy normal Heart rate increased Hypophagia Magnetic resonance cholangiopancreatography Nausea Pain Palpitations

Symptomtext

Began experiencing gripping stomach pain radiating to upper back 30 minutes to 1 hour after eating and at other times. Pain lasted from a few minutes to an hour or more. Also experienced hives on my legs and arms at the same time. On 11/9/21 went to ER for pain in stomach without having eaten in several hours. Given Protonix with no relief, sent home with Omeprazole. 11/9/21 to PCP for same symptoms and given Famotidine. Ultrasound on 11/12/21 - normal. 11/22/21 to PCP for continued abdominal pain - referred to Gastroenterologist. 12/20/21 - new symptoms of early am bowel movements along with heart palpitations, nausea, and shakiness which lasted through mid morning, at times all day. Weight loss ongoing since start of event, now at 10 plus pounds. 12/23/21 - barium swallow - normal. 12/24/21 - to local hospital ER for continued early am symptoms, continued weight loss. CT and Ultrasound done - all normal. MiraLAX, Bentyl, Zofran and omeprazole given. 12/28/2021 - to PCP who sent urgent referral for endocrinology and cardiology at local Hospital. Placed ZIO Patch on for 7 days. 1/5/2022-1/6/2022 - admitted to local Clinical Unit for same symptoms - Endoscopy, Colonoscopy and MRCP completed - all normal. Throughout all PCP, ER visits blood and urine tests continued to be normal. 1/8/2021 to local Hospital ER for am symptoms, heart rate at 133 BPMs, nausea, and shakiness. Consult with cardiology. Put on Metoprolol 1/2 of 25 mg tablet in am for tachycardia. 1/10/2021 Metoprolol stopped because blood pressure bottomed out. 1/14/2021 Cardiologist - EKG normal, Echocardiogram normal. 24 hour urine and 72 hour fecal test completed and both are normal. On Famotidine and Omeprazole now but told by GI to decrease as there is no sign of anything wrong showing in the numerous tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: See above.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fluticasone, Cetirizine, Gabapentin
Allergien: None
Vorherige Impfungen: -

VAERS 2062086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: CA
Alter: 91,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Injection site pain Limb injury Paraesthesia

Symptomtext

Site: Pain at Injection Site-Medium, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 2037861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NC
Alter: 60,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 07.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Burning sensation Condition aggravated Full blood count normal Headache Hypersensitivity Injection site pain Myalgia Pain Pain of skin Paraesthesia Sensitive skin Thyroid function test normal Vitamin D decreased

Symptomtext

After the Phizer COVID-19 booster I got the expected side effects of a sore arm at the injection site, some headaches, bad muscle aches and highly sensitive and aching skin. These side effects occurred about 1 day after the injection. I had the same side effects after the 2nd dose of the Phizer vaccine. With the second dose of the vaccine the side effects went away after a couple of days. However, after the booster injection not all side effects have gone away. The injection side pain and the bad muscle aches largely went away but the skin issues remain. It has now been about 6 weeks. The skin problem can happen anywhere on my body but it is most noticeable on my arms and legs. The legs are the most persistent. In my legs I have stinging skin pain and pins and needles feelings. The stinging at times gives the sensation of my legs being hot. The leg stinging skin is made worse by clothing touching my skin. The pins and needles feeling is worsened during hotter weather. Since the event started I have had my arms? skin badly ache and feel very sensitive to the touch along with pins and needle feelings. No visible skin rashes have been observed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No fever. Blood work normal (CBC) Thyroid function normal Slightly low vitamin D but not by much
Aktuelle Erkrankungen: None
Vorgeschichte: low back pain
Andere Medikamente: Famotidine 40mg/day Sertraline 25mg/day Trazodone 25 mg/day Saccharomyces Boulardi (supplement) 250mg/day
Allergien: None known.
Vorherige Impfungen: -

VAERS 2035565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OK
Alter: 29,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 04.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Back pain Condition aggravated Dizziness Headache Intermenstrual bleeding Vision blurred

Symptomtext

Vision blurred, severe headache, began spotting (menstrual), severe back pain, and dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Back pain.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2034944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: SC
Alter: 18,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthma Condition aggravated

Symptomtext

Between 7 pm 01/12/2022 and 10 pm 01/13/2022 patient had 6 asthma attacks, which were relieved with Albuterol inhaler. Patient advised not to receive anymore COVID-19 Pfizer vaccine in future.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Albuterol inhaler
Allergien: No
Vorherige Impfungen: -

VAERS 2554329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 51,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Hyperhidrosis Hypertension

Symptomtext

Headache, HYPERtension, Diaphoresis Narrative: Patient was monitored for 35 minutes, condition improved. Advised to consult primary care, go home. Spouse home and available to monitor

Weitere VAERSDATA-Felder

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

VAERS 2554238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 42,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Headache Myalgia Vomiting

Symptomtext

Headache, Myalgia & NauseaVomiting Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: yes, NAUSEA, HEADACHE AND MYALGIA AFTER 2ND PFIZER COVID VACCINE

VAERS 2515098

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Palpitations

Symptomtext

Palpitations Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2020788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: TX
Alter: 85,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 03.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / -

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

Drain site complication Dyspnoea Fatigue Haemoglobin decreased

Symptomtext

Patient placed in observation for shortness of breath/fatigue, inability to drain Pleurx, and hemoglobin drop

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: metastatic lung adenocarcinoma and loculated left pleural effusion with Pleurx drain in place
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 32,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 14.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Blood pressure increased Blood pressure measurement Dry mouth Dyspnoea Fatigue Gingival pain Gingival swelling Head discomfort Headache Heart rate Heart rate increased Inflammation Insomnia Oxygen saturation Oxygen saturation decreased Palpitations Swelling Symptom recurrence

Symptomtext

oxygen was going down/oxygen was down to low 80s; got gum recession from it, that is how bad they were swollen from it; head hurt; Sore gums; Toothache; his eyes he has to focus a bit to see; his whole body was swelling so bad that he could feel his body, organs, skull, and neck was so bad; when he lay down he could hear crackling and popping in his skull; couldn't sleep; inflammation; Dry mouth; heart rate would go up; shortness of breath; blood pressure 130/95; he always feels worn out.; heart palpitations; my symptoms came back worse; 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 32 year-old male patient received bnt162b2 (BNT162B2), administered in arm, administration date 14Nov2021 (Lot number: FH8030) at the age of 32 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "COVID-19", start date: Jul2021 (unspecified if ongoing), notes: I had COVID-19. I been described as a long hauler.; "Blood pressure high", start date: Jul2021 (unspecified if ongoing); "Heart palpitations", start date: Jul2021 (unspecified if ongoing), notes: Heart palpitations; "heart rate was up", start date: Jul2021 (unspecified if ongoing), notes: heart rate was up. There were no concomitant medications. The following information was reported: OXYGEN SATURATION DECREASED (hospitalization) with onset Nov2021, outcome "unknown", described as "oxygen was going down/oxygen was down to low 80s"; HEADACHE (non-serious) with onset Nov2021, outcome "unknown", described as "head hurt"; GINGIVAL PAIN (non-serious) with onset Nov2021, outcome "not recovered", described as "Sore gums"; TOOTHACHE (non-serious) with onset Nov2021, outcome "not recovered", described as "Toothache"; VISUAL IMPAIRMENT (non-serious) with onset Nov2021, outcome "not recovered", described as "his eyes he has to focus a bit to see"; SWELLING (non-serious) with onset Nov2021, outcome "unknown", described as "his whole body was swelling so bad that he could feel his body, organs, skull, and neck was so bad"; HEAD DISCOMFORT (non-serious) with onset Nov2021, outcome "unknown", described as "when he lay down he could hear crackling and popping in his skull"; INSOMNIA (non-serious) with onset Nov2021, outcome "unknown", described as "couldn't sleep"; INFLAMMATION (non-serious) with onset Nov2021, outcome "unknown", described as "inflammation"; DRY MOUTH (non-serious) with onset Nov2021, outcome "unknown", described as "Dry mouth"; GINGIVAL SWELLING (non-serious) with onset Dec2021, outcome "not recovered", described as "got gum recession from it, that is how bad they were swollen from it"; HEART RATE INCREASED (non-serious) with onset 2021, outcome "unknown", described as "heart rate would go up"; DYSPNOEA (non-serious) with onset 2021, outcome "unknown", described as "shortness of breath"; BLOOD PRESSURE INCREASED (non-serious) with onset 2021, outcome "unknown", described as "blood pressure 130/95"; FATIGUE (non-serious) with onset 2021, outcome "unknown", described as "he always feels worn out."; PALPITATIONS (non-serious) with onset 2021, outcome "unknown", described as "heart palpitations"; SYMPTOM RECURRENCE (non-serious) with onset 2021, outcome "unknown", described as "my symptoms came back worse". The patient was hospitalized for oxygen saturation decreased (start date: Nov2021, hospitalization duration: 3 day(s)). The patient underwent the following laboratory tests and procedures: blood pressure measurement: (2021) 130/95; heart rate: (2021) go up; oxygen saturation: (Nov2021) down to low 80s., notes: his oximeter would say his oxygen was down to low 80s. Therapeutic measures were not taken as a result of visual impairment. Therapeutic measures were taken as a result of dry mouth. Clinical Course: Patient got his first dose of the Pfizer BioNTech COVID-19 vaccine adult formulation (purple cap) on 14NOV2021 and within 10 days of receiving the vaccines, his symptoms came back worse. His doctor even wrote something down about an adverse reaction, he classified it as an auto-immune response as well and he even wrote an exemption from work to get the second dose of the Pfizer BioNTech COVID-19 vaccine adult formulation (purple cap) due to this adverse reaction. Regarding treatment it was stated as there was nothing he can do for his eyes, but for his dental health he brushes his teeth and keeps his mouth moisturized because he has dry mouth as well don't know dry mouth caused it, but none of this was going on before the vaccine. He says his gums are uncomfortable, it all started the last day before Thanksgiving, then for about a week he had these and was out of work an entire week. He clarifies he got off from work on Wednesday and started feeling it, then Thanksgiving night it got really, really bad. He says he has even got gum recession from it, that is how bad they were swollen from it. He says he was hospitalized at the end of 29Nov or 30Nov, and he was there three days. He says he couldn't sleep, when he tried to lay down he had bad swelling to his neck and his heart rate would go up, and he had shortness of breath. He says he had his oximeter on at home when he would try to sleep for about a half hour and his oximeter would say his oxygen was down to low 80s. Stated the only thing that really bothers him still are his gums and teeth, and a little his eyes, those are a little off, and he always feels worn out. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: Test Date: 2021; Test Name: Blood pressure; Result Unstructured Data: Test Result:130/95; Test Date: 2021; Test Name: Heart rate; Result Unstructured Data: Test Result:go up; Test Date: 202111; Test Name: oxygen; Result Unstructured Data: Test Result:down to low 80s.; Comments: his oximeter would say his oxygen was down to low 80s.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; COVID-19 (I had COVID-19. I been described as a long hauler.); Heart rate increased (heart rate was up); Palpitations (Heart palpitations)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2010718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: PA
Alter: 37,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 14.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Chest pain Lymph node pain

Symptomtext

I had under arm lymph node pain with the booster that made me see a doctor. I had some lymph node pain under my arm with the second dose as well. With the booster the lymph node pain traveled down into my lower chest area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None. I was told to take Ibuprofen and use a heating pad.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: I took my daily birth control pill.
Allergien: I am allergic to Penicillin.
Vorherige Impfungen: -

VAERS 2005860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Condition aggravated Dyspnoea Fatigue Fibromyalgia Headache Nasopharyngitis Pain Rhinorrhoea

Symptomtext

became ill with cold like symptoms and fibromyalgia flare-up and still on 1/5/2022 experiencing shortness of breath and cold symptoms (runny nose, headaches, fatigue, body aches) despite being treated with antibiotics and steroids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: fibromyalgia
Vorgeschichte: -
Andere Medikamente: methylphenidate 20mg (2 per day) gabapentin 100mg (2per day)
Allergien: penicillin biaxin peanuts
Vorherige Impfungen: -

VAERS 2001387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 16.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Blood test normal Breast pain Cardiac flutter Cardiac stress test normal Chest X-ray normal Chest pain Condition aggravated Echocardiogram Electrocardiogram normal Lymph node pain Lymphadenopathy Pain Palpitations

Symptomtext

2-3 days after receiving my booster, my arm was really sore up underneath my left armpit. My lymph nodes were really swollen. This happened during the 2nd vaccine as well. I didn't worry about it because they went away and they did. Then on 11/19, I felt sharp pains every 2-3 minutes where my lymph nodes are, into my breast and into the center of my chest. It was bothersome when I would walk. And I put it off for a while because I was afraid to go to the hospital at the time. I went to the doctor, and they gave me some antibiotics and gave me amoxicillin and that was 875 mg. I think it was 2-3 days after that, I just went to the ER because my heart was fluttering, racing, and I was in pain. It got to the point where I had to go because I wanted to know what that was. I went to the ER on New Years in the morning. They did a Chest X-ray, EKG, Stress Test, Ultrasound of the heart and everything came back negative. When I spoke to the Doctor, he said that sometimes the vaccine can have that affect on you where your heart can race and flutter. It was scary.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: Chest X-ray - negative EKG - negative Stress test - negative Ultrasound of Heart - negative Blood work for Clots - negative
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma (under control), High blood pressure, High cholesterol
Andere Medikamente: Hyzaar 100mg combination 100mg/12.5mg once daily Hydrochlorothiazide 12.5mg once daily Crestor 10mg once daily Pepcid OTC once daily Pro Air inhaler 4 puffs daily as needed
Allergien: Rice
Vorherige Impfungen: 2nd dose of Pfizer 04/09/2021- swollen lymph nodes under left arm and L breast was out of proportion to the right. L arm I could

VAERS 1999804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OK
Alter: 60,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dysgeusia Hypoaesthesia oral Palpitations Throat tightness

Symptomtext

Numbness is lips, and tongue. Tightness is throat. Metallic taste in mouth. Heart palpitations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes type 2, HBP, Autoimmune disease, Angina, Cardiomegaly
Andere Medikamente: Lisinopril, Hydroxychloroquine, Metformin, Montelukast
Allergien: Penicillin, Atorvastatin, mango
Vorherige Impfungen: -

VAERS 2510478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 24,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Migraine Pain Pain in extremity

Symptomtext

ARM PAIN, BODY ACHES, MIGRAINE Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1997465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Headache Palpitations

Symptomtext

Chest pain for 6 days, chest pain started 5 minutes after the injection, heart palpitations 2 days starting the next day after the injection, headaches 2 Days in a row the day after the injection. The chest pain did not progress.

Weitere VAERSDATA-Felder

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

VAERS 1997210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 35,0
Geschlecht: M
Eingang: 01.01.2022
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Blood magnesium Brain natriuretic peptide Chest X-ray Chest discomfort Chest pain Differential white blood cell count Electrocardiogram Full blood count Metabolic function test Nucleated red cells Palpitations Troponin I

Symptomtext

I experienced a pounding heartbeat and chest tightness for hours. After discussing with my primary care doctor, I was advised to go to the emergency department. Tests did not identify the issue and eventually the chest pain dissipated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: XR CHEST 2 VIEWS CBC WITH DIFFERENTIAL COMPREHENSIVE METABOLIC PANEL MAGNESIUM B-TYPE NATRIURETIC PEPTIDE TROPONIN I HIGH SENSITIVITY COMPLETE BLOOD COUNT COMPON AUTO 6 PART DIFF NUCLEATED RBC PERCENT NUCLEATED RBC ABSOLUTE ECG 12-LEAD
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1995394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 30,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Chills Dizziness Dyspnoea Headache Hyperacusis Immunisation Photophobia Pyrexia Vomiting

Symptomtext

Severe headache; Low grade fever; Vomiting; Joint pain; Chills; Sensitivity to light and sound; Sensitivity to light and sound; Dizziness; Shortness of breath; Booster (dose 3); This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old female patient (not pregnant) received BNT162B2 (BNT162B2), administered in arm left, administration date 13Dec2021 05:00 (Lot number: FH8030) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Postural orthostatic tachycardic syndrome" (unspecified if ongoing); "Peanut allergy" (unspecified if ongoing). Concomitant medication(s) included: AVIANE. Vaccination history included: BNT162B2 (dose 2, single; lot: EW0171; site: right arm; time: 10:00), administration date: 04May2021, when the patient was 29 years old, for COVID-19 immunization; BNT162B2 (dose 1, single; lot: ER8729; site: right arm; time: 10:00), administration date: 19Apr2021, when the patient was 29 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 13Dec2021 05:00, outcome "unknown", described as "Booster (dose 3)"; HEADACHE (non-serious) with onset 14Dec2021 13:00, outcome "recovering", described as "Severe headache"; PYREXIA (non-serious) with onset 14Dec2021 13:00, outcome "recovering", described as "Low grade fever"; VOMITING (non-serious) with onset 14Dec2021 13:00, outcome "recovering", described as "Vomiting"; ARTHRALGIA (non-serious) with onset 14Dec2021 13:00, outcome "recovering", described as "Joint pain"; CHILLS (non-serious) with onset 14Dec2021 13:00, outcome "recovering", described as "Chills"; PHOTOPHOBIA (non-serious), HYPERACUSIS (non-serious) all with onset 14Dec2021 13:00, outcome "recovering" and all described as "Sensitivity to light and sound"; DIZZINESS (non-serious) with onset 14Dec2021 13:00, outcome "recovering", described as "Dizziness"; DYSPNOEA (non-serious) with onset 14Dec2021 13:00, outcome "recovering", described as "Shortness of breath". Therapeutic measures were not taken as a result of headache, pyrexia, vomiting, arthralgia, chills, photophobia, hyperacusis, dizziness, dyspnoea. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient had no history of COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Peanut allergy; Postural orthostatic tachycardia syndrome
Andere Medikamente: AVIANE
Allergien: -
Vorherige Impfungen: -

VAERS 1993590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: TX
Alter: 53,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 23.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac stress test Chest pain Dyspnoea Dyspnoea exertional Echocardiogram Electrocardiogram abnormal Palpitations Ventricular extrasystoles

Symptomtext

Chest pain, Shortness of breath, palpitation. This symptoms started around 12/08/2022 Multiple premature ventricular beats on EKG, every third beat was a premature ventricular beat, about 30-35/min. 2D Echo Mild TR Exercise Stress Test: ST Elevation in anterolateral leads, about 2 mm and upsloping I was traveling when symptoms started, did those tests while traveling on 12/10/2021. Premature beats, mild dull chest pain, palpitation, exertional shortness of breath are persistent. I have appointment with cardiologist on 01/12/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: As mentioned above.
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: Hypertension
Andere Medikamente: Valsartan 320 mg daily Amlodipine 10 mg daily
Allergien: No Known Drug Allergy
Vorherige Impfungen: -

VAERS 1949036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 39,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 06.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Back pain Chills Decreased appetite Fatigue Gait inability Immediate post-injection reaction Injection site pain Migraine Muscle spasms Lethargy Muscular weakness Myalgia Vision blurred

Symptomtext

Patient after a few days she experienced lethargy, systemic muscle soreness and weakness

Weitere VAERSDATA-Felder

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

VAERS 1984984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: LA
Alter: 63,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Body temperature decreased Chills Fatigue Feeling cold Headache Nausea Pain Pain in extremity Tremor

Symptomtext

Approximately 11:45pm, developed severe chills and body shaking, temperature 93F, severe headache, nausea, severe full body ache, mild-mod arm pain. Tylenol taken approximately 9pm prior to developing the chills, and repeated about 3am in the midst of the severe chills. Used portable heater, overhead heater and blow dryer to try to heat my body up and diminish the coldness and chills. Chills and coldness lasted at least through 6-7am. I considered going to the Emerg Dept. Stayed in bed the whole next day extreme fatigue, headache, nausea, body aches, slightly cold, temp 96-97F. Continued to take Tylenol as directed on bottle. The following day, 2 days post injection, continue with headache, body aches but better than day prior. Three days post injection , headache remains, slight body aches, fatigue. I am 5-6 days post injection, still somewhat mildly fatigued with minor body aches . Each COVID Pfizer vaccine seems to have produced more severe symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: childhood asthma. hypothyroid.
Andere Medikamente: Synthroid 88mcg daily by mouth
Allergien: sulfa, Penicillin
Vorherige Impfungen: chills,headache, arm pain and body aches with 1st and 2nd COVID - Pfizer. The 3rd (booster) was the worse.

VAERS 1984657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Dysphagia Dyspnoea Swollen tongue

Symptomtext

Pt received booster, waited 15 min observation then left. Pt came back stating her tongue was swelling. Vitals were normal. Pt then had trouble swallowing and difficulty breathing. 911 called, epi administered, and Dr monitored until ambulance arrived. Pt taken to ED via ambulance.

Weitere VAERSDATA-Felder

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

VAERS 1981016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

moderat

Staat: TX
Alter: 38,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 27.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Condition aggravated Tinnitus

Symptomtext

My tinnitus has increased and it is constant ringing 24/7.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Tinnitus
Vorgeschichte: Tinnitus/ ptsd
Andere Medikamente: Na
Allergien: Na
Vorherige Impfungen: -

VAERS 1980770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 16.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Immunisation Lymph node pain Lymphadenopathy Menstrual disorder Pain

Symptomtext

It is very painful/swelling of her lymph nodes which began in one spot and now has traveled all over her body with throbbing pain; It is very painful/swelling of her lymph nodes which began in one spot and now has traveled all over her body with throbbing pain; It is very painful/ throbbing pain/ it was a constant stabbing pain, it was unbearable; I took the booster about 3 weeks ago; Swollen lymph nodes around my neck area/swollen lymph nodes are under her arm and legs/ swelling of her lymph nodes which began in one spot and now has traveled all over her body with throbbing pain; 3 days after taking the Booster dose, she got her period/ she has already been through menopause; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202101780834 (Pfizer). A 54 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Nov2021 (Lot number: FH8030) at the age of 54 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Menopause" (unspecified if ongoing), notes: she has already been through menopause. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose:1, Lot number:EN6205, anatomical location: left arm, Expiry: Unknown, She had nothing like this with the first 2 doses), administration date: 04Mar2021, when the patient was 53 years old, for Covid-19 immunization, reaction(s): "No reaction on previous exposure to Vaccine"; Covid-19 vaccine (Dose:2, Lot number:EP7533, anatomical location: left arm, She had nothing like this with the first 2 doses.), administration date: 25Mar2021, when the patient was 53 years old, for Covid-19 immunization, reaction(s): "No reaction on previous exposure to Vaccine". The following information was reported: IMMUNISATION (non-serious) with onset 16Nov2021, outcome "unknown", described as "I took the booster about 3 weeks ago"; LYMPHADENOPATHY (non-serious) with onset 16Nov2021, outcome "not recovered", described as "Swollen lymph nodes around my neck area/swollen lymph nodes are under her arm and legs/ swelling of her lymph nodes which began in one spot and now has traveled all over her body with throbbing pain"; LYMPH NODE PAIN (non-serious), CONDITION AGGRAVATED (non-serious) all with onset 12Dec2021, outcome "not recovered" and all described as "It is very painful/swelling of her lymph nodes which began in one spot and now has traveled all over her body with throbbing pain"; MENSTRUAL DISORDER (non-serious) with onset Nov2021, outcome "unknown", described as "3 days after taking the Booster dose, she got her period/ she has already been through menopause"; PAIN (non-serious) with onset 12Dec2021, outcome "not recovered", described as "It is very painful/ throbbing pain/ it was a constant stabbing pain, it was unbearable". Therapeutic measures were taken as a result of lymphadenopathy, lymph node pain, condition aggravated, pain. Additional Context: Patient stated that I took the booster about 3 weeks ago and I had swollen lymph nodes around my neck area and it was very painful and you could feel it under the hand and it was visible also and it has been 3 weeks. When took Advil (treatment), it went down but I couldn't indefinitely keep taking Advil (further clarification unknown). Patient said that she took the Covid-19 vaccine booster and all of her lymph nodes thorough out her body were swollen and almost a month and she was in pain. She did not understand what is going on as this did not happen with the first 2 doses. Patient said that the swollen lymph nodes started around her neck area. She said it was like there was a bulging that was rolling under her finger. She talked to some other people and found a couple of people that said it happened to them. She took Advil to treat her symptoms. The swollen Lymph nodes are all over her body now. Other people said that it did not happen like that with them. Yesterday, 12Dec2021, the swollen Lymph nodes were behind her neck and was throbbing pain. Advil did nothing. She said that it was a constant stabbing pain, it was unbearable. The swollen lymph nodes are under her arm and legs. She had nothing like this with the first 2 doses. Spoke to other people I know that had the side effects, and the same little ball, it started like a little ball, next to the clavicle, by the neck bone, like bowling ball, I spoke to other people and the same thing after while it went away. Since 16Nov2021, and was now moving all over, the left side of my body that I was getting lymph node swelling, all my neck area, back, and front, under my arm, and my leg, all on one side. Yesterday I had throbbing pain on my neck, like I was being stabbed on my neck, the swelling was actually visible to the eye too. How long does the swollen lymph nodes last. She reported that 3 days after taking the Booster dose, she got her period and was seeing the OB-GYN. I was menopausal, and 3 days after taking the vaccine, I had a 4-5 days period like before. She said that she has already been through menopause. Advil: Lot: R90541 Expiration: Sep2023. Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Menopause (she has already been through menopause)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1978727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

moderat

Staat: RI
Alter: 40,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 12.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Dizziness Ear pain Ear swelling Facial pain Fatigue Headache Lymph node pain Lymphadenopathy Neck pain Pain Palpitations Polymerase chain reaction SARS-CoV-2 test Swelling Swelling face

Symptomtext

Pain and swelling in lymph nodes; Pain and swelling in lymph nodes; Pain and swelling in lymph nodes, neck, face and ear on right side; Pain and swelling in lymph nodes, neck, face and ear on right side; Pain and swelling in lymph nodes, neck, face and ear on right side; Pain and swelling in lymph nodes, neck, face and ear on right side; Pain and swelling in lymph nodes, neck, face and ear on right side; Pain and swelling in lymph nodes, neck, face and ear on right side; Heart palpitations; dizziness; fatigue; body aches; headache; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 40 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 12Nov2021 15:00 (Lot number: Fh8030) at the age of 40 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Ff2590, Location of injection: Arm Right, Vaccine Administration Time: 03:00 PM), administration date: 22Oct2021, when the patient was 40 years old, for Covid-19 immunization. The following information was reported: LYMPH NODE PAIN (non-serious), LYMPHADENOPATHY (non-serious), outcome "not recovered" and all described as "Pain and swelling in lymph nodes"; NECK PAIN (non-serious), FACIAL PAIN (non-serious), EAR PAIN (non-serious), SWELLING (non-serious), SWELLING FACE (non-serious), EAR SWELLING (non-serious), outcome "not recovered" and all described as "Pain and swelling in lymph nodes, neck, face and ear on right side"; PALPITATIONS (non-serious), outcome "not recovered", described as "Heart palpitations"; DIZZINESS (non-serious), outcome "not recovered", described as "dizziness"; FATIGUE (non-serious), outcome "not recovered", described as "fatigue"; PAIN (non-serious), outcome "not recovered", described as "body aches"; HEADACHE (non-serious), outcome "not recovered", described as "headache". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of lymph node pain, lymphadenopathy, neck pain, facial pain, ear pain, swelling, swelling face, ear swelling, palpitations, dizziness, fatigue, pain, headache. Additional information: Patient received no other vaccine in four weeks and no covid prior vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20211205; Test Name: PCR; Result Unstructured Data: Test Result:Pending; Comments: Nasal Swab; Test Date: 20211205; Test Name: Nasal Swab; Test Result: Negative ; Comments: Binax
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1975286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: AR
Alter: 35,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood glucose normal Blood pressure abnormal Dizziness Hyperhidrosis Paraesthesia Vision blurred

Symptomtext

A few minutes after receiving the vaccine, the patient said he though he was having a reaction. He said that he was dizzy and that is vision was blurred. He started sweating profusely and said he felt like he was going to pass out. His blood pressure was 78/67 which is stated was very unusual. His blood sugar was 136. He continued to sweat profusely and said that his hands and fingers were tingling. We called for an EMT to come check him out. When the EMT arrived his blood pressure was back up within normal range and he was filling much better. The patient stayed at the pharmacy until he felt fully recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension.
Andere Medikamente: Patient stated he was on a blood pressure medication.
Allergien: No allergies that he is aware of.
Vorherige Impfungen: -

VAERS 1971900

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FH8030

moderat

Staat: PA
Alter: 40,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 22.11.2021
Beginn: 17.12.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / RA

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

Bronchitis Chest pain Headache Lower respiratory tract infection Malaise Pain Rhinorrhoea SARS-CoV-2 test

Symptomtext

Started getting sick on 12/17/2021, started with some slight aches and a nasal drip. Come Sunday, that turned into where I could feel it settle in my chest like I was getting a chest cold. I went Sunday to get a COVID-19 test and currently waiting for my results. On Monday, I called my PCP and we did a telehealth visit and I told her the aches, headaches, no fever, feels like everything is settling in my chest and a burning sensation in my chest. She said it could be early bronchitis and I was prescribed a z-pack for that. I actually called today because I'm getting worse and was told to go the med-express or ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 test waiting results.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ergocalciferol Vitamin D2; Levothyroxine; Biotin; Vitamin D3; Prenatal Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1971624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IN
Alter: 21,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chest pain Fatigue Pain

Symptomtext

Body aches, chest pain, and fatigue all for 1 day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sinus infection
Vorgeschichte: B12 deficiency
Andere Medikamente: Cefdinir, Mucinex D, Fluticasone nasal spray, Junel Fe birth control, Vitamin B12 1000 mcgs, and a multivitamin.
Allergien: N/A
Vorherige Impfungen: -

VAERS 1970723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Axillary pain Breast pain Dermatitis Gait inability Headache Immunisation Limb discomfort Myalgia Pain assessment Pain in extremity Paraesthesia

Symptomtext

Booster; First was having pain in her left arm; Then she started to be sore; there was inflamed skin between her left breast and armpit which from 29Nov2021 is bigger; feeling like needles poking or pinching her but only in the left side. she still felt the same poking like the needles in her left hip and butt in the left side and her left leg; inflamed skin between her left breast and armpit which from 29Nov2021 is bigger, growing more and it's painful; inflamed skin between her left breast and armpit which from 29Nov2021 is bigger, growing more and it's painful; She also has all of her left leg down; on her left hip feels like very hard pain where she cannot move it at all because it is painful; unable to walk; She also has a very strong headache that makes it hard to think; 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 29Nov2021 10:00 (Lot number: FH8030) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Allergic to the weather and pollen and all kinds of stuff" (unspecified if ongoing), notes: Allergic to the weather and pollen and all kinds of stuff; "Allergic to the weather and pollen and all kinds of stuff" (unspecified if ongoing), notes: Allergic to the weather and pollen and all kinds of stuff. Concomitant medication(s) included: CETIRIZINE HCL taken for seasonal allergy, seasonal allergy, start date: 29Nov2021, stop date: 30Nov2021. Vaccination history included: Bnt162b2 (1st dose, lot#EW0161), administration date: 14Apr2021, when the patient was 39 years old, for COVID-19 Immunization, reaction(s): "tired", "The brain felt similar as with this reaction to the booster shot; but was more like a cold, like a blood cold was running in for a little bit", "arm was sore", "had problems to breathe", "feeling the chest, like her heart is tired or her chest is tired"; Bnt162b2 (2nd dose, lot#EW0176), administration date: 05May2021, when the patient was 39 years old, for COVID-19 Immunization, reaction(s): "The brain felt similar as with this reaction to the booster shot; but was more like a cold, like a blood cold was running in for a little bit", "tired", "had problems to breathe", "arm was sore", "feeling the chest, like her heart is tired or her chest is tired". The following information was reported: IMMUNISATION (non-serious) with onset 29Nov2021, outcome "unknown", described as "Booster"; PAIN IN EXTREMITY (non-serious) with onset 29Nov2021, outcome "not recovered", described as "First was having pain in her left arm"; MYALGIA (non-serious) with onset 29Nov2021, outcome "not recovered", described as "Then she started to be sore"; DERMATITIS (non-serious) with onset 29Nov2021, outcome "not recovered", described as "there was inflamed skin between her left breast and armpit which from 29Nov2021 is bigger"; PARAESTHESIA (non-serious) with onset 29Nov2021, outcome "not recovered", described as "feeling like needles poking or pinching her but only in the left side. she still felt the same poking like the needles in her left hip and butt in the left side and her left leg"; LIMB DISCOMFORT (non-serious) with onset 2021, outcome "unknown", described as "She also has all of her left leg down"; ARTHRALGIA (non-serious) with onset 2021, outcome "unknown", described as "on her left hip feels like very hard pain where she cannot move it at all because it is painful"; GAIT INABILITY (non-serious) with onset 2021, outcome "unknown", described as "unable to walk"; HEADACHE (non-serious) with onset 2021, outcome "not recovered", described as "She also has a very strong headache that makes it hard to think"; BREAST PAIN (non-serious), AXILLARY PAIN (non-serious) all with onset 29Nov2021, outcome "not recovered" and all described as "inflamed skin between her left breast and armpit which from 29Nov2021 is bigger, growing more and it's painful". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Concomitant Products Cetirizine HCl. Patient taken it on 29Nov2021 and 30Nov2021, but not on 01Dec2021 or 02Dec2021. Patient did not visited the doctor till the time of reporting because of the event. This reaction really scares her. Normally they let her wait 15 minutes after vaccination in case of a reaction; but this time the nurse not said anything so they just left. Patient was thinking, because the nurse told her that she was a little hard and she was not relaxed completely, so she was assuming that was related to reaction initially; but then the reaction came more and more and she was pretty sure that the event was from the booster shot. Event onset was on 29Nov2021 after she was administered booster shot. First had pain in her left arm which she was assuming ok. Then she started to be sore; then there was inflamed skin between her left breast and armpit which was bigger from 29Nov2021, growing more and it was painful. Evening or night of 29Nov2021 in her neck on left side and in the brain, in the back of the head and all the left side of her head felt like needles poking or pinching her but only in the left side. On 01Dec2021 she was still felling the same poking like the needles in her left hip and butt in the left side and her left leg. She also had all of her left leg down and on her left hip feels like very hard pain where she cannot move it at all because it was painful; she had to stop to walk and everything, then with the pain she was unable to walk which has never happened to her before so it scares her a bit. She also had a very strong headache that makes it hard to think. When walking and everything the headache did not go away for anything. If she had to rate the pain from 1-10 it could be 6-7 right at the time of reporting. On 01Dec2021 was very bad. Outcome unknown, initially reported she thinks still the same; but then clarified that the needles felt in her brain she did not felt on the day of reporting; did not feel the needles feeling anywhere on the day of reporting; but the headache was still strong, pain was still in there and the inflamed sore skin area between her left breast and armpit was still there. She did not think that event will go away. On the day of reporting in the morning when she took a shower she could see inflamed sore skin area between her left breast and armpit was more, bigger and because of the sore area told her husband that she did not think this was going well. No additional Vaccines administered on same date of the Pfizer Suspect. She was supposed to get the flu shot but the nurse did not put it in the system so she did not get the flu shot. Patient not visited Emergency Room and Physician Office. Patient not received prior Vaccinations (within 4 weeks). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: pain scale; Result Unstructured Data: Test Result:6-7; Comments: rate the pain from 1-10 it could be 6-7 right now
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pollen allergy (Allergic to the weather and pollen and all kinds of stuff); Seasonal allergy (Allergic to the weather and pollen and all kinds of stuff)
Andere Medikamente: CETIRIZINE HCL
Allergien: -
Vorherige Impfungen: -

VAERS 1967958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain Condition aggravated Diarrhoea Fatigue Headache Injection site pain Myalgia Pain

Symptomtext

Injection on 11/29 @ 0900 09:00 - minimal injection site pain 18:00 - onset of generalized myalgia, headache 20:00 - mild fever (below 100 F) 11/30 @ 01:00 - acute onset of abdominal cramping - 7/10 pain, diarrhea 01:00-12:00 - abdominal cramping, diarrhea 11/29-11/30 all day - generalized myalgia, fatigue, headache 11/30 fell asleep at 19:00, woke up 12/1 @ 07:00 feeling 90% better. Mild fatigue/myalgia continued, diarrhea resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A - no doctor's office visit, absent leave from work for 1 day
Aktuelle Erkrankungen: None
Vorgeschichte: IBS, chronic low back pain
Andere Medikamente: Vyvanse, 40mg
Allergien: Tramadol - adverse rxn: nausea/emesis
Vorherige Impfungen: Mild reactions to most - if not all - previous COVID-19 and Flu vaccines, reactions were mild and included mild fever <100F, mya

VAERS 1967956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NJ
Alter: 17,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Palpitations

Symptomtext

Following her booster vaccine of Pfizer at 1440, patient stated feeling like her heart was racing and she appeared flushed. She complained of dizziness and patient and mother stated that she 'always feels like she's going to pass out' following any shot or when she gets blood drawn. 1440 BP: 153/85, HR: 113 appeared flushed, patient seated with feet extended above heart and given water to drink; EMS called 1445 BP: 146/86, HR: 112, patient finished water and said she was 'starting to feel better' 1455 BP: 151/83 HR: 88 color improving, less flush and EMS arrived to take over 1515 Patient stated feeling better at this point and was released by EMS with no visit to ED; mother drove patient home and was informed to monitor patient and if she continues to feel unwell or gets worse to take her to the ED.

Weitere VAERSDATA-Felder

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

VAERS 1967737

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FH8030

moderat

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 14.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Condition aggravated Tinnitus Vaccine positive rechallenge

Symptomtext

extreme tinnitus. Tinnitus started after the second shot and remained light. After the booster it's tripled in volume and unmanageable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: famcyclavir, SADBE
Allergien: NA
Vorherige Impfungen: -

VAERS 1967514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: VA
Alter: 30,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 17.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Atrioventricular dissociation Chest pain Electrocardiogram abnormal

Symptomtext

Chest pain exacerbated with deep inspiration. Sharp. Localized to upper left side of chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG with AV dissociation and repeat with possible ectopic atrial rhythm.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: prenatal vitamins, and valacyclovir 1000mg once daily
Allergien: PCN> hives
Vorherige Impfungen: -

VAERS 1963797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NM
Alter: 23,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Chest discomfort Dyspnoea Rash pruritic

Symptomtext

Chest tightness, shortness of breath, itchy rash (quarter size bumps).

Weitere VAERSDATA-Felder

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

VAERS 1963363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 07.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

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

Chest X-ray Chest pain Condition aggravated Dyspnoea Electrocardiogram Hypertension

Symptomtext

I experienced severe shortness of breath, extremely high blood pressure, severe chest pain. As I read the myocarditis symptoms people were experiencing it seemed like I was having the same issues. Went to urgent care and there was discussion of side effect of vaccine but not very serious. I had a similar less extreme side effect from the first dose, no side effect from the second dose, but booster was more serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: The urgent care did chest x-ray and ekg
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure, asthma, scardoisis
Andere Medikamente: I am taking regularly taking amlodopine for high blood pressure; asthma inhalers as needed
Allergien: sulfur, aspirin
Vorherige Impfungen: Pfizer first dose 3-30-2021

VAERS 1963249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: PA
Alter: 44,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 30.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / LA

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

Angiogram Cardiac stress test Chest discomfort Echocardiogram Electrocardiogram ambulatory Fibrin D dimer increased Limb discomfort Tachycardia

Symptomtext

Developed chest heaviness, 2 days later also heaviness in right arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Tachycardia (125-135 at times), elevated D-dimer.CTA chest, negative. Now following up with Cardiac workup. stress test, echo, and holter monitor.
Aktuelle Erkrankungen: None.
Vorgeschichte: IBS with constipation.
Andere Medikamente: Vitamin C, D, Zinc, Elderberry, B-complex, Calcium, Milk Thistle.
Allergien: Ultram; I had a local reaction to Flu shot and Hepatitis Booster vaccine.
Vorherige Impfungen: -

VAERS 1961567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IN
Alter: 56,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Adrenal insufficiency Blood pressure measurement Chest pain Cough Cystitis Haematuria Hypertension Immunisation Insomnia Malaise Mental impairment Pain Throat tightness

Symptomtext

Adrenal insufficiency; Brain is not working too well; didn't sleep too well; lots of blood in urine; symptoms of a bladder infection; Severe pain; Blood pressure got so high; booster; dry cough; chest pain; like more of a constriction in my throat too; pretty sick; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 56 year-old female patient received bnt162b2 (BNT162B2), administration date 01Dec2021 (Lot number: FH8030) at the age of 56 years as dose 3, single for covid-19 immunisation. Relevant medical history included: "Ehlers-Danlos syndrome" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Hashimoto's disease" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing); "Adrenal insufficiency" (unspecified if ongoing); "Coronary vasospasm" (unspecified if ongoing); "disabled" (unspecified if ongoing). Concomitant medication(s) included: RAYOS; LEXAPRO; TYLENOL; ASPIRIN [ACETYLSALICYLIC ACID]; VITAMIN D [ERGOCALCIFEROL]; VITAMIN B12 [CYANOCOBALAMIN]; SPIRONOLACTONE; DHEA; LEVOTHYROXINE; AMLODIPINE; HYDROCORTISONE. Vaccination history included: Covid-19 vaccine (MANUFACTURER UNKNOWN, dose 1, single), for COVID-19 immunisation; Covid-19 vaccine (MANUFACTURER UNKNOWN, dose 2, single). The following information was reported: ADRENAL INSUFFICIENCY (medically significant), outcome "unknown", described as "Adrenal insufficiency"; MENTAL IMPAIRMENT (medically significant), outcome "unknown", described as "Brain is not working too well"; CHEST PAIN (non-serious) with onset 01Dec2021, outcome "unknown", described as "chest pain"; THROAT TIGHTNESS (non-serious) with onset 01Dec2021, outcome "unknown", described as "like more of a constriction in my throat too"; HAEMATURIA (non-serious) with onset 03Dec2021, outcome "unknown", described as "lots of blood in urine"; MALAISE (non-serious) with onset 01Dec2021, outcome "unknown", described as "pretty sick"; CYSTITIS (non-serious) with onset 03Dec2021, outcome "unknown", described as "symptoms of a bladder infection"; COUGH (non-serious) with onset 01Dec2021, outcome "unknown", described as "dry cough"; HYPERTENSION (non-serious) with onset 02Dec2021, outcome "unknown", described as "Blood pressure got so high"; INSOMNIA (non-serious), outcome "unknown", described as "didn't sleep too well"; PAIN (non-serious), outcome "unknown", described as "Severe pain". The patient underwent the following laboratory tests and procedures: blood pressure measurement: high. Therapeutic measures were taken as a result of adrenal insufficiency and included up dose of hydrocortisone; chest pain and included up dose of hydrocortisone, nitrogycerine, and Macrobid; and hypertension and included nitroglycerine. Clinical course: The patient was just calling for 'assistance' because she had an adverse event from Pfizer before. She had the Pfizer booster on 01Dec2021 and she had chest pain from that within 1 to 2 hours afterwards, and then it kept, it would go away and then come back and she called the cardiologist office on Thursday (as reported) and her blood pressure got so high that she had to take Nitroglycerin (treatment) for her chest pain and high blood pressure from the Pfizer booster. On 05Dec2021 at 2:00 in the morning, she woke up, had lots of blood in urine and had symptoms of a bladder infection from just having had the Pfizer booster on 01Dec2021. She felt pretty sick from this booster that she received. She had to up dose her hydrocortisone with the chest pain after the Pfizer booster and she had to take Nitroglycerine. She takes Amlodipine and she took Macrobid (Intent: treatment). Her brain was not working too well because she didn't sleep too well. She had to take Nitroglycerin on 02Dec2021 with the direction of her cardiologist who was on a call and she normally takes her Amlodipine anyway and she had a up her dose of hydrocortisone because she had adrenal insufficiency. Then on 05Dec2021, she had such severe pain, just blood in urine. So, she have to wait until she sees what the doctors say. If it gets worse, she will have to go to the emergency room.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal association between the events and 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: Chest pain
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:High
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adrenal insufficiency; Coronary vasospasm; Disability; Ehlers-Danlos syndrome; Hashimoto's disease; Hypertension; Hypothyroidism
Andere Medikamente: RAYOS; LEXAPRO; TYLENOL; ASPIRIN [ACETYLSALICYLIC ACID]; VITAMIN D [ERGOCALCIFEROL]; VITAMIN B12 [CYANOCOBALAMIN]; SPIRONOLACTONE; DHEA; LEVOTHYROXINE; AMLODIPINE; HYDROCORTISONE
Allergien: -
Vorherige Impfungen: -

VAERS 1955555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 02.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Dysmenorrhoea Extra dose administered Heavy menstrual bleeding Loss of personal independence in daily activities Mobility decreased Pruritus

Symptomtext

Menstruation the week following my booster shot on December 2, 2021 was extremely painful and heavier than usual. I was unable to get out of bed, teach yoga classes or conduct my daily activities because the pain was debilitating. Advil did not relieve the pain. The debilitating pain lasted approximately 36 hours. Pain continued afterward for 48 hours but was manageable. I am still bleeding after 7 days. Also noteworthy is that following my first shot in the vaccination series with the Moderna vaccine on March 17, 2021, I had my first period after not having had any period nor spotting for 6 months. My periods have lasted 7-10 days since the first Moderna shot, which is unusual. In addition, I have had itchy patches appear on my torso, arms and legs which have itched with greater intensity two weeks following my booster shot. I had itchy patches appear following the Moderna shot series, too, but the patches following the booster are greater in number and more intense.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Exercise and allergy induced asthma, idiopathic hypersomnia, menorrhagia
Andere Medikamente: Adderall 2.5 Adderall 10 XR Singular Zyrtec Flonase Genexa allergy relief homeopathic tablets Vitamin D3 Iron supplement Vitamin B12 Tumeric Force supplement
Allergien: Allergic to corn and all corn derived products (eg corn starch, corn oil, corn syrup, corn products in medical preparations and foods, maltodextrins, etc.)
Vorherige Impfungen: -

VAERS 1954906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: GA
Alter: 68,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 15.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: UN / LA

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

Arthralgia Arthritis Condition aggravated Nail disorder Peripheral swelling

Symptomtext

The area of the inject on my upper arm was swelled up and I felt pain for about 2 days before then my arthritis increased. The 2 nails swelled up which was strange observation I witness. On the 3rd day the pain reduced and the swelling on my arm disappeared.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Arthritis
Andere Medikamente: Vitamin C, Multivitamin, Naproxen
Allergien: No
Vorherige Impfungen: -

VAERS 1954728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MN
Alter: 69,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 11.03.2021
Beginn: 16.12.2021
Tage bis Beginn: 280,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chemotherapy Condition aggravated Vaccine breakthrough infection

Symptomtext

Fully vaccinated with booster on 11/22/21. COVID infection breakthrough and inpatient hospital admit. Receiving chemo.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Patient has cancer and is actively receiving chemo
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1951407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Mobility decreased Pain in jaw

Symptomtext

24 hours after vaccine experienced acute pain on both sides where the jaw meets the ear. Unable to fully open mouth in order to eat and drink. Pain in Jaw. Unable to open jaw fully in order to eat/drink. Limited range of motion in Jaw. Symptoms continued for over 24 hours and then began to fade. Symptoms subsided completely within 72 hours.

Weitere VAERSDATA-Felder

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

VAERS 1948841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IN
Alter: 25,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain

Symptomtext

Patient experienced left-sided chest pain shortly after his first dose of vaccine was administered that did not resolve over the course of 30 minutes. Patient was taken to ER by family to be evaluated. Unsure at this time of outcome.

Weitere VAERSDATA-Felder

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

VAERS 1947855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

moderat

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Chest pain Dizziness Heart rate increased Palpitations

Symptomtext

Rapid heart rate at rest, dizziness, chest pain, heart palpitations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Strep throat
Vorgeschichte: -
Andere Medikamente: June?s, Zyrtec D, multi-vitamin, vitamin C, vitamin D, zinc, DIM, probiotic
Allergien: -
Vorherige Impfungen: -

VAERS 1947839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8030

moderat

Staat: KS
Alter: 20,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Adverse reaction Asthenia Delusion Fatigue Fear Feeling abnormal Hypoaesthesia Incomplete course of vaccination Malaise Mental impairment Myalgia Nausea Pain Paraesthesia Vertigo Vomiting

Symptomtext

I waited 30 minutes after the vaccine at the pharmacy and then left. At my home I started to feel terrible and started vomiting and could not stop vomiting for 24 hours. I had terrible muscle pain, vertigo, loss of sensation in the opposite hand, pins and needles all through my body, extreme fatigue, could not think, delusions. My parents took me to the hospital when they could not stop vomiting with over the counter meds and they were backed up for hours. The next morning I contacted an online virtual care doctor through telehealth app and he prescribed me dissolvable Zofran pills. I had to take double dose to finally stop the vomiting. I still feel nauseous, weak, brain fog and body aches. I have never felt sicker in my whole life despite having the regular flu many times in the past. I have not seen people report extreme vomiting so I believe this was an adverse reaction. I am terrified of ever having the second shot and most likely will not be doing it if I had this reaction on the first one. I literally felt like I was dying from the way I felt after receiving that vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: no tests had to call Urgent care telehealth doctor from bed
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1947092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Chills Diarrhoea Eating disorder Headache Immunisation Insomnia Myalgia Pyrexia Retching Tremor Vomiting

Symptomtext

Shaking; Vomiting/puking; Diarrhea; Joint pain; Fever; Chills; Muscle pain; Headache; I can't eat; Gagging; I haven't been able to sleep; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 20Nov2021 13:00 (Lot number: FH8030) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "High Blood Pressure" (unspecified if ongoing). Concomitant medication(s) included: RAMIPRIL taken for hypertension; AMLODIPINE taken for hypertension. Vaccination history included: Bnt162b2 (Dose 1, Single (The first two, patient got at the health department)), for COVID-19 immunization; Bnt162b2 (Dose 2, Single (The first two, patient got at the health department)), for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Nov2021 13:00, outcome "unknown", described as "Booster"; TREMOR (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "Shaking"; VOMITING (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "Vomiting/puking"; DIARRHOEA (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "Diarrhea"; ARTHRALGIA (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "Joint pain"; PYREXIA (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "Fever"; CHILLS (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "Chills"; MYALGIA (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "Muscle pain"; HEADACHE (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "Headache"; INSOMNIA (non-serious) with onset 21Nov2021 09:30, outcome "unknown", described as "I haven't been able to sleep"; RETCHING (non-serious) with onset 22Nov2021, outcome "unknown", described as "Gagging"; EATING DISORDER (non-serious) with onset 22Nov2021 01:00, outcome "unknown", described as "I can't eat". Additional information: Patient had no prior vaccination (4 Weeks). On 21Nov2021, since morning at 9:30 hours, patient had not been able to sleep. On 22Nov2021, at 01:00 hour (morning), patient was shaking so bad and mean puking, it was happening, and stated that this was supposed to be good for her. So, patient mean it just doesn't make any sense. Patient mean, that she can't eat, had diarrhea, vomiting, joint pain, fever, chills, muscle pain and headache. On 22Nov2021, patient opened the refrigerator to get even a drink and she just started gagging. Patient stated that this is how the government is helping us. Patient stated that she had to call and tell somebody that this booster shot, this was cruel and inhumane. 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: Blood pressure high
Andere Medikamente: RAMIPRIL; AMLODIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 1943620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 43,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 12.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: UN / UN

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

Anosmia Blood creatinine increased COVID-19 Chest X-ray abnormal Diarrhoea Dyspnoea Electrocardiogram abnormal Fibrin D dimer increased Headache Pneumonia SARS-CoV-2 test positive Sinus tachycardia Troponin

Symptomtext

Shortness of Breath Per pt, "I've tested positive for covid 9 days ago. I feel a lot better but my wife made me come in." HPI: This is a 43y.o. male with significant past medical history of HTN, T2DM, and morbid obesity that presented to the hospital with chief complaint of COVID-19 infection. He reports he became symptomatic on 11/17 and tested positive on 11/22. He has since had worsening headache, loss of smell, and diarrhea. He developed shortness of breath yesterday prompting him to seek ED evaluation. He denies any fever, chills, chest pain, palpitations, cough, abdominal pain, nausea, vomiting, constipation, or urinary complaints. In the ED, patient normotensive, afebrile, stable SPO2 on room air. Cr 1.78, troponin 0.05, d-dimer 755. EKG with sinus tachycardia. CXR with multifocal pneumonia. He has been admitted for further evaluation and management with ID consultation. Patient seen and examined only by the attending physician; NP only responsible for chart review in an effort to limit exposure given the patient's COVID positive status.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 30,0
Labordaten: Currently still in the hospital
Aktuelle Erkrankungen: Diabetes mellitus (CMS/HCC) ? Hypertension
Vorgeschichte: ? Diabetes mellitus (CMS/HCC) ? Hypertension
Andere Medikamente: amLODIPine (NORVASC) 10 MG PO Tab take 10 mg by mouth once daily. 11/26/2021 Unknown time lisinopril (PRINIVIL, ZESTRIL) 40 MG PO Tab
Allergien: none
Vorherige Impfungen: -

VAERS 1943476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: LA
Alter: 59,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 19.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: SYR / RA

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

Gait disturbance Mobility decreased Muscular weakness Pain in extremity

Symptomtext

Weakness and pain in both legs. Limited mobility as a result. Less pain after taking Gabapentin and MethylPREDNISolone tablets ; however, I am still experiencing difficulty walking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Centrum Silver Women 50+ Amlodipine Besylate 5 mg tab
Allergien: None
Vorherige Impfungen: -

VAERS 1943134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: FL
Alter: 40,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Arthralgia Limb injury Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 2546674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 12.12.2021
Impfdatum: 09.12.2021
Beginn: 20.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Angina pectoris Chest X-ray Chest pain Computerised tomogram thorax Headache Migraine

Symptomtext

Headache, Angina, Severe Migraine and crushing chest pain Narrative: 2 days after Booster vaccination employee experienced Severe migraine and "crushing chest pain" which she went to the ER for. She had a CT scan and CXR and given medication and a referral to Neurology

Weitere VAERSDATA-Felder

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

VAERS 1942034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Condition aggravated Dizziness Headache Impaired work ability Incorrect dose administered Nausea Pain Pyrexia

Symptomtext

patient given 0.5ml instead of the correct dose of 0.3ml. Patient experienced severe headache, body aches, fever, nausea and dizziness. She missed 1 shift from work. No medical attention needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: headaches, body aches, dizziness

VAERS 1941884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Angina pectoris Blood test abnormal Chest pain Chills Dizziness Fibrin D dimer Haemangioma of liver Headache Hepatic mass Immunisation Impaired driving ability Investigation Night sweats SARS-CoV-2 test

Symptomtext

booster dose; Liver Hemangioma" pushing on rib cage; constant chest/heart pain; constant chest/heart pain; night sweats (felt like buckets of water had been thrown on me); intense headache; unbelievable dizziness (could not drive for 6 days); unbelievable dizziness (could not drive for 6 days); D Dimer Blood Test was 3500+ (normal is 500).; they found masses on my liver; I had Extreme chills; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 08Nov2021 (Lot number: FH8030) at the age of 45 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU VACCINE VII, administration date 21Oct2021. Past drug history included: Amoxicillin, reaction(s): "known allergies", notes: known allergies: Amoxicillin. Vaccination history included: Bnt162b2 (Dose Number: 2, prev dose product=COVID 19, prev dose brand=Pfizer, prev dose lot number= ER8735, prev dose administration date= 20Apr2021, prev dose dose number=2, Vaccine location= Left arm), administration date: 20Apr2021, when the patient was 45 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, prev dose product=COVID 19, prev dose brand=Pfizer, prev dose lot number= ER8734, prev dose administration date= 30Mar2021, prev dose dose number=1, Vaccine location= Left arm), administration date: 30Mar2021, when the patient was 45 years old, for Covid-19 immunization. The following information was reported: HAEMANGIOMA OF LIVER (hospitalization) with onset 08Nov2021 22:00, outcome "recovering", described as "Liver Hemangioma" pushing on rib cage"; ANGINA PECTORIS (hospitalization, medically significant), CHEST PAIN (hospitalization) all with onset 08Nov2021 22:00, outcome "recovering" and all described as "constant chest/heart pain"; NIGHT SWEATS (hospitalization) with onset 08Nov2021 22:00, outcome "recovering", described as "night sweats (felt like buckets of water had been thrown on me)"; HEADACHE (hospitalization) with onset 08Nov2021 22:00, outcome "recovering", described as "intense headache"; DIZZINESS (hospitalization), IMPAIRED DRIVING ABILITY (hospitalization) all with onset 08Nov2021 22:00, outcome "recovering" and all described as "unbelievable dizziness (could not drive for 6 days)"; BLOOD TEST ABNORMAL (hospitalization) with onset 08Nov2021 22:00, outcome "recovering", described as "D Dimer Blood Test was 3500+ (normal is 500)."; HEPATIC MASS (hospitalization) with onset 08Nov2021 22:00, outcome "recovering", described as "they found masses on my liver"; CHILLS (hospitalization) with onset 08Nov2021 22:00, outcome "recovering", described as "I had Extreme chills"; IMMUNISATION (medically significant) with onset 08Nov2021 22:00, outcome "unknown", described as "booster dose". The patient was hospitalized for haemangioma of liver, angina pectoris, chest pain, night sweats, headache, dizziness, impaired driving ability, blood test abnormal, hepatic mass, chills (hospitalization duration: 1 day(s)). The events "liver hemangioma" pushing on rib cage", "constant chest/heart pain", "constant chest/heart pain", "night sweats (felt like buckets of water had been thrown on me)", "intense headache", "unbelievable dizziness (could not drive for 6 days)", "unbelievable dizziness (could not drive for 6 days)", "d dimer blood test was 3500+ (normal is 500).", "they found masses on my liver" and "i had extreme chills" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: fibrin d dimer: (08Nov2021) 3500+ (Notes: D Dimer Blood Test was 3500+ (normal is 500) and then they found masses on my liver and diagnosed me with liver cancer (NO pre-existing condition and NO family history of liver cancer and I'm NOT a drinker) but further tests: (08Nov2021) showed "liver hemangioma" pushing on rib cage and doctor suspected this is causing my chest/heart; sars-cov-2 test: (16Nov2021) negative, notes: Nasal Swab. Therapeutic measures were not taken as a result of haemangioma of liver, angina pectoris, chest pain, night sweats, headache, dizziness, impaired driving ability, blood test abnormal, hepatic mass, chills, immunisation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: Test Date: 20211108; Test Name: D-Dimer Blood Test; Result Unstructured Data: Test Result:3500+; Comments: D Dimer Blood Test was 3500+ (normal is 500) Then, they found masses on my liver and diagnosed me with liver cancer; Test Date: 20211108; Test Name: further tests; Result Unstructured Data: Test Result:showed "Liver Hemangioma" pushing on rib cage; Comments: showed "Liver Hemangioma" pushing on rib cage; Test Date: 20211116; Test Name: Nasal Swab; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1885347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Anxiety Asthenia Nervousness Palpitations Panic attack Dizziness Fatigue Immunisation Nausea

Symptomtext

the vaccine booster; got panic attack; more anxious nervous than before; nausea; dizziness; fatigue; This is a spontaneous report received from contactable Consumer or other non-HCP. The reporter is the patient. A 37-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Nov2021 19:15 (Lot number: FH8030) at the age of 37 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "no" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: No. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ew0185, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 07May2021, when the patient was 37 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ew0162, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 16Apr2021, when the patient was 37 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 10Nov2021 19:45, outcome "unknown", described as "the vaccine booster"; PANIC ATTACK (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "got panic attack"; ANXIETY (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "more anxious nervous than before"; NAUSEA (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "nausea"; DIZZINESS (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "dizziness"; FATIGUE (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "fatigue". The events "the vaccine booster", "got panic attack", "more anxious nervous than before", "nausea", "dizziness" and "fatigue" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were not taken as a result of immunisation, panic attack, anxiety, nausea, dizziness, fatigue. Additional information: 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 known allergies reported for the patient. No other medical history has been reported. Vaccine Facility information available. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: no
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1885347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Anxiety Asthenia Nervousness Palpitations Panic attack Dizziness Fatigue Immunisation Nausea

Symptomtext

the vaccine booster; got panic attack; more anxious nervous than before; nausea; dizziness; fatigue; This is a spontaneous report received from contactable Consumer or other non-HCP. The reporter is the patient. A 37-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Nov2021 19:15 (Lot number: FH8030) at the age of 37 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "no" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: No. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ew0185, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 07May2021, when the patient was 37 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ew0162, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 16Apr2021, when the patient was 37 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 10Nov2021 19:45, outcome "unknown", described as "the vaccine booster"; PANIC ATTACK (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "got panic attack"; ANXIETY (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "more anxious nervous than before"; NAUSEA (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "nausea"; DIZZINESS (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "dizziness"; FATIGUE (non-serious) with onset 10Nov2021 19:45, outcome "recovering", described as "fatigue". The events "the vaccine booster", "got panic attack", "more anxious nervous than before", "nausea", "dizziness" and "fatigue" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were not taken as a result of immunisation, panic attack, anxiety, nausea, dizziness, fatigue. Additional information: 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 known allergies reported for the patient. No other medical history has been reported. Vaccine Facility information available. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: no
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2546673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 46,0
Geschlecht: U
Eingang: 10.12.2021
Impfdatum: 09.12.2021
Beginn: 20.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Angina pectoris Chest X-ray Chest pain Computerised tomogram Headache Migraine

Symptomtext

Headache, Angina, Severe Migraine and crushing chest pain Narrative: 2 days after Booster vaccination employee experienced Severe migraine and "crushing chest pain" which she went to the ER for. She had a CT scan and CXR and given medication and a referral to Neurology

Weitere VAERSDATA-Felder

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

VAERS 1939420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 70,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Axillary pain Chills Condition aggravated Discomfort Fatigue Headache Influenza like illness Musculoskeletal stiffness Myalgia Neuralgia Oedema peripheral Poor quality sleep Tinnitus

Symptomtext

Booster given at 1PM no issues until 8:30 PM felt ?under the weather? as expected and went to bed?awoke in night and had headache and felt aches and pains in joints and muscles?took Advil gel cap?..slept fitfully due to headache and aches?.woke at 7:30AM Monday morning and same unrelenting headache, aches and pain in joints (couldn?t bend my fingers) and muscles too (flu like symptoms)?.tinnitus was very loud and would pulsate when I got up and walked around?.extreme fatigue, chills, nerve endings agitated causing uncomfortable reaction to touching cold surfaces?pain and swelling developed in right underarm area of arm received vaccination?.fever of 99.7 high for me since I run subnormal temp. Headache, tinnitus and swelling under arm continued as other symptoms eased? Slept as much as possible on Monday and called my doctor for advise on painful swelling in underarm area on Tuesday. Advised to take Advil every 8 hrs and call back if did not resolve in a couple of days?.did not ask to see me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Double ear infection on 11/08/21 and had taken LEVOFLOXIN 500mg tablets for 1 week?ended antibiotic 2 weeks prior to vaccination booster
Vorgeschichte: Seasonal Bronchitis and allergies
Andere Medikamente: Held all my medications (only take over the counter) day of vaccination?Claritin, allergy nasal spray (PRN), Nexium (every 2 days), Magnesium (as needed for fatigue), Vit D3 2x week, Vit A 3x week for eyes, Multi Vit 2x week (all vitamins t
Allergien: Penicillin, horse serum Tetanus, Erythromycin, Sulfa, Peanuts, avocado, crab, lactose intolerant
Vorherige Impfungen: First Shingles vaccine similar symptoms for 1 week but no swelling in under arm

VAERS 1936998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 76,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Dry skin Injection site erythema Injection site inflammation Injection site pain Injection site reaction

Symptomtext

#1: no soreness, no redness in left arm #2: Mild soreness in arm if pressure applied to injection site in evening of day of shot; all gone by morning #3: Moderate soreness in right arm if pressure applied to injection site; perception of mild swelling in muscle at injection site; soreness gone by morning of subsequent day. moderate inflammation about the size of a 50? coin at injection site with roughness on a medium pink inflammation at injection site still observed 7 days later when bandaid first removed. Smooth medium pink discoloration the size of a 50? coin observed 15 days later. Light pink discoloration the size greater than a quarter coin ovserved 19 days later. Slight pink after 23 days quarter sized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none except psoriasis diagnosed at age 20; no treatments and no problems
Andere Medikamente: none
Allergien: marijuana (headaches), none known
Vorherige Impfungen: -

VAERS 1935412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Dizziness

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Dizziness / Lightheadness-Mild, Additional Details: Patient did state she's not sure if it's in her head. I called her after a few hours and she said she's totally fine.

Weitere VAERSDATA-Felder

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

VAERS 1932143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 04.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain Dyspnoea

Symptomtext

Chest pain such as tightness in chest, difficulty when breathing in hard, soreness in chest.

Weitere VAERSDATA-Felder

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

VAERS 1931596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: GA
Alter: -
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Blood pressure measurement COVID-19 Chest X-ray Cough Dry mouth Dyspnoea Feeling abnormal Headache Hypertension Immunisation Nasal congestion Pain Pain in extremity SARS-CoV-2 test Thirst Vaccination failure Vaccination site swelling

Symptomtext

Had problems breathing; I was positive for COVID using a PCR test; I was positive for COVID using a PCR test; is very thirsty and is drinking a lot of liquids, her mouth is very dry; felt bad; Body aches/ felt bad and achy; My arm had pain; booster; Headache; Coughing; a stuffy nose; had swelling where the shot was; is very thirsty; Blood pressure high; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 58 year-old female patient received bnt162b2 (BNT162B2), administration date 26Nov2021 (Lot number: FH8030) at the age of 58 as dose 3 (booster), single, administration date 07Apr2021 (Lot number: ER8729) as dose 2, single and administration date 17Mar2021 (Lot number: EN6206) as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: VITAMINS NOS. The following information was reported: COVID-19 (medically significant), VACCINATION FAILURE (medically significant) all with onset 28Nov2021, outcome "unknown" and all described as "I was positive for COVID using a PCR test"; IMMUNISATION (non-serious) with onset 26Nov2021, outcome "unknown", described as "booster"; PAIN (non-serious) with onset 27Nov2021, outcome "not recovered", described as "Body aches/ felt bad and achy"; PAIN IN EXTREMITY (non-serious) with onset 27Nov2021, outcome "recovering", described as "My arm had pain"; DYSPNOEA (non-serious) with onset 29Nov2021, outcome "recovering", described as "Had problems breathing"; HEADACHE (non-serious) with onset 2021, outcome "recovering", described as "Headache"; COUGH (non-serious) with onset 2021, outcome "unknown", described as "Coughing"; NASAL CONGESTION (non-serious) with onset 2021, outcome "unknown", described as "a stuffy nose"; DRY MOUTH (non-serious) with onset 28Nov2021, outcome "not recovered", described as "is very thirsty and is drinking a lot of liquids, her mouth is very dry"; HYPERTENSION (non-serious) with onset 2021, outcome "unknown", described as "Blood pressure high"; FEELING ABNORMAL (non-serious) with onset 27Nov2021, outcome "unknown", described as "felt bad"; VACCINATION SITE SWELLING (non-serious) with onset 2021, outcome "unknown", described as "had swelling where the shot was"; THIRST (non-serious) with onset 2021, outcome "unknown", described as "is very thirsty". The event "had problems breathing" was evaluated at the emergency room visit. I am 90% that I have the new variant (omicron). Reason for no lot number: of COVID-19 Vaccine: Other: Consumer stated, "No, I just do not want, I am not going to deal with this anymore. I am doing this Pfizer a favor and right now, I am not happy the all those things you are asking me." Consumer stated, "I took the Pfizer shot and I went to on the 21st (not clarified), I am a crew member, I came back on the 25th (not clarified) and I took the booster on the 26th (not clarified) and then I was supposed to go back to on the 28th and I got positive for the virus, I got positive with the swab, the rapid test, I got positive with the PCR." In response to probing for safety report, consumer stated, "The reason I was calling Pfizer because I was staying in a hotel in (Place withheld) in (Place withheld) watching TV and I was seeing the CEO for Pfizer talking about 'all they know about the vaccine thing'. I was almost a 100% sure that I have the African virus (further clarification unknown, hence event captured as per verbatim). So, I just wanted to share with Pfizer for them maybe further do a test to make sure that what I had because I went to the ER and they told me it was not a test that can do it and they just write the test because I was having problem breathing, I had the exact symptoms the doctors in say, that they have it (further clarification unknown, hence event captured as per verbatim), I do not have fever. So, I was going to talk with someone in Pfizer for them to learn about what I was going through right now because there was something to share with them that I came back from there and then I got positive, you know what I am saying like I want to help Pfizer to figure out if I had that virus, because I am telling you, you know what I am talking about, I am trying to help Pfizer." The caller lives in (place withheld), and was currently 58 years old. The caller was calling about the Pfizer covid vaccine. The caller got both vaccines and has received the booster dose. The caller works in the (Place withheld) . The caller went to on the 22Nov2021 and got back the 25Nov2021. On 26Nov2021 the caller took the booster dose. On 27Nov2021 the caller had some. On 28Nov2021 the caller found out she was positive for covid. The caller went to the emergency room because she was having problems breathing. The caller believes she has the new Micron variant. The covid test that the caller did was a PCR test which was positive. The caller notes that she had the rapid covid test on 21Nov2021 at the clinic in the airport which was negative. On 26Nov2021 the caller got her booster dose of the vaccine, the third dose. On 27Nov2021 the caller had a little bit of pain in her arm. On 28Nov2021 when the caller had her rapid covid test the nurse said she was positive. The caller cried for an hour because they put you in a hotel to quarantine. The caller got to the hotel on 28Nov2021. On 29Nov2021 the caller was having problems breathing and coughed so much her lungs were hurting so she went to the emergency room because it was hard to breathe. The caller didn't have anything for pain or coughing. They did an X-ray on the caller's chest and it was clear. They did a PCR covid test when the caller was in the emergency room but they did the rapid test at the airport. The PCR was positive as well. The caller was taking ibuprofen for her headache and never had a fever or lost her taste or smell. Its getting a little better, the caller was on the 4th day of her Z pack. The caller asked the emergency room for the cocktail to help her but they didn't have it. The has not contacted the caller and the emergency room staff said that they reported that she was positive for covid and had recently been to place. The caller was from (Withheld) and has a doctor in (place withheld) but she doesn't consider her her doctor. The caller was in (Withheld) on 17Nov2021 to see her doctor and they did her blood work and checked her covid antibodies. The caller's antibodies were positive this time but they were negative in the past. The caller was unsure when her antibodies were checked previously, she was unsure if she had her covid vaccines yet at this point. The caller will have to ask her doctor about this. The caller clarifies that all of her symptoms and events happened in the . To fly back home the caller did the covid test on the 18Nov2021 that was negative. The caller has not been eating. The caller had swelling where the shot was. The caller cried so much she thinks that was why she had the coughing. The caller has had coughing, a stuffy nose, sneezing, and a runny nose. The caller's stuffy nose and runny nose alternate. The caller's daughter had the virus last year for Christmas and the caller took care of her daughter and monitored her temperature and oxygen level. The caller's daughter had a bad reaction to the virus and the caller never got the virus while she was taking care of her. The caller believes she had the variant from because she had been exposed to covid so many times previously and never got it. The caller's body was hurting and she thought it was from the vaccine. The caller takes Ibuprofen every 8 hours as advised by the doctor because she was having headaches too. The headache was in the back of the caller's neck. The caller was very thirsty and was drinking a lot of liquids, her mouth was very dry. The caller's blood pressure was very high when she went to the emergency room it was 136/101 and her oxygen was normal. On 17Nov2021 the caller went to see her doctor and they did her blood work and checked her antibodies. The caller's antibodies were positive this time but they were negative in the past. The caller was unsure when her antibodies were checked previously, she was unsure if she had her covid vaccines yet at this point. The caller will have to ask her doctor about this. The caller notes that she had the rapid covid test on 21Nov2021 at the clinic in the airport which was negative. On 26Nov2021 the caller got her booster dose of the vaccine, the third dose. On 28Nov2021 when the caller had her rapid covid test the nurse said she was positive. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (unspecified date) 136/101, notes: blood pressure was very high; chest x-ray: (28Nov2021) clear; sars-cov-2 test: (18Nov2021) negative; (28Nov2021) positive, notes: positive with the PCR; (21Nov2021) positive. Therapeutic measures were taken as a result of headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:136/101; Comments: blood pressure was very high; Test Date: 20211128; Test Name: Chest X-ray; Result Unstructured Data: Test Result:clear; Test Date: 20211118; Test Name: COVID-19 virus test; Test Result: Negative ; Test Date: 20211128; Test Name: PCR Test; Test Result: Positive ; Comments: positive with the PCR; Test Date: 20211121; Test Name: rapid covid test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1929145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IN
Alter: 78,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / -

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

Arthralgia Mobility decreased Pain Vaccine positive rechallenge

Symptomtext

Severe pain in the injection side shoulder. Not the injection site but rather the whole shoulder. The pain is constant but more severe at night in bed. It is very painful for me to roll over in bed. It is difficult to raise my arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure which is under control.
Andere Medikamente: Lisinopril, Allopurinal, AREDS -2, Multi -vitamin
Allergien: None
Vorherige Impfungen: Pfizer Covid shot on 3/9/2021. Same reaction

VAERS 1928762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: WV
Alter: 39,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Blepharospasm Chest X-ray normal Computerised tomogram normal Electrocardiogram abnormal Eye pain Headache Migraine Nausea Pyrexia Tinnitus Vomiting

Symptomtext

It started with a really bad slight headache work up with a severe migraine, fever, nausea. My chief concern was my headache, ringing of my ears (mainly in left ear). I decided to inform my husband went to Urgent care. The wait was so long we went to hospital had test ran for my migraine. I vomited from Friday, Saturday, Sunday and on Tuesday. I took Zofran which has not help with my vomiting, I have also exp sharp in my left eye cause it to twitch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: 1,0
Labordaten: EKG (abnormal), CT scan (normal results), Chest X-ray (normal)
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Tramadol, Adderall, Women's Probiotic, Daily Vitamins, B12,
Allergien: No
Vorherige Impfungen: 2nd Pfizer (flu like symptoms lasted 3 days)

VAERS 1928540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NH
Alter: 47,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 01.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Fatigue Lethargy Lymphadenopathy Migraine Oropharyngeal pain SARS-CoV-2 test negative Streptococcus test negative

Symptomtext

Severe migraine for 3 days after second vaccine (Pfizer) 4 days after second vaccine- lethargy, fatigue, swollen lymph nodes, sore throat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Rapid strep- negative Covid PCR test- negative
Aktuelle Erkrankungen: none
Vorgeschichte: migraines asthma
Andere Medikamente: multi vitamin amitriptyline prozac
Allergien: augmentin flu vaccine gluten
Vorherige Impfungen: Flu vaccine

VAERS 1928374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IL
Alter: 40,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Hypotension

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Hypotension-Mild

Weitere VAERSDATA-Felder

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

VAERS 2559302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Headache Hypertension

Symptomtext

Headache & HYPERtension Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: The patient reports getting sick after each dose

VAERS 2559302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Headache Hypertension

Symptomtext

Headache & HYPERtension Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: The patient reports getting sick after each dose

VAERS 1924264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: MA
Alter: 58,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 05.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysphagia Dyspnoea Eye swelling Hypoaesthesia Mouth swelling Swelling face Swollen tongue Throat tightness

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild

Weitere VAERSDATA-Felder

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

VAERS 1924063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IN
Alter: 22,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 21.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Angina pectoris Cardiac discomfort Cardiac monitoring normal Chest X-ray normal Chest discomfort Chest pain Heart rate increased Laboratory test normal

Symptomtext

Heart/chest pain, tightness of heart/chest and elevated heart rate. Symptoms occurred for approximately 10 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Heart tracing: Normal. Chest x-ray: Normal. Basic labs. Blood testing for heart dysfunction: None seen. Blood testing for inflammation/blood clots: None seen.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C
Allergien: N/A
Vorherige Impfungen: -

VAERS 1923843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: AZ
Alter: 48,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Chills Decreased appetite Dizziness Feeling abnormal Feeling hot Hyperhidrosis Injection site pain Lethargy Lymph node pain Migraine Nausea Pyrexia

Symptomtext

Migraine started at 2:30 same day as the vx. Shortly after became lethargic. By 10pm felt feverish but temp wasn?t taken. Overnight had severe chills, sweating, nausea and migraine which persisted until approx 3pm on Dec. 3rd. Dizziness persisted, also loss of appetite and brain fog. Awoke Dec. 4th with pain under left arm, armpit area (lymph node). Left side of my face was hot while the right side was a normal temp. Sweating excessively but no fever suspected. Still have loss of appetite. Dec. 5th Only remaining symptom is pain in armpit. Soreness at injection site has occurred throughout.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperthyroidism, recent dx, no tx Diabetes Hypertension
Andere Medikamente: Lisinopril Metformin Sertraline
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1923648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: FL
Alter: 45,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: Patient reported having some numbness and tingling in the extremity they recieved the vacination and in their neck area. Patient discribed sensation as mild and did not worsen or improve while spending 30 minutes in the store after receiving the vacination.

Weitere VAERSDATA-Felder

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

VAERS 2565320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 35,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Diarrhoea Myalgia Pyrexia Tremor

Symptomtext

Myalgia, Diarrhea, violent body shaking, fever, chills, Narrative: N/A

Weitere VAERSDATA-Felder

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

VAERS 2565309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain Chills Headache Pain Palpitations

Symptomtext

Headache, Palpitations, chills, body aches, abdominal cramps Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2565302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 30.11.2021
Beginn: 02.12.2021
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 Pain Pain in extremity

Symptomtext

left arm pain radiated to chest area.. Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1920747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 64,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anti-thyroid antibody increased Atrial fibrillation Blood electrolytes normal Blood thyroid stimulating hormone increased Echocardiogram normal Full blood count normal Metabolic function test Metabolic function test normal Myocardial necrosis marker normal Palpitations Sinus rhythm Tachycardia

Symptomtext

Also received influenza vaccine in right deltoid at same time (no vaccine information supplied). Five hours after COVID vaccine, developed palpitations and tachycardia. Went to ER and found to be in A-fib with RVR. No prior cardiac issues. Spontaneously converted back to sinus rhythm at 0830 11/30/21 in hospital. Complete cardiac work-up found to be normal, no ACS. Of note, markedly elevated Thyroid peroxidase antibody and slightly elevated TSH noted, prior thyroid testing normal. Normal CBC and CMP including electrolytes. No instigating factor identified by Cardiology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 3,0
Labordaten: See Item 18, complete normal cardiac enzymes and ECHO 11/30/21.
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, GERD
Andere Medikamente: Omeprazole 40mg daily, HCTZ/Lisinopril 25/20mg, ASA 325mg
Allergien: None
Vorherige Impfungen: -

VAERS 1920651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: MO
Alter: 31,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Dyspnoea Fatigue Heart rate increased

Symptomtext

The night I got the vaccine I had a weird thing happen with my heart rate. Just walking form my bed to the bathroom and my office, I was winded and my heart rate was elevated. My apple watch was reading 135 bpm. Then, my heart rate was bouncing around all over the place while I was at rest working at my desk. I also felt very tired. I decided not to move the next day except for when I had to. I took a shower and my heart rate was 169bpm. Then I felt like I had run a 5k in the dead of summer. I was so fatigued the rest of the day. This went on for multiple days. I did a telehealth with my doctor and she advised me that I was probably okay and gave me tips on how to lower my heart rate. She said if it does not get better, I should go to urgent care. Today, I am feeling better but it still elevates a bit when I go on a walk.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Flonase Zyrtec Haley birth control Spironolactone 50mg daily Adderall 20 mg daily Vitamin C Vitamin D Zinc Melatonin gummies
Allergien: None
Vorherige Impfungen: Moderna dose 2- 02/12/2021- experienced a more mild case of elevated heart rate for a couple of days.

VAERS 1917543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CT
Alter: 46,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 30.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / RA

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

Chest pain Fibrin D dimer increased Palpitations

Symptomtext

CHEST PAIN AND PALPITATIONS D- DIMER ELEVATED

Weitere VAERSDATA-Felder

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

VAERS 1916376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IN
Alter: 60,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injection site coldness Injection site discomfort Injection site hypoaesthesia Injection site paraesthesia

Symptomtext

Patient experienced numbness, coldness, tingling and sensitivity to pressure in left arm, below site of vaccination, within 1 minute of injection. Hands are equally warm, pulse is normal, no complaints of shortness of breath, local pain, or dizziness. Symptoms have maintained severity for 30 minutes, seem to be beginning to lessen, but are still occurring.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: No illnesses.
Vorgeschichte: Acid Reflux; Quadruple bypass surgery in 2012.
Andere Medikamente: Metformin; Gempride; Lisinopril; Citalopram; Metoprolol; Baby Aspirin; Vitamin D; Omeprazole.
Allergien: Allergies to statins; Seasonal allergies (all year round) not identified, takes Zyrtec.
Vorherige Impfungen: -

VAERS 1914553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: PA
Alter: 72,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Gait disturbance Headache Injected limb mobility decreased Neck pain Pain in extremity Tinnitus

Symptomtext

Severe pain in side, back and front of neck, head-back of head, side of head, side of face, jaw, ears....I felt like I had been beaten up about my head and neck. Ringing in the ears (which still persists), dizziness, unsteady on feet. Severe pain in left arm, not able to lift arm. All symptoms lasted for over a week, with tinnitus still present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: scoliosis-repaired
Andere Medikamente: Multivitamin Calcium Actonel 35 1x week allegra
Allergien: Sulfa, penicillin, codeine, propofol, tramadol, relafen, morphine
Vorherige Impfungen: TDAP-01/02/2015; age 66. First dose of Pfizer Covid vaccine-04/04/2021; age 71.

VAERS 1913834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: IL
Alter: 31,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 27.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Dehydration Electrocardiogram normal Fatigue Full blood count normal Headache Heart rate increased Lymph node pain Lymphadenopathy

Symptomtext

The day after the vaccine I had high heart rate even after being inactive or 10 minutes. I went to the hospital where everything came back normal but they gave me fluids for dehydration. I have also been experiencing fatigue, headaches and pain/swelling in the lymph nodes in my armpits. I am also still experiencing high heart rate while inactive after leaving the hospital. I have a follow up with my PCP scheduled for Saturday 12/4/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Complete blood work panel- 11/28/2021- normal EKG- 11/28/2021- normal
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Adderall XR 30mg daily 10mg Adderall booster as needed Claritin once daily
Allergien: Erythromycin Meloxicam
Vorherige Impfungen: -

VAERS 1913394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Axillary mass Headache Nausea Tremor Vomiting

Symptomtext

fluid under the armpit: a lump. also headach, shakes, nausea and vomitting

Weitere VAERSDATA-Felder

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

VAERS 1910024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Differential white blood cell count Full blood count Hypertension Metabolic function test Swelling face Troponin

Symptomtext

Facial fullness, chest tightness, hypertension starting ~45 minutes post administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Physical exam; trops; CBC w/diff; trops x 2; Chem7
Aktuelle Erkrankungen: N/A
Vorgeschichte: HTN
Andere Medikamente: Epi-pen; Methylprednisolone; Diphenhydramine; Famotidine
Allergien: Codeine, Percocet
Vorherige Impfungen: Similar reactions (anaphalyctic-type) to both previous COVID doses (one Pfizer, one Moderna).

VAERS 1908556

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CO
Alter: 47,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 24.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Complement factor C4 Condition aggravated Immune complex assay Lip swelling Swelling face Urticaria

Symptomtext

11/24 12pm: Booster dose of Pfizer mRNA after first two of Moderna (finished 5/5)] 11/26: 6:20pm - Photo evidence of hip welt?pretty sure it began there either 24th or 25th, but have no photos. Left hip welt began to grow?.I thought it might go to face. 11/26 11:30pm: Video - hip growing, spread and height, and appears to be non-pitting, blanching. 11/27 2:20am: Facial swelling begins on the left side of lips - lower more prominent but upper had begun. Took 20mg of Cetirizine quick dissolving tabs (2) 11/27 7:25am: Facial swelling has spread to both sides of upper and lower lips and cheek/upper chin/Jowl on left side?maybe a little on right. 11/27 8:15am: Blood draw for C1/C4 tests. Needle goes in without issue?I?m sure there was latex gloves, but I don?t recall?rubbing alcohol, gauze and red wrap...nothing I'd think would cause a reaction. 11/27 1pm: Slight itch at draw site has me notice the ?hive? around the draw site?PHOTOS 11/27 2:15pm: Another 20mgs of quick dissolving Cetirizine 11/27 4:40pm: Lips draining a little, cheeks still strong, especially the left one. Draw site has really spread and raised. Left hip welt is still present but might be going away a bit. PHOTOS 11/28 2:15am: Swelling is still present, but does seems to be getting better in lips?10mg of Cetirizine 11/28 10:30am: Swelling is still present but is draining?left cheek is really still solid. Took 10mg of Cetirizine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Awaiting the C1/C4 test results.
Aktuelle Erkrankungen: Angioedema on October 26th.
Vorgeschichte: Chronic angioedema of unknown origin...but in my lifetime I've experienced eye or lip swelling over 20 times.
Andere Medikamente: None
Allergien: Unknown cause of angioedema.
Vorherige Impfungen: -

VAERS 1905754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chest pain

Symptomtext

Chest pain/pressure beginning date of second vaccine until currently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1905052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Tachycardia

Symptomtext

Systemic: Tachycardia-Mild

Weitere VAERSDATA-Felder

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

VAERS 1902077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: MA
Alter: 18,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Flushing Hyperhidrosis Hypotension Visual impairment Vomiting

Symptomtext

Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Medium, Systemic: Visual Changes/Disturbances-Medium, Systemic: Vomiting-Medium

Weitere VAERSDATA-Felder

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

VAERS 1899976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 21,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Pyrexia Tremor

Symptomtext

Uncontrollable shaking( more than just chills). Fever of 102. Joint pain. Resting heart rate of 130 while sleeping

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Joint pain
Andere Medikamente: -
Allergien: Cat dander. Dust. Moxifloxicin
Vorherige Impfungen: -

VAERS 1899720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 59,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Muscle spasms Myalgia Pyrexia Rash Fear Head discomfort Illness Tremor

Symptomtext

Severe high temp 101.8 and weird muscle spasm in my head that lasted four days and continues now the fever was 28 hours and would not break! I will never take another vaccine I was so scared and very very sick 28 hours.

Weitere VAERSDATA-Felder

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

VAERS 1899545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MD
Alter: 33,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 20.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Musculoskeletal chest pain

Symptomtext

Extreme Tenderness in my ribs. It's hurts to bend or touch, lay down.; This is a spontaneous report from a contactable other healthcare professional, the patient. A 33-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FH8030) via an unspecified route of administration in the left arm on 20Nov2021 at 17:15 (at the age of 33-years-old) as a single dose for COVID-19 immunisation. Medical history included acne and sulfa allergy. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included spironolactone (MANUFACTURER UNKNOWN) for an unknown indication, from an unknown date and unknown if ongoing. The patient did not receive any other vaccine within four weeks prior to the COVID-19 vaccine. The patient previously received paracetamol; oxycodone hydrochloride; oxycodone terephthalate (PERCOCET) and experienced drug allergy. On 21Nov2021 at 08:00, the patient experienced extreme tenderness in her ribs; it hurt to bend, touch or lay down. No therapeutic measures were taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event extreme tenderness in ribs; it hurt to bend, touch or lay down was resolving at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acne; Sulfonamide allergy (Known allergies: Sulfa)
Andere Medikamente: SPIRONOLACTONE
Allergien: -
Vorherige Impfungen: -

VAERS 1897600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: PA
Alter: 27,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Hypoaesthesia Immediate post-injection reaction

Symptomtext

IMMEDIATELY AFTER INJECTION SHE INDICATED SHE HAD TROUBLE BREATING AND FELT NUMB ALL OVER HER BODY.PHARMCY TECHNICIAN CALLED 911 FOR PARAMEDICS IN THE MEANTIME I GAVE HER AN EPIPEN INJECTION WHICH SHE IMMEDIATELY INDICATED SHE FELT BETTER AND HAD IMPROVED BREATHING. THE PARAMEDICS CAME IN A FEW MINUTES AND CHECKED HER AND TOOK HER TO THE HOSPITAL. LATER IN THE DAY SHE STOPPED IN WITH A PRESCRIPTION FROM ER AND INDICATED SHE WAS FEELING BETTER.

Weitere VAERSDATA-Felder

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

VAERS 1896980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: NY
Alter: 68,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain Pain

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Medium, Additional Details: Chest pain-felt like getting vaccine in chest area/breast last night (pinch/stabbing pain) and then changed to more of a dull pain today. pain scale 5 and now dropped to 3

Weitere VAERSDATA-Felder

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

VAERS 1895088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: PA
Alter: 29,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Dizziness Dyspnoea

Symptomtext

Patient started to experience chest pain, difficulty breathing, and light-headedness approximately 5 minutes after receiving their first dose of the Pfizer COVID-19 vaccine. 10-15 minutes after dose administration, patients blood pressure was 108/56 mmHg which they stated was normal for them. I continued to observe and a few minutes later the patient stated their chest pain and light-headedness was worsening. I called 911 emergency personnel at 17:40 to the scene for further care, they arrived at 17:48 and took him to the hospital for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1893450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OH
Alter: 47,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dysphagia Dyspnoea Throat tightness

Symptomtext

Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Additional Details: Minutes after administeration of vaccine, patient reported that she thinks she is having trouble breathing and it is possible that her throat is swelling shut, she was unsure. Administered bendaryl to patient with a sip of water. After observation for 15-30 minutes, patient said that she feels fine. Patient said that she also has asthma which may have contributed to her symptom(s).

Weitere VAERSDATA-Felder

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

VAERS 1890409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: WA
Alter: 79,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 20.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Interchange of vaccine products Vertigo

Symptomtext

Prior vaccination with Moderna Covid on 2/9/21 and 3/9/21. Had onset of vertigo after her initial vaccinations which resolved over 1 month. No prior issue with balance or vertigo. The day after she had her Covid booster with Pfizer, she again had onset of vertigo.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis, hypertension, hypothyroid, celiac disease, asthma, double vision, status post cataract surgery
Andere Medikamente: Levothyroxine, amlodopine, atorvastatin,
Allergien: Nitrofurantoin, codeine, meperidine, naproxen, oxycodone
Vorherige Impfungen: Moderna Covid, 78 years, 2/9/21 and 3/9/21

VAERS 1890196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CO
Alter: 48,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspepsia Hypertension Migraine Rhinorrhoea

Symptomtext

Patient experienced high blood pressure over 160/90 several hours after vaccine. Patient still has high blood pressure 3 weeks after vaccine. They never had high blood pressure prior to vaccine. Patient also began having recurring migraines the next day after vaccine. Also had heartburn start shortly after, along with sinus drainage.

Weitere VAERSDATA-Felder

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

VAERS 1889186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NY
Alter: 58,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain Mobility decreased Neuralgia Paraesthesia

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: Tingling (specify: facial area, extremities)-Severe, Additional Details: Patient reported difficulty moving upper arm. Nerve pain in shoulder.

Weitere VAERSDATA-Felder

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

VAERS 1888690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

moderat

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: UN / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

My hands and feet fall asleep and I feel pins and needles. No treatment. What could possibly relieve this? A doctor cannot do anything for me.

Weitere VAERSDATA-Felder

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

VAERS 1888261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia Pharyngeal hypoaesthesia Throat tightness

Symptomtext

Throat tightness within 10 minutes of receiving injection. One hour later, experienced numbness and tingling in left arm, down to fingers. Shortly afterward, felt numbness/tingling in face. Arm and face numbness/ tingling lasted several hours, then subsided. Both then returned on and off for the rest of the day and during the second day. Three days after vaccination, facial numbness is more pronounced, and numbness has spread to neck/throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Went to urgent care on 11/19. No tests were done.
Aktuelle Erkrankungen: None
Vorgeschichte: Crohn's disease
Andere Medikamente: Sulfasalazine, low dose naltrexone
Allergien: Cipro, gluten, dairy
Vorherige Impfungen: -

VAERS 1888232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IN
Alter: 29,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood creatine phosphokinase Blood urine present Chromaturia Condition aggravated Extra dose administered Full blood count Metabolic function test Urine analysis abnormal

Symptomtext

24 hours after the 3rd covid Pfizer vaccine, patient developed brown-colored urine. Similar episode after receiving 2nd covid Pfizer vaccine, and the brown-colored urine self-resolved after 72 hours at that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Patient went to Urgent Care 48 hours after vaccine administration and was found to have 3+ blood on urine dipstick. CBC, CMP, and CPK are currently pending.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Brown-colored urine x72 hours, 28 years old, 1/8/21, Pfizer covid vaccine (2nd dose)

VAERS 1888083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MD
Alter: 20,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain upper Chills Dizziness Headache Nausea Pyrexia Tachycardia Tremor

Symptomtext

Fever, chills, nausea, tremors, stomach pain, headache, tachycardia (130 bpm resting) and dizziness; starting approximately, 10:00 pm, November 19, 2021, 9 hours post vaccination, and continuing through the night into November 20, 2021. Symptoms currently ongoing, less severe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Metoprolol Tartrate 25mg; Melatonin 3mg
Allergien: Codeine; Sulfa; Omnicef
Vorherige Impfungen: -

VAERS 1887971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: VA
Alter: 30,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dysmenorrhoea Injection site pain Injection site swelling Mobility decreased Pyrexia

Symptomtext

Low fever (101F?), pain in the injection site with swelling and limited mobility. Severe period cramps even though I had a period 2 weeks ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: High Cholesterol
Vorgeschichte: Asthma
Andere Medikamente: 8am: Bupropion XL 300mg, Vitamin D3 (1,000 iu), Garden of Life Once a Day Female Probiotics, Zyxal (generic) 25mg. 5pm: 2 Tylenol extra strength Arm implant Nexplanon 2 years in.
Allergien: Pineapple, fungus/mold, chocolate, shellfish, Aspirin and NSAIDS
Vorherige Impfungen: -

VAERS 1881296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OK
Alter: 37,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Flushing Hypertension Tachycardia

Symptomtext

Flushing, tachycardia, and hypertension. Required Benadryl 37.5 mg oral and IM Solumedrol 40 mg. which resolved tachycardia and hypertension

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: states had a "cold" with some left sided chest tightness and wheezing (COVID test neg per report)
Vorgeschichte: none
Andere Medikamente: none
Allergien: TDap immunizaion
Vorherige Impfungen: TDAP, Light headedness and racing heart approx. 2009

VAERS 1880552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

moderat

Staat: NY
Alter: 40,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Dyspnoea Fatigue Oropharyngeal pain Pain Rhinorrhoea Sinus congestion

Symptomtext

Body aches, Fatigue, Sore throat, Sinus/Nasal congestion, runny nose, Shortness of breath, Chest tightness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, Colon Cancer, Ulcerative colitis, Anxiety
Andere Medikamente: Ventolin HFA, clonopins, Nyquil, Tamiflu
Allergien: Walnuts
Vorherige Impfungen: -

VAERS 1880075

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: FL
Alter: 29,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Blood pressure normal Dizziness Heart rate normal Tremor

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Shakiness-Medium, Additional Details: patient said she is very anxious about possible reaction with pfizer vaccine short and long term. she felt better before leaving. Was given electrolytes and snacks because she stated she didn't have any food before vaccination. BP and HR were within normal range

Weitere VAERSDATA-Felder

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

VAERS 1878046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: WA
Alter: 14,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Crying Dizziness Fall Tremor

Symptomtext

Patient received 1st dose of Pfizer, patient fell face down on the floor 5 minutes after receiving the vaccine. She complained of dizziness, crying and shaking. Neurological and skin assessment done - no injuries sustained, she was alert and oriented x 4, crying and anxious. Vitals were within normal limits, legs were elevated and assisted to sitting position when dizziness relieved. She was released stable to family members.

Weitere VAERSDATA-Felder

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

VAERS 1877678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: WV
Alter: 18,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anal incontinence Hyperhidrosis Malaise Tremor Vomiting

Symptomtext

About 5 minutes post vaccination, the patient started vomiting. She said her hands were sweaty and they were shaking. She also deficated. Her mom was there and said she has a vomiting syndrome and diabetes. She also did not eat all day. She sat for about 20 minutes and was still feeling sick so her mom was going to take her to the ER because she thought it was from one of her other illnesses.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 1877330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: WA
Alter: 34,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 11.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Blood pressure increased Chest discomfort Dyspnoea Electrocardiogram normal Fatigue Feeling abnormal Headache Heart rate increased Mobility decreased X-ray normal

Symptomtext

Friday & Saturday, I felt bad and tired. Fatigued and I couldn't do very much. I had bad headaches. Sunday morning and I couldn't breathe very well, and I felt like there was a bar across my chest. When I got up my boyfriend was trying to watch me breathe and said it was bad. So, the nurse line suggested to call 911. Paramedics came and looked at me, and they said the BP and HR was high but within normal range and my O2 was normal as well. So, on Monday I was able to go to my primary to see another doctor. I had an ECG and an x-ray done and were both normal. They told me to schedule an appointment with my PCP, but she hasn't had availability for the last couple weeks. So, I'm trying to get help with my breathing and see if they can prescribe anything to help with that. Brother also had issues with Pfizer vaccination regarding the 2nd dose. Could be genetic but unsure at this time since both of us had a reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ECG - normal X-ray -normal
Aktuelle Erkrankungen: None
Vorgeschichte: PCOS
Andere Medikamente: Metformin 1000mg once daily
Allergien: Mild reaction to Naproxen Sodium Band-Aids
Vorherige Impfungen: Sick after second Pfizer - not too serious

VAERS 1876908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 10.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Condition aggravated Herpes zoster Influenza Injection site pain Myalgia Neck pain Rash

Symptomtext

Sire right arm at injection site and flu type symptoms the day after vaccine. Second day after vaccine sore neck/shoulder muscles which grew increasingly worse. Rash developed on 11/16/2021. Went to urgent care on 11/17/2021 and diagnosed with shingles.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: B12 D3 Collagen Amal powder Spriva inhaler
Allergien: None
Vorherige Impfungen: Sore arm at injection site, flu like symptoms.

VAERS 1876223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: NJ
Alter: 12,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Dysphagia Dyspnoea Flushing Hyperhidrosis Throat tightness

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: pt was given 1 shot of epipen 0.3 mg , called 911 , pt symptoms improved right after the epipen shot , his mom drove him to emergency room to monitor and follow up , the kid was ok before leaving the pharmacy

Weitere VAERSDATA-Felder

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

VAERS 1876213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Limb injury Pain Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 1874655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: IL
Alter: 47,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 12.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Arthralgia Injected limb mobility decreased Injection site discomfort

Symptomtext

I received the 3rd booster shot of the Pfizer vaccine on Friday. The only side effect on Saturday was some slight discomfort at the injection site on my left arm. On Sunday, the joint in my left shoulder became painful and I could not raise my left arm above my head. On Monday, the pain in the joint of my left shoulder become to subside.

Weitere VAERSDATA-Felder

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

VAERS 1874180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: CA
Alter: 36,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthma Chest pain Condition aggravated Dyspepsia Oedema peripheral

Symptomtext

patient has taken tylenol on the second day reffered to his doctor or emergency room

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: asthma
Vorgeschichte: Asthma
Andere Medikamente: The person felt heartburn at night on 11/12 then next day in the afternoon when he was taking the shower found a bump under his left armpit . It has become worse since then and patient has felt chest pain. Patient has asthma and his asthma
Allergien: N/A
Vorherige Impfungen: -

VAERS 1873257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: VA
Alter: 46,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Dizziness Dyspnoea Fatigue Heart rate increased Hepatic enzyme increased Laboratory test Night sweats Thyroid function test Tremor Herpes zoster Rash

Symptomtext

shingles outbreak rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: bronchitis and sinus infection
Vorgeschichte: fibromyalgia, HTN, chronic pain, migraines, allergies, TBI, PTSD, neuropathy
Andere Medikamente: venlafaxine, HCTZ/lisinopril combo 12.5/10, allegra, topamax, pantaprazole, atarax, oraphedrine, prebiotic
Allergien: latex, iodine, ketamine, hydrocodone, codeine, shellfish, benadryl, penicillin
Vorherige Impfungen: -

VAERS 1872971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 34,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Chest X-ray normal Chest discomfort Computerised tomogram head normal Dizziness Dyspnoea Electrocardiogram normal Fibrin D dimer normal Heart rate increased Hypertension Hypoaesthesia Immediate post-injection reaction Laboratory test normal Limb discomfort Magnetic resonance imaging head normal Magnetic resonance imaging spinal normal Nausea Neurological examination abnormal

Symptomtext

Immediate dizziness and vertigo following vaccine. After 4 hours onset of hives on chest and arms with difficulty breathing, and severe nausea and vomiting. Onset of neck rigidity, left leg heaviness and numbness. Went to Urgent Care for immediate treatment, and was given ondansetron for nausea and advised to go to ER if symptoms persisted. Condition worsened with onset of severe vertigo, facial numbness, rapid pulse, chest heaviness (difficulty breathing), and increased leg numbness and tingling. Went to ER for treatment and had high blood pressure (169/91).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: MRI Brain (W/WO Contrast), MRI Lumbar Spine (W/WO Contrast), MRI Thoracic Spine (W/WO Contrast), CT Head WO Contrast, Chest X-Ray, D-Dimer test, EKG, and multiple labs. All labs and tests came back clear. Neurology examined and noted decreased strength in left leg and advised outpatient EMG/NCS and follow up with neurologist.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ortho Tri-Cyclen
Allergien: PCN
Vorherige Impfungen: -

VAERS 2574028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Headache Tachycardia

Symptomtext

Headache & Tachycardia Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1869436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OK
Alter: 34,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia Sensory loss

Symptomtext

Tingling and loss of sensation in left hand.

Weitere VAERSDATA-Felder

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

VAERS 1869328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: UT
Alter: 45,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 03.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest pain Computerised tomogram Electrocardiogram

Symptomtext

On Nov 12, (9 days after injection) started having burning chest pain localized on left side of sternum.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: All Nov 14 2021 EKG - signs of pericarditis Blood tests for troponin-normal D-dimer - elevated CT Scan - normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Dietary supplements: fish oil, zinc, magnesium, MSM, D3
Allergien: None
Vorherige Impfungen: -

VAERS 1868611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 31.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Chills Condition aggravated Extra dose administered Fatigue Fibromyalgia Headache Injection site pain Pain Pyrexia Rhinorrhoea Swelling Upper-airway cough syndrome

Symptomtext

Initial vaccine (3/31/2021) and booster (11/13/2021) produced the same side effects. Very painful headache, significant body aches all over, post nasal drip/runny nose, chills, mild fever (only for a few hours at start of symptoms), pain at injection site with mild swelling, fatigue. Symptoms usually begin 8-10 hours after vaccine and last for 3-6 days. The worst part is the pain and fatigue, which could be a flare up of fibromyalgia symptoms at some point. Currently recovering from booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Fibromyalgia, GERD, IBS
Vorgeschichte: See item 11
Andere Medikamente: -
Allergien: None.
Vorherige Impfungen: -

VAERS 1868314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: KY
Alter: 47,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Abdominal pain upper Body temperature increased Crying Dyspnoea Gait disturbance Headache Muscle spasms Pain Pain in extremity Skin burning sensation Somnolence Tension Thinking abnormal

Symptomtext

The second shot felt wrong almost immediately. Sharp pain started shooting down my arm. Temp started being very noticeable. My arms started tensing up. Then my whole body has felt like it was totally having charley horses. I laid in the fetal position and cried. Temp wouldn?t go down it was 103.4 at its highest. Yesterday slept most of the day. The pains keep coming back. Temp came back 101.7. So then my skin burned. Every single part of me felt like my bones and muscle is going to burst thru my skin. Severe headache unlike even a migraine. Temp today is 99.4 but now I try to walk in my house and stumble. Can?t stay awake. Shortness of breath started just about an hour ago. Severe stomach pains. Continued can?t keep thought.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No however I did take the also mandated flu shot
Andere Medikamente: No
Allergien: Codiene and morphine.
Vorherige Impfungen: -

VAERS 1867917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 39,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Electrocardiogram normal Hypoaesthesia Paraesthesia Heart rate increased

Symptomtext

Patient received Pfizer COVID vaccine in right arm. Within 15 minutes, patient returned to the pharmacy saying his chest felt weird and he was having tingling/numbness in his left arm. Patient instructed to sit down. Pharmacist called 911. 911 operator instructed pharmacist to give patient 4 tablets of aspirin 81 mg to chew while waiting for paramedics to arrive. Patient complied. Paramedics arrived within 10 minutes and checked vital signs and did EKG, which they report as being within normal limits. Patient then left the store.

Weitere VAERSDATA-Felder

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

VAERS 1864532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest discomfort Chest pain Dizziness Flushing Hyperhidrosis Hypertension Visual impairment

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating-Mild, Systemic: Hypertension-Mild, Systemic: Visual Changes/Disturbances-Mild

Weitere VAERSDATA-Felder

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

VAERS 1861813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 29.03.2021
Beginn: 08.05.2021
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: SYR / LA

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

Heart rate increased Magnetic resonance imaging head normal Palpitations Visual impairment

Symptomtext

Approximately 3 weeks after second shot vision problem started to surface, 5-6 months after second shot heart pounding and rapid heart beats. Things I did not have before vaccinations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Three vision tests without resolve, one brain MRI results were unremarkable.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa drugs, erythromycin, ct dye
Vorherige Impfungen: -

VAERS 1860866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Muscle twitching Paraesthesia oral Pharyngeal paraesthesia

Symptomtext

Patient received Pfizer COVID-19 Vaccine to right deltoid at 0906. Patient was in observation area of the clinic, when RN received called from Pharmacist at 0930 with patient who had complaints of tingling to her mouth and throat. RN responded and Epinephrine 1mL was administered per protocol at 0934 to right vastus lateralis. Patient's initial vital sign assessment was: 1st blood pressure 149/93, 2nd blood pressure 139/85; heart rate was 70, O2 was 96% on room air. Patient airway was clear. RN stayed with patient to monitor and patient's PCP came to check on patient as well. Patient then report symptoms improving and was medically stable. PCP agreed to keep patient in the clinic longer for further observation to prevent ED visit. At 0955 patient started to complain of right arm involuntary twitching intermittently, noting it started about 1 minute ago. Pt unable to grasp RN hand; however patient was able to grasp with left hand and pushed down with her right and left leg with out any concerns. Patient denies any respiratory complaints and continues to be responsive. Patient did endorse this reaction occurred one other time after taking Reglan. RN called for provider assessment. Two doctors came to assess patient to rule out stroke. Patient was able to hold both arms above head showing muscle strength and tone. Doctor's direction was to bring patient to the ED for further observation. Patient was transferred to a wheelchair with minimal 1 person assistance. 2 RNs brought patient to the ED via wheelchair. Upon getting to the 2nd floor patient began to have gross twitching to bilateral arms and was still responsive. Shortly after the patient began to have full body gross twitching. One RN assisted with prevention of fall from wheelchair, while other RN called code blue, patient began minimally responding (able to open eyes on command, but unable to tell name) and was brought down to the ED with the code team.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: Blood work (HIV, CBC. Magnesium, BMP) No additional testing noted at this time.
Aktuelle Erkrankungen: Chronic low back pain
Vorgeschichte: Prediabetes Gastroparesis Asthma Sleep Apnea
Andere Medikamente: 1. Albuterol nebulizer 2. Vitamin D3 3. Ventolin inhaler
Allergien: 1. Amoxicillin 2. Metoclopramide 3. Penicillin 4. Reglan 5. Tigan
Vorherige Impfungen: -

VAERS 1860803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / AR

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

Dyspnoea Headache

Symptomtext

Patient stated that she couldn't breathe overnight after getting vax. Patient stated that she has asthma. Patient also reported headaches.

Weitere VAERSDATA-Felder

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

VAERS 1860532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: NJ
Alter: 50,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Dyspnoea

Symptomtext

Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Dizziness / Lightheadness-Mild

Weitere VAERSDATA-Felder

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

VAERS 1855768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CT
Alter: 38,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Hypersensitivity Pharyngeal paraesthesia Tryptase

Symptomtext

Chief Complaint Patient presents with ? Allergic Reaction Patient is a 38 y/o F with PMHx ankylosing spondylitis, migraine headaches who presents to ED at request of COVID-19 service line for evaluation of post-vaccination symptoms. Patient received her COVID-19 vaccine at 1:00PM. She was monitored for 30 minutes without any symptoms. At 2:00 p.m., patient began feeling a sensation of tingling in her throat. She subsequently called the COVID-19 vaccination hotline and was recommended to present to the ED for evaluation. She denies all other symptoms including headache, dizziness, lightheadedness, changes in vision or hearing, nausea, vomiting, chest pain or pressure, palpitations, shortness breath or difficulty breathing, wheezing, abdominal pain, pelvic pain, diarrhea, myalgias, arthralgias, paresthesias, rashes or lesions, skin pruritus. She does have an allergy to aspirin and penicillins with reported hives and shortness of breath characterized as anaphylaxis. The history is provided by the patient. No language interpreter was used. This is a new problem. The current episode started 1 to 2 hours ago. The problem occurs constantly. The problem has not changed since onset.Pertinent negatives include no chest pain, no abdominal pain, no headaches and no shortness of breath. Nothing aggravates the symptoms. Nothing relieves the symptoms. She has tried rest for the symptoms. The treatment provided no relief. Review of Systems Constitutional: Negative for chills and fever. HENT: Negative for congestion. Respiratory: Negative for shortness of breath. Cardiovascular: Negative for chest pain. Gastrointestinal: Negative for abdominal pain, diarrhea, nausea and vomiting. Genitourinary: Negative for dysuria. Musculoskeletal: Negative for back pain. Skin: Negative for rash. Neurological: Negative for dizziness, light-headedness and headaches. All other systems reviewed and are negative. Physical Exam ED Triage Vitals [11/03/21 1446] BP: (!) 147/107 Pulse: n/a Pulse from O2 sat: (!) 98 Resp: 18 Temp: 98.1 ?F (36.7 ?C) Temp src: Oral SpO2: 98 % BP (!) 141/96 | Pulse 76 | Temp 98.2 ?F (36.8 ?C) (Oral) | Resp 18 | SpO2 100% Physical Exam Vitals and nursing note reviewed. Constitutional: Appearance: Normal appearance. She is well-developed. HENT: Head: Normocephalic and atraumatic. Nose: Nose normal. Mouth/Throat: Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Conjunctiva/sclera: Conjunctivae normal. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: Normal heart sounds. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Normal breath sounds. Chest: Chest wall: No tenderness. Abdominal: General: Abdomen is flat. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: General: Normal range of motion. Cervical back: Normal range of motion and neck supple. Skin: General: Skin is warm and dry. Neurological: Mental Status: She is alert and oriented to person, place, and time. Psychiatric: Mood and Affect: Mood normal. Behavior: Behavior normal. Procedures Procedures Resident/APP MDM: 38 y/o F with PMHx ankylosing spondylitis, migraine headaches who presents to ED at request of COVID-19 service line for evaluation of post-vaccination symptoms. Patient received her COVID-19 vaccine at 1:00PM. She was monitored for 30 minutes without any symptoms. At 2:00 p.m., patient began feeling a sensation of tingling in her throat. She subsequently called the COVID-19 vaccination hotline and was recommended to present to the ED for evaluation. She denies all other symptoms including headache, dizziness, lightheadedness, changes in vision or hearing, nausea, vomiting, chest pain or pressure, palpitations, shortness breath or difficulty breathing, wheezing, abdominal pain, pelvic pain, diarrhea, myalgias, arthralgias, paresthesias, rashes or lesions, skin pruritus. She does have an allergy to aspirin and penicillins with reported hives and shortness of breath characterized as anaphylaxis. On initial presentation, patient well appearing in no acute distress. Vital Signs grossly unremarkable. Normotensive, afebrile, even, nonlabored respirations at 98% room air, 18 breaths per minute. Heart regular rate and rhythm, lungs clear throughout with vesicular breath sounds. No urticaria appreciated on the all layers of skin. Oropharynx without edema or swelling. No laryngeal tenderness. Limited differential includes: Hypersensitivity reaction, consider early anaphylactoid reaction. Consider anxiety. Plan: -labs include tryptase -125 mg IV Solu-Medrol, 25 mg IV Benadryl, 20 mg IV Pepcid. No acute or emergent need for epinephrine at present. If needed, consider of 0.3 mg epinephrine if secondary organ system involvement occurs -continue to monitor for clinical signs of anaphylaxis; if stable, discharged with short course of prednisone and strict return precautions Results: -7:57 PM patient feeling significantly improved. Will discharge home with continued use of Pepcid and or Benadryl every 4-6 hours as needed, 5 day course of prednisone 40 mg once daily, EpiPen autoinjector in strict return precautions/follow-up instructions. Patient verbalized understanding and is in agreement with this plan of care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: tryptase and CH50; not yet resulted
Aktuelle Erkrankungen: none noted
Vorgeschichte: Migraine without aura and without status migrainosus, not intractable Class 1 obesity due to excess calories without serious comorbidity with body mass index (BMI) of 31.0 to 31.9 in adult Radial styloid tenosynovitis of right hand Right wrist pain Stiffness of right wrist joint Abdominal pain Vulvodynia DDD (degenerative disc disease), lumbar Abnormal Pap smear of cervix
Andere Medikamente: Humira Relpax Junel Naprosyn
Allergien: ASA-hives, shortness of breath Penicillin-hives, shortness of breath
Vorherige Impfungen: -

VAERS 1854258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

moderat

Staat: MD
Alter: 89,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Cardiac murmur Fatigue Haemoglobin decreased Mobility decreased SARS-CoV-2 test negative Urinary tract infection White blood cell count abnormal

Symptomtext

Became very fatigued the day after her second covid shot. Could not pick her up. Transported to hospital by ambulance and a negative covid test was done. Admitted into hospital for supposedly a urinary tract infection. Her white blood cell count did come down but not sure if that was from antibiotics or her cll. She was supposed to get a procrit shot on friday for her cll if hemoglobin is below 10 which is was dangerously low at 7.5. Medicare does allow it to be given in hospital even though the oncology center is attached to the hospital. The oncologist checked with the pharmacy for the procrit shot amd the pharmacist said no she does not meet the criteria. Luckily it has gone back up to 8.6. They are not getting her out of bed either so she will need a rehab. also they said she has a heart murmer which i have never seen diagnosed for her before

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Please see above. Multiple blood work work done.
Aktuelle Erkrankungen: Cll luekemia, stage 3 kidney disease, skin cancer
Vorgeschichte: Cll leukemia, stage 3 kidney disease, skin cancer
Andere Medikamente: Baby aspirin, zoloft, zyrtec, amlodipine, levothyroxine, atorvastatin, tylenol pm, tylenol 650mg
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1853958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Patient experienced numbness and tingling to the lower extermity on the right arm upto her elbow after receiving the covid19 2nd vaccine. She said the numbness went away the same day in the evening and the tingling went away in the late afternoon on 11/6/21 (saturday). she has recovered from her tingling and numbness.

Weitere VAERSDATA-Felder

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

VAERS 1853604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Electrocardiogram normal Hypoaesthesia Paraesthesia

Symptomtext

Tingling and numbness - pins and needles sensation upper body, limbs and mouth approximately one hour after first dose administered. Cleared approximately 15 minutes later. Sensation appeared once again 30 minutes after clearing. Urgent care visit-advised to monitor symptoms at home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EKG-11/8/2021-normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Zoloft
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1850371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: RI
Alter: 25,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Injection site erythema Injection site mass Musculoskeletal chest pain Pain Pyrexia Tenderness

Symptomtext

Pt had a fever on 11/1 which completely resolved within 12 hours. 11/3 a red lump appeared at injection site along with SOB and "achiness". Also had pain along bilateral anterior ribs that were tender to palpation.

Weitere VAERSDATA-Felder

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

VAERS 1848904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort Arthralgia Diarrhoea Fatigue Feeling abnormal Extra dose administered Immediate post-injection reaction Injection site erythema Injection site inflammation Joint stiffness Pain Pain in extremity Paraesthesia Pruritus Pyrexia

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

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

VAERS 1848904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / UN

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

Abdominal discomfort Arthralgia Diarrhoea Fatigue Feeling abnormal Extra dose administered Immediate post-injection reaction Injection site erythema Injection site inflammation Joint stiffness Pain Pain in extremity Paraesthesia Pruritus Pyrexia

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

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

VAERS 1849138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

moderat

Staat: NM
Alter: 57,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Headache Palpitations Peripheral swelling

Symptomtext

Patient called with swollen arm from neck to hand, states it started this morning after receiving Pfizer Covid-19 booster in his right arm yesterday. Yesterday he had chest pain, heart pounding and headache that went away then he woke up this morning with arm swelling. I recommended he call his MD office and go to urgent care for further assessment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unk
Vorgeschichte: asthma, diabetes
Andere Medikamente: unk
Allergien: nkda
Vorherige Impfungen: -

VAERS 1842637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

moderat

Staat: FL
Alter: 35,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Discomfort Dysphagia Lymphadenopathy Throat tightness Tremor

Symptomtext

Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Chills-Mild, Systemic: Shakiness-Mild, Additional Details: Patient experienced discomfort when swallowing and stated it was probably due to her large lymph nodes. Rph asked if patient had trouble breathing and offered epinephrine but patient denied sob/dyspnea and could hold a conversation/answer questions. Rph called emergency services at 5:54 pm and paramedics arrived around 6:01 pm. Patient was alert and aware of her surroundings and was able to answer paramedic's questions. Rph expressed feelings of speedy recovery and asked patient to follow up.

Weitere VAERSDATA-Felder

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

VAERS 2725648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 55,0
Geschlecht: F
Eingang: 20.12.2023
Impfdatum: 23.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Pain in extremity

Symptomtext

Reaction to the shot in term of pain in the arm significantly worst then prior shots ON; This is a spontaneous report received from an Other HCP. A 57-year-old female patient received BNT162b2 (BNT162B2), on 23Nov2021 as dose 3 (booster), single (Lot number: FH8030) at the age of 55 years intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Hashimoto" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Sulfa, reaction(s): "allergy". Vaccination history included: BNT162b2 (dose 1, lot number unknown), administration date: 12Mar2021, for COVID-19 immunisation, reaction(s): "Reaction to the shot in term of pain in the arm significantly worst then prior shots ON"; BNT162b2 (dose 2, lot number unknown), administration date: 01Apr2021, for COVID-19 immunisation, reaction(s): "Reaction to the shot in term of pain in the arm significantly worst then prior shots ON". The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Reaction to the shot in term of pain in the arm significantly worst then prior shots ON".; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300414510 Same patient, partial same event, different dose;US-PFIZER INC-202300447636 Same patient/event, different dose;US-PFIZER INC-202300447641 same patient/product, different event/vaccine dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2719315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 57,0
Geschlecht: F
Eingang: 30.11.2023
Impfdatum: 26.11.2023
Beginn: 26.11.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: - / LA

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

Arthralgia Ear pain Headache Hypoaesthesia Pain in extremity Temporomandibular joint syndrome Wrong product administered

Symptomtext

TMJ; sore next and shoulder; earache when chewing; Headache; pain in the arm; numbness of left face; wrong vaccine administered; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 57-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 26Nov2023 at 18:00 as dose 6, single (Lot number: FH8030) at the age of 57 years, in left arm for covid-19 immunisation. The patient didn't receive bnt162b2 omi xbb.1.5 (COMIRNATY (2023-2024 FORMULA)). The patient's relevant medical history included: "Hashimoto" (unspecified if ongoing); "known allergies: sulfa" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Covid-19 vaccine (dose 1, unknown manufacture), for covid-19 immunisation, reaction(s): "pain in the arm"; Covid-19 vaccine (dose 2, unknown manufacture), for covid-19 immunisation, reaction(s): "pain in the arm"; Covid-19 vaccine (dose 3, unknown manufacture), for covid-19 immunisation, reaction(s): "pain in the arm"; Covid-19 vaccine (dose 4, unknown manufacture), for covid-19 immunisation, reaction(s): "pain in the arm"; Covid-19 vaccine (dose 5, unknown manufacture), for covid-19 immunisation, reaction(s): "pain in the arm". The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 26Nov2023, The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 26Nov2023, outcome "unknown", described as "wrong vaccine administered"; HEADACHE (non-serious) with onset 27Nov2023, outcome "not recovered"; TEMPOROMANDIBULAR JOINT SYNDROME (non-serious) with onset 27Nov2023, outcome "not recovered", described as "TMJ"; EAR PAIN (non-serious) with onset 27Nov2023, outcome "not recovered", described as "earache when chewing"; HYPOAESTHESIA (non-serious) with onset 27Nov2023, outcome "not recovered", described as "numbness of left face"; PAIN IN EXTREMITY (non-serious) with onset 27Nov2023, outcome "not recovered", described as "pain in the arm"; ARTHRALGIA (non-serious) with onset 27Nov2023, outcome "not recovered", described as "sore next and shoulder". Therapeutic measures were not taken as a result of temporomandibular joint syndrome, arthralgia, ear pain, headache, pain in extremity, hypoaesthesia. Additional information: The patient received any other medications within 2 weeks of vaccination included linzness. Reported Event: All on left side: TMJ, sore next and shoulder, earache when chewing, numbness of left face. Headache. Reaction to the shot in term of pain in the arm significantly worst then prior shots ON. Around 12 of 27Nov2023 symptoms started.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's disease; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2683519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 19.09.2023
Impfdatum: 09.07.2021
Beginn: 01.08.2023
Tage bis Beginn: 753,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia Blood test normal Feeling cold

Symptomtext

LOT NUMBER FOR BOOSTER FH8030

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: complaints of sudden joint pain, right side severe pain in the knee, and coldness could not be seen in blood work or explained
Aktuelle Erkrankungen: no
Vorgeschichte: stroke 2000 visually impaired from stroke
Andere Medikamente: -
Allergien: tramadol
Vorherige Impfungen: -

VAERS 2676532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 25.08.2023
Impfdatum: 21.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Injection site swelling

Symptomtext

CLIENT STATES THAT ON THE DAY OF THE VACCINE BEING ADMINISTERED TO HER, THE NURSE GIVING THE SHOT USED A STABBING TECHNIQUE IN HSR LEFT UPPER ARM. STATES SHE ASKED THE NURSE WHY DID SHE GIVE HER SHOT THAT WAY AND WAS TOLD THAT THIS IS THE WAY THAT SHE WAS SUPPOSED TO GIVE IT. CLIENT STATES THAT S DAYS LATER SHE WOKE UP TO A SWOLLEN ARM AT THE INJECTION SITE AND IT HAS NOT GONE AWAY SINCE THAT DAY. SHE PRESENTED TO OUR FACILITY ON 08/11/2023 AT WHICH TIME i MEASURED THE AREA NOTING IT TO BE APPROXIMATELY 2 AND A HALF INCHES WIDE AND 3 AND A HALF INCHES LONG. NOT WARM TO TOUCH JUST SWOLLEN. STATES SHE HAS BEEN TO THE ER 2 MONTHS AGO FOR ANOTHER REASON AND THE ER DOCTOR NOTICED THE AREA BUT NOTHING WAS DONE ABOUT IT AT THAT VISIT. SHE HAS ALSO BEEN UNDER THE CARE OF 2 DOCTORS REGARDING HER RIGHT SHOULDER BECAUSE OF A FALL ON THAT SHOULDER. BOTH DOCTORS HAVE SEEN THE LEFT ARM BEING SWOLLEN AND ARE CHECKING TO SEE WHAT CAN BE DONE ABOUT IT BECAUSE CLIENT STATES THAT SHE HAS BEEN TOLD IN TIMES PAST THAT SHE COULD NOT GET A MRI DONE WITH HAVING THE PACEMAKER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site swelling
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: pACEMAKER SINCE 03/22/2017; MILD STROKE IN 1997
Vorgeschichte: SEIZURES; PACEMAKER
Andere Medikamente: SEIZURE MEDS. BUT NOT TAKEN AT TIME OF VACCINATION
Allergien: DILAUDID, NUTS AND CITRUS FOODS
Vorherige Impfungen: -

VAERS 2667843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 08.08.2023
Impfdatum: 21.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Myalgia SARS-CoV-2 test

Symptomtext

muscle pain; prolonged weakness; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Nov2021 as dose 1, single (Lot number: FH8030) at the age of 60 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Depression" (unspecified if ongoing); "IBS" (unspecified if ongoing). Concomitant medication(s) included: LEXAPRO; GABAPENTINE. Past drug history included: Valtrex, reaction(s): "known allergies: Valtrex". No other vaccine in four weeks. The following information was reported: MYALGIA (disability) with onset 23Nov2021, outcome "not recovered", described as "muscle pain"; ASTHENIA (disability) with onset 23Nov2021, outcome "not recovered", described as "prolonged weakness". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Feb2022) Negative, notes: Nasal swab. Therapeutic measures were not taken as a result of myalgia, asthenia.; Sender's Comments: Based on the current available limited information in the case provided, the causal association between the events Myalgia, Asthenia and the use of suspect product cannot be fully 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: Myalgia
Hospital-Tage: -
Labordaten: Test Date: 202202; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Irritable bowel syndrome
Andere Medikamente: LEXAPRO; GABAPENTINE
Allergien: -
Vorherige Impfungen: -

VAERS 2647956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NC
Alter: 45,0
Geschlecht: F
Eingang: 21.06.2023
Impfdatum: 21.06.2021
Beginn: 01.12.2021
Tage bis Beginn: 163,0
Dosis: 3
Route/Site: IM / UN

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

Erythema Idiopathic urticaria Pruritus Sensitive skin Urticaria

Symptomtext

Within a month of receiving my Covid booster in 11/21 I starting feeling itchy all over my body. I could tell my body was starting to react to something and ultimately it would become hives. I had never experienced anything like this before! I also had not put anything different or new in my body. My skin then became overreactive to anything that scraped, touched, brushed or scratched me. I would get bright red welps & hives anywhere & everywhere all over my body. It was not isolated to one area. I have been dealing with the hives for 1.5 years now. I must take OTC allergy medication (Zyrtec, Allegra) 2x daily or my skin is uncontrollably itchy. I also receive monthly Xolair shots to control the hives from my Allergist.

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Praegender Schweregrund: Idiopathic urticaria
Hospital-Tage: -
Labordaten: 02/23/22 - Consult w/Dr. @ Asthma & Allergy. He diagnosed it as Idiopathic Urticaria 04/04/22 - Xolair shot 05/02/22 - Xolair shot 06/07/22 - Xolair shot 07/12/22 - Xolair shot 07/13/22 - Follow up @ Allergy & Asthma Center 08/09/22 - Xolair shot 10/14/22 - Follow up @ Allergy & Asthma Center 10/28/22 - Xolair shot 11/28/22 - Xolair shot 12/30/22 - Xolair shot 01/27/23 - Xolair shot 02/27/23 - Xolair shot 03/31/23 - Xolair shot 05/01/23 - Xolair shot 05/30/23 - Xolair shot 06/27/23
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes
Andere Medikamente: Metformin, Atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2637312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: OH
Alter: 63,0
Geschlecht: F
Eingang: 26.05.2023
Impfdatum: 16.11.2021
Beginn: 17.02.2022
Tage bis Beginn: 93,0
Dosis: 3
Route/Site: IM / AR

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

Alopecia Erythema Follicular disorder Lichen planopilaris Madarosis Pruritus Rash

Symptomtext

2/17/2022 I went in for a regular Dermatology visit. The doctor discovered I had Frontal Fibrosing Alopecia. I am losing my eyebrows and my hair from my sideburns back. My scalp is red and itchy. The follicles are being attacked by my body which causes the hair to fall out and not grow out in that particular follicle. There is no cure, but the medication prescribed to me is supposed to slow it down. The medication I was prescribed finasteride, a steroid solution to put on my scalp, RETIN A to use on my forehead for the bumps. I also was to start on ROGAINE. I was recently prescribed doxycycline. I stopped taking finasteride and doxycycline because of the side effects and the fact that this condition continues to progress. I am still using the topicals.

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Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's Disease; Irritable Bowel Syndrome; Osteoarthritis
Andere Medikamente: C-PAP; levothyroxine; magnesium; multivitamin; vitamin C; vitamin D
Allergien: Sulfa; seasonal allergies
Vorherige Impfungen: -

VAERS 2594289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 51,0
Geschlecht: F
Eingang: 10.03.2023
Impfdatum: 23.11.2021
Beginn: 01.04.2022
Tage bis Beginn: 129,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Insomnia Joint range of motion decreased Periarthritis X-ray

Symptomtext

I could not sleep at night; I developed frozen shoulder/ pain, non-movement; I developed frozen shoulder/ pain, non-movement; I developed frozen shoulder/ pain, non-movement; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old female patient received BNT162b2 (BNT162B2), on 23Nov2021 as dose 3 (booster), single (Lot number: FH8030) at the age of 51 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose: 2, lot number: ER8729), administration date: 15Apr2021, when the patient was 51-year-old, for COVID-19 immunization; BNT162b2 (Dose: 1, Lot number: it is either ER87B0 or it is ER87), administration date: 25Mar2021, when the patient was 51-year-old, for COVID-19 immunization. The following information was reported: PERIARTHRITIS (medically significant), ARTHRALGIA (medically significant), JOINT RANGE OF MOTION DECREASED (medically significant) all with onset Apr2022, outcome "unknown" and all described as "I developed frozen shoulder/ pain, non-movement"; INSOMNIA (non-serious), outcome "unknown", described as "I could not sleep at night". The event "i developed frozen shoulder/ pain, non-movement" required physician office visit. The patient underwent the following laboratory tests and procedures: X-ray: there is no broken bones, nothing. Therapeutic measures were taken as a result of periarthritis, arthralgia, joint range of motion decreased, insomnia. Clinical course: The patient was calling because she received three vaccines from the Pfizer from the start of the pandemic until last year and then after her last booster. She developed frozen shoulder which put her through an orthopedic doctor and physical therapy for almost 11 months now. The reason she was calling was she believed that the Pfizer vaccines mall three of the vaccines that she received, she felt that they attributed to the frozen shoulder. She was young person, physically active, not overweight. She believed that the vaccine caused her shoulder frozen. Apr2022 was when the frozen shoulder started. Pain, non-movement and after three months of pain, "the pain where I could not sleep at night". I went to orthopedic doctor for X-ray and doctor said "there is no broken bones, nothing." The patient went to an orthopedic doctor because of she had 3 months of pain. She did two cortisone shot in her shoulder over a six months period one on the front, waited three months at back of the shoulder with physical therapy. Her shoulder and her arm is at 95% which is great but the reason she was calling is in the last 4 months, she have met about 30 people, these are friends and colleagues across the country, females, males, different ages. They all reported to her that they have frozen shoulder (Further clarifications unknown) and they all have gone to doctors. They all just got the shocking that they are undergoing shoulder pain. The one thing they all have in common was they had three vaccines for COVID multiple times in the same arm that they all got frozen shoulder. So, it is definitely not coincidental. She thinks that if Pfizer have not received a complaint like this, Pfizer need to document that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: X-ray; Result Unstructured Data: Test Result:there is no broken bones, nothing
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2583315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NJ
Alter: 27,0
Geschlecht: F
Eingang: 17.02.2023
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Chills Fatigue Headache Hyperhidrosis Insomnia Myalgia Pyrexia Vaccination site pain

Symptomtext

low-grade fever; mild to intense headache; muscles soreness; fatigue; on and off sweats; chills; difficulty sleeping; mild soreness at the injection site; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 27-year-old female patient received BNT162b2 (BNT162B2), on 19Nov2021 at 10:45 as dose 3 (booster), single (Lot number: FH8030) at the age of 27 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: BLISOVI 24 FE oral taken for contraception, start date: 2018 (ongoing). Vaccination history included: BNT162b2 (DOSE 1; Lot number: EL3247; 10:00 in right arm), administration date: 04Mar2021, when the patient was 26-year-old, for COVID-19 immunization, reaction(s): "low-grade fever", "mild to intense headache", "muscles soreness", "fatigue", "on and off sweats", "chills", "difficulty sleeping", "mild soreness at the injection site"; BNT162b2 (DOSE 2; Lot number: EP6955; 09:30 in right arm), administration date: 25Mar2021, when the patient was 26-year-old, for COVID-19 immunization, reaction(s): "low-grade fever", "mild to intense headache", "muscles soreness", "fatigue", "on and off sweats", "chills", "difficulty sleeping", "mild soreness at the injection site". The following information was reported: CHILLS (non-serious) with onset 19Nov2021 at 21:00, outcome "recovered"; INSOMNIA (non-serious) with onset 19Nov2021 at 21:00, outcome "recovered", described as "difficulty sleeping"; FATIGUE (non-serious) with onset 19Nov2021 at 21:00, outcome "recovered"; PYREXIA (non-serious) with onset 19Nov2021 at 21:00, outcome "recovered", described as "low-grade fever"; VACCINATION SITE PAIN (non-serious) with onset 19Nov2021 at 21:00, outcome "recovered", described as "mild soreness at the injection site"; HEADACHE (non-serious) with onset 19Nov2021 at 21:00, outcome "recovered", described as "mild to intense headache"; MYALGIA (non-serious) with onset 19Nov2021 at 21:00, outcome "recovered", described as "muscles soreness"; HYPERHIDROSIS (non-serious) with onset 19Nov2021 at 21:00, outcome "recovered", described as "on and off sweats". Therapeutic measures were taken as a result of pyrexia, headache, myalgia, fatigue, hyperhidrosis, chills, vaccination site pain. Additional information: Following vaccination (primary dose, second dose, and both boosters), the patient experienced a low-grade fever, mild to intense headache, muscles soreness and fatigue, on and off sweats/chills, difficulty sleeping due to side effects after getting the vaccine, and mild soreness at the injection site. The onset of side effects began in the evening and continued through the night and into the next day. The patient recalls that the side effects following the 3rd (booster) dose were the most severe and lasted more than 24 hours. She took acetaminophen in all instances as recommended and recovered.; Sender's Comments: Linked Report(s) : US-PFIZER INC-PV202300029954 same patient/events, different dose;US-PFIZER INC-2021336635 same patient/events, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: BLISOVI 24 FE
Allergien: -
Vorherige Impfungen: -

VAERS 2555125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: OR
Alter: 47,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 07.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Pyrexia

Symptomtext

I had cold chilis, low grade fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2550355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 75,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 15.09.2022
Beginn: 24.12.2022
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Diarrhoea SARS-CoV-2 test positive

Symptomtext

Hospitalization: 12/24/2022 - 1/3/23 (10 days) Presentation to the ED: worsening diarrhea. COVID + date: 12/24/2022 Treatment: no treatment specific to COVID. Discharge to: SNF Moderna 002A21A 3/12/2021 Moderna 046B21A 4/9/2021. Pfizer FH8030 11/17/2021 Pfizer Bivalent GJ5342 9/15/2022

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Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, aortic stenosis, GERD, depression, hypertension, anxiety, gout, CVA, CHF
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2542031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TN
Alter: 25,0
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 01.12.2021
Beginn: 01.04.2022
Tage bis Beginn: 121,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Bone graft Bone infarction Bone pain Laboratory test normal Magnetic resonance imaging abnormal Osteonecrosis Surgery

Symptomtext

Patient received 2 Pfizer doses and 1 Pfizer booster in 12/01/2021. A few months after booster, patient complained of hip pain. Began PT & hip pain worsened. MRI was taken and revealed avascular necrosis of right femoral head pre-collapse stage. Not bilateral. Core decompression w/ bone grafting surgery was done July 25, 2022. After surgery, patient complained about knee pain. MRI ordered and showed bone infarct (avascular necrosis) at distal femur and proximal tibia. Treated with core decompression. Date of surgery was December 8, 2022. Patient is now complaining about right lower rib-fib and ankle pain. MRI ordered, scheduled for 01/07/2023. Patient was evaluated by hematologist to check for clotting disorders and variety of other causes. Labs were unremarkable and no clotting disorders identified. Negative for Lupus and Sjogren's syndrome. Patient was competitive athlete in teen years and early 20s. No serious injuries aside from left ankle medial malleolus fracture in 2017, which was surgically corrected in 2017 with ankle ORIF surgery. PATIENT HAS NO HISTORY OF ANY CLOTS OR MICRO CLOTS PRIOR TO RECEIVING COVID VACCINES.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: See Item 18.
Aktuelle Erkrankungen: None.
Vorgeschichte: Anxiety
Andere Medikamente: -Clonazepam 0.5 mg bid -Viibryd 20 mg qam -Vitamin D3 5,000 IU qam
Allergien: None.
Vorherige Impfungen: -

VAERS 2539030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 90,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 18.03.2021
Beginn: 25.09.2022
Tage bis Beginn: 556,0
Dosis: 3
Route/Site: - / -

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

Asthenia Blood culture Blood lactic acid COVID-19 Chest X-ray abnormal Culture urine Laboratory test Pleural effusion Pyrexia SARS-CoV-2 test positive Sepsis Troponin normal Urine abnormality Urine analysis abnormal Urostomy

Symptomtext

92y.o. male with a PMHx significant for bladder cancer, CKD (Stage 4), HTN, CAD, dementia. Pt presents to facility from SAR after patient was found to have multiple days of fever and generalized weakness. He had received tylenol with some relief, but fever persisted, according to family. Family had noticed that patient had cloudy urine in his urostomy bad and they had concern for infection. In the ED, patient was worked up for sepsis and covid-19 test was positive. He received IVF bolus, started on Vancomycin and Merrem, labs drawn and blood/urine cultures sent. Troponins were negative, Lactic acid 2.0, UA positive for bacteria, chest xray shows small pleural effusion. Upon arrival to the unit, patient had some difficulty with communication due to language barrier. He is not in acute distress, denies chest pain, shortness of breath, headache, dizziness, nausea, abdominal pain, diarrhea. Spoke with patient's son and daughter over the phone to discuss patient's home medications and history. Disposition - Pt stable for dc today home. Daughter refused home care . Pt to continue home meds except lasix. F/u with specialists

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Praegender Schweregrund: Pyrexia
Hospital-Tage: 4,0
Labordaten: 9/25 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2539027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 04.02.2021
Beginn: 25.09.2022
Tage bis Beginn: 598,0
Dosis: 3
Route/Site: - / -

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

Debridement Iliac artery occlusion Pain Peripheral artery stenosis SARS-CoV-2 test Surgery Wound Wound treatment

Symptomtext

This is a 74y.o. female with history of COPD, a-fib on xeralto, who presented on 9/25/2022 with occlusion at the level of the bilateral external iliac arteries and severe luminal caliber narrowing of the SFAs to the level of the mid popliteal arteries bilaterally.. Pt underwent procedure listed above which they tolerated well without complication, see operative report for full details. Patient recovered well. Hospital course significant for left wound that required operative groin washout and debridement. On HD#33, pain controlled, pt tolerating diet, voiding and ambulating independently, ready for discharge to home care with instruction to follow up as indicated below. Pt was educated on pain expectations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: 33,0
Labordaten: 9/25 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2531121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 29.11.2021
Beginn: 16.01.2022
Tage bis Beginn: 48,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Hypersomnia Oropharyngeal pain SARS-CoV-2 test positive Throat irritation

Symptomtext

I received my Pfizer booster for COVID-19 on 11/29/2021. On about 1/16/2022, I developed an itchy, sore throat. Not only that, but I had been dealing with fatigue for a while. I took some Tylenol, but the symptoms didn't go away. The symptoms continued on 1/17/2022, plus I had a little bit of a cough. I decided to take a BinaxNOW home antigen test on 1/18/2022, and I got a positive result. I isolated in my room. I was fatigued, so I spent quite a bit of time sleeping. Whenever I had to talk with people, I always did it outdoors and wearing an N95 mask. I tested every day after I got the positive result, and I didn't get a negative result until 1/24/2022. Even though I had tested negative, I still felt tired. The fatigue lasted possibly for a month after I tested negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 1/18/2022-1/23/2022--BinaxNOW Home Antigen Tests--Positive Results; 1/24/2022--BinaxNOW Home Antigen Test--Negative Result.
Aktuelle Erkrankungen: None.
Vorgeschichte: History of Breast Cancer (In Remission for 10 Years).
Andere Medikamente: Calcium; Letrozole; Biotin.
Allergien: Penicillin.
Vorherige Impfungen: -

VAERS 2525484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: 49,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 02.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / AR

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

Head discomfort Headache Vision blurred

Symptomtext

I had a headache, but it was on the crown of my head. It was a major pain, but it was a nagging consistent pressure. It wasn't a sensation I had never felt before in my head. I don't recall if I spoke with a doctor or not. I was able to take some aspirin and the sensation eventually went away. A few weeks ago, I began to notice blurred vision in my left eye. I am scheduled to see an eye doctor next week to address this issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Neuropathy
Andere Medikamente: BASAGLAR insulin pen; gabapentin; aspirin
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2515274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: RI
Alter: 47,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Erythema Pain Peripheral swelling Pruritus Skin warm

Symptomtext

11/7/2021 My left arm was red, swollen, aching, throbbing, felt like fever and itching. It just covered half of my arm. I went to the doctor on 11/9/2021 and she put me on antibiotics. It took about five days for it all to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: BACTRIM
Vorherige Impfungen: COVID, same reactions as this one.

VAERS 2515241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 22.11.2021
Beginn: 10.07.2022
Tage bis Beginn: 230,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Malaise No adverse event Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had no reaction to vaccine. I started feeling sick with a dry cough for a week prior to testing positive for COVID-19. Throughout the week, I tested multiple times for COVID-19 and each one was negative. I had a PCR test too and it was negative. On 07/10/2022, I tested positive with a home test for COVID-19. I went to an urgent care center and was given the prescription for PAXLOVID. It made the taste of my coffee icky. It knocked out the congestion in my chest fast and I did not rebound.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 10JUL2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Thyroid Disease
Andere Medikamente: N/A
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2514049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: VA
Alter: 49,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 19.11.2021
Beginn: 20.07.2022
Tage bis Beginn: 243,0
Dosis: 3
Route/Site: SYR / AR

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

COVID-19 Cough Fatigue Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I contracted COVID after a family vacation. (Interestingly, three of our four family members tested positive and were symptomatic. All four of us had received three Covid vaccines. The fourth never tested positive -despite sharing food, drinks, sleeping in close quarters, etc.) I tested positive with a home test. Symptoms were sore throat, cough, fever, tiredness, headache. I called my doctor's office and was prescribed Paxlovid. I finished the entire course. I tested positive for a total of 10 days, but felt much better around day 7 or 8.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home test
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety
Andere Medikamente: Sertraline, Bupropion HCL XL, Allegra, Emergen-C immune +, Prilosec
Allergien: N/A
Vorherige Impfungen: -

VAERS 2509437

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 18.11.2021
Beginn: 16.11.2022
Tage bis Beginn: 363,0
Dosis: 3
Route/Site: - / -

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

Pyrexia Rhinorrhoea

Symptomtext

fever, runny nose

Weitere VAERSDATA-Felder

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

VAERS 2490950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 24.03.2021
Beginn: 03.09.2022
Tage bis Beginn: 528,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Cough Malaise Myalgia SARS-CoV-2 test positive

Symptomtext

09/03/22 presents to ED for "cough and overall malaise myalgias". PMHx of "chronic left lower extremity thrombosis not on anticoagulation"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 09/03/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2477149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 02.12.2021
Beginn: 30.09.2022
Tage bis Beginn: 302,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Exposure to SARS-CoV-2 Fatigue Loss of personal independence in daily activities Metastases to central nervous system Metastatic malignant melanoma Nasal congestion Productive cough SARS-CoV-2 test positive

Symptomtext

"Provider d/c note: ""Patient is a pleasant 83 YO female who presented 9/30/2022 9:44 AM to inpatient rehab after primary admission to hospital for profound weakness due to covid 19. She says she began to notice symptoms on the evening of Sept 22 with stuffy nose that proceeded to a productive cough. Her husband had covid and she tested + at home on Sept. 23. By the next day she was profoundly weak and needed help getting around whereby she was able to do things independently with a walker previously. She has a hx of malignant melanoma with mets to the brain diagnosed in April 2022. She will have f/u MRI and CT scans as an ouptatinet in approx 3 weeks. She says she has begun to recover physically from the covid and is nearly back to the strength and function she had on discharge from inpatient rehab on her previous visit. She did however have trouble completing therapy at hospital due to fatigue. She says her cough improves daily and is down to only about 6 coughs / day."""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 7,0
Labordaten: COVID Detected PCR on 9/24/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Essential hypertension, benign Hypercholesterolemia Hypertension SVT (supraventricular tachycardia) (*) Endocrine Hypothyroidism Integumentary Psoriasis Psychological Depression Urinary Stage 3 chronic kidney disease (*) Other Obesity Vitamin B 12 deficiency Seizure (*) Mass of brain Chronic hyponatremia BMI 34.0-34.9,adult Acute left hemiparesis (*) History of malignant melanoma Metastatic melanoma (*) Oral mucositis due to radiation Abnormal PET scan of colon Brain metastases (*) Debility
Andere Medikamente: -
Allergien: Claritin, Naproxen Sodium, Penicillins
Vorherige Impfungen: -

VAERS 2473289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 13.06.2022
Beginn: 01.07.2022
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: SYR / LA

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

Albumin globulin ratio increased Anti-thyroid antibody positive Antinuclear antibody negative Anxiety Nausea Panic attack Rash pruritic Serum ferritin decreased Tri-iodothyronine increased Weight decreased

Symptomtext

Itchy rash, weight loss, nausea, panic attack, anxiety. Began in earnest 22 days after 4th vax..

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: Autoimmune thyroid panels reveal elevated anti-TPO and anti-TBG (no history of prior) antibodies, slightly elevated T3. Elevated A/G ratio. Very low ferritin. ANA panel currently negative, but will continue to monitor.
Aktuelle Erkrankungen: autoimmune hypo thyroiditis
Vorgeschichte: autoimmune hypothyroiditis, migraine headache, osteopenia
Andere Medikamente: Armour Thyroid (NDT) 30 mg T.I.D.. Occasional hydroxycodone/acetominophen 5/325 for headache (1-2/mo), occasional ibuprofen for headache, back and joint pain.
Allergien: Mild Allergy Ceftin (abx); severe allergy floroquinolone abx (ALL); bee stings (childhood allergy)
Vorherige Impfungen: -

VAERS 2467169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NJ
Alter: 35,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 23.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Vertigo

Symptomtext

Experienced vertigo after receiving the Pfizer booster. Woke up to severe dizziness/room spinning at approximately 3am on 11/25/21. Severe sensation lasted throughout the day, becoming more manageable and allowing for movement/walking around 6pm on 11/25/21. Symptoms became more mild, tapering each day, but persisted through 10/4/21. Took OTC Dramamine to assist with symptoms during that week. In the coming months, continued to experience mild feeling of lightheadedness on the right side when lying down for sleep. [Had never had an episode of vertigo previously; no issues following the Moderna 2-dose series.]

Weitere VAERSDATA-Felder

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

VAERS 2436488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 99,0
Geschlecht: M
Eingang: 09.09.2022
Impfdatum: 16.11.2021
Beginn: 03.08.2022
Tage bis Beginn: 260,0
Dosis: 3
Route/Site: SYR / UN

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

Fall Malaise

Symptomtext

Hospitalization for a fall and COVID-19 symptoms on dates 8/3/2022-8/16/2022. Treated with dexamethasone, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.?

Weitere VAERSDATA-Felder

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

VAERS 2416002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NC
Alter: 62,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 23.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / LA

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

Rash Rash erythematous Rash pruritic

Symptomtext

11-30-2021, I started having a red rash with pinhead bumps that covered from the wrist to almost my elbows on both arms. It was very itchy. I treated the areas with cortisone cream. It lasted for about 2.5 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto; Graves Disease
Andere Medikamente: Metformin; omeprazole; spironolactone; carvedilol; vitamin B12 inj; amlodipine; atorvastatin; losartan; biotin; melatonin; women's VITACRAVE multivitamin; EMERGEN-C
Allergien: Penicillin; CIPRO; SEPTRA; pneumonia vaccine 23; sulfa drugs
Vorherige Impfungen: Pneumonia Vaccine 23 - approx. 2015 - approx. 55 years old - The injection site became really swollen, red and itchy.

VAERS 2403863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 06.08.2022
Impfdatum: 18.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Cough Dysphonia Nasal congestion Pain in extremity Speech disorder

Symptomtext

sore arm; She is coughing up a lot of stuff and blowing out stuff; congested; hoarse; having a hard time talking; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old female patient received BNT162b2 (BNT162B2), on 18Nov2021 as dose 3 (booster), single (Lot number: FH8030) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Impaired immune system" (unspecified if ongoing), notes: she has an impaired immune system. There were no concomitant medications. Vaccination history included: moderna (DOSE 1, SINGLE, Lot number: 030L20A,, EXP: 16Jul2021, Dose and Route: Unknown dose; route is left arm , Time: Believes 20:00 because she cashed out of the pharmacy at 20:15), administration date: 26Jan2021, when the patient was 60-year-old, for Covid-19 Immunization; moderna (DOSE 2, SINGLE, LOT: 013M20A, EXP: 31Jul2021, Dose and Route: Unknown dose; route is left arm , Time: About 18:30-18:45), administration date: 23Feb2021, when the patient was 60-year-old, for Covid-19 Immunization; Flu vaccine (Previous Fall had to get flu); Pneumonia vaccine (second pneumonia). The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "sore arm"; COUGH (non-serious), outcome "unknown", described as "She is coughing up a lot of stuff and blowing out stuff"; NASAL CONGESTION (non-serious), outcome "unknown", described as "congested"; DYSPHONIA (non-serious), outcome "unknown", described as "hoarse"; SPEECH DISORDER (non-serious), outcome "unknown", described as "having a hard time talking".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Immune system disorder (she has an impaired immune system)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2388198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NE
Alter: 58,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 20.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / AR

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

Blood testosterone decreased Fatigue Positive airway pressure therapy Sleep apnoea syndrome Sleep study abnormal

Symptomtext

Within a month or so after receiving my third dose of Pfizer I began to notice that I was feeling extremely exhausted. Around the 15th of November of that same year (2021) I began taking a thyroid medication and I received my third dose of Pfizer on 11/20/2021. On 03/16/2022 I saw a doctor for my fatigue. He advised that I do a sleep apnea sleep study which I did in May of 2022. I began to use a C-PAP machine in June of 2022 but I am still feeling extreme exhaustion to the point where I am very fatigued after menial tasks like moving pillows from my bed or moving dishes around in the dish washer. I am scheduled to see my doctor again next week, 08/04/2022, to discuss this further. Since receiving my third dose in 2021, I have also received a fourth dose of Pfizer on 04/20/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Sleep study May 2022, Sleep apnea found; testosterone test, lowered levels of testosterone found 07/11/2022.
Aktuelle Erkrankungen: None.
Vorgeschichte: None
Andere Medikamente: Rosuvastatin calcium; levothyroxine sodium; MYRBETRIQ.
Allergien: None.
Vorherige Impfungen: -

VAERS 2367770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 11.04.2022
Beginn: 06.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia COVID-19 Headache Oropharyngeal pain SARS-CoV-2 test positive Sinus disorder

Symptomtext

I had a bad sore throat and headache. I took a home COVID-19 Test that came back positive. I called my Primary Care Physician who prescribed the Paxlovid and a Z-Pak that I have finished. I am feeling better but low on energy, a little sinus trouble.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Home COVID-19 Test
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure; High Cholesterol
Andere Medikamente: Atorvastatin; Amlodipine; Potassium Citrate; Claritin; Multivitamin; Biotin, Potassium Vitamin B-12 injection; Vitamin C
Allergien: Levaquin; Codeine
Vorherige Impfungen: -

VAERS 2367741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: NC
Alter: 30,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 22.11.2021
Beginn: 06.07.2022
Tage bis Beginn: 226,0
Dosis: 3
Route/Site: IM / UN

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

COVID-19 Nausea Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Vomiting and nausea with low grade fever on 7/3 Tested positive for covid on 7/6

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: Tested positive for covid on 7/6
Aktuelle Erkrankungen: head cold
Vorgeschichte: -
Andere Medikamente: Sertraline 50 mg
Allergien: -
Vorherige Impfungen: -

VAERS 2365986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: IL
Alter: 57,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 12.02.2022
Beginn: 01.03.2022
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: SYR / LA

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

Breast induration Joint swelling Limb discomfort Musculoskeletal stiffness Nipple pain Pain Skin discolouration

Symptomtext

To start the nurse was very evasive like she was hiding my injection it was weird, I didnt think anything about it and went home. then in march I started getting symptoms tenderness in my nipple area and Im a male underneath my nipples was very hard like I was growning breats and start get large , i was like this is strange and then I the fluid was so heavy in my arm like it didnt want to pass after weeks. Then my ankles start to overly swell ok this is also strange never happen before and severe stiffness with pain and darkness in skin color of my ankels and I still have these sympton today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nipple pain
Hospital-Tage: -
Labordaten: not test yet i have report it my doctor.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: mlodipine
Allergien: none
Vorherige Impfungen: -

VAERS 2362786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 24.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Gait disturbance Joint swelling Pain in extremity Peripheral swelling Rheumatoid arthritis Rheumatoid factor positive

Symptomtext

about two weeks after injections I noticed a swollen wrist that had no injury to it. That swelling resolved but then my feet began to swell and be painful to walk on. A few months later my right pinky finger swelled (feet continued to be an issue), then subsequent fingers swelled/painful. Wrist then became the same, and other areas off and on.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: RF confirmed rheumatoid arthritis. I had zero signs or symptoms prior to my booster.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Covid 19 pfizer 2nd dose on 2/10/21 - 49 yo breasts developed lumps and then my dermal filler areas became swollen.

VAERS 2362238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NJ
Alter: 44,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 02.12.2021
Beginn: 30.06.2022
Tage bis Beginn: 210,0
Dosis: 3
Route/Site: OT / LA

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

Chills Nasal congestion Pain Pyrexia Rhinorrhoea

Symptomtext

Fever; Chills; Body pains; Runny nose; Congestion; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44-year-old male patient received BNT162b2 (BNT162B2), on 02Dec2021 as dose 3 (booster), single (Lot number: FH8030) at the age of 44 years intramuscular, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1 SINGLE; Lot number: EN6203), administration date: 24Feb2021, when the patient was 43-year-old, for Covid-19 Immunisation; BNT162b2 (DOSE 2 SINGLE; Lot number: EP7534), administration date: 17Mar2021, when the patient was 43-year-old, for Covid-19 Immunisation. The following information was reported: PAIN (non-serious) with onset 30Jun2022, outcome "not recovered", described as "Body pains"; CHILLS (non-serious) with onset 30Jun2022, outcome "not recovered"; NASAL CONGESTION (non-serious) with onset 30Jun2022, outcome "not recovered", described as "Congestion"; PYREXIA (non-serious) with onset 30Jun2022, outcome "not recovered", described as "Fever"; RHINORRHOEA (non-serious) with onset 30Jun2022, outcome "not recovered", described as "Runny nose". Therapeutic measures were not taken as a result of pyrexia, chills, pain, rhinorrhoea, nasal congestion. Additional information: The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: No other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2361224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: AK
Alter: 60,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 21.12.2021
Beginn: 07.07.2022
Tage bis Beginn: 198,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Joint stiffness Joint swelling Laboratory test Musculoskeletal stiffness Neck pain Psoriatic arthropathy X-ray X-ray limb

Symptomtext

New onset of psoriatic arthritis with neck pain and stiffness starting approximately three weeks after immunization and severe knee stiffness, swelling and pain a month after that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: X-rays neck and knees 03/03/2022 Labs 03/29/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Plaque psoriasis Hearing loss
Andere Medikamente: None
Allergien: Naproxen, modafinil
Vorherige Impfungen: -

VAERS 2323234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: PA
Alter: 40,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 09.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 180,0
Dosis: 3
Route/Site: IM / LA

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

Body temperature increased Feeling hot Influenza Nasopharyngitis Oropharyngeal pain Pain Productive cough SARS-CoV-2 test negative

Symptomtext

On June 07, 2022 I woke up with a sore throat, I was warmer than usual. I took a home COVID 19 test. The second day I started coughing and had some phlegm, my temperature was elevated for three days. By day three the cough went away, no more aches or pains it felt like a light cold or flu. I had received a prescription of Paxlovid on June 8, 2022. By June 12, 2022 I was testing negative and feeling much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Home COVID 19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Losartan/HCTZ
Allergien: No
Vorherige Impfungen: -

VAERS 2318798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MO
Alter: 25,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 03.12.2021
Beginn: 11.06.2022
Tage bis Beginn: 190,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Dizziness Fatigue Impaired work ability Oropharyngeal pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I woke up I had a sore throat and saw I had sinus drainage but no spots or signs in my throat but did have congestion I became dizzy on Sunday 06/12/2022 and was fatigued and our of it then developed a fever of 101.4 I called out of work yesterday 06/13/2022 made an appointment with my PCP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Rapid Covid test was positive and a PCR test at urgent care positive as well
Aktuelle Erkrankungen: No.
Vorgeschichte: Sleep apnea Polycystic ovarian syndrome eczema hidradenitis sutpuratiza
Andere Medikamente: Zyrtec Wellbutrin Zoloft Spironolactone Birth control implant manufacture unknown Triamcinolone Eucrisa
Allergien: Cold induced urticaria
Vorherige Impfungen: -

VAERS 2310571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 06.06.2022
Impfdatum: 03.12.2021
Beginn: 08.01.2022
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain Diverticulitis Muscle spasms Pyrexia

Symptomtext

Developed Diverticulitus. Abdominal pain, fever, cramping . Ist vaccine does was 3/1/21. Diverticulitus developed with first incident on 8/2021, then 1/8 2022 just after the booster vaccination, then most severe in May 2022.

Weitere VAERSDATA-Felder

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

VAERS 2310101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 93,0
Geschlecht: F
Eingang: 06.06.2022
Impfdatum: 02.02.2021
Beginn: 19.05.2022
Tage bis Beginn: 471,0
Dosis: 3
Route/Site: IM / -

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

Asthenia COVID-19 Pain

Symptomtext

Patient presented to the ED with weakness and generalized pain. Was subsequently found to have COVID. Patient discharged on 5/24/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Dementia, CHF
Andere Medikamente: Keflex
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2306283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: PA
Alter: 65,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 20.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: - / RA

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

Dizziness Fall Rash macular Vertigo

Symptomtext

severe vertigo; constant dizziness; i trip down steps; severe skin blotches; The initial case was missing the following minimum criteria: ICH-Unspecified product. Upon receipt of follow-up information on (23May2022), this case now contains all required information to be considered valid. This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID: (005570). The reporter is the patient. A 65-year-old male patient received BNT162b2 (BNT162B2), on 20Nov2021 at 13:30 as dose 2, single (Lot number: FH8030) at the age of 65 years, in right arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Lot number/Expiry date: FF8891, Anatomical location: Left arm, Time the vaccination was given: 11: 00), administration date: 30Oct2021, when the patient was 65-year-old, for Covid-19 immunization. The following information was reported: FALL (non-serious) with onset 10Dec2021, outcome "not recovered", described as "i trip down steps"; RASH MACULAR (non-serious) with onset 10Dec2021, outcome "not recovered", described as "severe skin blotches"; DIZZINESS (non-serious) with onset 14Feb2022, outcome "not recovered", described as "constant dizziness"; VERTIGO (non-serious) with onset 14Feb2022, outcome "not recovered", described as "severe vertigo". Therapeutic measures were not taken as a result of vertigo, dizziness, fall, rash macular. Additional Information: Did the reported issue occur after use of a Pfizer product: Yes. If surgical treatment needed for the event: Was the surgery planned prior to taking the product: No, No. It was reported that, patient never got covid. Wish I never got vaccine, I suffer constant dizziness, even in bed. I am afraid I will have an accident falling. I avoid all activity. I was a very active person, not now. Government told me it was tested, that was a lie. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2303929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 24,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Nausea

Symptomtext

Sudden extreme nausea. Have been feeling nauseous on and off ever since, no real pattern to it. Night or day, before or after eating, etc.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control (ocella)
Allergien: None. Vegan for 6.5 years so maybe sensitive to animal byproducts?
Vorherige Impfungen: -

VAERS 2303531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MO
Alter: 98,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 26.04.2021
Beginn: 29.05.2022
Tage bis Beginn: 398,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

Case became extremally fatigued and disorientated on 05/29/2022, was taken to hospital, tested positive and was admitted.

Weitere VAERSDATA-Felder

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

VAERS 2292647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 23.04.2022
Beginn: 24.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test normal Extra dose administered Gait inability Joint swelling Pain X-ray

Symptomtext

Severe joint swelling - pain causing inability to walk, use stairs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Blood work normal, knee x-ray, pt, awaiting ortho eval.
Aktuelle Erkrankungen: Elevated BP due to BuPROPion
Vorgeschichte: None
Andere Medikamente: Bupropion XL
Allergien: Vitamin E Compazine (prochlorperazine)
Vorherige Impfungen: Each Covid vaccine some joint swelling but 4th dose was most severe and debilitating

VAERS 2286714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MA
Alter: 80,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 01.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Fatigue Headache

Symptomtext

headache; fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 80-year-old male patient received BNT162b2 (BNT162B2), on 11Feb2021 as dose 1, single (Lot number: EL9266), on 04Mar2021 as dose 2, single (Lot number: EN6205) and on 01Dec2021 as dose 3 (booster), single (Lot number: FH8030) at the age of 80 years for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: LISINOPRIL; ASPIRIN 81; ZETIA. The following information was reported: HEADACHE (non-serious), outcome "recovered"; FATIGUE (non-serious), outcome "recovered". Additional Information: Caller states he had a severe reaction to the fourth vaccine. Caller states he had a headache and fatigue which he had with the first 3 too but this one he was up all night long with dry heaves, dizziness, achiness and just not feeling well at all. Caller states he had Covid before any of the vaccines were available so he knows it is not a good thing to have. Treatment included Stay in bed a lot. Fourth Dose or Second Booster Dose taken on 11May2022 with Lot FP7557 or FP4554. Prior Vaccinations (within 4 weeks) was None. AE(s) following prior vaccinations was None. Patient's does not have any medical History (including any illness at time of vaccination). And no family Medical History Relevant to AE(s). AE(s) does not required visit to Emergency room or physician room. Generic zetia and statin are reported; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200720046 Same patient, same event, different dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's Medical History (including any illness at time of vaccination)? None
Andere Medikamente: LISINOPRIL; ASPIRIN 81; ZETIA
Allergien: -
Vorherige Impfungen: -

VAERS 2285096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: GA
Alter: 44,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 17.11.2021
Beginn: 03.05.2022
Tage bis Beginn: 167,0
Dosis: 3
Route/Site: SYR / LA

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

Allergy test Cough Fatigue Infection Upper-airway cough syndrome

Symptomtext

11/7/2021 vaccination. 05/02/2022 went for long walk with friend. 05/03/2022 Woke up tired, exhausted. Thought it was from the walk. Started to experience cough, persisted to include post nasal drip. I thought it was a cold. I never had a fever. I thought maybe then allergies; Sudafed but it wasn't relieving or making it go away. The persistence and intensity, I made appointment with allergies. Dr. stated that it wasn't allergies but rather a 'post infection state'; no tests to see what it was. No wheezing. Put on albuterol inhaler, Flonase and antihistamine spray, a steroid 6 day course, antibiotic for a month 10 day course. I have not had my follow up yet with allergist. Almost recovered. Residual cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Allergy/trey tests (last one was 5 years ago); inconclusive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; allergy induced (genetic) ('pretty bad')
Andere Medikamente: Vitamin supplements; inhaler PRN albuterol; ashwagandha
Allergien: Penicillin
Vorherige Impfungen: TT; never had such a reaction as I did this last time (11/07/2021) to my arm. Hard to move my arm. Don't remember happening last

VAERS 2284948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 18.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 164,0
Dosis: 3
Route/Site: SYR / RA

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

Cardiac stress test normal Chest discomfort Cholelithiasis Fatigue Pain SARS-CoV-2 antibody test positive SARS-CoV-2 test negative Surgery X-ray normal

Symptomtext

I had gallstones that blocked from kidney to gallbladder requiring a holiseptomy and I'm currently in recovery from this surgery. The other health event started more than 2.5 months ago and started with body aches and tiredness. Not sure if I got Covid. I tested a couple of times with home Covid test and it came back negative. I don't know what the cause of it was but it's still hanging around now. Last week I finally talked my doctor into getting an antigen test and it shows I have antibodies. I'm still having tightness in the chest and no one knows what's causing it and it's only on the left side and seems to be getting more constant now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home Covid test negative. Antigen test, I have antibodies. Chemical stress test, no heart condition. X-ray normal.
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure; metabolic syndrome
Andere Medikamente: Chondroitin sulfate; B12 500mg; Zyrtec 10mg; omeprazole 20mg; krill oil 1500mg; coQ10; magnesium; vit C; Viactiv; vit D3; irbesartan; probiotic; eye drops
Allergien: Penicillin; amoxicillin; hydrocodone; lisinopril
Vorherige Impfungen: -

VAERS 2284811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 33,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 06.12.2021
Beginn: 28.04.2022
Tage bis Beginn: 143,0
Dosis: 3
Route/Site: UN / UN

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

Chills Cough Hyperhidrosis Pain Pyrexia

Symptomtext

body aches, cough, fever, chills, sweats

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2275603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / AR

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

Chest discomfort Dizziness Impaired work ability Nausea

Symptomtext

I received the vaccination. I might have been in the store for another 5 minutes, and I left and I was walking home. I would say like 10-15 minutes after the vaccine as I was walking home, I started to experience tightness in my chest. I walked home very slowly and I probably took my albuterol then. I went home. I can?t remember if I had a headache because I had a headache for the first two. But I did not go to work the next day because I was very dizzy and nauseous. The chest tightness subsided and it was gone the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Allegra Digestive Enzyme Vitamin D3 3000mg Vitamin C 9500mg Zinc
Allergien: Environmental ? trees, grass, dust, cats, dogs Certain foods Bactrim Penicillin Cipro Flagel Codeine Eggs Sensitivities to medications in general Etc.
Vorherige Impfungen: Egg free flu vaccine (Fall/Winter 2020) - received vaccine and waited in store for 10 minutes, left and experienced chest tightn

VAERS 2273519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: KY
Alter: 65,0
Geschlecht: M
Eingang: 12.05.2022
Impfdatum: 22.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: SYR / AR

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

Blood glucose decreased Cold sweat Dizziness Echocardiogram normal Full blood count normal Hyperhidrosis Nervousness

Symptomtext

Couple of weeks after my booster I started experiencing low blood sugars, getting shaky, sweaty and clammy. I would have to drink some orange juice or have some proteins to get it up. It has happened several times, then in December I had an episode where I felt like I was going to pass out, I ate a few sweets incase in was my blood sugar went to ER and my blood sugar was 52. Around a month later I had another episode like that my blood sugar 118 and my blood pressure was 128/80 something both were normal. But because of that and the episodes being the same I don't believe that it was my blood sugar. I am still experiencing low bloods sugars even after I eat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 03/24/22 complete blood workup, normal. 03/30/22 echo, normal. Upcoming appointment w/Cardiologist on 05/16/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Low dose aspirin
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2270924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 89,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 09.02.2021
Beginn: 07.02.2022
Tage bis Beginn: 363,0
Dosis: UNK
Route/Site: - / -

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

Abdominal pain COVID-19 SARS-CoV-2 test positive

Symptomtext

02/07/22 presents to ED for "abdominal pain". PMHx of "HLD, hypothyroidism, GERD, Raynaud's, asthma, TIA, and mild dementia"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 02/07/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 28.11.2021
Beginn: 02.04.2022
Tage bis Beginn: 125,0
Dosis: UNK
Route/Site: SYR / -

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

Mechanical urticaria Pain in extremity

Symptomtext

Dermatographia, sore arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Ehlers Danlo's syndrome, asthma
Andere Medikamente: Lots
Allergien: Imitrex, box elder pollen, tobacco smoke, tramadol, white oak
Vorherige Impfungen: -

VAERS 2248104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 07.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: SYR / LA

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

Blood potassium decreased Blood test abnormal Dizziness Vertigo

Symptomtext

Vertigo; given Meclizine to treat dizzy symptoms. Followed up with doctor March 3rd. Symptoms had improved; with minimal vertigo symptoms remaining.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: bloodwork - 2/28. low potassium levels found; suggested to eat more fruits/veggies.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Vitamin D deficiency
Andere Medikamente: Vitamin D; Multi-Vitamin
Allergien: N/A
Vorherige Impfungen: swollen lymph nodes; 37. second dose of Pfizer Covid19 vaccine (EW0169) administered 04/07/21

VAERS 2246340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 52,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 23.11.2021
Beginn: 25.12.2021
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: IM / AR

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

Blood sodium decreased Blood test abnormal Fall Hyponatraemia Impaired work ability Malaise Memory impairment Red blood cell count abnormal Road traffic accident White blood cell count abnormal

Symptomtext

I wasn't feeling well all winter, I couldn't feel good but I have been anemic so I got an IV infusion. My sodium bottomed out and I ended up in the hospital. My sodium was normal prior to the booster. We spent Christmas out of the area and I was having memory lapses. On April 2 I had a small fall and April 3 I was in a car accident. April 5 I went to the ER. Right before the holiday I went back in. I was an emergency admit again. Everything was off, white count, red count, and I see all kinds of specialists. I left my job because I couldn't think anymore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: 4,0
Labordaten: Blood panels showed Hyponatremia in April 7, 2022.
Aktuelle Erkrankungen: Anemic
Vorgeschichte: Anemic
Andere Medikamente: Xanax; Amitriptyline; Gabapentin; Daily Vitamins; Zinc; B-12 Injections; Beta Blocker
Allergien: Morphine; Prednisone Steroids; SFRIs; Lexapro; Seroquel; Clozapine
Vorherige Impfungen: -

VAERS 2243740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 73,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 26.01.2022
Beginn: 11.04.2022
Tage bis Beginn: 75,0
Dosis: 4
Route/Site: SYR / RA

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

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

Symptomtext

04/11/2022 I woke up with a sore throat. I called the Hospital to get a PCR COVID test. Tested positive on 4/14/2022. On 4/15/2022 I received INV -MOLNUPIRAVIR 200mg. Stopped medication last night. I don't feel tired. I have a headache over my right eye, runny nose. I am not as exhausted as I was before. They gave me Benzonatate to take 3 times a day. I am not coughing as much any more. They sent me a diabetic tussin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID PCR Test. Positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Prostate Cancer; High Blood Pressure; Gout; Type 2 Diabetes; Indigestion/Heartburn
Andere Medikamente: Fish oil Calcium with Vitamin D Vitamin B 12 Vitamin D3 Allopurinol Alerted Atorvastatin Bayer Aspirin Lisinopril Metformin Montelukast Naproxen Pantoprazole Tropism Methocarbamol Oxycodone Gabapentin Lupron Prednisone Zytiga
Allergien: Cefadroxil
Vorherige Impfungen: -

VAERS 2237902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: IL
Alter: 92,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Contusion Pain in extremity

Symptomtext

really bad sore and bruised arm; really bad sore and bruised arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 92-year-old female patient received BNT162b2 (BNT162B2), on 30Nov2021 at 14:00 as dose 3 (booster), single (Lot number: FH8030) at the age of 92 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Macular degeneration" (unspecified if ongoing), notes: Macular degeneration diagnosed four years ago; "hearing problem" (unspecified if ongoing), notes: hearing problem diagnosed many many years ago, only has hearing in one ear; "very high fever" (unspecified if ongoing), notes: at one years old running a very high fever; "mastoid broke the year drum" (unspecified if ongoing), notes: a mastoid broke the year drum, deaf in one ear.; "Colostomy" (unspecified if ongoing), notes: Colostomy Diagnosed 27-28 years ago; "lost a weight" (unspecified if ongoing), notes: lost a weight; "poor sight" (unspecified if ongoing), notes: poor sight is very poor. The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose: 1, Lot number: FW0150, Anatomical Location: Right Arm, Expiry Date: Unknown), administration date: 03Apr2021, when the patient was 91-year-old, for COVID-19 Immunization, reaction(s): "No adverse effect"; BNT162b2 (Dose: 2, Lot number: EW0150, Anatomical Location: Right Arm, Expiry Date: unknown), administration date: 24Apr2021, when the patient was 91-year-old, for COVID-19 Immunization, reaction(s): "No adverse effect"; Flu shot (about 50 years ago a Flu shot, made her sick to her stomach, it didn't hurt her arm.), reaction(s): "sick to her stomach". The following information was reported: PAIN IN EXTREMITY (non-serious), CONTUSION (non-serious) all with onset 01Dec2021, outcome "not recovered" and all described as "really bad sore and bruised arm". Therapeutic measures were taken as a result of pain in extremity, contusion. Additional information: Caller went to withheld pharmacy, she got both of her shots for Covid, no problem. On 30Nov2021, she never felt it when the girl gave the shot to her. she did not feel 'bad' when getting the shot. The next day her arm felt bruised and sore, her arm started getting sore up to her shoulder, and was get so it, it was like bruise and it just kept getting worse and going down, down, now her whole arm was sore, when she pick something up it hurts, when she try to move some thing her arm hurts. she can't pick anything up, her arm hurts no matter what she does. Caller stated that since having the booster vaccine, she has had a "really bad sore and bruised arm." Caller stated that she had a doctor's appointment tomorrow to assess her arm. She is wondering if any other people have had this problem, what she can do for her side effects. Consumer enquired whether had any complaints of people after they got the booster shot having a sore arm. Consumer was informed about the role of Pfizer Drug Safety. Consumer was informed about the Pfizer Medical Information department and telephone# was shared as withheld, option 3, 8 AM to 9 PM, Monday to Friday. Spoke from attached document: "Cons -How long side effects last (v8.0" under "Side effects that had been reported with the vaccine include." Informed caller that Pfizer is unable to make treatment recommendations for individual patients. Referred caller to follow up with her HCP. Fulfillment offered and sent. Survey offered. Case narrative including clinical course, therapeutic measures, outcome and additional relevant information: Report was not related to a study or programme. The patient was also the reporter. HCP consent to contact was Yes. HCP Type was General practitioner. Other Conditions were Yes. No Investigations. NDC number and Expiry Date of Pfizer Covid-19 Vaccine was Unknown. Other Products were Yes. she used to be 5 foot 2 inches height but is now 5 foot 1 and half inch, happened over the last few years. she lost a weight, before the vaccine She has poor sight is very poor, she has to get the magnifying glass to look at the paper with her HCP information. Caller has macular degeneration, clarifies this is nothing to with vaccine. Caller called the drug store and they told her to call her doctor. She is going to her doctor tomorrow, then she thought she should also contact Pfizer. arm felt bruised and sore, started the day after receiving the vaccine. Treatment: she was using a roll on, something cold and it was not helping, didn't know the name of the roll on. Her arm hurts no matter what she does: if she reaches across the table she feels pain. Start: the next day. Hard for her to read vaccine card. Vaccine Card: Looks like they wrote the 30Nov2021, but she went 20Nov2021. She is checking her calendar. At her age it is kind of hard to remember things. Clarifies she had an appointment on 20Nov2021 and they canceled and she did receive the booster on 30Nov2021 as documented on her vaccine card. Second dose received 24Apr2021. Lot number: EWD150 or EW0150. Caller isn't sure if that is a D or Zero following EW in the lot number. Right Arm. No expiration dates listed. Indication: Allergic to so many things, her daughter went over the list with the Pfizer and the other one and the Pfizer was the only one she could use without having a problem. Her daughter is a physical therapist and she looked through the list of what the other two vaccines contain and she said Pfizer was the best one for her. Concomitant Medications was No, her ordinary medicine was what she was taking. No Investigations. since her arm was not getting better, she wanted to see what she could do for it. Vaccine Lot Expire Date was unknown. Additional Vaccines Administered on Same Date of the Pfizer Suspect was none. arm felt bruised and sore Time of Onset: (24-hour clock) was morning. hurts no matter what she does. Each day it was getting worse. No Emergency room visit. kept thought it was going to get better, has a regular appointment at the doctors tomorrow. No Physician Office visit. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) were none. Adverse Event Onset Age of flu shot was unknown. Vaccine/Brand Name and Vaccination Date was unknown. Family Medical History Relevant to AE(s) was none. Relevant Tests were None. NDC and UPC number of COVID-19 Vaccine was Unknown. Additional Context: Last name: Consumer stated, "withheld (When clarified as withheld consumer confirmed the same, contradictory information hence, not captured in tab; Initial confirmed as K hence captured)." Lot#: Consumer stated, "Oh god I do not know where my card is right now." Product details (Expiration date, NDC# UPC# and Treatment) and Pharmacy details could not be probed as consumer was unwilling to share further information. Hence further probing could not be done. Limited information available over the call. QR Comment: Reporter type could not be probed hence captured by default as Consumer or other non-health professional in tab. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Colostomy (Colostomy Diagnosed 27-28 years ago); Fever (at one years old running a very high fever); Hearing decreased (hearing problem diagnosed many many years ago, only has hearing in one ear); Macular degeneration (Macular degeneration diagnosed four years ago); Sight disability (poor sight is very poor); Trauma ear drum (a mastoid broke the year drum, deaf in one ear.); Weight loss (lost a weight)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2236033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 15.04.2022
Impfdatum: 15.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / AR

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

Arthralgia Exercise tolerance decreased Fatigue Gait disturbance Inflammatory marker test Laboratory test normal

Symptomtext

Joint pain, focused initially in knees and ankles and now primarily in ankles and feet. Significant pain and difficulty walking first thing in morning through early April (>4 months). I have not been able to exercise or walk or exercise recreationally, and I am paying for expensive on campus parking next to my office, which I used to never do. I used to walk 3-5 miles a day and also do yoga, etc. Some days pain was so severe when I got home, I would make sure I did everything I needed on the first floor before going upstairs so that I would not have to do the stairs more than once. I am now in PT, including icing and NSAIDs, which is helping considerably. After the first series, I had similar symptoms, plus approx 3 weeks of severe fatigue, and the pain from that event was largely resolving by the time I went in for the booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: My doctor did a suite of tests looking for inflammation a month ago; most were negative.
Aktuelle Erkrankungen: I had a previous similar adverse reaction to my initial vaccine series (3/22/21 and 4/12/21) which had mostly cleared by August, but I was still dealing with mild joint pain. This reaction is to my booster.
Vorgeschichte: I previously had an extended post-viral syndrome with Chikungunya in 2015 (my case was reported) that lasted about six months.
Andere Medikamente: Allegra
Allergien: Many seasonal allergies (pollen, mold, etc), corn, rye, dairy, gluten, crab
Vorherige Impfungen: -

VAERS 2225945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: AL
Alter: 53,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Balance disorder Fall Hypoaesthesia Muscular weakness Pain Phlebitis Vascular pain

Symptomtext

I noticed that I started to experience leg vein swelling gradually after receiving my vaccination for Dose 1 and Dose 2, but it became more noticeable after Dose 2 Pfizer-BioNTech April 10, 2021 lot EL3302. My veins are more visible in the legs with swelling, with pain that is throbbing and numbing pain. I can not determine if the pain is in the leg or the back, not sure where it is coming from. When I go to stand the leg will give out and cause a balance issue or fall issue. Upcoming visit with surgery on 04/18/2022 and will communication this issue with the physicians and neurologist to check for blood clots and to determined the cause of the leg vein swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: No.
Aktuelle Erkrankungen: No
Vorgeschichte: Back issues
Andere Medikamente: Descovy 200 mg/25mg l pill a day
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2219838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: OH
Alter: 80,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Vaccination site pain Weight

Symptomtext

she has feeling pain in the arm where she received the vaccine./caller's arm is extremely painful, not getting better at all.; Caller is tired today; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200506924 (Pfizer). A 80 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 11Jan2022 16:00 (Lot number: FH8030) at the age of 80 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE: 1, Lot number: EN6203 Expiration, date: 30Jun2021 Sees on vaccination card expires 6, hours. Dose and route: 0.3ml, syringe in arm), administration date: 04Mar2021, when the patient was 79 years old, for COVID-19 immunization; Bnt162b2 (DOSE: 2, Lot number: EN6207 Expiration, date: 31Jul2021 Sees on vaccination card, 30mcg / .3ml IM, vial diluted 30Mar at 1400 hours.), administration date: 30Mar2021, when the patient was 80 years old, for Covid-19 immunization, reaction(s): "Headache/After one of the first COVID-19 vaccine shots caller had a headache for 6 weeks or longer. Headache is gone now, took a long time. Caller clarifies this was after the 2nd dose.". The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 11Jan2022, outcome "not recovered", described as "she has feeling pain in the arm where she received the vaccine./caller's arm is extremely painful, not getting better at all."; FATIGUE (non-serious) with onset 2022, outcome "unknown", described as "Caller is tired today". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: 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: Fatigue
Hospital-Tage: -
Labordaten: Test Name: Weight; Result Unstructured Data: Test Result:Normal weight; Comments: Patient weight: declined to provide, states that she is keeping her weight a secret, but she's a normal weight; not skinny, but a normal weight.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2217928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 06.04.2022
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cough Headache Pain Rhinorrhoea

Symptomtext

Narrative: Patient was administered the vaccine and observed for 15 minutes without any issues. Two days later, on December 22, he contacted the clinic reporting that yesterday he had body aches, last night he started with a headache, nasal drainage and coughing, He was advised to monitor for worsening symptoms and to call back if no improvement in 48-72 hours. To date, 1/4/2022, there has not been any further communication from the patient. It would seem the reported ADE has resolved.

Weitere VAERSDATA-Felder

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

VAERS 2213614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 03.04.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fatigue Headache Rash

Symptomtext

Headache, fatigue, Rash- From lower neck to above neck

Weitere VAERSDATA-Felder

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

VAERS 2212192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MS
Alter: 33,0
Geschlecht: M
Eingang: 01.04.2022
Impfdatum: 26.03.2022
Beginn: 26.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Rash Rash erythematous Rash pruritic

Symptomtext

Rash that started the day I took the first shot. The rash started about an hour after taking the shot and it has gotten progressively worse over the last 6 days. The rash is very itchy, red and all over my body. Have tried creams, lotions, and steroid treatment with no improvement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin and Sulfa Medications
Vorherige Impfungen: -

VAERS 2210232

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FH8030

mild

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / AR

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

Ageusia Anosmia Back pain COVID-19 Ear infection Ear pain Exposure during pregnancy Myalgia Neck pain Oropharyngeal pain Pain in extremity Respiratory tract congestion SARS-CoV-2 test positive Tinnitus

Symptomtext

Received covid booster shot 12/4/2021 and developed a sore arm, sore back and neck muscles, sore throat, ear pair in left ear, congestion, (developed ringing in left ear that lasted 4 weeks). Had an appointment with urgent care nurse practitioner and she prescribed antibiotics for an ear infection.. The next day I noticed a loss of taste and smell and decided to get a rapid covid test which came back positive. My husband and son also became ill and tested positive for covid. I took a pregnancy test January 2022 and tested positive for pregnancy, which means I because pregnant around the same time I received the booster. Currently, I am still pregnant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Prenatal Vitamin Vitamin D Letrozole
Allergien: N/A
Vorherige Impfungen: -

VAERS 2209547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MO
Alter: 69,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 12.11.2021
Beginn: 23.12.2021
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: SYR / LA

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

Biopsy skin abnormal Erythema Hyperkeratosis Pain Rash Scab

Symptomtext

On December 23, 2021 around 10:00 I got done take a shower and my back stung at a certain part of my right shoulder and back. I thought it was a pimple. In the next 3-4 days, it formed a line and I initially thought it was a mild case of shingles. It looked like Chicken Pox or Shingles. In early January I made an appointment for January 27th with my Dermatologist. In between scheduling that I had a rash break out on my right ankle and then spread to other but those cleared up 8-10 minutes. The back rash never cleared up so I contacted my dermatologist. Some family members tested Positive with COVID so I rescheduled for March 2, 2022. The doctor did a biopsy. They called me and gave me results and that there was no further action that needed to be taken. Most of the scabbing is gone and there is some pinkness but from where skin was removed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Biopsy 03/02/2022 with MD. Results 03/17/2022 Benign Keratosis.
Aktuelle Erkrankungen: None.
Vorgeschichte: Stroke in 2009; High BP; Elevated Cholesterol.
Andere Medikamente: Lisinopril 20MG QD; Atorvastatin 20mg QD.
Allergien: Penicillin.
Vorherige Impfungen: -

VAERS 2204133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: 38,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 24.11.2021
Beginn: 20.12.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray Cough Diarrhoea Fatigue Laryngitis Nausea Oropharyngeal pain Pulmonary function test SARS-CoV-2 test

Symptomtext

Laryngitis, cough, sore throat, fatigue, diarrhea, nausea lasting over 3 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Covid Test Dec. 26th Chest X-ray Feb. 2nd and a Pulmonary Function Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Anxiety, Depression, disc herniations, history of neuroendocrine tumor of the pancreas.
Andere Medikamente: Clonopin, Cymbalta, Metformin, Topamax, Percocet, Valtrex, Aygestin, Vitamin B, Vitamin D, Multi-Vitamin, baby aspirin, Lunesta
Allergien: Sulfa, Latex, Steri-strips
Vorherige Impfungen: -

VAERS 2201707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TX
Alter: 84,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 11.11.2021
Beginn: 28.03.2022
Tage bis Beginn: 137,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Pain in extremity

Symptomtext

Patient called 3/28/22 to report arm was still sore from vaccine back in November, states now hurting up into shoulder area. Patient was advised of otc medications such as tylenol and ibuprofen to treat soreness but was encouraged to reach out to dr for evaluation to make sure soreness from vaccine back in November as pharmacy cannot diagnose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none reported
Aktuelle Erkrankungen: smoker
Vorgeschichte: smoker, no other health conditions reported, this was the booster vaccine
Andere Medikamente: none reported
Allergien: none reported
Vorherige Impfungen: -

VAERS 2198311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 74,0
Geschlecht: M
Eingang: 25.03.2022
Impfdatum: 22.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

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

Diarrhoea SARS-CoV-2 test

Symptomtext

diarrhea; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Nov2021 13:15 (Lot number: FH8030) at the age of 74 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: sulfa drugs" (unspecified if ongoing); "Dose Number 1: Moderna/ Dose Number 2: Moderna/ Dose Number 2: Pfizer booster" (unspecified if ongoing); "If Covid Prior Vaccination: Yes" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Moderna (prev_dose_product: COVID19,, prev dose brand:Moderna,, prev dose brand unknown:False,, prev dose lot number:006M20A,, prev dose lot unknown :False,, prev dose administration date:19Feb2021,, prev dose administration time:02:30PM, prev dose dose number:1,, prev dose vaccine location:Left arm), administration date: 19Feb2021, when the patient was 74 years old, for Covid-19 immunization; Moderna (Prev dose product:COVID 19,, Prev dose brand:Moderna,, Prev dose brand unknown:False,, Prev dose lot number:0061321A,, Prev dose lot unknown:False,, Prev dose administration date=19Mar2021,, Prev dose administration time=01:45PM, Prev dose dose number:2,, Prev dose vaccine location:Left arm,), administration date: 19Mar2021, when the patient was 74 years old, for Covid-19 immunization. The following information was reported: DIARRHOEA (non-serious) with onset 25Nov2021 12:00, outcome "not recovered", described as "diarrhea". The event "diarrhea" was evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of diarrhoea. Additional information: No other vaccine in four weeks. Prior vaccination had covid. Covid was tested post vaccination. Nasal swab test type post vaccination.15 Minute test. Patient stated he got diarrhea soon after taking the Pfizer booster (22Nov2021) and still have it (13Mar2022). Treatment for adverse event with Anti-Diarrhea Medication & Scheduled For Colonosc No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Date: 20220119; Test Name: 15 nimute test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Interchange of vaccine products; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2191492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NJ
Alter: 23,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 23.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: - / LA

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

Illness Malaise SARS-CoV-2 test Taste disorder

Symptomtext

horrible taste/ the food tasted like garbage; sick; he felt lousy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 23 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 23Nov2021 (Lot number: FH8030) at the age of 23 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Migraine", start date: 2011 (unspecified if ongoing), notes: started when he was 13 years old. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, States dose #2 of Pfizer BioNTech Covid 19 vaccine on 12Apr2021 in his upper left arm at roughly 3:30pm. Caller does not have NDC or expiry to provide. lot EW0161.), administration date: 12Apr2021, when the patient was 22 years old, for COVID-19 immunization, reaction(s): "States dose #1 of Pfizer BioNTech Covid 19 vaccine on 27Mar2021/ States dose #2 of Pfizer BioNTech Covid 19 vaccine on 12Apr2021"; Bnt162b2 (DOSE 1, SINGLE, States dose #1 of Pfizer BioNTech Covid 19 vaccine on 27Mar2021 in his upper left arm at 3:30. Caller does not have NDC or expiry to provide. lot ER8737.), administration date: 27Mar2021, when the patient was 22 years old, for COVID-19 immunization. The following information was reported: TASTE DISORDER (non-serious) with onset Dec2021, outcome "not recovered", described as "horrible taste/ the food tasted like garbage"; ILLNESS (non-serious) with onset Dec2021, outcome "unknown", described as "sick"; MALAISE (non-serious) with onset Dec2021, outcome "unknown", described as "he felt lousy". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of taste disorder. Additional information: Agent relays the caller is calling to report on her 23 year old son, (Name withheld). Agent relays the callers son received his booster dose of the Pfizer BioNTech Covid 19 vaccine sometime in Nov2021, like the day before Thanksgiving but caller did not have exact date. Agent relays the caller is reporting that 2 weeks later her son has a horrible taste after eating and reports it tastes like garbage when he eats. Agent relays the caller is asking for more information and he provided what he has and the caller would like to report the AE. Agent relays the caller is reporting her son has been experiencing this since Nov2021, it has not disappeared. Agent relays the caller did some research online and read like 6 patients reported the same thing and she wanted more information and to file a report as it seems like this is a rare event of the booster to her. Caller states it's like a side effect of long haul Covid symptoms, that garbage tasting thing and it has not gone away. States her son has not been out of the house for 2 years other than to get the vaccine and to stress to that point she means literally, she is immunocompromised with severe asthma. States he has not worked and is living at home and has nowhere, it's not like he got Covid between. States she made him get a PCR test maybe 3 weeks after his booster and it came back negative. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Test Name: Covid PCR test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine (started when he was 13 years old)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2191472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 40,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 12.11.2021
Beginn: 12.12.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: - / LA

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

Pain in extremity

Symptomtext

Pain in my left Arm that is limiting my capacity to use my left arm.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-healthcare professional). The reporter is the patient. A 40 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 12Nov2021 14:45 (Lot number: FH8030) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Type II diabetes" (unspecified if ongoing); "GERD" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN; SIMVASTATIN. Vaccination history included: Bnt162b2 (Dose Number: 2, single, Batch/Lot No: EL9269, Location of injection: Arm Left, Vaccine Administration Time: 01:15 PM), administration date: 05Feb2021, when the patient was 40 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, single, Batch/Lot No: EL3249, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 15Jan2021, when the patient was 39 years old, for COVID-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 12Dec2021 14:45, outcome "not recovered", described as "Pain in my left Arm that is limiting my capacity to use my left arm.". Therapeutic measures were not taken as a result of pain in extremity. Additional information: Facility where the most recent COVID-19 vaccine was administered included Public Health Clinic/Veterans Administration facility. The patient received any other vaccines within 4 weeks prior to the COVID vaccine was Unknown. The patient received medications within 2 weeks of vaccination included Metformin 500 mg and simvastatin20 mg. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD; Type II diabetes mellitus
Andere Medikamente: METFORMIN; SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2189107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: IN
Alter: 61,0
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 01.12.2021
Beginn: 02.02.2022
Tage bis Beginn: 63,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Fatigue Headache Impaired work ability

Symptomtext

Extremely tired, chills, headaches. Took Tylenol and Nyquil. Lasted about 1 week. I have had post COVID headaches and some issues with clarity when working.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: mild copd
Andere Medikamente: multi vitamin, eye promise tablets.
Allergien: -
Vorherige Impfungen: headaches, chills, and extreme tiredness. 61 yrs Pfizer EN6199 3/11/21 first vaccine

VAERS 2184622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: 49,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 24.11.2021
Beginn: 14.02.2022
Tage bis Beginn: 82,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Gait disturbance Hypoaesthesia

Symptomtext

Four weeks ago, the tip of my right thumb went numb. Over the course of the next week the numbness extended to my entire hand and patches of numbness on my arm. The numbness spread to my left hand and arm and to my feet as well. At this point my right arm is numb 24/7. The numbness has affected my gait. I had a previous knee injury that has flared up. My dr. put me on a heavy inflammatory steroid which didn't help the numbness but did help the knee pain while I was taking it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Reflex sympathetic dystrophy
Andere Medikamente: Omeprazole; testosterone gel; methadone; oxycodone; aspirin; hydrochlorothiazide; iron supp
Allergien: None
Vorherige Impfungen: -

VAERS 2181818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 19.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Alopecia Blister Blood pressure measurement Feeling abnormal Hypoaesthesia Nerve conduction studies Pain Joint swelling Pain in extremity Peripheral swelling Rash

Symptomtext

she can''t lift her left arm, she has excruciating pain; rash on her hands and the tops of her feet; her ankles are super swollen and her hands are swollen; her ankles are super swollen and her hands are swollen; her right hand is numb and painful; her right hand is numb and painful; hair is falling out like crazy; has blisters under her left arm, it was so painful; she is in extreme agony; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 19Dec2021 13:00 (Lot number: 331308A) at the age of 51 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "left shoulder surgery", start date: Aug2021 (unspecified if ongoing), notes: has been going to physical therapy. There were no concomitant medications. Vaccination history included: Bnt162b2 (dose 1, single, Batch /lot number: FH8030, anatomical location: left arm), administration date: 28Nov2021, when the patient was 51 years old, for Covid-19 Immunization, reaction(s): "she had throbbing for a couple of days". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Dec2021, outcome "not recovered", described as "she can''t lift her left arm, she has excruciating pain"; RASH (non-serious) with onset Dec2021, outcome "unknown", described as "rash on her hands and the tops of her feet"; JOINT SWELLING (non-serious), PERIPHERAL SWELLING (non-serious) all with onset Dec2021, outcome "not recovered" and all described as "her ankles are super swollen and her hands are swollen"; HYPOAESTHESIA (non-serious), PAIN IN EXTREMITY (non-serious) all with onset Dec2021, outcome "recovered" (Dec2021) and all described as "her right hand is numb and painful"; ALOPECIA (non-serious) with onset Dec2021, outcome "not recovered", described as "hair is falling out like crazy"; BLISTER (non-serious) with onset Dec2021, outcome "unknown", described as "has blisters under her left arm, it was so painful"; FEELING ABNORMAL (non-serious) with onset Dec2021, outcome "unknown", described as "she is in extreme agony". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient too no Prior Vaccinations (within 4 weeks), had no AE(s) following prior vaccinations. Caller (patient) stated that on the 19th she got her 2nd one and ever since then she can't even tell there are so many things wrong. Caller relays she had left shoulder surgery in Aug2021 and has been going to physical therapy and has been making a lot of progress. Caller states that now she can't lift her left arm, she had excruciating pain. Caller provides that started yesterday, that it can't get any worse, any way she moves it feels like there was an impingement, she doesn't know how to explain it. Caller states it's bad, that she had made so much progress for this to happen and she can't do anything and she Was like oh my God. Caller relays that she and her physical therapist were close and he was like you need to go to urgent care and she said no there are crazy people there to see if they have covid and she was just going to wait and see and the next day then her hand goes numb and her ankles are still very swollen. Caller relays she took her blood pressure and it's normal and she had normal salt intake and was not a big salt person and doesn't eat a lot of foods with salt so she doesn't think that was it. Caller relays she had a rash on her hands and the tops of her feet that started like 3 days after the 2nd vaccine. Caller states her ankles are super swollen and her hands were swollen and they had been that way since the next day after the 2nd vaccine. Caller states her right hand was numb and painful and that started the day before yesterday and that was now gone, it went away 24 hours later. Caller relays she did had neurological and had to have a full nerve conduction test and possible cervical spine surgery which she doesn't think she will do. Caller stated she had not had numbness or tingling since seeing her neurologist a few months back. Caller relays her hair was falling out like crazy, she noticed that yesterday. Stated she had thick, beautiful hair and it was overnight and she doesn't know if one goes with the other, she had an appointment to see her surgeon that did her shoulder surgery but she had come so far and now she can barely move it. Caller stated with the swelling and rash she also had blisters under her left arm, it was so painful and she was like squeezing all over her arm like what the heck. States she had 2 big blisters and it's all red underneath. Caller states she called her pharmacist and they said to call Pfizer and tell us what she was experiencing. Caller states she was about 5 foot 2 and a half, she was 200 pounds before physical therapy and now she was down to 169 and she could hop on her bike and was almost up to 9 miles now. Caller states she feels like she was falling apart at the seams now that she was 50. Caller stated she called the surgeon and will see him Thursday, she wanted to see him today but he was not it and was told that someone would call her and her physical therapist wants her to come in and see him also. Caller relays she was in extreme agony and he wants to look at it and she had a feeling he will tell her to go to the ER. Dose #1 on 28Nov2021 in her left arm, like a moron, around lunch time. Stated she had throbbing for a couple of days but no side effects at all and now she was experiencing everything under the sun. Caller does not have NDC or expiry to provide. Dose #2 on 19Dec2021 in her right arm at around 1pm. Caller does not have NDC or expiry to provide. Caller stated with her left arm what was weird was that she alternates twice a week with ice and heat. She texted a picture to her physical therapist this morning and he said it looks like burns and she uses a heating pad but it auto turns off after 20 minutes and she had it on medium heat so there was no way she had blisters the way she does and she was not able to move her arm for anything. Caller states it's so bizarre she had come so far with her recovery with PT and now the pain was so unbearable she can't stop crying, it's really shitty, she didn't even want it and her primary was mad at her and she started crying as she was scared as she doesn't feel they know enough about it and just don't know. Caller stateD what was very sad, one the girls she used to work with her husbands friends wife she had her left side of her face paralyzed and she couldn't shut her eye to sleep and she has to tape her eye shut. Caller states how crazy. She doesn't know if this was reported and she doesn't know enough to report on it. Caller states her friend said she's not getting it, she was regretting getting it with so many problems she was having since her 2nd one and she was scared. States her hair, not for nothing but it's her pride and joy, it's beautiful thick red hair and her ponytail looks like a pathetic little reed. She lost her hair on Saturday and today is Tuesday. Stated she noticed it Saturday and it was ok and on Sunday she felt like it was thin and yesterday she kept running her fingers through and it was coming out in handfuls, she was scared to wash her hair, that when she washed it on Saturday it was coming out in crumples and she does dye her hair every 6 weeks but never ever had it done this. Her hair came out like normal in the shower and this was abnormal. The events did not led the patient to Emergency Room and No Physician Office. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:normal; Test Date: 2021; Test Name: full nerve conduction test; Result Unstructured Data: Test. Result:Unknown results.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shoulder arthroscopy (has been going to physical therapy.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2181642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MS
Alter: 57,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Dizziness Feeling abnormal

Symptomtext

light headedness; she just has a weird feeling; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. A 57 year-old female patient received bnt162b2 (COMIRNATY), administered in deltoid left, administration date 01Dec2021 09:00 (Lot number: FH8030, Expiration Date: 31Mar2022) at the age of 57 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "has sinus problems" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1, single, lot No: FF2593, expiry date:30Mar2022, Time the Vaccination Was Given:2:00pm, Anatomical Location of Administration: left deltoid), administration date: 10Nov2021, when the patient was 57 years old, for Covid-19 Immunization, reaction(s): "when she took the 1st dose of the vaccine she lost hearing in her left ear for three days and felt stopped up". The following information was reported: DIZZINESS (non-serious) with onset 02Dec2021 10:00, outcome "not recovered", described as "light headedness"; FEELING ABNORMAL (non-serious) with onset 02Dec2021, outcome "unknown", described as "she just has a weird feeling". Additional information: Caller states the lightheadedness began this morning about a couple of hours ago at 10:00am and when she took the 1st dose of the Pfizer Covid vaccine she was pressured into getting it and at that time she could not work unless she got it which her work changed yesterday; states when she took the 1st dose of the vaccine she lost hearing in her left ear for three days and felt stopped up; States she does not know when the hearing loss began and felt like her ear was stopped up like a cotton ball was there but she did not loose hearing and was not able to being able to hear like if you are flying on a plane the pressure changes and it felt like that; states she does not know when the hearing issue began but it was just a few days after the 1st dose of the vaccine and is not ongoing but lasted like 3 days. States the lightheadedness is ongoing and about the same and even talking to the agent she just has a weird feeling not dizzy and just lightheaded. Caller states the lightheadedness began this morning about a couple of hours ago at 10:00am and when she took the 1st dose of the Pfizer Covid vaccine she was pressured into getting it and at that time she could not work unless she got it which her work changed yesterday; states when she took the 1st dose of the vaccine she lost hearing in her left ear for three days and felt stopped up; states she took a nasal congestion tablet and Flonase and with blowing her nose those products did not work and she could not hear from her left ear and it was stopped up. AE(s) does not require a visit to emergency room/physician office. Additional vaccines administered on same date of the Pfizer suspect was none. Prior vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) was none. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sinus disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2180689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 78,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Pain in arm, at injection site. confirmed she did not have pain in joint, ruling out intraarticular injection. Pain has remained consistent since receiving shot in November.

Weitere VAERSDATA-Felder

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

VAERS 2179306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 48,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Fatigue Off label use Pain Product use issue Vaccination site pain

Symptomtext

Soreness at injection site; Body aches; General fatigue; Most recent dose details product=COVID 19, other vaccine same date product=Influenza Quad Valent; Most recent dose details product=COVID 19, other vaccine same date product=Influenza Quad Valent; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 48 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 01Dec2021 11:30 (Lot number: FH8030) at the age of 48 years as dose 1, single for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), administered in arm right, administration date 01Dec2021 (Batch/Lot number: unknown) as dose 1, single for immunisation. Relevant medical history included: "Insomnia" (unspecified if ongoing). Concomitant medication(s) included: LUNESTA; IBUPROFEN; TRUVADA. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 01Dec2021, outcome "unknown" and all described as "Most recent dose details product=COVID 19, other vaccine same date product=Influenza Quad Valent"; VACCINATION SITE PAIN (non-serious) with onset 01Dec2021 19:00, outcome "not recovered", described as "Soreness at injection site"; PAIN (non-serious) with onset 01Dec2021 19:00, outcome "not recovered", described as "Body aches"; FATIGUE (non-serious) with onset 01Dec2021 19:00, outcome "not recovered", described as "General fatigue". The action taken for influenza vaccine was unknown. Therapeutic measures were taken as a result of vaccination site pain, pain, fatigue. Additional Information: The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to COVID vaccine. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were taken as a result of vaccination site pain, pain and fatigue which included treatment with ADVIL. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Insomnia
Andere Medikamente: LUNESTA; IBUPROFEN; TRUVADA
Allergien: -
Vorherige Impfungen: -

VAERS 2179275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 47,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / LA

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

Fatigue Headache Pain Pain assessment Vaccination site pain

Symptomtext

Soreness at injection site (3 on pain scale of 1-10); body aches (2 on pain scale); headache (3 on pain scale); tiredness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from a sales representative. The reporter is the patient. A 47 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 16Nov2021 17:15 (Lot number: FH8030) at the age of 47 years as dose 3(booster), single for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), intramuscular, administered in arm right, administration date 16Nov2021 17:15 (Batch/Lot number: unknown) as dose number unknown, single. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, Date: 16Mar2021, Site of Injection: Left upper arm, Lot: EP6955(Pfizer)), administration date: 16Mar2021, when the patient was 47 years old, for Covid-19 immunization; Bnt162b2 (Dose: 2, Date: 06Apr021, Site of Injection: Left upper arm, Lot: EP0955(Pfizer)), administration date: 06Apr2021, when the patient was 47 years old, for COVID-19 immunisation. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 17Nov2021, outcome "recovered" (17Nov2021), described as "Soreness at injection site (3 on pain scale of 1-10)"; PAIN (non-serious) with onset 17Nov2021, outcome "recovered" (17Nov2021), described as "body aches (2 on pain scale)"; HEADACHE (non-serious) with onset 17Nov2021, outcome "recovered" (17Nov2021), described as "headache (3 on pain scale)"; FATIGUE (non-serious) with onset 17Nov2021, outcome "recovered" (17Nov2021), described as "tiredness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site pain, fatigue. Therapeutic measures were taken as a result of pain, headache. Additional information: Concomitant Drugs; List below concomitant drugs taken within two weeks before the event onset. Exclude all drugs only administered more than two weeks before the event, and any drug used to treat the event or taken after event onset: was not provided. Patient's Medical History (including any illness at time of vaccination) was not provided. Family Medical History Relevant to AE (s) was not provided. RELEVANT TESTS List other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebro-spinal fluid culture, pleural fluid culture, urine culture, diagnostic imaging, (e.g., chest X-ray, MRI). If COVID-19 testing has been conducted, provide test dates and results was not provided. Specific relevant test for Thromboembolic event with Thrombocytopenia was not provided. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20211117; Test Name: pain scale; Result Unstructured Data: Test Result:2/3; Comments: body aches headcahe; Test Date: 20211117; Test Name: pain scale; Result Unstructured Data: Test Result:3; Comments: soreness injection site
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Feeling abnormal Headache Inflammation Urticaria

Symptomtext

inflammation/had inflammation on hands and feet and face; head fogginess; hives on her back and chest/ few hives and raised welts on her back; headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 61 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 02Dec2021 (Lot number: FH8030) at the age of 61 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Allergy medication" (unspecified if ongoing), notes: She would take an allergy medication periodically prior to this. only take it if she needs. There were no concomitant medications. The following information was reported: URTICARIA (non-serious) with onset 02Dec2021, outcome "recovering", described as "hives on her back and chest/ few hives and raised welts on her back"; HEADACHE (non-serious) with onset 02Dec2021, outcome "recovering", described as "headache"; FEELING ABNORMAL (non-serious) with onset 03Dec2021, outcome "recovering", described as "head fogginess"; INFLAMMATION (non-serious) with onset 04Dec2021, outcome "recovering", described as "inflammation/had inflammation on hands and feet and face". Therapeutic measures were taken as a result of urticaria. Additional information: Patient stated that she received her first dose of the vaccine last 02Dec2021 and on the same day she developed hives on her back and chest, experiences headache. She had head fogginess that started the next day on 03Dec2021 and then, she also had inflammation on her hand and a little on her face and feet started on 04Dec2021. She also stated that the hives lasted for two weeks. She took an allergy medication ?Allegra', to offset it when she started feeling the reaction on 03Dec2021, and the hives are just starting to feel better on 10th day, she would only take medicine if she needs to. She would take an allergy medication periodically prior to this. She just doesn't like taking medications and she would only take it if she needs to. She wanted to know if she can get her 2nd dose after experiencing this side effects. She does not think she is a candidate for second dose and wanted to ask someone guidance about getting second dose based on her symptoms. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (She would take an allergy medication periodically prior to this. only take it if she needs.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: 45,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 16.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Arthralgia Asthenia Back pain Blood pressure abnormal Blood pressure measurement Dizziness Fatigue Headache Laboratory test Malaise Myalgia Neck pain Nervousness Somnolence

Symptomtext

I am sick; Feeling weak, tired and drowsy; I am having terrible headaches; Feeling weak, tired and drowsy; Feeling weak, tired and drowsy; dizzy; nervous; "has blood pressure" everyday; had shoulder, back, neck, and knee pain; had shoulder, back, neck, and knee pain; had shoulder, back, neck, and knee pain; had shoulder, back, neck, and knee pain; muscle pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program . The reporter is the patient. A 45 year-old male patient received bnt162b2 (COMIRNATY), administration date 16Nov2021 (Lot number: FH8030) at the age of 45 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Osteoarthritis" (unspecified if ongoing), notes: Verbatim: Osteoarthritis; "Spinal stenosis" (unspecified if ongoing), notes: Verbatim: Spinal stenosis; "Migraine headache" (unspecified if ongoing), notes: Verbatim: Migraine headache; "Hypersensitivity" (unspecified if ongoing), notes: Verbatim: Allergy. The patient's concomitant medications were not reported. The following information was reported: MALAISE (non-serious), outcome "unknown", described as "I am sick"; ASTHENIA (non-serious), FATIGUE (non-serious), outcome "not recovered" and all described as "Feeling weak, tired and drowsy"; HEADACHE (non-serious), outcome "unknown", described as "I am having terrible headaches"; SOMNOLENCE (non-serious), outcome "unknown", described as "Feeling weak, tired and drowsy"; DIZZINESS (non-serious), outcome "unknown", described as "dizzy"; NERVOUSNESS (non-serious), outcome "unknown", described as "nervous"; BLOOD PRESSURE ABNORMAL (non-serious), outcome "unknown", described as ""has blood pressure" everyday"; ARTHRALGIA (non-serious), BACK PAIN (non-serious), NECK PAIN (non-serious), ARTHRALGIA (non-serious), outcome "unknown" and all described as "had shoulder, back, neck, and knee pain"; MYALGIA (non-serious), outcome "unknown", described as "muscle pain". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache, arthralgia, back pain, neck pain, arthralgia, myalgia. Additional Information: No prior vaccinations. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: "has blood pressure" everyday; Result Unstructured Data: Test Result:unknown result; Comments: "has blood pressure" everyday; Test Date: 202110; Test Name: Lab test; Result Unstructured Data: Test Result:Unknown result; Comments: Only in Oct
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Verbatim: Allergy); Migraine headache (Verbatim: Migraine headache); Osteoarthritis (Verbatim: Osteoarthritis); Spinal stenosis (Verbatim: Spinal stenosis)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: AZ
Alter: 49,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Axillary pain Fatigue Headache Lymph node pain Lymphadenopathy Malaise Swelling

Symptomtext

Malaise; right ancillary lymph node swelling and pain/Armpit swelling and pain; right ancillary lymph node swelling and pain/Armpit swelling and pain; headache (stingy like a migraine); fatigue; Armpit swelling and pain is unique to third shot.; Armpit swelling and pain is unique to third shot.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 16Nov2021 09:30 (Lot number: FH8030) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "COVID-19", start date: Jan2021 (unspecified if ongoing), notes: Had covid in Jan 2021. Concomitant medication(s) included: INFLUENZA VACCINE, administration date 11Oct2021. Vaccination history included: Bnt162b2 (Dose 2, Batch/Lot No: EW0172, Location of injection: Right : Arm, Vaccine Administration Time: 12:00 PM), administration date: 28Apr2021, when the patient was 48 years old, for COVID-19 Immunization; Bnt162b2 (Dose 1, Batch/Lot No: EP8834, Location of injection: Right Arm, Vaccine Administration Time: 10:30 AM), administration date: 06Apr2021, when the patient was 48 years old, for COVID-19 Immunization, reaction(s): "Had same kind of headache with first". The following information was reported: MALAISE (non-serious) with onset 16Nov2021 18:00, outcome "not recovered", described as "Malaise"; LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 16Nov2021 18:00, outcome "not recovered" and all described as "right ancillary lymph node swelling and pain/Armpit swelling and pain"; HEADACHE (non-serious) with onset 16Nov2021 18:00, outcome "recovered" (18Nov2021), described as "headache (stingy like a migraine)"; FATIGUE (non-serious) with onset 16Nov2021 18:00, outcome "not recovered", described as "fatigue"; SWELLING (non-serious), AXILLARY PAIN (non-serious) all with onset 16Nov2021 18:00, outcome "not recovered" and all described as "Armpit swelling and pain is unique to third shot.". Therapeutic measures were not taken as a result of malaise, lymphadenopathy, lymph node pain, headache, fatigue, swelling, axillary pain. Additional information: patient was not tested for covid post vaccination. had no known allergies. Vaccination facility: Pharmacy or Drug Store. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Had covid in Jan 2021)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

mild

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Injection site erythema Injection site pain Injection site swelling Injection site warmth Pruritus

Symptomtext

warm to the touch; swelling, red raised area that was underneath the injection site in my left arm; swelling, red raised area that was underneath the injection site in my left arm; painful; itchy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Nov2021 14:30 (Lot number: Fh8030) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetes" (unspecified if ongoing), notes: Other medical history: Diabetes; "High Blood Pressure" (unspecified if ongoing), notes: Other medical history: High Blood Pressure; "High Cholesterol" (unspecified if ongoing), notes: Other medical history: High Cholesterol. Concomitant medication(s) included: METFORMIN; LISINOPRIL; ATORVASTATIN. Past drug history included: Coedine, reaction(s): "Drug allergy", notes: Known Allergies: Coedine; Sulfur, reaction(s): "Drug allergy", notes: Known Allergies: Sulfur; Pyridium, reaction(s): "Drug allergy", notes: Known Allergies: Pyridium. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0153, Location of injection: Arm Left, Verbatim: I never had this side effect with the two previous vaccines other than a sore arm for a day.), administration date: 12Apr2021, when the patient was 64 years old, for Covid-19 Immunization, reaction(s): "sore arm"; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8727, Location of injection: Arm Left, Verbatim: I never had this side effect with the two previous vaccines other than a sore arm for a day.), administration date: 22Mar2021, when the patient was 64 years old, for Covid-19 Immunization, reaction(s): "sore arm". The following information was reported: INJECTION SITE WARMTH (non-serious) with onset 11Nov2021, outcome "recovering", described as "warm to the touch"; INJECTION SITE ERYTHEMA (non-serious), INJECTION SITE SWELLING (non-serious) all with onset 11Nov2021, outcome "recovering" and all described as "swelling, red raised area that was underneath the injection site in my left arm"; INJECTION SITE PAIN (non-serious) with onset 11Nov2021, outcome "recovering", described as "painful"; PRURITUS (non-serious) with onset 11Nov2021, outcome "recovering", described as "itchy". Therapeutic measures were not taken as a result of injection site warmth, injection site erythema, injection site swelling, injection site pain, pruritus. Additional information included: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had swelling, red raised area that was underneath the injection site in my left arm. It was 5 inches across, warm to the touch, painful and itchy. The patient still had it but it seemed to be getting better. The patient never had that side effect with the two previous vaccines other than a sore arm for a day. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Other medical history: High Blood Pressure); Diabetes (Other medical history: Diabetes); High cholesterol (Other medical history: High Cholesterol)
Andere Medikamente: METFORMIN; LISINOPRIL; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2176155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 20.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / RA

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

Headache Lymph node pain Lymphadenopathy SARS-CoV-2 test

Symptomtext

Headache; swollen lymph nodes in right underarm and right breast with pain; swollen lymph nodes in right underarm and right breast with pain; This is a spontaneous report received from contactable reporter(s) (Other HCP) Nurse. The reporter is the patient. A 46-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 20Oct2021 13:00 (Lot number: FH8030) at the age of 46 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Allergy to Penicillin" (unspecified if ongoing); "Allergy to sulfa" (unspecified if ongoing). Concomitant medication(s) included: FLU VACCINE VII, administration date 21Sep2021. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL9266, Location of injection: Arm Right, Vaccine Administration Time: 12:00), administration date: 16Feb2021, when the patient was 45 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3249, Location of injection: Arm Right, Vaccine Administration Time: 12:00), administration date: 26Jan2021, when the patient was 45 years old, for Covid-19 Immunization. The following information was reported: HEADACHE (non-serious) with onset 22Oct2021 17:00, outcome "unknown", described as "Headache"; LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 22Oct2021 17:00, outcome "unknown" and all described as "swollen lymph nodes in right underarm and right breast with pain". The events "headache", "swollen lymph nodes in right underarm and right breast with pain" and "swollen lymph nodes in right underarm and right breast with pain" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. It was unknown if therapeutic measures were taken as a result of headache, lymphadenopathy, lymph node pain. Additional information: if covid prior vaccination No. if covid tested post vaccination was yes No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20211021; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2173741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MO
Alter: 55,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 22.05.2021
Beginn: 07.03.2022
Tage bis Beginn: 289,0
Dosis: 3
Route/Site: IM / RA

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

Cough Ear pain Fatigue Headache Myalgia Nausea Pyrexia Respiratory tract congestion Vomiting

Symptomtext

Symptoms were; fever, cough, congestion, fatigue, headache, muscle aches, nausea, vomiting and left ear ache. Treated in hospital with Remdesivir and increased prednisone dosage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: 3,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Lupus
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2171872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 05.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: SYR / AR

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

Ageusia Anosmia Arthralgia COVID-19 Chills Exposure to SARS-CoV-2 Headache Injection site pain Malaise Pain SARS-CoV-2 test positive

Symptomtext

I had very little side effects from the booster shot compared to the second covid vaccine I had received approximately 8 months prior. I just had a mild headache and mild ache at injection site vs. chills, headache, joint pain, body aches, severe pain at injection site. 3 weeks later, I was feeling under the weather, but would test negative when using an at home covid test kit. Then, my boyfriend, whom I live with, tested positive for covid and we did not isolate him nor avoid direct contact. I was feeling ill for over a week and tested every other day but continued to test negative. Finally, on Jan 9, 2022, I lost my sense of smell and taste and got a covid positive result

Weitere VAERSDATA-Felder

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

VAERS 2161696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MA
Alter: 50,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 17.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: - / LA

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

Burning sensation Nail discolouration Pain in extremity Raynaud's phenomenon SARS-CoV-2 test Swelling

Symptomtext

Bilateral 8 toes, except big toe is bluish red; Bilateral 8 toes, except big toe is/swollen; Bilateral 8 toes, except big toe is/burning feeling; Bilateral 8 toes, except big toe is/painful; Looks like Raynaud's phenomenon.; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 50 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 17Nov2021 (Lot number: FH8030) at the age of 50 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: VIT B12; ADVIL. Past drug history included: Metoclopramide, reaction(s): "known allergies: Metoclopramide", notes: known allergies: Metoclopramide. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0172, Location of injection: Arm Left), administration date: 03May2021, when the patient was 50 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0153, Location of injection: Arm Left), administration date: 12Apr2021, when the patient was 50 years old, for COVID-19 Immunization. The following information was reported: NAIL DISCOLOURATION (non-serious) with onset Dec2021, outcome "recovering", described as "Bilateral 8 toes, except big toe is bluish red"; SWELLING (non-serious) with onset Dec2021, outcome "recovering", described as "Bilateral 8 toes, except big toe is/swollen"; BURNING SENSATION (non-serious) with onset Dec2021, outcome "recovering", described as "Bilateral 8 toes, except big toe is/burning feeling"; PAIN IN EXTREMITY (non-serious) with onset Dec2021, outcome "recovering", described as "Bilateral 8 toes, except big toe is/painful"; RAYNAUD'S PHENOMENON (non-serious) with onset Dec2021, outcome "recovering", described as "Looks like Raynaud's phenomenon.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of nail discolouration, swelling, burning sensation, pain in extremity, raynaud's phenomenon. Additional information: It was reported that she had bilateral 8 toes, except big toe is bluish red, swollen, burning feeling and painful looks like Raynauds Phenomenon. No other vaccine in four weeks. other medications in two weeks included Vit B12, Advil as needed. No covid prior vaccination, she had covid tested post vaccination. AE treatment included Advil and Atenolol. No other medical history and no hospitalization prolonged. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history None
Andere Medikamente: VIT B12; ADVIL
Allergien: -
Vorherige Impfungen: -

VAERS 2161522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

mild

Staat: OK
Alter: 17,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Erythema Pruritus

Symptomtext

Upper arm got red and itchy immediately after; Upper arm got red and itchy immediately after; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 17 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 27Nov2021 12:00 (Lot number: Fh8030) at the age of 17 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Known Allergies: Latex" (unspecified if ongoing); "COVID-19" (unspecified if ongoing). Concomitant medication(s) included: LEVOXYL; ADDERALL; PROZAC. The following information was reported: ERYTHEMA (non-serious), PRURITUS (non-serious) all with onset 27Nov2021 12:00, outcome "recovered" (2021) and all described as "Upper arm got red and itchy immediately after". Therapeutic measures were not taken as a result of erythema, pruritus. Additional information: The patient had not received any other vaccine within 4 weeks prior to the vaccine, and not tested COVID post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Latex allergy
Andere Medikamente: LEVOXYL; ADDERALL; PROZAC
Allergien: -
Vorherige Impfungen: -

VAERS 2161418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 12.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: - / LA

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

Bladder pain Gait disturbance Ovulation pain

Symptomtext

sharp pain in my ovary and in my bladder and the pain was going towards my legs; its my ovary, its pushing on my bladder; I had problems walking; I keep limping when I walk and on the first day I couldn't walk at all; sharp pain in my ovary and in my bladder and the pain was going towards my legs; its my ovary, its pushing on my bladder; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 36 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 12Nov2021 (Lot number: FH8030) at the age of 36 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU. Vaccination history included: Bnt162b2 (Dose 1, Pfizer EL9269), administration date: 09Feb2021, when the patient was 35 years old, for COVID-19 Immunization; Bnt162b2 (Dose 2, EN6108), administration date: 02Mar2021, when the patient was 35 years old, for COVID-19 Immunization. The following information was reported: OVULATION PAIN (non-serious), BLADDER PAIN (non-serious) all with onset 17Nov2021, outcome "unknown" and all described as "sharp pain in my ovary and in my bladder and the pain was going towards my legs, its my ovary, its pushing on my bladder"; GAIT DISTURBANCE (non-serious) with onset 17Nov2021, outcome "unknown", described as "I had problems walking; I keep limping when I walk and on the first day I couldn't walk at all". The events "sharp pain in my ovary and in my bladder and the pain was going towards my legs, its my ovary, its pushing on my bladder", "i had problems walking; i keep limping when i walk and on the first day i couldn't walk at all" and "sharp pain in my ovary and in my bladder and the pain was going towards my legs, its my ovary, its pushing on my bladder" were evaluated at the emergency room visit. Additional information: Reporter was just trying to report one of the possible side effect and she was trying to do this online but for some reasons website would not let her. It just keeps switching, its like just blinking-blinking and it wouldn't let her choose anything. So, that's why reporter called. She wanted to do this in website. Pfizer COVID-19 vaccine and actually specifically she was talking about Pfizer booster which is the same she feel. Consumer confirmed the starting date of events as 17Nov2021. Patient started experiencing a sharp pain in her ovary and in her bladder and the pain was going towards her legs and she had problems walking. So, actually she had to take couple of days off. Patient was a teacher. So, she had to take couple of days off. So, patient can go to emergency room and obviously because of the shortage she was not able to see the doctor right away so she conduct a work again that day. Again, started feeling the same way and went to emergency room on Friday where she spent the whole entire day (Further clarification unknown) and they could not understand what was happening to her and the pain still persisted. Its not as sharp as the first couple of days but she have never experienced anything like that. So, she can tell that its her ovary, its pushing on her bladder. Its on her bladder consistently was in a sharp pain and the pain radiates towards her legs. So, patient keep limping when she walks and on the first day she could not walk at all. Second shot was EN61 I think its 08. It might be 88. She think its 08 (Not clarified) and the date was 02Mar2021. Booster shot was FH8030 number 3, 12Nov2021. Well, that says 8030 and then that says the number like a 3. Patient don't know if its might a 30 (Not clarified). She guess, they just marked that its her third shot. No lab test. They give her some kind of pain killers when she was in the emergency room but it didn't effect her what so ever. So, then they couldn't find the reason. They didn't, she meant they just did some test thus, no medication was given to her. She was prescribed Naproxen which was the Ibuprofen but nothing else. She have never purchased it. So, she can give you the name. Its the same as Ibuprofen because she have a side effect from Naproxen so she never got it. It was ordered but she never got that. She had the flu shot two weeks no, one week before her booster shot. She didn't had her vaccination before my prior vaccinations like her original COVID-19 vaccination but she did had a flu shot 1 week actually 1 week and half before her booster. She just really wanted to make sure that she don't even know if its kind of after the just wanted to do her part and just report things. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2151288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 35,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Headache Pain Pyrexia Vomiting

Symptomtext

I woke up the next morning with chills, fever, headache, body aches, and vomiting. It was worse and lasted longer but I did not contact my PCP or treatment. The symptoms did subside in about 4-5 days.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid Disease
Andere Medikamente: Lasix 20mg one time a day, Phentermine 37.5 MG once a day, Furosemide 20mg once a day.
Allergien: None
Vorherige Impfungen: -

VAERS 2138017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Rash

Symptomtext

Rash in the Arm

Weitere VAERSDATA-Felder

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

VAERS 2137079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

mild

Staat: NJ
Alter: 68,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 01.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Chills Cough Inflammation Influenza like illness Malaise Oesophagogastroduodenoscopy Pain in extremity Pulmonary pain SARS-CoV-2 test negative Sneezing

Symptomtext

After second vaccine El3246 developed flu like symptoms lasting up to 3 hrs this re occurred every 3 days continuously for 9 months. Symptoms were headache, nausea, chills, joint pain . Stomach distress diagnosed with gastritis relieved by PPI . Booster vaccine iFH8030 11/20/21 3 hrs post injection severe left knee pain lasting 12 hrs. Followed by random joint pains in hands, back, neck. Flu like symptoms again tested PCR negative x 3 . I am a health care RN wearing a KN 95 12hrs.. a day. Basically I have not felt well since second vaccine . Currently experiencing daily chills, sometimes sneezing, lung pain and cough, no temperature elevation ever. I never know if I am experiencing a new viral exposure daily-then symptoms dissipate after several hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Had EGD for gastric symptoms . Also 2 weeks ago has inflammation of my trochanter and knee left side required 2 weeks of PT.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: No prescriptions. Vitamin A,E,D3,B12,D2 Probiotic, Evening oil of Primrose
Allergien: Sulfa,Penicillin,Macrodantin, Avalox, Prozac, Cipro Chicken,soy,gluten,dairy Latex
Vorherige Impfungen: -

VAERS 2130736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: TN
Alter: 63,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Site: Pain at Injection Site-Medium

Weitere VAERSDATA-Felder

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

VAERS 2129109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 59,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 03.12.2021
Beginn: 28.01.2022
Tage bis Beginn: 56,0
Dosis: 3
Route/Site: SYR / LA

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

Adverse drug reaction Dizziness Fatigue Nausea Pain in extremity

Symptomtext

The evening of the injection (December 3, 2021) and next day I felt lightheaded, nauseous, fatigued and my left arm hurt. On January 28th, upon taking medication for Chronic Lyme & Bartonella, the left side of my face swelled. My left leg swelled and was very painful. This swelling lasted about 4 days. I have never had that reaction to the Lyme medications before. It's curious that the swelling and pain occurred on the same side as all three of my COVID-19 injections,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Lyme and Bartonella Hypothyroidism
Andere Medikamente: Levothyroxine
Allergien: sulfa and dicloxacillin
Vorherige Impfungen: -

VAERS 2122890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: GA
Alter: 70,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 15.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / LA

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

Mouth ulceration Pyrexia

Symptomtext

After the Booster, I had high fever for 3 days and 2 nights (same thing with the 2nd shot). Then fever went completely away and my mouth was full of ulcers. Was prescribed ACYCLOVIR for 5 days by Teledoc through my Insurance Co. Ulcers lasted longer than the 5 days of the Anti Viral drug.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: no tests - used Teledoc
Aktuelle Erkrankungen: none
Vorgeschichte: Pre-diabetes No medications. Meds for hypothyroidism. Meds for high cholesterol. meds for Meniere's of inner ear.
Andere Medikamente: Levothyroxine, Diazepam, Meloxicam, Rosuvastatin
Allergien: Latex
Vorherige Impfungen: -

VAERS 2122660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Blood glucose Chills Fatigue Glycosylated haemoglobin increased Illness Lymphadenopathy Pyrexia

Symptomtext

fatigue; swollen lymph node under right arm; very sick for two nights; Fever; chills; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 01Nov2021 13:00 (Lot number: FH8030) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Cholesterol", start date: 2015 (unspecified if ongoing), notes: Diet and exercise controlled 17Jun21 - A1C was 6.8 and Glucose mg/DL was 1. Family history included: "DM", start date: 2018 (unspecified if ongoing), notes: Diet and exercise controlled, 6/17/21 - A1C was 6.8 and, Glucose mg/DL was 149; "HBP", start date: 2003 (unspecified if ongoing). Concomitant medication(s) included: COZAAR taken for hypertension, start date: 2012 (ongoing); HCTZ taken for hypertension, start date: 2012 (ongoing); PRAVASTATIN taken for blood cholesterol, start date: 2015 (ongoing). Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0171, Location of injection: Arm Right, Vaccine Administration Time: 13:00 PM, Second dose had slight pain in arm, vaccine was administered, a little feverish that night, took one advil.), administration date: 28Apr2021, when the patient was 54 years old, for COVID-19 immunization, reaction(s): "slight pain in arm", "little feverish"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0151, Location of injection: Arm Right, Vaccine Administration Time: 13:00 PM), administration date: 07Apr2021, when the patient was 54 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 01Nov2021, outcome "recovered" (03Nov2021), described as "Fever"; CHILLS (non-serious) with onset 01Nov2021, outcome "recovering", described as "chills"; FATIGUE (non-serious) with onset 02Nov2021 02:30, outcome "recovering", described as "fatigue"; LYMPHADENOPATHY (non-serious) with onset 02Nov2021 02:30, outcome "recovering", described as "swollen lymph node under right arm"; ILLNESS (non-serious) with onset 02Nov2021 02:30, outcome "recovering", described as "very sick for two nights". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Therapeutic measures were not taken as a result of chills, fatigue, lymphadenopathy. Additional information: It was reported that, facility type reported as Pharmacy or Drug Store. She did not receive any other vaccines within 4 weeks. She had received other medications within 2 weeks. She was not tested covid post vaccination. She had no covid prior vaccination. No known allergies were reported. Vaccine was not administered at Military Facility. Prior vaccinations (within 4 weeks) reported as none. Relevant tests and Specific relevant tests reported as none. Antibody test to platelet factor IV. Family medical history relevant to adverse events: HBP, Stroke/CVA, Cardiac Arrest, Diet controlled DM. After receiving third dose/booster she was very sick for two nights, fever and chills, Monday and Tuesday night. She was in bed all Tuesday with fatigue. Fever subsided by Wednesday morning, that was when she noticed the swelling under her armpit. She thought that it was lymph node. For the fever, she took one Advil (200mg) every 6 hours and did not exceed 3 a day. She emailed her PCP and would keep an eye on the swelling and follow up by weekend or early next week. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20210617; Test Name: Glucose; Test Result: 149 mg/dl; Test Date: 20210617; Test Name: A1C; Result Unstructured Data: Test Result:6.8
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Cholesterol (Diet and exercise controlled 17Jun21 - A1C was 6.8 and Glucose mg/DL was 1); Diabetes mellitus (Diet and exercise controlled 6/17/21 - A1C was 6.8 and Glucose mg/DL was 149)
Andere Medikamente: COZAAR; HCTZ; PRAVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2121131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NC
Alter: 43,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 23.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Burning sensation Joint range of motion decreased Muscle spasms Neuralgia Pain

Symptomtext

Patient came into pharmacy on 2/17/22 stating he wanted to report issues from his first Pfizer covid 19 dose on 11/23/21. Patient originally called to report but they directed him to come to pharmacy store level and they asked patient to get a claim number which he did not have. Patient stated 3 days after receiving 1st Pfizer dose he had burning/stinging pain, deep soreness, pulsating pain, and muscle spasms. Patient stated no issues with 2nd dose of Pfizer which he had administered in right arm.Patient followed up with physician who told him nerve was struck possibly during vaccine administration causing nerve pain. Patient was prescribed muscle relaxers and physical therapy by physician which patient states is still ongoing as of 2/17/22. Patient states left arm where area of vaccination occurred starting to heal with range of motion getting better with physical therapy but they are continuing to work on building strength back in his left arm. Patient stated left arm is his dominant arm and he had no issues with mobility or pain in his left arm prior to getting the vaccine. Patient wanted to report to us but did not state any legal action or requesting compensation or treatment compensation. Patient was thankful he received 2 doses of Covid vaccine prevented him from getting covid during December and at work when it was going around. Patient inquired when he was eligible for a booster vaccine which HCP wrote down date in 5 months from 2nd dose of Pfizer on her business card and gave to patient. Also offered to mail patient gift card for customer loyalty for using our pharmacy for vaccines for customer service.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: asthma, diabetes
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 2116862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: WA
Alter: 42,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 10.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Arthralgia Blood test normal Fatigue Menstruation irregular Pyrexia Rash

Symptomtext

After i got the booster I had extreme fatigue and every joint in my body felt as if was on fire, i had a fever as well, it caused my period to last a few extra days. I had extreme anxiety and it lasted for three to four days. I had skin rashes as well. I saw a doctor and he did some blood work an everything came back normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Blood work. nothing came back
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2108908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 47,0
Geschlecht: U
Eingang: 12.02.2022
Impfdatum: 22.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Rash SARS-CoV-2 antibody test

Symptomtext

Rash; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 47 year-old patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), intramuscular, administered in deltoid left, administration date 22Nov2021 (Lot number: FH8030) at the age of 47 years as dose 2, single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162B2 (Dose 1; Lot number: FF8841; at 17:00 intramuscularly in the left shoulder), administration date: 14Oct2021, when the patient was 47 years old, for COVID-19 immunization, reaction(s): "Splotchy, red, and itchy raised rash under both arms and along side of torso", "Splotchy, red, and itchy raised rash/ rash mainly on right inner thigh near groin, smaller rash on left of inner side groin", "Splotchy, red, and itchy raised rash", "extremely itchy and dry elbows", "extremely itchy and dry elbows/ itchy and red rash on both ankles and up and down both thighs/small itchy rash on back waist", "rash under arm", "rash thighs & calves". The following information was reported: RASH (medically significant), outcome "recovering", described as "Rash". The clinical course was reported as follows: Upon receiving the first dose of the Pfizer COVID-19 vaccination shot, the patient began feeling extremely dry areas on the elbow. The dryness began a few days after my first dose. The dry progressed to a rash. The rash was red with small red bumps. This rash progressed into Nov2021 to areas on flanks on the side of torso as well into my waistline. A few days later, the patient began noticing areas on the back of the ankles and further areas around waistline. The patient began using hydrocortisone uptime on the areas around 03Nov2021/04Nov2021. A few days later, the patient noticed a rash on the right side of the thighs which progressed to the left side down. The symptoms began to subside in late Nov2021/early Dec2021. The patient underwent the following laboratory tests and procedures: sars-cov-2 antibody test: (30Aug2021) positive, notes: 65.6 U/mL.; Sender's Comments: Based on the information currently available, a possible contributory role of the suspect drug in the reported event cannot be completely ruled out 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

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Date: 20210830; Test Name: COVID antibody test; Test Result: Positive ; Comments: 65.6 U/mL
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TN
Alter: 44,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 12.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Biopsy Blood test Urticaria

Symptomtext

Broke out with hives; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 44 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 12Nov2021 16:00 (Lot number: FH8030) at the age of 44 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Seasonal allergy" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Auto-brewery syndrome" (unspecified if ongoing); "COVID-19", start date: 14Aug2021 (not ongoing). The patient took concomitant medications. Past drug history included: Azithromycin, reaction(s): "Drug allergy"; Azithromycin, reaction(s): "Hives". The following information was reported: URTICARIA (medically significant) with onset 14Nov2021 08:00, outcome "not recovered", described as "Broke out with hives". The event "broke out with hives" was evaluated at the physician office visit. Therapeutic measures were taken as a result of urticaria. Additional information: the patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Treatment received for the adverse event included Benadryl injection, steroid injection, steroid tabs.; 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 the reported event URTICARIA 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: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Auto-brewery syndrome; COVID-19; Hypertension; Seasonal allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TN
Alter: 44,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 12.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Biopsy Blood test Urticaria

Symptomtext

Broke out with hives; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 44 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 12Nov2021 16:00 (Lot number: FH8030) at the age of 44 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Seasonal allergy" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Auto-brewery syndrome" (unspecified if ongoing); "COVID-19", start date: 14Aug2021 (not ongoing). The patient took concomitant medications. Past drug history included: Azithromycin, reaction(s): "Drug allergy"; Azithromycin, reaction(s): "Hives". The following information was reported: URTICARIA (medically significant) with onset 14Nov2021 08:00, outcome "not recovered", described as "Broke out with hives". The event "broke out with hives" was evaluated at the physician office visit. Therapeutic measures were taken as a result of urticaria. Additional information: the patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Treatment received for the adverse event included Benadryl injection, steroid injection, steroid tabs.; 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 the reported event URTICARIA 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: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Auto-brewery syndrome; COVID-19; Hypertension; Seasonal allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2099675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: RI
Alter: -
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 11.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: SC / -

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

Allergy test Urticaria

Symptomtext

3 Pfizers, 1/24/21, 2/17/21; booster 11/11/21. Hives began 12/05/21. Saw an allergist after an ER visit on 12/25. Allergist noted increased patient volume with hives within 4-6 weeks of booster. I take a Zyrtec daily to manage the hives. Will monitor-hope this 'hyper response to the booster' will fade with time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Standard allergy panels
Aktuelle Erkrankungen: none
Vorgeschichte: Osteoporosis
Andere Medikamente: Prolia, Multivitamin, Vitamin D, Calcium supplement, cranberry extract.
Allergien: Sulfa, naprosen, birth control pills (caused DVT)
Vorherige Impfungen: -

VAERS 2201211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Decreased appetite Fatigue Headache Night sweats Pain Pain in extremity Pyrexia

Symptomtext

Narrative: Headache, fever, arm pain, body aches, chills, fatigue, loss of appetite, night sweats

Weitere VAERSDATA-Felder

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

VAERS 2091104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 44,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 05.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Asthenia Dizziness Fall Headache Myalgia

Symptomtext

About 1 week after 1st dose started to receive chronic headaches and periods of dizziness to the point of falling over. Once every couple weeks. Muscle and joint soreness. Loss of strength. All of these ailments continue today's date. Has not seen a doctor yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Has not seen a medical provider. Does not have insurance.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Penicillin
Vorherige Impfungen: Pfizer

VAERS 2090385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TX
Alter: 16,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injection site bruising

Symptomtext

Site: Bruising at Injection Site-Mild, Additional Details: Mom does not want to provide any information as Dr is monitoring her health but wants to make sure issue gets resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2206324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 30.11.2021
Beginn: 22.12.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Cough Fatigue Laboratory test Myalgia Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 12/17/20 , Pfizer, dose #1 NON-CLINIC 01/06/2021, Pfizer, dose #2 NON-CLINIC 11/30/2021, Pfizer, dose #3 12/23 COVID swab, result: detected 12/22 pt cc: cough, chills, fatigue, fever, myalgias, rhinorrhea, sore throat exposure: unknown 12/23 SARS-COV-2 Variant Sequencing: pending

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 12/23 COVID swab, result: detected 12/23 SARS-COV-2 Variant Sequencing: pending
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2076177

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: LA
Alter: 34,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Cold sweat Dizziness Fatigue Pyrexia

Symptomtext

High fever for 2 days- 102.5-103. Treated with Tylenol 1000 mg every 4 hours and Aleve 440mg every 6 hours alternating doses. I was unable to care for my baby the day after. I was having to feed her while laying on the floor. I would get up to give her bite due to dizziness and high fevers. I was having cold sweats, dizziness, and unbelievable exhaustion. This lasting 48 hours. After 48 hours I had a low grade temp for a week which was bearable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: ADHD
Andere Medikamente: Adderall
Allergien: none
Vorherige Impfungen: -

VAERS 2075478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TN
Alter: 60,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 02.04.2021
Beginn: 16.01.2022
Tage bis Beginn: 289,0
Dosis: 3
Route/Site: IM / UN

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

Headache Nausea Productive cough Rhinorrhoea

Symptomtext

Patient presented with history of 9 day worsening symptoms. Patient experienced productive cough, headache, runny nose, and nausea. Patient required up to 5L of nasal cannula. Patient received dexamethasone 6 mg IV once.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: renal insufficiency pre-diabetes hypertension hyperlipidemia
Andere Medikamente: None listed
Allergien: penicillins
Vorherige Impfungen: -

VAERS 2068560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: SD
Alter: 37,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Disturbance in attention Dizziness Feeling drunk

Symptomtext

About 30 minutes after the booster shot (i had the first 2 shots with no side effects) I got very dizzy, couldn't concentrate. It felt like i had been drinking, I had not had anything to drink before or after the shot other than water. It lasted for about 3 hours and then went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Centrum multi vitamin.
Allergien: None.
Vorherige Impfungen: -

VAERS 2065822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NJ
Alter: 62,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 01.04.2021
Beginn: 01.07.2021
Tage bis Beginn: 91,0
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Botulinum toxin injection Computerised tomogram normal Headache Magnetic resonance imaging head normal Magnetic resonance imaging neck

Symptomtext

3 months after my 2nd vaccine I started getting headaches. They were just in the front and temples at 1st but soon became ALL over my head, including the back where your head hits the pillow. They got more and more intense. They got even worse after my booster shot, serious every day non-stop pain. I went to every type of doctor to determine the cause: ENT, Allergist, Cardiologist, Dentist, Oral Surgeon, PCP, Orthopedist, Neurologist. I had blood work for everything, also a head Cat scan, neck and brain MRI?s and nothing was found. I was given migraine injections which did nothing for the pain, I was taken off some medications which, again, did nothing for the pain even after being off them 60 days and longer. Finally, I was given Botox injections all over my head and neck which almost completely removed the headaches for 30 days, but I still had pain in the back of the head where your head hits the pillow. I?ve NEVER had headaches like this before. No one could can them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Cat Scan on head neck and head MRI several blood tests to check hormones, vitamin levels, serotonin levels
Aktuelle Erkrankungen: None
Vorgeschichte: Pulmonary Fibrosis, High blood pressure, high triglycerides
Andere Medikamente: Singular, Topamax, Trilipix, Atenenol, Klonopin, Zoloft, Pravastatin, Protonix, Lipitor, Lovaza
Allergien: None
Vorherige Impfungen: -

VAERS 2065284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: 72,0
Geschlecht: U
Eingang: 25.01.2022
Impfdatum: 20.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: - / LA

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

Erythema of eyelid Eye infection Eyelids pruritus Gastrointestinal disorder Gastrointestinal pain

Symptomtext

Sensitivity of the lower GI tract. I can't eat any tomatoes or tomato sauce, just like the last time I had the 2nd Pfizer shot. I have Lower GI cramps and also my eyelids turned really red & itchy. I got an eye infection after that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eyelids pruritus
Hospital-Tage: -
Labordaten: I went to opthamologist. prescribed eye antibiotic 1/12/2022
Aktuelle Erkrankungen: herpes 2 outbreak MID OCT-NOV
Vorgeschichte: diverticulosis,herpes 2, asthma, osteoarthritis
Andere Medikamente: Levothyroxine azelastine nasal spray, fluticasone 88 estradiol patch 0.375; valacyclovir 500 mg Liothyronine .5 mcg, once perday Buspirone 15 mg at bedtime albuterol inhaler, 2 puffs once per day and PRN. Vitamins: C 1000, B-50 complex, B-
Allergien: naproxen, penicillin, aspirin, Motrin, tylenol, demerol, xanax, valium
Vorherige Impfungen: -

VAERS 2063871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 03.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: SYR / RA

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

Abdominal discomfort Herpes zoster Hypoaesthesia Neuralgia Rash

Symptomtext

Shingles, rash, nerve pain, numbness and digestive upset. Started on 12/26/2021. Diagnosed by doctor on 12/29/2021. Symptoms still lingering to present date.

Weitere VAERSDATA-Felder

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

VAERS 2061856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Arthralgia Blood test Electroencephalogram Fatigue Gait disturbance Illness Immunisation Inflammation Limb injury Lymphadenopathy Musculoskeletal stiffness Nasopharyngitis Pain in jaw Paranasal sinus discomfort Pharyngeal swelling SARS-CoV-2 test

Symptomtext

the booster shot; legs are stiff and can't walk this morning; Inflammation/my legs feel like they are highly inflamed and its hard to me bend my knee; legs are stiff and can't walk this morning/legs are now starting to get a lot more stiff/mass inflammation effect and that include the fact my hands are very arthritic you know they are stiff; Fatigue/Tiredness; have been pretty sick; Classic cold symptoms; Sinus pressure; My glands were swollen, my throat was swollen; My glands were swollen, my throat was swollen; Pain in my joint of my jaw; Mass inflammation effect and that include the fact my hands are very arthritic you know they are stiff; Injured my shoulder; My glands were swollen, my throat was swollen; My glands were swollen, my throat was swollen; This is a spontaneous report received from a contactable Consumer or other non HCP from medical information team. The reporter is the patient. A 63 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 29Nov2021 16:20 (Lot number: FH8030) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), administration date 13Oct2021 (Batch/Lot number: unknown) as dose number unknown, single for immunisation; botulinum toxin type a (BOTOX) (Batch/Lot number: unknown). Relevant medical history included: "back and shoulder issues" (unspecified if ongoing), notes: verbatim: back and shoulder issues; "back and shoulder issues" (unspecified if ongoing), notes: verbatim: back and shoulder issues; "anti-inflammatory" (unspecified if ongoing). Concomitant medication(s) included: CARMEN [CARBOPLATIN] taken for inflammation; DHEA; DANDELION taken for liver disorder. Vaccination history included: Covid-19 vaccine (Dose number: 1, MANUFACTURER UNKNOWN), for COVID-19 immunization; Covid-19 vaccine (Dose number: 2, MANUFACTURER UNKNOWN), for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 29Nov2021, outcome "unknown", described as "the booster shot"; GAIT DISTURBANCE (non-serious) with onset 2021, outcome "unknown", described as "legs are stiff and can't walk this morning"; INFLAMMATION (non-serious) with onset 2021, outcome "unknown", described as "Inflammation/my legs feel like they are highly inflamed and its hard to me bend my knee"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 2021, outcome "unknown", described as "legs are stiff and can't walk this morning/legs are now starting to get a lot more stiff/mass inflammation effect and that include the fact my hands are very arthritic you know they are stiff"; FATIGUE (non-serious) with onset 2021, outcome "unknown", described as "Fatigue/Tiredness"; ILLNESS (non-serious) with onset 2021, outcome "unknown", described as "have been pretty sick"; NASOPHARYNGITIS (non-serious) with onset 2021, outcome "unknown", described as "Classic cold symptoms"; PARANASAL SINUS DISCOMFORT (non-serious) with onset 2021, outcome "unknown", described as "Sinus pressure"; LYMPHADENOPATHY (non-serious), PHARYNGEAL SWELLING (non-serious), LYMPHADENOPATHY (non-serious), PHARYNGEAL SWELLING (non-serious) all with onset 2021, outcome "unknown" and all described as "My glands were swollen, my throat was swollen"; PAIN IN JAW (non-serious) with onset 2021, outcome "unknown", described as "Pain in my joint of my jaw"; ARTHRALGIA (non-serious) with onset 2021, outcome "unknown", described as "Mass inflammation effect and that include the fact my hands are very arthritic you know they are stiff"; LIMB INJURY (non-serious) with onset 2021, outcome "unknown", described as "Injured my shoulder". The events "legs are stiff and can't walk this morning", "inflammation/my legs feel like they are highly inflamed and its hard to me bend my knee", "legs are stiff and can't walk this morning/legs are now starting to get a lot more stiff/mass inflammation effect and that include the fact my hands are very arthritic you know they are stiff", "fatigue/tiredness", "have been pretty sick", "classic cold symptoms", "sinus pressure", "my glands were swollen, my throat was swollen", "my glands were swollen, my throat was swollen", "pain in my joint of my jaw", "mass inflammation effect and that include the fact my hands are very arthritic you know they are stiff", "injured my shoulder", "my glands were swollen, my throat was swollen" and "my glands were swollen, my throat was swollen" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. The action taken for botulinum toxin type a was unknown. Therapeutic measures were taken as a result of gait disturbance, inflammation, musculoskeletal stiffness, fatigue, illness, nasopharyngitis, paranasal sinus discomfort, lymphadenopathy, pharyngeal swelling, pain in jaw, arthralgia, limb injury, lymphadenopathy, pharyngeal swelling. Additional information: She went to the ER last night 06Jan2022. She had blood work done which was normal. She has done 2 COVID PCR tests which were both negative. Its the Ibuprofen, she has been using heat pads she has been using ice packs that's pretty much it and then the sleeping pills just because she can normally get 3 or 4 hours of sleep every night and the Arnicre which is the topical anti-inflammatory. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: blood work; Result Unstructured Data: Test Result:Normal; Test Name: EEG; Result Unstructured Data: Test Result:perfect; Test Name: COVID PCR test; Test Result: Negative; Test Name: COVID PCR test; Test Result: Negative.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back disorder (verbatim: back and shoulder issues); Inflammation; Shoulder discomfort (verbatim: back and shoulder issues.)
Andere Medikamente: CARMEN [CARBOPLATIN]; DHEA; DANDELION.
Allergien: -
Vorherige Impfungen: -

VAERS 2056980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: LA
Alter: 42,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Axillary pain Immunisation Lymphadenopathy

Symptomtext

swelling in arm pit/Swollen lymph nodes; noticed irritation and soreness under his arm which he thought it was like the vaccine was radiating under his arm; booster; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 42 year-old male patient received bnt162b2 (BNT162B2), administration date 29Dec2021 (Lot number: FH8030) at the age of 42 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (first dose , LOT: EL0142, first dose injected in his arm), administration date: 08Jan2021, when the patient was 41 years old, for COVID-19 immunization; Bnt162b2 (second dose , LOT: EL9265), administration date: 28Jan2021, when the patient was 41 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 29Dec2021, outcome "unknown", described as "booster"; LYMPHADENOPATHY (non-serious) with onset 30Dec2021, outcome "not recovered", described as "swelling in arm pit/Swollen lymph nodes"; AXILLARY PAIN (non-serious) with onset 30Dec2021, outcome "unknown", described as "noticed irritation and soreness under his arm which he thought it was like the vaccine was radiating under his arm". Therapeutic measures were not taken as a result of lymphadenopathy. Additional information: Patient reported this morning he woke up and showered and noticed pretty significant swelling under his arm pit. He says he had done no treatment other than stretching his arm, it was swollen lymph nodes. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2218738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Rash pruritic

Symptomtext

PRURITIC RASH Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2050894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

mild

Staat: PA
Alter: 52,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 13.11.2021
Beginn: 20.12.2021
Tage bis Beginn: 37,0
Dosis: 1
Route/Site: SC / LA

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

Pruritus Rash Scab Skin weeping Urticaria

Symptomtext

Approximately 30 days after vaccine, left arm itchy and hives. By January, 12inch rash on arm that oozes in elbow crease and crusty.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: High cholesterol, genetic; anemia
Andere Medikamente: Praulent 150mg, trazadone, lexapro, co-enzyme 10, vitamin d, biotin, calcium, l-lysine, baby asa, resveratrol, Mg, b12
Allergien: PCN, sulfa drugs, latex, wheat, iodine,
Vorherige Impfungen: -

VAERS 2047474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: OK
Alter: 49,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 22.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

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

Pruritus Swelling Urticaria

Symptomtext

Hives and terrible itching and swelling

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Testosterone Anastrazole NP THYROID 120mg Anusol 2.5 Bayer low dose aspirin Nasocort Claritin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2039515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MS
Alter: 35,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 09.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

Widespread hives that began 12/27/21 with one patch on my right hip. Has spread to left hip, right thigh, both butt cheeks, both lower legs and chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal multivitamin Vitamin D3 Zyrtec 10mg Norethindrone 0.35
Allergien: Adhesive bandages, neosporin
Vorherige Impfungen: -

VAERS 2037851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: IN
Alter: 60,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Back pain Chills Fatigue Myalgia Pyrexia

Symptomtext

Fever; chills; muscle, back and joint pain; fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A. None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Prilosec 20mg QD Levothyroxine 50 mg QD Liothronine 10 mg QD Aller tec 10mg QD Vitamin D 1000 IU QD
Allergien: Penicillin, sulfa, keflex, tree nuts, soybean, sunflower, sesame seeds, peanuts, legumes
Vorherige Impfungen: Moderna COVID-19 vaccine on 12/30/2020 and 1/27/2021

VAERS 2030773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8030

mild

Staat: OR
Alter: 43,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 10.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Axillary pain Breast tenderness Lymphadenopathy

Symptomtext

Breast/armpit tenderness, lymph node swelling moderate side effect 5 out of ten.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Allegra, magnesium
Allergien: Dust, penicillin, tomatoes, cucumbers
Vorherige Impfungen: Similar adverse event with my second covid vaccine at the same site. This time is worse.

VAERS 2029030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MO
Alter: 46,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Injection site pain Myalgia Pyrexia

Symptomtext

Soreness at injection site and fever of 99.8?f. As well as muscle aches and fatigue.

Weitere VAERSDATA-Felder

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

VAERS 2028719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: ID
Alter: 53,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Dermatitis allergic Feeling abnormal Peripheral coldness Rash Rash pruritic Urticaria

Symptomtext

I received my Pfizer COVID-19 booster vaccine (Pfizer FH8030) on Dec 6th 2021 at Primary Health facility and my rashes/hives began to occur that evening; approximately 6 hours after receiving the shot. These first began in the lower portion of my back. They are raised bumps and seem big. Sometimes, I would get many of these bumps in cluster forms and these clusters tend to become very problematic since they don't seem to heal. More of these bumps tend to raise up in the clusters continuing to make them larger and harder over time. However, I also get several bumps that would seem to rise up in certain areas at a time. Such as getting several on the back of my neck, then on my upper legs, then, my lower arms, etc. Throughout this time, the old ones didn't go away so as new ones kept coming, there was not any area of my body that didn't end up with these rash/hive like large raised bumps. They itch a lot, especially when some were about to break through the skin, which would often occur each evening. When I would run my finger over the newly affected area, it would sting. One week after receiving my booster, I went into Primary Health facility to have them looked at my skin condition. Since I also had this experience after I received my second portion of the vaccine earlier in the year (I will also explain that), the doctor agreed that it seemed that it was the vaccine that triggered this allergic response. He checked me for any signs of anaphylaxis, and everything seemed fine at that time. He provided me with a prescription of Prednisone 20mg tablets on a taper (60mg for 3 days, 40mg for 3 days, and 20mg for 4 days). The Prednisone made the condition reside, so I had hopes this was enough to clear it all out. However, after I was done with the treatment on Dec 23rd 2021, the rash/hive bumps all rose back up and began to spread again. At this time, I decided to go see my dermatologist, but since it was now the holidays, I couldn't get in for another week. On Jan 6th 2022, I was able to see my dermatologist who after examination, provided me with a 6 week taper shot of Kenalog (Triamcinolone). This treatment was what finally resolved this allergy skin reaction last time, so I have hopes it clears it out this time. Previous reaction: My previous experience with this allergic skin reaction began 3-4 days after I had received the second dose of the Pfizer COVID-19 vaccine (Pfizer EL9266) on Feb 23, 2021. My first dose of the Pfizer COVID-19 vaccine (Pfizer EL9269) was received on Feb 2, 2021. The only reaction I had to the first dose was that my left arm was freezing cold for nearly 30 minutes after the dose. So, I was monitored by a Dr. there until my arm warmed up. Both doses were received at Primary Health facility. The above description is very similar to this earlier experience. The main difference is the timing of treatments and the lack of connecting the rash/hives to the vaccine. I have never had any allergic reaction to any medications or foods before, so personally, I didn't make the connection. When I finally wondered about a connection, the doctors I spoke with didn't think it was connected, so we brainstormed other different things I may have been using that week that may have triggered the rash/hives. At that time we all decided that Tea Tree Oil must be it, since I began to use it one day before the rashes began. Therefore, I never mentioned it in these check ins. However, the rashes did not subside when I stopped using the Tea Tree Oil after the one day. But, I figured they would clear up on their own. It was 3 weeks later after my body had become covered by these rash/hives and I had a rash cluster covering nearly the entire lower portion of my right arm and hand (even though I had all my vaccines in my left arm). I was miserable and could feel my body fighting hard against this allergic response. At this 3 week point of having the relief, went in to the Primary Health facility to have them looked at my skin condition. At this time, they placed me on a PredniSONE taper (These were 10mg tablets, so the taper was something like: 40mg for 3 days, 30mg for 3 days, 20mg for 3days, 10mg 1 days). At the end of this treatment (last day of treatment: Apr 11, 2021), my rashes had slowed, but not subsided. I was also referred to Dermatology Center where I was seen on Apr 8, 2021, who prescribed a 0.1% Triamcinolone Acetonide ointment. He was certain that the rashes would clear up and had no connection to the vaccines. A week after completing the PredniSONE, the rashes/hives began to spread intensely again, so I went back to the Dermatology Center on Apr 20, 2021 where they then prescribed me with a 6 week taper shot of Kenalog (Triamcinolone), as well as 0.05% Clobetasol Propionate solution to be mixed in with CeraVe skin cream. This treatment was what finally resolved this allergy skin reaction. This entire first experience with the rash/hive allergic reaction lasted a total of 3 months and was quite miserable. I also want to mention that I was not utilizing anything different during my second rash outbreak on Dec 6th 2021, so the only thing I could correlate to the allergic reaction was the vaccine. I apologize for the length of this description, but I want to be sure all the facts that pertain to this (that I can recall or collect) are included.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Other than above mentioned ones, I am working with my Dermatologist to arrange tests to verify allergic reactions.
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-hypertension
Andere Medikamente: Multi-vitamins, Ginger root, Black Cohosh
Allergien: No other experiences other than the Pfizer COVID-19 Vaccine.
Vorherige Impfungen: -

VAERS 2028355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 12.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 52,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Cough Fatigue Myalgia Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

fatigue, congestion, sore throat, cough, myalgias + COVID test

Weitere VAERSDATA-Felder

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

VAERS 2028349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 12.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 52,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

congestion, sore throat + COVID test

Weitere VAERSDATA-Felder

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

VAERS 2027375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: -
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Body temperature Chills Hypersensitivity Overdose Pain in extremity Poor quality product administered Product preparation error Pyrexia

Symptomtext

Allergic Reaction; received possibly the whole undiluted vial of the vaccine / was possibly 90 - 120 mcg of vaccine given to the patient; Please provide the stage of medication error (e.g., prescribing, dispensing, preparation, and administration): preparpation and administration; received possibly the whole undiluted vial of the vaccine / was possibly 90 - 120 mcg of vaccine given to the patient; mild fever; chills; sore arm; This is a spontaneous report received from contactable reporter(s) (Physician) from medical information team. A 58 year-old female patient received bnt162b2 (COMIRNATY), intramuscular, administered in arm left, administration date 16Nov2021 (Lot number: FH8030) as dose 2, single for covid-19 immunisation. Relevant medical history included hypertension (ongoing); osteoarthritis (ongoing); prediabetes (ongoing); Allergic reactions (ongoing); hypercholesterolemia (ongoing); High cholesterol (unspecified if ongoing); Allergy symptoms (unspecified if ongoing). Concomitant medication(s) included ATORVASTATIN taken for blood cholesterol increased (ongoing); ALLEGRA taken for hypersensitivity (ongoing); HYDROCHLOROTHIAZIDE taken for hypertension (ongoing). Vaccination history included Bnt162b2 (Dose:01, Batch/Lot# 301558A, Time: 13:00, Site and Route of injection, Anatomical Site of injection: Left upper arm, Route of administration: Intramuscular, Batch/Lot number: 301558A / PAA173398), administration date 19Oct2021, when the patient was 58 years old, for COVID-19 Immunization, reaction(s) mild fever, chills. The following information was reported OVERDOSE (non-serious), PRODUCT PREPARATION ERROR (non-serious) all with onset 16Nov2021, outcome unknown; POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 16Nov2021, outcome unknown; PYREXIA (non-serious) with onset 16Nov2021, outcome recovered (2021); CHILLS (non-serious) with onset 16Nov2021, outcome recovered (2021); PAIN IN EXTREMITY (non-serious) with onset 16Nov2021, outcome recovered (2021); HYPERSENSITIVITY (non-serious) with onset 16Nov2021 21:00, outcome recovered (2021). Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of hypersensitivity. Phone out 3:40 pm ? Reporter provided an update that the patient is still OK and doing fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result: Unknown results; Test Name: Fever; Result Unstructured Data: Test Result: Unknown results.
Aktuelle Erkrankungen: Allergic reaction; Hypercholesterolemia; Hypertension; Osteoarthritis; Prediabetes
Vorgeschichte: Allergy; High cholesterol
Andere Medikamente: ATORVASTATIN; ALLEGRA; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2555412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Feeling abnormal Myalgia

Symptomtext

Myalgia Brain fog Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2517641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Headache Injection site pain Pyrexia

Symptomtext

Headache, Fever, Chills, Injection site soreness Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2516630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Fatigue Headache Injection site pain Myalgia Pyrexia Rash

Symptomtext

Confusion, Headache, Myalgia, Fever, SkinRash, Rash, FATIGUE, INJECTION SITE PAIN Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2516628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue

Symptomtext

FATIGUE Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2025538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 31.12.2021
Beginn: 08.01.2022
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Bursitis Compression garment application Joint swelling Myalgia Pain Pain in extremity

Symptomtext

Sore arm muscle and pain when reaching high. Vaccine induced bursitis of both elbows with pain and swelling. Using ibuprofen and ice packs along with compression sleeves until symptoms resolve. Have called to inform my MD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: No tests nor results as yet.
Aktuelle Erkrankungen: Herpes
Vorgeschichte: Herpes
Andere Medikamente: None
Allergien: Opioids
Vorherige Impfungen: -

VAERS 2658677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 14.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Injection site pain Myalgia

Symptomtext

Myalgia Fatigue, injection site soreness Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2554328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Headache Myalgia Nausea Vomiting

Symptomtext

Headache, Myalgia & NauseaVomiting Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2552207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Decreased appetite Diarrhoea Headache Pain in extremity Rhinorrhoea

Symptomtext

Headache, Diarrhea, Sore arm, runny nose, and no apetite Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2517691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Lymphadenopathy Pyrexia

Symptomtext

Arthralgia, Fever, Swollen lymph node Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2517685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cough Fatigue Headache Injection site pain Myalgia Oropharyngeal pain Pyrexia Wheezing

Symptomtext

Headache, Myalgia, Fever, CoughWheeze, Fatigue, injection site soreness, sore throat Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2020847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: KS
Alter: 52,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 15.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Back pain Influenza like illness Injection site pain Lymph node pain Lymphadenopathy Mammogram Neck pain Pyrexia Ultrasound breast

Symptomtext

I experienced severe pain at the injection site, which was different than previous vaccines. That started approximately 12 hours following injection. I also experienced low-grade fever and mild flu like symptoms 24 hours following injection. I awoke 36 hours after my injection with severe pain in my left arm pit and breast as well as worsening pain in my left arm at the injection site. I also had pain on the left side of my neck and back. The lymph nodes in my left armpit and breast were enlarged and painful for 8 days following the booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: No tests. Breast ultrasound and mammogram to confirm that it was just enlarged lymph nodes.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Celexa, Vitamin D3, Topomax
Allergien: NKA
Vorherige Impfungen: -

VAERS 2018863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NJ
Alter: 56,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 26.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Body temperature Bone pain Chills Illness Immunisation Injection site pain Pain Pyrexia

Symptomtext

Booster; Booster dose/third dose: got really, really sick; Booster dose/third dose: severe chills; Booster dose/third dose: fever; Booster dose/third dose: severe body aches; Booster dose/third dose: her bones hurt like in her thighs; Booster dose/third dose: Where the injection was administered in her right arm shoulder was very sore; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 56 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 26Nov2021 13:00 (Lot number: FH8030) at the age of 56 years as dose 3 (booster), 0.3 ml single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE: 1, Lot: ER8731, NDC: Unknown, not on the CDC vaccine record card., Expiry: 31Jul2021, Lot/Expiry information was on sticker on the CDC vaccine record card., Dose: 0.3mL injection to right arm shoulder, Administered at a mega site.), administration date: 23Apr2021, when the patient was 55 years old, for COVID-19 immunization, reaction(s): "First dose: some mild soreness in right arm shoulder"; Bnt162b2 (DOSE: 2, Second dose: Date administered: 14May2021, Lot: EW0173, NDC: Unknown, not on the CDC vaccine record card., Expiry: 31Aug2021, Lot/Expiry information was on sticker on the CDC vaccine record card., Dose: 0.3mL injection to right arm shoulder, Administered at a mega site., mega site that was run., When went to mega site 0.3mL for first and second vaccine), administration date: 14May2021, when the patient was 55 years old, for COVID-19 immunization, reaction(s): "Second dose: some soreness in the right arm shoulder."; Bnt162b2 (DOSE: 2), administration date: 14May2021, when the patient was 55 years old, for Covid-19 immunization, reaction(s): "Second dose: body aches". The following information was reported: IMMUNISATION (non-serious) with onset 26Nov2021 13:00, outcome "unknown", described as "Booster"; ILLNESS (non-serious) with onset 26Nov2021, outcome "recovered" (30Nov2021), described as "Booster dose/third dose: got really, really sick"; CHILLS (non-serious) with onset 26Nov2021, outcome "recovered" (30Nov2021), described as "Booster dose/third dose: severe chills"; PYREXIA (non-serious) with onset 26Nov2021, outcome "recovered" (30Nov2021), described as "Booster dose/third dose: fever"; PAIN (non-serious) with onset 26Nov2021, outcome "recovered" (30Nov2021), described as "Booster dose/third dose: severe body aches"; BONE PAIN (non-serious) with onset 26Nov2021, outcome "recovered" (30Nov2021), described as "Booster dose/third dose: her bones hurt like in her thighs"; INJECTION SITE PAIN (non-serious) with onset Nov2021, outcome "recovered" (2021), described as "Booster dose/third dose: Where the injection was administered in her right arm shoulder was very sore". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of illness, chills, pyrexia. Additional information: Dosage text: Unknown strength/volume/dose injection to right arm shoulder at time of appointment: 13:00. Dates for First dose: some mild soreness in right arm shoulder: (From: 24Apr2021 To: 25Apr2021). Dates for Second dose: some soreness in the right arm shoulder.: (From: 15 May 2021 To: 16May2021). Dates for Second dose: body aches: (From: 15May2021 To: 16May2021).Additional Context: This consumer is the patient who called regarding the booster dose of Pfizer Covid-19 Vaccine she was administered. She got really, really sick for 4 days so she just wanted to get some feedback. She did call her doctor when it happened. Now its like, she believes in vaccinations, but she is really super afraid to get a booster again. She wouldn't say she had adverse reaction, it falls over into side effects categories. She is fine now, recovered completely from all events, but she is very nervous about getting any additional booster doses of the Pfizer Covid-19 Vaccine and wanted some feedback from Pfizer about these events and future booster doses of the Pfizer Covid-19 Vaccine. Reporter: Address/Fax/Email: Unknown. Caller mentioned being in (withheld) state, but did not verify this as part of her address. After being administered the booster dose of Pfizer Covid-19 Vaccine caller reported: Onset dates 26Nov2021, onset times unknown: got really, really sick; severe chills like she has never had in her life, she felt like she was almost convulsing, could not keep her body still. She took Advil which seemed to calm it down a bit. Even though she was on Advil and Tylenol for 4 days she had a fever of 101 degrees Fahrenheit while on those medications. She also had severe body aches and like her bones hurt like in her thighs. Onset date: Unknown if 26Nov2021 or 27Nov2021. Onset time unknown. Where the injection was administered in her right arm shoulder was very sore- she would say event lasted for a full week until unknown date in 2021 and she recovered completely; this event with the arm was expected, that was the least of her worries. After being administered the first dose of Pfizer Covid-19 Vaccine caller reported: Onset date of 24Apr2021 at unknown onset time: some mild soreness in right arm shoulder, which was nothing to worry about. She recovered completely by 25Apr2021. After being administered the second dose of Pfizer Covid-19 Vaccine caller reported: Onset date of 15May2021 at unknown onset time: some soreness in the right arm shoulder. Onset date of 15May2021, onset time: unknown other than a full 12 hours after administration of second dose of Pfizer Covid-19 Vaccine: body aches which were not severe. She took 1 Advil for these events and the Advil cured her, she was back to normal, over the body aches; She recovered completely from these events by 16May2021. Thats why she felt really positive about getting the booster dose later. Pfizer Covid-19 Vaccine: Caller initially reported product name as the Booster; then clarified the Pfizer Booster, then clarified as Pfizer for Booster Covid-19 Vaccine; finally clarified as Pfizer Covid-19 Vaccine, with her primary report purpose regarding the booster dose of the Pfizer Covid-19 Vaccine. Regarding testing/treatment/medical interventions caller reported the only other relevant information was that she had a telemed appointment with her doctor because she did not feel well enough to go to his office relative to the events experienced with the booster dose of the Pfizer Covid-19 Vaccine. Tylenol: Strength: 500mg each Lot: ALA071 Expiry: Jul2023 NDC: Unknown, did not find this information on packaging. UPC: 300450488282 While looking for the Advil Liquigels Lot/NDC/UPC/Expiry caller reported that the print is so small, wanted to see if she still had the cardboard box which might be bigger, but she did not have the box; might have to get the old magnifying glass: then provided as: Advil Liquigels: Strength: 200mg each Lot: R75211 Expiry: Sep2022 UPC/NDC: Unknown, caller did not see this information on the bottle, and did not have outer packaging/cardboard box any longer. It says Distributed by Pfizer (name withheld), (state withheld)- she did not realize Pfizer made Advil. No emergency Room visit. Physician Office Telemed visit only with events Booster dose/third dose: got really, really sick; Booster dose/third dose: severe chills; Booster dose/third dose: fever; Booster dose/third dose: severe body aches; Booster dose/third dose: her bones hurt like in her thighs; Booster dose/third dose: Where the injection was administered in her right arm shoulder was very sore. Not hospitalized. No prior vaccinations (within 4 weeks). She had never even had a flu shot and never had any adverse events following prior immunizations. No underlying health issues, she was a relatively healthy person. No family medical history relevant to ae. No relevant tests. Reporter mentioned her family and friends all got the Pfizer booster and did relatively well so thats why she herself was really shocked at how sick she got. She has concerns about getting any future booster doses of Pfizer Covid-19 Vaccine. Her doctor had a suggestion about maybe getting antibody test first before the next booster. Caller did not want to report further information regarding her family and friends that all got the Pfizer booster: lots/ndcs/expiries: not provided, caller did not want to report further information. Is there a Product Complaint: Yes Description of Product Complaint: Consumer was the patient reporting adverse events with Pfizer Covid-19 Vaccine. During that report caller mentioned treatment of those events where she mentioned: Even though she was on Advil and Tylenol for 4 days she had a fever of 101 degrees Fahrenheit while on those medications. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101886117 similar report from same reporter;US-PFIZER INC-202101886121 similar report from same reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result:101 Fahrenheit; Comments: he had a fever of 101 degrees Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: TX
Alter: 36,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Interchange of vaccine products Lymphadenopathy Movement disorder Off label use Pain

Symptomtext

Severe swollen lymph node in armpit; Dose 1: Moderna; Dose 2: Moderna; Dose 1: Moderna; Dose 2: Moderna; hindered my movement; hurt badly; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 36-year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection), administered in arm left, administration date 07Dec2021 (Lot number: FH8030) at the age of 36 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Endometriosis" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: 013M20A, Location of injection: Arm Left), administration date: 03Feb2021, when the patient was 35 years old, for COVID-19 immunization; Moderna (Dose Number: 1, Batch/Lot No: 027120A, Location of injection: Arm Left), administration date: 06Jan2021, when the patient was 35 years old, for COVID-19 immunization. The following information was reported: LYMPHADENOPATHY (non-serious) with onset 08Dec2021, outcome "recovered" (Dec2021), described as "Severe swollen lymph node in armpit"; OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 08Dec2021, outcome "recovered" (Dec2021) and all described as "Dose 1: Moderna; Dose 2: Moderna"; MOVEMENT DISORDER (non-serious) with onset 08Dec2021, outcome "recovered" (Dec2021), described as "hindered my movement"; PAIN (non-serious) with onset 08Dec2021, outcome "recovered" (Dec2021), described as "hurt badly". Therapeutic measures were not taken as a result of lymphadenopathy, off label use, interchange of vaccine products, movement disorder, pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Endometriosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 20.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Body temperature Clostridial infection Culture stool Diarrhoea Immunisation Insomnia Neck pain Pain in extremity Pyrexia Vomiting Weight decreased

Symptomtext

stated that she could not sleep; Vomiting/ Vomiting was reported as worsened; Diarrhea; Patient received third dose of vaccine; neck sore; left arm sore; stated that her weight has went down; clostridium; low grade fever; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 84 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 20Nov2021 16:30 (Lot number: FH8030) at the age of 83 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Clostridium difficle", start date: 08Oct2021 (ongoing). Concomitant medication(s) included: LISINOPRIL; VANCOMYCIN taken for infection (ongoing). Vaccination history included: Bnt162b2 (Dose Number:01, Lot number:EN6198), administration date: 04Mar2021, when the patient was 83 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number:02, Lot number:EN6208), administration date: 25Mar2021, when the patient was 83 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (medically significant) with onset 20Nov2021, outcome "unknown", described as "Patient received third dose of vaccine"; CLOSTRIDIAL INFECTION (medically significant) with onset Nov2021, outcome "not recovered", described as "clostridium"; NECK PAIN (non-serious) with onset 20Nov2021, outcome "recovered" (21Nov2021), described as "neck sore"; WEIGHT DECREASED (non-serious) with onset Nov2021, outcome "unknown", described as "stated that her weight has went down"; INSOMNIA (non-serious) with onset 21Nov2021, outcome "recovered" (2021), described as "stated that she could not sleep"; PYREXIA (non-serious) with onset Nov2021, outcome "unknown", described as "low grade fever"; PAIN IN EXTREMITY (non-serious) with onset 20Nov2021, outcome "recovered" (2021), described as "left arm sore"; VOMITING (non-serious) with onset 21Nov2021, outcome "recovered" (2021), described as "Vomiting/ Vomiting was reported as worsened"; DIARRHOEA (non-serious) with onset 21Nov2021, outcome "recovered" (2021), described as "Diarrhea". The patient underwent the following laboratory tests and procedures: body temperature: (Nov2021) low grade fever; culture stool: (14Oct2021) clostridium. Therapeutic measures were not taken as a result of neck pain, insomnia, pain in extremity, vomiting, diarrhoea. The reporter stated that she was fine and went for her Covid booster on Saturday around 4:30pm. Stated that she did shopping, had something to eat, went to bed and at 2:30am woke up. Her arm and neck were sore like someone was pushing on her chest. Stated that she came down with a very bad case of diarrhoea. On Sunday morning she could not sleep. She woke up on 2:30 Sunday morning and had to stay awake until 5:30 and tried to go to sleep again. All day was bad, she had diarrhoea and was wiped out. All she wanted to do was go to bed. Stated that Sunday and this morning she had to go to the bathroom and had diarrhoea and vomiting. She had to put some food down and it came up. In morning the diarrhoea seems to be letting up. She went to the bathroom at 6:45 and 7:30 and she had not gone in the past 1.5 hours with no diarrhoea or vomiting. She cannot hold any food on her stomach, her weight has gone down. Wanted to know if this was a side effect from this. Event details was stated that her arm was sore under it about 3 hours after the shot, it was sore if one touches it, her neck was no longer this morning when she woke up. She could not sleep from off and on going to the bathroom, she tried to have a little coffee and it came up. There was no treatment. Patient experienced left and neck arm soreness, diarrhoea, vomiting and could not sleep. Patient wants to know if these are normal side effects from the vaccination. Patient stated that when she eats something, it usually comes out after the meal. The patient added that last night she just had a potato. She tried to eat something, whatever she put in there it all come out. Patient received her vaccination on Saturday at 4:30 or 4:45PM, everything started at 2:30AM in the morning. At first, there was no vomiting, later on the second day in the afternoon and in morning, she experienced vomiting. The reporter added that, she only took her medications yesterday for thyroid and Lisinopril after finishing throwing up, she was still down. Patient stated that it was terrible yesterday. Patient mentioned that she still has diarrhoea and was not able to eat. The patient afraid she had lost weight just over 2 days. Patient asked recommendations on what to do, if these were normal side effects. patient stated that her husband went with her, and he was fine. The reporter cannot remember being so sick for three days. Could not hold food down. Had diarrhoea, low grade fever, pain in neck and arm. Spent one and half day in bed. Took three days before and felt somewhat better. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: Body temperature; Result Unstructured Data: Test Result:low grade fever; Test Date: 20211014; Test Name: Stool specimen; Result Unstructured Data: Test Result:Clostridium
Aktuelle Erkrankungen: Clostridium difficile infection
Vorgeschichte: -
Andere Medikamente: LISINOPRIL; VANCOMYCIN
Allergien: -
Vorherige Impfungen: -

VAERS 2018195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 02.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

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

Allodynia Back pain Burning sensation

Symptomtext

low back pain with allodynia in area - burning feeling with no rash/redness/swelling. Started on Medrol Dose Pack started on 12/29/21. Finished steroid 6 days later. No continued back pain or sensitivity at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: migraine
Andere Medikamente: Zomig 5mg PRN for migraine
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2012970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8030

mild

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 30.11.2021
Beginn: 28.12.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: SYR / LA

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

Erythema Eye infection Eyelid pain Hordeolum Swelling of eyelid

Symptomtext

swelling on eyelid, redness, pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eyelid pain
Hospital-Tage: -
Labordaten: diagnosis: stye in eye, infected gland
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2010827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Injection site haemorrhage Injection site reaction Muscle spasms

Symptomtext

Next day, found a very unique square form around my shot/injection site. A perfect square about 1 inch x 1 inch formed. 4 red dots (my blood) followed with a perfect straight dotted lines down, sideways to each dot forming a perfect square - never seen anything like that. Went to pharmacy after day 3 but it had slightly faded but staff said they have never seen anything like that and finally Pharmacist came - said it was just a bruise - how I reacted to it.... hesitant to take 2nd Covid vaccine.... was planning for tomorrow but very concerned. Did not have any other side effects but cramps on calves but that could have been anything.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site haemorrhage
Hospital-Tage: -
Labordaten: No medical tests - but did consult with pharmacist that injected me with vaccine.
Aktuelle Erkrankungen: Horrible flu / RSV - mimicked Covid-19 but tested negative twice - lasted an entire month in Oct - Nov 2021
Vorgeschichte: Bronchiactisus, mild ashtma
Andere Medikamente: Tumeric - dash only
Allergien: Pennicillin, sulfa
Vorherige Impfungen: Flu vaccines - horrible - extreme swollen non functional arm for 3+ weeks.

VAERS 1952643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood test Computerised tomogram Heart rate increased Injection site rash Mass Pain Pyrexia Rash

Symptomtext

Covid arm, rash below injection sight. Began 12/3 and grew larger through 12/7. Contacted after hours family doctor due to rash and heart rate. Rash went away 2-3 days and then returned. Increased heart rate beginning 12/4 through 12/7. Resting would not drop below 90-120. Standing would immediately cause heart rate to jump to 140 and above. Went to ER on 12/6 but they just diagnosed as increased heart rate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 12/6 - Bloodwork Ct scan
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Multivitamin
Allergien: Iodine (uv contrast)
Vorherige Impfungen: -

VAERS 1952643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Blood test Computerised tomogram Heart rate increased Injection site rash Mass Pain Pyrexia Rash

Symptomtext

Covid arm, rash below injection sight. Began 12/3 and grew larger through 12/7. Contacted after hours family doctor due to rash and heart rate. Rash went away 2-3 days and then returned. Increased heart rate beginning 12/4 through 12/7. Resting would not drop below 90-120. Standing would immediately cause heart rate to jump to 140 and above. Went to ER on 12/6 but they just diagnosed as increased heart rate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 12/6 - Bloodwork Ct scan
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Multivitamin
Allergien: Iodine (uv contrast)
Vorherige Impfungen: -

VAERS 2006285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: LA
Alter: 37,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 10.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Rash Vaccine positive rechallenge

Symptomtext

Acute onset of rash of the bilateral arms, biceps/forearms and left rib cage. Symptoms reportedly occurred at the time of initial injection on 17 November as well but were increased w/ 2nd dose

Weitere VAERSDATA-Felder

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

VAERS 2005786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 22.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain lower Computerised tomogram abnormal Epiploic appendagitis Peripheral swelling Pruritus Rash

Symptomtext

Legs swelled up with rash and itching. Pain in left lower abdomen. CT Scan showed Appendagitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: -
Labordaten: CT Scan
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2002659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: NY
Alter: 34,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 01.11.2021
Beginn: 29.12.2021
Tage bis Beginn: 58,0
Dosis: 2
Route/Site: IM / RA

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

Chills Headache Swelling

Symptomtext

swelling, headache, chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: men's 1 a day
Allergien: none
Vorherige Impfungen: -

VAERS 2508188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Fatigue Headache Pain in extremity

Symptomtext

Headache ARM PAIN, CHILLS, FATIGUE, WEAKNESS Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2508182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Headache Pain Pyrexia

Symptomtext

Headache, Fever, BODY ACHES, FATIGUE Narrative:

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

VAERS 1997233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NC
Alter: 67,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 01.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Back pain Blindness unilateral Bone pain Computerised tomogram normal Electrocardiogram normal Gait disturbance Injection site pain Ophthalmological examination normal Pain in extremity Scan with contrast normal Slit-lamp examination

Symptomtext

Dec. 2 , in early morning, started having sharp pains in both shoulders, next morning noticed issues with both knees, very difficult to walk, it's as if bones were acheing. Took NSaID, didn't help, took Tylenon Extra Strength, no help> I RAREly need any pain medications, very physically active, The pain continued tomy lower back, carried down into my hip socket on L. side, couple days later, started moving down my leg clear to my ankle. Took many Epsom salt soaks, ice packs, heating pads, rest (not something I've had to do in the past - EVER) This went on for over 2 weeks or more. Pain finally started to subside when one morning, I had an episode of partial vision loss in left eye - vision came back after 30 seconds or so. Had another episode 1 1/2 hours later - went to ER immediately.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: ER - Did slit lamp and woods lamp STAT, did not do any stroke test, raising arm, tongue out, etc. Told me to call Eye Dr. Saw them, did eye exam, couldn't find anything, said it could be occular migrane - never have had a migrain or occular issue before. 2 days later, I call Dr on call eye and he said to go to ER, said they don't have the equipment at this ER to do as thorough of a test. Was concerned that it could be an eye stroke. Went the Health Center - Had CT scan with contrast and an EKG - found nothing. Told me to contact Neurology and they would call ahead. Neurology could not see me until 10 days later because of holidays. Sent me back to ER - 6:00 pm - 4:00 A.M before they could do MRI -
Aktuelle Erkrankungen: Nothing
Vorgeschichte: Hypothyroid - being treated with daily Synthroid - checked every 6 months
Andere Medikamente: Synthroid 100 mcg. Magnesium Chloride & Calcium
Allergien: Sulfa - slight rash - as a child
Vorherige Impfungen: -

VAERS 1995577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: WA
Alter: 58,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 07.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chills Fatigue Hair injury Illness Immunisation Influenza like illness Myalgia Pain Pain in extremity

Symptomtext

Flu like symptoms; chills; his hair hurt; sick; Received booster shot on 07Dec21 with ongoing leg and large muscle pain/muscle pain was in his legs and arms; booster; Received booster shot on 07Dec21 with ongoing leg and large muscle pain; fatigue; Achy/everything hurt; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from information team. The reporter is the patient. A 58 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Dec2021 10:00 (Lot number: FH8030) at the age of 58 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "muscle relaxer" (unspecified if ongoing). Concomitant medication(s) included: METHOCARBAMOL taken for muscle relaxant therapy. Vaccination history included: Bnt162b2 (Dose of Covid-19 Shot, Lot- EW0171: Exp- Unknown; Administered in left arm), administration date: 23Apr2021, when the patient was 58 years old, for COVID-19 Immunization, reaction(s): "slight fatigue", "muscle soreness"; Bnt162b2 (Second Dose of Covid-19 Shot, Lot- EW0183; Exp- Unknown; Administered in left arm), administration date: 17May2021, when the patient was 58 years old, for COVID-19 Immunization, reaction(s): "slight fatigue", "muscle soreness". The following information was reported: IMMUNISATION (non-serious) with onset 07Dec2021 10:00, outcome "unknown", described as "booster"; PAIN IN EXTREMITY (non-serious) with onset 07Dec2021, outcome "not recovered", described as "Received booster shot on 07Dec21 with ongoing leg and large muscle pain"; MYALGIA (non-serious) with onset 07Dec2021 10:00, outcome "not recovered", described as "Received booster shot on 07Dec21 with ongoing leg and large muscle pain/muscle pain was in his legs and arms"; INFLUENZA LIKE ILLNESS (non-serious) with onset 08Dec2021, outcome "recovering", described as "Flu like symptoms"; PAIN (non-serious) with onset Dec2021, outcome "unknown", described as "Achy/everything hurt"; FATIGUE (non-serious) with onset 07Dec2021, outcome "not recovered", described as "fatigue"; CHILLS (non-serious) with onset 08Dec2021, outcome "unknown", described as "chills"; HAIR INJURY (non-serious) with onset 08Dec2021, outcome "unknown", described as "his hair hurt"; ILLNESS (non-serious) with onset 08Dec2021, outcome "unknown", described as "sick". No follow-up attempts are possible. No further information is expected. Follow-up (21Dec2021): This is a spontaneous follow-up report received from a same contactable consumer. This 58 year old female consumer (patient) reporter for her self that: Updated information: Events Added. Historical vaccine details updated. Vaccination facility information updated. Concomitant information updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Muscle relaxant therapy
Andere Medikamente: METHOCARBAMOL
Allergien: -
Vorherige Impfungen: -

VAERS 1995389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 13.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Headache Immunisation Pain in extremity

Symptomtext

Booster; Headache; Some arm pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 47 year-old female patient received bnt162b2 (BNT162B2), administration date 13Dec2021 (Lot number: FH8030) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Manufacturer Unknown), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 13Dec2021, outcome "unknown", described as "Booster"; HEADACHE (non-serious) with onset Dec2021, outcome "unknown", described as "Headache"; PAIN IN EXTREMITY (non-serious) with onset Dec2021, outcome "unknown", described as "Some arm pain". Additional information: The patient received the Pfizer-BioNTech COVID-19 Vaccine booster dose on Monday and had headache now, 3 days later and asked for information how to treat this. Patient mentioned she would still need to contact her Doctor. E-transmitting potential AE for review (47 years old, Female). Response: Checked EUA, Revised: 16Dec2021. Spoke from attached documents and explained that Pfizer is unable to make treatment recommendations specific for individual patients, referred to HCP for further guidance. Follow-up received on 17Dec2021: This is a spontaneous follow-up report received from the same contactable consumer. This 47-year-old female consumer (patient) reported for herself that: Updated Information: New event added. Additional Information: This report is not related to a study or programme. Reporter seriousness for Severe headache and Arm pain: Unspecified. Reporter states that: She received the Pfizer vaccine, the booster on Monday and she had severe headache since then. Patient wanted to confirm whether she should go to the ER. Patient had queried if this Is major cause of concern and what should she do. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1995286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Chills Immunisation Lymph node pain Pain Pyrexia

Symptomtext

booster; Sore underarm (lymph node); Chills; Fever; Body ache; This is a spontaneous report received from a non-contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 32-year-old female patient (not pregnant) received bnt162b2 (BNT162B2, solution for injection) (Lot number: FH8030) as dose 3 (booster), single for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8732), for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8732), for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "booster"; LYMPH NODE PAIN (non-serious), outcome "recovered", described as "Sore underarm (lymph node)"; CHILLS (non-serious), outcome "recovered", described as "Chills"; PYREXIA (non-serious), outcome "recovered", described as "Fever"; PAIN (non-serious), outcome "recovered", described as "Body ache". Therapeutic measures were not taken as a result of lymph node pain, chills, pyrexia, pain. Additional information: The patient was neither diagnosed with COVID-19 Prior to vaccination, nor been tested for COVID-19 Since the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1995273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MD
Alter: 67,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 05.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Arthralgia Asthenia Blood test Bone pain Chills Contusion Dizziness Dysstasia Immunisation Lethargy Muscular weakness Myalgia Osteoarthritis Pain Pain in extremity Tenderness Vaccination site nodule Vaccination site pruritus

Symptomtext

booster dose; muscle weakness to the point she needs to use a cane to ambulate and her knees throb at night while in bed.; her knees were throbbing which has never happened before/She ached all over; she felt dizzy/ she felt lightheaded like she felt like if she turned her head too fast; arm is still itchy and tender; she felt like they were bruised on the bottom; Every bone, muscle and joint in her body was aching; hard to stand on her feet; chronic hip and back pain has tripled; leg weakness; She was extremely lethargic; Chills; Her feet in particular, she felt like they were bruised on the bottom/heel pain; Every bone, muscle and joint in her body was aching; Every bone, muscle and joint in her body was aching; giant knot up under the injection site; It also itched like she had a thousand mosquito bites, her whole arm itched / her arm is still itchy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 67 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 05Dec2021 (Lot number: FH8030) at the age of 67 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (ongoing); "Blood pressure high" (ongoing); "Osteoarthritis" (unspecified if ongoing). Concomitant medication(s) included: TELMISARTAN taken for hypertension; LEVOTHYROXINE taken for thyroid disorder. Vaccination history included: Bnt162b2 (1st dose, Route, Anatomical Location: Upper Left arm), administration date: 16Feb2021, when the patient was 66 years old, for COVID-19 immunization, reaction(s): "she had minor side effects with the primary series of the Pfizer Covid Vaccine"; Bnt162b2 (2nd dose, Lot number: ENG198 or EN6198. , Route, Anatomical Location: Upper Left arm), administration date: 09Mar2021, when the patient was 66 years old, for COVID-19 immunization, reaction(s): "she had minor side effects with the primary series of the Pfizer Covid Vaccine". The following information was reported: IMMUNISATION (non-serious) with onset 05Dec2021, outcome "unknown", described as "booster dose"; MUSCULAR WEAKNESS (non-serious) with onset Dec2021, outcome "unknown", described as "muscle weakness to the point she needs to use a cane to ambulate and her knees throb at night while in bed."; PAIN (non-serious) with onset Dec2021, outcome "unknown", described as "her knees were throbbing which has never happened before/She ached all over"; DIZZINESS (non-serious) with onset Dec2021, outcome "unknown", described as "she felt dizzy/ she felt lightheaded like she felt like if she turned her head too fast"; TENDERNESS (non-serious) with onset Dec2021, outcome "not recovered", described as "arm is still itchy and tender"; CONTUSION (non-serious) with onset Dec2021, outcome "unknown", described as "she felt like they were bruised on the bottom"; BONE PAIN (non-serious), ARTHRALGIA (non-serious), MYALGIA (non-serious) all with onset Dec2021, outcome "unknown" and all described as "Every bone, muscle and joint in her body was aching"; DYSSTASIA (non-serious) with onset Dec2021, outcome "unknown", described as "hard to stand on her feet"; OSTEOARTHRITIS (non-serious) with onset Dec2021, outcome "unknown", described as "chronic hip and back pain has tripled"; ASTHENIA (non-serious) with onset Dec2021, outcome "not recovered", described as "leg weakness"; LETHARGY (non-serious) with onset Dec2021, outcome "unknown", described as "She was extremely lethargic"; CHILLS (non-serious) with onset Dec2021, outcome "unknown", described as "Chills"; PAIN IN EXTREMITY (non-serious) with onset Dec2021, outcome "unknown", described as "Her feet in particular, she felt like they were bruised on the bottom/heel pain"; VACCINATION SITE NODULE (non-serious) with onset Dec2021, outcome "recovering", described as "giant knot up under the injection site"; VACCINATION SITE PRURITUS (non-serious) with onset Dec2021, outcome "not recovered", described as "It also itched like she had a thousand mosquito bites, her whole arm itched / her arm is still itchy". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The caller mentions she had a very mild reaction with the first shot and then it was a little more stringent on the second shot and lasted a few more days. Her feet in particular, she felt like they were bruised on the bottom. It was hard to stand up on her feet, especially on her left heel. She had severe heel pain, it felt like someone hit her with a hammer just on her heel. All of her joints in her feet ached all over. She has not had knee pain before. However, when she laid down at night, her knees were throbbing which has never happened before. She also had the chills. She had no fever, but just chills off and on for the first few days. She is still experiencing leg weakness. It's like the muscle in her legs are still weak, it is hard for her to stand up. She has to really be careful or she will fall backwards, it's like her legs don't want to lift her. She has always had chronic hip and back pain but it feels like the pain has tripled and it hasn't gone away. If she would go back to the normal former pain level she had, that would be a relief. Prior Vaccinations (within 4 weeks) was none. She does get blood work done every 3 months for her regular doctor though. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: blood work; Result Unstructured Data: Test Result:Unknown; Comments: She does get blood work done every 3 months for her regular doctor though.
Aktuelle Erkrankungen: Blood pressure high; Hypothyroidism
Vorgeschichte: Medical History/Concurrent Conditions: Osteoarthritis
Andere Medikamente: TELMISARTAN; LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1993249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: WI
Alter: 26,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Hypoaesthesia Hypoaesthesia oral Muscle twitching Pain

Symptomtext

Patient received her 1st COVID-19 vaccination on 12/17/2021 at 12:00 pm. Around 10:00 pm on 12/17/2021, she began to notice body aches. Around 3:00 am on 12/18/2021, she began to notice numbness to the left-side of her face including her lip, cheek and chin as well as, on the inside of her left mouth. She then noticed twitching to her left cheek brought on by smiling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Evaluated in urgent care on 12/18/2021. No labs or imaging performed. Continued to monitor and referred to neurology.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma, PCOS
Andere Medikamente: Albuterol, Fluoxetine, Metformin, Prenatal vitamins, Tylenol, Ibuprofen.
Allergien: Acetaminophen with Codeine, Nitrofurantoin, Opioids, Zoloft.
Vorherige Impfungen: -

VAERS 1993234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: VA
Alter: 32,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Back pain Hypoaesthesia Rash

Symptomtext

Patient began experiencing back pain and numbness starting on 12/22/21 about 2 hour after receiving vaccines. She used Tylenol and motrin to help with pain. Pain has continued and she began to use icy hot patches. Patient developed rash this morning and called pharmacy to ask what they should do. Patient believes that they may have shingles and is going to be checked out by a doctor.

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

VAERS 1992986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 16.11.2021
Beginn: 20.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chest discomfort Cough Dizziness postural Ear pain Exposure to SARS-CoV-2 Fatigue Headache Oropharyngeal pain Pyrexia Rash Rhinorrhoea SARS-CoV-2 test positive Sinus congestion Swelling of eyelid

Symptomtext

Tested positive for COVID after vaccination 12/24/2021. 12/20/2021 was first day of symptoms. I was exposed on Saturday 12/18/2021. In the beginning, my first symptoms were runny nose, sinus congestion, headache and sore throat, and earaches. And then after several days (4 days), I developed a cough, and I was also very tired. I had a fever which was 101. I felt dizziness when I stood up. The next day when I woke up, my chest felt like I had a brick on my chest, it was very heavy. A few days later, I developed a rash on my hands and arms and on my face near the outside of my eyes. There was swelling as well near my eyes. I called the on-call doctor when I got the positive test in the evening, so I had a plan on the weekend. I was told to just treat it as any cold and to go to the ER if I had any difficulty breathing or if things got worse. She also suggested cough syrup and gargling and Tylenol for any pain as well. I also spoke with my doctor today because I haven't been getting any better or worse and she was concerned because I could develop pneumonia, so she prescribed me more prescriptions? albuterol sulfate inhaler 2 puffs 3 times daily, azithromycin 250mg 6 doses, Methylprednisolone 4mg 21 tabs, Benzonatate as needed. For the rash as well, I was also taking Claritin to help with the rash. I had gotten rashes with each of my vaccines, so I took the Claritin to help with those as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness postural
Hospital-Tage: -
Labordaten: COVID test lateral flow -12/24/2021 - positive
Aktuelle Erkrankungen: Cold in October - not COVID
Vorgeschichte: None
Andere Medikamente: Rosuvastatin 10mg daily Larin 1/20 one tab daily Multivitamin Fish Oil capsules 2 daily
Allergien: Avocados, Mangos
Vorherige Impfungen: -reaction to most vaccinations -1st & 2nd Moderna - rashes and swelling on arm where vaccine was received - 08/2021 flu vaccine

VAERS 1992600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 03.11.2021
Beginn: 20.12.2021
Tage bis Beginn: 47,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Fatigue Headache Myalgia Nasal congestion Pain Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

On 12/20/2021 me, my husband, and daughter all started having symptoms. I was feeling achy and sniffly and we went and got tested on 12/21/2021 which was negative. I had body aches, a headache, sneezing, and sniffling, but no cough. 3 days later we tested again, and we all tested positive, and they told us to quarantine for 10 days. We all started feeling a lot better quickly. It lasted about 7 days. I am better and I was least affected with the symptoms. It did feel like someone beat me up and I had muscle aches, headaches, nasal congestion, fatigue, and tiredness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID - positive result
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism; Depression
Andere Medikamente: Levothyroxine; Zoloft; Trazodone; Lexapro
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1992513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Feeling hot Impaired work ability Muscular weakness Nasal congestion Oropharyngeal pain Pain SARS-CoV-2 test negative SARS-CoV-2 test positive Sensory disturbance

Symptomtext

12/17 I started to have the sore throat. That was continuous, then on 12/22, I started to have a stuffy nose, 12/23 was more stuffy nose so I went to go do a Covid test. At the time, they only have a PCR so I did that, and the next day I also came back to do the rapid test 12/24 as well. And that came back negative. And my nose was still stuffy. Also starting 12/22 I got body aches but it's like body aches without a fever. It's not strong pain but it felt like my muscles were shrinking feeling. It's different from outside and inside. Strange feeling inside. 12/26 I was also feeling feverish and the highest was 99.8. So I went to see my doctor on Monday 12/27 and she couldn't tell. I told my doctor that I had a runny nose and sore throat and she said it could be a cold or Covid. The test results for the PCR came on the 12/28 and came back positive. And I notified work and I didn't go. Yesterday 12/29, I took a test again and it came back negative for rapid and the results for the PCR came back 12/30 negative as well. I still have coughing and stuffy nose. But I no longer have that strange pain feeling. Sore throat has improved but the stuffy nose I still have.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID PCR Test 12/23/2021, positive. COVID Rapid Test 12/24/2021, negative. COVID Rapid Test 12/29/2021, negative. COVID PCR Test 12/29/2021, negative.
Aktuelle Erkrankungen: None
Vorgeschichte: Hx of skin cancer (2 years ago)
Andere Medikamente: Women's Multivitamin; Vitamin C; Vitamin D; Vitamin E
Allergien: Alcohol; Morphine
Vorherige Impfungen: -

VAERS 1989122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: NC
Alter: 33,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 22.11.2021
Beginn: 28.12.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: UN / AR

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

Rash Rash erythematous

Symptomtext

I've had a red rash (1/2 inch) pop up on my left forearm and both legs. It looks like a patch of dry skin, but it does not itch or burn.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: HFMD
Vorgeschichte: Asthma
Andere Medikamente: Claritin, Singular, Flonase, Azelastine, Junel, Vitamin C, Multivitamin, Align Probiotic, Restasis, Vitamin D
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1988787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Pruritus Rash

Symptomtext

Itching , small bumps on and off

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: penicillin?
Vorherige Impfungen: -

VAERS 1982086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 03.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Pain Pain in extremity Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

After 24 hour, body ache, sore arm, and fatigue. Then on Dec 18th, I was fatigue and had a dry cough. I had a running nose. These symptoms are still ongoing. I got a COVID-19 test on the Dec 20th, negative. On the Dec 24th got 3 COVID-19 test, positive results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Unithroid
Allergien: N/A
Vorherige Impfungen: -

VAERS 1982059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 17.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Erythema Gingival pain Gingival swelling Oral pain Toothache

Symptomtext

Mild mouth/teeth pain beginning on 12/19/21. Progressively got worse as the days went on. By 12/22/21, right side of mouth/gums felt sore, swollen and painful, couldn?t chew food. Unable to get in to see my dentist (no appnts available until 1/5/22) so based on symptoms, was prescribed antibiotics over the phone in case of infection or abscess. Made an appnt with primary care that day who said gums looked red and swollen. Said to take the antibiotics prescribed from dentist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Gingival pain
Hospital-Tage: -
Labordaten: None, just regular exam by pcp.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Eye drops
Allergien: Amoxicillin, Flonase
Vorherige Impfungen: -

VAERS 1980922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: IN
Alter: 35,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Headache Injection site pain Malaise

Symptomtext

Headache at 8pm on day of vaccine persisting through day 2-3 post vaccine. General malaise intermittently. Left arm pain throughout deltoid for 3 days post vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sore throat on 12/18/21 suspected to be viral with Covid negative PCR and antigen testing
Vorgeschichte: Asthma, Moderate environmental allergies
Andere Medikamente: Singular, Albuterol, Cetirizine, Alrex, Olopatadine
Allergien: Keflex, Mango
Vorherige Impfungen: -

VAERS 1980794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: MI
Alter: 41,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Haematoma Immunisation Joint swelling Pain

Symptomtext

about 24 hours after getting it my shoulder swelled up. I have like a large Hematoma on the outside of it so a large swelling on the outside of my shoulder; about 24 hours after getting it my shoulder swelled up. I have like a large Hematoma on the outside of it so a large swelling on the outside of my shoulder; I can''t put any weight on my arm or lift without having shooting pains; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 10Dec2021 (Lot number: FH8030) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Blood pressure" (unspecified if ongoing), notes: Verbatim: Blood pressure. Concomitant medication(s) included: LISINOPRIL taken for blood pressure measurement. Vaccination history included: Bnt162b2 (Dose 1), for Covid-19 immunization; Bnt162b2 (Dose 2), for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 10Dec2021, outcome "unknown", described as "booster"; JOINT SWELLING (non-serious), HAEMATOMA (non-serious), outcome "unknown" and all described as "about 24 hours after getting it my shoulder swelled up. I have like a large Hematoma on the outside of it so a large swelling on the outside of my shoulder"; PAIN (non-serious), outcome "unknown", described as "I can''t put any weight on my arm or lift without having shooting pains". Therapeutic measures were taken as a result of joint swelling, haematoma, pain. Additional information: Yesterday around 4 o'clock so about 24 hour after my booster shot (10Dec2021). Anatomical site of administration: Left shoulder. The number looks like 4335, that's the only number on here and on the back there is a number that says FH8030, I am not sure which one the Lot number would be. I have FH8030. No lab test (within 2 weeks). Patient was still experiencing the problem. Treatment: Taking Ibuprofen, putting ice on it as well. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure (Verbatim: Blood pressure)
Andere Medikamente: LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1980718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8030

mild

Staat: CT
Alter: 44,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Headache Lymphadenopathy Vaccination site pain

Symptomtext

Swollen lymph nodes in left armpit; a mild headache; Sore Arm at injection site; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 23Nov2021 16:00 (Lot number: FH8030) at the age of 44 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Batch/Lot No: EP6955, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 31Mar2021, when the patient was 43 years old, for COVID-19 Immunization; Bnt162b2 (DOSE 1, SINGLE, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 10:30 AM), administration date: 10Mar2021, when the patient was 43 years old, for Covid-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 23Nov2021 20:00, outcome "recovering", described as "a mild headache"; VACCINATION SITE PAIN (non-serious) with onset 23Nov2021 20:00, outcome "recovering", described as "Sore Arm at injection site"; LYMPHADENOPATHY (non-serious) with onset 24Nov2021 01:00, outcome "unknown", described as "Swollen lymph nodes in left armpit". Therapeutic measures were not taken as a result of headache, vaccination site pain, lymphadenopathy. Additional information: Other vaccine in four weeks: No. other medications in two weeks: None. covid prior vaccination: No. covid tested post vaccination: No. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1979818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8030

mild

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Burning sensation Rash

Symptomtext

I started having rashes all over my body a week after the first dose. I didn?t pay much attention and thought it was temporary, maybe related to the vaccine. I have never been allergic to anything of have a history of rashes. After receiving the second dose, which I postponed taking because of the rash, i broke out in severe rashes over both my legs. My legs felt like they were burning. These have continued ever since. Benadryl, which i have taken daily has no relief effect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: I did do a series of blood test a week prior to taking the second dose. All blood work was normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1978981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: NJ
Alter: 80,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Headache

Symptomtext

Dizziness, headache

Weitere VAERSDATA-Felder

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

VAERS 1978773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8030

mild

Staat: RI
Alter: 74,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Immunisation Pruritus Rash

Symptomtext

itching got really annoying; rash spread to different parts of my body; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 13Nov2021 12:00 (Lot number: fh8030) at the age of 74 years as dose 3(booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (prev dose product=COVID 19, prev dose brand=pfizer, prev dose brand unknown=False, prev dose lot number=fl9262, prev dose lot unknown=False, prev dose administration date=17Mar2021, prev dose administration time=03:00PM , prev dose dose number=2, after 2nd shot got minor itching), administration date: 17Mar2021, when the patient was 74 years old, for COVID-19 immunization, reaction(s): "got minor itching", "some minor rash,mostly on back of"; Bnt162b2 (prev dose product=COVID 19, prev dose brand=pfizer, prev dose brand unknown=False, prev dose lot number=en6201, prev dose lot unknown=False, prev dose administration date=24Feb2021, prev dose administration time=02:00PM , prev dose vaccine location= Left arm, prev dose dose number=1), administration date: 24Feb2021, when the patient was 74 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 13Nov2021 12:00, outcome "not recovered", described as "Booster"; PRURITUS (non-serious), outcome "not recovered", described as "itching got really annoying"; RASH (non-serious), outcome "not recovered", described as "rash spread to different parts of my body". The events "booster", "itching got really annoying" and "rash spread to different parts of my body" were evaluated at the physician office visit. Therapeutic measures were taken as a result of immunisation, pruritus, rash. Additional Information:It was reported that patient did not had any other vaccine in four weeks. And The patient was not diagnosed with SARS-CoV-2 infection before or after vaccination. And had no known allergies. Other medical history: none After 2nd shot got minor itching and some minor rash, mostly on back of arms, After 3rd shot itching got really annoying and rash spread to different parts of my body. Using anti itching creams. seems to help, but problem is still intermitant. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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