VAERS Reports FJ 4991

VAERS 2644568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 13.06.2023
Impfdatum: 21.07.2022
Beginn: 13.12.2022
Tage bis Beginn: 145,0
Dosis: 4
Route/Site: IM / LA

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

Acute respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE

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

VAERS 2635446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 06.04.2022
Beginn: 13.06.2022
Tage bis Beginn: 68,0
Dosis: 4
Route/Site: - / -

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

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

VAERS 2600080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: FL
Alter: 80,0
Geschlecht: F
Eingang: 21.03.2023
Impfdatum: 06.08.2022
Beginn: 14.03.2023
Tage bis Beginn: 220,0
Dosis: 4
Route/Site: SYR / UN

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

Acute respiratory failure COVID-19 Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Respiratory failure Tachypnoea

Symptomtext

Hospitalization for dyspnea acute on chronic hypoxemic respiratory failure, tachypnea with COPD exacerbation likely due to COVID on dates 3/14/2023-3/17/2023. Treated with dexamethasone, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2584254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: NY
Alter: 87,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 15.09.2022
Beginn: 22.01.2023
Tage bis Beginn: 129,0
Dosis: 4
Route/Site: IM / RA

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

Acute respiratory failure Atelectasis Blood gases Blood lactic acid Body temperature decreased COVID-19 Cerebral haemorrhage Cerebral mass effect Chest X-ray abnormal Computerised tomogram head abnormal Endotracheal intubation Fall Fraction of inspired oxygen Lactic acidosis Leukocytosis Mechanical ventilation SARS-CoV-2 test positive Sepsis

Symptomtext

1/22/2023-Brought in EMS, presents to ED, had been found unresponsive at bottom of stairs. HR in 60, while obtaning CT dropped to 30's, 1 amp Atropine given. Temp-85.8, BP 194/91.Covid + test. Intubated. CT- LArge intraparenchymal Hemmorhage R cerebral hemisphere, centered R temporal and occipital lobes .2x5.9 cm. 1.9cm r to L midline shift. Evidence of impending transtentorial herniation and brainstem deviation to the left. CXR-small desnity upper left lung, atelectasis. Admit to trauma, acute hypoxic resp failure s/t fall, intraparencymal hemorrhage. WBC 18.4 1/23/2023- Vent-AC VC 400/14/100 Fio2/5 Peep. Comfort care patient has been made DNR. Sepsis d/t Covid leukocytosis 18.4, lactic acidosis 2.4. 1/23/2023-Levophed to keep MAP above 65 WBC 13.2. ABG 7.353/43.4/24.1 on 100% Fio2 AC VC vent. 1/24/2023-Terminal exubation @1257.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism and HTN
Andere Medikamente: -
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2578132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 08.02.2023
Impfdatum: 13.05.2022
Beginn: 22.01.2023
Tage bis Beginn: 254,0
Dosis: 2
Route/Site: - / -

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

Angiogram pulmonary abnormal Blood culture positive Blood gases abnormal COVID-19 COVID-19 pneumonia Central venous catheterisation Chest X-ray abnormal Chills Cough Death Decreased appetite Diarrhoea Dyspnoea Fatigue Hypophagia Hypotension Hypoxia Incontinence

Symptomtext

Discharge Provider: MD;* Primary Care Physician at Discharge: MD Admission Date: 1/22/2023 PRESENTING PROBLEM: Multifocal pneumonia [J18.9] HOSPITAL COURSE: Patient is a 65 y.o. female with a history of mantle cell lymphoma, pulmonary emboli on Eliquis and GAD who presented with cough and shortness of breath. Patient stated she has not been feeling well since the beginning of the month. She stated she has fever, chills, cough, persistent diarrhea, decreased appetite and malaise. On 1/5/2023 she was diagnosed with COVID and treated with molnupiravir. She endorsed being incontinent due to perfuse diarrhea and had little oral intake. The diarrhea has resolved but she continues with a cough, increasing shortness of breath and fatigue. Her husband called 911 and EMS arrived. Patient was found to be hypoxic and placed on 4L 02 to maintain sats above 90%. Upon arrival to the emergency department patient was found to be hypotensive and was given a 1 L bolus of IV fluids. She was hypoxic and placed on 2 L of oxygen to maintain sats above 90%. COVID PCR positive. Lab work was relatively unremarkable. Blood gas did demonstrate hypoxia. Chest x-ray demonstrated extensive bilateral airspace opacities suspicious for multifocal pneumonia. Blood cultures were drawn and she was given IV Rocephin, azithromycin and vancomycin. She was admitted with hospitalist services for further care and treatment of COVID-19, multifocal pneumonia and hypoxia. Patient was started on IV cefepime and vancomycin. Patients diarrhea returned and then subsided without testing. Blood cultures positive for Staph hominis. Repeat blood cultures obtained. ID consulted and suspected patient has bacterial super infection after COVID, ID recommendations were followed. She completed a 10 day course of antibiotics. Her oxygen needs waxed and waned. She was diuresed with lasix. She had to be moved to ICU for hypotension and was given fluid boluses and intermittently levophed was used to maintain blood pressure. She slowly started to improve and oxygen demand was decreasing. Then February 3 and 4 her oxygen demand significantly increased requiring HFNC on the evening of 2/4. CTA indicated worsening Covid pneumonia and ruled out PE. Patient wishes were reviewed and she continued to be adamant about not wanting intubation. VICU and ID were participating in care. She was again started on broad spectrum antibiotics. She had intermittent hypotension and maintaining peripheral access was difficult. A PICC line was placed, and supportive care with pressers continued. Due to worsening need for oxygen and hypotension goals of care were again discussed and Hospice was consulted for further assistance on February 6th. Patient and husband made plan to discharge home with hospice, but unfortunately after completion of plans and being left alone her oxygen needs increased and were being met by HFNC at 95% and a venti mask. She was made comfort measures on 2/6 in the evening and passed away at 7:03 on 2/7/23 with husband and granddaughter at bedside. Hospice was notified.

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Praegender Schweregrund: Death
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: GERD (gastroesophageal reflux disease) Hypercholesteremia GAD (generalized anxiety disorder) Depression Hyperlipidemia Fibromyalgia Osteoarthritis Mantle cell lymphoma, lymph nodes of inguinal region and lower limb (HCC) Personal history of colonic polyps Family history of malignant neoplasm of gastrointestinal tract S/P autologous bone marrow transplantation (HCC) Chronic pain Pain in joint Dehydration History of lumbar fusion Stage 3a chronic kidney disease (HCC) Hypophosphatemia Rash Multifocal pneumonia COVID-19 Pulmonary emboli (HCC) Acute respiratory failure with hypoxia (HCC) Leukocytosis Hypotension Adrenal insufficiency (HCC) Encounter for end of life care
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acetaminophen (TYLENOL) 650 MG extended release tablet acyclovir (ZOVIRAX) 400 MG tablet busPIRone (BUSPAR) 5 MG tablet ELIQUIS 5 MG tablet famotidine (PEPCID) 20 MG tablet fentaNYL (DURAGESIC) 25 MCG/H
Allergien: Adhesive TapeRash Bee VenomHives Crestor [Hmg-coa-r Inhibitors]Myalgia Obinutuzumab
Vorherige Impfungen: -

VAERS 2545079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: CT
Alter: 58,0
Geschlecht: M
Eingang: 28.12.2022
Impfdatum: 23.05.2022
Beginn: 27.09.2022
Tage bis Beginn: 127,0
Dosis: 4
Route/Site: IM / RA

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

Acute myocardial infarction Angiogram Blood test Catheterisation cardiac Echocardiogram Magnetic resonance imaging heart X-ray

Symptomtext

Non-St Elevated Myocardial Infarction. X-rays, blood work, cardiac catheterization, CT angiogram, echo comprehensive (9/28/22); cardiac MRI (11/28).

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: asthma, hypertension
Andere Medikamente: Singulair, Crestor, Zoloft, Hydrochlorothiazide, Valsartan, multi-vitamin, niacin, potassium
Allergien: n/a
Vorherige Impfungen: slight fever

VAERS 2520473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: ID
Alter: 63,0
Geschlecht: M
Eingang: 30.11.2022
Impfdatum: 26.05.2022
Beginn: 20.09.2022
Tage bis Beginn: 117,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Cardiac arrest Dialysis Impaired work ability Intensive care Malaise Oropharyngeal pain Pulmonary embolism Renal failure Resuscitation SARS-CoV-2 test positive Syncope

Symptomtext

On September 20, 2022, I came down with symptoms that were confirmed to be COVID-19 by my home test. On day 9, I went into cardiac arrest due to a pulmonary embolism. I did not have any symptoms other than a slight sore throat. I was planning to go back to work the following Monday. My wife found me collapsed in the bathroom and we called the ambulance. I went into cardiac arrest in the emergency room. They did CPR for about 40 minutes. They administered TPA and my heart restarted. I was in ICU for four days under critical care. I was then in the hospital for an additional 2 weeks. As of today, I have no brain damage. I did have kidney failure while in the hospital and I am on dialysis two days a week.

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; calcium; vitamin D3; fish oil; magnesium
Allergien: Sensitivity to CIPRO
Vorherige Impfungen: -

VAERS 2507381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 26.04.2022
Beginn: 11.10.2022
Tage bis Beginn: 168,0
Dosis: 4
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Asthenia Bladder catheterisation Blood creatinine normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Hypophagia Hypoxia Lung opacity Pyrexia SARS-CoV-2 test positive Urinary retention

Symptomtext

Clinical Summary Patient is a 82 y.o. male with a history of CVA with left sided weakness who presented to RMH 10/11/2022 with 1 day of SOB, fever and increased weakness. Found hypoxemic and COVID-19 positive. Course prolonged by placement and need for isolation. Patient stabilized and discharge to facility. 1. Acute Hypoxemic Respiratory Failure: due to COVID. Weaned off O2 10/13/22. 2. COVID-19 Pneumonia: Vaccinated. Symptoms started 10/10/22. Tested positive on 10/11/22. CXR 10/11/22 showed left hazy opacity course markings. Pt family declined remdesivir. COVID 19 pneumonia only, no sepsis. Decadron discontinued 10/17/22. 3. AKI: Cr 1.1 on admit. Baseline 0.7. Likely pre-renal due to poor po intake in addition to loss of autoregulation. Held home ACEi on admit. Resolved to normal on 10/13/22. Resumed home medications on discharge. 4. Urinary Retention: with history of BPH s/p TURPT in the past. Has had foley in the past. Foley placed on admit. Voiding trial when more ambulatory at IPR. 5. CVA: with left sided weakness. 6. HTN: Continued home meds. 7. Waldenstrom's Macroglobulinemia: per history no longer on treatment. 8. Code status: DNR CCA DNI discussed on admit

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

VAERS 2501864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: NY
Alter: 83,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 01.04.2022
Beginn: 21.05.2022
Tage bis Beginn: 50,0
Dosis: 2
Route/Site: IM / LA

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

Acidosis Anion gap Atelectasis Blood bicarbonate decreased Blood creatinine increased Blood gases Blood potassium increased Bradycardia COVID-19 Catheter placement Chest X-ray abnormal Computerised tomogram abdomen abnormal Death Dialysis Endotracheal intubation Hypotension Intensive care Intraosseous access placement

Symptomtext

5/21/2022-Presents Ed via EMS, at home intially sinus brady hypotensive transcutaneously paced. Hr-40, systolic around 70 mmHg on norepinephrine mcg/min. Intubated. Had IO of R shoulder due to inability to place IV access. Admit hemodynamically significant bradycarida in the setting of severe mtabolic derangeent and metabolic acidosis. Potassium 7 and creatnine above 6 . CXR: bibasilar linear atelectasis. Covid + test. Hemodialsysi catheter via IJ for emergenct dislaysis. Pancreatits based on abd CTand lipase over 4000. Transfered to ICU. Temporary venous pacemaker placed along with hemodialysis catheter. Vent settings Fio2 100% resp 16 ABG: 6.9/27.2 bicarb less then 6 and anion gap more then 19 Ordered IV meropenem and pressor support. 5/22/2022-Bicarb drip started , acidosis improving. Monoclonals and steroids not recommended due to amount of renal failure. Vent settings Fio2 50% resp 10 Family discussion, Patient made palliative. Terminal exubation. Time of death 1600.

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Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PE, Breast cancer, renal carcnoma status post nephrectomy, type 2 DM, HTN and A fib.
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2315078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: NY
Alter: 87,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 08.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

Blister Chills Confusional state Eye swelling Hypersensitivity Insomnia Malaise Near death experience Pruritus Rash macular Stress Swelling face Thermal burn Weight

Symptomtext

She states she is going to die and going crazy; looks like burns to left arm, shoulder, left side of chest and breast, neck, ear, and face; itchy; Her eyes are closed and can barely see they're swollen; chills; malaise; state of confusion; "burned victim" at her whole arm for about 2 weeks and 10 days; "I look like I have an elephant face, I have this red black splotches all over."; "I look like I have an elephant face, I have this red black splotches all over."; She reported her entire left arm had an allergic reaction; exasperated; not sleeping; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-healthcare professional) from medical information team. The reporter is the patient. An 87-year-old female patient received BNT162b2 (BNT162B2), on 08Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 87 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroid" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID taken for hypothyroidism. Vaccination history included: BNT162b2 (Dose 1, Lot number: EL9262 or GL9265), administration date: 25Jan2021, when the patient was 86-year-old, for COVID-19 immunisation, BNT162b2 (Dose 2, Lot number: EN5318 or GN5318), administration date: 16Feb2021, when the patient was 86-year-old, for COVID-19 immunisation, reaction(s): "thought this was a rash like her second one"; BNT162b2 (Dose 3, Lot number: FF3592), administration date: 28Sep2021, when the patient was 86-year-old, for COVID-19 immunisation. The following information was reported: NEAR DEATH EXPERIENCE (medically significant), outcome "unknown", described as "She stated she is going to die and going crazy", BLISTER (non-serious), outcome "unknown", described as "looks like burns to left arm, shoulder, left side of chest and breast, neck, ear, and face", PRURITUS (non-serious), outcome "unknown", described as "itchy", EYE SWELLING (non-serious), outcome "unknown", described as "Her eyes are closed and can barely see they're swollen", CHILLS (non-serious), outcome "unknown", MALAISE (non-serious), outcome "unknown", CONFUSIONAL STATE (non-serious), outcome "unknown", described as "state of confusion"; THERMAL BURN (non-serious), outcome "recovered", described as ""burned victim" at her whole arm for about 2 weeks and 10 days", SWELLING FACE (non-serious), RASH MACULAR (non-serious), outcome "unknown" and all described as ""I look like I have an elephant face, I have this red black splotches all over."", HYPERSENSITIVITY (non-serious), outcome "unknown", described as "She reported her entire left arm had an allergic reaction", STRESS (non-serious), outcome "unknown", described as "exasperated", INSOMNIA (non-serious), outcome "unknown", described as "not sleeping". The events "she stated she is going to die and going crazy", "looks like burns to left arm, shoulder, left side of chest and breast, neck, ear, and face", "itchy", "her eyes are closed and can barely see they're swollen", "chills" and "malaise" required physician office visit. The patient underwent the following laboratory tests and procedures: Weight: Unknown result, notes: 10-112 pounds. Therapeutic measures were not taken as a result of insomnia. Clinical Information: She stated she would like to document the facts as that was one of the reasons she was calling. She stated Pfizer should have to know what was happening and then she would like to be transferred to get her questions answered. She stated she has been in excellent health until now and has only had to take one medication for her hypothyroid. Caller stated contact was best in the afternoon as she was at the senior centre in the mornings. Caller stated her skin looks burned on her left arm to shoulder to left side of chest or breast, neck to ear to left to right side of her face. This started 3 days after her 2nd COVID-19 vaccine booster. Caller stated her doctor still doesn't know about this. Caller stated she was in such a state of confusion. She stated she had all the reactions but those passed like chills and malaise. Her left arm was itchy from the stupid vaccine and stated she would scratch and forget this. She stated at her age she can't address things as she just ignores them. She stated one morning she got up 10 days to 2 weeks later and her skin looked like burnt roast beef. She stated the weather was warm and she was taking off her winter clothes. She stated there was another small area that was all red or dark brown. She stated this started about 2 and a half weeks ago to her face. She stated last week or week before she saw her internist who referred her to a dermatologist. She stated she has to wait weeks for an appointment. She went to the dermatologist yesterday and she had never seen this before either. The dermatologist wanted to give the caller creams to try but the caller just wanted her to flush the vaccine out of her body. Caller told the dermatologist she would call Pfizer and the dermatologist told her she would be wasting her time. Caller stated this was systemic in her body and will continue until this was flushed out. She stated she received all 4 COVID-19 Vaccines in her left arm and has 4 tiny scar spots. Indication for 4th dose of COVID-19 vaccine: She stated because omicron numbers were going up and no one was wearing masks. She was bombarded with 4th dose and being 88 and high risk. She was told she could go shopping and not have to worry. She stated she was stupid and shouldn't have received the 4th dose. No, she stated she has only ever taken one medication. She stated she has never taken a flu shot or the any other shots that are offered at her yearly physical. She stated she went blind for the 4th dose of the COVID-19 Vaccine. She stated if she had used her brain she would have never had to go through this. She stated the Polyethylene Glycol was not put on the website until after the first 2 deaths from 4th dose. stated this was worth waiting for. She stated she was deathly ill and has not slept in weeks from the incessant itching. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200793431 similar report from same reporter

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Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: Test Name: Weight; Result Unstructured Data: Test Result:Unknown result; Comments: 10-112 pounds
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 2308949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

kritisch

Staat: IL
Alter: 83,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 03.06.2022
Beginn: 03.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Epistaxis Nervousness Respiratory arrest Unresponsive to stimuli

Symptomtext

Patient went to stand after vaccine and sat back down in chair, became unresponsive to stimuli and seemed to stop breathing. She regained consciousness with a bloody nose and feeling "shaky". Offered water and cold cloth on neck. EMTs arrived and assessed patient. Patients vitals seemed stable and they offered she could go to hospital or not. Patient chose to go and was taken by EMTs to ER. Has a history of cardiac issues

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Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: A-fib
Andere Medikamente: -
Allergien: suklfa
Vorherige Impfungen: -

VAERS 2262686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

kritisch

Staat: CA
Alter: 81,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 25.04.2022
Beginn: 26.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Alanine aminotransferase normal Angiogram cerebral normal Anticoagulant therapy Antiplatelet therapy Arteriogram carotid normal Aspartate aminotransferase normal Asthenia Balance disorder Basophil percentage Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood magnesium normal Blood potassium normal

Symptomtext

Day 1: fever to 100 Day 2: lnner ear feeling of instability Day 3: Lower extremity weakness and unstable gait Day 4: Sent to ER-CVA identified

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Result type: Consultation Note Result date: April 30, 2022 07:40 PDT Result status: Auth (Verified) Result Title/Subject: Neurology Consultation Note Performed By/Author: DO, on April 30, 2022 07:42 PDT Verified By: DO, on April 30, 2022 08:49 PDT Encounter info: Emergency - IP, 04/29/2022 - * Final Report * Patient: Age: 81 Years Gender: Female Author: DO Date of Service: 04/30/2022 Reason for Consultation: Weakness History of Present Illness: 81-year-old female with history of Sjogren's disease, lupus, TIA, hypertension, and hyperlipidemia presents with weakness. PT states that 2 days ago she felt off balance and her legs buckled up on her. She later realized that her L leg was weaker. she takes daily Aspirin. Review of Systems: All 10 point ROS systems were Negative except for stated in HPI Problem List/Past Medical History: Ongoing HTN - Hypertension Hx of Sjogren's disease Lupus erythematosus Sjogren's syndrome TIA Historical Procedure/Surgical History: tribectomy (01/01/2012), hysterectomy (01/01/1978). Medications: Active Medication Orders: PRN Medications acetaminophen (Tylenol) 650 mg Q4H PR acetaminophen 650 mg Q4H PO bisacodyl (Dulcolax) 10 mg daily PO lactulose 20 g QID PO magnesium hydroxide (Milk of Magnesia) 30 mL daily PO Medications aspirin 81 mg daily PO docusate (Colace) 250 mg QHS PO famotidine (Pepcid) 20 mg BID PO senna 2 tab QAM PO Allergies: codeine (Nausea) ciprofloxacin (HA - Headache) Objective: Vitals & Measurements: T: 36.2 ?C (Oral) TMIN: 36.2 ?C (Oral) TMAX: 36.7 ?C (Oral) HR: 65 (Monitored) RR: 18 BP: 128/60 SpO2: 96% WT: 53.2 kg WT: 53.2 kg Physical Exam: Pt was examined with the help of bedside nurse. General: Alert, in no acute cardiopulmonary distress. Eyes: no scleral icterus, no proptosis Musculoskeletal: Normal tone, No significant atrophy, CV: no palpitations, No significant edema Pulm: Non-labored breathing , No cyanosis Psych: Appropriate affect and mood, No significant anxiety Skin: No erythema or vesicular lesions Neurologic: Mental Status: AAO to person, place, time, able to provide detailed history and answer questions appropriately Language and speech: normal for naming, repetition and fluency, No dysarthria Cranial nerves Visual fields full to finger confrontation, Pupils are round and reactive bilaterally, EOMI, No facial asymmetry, Sensation is intact to touch in V1-V3 distribution bl, Hearing is intact to voice, moves head bl direction without difficulty Motor: Moves all extremities spontaneously. Able to raise both arms and hold antigravity for 10s. Able to raise both legs and hold antigravity for 5s. L leg drift No abnormal movement noticed today. Appropriate muscle bulk and tone for age. Sensation: intact to touch in bl UE and LE Coordination: intact for finger to nose Gait: Deferred for safety Laboratory, Imaging and Studies: Lab Results: 30-APR 05:01 WBC 4.2 HGB 12.1 HCT 35.8 PLT 253 PMN 50 Lymph 34 Mono 8 Eos 7 Baso 1 Na 142 K 3.9 Cl 106 CO2 27 BUN 15 Cr 0.7 CrCl 52.94 AG 9 Glu 87 Ca 8.8 Mg 1.9 ALT 7 AST 13 AlkPhos 58 TBili 0.5 TP 7.0 Alb 3.8 29-APR 15:23 WBC 4.6 HGB 12.6 HCT 37.6 PLT 259 PMN 58 Lymph 27 Mono 9 Eos 5 Baso 1 Na 141 K 4.0 Cl 104 CO2 30 BUN 20 Cr 0.8 AG 7 Glu 95 Ca 9.2 Mg 2.0 ALT 9 AST 15 AlkPhos 62 TBili 0.3 TP 7.0 Alb 4.1 Troponin-HS 5.6 Imaging Results: XR Chest 1 View Performed By/Author: MD, on 29 APR 2022 17:03 PDT IMPRESSION: No acute disease. CTA Head/Neck w/+ w/o IV Con Performed By/Author: MD, on 29 APR 2022 17:27 PDT IMPRESSION: No acute abnormality. These findings were discussed with Dr. on 4/29/2022 17:35 PM. This exam was performed using dose optimization techniques including automated exposure control, adjustment of mA and/or kV according to patient size, and/or iterative reconstruction. MRI Brain w/o Contrast Performed By/Author: MD, on 29 APR 2022 19:43 PDT IMPRESSION: Small acute right periventricular infarct. Studies: ECG- 12 Lead April 29, 2022 15:24 PDT * Preliminary Report * IMPRESSION: Normal sinus rhythm.Left axis deviation.Left bundle branch block.Abnormal ECG.When compared with ECG of 04-SEP-2021 11:43,.No significant change was found.. PRELIM RESULT Assessment and Plan 81-year-old female with history of Sjogren's disease, lupus, TIA, hypertension, and hyperlipidemia presents with weakness. SS 1. MRI brain shows small acute Right periventricular infarct. CTA head/neck shows no LVO. Diagnosis acute CVA. Etiology small vessel disease given location. Recommendations: - TTE w/ bubble - Telemetry while inpatient - PT/OT/SLP - Antiplatelet: Aspirin 81mg PO daily , Plus Plavix 75 mg daily for 21 days - Anticoagulation: no known indication - HTN: long-term goal normotension, outside the window for permissive HTN - HLD: high-intensity statin for goal LDL <70 - DM: A1C goal <6.5 Teleneurology will sign off Please call for any neurological question/concern. Thank you for your consult Patient/family express understanding and agree with plan. DO
Aktuelle Erkrankungen: Past medical history: allergic rhinitis, Sjogren's, DJD, Glaucoma, TIA 2009, 6/19, 4/20, leukopenia, recurrent shingles 10/2016, depression, LBP
Vorgeschichte: Sjogren's, Mild HTN, AR, LBP
Andere Medikamente: Medications: xalatan, nasonex-not using. ASA 81mg/d, crestor 5mg, norvasc 2.5mg/d. pilocarpine, refresh eye drops
Allergien: Allergies: quinolones-vomitting, immuran, diarrhea-?plavix, sertraline-diarrhea
Vorherige Impfungen: Moderna COVID vax, 8/19/21, age 81, fever and malaise x 24hrs

VAERS 2189978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

kritisch

Staat: CT
Alter: 55,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 17.03.2022
Beginn: 18.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Angiocardiogram Fibrin D dimer increased Pulmonary embolism

Symptomtext

Pulmonary embolus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: elevated d-dimer, CTA DONE ON 3/21/22
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None
Allergien: Platinum, micronized progesterone, phenobarbital
Vorherige Impfungen: -

VAERS 2642445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 08.06.2023
Impfdatum: 23.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Arthralgia Burning sensation Decreased appetite Dizziness Fatigue Hyposmia Interchange of vaccine products Menstruation delayed Menstruation irregular Migraine Myalgia Nausea Post-acute COVID-19 syndrome SARS-CoV-2 test Syncope Vision blurred

Symptomtext

fainted in shower; Interchange of vaccine products; may have "long- covid"; migraines; diminished smell continues; fatigue; nausea; joint pains; burning sensation legs/arms; muscle pains; dizziness; blurry vision; loss of appetite; menstrual irregularities- delay/ early; menstrual irregularities- delay/ early; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 42-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Jul2022 as dose 4 (booster), single (Lot number: FJ4991) for covid-19 immunisation. The patient's relevant medical history included: "endometriosis" (unspecified if ongoing); "severe varicose veins with treatment" (unspecified if ongoing); "bell's palsy" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Moderna covid-19 vaccine (DOSE 1, SINGLE, happened after receiving each vaccine and is occurring now.), administration date: Feb2021, when the patient was 41 years old, for COVID-19 immunization, reaction(s): "diminished smell continues", "joint pains", "burning sensation legs/arms", "burning sensation legs/arms", "loss of appetite", "dizziness", "fatigue", "menstrual irregularities- delay/ early", "migraines", "muscle pains", "nausea", "fainted in shower", "blurry vision"; Moderna covid-19 vaccine (DOSE 2, SINGLE, happened after receiving each vaccine and is occurring now.), administration date: Feb2021, when the patient was 41 years old, for COVID-19 immunization, reaction(s): "fainted in shower"; Moderna covid-19 vaccine (DOSE 2, SINGLE, happened after receiving each vaccine and is occurring now.), administration date: Mar2021, when the patient was 41 years old, for COVID-19 immunization, reaction(s): "diminished smell continues", "joint pains", "burning sensation legs/arms", "burning sensation legs/arms", "loss of appetite", "dizziness", "fatigue", "menstrual irregularities- delay/ early", "migraines", "muscle pains", "nausea", "blurry vision"; Moderna covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE, happened after receiving each vaccine and is occurring now.), administration date: Oct2021, when the patient was 42 years old, for COVID-19 immunization, reaction(s): "diminished smell continues", "joint pains", "burning sensation legs/arms", "burning sensation legs/arms", "dizziness", "fatigue", "migraines", "muscle pains", "nausea", "fainted in shower", "blurry vision"; Moderna covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE, happened after receiving each vaccine and is occurring now.), administration date: Feb2021, when the patient was 41 years old, for COVID-19 immunization, reaction(s): "loss of appetite"; Moderna covid-19 vaccine (DOSE 1, SINGLE, happened after receiving each vaccine and is occurring now.), administration date: Oct2021, when the patient was 42 years old, for COVID-19 immunization, reaction(s): "menstrual irregularities- delay/ early". The following information was reported: SYNCOPE (medically significant), outcome "not recovered", described as "fainted in shower"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown"; POST-ACUTE COVID-19 SYNDROME (non-serious), outcome "not recovered", described as "may have "long- covid""; MIGRAINE (non-serious), outcome "not recovered", described as "migraines"; HYPOSMIA (non-serious), outcome "not recovered", described as "diminished smell continues"; FATIGUE (non-serious), outcome "not recovered"; NAUSEA (non-serious), outcome "not recovered"; ARTHRALGIA (non-serious), outcome "not recovered", described as "joint pains"; BURNING SENSATION (non-serious), outcome "not recovered", described as "burning sensation legs/arms"; MYALGIA (non-serious), outcome "not recovered", described as "muscle pains"; DIZZINESS (non-serious), outcome "not recovered"; VISION BLURRED (non-serious), outcome "not recovered", described as "blurry vision"; DECREASED APPETITE (non-serious), outcome "not recovered", described as "loss of appetite"; MENSTRUATION IRREGULAR (non-serious), MENSTRUATION DELAYED (non-serious), outcome "not recovered" and all described as "menstrual irregularities- delay/ early". The events "fainted in shower", "may have "long- covid"", "migraines", "diminished smell continues", "fatigue", "nausea", "joint pains", "burning sensation legs/arms", "muscle pains", "dizziness", "blurry vision", "loss of appetite" and "menstrual irregularities- delay/ early" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: If covid tested post vaccination: Yes. It was unknown if therapeutic measures were taken as a result of syncope, post-acute covid-19 syndrome, migraine, hyposmia, fatigue, nausea, arthralgia, burning sensation, myalgia, dizziness, vision blurred, decreased appetite, menstruation irregular, menstruation delayed. Clinical course: Reported on 04Jun2023 that second covid booster (4th covid vaccine dose) was Pfizer's. All other doses (3) were Moderna. The patient got Covid in early Apr2023. Nowfelt they may have "long- covid" as they are experiencing migraines, diminished smell continues, fatigue, nausea, joint pains, burning sensation legs/arms, muscle pains, dizziness/blurry vision, fainted in shower, loss of appetite, menstrual irregularities- delay/ early - indicates these irregularities happened after receiving each vaccine and was occurring now. The patient seek medical care by primary physician. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Positive ; Comments: If covid tested post vaccination: Yes
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bell's palsy; Endometriosis; Varicose veins
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2578702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: VA
Alter: 20,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: -
Beginn: 11.09.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

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

Anxiety Depression Fatigue Ischaemic stroke

Symptomtext

On 9/11/2022 I experience an ischemic stroke after receiving my booster shot for covid-19. I received the Pfizer shot for all 3 doses. I was lucky enough to not suffer any long term deficits, however, I now have to live with extreme fatigue, anxiety and depression due to the stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No alcohol use, smoking, pregnancy, or drug use.
Vorgeschichte: PFO(patent formen ovale)
Andere Medikamente: Plavix
Allergien: Carrots, peaches, cherries, pollen, apples
Vorherige Impfungen: -

VAERS 2518038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FJ4991

schwer

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 19.07.2022
Beginn: 02.11.2022
Tage bis Beginn: 106,0
Dosis: 4
Route/Site: - / -

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

Angiogram abnormal Anxiety Blood culture positive COVID-19 Chest pain Cholecystitis Cholecystostomy Computerised tomogram abdomen abnormal Condition aggravated Duodenal ulcer Dyspnoea Dyspnoea exertional Electrocardiogram QT prolonged Endotracheal intubation Enterococcus test positive Extubation Gastric ulcer Gastric ulcer haemorrhage

Symptomtext

Admit Date: 11/2/2022 5:13 PM Discharge Date: 11/20/2022 COVID positive Date 11/2/2022 Admitting Physician: DO Attending Physician: MD, Discharge Clinician: MD, Primary Care Provider at Discharge: MD Hospital Course: Patient is a 86 y.o. male HTN, HLD, adult acne on intermittent doxycyline therapy presented to emergency room complaining of worsening shortness of breath and dyspnea on exertion for 2 days. Patient also had nausea, and poor oral intake besides moderate sharp substernal chest pain noted while walking in hardware store 2 days ago. Denies active chest pain. Patient found to be hypoxic desaturating to the 80s while ambulating. Patient tested positive for COVID. Patient was continued on respiratory isolation. Patient was started on dexamethasone and remdesivir. Infectious diseases recommended discontinuing dexamethasone and remdesivir due to low cycle threshold (of 36). Patient had persistent positive blood cultures with Enterococcus and Klebsiella bacteremia. Patient was initially placed on IV vancomycin and IV Zosyn. After sensitivities were available patient was transitioned to IV Zosyn. Repeat blood cultures remained negative. CT scan of the abdomen showed cholecystitis with possible perforation and abscess. IR was consulted and placed image guided cholecystostomy drain. Patient was taking aspirin 650 mg daily along with naproxen for back pain. Patient developed multiple bloody bowel movements overnight. CT angiogram was positive for active extravasation of contrast into the gastric body. Gastroenterology performed EGD which found gastric and duodenal ulcers which were treated. Gastroenterology team recommended IV Protonix for 72 hours. Patient also had thrombocytopenia for which she received 2 units of platelets. Developed acute drop in hemoglobin down to 5.4. Patient was transferred to intensive care unit. He was given 6 units of PRBC, 1 unit of FFP and 1 unit of platelets. He was intubated and EGD was performed. EGD showed actively bleeding gastric ulcer and ulcer was treated with clips and epinephrine. After intubation, the patient was hypotensive and started on pressors. He was extubated after EGD. The patient has been off pressors since 11/13/22. His course was complicated by anxiety and HTN. His home blood pressure medications have been resumed. The patient was transferred out of the ICU to the hospitalist service on 11/15/2022. Patient's hemoglobin remained stable after transfer out of intensive care unit. Patient was continued on IV Zosyn. Patient had elevated QTC interval. Repeat EKG with improvement in QTC. Infectious diseases recommended transitioning patient to oral Cipro and Augmentin to finish total 6 weeks of antibiotics until December 17th, 2022. Patient will need Infectious diseases follow-up in 2-4 weeks. Patient complained of mild diarrhea on antibiotics which resolved by itself. Patient had elevated blood pressures and continued to have high blood pressure despite increasing losartan. Patient was continued on metoprolol. Hydralazine was added for better blood pressure control. Patient was discharged to Subacute rehab in stable condition as recommended by therapy.

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Praegender Schweregrund: Intensive care
Hospital-Tage: 18,0
Labordaten: -
Aktuelle Erkrankungen: office visit Visit Diagnoses Shortness of breath - Primary Slurred speech Abnormal gait HPI: Patient is a 86 y.o. man presenting with new onset of shortness of breath, chest pain, change in speech, and change in ability to ambulate; he called into the office and was scheduled for an acute 15 min appointment; In the office today he has slightly slurred speech and reports, "I did have some chest pain but its not as bad but it reminds of me when I had my pericarditis a couple of years ago" He tested negative for Covid; the shortness of breath began abruptly on Monday after he attended physical therapy. Due to patient's acute change from baseline I cannot rule out a stroke and I believe stat CT of head is indicated. Additionally, I think he needs to have troponin level drawn due to chest pain along with stat chest xray and ekg. Notified the transfer center of patient's impending arrival. They agreeable to plan. Follow up instructions: Discussed all diagnoses, treatments, and recommendations with patient. Patient exhibited full understanding off plan. All answers and questions were answered prior to discharge
Vorgeschichte: Essential hypertension High cholesterol Glaucoma Bacteremia due to Enterococcus faecium and Klebsiella pneumoniae secondary to cholecystitis and possible liver abscess Acute respiratory failure with hypoxia (HCC) Acute cholecystitis Hypomagnesemia Gastrointestinal hemorrhage associated with gastric ulcer Acute blood loss anemia Diarrhea Chronic back pain Hypokalemia Physical deconditioning Allergic rhinitis Osteoarthritis IFG (impaired fasting glucose) Failed back syndrome of lumbar spine Controlled type 2 diabetes mellitus without complication, without long-term current use of insulin (HCC) Facial droop Demand ischemia (HCC) Electrolyte abnormality Pain Rash Gastric ulcer Macular degeneration
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet Brimonidine Tartrate-Timolol (COMBIGAN) 0.2-0.5 % SOLN cal
Allergien: Statins
Vorherige Impfungen: -

VAERS 2513068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: WI
Alter: 89,0
Geschlecht: M
Eingang: 21.11.2022
Impfdatum: 25.08.2022
Beginn: 07.11.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: UN / UN

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

Asthenia Bladder catheterisation Brain natriuretic peptide increased COVID-19 Chest X-ray abnormal Cough Culture urine negative Echocardiogram Haemorrhage urinary tract Laboratory test Malaise Oropharyngeal pain Pulmonary congestion Pulmonary oedema Respiratory tract congestion SARS-CoV-2 test positive Urine analysis abnormal

Symptomtext

Information provided in this adverse event note, is per web report received by Regulatory Authority from submitting facility. Covid-19 vaccination information is provided by information that is in Regulatory Authority Immunization Registry. PER WEB REPORT received: ?Hospitalized 11/7/2022 presented with increased weakness for the past 1 to 2 days. Associated symptoms included chest congestion, throat soreness, nonproductive cough. He denies any associated headaches, dizziness or lightheadedness, fever or chills, sinus congestion or runny nose, chest pain or shortness of breath or palpitations, nausea or vomiting, stomach pain, urinary symptoms, diarrhea, or increased leg swelling. Patient?s chest x-ray does show vascular congestion and mild interstitial edema. However, patient overall did not appear to be fluid overloaded. BNP mildly elevated at 721, though without available reference to compare. I suspect that this value is elevated at his baseline. Blood pressure overall well controlled at home, per wife. It is possible that recent COVID-19 infection may be causing increased cardiac stress. Patient positive for COVID-19 (vaccinated x4) [Janssen 3/19/2021 1805031 / public; Pfizer 11/30/21 FH8027; Pfizer tris 12+ 4/21/2022 (lot number not available in IR); Pfizer tris+ 8/25/2022 FJ4991] Symptom onset 11/5/2022. Weakness is likely secondary to COVID infection. He has not required any oxygen in the hospital and vital signs are very stable. Does not appear to be a good candidate for steroids at this time. Patient had episode of urine with some bloody clots in it. However today Foley bag had no evidence of blood or clots in it. Patient denies any urinary symptoms, UA did show some blood but culture was not indicated, unlikely that this is UTI.?

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Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: Chest X-ray, Lab work, Echo Cardiogram
Aktuelle Erkrankungen: unknown
Vorgeschichte: CAD s/p multiple stent placement procedures, HTN, Hyperlipidemia, Heart block s/p pacemaker
Andere Medikamente: unknown
Allergien: it is not known if this patient has any allergies
Vorherige Impfungen: -

VAERS 2490107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FJ4991

schwer

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
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 Dyspnoea Injection site erythema Injection site swelling Pallor Throat tightness Vomiting

Symptomtext

Anaphylactic type reaction requiring Epipen. Shortness of breath, closure of airways, vomiting, pale face, redness and swelling at injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Previously J&J vaccine, reaction was redness and swelling and rash at injection site but no SOB

VAERS 2480452

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 05.04.2022
Beginn: 18.09.2022
Tage bis Beginn: 166,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Chest X-ray normal Illness Loss of consciousness Malaise Oxygen saturation decreased Syncope

Symptomtext

I experienced COVID-19 after my vaccine. I had PAXLOVID. I caught Covid on a trip I took. I went to urgent care three times to get chest x-ray because my oxygen level were so low. I felt very ill. I also fainted and passed out. The third time I went to the ER is because I needed albuterol which helped me a lot. This is the sickness I ever been in my life and I am still not very well.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Chest x-ray; negative.
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis
Andere Medikamente: Vitamins
Allergien: Dairy; iodine; contrast dye; antibiotics
Vorherige Impfungen: With Moderna second vaccine, had severe dizziness and that is why I switched to Pfizer for the third shot.

VAERS 2464930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: -
Alter: 25,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 21.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Anticoagulant therapy Antinuclear antibody positive Arthralgia Chest pain Choking sensation Computerised tomogram Deep vein thrombosis Dizziness Dyspnoea Electrocardiogram T wave abnormal Electrocardiogram ambulatory abnormal Fibrin D dimer increased Heart rate irregular Hepatic enzyme increased Hypoaesthesia Laboratory test Limb mass Malaise

Symptomtext

06/21/22 - Day of second dose. Within the first 15 minutes I felt dizzy and unwell. The pharmacist handed me a bottle of water and I waited an additional 15 minutes. Afterward I felt safe to go home. Later that day I went to the ER with chest pain. I had a normal EKG and was sent home. 06/23/22 - The chest pain was worse and I also felt short of breath. I went to an ER and was given Ibuprofen 800 after they determined I wasn't having an emergency via EKG and CT scan following an elevated d-dimer. Around this time I noticed a small palpable mass behind my left knee. 07/07/22 - Concerning chest pain, ER, sent home after an unremarkable x-ray. 07/12/22 - First appointment with new PCP. I'm referred to a cardiologist. 07/14/22 - Fasting labs. Unremarkable aside from mildly elevated liver enzymes. 07/21/22 - Chest and pain, bounding pulse, ER, kept overnight after they found elevated troponin. EKG was also abnormal, nonspecific t wave abnormality. 07/22/22 - Cardiology consult. EKG was borderline, I was never given a copy so I don't remember the specifics. 08/08/22 - Normal stress echo. Given a Holler monitor to wear for two weeks. No abnormal findings other than PVCs. I was never given the exact amount and don?t have access to the data. Late August I noticed pain in my left knee. 09/02/22 - I was diagnosed with a DVT. I was given Xarelto, 15mg to take twice a day for 21 days. 09/03/22 - Hospitalized after complaints of chest pain that differed from my usual and tachycardia. They did not find anything immediately concerning and I was released the next afternoon. 09/14/22 - Met with PCP. Referred to hematologist. 09/21/22 - Hematologist took labs, concerned about possible autoimmunity. As of 09/29/22 I have access to a few of the results. My ANA is 1:320, homogenous. I?ll know more 10/05/22, my next appointment. All of the symptoms I can remember: chest pain, shortness of breath, erratic heart rate that would dramatically change when I?d move around even slightly, random episodes of tachycardia, PVCs, stabbing pains and numbness in my extremities, increased vein visibility, a throat sensation that felt like being choked, inability to breathe deeply. As of 09/29/22 my remaining symptoms are PVCs and occasional cold/numb extremities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: 07/14/22 - Elevated liver enzymes 07/21/22 - Elevated troponin, abnormal EKG - nonspecific t wave abnormality 08/08/22 - Two week Holter monitor shows PVCs 09/02/22 - DVT 09/21/22 - Positive ANA, 1:320 Homogenous
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2433709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FJ4991

schwer

Staat: FL
Alter: 60,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 20.07.2022
Beginn: 24.07.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Computerised tomogram Electromyogram Fall Gait inability Guillain-Barre syndrome Hypoaesthesia Immediate post-injection reaction Limb discomfort Magnetic resonance imaging Mobility decreased Monoplegia Paraesthesia Peroneal nerve palsy Pyrexia Sleep disorder Walking aid user

Symptomtext

It started fever imidiatley after vaccine, and 4 days later I woke ip at 4 in the morning and my body was just numb, When I went to pull my legs over the side of the bed I just fell straight to the floor. I had to crawl to my roommates door and can barely knot on his door for help. EMS picked me up My right leg feels like a bag of cement and pins and needles but my left leg is totally paralized and now have dropped foot. Physical therapy gave a drop foot support and can use a walker. I am trying to use a cane but I can't use a cane that well. I'm waiting to see if i can get IgG injection done. I was admitted to the Clinic. on 7/24/22 to 8/22/22 and diagnosed there by Dr. with GBS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 28,0
Labordaten: EMG test, Blood work, MRI, CT scan all done while I was admitted at the Clinic
Aktuelle Erkrankungen: NO
Vorgeschichte: Chronic Migranes, PTSD, Depression, FIbromyalgia, Hypothyroid
Andere Medikamente: Duloxitin, Cympalta, Sumatriptan, Levothyroxin, Gabapentin
Allergien: NO
Vorherige Impfungen: flu shot malase and my arm would hurt

VAERS 2428705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: NJ
Alter: 66,0
Geschlecht: F
Eingang: 04.09.2022
Impfdatum: 01.05.2022
Beginn: 20.05.2022
Tage bis Beginn: 19,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Cardiac stress test Chest X-ray Echocardiogram Pericardial effusion Pericarditis

Symptomtext

Developed pericarditis June 4, 2022 . Was hospitalized after fluid was found around my heart .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Stress test, chest X-ray, blood work, echo cardio gram. May 24, 2022-June 6, 2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Synthroid, calcium d3, estrace
Allergien: Peanuts, Avalon, penicillin
Vorherige Impfungen: -

VAERS 2412859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: PA
Alter: 17,0
Geschlecht: F
Eingang: 16.08.2022
Impfdatum: 16.08.2022
Beginn: 16.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Altered state of consciousness Dry mouth Erythema Eye movement disorder Head titubation Presyncope

Symptomtext

AFTER GIVING THE SHOT, WHILE EXPLAINING THE AFTER CARE TO THE PATIENT AND HER MOM, (WHO WAS PRESENT IN THE CONSULTATION ROOM), WE NOTICED THE PATIENT WAS ABOUT TO PASS OUT. HER HEAD STARTED FALLING TO ONE SIDE, HER EYES ROLLED UP AND HER HEAD WENT BACK. HER FACE AND NECK COLOR TURNED RED . WE HELD AN ICE PACK TO HER NECK AND FOREHEAD , RAISED HER LEGS WITH AN ADDITIONAL CHAIR WHILE SUPPORTING HER HEAD AND BACK (RESTING IN THE CHAIR WHERE THE VACCINE WAS GIVEN). ONE RX TECH CALLED FOR MEDICAL HELP. THE PATIENT WAS IN AND OUT OF CONSCIOUSNESS, HER MOUTH WAS DRY. SHE NODDED HER HEAD FOR SOME WATER WHICH SHE TOOK SIPS OF IN BETWEEN TAKING DEEP BREATHS, IN THE MEANTIME THE PARAMEDICS ARRIVED AND SPOKE TO HER TO FIGURE OUT HER CONDITION AND HOW IT HAPPENED. SHE WAS THEN TRANSPORTED VIA AN AMBULANCE TO THE ER OF THE LOCAL HOSPITAL WHERE SHE WAS GIVEN FURTHER CARE. IN ABOUT AN HOUR AND HALF, WE CHECKED WITH HER MOM WHO CONFIRMED THAT SHE WAS DOING MUCH BETTER AND HER COLOR WAS BACK

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: UNKNOWN OR NOT RELEASED BY MEDICAL STAFF AT HOSPITAL
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: BIRTH CONTROL TABLETS
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 2404084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: GA
Alter: 43,0
Geschlecht: F
Eingang: 07.08.2022
Impfdatum: 07.08.2022
Beginn: 07.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Feeling cold Paraesthesia Seizure Thirst

Symptomtext

Approximately 15 minutes after the patient received her vaccination, she complained of feeling thirsty, cold, and tingly all over. She had no difficulty breathing, loss of consciousness, or hives. I spoke with her and asked if she wanted me to call the ambulance and she stated no because she wanted to wait to see if she would feel better after drinking a bottle of water. I contacted Pfizer customer service number to see if they had any advice but the agent stated that Pfizer's medical reporting line is only open Monday thru Friday from 8-9pm. Minutes later the patient began having convulsions and we immediately contacted the emergency number and they came to the store to provide further medical treatment. It took approximately 45 minutes before the patient was transported to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No other illnesses reported
Vorgeschichte: None
Andere Medikamente: Patient is not taking any medications.
Allergien: No know allergies
Vorherige Impfungen: -

VAERS 2630860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: CO
Alter: 16,0
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fall Loss of consciousness Pallor

Symptomtext

Patient was given vaccine (Pfizer Biotech) around 1:00 pm on 07/29/2022, got up from chair and stood for a moment. Patient turned pale, blacked out and feel forward. Patient quickly come to and in 15 mins was back to normal

Weitere VAERSDATA-Felder

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

VAERS 2388799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Loss of consciousness Syncope Tonic clonic movements

Symptomtext

PT HAD SYNCOPE ~10 MIN AFTER VACCINATION. TEMPORARY LOSS OF CONSCIOUSNESS, TONIC-CLONIC ARM MOVEMENTS FOR ~5-10 SECONDS. PT REGAINED CONSCIOUSNESS ABOUT 30-60 SECONDS AFTER ONSET.

Weitere VAERSDATA-Felder

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

VAERS 2388213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: FL
Alter: 13,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fall Head injury Limb injury Loss of consciousness Nervousness

Symptomtext

Patient received vaccine with her siblings. No history of dizziness or fainting previously. She went to join her siblings while mother asked about how long they should wait, and while we spoke child passed-out and fell into a fixture. Mother indicated she herself has a history of dizziness, fainting with needles but had not indicated child ever experienced this though she said she had been nervous earlier about getting vaccine. Pharmacist examined child because child hit her leg and head on a fixture as she fell, but no cuts or anything are visible. No medical attention has been sought as of this point in time.

Weitere VAERSDATA-Felder

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

VAERS 2364141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

schwer

Staat: OH
Alter: 26,0
Geschlecht: M
Eingang: 10.07.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling hot Loss of consciousness

Symptomtext

After administerigng the vaccine, the patient sat in the waiting area. After about 5 minutes, the patient passed out on the floor. The pharmacist went to assist the patient. The patient felt like they were hot and light headed. The pharmacist checked the temperature of the patient and it was fine. The pharmacist asked for assistance from a technician and checked the patient's blood pressure. The patient was asked to move to the floor to prevent further falls, but did not want to. The patient's blood pressure was checked every 3 minutes for approximately 45 minutes. The patient was feeling better at that point and said they wanted to leave.

Weitere VAERSDATA-Felder

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

VAERS 2359814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: -
Alter: 12,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 05.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Back pain Nausea Pain in extremity Presyncope Pyrexia

Symptomtext

Sore arm started with in 1 hour of dose. The next morning there was a Low grade fever, wave of nausea, sore lower back, weak, and almost fainted.

Weitere VAERSDATA-Felder

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

VAERS 2356858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

schwer

Staat: IL
Alter: 39,0
Geschlecht: M
Eingang: 03.07.2022
Impfdatum: 03.07.2022
Beginn: 03.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Hyperhidrosis Pallor Syncope

Symptomtext

Patient state he felt dizzy about five minutes after the shot. He collapsed but didnt lose consciousness. When he sat up he was very pale and sweating. We had him sit with his feet up and gave him a glass of water. After about 10 minutes his color returned and he said he felt better and left with his wife

Weitere VAERSDATA-Felder

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

VAERS 2335354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: TN
Alter: 14,0
Geschlecht: M
Eingang: 25.06.2022
Impfdatum: 25.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Presyncope Vaccination site haemorrhage

Symptomtext

Upon vaccine administration, patient began to bleed a good amount. Vaccine administrator cleaned up his arm and then he appeared to have a vasovagal response. Patient sat back down in chair, his dad lifted his legs to help the blood flow to his head. We provided cold water, and pharmacist applied a cool/damp paper towel to his forehead. Patient's dad periodically checked his pulse manually and we both monitored to be sure his condition improved. After about 15 or 20 minutes, patient was feeling better. We gave another bottle of cold water and he and his dad sat in the waiting area for 5 or 10 more minutes. Patient was able to walk out of the store afterward and seemed to be just fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no known illnesses
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no known medication allergies
Vorherige Impfungen: -

VAERS 2322423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: MS
Alter: 17,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 16.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal discomfort Feeling hot Pallor Syncope Vision blurred

Symptomtext

Two minutes after I gave patient her vaccine, she fainted. Her mother and brother caught and sat her in the chair. Patient became alert as she sat in the chair. Then patient became pale in the face and hot, so her brother bought her some water to drink and place bottle on her head to keep cool. Patient then began to have blurry vision and upset stomach. I called the ambulance. After the ambulance checked on her, mother said that patient was okay and she was taking her to the doctor.

Weitere VAERSDATA-Felder

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

VAERS 2314396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: WY
Alter: 28,0
Geschlecht: M
Eingang: 09.06.2022
Impfdatum: 08.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea Erythema Eye movement disorder Fall Feeling abnormal Head injury Loss of consciousness Stridor Swelling Syncope

Symptomtext

The patient was given his first dose of the vaccine around 5:07. Afterwards, he came out of the waiting room to the front of the pharmacy counter and said he feels weird. The patient then collapsed and hit his head. I responded to his side and he came to. Very shortley after, his eyes rolled back into his head. He was turning read, and had significant buldging in his neck. His breathing was very labored and making a strider like noise. I adminstered an epi-pen at 5:09 pm into his right outer thigh and he immediately started breathing and coming to. He remained stable until EMS arrived and was transported to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None to my knowledge.
Vorgeschichte: None to my knowledge.
Andere Medikamente: None to my knowledge.
Allergien: Allergies to mangos but not disclosed until after the fact.
Vorherige Impfungen: -

VAERS 2310723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 06.06.2022
Impfdatum: 04.05.2022
Beginn: 30.05.2022
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: SYR / RA

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

Anticoagulant therapy Deep vein thrombosis Dyspnoea Dyspnoea exertional Hypersensitivity Pain in extremity Thrombosis Ultrasound Doppler abnormal

Symptomtext

On May 19th, went for my typical job of about 3 miles. I barely got 1/2 mile and was completely out of breath and could only go 1-2 blocks thereafter with needing a break to barely get home. Then on Monday May 30th, woke up at 5am with a deep calf pain. It wasnt a cramp or strain or pull from prior exercises; it felt very different. Monitored rest of Monday, Tuesday seemed to lesson a little but came back in the evening and kept me up most of the night with constant pain. Went to urgent care on Wednesday June 1st. Received an ultrasound that determined I had a blood clot in my right calf. It was 5cm and by Friday for my 2nd ultrasound, grown to 14cm. I have been put on Xarelto 15mg, 2x/day for next 3 weeks then going to 20mg, 1x/day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: 1. June 1st @ 6pm - ultrasound of the right calf. Results: acute DVT - 5cm nonobstructing clot in the gastrocnemius vein. 2. June 3rd @ 12N - ultrasound of the right calf. Results: Thrombus within the peroneal vein now measuring up to 14cm in length.
Aktuelle Erkrankungen: None or just common outdoor allergies
Vorgeschichte: None
Andere Medikamente: Omaprozale: 40mg Flonase for allergies
Allergien: None
Vorherige Impfungen: -

VAERS 2309688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: PA
Alter: 33,0
Geschlecht: M
Eingang: 05.06.2022
Impfdatum: 08.05.2022
Beginn: 08.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling hot Hot flush Loss of consciousness Malaise Nausea

Symptomtext

In the first 10 minutes after vaccine, patient began feeling ill. He complained of nausea and feeling hot and flushed. He did briefly loose consciousness for less than one minute. We did call 911 or EMS to be safe. They decided to dispatch an ambulance from Hospital. Instructed me to monitor the patient for any changes and not to let him eat or drink anything. When EMS arrived the patient was feeling better. He never had trouble breathing or tongue swelling. The EMS agents spoke with the patient and decided he did not have a reaction that required their services and he refused their care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None that I am aware of.
Aktuelle Erkrankungen: -
Vorgeschichte: None listed.
Andere Medikamente: None reported.
Allergien: NKA
Vorherige Impfungen: -

VAERS 2296527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: WA
Alter: 17,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 25.05.2022
Beginn: 25.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Lacrimation increased Loss of consciousness Nausea Vomiting

Symptomtext

Patient was accompanied by her mother to come receive Pfizer booster #1. After immunization, patient and mom were sitting in observation when mom asked for the bathroom because the patient was feeling nauseous and might throw up. As mom walked the patient toward the bathroom away from pharmacy department, the patient started to slouch, and I ran over to help because she looked like she was about the pass out. Mom and I lowered her to the floor next to meat department. Mom had a sports drink ready for her to sip as she quickly regained consciousness. The patient then vomited onto the floor. We provided paper towels, cleaning wipes and trash to help with clean up. Mom informed me the patient has history of syncope/NV with shots and blood draw. Mom was very calm and prepared for the incident. I let her know they both handled the situation well but, in the future, please feel free to request to stay inside our vaccine room for private observation as the patient was clearly embarrassed and was teary. Later that day Mom posted on the social media page that she felt the store associates handled the patient's incident with support and kindness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NO
Vorherige Impfungen: -

VAERS 2277735

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

schwer

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 14.05.2022
Impfdatum: 14.05.2022
Beginn: 14.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fasting Hypotension Syncope

Symptomtext

patient fainted 10 min after shot. paramedics were called. bp was low at 80. father stated patient has been in fasting state since last nite. systolic went up to 110 and patient refused transport to hospital

Weitere VAERSDATA-Felder

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

VAERS 2276426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: NC
Alter: 37,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 09.05.2022
Beginn: 12.05.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LL

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

Fatigue Insomnia Menstruation irregular Pain Thrombosis

Symptomtext

Fatigue, mild body aches, trouble sleeping, light menstrual bleeding with blood clots 10 days prior to end of birth control and expected start of menstrual cycle

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Junel fe, daily, Iron, every 2 days, Loratadine, daily, Levalbuterol, as needed
Allergien: N/A
Vorherige Impfungen: -

VAERS 2273350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: GA
Alter: 15,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 12.05.2022
Beginn: 12.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness Pallor

Symptomtext

PATIENT GOT UP TO LEAVE AND PASSED OUT. CAREGIVER CAUGHT HER. SHE WAS PALE AND SAID SHE FELT WHOOZY. SHE WAS GIVEN WATER AND A POPSICLE AND PROPPED HER FEET UP. SHE REMAINED IN THE PHARMACY FOR 15 ADDITIONAL MINUTES.

Weitere VAERSDATA-Felder

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

VAERS 2267043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: NH
Alter: 89,0
Geschlecht: M
Eingang: 07.05.2022
Impfdatum: 03.05.2022
Beginn: 07.05.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / -

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

Angiocardiogram Angiogram Angiogram cerebral Facial paralysis Full blood count Metabolic function test Speech disorder

Symptomtext

4 days after vaccination, developed TIA symptoms of difficulty speaking and left sided facial droop

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: All initial imaging and labs done on ED visit 5/7/2022. CT Angiogram head and neck, chest CT, BMP, CBC
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, pulmonary fibrosis
Andere Medikamente: Aspirin 81mg Daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 2263968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

schwer

Staat: NY
Alter: 73,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 04.05.2022
Beginn: 04.05.2022
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 Disorientation Ear pain Facial pain Fatigue Headache Influenza like illness Loss of consciousness Myalgia Pain Pyrexia

Symptomtext

Patient complained of fatigue, body aches, and other flu-like symptoms starting about 12 hours after vaccination. The following day (5/1), the patient states she passed out for 12 hours, had pain that was severe and radiated throughout the head, ear, and face. Full body muscle aches so severe in the back, the patient worried it may have been her kidneys. Also experienced a fever. The patient thought about going to the hospital, but did not. Starting 5/2, patient was experiencing some disorientation and issues with hand coordination. Fatigue and muscle aches continue, but less severe, same with the pain.

Weitere VAERSDATA-Felder

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

VAERS 2259975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: GA
Alter: 31,0
Geschlecht: M
Eingang: 01.05.2022
Impfdatum: 12.04.2022
Beginn: 30.04.2022
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: SYR / LA

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

Bell's palsy

Symptomtext

Bell's Palsy, developed less than three weeks after administration, currently ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known
Vorgeschichte: High blood pressure
Andere Medikamente: Wellbutrin, Methoprolol, Melatonin
Allergien: None known
Vorherige Impfungen: -

VAERS 2254612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 01.04.2022
Beginn: 02.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blood culture Blood test Chest X-ray Chills Decreased appetite Fear Feeling abnormal Feeling cold Hypotension Impaired driving ability Loss of consciousness Loss of personal independence in daily activities Pain Pyrexia Vomiting

Symptomtext

A severe reaction of a fever in the following afternoon, so cold-teeth chattered, every cell in the body ached, temperature of 103.9, vomiting, after 6 days blood pressure was so low 77/55 she was blacking out, urged to go to emergency, severe brain fog, now every afternoon around 3pm her temperature is elevated and has been consistent since she had the booster shot. The fever is the same as when she was diagnosed with Latent Tuberculosis in 2011. Brain fog is so severe she cannot drive, fix a meal or handle bills or take a shower for fear of fainting. She has no appetite.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Chest xray, blood culture and numerous blood tests
Aktuelle Erkrankungen: none
Vorgeschichte: Patient was diagnosed with TB at 15 years old. She had a bump on her neck but doctors would not biopsy it. Patient's father was a medical doctor in another country as well as a pathologist. Her father put her on a regimen of very strong drugs that he knew were effective in another country. Doctors were unwilling to prescribe these drugs. November 1, 2014 she began taking: Isoniazid, 300 miligrams, Ethambutol, 400 miligrams, Tyrazinamide 500 miligrams and Clarithromycin 500 miligrams. She was no longer taking these drugs when she got the vaccines.
Andere Medikamente: Vitamin B6 and B12
Allergien: none
Vorherige Impfungen: -

VAERS 2233740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: MA
Alter: 78,0
Geschlecht: F
Eingang: 14.04.2022
Impfdatum: 13.04.2022
Beginn: 13.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Syncope

Symptomtext

She waited at the pharmacy for 15 min after getting the vaccine and then left. She had faint in the parking lot. Her daughter let us know the situation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: She was fine and she did not feel sick.
Vorgeschichte: She reported diabetes and heart disease
Andere Medikamente: None
Allergien: Mone
Vorherige Impfungen: -

VAERS 2228434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

schwer

Staat: ME
Alter: 62,0
Geschlecht: M
Eingang: 12.04.2022
Impfdatum: 05.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / -

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

Chest pain Echocardiogram abnormal Electrocardiogram abnormal Full blood count Metabolic function test Pericarditis Troponin

Symptomtext

pt had chest pain within 24 hours and went to ER showing abnormal EKG,seen in follow up outpatient with ongoing chest pain day 3 and still changes in EKG. echo showed pericardias inflammation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: echo, ekg, troponin, cbc, cmp
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: allopurinal and lipitor
Allergien: none
Vorherige Impfungen: -

VAERS 2223685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

schwer

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Adhesive tape use Haemorrhage Skin wound Syncope

Symptomtext

Approximately 10 minutes after getting the vaccine, patient fainted in the parking lot and bleeding on the back of his head and woke up in less than a minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Paramedic arrived within minutes and took him to the hospital . And the wound was seal with glue.
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: n/a
Allergien: sulfa meds
Vorherige Impfungen: -

VAERS 2198427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

schwer

Staat: TX
Alter: 21,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 24.03.2022
Beginn: 24.03.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / RA

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

Loss of consciousness Syncope Wound Wound haemorrhage

Symptomtext

Patient came in to get 1st dose of Adult COVID 19 Vaccine, Pfizer brand. The tech inject 0.3 ml pfizer syringe into right deltoid at - 6:08pm and the patient then got up and sat down in waiting area chair where he then fainted after sitting there for 1 minute at -6:10pm. Patient was on floor for 3-5 seconds and regained consciousness where he stated," what happened?" Medical professional asked him to stay on the floor and he wanted to sit on the chair he cut his upper left eyebrown 1/4th inch and was bleeding a bit, aling with a cut 1/2 inch on upper left shoulder. He sat and applied pressure to eyebrow and bleeding stopped. He drank water and waited with medical professional for paramedics which arrive-6:18pm & took patient outside on stretcher.

Weitere VAERSDATA-Felder

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

VAERS 2671696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: TN
Alter: 29,0
Geschlecht: F
Eingang: 15.08.2023
Impfdatum: 22.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chest discomfort Chest pain Dizziness Palpitations Pyrexia

Symptomtext

Chest pain and tightness. Racing heart and palpitations. Fever and lightheaded. All started within 24 hours of vaccine and lasted for week. The chest pain, tightness, and lightheadedness still occurs at times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Merina IUD
Allergien: Peanuts and cashews.
Vorherige Impfungen: -

VAERS 2663525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 31.07.2023
Impfdatum: 08.07.2022
Beginn: 06.02.2023
Tage bis Beginn: 213,0
Dosis: 3
Route/Site: IM / LA

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 2639756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 01.06.2023
Impfdatum: 24.05.2022
Beginn: 01.10.2022
Tage bis Beginn: 130,0
Dosis: 4
Route/Site: IM / LA

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

Hypertension

Symptomtext

In October 2022, my blood pressure was high, 142/92, I was put on a monitor. In April 2023, it was 152/96 and in May of 2023 it was 170/90. I've been given a water pill to help and I have changed my diet and it has helped. There are no symptoms. The only way I know is when I check my pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Sepsin; Epinephrin
Vorherige Impfungen: -

VAERS 2621649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WA
Alter: 61,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 16.07.2022
Beginn: 01.09.2022
Tage bis Beginn: 47,0
Dosis: 4
Route/Site: IM / LA

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

Blood test Oral pain Paraesthesia oral

Symptomtext

I had tingling of my tongue and soreness in my upper and lower pallet of my mouth.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: Bloodwork
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid; pravastatin; multivitamin
Allergien: Cephalosporin
Vorherige Impfungen: -

VAERS 2611405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: NC
Alter: 68,0
Geschlecht: M
Eingang: 07.04.2023
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / AR

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

Dyspnoea exertional Fatigue Pyrexia

Symptomtext

I received three vaccines on 09/08/2022 the COVID-19, DTap and Influenza. I had a fever and extreme tiredness within hours of receiving the vaccines. I just rested and let my system do its thing. I felt better within a day. Six months later, I began having shortness of breath on exertion. My doctor believes it is due to being shut in since the pandemic. The shortness of breath is getting better as I am trying to get out more.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Congestive Heart Failure; High Cholesterol
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2610795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WA
Alter: 68,0
Geschlecht: M
Eingang: 06.04.2023
Impfdatum: 01.04.2022
Beginn: 07.12.2022
Tage bis Beginn: 250,0
Dosis: 4
Route/Site: IM / AR

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

Angiogram abnormal Arterial occlusive disease Cardiac stress test abnormal Chest pain Dizziness

Symptomtext

It was chest pain. In Mid-March I had dizzy spells. I saw my PCP in December who referred my to a Cardiologist three times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: JAN2023 - Stress Test - confirmed symptoms; 20MAR2023 -Angiogram - blockage in two arteries approximately 50%
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Albuterol Aerosol for Asthma PRN
Allergien: Nuts; Fish
Vorherige Impfungen: -

VAERS 2565843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ 4991

moderat

Staat: ID
Alter: 62,0
Geschlecht: M
Eingang: 23.01.2023
Impfdatum: 17.05.2022
Beginn: 22.05.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: IM / LA

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

Condition aggravated Epistaxis Haemorrhage Hypertension Laboratory test Sleep study

Symptomtext

High Blood pressure spikes lasting for a week. Uncontrollable bleeding right nasal. BP as high as 200/118. Three ER visits. Prescribed Clonidine 0.1 mg daily until it relented. Saw cardiologist. Upped candesartan to 24 mg and Amlodipine to 7.5 mg daily and started Spironolactone 25 mg daily. Off Clonidine as it subsided. Excellent BP all summer and fall. Got the second Pfizer bivalent booster on January 14, 2023 (lot#GL2042) and in 3 days I began the high BP spikes again. 196/115. Still had the Clonidine and started taking to control my BP. Took me a week of use until the BP spikes have subsided. I suspect the Pfizer boosters are interfering with the ACE inhibitor drug Candesartan. That?s why it takes a few days for my BP to spike. ???? No question in my mind that the Pfizer boosters caused this. People with high BP problems should be warned. I need to find another alternative to help prevent Covid infections now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Sleep study and labs at ER and by Cardiologist.
Aktuelle Erkrankungen: High BP, sleep apnea but use a CPAP
Vorgeschichte: High BP
Andere Medikamente: Candesartan 16 mg, Amlodipine 5mg, Aspirin 81 mg, Omeprazole 20 mg, Zetia 5 mg, Zyrtec 20 mg, Lexipro 2.5 mg
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2560893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 15.07.2022
Beginn: 19.12.2022
Tage bis Beginn: 157,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Contusion Cyanosis Discomfort Disorientation Dizziness Exercise tolerance decreased Fatigue Headache Insomnia Loss of personal independence in daily activities Mobility decreased Oxygen saturation decreased Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I received my second Pfizer COVID-19 booster on 7/15/2022. On 12/19/2022, I woke up with a heaviness in my body that was centered in my chest. I then took a home antigen test, and I got a positive result. My husband had tested positive two days prior, so I was expecting it. I felt unable to function, so I pretty much stayed in bed the whole time, except the times I would get up to fix food. I had a headache and disorientation. About 6 days in, I had an episode in which my oxygen level went down to 86. I became disoriented, so I had a lie down for about an hour. After about an hour, my oxygen level was normal again, so I got back up and went to the kitchen to do some work. When I went to the kitchen, I felt faint and disoriented again. Not only that, but my left thumb had turned blue! The area from the base of the thumb to the knuckle was purplish black, kind of like a bruise. There was no pain, though. I had another lie down, and I did not get back up. Thankfully, it didn't happen again after that. During my illness, I felt like I had congestion in the chest, but I couldn't cough it up. I avoided coughing, because I was afraid coughing would make it worse. I felt unable to function, because I had really intense fatigue. Despite my fatigue, though, I had trouble sleeping. Most nights, I would be awake until 4 AM. However, I was still able to eat; my senses of smell and taste were not affected by the virus. During my illness, I took echinacea tea, elderberry gummies, manuka honey, and ADVIL. I tested myself on day 8, day 12, and day 16, and it wasn't until day 16 that I got a negative result. At the time of this writing, I sort of still have some residual symptoms. I do my normal pre-COVID-19 activities (e.g. grocery shopping) every other day, and I'm always exhausted on the days in between. Prior to COVID-19, I would sometimes walk for a mile, but I have not been able to do that since getting sick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 12/19/2022, 12/27/2022, 12/31/2022 home antigen tests, positive results; 1/5/2022 home antigen test, negative result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Stage 1 Hypertension.
Andere Medikamente: Multivitamins; coQ10; glucosamine; fish oil; turmeric; probiotic.
Allergien: None.
Vorherige Impfungen: -

VAERS 2548802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OH
Alter: 60,0
Geschlecht: M
Eingang: 03.01.2023
Impfdatum: 09.06.2022
Beginn: 24.12.2022
Tage bis Beginn: 198,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Tested COVID-19 positive, resulted in hospital stay and abnormal chest x-ray. Symptoms include cough and shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: Nasal swab collected 12/24/2022 detected 2019 Novel Coronavirus RNA on 12/24/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular disease and hypertension.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2546971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: MI
Alter: 56,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 20.05.2022
Beginn: 04.07.2022
Tage bis Beginn: 45,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cardiac stress test normal Chest X-ray normal Chest pain Computerised tomogram head normal Dyspnoea Electromyogram normal Laboratory test Nasal congestion Paraesthesia Paranasal sinus hypersecretion Pyrexia SARS-CoV-2 test positive

Symptomtext

7/4/2022 in the afternoon Sinus drainage and stuffy nose were noticed. Fever peaking at 102 at 10 PM. 7/5 tested positive on at home COVID-19 test. Televisit with doctor who advised to treat symptomatically. Fever broke 7/6 but stuffy nose lingered for about 10 days. 8/2 shortness of breath and chest pains that lingered until September and October. PCP had 2 Chest x-rays, CT scan of sinuses and referral to pulmonologist after a had a breathing test. Tingling in left arm and leg, had an EMG.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 7/5 tested positive on at home COVID-19 test. Chest x-ray 9/27 clear, 12/13 Chest X-ray, clear, CT scan of sinuses date unknown, breathing test 12/13 results unknown, Stress test 11/15, normal, EMG 11/2 normal
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Metoprolol
Allergien: ROCEPHIN; LEVAQUIN
Vorherige Impfungen: -

VAERS 2543648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OH
Alter: 84,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 22.04.2022
Beginn: 07.11.2022
Tage bis Beginn: 199,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

Tested COVID-19 positive, resulted in hospital admission. Symptoms include fever, sore throat, cough, shortness of breath, chest pain, and diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Nasopharyngeal SARS-CoV-2 antigen test collected 11/7/2022 tested positive for COVID-19 antigen on 11/7/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes, hypertension, cancer, cerebrovascular disease, and former smoker.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2524122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: MO
Alter: 64,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 05.06.2022
Beginn: 04.07.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Hypertension Malaise Migraine Oropharyngeal pain Palpitations SARS-CoV-2 test positive

Symptomtext

After receiving the vaccine, I had a migraine headache, and this happened after each COVID-19 vaccine. On 07/04/2022 I started not feeling well with a sore throat. On 07/06/2022 I tested positive with a home test for COVID-19. I contacted my doctor and was prescribed PAXLOVID. I rebound after taking the full prescription and was sick for a week. I also experienced a racing heart, high blood pressure, heart palpitations and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 06JUL2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Migraines
Andere Medikamente: N/A
Allergien: Sulfa; COMPAZINE
Vorherige Impfungen: -

VAERS 2514088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 23.05.2022
Beginn: 07.10.2022
Tage bis Beginn: 137,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Dyspnoea Pain Respiratory tract congestion SARS-CoV-2 test negative SARS-CoV-2 test positive Taste disorder

Symptomtext

I tested positive for COVID-19 on 10/07/2022. I had body aches, congestion, and I had a hard time breathing, I had altered taste, but I didn't lose my sense of smell. I called my doctor, and she told me to treat my symptoms with over-the-counter medication. I took ALKA-SELTZER PLUS, and ROBITUSSIN. She didn't call in PAXLOVID. I am feeling much better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 07OCT2022 COVID-19 test positive; 17OCT2022 rapid COVID-19 test negative; 17OCT2022 PCR COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Atorvastatin; tolterodine; METAMUCIL; vitamin D3; OSTEO BI-FLEX; vitamin C; multivitamin; baby aspirin; cetirizine; ALEVE; elderberry gummy
Allergien: N/A
Vorherige Impfungen: -

VAERS 2513900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: NH
Alter: 67,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 21.05.2022
Beginn: 06.09.2022
Tage bis Beginn: 108,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chest X-ray abnormal Exposure to SARS-CoV-2 Foreign body in throat Malaise Pneumonia Respiratory tract congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

On 09/07/2022, I had been to a family event and travelled out of town. When I returned home, I tested positive for COVID-19. I maintained mild symptoms and quarantined as recommended. I was still dealing with some congestion from the COVID-19, but two weeks later, I was diagnosed with pneumonia. They did not feel that it was related to my COVID-19 diagnosis. After recovering from Pneumonia, I had a pre-planned trip abroad from 10/21/2022 to 10/31/2022 which I followed through with. Someone on my tour group was COVID-19 positive and I subsequently contracted COVID-19 again. On 10/29/2022, I felt like I had cotton in my throat, and it was itchy. I thought it was allergy issues since I had just recently recovered from COVID-19. I landed home on 10/30/2022 and tested positive for COVID-19 in the early hours of 10/31/2022. I still had mild symptoms and my doctor did not recommend Paxlovid. I quarantined again for the recommended amount of time and continued to wear a mask until I tested negative on 11/09/2022. Although I still continue to wear a mask out in public.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: 07SEP2022 - At Home COVID-19 Test - Positive; 16SEP2022 - At Home COVID-19 Test - Negative; 04OCT2022 - Chest X-Ray - Pneumonia Diagnosed; 31OCT2022 - At Home COVID-19 Test - Positive; 09NOV2022 - At Home COVID-19 Test - Negative
Aktuelle Erkrankungen: Allergy Symptoms
Vorgeschichte: None
Andere Medikamente: Nasacort; Zyzol; Claritin; Prozac; Vitamin D; Calcium
Allergien: Environmental Allergies
Vorherige Impfungen: -

VAERS 2510979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 15.04.2022
Beginn: 29.07.2022
Tage bis Beginn: 105,0
Dosis: 4
Route/Site: IM / RA

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

Asthenia Bone pain Cough Exercise tolerance decreased Eye pain Fatigue Gait disturbance Headache Hypophagia Impaired healing Loss of personal independence in daily activities Malaise Middle insomnia Mobility decreased Neck pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I received my second Pfizer booster for COVID-19 on 4/15/2022. On 7/29/2022, I was at a rehabilitation session and felt too fatigued to do the exercises; I ended up going home early, because I couldn't even last for 3 minutes. They gave an antigen test, which yielded a negative result. Then on 7/30/22, at about midnight or so, I woke up with a fever, a cough, and a headache on the right side of my head and neck. By the time I woke up later in the morning, I was barely able to get out of bed and shuffle to the bathroom. I took another antigen test and got another negative result. I kept taking antigen tests over the weekend and getting negative results each time. It wasn't until 8/1/2022 or 8/2/2022 that I finally got a positive result. I ended up being sick for 3 weeks. I normally go to rehabilitation sessions 2 days a week, but I was unable to go to my sessions during those 3 weeks that I was sick. I had a fever that would break and then come back. For a whole week, I had a deep-bone body ache from head to toe, and I couldn't shake it. When I had the headache, my eyes also ached. I spent most of the time sleeping for 10-16 hours at a stretch, because I was so fatigued. I had a terrible cough. I treated my symptoms with OTC medicines like NYQUIL, DAYQUIL, ibuprofen, and TYLENOL. The medicines didn't help much with the deep-bone ache, but they did help break the fever. During my illness, I was under the guidance of an RN, who advised me regarding what actions to take. I'm normally very active and walk 5+ miles a day, but during my illness, I was barely able to shuffle around my apartment. My kids and their spouses brought food and drinks, but I spent most of the time sleeping. I did the bare minimum with regard to movements, eating, drinking, medicating, and toileting. My recovery was very slow. I didn't leave my apartment except to go to the patio to get some sunlight, and even that was exhausting. I didn't begin to really feel like I was recovering until the last week of August and the first week of September 2022. I'm doing much better now, but my energy and stamina levels aren't what they were prior to the illness. On good days, I can walk a mile and a half. I was able to gradually work my way back up to 15 minutes max on the exercise bike at the rehab facility. Even now, though, I don't feel like I have completely recovered, because I can overexert myself without realizing it, and I'll be down for about 2-3 days afterwards. This often seems to happen after the rehab sessions, because I do have to work during those sessions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Chronic Kidney Disease (Both Kidneys); Early Onset Osteoporosis; Collagenous Colitis; Hypothyroidism; Barrett's Esophagus; Internal Hemorrhoids; Bone Spurs; Closed Fractures in the Spine, Both Clavicles, Left Rotator Cuff, and Right Elbow; Expressive Dysphasia; History of Breaking Both Feet on 3 Separate Occasions; Pre-Diabetes; Proneness to Gout; Hyperlipidemia; Hypoglycemia; Anemia; Sleep Apnea; Lesion of Ulnar Nerve (Left Arm); Myoclonus; Nephrosclerosis (Both Kidneys); Traumatic Brain Injury (Sustained in August 2011).
Andere Medikamente: Colestipol; levothyroxine; calcium; potassium; gabapentin; amitriptyline; allopurinol; melatonin; LUNESTA; KLONOPIN; vitamin D3; PRILOSEC; LAMICTAL; hydrocodone; ZOFRAN; ketotifen fumarate eye drops.
Allergien: Sulfa drugs.
Vorherige Impfungen: -

VAERS 2485668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 19.04.2022
Beginn: 01.09.2022
Tage bis Beginn: 135,0
Dosis: 4
Route/Site: SYR / LA

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

Ageusia Anosmia Bed sharing Chest pain Cough Malaise Pyrexia SARS-CoV-2 test positive Sleep disorder

Symptomtext

I had my vaccination on 04/19/2022. On 09/01/2022 I had burning sensation in chest. I went to bed and woke up at 04:00 AM with a fever and felt unwell. I was COVID-19 Negative on 09/02/2022. I made appointment with primary doctor on 09/03/2022 and tested COVID-19 Positive. I lost my taste of smell and taste with coughing. I was not prescribed any course of medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 09/03/2022 COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: GERD
Andere Medikamente: Omeprazole; Pepcid; Multivitamin; Fiber; Osteoporosis Injections
Allergien: Protonix
Vorherige Impfungen: -

VAERS 2478885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 12.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Blood cholesterol increased Blood glucose normal C-reactive protein normal Cardiac stress test Chest X-ray normal Cortisol normal Decreased appetite Dyspnoea exertional Echocardiogram Electrocardiogram abnormal Fatigue Fibrin D dimer normal Full blood count normal Glycosylated haemoglobin increased Laboratory test normal Loss of personal independence in daily activities Low density lipoprotein normal

Symptomtext

After 3rd vaccine, the next day because extremely exhausted and weak. It was very difficult to perform basic daily tasks. Short of breath - especially when climbing stairs. Nausated. Lack of appetite. This continued for several days. 1st MD consult via telehealth. I was told my condition was too complicated and needed to be physically seen. The following day, I was seen by my MD. EKG showed sinus brady 40's. Cardiologist referral was made. Also, my endocrinologist was consulted. He recommend my hydrocortisone dose to be tripled for a few days while I am experiencing these symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: 7-18-2022 EKG: SinusBrady 47; CXR: Lungs Clear. D-Dimer, CBC were WNL. CMP: BG slightly elevated (106). 8/8/2022 Thyroid panel WNL, AM Cortisol 14.2, HgbA1C 6.1, Total Cholesterol 223, LDL 128 8/13/2022 CRP, Sed Rate, Vit B level WNL 8/15/2022 Seen by cardiologist 8/15/2022 BMP WNL, Covid test: neg 8/22/2022 Stress Test - low probability of ischemia 10/13/2022 Echocardiogram: Pending results
Aktuelle Erkrankungen: Major back surgery 5/4/2022.
Vorgeschichte: Addison's Disease. Asthma
Andere Medikamente: Hydrocortisone 15mg, Ultram 50mg, MVI
Allergien: Allergies: Latex, Betadine, Erythromycin, Seravent
Vorherige Impfungen: -

VAERS 2459888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: TX
Alter: 62,0
Geschlecht: M
Eingang: 25.09.2022
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Mobility decreased

Symptomtext

PATIENT CANNOT LIFT HIS LEFT ARM SINCE 07/15/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: DIARRHEA, DIVERTICULAR DISEASE OF GI TRACT, OSTEOMALACIA
Vorgeschichte: DIARRHEA, DIVERTICULAR DISEASE OF GI TRACT, OSTEOMALACIA
Andere Medikamente: -
Allergien: PENICILLIN, VICODIN, ACETAMINOPHEN, MORPHINE DERIVATIVES
Vorherige Impfungen: -

VAERS 2446424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OH
Alter: 84,0
Geschlecht: F
Eingang: 15.09.2022
Impfdatum: 10.05.2022
Beginn: 18.07.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: IM / RA

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

Angiogram cerebral normal Arteriogram carotid normal Asthenia Blood sodium normal COVID-19 Dehydration Eyelid ptosis Fatigue Horner's syndrome Hypokalaemia Hyponatraemia Leukopenia Macrocytosis Neurological symptom Pain of skin Physical deconditioning SARS-CoV-2 test positive Urine analysis normal

Symptomtext

84 yo F with a h/o metastatic breast cancer ( to ilium ) and NPH ( with VP shunt, follows with dr) has been admitted to the hospital due to generalized weakness and stroke like symptoms . She is incidentally found to have COVID-19 infection. COVID - 19 virus infection Generalized fatigue - Positive test from home kit on 7/12/22 - Completed paxlovid - no respiratory issues but fatigue which seems to be improving - patient near baseline prior to discharge on PT/OT eval and she is gradually improving - resume OP PCP f/u for current update on COVID19 vaccination - PT/OT recommends HHC on discharge Acute Right Sided Horner's Syndrome- improved - Ptosis with associated with intense ipsilateral scalp pain, improved - no internal carotid artery dissection on CTA head and neck, stroked ruled out and this was her 4 the episode of stroke of symptoms per patient requiring further w/u and they were all negative. - no acute process on CTA Head & Neck - PT/OT consulted for deconditioning and felt stable for discharge to HHC Metastatic Breast Cancer - Left breast with Metastatis to the right iliac wing - On ibrance/letrozole , continue on discharge -resume OP hem/onc f/u - overall prognosis guarded Hypokalemia-resolved - Monitor and replete - check mag level Hyponatremia - likely from dehydration and use of diuretic at home - Na 128>139>137 Chronic Leukopenia Macrocytosis - Due to ibrance - WBC improving Hx of bladder incontinence Recurrent UTI - s/p recent antibiotic course few days bac - UA normal on admission Hx of Hydrocephalous - titratable VP shunt -shuntogram xrays look stable on this admission -resume OP f/u with dr as discussed Physical deconditioning - PT/OT consulted and recommends HHC - husband thinks patient at his baseline currently and can handle with some help at home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 3,0
Labordaten: as above
Aktuelle Erkrankungen: -
Vorgeschichte: metastatic breast ca GERD neuropathy OAB skin ca NPH
Andere Medikamente: Tylenol pr ASA 81mg daily atenolol Ca/Vit D3 d-mannose docusate prn esomeprzole estradiol vaginally fexofenadine lactobacillus letrozole losartan methenamine hippurate mirabegron nystatin/triam cream topically prn palbociclib x3 weeks. Off
Allergien: amoxicillin sulfa doxycycline propoxyphene
Vorherige Impfungen: -

VAERS 2446404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OH
Alter: 83,0
Geschlecht: F
Eingang: 15.09.2022
Impfdatum: 21.05.2022
Beginn: 06.08.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: IM / RA

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

Atrial fibrillation COVID-19 Computerised tomogram thorax normal Condition aggravated Cough Dyspnoea Fatigue Febrile neutropenia Neutrophil count decreased Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

84 y.o. female patient of MD with history of cholangiocarcinoma, paroxysmal atrial fibrillation on long-term anticoagulation, essential hypertension, hyperlipidemia, coronary artery disease, ascending aortic aneurysm who presented with fever and cough in context of positive home COVID testing. Covid-19 Virus Infection Date of onset of symptoms: ~8/5/2022 Symptoms present on admission: Fever, cough, sore throat, fatigue, shortness of breath. Date of covid positive test: 8/6/2022 Vaccination status: vaccinated +2 boosters Imaging: CT chest is without evidence of consolidation Oxygen requirements on admission: None Medical therapy: not indicated, was sent for Paxlovid, but this is an outpatient therapy only to prevent hospitalization Consultants following: Infectious disease, Oncology Given overall immunosuppression - MAB and Neupogen given per ID and oncology Neutropenic fever On admission was not febrile however on day 1 had fever of 100.4 Absolute neutrophil count: 723 With known source of viral COVID infection as likely cause of fever will hold off on antibiotics for now pending ID input Hematology/oncology following ID following Cholangiocarcinoma S/p chemotherapy (just finished earlier this week) Atrial fibrillation with rapid ventricular response Heart rate near 130 on admission Likely due to COVID infection Continue home Xarelto, carvedilol Continue low-dose Cardizem drip for rate control, wean as tolerated Increased BB Essential hypertension Increased coreg given rapid HR Will continue ARB and stop hydrochlorothiazide given relative hypotension and hypokalemia on admission

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: as above
Aktuelle Erkrankungen: Pt was on chemotherapy for locally advanced adenocarcinoma, clinically c/w intrahepatic cholangiocarcinoma
Vorgeschichte: atrial fibrillation ascending aortic aneurysm GERD Hyperlipidemia left anterior fascicular block liver CA-locally advanced w/ intrahepatic cholangiocarcinoma pulmonary HTN macular degneration
Andere Medikamente: alprazolam 0.25mg daily carvedilol 6.25mg BID Vitamin D3 1000 units daily cyanocobalamin 1000mcg daily ferrous sulfate 325mg daily fluticasone 110mcg MDI one puff daily HCTZ 12.5mg daily losartan 50mg daily ondansetron 4mg po/SL Q 8hours pr
Allergien: metoprolol amlodipine diltiazem nitrofurantoin benzonatate augmentin
Vorherige Impfungen: -

VAERS 2431239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OK
Alter: 86,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 19.08.2022
Beginn: 07.09.2022
Tage bis Beginn: 19,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pt admitted to hospital, not related to +Covid test. Only s/s = SOB, SARS test completed for discharge.

Weitere VAERSDATA-Felder

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

VAERS 2431083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 08.06.2022
Beginn: 24.08.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Chest X-ray normal Cough Dyspnoea Hypoxia SARS-CoV-2 test positive

Symptomtext

an 83-year-old female with a history of advanced COPD with Pseudomonas colonization, hypertension, dyslipidemia, GERD and osteoporosis, who presented with increasing shortness of breath, cough and hypoxia on 08/24. At the time of admission, chest x-ray was negative for infiltrate. Patient is fully vaccinated against COVID, however COVID test was positive on 08/24. Patient was placed in severe respiratory isolation. Patient was continued on Spiriva, Symbicort and DuoNebs. The patient also is on daily azithromycin and alternating colistin/TOBI treatments. Patient was continued on colistin. Patient had been started on Prednisone prior to admission, which was transitioned to IV Solumedrol. Patient was also started on Remdesivir. Pulmonary was consulted. She was continued on IV Remdesivir (completed 5 days), breathing treatments as well as steroids with slow improvement in her respiratory status. She was transitioned back to prednisone on 08/29. As the patient had clinically improved, having completed treatment with remdesivir, and being transitioned to oral prednisone she was discharged to home on 8/30/22. She was seen by pulmonary rehab on day of discharge, and will require 2 L oxygen with activity only. She will be discharged home on 8/30/22. She will be placed on a tapering dose of Prednisone at discharge, and should follow-up with her PCP in 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Bronchiectasis without complication (HCC) Spinal stenosis of lumbar region with neurogenic claudication COPD, very severe (HCC) Rosacea Age-related osteoporosis with current pathological fracture with routine healing Personal history of colonic polyps GERD (gastroesophageal reflux disease) Hyperlipidemia, unspecified hyperlipidemia type Early dry stage nonexudative age-related macular degeneration of both eyes Posterior vitreous detachment of right eye History of Pulmonary Mycobacterium avium-intracellulare infection (HCC) Keratoconjunctivitis sicca (HCC) Filamentary keratitis of right eye Valvular insufficiency Pseudomonas aeruginosa colonization Essential hypertension Opioid use Iron deficiency anemia Macular degeneration IBS (irritable bowel syndrome) COVID Generalized weakness Trigger ring finger of left hand Cachexia (HCC) History of pulmonary embolism History of positive PPD Breast lump Secondary adrenal insufficiency (HCC) IgG deficiency (HCC) Suspected pulmonary hypertension Finger pain, left COPD exacerbation (HCC) Chronic respiratory failure with hypoxia (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ALBUTEROL 108 (90 Base) MCG/ACT inhaler atorvastatin (LIPITOR) 40 MG tablet azithromycin (ZITHROMAX) 250 MG tablet Carboxymethylcellulose Sodium (ARTIFICIAL TEARS OPTH) cholecalciferol (VITAMIN D3) 50 M
Allergien: Sulfa DrugsRash, Throat swelling AmoxicillinDiarrhea Tape AdhesiveRash, Other
Vorherige Impfungen: -

VAERS 2413455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 17.08.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chest pain Muscular weakness Nausea Pain Pyrexia

Symptomtext

Immediate fever , nausea , weakness , chest pain . Fever lasted up to 4 days . Pain lasted for couple of weeks. Weakness of left shoulder and arm still in place to the date .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Myasthenia gravis
Vorgeschichte: Myasthenia gravis
Andere Medikamente: Mestinon , prednisone
Allergien: None
Vorherige Impfungen: -

VAERS 2412365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WA
Alter: 77,0
Geschlecht: F
Eingang: 16.08.2022
Impfdatum: 16.05.2022
Beginn: 03.08.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Dyspnoea Headache Hypersomnia Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

05/16/2022 I had my vaccination. On 08/1/2022 we went to the doctors for my husband and stayed at a hotel. There was no air conditioning and it was in the 90's. The room was very hot and could not stay there that long. I think it allowed the germs to breath and believe where we got COVID-19. 08/02/2022 We went to my husbands doctor for his appointment. On Tuesday night, my husband was coughing and hacking. 08/03/2022 I woke up with a cough, labored breathing, headache and sore throat. I slept a lot. My husbands cough was getting worse with a temperature of 102. We tested and were COVID-19 Positive. We were prescribed Plaxovid. I am feeling much better and tested negative 08/16/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Allergies
Andere Medikamente: Esterase; Hydrochloride
Allergien: Almost all pain medications.
Vorherige Impfungen: Flu shots a sore arm. COVID-19 vaccinations sore arm.

VAERS 2404464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: MN
Alter: 25,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Mobility decreased Pain

Symptomtext

Patient reports pain with motion in arm and ack of mobility

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Recommended to see her primary
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2388861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: AZ
Alter: 71,0
Geschlecht: M
Eingang: 06.08.2022
Impfdatum: 04.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Blood test normal Chemotherapy Full blood count normal Infection Injected limb mobility decreased Pain in extremity COVID-19 Drug ineffective SARS-CoV-2 test Injection site erythema Injection site pain Injection site swelling Injection site warmth Nerve injury Pain

Symptomtext

left arm from shoulder to elbow is severely swollen & painful/Arm & fingers are painful; left arm from shoulder to elbow is severely swollen & painful; Unable to move fingers on left hand; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old male patient received BNT162b2 (BNT162B2), on 04Jul2022 at 13:00 as dose number unknown, single (Batch/Lot number: unknown) at the age of 71 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Multiple myeloma" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INJECTED LIMB MOBILITY DECREASED (non-serious) with onset 07Jul2022 at 10:00, outcome "not recovered", described as "Unable to move fingers on left hand"; ARTHRALGIA (non-serious) with onset 07Jul2022 at 10:00, outcome "not recovered", described as "left arm from shoulder to elbow is severely swollen & painful"; PAIN IN EXTREMITY (non-serious) with onset 07Jul2022 at 10:00, outcome "not recovered", described as "left arm from shoulder to elbow is severely swollen & painful/Arm & fingers are painful". Therapeutic measures were not taken as a result of pain in extremity, arthralgia, injected limb mobility decreased. Additional information: It was unknown if the patient had any other medication within the two weeks of vaccination. The patient had no known allergies. It was reported that 4 weeks post vaccine injection, left arm from shoulder to elbow was severely swollen and painful. The patient has lost movement in all fingers. Arm and fingers are painful. Unable to move fingers on left hand. Have had doctors look at it but nobody knows what it was. The patient wanted help. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Multiple myeloma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2403130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 19.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Condition aggravated Exercise tolerance decreased Inflammation Migraine Muscle strain Muscle tightness Myalgia Plantar fasciitis X-ray

Symptomtext

Severe migraine lasting several weeks. Re-onset of severe inflammatory response in lower extremities, causing muscle tightness and pain, including plantar fasciitis and athletic pubalgia (previously diagnosed one week following first COVID booster shot). Prior to the boosters, I never experienced plantar fasciitis or pubic pain. Before the boosters, I ran 6 miles per day, but due to the inflammation and muscle tightness, I am unable to run for more than 2 minutes at a time without further aggravating the inflammation. My orthopedist prescribed Diclofenac 75 mg for 2 weeks to address the inflammation since I am not able to take prednisone. The Diclofenac has helped, but not fully resolved the issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: X-rays and exam by orthopedist and physical therapy.
Aktuelle Erkrankungen: None.
Vorgeschichte: Chronic Migraine, Sensory Processing Disorder
Andere Medikamente: Gabapentin, Modafinil, Atenolol, Omeprazole, Cyclobenzaprine, Vitamin B2, Vitamin B12, Vitamin D, Zyrtec, Levonor-Eth Estrad 0.15-0.03 PRN: Cambia, Remeron, Nurtec
Allergien: Sulfa, Codeine, Zofran
Vorherige Impfungen: COVID19 Pfizer/BioNTech, Booster #1, about a week after developed severe athletic pubalgia and plantar fasciitis; unable to run

VAERS 2393113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ 4991

moderat

Staat: AZ
Alter: 52,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 03.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Pain in extremity Paraesthesia

Symptomtext

Left arm aching and tingling and soreness weeks after injection. Is NOT happening in other arm that did not receive injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: B12, Vitamin D Multi vitamin
Allergien: No known
Vorherige Impfungen: -

VAERS 2388320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 22.04.2022
Beginn: 16.06.2022
Tage bis Beginn: 55,0
Dosis: 4
Route/Site: IM / LA

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

Blood test normal Bradycardia COVID-19 Cardiac monitoring abnormal Chest X-ray Contusion Feeding disorder Fluid intake reduced Gingival discolouration Headache Hyperaesthesia Injected limb mobility decreased Lip exfoliation Lung disorder Malaise Musculoskeletal disorder Oropharyngeal discolouration Oropharyngeal pain

Symptomtext

I had a sore arm the next day after vaccination. The first week was the worse. I could not touch my left arm and I had to use my right hand to lift my left arm. This lasted for 2 weeks. I did take Tylenol for pain but did help. I did have long effects after getting COVID-19 in November 2020. I did have to get put on O2 for 3 months. Then, I caught COVID-19 again 06/16/2022. I takes me longer to test positive. My husband tested positive. It took me 8 days before I tested positive since symptoms. I had runny nose and sore throat. It took a total of 17 tests. I went to my doctor and was prescribed Paxlovid. I was showing abnormal bruising and blood vessels busting that looked like scratch marks. I went to the ER and had a chest x-ray, COVID-19 test, blood work, heart monitor which indicated bradycardia. Nothing was found on why my blood vessels were doing that and the doctor thinks that I could have something to do with COVID-19. My throat turned all white and moved from my uvula and lower part of my throat and even around my gums. My lips started peeling. I could not eat or drink. It went into my lungs. I used an oral mouth wash 4 times a day then Neosporin on my lips. I also went to my doctor and was tested for strep which was negative. I tested negative on 6/24/2022. Then on 7/2/2022, I tested positive with a rebound effect of COVID-19 and symptoms of headache and runny nose came back. My symptoms lasted for 2 weeks after the rebound.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: COVID-19 test; Blood work - normal; Heart monitor - bradycardia; Strep test - negative
Aktuelle Erkrankungen: None
Vorgeschichte: Back pain; Hypothyroidism
Andere Medikamente: Levothyroxine ; Potassium; Nasal Spray; Magnesium; Vitamin D
Allergien: Penicillin; Latex
Vorherige Impfungen: -

VAERS 2379109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: VA
Alter: 62,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 15.04.2022
Beginn: 10.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Chills Fatigue Feeling abnormal Headache Impaired work ability Malaise Muscular weakness Night sweats Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Throat irritation Tremor

Symptomtext

On the morning of the July 10th I woke up with mild headache and very scratchy throat, but I also have seasonal allergies so thought it might be that. I have a 6 week old grandchild and my main concern was to test before going over there, but tested negative for COVID-19, I was worried the headache might turn into a migraine so I took my migraine medication preemptively. Monday, Tuesday, Wednesday I continued to have a low grade headache and sore throat, but Thursday morning when I woke up I had a definite headache, a very bad sore throat and a fever of 101.8. I took an at home COVID-19 test and it came back immediately positive. I talked to the nurse practitioner at doctor's office, and prescribed Paxlovid but to not take my Lipitor, or Lunesta, or Xanax. My fever continued and the chills were so bad that my hands were shaking, I was struggling to notify my employment because my hands were shaking so bad. The nurse practitioner wanted me to have a tele-health appointment and she re-iterated about the medications, she checked on my fever which was still high, and told me to stay hydrated. I continued to work when I could but I was still really tired. By Monday, the fever the was gone and the sore throat. I'm still having bad night sweats, Tuesday by noon I was eating peanut butter toast and suddenly felt weak in the knees and knew I would pass out if I didn't go sit down. I took my blood pressure, it was 86/60. I immediately called my doctor and they were surprised that I had still been working (I work from home and had a lot of deadlines). They suggested complete bedrest and not to go back to work at all until the following Monday. I am experiencing brain fog and fatigue and still not feeling better. I have stopped taking my blood pressure medication and will not start again until my blood pressure gets back to normal. Overall this experience has been going on for about 3 weeks. This morning my blood pressure was 99/61 and my heart rate was 80.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: at home COVID-19 test
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma; High blood pressure; Hypoglycemia; Hypothyroid; Anxiety; Migraines; Panic Attacks; Insomnia
Andere Medikamente: Lunesta; Armour Thyroid; Oestradiol ; Lisinopril; Lipitor; Percocet; Xyzal; Xanex as needed; Vitamin D; CBD drops; Imitrex as needed
Allergien: Seasonal Allergies
Vorherige Impfungen: "Covid arm" after every Pfizer COVID-19 vaccine

VAERS 2374778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OR
Alter: 63,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 19.04.2022
Beginn: 18.06.2022
Tage bis Beginn: 60,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Cough Fatigue Headache Mobility decreased Musculoskeletal stiffness Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Started out with fatigue and a cough that was different then my normal cough. Then I started feeling a headache and a stiff neck and then I lost smell and taste at that point. And just over the day the symptoms got worse. I had body aches. I began to feel better around the 6/26. but 6/27 i still had a cough and fatigue. The whole time i was running a low grade fever. On 6/28 the fever came back. The cough got worse the fatigue got worse and all the symptoms came back. On the 6/18 we went to urgent care and that is when i found out i had COVID-19. On the 6/30 we called the doctor and they had me retest and it was very positive and stated i had a rebound case. They put on the Paxlovid on the 6/18. The rebound case lasted until 7/11, that was my first day with no fever. And everything at that point got better. This week my smell is starting to come back and i am feeling pretty normal. I was in bed for the first 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID-19- positive 6/18/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Stiff Persons Syndrome; Fibromyalgia; osteoporosis
Andere Medikamente: Rituxan; Percocet, Baclofen; Prozac; Lunesta; Hydrocortisone; Genatropin; Calcium; B12; Women's Multi Vitamin; Vitamin C; B1; Biotin; Aspirin; Benadryl; Azelastine
Allergien: Penicillin; Morphine; Indocin; Butazolicidin; Erythromycin; Slagal; Levhuqin; Plaquenil; Omeprazole; Honey Bees; Yellow Jackets
Vorherige Impfungen: -

VAERS 2372395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 30.06.2022
Beginn: 07.07.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: SYR / AR

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

Biopsy skin abnormal Condition aggravated Granuloma annulare

Symptomtext

After about a week post vaccination I did see my symptoms begin to come back that was occurring prior to this vaccination post my 3rd dose of pfizer. I did not reach out to my dermatologist yet for care. I have just been using Minocycline to help with symptoms however my doctor did say that if my symptoms did not improve they would recommend hydroxychloroquine. I did previously have steroid injections on areas where my symptoms were raised, and I did see some improvement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Biopsy Test: Diagnosed Granuloma Annular
Aktuelle Erkrankungen: N/A
Vorgeschichte: Lymphocytic Colitis; West Nile Virus
Andere Medikamente: Fluoxetine HCL; Minocycline;
Allergien: N/A
Vorherige Impfungen: Pfizer Vaccine #3 Date:12/09/2021 Lot: 330308D : I started to notice after my vaccine discoloration in my skin near my pelvic ar

VAERS 2370194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: PA
Alter: 76,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 21.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Blood test normal Burning sensation Electromyogram normal Erythema Hypoaesthesia Nervous system disorder Neuropathy peripheral Paraesthesia

Symptomtext

Peripheral neuropathy; I had a CNS reaction; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 77-year-old female patient received BNT162b2 (BNT162B2), on 13Oct2021 as dose 3 (booster), single (Lot number: 330130BA) and on 21May2022 as dose 4 (booster), single (Lot number: FJ4991, Batch number: RA11133) at the age of 76 years for covid-19 immunisation. The patient's relevant medical history included: "Thyroid" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 2), for COVID-19 Immunization, reaction(s): "do not have the problem with the first two"; Bnt162b2 (Dose 1), for COVID-19 Immunization, reaction(s): "do not have the problem with the first two". The following information was reported: NERVOUS SYSTEM DISORDER (non-serious) with onset 2021, outcome "unknown", described as "I had a CNS reaction"; NEUROPATHY PERIPHERAL (medically significant) with onset 2021, outcome "unknown", described as "Peripheral neuropathy". Therapeutic measures were not taken as a result of neuropathy peripheral, nervous system disorder. Clinical course: The patient had a CNS reaction very severe and resulted in peripheral neuropathy. The patient wants to make sure they understand that the vaccine has caused some serious problem. The patient does not have the problem with the first two, but the two boosters have lastly peripheral neuropathy. Second one which really almost killed me was administered on 21May2022. The patient believed it was my left arm. The patient has nothing other than thyroid medication and the only med and disease. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2370194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: PA
Alter: 76,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 21.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Blood test normal Burning sensation Electromyogram normal Erythema Hypoaesthesia Nervous system disorder Neuropathy peripheral Paraesthesia

Symptomtext

Peripheral neuropathy; I had a CNS reaction; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 77-year-old female patient received BNT162b2 (BNT162B2), on 13Oct2021 as dose 3 (booster), single (Lot number: 330130BA) and on 21May2022 as dose 4 (booster), single (Lot number: FJ4991, Batch number: RA11133) at the age of 76 years for covid-19 immunisation. The patient's relevant medical history included: "Thyroid" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 2), for COVID-19 Immunization, reaction(s): "do not have the problem with the first two"; Bnt162b2 (Dose 1), for COVID-19 Immunization, reaction(s): "do not have the problem with the first two". The following information was reported: NERVOUS SYSTEM DISORDER (non-serious) with onset 2021, outcome "unknown", described as "I had a CNS reaction"; NEUROPATHY PERIPHERAL (medically significant) with onset 2021, outcome "unknown", described as "Peripheral neuropathy". Therapeutic measures were not taken as a result of neuropathy peripheral, nervous system disorder. Clinical course: The patient had a CNS reaction very severe and resulted in peripheral neuropathy. The patient wants to make sure they understand that the vaccine has caused some serious problem. The patient does not have the problem with the first two, but the two boosters have lastly peripheral neuropathy. Second one which really almost killed me was administered on 21May2022. The patient believed it was my left arm. The patient has nothing other than thyroid medication and the only med and disease. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2368088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 12.04.2022
Beginn: 27.05.2022
Tage bis Beginn: 45,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chest pain Chills Cough Decreased appetite Disorientation Fatigue Headache Insomnia Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 with symptoms of severe headache, body aches, fever 100.1 to 100.6, insomnia, urge to cough, congestion, chest pain, lack of appetite, disorientation, chills, and fatigue. I was not able to take PAXLOVID due to taking rosuvastatin. The fever resolved after 5 days. My symptoms began to resolve after 9 days of illness. I am still experiencing lingering fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 rapid antigen test was positive on 05/27/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Osteoarthritis; Left Hip Replaced; Mitro Valve Prolapse; Super Ventricular Tachycardia; Kidney Stones; Inflammation Marker in the body, and elevated IGE; Seasonal Allergies; High Cholesterol
Andere Medikamente: Vitamin D3; vitamin E; vitamin B complex; rosuvastatin; zoledronic IV
Allergien: Grasses; weeds; pollen; pet dander; sulfa; BACTRIM; CLEOCIN; DURICEF; MACROBID; PLAQUENIL
Vorherige Impfungen: Flu vaccine 10/2022 I experienced 4 days of fever, body aches, and flu like symptoms.

VAERS 2367977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: IL
Alter: 73,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 20.04.2022
Beginn: 01.05.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: SYR / RA

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

Back pain Loss of personal independence in daily activities Mobility decreased Muscle spasms Pain Pain in extremity

Symptomtext

3 weeks after receiving my vaccine. I began to have pain in my lower back and shooting pain down my right leg to the lower calf. The pain occurred at night when sleeping and when walking I can have the shooting pain down the leg. I am experiencing muscle spasms along with the shooting pain. I have since been seeing a chiropractor for this pain. The doctor has changed my medications. I have been taking arthritis TYLENOL, extra strength, and blue emu cream and one for muscle spasm. It is getting better but the pain is not gone. I am unable to perform activities that I used to do. It is difficult to climb the stairs and an I'm unable to garden anymore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Arthritis; Acid Reflux
Andere Medikamente: Trospium chloride; ARNUITY ELLIPTA; LIPITOR; TYLENOL; tension headache relief; vitamin supplements
Allergien: Aspirin; seafood
Vorherige Impfungen: -

VAERS 2367507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 11.04.2022
Beginn: 14.04.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / AR

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

Blood glucose decreased Blood test abnormal Dyspnoea Exercise tolerance decreased Feeling abnormal Shoulder arthroplasty Sleep disorder

Symptomtext

While I was in recovery during a reverse shoulder replacement I had a difficult time breathing. During the night you could not sleep and had to have VALIUM and breathing treatments. I could not catch a breath. This continued. I thought it could have been surgery but now I am wondering if it has something to do the the vaccine. I still do not feel completely normal. I get winded very easily. The day before surgery, I walked 2 miles on a treadmill. Now I can no longer do that. I also have low blood sugar. I am now on more medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood work abnormal.
Aktuelle Erkrankungen: None
Vorgeschichte: COPD; Arthritis
Andere Medikamente: ADVAIR; SPIRIVA; nebulizer; MYRBETRIQ; multivitamin; LUNESTA; NORCO
Allergien: BACTRIM
Vorherige Impfungen: -

VAERS 2366331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 11.04.2022
Beginn: 11.06.2022
Tage bis Beginn: 61,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Musculoskeletal chest pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

Started with a runny nose and post nasal drip and coughing, I had just flown back home and originally thought it was my allergies starting up as soon as I got home. I coughed through the night and all the next day, which was Sunday. I coughed so much my ribs hurt, and the runny nose just wouldn't stop. I took some cough and cold medicine but it didn't really work. Monday I developed a low grade fever, the highest was 100.8 F. I took a home test and tested positive for COVID-19. Then I texted with my doctor, she said to go in the morning to the ER and ask for the monoclonal antibodies treatment. At that point my husband was still negative. We went at about 5:30 in the AM on Tuesday and my husband tested positive at that time. He never got sick, but we both received the MAB treatment. The overall time period was about a week. It was pretty mild, I never got too sick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: COVID-19 home test
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure; mild asthma
Andere Medikamente: Atenolol; SYNTHROID; ZYRTEC; baby aspirin; PREVACID; ACTONEL; SYMBICORT; EDARBI; LIPITOR; FLONASE; azelastine nasal spray; calcium plus D3; vitamin C; women's multivitamin; vitamin D3; coQ10; turmeric; LIPO-FLAVONOID
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2366307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: PA
Alter: 63,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 11.03.2022
Beginn: 15.06.2022
Tage bis Beginn: 96,0
Dosis: 4
Route/Site: IM / LA

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

Back pain Chest X-ray normal Cough Dizziness Dyspnoea Obstructive airways disorder Painful respiration

Symptomtext

I had pain when I was breathing in I had constricted airways, my back hurt where my lungs are. I had shortness of breath, light headed. I called my doctor because my inhaler was not working and made an appointment to go in for a reassessment of my breathing medication. He prescribed new medications and a steroid to help clear my lungs. I am feeling better but I am still coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest X-Ray - Normal
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure
Andere Medikamente: Ibersartan
Allergien: No
Vorherige Impfungen: -

VAERS 2364002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: IL
Alter: 51,0
Geschlecht: F
Eingang: 09.07.2022
Impfdatum: 09.07.2022
Beginn: 09.07.2022
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 Immediate post-injection reaction Nausea Paraesthesia Sensory disturbance Throat tightness

Symptomtext

The patient received the vaccine and immediately after administration reported feeling lightheaded, dizzy, tingling in her left arm, nausea, neck sensation, minor throat constriction, and chest pain. We, myself and (the staff pharmacist), immediately offered to call 911 and offered an EPI PEN. The patient denied the EPI PEN and denied our offer to call an ambulance. We took the patient's blood pressure, and it was 116/82. She was conscious and responding to questions and denied once more the offer for us to call her ambulance. We had the patient sit in a chair with support and monitored her while she contacted a family member to take her to the ER. We took her blood pressure again and it came back at 108/82. We insisted she seek immediate medical attention. She insisted her sister/friend, take her to the emergency room. She called friend and friend picked her up to take her immediately to the emergency room at our insistence. The patient departed our pharmacy at approximately 5PM stating she would have friend drive her to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Unknown.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Tamsulosin 0.4 mg Hydroxyzine HCl 25 mg Albuterol HFA 8.5 gm Solifenacin 10 mg Phentermine 37.5 mg Polyethylene glycol 3350 NF powder Carbamazepine 200 mg Victoza 18mg/3mL INJ pen Estradiol 0.01% vaginal cream 42.5 gm Epinephrine 0.3 mg I
Allergien: Sumatriptan (reaction unknown) Iodides
Vorherige Impfungen: -

VAERS 2363125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 24.05.2022
Beginn: 14.06.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: IM / LA

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

Chest X-ray normal Chest discomfort Computerised tomogram thorax normal Dyspnoea Electrocardiogram normal Fibrin D dimer Full blood count normal Metabolic function test normal Stress echocardiogram normal

Symptomtext

onset of breathing difficulties, tightening in chest and heaviness in chest about 3 weeks after my 2nd booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: lung x ray and ecg on 6/16/2022 ecg, cbc, d-dimer, comprehensive metabolic panel on 6/26/2022 chest CT scan on 6/29/2022 echo stress w/ continuous ecg monitoring 7/6/2022 **all clear**
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: vytorin 10/40 multi vitamin calcium
Allergien: vibramyacin bactrim
Vorherige Impfungen: temperature and extreme fatigue - 69 years old Booster #1 (Pfizer) 10/20/21 temperature, body aches, fatigue - 69 years old, P

VAERS 2362298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: PA
Alter: 58,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 18.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / LA

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

Discomfort Idiopathic environmental intolerance Insomnia Loss of personal independence in daily activities Paraesthesia SARS-CoV-2 test

Symptomtext

pins and needles sensation/prickling; entire body has become hyper sensitive to energy emissions from all types of electronics and wi-fi; cannot sleep; quit my office job/quality of life is terrible; extreme full body discomfort; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 58-year-old female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE), on 18Apr2022 as dose number 4 (booster), single (Lot number: FJ4991) at the age of 58 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Sjogren's" (unspecified if ongoing); "bipolar 2" (unspecified if ongoing), notes: bipolar 2; "mild distal peripheral neuropathy in my feet" (unspecified if ongoing), notes: mild distal peripheral neuropathy in my feet. Concomitant medication(s) included: LAMOTRIGINE; KLONOPIN; ELAVIL [ALLOPURINOL]; MARIJUANA. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: ER8734, Location of injection: Arm Left), administration date: 25Mar2021, when the patient was 57-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: ER8731, Location of injection: Arm Left), administration date: 17Apr2021, when the patient was 57-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 3, Batch/Lot No: FH8020, Location of injection: Arm Left), administration date: 17Oct2021, when the patient was 58-year-old, for COVID-19 immunization. The following information was reported: INSOMNIA (disability) with onset 20Apr2022, outcome "not recovered", described as "cannot sleep"; IDIOPATHIC ENVIRONMENTAL INTOLERANCE (disability) with onset 20Apr2022, outcome "not recovered", described as "entire body has become hyper sensitive to energy emissions from all types of electronics and wi-fi"; DISCOMFORT (disability) with onset 20Apr2022, outcome "not recovered", described as "extreme full body discomfort"; PARAESTHESIA (disability) with onset 20Apr2022, outcome "not recovered", described as "pins and needles sensation/prickling"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (disability) with onset 20Apr2022, outcome "not recovered", described as "quit my office job/quality of life is terrible". The events "pins and needles sensation/prickling" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown, notes: Since the vaccination, has the patient been tested for COVID-19?:Yes; Negative, notes: Negative. Therapeutic measures were not taken as a result of paraesthesia, idiopathic environmental intolerance, insomnia, loss of personal independence in daily activities, discomfort. Additional information: Within 72 hours of receiving second Pfizer booster on 18Apr2022, pins and needles sensation began in hands when and after holding my cellphone. Since that time, entire body became hyper hypersensitive to energy emissions from all types of electronics and wi-fi, including computers, laptops, cellphones, internet, computerized system in her hybrid car, smart meters, outdoor overhead electrical and cable wires, LED lightbulbs, and even simple electronics such as a floor fan and digital alarm clock. She had to quit office job because she was surrounded by electronics and radio waves that were causing extreme full body discomfort- prickling and pins and needles, even on face, but especially on hands, arms and upper chest. She cannot use electronics at home, and cannot even work at a remote job. She cannot sleep in bed because the high wires attached to her house outside the bedroom caused intense pins and needles all over the body. Her quality of life was terrible. The patient did not receive other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: COVID-19; Result Unstructured Data: Test Result:Unknown; Comments: Since the vaccination, has the patient been tested for COVID-19?:Yes; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative; Comments: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bipolar II disorder (bipolar 2); Peripheral neuropathy (mild distal peripheral neuropathy in my feet); Sjogren's
Andere Medikamente: LAMOTRIGINE; KLONOPIN; ELAVIL [ALLOPURINOL]; MARIJUANA
Allergien: -
Vorherige Impfungen: -

VAERS 2359842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Hypoaesthesia Injection site hypoaesthesia Injection site pain Injection site paraesthesia Paraesthesia

Symptomtext

4th dose in series injected left IM deltoid around 10am. Patient later reported back at 1:45pm same day, experiencing soreness at the injection site, along with tingling and numbness that radiated from the injection site down to the hand. Patient was concerned whether that this was a normal side effect. I informed patient that these side effects have been reported in the past and referred patient to advice nurse to see if further evaluation same day is needed. Patient called advice nurse and informed me that this is a rare side effect, and that the nurse instructed patient to continue self-monitoring and to report back if side effects worsen. Unclear if patient has recovered from side effects and the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported
Andere Medikamente: unknown
Allergien: none reported
Vorherige Impfungen: -

VAERS 2356819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

moderat

Staat: MA
Alter: 77,0
Geschlecht: M
Eingang: 03.07.2022
Impfdatum: 21.06.2022
Beginn: 02.07.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: IM / LA

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

Injected limb mobility decreased Pain in extremity

Symptomtext

The patient has arm pain and limited range of motion for couple of weeks after vaccination. Pharmacist didn't see any redness or bruise near vaccination site.

Weitere VAERSDATA-Felder

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

VAERS 2356280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 22.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / -

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

Confusional state Dyspnoea Illness Malaise Pyrexia Vomiting

Symptomtext

Fever; Shortness of breath; I started throwing up/she is puking; I am totally out of it; I felt like a truck ran me over; Sick; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received BNT162b2 (BNT162B2), on 22Jun2022 as dose 4 (booster), single (Lot number: FJ4991) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN), for Covid-19 immunization; Covid-19 vaccine (DOSE 2; MANUFACTURER UNKNOWN), for Covid-19 immunization; Covid-19 vaccine (DOSE 3; MANUFACTURER UNKNOWN), for Covid-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 23Jun2022, outcome "unknown", described as "Fever"; CONFUSIONAL STATE (non-serious) with onset 23Jun2022, outcome "unknown", described as "I am totally out of it"; MALAISE (non-serious) with onset 23Jun2022, outcome "unknown", described as "I felt like a truck ran me over"; VOMITING (non-serious) with onset 23Jun2022, outcome "unknown", described as "I started throwing up/she is puking"; DYSPNOEA (non-serious) with onset 23Jun2022, outcome "unknown", described as "Shortness of breath"; ILLNESS (non-serious) with onset 23Jun2022, outcome "unknown", described as "Sick". Additional information: It was reported that the caller experienced side effects of the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2342006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: NJ
Alter: 35,0
Geschlecht: M
Eingang: 29.06.2022
Impfdatum: 28.05.2022
Beginn: 22.06.2022
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: IM / -

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

Blood test Chest X-ray normal Chest discomfort Chest pain Dizziness Electrocardiogram Inappropriate schedule of product administration Palpitations Paraesthesia

Symptomtext

Patient is a hospital employee who received dose 1 (11/27/2021) and dose 2 (05/28/2022) of Pfizer vaccine at a local pharmacy store. Presented to hospital emergency room on 6/22/2022 at 10AM. Sections of medical record copied below from ED physician assistant notes. Chief complaint "Patient presents with palpitations. Pt states he woke up at 2am with palpitations (heart racing). He said the started to feel tingling in his L face, L shoulder and hand. He denies chest pain/SOB. The "heart racing" feeling improved but then returned. He states he is vaccinated x3 but does not have his card with him. " History "35-year-old male presents for evaluation of palpitations that began around 2 PM this morning he woke up from sleep because his heart was racing and felt like it was pounding in his chest. He felt pins and needle sensation in his left shoulder radiating down his left upper extremity and into his neck. He got up tried to drink some water and felt lightheaded as though he was going to pass out. He also reports discomfort to his left chest described as a dull ache that does not radiate. " ED Course Wed Jun 22, 2022 "1035AM EKG interpreted by me: sinus rhythm at 75 bpm;no ST/T changes; Qtc 405 (-)Brugada (-)WPW 1132AM CXR as read contemporaneously by me: no acute cardiopulmonary disease no pericardial effusion 1235PM Pt resting comfortably in bed. Complains of continued chest pain and paresthesias. Exam remains non-focal. Additional treatment with toradol 15 mg IV ordered 1320PM Pt counseled that all blood work and imaging studies are unremarkable. Vital signs remain stable and he is in no acute distress. Provided with cardiology f/u and given strict return precautions"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, CXR, blood work.
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2341945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / AR

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

Abdominal pain Asthenia Colitis Colonoscopy abnormal Fatigue Gait disturbance Gastrointestinal disorder Headache Large intestine polyp Pain Precancerous lesion of digestive tract Procedural nausea Procedural pain Pyrexia Retching Tremor Weight decreased

Symptomtext

05/02/2022 I received the vaccination and I did not feel I had a severe reaction, I did however have issues with achiness, fatigue, and overall slightly painful. I did then have a lot of gastrointestinal problems later on and also headaches and fatigue. The most noticeable reaction is that my legs are trembling and it is hard to walk due to increase weakness. Low grade fever every now and then, and weight loss as well. I have been receiving care from my physicians who did a colonoscopy that found slight inflammation and pre cancerous polyps. My symptoms had gotten worse from the procedure as well. They are looking into Addison's Disease. I did have 2 emergency visits due to dry heaving and abdominal pain after my procedure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Colonoscopy: precancerous polyps.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Sjogren's syndrome
Andere Medikamente: Potassium; Vitamin D
Allergien: Iodine; Ampicillin; Doxycycline; Selsa antibiotics; Erythromycin; Ciprofloxacin; Lidocaine; Metronidazole; Quinacrine; Hydroxychloroquine; Latex; Estrogen
Vorherige Impfungen: Flu Shots: causing reaction for 24-48 hours afterwards.

VAERS 2339219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 24.05.2022
Beginn: 05.06.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: SYR / LA

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

Chest X-ray normal Dyspnoea Electrocardiogram normal

Symptomtext

difficulty taking a very deep breath, not short of breath. came on slowly but every day starting on July 15th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: Metprolol, Gabaoentin, Tapazole, Silymarian, D-mannnose, Turmeric
Allergien: none
Vorherige Impfungen: -

VAERS 2337016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 28.06.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / -

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

Injected limb mobility decreased Injection site pain

Symptomtext

Pain at arm injection limit motion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Metformin 1000mg 2X Daily
Allergien: Shrimp
Vorherige Impfungen: -

VAERS 2337011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 28.06.2022
Impfdatum: 24.04.2022
Beginn: 02.05.2022
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / LA

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

Electrocardiogram Hypoaesthesia Hypotonia Injection site pain Limb discomfort Mobility decreased

Symptomtext

Off and on since 1st injection lasting minutes to hours: numbness in arm, inability to make a fist, arm feels limp/heavy, pinching, burning sensation from injection site down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: ECG on 5/24/22
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Clindamycin (topical for acne), Wynzora (topical for psoriasis)
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2329675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

moderat

Staat: -
Alter: 25,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 21.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Costochondritis Dyspnoea

Symptomtext

Chest pain, shortness of breath. Diagnosed costochondritis.

Weitere VAERSDATA-Felder

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

VAERS 2325817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: SC
Alter: 26,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 21.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Dizziness Dyspnoea

Symptomtext

Patient experienced shortness of breath, dizziness, chest tightness and was light-headed.

Weitere VAERSDATA-Felder

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

VAERS 2325679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 23.05.2022
Beginn: 10.06.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: SYR / RA

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

Bronchitis COVID-19 Cough Headache Oropharyngeal pain Pneumonia SARS-CoV-2 test positive

Symptomtext

05/23/2022 Vaccination 06/10/2022 Started to experience sore throat, mild. 06/11/20232 HA, cough. Took at home COVID test, negative 06/13/2022 Rapid COVID; Positive 06/14/2022 PCR; I did not get the results till late on 06/15/2022. I had called the pharmacy as it was not posted and it was 48 hours since I took the test. The pharmacy mentioned it 'could be due the store losing power'. I felt that it took a long time to get the results, even though I was taking the necessary precautions to isolate. The health department didn't provide enough information on how to protect my family other then using a different sink when washing hands. I was not given any guidelines on how many days I was contagious, etc. I would have benefited from having that information up front when testing positive. 06/20/2022 COVID- *bronchitis and touch of pneumonia. Still have not recovered from COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: COVID; +
Aktuelle Erkrankungen: n/a
Vorgeschichte: High blood pressure, anxiety, osteopenia, high cholesterol
Andere Medikamente: Amlodipine, Calex, pravastatin, chloromax, calcium w/ Vit D, juice max
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2324203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CO
Alter: 67,0
Geschlecht: F
Eingang: 20.06.2022
Impfdatum: 11.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: IM / RA

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

Abdominal pain Anion gap Blood bicarbonate Blood glucose increased Blood ketone body Blood lactic acid increased Blood pH decreased Dehydration Diabetic ketoacidosis Fluid intake reduced Hypophagia Malaise Mental status changes Metabolic abnormality management Myalgia Nausea Treatment noncompliance Urine ketone body present

Symptomtext

Patient presented to hospital emergency department with slightly altered mentation and a 4-day history of nausea, vomiting, abdominal pain, and myalgias. Patient was found to be in diabetic ketoacidosis. Likely precipitating factors included minimal food and fluid intake, failure to administer routine insulin detemir, and continuation of daily dapagliflozin associated with severe malaise and dehydration following COVID-19 booster. Patient was given IV fluids and insulin with subsequent resolution of metabolic abnormalities and symptoms. Patient was discharged with comprehensive follow-up care plan in place.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: 6/16/22: Arterial pH 7.13 Bicarbonate arterial 4.3 mmol/L Blood glucose 253 mg/dL Venous lactate 4.8 mmol/L Anion gap 30 Urine ketones (+) Beta hydroxybutyrate >8 mmol/L
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes mellitus Hypertension Hyperlipidemia Sciatica/Left hip pain
Andere Medikamente: Insulin detemir Dapagliflozin Metformin Lisinopril Aspirin Gabapentin
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2322837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: NC
Alter: 71,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 20.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

Condition aggravated Hypoaesthesia Paraesthesia SARS-CoV-2 test COVID-19 Drug ineffective

Symptomtext

Peripheral numbness feet, legs; tingling in hands; right foot/leg and fingers were affected and right leg worse; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 20May2022 at 10:30 as dose 4 (booster), single (Lot number: FJ4991) at the age of 71 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Pancreatic carcinoma" (unspecified if ongoing); "known allergies: Shellfish" (unspecified if ongoing); "Physical therapy" (unspecified if ongoing). Concomitant medication(s) included: CALCIUM; VIT D3; ASPIRIN [ACETYLSALICYLIC ACID]; PANTOPRAZOLE. Vaccination history included: BNT162b2 (other vaccine same date product=Covid pfizer,, other vaccine same date lot number=FF2588,, other vaccine same date vaccine date=20May2022,, other vaccine same date dose number=3,, other vaccine same date vaccine location=Right arm), administration date: 20May2022, for covid-19 immunization. The following information was reported: HYPOAESTHESIA (non-serious), outcome "not recovered", described as "Peripheral numbness feet, legs"; PARAESTHESIA (non-serious), outcome "not recovered", described as "tingling in hands"; CONDITION AGGRAVATED (non-serious), outcome "not recovered", described as "right foot/leg and fingers were affected and right leg worse". The events "peripheral numbness feet, legs", "tingling in hands" and "right foot/leg and fingers were affected and right leg worse" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of hypoaesthesia, paraesthesia, condition aggravated. Additional information: Peripheral numbness feet, legs and tingling in hands. Started after first dose but didn't equate it with vaccine until after the most recent booster. Initially in left foot/leg only about two three weeks after shot. A week after the 4th booster my right foot/leg and fingers were affected and right leg worse. Then connected the dots from beginning. No other vaccines in four weeks. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 202202; Test Name: Nasal Swab; Test Result: Positive ; Test Date: 202204; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pancreatic cancer; Physical therapy; Shellfish allergy
Andere Medikamente: CALCIUM; VIT D3; ASPIRIN [ACETYLSALICYLIC ACID]; PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2320496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: KS
Alter: 18,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 15.06.2022
Beginn: 15.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Burning sensation Paraesthesia

Symptomtext

Patient described burning and tingling in right arm down to fingertips that lasted about 10 minutes. Symptoms resolved without intervention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: No Known Health Condiditions
Andere Medikamente: Xulane Patch
Allergien: NKA
Vorherige Impfungen: -

VAERS 2317675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WA
Alter: 74,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 15.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / LA

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

Condition aggravated Extra dose administered Fibromyalgia Limb discomfort Musculoskeletal discomfort Neuropathy peripheral No reaction on previous exposure to drug Polyneuropathy

Symptomtext

I had Peripheral Neuropathy in my feet for many years. It was well managed and little trouble. I am not diabetic. Similarly I have had fibromyalgia. I worsened in symptoms of both shortly after the second booster shot and I had additional discomfort in legs and lower back. These kept getting more serious. This became cause for a trip to the ER on 5th May. This result in a new diagnosis of Polyneuropathy and a prescription for Gabapentin. As of today, 13th June, symptoms are worsened and/or break through the medication. Note that this was my second booster shot for Covid and that I had *absolutely* no reaction to any of the other three shots. All were administered at the same pharmacy. I did notice that the second booster shot was "Grey cap" and the earlier three shots were "Purple cap"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Osteoporosis, Fibromyalgia, Peripheral Neuropathy
Andere Medikamente: Estradiol, Ibuprofen, Centrum silver, Calcium
Allergien: none known
Vorherige Impfungen: -

VAERS 2317389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CO
Alter: 58,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 05.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Dyspnoea Fatigue Pulmonary congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

My symptoms began approximately 2-3 days after my vaccine. My symptoms mimicked common seasonal allergies so I didn't think too much about it. I began to develop chest congestion, trouble breathing, intense coughing and fatigue. This was a clue that I needed to get tested. First day I found out I was positive, I did have an appointment with my nurse practitioner via virtual appointment. They prescribed the PAXLOVID. This medication has been significant for me. I would compare it to a very bad chest cold. The symptoms are lingering today. I was also on prednisone. I believe the medication has helped me from getting severely sick. The cough has been utterly exhausting. I have been able to work through it. The level of fatigue and exhaustion was extremely high the first few days. The chest congestion is much better today (I am on day 4). The runny nose is still here.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Hemochromatosis
Andere Medikamente: Montelukast; ALLEGRA D; atorvastatin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2258954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: NV
Alter: 78,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 26.04.2022
Beginn: 12.05.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / -

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

Arthralgia Chest pain Dyspnoea Condition aggravated Lymphadenopathy Tinnitus

Symptomtext

Developed tinnitus after first two rounds of COVID-19 vaccine and ENT prescribed lipo-flavonoid that seemed to be resolving issues. After receiving booster tinnitus increased in severity and is now in both ears. On May 12th I noticed a swollen lymph node. Went to urgent clinic. Urgent care doctor instructed me to monitor it. Urgent clinic doctor seemed certain that it was due to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: PSVT; Osteoporosis; Asthma; COPD; Allergies
Andere Medikamente: Verapamil; montelukast; PROVENTIL; MUCINEX; nasal spay
Allergien: Codeine; morphine; sulfa
Vorherige Impfungen: First two COVID-19 vaccines I experienced tinnitus in one ear.

VAERS 2258954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

moderat

Staat: NV
Alter: 78,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 26.04.2022
Beginn: 12.05.2022
Tage bis Beginn: 16,0
Dosis: UNK
Route/Site: IM / UN

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

Arthralgia Chest pain Dyspnoea Condition aggravated Lymphadenopathy Tinnitus

Symptomtext

Developed tinnitus after first two rounds of COVID-19 vaccine and ENT prescribed lipo-flavonoid that seemed to be resolving issues. After receiving booster tinnitus increased in severity and is now in both ears. On May 12th I noticed a swollen lymph node. Went to urgent clinic. Urgent care doctor instructed me to monitor it. Urgent clinic doctor seemed certain that it was due to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: PSVT; Osteoporosis; Asthma; COPD; Allergies
Andere Medikamente: Verapamil; montelukast; PROVENTIL; MUCINEX; nasal spay
Allergien: Codeine; morphine; sulfa
Vorherige Impfungen: First two COVID-19 vaccines I experienced tinnitus in one ear.

VAERS 2314551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 09.06.2022
Impfdatum: 08.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysphagia Erythema Hypoaesthesia oral Paraesthesia oral Throat irritation

Symptomtext

Patient experienced scratchy throat 5 to 10 min after receiving the two vaccinations. She came over to the pharmacy counter and I told her to sit down in front of me for a little bit. After another 10 min she complained that her tongue and lips felt numb and tingled, and was having slight difficulty swallowing. Her chest looked red. At this point I called for EMS and continued to monitor. She never had full blown anaphylactic symptoms, and an Epipen was never used. After being evaluated by EMS in the ambulance she declined futher treatment and drove herself home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Cystic Fibrosis
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 2313185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WA
Alter: 73,0
Geschlecht: M
Eingang: 08.06.2022
Impfdatum: 03.05.2022
Beginn: 03.06.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: SYR / LA

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

Atrial fibrillation Blood test Chest X-ray Electrocardiogram Laboratory test Palpitations

Symptomtext

I went into atrial fibrillation a month after receiving my vaccination. My heart was racing out of my chest. I went to the hospital, and they performed bloodwork, EKG, chest x-ray, and some other tests to confirm I wasn't having a heart attack or anything. They then gave me steroid drugs to decelerate my heart rate. They gave me medicated diltiazem to slow down my heart rate. They monitored me for a bit after that, and once it was back down to normal, I was sent home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Bloodwork, EKG, Chest X-Ray: 06/03/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes
Andere Medikamente: Fish Oil Melatonin 5mg Bayer Aspirin 81mg Centrum Silver Multivitamin Vitamin D3 50mg Pantoprazole SOD 40mg Pravastatin Sodium 10mg Lisinopril 5mg Metformin 500mg Doxazosin Mesylate 8mg Finasteride 5mg Acetaminophen 500mg
Allergien: Decongestants
Vorherige Impfungen: -

VAERS 2313068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: MS
Alter: 65,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 06.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain upper Coxsackie viral infection Headache Herpes zoster Pneumonia Rash Respiratory tract congestion

Symptomtext

My second dose of the Covid vaccine was in April 2021. In September that year, I got shingles which I've never had. I was sick for three weeks. I didn't associate it with the vaccine. But then I also contracted coxsackie virus and pneumonia within the next three months. In December I had my third dose and was fine so I proceeded with my fourth dose on 06/06/20222. I went in that Monday to receive the vaccine and by Tuesday, the next day I had broken out with shingles again. I've spoken with my doctor and I have an upcoming appointment. Although I'm not feeling too badly, the rash is almost identical to the one I had when I had shingles in September of 2021 and I'm having other similar symptoms such as congestion, headache and slight stomach pain. I had my shingles vaccine in April of 2022 which, I believe helped lessen the severity of this outbreak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma; Hypothyroidism
Andere Medikamente: Levothyroxine 112mg; AMBIEN 10mg; SINGULAIR; ANORO ELLIPTA inhaler; CLARITIN; FLOVENT inhaler; vitamin B2; melatonin; milk thistle; vitamin D
Allergien: Amoxicillin sensitivity; CAPRYL sensitivity; LEVAQUIN sensitivity; ibuprofen sensitivity
Vorherige Impfungen: Second dose of Pfizer. 04/24/2021. 64 years of age. Shingles outbreak within 5 months.

VAERS 2303790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 28.05.2022
Beginn: 28.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Asthma Chest discomfort Cough Dyspnoea

Symptomtext

persistent cough; Asthma exacerbation; chest tightness; difficulty breathing; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28May2022 at 11:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 37 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Mild asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose: 1, Manufacturer unknown), for Covid-19 Immunization; Covid-19 vaccine (Dose: 2, Manufacturer unknown), for Covid-19 Immunization; Covid-19 vaccine (Dose: 3, Manufacturer unknown), for Covid-19 Immunization. The following information was reported: ASTHMA (medically significant) with onset 28May2022 at 19:00, outcome "recovering", described as "Asthma exacerbation"; CHEST DISCOMFORT (medically significant) with onset 28May2022 at 19:00, outcome "recovering", described as "chest tightness"; DYSPNOEA (medically significant) with onset 28May2022 at 19:00, outcome "recovering", described as "difficulty breathing"; COUGH (medically significant) with onset 28May2022 at 19:00, outcome "recovering", described as "persistent cough". The events "persistent cough", "asthma exacerbation", "chest tightness" and "difficulty breathing" required emergency room visit. Therapeutic measures were taken as a result of cough, asthma, chest discomfort, dyspnoea. Clinical course: The patient had no known allergies. She did not receive other vaccine in four weeks. She did not have covid prior vaccination and did not tested for covid post vaccination. The patient was treated with dexamethasone. Follow-up attempts are completed. 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: Mild asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2310575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OR
Alter: 68,0
Geschlecht: M
Eingang: 06.06.2022
Impfdatum: 14.04.2022
Beginn: 29.05.2022
Tage bis Beginn: 45,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Asthenia COVID-19 Cough Dyspnoea Headache Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID break through Case. I received my 2nd booster shot on 04/14/2022. I tested positive for COVID 05/28/2022. I was also positive on 05/30/2022. My symptoms on 05/28/2022 were fever, headache, lack of energy, cough, joints aches, shortness of breath. I did a tele health on 05/29/2022 and my doctor prescribed me PAXLOVID and Aspirin. I took it for 5 days. As of now am still testing positive. My headache, cough, fever, joint aches are gone. I just have lack of energy. I will take a COVID home test on 06/09/2022 because am planning to travel if it's not negative I will not travel.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID home test
Aktuelle Erkrankungen: headaches frequently
Vorgeschichte: none
Andere Medikamente: Regular med - aspirin, eye drop for glaucoma
Allergien: none
Vorherige Impfungen: -

VAERS 2307424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 09.05.2022
Beginn: 09.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Blood test normal Body temperature increased Chest discomfort Confusional state Cough Dyspnoea Electrocardiogram normal Fatigue Feeling abnormal Feeling cold Feeling hot Full blood count normal Hyperhidrosis Immunisation reaction

Symptomtext

That evening after the vaccine around 06:30PM ET I told my husband I felt cold, then I felt hot. I took my temperature and it was 104F. I got in the floor because the bed was soaking wet because I was sweating so bad. That whole week I felt extremely tired and had extreme brain fog and confusion, a dry hacking cough a heaviness in my chest that made me feel like I could not get my breath. I called the doctor on Monday to make an appointment. I went in on Tuesday, the doctor did a complete check up. He ran an EKG, had a complete CBC blood panel work up done. Everything came back negative. My doctor feels that I had an adverse reaction to the second booster shot and that it may take a couple weeks for me to get over this. To this day I am still experiencing some brain fog and I still have times that I cannot get enough air in my lungs. I have fatigue now and that is not me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG negative. Complete CBC blood panel negative.
Aktuelle Erkrankungen: No
Vorgeschichte: Allergies
Andere Medikamente: Lisinopril 20mg; metformin HCL 500mg; vitamin D3; Allergy-Cyr; Livalo; allopurinol 100mg 300mg; levothyroxine 25mcg; amlodipine 10mg; cinnamon
Allergien: Penicillin; erythromycin; scopolamine
Vorherige Impfungen: -

VAERS 2301695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 29.05.2022
Impfdatum: 28.05.2022
Beginn: 28.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Erythema Hyperhidrosis Nausea

Symptomtext

PATIENT GOT PFIZER AS THE SECOND BOOSTER AFTER GETTING J&J 2 TIMES. PATIENT COULD NOT BREATHE. PATIENT TURNED RED AND WAS NAUSEOUS AND SWEATING. WE CALL 911 AND PATIENT GOT BETTER AFTER 10-15 MINUTES WITHOUT ANY MEDICATION GIVEN. I CALLED TO FOLLOW UP. PATIENT FEELS WELL AND DID NOT HAVE ANY SIDE EFFECTS AFTER THAT.

Weitere VAERSDATA-Felder

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

VAERS 2298743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 12.05.2022
Beginn: 21.05.2022
Tage bis Beginn: 9,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Condition aggravated Cough Fatigue Headache Malaise Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I received my 2nd booster shot on 05/12/2022 and my COVID symptoms started on 05/21/2022 in the morning around 8-9:00AM runny nose , and i got really tired. I couldn't stay awake. cough , headache, sore throat. on 05/22/2022 i did home test which was negative and 05/24/2022 it was negative. i also went to health department in the evening on 05/24/2022 . and i received my test result on 05/25/2022 was positive. I did telehealth with my doc he prescribed me oral medication, inhaler. i am in the process of recovery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: PCR COVID HOME TEST
Aktuelle Erkrankungen: headaches normal
Vorgeschichte: asthma, hypertension,
Andere Medikamente: regular meds - cintriod, losartan, cingular vigal , breo- inhaler, qnasal ( nasal spray
Allergien: none
Vorherige Impfungen: -

VAERS 2296788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WI
Alter: 65,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 21.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered Injected limb mobility decreased Injection site pain

Symptomtext

PATIENT DESCRIBES A PAIN NEAR THE INJECTION SITE A COUPLE OF HOURS AFTER ADMINISTRATION BUT NOTED ZERO DISCOMFORT IMMEDIATELY AFTERWARDS. THE PAIN HAS BEGUN TO SPREAD UP INTO HER SHOULDER AND NECK AS TIME GOES ON. SHE REPORTS PAIN WITH SLEEPING ON HER RIGHT ARM AND IS LIMITED ON RANGE OF MOTION.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: HYPERTENSION
Andere Medikamente: N/A
Allergien: PENICILLIN, ACE INHIBITORS
Vorherige Impfungen: -

VAERS 2292726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: VA
Alter: 55,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 09.05.2022
Beginn: 19.05.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / RA

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

Cough Dyspnoea Exposure to SARS-CoV-2 Exposure via direct contact Headache Influenza like illness Pain SARS-CoV-2 test SARS-CoV-2 test negative Sinus congestion Suspected COVID-19 Upper-airway cough syndrome

Symptomtext

My nephew was infected, and I was in contact with him last week and three days later I started having sob, headache, ache cough sinus congestion postnasal drip flu like symptoms. I haven't had a fever at all. On Friday May 20 I took a home test then call my Dr about getting PCR test and they referred me to the urgent care and they don't have them at my PCPS office. They did a rapid at the urgent care it was negative, and they sent off samples for the PCR and it was also negative. They instructed me to rest and to push fluids. They told me they were unable to do anything without a positive test. Called my Dr and they thought I do have COVID but I was testing too soon for a positive test. The Dr said she was going to treat as if I had COVID I was put on an antibiotic and cough syrup. I have an inhaler that I take it whenever my asthma starts to act up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Celiac IBSD Nash Chiari type 1 Asthma Hypothyroid Osteoarthritis Chronic migraines Obesity psoriasis
Andere Medikamente: Butropion 75mg2x a day Topiramate 50mg 2x a day Celecoxib 200mg 2x a day Montelukast 10mg 1x a day Rosuvastatin 20mg 1x a day Citalopram 40mg 1x a day Levothyroxine 0.125mg 1x a day Dicyclomine 10mg 1 a day 4x day as directed Albut
Allergien: Tetrytol Levaquin
Vorherige Impfungen: -

VAERS 2290180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: VA
Alter: 84,0
Geschlecht: M
Eingang: 22.05.2022
Impfdatum: 20.05.2022
Beginn: 21.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Immunisation reaction Mobility decreased Muscular weakness Pyrexia Rash

Symptomtext

Patient broke out in a rash over chest, back and arms and experienced muscle weakness in legs and arms and was unable to move out of the bed at 3:00 am on Saturday 5/21/2022. Patient also had a fever of 101 degrees Fahrenheit. Patient's wife called EMS where the rescue squad came to evaluate. He was told to take Tylenol and did take two Tylenol. Patient's wife states that EMS told her it was a reaction to the COVID vaccine. As of Sunday at roughly 12:15 pm, the patient's wife reported that the rash was gone and that he can now move arms and legs with no issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No known other illnesses
Vorgeschichte: Unknown
Andere Medikamente: Ropinirole, levothyroxine, metoprolol succinate, tamsulosin
Allergien: No known drug allergies
Vorherige Impfungen: Patient had a reaction to the second Shingrix vaccine when he was 83 years old. He had a red rash develop on both sides of the

VAERS 2290061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: OH
Alter: 17,0
Geschlecht: F
Eingang: 22.05.2022
Impfdatum: 21.05.2022
Beginn: 21.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperventilation Pallor Respiration abnormal Tremor Visual impairment

Symptomtext

About 2-3 minutes after receiving vaccine, patient became a little dizzy, wash visibly shaky, and face went pale. She was also hyperventilating a little. She mentioned her vision was starting to go dark around the edges. Patient was seated at this time. Her mother alerted us right away, we grabbed the emergency use bag and went out to monitor her. Patient was responsive and we observed no swelling or trouble breathing. Patient mentioned she could breathe fine as well. Pharmacist had patient count her breathing (4 sec inhale, hold 4 seconds, 4 sec exhale, hold 4 sec), while instructing a coworker to grab a cold water. Patient was wearing a smart watch that showed her pulse, so pharmacist was keeping an eye on that as well (in the few minutes we were with her the highest pulse pharmacist saw was 78). We administered a dose of benadryl 50m to the patient at mother's request. Once the patient's breathing returned to normal (about 2-3 more minutes) the color came back to her face. Had patient wait about 15 more minutes, after symptoms resolved before letting them leave the store.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: check pulse from patient's smart watch.
Aktuelle Erkrankungen: none mentioned on VAR
Vorgeschichte: none reported
Andere Medikamente: unknown (tried to call patient 4 times 5/21/22 and 5/22/22)
Allergien: none known
Vorherige Impfungen: -

VAERS 2284990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 20.04.2022
Beginn: 15.05.2022
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain COVID-19 Cough Dyspnoea Fatigue Malaise Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 5/15/2022 with symptoms of sore throat, congestion, and when I woke up Monday my whole body was aching, fatigue, cough, minor difficulty breathing, and intermittent abdominal pain. I was prescribed Paxlovid 05/18/2022 which leaves a terrible metallic taste in my mouth. The sore throat and body aches have abated, but I am still feeling very ill.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 05/18/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Vitamin C; vitamin D3; vitamin K2; B12 liquid; chlorophyll drops; Synthroid; Dulera inhaler
Allergien: Penicillin; sulfa
Vorherige Impfungen: -

VAERS 2276406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

moderat

Staat: NM
Alter: 73,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 29.04.2022
Beginn: 02.05.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Asthenia Confusional state Dyspnoea Gait disturbance Hyperhidrosis Incontinence Neck pain Pain in extremity Pelvic pain Sleep disorder Vomiting Wheezing

Symptomtext

Woke at 2:30 AM bathed in sweat, intense,severe pain neck, shoulders, hands, feet, pelvis. Profound weakness, difficulty walking. Incontinence, vomiting. Shortness of breath, wheezing, confusion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Stenosis, Osteoarthritis, PVD, Neuropathy
Andere Medikamente: Ibuprofen, Metapropol, Loratidine, Simvastatin, Levothyroid, Fluoxetine, Gabapentin, Omeprazole, Mulit Vits, Calcium, Vit D, Hydrocodone, Probiotics
Allergien: Demeral
Vorherige Impfungen: -

VAERS 2273500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

moderat

Staat: WA
Alter: 75,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 06.04.2022
Beginn: 24.04.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chills Dehydration Diarrhoea Fatigue Feeding disorder Foreign travel Nasal congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

I was out of the country. I started to have nasal congestion, chills, fever. I was extremely fatigued the next day. That progressed to having diarrhea and being unable to eat and became dehydrated. My wife went to the pharmacy and got fluimucil, Imodium, and dioralyte. I had fever and chills for 3 days. I had diarrhea for 8 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: covid test- positive
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: propecia flonase Allopurinol finasteride
Allergien: pork soy milk turkey
Vorherige Impfungen: -

VAERS 2268897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 10.04.2022
Beginn: 01.05.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: SYR / LA

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

Asthma Blood potassium increased Blood test COVID-19 Chest discomfort Condition aggravated Dyspnoea Metabolic function test Nasopharyngitis Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

I woke up Sunday and felt like I had a cold. I had a scratchy throat and runny nose and on Monday, I still had the sore throat, runny nose and body aches. On Tuesday, the symptoms triggered my asthma, and I was still having all of those symptoms even on Wednesday. On Thursday, most symptoms had gone away but I was having chest tightness and my asthma symptoms got worse. By Sunday I was having trouble breathing so I was using a peak flow meter even though my O2 sat stayed at 99%. My numbers are coming up with the peak flow meter and I am still taking Prednisone. I am feeling better, but my nose is still runny, and I still feel like I am having an asthma problem.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID-19 Test - Positive Blood Test - BMP Potassium was high in the morning and they redrew in the afternoon, and it was normal
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetic Type 1 Asthma Hashimoto's Disease
Andere Medikamente: Novolog Insulin Sliding Scale Levothyroxine 112mcg Lipitor 10 mg Monoculist 10 mg Zyrtec Aspirin 81 mg Flovent Inhaler 110 mcg Estradiol Patch .025 mg Testosterone Gel Vitamin K with D3
Allergien: Sulfa Wheat
Vorherige Impfungen: Flu shot in the 1995 - whole arm swelled up

VAERS 2267658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: AZ
Alter: 62,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 01.04.2022
Beginn: 03.05.2022
Tage bis Beginn: 32,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Influenza virus test negative SARS-CoV-2 test positive

Symptomtext

Covid positive with COVID pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Influenza negative, COVID positive
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, hypertension
Andere Medikamente: advair, montelukast, lisinopril, premarin
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2267160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ 4991

moderat

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 08.05.2022
Impfdatum: 03.04.2022
Beginn: 24.04.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: - / -

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

Angiogram abnormal Cardiac stress test abnormal Catheterisation cardiac abnormal Chest pain Coronary arterial stent insertion Coronary artery occlusion

Symptomtext

4/24/22 - chest pain under stress and ay high altitude 4/28/22 - "flunked" stress test ordered by cardiologist 5/2 /22 - Cath study/angiogram. 80% occlusion of LAD found. Stent inserted. Feeling fine now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: See above.
Aktuelle Erkrankungen: Cardiomyopathy
Vorgeschichte: Cardiomyopathy
Andere Medikamente: Too many to list
Allergien: None
Vorherige Impfungen: -

VAERS 2262384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 08.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: IM / LA

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

Chest X-ray normal Cough Electrocardiogram abnormal Electrocardiogram ambulatory Fatigue Insomnia Myalgia Palpitations Rhinorrhoea SARS-CoV-2 test negative Ventricular extrasystoles

Symptomtext

I don't know whether this would count as an adverse event but 2 weeks after receiving my 2nd booster (4th vaccine injection), I developed a cough, runny nose, significant palpitations, and fatigue with muscle aches that lasted 3 days. The palpitations were so frequent that it was hard to sleep. I still have the cough and occasional palpitations as of May 3rd. I took a Covid test (PCR) which was negative. I saw Urgent Care (Dr.) on Monday 4/25/22 who ran an EKG and did a Chest x-ray. My lungs were clear and my EKG was normal except for a PVC. He thought I was having multiple PVCs and referred me to a cardiologist who placed me on a Holter monitor for 2 weeks (I'm still wearing it so I don't have results). As of today, the PVCs are much reduced but still occurring and I still have a cough but not frequently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Negative Covid test (PCR) - 4/24/2022 EKG - 4/25/2022 Chest x-ray - 4/25/2022 Holter monitor x 2 weeks (in progress) - placed 4/29/2022
Aktuelle Erkrankungen: -
Vorgeschichte: skin form of lupus (in remission - no meds); osteoarthritis; scoliosis; mitral valve prolapse (no regurgitation); allergic rhinitis
Andere Medikamente: Flonase nasal spray, estradiol patch, Astelin nasal spray, Zyrtec, Vit. C, multivits for women over 50, magnesium, tumeric capsule (1000 mg), ursodiol, tylenol as needed
Allergien: Allergic to sulfa drugs and levaquin Allergic to peanuts
Vorherige Impfungen: sore arm, fatigue, achiness for 24-48 hrs following the first 3 covid vaccinations

VAERS 2258309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: WI
Alter: 46,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 27.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Arthralgia Cardiac flutter Chest X-ray Chest pain Dyspnoea Electrocardiogram Fatigue Fibrin D dimer Full blood count Laboratory test Myalgia Nausea Pain in extremity Pulmonary pain Sleep disorder

Symptomtext

Severe new persistent Left sized chest pain, severe persistent left sized lung pain, nausea, chest fluttering, abnormal fatigue, inability to lay on left side due to lung pain, shortness of breath, muscle ache in left arm , generalized severe joint pain and pain in hands like being sliced with razor blades.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CBC, d dimer, chem 8, 12 lead ecg, cxr, ED visit r/o stemi work up for pe, dvt. Primary md to follow up with cardiac mri and stress test as pain persists in lung and chest after discharge from ED.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma controlled for years
Andere Medikamente: None
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2256850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 18.04.2022
Beginn: 25.04.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: SYR / LA

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

Condition aggravated Erythema Inflammation Loss of personal independence in daily activities Pain Pain in extremity Psoriasis Trismus

Symptomtext

Incredibly painful exacerbation and onset of new psoriasis legions. My usual topical ointments also seem to worsen the pain. This happened with all three prior Pfizer COVID vaccines as well EXCEPT with the first booster. The intense pain lasted a good many weeks with vaccines #1 and #2. Hoping this #4 response is shorter-lived. The pain (and redness) is intense. ALSO, with the #1 vaccine, I suffered for about 3 weeks with an inflammatory reaction in my left jaw--the pain was so severe, I was on liquids and soft foods and could barely open my mouth wide enough for a toothbrush. I could not use my electric toothbrush during that time. And much worse with #1 and #2 and intermittently at a lower pain level ever since, I now live with painful squeezing in the tips of my toes and painfully squishy fingertips (I'm a guitarist and this has now limited my playing considerably). BUT, I did have one month of non-squishy/non-painful fingertips about 5 mos after vaccine #3 (first booster), when it ALL resolved. But having just gone for the second booster (vax #4), I'm right back to where I was before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Discussed with my group of doctors (PCP, derm, rheum) but no specific tests performed. Derm confirmed for me that the psoriasis exacerbation was most likely from the vaccine. I also sought help from a vascular surgeon about the intensely painful squeezing of toes (most occurrences in the night) but he found my peripheral pulses to be good.
Aktuelle Erkrankungen: Psoriatic arthritis, Psoriasis, Fluctuating IBS, Degenerative Disc Disease, Coccydinia, Lichen Sclerosis
Vorgeschichte: Psoriatic arthritis, Psoriasis, Fluctuating IBS, Degenerative Disc Disease,
Andere Medikamente: Simponi (injectable), Benicar, Metoprolol, Tacrolimus Ointment, Hydrocortisone Ointment, Calcipotriene Cream, Vitamin B12, Vitamin D3
Allergien: Penicillin, Levaquin family, Latex, Indocyn, NSAIDs
Vorherige Impfungen: -

VAERS 2248015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: IA
Alter: 78,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 18.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

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

Arrhythmia Blood test Cardiac monitoring Electrocardiogram Fatigue Feeling abnormal

Symptomtext

04/18/202 I received my booster 4. I started to experience adverse event from 04/21/2022 I felt tired, My heart would not stay in a regular rhythm. I tried to rest but it wont not help. I felt poorly and I had my friend to take me to ER they did EKG, blood work and they hooked me up to a heart monitor. I happened yesterday morning. It was happening for couple of days. I was admitted in the ER for 7 hours. The doctor said they had seen other patients with the same issue after the 4th booster. They suggested I should take magnesium.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: EKG, Bloodwork
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Eliquis; Metoprolol
Allergien: Morphine; Darvon
Vorherige Impfungen: Vaccine 1, 2, 3 headache, sore arm and tired feeling.

VAERS 2245941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: NC
Alter: 61,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 08.04.2022
Beginn: 09.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Herpes zoster Paraesthesia

Symptomtext

It started the following day. It was a tingling sensation on my scalp and my face. I have had it before so I knew it was shingles. I still have it today. I am currently on Valtrex to treat it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes type II, Chronic Kidney Disease, Hypertension, Hyperlipidemia
Andere Medikamente: Lantus, Ozempic, Lokelma, Avapro, Synthroid, Lipitor (Atorvastatin) , Vitamin E, Vitamin D with calcium, Vitamin C, Aspirin, Coreg
Allergien: None
Vorherige Impfungen: -

VAERS 2226043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: TN
Alter: 59,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 22.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Deafness unilateral Tinnitus

Symptomtext

I starting having ringing in both ear. It is still ongoing since my last vaccine. I have been to audiologist about this. They said I have a little loss of hearing in my right ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Aspirin; Latex
Vorherige Impfungen: -

VAERS 2182787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

moderat

Staat: CT
Alter: 26,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 14.03.2022
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Body temperature Pain in extremity Pyrexia Chills Dizziness Hyperhidrosis Tachycardia

Symptomtext

fever over 100F; Sore arm; 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), administered in arm left, administration date 14Mar2022 06:30 (Lot number: Fj4991) at the age of 26 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Attention deficit hyperactivity disorder" (unspecified if ongoing); "Known Allergies: sulfa drugs" (unspecified if ongoing); "if covid prior vaccination: Yes" (unspecified if ongoing). Concomitant medication(s) included: ADDERALL. Past drug history included: Morphine, reaction(s): "Known Allergies: Morphine". Vaccination history included: Bnt162b2 (Dose 1, lot number=Fk9895, administration time=05:00 PM, vaccine location=Left arm), administration date: 18Feb2022, when the patient was 26 years old, for Covid-19 immunization, reaction(s): "I almost fainted immediately after the first dose/Felt faint for a few days", "my arm and fingers on the left side went numb", "Severe chills", "fever over 100F", "Sore arm". The following information was reported: PYREXIA (non-serious), outcome "unknown", described as "fever over 100F"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Sore arm". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: No other vaccine received in four weeks. Other medications in two weeks: Generic Adderall IR. After second dose, patient had fever over 100F and Sore arm. No loss of touch in arm or hand. Not tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Name: fever; Result Unstructured Data: Test Result:100 Fahrenheit; Comments: fever over 100F
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD; COVID-19; Sulfonamide allergy
Andere Medikamente: ADDERALL
Allergien: -
Vorherige Impfungen: -

VAERS 2182787

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge Fj4991

moderat

Staat: CT
Alter: 26,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 14.03.2022
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Body temperature Pain in extremity Pyrexia Chills Dizziness Hyperhidrosis Tachycardia

Symptomtext

fever over 100F; Sore arm; 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), administered in arm left, administration date 14Mar2022 06:30 (Lot number: Fj4991) at the age of 26 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Attention deficit hyperactivity disorder" (unspecified if ongoing); "Known Allergies: sulfa drugs" (unspecified if ongoing); "if covid prior vaccination: Yes" (unspecified if ongoing). Concomitant medication(s) included: ADDERALL. Past drug history included: Morphine, reaction(s): "Known Allergies: Morphine". Vaccination history included: Bnt162b2 (Dose 1, lot number=Fk9895, administration time=05:00 PM, vaccine location=Left arm), administration date: 18Feb2022, when the patient was 26 years old, for Covid-19 immunization, reaction(s): "I almost fainted immediately after the first dose/Felt faint for a few days", "my arm and fingers on the left side went numb", "Severe chills", "fever over 100F", "Sore arm". The following information was reported: PYREXIA (non-serious), outcome "unknown", described as "fever over 100F"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Sore arm". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: No other vaccine received in four weeks. Other medications in two weeks: Generic Adderall IR. After second dose, patient had fever over 100F and Sore arm. No loss of touch in arm or hand. Not tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Name: fever; Result Unstructured Data: Test Result:100 Fahrenheit; Comments: fever over 100F
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD; COVID-19; Sulfonamide allergy
Andere Medikamente: ADDERALL
Allergien: -
Vorherige Impfungen: -

VAERS 2196561

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

moderat

Staat: IL
Alter: 33,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Back pain Chest pain Chills Dysgeusia Gait disturbance Headache Mobility decreased Pain Pyrexia Taste disorder Tremor

Symptomtext

12 hours after receiving the vaccine, I developed severe body aches, including my right knee almost unable to move/walk. I spiked a fever up to 101.8, chills with shivering/tremors, and a headache. Over 24 hours later, I am still experiencing significant body/joint aches. I also have developed a metallic taste in my mouth and anything I eat or drink tastes metallic. I have had chest pains and severe upper left and middle back pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, anxiety/ADHD, endometriosis
Andere Medikamente: Losartan, hydrochlorothiazide, buspirone
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2679106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 61,0
Geschlecht: M
Eingang: 04.09.2023
Impfdatum: 16.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Contusion Pruritus Skin haemorrhage Skin necrosis

Symptomtext

looks like if you are on a blood thinner where you have those kind of skin necrosis only he is not on a blood thinner.; itching did not start until the 2nd dose for the itching and now this skin pattern where it is easy to bleed started much later and he has patching that was there he thought from the itching; itching has increased dramatically; noticed as of late there is a larger pattern of bruising/patching that is bruised; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old male patient received BNT162b2 (BNT162B2), on 16Jun2022 as dose 3 (booster), single (Lot number: FJ4991) at the age of 61 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (dose 1, lot number: EP6955), administration date: 19Mar2021, when the patient was 60-year-old, for COVID-19 Immunization, reaction(s): "rash on left arm above his wrist on forearm", "itching all over the body after rash formed"; BNT162b2 (Dose 2), administration date: 09Apr2021, when the patient was 60-year-old, for COVID-19 Immunization, reaction(s): "itching did not start until the 2nd dose for the itching and now this skin pattern where it is easy to bleed started much later and he has patching that was there he thought from the itching", "itching has increased dramatically", "looks like if you are on a blood thinner where you have those kind of skin necrosis only he is not on a blood thinner", "noticed as of late there is a larger pattern of bruising/patching that is bruised". The following information was reported: SKIN NECROSIS (medically significant), outcome "unknown", described as "looks like if you are on a blood thinner where you have those kind of skin necrosis only he is not on a blood thinner."; SKIN HAEMORRHAGE (non-serious), outcome "unknown", described as "itching did not start until the 2nd dose for the itching and now this skin pattern where it is easy to bleed started much later and he has patching that was there he thought from the itching"; PRURITUS (non-serious), outcome "not recovered", described as "itching has increased dramatically"; CONTUSION (non-serious), outcome "unknown", described as "noticed as of late there is a larger pattern of bruising/patching that is bruised". The events "looks like if you are on a blood thinner where you have those kind of skin necrosis only he is not on a blood thinner.", "itching did not start until the 2nd dose for the itching and now this skin pattern where it is easy to bleed started much later and he has patching that was there he thought from the itching", "itching has increased dramatically" and "noticed as of late there is a larger pattern of bruising/patching that is bruised" required physician office visit. Clinical course: After his 2nd dose, he thought itching was a side effect and he has that on file and after that, now it is probably to the top level of boosters that he has had and where he is supposed to be and the condition of itching has increased dramatically and he has the skin condition to his forearms and it accelerated enough that it looks like if you are on a blood thinner where you have those kind of skin necrosis only he is not on a blood thinner. He is seeing a dermatologist. The itching did not start until the 2nd dose for the itching and now this skin pattern where it is easy to bleed started much later and he has patching that was there he thought from the itching. The itching increased dramatically and he does not know when it began to increase dramatically but guesses it is when he first noticed it was just there and did not notice it being increased but noticed as of late there is a larger pattern of bruising, bleeding and patching that is bruised.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300290354 same patient/vaccine, different dose/event;US-PFIZER INC-2021412848 same patient/vaccine, different dose/event;US-PFIZER INC-202300290360 same patient/vaccine, different dose/event;US-PFIZER INC-202300290361 same patient/vaccine, different dose/event;

Weitere VAERSDATA-Felder

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

VAERS 2652056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 03.07.2023
Impfdatum: 30.06.2022
Beginn: 01.01.2023
Tage bis Beginn: 185,0
Dosis: 4
Route/Site: IM / AR

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

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

Symptomtext

One day in January 2023, I woke up with a slight cough and extreme fatigue. I took a home antigen test and got a positive result. I called my doctor, who asked me if I wanted Paxlovid. When she explained the possible side effects to me, I decided not to take it. She instead prescribed me a nasal spray and a steroid. I self-isolated at home for about two weeks. The symptoms were very mild. I never developed any symptoms besides the cough and fatigue, both of which remained mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: JAN2023 - Home Antigen Test - Positive Result
Aktuelle Erkrankungen: None
Vorgeschichte: COPD; Hypertension; Pre-Diabetes
Andere Medikamente: Multivitamin; Vitamin D3; Fiber Pills; Calcium; Vitamin C; Glipizide; Fluticasone Propionate Inhaler; Losartan
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2647187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: DE
Alter: 60,0
Geschlecht: F
Eingang: 20.06.2023
Impfdatum: 16.06.2022
Beginn: 02.02.2023
Tage bis Beginn: 231,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Bronchitis COVID-19 Fatigue Malaise Oropharyngeal pain Pain in extremity SARS-CoV-2 test positive Sneezing

Symptomtext

I had a sore arm and fatigued for about two days after receiving the vaccine. I began not feeling well on 01/31/2023 with sneezing and sore throat. I tested positive for COVID-19 on 02/02/2023. I contacted my doctor and got a prescription for prednisone and an antibiotic. I also had bronchitis too. As of today, I am feeling better but for four months since having COVID-19, I had extreme fatigue and really bad joint pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 02FEB2023 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: N/A
Allergien: Seasonal Allergies
Vorherige Impfungen: -

VAERS 2644758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 13.06.2023
Impfdatum: 24.05.2022
Beginn: 25.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Asthenia Fatigue Hyperhidrosis Lyme disease Malaise Nasopharyngitis Pain

Symptomtext

I experienced generalized achiness, malaise, sweats and total lack of energy. This began within 24 hours of booster. Within a week I had joint pain in ankles, knees and wrists. I continued to be very tired. I got an NSAID and advised to hydrate well. This lasted about 3 three weeks. I had already diagnosed previously with lime disease but this seemed to be a flare up. This past weekend I another flare up. I also have a cold at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Depression; Anxiety
Andere Medikamente: Amlodipine; Escitalopram; Turmeric; Vitamin B3; Ashwagandha; Zinc; Vitamin K; Super beets; Ubiquinol; Elderberry
Allergien: Penicillin; Sulfa; Peaches; Pears; Plums; Apples; Cherries; Latex
Vorherige Impfungen: Shingles, massive swelling at injection site, 2016.

VAERS 2644587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AZ
Alter: 59,0
Geschlecht: F
Eingang: 13.06.2023
Impfdatum: 12.06.2022
Beginn: 27.02.2023
Tage bis Beginn: 260,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chest discomfort Cold sweat Cough Dizziness Feeling abnormal Feeling cold Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

2/27/23 I woke up with a sore throat. I then became cold, clammy and lightheaded. I did not feel like I was with it. I began feeling a tightness in my chest and a headache that was unbelievable. I took a Tylenol. I went to Urgent Care and tested positive for COVID. I was prescribed Paxlovid and began taking it that day. I continued with a cough for two weeks. I took 2 at home COVID tests that were positive and then one that was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 27FEB23- COVID Test-Positive; 7MAR23-At Home COVID Test-Positive; 15MAR23- At Home COVID Test-Positive; 21MAR23-At Home COVID Test-Negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Collagen
Allergien: None
Vorherige Impfungen: -

VAERS 2636066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 75,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 27.10.2022
Beginn: 14.02.2023
Tage bis Beginn: 110,0
Dosis: 4
Route/Site: IM / RA

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

Alanine aminotransferase increased Aneurysm repair Angiogram cerebral normal Angiogram normal Anticoagulant therapy Aphasia Aspartate aminotransferase increased Atelectasis Autoimmune hepatitis Blood lactic acid normal Constipation Diplopia Endotracheal intubation Headache Hepatitis viral test negative COVID-19 Chest X-ray normal Computerised tomogram abdomen

Symptomtext

2/14/2023-Presents to ED, c/o headache, aneurysm repair previous week. Blurry and double visions. Aphasia. Afebrile BO 147/91. Covid + test. CXR- no pulm disease . 95% on 4/L NC, desat to 83% on 6/L NC, intubated (40% mechanical ventilation). CT/CTA- no artery occlusion. Cerebral angio completed (robust flow to b/l PCA's). Remdesivir. 2/16/2023- Remained intubated, awake and following commands. Chest CT-small effusions and basal atelectasis. Cont on heparin gtt. Exubated. Hemo stable. WBC 11.9 afebrile but on decadron. Remdesivir d/c AST-73 ALT-91 Lipase- 466 Remains on ceftriaxone 2/18/2023- Remains on RA. Uprendng transaminase transaminitis AST 117 and ALT 124 Lipase now 857 CT abd-post/op chole clips in plac show no complications of pancreatitis. GI consult_ increase in lipase r/t constipation and UTI. bowel regimen. 2/20/2023 WBC wnl. Downtreding LFT's AST 72 and ALT 116 2/23/2023- Remains on RA. Hemo stable. WBC-9.6 ALT-137 AST -74. Lactic acid negative. Hepatitis serologies negative . Afebrile. D/c to home follow for autoimmune hepatitis outpatient basis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cerebral aneurysm repair, HTN, CAD w stent, A fib.
Andere Medikamente: -
Allergien: PCN
Vorherige Impfungen: -

VAERS 2635570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TX
Alter: 79,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 20.05.2022
Beginn: 13.01.2023
Tage bis Beginn: 238,0
Dosis: 4
Route/Site: SYR / LL

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

Computerised tomogram Magnetic resonance imaging Pain Pancreatitis Somnolence X-ray

Symptomtext

I woke up early did housework I got sleepy layed on the couch an hour later I wloke up with a bad pain and called EMS. I was taken to the Hospital and was there from 13JAN2023 to 17JAN2023.

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Praegender Schweregrund: Pain
Hospital-Tage: 5,0
Labordaten: Xrays; CAT Scan; MRI; Diagnosis - Pancreatitus
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol
Andere Medikamente: Calcium; Glucosamine Condroitin; Allegra; Atorvastatin
Allergien: Cedar
Vorherige Impfungen: -

VAERS 2633504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 18.05.2023
Impfdatum: 17.05.2022
Beginn: 16.04.2023
Tage bis Beginn: 334,0
Dosis: 4
Route/Site: IM / LA

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

Cough Eye discharge Eye infection Fatigue Malaise No adverse event SARS-CoV-2 test negative Swelling of eyelid

Symptomtext

I did not have a adverse reaction to the vaccine. On 04/16, I began not feeling well and tired all day. I developed a cough on 04/17. On 04/21, I woke up with my left eye was swollen and glued shut like I had conjunctivitis. I went to an urgent care facility and got antibiotics for the infection. The eyedrops they gave me for the eyes did not work so I had to get another prescription. I tested negative for COVID-19 on 04/16/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 16APR2023 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Atorvastatin; CoQ10; Vitamin C
Allergien: Keflex
Vorherige Impfungen: -

VAERS 2629091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 78,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 03.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: SYR / LA

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

Feeling abnormal Influenza like illness Pyrexia

Symptomtext

I felt like I had a flu, I had a high fever of 104. I took an asprin and I took a nap but I thought I wasn't gonna wake up, I went to the doctor because I thought I had an infection from my previous heart valve replacement. I wasn't myself for a week or so.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes 2; Heart velv; Heart attack
Andere Medikamente: Ozampec; Losartan; Omeprazol; Loratadine; Aspirin; Travoprost; Benadryl; Lovastatin; Vitamin D3; Biotin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2626445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MA
Alter: 67,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 26.04.2022
Beginn: 25.12.2022
Tage bis Beginn: 243,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

It started with a sore throat then a headache and fever. I went to urgent care locally. I was given a COVID-19 test and it was positive. I emailed my PCP and I was emailed back to take PAXLOVID and took it for five days and then I was back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 31DEC2022 COVID-19 test, positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Atenolol; valproic acid; multivitamin; vitamin C; vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2619883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 78,0
Geschlecht: M
Eingang: 24.04.2023
Impfdatum: 22.04.2022
Beginn: 21.02.2023
Tage bis Beginn: 305,0
Dosis: 4
Route/Site: IM / -

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

COVID-19 Headache Lethargy Pyrexia SARS-CoV-2 test positive

Symptomtext

After receiving the vaccination I attended a cruise vacation and it was determined that I had COVID. I experienced a headache, lethargy and fever. I also needed to be quaratined.

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: I received a COVID Test of which determined a positive status.
Aktuelle Erkrankungen: No other illnesses at the time of vaccination.
Vorgeschichte: No chronic or long standing health conditions.
Andere Medikamente: At the time of the vaccination I was taking a Multi Vitamin, Vitamin D, Vitamin C, Calcium, Zeaxanphin Lutein, Fish Oil, Tumeric, Cinnamon, Biotin, Co Q 10, Pravastatin, HCTZ, Potassium, Synthroid, Amlodipine, and Besylate
Allergien: No allergies to medications and or foods.
Vorherige Impfungen: sore arm with flu vaccination and shingles vaccine

VAERS 2619398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

mild

Staat: WI
Alter: 68,0
Geschlecht: M
Eingang: 22.04.2023
Impfdatum: 26.01.2021
Beginn: 18.04.2023
Tage bis Beginn: 812,0
Dosis: 4
Route/Site: - / -

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

Arthralgia Dysgeusia Fatigue Headache Oropharyngeal pain Perfume sensitivity Respiratory tract congestion

Symptomtext

Sore throat, congestion, achy joints, fatigue, head ache, metallic taste, sensitive to certain smells

Weitere VAERSDATA-Felder

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

VAERS 2619115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 53,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 19.04.2022
Beginn: 01.07.2022
Tage bis Beginn: 73,0
Dosis: 4
Route/Site: IM / RA

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

Dry eye Eczema Eczema eyelids Eye disorder Eye pain Gastric disorder Intraocular pressure test Punctal plug insertion

Symptomtext

Starting in Jul 22 severe dry eyes symptoms started with eye sensitives. My eyes hurt and felt like a punch in the eye even. Any kind of pressure made it hurt worst even with warm and cold compress. On 10Aug went to Optometrist and he said there is a lot of dryness and gave me a topical steroid but I stopped it because it burned my eyes really bad. 31Aug I went to the ER because my eyes and there was an Optometrist Dr. He gave me a medicine - eye drops and night time gel. Three weeks later, it was better and the Optometrist put me on Pataday and regular eye drops. I am going start on Restasis soon. They put plug in my eyes on 26Sep22. I also had eczema which started on my eye lids and under my eye and moved up to my forehead and around my lips and neck. I got a steroid shot . I got Desonide and Dupixen. Today is my second day of Dupixen. 21Dec2022 saw my Gastroenterologists because of of stomach issues. 28Dec and 2Mar, I had another set of plugs . Feb23 I started realizing that I could not take diary products.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: 10Aug22 Eye Exam testing the pressure on my eyes and cornea was very dry; 31Aug22 same Eye Exam testing the pressure on my eyes and cornea was very dry
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Autoimmune Disease; Thyroid; Anxiety
Andere Medikamente: Levoxyl; Nifedipine; Lamotrigine; Klonopin; Celexa; Vitamin A ( sometimes)
Allergien: Slight Intolerance of Gluten; Diary; Dilaudid; Losartan
Vorherige Impfungen: -

VAERS 2616834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CT
Alter: 70,0
Geschlecht: M
Eingang: 18.04.2023
Impfdatum: 11.04.2022
Beginn: 22.01.2023
Tage bis Beginn: 286,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Headache Nasal congestion Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

On Sunday night 22JAN2023 I started to feel stuffy followed by a headache the next morning with continued symptoms I took a home COVID-19 test which was positive later in the day I called my family physician, he told me he would prescribe PAXLOVID because of my age and condition. I started PAXLOVID symptoms continued for several days but within one week I was well and symptoms were never worse than a typical head cold. Being the generous I gave it to my wife and she followed with the same symptoms a week later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 23JAN20232 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis; Hypertension; Gout; High Cholesterol; Enlarged Prostate
Andere Medikamente: MOBIC; atenolol; alopurinol; FLOMAX; CRESTOR; TYLENOL
Allergien: None
Vorherige Impfungen: -

VAERS 2616782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 74,0
Geschlecht: F
Eingang: 18.04.2023
Impfdatum: 14.04.2022
Beginn: 29.11.2022
Tage bis Beginn: 229,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Oropharyngeal pain Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On 11/29/2022, I first had symptoms of body ache, runny nose sore throat and a little congestion. The fever was not very high. I was a at a dinner with 5 people having COVID-19. I contacted my doctor the next day. She got a prescription for Paxlovid. It was drastically better. I still had a runny nose. Two weeks after I got that runny nose again and tested positive. I just isolated for 10 days; I took Tylenol if I needed it. I didn't need anything really.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 29NOV2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; COPD
Andere Medikamente: Claritin; Seroquel; Atorvastatin; Budesonide; Inhaler Symbicort; Pantoprazole; Women's Multivitamin; Vitamin D
Allergien: Cephalosporin
Vorherige Impfungen: -

VAERS 2613121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 65,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 05.04.2022
Beginn: 01.08.2022
Tage bis Beginn: 118,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Fatigue Headache Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

I felt tired and sickly for about 24 hours after receiving the vaccine. I had a headache, feverish, feeling ill and tired when I tested positive for COVID-19 in 08/2022. I contacted my doctor and got a prescription for Paxlovid. I tolerated the medication, but it left a terrible taste in mouth. As of today, I do not have any lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: AUG2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 2612597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MN
Alter: 66,0
Geschlecht: M
Eingang: 10.04.2023
Impfdatum: 04.04.2022
Beginn: 03.01.2023
Tage bis Beginn: 274,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Cough Fatigue Headache Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 1/3/23. I had a cough, congestion, fatigue, fever, and a headache. I contacted my doctor and was prescribed 5 days' worth of PAXLOVID. After taking PAXLOVID for a couple days I felt a lot better. I am feeling much better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 03JAN2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Meniere's Disease
Andere Medikamente: Fish oil
Allergien: Amoxicillin; hornets; wasps; crab; hazelnuts
Vorherige Impfungen: -

VAERS 2612469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 76,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 08.04.2022
Beginn: 08.04.2023
Tage bis Beginn: 365,0
Dosis: 3
Route/Site: SYR / UN

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

Diarrhoea Faecal fat test Pancreatic failure

Symptomtext

I had my vaccination on 04/08/2022. I started to experience diarrhea almost immediately and it lasted for months. I contacted my physician and they referred me to a gastroenterologist. In 2022 I was given a fat and fecal test which determined I have Exocrine Pancreatic Insufficiency. I have changed my diet and with medication I am feeling better on 04/10/2023. I am still having follow up appointments with my gastroenterologist to monitor my diagnosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 2022 Fecal - Fat content test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Herpes; Leaky bladder
Andere Medikamente: N/A
Allergien: Codeine; Penicillin; Sulfa
Vorherige Impfungen: -

VAERS 2585929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 23.02.2023
Impfdatum: 06.05.2022
Beginn: 06.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Pain in extremity

Symptomtext

just a sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 74-year-old female patient received BNT162b2 (BNT162B2), on 06May2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 74 years for covid-19 immunisation. The patient's relevant medical history included: "Cirrhosis From Hepatitis C" (unspecified if ongoing); "Hepatitis C" (unspecified if ongoing), notes: Hepatitis C She got this from a hospital 40 years ago.; "Encephalopathy" (ongoing); "She was in a car accident" (unspecified if ongoing), notes: She was in a car accident. Concomitant medication(s) included: XIFAXAN taken for encephalopathy, start date: 2020; ZINC; GENERLAC taken for hepatic cirrhosis; LACTULOSE taken for hepatic cirrhosis. Vaccination history included: BNT162b2 (Dose: 01, Lot: EN6199, NDC/Expiry: Unknown, this is not on the CDC vaccine record card., Sore arm: From date: 06Mar2021, Stop date: Unknown other than a couple of days later. , Outcome: Recovered completely.), administration date: 06Mar2021, when the patient was 73-year-old, for COVID-19 immunization, reaction(s): "Sore arm"; BNT162b2 (Dose: 02, Lot: ER8733, NDC/Expiry: Unknown, this is not on the CDC vaccine record card., Administered at 14:00., Sore arm: From date: 30Mar2021, Stop date: Unknown other than a couple of days later. , Outcome: Recovered completely.), administration date: 30Mar2021, when the patient was 73-year-old, for COVID-19 immunization, reaction(s): "Sore arm"; BNT162b2 (Dose: 03, Lot: FH8020, NDC/Expiry: Unknown, this is not on the CDC vaccine record card., Administering facility name on CDC vaccine record card: Withheld, Sore arm: From date: 22Oct2021, Stop date: Unknown other than a couple of days later. , Outcome: Recovered completely), administration date: 22Oct2021, when the patient was 74-year-old, for COVID-19 immunization, reaction(s): "Sore arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 06May2022, outcome "recovered" (2022), described as "just a sore arm". Therapeutic measures were not taken as a result of pain in extremity.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300073682 same patient, different dose and event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Encephalopathy
Vorgeschichte: Medical History/Concurrent Conditions: Hepatic cirrhosis; Hepatitis C (Hepatitis C She got this from a hospital 40 years ago.); Motor vehicle accident (She was in a car accident)
Andere Medikamente: XIFAXAN; ZINC; GENERLAC; LACTULOSE
Allergien: -
Vorherige Impfungen: -

VAERS 2582307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FJ4991

mild

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 15.02.2023
Impfdatum: 16.08.2022
Beginn: 01.02.2023
Tage bis Beginn: 169,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chills Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID on Feb. 1, 2023. My head was really congested, and I had body aches, both my head and chest were congested. The second day I started getting chills, and the third day went away, fourth day still congested. Since it's been over seven day I tested again, and it was negative. I called my doctor and let them I tested positive, and they prescribed me Paxlovid, but I didn't take it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 01FEB23 - COVID - 19 Test - Positive 08FEB23 - COVID - 19 Test - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2573872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WV
Alter: 51,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 17.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / LA

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

Arthralgia

Symptomtext

pain in and under left shoulder/blade; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient received BNT162b2 (BNT162B2), on 17Jul2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 51 years intramuscular, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Date/time: 09Apr2021, Time(24 hr): 21:00, Site and route of injection: Left upper arm, Route of administration: Intramuscular, Batch/Lot number: EW0150), administration date: 09Apr2021, when the patient was 51-year-old, for Covid-19 immunization; BNT162b2 (DOSE 2, SINGLE, Date/time: 30Apr2021, Time(24 hr): 20:45, Site and route of injection: Left upper arm, Route of administration: Intramuscular, Batch/Lot number: EW0169), administration date: 30Apr2021, when the patient was 51-year-old, for Covid-19 Immunization; BNT162b2 (DOSE 3(BOOSTER), SINGLE, Date/time: 21Nov2021, Time(24 hr): 14:30, Site and route of injection: Left upper arm, Route of administration: Intramuscular, Batch/Lot number: FH8030), administration date: 21Nov2021, when the patient was 51-year-old, for Covid-19 Immunization. The following information was reported: ARTHRALGIA (non-serious), outcome "unknown", described as "pain in and under left shoulder/blade". Additional information: Pain in and under left shoulder/blade, was sudden onset. Made me concerned it could be something else. Can't remember how long it lasted. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : PFIZER INC-202201349553 same patient, different dose and event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Immunocompromised; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's medical history: None.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2552458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 07.07.2022
Beginn: 24.08.2022
Tage bis Beginn: 48,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Headache Malaise Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a headache and sore body for a couple days after the vaccine. On 08/24/2022, I did not feel well with a runny nose. On 08/25/2022, I tested positive for COVID-19 with a home test. I had a bad cough, congestion, fever and achiness. I contacted my primary care physician but they could not see me so I contacted my neurologist, and I went to the hospital for monoclonal antibody infusion. The infusion helped stop me progressing in my illness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 25AUG2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: N/A
Allergien: Opioids
Vorherige Impfungen: -

VAERS 2552075

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 64,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 22.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Injection site erythema Injection site warmth Skin warm

Symptomtext

Shot site, 3 inches+ surrounding, red and hot to the touch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Small left ovarian cyst ultra sound detected 2010-06-09 1.7 x 1.6 x 1.7 cm. Reconfirmed 2017-12-22, "up to 10 mm".
Andere Medikamente: 1 Centrum Silver Women 50+ 1 tablet orally once every 3 days 2 B12 500mcg 1 tablet orally once daily 3 B-Complex w/ C (150mg) 1 tablet orally once every 3 days 4 C 500MG 1 tablet orally once daily
Allergien: PENICILLINS
Vorherige Impfungen: -

VAERS 2547064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: RI
Alter: 78,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 18.07.2022
Beginn: 26.12.2022
Tage bis Beginn: 161,0
Dosis: 4
Route/Site: SYR / LA

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

Asthenia COVID-19 Chills Eye pruritus Fatigue Loss of personal independence in daily activities Pain Pain of skin SARS-CoV-2 test positive Somnolence

Symptomtext

On 12/26/2022 I was very exhausted and weak, everything hurt. I couldn't make my bed. I had chills and wanted to sleep. I felt so weak. I took a shower and went to bed. My hair hurt, I couldn't touch my hair and my eyes were so itchy. I took a COVID-19 test and it was positive. I called my doctor immediately and she prescribed PAXLOVID after a consultation. I have been taking it now with no side effects except for the bitter taste in my mouth. My symptoms now just feel like a have a cold. I feel tired, just to make soup and a sandwich for lunch made me feel extremely tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes; Left Lung removed; Bladder Cancer
Andere Medikamente: NOVOLOG; TOUJEO slide scale; SYNTHROID hydrochlorothiazide; vitamin A; vitamin D; iron; vitamin B12; metoprolol; multivitamin; vitamin B complex
Allergien: Egg; latex; sensitivity to all medications; gabapentin; NEURONTIN; blood pressure medications; contrast dyes
Vorherige Impfungen: -

VAERS 2543580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TX
Alter: 72,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 21.06.2022
Beginn: 09.11.2022
Tage bis Beginn: 141,0
Dosis: 4
Route/Site: SYR / LA

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

Cough Facial pain Headache Influenza Influenza B virus test positive Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative Sneezing

Symptomtext

I received my 4th dose on 06/21/2022. My Influenza symptoms started in the morning around 08:00AM on 11/09/2022. I had a stuffy head, runny nose, coughing, achy face, severe head, and sneezing. On 11/13/2022 I went to the clinic where they did few tests. They did flu and COVID-19. I was positive for Influenza B. I was taking MUCINEX AM/PM before I went to the clinic. They just advised me to continue taking MUCINEX and to drink plenty of fluids. Over all it lasted for 1 month. It just subsided 1 week ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial pain
Hospital-Tage: -
Labordaten: 27DEC2022 COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis; Fibromyalgia
Andere Medikamente: Carvedilol; olmesartan; frusemide
Allergien: None
Vorherige Impfungen: -

VAERS 2537751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: UT
Alter: 74,0
Geschlecht: M
Eingang: 20.12.2022
Impfdatum: 20.06.2022
Beginn: 27.09.2022
Tage bis Beginn: 99,0
Dosis: 4
Route/Site: IM / RA

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

Body temperature increased COVID-19 Decreased appetite Fatigue Feeling abnormal Influenza like illness Nausea Pain SARS-CoV-2 test positive

Symptomtext

I started feeling poorly on 11/26/22 and took my temperature, it was 101.5F. I felt like I had the flu. I awoke with body aches, still feeling bad, my temperature did come down some. I felt nauseous and more like I had the flu or bad a bad cold. I use my home COVID-19 test that came back positive but waited until later in the day to take a second test. The second test also showed positive, so I called my doctor and had a telehealth visit and was prescribed PAXLOVID, after three days I could eat. After the five days of PAXLOVID, I felt better but the fatigue lasted for three weeks, once it was gone, I have been feeling more like myself.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test positive
Aktuelle Erkrankungen: No
Vorgeschichte: Type II Diabetes; High Cholesterol; High Blood Pressure
Andere Medikamente: Pioglitazone; metformin; LANTUS; atorvastatin; propranolol; valsartan; lorazepam; omeprazole; vitamin C; AIRBORNE immune: CENTRUM SILVER; probiotic; ALLERCLEAR; ALLERFLO
Allergien: No
Vorherige Impfungen: -

VAERS 2537254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 20.12.2022
Impfdatum: 12.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Asthma Nausea Vomiting

Symptomtext

Asthma; I got sick to my stomach and was throwing up; I got sick to my stomach and was throwing up; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received BNT162b2 (BNT162B2), on 12Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 71 years for covid-19 immunisation. The patient's relevant medical history included: "blood pressure" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot Number: EL9264), administration date: 01Apr2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "First two shots, I fell and had hard time getting up"; BNT162b2 (DOSE 2, SINGLE; Lot Number: EW0171), administration date: 29Apr2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "First two shots, I fell and had hard time getting up"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: 0308D), administration date: 10Dec2021, when the patient was 71-year-old, for COVID-19 immunization, reaction(s): "asthma", "I got sick to my stomach and was throwing up", "I got sick to my stomach and was throwing up". The following information was reported: ASTHMA (non-serious) with onset 2022, outcome "unknown"; NAUSEA (non-serious), VOMITING (non-serious) all with onset 2022, outcome "unknown" and all described as "I got sick to my stomach and was throwing up". Therapeutic measures were not taken as a result of asthma, nausea, vomiting. Additional information: The patient was taking blood pressure medication and stopped after the second dose as it may drop the blood pressure. After receiving the vaccinations couple of hours later, the patient got sick to stomach and was throwing up. The patient was not taking any regular medications.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201375592 same patient/reporter, different vaccine;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2533209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 13.06.2022
Beginn: 23.11.2022
Tage bis Beginn: 163,0
Dosis: 3
Route/Site: IM / LA

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

Dry throat Headache Influenza virus test negative Pain SARS-CoV-2 test negative Streptococcus test negative Thirst

Symptomtext

Began having headache for an entire week and on 11/23/2022 began hurting all over and headache got worse. Also began having unquenchable thirst and just felt dry. Went to urgent care on 11/25/2022. Tested negative for COVID-19, flu, and strep. Urgent care put me on antibiotic and steroid. Also experienced sore throat, congestion, and cough intermittently. Also used OTC sinus meds and TYLENOL for congestion and achiness. Some days I can't taste foods and somedays I can. Still experiencing insomnia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 negative; flu negative; Strep negative
Aktuelle Erkrankungen: No
Vorgeschichte: Heart valve repair; Hypothyroidism
Andere Medikamente: Aspirin; metropole; levothyroxine; vitamin D3; ca; acid reflux medication; SENECA multivitamin
Allergien: VICODIN
Vorherige Impfungen: Arm soreness post COVID-19 vaccine

VAERS 2522034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 62,0
Geschlecht: M
Eingang: 02.12.2022
Impfdatum: 04.06.1959
Beginn: 01.06.2022
Tage bis Beginn: 23.008,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Headache Malaise Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had symptoms of a call like congestion, coughing and a headache. I completed a COVID-19 Home test which was positive. I called my doctor and they prescribed Paxlovid which I started taking it the next day. My symptoms improved in about 2 days. The symptoms improved with some lingering symptoms like congestion and coughing. I was symptom free about 5- or 6-days in. I do feel that I have completed recovered from the symptoms of that infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID 19 Test Home-October 01, 2022-Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Breakthrough case of Flu 10 to 12 years ago

VAERS 2520029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 73,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 26.05.2022
Beginn: 30.08.2022
Tage bis Beginn: 96,0
Dosis: 4
Route/Site: SYR / LA

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

Angiogram retina abnormal Blindness COVID-19 Cough Fatigue Malaise Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

COVID-19 case, I started feeling symptoms on 8/30 I had sore throat, coughing, mild fever, fatigue. Not too bad but definitely sick. Sneezing with a lot of congestion. Acute symptoms lasted about a week. Then another week of further resolution of coughing. On the November holiday 2022 I experienced a sudden acute loss of vision in 1 eye. I couldn't see so went to the ER and was sent to the Ophthalmology clinic. It started to resolve in a few hours but still obscured. They are looking into it without rational as to why it happened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test positive 9/1 and negative on 8/31; Retinal angiogram a bit of left eye changes but other than that normal.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Vitamins B; multivitamins; C; DKA mixture; cod liver oil; TYLENOL; ALEVE
Allergien: Gluten; grains; milk; dairy; bee stings
Vorherige Impfungen: -

VAERS 2518831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MO
Alter: 82,0
Geschlecht: M
Eingang: 29.11.2022
Impfdatum: 14.05.2022
Beginn: 25.11.2022
Tage bis Beginn: 195,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fall Knee arthroplasty Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Surgery

Symptomtext

symptoms: fever, congestion Admitted to hospital for scheduled knee replacement on 11/04/2022, slipped out of chair, required more surgery on 11/22/2022, tested positive for COVID-19 11/25/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: unable to access that information due to regulations
Aktuelle Erkrankungen: this information was not provided
Vorgeschichte: high blood pressure
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2518352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OH
Alter: 68,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 27.05.2022
Beginn: 14.10.2022
Tage bis Beginn: 140,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal discomfort Abdominal pain upper Blood test normal COVID-19 Cardiomegaly Chest X-ray abnormal Chills Cough Headache Nausea Rhinorrhoea SARS-CoV-2 test positive Vomiting

Symptomtext

No immediate reactions. 14 Oct 2022 upset stomack, cold flashes, runny nose. At home Coved Test positive. Oct 20 another at home Covid Test positive. Sypmptoms getting worse. Cannot hold down energy drink or water. Continuous Headached and stomach ache. Oct 21, Taken to Hospital by ambulance. ER put me on Zofran IV with Benderyl. After four hours Nauseau had passed. Sent home with 10 mg Metoclopramide. However, continuous coughing continues to 11/28/2022

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Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Chest Xray showed slightly enlarged heart. Blood tests were normal
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure and Cholesterols
Andere Medikamente: Lipitor, Mircardisin
Allergien: None
Vorherige Impfungen: -

VAERS 2517956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TN
Alter: 64,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 27.05.2022
Beginn: 07.10.2022
Tage bis Beginn: 133,0
Dosis: 4
Route/Site: IM / RA

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

Bronchitis Chills Cold sweat Nausea Pyrexia Respiratory tract congestion

Symptomtext

I had allergy like symptoms fever congestion and bronchitis and then experienced 4 days of nausea and cold sweats and chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Azithromycin
Vorgeschichte: Hypothyroid: High blood pressure
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2517401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 41,0
Geschlecht: F
Eingang: 26.11.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Diarrhoea Discomfort Feeling abnormal Hot flush Sensation of foreign body

Symptomtext

About 5 minutes after receiving the vaccine, I felt a hot flush throughout my body. Then I had diarrhea and felt like there was something in my throat. I felt uncomfortable and like something just wasn't right. It's hard to describe. I went to the ER and they found my vitals were normal. I sat there for a few hours and then went home. I continued to feel strange and like there was something in my throat for about a week afterwards, on and off. The feeling eventually went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: no tests were done.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Spironolactone, Doxycycline
Allergien: Allergic to Macrobid, Scopolomine, Reglan. Also allergic to eggs, cows milk, chicken, red peppers
Vorherige Impfungen: -

VAERS 2517215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 26.11.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / LA

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

Balance disorder Dementia Alzheimer's type Disorientation Disturbance in attention Dizziness Electroencephalogram Fatigue Feeling abnormal Heart rate increased Magnetic resonance imaging head Vaccination site pain Vertigo positional

Symptomtext

She has a weird kind of like vertigo; it makes her arm a little sore; she has problems thinking, brain fog when she is playing piano and stuff; disoriented; brain fog; rapid heartbeat; over the last six months she was thinking she was get Alzheimer's; dizziness; unbalanced issues; fatigue; 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 72-year-old female patient received BNT162b2 (BNT162B2), on 02May2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 71 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 (1st dose: Date: 25Jan2021. , Time: not probed. , Route of Administration: intramuscular. , Batch/Lot number: EL9263.), administration date: 25Jan2021, when the patient was 70-year-old, for COVID-19 Immunization, reaction(s): "All her vaccine doses would be given on left side/it makes her arm a little sore", "She has had dizzy spells for over a year"; BNT162b2 (2nd dose: Date: 15Feb2021. , Time: not probed. , Anatomical Site of injection: left arm. , Route of Administration: intramuscular. , Batch/Lot number: EN6201.), administration date: 15Feb2021, when the patient was 70-year-old, for COVID-19 Immunization, reaction(s): "All her vaccine doses would be given on left side/it makes her arm a little sore", "She has had dizzy spells for over a year"; BNT162b2 (3rd dose: Date: 21Sep2021. , Time: not probed. , Anatomical Site of injection: left arm. , Route of Administration: intramuscular. , Batch/Lot number: FC3183.), administration date: 21Sep2021, when the patient was 70-year-old, for COVID-19 Immunization, reaction(s): "All her vaccine doses would be given on left side/it makes her arm a little sore", "She has had dizzy spells for over a year". The following information was reported: VERTIGO POSITIONAL (non-serious) with onset 02May2022, outcome "not recovered", described as "She has a weird kind of like vertigo"; FEELING ABNORMAL (non-serious) with onset 2022, outcome "unknown", described as "brain fog"; DISORIENTATION (non-serious) with onset 2022, outcome "unknown", described as "disoriented"; DIZZINESS (non-serious) with onset 2022, outcome "not recovered"; FATIGUE (non-serious) with onset 2022, outcome "not recovered"; VACCINATION SITE PAIN (non-serious) with onset 2022, outcome "not recovered", described as "it makes her arm a little sore"; DEMENTIA ALZHEIMER'S TYPE (medically significant) with onset 2022, outcome "not recovered", described as "over the last six months she was thinking she was get Alzheimer's"; HEART RATE INCREASED (non-serious) with onset 2022, outcome "unknown", described as "rapid heartbeat"; DISTURBANCE IN ATTENTION (non-serious) with onset 2022, outcome "unknown", described as "she has problems thinking, brain fog when she is playing piano and stuff"; BALANCE DISORDER (non-serious) with onset 2022, outcome "not recovered", described as "unbalanced issues". The events "over the last six months she was thinking she was get alzheimer's", "dizziness", "unbalanced issues", "fatigue", "she has a weird kind of like vertigo", "it makes her arm a little sore", "she has problems thinking, brain fog when she is playing piano and stuff", "disoriented" and "brain fog" required physician office visit. The patient underwent the following laboratory tests and procedures: Electroencephalogram: negative; Heart rate increased: rapid heartbeat; Magnetic resonance imaging head: negative; negative. Clinical Course: This was a booster dose because patient have had 5 doses. Patient had the dizziness coming on for a while and it got worse with the last two that she got. Her symptoms are dizziness and unbalanced issues, rapid heartbeat. Patient had to been to every doctor known to man. Patient had been to two neurosurgeons, neurologist, heart doctor, breathing doctor, 3 ENT's and no one can find anything wrong with her. They just kept asking her if she have had Covid. Patient did not have Covid. She read the symptoms online, they are not going away, she has had them now for the last 6 months, they are getting worse and worse and she doesn't know what to do. She would like to know, since enough people know have it that they must know about this, if this is going to go away? She knew when it came out they didn't know what side effects would be, but she is hoping they will have information now. She just had her last COVID vaccine a few months ago. Her symptoms have something to do with position and movement of her head, it gets worse. She has a handwritten vaccine card, NDC/EXP were not provided for her doses of the vaccine. All her vaccine doses would be given on left side because she is right-handed and it makes her arm a little sore, so she thinks they were all given in left arm. After her fourth dose was given 02May2022, it has been since that it got really bad. She has a weird kind of like vertigo, but the world doesn't spin, it has to do with position of her head and gets better when she lays down and doesn't move, when she was immobile. She can be in the car driving and it happens. It seems to happen more in the car for some weird reason, maybe movement. At first when she started getting it, it was occasional, and she didn't think about it. The last six months it has been all the time, and it doesn't go away. She has had dizzy spells for over a year. When she first had it, they would last 30 seconds then be gone. She was very physical and rides horses, and over the last six months she was thinking she was get Alzheimer's, she has problems thinking, brain fog when she is playing piano and stuff. It seems to be positional, with her head and neck and arms. She thought it had to do with her back, so she went to the two neurologists and two neurosurgeons. They said her symptoms are similar to COVID if that is what is being reported, but she didn't have COVID, and did not have reactions to COVID shot other than a sore arm. She had four shots, and it is horrible now, the dizzy spells don't go away. The doctors couldn't find anything wrong with her. She has dizzy spells, unbalance issues, if she moves her head too fast from one side to the other or up and down, it is like a carnival ride or something.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Name: EEG; Test Result: Negative ; Test Name: rapid heartbeat; Result Unstructured Data: Test Result:rapid heartbeat; Test Name: brain MRI; Test Result: Negative ; Test Name: MRA; Test Result: Negative
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 2514065

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AK
Alter: 56,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 06.04.2022
Beginn: 29.07.2022
Tage bis Beginn: 114,0
Dosis: 4
Route/Site: IM / LA

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

Back pain COVID-19 Decreased appetite Fatigue Feeling abnormal Headache SARS-CoV-2 test positive

Symptomtext

I had recently traveled out of state and attended a crowded ball game on 07/27/2022. I traveled home by flight on 07/28/2022. On 07/29/2022, I began developing symptoms in the late afternoon. Nothing major, but I knew something was wrong, so I took an at home COVID-19 test and it was negative. I woke up the next day, on 07/30/2022, and still didn't feel right so I took another test, and it was positive. I was incredibly fatigued, had no appetite, I had terrible back pain, along with the worst headache I've had in my life. I called my local hospital on 08/03/2022 because of the terrible headache that would not go away. They wanted me to come in to be seen, but I was concerned about going since my oxygen levels were fine. I ended up drinking two bottles of PEDIALYTE to rehydrate and the next morning my headache was gone. I was still fatigued for a good two weeks after that, but my appetite slowly came back, and my other symptoms dissipated in that time as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: 29JUL2022 at home COVID-19 test negative; 30JUL2022 at home COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid Condition
Andere Medikamente: Levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 2512747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NC
Alter: 54,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 21.05.2022
Beginn: 15.10.2022
Tage bis Beginn: 147,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chills Decreased appetite Dizziness Fatigue Headache Impaired work ability Nausea Pain Paranasal sinus hypersecretion Parosmia Pyrexia SARS-CoV-2 test positive Taste disorder Weight decreased

Symptomtext

Symptoms started on Saturday, 10/15/2022: sinus drainage, headache, nausea, fever, dizziness, chills, body aches, fatigue, loss of appetite. Diagnosed on 10/18/2022 as Covid positive. Took 5 days of Paxlovid medication. Returned to work on 10/24/2022 still with fatigue, nausea, weight loss and dizziness. My sense of taste and smell was still intact; however, they became hyper-sensitive causing an increase in nausea and continued loss of appetite.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Diagnosed as Covid positive on 10/18/2022
Vorgeschichte: High blood pressure
Andere Medikamente: Carvedilol blood pressure med.
Allergien: N/A
Vorherige Impfungen: -

VAERS 2511939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AZ
Alter: 75,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 25.10.2022
Beginn: 13.11.2022
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: SYR / RA

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

COVID-19 Chills Cough Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On Novemer 13 came down with chills. The following day had chills, cough, congestion and tested with at home antigen test and was positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: n/a
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: chills, feeling poorly following for a couple days after vaccinations

VAERS 2507189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MD
Alter: 56,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 20.04.2022
Beginn: 09.10.2022
Tage bis Beginn: 172,0
Dosis: 4
Route/Site: SYR / AR

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

COVID-19 Fatigue Headache Nasopharyngitis Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Starting 10/09/2022, I woke up with a headache and thought I was tired. My fatigue increased and I started developing a sore throat and cold like symptoms. The headache worsened and I took a test that evening (COVID-19 was positive). On Monday, the symptoms were increasing and I had a sore throat, fever, headache and fatigue. I called the doctor and I was put on PAXLOVID due to a lower immune response, having asthma and due to having the last dose 6 months prior. I started the PAXLOVID that day and my symptoms went away really quickly which was great. I finished it 10/15/2022 and on 10/17/2022 I tested negative. On 10/19/2022, I tested positive again for COVID-19 and I continued to test positive until 10/26/2022. I am unsure when I was negative because I stopped testing by then. I felt great after 10/19 but continued to test positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 at home test (10/09/2022): positive; COVID-19 at home test (10/17/2022): negative; COVID-19 at home test (10/19/2022-10/26/2022): positive when tested every other day.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Allergies
Andere Medikamente: Atorvastatin; SINGULAIR; ALLER-FEX; ALLER-CORT; NAPHCON A; vitamin D; ADVAIR DISKUS; estrogen cream
Allergien: None
Vorherige Impfungen: -

VAERS 2504357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

mild

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 31.05.2022
Beginn: 15.06.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: SYR / LA

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

Erythema Pruritus Rash Urticaria

Symptomtext

My skin became very itchy with the 3 one. It was itchy before but after the third one I developed hives on my face, neck and leg. On my face and neck it was very red, blood red. It was so bad that my husband rushed me to the emergency room. The first rash/hives that appeared was on the back of my left leg only. Then after that they progressively got worse. I?ve seen 2 dermatologists, and one allergist. None of them even brought this up to me. I started talking to a friend who had the exact, same thing. Her allergist suggested that it could be a reaction that she had. I?ve never had to be this careful of covering up my skin for even 5 mins when I just go outside. My face hasNever gotten red like this. My entire body has to be covered up. I?ve had the 4 shots over 2 1/2 years a just got the new one also.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: I?ve seen 2 dermatologists, and from this August-October I?ve seen a dermatologist, allergist, and one emergency room.
Aktuelle Erkrankungen: None
Vorgeschichte: Trigeminal neuralgia/high blood pressure
Andere Medikamente: Lamotrogine, bupropion, losartan
Allergien: Fluroquinolones
Vorherige Impfungen: -

VAERS 2503156

NOVAVAX · COVID19 (COVID19 (NOVAVAX)) · Charge FJ4991

mild

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 06.05.2022
Beginn: 28.08.2022
Tage bis Beginn: 114,0
Dosis: 4
Route/Site: SYR / LA

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

Asthenia COVID-19 Exposure to SARS-CoV-2 Fatigue Laryngitis Nasopharyngitis Oropharyngeal pain Pain Productive cough SARS-CoV-2 test positive Sinusitis Throat clearing

Symptomtext

On 08/27/2022 I was getting over a regular cold. I was exposed to COVID. I began feeling more tired than usual, ached slightly, my throat was slightly sore. On 8/28/2022 I tested positive for COVID with home test. I continued to be tired, low energy and achy. I tested a week later and my COVID home test was negative. I spoke with my physician on 9/1/22, telehealth. He had me take Vitamin D, Vitamin C and Zinc. Around 9/8/22, I developed sinusitis, constantly coughing up phlegm, blowing nose and clearing my throat. Around 9/17/22 I developed laryngitis. I was not as tired but felt worse. I had a telehealth visit on 9/20/22 with my physician. I was started on amoxicillin 500mg, three times a day for seven days. After I completed the antibiotic, I began to feel like myself and regaining strength. I have now completely recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home COVID tests, both negative and positive tests.
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-diabetic; high cholesterol
Andere Medikamente: Aspirin; Repatha; Tamsulosin; Metformin; Potassium Sulfate; Cinnamon Pills;
Allergien: None
Vorherige Impfungen: -

VAERS 2502089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 20.07.2022
Beginn: 22.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Dizziness Fatigue Lethargy Loss of personal independence in daily activities Nausea Pyrexia Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

Starting the Friday after the vaccine, I got nauseous and dizzy and this lasted all day. I woke up the next day with a runny nose and later that day developed a scratchy throat. The next day, I tested myself for COVID-19 at home and it was positive. I contacted my doctor the next day (on Monday) and she prescribed me PAXLOVID. I started it that evening. The fever was bad at this point. It took a few days before I started getting some relief. By the time the PAXLOVID was done, I felt better. However, it took a total of 2 weeks to stop testing positive for COVID-19. To this day, I am still experiencing fatigue and lethargy. Its been hard to even do normal daily activities without being tired out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: At-home COVID-19 test: positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; High Blood Pressure; High Cholesterol; Diabetes; Obesity
Andere Medikamente: JARDIANCE; rosuvastatin; metformin; ezetimibe; hydrochlorothiazide; losartan; TOUJEO insulin; nifedipine; vitamin D2 weekly; BAYER aspirin; magnesium glycinate; MICRO C
Allergien: Dairy; eggs; chicken; numerous environmental allergens
Vorherige Impfungen: -

VAERS 2497925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 03.05.2022
Beginn: 30.08.2022
Tage bis Beginn: 119,0
Dosis: 4
Route/Site: IM / RA

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

Bed sharing Cough Fatigue Feeling cold Malaise Nasal congestion Pulmonary congestion Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

On 8/30/2022 in the evening, I was not feeling well. I was sneezing, I had congestion. I was coughing. I had congestion in my chest and in my nose. I felt cold. I did not have a fever. I was extremely tired. I just felt very cold. I took a COVID-19 home test and tested positive on 8/31/2022. I called my doctor on 8/31/2022 and she prescribed PAXLOVID for the 5 days and I took it for the 5 days. I had a negative COVID-19 test on 9/10/2022 and my symptoms resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 8/31/2022 COVID-19 home test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; High Cholesterol; Thyroid; Diabetes
Andere Medikamente: SYNTHROID; lovastatin; metformin XR; PULMICORT; alphabetic multivitamins; ZYRTEC; PEPCID AC
Allergien: Environmental allergies; trees; hay fever; lactose intolerant; amoxycillin; erythromycin; codeine
Vorherige Impfungen: -

VAERS 2495375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NC
Alter: 40,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 21.07.2022
Beginn: 06.10.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Feeling abnormal Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

I took my vaccination on 07/21/2022. On 10/06/2022 I woke up with a sore throat and I felt awful. The following day 10/07/2022 the pain was horrible. I tested COVID-19 Positive on that day. The doctor put me on Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 10/07/2022 - COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Asthmatic
Andere Medikamente: Losartan
Allergien: Aspirin; Latex; Eggs; Peanuts; Berries
Vorherige Impfungen: flu due to egg allergies

VAERS 2494004

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WI
Alter: 63,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 28.04.2022
Beginn: 02.10.2022
Tage bis Beginn: 157,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Hypophagia Nausea Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

In the afternoon I noticed that I was getting a sore throat. It was moderate. I completed a COVID 19 home test on October 3rd and it was positive. On October 3rd, I did a tele visit with the doctor and I was not feeling really bad, so she did not prescribe. I was in bed for 2 days with nausea really bad. I could not eat or drink anything. By the 6th I felt a lot better. I never got a temperature above 99 degrees. I was tired afterwards for a couple of weeks but have since completely recovered.

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

VAERS 2492932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 08.04.2022
Beginn: 29.07.2022
Tage bis Beginn: 112,0
Dosis: 4
Route/Site: IM / LA

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

Blood test abnormal COVID-19 Cough Diarrhoea Fatigue Head discomfort Nasopharyngitis Renal impairment SARS-CoV-2 test positive

Symptomtext

On 7/29/2022, I started having like a head cold, stuffy head, not a big deal and a cough. Around 3 days later, I took a COVID-19 home test and it was positive with 5 seconds. I reported online to my doctor's office that I had COVID-19. A doctor called me back and prescribed a specialized reduced prescription of Paxlovid because I have a reduced kidney function. I had diarrhea and I was extremely tired during that time. Five days later, I tested again, and the results were negative, and symptoms were gone. I just recently started having recurring diarrhea about every 10 or 15 days. It started in September. The doctor thought that maybe there is a relation with me having COVID-19, because I had the diarrhea when I had COVID-19. I have an appointment with my doctor to follow up on this.

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Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 7/31/2022 - COVID-19 home test- positive blood work- because I have a reduced kidney function
Aktuelle Erkrankungen: N/A
Vorgeschichte: thyroid deficiency; High cholesterol
Andere Medikamente: Levothyroxine; Rosuvastatin; Omeprazole; Trazodone; Melatonin; Multivitamin; Calcium Citrate; Baby Aspirin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2489910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 12,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 26.04.2022
Beginn: 04.09.2022
Tage bis Beginn: 131,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Oropharyngeal pain Pyrexia Rash SARS-CoV-2 test positive

Symptomtext

He tested positive for COVID-19 on 9/14/22. He had a sore throat, cough, slight fever, and really fatigued. Within a couple hours of testing positive, he started taking PAXLOVID and he will be taking it for five days. PAXLOVID worked great because he is feeling much better now. He did get a small rash and it is hard to tell if it was from the medication or COVID-19.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 09OCT22 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Albuterol; QVAR
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2489484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 76,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 18.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

Eczema Full blood count Haemoglobin Investigation Laboratory test Pruritus Rash papular

Symptomtext

experienced a papular rash on his chest, back, legs, and arms; itching/little scalp itching; eczema/spongiotic dermatitis; This is a spontaneous report received from contactable reporter (Physician) from medical information team and product quality group. The reporter is the patient. A 76-year-old male patient received BNT162b2 (BNT162B2), on 18Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 76 years, in right arm for COVID-19 immunisation. The patient's relevant medical history included: "back pain" (unspecified if ongoing); "sleep" (unspecified if ongoing); "Allergic rhinitis" (unspecified if ongoing); "Surgery in left arm" (unspecified if ongoing); "COVID-19" (unspecified if ongoing), notes: in the past. Concomitant medication(s) included: LORTAB [LORATADINE] taken for back pain, sleep disorder (ongoing); FINASTERIDE (ongoing); FLUTICASONE taken for rhinitis allergic; VITAMIN D [VITAMIN D NOS] nasal; B12-VITAMIIN oral. Vaccination history included: BNT162b2 (dose 1, single, LOT: EH9899), administration date: 21Dec2020, when the patient was 75-year-old, for COVID-19 Immunization; BNT162b2 (dose 2, single, LOT: EL1284), administration date: 12Jan2021, when the patient was 75-year-old, for COVID-19 Immunization; BNT162b2 (dose 3, single, LOT: FF2888 (looks like), Anatomical location: Probably in right arm), administration date: 26Sep2021, when the patient was 76-year-old, for COVID-19 Immunization; flu (Dose number: Unknown, Manufacturer: unknown), administration date: 03Oct2022, when the patient was 77-year-old. The following information was reported: ECZEMA (medically significant) with onset Apr2022, outcome "unknown", described as "eczema/spongiotic dermatitis"; RASH PAPULAR (medically significant) with onset Apr2022, outcome "not recovered", described as "experienced a papular rash on his chest, back, legs, and arms"; PRURITUS (medically significant) with onset Apr2022, outcome "recovering", described as "itching/little scalp itching ". The events "experienced a papular rash on his chest, back, legs, and arms", "itching/little scalp itching " and "eczema/spongiotic dermatitis" required physician office visit. The patient underwent the following laboratory tests and procedures: Full blood count: Ok, notes: All blood counts and chemistry counts have been ok; Hemoglobin: low, notes: very slight low but not much; Alpha-gal test: Negative; Chemistry: Ok, notes: All blood counts and chemistry counts have been ok. Therapeutic measures were taken as a result of rash papular, pruritus, eczema. Clinical course details: Patient described the rash as pretty severe dermatologically but not life-threatening. Patient stated that he received Dupixent on 12Oct2022 and will receive his next dose on 26Oct2022. Patient mentioned that Dupixent made his rash worse, but the itching has become better. Patient stated that he received Dupixent on 12Oct2022 and will receive his next dose on 26Oct2022. Patient mentioned that he was schedule for the bivalent vaccine in Nov2022. Patient mentioned that it has been 6 months when he had the rashes. Shortly thereafter, broke out in papular rash on chest, back of legs, arms, soles of feet and so on. Patient was very itchy and had 2 skin boxes that showed either eczema or drug reaction. Patient can't really tell the difference if it was eczematous reaction or drug reaction from the biopsy. Also had an Alpha-gal test that was negative. Patient was not aware of anything to likely have caused this. Patient has been on some long-term medication like, Finasteride 5mg a day, for several years. Patient had some chronic back issues that required him to take low dose Lortab in the middle of the night, for back pain and sleep. Patient has been on that several years. Patient thought it was a little unusual to experience a drug reaction for that length of time. Patient had seen 2 different dermatologists, and one put him on Dupixent. Patient had the rash probably within the end of the month (Apr2022), not the same day. Patient didn't get short of breath but was very itchy. Patient was on the actual back and front and back of legs, feet and arm, not much on the face. Patient maybe had a little scalp itching and still some trouble with the itching. The pathologist called them spongiotic dermatitis. Didn't sense any fungal element.; Sender's Comments: Based on available information and temporal association the causal role of suspect drug cannot be excluded for reported events Case will be reviewed on receipt of FU information. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate,Linked Report(s) : US-PFIZER INC-202201247037 Same patient/product, different dose/event;

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Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Test Name: Blood counts; Result Unstructured Data: Test Result:Ok; Comments: All blood counts and chemistry counts have been ok.; Test Name: Hemoglobin; Result Unstructured Data: Test Result:low; Comments: very slight lowbut not much; Test Name: Alpha-gal test; Test Result: Negative ; Test Name: Chemistry; Result Unstructured Data: Test Result:Ok; Comments: All blood counts and chemistry counts have been ok.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic rhinitis; Back pain; COVID-19 (in the past); Sleep disorder; Surgery
Andere Medikamente: LORTAB [LORATADINE]; FINASTERIDE; FLUTICASONE; VITAMIN D [VITAMIN D NOS]; B12-VITAMIIN
Allergien: -
Vorherige Impfungen: -

VAERS 2488388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 15.04.2022
Beginn: 29.06.2022
Tage bis Beginn: 75,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia COVID-19 Cough Malaise Nasal disorder SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. I started feeling sick after I got home from a trip on 06/29/2022 with nose, coughing and feeling weak. On 07/02/2022, I tested positive with a home test for COVID-19. I contacted a doctor with my insurance company and was going to get a prescription for PAXLOVID but never got it. I didn't take anything for my symptoms.

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Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 02JUL2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: PROLIA; vitamin C; vitamin D; vitamin E; vitamin B12
Allergien: Antihistamines
Vorherige Impfungen: The 2nd Shingles vaccine at age 56, I had a fever, nauseated and felt bad in general which lasted about one day.

VAERS 2484936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 14.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Asthenia Body temperature Chills Nausea Pyrexia Vomiting

Symptomtext

nausea; vomit; fever; chills; weakness; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team, Program ID. The reporter is the patient. A 69-year-old female patient received BNT162b2 (BNT162B2), on 14Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 69 years, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "Addison's disease" (ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose 1 of the Covid Vaccine: Administered to the caller on 21Jan2021; Lot Number: EL1284), administration date: 21Jan2021, when the patient was 68-year-old, for Covid-19 immunization; BNT162b2 (Dose 2 of the Covid Vaccine: Administered to the caller on 11Feb2021; Lot Number: EN5318), administration date: 11Feb2021, when the patient was 68-year-old, for Covid-19 immunization; BNT162b2 (Dose 3 (Booster) of the Covid Vaccine: Administered to the caller on 11Oct2021; Lot Number: 30155DA.), administration date: 11Oct2021, when the patient was 68-year-old, for Covid-19 immunization; Flu vaccines (Caller states that she gets Flu vaccines yearly and gets fatigue for one day. Dates, Lot Numbers, Expiry Dates for Flu Vaccines was unknown.), for Immunization, reaction(s): "gets fatigue for one day". The following information was reported: CHILLS (non-serious) with onset 15Apr2022, outcome "recovered" (15Apr2022); PYREXIA (non-serious) with onset 15Apr2022, outcome "recovered" (15Apr2022), described as "fever"; NAUSEA (non-serious) with onset 15Apr2022, outcome "recovered" (15Apr2022); VOMITING (non-serious) with onset 15Apr2022, outcome "recovered" (15Apr2022), described as "vomit"; ASTHENIA (non-serious) with onset 15Apr2022, outcome "recovered" (15Apr2022), described as "weakness". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: It was reported that the patient had no investigations relevant tests. The patient did not have any prior vaccinations within four weeks prior to the first administration date of the suspect vaccine. Caller stated that she got Flu vaccines yearly and got fatigue for one day. Dates, NDC, Lot Numbers, Expiry Dates for Flu Vaccines was unknown by the caller. The patient did not administer additional vaccines on same date of the Pfizer suspect. The patient reported that she had her last covid booster on 14Apr2022, about 12 hours after the vaccine, she had nausea, vomiting, fever, chills, and weakness. Time the vaccination was given was reported as around 1000. Caller stated that all of these symptoms began in the early morning on 15Apr2022 and lasted for around 8-10 hours. She was scheduled to have another booster on 21Oct2022. Stated that she was going to be getting her fifth shot, third booster vaccine this Friday. Her question was, was it safe for her to have another booster. The caller was wondering if with this new variant vaccine has anyone reported these same side effects. When prompted for specific seriousness criteria related to all of her symptoms the caller replied with no. Caller stated that she did have Addison's disease and was diagnosed with this condition about 27 years ago when she was about 42 years old and was on unspecified steroid medications. Stated that anything that dehydrates her, like vomiting, she usually has to go to the Emergency Room. States that she did not have to go to the Emergency Room or physician office with these above-mentioned events that started on 15Apr2022. Caller denied any other medications, labs, testing, or treatments relevant to these events.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220415; Test Name: Fever; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: Addison's disease
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2481110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 54,0
Geschlecht: M
Eingang: 17.10.2022
Impfdatum: 16.07.2022
Beginn: 15.09.2022
Tage bis Beginn: 61,0
Dosis: 4
Route/Site: IM / LA

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

Back pain Bursitis

Symptomtext

On 9/15/2022 I started to notice the pain in my lower back. It was gradual at first and it increased overtime. On 10/10/2022, I went to see my rheumatologist. He gave me 2 cortisone shots on my hips. He diagnosed me with Bursitis. I have not recovered from the adverse event I have to return for a follow up.

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Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: N/A
Vorgeschichte: Sickle cell anemia; Rheumatoid arthritis
Andere Medikamente: Folic acid; spironolactone; hydralazine; pravastatin; amlodipine besylate; carvedilol; methotrexate
Allergien: N/A
Vorherige Impfungen: -

VAERS 2480576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 71,0
Geschlecht: M
Eingang: 17.10.2022
Impfdatum: 15.04.2022
Beginn: 30.07.2022
Tage bis Beginn: 106,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Feeling abnormal Headache Malaise Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

07/30/2022 I started to not feel well that evening. I had a sore throat and started to get fever. I took Covid home test the next day, which was negative. I had a positive PCR test om 8/31/22 at a health facility. I had a cough, sore throat, headache and a fever 101- 102 and was tired. I took Delsum and it helped my cough. My cough was a clear mild cough. I took some Tylenol a few times with a headache. 08/1/2022 I had a telehealth with my doctor and she prescribed Paxlovid. It was 08/03/2022 before I was able to start the Paxlovid. The symptoms slowly abated. The cough lasted for about a month, slowly weakening. I was still tired did not feel like I had energy and did not feel like myself for about 5 weeks. By Day 12, I tested negative for the first time. Day 15, I had a positive COVID home test. I continued to test positive for 4-5 days before I tested negative again.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID tests, negative COVID tests, Positive
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood pressure
Andere Medikamente: Tamsulosin; Crestor; Losartan; Vitamin D; Vitamin B12; Baby aspirin
Allergien: Keflex; penicillin
Vorherige Impfungen: -

VAERS 2478568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: PA
Alter: 61,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 20.05.2022
Beginn: 21.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: UN / LA

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

Scratch Skin erosion Urticaria

Symptomtext

No symptoms for first 24 hrs, then I started noticing what I thought were bug bites on all 4 of my extremities. After taking benadryl and scratching myself raw, I went to the Dr.s 72 hours post shot. This was my first Pfizer booster. All 3 previous shots were Moderna. I was diagnosed with hives and treated with a course of prednisone, which resolved the hives within 48 hrs.

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Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: none.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: multi-vitamin, progesterone, estrogen patch, gabapentin, fish oil, zyrtec,
Allergien: allergic to Zofran, dust, mold,
Vorherige Impfungen: -

VAERS 2473309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 24.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia

Symptomtext

Left shoulder pain

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Awaiting
Aktuelle Erkrankungen: None
Vorgeschichte: Heart disease Obesity
Andere Medikamente: Attorvasttatin Carvedilol Lisinopril Cetirizine Bayer asprin Valacyclovir Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 2472436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 08.04.2022
Beginn: 19.09.2022
Tage bis Beginn: 164,0
Dosis: 4
Route/Site: - / RA

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

COVID-19 Cough Dysgeusia Fatigue Myalgia Drug ineffective SARS-CoV-2 test Nasal congestion SARS-CoV-2 test positive

Symptomtext

Positive for COVID-19. Symptoms included stuffy nose, cough, muscle aches, metallic taste in mouth, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Positive on COVID-19 home antigen test.
Aktuelle Erkrankungen: None
Vorgeschichte: Ankylosing spondylitis
Andere Medikamente: Humira (adalimumab), Red Yeast Rice, 1-Day Men's Over 50 Multivitamin, Vitamin D 5000 units/day
Allergien: None
Vorherige Impfungen: -

VAERS 2472436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 08.04.2022
Beginn: 19.09.2022
Tage bis Beginn: 164,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Cough Dysgeusia Fatigue Myalgia Drug ineffective SARS-CoV-2 test Nasal congestion SARS-CoV-2 test positive

Symptomtext

Positive for COVID-19. Symptoms included stuffy nose, cough, muscle aches, metallic taste in mouth, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Positive on COVID-19 home antigen test.
Aktuelle Erkrankungen: None
Vorgeschichte: Ankylosing spondylitis
Andere Medikamente: Humira (adalimumab), Red Yeast Rice, 1-Day Men's Over 50 Multivitamin, Vitamin D 5000 units/day
Allergien: None
Vorherige Impfungen: -

VAERS 2472038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 54,0
Geschlecht: M
Eingang: 07.10.2022
Impfdatum: 07.04.2022
Beginn: 23.08.2022
Tage bis Beginn: 138,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Malaise Pyrexia SARS-CoV-2 test positive Sneezing

Symptomtext

I tested positive for COVID-19, August 23, 2022. I had really mild symptoms. I was sneezing a lot and a slight fever around 99. I contacted my doctor the same day and he prescribe me Paxlovid the same day. I was instructed to take the Paxlovid for five days straight.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: I tested positive for COVID-19, August 23, 2022, and my doctor prescribe me Paxlovid the same day.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Fluoxetine; Flonaxx; Vitamin D; Fish oil pill,
Allergien: Penicillin; Raw potatoes
Vorherige Impfungen: -

VAERS 2470132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 05.04.2022
Beginn: 13.09.2022
Tage bis Beginn: 161,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Depressed mood Disturbance in attention Fatigue Nasopharyngitis Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I woke up to 9/13/2022 with a very runny nose at 03:00AM. My nose was running like a faucet that I could not turn off. I decided to take the 3 at home test that I received in the mail and instantly they came back positive. I decided to order 2 more and they arrived the next day on 09/14/2022 and those results were positive. I was able to contact my primary care doctor via telehealth and he prescribed Paxlovid that day. I was very fatigue and just felt completely down, it felt as if I had a head cold. Now my concentration has not been the same and I am still feeling fatigue after 10 days of testing negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 3 At home Covid test 09/13/2022 -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2469939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 68,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 04.04.2022
Beginn: 11.07.2022
Tage bis Beginn: 98,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Feeling abnormal Headache Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had congestion in my chest, sore throat, headache, general exhaustion. I got a runny nose and a dry cough. I felt pretty crummy. The simplest way to describe it was that every molecule in my body was a t war with every molecule in my body. I felt terrible for a couple of days. I took Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Pre-Diabetic
Andere Medikamente: Lisinopril; Baby Aspirin; Collagen tablet; Vitamin E; Vitamin D; CoQ10; Turmeric
Allergien: N/A
Vorherige Impfungen: -

VAERS 2469699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: ID
Alter: 71,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 21.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Biopsy skin Blood test Dry skin Rash Rash erythematous Rash papular Rash pruritic Skin exfoliation Thyroid function test Viral infection

Symptomtext

A couple days after getting the vaccine I started breaking out in a rash. It started on my ankle, in the course of a week it went from my feet to the top of my head. It was raised bumps that were red and fluid filled. It presented itself differently on different parts of my body. It showed up in patches, I was itchy, it felt like sandpaper. Some areas dried up and flaked off like dandruff others the skin peeled off. I went to my PCP who ran blood test, thyroid test, skin biopsy. The test only showed that I had a rash. I was treated for a general rash. I have seen my PCP, an Endocrinologist and an Allergist who have all come to the same conclusion that I have had a viral infection reaction. I was taking prednisone for a while it helped with the itching. The rash came back after the three week treatment. I was given a cortisone shot and this completely wiped out the rash. I was given betamethasone ointment to put on the rash. It is helping with my hands as we are nearing the five week period of when the shots normally wear off.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Blood test; Thyroid test; Skin biopsy
Aktuelle Erkrankungen: No
Vorgeschichte: Heart Disease; Lower Back Issues; Pre Diabetic
Andere Medikamente: LIPITOR; lisinopril; low dose aspirin; krill oil; vitamin D3; famotidine; lutein/zeaxanthin; coQ10
Allergien: BENZONE
Vorherige Impfungen: -

VAERS 2468957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 02.04.2022
Beginn: 03.09.2022
Tage bis Beginn: 154,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Fatigue Headache Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On 09/02/2022 I had headaches, congestions, extremely tired. The same day we did COVID-19 home test and was positive. I went to urgent care they prescribed us Paxlovid for 5 days. They told me to take acetaminophen as needed. After 5 days I had a rebound. They prescription of Paxlovid again for 5 days. After that we had conference with my doctor on 09/20/2022. She said she will give me Paxlovid again but we didn't go that route. I had to let it fight it by it's own. On 09/25/2022 we tested negative for COVID-19. I stated recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test_ Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Diverticulosis
Andere Medikamente: Armodafinil; Atorvastatin ; Amlodipine; Lateroprol; Omeprazole; Testosterones; Calcium
Allergien: Antibiotics free; Aspirin; Citfroxine; No sugars; Codeine ; Morphine; oxycodone; Tree nuts;
Vorherige Impfungen: -

VAERS 2468631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OH
Alter: 61,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 01.04.2022
Beginn: 09.07.2022
Tage bis Beginn: 99,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Chills Cough Feeling abnormal Headache Hyperhidrosis Pain SARS-CoV-2 test positive Sneezing Throat clearing

Symptomtext

I was driving home and that morning I noticed I was clearing my throat a lot. An hour into the drive I started getting chills, sweats, body aches. I had to stop frequently at rest areas. I felt really bad by the time I got home. It took me an extra 2 hours to get home. I tested COVID-19 positive as soon as I got home. I drove myself into base and got a PCR test. I went home and tried to sleep, My symptoms continued. The nurse practitioner called and told me that I was prescribed PAXLOVID. I had a headache that was constant but weak. I was sneezing and coughing a lot. With the body aches and chills started subsiding Wednesday night. By Friday I felt a lot better. By Saturday I was able to return to my normal activities. I was also taking TYLENOL and oscillococcinum.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home COVID-19 test - positive; PCR COVID-19 test- positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Exercised Induced Asthma; Type II Diabetic; Stage 3 Kidney Disease
Andere Medikamente: Metformin; HCTZ; losartan; cetirizine; JANUVIA; NEXIUM; baby aspirin; vitamin D3; coQ10; vitamin B12; iron; monthly dose of REPATHA
Allergien: N/A
Vorherige Impfungen: -

VAERS 2450266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MD
Alter: 71,0
Geschlecht: F
Eingang: 01.10.2022
Impfdatum: 25.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Pyrexia SARS-CoV-2 test Vaccination failure Diarrhoea Faeces pale

Symptomtext

clay colored stools; loose stools; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 25Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 71 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "Pre DM" (unspecified if ongoing), notes: Pre DM; "Lung disease/interstitial screening from prior toxic exposure" (unspecified if ongoing), notes: Lung disease (please specify) interstitial screening from prior toxic exposure.; "NAFLD" (unspecified if ongoing), notes: NAFLD; "oxalate stones" (unspecified if ongoing), notes: Kidney disease (please specify) oxalate stones.; "familial hyperlipidemia" (unspecified if ongoing); "Gout" (unspecified if ongoing); "Is the patient a smoker/ former smoke? No" (unspecified if ongoing), notes: Is the patient a smoker/ former smoke? No. Concomitant medication(s) included: TENORMIN; SYNTHROID; NORVASC; CLONIDINE; LOSARTAN; POTASSIUM CITRATE; VITAMIN D3. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6201; Route of administration: Intramuscular; Site of injection: Left arm), administration date: 12Feb2021, when the patient was 70-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: EN6198; Route of administration: Intramuscular; Site of injection: Left arm), administration date: 05Mar2021, when the patient was 70-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: FF2593; Route of administration: Intramuscular; Site of injection: Left arm), administration date: 23Oct2021, when the patient was 71-year-old, for COVID-19 Immunization. The following information was reported: FAECES PALE (non-serious) with onset 2022, outcome "unknown", described as "clay colored stools"; DIARRHOEA (non-serious) with onset 2022, outcome "unknown", described as "loose stools". Additional information: Patient was not hospitalized or admitted to an Intensive Care Unit. Patient was not still (at the time of this report) hospitalized. Patient did not display clinical signs at rest indicative of severe systemic illness and did not require supplemental oxygen (including high flow or ECMO) or received mechanical ventilation. New or worsened symptoms/signs during the COVID-19 illness included clay-colored stools and loose stools. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Familial hyperlipidemia; Gout; Hypertension; Kidney stones (Kidney disease (please specify) oxalate stones.); Lung disease (Lung disease (please specify) interstitial screening from prior toxic exposure.); Non-alcoholic fatty liver (NAFLD); Nonsmoker (Is the patient a smoker/ former smoke? No); Pre-diabetes (Pre DM)
Andere Medikamente: TENORMIN; SYNTHROID; NORVASC; CLONIDINE; LOSARTAN; POTASSIUM CITRATE; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 2450266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MD
Alter: 71,0
Geschlecht: F
Eingang: 01.10.2022
Impfdatum: 25.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / LA

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

COVID-19 Pyrexia SARS-CoV-2 test Vaccination failure Diarrhoea Faeces pale

Symptomtext

clay colored stools; loose stools; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 25Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 71 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "Pre DM" (unspecified if ongoing), notes: Pre DM; "Lung disease/interstitial screening from prior toxic exposure" (unspecified if ongoing), notes: Lung disease (please specify) interstitial screening from prior toxic exposure.; "NAFLD" (unspecified if ongoing), notes: NAFLD; "oxalate stones" (unspecified if ongoing), notes: Kidney disease (please specify) oxalate stones.; "familial hyperlipidemia" (unspecified if ongoing); "Gout" (unspecified if ongoing); "Is the patient a smoker/ former smoke? No" (unspecified if ongoing), notes: Is the patient a smoker/ former smoke? No. Concomitant medication(s) included: TENORMIN; SYNTHROID; NORVASC; CLONIDINE; LOSARTAN; POTASSIUM CITRATE; VITAMIN D3. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6201; Route of administration: Intramuscular; Site of injection: Left arm), administration date: 12Feb2021, when the patient was 70-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: EN6198; Route of administration: Intramuscular; Site of injection: Left arm), administration date: 05Mar2021, when the patient was 70-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: FF2593; Route of administration: Intramuscular; Site of injection: Left arm), administration date: 23Oct2021, when the patient was 71-year-old, for COVID-19 Immunization. The following information was reported: FAECES PALE (non-serious) with onset 2022, outcome "unknown", described as "clay colored stools"; DIARRHOEA (non-serious) with onset 2022, outcome "unknown", described as "loose stools". Additional information: Patient was not hospitalized or admitted to an Intensive Care Unit. Patient was not still (at the time of this report) hospitalized. Patient did not display clinical signs at rest indicative of severe systemic illness and did not require supplemental oxygen (including high flow or ECMO) or received mechanical ventilation. New or worsened symptoms/signs during the COVID-19 illness included clay-colored stools and loose stools. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Familial hyperlipidemia; Gout; Hypertension; Kidney stones (Kidney disease (please specify) oxalate stones.); Lung disease (Lung disease (please specify) interstitial screening from prior toxic exposure.); Non-alcoholic fatty liver (NAFLD); Nonsmoker (Is the patient a smoker/ former smoke? No); Pre-diabetes (Pre DM)
Andere Medikamente: TENORMIN; SYNTHROID; NORVASC; CLONIDINE; LOSARTAN; POTASSIUM CITRATE; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 2461861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NJ
Alter: 62,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 25.07.2022
Beginn: 20.09.2022
Tage bis Beginn: 57,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Nasal congestion Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

The symptoms were mild and started out with a sore throat. Very congested with a bit of a cough, achy. It started on a Monday and by Thursday the sore throat went away, the only thing that stayed was the congestion and the cough. Today I'm still a bit stuffy but not bad. It was all very mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 self test- positive
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma; Hypothyroidism
Andere Medikamente: Thyroid medication
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2446379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OH
Alter: 84,0
Geschlecht: F
Eingang: 15.09.2022
Impfdatum: 12.04.2022
Beginn: 28.06.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: UN / UN

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

COVID-19 Diarrhoea Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Tested COVID positive- symptoms include nausea/vomiting and diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 1,0
Labordaten: Nasopharyngeal swab collected on 6/29/2022 detected 2019 Novel Coronavirus RNA on 6/9/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic lung disease, hypertension, cardiovascular disease, and autoimmune condition.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2362244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 71,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 29.06.2022
Beginn: 01.02.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Abdominal distension Abdominal pain Arthralgia Asthenia Balance disorder Body temperature Decreased appetite Dizziness Eye irritation Headache COVID-19 SARS-CoV-2 test Vaccination failure Injection site swelling Lethargy Pyrexia Tinnitus Urticaria

Symptomtext

COVID-19/Covid-19 test positive; COVID-19/Covid-19 test positive; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 29Jan2021 at 08:30 as dose 1, single (Lot number: EL0142), in right arm, on 19Feb2021 at 08:30 as dose 2, single (Lot number: EL926), in right arm and on 29Jun2022 at 10:30 as dose 3 (booster), single (Lot number: FJ4991) at the age of 71 years, in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Migraine", start date: 2004 (ongoing); "Asthma", start date: 1980 (ongoing); "Takotsubo", start date: 2014 (ongoing), notes: Illness/AE: Takotsubo; "Cardiac spasm" (ongoing), notes: Illness/AE: Cardiac spasm; "Hiatal hernia with GERD", start date: 2019 (ongoing), notes: Hiatal hernia with GERD, Pertinent details: Had LINX surgery; "Fibromyalgia", start date: 1999 (ongoing); "Osteopenia/ perosis with joint pain" (ongoing), notes: Osteopenia/ perosis with joint pain; "Osteopenia/ perosis with joint pain" (ongoing), notes: Osteopenia/ perosis with joint pain; "Allergy" (unspecified if ongoing); "Leg cramps" (unspecified if ongoing); "arthritis" (unspecified if ongoing); "sleep" (unspecified if ongoing), notes: sleep; "Blood pressure" (unspecified if ongoing); "constipation" (unspecified if ongoing); "Brain fog" (unspecified if ongoing); "Prevent bladder infections" (unspecified if ongoing); "Low vit-D" (unspecified if ongoing); "Osteoporosis" (unspecified if ongoing); "High cholesterol" (unspecified if ongoing); "Overactive bladder" (unspecified if ongoing); "Heart" (unspecified if ongoing), notes: Heart; "Prevent bladder infections" (unspecified if ongoing), notes: Prevent bladder infections; "Hiatal hernia with GERD", start date: 2019 (ongoing), notes: Hiatal hernia with GERD, Pertinent details: Had LINX surgery; "Prevent covid" (unspecified if ongoing), notes: Prevent covid; "Back pain" (unspecified if ongoing); "Hives", start date: 29Jun2022, stop date: 02Jul2022, notes: Duration of hives: 29Jun2022-02Jul2022; "Headaches" (unspecified if ongoing), notes: Headaches. Concomitant medication(s) included: OXYBUTYNIN oral taken for hypertonic bladder (ongoing); LYRICA oral taken for fibromyalgia (ongoing); CRESTOR oral taken for blood cholesterol increased (ongoing); MVI 118 oral (ongoing); CALCIUM oral taken for osteoporosis (ongoing); TURMERIC + oral taken for arthralgia (ongoing); D3 oral taken for hypovitaminosis; ASA oral taken for cardiac disorder (ongoing); METHENAMINE oral taken for cystitis (ongoing); COENZYME Q10+ oral taken for cardiac disorder (ongoing); B COMPLEX [VITAMIN B COMPLEX] oral taken for confusional state, arthralgia (ongoing); FIBER oral taken for constipation (ongoing); MAGNESIUM oral taken for muscle spasms (ongoing); VERAPAMIL oral taken for stress cardiomyopathy, cardiac disorder (ongoing); SINGULAIR oral taken for asthma (ongoing); BACOFEN oral taken for arthralgia, arthritis, muscle spasms (ongoing); ZERICA oral taken for covid-19 immunisation, start date: 2021; ALBUTEROL HFA taken for asthma (ongoing); FLONASE [FLUTICASONE PROPIONATE]; OXYCODON oral taken for back pain, arthralgia (ongoing); PRILOSEC [OMEPRAZOLE MAGNESIUM] oral taken for gastrooesophageal reflux disease (ongoing); BENADRYL oral taken for hypersensitivity, urticaria; ZYRTEC ALLERGY oral taken for hypersensitivity (ongoing); MELATONIN oral taken for sleep disorder (ongoing); UBRELVY oral taken for migraine, headache. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Feb2022, outcome "unknown" and all described as "COVID-19/Covid-19 test positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Negative, notes: I Had numerous other covid tests (nasal) & all other were negative & due to being admitted to Hospital; (Feb2022) Positive. Clinical course: The patient was sick for 4 days & (Illegible) that when had covid in early Feb2022. No follow-up attempts are possible. No further information is expected.; 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 events of vaccination failure and COVID-19 cannot be ruled out given the known suspect product profile and temporal association.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Negative ; Comments: I Had numerous other covid tests (nasal) & all other were negative & due to being admitted to Hospital.; Test Date: 202202; Test Name: Covid-19 Test; Test Result: Positive
Aktuelle Erkrankungen: Asthma; Fibromyalgia; GERD (Hiatal hernia with GERD Pertinent details: Had LINX surgery); Hiatal hernia (Hiatal hernia with GERD Pertinent details: Had LINX surgery); Hives (Duration of hives: 29Jun2022-02Jul2022); Joint pain (Osteopenia/ perosis with joint pain); Migraine; Osteopenia (Osteopenia/ perosis with joint pain); Spasm coronary artery (Illness/AE: Cardiac spasm); Takotsubo syndrome (Illness/AE: Takotsubo)
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Arthritis; Back pain; Bladder infection (Prevent bladder infections); Bladder infection; Blood pressure; Confusion; Constipation; COVID-19 immunization (Prevent covid); Headache (Headaches); Heart disorder (Heart); High cholesterol; Leg cramps; Osteoporosis; Overactive bladder; Sleep disorder (sleep); Vitamin D deficiency
Andere Medikamente: OXYBUTYNIN; LYRICA; CRESTOR; MVI 118; CALCIUM; TURMERIC +; D3; ASA; METHENAMINE; COENZYME Q10+; B COMPLEX [VITAMIN B COMPLEX]; FIBER; MAGNESIUM; VERAPAMIL; SINGULAIR; BACOFEN; ZERICA; ALBUTEROL HFA; FLONASE [FLUTICASONE PROPIONATE]; OXYCODO
Allergien: -
Vorherige Impfungen: -

VAERS 2362244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 71,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 29.06.2022
Beginn: 01.02.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Abdominal distension Abdominal pain Arthralgia Asthenia Balance disorder Body temperature Decreased appetite Dizziness Eye irritation Headache COVID-19 SARS-CoV-2 test Vaccination failure Injection site swelling Lethargy Pyrexia Tinnitus Urticaria

Symptomtext

COVID-19/Covid-19 test positive; COVID-19/Covid-19 test positive; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 29Jan2021 at 08:30 as dose 1, single (Lot number: EL0142), in right arm, on 19Feb2021 at 08:30 as dose 2, single (Lot number: EL926), in right arm and on 29Jun2022 at 10:30 as dose 3 (booster), single (Lot number: FJ4991) at the age of 71 years, in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Migraine", start date: 2004 (ongoing); "Asthma", start date: 1980 (ongoing); "Takotsubo", start date: 2014 (ongoing), notes: Illness/AE: Takotsubo; "Cardiac spasm" (ongoing), notes: Illness/AE: Cardiac spasm; "Hiatal hernia with GERD", start date: 2019 (ongoing), notes: Hiatal hernia with GERD, Pertinent details: Had LINX surgery; "Fibromyalgia", start date: 1999 (ongoing); "Osteopenia/ perosis with joint pain" (ongoing), notes: Osteopenia/ perosis with joint pain; "Osteopenia/ perosis with joint pain" (ongoing), notes: Osteopenia/ perosis with joint pain; "Allergy" (unspecified if ongoing); "Leg cramps" (unspecified if ongoing); "arthritis" (unspecified if ongoing); "sleep" (unspecified if ongoing), notes: sleep; "Blood pressure" (unspecified if ongoing); "constipation" (unspecified if ongoing); "Brain fog" (unspecified if ongoing); "Prevent bladder infections" (unspecified if ongoing); "Low vit-D" (unspecified if ongoing); "Osteoporosis" (unspecified if ongoing); "High cholesterol" (unspecified if ongoing); "Overactive bladder" (unspecified if ongoing); "Heart" (unspecified if ongoing), notes: Heart; "Prevent bladder infections" (unspecified if ongoing), notes: Prevent bladder infections; "Hiatal hernia with GERD", start date: 2019 (ongoing), notes: Hiatal hernia with GERD, Pertinent details: Had LINX surgery; "Prevent covid" (unspecified if ongoing), notes: Prevent covid; "Back pain" (unspecified if ongoing); "Hives", start date: 29Jun2022, stop date: 02Jul2022, notes: Duration of hives: 29Jun2022-02Jul2022; "Headaches" (unspecified if ongoing), notes: Headaches. Concomitant medication(s) included: OXYBUTYNIN oral taken for hypertonic bladder (ongoing); LYRICA oral taken for fibromyalgia (ongoing); CRESTOR oral taken for blood cholesterol increased (ongoing); MVI 118 oral (ongoing); CALCIUM oral taken for osteoporosis (ongoing); TURMERIC + oral taken for arthralgia (ongoing); D3 oral taken for hypovitaminosis; ASA oral taken for cardiac disorder (ongoing); METHENAMINE oral taken for cystitis (ongoing); COENZYME Q10+ oral taken for cardiac disorder (ongoing); B COMPLEX [VITAMIN B COMPLEX] oral taken for confusional state, arthralgia (ongoing); FIBER oral taken for constipation (ongoing); MAGNESIUM oral taken for muscle spasms (ongoing); VERAPAMIL oral taken for stress cardiomyopathy, cardiac disorder (ongoing); SINGULAIR oral taken for asthma (ongoing); BACOFEN oral taken for arthralgia, arthritis, muscle spasms (ongoing); ZERICA oral taken for covid-19 immunisation, start date: 2021; ALBUTEROL HFA taken for asthma (ongoing); FLONASE [FLUTICASONE PROPIONATE]; OXYCODON oral taken for back pain, arthralgia (ongoing); PRILOSEC [OMEPRAZOLE MAGNESIUM] oral taken for gastrooesophageal reflux disease (ongoing); BENADRYL oral taken for hypersensitivity, urticaria; ZYRTEC ALLERGY oral taken for hypersensitivity (ongoing); MELATONIN oral taken for sleep disorder (ongoing); UBRELVY oral taken for migraine, headache. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Feb2022, outcome "unknown" and all described as "COVID-19/Covid-19 test positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Negative, notes: I Had numerous other covid tests (nasal) & all other were negative & due to being admitted to Hospital; (Feb2022) Positive. Clinical course: The patient was sick for 4 days & (Illegible) that when had covid in early Feb2022. No follow-up attempts are possible. No further information is expected.; 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 events of vaccination failure and COVID-19 cannot be ruled out given the known suspect product profile and temporal association.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Negative ; Comments: I Had numerous other covid tests (nasal) & all other were negative & due to being admitted to Hospital.; Test Date: 202202; Test Name: Covid-19 Test; Test Result: Positive
Aktuelle Erkrankungen: Asthma; Fibromyalgia; GERD (Hiatal hernia with GERD Pertinent details: Had LINX surgery); Hiatal hernia (Hiatal hernia with GERD Pertinent details: Had LINX surgery); Hives (Duration of hives: 29Jun2022-02Jul2022); Joint pain (Osteopenia/ perosis with joint pain); Migraine; Osteopenia (Osteopenia/ perosis with joint pain); Spasm coronary artery (Illness/AE: Cardiac spasm); Takotsubo syndrome (Illness/AE: Takotsubo)
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Arthritis; Back pain; Bladder infection (Prevent bladder infections); Bladder infection; Blood pressure; Confusion; Constipation; COVID-19 immunization (Prevent covid); Headache (Headaches); Heart disorder (Heart); High cholesterol; Leg cramps; Osteoporosis; Overactive bladder; Sleep disorder (sleep); Vitamin D deficiency
Andere Medikamente: OXYBUTYNIN; LYRICA; CRESTOR; MVI 118; CALCIUM; TURMERIC +; D3; ASA; METHENAMINE; COENZYME Q10+; B COMPLEX [VITAMIN B COMPLEX]; FIBER; MAGNESIUM; VERAPAMIL; SINGULAIR; BACOFEN; ZERICA; ALBUTEROL HFA; FLONASE [FLUTICASONE PROPIONATE]; OXYCODO
Allergien: -
Vorherige Impfungen: -

VAERS 2436924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 04.08.2022
Beginn: 08.09.2022
Tage bis Beginn: 35,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Chills Cough Fatigue Nasal congestion Oropharyngeal pain Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I received sore throat; fever; fatigue; cough; runny and stuffy nose; chills; body aches and I'm taking over the counter Sudafed. I still have symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: I tested positive COVID 19 on 09/08/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2434633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MA
Alter: 56,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 19.07.2022
Beginn: 19.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Immediate post-injection reaction Myalgia Pain in extremity

Symptomtext

PATEINT REPORTED EVENT TO PHARMACY 9/8/22. THE PATIENT STATES THAT THE ARM WAS SORE FROM THE VACCINE IMMEDIATELY AFTER THE VACCINE AS EXPECTED, BUT THE SORENESS NEVER SUBSIDED AND STATES THAT THE PAIN GOT WORSE THIS MOST RECENT WEEK. WHEN SDESCRIBING THE PAIN, HE SAYS IT IS DULL, AND IS EXACERBATED BY PHYSICAL ACTIVITY/EXERCISE. THE PAIN IS LOCALIZED TO THE MUSCLE BUT HE CANNOT PINPOINT. THERE IS NO REDNESS OR HEAT AT THE INJECTION SITE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: PATIENT RECOMMENDED TO CONTACT MD FOR FOLLOW UP
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2424239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: MO
Alter: 46,0
Geschlecht: M
Eingang: 30.08.2022
Impfdatum: 26.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Hypoaesthesia Injection site pain Pain Pain in extremity

Symptomtext

pt states that arm was sore/painful the next day. Says his right arm 2 months later still hurts at injection site, especially if touched. Has shooting pain / pain in arm from right trapezius down to right hand finger times along with numbness. States has not seen doctor yet. Took his primary Dr's info. Contacted Dr office and employee is coordinating office getting him in to be checked out and aware of the adverse event from the booster shot. Patient denied have any other sort of accident to neck/back/arm that could account for the pain and numbness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: Pt to still be seen by Dr. Unknown if any permanent issue yet.
Aktuelle Erkrankungen: pt says no immediate injuries around vaccination time
Vorgeschichte: pt says no long standing health conditions or other neck, back, arm conditions
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2424025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: NH
Alter: 83,0
Geschlecht: F
Eingang: 30.08.2022
Impfdatum: 28.08.2022
Beginn: 29.08.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Immunisation reaction Injection site reaction Rash erythematous

Symptomtext

Patient presented to the pharmacy two days after vaccination with a red rash on her upper left arm. She followed up with her primary care provider who explained she had symptoms of "COVID arm". The provider recommended OTC Tylenol.

Weitere VAERSDATA-Felder

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

VAERS 2420087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MN
Alter: 25,0
Geschlecht: F
Eingang: 25.08.2022
Impfdatum: 14.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Joint range of motion decreased Pain Pain in extremity

Symptomtext

pt reports day of vaccination having typical mild arm soreness with movement but the next 5 days had severe arm pain and now has had persistent arm pain and decreased ROM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: dysmenorrhea, endometriosis, PCOS, migraine
Andere Medikamente: unknown
Allergien: azithromycin
Vorherige Impfungen: -

VAERS 2419416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: VA
Alter: 83,0
Geschlecht: M
Eingang: 24.08.2022
Impfdatum: 21.07.2022
Beginn: 07.08.2022
Tage bis Beginn: 17,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Foreign travel Malaise Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

While on a tour to PRIVATE I contracted COVID on or about August 7, 2022. Upon arriving in PRIVATE on August 9, 2022, for another tour in PRIVATE I became very sick with sneezing, runny nose, sore throat and dry cough. My spouse went to a local pharmacy and purchased OTC meds for my symptoms plus 4 home-style COVID antigen testing kits. I tested positive, and reported same to our tour company and to the hotel.. The tour company canceled our tour and the hotel accepted our request to remain longer in our assigned room (for up to 7 day, with no daily service and meals only by Room Service. The hotel also arranged for a nurse from a local medical facility to come to our room on August 10th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID 19 Antigen test (nasal swab) was positive on August 10th.
Aktuelle Erkrankungen: none.
Vorgeschichte: high cholesterol, diarrhea, migraine.
Andere Medikamente: rosuvastatin, aspirin, gabapentin ,losartan, atrovent, nasacort, fiorinal, lomotil, viberzi, valium, qulipta.
Allergien: none.
Vorherige Impfungen: -

VAERS 2417264

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge FJ4991

mild

Staat: IN
Alter: 56,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 28.07.2022
Beginn: 28.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Headache

Symptomtext

Within a few hours of getting the 1st booster shot, I developed a headache that has lingered on every day since then.

Weitere VAERSDATA-Felder

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

VAERS 2415236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 18.08.2022
Impfdatum: 17.05.2022
Beginn: 12.06.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: SYR / -

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

Drug hypersensitivity Eye swelling Food allergy Lip swelling Swelling of eyelid Urticaria

Symptomtext

I always had an allergy to tree nuts. After the booster I developed new allergies and the current ones got worse. My left eye began to swell up multiple times. Anytime I had aspirin or advil cold and sinus. My lips swelled up 2 times. When I had coconut products my body began to hive up. I've had the tree nut allergy but never developed hives. I am 43 years old and have used Aspirin and Advil cold and sinus for 20 years at least. After the vaccine I've developed an allergy to these medicines. My eye completely shuts down, eye lids swell up, only on my left eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: I have an allergist appointment 8/25 with my Dr. I've documented 3 incidents where my left eye has swollen after use of Advil cold and sinus and aspirin. I will verify this with the allergist and testing.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, High blood pressure
Andere Medikamente: Montelukast, Lisinopril, Aspirin, Advil Cold and Sinus, Albuterol
Allergien: Tree nuts, coconut. I received the first 2 Pfizer vaccines 2/28/21 and 3/21/21. After the booster on 5/17/22 I developed an allergy to Aspirin and Advil cold and sinus, both NSAID's. I was given Pfizer (FJ4991) at Pharmacy.
Vorherige Impfungen: -

VAERS 2415223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 15.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / RA

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

Rash

Symptomtext

PATIENT DEVELOPED RASH ALL OVER HER FACE. SHE TOOK SOME BENADRYL BUT THE RASH DID NOT IMPROVE.

Weitere VAERSDATA-Felder

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

VAERS 2412890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 37,0
Geschlecht: F
Eingang: 16.08.2022
Impfdatum: 06.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / RA

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

Pruritus Rash Urticaria

Symptomtext

ITCHING,RASH AND HIVES ON THE BACK,UNDER ARM, LEGS...SYMPTOMS COME AND GO

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2407446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 20.07.2022
Beginn: 21.07.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Hypotonia Injection site pain Muscle spasms

Symptomtext

Severe charlie horse in right calf lasting only a minute or two, arm at injection nearly limp, extremely sore two days following, feeling of weakness next day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: mental illness synocope unspecified psychosis one month prior
Vorgeschichte: no
Andere Medikamente: Risperdone .5mg twice daily
Allergien: no
Vorherige Impfungen: -

VAERS 2407441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AZ
Alter: 65,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 08.05.2022
Beginn: 24.06.2022
Tage bis Beginn: 47,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Malaise Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

First came down with a soar throat, then took a test and was positive for covid. I went to urgent care I was prescribed paxlovid, few days he had a fever. After few days I was feeling better and tested negative. 5 days later he started to feel sick with body aches and re -tested and I was positive again for covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: antigen test
Aktuelle Erkrankungen: none
Vorgeschichte: dilated cardio myopic mitral valve regurgitation
Andere Medikamente: carvedilol 3.1 ML Lisinopril 5 ML Crestor 20 ML omeprazole 20 ML Aspirin Zyrtec Metamucil vitamin B12 vitamin D3
Allergien: Biaxin
Vorherige Impfungen: -

VAERS 2407206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AZ
Alter: 78,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 06.05.2022
Beginn: 24.07.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

On 7-24-2022, I had a sore throat. The following morning I had the sniffles. On 7-26, I used a home COVID-19 test with negative results. On 7-27, I tested positive with a home COVID-19 test. I contacted my primary care physician on 7-27 thru their internet portal. She responded back on 7-29 thru the portal and told me to take aspirin or TYLENOL for fever (don't know if I ever had one) and drink a lot of non caffeinated fluids. She did not order any medications or tests. I tested negative on 8-6-2022 with a home COVID-19 test. I am reporting a breakthrough case of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 7-26-2022 home COVID-19 test with negative results. 7-27-2022 home COVID-19 test with positive results. 8-6-2022 home COVID-19 test with negative results.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; High Cholesterol; Anxiety; Depression; Restless Legs
Andere Medikamente: Multivitamin; calcium; vitamin D3; vitamin B complex; vitamin C; magnesium; echinacea purpurea; iron supplement; OSTEO BIOFLEX; baby aspirin; bupropion; lisinopril/HCTZ; escitalopram; ropinirole; ibandronate sodium; zolpidem
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2406918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NJ
Alter: -
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 13.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: - / LA

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

Purpura Rash

Symptomtext

skin rashes similar to purpuric skin rash in the palm, in the hands, parts of stomach, thigh and in the legs; skin rash in the palm, in the hands; skin rashes...parts of stomach; skin rashes...thigh and in the legs; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old male patient received BNT162b2 (BNT162B2), on 13Jul2022 at 18:45 as dose 4 (booster), single (Lot number: FJ4991), in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: VITAMIN B12 [CYANOCOBALAMIN]; COD LIVER OIL [COD-LIVER OIL]; VITAMIN K2 MK7. Vaccination history included: BNT162b2 (DOSE 3, SINGLE; Lot No: FD0810; Injection site: Arm Left; Vaccine Administration Time: 02:30 PM), administration date: 22Oct2021, when the patient was 58-year-old, for COVID-19 immunisation; Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunisation. The following information was reported: RASH (non-serious) with onset 23Jul2022, outcome "not recovered", described as "skin rash in the palm, in the hands"; PURPURA (non-serious) with onset 23Jul2022, outcome "not recovered", described as "skin rashes similar to purpuric skin rash in the palm, in the hands, parts of stomach, thigh and in the legs"; RASH (non-serious) with onset 23Jul2022, outcome "not recovered", described as "skin rashes...parts of stomach"; RASH (non-serious) with onset 23Jul2022, outcome "not recovered", described as "skin rashes...thigh and in the legs". Therapeutic measures were taken as a result of purpura, rash, rash, rash. Additional information: The patient did not receive any other vaccines within 4 weeks. No covid prior vaccination and no covid tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to plants; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: VITAMIN B12 [CYANOCOBALAMIN]; COD LIVER OIL [COD-LIVER OIL]; VITAMIN K2 MK7
Allergien: -
Vorherige Impfungen: -

VAERS 2405971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NC
Alter: 69,0
Geschlecht: M
Eingang: 09.08.2022
Impfdatum: 06.05.2022
Beginn: 30.07.2022
Tage bis Beginn: 85,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Foreign travel Malaise SARS-CoV-2 test positive

Symptomtext

Returned from away on Wednesday 7/27/22, I felt fine. On Saturday 7/30/22 I started coughing (dry hacking cough -on occasion). On Sunday 7/31/22 I was also coughing (dry hacking cough - on occasion but a little more frequent) I took an at-home covid test on 7/31/22 but it was negative. On Monday 8/1/22 still coughing, I took another at-home covid test - it was positive. On Tuesday 8/2/22 I had a telehealth meeting with my Primary Care Physician, I was prescribed a 5-day regiment of Merck's Lagevrio 200mg. My coughing symptoms improved overnight and improved by next morning. Saturday 8/6/22 my symptoms are very mild, but I still tested positive. It is Tuesday 8/9/22 and I still have mild coughing on occasion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Sarcoidosis (likely a mild impact to my lungs) Cardiomyopathy
Andere Medikamente: Xarelto 20mg daily Carvedolil 6.25mg twice daily Lisinopril 2.5mg nightly Montelukast 10mg nightly Multi-Vitamins Vitamin D3
Allergien: Amoxicillin Erythromicin
Vorherige Impfungen: -

VAERS 2405499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MS
Alter: 34,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 02.08.2022
Beginn: 03.08.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Urticaria Vaccination site movement impairment Vaccination site pain Vaccination site swelling

Symptomtext

broke out in hives all over my back; have a painful knot in my left armpit that's swollen and hard for me to move my arm; have a painful knot in my left armpit that's swollen and hard for me to move my arm; have a painful knot in my left armpit that's swollen and hard for me to move my arm; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Aug2022 at 15:15 as dose 3 (booster), single (Lot number: FJ4991) at the age of 34 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Osteoarthritis" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "IBS" (unspecified if ongoing). Concomitant medication(s) included: TRAZODONE; FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]; CELEBREX; PROTONIX [PANTOPRAZOLE SODIUM SESQUIHYDRATE]; VITAMIN D [VITAMIN D NOS]. Past drug history included: Amitriptyline, reaction(s): "known allergies: Amitriptyline". Vaccination history included: BNT162b2 (Prev dose product=COVID 19,, Prev dose brand=Pfizer,, Prev dose brand unknown=False,, Prev dose lot unknown=True,, Prev dose lot unknown reason=Obscured by other product labelling, Prev dose administration date=15Sep2021,, Prev dose dose number=2,, Prev dose vaccine location=Left arm,), administration date: 15Sep2021, when the patient was 33-year-old, for COVID-19 Immunization; BNT162b2 (prev dose product=COVID 19, prev dose brand=Pfizer,, prev dose brand unknown=False,, prev dose lot number=EW0175,, prev dose lot unknown=False,, prev dose administration date=14Aug2021,, prev dose dose number=1,, prev dose vaccine location=Right arm), administration date: 14Aug2021, when the patient was 33-year-old, for COVID-19 Immunization. The following information was reported: URTICARIA (non-serious) with onset 03Aug2022, outcome "recovering", described as "broke out in hives all over my back"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE SWELLING (non-serious), VACCINATION SITE MOVEMENT IMPAIRMENT (non-serious) all with onset 03Aug2022, outcome "recovering" and all described as "have a painful knot in my left armpit that's swollen and hard for me to move my arm". Therapeutic measures were not taken as a result of urticaria, vaccination site pain, vaccination site swelling, vaccination site movement impairment. Additional information: patient did not received other vaccine in four weeks. No treatment received for ae. Patient did not had covid prior vaccination and covid was not tested post vaccination patient has Known allergies with Amitriptyline Other medications in two weeks reported as Trazodone. Flexeril. Celebrex. Protonic. Vitamin D and Other medical history is reported as Osteoarthritis. Fibromyalgia. IBS. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fibromyalgia; Irritable bowel syndrome; Osteoarthritis
Andere Medikamente: TRAZODONE; FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]; CELEBREX; PROTONIX [PANTOPRAZOLE SODIUM SESQUIHYDRATE]; VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2405563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 22,0
Geschlecht: F
Eingang: 06.08.2022
Impfdatum: 05.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Burning sensation Headache Pharyngeal swelling Pruritus Skin discolouration Swollen tongue

Symptomtext

Started w/ headache 15 minutes after shot was given. Progressed to face and neck burning and itching 10 minutes later. Soon progressed to throat and tongue swelling. 50 minutes later her toes started turning purple. She was given (2) ibuprofen 200mg and 25mg benadryl. 911 was called and she was taken to the ER.

Weitere VAERSDATA-Felder

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

VAERS 2403979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 06.08.2022
Impfdatum: 17.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

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

Fatigue Headache Tongue cyst

Symptomtext

Bad headache and fatigue. White cyst-like pimple in the middle of the top of my tongue. Doctor visit on 7/25/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, diabetes, heart condition
Andere Medikamente: Flonase, Tirosint, Pantoprazole, Flovent, Losartan, Metoprolol, Zetia, Aspirin 81mg, Spirolactone
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2403510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MA
Alter: 18,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 05.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Fall Hypoacusis Visual impairment Vomiting

Symptomtext

Around 3:15-3:20pm, after patient had received her first dose of Pfizer Covid vaccine, she was reading paperwork about her vaccine and started to feel anxious. her vision and hearing started to be affected/muffled and she came up to the counter to let the pharmacy staff know. After doing so, she did not make it back to her chair before falling to the ground. Rx technician witnessed this. 911 was called by front store management and EMS was en route. Patient states she may have lost consciousness for a few seconds but remembers being helped up and seated in chair. 911 operator instructed pharmacist not to administer epinephrine. A short time later, the patient vomited. With her permission, her father was informed and left work to meet her at the pharmacy. She contacted him when EMS arrived to discuss whether she should go to the hospital as she was feeling much better. She declined going to hospital and was monitored by pharmacy staff until her father arrived about an hour later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None per VAR form or discussed by patient with pharmacist
Vorgeschichte: None per VAR form or discussed by patient with pharmacist
Andere Medikamente: Unknown as patient does not fill medications with us
Allergien: None per VAR form
Vorherige Impfungen: -

VAERS 2403091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Fall Fatigue

Symptomtext

Dizziness, fell after vaccine, fatigue

Weitere VAERSDATA-Felder

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

VAERS 2402935

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AZ
Alter: 72,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 05.05.2022
Beginn: 04.08.2022
Tage bis Beginn: 91,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Headache Nausea Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

Started having a headache with a lot of sneezing, cough, and with sore throat and chest congestion. After 2 days of it not subsiding, I tested at home 2 days later and it was negative. Two days after that I started feeling nauseas so I took another home test and tested positive. Had telehealth visit and was prescribed PAXLOVID. Still feeling feverish at this point.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Home COVID-19 test negative. Two days later my home COVID-19 test was positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic; Hiatal Hernia
Andere Medikamente: Atorvastatin; pantoprazole; lisinopril; fish oil; calcium; horse chestnut; PRESERVISION; aspirin
Allergien: Dairy
Vorherige Impfungen: -

VAERS 2401974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 51,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 20.07.2022
Beginn: 02.08.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: SYR / LA

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

Bladder pain Chills Constipation Dysuria Pain Pyrexia

Symptomtext

Difficulty urinating - feeling of a full bladder, but unable to urinate freely. Pain as if bladder is overly full. Constipation - unable to defecate at all from 8/2-8/5. Slowly recovering Fever and chills - 8/2-8/4 Body aches - 8/2 - 8/4 - managed with 600mg ibuprofen every 6 hours (4 x per day)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bladder pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Hammer Nutrition Tissue Rejuvenator (Glucosamine and Chondroitin) Hammer Nutrition Super Antioxidant
Allergien: None
Vorherige Impfungen: -

VAERS 2400358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OR
Alter: 75,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 03.05.2022
Beginn: 18.07.2022
Tage bis Beginn: 76,0
Dosis: 4
Route/Site: SYR / AR

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

COVID-19 Cough Fatigue Feeling abnormal Headache Hypersomnia Oropharyngeal pain SARS-CoV-2 test positive Sinus congestion Sneezing

Symptomtext

I felt tired, sinus plugged up, headache and sneezing on 07/18/2022. I slept all afternoon and when I woke I still felt bad. I went ahead and took a home test and it was positive. Around day three I did have a sore throat and some coughing, headache lasted about three days, fatigue lasted about a week. I talked to my doctor on 07/20/2022 and got a prescription of Paxlovid and started on the evening of the 20th. As of today I still do have fatigue that is lingering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Home Test Positive 07/18/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Blood Clots; G6PD; Low Thyroid; Osteopenia
Andere Medikamente: Warfarin; Levothyroxine; Calcium Magnesium; Alphalopick Acid; Frelenium; Vitamin D; Vitamin B12
Allergien: Sulfa; Demerol; Quinine
Vorherige Impfungen: -

VAERS 2399293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TN
Alter: 62,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 27.07.2022
Beginn: 28.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Rash

Symptomtext

client recieved covid vaccine 2 days prior to july 27th when she saw my fellow NP for a rash that started locally and then was spreading. the NP @ that time put her on prednisone and the client is following up today with worsening of the rash and no improvement with prednisone. looks just like a drug eruption.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: thyroid disorder, osteopenia, inosmnia,
Andere Medikamente: aldactone, banophen, lunesta, boniva, synthroid, zoloft, lamisil
Allergien: none
Vorherige Impfungen: -

VAERS 2398047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: DE
Alter: 82,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 09.07.2022
Beginn: 24.07.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Headache Hypersomnia Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a headache and sore throat on night of July 24th. I had runny nose and was really tired. I slept most of the next day. I called the doctor to get medication. I was warned about Paxlovid causing rebound case. I still have a runny nose. I am just taking it easy and laying low.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes; Cardio Vascular Disease
Andere Medikamente: Synthroid; Atenolol; Metformin; Nexium; Valsartan; Zyrtec; Zetia; Fenofibric; Aspirin
Allergien: Cipro; Seasonal environment
Vorherige Impfungen: -

VAERS 2397968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IN
Alter: 66,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 11.07.2022
Beginn: 27.07.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Nasal congestion Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Symptoms began on Wednesday; nasal congestion and sore throat. It continued into Thursday. I did two at home tests and they were both positive. I contacted my doctor on Friday. They arranged for an infusion on Saturday, July 30th. Since I take amiodarone I was advised not to take PAXLOVID. I had the infusion and as of today my symptoms are much better. No sore throat and a bit of a runny nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Home COVID-19 tests, 3, all positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: PKD Kidney Disease; Psoriatic Arthritis; AFIB under control
Andere Medikamente: ENBREL; ramipril; propranolol; amiodarone
Allergien: N/A
Vorherige Impfungen: -

VAERS 2397664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 30.07.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

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

Arthralgia Chest discomfort Dysgeusia Fatigue Joint swelling Pain

Symptomtext

Extreme fatigue, overall body soreness, finger joint swelling and pain, metallic taste in mouth, some mild chest tightness.

Weitere VAERSDATA-Felder

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

VAERS 2400271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TX
Alter: -
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: -
Beginn: 18.07.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Bladder catheterisation Pain in extremity Urinary incontinence

Symptomtext

Received 2nd Pfizer COVID booster on 07/15/22...On 7/17/22, developed severe leg pains, bilaterally. Also, developed incontinence and needed foley catheter by 07/22/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2395182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 58,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 24.04.2022
Beginn: 26.06.2022
Tage bis Beginn: 63,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Dizziness Feeling abnormal Headache Nasopharyngitis Pain Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

Started with cold symptoms, scratchy throat, runny nose, body aches, headache, cough. Went to work on 06.26.22 and rapid test was positive - treated with Paxlovid but only took 2.5 days before feeling lightheaded, foggy so stopped taking the antiviral

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Rapid Covid test done at clinic - positive
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, HTN, Hypothyroid, Hypercholesterolemia
Andere Medikamente: Glucophage, Actos ,Synthroid, Lisinopril, Zocor, Vitamin D, Magnesium
Allergien: Sulfa, Ampicillin, Sudafed, Levaquin
Vorherige Impfungen: -

VAERS 2395157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 63,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 27.04.2022
Beginn: 01.05.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: SYR / LA

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

Blood pressure increased Headache Magnetic resonance imaging head normal

Symptomtext

After few weeks of the vaccine persistent headaches occurred for 2 weeks. I took all kinds of medications but didn't work. 06/01/2022 I went to the clinic they ordered MRI of my brain but they didn't find anything that should be noted for. They told me to use FLONASE. I noticed my blood pressure was elevated. 07/14/2022 I had a follow up with my doctor for something else. I noticed my blood pressure was high again. My doctor advised me to change my diet and my doctor also prescribed me losartan. Now that my blood pressure is being normalized my headaches reduced. I will be following up with my doctor on 08/04/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid; Hypercholesterolemia; Arthritis; Allergic Rhinitis; Migraines
Andere Medikamente: Estradiol; meloxicam; simvastatin; SINGULAIR; levothyroxine
Allergien: Thimerosal; nickel
Vorherige Impfungen: -

VAERS 2394993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MN
Alter: 70,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 24.04.2022
Beginn: 12.07.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Dysphonia Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

Covid diagnosed by home antigen test after symptoms of headache, sore throat, hoarse voice, and cough. Called physician office and had virtual visit after which she prescribed Paxlovid at a reduced dose. Paxlovid, reduced dose, begun on Friday 7/15 with symptom improvement that day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: At home antigen test, 7/13/22, positive for Covid 19
Aktuelle Erkrankungen: none
Vorgeschichte: obesity
Andere Medikamente: None
Allergien: erythromycin sulfa
Vorherige Impfungen: -

VAERS 2394942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 86,0
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: 27.04.2022
Beginn: 10.07.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / -

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

COVID-19 Fatigue Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

On July 10, 2022 I had an extreme sore throat that hurt worse than anything I had ever experienced. I took a home COVID-19 test on July 11, 2022, that came back positive. I waited to take a second a test that also came back positive. I called my Primary Care Physician and requested a prescription for the PAXLOVID. I started taking the antiviral on July 12, 2022 and quarantined for 5 days and I am feeling better the fatigue is going away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: Interstitial Lung Disease asymptomatic; Hypertrophic Obstructive Cardiomyopathy
Andere Medikamente: Famotidine acid controller; metoprolol; simvastatin; clopidogrel; losartan; mature multivitamin; vitamin D3
Allergien: Penicillin
Vorherige Impfungen: 1955 Influenza vaccine

VAERS 2393889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 66,0
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: 22.04.2022
Beginn: 01.06.2022
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: SYR / LA

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

Abdominal discomfort COVID-19 Fatigue Headache Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Sore throat Headache Runny nose Upset stomach General fatigue lasting for over 3 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Tested positive for COVID 19, via at home test kit, as of 06/30/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure COPD Artery plaque/stent
Andere Medikamente: Metoprolol Tartrate ?50mg ??2xdaily Lisinopril ??10mg ??1xdaily Rosuvastatin Calcium ?20mg ??1xdaily Clopidogrel ??75mg ??1xdaily Isosorbide Mononitrate?30mg??1xdaily Asprin ???81mg ??1xdaily Stiolto Respimat??2.5/2.5mcg?INH 4GM
Allergien: None
Vorherige Impfungen: -

VAERS 2393185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 27.07.2022
Impfdatum: 24.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain Urine analysis

Symptomtext

Abdominal pain, possible mesenteric lymphadenitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Doctor exams and urine test.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2391413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WI
Alter: 52,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 19.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: SYR / -

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

Fatigue Headache

Symptomtext

Extreme tiredness and fatigue plus headaches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None I have not gone to the doctor
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Synthroid
Allergien: -
Vorherige Impfungen: -

VAERS 2390997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MS
Alter: 60,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 14.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Chills Cough Diarrhoea Fatigue Headache Myalgia Nausea Pyrexia SARS-CoV-2 test positive

Symptomtext

Nausea, diarrhea, fever, chills, muscle aches, fatigue, severe cough, really bad headache, and I'm still having problems. July 22nd COVID-19 at home test that morning and it was positive. At the doctor that afternoon and it was positive. They put me on PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: July 22nd COVID-19 at home test that morning and it was positive.
Aktuelle Erkrankungen: I had the flu about 2 months ago
Vorgeschichte: High blood pressure; high cholesterol; diabetes; neuropathy; congenital heart disease; history of strokes (2)
Andere Medikamente: MEVACOR; NAPROSYN; PLAVIX; TRICOR; SINGULAIR; NEURONTIN; ZOLOFT; LASIX; lisinopril; metoprolol; CENTRUM silver
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2390954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 6,0
Geschlecht: M
Eingang: 26.07.2022
Impfdatum: 21.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Chills Pyrexia

Symptomtext

Patent has fever and chills for 2 days

Weitere VAERSDATA-Felder

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

VAERS 2388269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 10.04.2022
Beginn: 26.06.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Asthenia COVID-19 Dizziness Fatigue Nausea Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

About midnight, early morning of June 26th, I had fever, nausea, fatigue and light headed and body aches primarily in the joints. After about 4 days I didn't have any fever but still had the joint aches and extreme fatigue for about a week. I began PAXLOVID on June 30 after testing positive at home and speaking with doctor. As of today, July 25th, I still have low energy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Home antigen COVID-19 test, positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Migraines; Arthritis
Andere Medikamente: Amlodipine; benazepril; pravastatin; estradiol; duloxetine; melatonin; TYLENOL; FLONASE; EMGALITY; BOTOX; IMITREX; vitamin C; vitamin D; riboflavin; magnesium
Allergien: Sulfa; bacitracin; kiwi; nickle
Vorherige Impfungen: -

VAERS 2388081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 18.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: - / LA

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

Arthropod bite Injection site swelling Pruritus Tongue disorder Urticaria

Symptomtext

I had swelling at the injection site. Then saturday, i started itching a welp which was on the opposite arm of the injection site. I started feeling like I had a bite, or i was bitten by something, an ant or mosquito. I was in a weird part of my arm. I went to a movie t about noon, and all down my arm and down the side of my back started to itch. At that point, I was sitting next to someone, nothing weird about that. When I got home, it started to spread down the back of my leg, my butt cheek and down my thigh, it spread over to the other leg in the same area. and by evening, it went to my calves. So I took benadryl to go to sleep, cause it was unbareable. I didnt really know what hives were, so I looked it up. Woke up on Sunday morning, it was activated all over everywhere. I couldnt take benadryl , so i went and brought allegra and I took that. By the time I took that, it had gotten so much worst. In my feet, between my toes, my palms, my face, I can feel my tongue get a little thick. I started to get nervous. By then I had already taken allegra, soon as it kicked in, it went away. This morning, it was worst. I was welted everywhere, but my torso is not welted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site swelling
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Asprin and Latex
Vorherige Impfungen: Flu shot- home for days with the flu Pfizer- little sick

VAERS 2387572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AZ
Alter: 73,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 10.04.2022
Beginn: 10.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Acoustic stimulation tests Body temperature Chills Deafness Headache Pyrexia SARS-CoV-2 test Sinus pain Tinnitus

Symptomtext

headache; 6 hours after Phizer COVID 19 Booster vaccine I started getting chills; 100 degree fever; sinus pain; hearing loss; loud tinnitus in both ears; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Apr2022 at 11:00 as dose 3 (booster), single (Lot number: FJ4991) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Birt Hoggs Dube Syndrome" (unspecified if ongoing); "Valley Fever" (unspecified if ongoing); "Egg white allergy" (unspecified if ongoing), notes: Allergy: Egg white allergy; "if covid prior vaccination : yes" (unspecified if ongoing), notes: if covid prior vaccination : yes. Concomitant medication(s) included: ARMOUR THYROID. Vaccination history included: BNT162b2 (Dose 2, COVID-19,, lot number=301458A,, administration date=28Sep2021,time=11:00 AM,, vaccine location=Left arm,), administration date: 28Sep2021, when the patient was 72-year-old, for COVID-19 immunization; BNT162b2 (Dose 1, COVID 19,, lot number=FC3184,, administration date=06Sep2021, time=12:00 PM,, vaccine location=Left arm), administration date: 06Sep2021, when the patient was 72-year-old, for COVID-19 immunization. The following information was reported: PYREXIA (disability) with onset 10Apr2022 at 17:00, outcome "recovered" (12Apr2022), described as "100 degree fever"; CHILLS (disability) with onset 10Apr2022 at 17:00, outcome "recovered" (12Apr2022), described as "6 hours after Phizer COVID 19 Booster vaccine I started getting chills"; HEADACHE (disability) with onset 10Apr2022 at 17:00, outcome "recovered" (12Apr2022); DEAFNESS (disability) with onset 10Apr2022 at 17:00, outcome "not recovered", described as "hearing loss"; TINNITUS (disability) with onset 10Apr2022 at 17:00, outcome "not recovered", described as "loud tinnitus in both ears"; SINUS PAIN (disability) with onset 10Apr2022 at 17:00, outcome "recovered" (12Apr2022). The events "headache", "6 hours after phizer covid 19 booster vaccine i started getting chills", "100 degree fever", "sinus pain", "hearing loss" and "loud tinnitus in both ears" required physician office visit. The patient underwent the following laboratory tests and procedures: Acoustic stimulation tests: (22Jun2022) Unknown results; Body temperature: (unspecified date) 100 degree, notes: 100 degree fever; SARS-CoV-2 test: (18Jul2022) Negative, notes: Nasal Swab. Therapeutic measures were taken as a result of headache, chills, pyrexia, sinus pain, deafness, tinnitus. Clinical course: Covid prior vaccination reported as yes. Covid tested post vaccination reported yes. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220622; Test Name: Audiology test; Result Unstructured Data: Test Result:Unknown results; Test Name: Fever; Result Unstructured Data: Test Result:100 degree; Comments: 100 degree fever; Test Date: 20220718; Test Name: I-Health; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Birt-Hogg-Dube syndrome; COVID-19 (if covid prior vaccination : yes); Egg allergy (Allergy: Egg white allergy); Valley fever
Andere Medikamente: ARMOUR THYROID
Allergien: -
Vorherige Impfungen: -

VAERS 2387481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Arthralgia Body height decreased Headache Illness Malaise Neck pain Pain Pain in extremity Pyrexia Vaccination site pain

Symptomtext

she is shrinking; not feeling well; little more physically ill; low grade fever like 1/2 a degree; achy all over; headache; pain in her arm and shoulder by the injection site; left arm and shoulder pain/arm had gotten pretty sore; shoulder pain/shoulder was achy; pain running up her neck/neck and shoulder was achy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66-year-old female patient received BNT162b2 (BNT162B2), on 13Jul2022 at 09:30 as dose 4 (booster), single (Lot number: FJ4991) at the age of 66 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "for bone density" (unspecified if ongoing); "thyroid" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE taken for thyroid disorder, start date: 1980; FOSAMAX taken for bone density abnormal; FISH OIL; VITAMIN D3. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Pfizer COVID-19 Vaccine:, Lot number: EN6199, Date Received: 02Mar2021, She didn't have any side effects at all with this 1st dose.), administration date: 02Mar2021, when the patient was 64-year-old, for Covid-19 immunization; BNT162b2 (DOSE 2, SINGLE, Pfizer COVID-19 Vaccine:, Lot number: EK or ER 8732, Date Received: 20Mar2021, She had a little bit of soreness in her arm after her 2nd and 3rd dose of the COVID-19 Vaccine.), administration date: 20Mar2021, when the patient was 64-year-old, for Covid-19 immunization, reaction(s): "soreness in her arm"; BNT162b2 (DOSE 3(BOOSTER), SINGLE, Pfizer COVID-19 Vaccine:, Lot number: 331708A, Date Received: 15Dec2021, She had a little bit of soreness in her arm after her 2nd and 3rd dose of the COVID-19 Vaccine.), administration date: 15Dec2021, when the patient was 65-year-old, for Covid-19 immunization, reaction(s): "soreness in her arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 13Jul2022, outcome "recovered" (15Jul2022), described as "left arm and shoulder pain/arm had gotten pretty sore"; VACCINATION SITE PAIN (non-serious) with onset 13Jul2022, outcome "recovered" (15Jul2022), described as "pain in her arm and shoulder by the injection site"; NECK PAIN (non-serious) with onset 13Jul2022, outcome "recovered" (15Jul2022), described as "pain running up her neck/neck and shoulder was achy"; ARTHRALGIA (non-serious) with onset 13Jul2022, outcome "recovered" (15Jul2022), described as "shoulder pain/shoulder was achy"; PAIN (non-serious) with onset 14Jul2022, outcome "recovered" (15Jul2022), described as "achy all over"; HEADACHE (non-serious) with onset 14Jul2022, outcome "recovered" (15Jul2022); ILLNESS (non-serious) with onset 14Jul2022, outcome "recovered" (15Jul2022), described as "little more physically ill"; PYREXIA (non-serious) with onset 14Jul2022, outcome "recovered" (15Jul2022), described as "low grade fever like 1/2 a degree"; MALAISE (non-serious) with onset 14Jul2022, outcome "recovered" (15Jul2022), described as "not feeling well"; BODY HEIGHT DECREASED (non-serious), outcome "unknown", described as "she is shrinking". Additional information: Patient is calling about the Pfizer COVID-19 Vaccine her 3rd booster but clarifies this was her 4th dose. Patient wanted to report the side effects. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200975335 same reporter/patient/product, different dose/AE;US-PFIZER INC-202200975336 same reporter/patient/product, different dose/AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bone density abnormal; Thyroid disorder
Andere Medikamente: LEVOTHYROXINE; FOSAMAX; FISH OIL; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 2379407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 66,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 21.04.2022
Beginn: 24.06.2022
Tage bis Beginn: 64,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Malaise Myalgia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 06/24/2022 with symptoms of cough, muscle aches, and congestion. I was prescribed Paxlovid, Pednisone, and Trilogy Inhaler on 06/27/2022. I was ill for 10 days before my symptoms began to resolve. I am still experiencing a lingering cough and needing to use the inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 06/25/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Hyperthyroidism
Andere Medikamente: Synthroid; Livalo
Allergien: N/A
Vorherige Impfungen: -

VAERS 2379271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MD
Alter: 95,0
Geschlecht: M
Eingang: 22.07.2022
Impfdatum: 20.04.2022
Beginn: 07.07.2022
Tage bis Beginn: 78,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Malaise Rhinorrhoea SARS-CoV-2 test positive Symptom recurrence

Symptomtext

A dry cough started on July 7. Tested positive for COVID. Called Doctor who prescribed PAXLOVID. Symptom disappeared in two days. However on 07/21 cough returned along with runny nose. Vitals remain stable and Oxygen level is normal. Appetite is good, but he seems to be more tired than usual. Tested today and was again positive for COVID. Symptoms have lessened, however.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: hydrocephalus has a shunt bph glaucoma dementia atrial fibrillation
Andere Medikamente: Timolol Maleate eye drops Multivitamin Vitamin D Calcium Caltrate with D
Allergien: sulfa drugs
Vorherige Impfungen: -

VAERS 2379262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 56,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 20.04.2022
Beginn: 16.06.2022
Tage bis Beginn: 57,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Feeling abnormal Haemoptysis Headache Nasopharyngitis Oropharyngeal pain Paranasal sinus hypersecretion Productive cough SARS-CoV-2 test positive Sinus headache

Symptomtext

June 13th - developed sore throat, felt like a cold was starting. Test negative on Home Testing kit. June 14th - sore throat, tired, didn't feel good, cough Tested negative on home testing kit. June 15th - sore throat, tired, cough with phlegm, headache. Didn't test June 16th - woke up with sinus headache, felt like a sinus infection was starting, drainage, coughing with blood and phlegm. I made an appointment for urgent care but decided to test to make sure it wasn't covid. I tested positive. Called doctor's office. Taking ibuprofen, and Mucinex. Drank water and sports drink. June 17th - internet appointment with Dr office. Prescribed Paxlovid and Benzonatate. Took ibuprofen, Dayquil and NightQuil, Afrin, used humidifier. June 21st - tested negative

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: June 13, 14, 15 and 21 - home Covid test kit
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Flonase, Albuterol, Flovent, Chiral Balance: Woman's Am & PM and D-Chiro-Inositol, Centrum Silver Multivitamin Women 50+, Align DualBiotic, Prebiotic + Probiotic
Allergien: Tetnus
Vorherige Impfungen: Tetnus. Fever and swelling at site.

VAERS 2379138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AL
Alter: 78,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 21.04.2022
Beginn: 02.07.2022
Tage bis Beginn: 72,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Malaise Nasal congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

07/02/2022 I was supposed to go to friend?s house and was feeling ill. I took a test it was negative, and I thought it was just allergies. I went to Cough, nasal congestion, and slight fever 07/03/2022 I went to urgent care, and I was positive, and the doctor gave me the antiviral. I isolated for more than 15 days I had recovered on July 9th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Myrbetriq; D3, Calcium; Eye Vitamin; Magnesium; Melatonin; Vitamin E; Fish Oil; Vitamin C; Multivitamin; Zinc
Allergien: N/A
Vorherige Impfungen: -

VAERS 2377311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MD
Alter: 87,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 18.04.2022
Beginn: 01.07.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Fatigue Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Had a sore throat, then a runny nose, was very tired, but no fever. Used a rapid home test. It was positive. Called Dr. He prescribed Paxlovid. Took the Med. Symptoms stopped the next day. Masked and isolated self for five days. felt fine. After one week tested negative. Have had no symptoms since that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Positive COVID home test on 07/01/2022; negative COVID home test on 07/08/2022
Aktuelle Erkrankungen: none
Vorgeschichte: endometrial cancer in remission
Andere Medikamente: timolol maleate eyedrops eliquis anastrazole multivitamin Calcium Caltrate with Vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 2377307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 20.07.2022
Beginn: 21.07.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Rash

Symptomtext

Patient started getting a rash all over face in the morning

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: shampoo preservative
Vorherige Impfungen: Patient had similar reaction after 1st Covid Pfizer Vaccination. Patient was 47 at the time, and she ended up going to the ER.

VAERS 2376812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

mild

Staat: RI
Alter: 62,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 29.06.2022
Beginn: 21.07.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Malaise

Symptomtext

I got Covid. Was treated with paxlovid. Too many side effects

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: I got Covid.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Diabeties Depression
Andere Medikamente: Celexa Buspirone Magniseum Multi vitamin Crestor Metformin
Allergien: Wellbutrin Percoset
Vorherige Impfungen: -

VAERS 2376619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 53,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 20.04.2022
Beginn: 25.04.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: SYR / LA

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

Headache Laryngitis Malaise Oropharyngeal pain Pyrexia

Symptomtext

I wasn't feeling well on Saturday. I woke up Sunday morning with a high fever of 102. I had a headache and then two days later I had a sore throat. I had some laryngitis. I'm not sure how long the fever lasted and I had the laryngitis for 2 weeks. Tuesday was when I went to go see the doctor because I must have still had the fever. The temperature was going down because of TYLENOL, but 5 hours later it would go back up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Seizures; Pulmonary Sarcoidosis; Left Vocal Chord Paralysis
Andere Medikamente: VIMPAT; LAMICTAL; TOPAMAX; ONFI; SYNTHROID
Allergien: CIPRO; KEFLEX; PYRIDIUM; red dye #40; COLACE; iodine contrast
Vorherige Impfungen: -

VAERS 2373859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NV
Alter: 70,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 01.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Extra dose administered Fatigue Feeling abnormal Headache Loss of personal independence in daily activities Oropharyngeal pain Rash Rash macular SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I received my second booster on 05/01/2022 and on 05/02/2022 I woke up with spots on my body. Over the next few days the rash became worse. I was embarrassed to go out anywhere because I felt like I looked like I had leprosy. I visited a dermatologist clinic and seen an apn, she did look at one red spot that was on my arm and gave me samples of Dove laundry soap, told me to hydrate and change my soap. I still have the rash to this day but not as bad as they once were. I also had a breakthrough of COVID-19, I tested positive on 06/17/2022. I woke up with a really bad sore throat, headache and just overall felt bad. I took a home test that was positive at that point I went to urgent care and received a prescription Paxlovid. Within 2-3days after starting medication I started feeling better. As of today I am still dealing with fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol
Andere Medikamente: Gabapentin; Atorvastatin; Escitalopram; Clomazetam; Melatonin
Allergien: None
Vorherige Impfungen: -

VAERS 2373845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 65,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 18.04.2022
Beginn: 11.06.2022
Tage bis Beginn: 54,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Exposure to SARS-CoV-2 Nasopharyngitis Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

04/18/2022 vaccination. 06/11/2022 I had a sore throat like a cold coming on. My husband tested COVID-19 5 days ahead of me. 06/12/2022 I tested COVID-19 positive. I got on a test to treat program; a clinic at a pharmacy. Didn't recommend unless I had more symptoms as I didn't have any other risk factors. I did not take the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Seasonal Allergies
Andere Medikamente: ZYRTEC
Allergien: N/A
Vorherige Impfungen: -

VAERS 2373802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 73,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 18.04.2022
Beginn: 08.07.2022
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

My first symptoms started in the evening and I had a runny nose, scratchy throat, and cough. the next morning and they did a COVID-19 test that came back positive. I contacted my doctor, and she prescribed Paxlovid. Within 12 hours of starting the medicine I was filling significantly better. Most of my symptoms subsided except I still feel fatigued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Calcium; Fosamax
Allergien: N/A
Vorherige Impfungen: -

VAERS 2373784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MO
Alter: 69,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 15.04.2022
Beginn: 28.05.2022
Tage bis Beginn: 43,0
Dosis: 4
Route/Site: SYR / AR

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

COVID-19 Cough Ear infection Headache Middle ear effusion Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

I started getting symptoms scratchy throat so I thought it was allergies. I took a COVID-19 test the next day that was negative. Then my symptoms progressed. I took another test that was also negative. I went to the doctor and was prescribed an antibiotic. The next day, I ran a fever of 101 and body aches. I had a headache also. I took another COVID-19 test that showed positive. I did have a cough with congestion. My ears were affected as well. I sent a message to my doctors office and was told that I did have fluid in my ears during the previous visit. I did have an ear infection. I went to an ENT and was prescribed Prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: Neuropathy; Osteoporosis; Arthritis; GERD
Andere Medikamente: Calcium; Vitamin D; Magnesium; Probiotic; Nexium
Allergien: Certain Antibiotics to side affects
Vorherige Impfungen: -

VAERS 2372787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered Injection site pain Joint range of motion decreased Pain Product administered at inappropriate site

Symptomtext

Patient felt vaccine given too high on arm. It hurt when given and continues to hurt. She cannot lift arm over her head without pain

Weitere VAERSDATA-Felder

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

VAERS 2372759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: PA
Alter: 67,0
Geschlecht: M
Eingang: 18.07.2022
Impfdatum: 29.04.2022
Beginn: 15.06.2022
Tage bis Beginn: 47,0
Dosis: 4
Route/Site: IM / LA

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

Cough Malaise

Symptomtext

Started with cough on the 13th the next day cough persisted the morning of 15th I knew I was not well, spoke with physician assistant who instructed to take covid home test, once diagnosed I was given paxlovid within 3-5 days I started to feel better

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: aspirin, meloxicam, metoprolol, 80mg atorvastatin, 10mg lisinotril
Allergien: morphine
Vorherige Impfungen: -

VAERS 2372454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OR
Alter: 55,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 17.04.2022
Beginn: 14.07.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Headache Lacrimation increased Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 07/14/2022 with symptoms of cough, runny nose, sore throat, congestion, headache, fatigue, and watery eyes. I was prescribed PAXLOVID on 07/15/2022. My sore throat, watery eyes, and congestion began to improve after taking PAXLOVID. I am not fully recovered yet, but my symptoms are improving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 07/14/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: Hydrochlorothiazide; cetirizine
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2372269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TN
Alter: 54,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 16.07.2022
Beginn: 17.07.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Fatigue Headache Injection site erythema Injection site pain Injection site swelling Pain

Symptomtext

Within 20 hours of receiving the Pfizer-BioNTech COVID-19 Vaccine EUA, I began experiencing the following symptoms: extreme fatigue headaches swelling, pain, and redness at injection site body aches joint soreness All these symptoms are continuing at 42 hours post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Wood betony tincture, herbal tincture with elderberry, kalmegh, and other herbs
Allergien: Gluten and dairy sensitive. Sensitive to novocaine, lidocaine, and other caines.
Vorherige Impfungen: -

VAERS 2372089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 14,0
Geschlecht: M
Eingang: 18.07.2022
Impfdatum: 17.07.2022
Beginn: 18.07.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Hyperhidrosis Nausea Vomiting

Symptomtext

Nausea, vomiting and sweating.

Weitere VAERSDATA-Felder

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

VAERS 2371931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OK
Alter: 46,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 14.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Diarrhoea Epistaxis Erythema of eyelid Eye pain Eyelid function disorder Eyelid irritation Increased upper airway secretion Oropharyngeal discomfort Scleral discolouration Swelling of eyelid

Symptomtext

At approximately 33 hours after receiving the vaccine, my left eye began to hurt and I had difficulty closing my eyes and when I went to look at my eye, it was extremely red and the white area was yellowish and swollen with red looking veins. The bottom and corners of my eyes were blood red and extremely irritated and swollen. My right eye had very dark red looking veins but it was not as extensive and painful as my left eye. I also started having diarrhea on July 16 at approximately 9am. I also have a constant tickle in my throat since the night of the 15th and am producing small gobs of mucus. My nose started bleeding June 16 at approximately 9am.

Weitere VAERSDATA-Felder

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

VAERS 2371664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MO
Alter: 50,0
Geschlecht: M
Eingang: 16.07.2022
Impfdatum: 28.05.2022
Beginn: 29.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / LA

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

Myalgia Pain

Symptomtext

Left deltoid has been aching for 6 weeks since injection; some sharp pain during movement; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 50-year-old male patient received BNT162b2 (BNT162B2), on 28May2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 50 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin. The patient took concomitant medications. Vaccination history included: Comirnaty (Primary immunization complete, DOSE 1,2 and 3), for COVID-19 IMMUNISATION. The following information was reported: MYALGIA (non-serious) with onset 29May2022, outcome "not recovered", described as "Left deltoid has been aching for 6 weeks since injection"; PAIN (non-serious) with onset 29May2022, outcome "not recovered", described as "some sharp pain during movement". Therapeutic measures were not taken as a result of myalgia, pain. Additional information: The patient was not given other vaccine in fourweeks. Other medications were given in two weeks but do not know details. The reporter stated that the patient experienced Left deltoid ache for 6 weeks since injection and some sharp pain during movement. All prior Comirnaty doses (N=3) have been in the left deltoid.The patient had other medical history but do not have details. No statement required. FU will be conducted.

Weitere VAERSDATA-Felder

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

VAERS 2370674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TN
Alter: 76,0
Geschlecht: M
Eingang: 15.07.2022
Impfdatum: 14.04.2022
Beginn: 09.07.2022
Tage bis Beginn: 86,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Nasopharyngitis Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I was feeling achy, had a cough, and fatigued, it felt like had a mild head cold. I took a home COVID-19 test it came positive and was unable to connect with my doctor until Monday. Once I had my telehealth visit my doctor prescribed LAGEVRIO that I started taking Monday evening. I still feel tired, slight cough and congestion but getting better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Atorvastatin; levothyroxine; olmesartan medoxomil; amlodipine; vitamin D3; coQ10; folic acid; omega krill oil; vitamin B complex; omeprazole; TYLENOL PM
Allergien: No
Vorherige Impfungen: -

VAERS 2370598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: LA
Alter: 51,0
Geschlecht: M
Eingang: 15.07.2022
Impfdatum: 14.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: IM / AR

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

Rash

Symptomtext

I had a non itching rash that developed on my body two weeks after the vaccine. At first I did not worry about because it was not itching. I honestly thought it may be poison ivy because I am an outdoors type person. Once it started to spread all over my body I sought medical attention. I was prescribed two topical steroid medications clobetasol propionate cream 05% and triamcinolone acetonide cream 0.1% to use.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Metformin; lisinopril/HCTZ; atorvastatin; ONE A DAY men's
Allergien: Sulfa drugs; KEFLEX
Vorherige Impfungen: -

VAERS 2369075

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CT
Alter: 63,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 13.04.2022
Beginn: 21.06.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Ear pain Hypersomnia Oropharyngeal pain Pain Pain in extremity Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had a sore arm after the vaccine but that is all. I tested positive for COVID-19 on 06/21/22. I had congestion, coughing, slept for the whole day, my throat felt like I was swallowing broken glass and body aches. I took Tylenol to help me with my symptoms. My doctor ordered the monoclonal injection. I felt better for one or days. Then my throat started hurting and both ears hurt. I went to a urgent care center for antibiotics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Home test for COVID-19 was positive 06/21/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Heart "missed shape heart"
Andere Medikamente: Doxazosin; Eliquis; Pantoprazole; Levothyroxine; Losartan; Rosuvastatin; Diltiazem; Famotidine; Saint John wort and Tylenol
Allergien: Sulphar
Vorherige Impfungen: -

VAERS 2368798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 11.04.2022
Beginn: 23.06.2022
Tage bis Beginn: 73,0
Dosis: 4
Route/Site: IM / AR

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

Ageusia COVID-19 Fatigue Headache Nasal congestion Oropharyngeal pain Pain Paranasal sinus hypersecretion SARS-CoV-2 test positive

Symptomtext

On 06/23/2022 I began experiencing an extremely sore throat and some really bad sinus drainage with stuffiness. My daughter and I worked out the day before and I expected some soreness, but I realized that it was more like a body ache than the expected soreness. I was also experiencing a headache. I took some Advil and tried to gargle with salt water. On Saturday, I went on a few mile run with my daughter and when I returned home I was extremely exhausted and had to sleep for a few hours. I noticed a slight loss of taste but no loss of smell. I then started testing myself for COVID-19 over the next few days on 06/27/2022, a home test turned up positive. I then arranged for a telehealth visit with my doctor. She advised rest and hydration and symptom treatment with over the counter medication. Over the next few days, I was still experiencing a pretty sore throat but my body aches were getting better. At this point, my symptoms are basically gone with the exception of some very noticeable fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home COVID-19 test-positive-06/27/2022
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Women's multivitamin
Allergien: None.
Vorherige Impfungen: -

VAERS 2366413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 05.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Pain in extremity Peripheral swelling

Symptomtext

Pt was vaccinated with her first Pfizer Covid shot on 7/5/2022. She reported on 7/12/22 that her arm was swelling at first. After 3 days, the swelling came down and her arm started to be painful. Her pain also spread to shoulder area. Advised patient to call her primary care doctor or go to Urgent Care. In case of emergency, she is to call.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: n/1
Aktuelle Erkrankungen: NONE REPORTED
Vorgeschichte: Calcification of bilateral urethers COPD
Andere Medikamente: UNKNOWN
Allergien: ASPIRIN BACTRIM BIAXIN BREO ELLIPTA CECLOR CODEINE IODINE LEVAQUIN PENICILLIN ZITHROMAX
Vorherige Impfungen: -

VAERS 2366239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: KS
Alter: 79,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 11.04.2022
Beginn: 07.06.2022
Tage bis Beginn: 57,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Insomnia Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

I had a sore throat, congestion and had a difficulty sleeping for 3 days, coughing, sneezing, body aches. I used MUCINEX D to help with the congestion at night. I used a home COVID-19 test that once it showed positive called my doctor. He advised me to quarantine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Omeprazole; pravastatin; RESTASIS; cholestyramine
Allergien: No
Vorherige Impfungen: -

VAERS 2366123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 01.04.2022
Beginn: 04.07.2022
Tage bis Beginn: 94,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Chest discomfort Diarrhoea Gastrointestinal disorder Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Vomiting

Symptomtext

Low grade temperature, minor runny nose and sore throat, not a big deal. Major gastrointestinal stuff; 12 hours of vomiting and I'm on day 7 of diarrhea. I started to feel it in my chest yesterday and called my doctor, it feels like the Valley Fever. I was given PAXLOVID last night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 rapid home test -positive.
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure; Valley fever
Andere Medikamente: Labetalol; fluconazole
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2364615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 64,0
Geschlecht: M
Eingang: 11.07.2022
Impfdatum: 03.06.2022
Beginn: 04.07.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Fatigue Headache Lacrimation increased Oropharyngeal pain Productive cough Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

On 7-3, 2022 I started having fatigue. The following morning I began having a runny nose, head congestion and watery eyes. I took a home Covid19 test and it was positive. Four hours later I took another home Covid19 test and it was positive as well. On 7-5, I started having a headache, sore throat and productive cough. I called to get a doctors appointment but could not get in to be seen. On 7-6, I went to a minute clinic and they tested me for Covid19 at the clinic. It came back positive as well. I was prescribed Molnupiravir. I am doing better today with still light fatigue and productive cough remaining. I am reporting my breakthru case of Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 7-4-2022 Two home Covid 19 tests - both positive 7-6-2022 Clinic- Covid19 test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-Diabetes, Hyperlipidemia, HTN, COPD
Andere Medikamente: Metformin, Lipitor, Prinivil, Norvasc, Allegra, Vit D3, Flonase, Combivent Respimat inhaler
Allergien: None
Vorherige Impfungen: -

VAERS 2364376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 73,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 07.04.2022
Beginn: 13.06.2022
Tage bis Beginn: 67,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Fatigue Feeling abnormal Nasal congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

I woke up feeling more stuffy than normal so I took a home COVID-19 test and it came back negative. I was tired but the rest of the day was okay. The next day I had a scratchy throat and felt bad so I took the home COVID-19 test again and this time it came back positive. I called my doctor, we had a telehealth visit and she prescribed PAXLOVID. I started taking it the night. I slept through the night and the next day I felt so much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Baby aspirin; losartan
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 2364354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 60,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 09.04.2022
Beginn: 08.07.2022
Tage bis Beginn: 90,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Exposure to SARS-CoV-2 Headache SARS-CoV-2 test positive Throat irritation

Symptomtext

I was exposed to COVID-19 on July 6, 2022 so I tested that evening using my home COVID-19 test it came back negative. On July 8, 2022 I woke up with a scratchy throat took a home COVID-19 test it had a faint positive line so I went in to the local urgent care they used a rapid COVID-19 test that came back positive. I came home and quarantined from everyone. I took over the counter medications, MUCINEX, elderberry gummies, TYLENOL. I had a slight cough, headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Home COVID-19 test, rapid COVID-19 test.
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure; Pre-Diabetic
Andere Medikamente: Valsartan; atorvastatin
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2364351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 11.07.2022
Impfdatum: 10.04.2022
Beginn: 30.06.2022
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Cough Dizziness Fatigue Headache Nasal congestion Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case. Chest congestion, stuffy nose, sinus swollen, cough, fatigue, dizziness, occasional headaches. Took a home test on 06/30/2022 and tested positive. Still has Covid. Messaged Dr. through health portal. Wondered if I should take PAXLOVID, but my Dr. advised against it and wanted me to rest and quarantine. A Cardiologist from the patient portal contacted me and recommended me to keep watch on my Blood Oxygen levels and if it got below 88, to head to the ER. Still testing positive for COVID on 07/11/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Home test - positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Spinal Stenosis; Degenerative Disc Disease; Neuropathy.
Andere Medikamente: Metformin; gabapentin; benazepril; amlodipine; CRESTOR; vitamin K; potassium; calcium magnesium mix; vitamin C; vitamin D; zinc; multivitamin; vitamin E; turmeric; curcumin; triple omega 369; coQ10; ibuprofen.
Allergien: N/A
Vorherige Impfungen: -

VAERS 2364020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 72,0
Geschlecht: M
Eingang: 09.07.2022
Impfdatum: 06.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Chills Pyrexia

Symptomtext

chills and fever starting about 36 hours after injection, lasting about 24 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: mild idiopathic interstitial pulmonary disease
Andere Medikamente: cetrizine 10mg daily
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2362809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CO
Alter: 72,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 07.04.2022
Beginn: 27.06.2022
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: IM / LA

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

Bronchitis COVID-19 Cough Ear infection Feeling abnormal Headache Lethargy Malaise Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

6/27/2022 about noon I started to feel bad. Lethargy, headache, and a cough developed overnight. 6/28 all symptoms got worse over the course of the day. 6/29 Symptoms got worse and I took home COVID 19 test, positive. 6/30 cough and fever improved. 7/1 Tested again and it was positive. 7/6 went to see doctor, who prescribed antibiotics to combat ear and bronchial infections. 7/7 symptoms improving but congestion lingers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 6/29 and 7/1 at home COVID 19 tests, positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Lung Scaring;
Andere Medikamente: Omeprizol; Atorvastatin; Ramipril; Aspirin
Allergien: No
Vorherige Impfungen: -

VAERS 2362670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 07.04.2022
Beginn: 14.06.2022
Tage bis Beginn: 68,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

COVID positive on 6/14/2022 . Symptoms - Sore throat and cough. Prescribed Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: PCR Test
Aktuelle Erkrankungen: NA
Vorgeschichte: High Blood Pressure, High Cholesterol
Andere Medikamente: Lipitor, Metoprolol, Hydrochloride
Allergien: NA
Vorherige Impfungen: -

VAERS 2361271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WI
Alter: 68,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 16.04.2022
Beginn: 29.06.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia COVID-19 Cough Decreased appetite Dysphonia Feeling abnormal Nausea Oropharyngeal pain SARS-CoV-2 test positive Taste disorder Throat irritation Vomiting

Symptomtext

On Wednesday June 29 I started feeling "odd" and as Friday progressed I felt worse. I did not run fever but my throat was scratchy, sore and hoarse. I began to have a terrible cough. I took home COVID-19 test and it was positive. I called the on-call nurse and got Paxlovid. I began to take it Saturday and within 24 hours I was very nauseous and had bad taste in my mouth. I also had no energy and no appetite. I believe the COVID-19 symptoms were gone, except for my cough, but the side effects from Paxlovid were horrible. I was so nauseous after dinner I vomitted my dinner and decided not to take my last dose of Paxlovid. Today I did another home test and it was negative. I have started to feel better today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: Home COVID-19 test, negative; Home COVID-19, positive (July 1st), Home COVID-19 test, negative (July7th)
Aktuelle Erkrankungen: N/A
Vorgeschichte: Breast Cancer; High Blood Pressure; Acid Reflux
Andere Medikamente: Lisinopril; Pantoprazole; Anastrozole; Calcium; Vitamin D; Iron; Ibuprofen; Benadryl
Allergien: Prednisone;
Vorherige Impfungen: -

VAERS 2361007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: SC
Alter: 72,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 06.04.2022
Beginn: 05.07.2022
Tage bis Beginn: 90,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Dysphonia Head discomfort Malaise Pyrexia SARS-CoV-2 test positive Throat irritation

Symptomtext

My throat was scratchy and I was hoarse, As the day progressed I had increased hoarseness and scratchiness. I tested at around 03:00AM on July 6th and it was positive. Once I realized I was positive I moved out of my bedroom to isolate. I started taking Theraflu for the cough. I sent a message to my doctor later on that morning and since the symptoms were not so bad she advised me to isolate. Later that morning, I developed a fever of 99.4. Yesterday I started coughing and my head was stopped up. I went to pharmacy and got me some chest rub and cough drops. I am still recovering from my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 Home Test-July 6th, 2022-Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Spinal Synopsis
Andere Medikamente: Levothyroxine; Intermittent Tramadol; Tylenol Arthritis; Vitamin C; Multi Vitamin; Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 2359714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AZ
Alter: 69,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 04.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 17,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Head discomfort Lethargy Oropharyngeal discomfort SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 4/21/22. I developed a tickle in my throat and extreme fatigue. Reached out to my doctor on 4/26/22. Had a stuffy head and lethargic. Developed a dry cough about 6 days later. I tested negative on the 10th day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High BP; Type 2 Diabetes
Andere Medikamente: Lothedapine; Aspirin; Gemfibrozil; Iron; Krill Oil; Vitamin C; Claritin; Multi-vitamin; Zinc; Testosterones; Vitamin D; Probiotic
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2359670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 76,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 05.04.2022
Beginn: 29.05.2022
Tage bis Beginn: 54,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Head discomfort Malaise Nasal congestion Pain SARS-CoV-2 test positive Sinus congestion

Symptomtext

5/29/2022 Nasal congestion, sinus and head fullness, with a slight cough. 5/30 Symptoms increased in intensity, with fatigue and mild body aches. At home test Positive. Sought care on 5/30. Urgent care performed an antigen test for COVID 19. Doctor prescribed Molnupiravir and benzonatate. 6/2 Started to feel better. Cough lessened as did nasal congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 5/30 At home COVID 19 test and Antigen test both positive.
Aktuelle Erkrankungen: No
Vorgeschichte: high cholesterol; mild asthma; osteoarthritis;
Andere Medikamente: Pravastatin; low dose aspirin; Levothyroxine; Singular; Metoprolol; Claritin; Calcium; Vitamin D; Benefiber; Probiotic; Ubiquinol; Fish oil
Allergien: Clindamycin; Vicodin
Vorherige Impfungen: -

VAERS 2357686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 04.04.2022
Beginn: 01.07.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Fatigue Headache Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sinusitis

Symptomtext

I had major headache and congestion. I felt very fatigue. I had sinus infection, sore throat, and nasal drainage. I tested positive for COVID-19. I did not received treatment and I still have all the symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin supplements
Allergien: None
Vorherige Impfungen: -

VAERS 2356309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 21.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Erythema Investigation Vaccination site rash Vaccination site warmth

Symptomtext

Left upper arm Red at the site hard and hot, about the size of a lime; Left upper arm Red at the site hard and hot, about the size of a lime; Left upper arm Red at the site hard and hot, about the size of a lime; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Jun2022 at 11:30 as dose 3 (booster), single (Lot number: FJ4991) at the age of 53 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "latex: allergy" (unspecified if ongoing). Concomitant medication(s) included: FAMOTIDINE; LEVOCETIRIZINE; LEVOTHYROXINE; OLMESAR. Vaccination history included: BNT162b2 (Dose 2, Batch/Lot No: FG3527, Location of injection: Arm Left, Vaccine Administration Time: 03:00 PM), administration date: 09Nov2021, when the patient was 53-year-old, for COVID-19 immunization; BNT162b2 (Dose 1, Batch/Lot No: FF2590, Location of injection: Arm Left, Vaccine Administration Time: 03:00 PM), administration date: 12Oct2021, when the patient was 53-year-old, for COVID-19 immunization. The following information was reported: VACCINATION SITE WARMTH (non-serious), VACCINATION SITE RASH (non-serious), ERYTHEMA (non-serious) all with onset 21Jun2022 at 12:00, outcome "not recovered" and all described as "Left upper arm Red at the site hard and hot, about the size of a lime". The events "left upper arm red at the site hard and hot, about the size of a lime" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site warmth, vaccination site rash, erythema. Additional information: The patient had not received other vaccine in 4 weeks. Patient had other medications in 2 weeks with famotidine, levocetirizine, levothyroxine and olmesar. The patient was visited to doctor or other healthcare professional office/clinic visit for adverse event. The patient had no covid prior vaccination and covid tested post vaccination. Patient had latex allergy and no food allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site rash
Hospital-Tage: -
Labordaten: Test Date: 20220621; Test Name: about the size of a lime; Result Unstructured Data: Test Result:the size of a lime
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Latex allergy
Andere Medikamente: FAMOTIDINE; LEVOCETIRIZINE; LEVOTHYROXINE; OLMESAR
Allergien: -
Vorherige Impfungen: -

VAERS 2335331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 02.07.2022
Impfdatum: 07.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Contusion Injection site bruising Injection site induration Pain Injection site mass Injection site pain

Symptomtext

Patient reported hard, painful, and bruised lump on arm area where she received vaccine. Patient stated that pharmacy staff did not ask for her identification card.

Weitere VAERSDATA-Felder

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

VAERS 2335331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 02.07.2022
Impfdatum: 07.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Contusion Injection site bruising Injection site induration Pain Injection site mass Injection site pain

Symptomtext

Patient reported hard, painful, and bruised lump on arm area where she received vaccine. Patient stated that pharmacy staff did not ask for her identification card.

Weitere VAERSDATA-Felder

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

VAERS 2347546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 19.05.2022
Beginn: 20.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Herpes zoster Pain Rash Skin test

Symptomtext

I developed a rash after 4th dose. 2 days later I felt it stronger underneath my arm and back. I was pretty sure it was Shingles and went to urgent care on 5/31/2022. I already started taking gabapentin 100 mg, then they prescribed acyclovir 1 gram twice daily for 1 week. Saw PCP 06/24/2022 and my gabapentin was raised to 300mg daily, valacyclovir HCL 1 gram twice daily I was diagnosed with Herpetic pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Skin scraping to confirm that I have shingles.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Joint problems; Hip Replacement; Knee replacement
Andere Medikamente: Magnesium; calcium; cod liver oil; vitamin core minerals; vita antioxidant; vitamin C; turmeric; boswellia; vitamin D; PURE ligament restore; joint complex; bromelain; bone builder
Allergien: Narcotic;
Vorherige Impfungen: -

VAERS 2347419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MD
Alter: 69,0
Geschlecht: M
Eingang: 01.07.2022
Impfdatum: 30.03.2022
Beginn: 13.05.2022
Tage bis Beginn: 44,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Cough Head discomfort Myalgia Nasal congestion Oropharyngeal pain Productive cough Pulmonary congestion Pyrexia Rhinorrhoea SARS-CoV-2 test

Symptomtext

I began with a sore throat; the next day, I had a stuffy and runny nose, a heavy cough, head congestion, and a worse sore throat. I went to the pharmacy to get a PCR COVID-19 test done on 05/13/2022. That next day on Saturday, it was worse that became a fever, body chills and muscle aches. As the days went on, my symptoms got worse including body chills, muscle aches, and more. I went to the doctor on 05/16/2022 to get my first dose of Paxlovid to begin my 5-day regime as well as an antibiotic for my chest congestion (I kept coughing up phlegm). The Paxlovid put a metallic taste in my mouth, but by day 2 or 3 of the regime, I was definitely feeling way better. After the regime was completed, I felt better and resumed my day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 Test: 05/13/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; High Blood Pressure; Cholesterol
Andere Medikamente: Atorvastatin; Amlodipine; Tamsulosin; Omeprazole; Losartan Potassium; Levothyroxine; Fluticasone Propionate & Salmeterol Inhaler; Centrum Silver; Vitamin D; Vitamin B-Complex
Allergien: N/A
Vorherige Impfungen: -

VAERS 2344751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 18.05.2022
Beginn: 23.06.2022
Tage bis Beginn: 36,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of sore throat and a cough. That progressed to a worse cough, fever, and, tiredness. The next day, I took an at home COVID-19 test that was negative. On 6/25/2022, I went to a drive thru and received a positive COVID-19 test. I contacted my doctor and received a prescription for a cough medicine and PAXLOVID. I feel like the PAXLOVID is helping. I still have a cough but it is not as bad as it was.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis
Andere Medikamente: Vitamins
Allergien: KEFLEX
Vorherige Impfungen: -

VAERS 2342456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 75,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 31.05.2022
Beginn: 01.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Discomfort Pruritus Seborrhoeic keratosis Urticaria

Symptomtext

I got my second booster May 31,2022 and the hives came back like immediately and a sudden eruption on my arms and mostly on my back. My husband noticed my back first and I had someone to take a picture and show it to me. I see a massage therapist at least once a month and she said it was dramatically different from the last visit. This gave me major concern so I went back to see my doctor It caused me to see a dermatologist June 24,2022 which diagnosed me with seborrheic keratosis and hives as well as Lesra Treale. The hives itch and were very uncomfortable. Hydroxyzine was prescribed and it dose help at night with the itching. Still currently dealing with this and I do have a follow up schedule.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Multi Vitamin; Vitamin D
Allergien: NA
Vorherige Impfungen: -

VAERS 2341985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NC
Alter: 53,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 29.03.2022
Beginn: 25.06.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Decreased appetite Exposure to SARS-CoV-2 Headache Heart rate increased Nausea Oropharyngeal pain Pain Productive cough SARS-CoV-2 test negative Sneezing

Symptomtext

I noticed that my heart rate was increased and it was very abnormal and alarming. I started having a sore throat and headache, and my body was achy. My spouse tested positive that Tuesday so I tested again since I had tested the two days prior and I was negative for COVID-19. I had severe joint pain, I was sneezing, I was coughing up yellow liquid. I was not interested in food not to the point of being nauseous but I was really turned off to food. I called my health care provider and I got prescribed PAXLOVID and a Z-PAK since I had a productive cough and I was given a steroid for my joint pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID-19 home test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Prior Breast Cancer History
Andere Medikamente: Testosterone cream; multivitamin
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2339488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OH
Alter: 17,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Eye movement disorder Headache Hyperhidrosis Pallor

Symptomtext

About 10 minutes after vaccination, patient was sitting in waiting room and became very pale and light headed. Mom asked if there was somewhere she could lay down. Mom reported daughter's eyes started to roll slightly back in head very briefly. Patient then moved to sitting position on the floor and I came out and had pt lay on floor with feet elevated. Patient was talking and alert. She was sweaty. Patient was given cold towel for head and remained alert, but in lying position with feet elevated for 15 min. Patient was then moved to sitting position on floor and given apple juice. Patient was then moved to sitting position in chair for another 10 minutes. Patient fully recovered from episode with report of slight headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: non reported
Andere Medikamente: no known
Allergien: none reported
Vorherige Impfungen: -

VAERS 2329649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

mild

Staat: TX
Alter: 21,0
Geschlecht: M
Eingang: 23.06.2022
Impfdatum: 22.06.2022
Beginn: 22.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blindness transient Blood glucose normal Dizziness Electrocardiogram normal Hyperhidrosis Vomiting

Symptomtext

PATIENT HAD TRANSIENT VISION LOSS , DIZZINESS, VOMITING AND PERFUSE SWEATING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: AMBULANCE CHECKED BLOOD SUGAR AND HEART EKG AND NORMAL
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: -
Allergien: none
Vorherige Impfungen: -

VAERS 2326003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

mild

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 12.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Blood test Electrocardiogram abnormal Fatigue Gingival discomfort Headache Mastication disorder Nausea Noninfective gingivitis Oral discomfort Oral herpes Pyrexia Rash SARS-CoV-2 test negative Stomatitis Urticaria Viral infection

Symptomtext

Nausea, 102 fever for 3 days, headache, exhaustion, irregular EKG, viral infection, rash, hives, mouth sores, cold sores, burning mouth and gums, unable to chew, sores on gums

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 6/14/2022 Covid tests at at Immediate Care and hospital result negative. EKG 6/14/2022 at Immediate Care and hospital, 6/14/2022 blood work hospital. 6//17/2022 Prednisone 20 mg prescribed by primary doctor. 6/18/2022 hospital Blood work and IV Prednisone and Benadryl, Prednisone prescription 40 mg prescribed by doctor at hospital
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, high cholesterol, high triglycerides, migraines, arthritis
Andere Medikamente: Daily Irbesartan 300 mg daily = High BP Atorvastatin 20 mg daily = High Cholesterol Hydrochlorothiazide 25 mg daily = High BP Meloxicam 7.5 mg = Arthritis pain Levothyroxine 25 mcg daily (aka Synthroid) = Low metabolism /thyroid Nadolol
Allergien: Allergies and medications unable to tolerate Amoxicillin (oral thrush) Acyclovir (for infection, hives) Nystatin (rinse for oral thrush hives) Iodine Tramadol (extreme nausea, dizzy) Azor (headaches) Viibryd (sickly, dizzy, nightmares) Effexor (insomnia) Ultram Topamax (extreme mood swings, uncontrollable crying) Codeine (extreme nausea) Hydrocodone (extreme nausea) Oxycodone (extreme nausea) OxyContin (extreme nausea) Depakote Dilaudid (shallow breathing) Gabapentin (nauseous, dizzy) Lyrica 75 mg (extreme anger, no pain relief) Naproxen 500 mg 2 times a day with Imitrex for migraine (stomach pains, heartburn) Omeprazole 20 mg 1 pill per day while taking Naproxen (nausea, gas) Amlodpine Besylate 10 mg daily Stopped 5/4/21 Swelling Shellfish (anaphylactic shock) Walnuts (migraines) Red grapes (migraines) Alcohol any kind (migraines)
Vorherige Impfungen: -

VAERS 2325626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 73,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 09.05.2022
Beginn: 20.06.2022
Tage bis Beginn: 42,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Pain Productive cough SARS-CoV-2 test positive Sneezing Throat irritation

Symptomtext

some cough and phlegm frequent sneezing body aches, particularly arms and shoulders minor scratchy throat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: home rapid test was positive
Aktuelle Erkrankungen: none
Vorgeschichte: rheumatoid arthritis fibromyalgia reflux elevated blood pressure
Andere Medikamente: Humira Vyvanse Cymbalta tramadol Vit B's Vit D Magnesium/Calcium 2:1 Ubiquitol Fish Oil flax oil Iron probiotics
Allergien: Celebrex
Vorherige Impfungen: -

VAERS 2324403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OR
Alter: 73,0
Geschlecht: F
Eingang: 20.06.2022
Impfdatum: 02.06.2022
Beginn: 12.06.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Injection site bruising Injection site nodule

Symptomtext

Patient reported a large bruise nearby the site of injection, first noted on Sunday, 6/12/22. Pt was unsure weather it was a side effect 10 days after the shot or something else that was causing it. Pt also described a feeling of "a knot" underneath the bruise when examined it with her fingers. Pt was referred to contact and consult with her provider.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2317351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: AZ
Alter: 55,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 28.05.2022
Beginn: 07.06.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Cough Fatigue Headache Hypersomnia Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

On 6-7-2022, I started having a cough and sore throat. On 6-8, I noticed fatigue and slept a lot. On 6-9, I starting having a headache and running fever up to 100.5 but felt a little better. I was still having these symptoms on 6-10, so I took a home Covid test which was positive. I called and had a telehealth visit with my PCP office that day. I was prescribed PAXLOVID. I started taking that on 6-10. I have been coughing more today but I am feeling slightly better with no headache. I am reporting a breakthrough case of Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home Covid test on 6-10-2022 - positive result.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; ankylosing spondylitis; Migraines
Andere Medikamente: DEXILANT; XYZAL; zinc supplement; B complex supplement; vit D; vit C supplement
Allergien: Codeine; allergy to mold; mulberry plant; cats; dogs; ragweed
Vorherige Impfungen: -

VAERS 2317268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: PA
Alter: 62,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 20.05.2022
Beginn: 09.06.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Feeling abnormal Headache Nausea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID-19 Case: I started to have a slight bout of nausea, headache that was concentrated on the back of my head. I just remember feeling off. I did not take anything. My husband tested positive 2 days earlier so I decided to do a home rapid test and it came back positive 06/10/2022. I called my primary care physician to request the antiviral. I was given Paxlovid which I am still taking. I do experience a raw feeling in the back of my nasal passage. My symptoms are not too bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 06/10/2022. Rapid test: Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure, High Cholesterol, Diabetes, LPP, Asthma
Andere Medikamente: Low Dose Aspirin, Rosuvastatin, Metoprolol, Gabapentin, Finasteride, Cranberry, Hydroxychloroquine
Allergien: Lovonox, Losartan, Levaquin, Molds, Dogs
Vorherige Impfungen: -

VAERS 2317177

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: DE
Alter: 59,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 10.05.2022
Beginn: 30.05.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Exposure to SARS-CoV-2 Fatigue Headache Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

Symptoms started on the 30th with sore throat, headache, tiredness and aches and pains. My husband already tested positive that's why I was suspicious it was Covid. The first test I did was negative but then I tested again on June 1st and it was positive. On May 29th in the morning our neighbor told use he had tested positive and we had been with him days before. The doctor gave me PAXLOVID 5 day treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home Covid May 30th, 31st - negative. At home Covid June 1st - positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Slipped disk in March; hypothyroid
Andere Medikamente: SYNTHROID; WELLBUTRIN; fluoxetine
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2316690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 11.06.2022
Impfdatum: 16.04.2022
Beginn: 18.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pain Rash macular Skin exfoliation

Symptomtext

Appearance of 3 red, scaley blotches, and persistent muscle pain in the are of the injection in the deltoid muscle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2313779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 09.06.2022
Impfdatum: 11.04.2022
Beginn: 23.05.2022
Tage bis Beginn: 42,0
Dosis: 4
Route/Site: - / LA

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

Fatigue Pain Paranasal sinus discomfort Sinus congestion Throat irritation

Symptomtext

Scratchy throat; sinus pressure; sinus pressure and congestion; achy; tired; 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 11Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: 301308A; Anatomical Location: Left arm), administration date: 25Aug2021, when the patient was 62-year-old; Covid-19 vaccine (DOSE 1, MANFACTURER UNKNOWN), for Covid-19 immunization; Covid-19 vaccine (DOSE 2, MANFACTURER UNKNOWN), for Covid-19 immunization. The following information was reported: THROAT IRRITATION (non-serious) with onset 23May2022, outcome "recovered with sequelae", described as "Scratchy throat"; PAIN (non-serious) with onset 23May2022, outcome "recovered with sequelae", described as "achy"; PARANASAL SINUS DISCOMFORT (non-serious) with onset 23May2022, outcome "recovered with sequelae", described as "sinus pressure"; SINUS CONGESTION (non-serious) with onset 23May2022, outcome "recovered with sequelae", described as "sinus pressure and congestion"; FATIGUE (non-serious) with onset 23May2022, outcome "recovered with sequelae", described as "tired". Therapeutic measures were taken as a result of throat irritation, paranasal sinus discomfort, sinus congestion, pain, fatigue. Additional information: The patient had no known allergies. It was unknown if patient received any medication within two weeks of vaccination. Therapeutic measures were taken as a result of the events which included treatment with Paxlovid from 24May2022 to 29May2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2313477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 13,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 08.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Electrocardiogram Malaise Speech disorder

Symptomtext

Patient did not feel well after receiving vaccine. She was seated. She was alert but said she did not feel like she could talk. She was able to respond to commands. 911 was called immediately as a precautions and paramedics arrived after about 7 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Paramedics ran a ECG in ambulance and PT was in their custody.
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2313444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 11.05.2022
Beginn: 11.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Headache Hyperhidrosis Pallor Sight disability

Symptomtext

About 5 minutes after the vaccine, the patient complained of "bad headache, sweating, very dizzy, can't see". Patient looked very pale but was still responsive and able to answer questions. We called 911. Paramedics arrived about 20 minutes later. Paramedics check patient's blood pressure, pulse, lung, and everything was within normal limits. Paramedics asked patient if she had any rash, itching, difficulty breathing, swollen tongue, lips, which she denied. Paramedics told patient everything was normal, and asked patient if she wanted to go to the hospital which patient declined. Patient left pharmacy with her mom afterwards.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Blood pressure, pulse, lung check.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: PATIENT STATED SHE'S NOT ON ANY MEDICATION.
Allergien: MENINGITIS VACCINE PER PATIENT (DIZZY AND LIGHTHEADED)
Vorherige Impfungen: Meningitis vaccine

VAERS 2313073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IL
Alter: 53,0
Geschlecht: M
Eingang: 08.06.2022
Impfdatum: 25.04.2022
Beginn: 01.06.2022
Tage bis Beginn: 37,0
Dosis: 3
Route/Site: IM / LA

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

Body temperature increased COVID-19 Diarrhoea Fatigue Nausea Respiratory tract congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

I contracted COVID-19 on 6/01/2022 with symptoms of scratchy throat, congestion, nausea, mild diarrhea, low grade temp, and fatigue. I was prescribed PAXLOVID on 06/03/2022 and my symptoms began to improve after 4 days. The PAXLOVID leaves a bad taste in my mouth, and also gives me an upset stomach. I am still experiencing lingering fatigue at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 06/02/2022
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Acetaminophen; Ibuprofen; PEPCID AC
Allergien: No
Vorherige Impfungen: -

VAERS 2312799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OR
Alter: 60,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 21.04.2022
Beginn: 25.05.2022
Tage bis Beginn: 34,0
Dosis: 4
Route/Site: SYR / RA

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

Dizziness Nausea Vertigo

Symptomtext

Diagnosed with vertigo.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 5/28/2022?went in to see the doctor for dizziness, light-headedness, and nausea.
Aktuelle Erkrankungen: None
Vorgeschichte: Breast cancer survivor.
Andere Medikamente: MetFormin, Cardio Tonic, CoQ10, D3, Cell Guardian, Magnesium, Probiotic, Jade Screen teapills, Omega fish oils.
Allergien: Latex
Vorherige Impfungen: -

VAERS 2312385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 59,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 09.05.2022
Beginn: 31.05.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Feeling cold Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

We have been on vacation since, 5/21/22. On 5/31/22, we were staying at my inlaws, I had a runny nose and slight cough that I attributed to allergies or the sniffles after get wet and cold on 5/30/22. On 6/1/22, my nose was running again and I was tired, but we went golfing. On 6/2/22, I took a Home Covid Self Test, just to rule out Covid. It was positive. I made an appointment online at a nearby Clinic to get a Rapid Antigen Test. I was able to be tested that afternoon. Again, I tested positive. Because of my Type 2 Diabetes, the Nurse Practitioner said I was eligible for an antiviral medication. My symptoms are gone, as is the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 6/2/22 Home Covid Self Test (positive) 6/2/22 Rapid Antigen Test (positive) 6/6/22 Home Covid Self Test (slightly positive)
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Type 2
Andere Medikamente: Metformin, Rosuvastatin, Ramipril, Glimepiride, Multivitamin, Calcium, Vitamin D, Vitamin C, Fish Oil, Aller-fex (generic Allegra)
Allergien: Fentanyl, Ibuprofen, Aspirin (slight)
Vorherige Impfungen: -

VAERS 2311728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 27.04.2022
Beginn: 15.05.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: IM / RA

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

Abdominal discomfort Abdominal pain upper COVID-19 Dizziness Ear congestion Ear pain Fatigue Hunger Inner ear disorder Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of sore throat, runny nose, and extreme tiredness. I did get a low grade fever of 100 with an upset stomach. I would get hungry then my stomach would hurt. I took an at home COVID-19 test that the first one was negative then I repeated a few days later and it was positive. I did a telehealth visit on 6/1/2022 because I had some questions. I was experiencing some dizziness so was advised to take antihistamines and MUCINEX. I had an inner ear issues with an ear ache and some congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Synthroid; calcium; multivitamins; Benadryl
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 2308347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 72,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 03.05.2022
Beginn: 23.05.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Dry throat Fatigue Feeling abnormal Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing Throat irritation

Symptomtext

It started with a dry, scratchy throat, congestion, runny nose, and sneezing. Eventually, I had a fever, fatigue, very achy, coughing, and COVID-19 fog. It lasted a week, most of the symptoms went away except the fatigue. I was still coughing when I talked. I went to a clinic to get a PCR test on the 25th of May, to confirm the results of the at home test on the 24th of May. The results were positive and I was referred to my doctor to get a prescription of PAXLOVID and take a lot of fluids and zinc. I did not take the PAXLOVID because I started to feel better, I am still quarantining due to still being positive for COVID-19 after 11 days of quarantining.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: PCR test positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin D; multivitamin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2307450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: IN
Alter: 69,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 18.05.2022
Beginn: 19.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Fatigue Feeling abnormal Headache Myalgia Nausea Pyrexia Somnolence

Symptomtext

Severe aching of almost every muscle in my body. Initial fever which faded after 3-4 hours. Some nausea,no vomiting. Intense headache off and on for 4 days. Some tiredness,sleepiness,but not like others have had. Aching of muscles continued for 4 days, finally relenting by the middle of 4th day. Foggiest of mind for several days after all that. Back to normal self and function after about 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Mild bronchitis
Vorgeschichte: None
Andere Medikamente: Finofibrate 48mg,1000mg fish oil, adult vitamin,rested legs herbal supplement / day
Allergien: Penicillin, sulfa, morphine
Vorherige Impfungen: All Covid vaccines resulted in similar reaction. #1 was on 3/2/2021. #2 was 3/33/2021, #3 was 12/2/2021, #4 was 5/18/2022

VAERS 2306701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

mild

Staat: VA
Alter: 53,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 19.04.2022
Beginn: 26.04.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Clostridium test positive Colitis Culture stool positive Magnetic resonance imaging Myalgia Nasopharyngitis SARS-CoV-2 test positive Urine analysis

Symptomtext

On April 26, 2022, I experienced cold like symptoms following by muscle aches. I saw my primary care on May 29, 2022, who prescribed amoxicillin. My doctor recommended that I test for covid during the telehealth visit and I tested positive on May 29, 2022. I started the Paxloid on May 30, 2022. I continued the amoxicillin with the Paxloid since I had already started it. On May 12, 2022, I went to the Emergency Room and was diagnosed with colitis. The hospital took stool sample and I tested positive for C Diff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Stool sample, urine test, and I think it was a MRI.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Sertraline, Bupropion, Linzess, Dupliexent, Multi Vitamin, Vitamin D3, Rosuvastin Calcium, and Fiber supplement.
Allergien: -
Vorherige Impfungen: -

VAERS 2296250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: PA
Alter: 45,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 23.05.2022
Beginn: 25.05.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Injection site pustule Injection site rash Injection site swelling Injection site warmth Skin weeping

Symptomtext

Rash, warm, swollen skin at injection site, oozing pus, painful joints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None yet, but will be going to Urgent care as soon as they open.
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity, diabetes, stroke
Andere Medikamente: Zoloft, Topamax, metoprolol, lisinopril, lipitor
Allergien: Pork, bananas, effector, latex
Vorherige Impfungen: -

VAERS 2294372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 58,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 12.04.2022
Beginn: 20.05.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine but I did contract COVID. I started having symptoms on May 20 and tested positive on May 23. I'm taking Tylenol and Sudafed. I have prescription for benzonatate for the cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Antigen test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Topical prescriptions twice a week; estradiol cream; clobetasol ointment
Allergien: Antibiotics
Vorherige Impfungen: -

VAERS 2290944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 29.04.2022
Beginn: 18.05.2022
Tage bis Beginn: 19,0
Dosis: UNK
Route/Site: SYR / LA

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

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

Tested Positive for Covid on May 20, symptoms since May 18 but negative on May 18 and May 19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: see above
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, high cholesterol, obese
Andere Medikamente: Amlodipine Besylate / Benazepril, Rovustatin, Tadalafil
Allergien: none
Vorherige Impfungen: -

VAERS 2290860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 12.04.2022
Beginn: 11.05.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: IM / LA

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

Anosmia Body temperature increased COVID-19 Cough Diarrhoea Dysgeusia Fatigue Feeling abnormal Hypophagia Nasal congestion Oropharyngeal pain Pain Parosmia Respiratory tract congestion SARS-CoV-2 test positive Somnolence Vaccine breakthrough infection Weight decreased

Symptomtext

Breakthrough case of Covid - sx began 05/11/2022 Sx began with a sore throat, the next day I started to get achy. Then I got, the aches turned into shooting pain randomly. I lost some of my sense of smell and I had like phantom odors, smelling things that were not there. A couple days after that I had a temp of 100, but it never went higher than that. Around the 05/16/2022 I had a metallic sour taste in my mouth and that just went away. The sx built on top of each other. My nose and sinuses were stuffy all of the time. I did not get a cough until about 05/19/2022 - it a dry hacking cough. I had an absolute horrible tiredness that I still have, it is to the point that I can not do anything. I felt a little foggy headed most of the time and I slept for about 5 days I slept for about 14 hours per night. I lost some weight because I was not eating. My doctor gave me codeine cough syrup, Mucinex and she gave me Paxlovid on 05/16/2022. Oh and the first 6 days I had really bad diarrhea that Imodium did not help. Currently I still have the exhaustion that does not go away, a dry cough that is getting better and I have congestion in the morning and at night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 05/13/2022 $ 05/15/2022 - home tests both were positive
Aktuelle Erkrankungen: no
Vorgeschichte: Chronic pain, blood clotting D/O (protein C deficiency)
Andere Medikamente: Eliquis, singular, multi-vitamin, turmeric, resveratrol, Vitamin C & D, CoQ10, Krill Oil, magnesium, biotin, B complex, oxycodone
Allergien: shellfish
Vorherige Impfungen: -

VAERS 2289495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WI
Alter: 68,0
Geschlecht: F
Eingang: 21.05.2022
Impfdatum: 11.05.2022
Beginn: 13.05.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Chills Fatigue Lymphadenopathy Nausea Night sweats Pain in jaw Pyrexia

Symptomtext

PT REPORTS CHILLS, FEVER, NAUSEA NUGHTSWEATS THAT DISAPPEARED WITHIN THE FIRST 24 HOURS AFTER ADMINISTRATION. FATIGUE LASTED 48 HOURS. WITHIN 48 HOURS AFTER VACCINE ADMINISTRARTION PATIENT REPORTED FEELING LYMPH NODE SWELLING/JAW PAIN ON THE SIDE OF THE FACE. PT USED COLD COMPRESSES TO CONTROL THE SWELLING, THE SWEELING AND PAIN LASTED ONE WEEK UNTIL IT STARTED TO SUBSIDE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: NON-HODGKINS LYMPHOMA MASS BY THE RIGHT URETER BACK COMPRESSION FRACTURES
Andere Medikamente: IVIG, BRIMONIDINE, LATANOPROST, ACYCLOVIR, HYDROCHLOROTHIAZIDE, POTASSIUM CHLORIDE, DILTIAZEM, CETIRIZINE, HYDROCODONE-APAP, OXYCODONE-APAP, ACETAMINOPHEN, PROBIOTIC, MULTICAPS, MCHC, MAGNESIUM GLYCINATEVITAMIN a AND D3, ARTIC OILS BILBERRY
Allergien: ADHESIVES, LATEX, PROMETRIUM, BENZONATATE, MMR VACCINE, METORPOLOL, RITUXIMAB, SMZ-TMP, NITROFURANTOIN, DUSTMITES, RAGWEED, GRASS, BIRCH, OAK, CATS, DOGS, MOLDS, ARTIFICIAL, COLORS, DYES, CORN SYRUP, MILK AND DERIVATIVES.
Vorherige Impfungen: -

VAERS 2284846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NM
Alter: 77,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 27.04.2022
Beginn: 15.05.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sinus disorder

Symptomtext

Contracted COVID 19, runny nose, sinus problems, fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Tested positive COVID 19
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: LIPTOR
Allergien: Airborne allergy
Vorherige Impfungen: -

VAERS 2284835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OH
Alter: -
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 11.05.2022
Beginn: 11.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain upper Arthralgia Back pain Blood test Feeling abnormal Full blood count Hunger Hypophagia Liver function test abnormal Metabolic function test Nausea Pain

Symptomtext

A few hours receiving my 4th vaccine shopped in the pharmacy for about 15 minutes then I went home. I started having joint pian and hurting all over. I thought it was normal and the pharmacist told me to expect Flu like symptoms. I took Tylenol when I got home, and I started having pain in the upper right side of my abdomen and in my lower back as well. I was also very hungry but nauseated so I was having issues eating. I have been drinking plenty of fluids and plenty of water just naturally (sugar free stuff only) because it is very hot this time of year. I was feeling so crappy so finally Monday I called my family Dr but they didn?t tell me anything because they didn?t know what was going. My dr thought I had a uti and then she ran some test. Blood work CVC and a comprehensive metabolically panel These test looked fine with the exception of my liver so she said no more Tylenol . I am currently feeling really crappy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: See above
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Shingles-I felt like I had a really bas case of the Flu Chills In lots of pain at night body/head all over aches and was in the

VAERS 2283188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 62,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 12.04.2022
Beginn: 11.05.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Headache Oropharyngeal pain Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

First sign that I had was a runny nose. I thought that was just normal runny nose but Tuesday night & Wednesday morning I had a little sore throat. I thought I just had post nasal drip. Around noon on Wednesday I felt tired and not myself, so I did an at home rapid COVID-19 test and it was positive. I felt feverish, headache, cough, runny nose, body aches, sore throat and tired. I contacted my doctor on Thursday and she prescribed me Paxlovid and I started taking it on Thursday and took the last dose this morning. Because I have some kidney issues because of medications I take it was a reduced dose. Today I still have a little bit of post nasal drip and cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home Rapid COVID-19 Test on 05/11/2022 Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Type 2 Hypertension Gout High Cholesterol
Andere Medikamente: Melatonin 5mg 2 nightly Tartary extract 2500mg Metoprolol Titrate 50mg Camulosine HCL .8mg Hydrochlorothiazide 25mg Triamterene 37.5mg Synthroid 37.5mg/mcg Atoravastim 40mg Alopurinol 100mg Metformin 500mg
Allergien: None
Vorherige Impfungen: -

VAERS 2283083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 12.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Computerised tomogram abnormal Epidural injection Gait disturbance Inflammation Magnetic resonance imaging Pain in extremity Stenosis

Symptomtext

A history of pain in my leg became exacerbated. I never take pain meds but I needed them for this. I went to see the doctor because the pain was much different. I saw him in the middle of May after the shot. At first I thought it was totally unrelated but this was much worse than I ever had and is continuing to get worse. Initially my sports medicine doctor ordered an MRI. Then I started having really bad pain and the doctor ordered a CT and the scan showed stenosis. The physical therapist that I was sent to indicated that I had a lot of inflammation. She stated that it could be caused by the vaccine. The pain in my leg is affecting my life. I had an epidural completed today but I am still having issues with walking. My symptoms became really bad on April 26.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: MRI-does not recall actual dates; CT scan-Stenosis was identified-does not recall actual dates.
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis; hypertension; migraines; hypothyroid
Andere Medikamente: Vitamin D3 Zetia Losartan Magnesium Fish Oil Ranexa Crestor Co Q 10 Xiidra
Allergien: Azithromycin; KEFLEX; latex; fosfomycin tromethamine; ZITHROMAX; codeine; VERSED
Vorherige Impfungen: -

VAERS 2282890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 12.04.2022
Beginn: 12.05.2022
Tage bis Beginn: 30,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Sinus congestion Sneezing

Symptomtext

I woke up with a sore throat followed in the next two days sneezing sinus congestion body aches fever 102.2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Covid test positive.
Aktuelle Erkrankungen: No.
Vorgeschichte: Lichen sclerosis
Andere Medikamente: Rosuvastatin; alendronate sodium; D3; B12; biotin; calcium; melatonin; Nocdurna; clobetasol
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2281387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MO
Alter: 60,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 10.04.2022
Beginn: 13.05.2022
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

It was a runny nose and minor sore throat that started 4/13 and my wife also had symptoms and already tested positive. So I did a home test and tested positive. I really don't have any symptoms now so they lasted a couple of days at the most. Doctor put me on Paxlovid and I started that on 4/14/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: At home Covid test - positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; hypertension; CLL; high cholesterol; GERD
Andere Medikamente: Vitamin C 750mg, Metformin, Crestor, HCTZ, Protonic, Potassium, Cozaar, Centrum Silver
Allergien: No
Vorherige Impfungen: -

VAERS 2280930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 05.05.2022
Beginn: 06.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Dyskinesia Fatigue

Symptomtext

Extreme fatigue 3 days since the shot. Haven't been able to open left side of my mouth all the way.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma, high blood pressure
Andere Medikamente: Lisinopril 10MG, Bupropion, Wixela
Allergien: shellfish, penicillin, Clindamycin, Hydrochloride
Vorherige Impfungen: -

VAERS 2280895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CT
Alter: 75,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 06.05.2022
Beginn: 11.05.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Chest discomfort Cough Discomfort Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Fatigue Immunisation reaction Oropharyngeal discomfort SARS-CoV-2 test positive Stress cardiomyopathy Upper-airway cough syndrome Vaccine breakthrough infection

Symptomtext

Breakthrough Case of COVID and adverse reaction to the vaccine, So on Tuesday, 05/10/2022, took an at home test for COVID and it came out negative, because I had a tickle in my throat and cough and post nasal drip. then Wednesday on the 05/11/2022 I was feeling very tired, and by supper time I was feeling pressure in my upper back, chest, and left arm. So by that time, I went to urgent care in town and they did an EKG and they did not like what they saw and they sent me to the ER in town, at this point I was still testing negative for COVID, they also took an EKG and did not like the results so they sent me to another hospital for possible heart attack. So they determine that I did not have any blockages and they took another COVID test and this one came back positive. On the 13th they did an echo which showed decrease left ventricular ejection fraction. They diagnosed with Takotsubo Cardiomyopathy, and started me on remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 4,0
Labordaten: EKG, ECHO, COVID test.
Aktuelle Erkrankungen: None
Vorgeschichte: Imuno Compromised due to Breast Cancer in 2020
Andere Medikamente: Anastrozole; atorvastatin; multivitamin; calcium 600mg; vitamin D3 15 mcg; Synthroid; amlodipine; metoprolol.
Allergien: Aspirin; ibuprofen
Vorherige Impfungen: -

VAERS 2280737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: KY
Alter: 68,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 11.04.2022
Beginn: 10.05.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Chills Dry mouth Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Sleep disorder

Symptomtext

I woke up at 11:30 at night and had fever, chills, dry mouth, and a sore throat with headache. I was only sick for about 8 hours, I called the Dr in the morning and she ordered Paxlovid for 5 days and I took another test on Sunday and was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid Test Positive home test on 5/10/22; Covid Test Positive home test on 5/14/22; Covid Test Negative home test on 5/15/22
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Coronary Artery Disease
Andere Medikamente: Lisinopril Ezetimibe Multivitamin Calcium with D3 Omega 3 with Fish Oil CoQ10 Biotin D3 with K2
Allergien: None
Vorherige Impfungen: -

VAERS 2278590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TN
Alter: 50,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 13.05.2022
Beginn: 15.05.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Pain in extremity Swelling Tenderness

Symptomtext

The patient stated that she had swelling, soreness, and tenderness under her arm. I spoke with her again on 5/16/22 and she stated that it felt better and was subsiding. I told her if it continues or gets worse to call or go in to see her primary care doctor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: n/a
Allergien: nkda
Vorherige Impfungen: -

VAERS 2277862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 77,0
Geschlecht: M
Eingang: 15.05.2022
Impfdatum: 12.05.2022
Beginn: 12.05.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Chills Cough Decreased appetite Delirium Headache Nasal congestion Pain Productive cough Pyrexia SARS-CoV-2 test

Symptomtext

Three days of high fever (102.6 at its highest). Delirium. Body aches, chills, headaches, stuffy nose and sinuses, bad cough, flem and loss of appetite. Treatment: regular administration of tylenol, fluids. My wife and a good friend have had similar reactions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid test (5/14/2022), regular temperature checks.
Aktuelle Erkrankungen: None
Vorgeschichte: Minor heart issues
Andere Medikamente: Allopurinol Plavix Baby Aspirin Atorvistain
Allergien: None
Vorherige Impfungen: Soreness.

VAERS 2277555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: -
Geschlecht: F
Eingang: 14.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Fatigue Lip swelling Mouth swelling Swelling face

Symptomtext

Extreme swelling inside my upper and lower lip; Started to feel like a swelling inside my mouth and cheeks and around and under my tongue; Fatigue; Extreme swelling inside my upper and lower lip; Started to feel like a swelling inside my mouth and cheeks and around and under my tongue; Extreme swelling inside my upper and lower lip; Started to feel like a swelling inside my mouth and cheeks and around and under my tongue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FJ4991) for covid-19 immunisation. The patient's relevant medical history included: "Acid reflux" (unspecified if ongoing). Concomitant medication(s) included: PEPCID AC taken for gastrooesophageal reflux disease. Past drug history included: Omeprazole. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer), for COVID-19 immunization; Bnt162b2 (Dose 3 (Booster)), for COVID-19 Immunization. The following information was reported: LIP SWELLING (non-serious), SWELLING FACE (non-serious), MOUTH SWELLING (non-serious), outcome "unknown" and all described as "Extreme swelling inside my upper and lower lip; Started to feel like a swelling inside my mouth and cheeks and around and under my tongue"; FATIGUE (non-serious), outcome "unknown". Therapeutic measures were taken as a result of lip swelling, mouth swelling. Additional information: Reporter stated that after the booster shot and patient was not sure if this was a true side effect or this was from something else but patient had extreme swelling inside her upper and lower lip, similar to Canker sores but not truly a Canker sore because patient have been rinsing with a rinse that she suggested and they were subsiding a lot more quickly than they ever have, you know when patient was younger. Patient received this vaccine on Tuesday and by Wednesday evening patient started to feel like a swelling inside my mouth and cheeks and around and under my tongue and it was so similar to Canker sores and my pharmacist said that patient should call you to report it just for your data collecting evidence." Reporter stated, "Yes, that was correct and it still exists today which was now Saturday. Again, patient did not know if it was truly related. Patient normally take a drug for acid reflux but because patient was going for endoscopy this coming Thursday, patient was off Omeprazole and my doctor put me on Pepcid, just to kind of calm some of the acid reflux. So, patient do not know if the sores have anything to do with, you know more acidity in my mouth or not or if it was a true reaction. But my pharmacist said that patient should report it anyway because if you received any other call that have the same side effects then it would be helpful to know that I had a similar side effect." Reporter stated, "She gave me the whole print out and because I had the other vaccines, patient have a list of all the side effects but she said you were still collecting data for the second booster. This occurred after the second booster, patient know what all the other side effects are but patient only experienced a little bit of fatigue but nothing like the initial vaccine." 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: Acid reflux (esophageal)
Andere Medikamente: PEPCID AC
Allergien: -
Vorherige Impfungen: -

VAERS 2277529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: -
Geschlecht: M
Eingang: 14.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Fatigue

Symptomtext

A little bit of fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FJ4991) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 3 booster, Unknown manufacturer), for Covid-19 Immunization; Covid-19 vaccine (Primary immunization series complete, Unknown manufacturer), for Covid-19 Immunization. The following information was reported: FATIGUE (non-serious), outcome "unknown", described as "A little bit of fatigue". Additional information: "Reporter stated, "I reside in (withheld) and my pharmacist advised me to give you a call because you are still collecting data regarding the second booster and I wanted to let you know that after the booster shot and I am not sure if this was a true side effect or this was from something else but I had extreme swelling inside my upper and lower lip, similar to Canker sores but not truly a Canker sore because I have been rinsing with a rinse that she suggested and they are subsiding a lot more quickly than they ever have, you know when I was younger. I received this vaccine on Tuesday and by Wednesday evening I started to feel like a swelling inside my mouth and cheeks and around and under my tongue and it is so similar to Canker sores and my pharmacist said that I should call you to report it just for your data collecting evidence." When paraphrased the concern: Reporter stated, "Yes, that is correct, and it still exists today which is now Saturday. Again, I do not know if it is truly related. I normally take a drug for acid reflux but because I am going for endoscopy this coming Thursday, I am off Omeprazole and my doctor put me on Pepcid, just to kind of calm some of the acid reflux. So, I do not know if the sores have anything to do with, you know more acidity in my mouth or not or if it was a true reaction. But my pharmacist said that I should report it anyway because if you received any other call that have the same side effects then it would be helpful to know that I had a similar side effect." When informed the role of Pfizer Drug Safety and about Pfizer Medical Information Department for the questions: Reporter stated, "She gave me the whole print out and because I had the other vaccines, I have a list of all the side effects but she said you were still collecting data for the second booster. This occurred after the second booster, I know what all the other side effects are but I only experienced a little bit of fatigue but nothing like the initial vaccine." When again informed the role of Pfizer Drug Safety and for the questions contact details can be provided: Reporter stated, "Do you want me to call them and report this again or will you, it has been reported?" When asked for permission for further probing: Reporter stated, "No, I do not have the time right now but I just wanted to give you a call to let you know what I experienced." Reporter stated, "My husband had the vaccine, the same, we got at the same time and he did not have any side effects except for, you know a little bit of fatigue but he did not have any sore in his mouth or anything." Reporter was unwilling to complete the report. Thus, further probing could not be done and product details and pharmacy details were unknown. Limited information available over the call". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2276442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MD
Alter: 67,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 10.05.2022
Beginn: 10.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Pruritus Swelling Urticaria

Symptomtext

Intense itching, hives, and swelling on left side of body

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril/HCTZ, carvediolol, diltiazem XR,
Allergien: Calcium channel blockers, clindamycin, macrolides, ketolides, salicylates, vancomycin
Vorherige Impfungen: -

VAERS 2275381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 06.04.2022
Beginn: 06.05.2022
Tage bis Beginn: 30,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Cough Headache Lacrimation increased Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test Sneezing Vaccination failure

Symptomtext

4 days after my last dose of Paxlovid my symptoms returned/I took a Covid antigen test when I took the last Paxlovid dose, and it was still positive; 4 days after my last dose of Paxlovid my symptoms returned/I took a Covid antigen test when I took the last Paxlovid dose, and it was still positive; runny nose; sore throat; sneezing; watery eyes; headache; fever; cough; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Mar2021 at 11:00 as dose 1, single (Lot number: EN6207), in left arm, on 06Apr2021 at 11:00 as dose 2, single (Lot number: EWD150), in left arm, on 12Oct2021 at 10:00 as dose 3 (booster), single (Lot number: 30145BA), in left arm and on 06Apr2022 at 18:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 64 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "melanoma" (unspecified if ongoing), notes: Other medical history: melanoma; "brain cavernoma" (unspecified if ongoing), notes: Other medical history: brain cavernoma. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 06May2022, outcome "not recovered" and all described as "4 days after my last dose of Paxlovid my symptoms returned/I took a Covid antigen test when I took the last Paxlovid dose, and it was still positive"; COUGH (non-serious) with onset 2022, outcome "not recovered"; PYREXIA (non-serious) with onset 2022, outcome "not recovered", described as "fever"; HEADACHE (non-serious) with onset 2022, outcome "not recovered"; RHINORRHOEA (non-serious) with onset 2022, outcome "not recovered", described as "runny nose"; SNEEZING (non-serious) with onset 2022, outcome "not recovered"; OROPHARYNGEAL PAIN (non-serious) with onset 2022, outcome "not recovered", described as "sore throat"; LACRIMATION INCREASED (non-serious) with onset 2022, outcome "not recovered", described as "watery eyes". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06May2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Therapeutic measures were not taken as a result of rhinorrhoea, oropharyngeal pain, sneezing, lacrimation increased, headache, pyrexia, cough. Clinical course: No known allergies reported. Device timestamp was 06May2022. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20220506; Test Name: antigen test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cavernoma (Other medical history: brain cavernoma); Melanoma (Other medical history: melanoma)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2242029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: VA
Alter: 10,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 18.04.2022
Beginn: 18.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Nausea Pain Somnolence Product administered to patient of inappropriate age

Symptomtext

Sleepiness; Nausea; 10 years old patient who was administered the Pfizer COVID-19 Vaccine Gray Cap/ administered the adult dose the grey cap to a 10-year-old; This is a spontaneous report received from contactable reporter(s) (Pharmacist and Physician) from medical information team. A 10-year-old female patient received BNT162b2 (BNT162B2), on 18Apr2022 at 16:00 as dose number unknown 0.3 ml, single (Lot number: FJ4991, Expiration Date: 30May2022) at the age of 10 years, in left deltoid for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 18Apr2022 at 16:00, outcome "unknown", described as "10 years old patient who was administered the Pfizer COVID-19 Vaccine Gray Cap/ administered the adult dose the grey cap to a 10-year-old"; SOMNOLENCE (non-serious), outcome "recovered", described as "Sleepiness"; NAUSEA (non-serious), outcome "recovered". Additional information: The reporter had an error, administered the adult dose the grey cap to a 10-year-old. Expiration date said Sep2021, this one got pushed back so it should be extended to 30May2022. The patient provided information to you regarding the reported adverse event(s) with the use of the product. This occurred outside facility, patient complained if sleepiness, nausea one week later called to say improved. Unsure if causal, patient did not come into office. Follow-up (18Apr2022): This is a spontaneous follow-up report received from the contactable Pharmacist. This Pharmacist reported for a 10-Year-old female patient that: Reporter information. Patient details (demographics). Product coding updated, Product details. Follow up (20Apr2022): New information received in response to the mail trail sent regarding the confirmation of below mentioned query which included reporter details. Follow-Up (02May2022): Follow-up attempts are completed. No further information is expected. Follow-up (10May2022): This is a spontaneous follow-up report received from a contactable Physician. This Physician reported for a patient in response to HCP letter sent via follow-up letter which included that: Updated information included: New event "sleepiness, nausea". At risk was removed. Additional information: Did the patient provide information to you regarding the reported adverse event(s) with the use of the product: Yes, This occurred outside facility, patient complained if sleepiness, nausea one week later called to say improved. Unsure if causal, patient did not come into office.

Weitere VAERSDATA-Felder

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

VAERS 2242029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: VA
Alter: 10,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 18.04.2022
Beginn: 18.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Nausea Pain Somnolence Product administered to patient of inappropriate age

Symptomtext

Sleepiness; Nausea; 10 years old patient who was administered the Pfizer COVID-19 Vaccine Gray Cap/ administered the adult dose the grey cap to a 10-year-old; This is a spontaneous report received from contactable reporter(s) (Pharmacist and Physician) from medical information team. A 10-year-old female patient received BNT162b2 (BNT162B2), on 18Apr2022 at 16:00 as dose number unknown 0.3 ml, single (Lot number: FJ4991, Expiration Date: 30May2022) at the age of 10 years, in left deltoid for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 18Apr2022 at 16:00, outcome "unknown", described as "10 years old patient who was administered the Pfizer COVID-19 Vaccine Gray Cap/ administered the adult dose the grey cap to a 10-year-old"; SOMNOLENCE (non-serious), outcome "recovered", described as "Sleepiness"; NAUSEA (non-serious), outcome "recovered". Additional information: The reporter had an error, administered the adult dose the grey cap to a 10-year-old. Expiration date said Sep2021, this one got pushed back so it should be extended to 30May2022. The patient provided information to you regarding the reported adverse event(s) with the use of the product. This occurred outside facility, patient complained if sleepiness, nausea one week later called to say improved. Unsure if causal, patient did not come into office. Follow-up (18Apr2022): This is a spontaneous follow-up report received from the contactable Pharmacist. This Pharmacist reported for a 10-Year-old female patient that: Reporter information. Patient details (demographics). Product coding updated, Product details. Follow up (20Apr2022): New information received in response to the mail trail sent regarding the confirmation of below mentioned query which included reporter details. Follow-Up (02May2022): Follow-up attempts are completed. No further information is expected. Follow-up (10May2022): This is a spontaneous follow-up report received from a contactable Physician. This Physician reported for a patient in response to HCP letter sent via follow-up letter which included that: Updated information included: New event "sleepiness, nausea". At risk was removed. Additional information: Did the patient provide information to you regarding the reported adverse event(s) with the use of the product: Yes, This occurred outside facility, patient complained if sleepiness, nausea one week later called to say improved. Unsure if causal, patient did not come into office.

Weitere VAERSDATA-Felder

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

VAERS 2274122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 12.05.2022
Impfdatum: 30.03.2022
Beginn: 03.05.2022
Tage bis Beginn: 34,0
Dosis: 4
Route/Site: SYR / RA

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

Asthenia COVID-19 Cough Headache Oropharyngeal pain SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

On 5/3/2022, began experiencing symptoms: Post-Nasal Drip, Sore Throat, Cough, Headache, Weakness, Low Energy, No Stamina.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: PCR test on 5/8/2022 showed ?Positive? for COVID-19.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Type 2 Fatty Liver Disease Coronary Artery Disease Chronic Kidney Disease Recurring Kidney Stones
Andere Medikamente: Clopidogrel 75 mg Cycloset 4 mg Desloratadine 5 mg Farxiga 10 mg Fenofibrate 145 mg Finasteride 5 mg Glimepiride 2 mg Hydrocortisone 10 mg Potassium Citrate 1620 mg Rosuvastatin 40 mg Testosterone Gel 1.62% Trulicity 3 mg/0.5mL Vascepa 1 gr
Allergien: Iodine IVP
Vorherige Impfungen: -

VAERS 2273468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: PA
Alter: 59,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 04.05.2022
Beginn: 09.05.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Nasal congestion Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sinus operation Throat irritation

Symptomtext

I actually had a better reaction in my arm than previous vaccines. But I began experiencing a scratchy throat and some drainage and since my husband had already tested positive for Covid, I went to Urgent Care to be tested for Covid where I tested positive. I have been experiencing some stuffiness and congestion and one night of fever, but not much beyond that. At Urgent Care I was prescribed Paxlovid and have been taking that ever since.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Covid test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Joint Pain
Andere Medikamente: Multi vitamin Ibuprofen Joint supplement
Allergien: Sulfa
Vorherige Impfungen: Flu vaccine give me a large localized reaction on my arm.

VAERS 2269058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 66,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.05.2022
Beginn: 06.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Immediate post-injection reaction Injection site erythema Injection site pain Injection site swelling Myalgia Pain in extremity

Symptomtext

Injection site pain ongoing as of today's date; tiredness ongoing as of today's date; muscle pain; joint pain, injection site slight swelling and redness immediately following injections; arm pain ongoing as of today's date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: arthritis
Andere Medikamente: Levothyroxine, Spironolactone/HCTZ, Celebrex, Sertraline, Naloxone, Lisinopril
Allergien: Erithromycin, Shingrex vaccine
Vorherige Impfungen: -

VAERS 2268885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 10.05.2022
Beginn: 10.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Pruritus Urticaria

Symptomtext

Two days after booster started getting hives. Itchy small clusters of hives. Took antihistaminesand used cortisone cream. So far lasted five days.

Weitere VAERSDATA-Felder

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

VAERS 2267073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: CA
Alter: 82,0
Geschlecht: F
Eingang: 07.05.2022
Impfdatum: 06.05.2022
Beginn: 06.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Headache Myalgia Pyrexia Wheezing

Symptomtext

the patient started to have symptoms of headache, low grade fever, muscle aching and wheezing 12 to 15 hours after receiving the Pfizer 2nd booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Her doctor gave her a prednisone script
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: adhesive tape
Vorherige Impfungen: -

VAERS 2266556

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: TX
Alter: 82,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Pain in extremity Peripheral swelling Pruritus Pyrexia Vomiting

Symptomtext

pt arm was very swollen and very red with unusual soreness. pt ran 101.01 fever for 2 days. pt vomitted same night as vaccine and has been itchy for 4 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: none
Allergien: some but list not provided
Vorherige Impfungen: -

VAERS 2266106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: DE
Alter: 53,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 31.03.2022
Beginn: 04.05.2022
Tage bis Beginn: 34,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Cough Diarrhoea Inflammation Muscle spasms SARS-CoV-2 test positive Sinus disorder Sneezing Throat irritation

Symptomtext

I had a scratchy throat, inflamed sinuses, a mild cough, sneezing, and a little bit of diarrhea. I had severe leg cramps last night. I have cramps in my finger and hands as well. I called Telehealth and they prescribed me with prednisone and Flonase. Then they added azithromycin and cough syrup for me to take as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 Test- Negative (5/5/2022) COVID-19 Test- Positive (5/6/2022)
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure Obesity
Andere Medikamente: Lisinopril Vitamin D Omega 3 Multivitamin Biotin
Allergien: Penicillin Nickel Cobalt Gold
Vorherige Impfungen: -

VAERS 2264633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 28.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

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

Rash

Symptomtext

When I had the vaccine and when I get a booster, I get a rash in the same spot on my leg. It eventually goes away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium, Multivitamin
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2264582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 21,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 01.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Bone pain Chills Fatigue Headache Myalgia Pyrexia Rash Rash macular

Symptomtext

Extreme bone and muscle soreness next two days. Fever, chills. Exhaustion. Splotchy rash showed up all over body. Is still here 4 days later. Extreme headache next day.

Weitere VAERSDATA-Felder

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

VAERS 2263380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 16.04.2022
Beginn: 16.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site erythema Injection site pruritus Injection site swelling Skin exfoliation Skin wrinkling Swelling

Symptomtext

Large red area approximately 2.5 inches at injection site which which was swollen along with swollen left arm pit. Redness has remained for 3 weeks since receipt of injection as well as itching. Skin in that area appears wrinkled and is now peeling. Redness and itching still remain along with small swelling under left armpit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Mesalamine
Allergien: No
Vorherige Impfungen: -

VAERS 2259786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 43,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 26.04.2022
Beginn: 27.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Headache Injection site pain Lymph node pain Lymphadenopathy Nausea SARS-CoV-2 test Uterine spasm Vaginal haemorrhage Vaccination site pain

Symptomtext

Extreme pain in injection site for 3 days; extreme pain in Lymph nodes under left arm for 3 days; Headache; nauseous; vaginal bleeding; Uterine cramps; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Apr2022 at 12:00 as dose 3 (booster), single (Lot number: FJ4991) at the age of 43 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "MDD" (unspecified if ongoing); "GAD" (unspecified if ongoing); "Adenomyosis" (unspecified if ongoing); "Cow's milk" (unspecified if ongoing), notes: known allergies: Cow's milk. Concomitant medication(s) included: LITHIUM; PRISTIQ; KLONOPIN. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: FC3183 , Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 10Sep2021, when the patient was 42-year-old, for COVID-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: FC3183 , Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 20Aug2021, when the patient was 42-year-old, for COVID-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "Extreme pain in injection site for 3 days"; HEADACHE (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering"; UTERINE SPASM (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "Uterine cramps"; LYMPH NODE PAIN (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "extreme pain in Lymph nodes under left arm for 3 days"; NAUSEA (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "nauseous"; VAGINAL HAEMORRHAGE (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "vaginal bleeding". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site pain, lymph node pain, headache, nausea, vaginal haemorrhage, uterine spasm. Additional information: Patient was taking multivitamins and vitamins. No Other vaccine in four weeks. No COVID prior vaccination. Follow-up attempts completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20220430; Test Name: Nasal Swab; Test Result: Negative ; Comments: COVID test post vaccination COVID test type post vaccination=Nasal Swab,
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adenomyosis; Cow's milk allergy (known allergies: Cow's milk); Gadolinium deposition disease; Major depressive disorder
Andere Medikamente: LITHIUM; PRISTIQ; KLONOPIN
Allergien: -
Vorherige Impfungen: -

VAERS 2259786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 43,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 26.04.2022
Beginn: 27.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Headache Injection site pain Lymph node pain Lymphadenopathy Nausea SARS-CoV-2 test Uterine spasm Vaginal haemorrhage Vaccination site pain

Symptomtext

Extreme pain in injection site for 3 days; extreme pain in Lymph nodes under left arm for 3 days; Headache; nauseous; vaginal bleeding; Uterine cramps; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Apr2022 at 12:00 as dose 3 (booster), single (Lot number: FJ4991) at the age of 43 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "MDD" (unspecified if ongoing); "GAD" (unspecified if ongoing); "Adenomyosis" (unspecified if ongoing); "Cow's milk" (unspecified if ongoing), notes: known allergies: Cow's milk. Concomitant medication(s) included: LITHIUM; PRISTIQ; KLONOPIN. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: FC3183 , Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 10Sep2021, when the patient was 42-year-old, for COVID-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: FC3183 , Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 20Aug2021, when the patient was 42-year-old, for COVID-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "Extreme pain in injection site for 3 days"; HEADACHE (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering"; UTERINE SPASM (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "Uterine cramps"; LYMPH NODE PAIN (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "extreme pain in Lymph nodes under left arm for 3 days"; NAUSEA (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "nauseous"; VAGINAL HAEMORRHAGE (non-serious) with onset 27Apr2022 at 09:00, outcome "recovering", described as "vaginal bleeding". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site pain, lymph node pain, headache, nausea, vaginal haemorrhage, uterine spasm. Additional information: Patient was taking multivitamins and vitamins. No Other vaccine in four weeks. No COVID prior vaccination. Follow-up attempts completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20220430; Test Name: Nasal Swab; Test Result: Negative ; Comments: COVID test post vaccination COVID test type post vaccination=Nasal Swab,
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adenomyosis; Cow's milk allergy (known allergies: Cow's milk); Gadolinium deposition disease; Major depressive disorder
Andere Medikamente: LITHIUM; PRISTIQ; KLONOPIN
Allergien: -
Vorherige Impfungen: -

VAERS 2260431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: ID
Alter: 50,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 16.04.2022
Beginn: 26.04.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Dizziness Exposure to SARS-CoV-2 Fatigue Nasal congestion Nasopharyngitis Nausea Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I knew I had been exposed to COVID-19. Tuesday morning I woke up with sore throat and stuffy nose. I took a home test early morning, it had a faint positive line waited and took another home test later and still a faint line, went to the doctor's office to have test and it was positive. I had 3-4 days very sore throat, congestion. Wednesday Paxlovid started taking that night, cold symptoms eased up, still have fatigue and some dizziness and nauseous.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: COVID-19 Test 04/26/2022- positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's Thyroiditis; IBS
Andere Medikamente: Levothyroxine, Liothyronine, Singular, Allegra, Vitamin C, Cod Liver Oil, St. Johns Wart, Calcium Magnesium Zinc, Manganese B-12, Multi-Vitamin 50+
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2258605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 12.04.2022
Beginn: 19.04.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: SYR / LA

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

Burning mouth syndrome Burning sensation Decreased appetite Dyspepsia Fatigue

Symptomtext

Starting about 1 week after receiving the vaccine, I became very tired, lost my appetite and had developed indigestion. I tried taking some antacids but they didn't seem to help (I usually never get indigestion). Within a few days, it seemed to go away. However, I have had a burning sensation in my mouth off and on for the past 2 years. They're thinking its called burning mouth syndrome but unsure 100%. I am unsure if it started right after receiving my first dose or not. However, its been intermittent and bothersome. The dentist and my PCP have both given me gels, rinses and compounds for it but nothing has helped. Most recently I have been given magic mouth wash (special compound the pharmacist has to make) which hasn't helped. I am going to go to a specialist but won't get in until August.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Liquid Vitamin D3 with K2 and Pro Bono (bone retention dietary supplement)
Allergien: Penicillin; OTC allergy medicine
Vorherige Impfungen: Flu vaccine (12 years ago): felt like I caught the flu, Shingrix: extremely sore arm, fatigued and trembling inside of my head t

VAERS 2258598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NH
Alter: 75,0
Geschlecht: M
Eingang: 29.04.2022
Impfdatum: 14.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 8,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Influenza virus test Malaise Pain Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

I tested positive for COVID-19 04/23/2022. My symptoms was mild and lasted about 4 day. I had a running nose, coughing, sneezing, body aches and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test, flu and PCR.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Pravastatin 40mg; Triamterene 37.5mg; Diltiazem 300mg; Vitamin D3 IU; Lorazepam.
Allergien: No
Vorherige Impfungen: Shingle few years ago.

VAERS 2258449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NJ
Alter: 72,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 19.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Flushing Urticaria

Symptomtext

Broke out in hives 3 days after receiving shot. Mainly located on torso. flushing of the face and neck. More prominent in morning

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HBP, Hogh Cholesterol
Andere Medikamente: Fish oil, calcium, vit. D, Vit. C, Metoprolol, Telmisartan, Crestor
Allergien: None
Vorherige Impfungen: -

VAERS 2256863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: KS
Alter: 71,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 13.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / RA

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

Blood creatinine decreased Blood test normal Blood urea decreased Pruritus Rash

Symptomtext

04/15/2022 ? A few days after my vaccine I began to itch at the bottom base of my skull, and moved up towards the sides of my ears in my hairline. I also now have a bit of a rash on the left and right sides of my forehead. It started to go down my back towards the lower spine, and on the left side of my body as well. I also had some visual rash forming on my chest as well that was itching very badly as well. I was given a prescription for a cream and then when seeing a dermatologist I was given a liquid prescription, clobetasol scalp solution, to help with itching and rash formation in my hairline. It has been helping to soothe the itching. The patch on my chest has cleared up, my side and back are still itching. I have seen general improvement on my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Blood work: Returned with normal numbers. Additional blood test by primary care: Showed a 7 for BUN levels and creatinine was slightly low as well.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Calcification of Heart Artery; History of Hip Replacement; Eye Pressure; Family History of Melanoma.
Andere Medikamente: Baby Aspirin 81mg; Calcium 500mg Vitamin D 500mg; Multivitamin; Atorvastatin 10mg; Triamcinolone Acetonide 0.1%; Clobetasol 0.05% Scalp Solution; Latanoprost Eye Drops; Melatonin 5mg; Zyrtec 10mg; Pepsid AC 20mg; Flonase 50mcg; Sustain Ultr
Allergien: Adderall; Pneumonia vaccines causing swelling in shoulder; Rosuvastatin; Meloxicam; Pravastatin; Mobic; Dextroamphetamine; Crestor; Amphetamine; Prednisolone Acetate.
Vorherige Impfungen: Pneumonia vaccine, Unknown Date, causing swelling in shoulder.

VAERS 2252294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: UT
Alter: 39,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 19.04.2022
Beginn: 25.04.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pruritus Injection site rash

Symptomtext

PATIENT SHOWED A SMALL RASH AND ITCHING AT A SITE ADJACENT TO INJECTION SITE ON ARM. HE NOTICED IT APPROXIMATELY 1 WEEK LATER. NO TREATMENT GIVEN. RASH IS GRADUALLY DISAPPEARING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE KNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: NONE REPORTED
Allergien: NONE KNOWN
Vorherige Impfungen: -

VAERS 2252090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ 4991

mild

Staat: MA
Alter: 72,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 05.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Fatigue Full blood count normal Impaired work ability Laboratory test normal Liver function test normal Loss of personal independence in daily activities Red blood cell sedimentation rate normal Renal function test normal Thyroid function test normal Urine analysis normal

Symptomtext

fatigue interfering with daily activities and work

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Administered - all results normal April 12 & 15 Full PEx and labs done by PCP, i.e., CBC, thyroid, urine CVS, Sed Rate, renal, liver
Aktuelle Erkrankungen: None symptomatic
Vorgeschichte: Hypertension, essential Hypercholesterolemia osteopenia
Andere Medikamente: lisinopril 10 MG QD, rosuvastatin 5 MG QD, Vit D-3 800 IU QD, Vit B-12 2,500 mcg QD, Calcium carbonate 600 MG QD
Allergien: Penicillin Sulfa
Vorherige Impfungen: -

VAERS 2251813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 62,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 17.03.2022
Beginn: 20.03.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

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

Contusion Pain in extremity

Symptomtext

arm is hurting, like there is a bruise; arm is hurting, like there is a bruise; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old male patient received BNT162b2 (BNT162B2), on 17Mar2022 as dose 3 (booster), single (Lot number: FJ4991) at the age of 62 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Single, LOT- EW0187), administration date: 23May2021, when the patient was 61-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, Single, LOT- EW0180), administration date: 06Jun2021, when the patient was 61-year-old, for COVID-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious), CONTUSION (non-serious) all with onset 20Mar2022, outcome "not recovered" and all described as "arm is hurting, like there is a bruise". Additional information: No other products reported. No investigations reported. Reporter stated he was listening to the radio right now and stated he was getting a reaction to the Pfizer Covid shot. Stated he got had shot on 17Mar2022 and his arm was still like it was bruised, clarified there was no bruise but it felt like a bruise, started about 3 days after the shot, stated it was his left arm. Stated that it was his third dose. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other conditions: no
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2246211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 66,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / AR

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

Blood test abnormal Petechiae Rash Rash pruritic Tenderness

Symptomtext

I started to notice tenderness spreading from mid-low thoracic area of back. I woke up with a rash on my back and it spread from my back to my shoulders and chest throughout the day, and then the day after I was covered from head to toe in the rash. This rash came with horrible itching and pain. The rash is now subsiding quite a bit however the itching is still constant and all over. I went to urgent care and was not given any prescriptions. I was told to use Calamine lotion and Benadryl. the Benadryl did not help much and the lotion did not help and caused dryness of skin. I was given another prescription for an antihistamine that has helped very little and aloe vera seems to help with itching on the back. I went to urgent care a second time because there were blood spots on my chest. I saw my rheumatologist as well who did not know as to why or where my rash came from. I am still continuing to have itching everywhere and the rash is slowly going away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Blood Tests: Several abnormal blood results.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Rheumatoid Arthritis, Sjogren's, Fibromyalgia, COPD, Glaucoma
Andere Medikamente: Lipitor, Clozapine, Cymbalta, Pamoate, Trelegy, Eye Drops
Allergien: Morphine Drugs, Sulfa Drugs, Iodine, Amoxycillin, Blueberries, Cranberries, Kiwi, Olive Oil, Pinto Beans, Sugar, Walnuts, Sunflower Seeds
Vorherige Impfungen: -

VAERS 2244094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 01.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

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

Symptomtext

Developed Covid symptoms and tested negative on April 11, 2022. Tested positive on April 13, 2022. Began Paxlovid treatment on April 15, 2022 for five days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Labs performed at Hospital on April 15, 2022.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure and Cholesterol
Andere Medikamente: Atorvastatin 40 MG/day Metoprolol ER Succinate 100 MG/day Lisinopril 40 MG/day 1 low dose aspirin/day
Allergien: None
Vorherige Impfungen: -

VAERS 2243097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OR
Alter: 58,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 18.03.2022
Beginn: 18.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Abdominal pain

Symptomtext

Immediately after receiving the shot, I experienced sharp pain in my abdomen/the pain has progressed and keeps getting worse and worse; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Mar2022 at 13:15 as dose 4 (booster), single (Lot number: FJ4991) at the age of 58 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High BP" (unspecified if ongoing); "Diabetes" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL; SPIRONOLACTONE; METFORMIN; PRAVASTATIN. Vaccination history included: BNT162b2 (Dose Number: 3, Batch/Lot No: FC3183, Location of injection: Arm Right, Vaccine Administration Time: 03:15 AM), administration date: 24Sep2021, when the patient was 57-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: EN6198, Location of injection: Arm Right, Vaccine Administration Time: 12:00 AM), administration date: 27Feb2021, when the patient was 56-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL9269, Location of injection: Arm Left, Vaccine Administration Time: 01:00 AM), administration date: 06Feb2021, when the patient was 56-year-old, for Covid-19 immunization. The following information was reported: ABDOMINAL PAIN (non-serious) with onset 18Mar2022 at 13:15, outcome "not recovered", described as "Immediately after receiving the shot, I experienced sharp pain in my abdomen/the pain has progressed and keeps getting worse and worse". The events "immediately after receiving the shot, i experienced sharp pain in my abdomen/the pain has progressed and keeps getting worse and worse" required physician office visit and emergency room visit. Therapeutic measures were not taken as a result of abdominal pain. Additional Information: : Immediately after receiving the shot, I experienced sharp pain in my abdomen. I did not tell the pharmacy technician who gave me the shot because I thought this was temporary and it would subside. Unfortunately the pain has progressed and keeps getting worse and worse. Facility type vaccine: Pharmacy or Drug Store. If other vaccine in four weeks: No. If covid prior vaccination: No. If covid tested post vaccination: No. Known allergies: Unknown. Other medical history: Diabetes, High BP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Diabetes
Andere Medikamente: METOPROLOL; SPIRONOLACTONE; METFORMIN; PRAVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2238100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: MD
Alter: 61,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 14.04.2022
Beginn: 16.04.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Cyanosis Rash erythematous

Symptomtext

Reddish blue rash from hand all the way up to the elbow on right arm. No tingling or numbness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: cholesterol, anxiety, diabetes, acid reflux
Andere Medikamente: Temazepam , potassium choride, clopidogrel, gabapentin, hctz, novolog, omeperazole, doxazosin, sertraline, rosuvastatin,
Allergien: nka
Vorherige Impfungen: -

VAERS 2237809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 07.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

Abdominal pain upper Back pain Blood pressure measurement Body temperature Erythema Pain in extremity Skin odour abnormal Vaginal odour

Symptomtext

that her arms feels weepy, it is red, and she has a lot of pain/She says her right arm is red and lumpy; that her arms feels weepy, it is red, and she has a lot of pain; feel pain in her back, her stomach; feel pain in her back, her stomach/stomach is hurting; she noticed a funny weird odor coming from her privates and rectum; she noticed a funny weird odor coming from her privates and rectum/she also developed an odor which she never had before; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID: (159558). The reporter is the patient. A 67-year-old female patient received BNT162b2 (BNT162B2), on 07Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 67 years, in right arm for covid-19 immunisation; varicella zoster vaccine rge (cho) (SHINGRIX), on 07Apr2022 as dose number unknown, 50 ug single (Lot number: VL10PK), in right arm for herpes zoster. The patient's relevant medical history included: "Fibromyalgia" (unspecified if ongoing); "Blood pressure high" (unspecified if ongoing); "for her stomach" (unspecified if ongoing); "she got a little brace on her left arm for arthritis in her shoulder bone" (unspecified if ongoing), notes: she got a little brace on her left arm for arthritis in her shoulder bone. Concomitant medication(s) included: METOPROLOL SUCCINATE oral taken for hypertension; OMEPRAZOLE oral taken for abdominal discomfort; LISINOPRIL oral taken for hypertension; AMLODIPINE BESYLATE oral taken for hypertension; ISOSORBIDE DINITRATE oral taken for hypertension. Vaccination history included: BNT162b2 (first dose, 24Feb2021, it was Pfizer EL9262; Expiry date: May2021), administration date: 24Feb2021, when the patient was 66-year-old, for COVID-19 immunization; BNT162b2 (second dose; LOT: EN6199; Expiry date: Jun2021), administration date: 17Mar2021, when the patient was 66-year-old, for COVID-19 immunization; BNT162b2 (third dose or first booster of Pfizer COVID-19 vaccine was given 25Sep2021 of Pfizer LOT: E3592, which she says she can't make it out, it is, either an F or a T, clarified to LOT: FE3592.), administration date: 25Sep2021, when the patient was 66-year-old, for COVID-19 immunization; Shingrix (had a dose of this before in 2019), administration date: 2019, for Shingles vaccine, reaction(s): "No adverse event". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 07Apr2022, outcome "unknown", described as "that her arms feels weepy, it is red, and she has a lot of pain"; ERYTHEMA (non-serious) with onset 07Apr2022, outcome "unknown", described as "that her arms feels weepy, it is red, and she has a lot of pain/She says her right arm is red and lumpy"; BACK PAIN (non-serious) with onset Apr2022, outcome "unknown", described as "feel pain in her back, her stomach"; ABDOMINAL PAIN UPPER (non-serious) with onset Apr2022, outcome "unknown", described as "feel pain in her back, her stomach/stomach is hurting"; VAGINAL ODOUR (non-serious) with onset Apr2022, outcome "unknown", described as "she noticed a funny weird odor coming from her privates and rectum"; SKIN ODOUR ABNORMAL (non-serious) with onset Apr2022, outcome "unknown", described as "she noticed a funny weird odor coming from her privates and rectum/she also developed an odor which she never had before". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of erythema, pain in extremity. Additional Information: The caller is a consumer. She indicates that yesterday she received both the pfizer covid 19 vaccine (gray cap, 2nd booster, 4 doses so far in total) and the Shingrix vaccine (Shingles Vaccination). She received both vaccines in the same arm. She indicates that her arms feels weepy, it is red, and she has a lot of pain. she also mentioned that after getting the vaccine she started to feel pain in her back, her stomach, and she noticed a funny weird odor coming from her privates and rectum. she wiped and she smelled very bad. she wants to know if these are side effects of the 2nd booster. Other Medical Conditions: Caller says she has fibromyalgia, maybe that is why she is hurting so. No further details provided about her fibromyalgia. Concomitant medications: Caller says she had taken her medications before going to get her shots, which were not new medications, she takes them every day in the morning and evening. She says she took them before she went pharmacy, which was around 09:30. She says she took her Metoprolol Succinate 25mg, she took that and took her Omeprazole for her stomach which is 40mg, and she took her Lisinopril tablet which is 40mg, and she took her blood pressure Amlodipine besylate 5mg tablets, that's what she took before she went. Caller says for her Lisinopril she was taking 40mg once a day, then the day before yesterday her blood pressure was 189/90 something and her doctor increased it but she didn't increase it so she took only 40mg yesterday instead of taking the 80mg a day. Caller clarifies that when she went to the doctor's office the day before yesterday and they increased her medication to 80mg, so her dose was increased to two instead of one tablets a day. Additional information on concomitant drugs: Caller says she has been on Metoprolol succinate for a long time, a couple years, probably started it two years ago; Dosage text: 25mg once a day in the morning by mouth; Omeprazole: Caller says this is like Prilosec, it is the generic for that, which she has been on it forever but she doesn't know when she started, been on it for like four years, Dosage text: 40mg once a day by mouth; Lisinopril: Caller says that she started taking Lisinopril about two years ago. Dosage text: 40mg once a day by mouth; Amlodipine besylate: Caller says she started taking it probably about two years ago for her blood pressure. Dosage text: 5mg once a day in the morning by mouth; Isosorbide Dinitrate: Caller says she thinks her heart doctor put her on it almost three years ago. Dosage text: 10mg, one in the morning and one in the evening by mouth. caller who yesterday went to (Name withheld) pharmacy and got her second booster dose of Pfizer COVID-19 vaccine and also a shingles shot in her right arm. Agent reports caller said that it is all weepy and it's all red and in a lot of pain. Agent reports caller says she took Advil last night and it didn't help her. Agent reports caller says she also developed an odor which she never had before. Agent says caller wants to confirm if this is a side effect for Pfizer COVID-19 vaccine second booster. Caller clarifies that yesterday was her second booster or fourth dose of the Pfizer COVID-19 vaccine and along with that she got her shingles shot, which later was clarified to Shingrix. Pfizer COVID-19 vaccine: Caller says she got her first dose 24Feb2021, it was Pfizer EL9262 with EXP: May2021. She says NDC was not provided on her handwritten vaccine card for this dose. She says her second dose of Pfizer COVID-19 vaccine was 17Mar2021 of LOT: EN6199, EXP: Jun2021 and was also given at same location. She says NDC was not provided. Caller says her third dose or first booster of Pfizer COVID-19 vaccine was given 25Sep2021 of Pfizer LOT: E3592, which she says she can't make it out, it is either an F or a T, clarified to LOT: FE3592. She says the NDC/EXP are not provided for her third dose which was given at (Name withheld) store number (Number withheld) . She says she got her Pfizer COVID-19 fourth dose or second booster yesterday, which on the prescription it says it was for 12 plus and gray cap. She provides LOT: FJ4991 or 4091, and clarifies that LOT is handwritten and after the four it has a 9 or a 0 which is connected to the other nine after that. EXP: Unknown, not provided on handwritten vaccine card. Caller provides NDC: 59267-1025-01 from the paperwork (Name withheld) gave her for the Pfizer COVID- 19 vaccine. Shingrix: Caller says that the only information she has on this shot she got yesterday is that it was a shingles single dose VL10PK with NDC: 58160-0823-11, refrigerated. She says she thinks she had a dose of this before in 2019, and they told her she doesn't need another one again that this second one should last. She says she thinks had the first one in 2019, and she was ok when had it, but this one seems to make her sick, though she doesn't know which it would be, the shingles or COVID-19 vaccine. Caller says she doesn't have NDC/LOT/EXP to provide for her previous dose of the Shingrix vaccine. AE: Caller says her stomach is hurting. She says her vaccine doses were done in her right arm because she got a little brace on her left arm for arthritis in her shoulder bone or something like. She says they said she could do both shots in her right arm. She says her right arm is red and lumpy, she put ice on it yesterday. She says they said she could rub it, and she put an ice pack on it because it was hard and had pain inside, so she just stopped. She says she had a temperature of 99.3 degrees Fahrenheit this morning when she checked it. She says the pain is still there so she looked in the mirror and her arm was red. She says she didn't look at it last night, she put the ice pack on it and it was lumpy and hard in both areas where he gave her the shots. She says that it is just a hot long red line kind of like one and a half inches down, and across it is three inches long on her right arm. Advil Liqui-Gels AE/PC: Caller says she took Advil yesterday to see if that would help after she tried to put ice on it. She clarifies it was Advil gel caps that are green, 200mg, and she took one Advil Liqui-Gels and it didn't help her. Advil Liqui-Gels UPC: Unknown, caller says the barcode is not on the bottle, LOT: R94350, EXP: Jul2024, PAA 083151. AE Treatment: Caller says she has just been rubbing it to make the medicine circulate, she thought maybe must in one place that didn't go all way thru. She says when he gave her the Pfizer shot he did it real slow and didn't punch it in to make sure the medication goes thru, he injected it real, real slow, not fast like other shot where they stuck you and that is it. She says this one for both shots he did real, real slow. She says she walked home yesterday and it was hurting then, the pharmacy was just right down the street about a half mile or so, and her arm was hurting bad. She says she got home and laid down and got up and put an ice pack on it, then after that thought she would go ahead and take Advil since the ice pack was too hard, it was in the freezer and when she put on her arm it was hurting real bad, it couldn't touch. The patient reported a product complain. Description of Product Complaint: Description of complaint: Advil Liqui-Gels: Caller says she took Advil yesterday to see if that would help after she tried to put ice on it. She clarifies it was Advil gel caps that are green, 200mg, and she took one Advil Liqui-Gels and it didn't help her. Advil Liqui-Gels UPC: Unknown, caller says the barcode is not on the bottle, LOT: R94350, EXP: Jul2024, PAA 083151. Product strength and count size dispensed: 200mg, 20 gel caps No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Test Date: 20220406; Test Name: blood pressure; Result Unstructured Data: Test Result:189/90; Test Date: 20220408; Test Name: temperature; Result Unstructured Data: Test Result:99.3 Fahrenheit; Comments: this morning
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis (she got a little brace on her left arm for arthritis in her shoulder bone); Blood pressure high; Fibromyalgia; Stomach discomfort
Andere Medikamente: METOPROLOL SUCCINATE; OMEPRAZOLE; LISINOPRIL; AMLODIPINE BESYLATE; ISOSORBIDE DINITRATE
Allergien: -
Vorherige Impfungen: -

VAERS 2236500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: WA
Alter: 70,0
Geschlecht: F
Eingang: 15.04.2022
Impfdatum: 15.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Injection site pain Product administered at inappropriate site

Symptomtext

The following patient came in today for a Pfizer IM vaccine. Both tech and I explained to the patient the correct area of deltoid administration is two fingers down and above the armpit, in that triangle area. The patient insisted on us doing it lower to "avoid the tendons" - I explained that if I did it any lower it may actually hit tendons/nerves. I indicated with my glove where I would give the vaccine, which is in the correct area, and the patient said "that was acceptable" - however, when I gave it the patient said "it hurt and it was not in the correct muscle." DPM and PCP pharmacists have been notified and suggested a report to be made for documentation purposes. Tried to reach the patient but unable to reach by phone.

Weitere VAERSDATA-Felder

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

VAERS 2233910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: MD
Alter: 59,0
Geschlecht: F
Eingang: 14.04.2022
Impfdatum: 06.04.2022
Beginn: 10.04.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pain Injection site pruritus

Symptomtext

Over 3 days prior to the administration, patient is experiencing itching and mild pain at injection site. This adverse is still occurring after week. You tried hydrocortisone for a couple without resolution

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: ask during dermatologist appointment
Aktuelle Erkrankungen: none
Vorgeschichte: DM, blood pressure, seizures, cholesterol, anxiety
Andere Medikamente: DM, blood pressure, seizures, cholesterol, anxiety
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2233877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 14.04.2022
Impfdatum: 05.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal distension Headache Intermenstrual bleeding

Symptomtext

Since getting my third booster shot I started getting bloated, headaches, bleeding (period) and its already past the time I usually have it. I have been bleeding since the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Mushrooms, Sulfa drugs, amoxicillin, penicillin
Vorherige Impfungen: T dap

VAERS 2228784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: GA
Alter: 75,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Lethargy Pain in extremity Peripheral swelling

Symptomtext

arm aching, arm swollen, lethargic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: zyrtec, vitamin d
Allergien: -
Vorherige Impfungen: Pfizer 75 10/11/2021 lethargic

VAERS 2226825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Chills Nausea

Symptomtext

Nausea and intermittent chills for ca. 2 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Depression, back injury
Andere Medikamente: 1300 mg tylenol Metoprolol ER 50 mg Sertraline Bupropion Valacyclovir Losartan Synthroid Multivitamin, vit D, glucosamine/chondroitin
Allergien: Food: fennel
Vorherige Impfungen: -

VAERS 2225832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 09.04.2022
Beginn: 09.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Headache Pain Pyrexia

Symptomtext

Fever and achiness at 6 hours after vaccine. Headache now at 48 hour mark. Headache will not subside despite multiple doses of Tylenol

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HBP
Andere Medikamente: Lisinopril 5 mg daily Vitamin D 200 mcg daily
Allergien: Sulfa drugs contrast dye Iodine (shellfish)
Vorherige Impfungen: -

VAERS 2214917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

mild

Staat: FL
Alter: 26,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Oropharyngeal pain Pain in extremity

Symptomtext

stated her throat was hurting--took benadryl and it subsided. also stated her arm was hurting in some areas and numb from her elbow down stayed longer than 15 minutes with the arm not getting better

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: may have autoimmune disorder not currently identified
Vorgeschichte: -
Andere Medikamente: benadryl
Allergien: lactose, mildly to other foods and pollens
Vorherige Impfungen: -

VAERS 2214517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 30.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: SYR / LA

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

Blood test Eye pain Ocular discomfort Vision blurred

Symptomtext

Pain, discomfort, blurred vision in left and right eye. No treatment yet. No outcome yet. Might be MS exacerbation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: Blood work (4/4/22) and Visual field test (pending schedule)
Aktuelle Erkrankungen: None
Vorgeschichte: Multiple sclerosis
Andere Medikamente: Birth control pill, vitamin D, Tumeric, prenatal multivitamin
Allergien: None
Vorherige Impfungen: MS exacerbation, optic neuritis, 9-11-21, flu quad.

VAERS 2213937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: GA
Alter: 60,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 01.04.2022
Beginn: 02.04.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Erythema Lymphadenopathy Pain Swelling

Symptomtext

Patient states that around 24 hours after she received the second Pfizer covid vaccine she started to experience swelling in the lymph nodes of her left armpit. Three days later she is still having some pain and swelling and redness on the left side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Hip Pain
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2195009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OR
Alter: 63,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 21.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Myalgia

Symptomtext

Administered 4th dose of Pfizer when patient was not immunocompromised per current guidelines, reported muscle pain that went away with Aleve

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: HTN
Andere Medikamente: Lisinopril
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2195005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

mild

Staat: OR
Alter: 63,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Myalgia

Symptomtext

Administered 4th dose of Pfizer when patient was not immunocompromised per current guidelines, reported muscle pain that went away with Aleve

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: See above
Andere Medikamente: Dorzoloamide, Timolol, Metformin, HCTZ, Lisinopril, Amlodipine, Flomax
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2710775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CO
Alter: 68,0
Geschlecht: F
Eingang: 07.11.2023
Impfdatum: 06.06.2022
Beginn: 25.06.2023
Tage bis Beginn: 384,0
Dosis: UNK
Route/Site: - / -

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

Diffuse large B-cell lymphoma Positron emission tomogram abnormal

Symptomtext

I now have Diffuse Large B cell Lymphoma

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diffuse large B-cell lymphoma
Hospital-Tage: -
Labordaten: I have had a Petscan that shows the Lymphoma throughout my body.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood sugar and cholesterol
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2782555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 27.10.2023
Impfdatum: 11.05.2022
Beginn: 27.09.2022
Tage bis Beginn: 139,0
Dosis: 4
Route/Site: OT / -

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test positive

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; Moderna bivalent booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 64-year-old male patient received bnt162b2 (BNT162B2), on 11May2022 at 14:11 as dose 4 (booster), single (Lot number: FJ4991) at the age of 64 years intramuscular, in arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 01Apr2021 at 12:40 as dose 1, single (Lot number: EP7534), in arm, on 22Apr2021 at 15:42 as dose 2, single (Lot number: ER8737), in arm and on 30Aug2021 at 10:22 as dose 3 (booster), single (Lot number: FE3592), in arm, all intramuscular for covid-19 immunisation; davesomeran, elasomeran (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), on 27Sep2022 as dose 5 (booster), single (Lot number: AS716413) for covid-19 immunisation. The patient's relevant medical history included: "GERD" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 27Sep2022, outcome "recovered", described as "Moderna bivalent booster"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 14Aug2023 at 14:00, outcome "recovered" (19Aug2023) and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Aug2023) Positive, notes: 2 noon; (19Aug2023) Negative; (21Aug2023) Negative; (26Aug2023) Positive, notes: am; (27Aug2023) Positive; (28Aug2023) Positive; (29Aug2023) Positive; (30Aug2023) Positive; (31Aug2023) Positive; (01Sep2023) Positive; (02Sep2023) Positive; (03Sep2023) Positive; (04Sep2023) Positive; (05Sep2023) Positive; (06Sep2023) Positive; (07Sep2023) Positive; (08Sep2023) Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid from 14Aug2023 to 19Aug2023. Based on Investigational Results of Lot number # FE3592, EP7534, ER8737: Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EP7534, ER8737, FE3592, FJ4991 were investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EP7534, fill lot EP7532, and the formulated drug product lot EP7528. The final scope included the reported finished goods lot ER8737, fill lot EW3426, and the formulated drug product lot EP8586. The final scope was determined to be the reported finished goods lot FE3592, fill lot FF2553, and the bulk formulated drug product lot FA9141. The final scope was determined to be the reported finished goods lot FJ4991, fill lot FJ4988, and the bulk formulated drug product lot FJ4985. A complaint sample was not returned, and photographs were not received. There were no deviations that may have caused a complaint of this nature. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Based on Investigational Results of Lot number # FJ4991: Conclusion of Previously Completed Investigation (FCI/SI/OffCI): The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE INJECTABLE lot FJ4991 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FJ4991, fill lot FJ4988, and the bulk formulated drug product lot FJ4985. A complaint sample was not returned. The following potential quality issue was identified during the investigation: all test points of TFF permeate stream flow meters failed during their annual calibration. A manufacturing investigation under PR 7130626 is investigating the reported complaint. Any quality issues identified, root cause or corrective/preventative actions assigned, and the final quality of the batch will be documented in the manufacturing investigation PR 7130626. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received. Follow-up (21Oct2023): Follow-up attempts are completed. No further information is expected. Follow-up (19Oct2023): This is a spontaneous follow-up report received from a contactable consumer. This consumer (Patient) reported in response to Non-HCP letter sent that included: Updated information: Reporter & patient name updated. Patient height & weight added. Lab test added. Suspect recoded & new suspect added. New event added as Moderna bivalent booster. Drug ineffective & COVID-19 events onset/stop date added and outcome updated. Follow-up (23Oct2023): This is a follow-up report from product quality group providing investigation results. Updated information included: Investigation results reported for lot number FE3592, FJ4991, EP7534, ER8737.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300285847 same patient, different drug/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230814; Test Name: Tested covid; Test Result: Positive ; Comments: 2 noon; Test Date: 20230819; Test Name: Tested covid; Test Result: Negative ; Test Date: 20230821; Test Name: Tested covid; Test Result: Negative ; Test Date: 20230826; Test Name: Tested covid; Test Result: Positive ; Comments: am; Test Date: 20230827; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230828; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230829; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230830; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230831; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230901; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230902; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230903; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230904; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230905; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230906; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230907; Test Name: Tested covid; Test Result: Positive ; Test Date: 20230908; Test Name: Tested covid; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD; High cholesterol
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2687314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CO
Alter: 66,0
Geschlecht: F
Eingang: 27.09.2023
Impfdatum: 12.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / RA

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

Trigger finger

Symptomtext

HAS BEEN EXPERIENCING TRIGGER FINGER IN LEFT HAND AFTER COVID VACCINATIONS. MOST OFFTENC OCCURING AFTER HOLDING FORKS AND KNIFFS (FINE MOTOR ACTIVITIES) HAS HAPPENED UP TO 4 TIMES DURING ONE MEAL. OCCASIONALLY RIGHT HAND HAS SIMILAR ISSUES AND PAIN. PATIENT HAS BEEN USING A BRACE AS WELL. HAS HAD SOME UPPER ARM PAIN AS WELL, MORE IN THE LEFT ARM THAN IN THE RIGHT. Had a friend report similar events after the vaccines prompting her to come in for the same.

Weitere VAERSDATA-Felder

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

VAERS 2675230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

gering

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 22.08.2023
Impfdatum: 09.07.2022
Beginn: 01.08.2023
Tage bis Beginn: 388,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Drug ineffective

Symptomtext

COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Jul2022 as dose 4 (booster), single (Lot number: fj4991) at the age of 61 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2023, outcome "unknown" and all described as "COVID-19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid from 10Aug2023 to 15Aug2023.; Sender's Comments: Based on the known the information available the Causal relation between the events Drug ineffective, Covid 19 and suspect drug cannot be excluded completely

Weitere VAERSDATA-Felder

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

VAERS 2671015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

gering

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 14.08.2023
Impfdatum: 17.04.2022
Beginn: 03.12.2022
Tage bis Beginn: 230,0
Dosis: 4
Route/Site: - / RA

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

COVID-19 Interchange of vaccine products Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; vaccine brand other=Moderna; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Dec2020 as dose 1, single (Lot number: EH9899), in right arm, on 11Jan2021 as dose 2, single (Lot number: EL1283), in left arm, on 28Sep2021 as dose 3 (booster), single (Lot number: FF2587), in left arm and on 17Apr2022 as dose 4 (booster), single (Lot number: Fj4991) at the age of 64 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 03Dec2022 as dose 5 (booster), single (Lot number: 041H22A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hyperlipidemia" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 03Dec2022, outcome "unknown", described as "vaccine brand other=Moderna"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient received Paxlovid as treatment from 02Aug2023 to 07Aug2023. The patient started Paxlovid day 2 of COVID 19, 2 days after 5 day course of Paxlovid (day 7 of onset of symptoms), developed sore throat & runny nose, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hyperlipidemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2667710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: TN
Alter: 68,0
Geschlecht: F
Eingang: 08.08.2023
Impfdatum: 06.07.2022
Beginn: 11.10.2022
Tage bis Beginn: 97,0
Dosis: 1
Route/Site: - / -

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

Breakthrough COVID-19

Symptomtext

Breakthrough Covid-19 Infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breakthrough COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Not listed
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2642453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 08.06.2023
Impfdatum: 23.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Drug ineffective Interchange of vaccine products SARS-CoV-2 test Suspected COVID-19

Symptomtext

Got Covid in early Apr2023; Got Covid in early Apr2023; Interchange of vaccine products; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). A 42-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Jul2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 42 years for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), in Feb2021 as dose 1, single (Batch/Lot number: unknown), in Mar2021 as dose 2, single (Batch/Lot number: unknown) and in Oct2021 as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "endometriosis" (unspecified if ongoing); "severe varicose veins with treatment" (unspecified if ongoing); "history of bell's palsy" (unspecified if ongoing); "Allergy" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 23Jul2022, outcome "unknown"; DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant) all with onset Apr2023, outcome "unknown" and all described as "Got Covid in early Apr2023". The event "got covid in early apr2023" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown Results. It was unknown if therapeutic measures were taken as a result of drug ineffective, suspected covid-19. Clinical course: Patient had no prolonged hospitalization. It was unknown that patient received any other vaccines within 4 weeks prior to the COVID vaccine. There were other medications the patient received within 2 weeks of vaccination. Seeking medical care by primary physician. Prior to vaccination, the patient was not diagnosed with COVID-19. It was unknown if the patient had any known allergies. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300211339 same patient and drug, different event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Drug ineffective
Hospital-Tage: -
Labordaten: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Bell's palsy; Endometriosis; Varicose veins
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2642405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 07.06.2023
Impfdatum: 23.07.2022
Beginn: 01.04.2023
Tage bis Beginn: 252,0
Dosis: 4
Route/Site: OT / -

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

Menstruation irregular Post-acute COVID-19 syndrome SARS-CoV-2 test

Symptomtext

menstrual irregularities-delay/early-indicates these irregularities happened after receiving each vaccine and is occurring now; Got Covid in early April 2023/migraines/diminished smell continues/fatigue/nausea/joint pains/burning sensation legs/arms/muscle pains/dizziness/blurry vision/fainted in shower/loss of appetite; This spontaneous case was reported by a non-health professional and describes the occurrence of MENSTRUATION IRREGULAR (menstrual irregularities-delay/early-indicates these irregularities happened after receiving each vaccine and is occurring now) and POST-ACUTE COVID-19 SYNDROME (Got Covid in early April 2023/migraines/diminished smell continues/fatigue/nausea/joint pains/burning sensation legs/arms/muscle pains/dizziness/blurry vision/fainted in shower/loss of appetite) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 prophylaxis. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for COVID-19 vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19 previously. It was unknown if the patient received any other vaccines within 4 weeks prior to the COVID-19 vaccine or not. The patient's past medical history included Varicose veins (severe varicose veins with treatment). Concurrent medical conditions included Endometriosis and Bell's palsy. On 23-Jul-2022, the patient received fourth dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form and first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In April 2023, the patient experienced POST-ACUTE COVID-19 SYNDROME (Got Covid in early April 2023/migraines/diminished smell continues/fatigue/nausea/joint pains/burning sensation legs/arms/muscle pains/dizziness/blurry vision/fainted in shower/loss of appetite). On an unknown date, the patient experienced MENSTRUATION IRREGULAR (menstrual irregularities-delay/early-indicates these irregularities happened after receiving each vaccine and is occurring now). At the time of the report, MENSTRUATION IRREGULAR (menstrual irregularities-delay/early-indicates these irregularities happened after receiving each vaccine and is occurring now) had not resolved and POST-ACUTE COVID-19 SYNDROME (Got Covid in early April 2023/migraines/diminished smell continues/fatigue/nausea/joint pains/burning sensation legs/arms/muscle pains/dizziness/blurry vision/fainted in shower/loss of appetite) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In April 2023, SARS-CoV-2 test: Positive. No concomitant medication information was provided. It was reported that the patient had received fourth dose (second booster) of Pfizer vaccine on 23-Jul-2022 with lot number FJ4991. At the time of reporting, the patient felt like she might have long-Covid symptoms as the patient was experiencing migraines, diminished smell continued, fatigue, nausea, joint pains, burning sensation in legs/arms, muscle pains, dizziness/blurry vision, fainted in shower, loss of appetite and menstrual irregularities-delay/early. The patient indicated that these irregularities happened after receiving each vaccine and were occurring at the time of reporting as well. Patient was seeking medical care from primary physician. Treatment medication information was not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Menstruation irregular
Hospital-Tage: -
Labordaten: Test Date: 202304; Test Name: COVID-19 test; Test Result: Positive
Aktuelle Erkrankungen: Bell's palsy; Endometriosis
Vorgeschichte: Medical History/Concurrent Conditions: Varicose veins (severe varicose veins with treatment); Comments: Prior to the vaccination, the patient was not diagnosed with COVID-19 previously. It was unknown if the patient received any other vaccines within 4 weeks prior to the COVID-19 vaccine or not.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2639130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: NM
Alter: 67,0
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 18.07.2022
Beginn: 10.08.2022
Tage bis Beginn: 23,0
Dosis: 4
Route/Site: IM / RA

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

Eye discharge Magnetic resonance imaging abnormal Multiple sclerosis Optic neuritis Vision blurred

Symptomtext

Experienced Optic Neuritis on left eye. A dark brown film covered my left eye, which when looking at a person, I could not see their face and it was accompanied by a blurry peripheral view. For 3 days, the brown film was light until it became darker and I could not see a person's face and lasted around 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye discharge
Hospital-Tage: -
Labordaten: I had several eye tests on August 16, 17 and 24, 2022. An MRI was taken on October 4, 2022. The MRI results verified that I had Multiple Sclerosis (MS), which affected my Optic Nerve.
Aktuelle Erkrankungen: No
Vorgeschichte: Sinusitis
Andere Medikamente: Omeprazole, Flovent, Montelukast, Vitamin D3, Calcium Citrate
Allergien: Tizanidine
Vorherige Impfungen: -

VAERS 2634300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: OR
Alter: 74,0
Geschlecht: F
Eingang: 19.05.2023
Impfdatum: 16.05.2022
Beginn: 09.09.2022
Tage bis Beginn: 116,0
Dosis: 4
Route/Site: IM / UN

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

Bowel movement irregularity Cholelithiasis Magnetic resonance imaging abdominal abnormal Ultrasound abdomen abnormal

Symptomtext

In September of 2022, I started having trouble with bowel movement. I was advised to go to urgent care or emergency department. After an MRI and Ultrasound, it was recommended that I have a gallbladder removal. The surgeon stated I had a very large gallstone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bowel movement irregularity
Hospital-Tage: 2,0
Labordaten: MRI, abnormal, 09/2022; Ultrasound, abnormal, 09/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Osteoporosis; Low Thyroid; Morbid Obesity
Andere Medikamente: Calcium; vitamin D3; losartan; levothyroxine; atorvastatin
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2629463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

gering

Staat: CA
Alter: 50,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 14.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / RA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 51-year-old male patient received BNT162b2 (BNT162B2), on 14Jul2022 as dose number unknown, single (Lot number: Fj4991) at the age of 50 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Obesity" (unspecified if ongoing). The patient had no known allergy. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 including Paxlovid from Apr2023 to 03May2023. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2624851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 23.08.2022
Beginn: 30.12.2022
Tage bis Beginn: 129,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 4 vaccines Moderna 3/1/21 Lot# 010A21A; Moderna 3/29/21 Lot# 007B21A; Moderna 11/7/21 Lot# 039F21A; Pfizer 8/23/22 Lot# FJ4991

Weitere VAERSDATA-Felder

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

VAERS 2621118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: TX
Alter: -
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

Vaccination site erythema Vaccination site ulcer

Symptomtext

Half inch diameter redness; non healing sore at the inoculation site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 83-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FJ4991), in right arm for covid-19 immunisation. The patient's relevant medical history included: "COPD" (unspecified if ongoing), notes: Other medical history: COPD, High Blood Pressure, Gout, Anemia; "High Blood Pressure" (unspecified if ongoing), notes: Other medical history: COPD, High Blood Pressure, Gout, Anemia; "Gout" (unspecified if ongoing), notes: Other medical history: COPD, High Blood Pressure, Gout, Anemia; "Anemia" (unspecified if ongoing), notes: Other medical history: COPD, High Blood Pressure, Gout, Anemia. Concomitant medication(s) included: IRON; CALCIUM; LOSARTAN; B-12; SIMVASTATIN; ALLOPUR. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer.), for COVID-19 immunization; Bnt162b2 (product: Pfizer-BioNTech,, lot number: 30/4s8a,, dose number: DOSE 3 (BOOSTER), SINGLE, vaccine location: left arm), for COVID-19 immunization. The following information was reported: VACCINATION SITE ERYTHEMA (non-serious), outcome "not recovered", described as "Half inch diameter redness"; VACCINATION SITE ULCER (non-serious), outcome "not recovered", described as "non healing sore at the inoculation site". Therapeutic measures were not taken as a result of vaccination site erythema, vaccination site ulcer. Additional information: Half inch diameter redness and non healing sore at the inoculation site since the day of the third booster on Jul2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anemia (Other medical history: COPD, High Blood Pressure, Gout, Anemia); Blood pressure high (Other medical history: COPD, High Blood Pressure, Gout, Anemia); COPD (Other medical history: COPD, High Blood Pressure, Gout, Anemia); Gout (Other medical history: COPD, High Blood Pressure, Gout, Anemia)
Andere Medikamente: IRON; CALCIUM; LOSARTAN; B-12; SIMVASTATIN; ALLOPUR
Allergien: -
Vorherige Impfungen: -

VAERS 2621075

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: WI
Alter: 54,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 22.04.2022
Beginn: 01.06.2022
Tage bis Beginn: 40,0
Dosis: UNK
Route/Site: IM / RA

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

Angiogram Dysgraphia Feeling abnormal Loss of personal independence in daily activities Magnetic resonance imaging

Symptomtext

I?m not sure of exact date but shortly after last booster . I wasn?t feeling right and my handwriting was bad .I kept thinking it would get better. I lived with it for awhile until my family noticed I wasn?t getting better . I didn?t want to deal with it during the holidays so waited until Jan 2023. My life has completely changed . I was going to be a traveling surgical tech in July and now I?m not even going to be a tech any more I?m moving near family as soon. I need help with life things .I was so independent and now I?m not

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Praegender Schweregrund: Angiogram
Hospital-Tage: -
Labordaten: MRI CTA OT and PT
Aktuelle Erkrankungen: None at the time
Vorgeschichte: None at the time
Andere Medikamente: Clindimycin Peroxide Gel Losartan 50mg
Allergien: PCN
Vorherige Impfungen: -

VAERS 2619868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 08.04.2022
Beginn: 01.06.2022
Tage bis Beginn: 54,0
Dosis: 4
Route/Site: IM / LA

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

Deafness bilateral Deafness neurosensory Tinnitus

Symptomtext

A few days after the vaccine I started having Tinnitus. This is ongoing.

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Praegender Schweregrund: Deafness bilateral
Hospital-Tage: -
Labordaten: You saw, Audiologist on Wednesday October 19, 2022. The following issues were addressed: Sensorineural hearing loss (SNHL) of both ears, Tinnitus of both ears, and Tinnitus of right ear. October 19th. This was after seeing my primary care doctor, DO on 6/9/22 .
Aktuelle Erkrankungen: Crohn's
Vorgeschichte: Crohn's
Andere Medikamente: Gabapentin, Effexor, Flonase, Multivitamin, B-12, Humira, Xyrte,, Riztriptan.
Allergien: Sulfa, Norco, Shingles Vaccine
Vorherige Impfungen: Shingles Vaccine

VAERS 2615398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: WI
Alter: 89,0
Geschlecht: M
Eingang: 14.04.2023
Impfdatum: 22.07.2022
Beginn: 22.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / AR

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

Peripheral swelling

Symptomtext

The booster before my leg swelled up from my mid-calf down to my foot. I went to urgent care to get it checked. There was no blockage of a blood clot. It subsided after being but on an antihistamine and Lasix. It was gone in 4 to 5 days I took Benadryl with this most recent dose to offset, this was on 10/06/2022 Lot# GH9693 Pfizer-Bivalent. The reaction was the same but not as severe. It down my leg between the knee and ankle. It was slight swelling, I reported to the doctor, and he told me take the medication I had before on the last dose. It helped and within 48 hours it was back down to normal size.

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Praegender Schweregrund: Peripheral swelling
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Rheumatoid Arthritis
Andere Medikamente: Vitamin B12; Vitamin D; Calcium; Vitamin E; Multivitamins; Omega 3 Fish Oil
Allergien: A Statin Drug - Unsure
Vorherige Impfungen: -

VAERS 2613123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: NV
Alter: 79,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 09.04.2022
Beginn: 15.03.2023
Tage bis Beginn: 340,0
Dosis: N/A
Route/Site: IM / RA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

None after shots. Paxlovid after testing positive.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Paxlovid after testing positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Heart - Left Bundle Branch Block
Andere Medikamente: Atorvastatin Carvedilol Entresto Folic Acid Omeprazole Aspirin 81mg Methotrexate GNC multi vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2611623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: AZ
Alter: 81,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: -
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: SYR / LA

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

Barium swallow normal Blood test normal Hunger Renal function test normal Taste disorder Thyroid function test normal Weight decreased

Symptomtext

In the beginning of August 2022, I noticed that my clothing was a little bit bigger on me. I didn't pay too much attention to that. I did look at the scale and noticed I had lost 4 lbs. It was summer time and I don't eat too much when it's hot. I went to my cardiologist at the end of the month that was a routine visit. I got on his scale and I was down from 183 to 167 lbs. I didn't think too much of it. Suddenly it was not until September or so where I noticed I was just losing weight. I was losing 3lbs every 3 days maybe, around a pound a day. All of a sudden, I found that I was unable to swallow certain things. When eating breakfast with my favorite foods, and I would try to eat them and I cannot get myself to swallow it because it disgusts me. I would spit it out and try again with other foods. The same thing happened a week later with eggs. The same instance happened with potatoes. I threw it away with disgust. I tried different foods and nothing was working and I continued to lose weight. I lost interest in food because they didn't taste right. In January 2023, I finally decided I couldn't do this and I had lost 48lbs. I was also very hungry. I went to see my PCP. I made the mistake of saying I had trouble swallowing foods. Mechanically I had no problems swallowing, I just couldn't stand to swallow specific foods because they did not taste good to me. For example, I love chocolate and I could no longer stand the taste of the chocolate. The doctor sent me to get a barium swallow test, and it was completely negative which I knew it was going to be. I went to see a speech pathologist as well, and she determined I did not have a swallowing problem. Both of these I knew. The doctor wanted me to see an ENT, and I said I didn't think I had ENT problems. She mentioned a neurologist as well, and I noted I didn't want to do that either. I declined those two tests. I'm still losing weight. It has been since August 2022 and now we're into April 2023. I'm still losing weight, not at the same rate I was in the beginning, but I am now at 131. I'm eating much better now. I've been taking meal supplements by Pro Caps and Ensure as supplements. For these supplements, they are bigger pills, but I do not have trouble swallowing them.

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Praegender Schweregrund: Barium swallow normal
Hospital-Tage: -
Labordaten: Barium Swallow Test - Negative; Blood work - Normal; Speech Pathology Examination - No swallowing difficulties; Thyroid Testing - Normal; Kidney Panel - Normal
Aktuelle Erkrankungen: None
Vorgeschichte: Cardiac Arrhythmia Vtach; Stage 3 Kidney Failure; Thyroid Nodules
Andere Medikamente: Flecainide; Metoprolol; Simvastatin; Multivitamin; Acetyl Carnitine; Ginger; COQ10; Turmeric; Omega 3; Ocuvite; Azafrin; Resveratrol; Vitamin B Complex; Cranberry; Calcium; Vitamin D3; Vitamin K2 MK-7; Probiotic; Quercetin with Bromelain (P
Allergien: Seasonal Allergies
Vorherige Impfungen: -

VAERS 2611520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: WA
Alter: 73,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 31.03.2022
Beginn: 01.03.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Blood test Plasma cell myeloma Positron emission tomogram

Symptomtext

I had several unusual health events; multiple myeloma (Blood Cancer )

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Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Pet scan Blood Test
Aktuelle Erkrankungen: -
Vorgeschichte: mild heart condition, mild thyroid condition; sleep apnea ; restless leg syndrome; breast cancer 03/21.
Andere Medikamente: Allopurinol; ciclopirox; ezetimabe; Gabapentin; levothyroxine; pantoprazole; Spironolactone; Alprazolam; Metoprolol; Rosuvastatin; advil; Biotin; Baby Aspirin; B12, D3, Gasx; Tylenol; Vitamin C, Daily Multi Vitamins; Benefiber; Miralax;
Allergien: Epiephrine, Prednisone Oxycodne
Vorherige Impfungen: -

VAERS 2610909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MT
Alter: 79,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 04.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: IM / RA

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

Gingival bleeding Stomatitis

Symptomtext

Ten days started having bleeding gums with mouth sores. Saw doctor and was given chlorhexidine gluconate oral rinse, but the rinse only made sores worse. Gums are still too sore to wear partial.

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Praegender Schweregrund: Gingival bleeding
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hadn't been feeling well and took a COVID-19 test and was negative.
Vorgeschichte: Blood clots.
Andere Medikamente: Magnesium; vitamin D; calcium; TYLENOL; XARELTO; AREDS eye drops.
Allergien: Environmental; sulfa; penicillin; codeine; myosin; iodine; morphine.
Vorherige Impfungen: Shingles gave me a breakout in a rash in 2018

VAERS 2604386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

gering

Staat: MA
Alter: 71,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 08.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received BNT162b2 (BNT162B2), on 08Apr2022 at 13:00 as dose 4 (booster), single (Lot number: fj4991) at the age of 71 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "known allergies: dairy" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Oct2022) negative; (Oct2022) Positive, notes: Next day, turned positive in 20 seconds; (Oct2022) Positive, notes: positive until day 14,. Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202210; Test Name: SARS-CoV-2 test; Test Result: Negative ; Test Date: 202210; Test Name: SARS-CoV-2 test; Test Result: Positive ; Comments: Next day, turned positive in 20 seconds; Test Date: 202210; Test Name: SARS-CoV-2 test; Test Result: Positive ; Comments: positive until day 14,
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Milk allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2604383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CO
Alter: 60,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 26.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Feb2021 as dose 1, single (Lot number: EC9266), in left arm, on 06Mar2021 as dose 2, single (Batch/Lot number: unknown), in left arm, on 27Oct2021 as dose 3 (booster), single (Lot number: FE3592), in left arm and on 26Jul2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 60 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "History of vsd" (unspecified if ongoing); "known allergies: sulfa" (unspecified if ongoing); "history of breast cancer, stage 1" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Codine, reaction(s): "known allergies: Codine". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: 4 days after negative test; Negative. Therapeutic measures were taken as a result of vaccination failure, covid-19 which included PAXLOVID from 06Mar2023 to 11Mar2023. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: 4 days after negative test; Test Name: Covid-19 test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer stage I; Sulfonamide allergy; Ventricular septal defect
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2603102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 13.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An elderly female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Feb2021 as dose 2, single (Lot number: EN5318), in right arm, on 19Sep2021 as dose 3 (booster), single (Lot number: 30145BA), in right arm and on 13Jul2022 as dose 4 (booster), single (Lot number: FJ4991), in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment; Negative, notes: negative for COVID; Positive, notes: COVID test positive again. Therapeutic measures were taken as a result of drug ineffective, covid-19 (Paxlovid from 11Feb2023 to 16Feb2023).

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive; Comments: COVID 19 Treatment; Test Name: Covid-19 test; Test Result: Negative; Comments: negative for COVID; Test Name: Covid-19 test; Test Result: Positive; Comments: COVID test positive again.
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 2593564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 17.06.2022
Beginn: 01.12.2022
Tage bis Beginn: 167,0
Dosis: 4
Route/Site: - / -

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

Illness SARS-CoV-2 test Weight

Symptomtext

she was really sick in Dec2022 and tested negative for Covid; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP) from product quality group, Program ID: The reporter is the patient. A 61-year-old female patient received BNT162b2 (BNT162B2), on 17Jun2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 60 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes", start date: 2008 (unspecified if ongoing), notes: After hysterectomy; "hysterectomy" (unspecified if ongoing). Concomitant medication(s) included: INSULIN taken for type 2 diabetes mellitus (ongoing). Vaccination history included: BNT162b2 (dose 3, single), administration date: 06Nov2021, when the patient was 60-year-old, for COVID-19 immunization; BNT162b2 (dose 2, single, LOT: ER8733 EXP: unknown, Anatomical location: either right or left arm), administration date: 24Mar2021, when the patient was 59-year-old, for COVID-19 Immunization; BNT162b2 (dose 1, single, LOT: EN6203, EXP: unknown , Anatomical location: either right or left arm), administration date: 03Feb2021, when the patient was 59-year-old, for Covid-19 immunization. The following information was reported: ILLNESS (non-serious) with onset Dec2022, outcome "unknown", described as "she was really sick in Dec2022 and tested negative for Covid". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Patient was really sick in Dec2022 and tested negative for Covid. She got sick the first week in December and took 4 Covid test and they were negative. Her husband was sick in Dec2022, but it was influenza A. Sender's Comments: Linked Report(s) : US-PFIZER INC-202300094230 same reporter, product, different dose, events;US-PFIZER INC-202300094238 same reporter, product, different dose, events;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Illness
Hospital-Tage: -
Labordaten: Test Date: 202212; Test Name: COVID test; Test Result: Negative; Comments: took 4 COVID test and they were negative; Test Name: Weight; Result Unstructured Data: Test Result:170-175; Comments: 170-175 pounds right now
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes (After hysterectomy); Hysterectomy
Andere Medikamente: INSULIN
Allergien: -
Vorherige Impfungen: -

VAERS 2593531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: NC
Alter: -
Geschlecht: M
Eingang: 09.03.2023
Impfdatum: 15.07.2022
Beginn: 01.02.2023
Tage bis Beginn: 201,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old male patient received BNT162b2 (BNT162B2), on 06Feb2021 at 11:00 as dose 1, single (Lot number: EM9809), in left arm, on 27Feb2021 at 11:00 as dose 2, single (Lot number: EN6203), in left arm, on 26Sep2021 as dose 3 (booster), single (Lot number: EW0183), in left arm and on 15Jul2022 as dose 4 (booster), single (Lot number: FJ4991), in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Feb2023, outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Feb2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 and included Paxlovid from 21Feb2023 to 25Feb2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202302; Test Name: COVID test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2592713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: GA
Alter: 74,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 14.07.2022
Beginn: 04.08.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: - / LA

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

Dry eye Eczema Joint range of motion decreased SARS-CoV-2 test Vision blurred

Symptomtext

blurred vision in my left eye due to extreme dryness; blurred vision in my left eye due to extreme dryness; have difficulty raising and lowering my arms at times; arms and legs below the knees developed small sores that then became rough textured rash that sort of looked like eczema; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 74-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Jul2022 at 14:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 74 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hyprthyroidism" (unspecified if ongoing); "cancer" (unspecified if ongoing); "CHF" (unspecified if ongoing), notes: CHF. The patient took concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EL3246, Vaccine location: Left arm), for COVID-19 immunization; Bnt162b2 (DOSE 2, SINGLE; Lot number: EL3246, Vaccine location: Left arm), for COVID-19 immunization; Bnt162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: FE3590, Vaccine location: Left arm), for COVID-19 immunization. The following information was reported: ECZEMA (non-serious) with onset 04Aug2022 at 12:00, outcome "not recovered", described as "arms and legs below the knees developed small sores that then became rough textured rash that sort of looked like eczema"; VISION BLURRED (non-serious), DRY EYE (non-serious) all with onset 2023, outcome "unknown" and all described as "blurred vision in my left eye due to extreme dryness"; JOINT RANGE OF MOTION DECREASED (non-serious) with onset 2023, outcome "unknown", described as "have difficulty raising and lowering my arms at times". The events "arms and legs below the knees developed small sores that then became rough textured rash that sort of looked like eczema" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of eczema. Additional information: For about two weeks the patient's arms and legs below the knees developed small sores that then became rough textured rash that sort of looked like eczema but not quite. Her dermatologist ordered creams to apply, but after three tubes of use there were no changes. Has not abated as of this date. She also now have blurred vision in her left eye due to extreme dryness. She had difficulty raising and lowering her arms at times. She was a retired nurse and this skin condition does not look like any eczema she had ever seen. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Other medications the patient received within 2 weeks of vaccination were prescribed medications.

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Praegender Schweregrund: Dry eye
Hospital-Tage: -
Labordaten: Test Date: 20230113; Test Name: iHealth; Test Result: Negative; Comments: Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer; Congestive heart failure (CHF); Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2588976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 78,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 16.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 78-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jul2021 at 12:00 as dose 1, single (Lot number: EW0191), in left arm, on 14Dec2021 at 12:00 as dose 2, single (Lot number: 33130BA), in left arm and on 16Jul2022 at 12:00 as dose 3 (booster), single (Lot number: FJ4991) at the age of 78 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "occasional high blood pressure" (unspecified if ongoing), notes: Takes Olmesartan Medoximil 10 mg PRN. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid (Lot number: GG0133) from 20Feb2023 to an unknown date in Feb2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300081211 Same patient, different product and event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Takes Olmesartan Medoximil 10 mg PRN)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2588690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 28.02.2023
Impfdatum: 21.07.2022
Beginn: 30.12.2022
Tage bis Beginn: 162,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 4 vaccines Pfizer 2/24/21 Lot# En6200 ; Pfizer 3/17/21 Lot# Er2613; Pfizer 10/20/21 Lot# Ff2590; Pfizer 7/21/22Lot# FJ4991

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

VAERS 2585361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

gering

Staat: PA
Alter: -
Geschlecht: M
Eingang: 22.02.2023
Impfdatum: 22.07.2022
Beginn: 06.02.2023
Tage bis Beginn: 199,0
Dosis: 4
Route/Site: - / RA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received BNT162b2 (BNT162B2), on 08Feb2021 at 14:00 as dose 1, single (Lot number: en5318), in right arm, on 01Mar2021 as dose 2, single (Lot number: fn6200), in right arm, on 27Sep2021 at 11:00 as dose 3 (booster), single (Lot number: 30145ba), in right arm and on 22Jul2022 as dose 4 (booster), single (Lot number: fj4991), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes type II" (unspecified if ongoing), notes: Other medical history: Diabetes type II. The patient's concomitant medications were not reported. Past drug history included: Ciproflaxin, reaction(s): "Known allergies: Ciproflaxin", notes: Known allergies: Ciproflaxin. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 06Feb2023, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06Feb2023) Positive; (10Feb2023) Negative; (14Feb2023) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19 (Paxlovid).

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230206; Test Name: Covid-19 Test; Test Result: Positive ; Test Date: 20230210; Test Name: Covid-19 Test; Test Result: Negative ; Test Date: 20230214; Test Name: Covid-19 Test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type 2 diabetes mellitus (Other medical history: Diabetes type II)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2585344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: IL
Alter: 51,0
Geschlecht: F
Eingang: 22.02.2023
Impfdatum: 20.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

COVID-19; COVID-19; Interchange of vaccine products; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 20Jun2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 51 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 26Jan2021 as dose 1, single (Lot number: 013L20A), in left arm, on 26Feb2021 as dose 2, single (Lot number: 012A21A), in left arm and on 03Nov2021 as dose 3 (booster), single (Lot number: 017F21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "History of cancer" (unspecified if ongoing), notes: History of cancer with chemotherapy 13 years before this report; "Chemotherapy" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 20Jun2022, outcome "unknown"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient was treated with PF-07321332, ritonavir (PAXLOVID), from 08Feb2023 (Lot number: GF5593) to 12Feb2023. Therapeutic measures were not taken as a result of interchange of vaccine products.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer (History of cancer with chemotherapy 13 years before this report); Chemotherapy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2574677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

gering

Staat: VA
Alter: 81,0
Geschlecht: M
Eingang: 03.02.2023
Impfdatum: 22.07.2022
Beginn: 21.08.2021
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Interchange of vaccine products; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 82-year-old male patient received BNT162b2 (BNT162B2), on 21Aug2021 as dose 3 (booster), single (Lot number: fd8448) and on 22Jul2022 at 13:00 as dose 4 (booster), single (Lot number: fj4991) at the age of 81 years, in left arm for covid-19 immunisation; coviD-19 vaccine nrvv MVa (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), on 20Dec2022 at 13:00 as dose 5 (booster), single (Lot number: a57167b), in left arm for covid-19 immunisation; coviD-19 vaccine nrvv ad (chadox1 ncov-19) (ASTRAZENECA COVID-19 VACCINE), on 05Nov2020 at 11:00 as dose 1, single (Lot number: a03324) and on 03Dec2020 at 10:00 as dose 2, single (Batch/Lot number: unknown), in left arm for covid-19 immunisation. The patient's relevant medical history included: "mild diabetes" (unspecified if ongoing); "heart disease" (unspecified if ongoing); "spinal stenosis" (unspecified if ongoing); "known allergies sulfa" (unspecified if ongoing), notes: known allergies sulfa. Concomitant medication(s) included: ATORVASTATIN, start date: Jan2021, stop date: 16Jan2023; OMEPRAZOLE, start date: Jan2022; METOPROLOL TARTRATE, start date: Jan2020; CELECOXIB, start date: 16Nov2022; ASPIRIN [ACETYLSALICYLIC ACID], start date: Jan2018. Past drug history included: Avelox, reaction(s): "known allergies avelox". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 21Aug2021, outcome "not recovered"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jan2023, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Still testing positive 15 days; Positive. Therapeutic measures were taken as a result of drug ineffective, COVID-19: the patient received Paxlovid from 17Jan2023 to 21Jan2023 for treatment of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Positive ; Comments: Still testing positive 15 days; Test Name: Covid-19 Test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Heart disease, unspecified; Spinal stenosis; Sulfonamide allergy (known allergies sulfa)
Andere Medikamente: ATORVASTATIN; OMEPRAZOLE; METOPROLOL TARTRATE; CELECOXIB; ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2566745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: TN
Alter: 65,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 25.07.2022
Beginn: 12.12.2022
Tage bis Beginn: 140,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough SARS-CoV-2 test positive Throat irritation

Symptomtext

My COVID-19 infection symptoms started on 12/12/2022 in the morning at 8:00Am. I had a scratchy throat and cough. On 12/14/2022 I did a COVID-19 home test which was positive. On the same day I went to a health facility where I got retested for COVID-19 infection, it was positive again. On 12/15/2022 I did a telehealth with my doctor he prescribed me with PAXLOVID for 5 days, and a cough syrup.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 14DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; Cholesterol
Andere Medikamente: Participant didn't want to disclose medication information.
Allergien: Lactose intolerance
Vorherige Impfungen: -

VAERS 2558214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 21.07.2022
Beginn: 21.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; Interchange of vaccine products; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Jul2022 at 14:15 as dose 3 (booster), single (Lot number: FJ4991) at the age of 61 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 02Mar2021 at 09:30 as dose 1, single (Batch/Lot number: unknown), in left arm, on 29Mar2021 at 12:45 as dose 2, single (Batch/Lot number: unknown), in left arm and on 04Dec2022 at 11:00 as dose 4 (booster), single (Batch/Lot number: unknown), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Osteoporosis" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 21Jul2022 at 14:15, outcome "unknown"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 31Dec2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (31Dec2022) Positive; (01Jan2023) Positive; (06Jan2023) Negative; (07Jan2023) Negative; (09Jan2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Got COVID on 31Dec2022 tested positive just past midnight about 00:30 AM on 01Jan2023. Treated with Paxlovid. Got better and tested negative on 06Jan2023 and 07Jan2023. On 09Jan2023 tested Positive for COVID again. Patient did not have the known allergies.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221231; Test Name: Got Covid; Test Result: Positive ; Test Date: 20230101; Test Name: Got Covid; Test Result: Positive ; Test Date: 20230106; Test Name: Got Covid; Test Result: Negative ; Test Date: 20230107; Test Name: Got Covid; Test Result: Negative ; Test Date: 20230109; Test Name: Got Covid; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Osteoporosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2550949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: VA
Alter: 69,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 21.07.2022
Beginn: 01.12.2022
Tage bis Beginn: 133,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Jul2022 as dose 3 (booster), single (Lot number: FJ4991) at the age of 69 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Osteopenia" (unspecified if ongoing), notes: Osteopenia, not on meds; "Adult pertussis" (unspecified if ongoing), notes: adult pertussis about 20 years ago. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient had no known allergies. Treatment of COVID-19 with Paxlovid (Lot number: Lot 2707493) from 26Dec2022 to 28Dec2022.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Osteopenia (Osteopenia, not on meds); Pertussis (adult pertussis about 20 years ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2547547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: PA
Alter: 59,0
Geschlecht: M
Eingang: 31.12.2022
Impfdatum: 11.05.2022
Beginn: 01.12.2022
Tage bis Beginn: 204,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old male patient received BNT162b2 (BNT162B2), on 26Sep2021 at 13:00 as dose 3 (booster), single (Lot number: 30145BA), in left arm and on 11May2022 at 13:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 59 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (13Dec2022) Negative, notes: Took Paxlovid for 5 days. Tested negative two days later; (Dec2022) Positive, notes: positive for Covid (again). Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221213; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Took Paxlovid for 5 days. Tested negative two days later; Test Date: 202212; Test Name: Covid-19 Test; Test Result: Positive ; Comments: positive for Covid (again).
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2540788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: NV
Alter: 69,0
Geschlecht: M
Eingang: 22.12.2022
Impfdatum: 20.06.2022
Beginn: 25.11.2022
Tage bis Beginn: 158,0
Dosis: 4
Route/Site: IM / RA

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

Blood glucose normal COVID-19 SARS-CoV-2 test positive Sinus congestion Throat irritation

Symptomtext

My initial time that I thought I was getting it was 11/25/2022. I had a very minor irritation in my throat, and I was slightly congested in my sinuses. I did not develop a fever. My first at home COVID-19 test was 11/27/2022. I checked my temperature twice a day and I called the doctor on Monday 11/28/2022. He prescribed prednisone and PAXLOVID, but I never took it. I took MUCINEX to treat my symptoms. I began to feel better after about 3 days or 4 days afterwards. Within 5 days all my symptoms were gone but I continued to test positive until 12/08/2022. During this time my blood glucose levels have been higher than normal. I am in the 135 mid-range and I have a follow up appointment with my doctor in February regarding this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood glucose normal
Hospital-Tage: -
Labordaten: COVID-19 home test 11/27/2022 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Seasonal allergies
Andere Medikamente: Multivitamin; metformin; allergy shots 2 injections
Allergien: Several antibiotics; MSG; unknown food allergy
Vorherige Impfungen: -

VAERS 2539127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 26.12.2020
Beginn: 09.10.2022
Tage bis Beginn: 652,0
Dosis: 4
Route/Site: - / -

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

Delivery Maternal exposure before pregnancy

Symptomtext

Delivery Date: 10/10/2022 Delivery Time: 9:27 AM Gestational Age(weeks days/7): 39 6/7 Method of Delivery: Vaginal, Spontaneous Baby:

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

VAERS 2533729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 54,0
Geschlecht: U
Eingang: 16.12.2022
Impfdatum: 21.07.2022
Beginn: 27.11.2022
Tage bis Beginn: 129,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

interchange of vaccine products; COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 54-year-old patient received BNT162b2 (BNT162B2), on 21Jul2022 at 13:15 as dose 4 (booster), single (Lot number: FJ4991) at the age of 54 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 10Feb2021 at 14:30 as dose 1, single (Lot number: 038K20A), in left arm, on 22Mar2021 at 12:00 as dose 2, single (Lot number: 007B21A), in left arm and on 01Nov2021 at 15:45 as dose 3 (booster), single (Lot number: 939905), in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 27Nov2022, outcome "not recovered" and all described as "COVID 19 Treatment"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (27Nov2022) Positive, notes: I tested positive on 27Nov2022; (10Dec2022) Positive, notes: tested positive again on 10Dec2022. Clinical details: It was reported, the patient tested positive on 27Nov2022 and started Paxclovid (Lot number: GF3197) on 28Nov2022 to 03Dec2022. Then tested positive again on 10Dec2022 07:00 AM. No other medication in 2 weeks. Patient was not recovered and No treatment received. Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221127; Test Name: Covid-19 test; Test Result: Positive ; Comments: I tested positive on 27Nov2022; Test Date: 20221210; Test Name: Covid-19 test; Test Result: Positive ; Comments: tested positive again on 10Dec2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2533887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: VA
Alter: 15,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 14.05.2022
Beginn: 30.05.2022
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / AR

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

Computerised tomogram Laboratory test normal Menstrual disorder Oligomenorrhoea Polymenorrhoea

Symptomtext

Two weeks after her second Covid dose, patient is on a permanent menstrual cycle, with 3-4 days break in between. She has had all her labs and everything checks out fine. She was seen by a GYN and she suggested birth control to stop the bleeding, but even that does not stop it. For the record, her period started at 12, and for the past 2 years , she has been on a regular cycle.

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Praegender Schweregrund: Computerised tomogram
Hospital-Tage: -
Labordaten: She had a CT in July 2022, when we were concerned for having her 3rd period in the month of June. She had a full lab workout in Aug 2022.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2533319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: VA
Alter: 71,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 04.04.2022
Beginn: 26.08.2022
Tage bis Beginn: 144,0
Dosis: 4
Route/Site: IM / LA

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

Blood test abnormal Blood thyroid stimulating hormone increased Depression Onychoclasis Temperature intolerance

Symptomtext

I had abnormal blood work on 8/26/22. My doctor decided to have more blood work done on 11/22/22 and my Thyroid Stimulating Hormone was still high. In the weeks leading up to this, I noticed some split fingernails and was having depression. I was not able to lose weight and had some sensitivity to cold. I am still dealing with this and just started taking an increased dose for depression.

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Praegender Schweregrund: Blood test abnormal
Hospital-Tage: -
Labordaten: 26AU2022 Blood Panel - Thyroid Stimulating Hormone 4.5mclu; 22NOV2022 Blood Panel - Thyroid Stimulating Hormone 6.6mclu
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Idiopathic Hyponatremia
Andere Medikamente: Vitamin D; Vitamin D3; Multivitamin; Biotin; Claritin; Nexium; Baclofen; Nifedipine; Atenolol; Levothyroxine; Paxil
Allergien: Codeine; Hydrocodone
Vorherige Impfungen: -

VAERS 2530591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: FL
Alter: 53,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 04.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 24Mar2021 at 10:00 as dose 1, single (Lot number: EN6204), in left arm, on 07Apr2021 at 10:00 as dose 2, single (Lot number: EP6955), in left arm, on 04Nov2021 at 13:00 as dose 3 (booster), single (Lot number: Ff2588), in left arm and on 04Jul2022 at 12:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 53 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Past drug history included: Bactrim, reaction(s): "known allergies: Bactrim", notes: Known allergies : Bactrim. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19 which included Paxlovid treatment from 26Nov2022 to 01Dec2022. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE INJECTABLE lot FJ4991 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FJ4991, fill lot FJ4988, and the bulk formulated drug product lot FJ4985. A complaint sample was not returned. The following potential quality issue was identified during the investigation: all test points of TFF permeate stream flow meters failed during their annual calibration. A QAR was opened and a child record of the quality investigation was opened to track the product quality impact of lots that ran on the TFF skid from its previous calibration to the annual recalibration activities, including reported finished goods lot FJ4991. This investigation will be updated pending the closure of the action item for impact assessment. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE INJECTABLE lot FF2588 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FF2588, fill lot FF2557, and the bulk formulated drug product lot FE5319. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot EP6955 was investigated. The investigation included a review of manufacturing and packaging atch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EP6955, fill lot EP6954, and the formulated drug product lot EP6953. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EN6204 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EN6204, fill lot EN5335, and the formulated drug product lot EN5325. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201355572 Same patient, same drug/different dose, different AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2526196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: WV
Alter: 51,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 17.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Apr2021 as dose 1, single (Lot number: EW0150), in left arm, on 30Apr2021 as dose 2, single (Lot number: EW0169), in left arm, on 21Nov2021 as dose 3 (booster), single (Lot number: FH8030), in left arm and on 17Jul2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 51 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Bmi >40" (unspecified if ongoing), notes: Bmi >40; "Early arthritis" (unspecified if ongoing); "Cold/exercise induced asthma" (unspecified if ongoing); "Cold/exercise induced asthma" (unspecified if ongoing); "Minor heart murmur" (unspecified if ongoing); "Surgical plates/screws in left radius" (unspecified if ongoing), notes: surgical plates/screws in left radius; "Bivalves allergy" (unspecified if ongoing), notes: Bivalves allergy. The patient's concomitant medications were not reported. Past drug history included: Amoxicillin, reaction(s): "Allergy"; Marijuana, reaction(s): "Allergy"; Gin, reaction(s): "Allergy"; Juniper, reaction(s): "Allergy". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures, Paxlovid from 02Dec2022, were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Cold induced asthma; Exercise induced asthma; Heart murmur; Insertion of surgical hardware (surgical plates/screws in left radius); Obesity (Bmi >40); Shellfish allergy (Bivalves allergy)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2526192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: TX
Alter: -
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 24.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 24Jun2022 at 15:00 as dose 4 (booster), single (Lot number: FJ4991), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Osteoporosis" (unspecified if ongoing); "slipped discs" (unspecified if ongoing); "kidney stones" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Amoxicillin, reaction(s): "Known allergy: Amoxicillin causes a severe stomach ache", notes: Amoxicillin causes a severe stomach ache. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient treated with Paxlovid (anti-viral) for COVID-19 treatment from 30Nov2022 to unknown date. She did not take other medication in 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kidney stones; Osteoporosis; Slipped disc
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2520090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: FL
Alter: 12,0
Geschlecht: M
Eingang: 30.11.2022
Impfdatum: 23.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Muscle contractions involuntary Muscle twitching

Symptomtext

Fasciculation in face arms and legs. My son started having these twitches within 2 hours of the first dose of the vaccine. He is still intermittently experiencing twitching of the face, arms and legs with no other medical reason.

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Praegender Schweregrund: Muscle contractions involuntary
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: My son received the first dose of the Pfizer vaccine.A couple hours later he started having a twitch in his arm, eye and face. The twitch lasted for a few days and then subsided. It comes back randomly with no other medical explanation. pfizer covid vaccine lot number fj4991
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2514840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 14.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Jan2021 as dose 1, single (Lot number: EZ9263), in left arm, on 16Feb2021 as dose 2, single (Lot number: FL9267), in left arm, on 13Oct2021 as dose 3 (booster), single (Lot number: 30155BA), in left arm and on 14Apr2022 at 10:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of covid-19. Clinical course: Paxlovid, Treatment start date 12Aug2022, Treatment stop date=16Aug2022, Treatment of COVID -19.

Weitere VAERSDATA-Felder

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

VAERS 2514035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CO
Alter: 61,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 14.10.2022
Beginn: 12.11.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Positive COVID test on 11/14/22 (first symptoms 11/12/22)

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home COVID test 11/14/22
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Zyrtec (Cetirizine Hdrochloride 10mg), Psyllium Husk capsules 1,500 mg), Multivitamin with Biotin Collagen Keratin B Vitamins and Bamboo Extract, "Full Spectrum" CBD oil
Allergien: Steroids, all caines, nickel, methylparaben
Vorherige Impfungen: -

VAERS 2513028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: NH
Alter: 64,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 13.05.2022
Beginn: 18.08.2022
Tage bis Beginn: 97,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Feeling abnormal Impaired work ability Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On August 18, I was at work and my noses started to run. I took a test around 4PM and I knew my manager had COVID-19. My manager was home with it, but we all knew she had tested positive. It ran through our entire office. I went home and wasn't feeling the greatest tested for COVD-19 and it was positive. I then contacted the doctor through telehealth and was given PAXLOVID. Within 24 hours I was starting to recover. I felt bad all the way until Tuesday, and I was able to return on Thursday, August 25.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2512954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: -
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 21.04.2021
Beginn: 31.10.2022
Tage bis Beginn: 558,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Joint injury SARS-CoV-2 test positive

Symptomtext

Pt to ED 10/24 for hip injury. Pt tested for COVID prior to discharge, COVID+ 10/31 , no anti-COVID rx needed. Pt discharged 11/1.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 9,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Hepatic cirrhosis (CMS/HCC) Hepatic cirrhosis (CMS/HCC) Gastroesophageal reflux disease with esophagitis without hemorrhage GERD (gastroesophageal reflux disease) Uncontrolle Chronic left-sided low back pain with left-sided sciatica Open-angle glaucoma of both eyes Osteopenia determined by x-ray Abnormal electrocardiogram (ECG) (EKG) Hypokalemia Hypomagnesemia Cystitis AMS (altered mental status) Hyperammonemia (CMS/HCC) Hepatic encephalopathy (CMS/HCC) Obesity (BMI 30-39.9) Anemia Proteins serum plasma low Tremor Pedal edema Thrombocytopenia (CMS/HCC) COVID-19 Gait instability AKI (acute kidney injury) (CMS/HCC) Anxiety Urine culture positive Transaminitis Hypokalemia Hypomagnesemia Normocytic anemia
Andere Medikamente: amLODIPine (NORVASC) 10 MG PO Tab aspirin 81 MG amLODIPine (NORVASC) 10 MG PO Tab aspirin 81 MG PO Chew Tab docusate (COLACE) 100 MG PO Cap hydroCHLOROthiazide (HYDRODIURIL) 12.5 MG PO Tab lactulose (CEPHULAC) 10 GM/15ML PO Solution levothy
Allergien: None
Vorherige Impfungen: -

VAERS 2505439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 14.05.2022
Beginn: 11.11.2022
Tage bis Beginn: 181,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

covid vaccine breakthrough case dose 1 Pfizer 2/25/21 EN6198 dose 2 Pfizer 3/18/21 EN6205 dose 3 Pfizer 10/24/21 FH8020

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ 11/10/22 at home
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2503901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: AL
Alter: 74,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 19.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 75-year-old male patient received BNT162b2 (BNT162B2), on 10Feb2021 as dose 1, single (Lot number: EN5318), in left arm, on 31Mar2021 as dose 2, single (Lot number: EN6205), in left arm, on 27Sep2021 as dose 3 (booster), single (Lot number: FD8448), in right arm and on 19Jul2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 74 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Slightly elevated blood pressure" (unspecified if ongoing), notes: Rx treated. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 which was Paxlovid treatment.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201286149 Same reporter/patient, same drug, different AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Rx treated)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2498749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 65,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 09.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 65-year-old male patient received BNT162b2 (BNT162B2), on 14Jan2021 as dose 1, single (Lot number: el3302), on 04Feb2021 as dose 2, single (Lot number: en5318), on 01Sep2021 as dose 3 (booster), single (Lot number: en0173) and on 09May2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 65 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "CAD" (unspecified if ongoing); "GERD" (unspecified if ongoing); "known allergies: penicillin" (unspecified if ongoing), notes: known allergies: penicillin. Concomitant medication(s) included: ROSUVASTATIN CALCIUM; PRILOSEC [OMEPRAZOLE]; ASPIRIN 81. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Oct2022) Negative, notes: Negative test on day 5; (Oct2022) Positive, notes: positive test 2 days afterwards. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient received Paxlovid as treatment for COVID 19, Treatment start date was on 22Oct2022 and Treatment stop date was on 26Oct2022

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202210; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Negative test on day 5; Test Date: 202210; Test Name: COVID-19 Test; Test Result: Positive ; Comments: positive test 2 days afterwards
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Coronary artery disease; GERD; Penicillin allergy (known allergies: penicillin)
Andere Medikamente: ROSUVASTATIN CALCIUM; PRILOSEC [OMEPRAZOLE]; ASPIRIN 81
Allergien: -
Vorherige Impfungen: -

VAERS 2491597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: ID
Alter: 55,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 19.07.2022
Beginn: 01.08.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: SYR / -

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

Acoustic stimulation tests abnormal Deafness unilateral Hearing aid user Impaired work ability Magnetic resonance imaging head normal Tinnitus

Symptomtext

Received the vaccine on July 19, 2022, around the 2-3 week in August 2022, I noticed I couldn't hear out of my right ear and the mild tinnitus that I have had gotten worse. I called my ENT and the "soonest" I could get in was September 30, which I also had an audio testing done. I now have to get hearing devices in the hope that the devices will help...WHICH IS NOT COVERED BY INSURANCE!!! I work at our local school district as a tutor and had to resign from the job, as I couldn't do my job BECAUSE I COULDN'T HEAR THE STUDENTS!

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Praegender Schweregrund: Acoustic stimulation tests abnormal
Hospital-Tage: -
Labordaten: I had a hearing test in September 2020 and my word recognition on my right ear was 72%, I had a hearing test in September 2022 and my word recognition DROPPED to 20%. I've seen two ENTs (second was for a second opinion) and both have said the hearing loss is PERMANENT. I've had an MRI on the right side, which should everything being normal. I was told by both ENTs and the audiologist that they have seen an INCREASE on people saying they have gotten tinnitus, the tinnitus has increased and there has been hearing loss.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: penicillin
Vorherige Impfungen: flu 2020; flu 2010, and another flu shot don't remember the year

VAERS 2490835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: IL
Alter: 64,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 14.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 64-year-old male patient received BNT162b2 (BNT162B2), on 10Mar2021 as dose 1, single (Lot number: ER8131), in left arm, on 30Mar2021 as dose 2, single (Lot number: EW0175), in left arm, on 11Nov2021 as dose 3 (booster), single (Lot number: FH8020), in left arm and on 14Jul2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 64 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: CALCIUM CITRATE; CHONDROITIN; FISH OIL OMEGA 3; GLUCOSAMINE; VITAMIN D3. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient had no known allergies. He received other medication in two weeks as Multivitamin. Patient was treated with Paxlovid (anti-viral) for covid-19 from 11Oct2022 to 16Oct2022.

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Praegender Schweregrund: COVID-19
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: CALCIUM CITRATE; CHONDROITIN; FISH OIL OMEGA 3; GLUCOSAMINE; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 2480370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

gering

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 16.04.2022
Beginn: 16.10.2022
Tage bis Beginn: 183,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

covid breakthrough case

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ 10/16/22
Aktuelle Erkrankungen: -
Vorgeschichte: A. fib on Xarelto, CHF, GERD, chronic back pain,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ 4991

gering

Staat: PA
Alter: 68,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 01.04.2022
Beginn: 01.09.2022
Tage bis Beginn: 153,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Feb2021 at 15:00 as dose 1, single (Lot number: EN 6203), in left arm, on 18Mar2021 at 15:00 as dose 2, single (Lot number: ER 8727), in left arm, on 28Sep2021 at 14:30 as dose 3 (booster), single (Lot number: FE 2592), in left arm and on 01Apr2022 at 15:00 as dose 4 (booster), single (Lot number: FJ 4991) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "known allergy: Sulfa drugs" (unspecified if ongoing), notes: known allergy: Sulfa drugs; "hypothyroid" (unspecified if ongoing), notes: hypothyroid; "obesity" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (01Oct2022) positive, notes: tested positive. Therapeutic measures were taken as a result of vaccination failure, covid-19 as anti-viral drug Paxlovid.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221001; Test Name: tested positive; Test Result: Positive ; Comments: tested positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Hypothyroidism (hypothyroid); Obesity; Sulfonamide allergy (known allergy: Sulfa drugs)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: SC
Alter: 63,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 19.05.2022
Beginn: 02.10.2022
Tage bis Beginn: 136,0
Dosis: 4
Route/Site: - / LA

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

Body temperature COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 positive; COVID 19 positive; This is a spontaneous report received from contactable reporter (Consumer or other non HCP) from product quality group. The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Mar2021 as dose 1, single (Lot number: EN6207), on 06Apr2021 as dose 2, single (Lot number: EW0150), in right arm, on 02Dec2021 as dose 3 (booster), single (Lot number: 552590), in left arm and on 19May2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 63 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: COVID-19 (medically significant) with onset 02Oct2022, outcome "not recovered", described as "COVID 19 positive"; VACCINATION FAILURE (medically significant) with onset 02Oct2022, outcome "not recovered", described as "COVID 19 positive ". The patient underwent the following laboratory tests and procedures: Body temperature: (10Oct2022) 101, notes: fever of 101; SARS-CoV-2 test: (02Oct2022) Positive; (08Oct2022) Negative; (10Oct2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. The patient was COVID 19 positive on 02Oct2022. She took Paxlovid for 5 days as directed. She then tested negative on 08Oct2022 and felt great. On 10Oct2022, she felt really sick again with a fever of 101 and tested positive.

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Praegender Schweregrund: Body temperature
Hospital-Tage: -
Labordaten: Test Date: 20221010; Test Name: fever of 101; Result Unstructured Data: Test Result:101; Comments: fever of 101; Test Date: 20221002; Test Name: COVID TEST; Test Result: Positive ; Test Date: 20221008; Test Name: COVID TEST; Test Result: Negative ; Test Date: 20221010; Test Name: COVID TEST; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2472428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

gering

Staat: WA
Alter: 51,0
Geschlecht: F
Eingang: 08.10.2022
Impfdatum: 25.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Jun2022 at 10:00 as dose 4 (booster), single (Lot number: fj4991) at the age of 51 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. No Known allergies and other medication in 2weeks reported as No. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Treatment of COVID-19; (unspecified date) Negative, notes: negative test from first infection; (02Oct2022) Positive, notes: positive covid test result 7 days after negative test from first infection. (8 days after end of Paxlovid course. Therapeutic measures were taken as a result of drug ineffective, covid-19 with Anti-viral Paxlovid COVID 19 Treatment started on 20Sep2022 and stopped on 24Sep2022 with Lot number 2815071.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Virus test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Name: COVID-19 Virus test; Test Result: Negative ; Comments: negative test from first infection; Test Date: 20221002; Test Name: COVID-19 Virus test; Test Result: Positive ; Comments: positive covid test result 7 days after negative test from first infection. (8 days after end of Paxlovid course
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 2469461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

gering

Staat: UT
Alter: 63,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 27.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27May2022 as dose 4 (booster), single (Lot number: Fj4991) at the age of 63 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: DIVIGEL taken for hormone replacement therapy; PROGESTERONE taken for hormone replacement therapy. Past drug history included: Neosporin, reaction(s): "known allergy: Neosporin". The following information was reported: COVID-19 (medically significant), DRUG INEFFECTIVE (medically significant), outcome "recovering" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Poitive, notes: I tested positive; Negative, notes: I tested positive (after previously testing negative once the paxlovid was completed). Therapeutic measures were taken as a result of covid-19, drug ineffective. Clinical course: It was reported that patient received other medication in two weeks. Anti-viral details are as follows: Patient was taking Paxlovid from 20Sep2022 to 25Sep2022 to treat covid-19. Covid rebound. On day 7 after completing the paxlovid, Patient became ill again with covid symptoms and tested positive (after previously testing negative once the paxlovid was completed.) Experienced congestion, mild cough, significant fatigue and malaise.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Result Unstructured Data: Test Result:Poitive; Comments: I tested positive; Test Name: Covid-19 test; Test Result: Negative ; Comments: I tested positive (after previously testing negative once the paxlovid was completed)
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: DIVIGEL; PROGESTERONE
Allergien: -
Vorherige Impfungen: -

VAERS 2466640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: 98,0
Geschlecht: M
Eingang: 01.10.2022
Impfdatum: 27.05.2022
Beginn: 28.09.2022
Tage bis Beginn: 124,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 4 vaccines Pfizer 1/16/21 Lot# El0142; Pfizer 2/6/21 Lot# El3248; Pfizer 10/21/21 Lot# FE3590; Pfizer 5/27/22 Lot# FJ4991

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

VAERS 2466522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 01.10.2022
Impfdatum: 22.05.2022
Beginn: 01.09.2022
Tage bis Beginn: 102,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Mar2021 as dose 1, single (Lot number: EN6199), in left arm, on 27Mar2021 as dose 2, single (Lot number: ER8732), in left arm, on 16Oct2021 as dose 3 (booster), single (Lot number: FF8841), in left arm and on 22May2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "Known allergies: Sulfa drugs" (unspecified if ongoing), notes: Known allergies: Sulfa drugs. Concomitant medication(s) included: LEVOTHYROXINE; MONTELUKAST. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Sep2022) Positive, notes: Treatment of COVID-19; Total number of days since initial positive test is 16; (20Sep2022) Negative, notes: COVID rebound - positive test with symptoms three days after negative test and six days after finishing Paxlovid,; (23Sep2022) Positive, notes: COVID rebound - positive test with symptoms three days after negative test and six days after finishing Paxlovid; (28Sep2022) Positive, notes: Still testing positive five days after the test indicating rebound. Total number of days since initial positive test is 16. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Treatment included Paxlovid from 12Sep2022 to 17Sep2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202209; Test Name: COVID-19 test; Test Result: Positive ; Comments: Treatment of COVID-19; Total number of days since initial positive test is 16.; Test Date: 20220920; Test Name: COVID-19 test; Test Result: Negative ; Comments: COVID rebound - positive test with symptoms three days after negative test and six days after finishing Paxlovid,.; Test Date: 20220923; Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID rebound - positive test with symptoms three days after negative test and six days after finishing Paxlovid.; Test Date: 20220928; Test Name: COVID-19 test; Test Result: Positive ; Comments: Still testing positive five days after the test indicating rebound. Total number of days since initial positive test is 16.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Hypothyroidism; Sulfonamide allergy (Known allergies: Sulfa drugs)
Andere Medikamente: LEVOTHYROXINE; MONTELUKAST
Allergien: -
Vorherige Impfungen: -

VAERS 2465338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 03.05.2022
Beginn: 26.09.2022
Tage bis Beginn: 146,0
Dosis: 4
Route/Site: - / -

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

Asthenia COVID-19 Fall Gait disturbance Loss of personal independence in daily activities SARS-CoV-2 test positive Urinary tract infection

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 9/26/2022 Discharge Date: 09/28/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: General weakness Generalized weakness COVID-19 HOSPITAL COURSE: Patient is a 78 y.o. female who presents today with weakness becoming progressively worse. Patient normally is ambulatory and able to complete her ADLs with minimal assistance. This has become increasingly difficult this past week and she fell out of bed and get up last night. Her husband brought her to the emergency department for evaluation she was found to have acute urinary tract infection and COVID positive. In the face of her Parkinson's it is likely that we may be able to bring her back with some fluids and antibiotics, however, it is also possible she may require rehab in the form of home health care or subacute rehab. We will order physical and occupational therapy evaluations and continue Rocephin therapy started in the emergency department.. 9/28: Patient had an uneventful hospital stay. She did not show any respiratory issues related to her COVID positive test. The fluids were hep-locked, patient was tolerating oral. Patient was transition to Keflex to complete 3 days of therapy for urinary tract infection. She will follow-up with her primary care provider. Patient was seen by Physical therapy and Occupational therapy with arrangements for home therapies. Patient otherwise has remained hemodynamically stable, afebrile, room air oxygen. I discussed the case with the patient's husband who is wanting to take her home. Patient is stable for discharge. Patient was given COVID-19 discharge instructions. Patient will continue Sinemet, and follow-up with her primary care provider, also consider neurology referral as well.

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Praegender Schweregrund: Asthenia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia Osteoporosis Parkinson's disease (HCC) Frequent UTI Parkinson disease (HCC) S/P deep brain stimulator placement Chronic bilateral low back pain without sciatica Age-related osteoporosis without current pathological fracture Occlusion and stenosis of bilateral carotid arteries Generalized weakness Acute cystitis without hematuria COVID-19 Statin started by Vascular Surgery with Rx to be taken over by patient's PCP
Andere Medikamente: Carbidopa-Levodopa ER (RYTARY) 23.75-95 MG CPCR cephALEXin (KEFLEX) 250 MG capsule multivitamin with mineral (THERA M PLUS) tablet MYRBETRIQ 50 MG 24 hr tablet
Allergien: Atorvastatin Calcium [Atorvastatin]Other Sulfa DrugsHives Haldol [Haloperidol] Phenergan [Promethazine] Reglan [Metoclopramide]
Vorherige Impfungen: -

VAERS 2464223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: VA
Alter: 58,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 10.06.2022
Beginn: 01.09.2022
Tage bis Beginn: 83,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 11Mar2021 as dose 1, single (Lot number: 6N6208), on 31Mar2021 as dose 2, single (Lot number: ER8732), on 20Aug2021 as dose 3 (booster), single (Lot number: FC3180), in left arm and on 10Jun2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 58 years, in left arm for covid-19 immunisation. Patient was not pregnant at the time of vaccination. The patient's relevant medical history included: "Rheumatoid arthritis" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). Patient medical history included Rheumatoid Arthritis and known allergies to Penicillin and Macrodantin. Concomitant medication(s) included: ADVIL 12 HORAS; METHOTREXATE; MUCINEX; ORENCIA; SUDAFED 12 HOUR; TYLENOL. Past drug history included: Macrodantin, reaction(s): "Drug allergy". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19. Patient received the vaccine. Other medication in 2 weeks included Methotrexate, Orencia, Tylenol, Advil, Sudafed, Mucinex. Patient received Paxlovid (Lot number- 1919252A) from 13Sep2022 to 18Sep2022 for treatment of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 antigen test; Test Result: Positive ; Comments: Treatment of COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Rheumatoid arthritis
Andere Medikamente: ADVIL 12 HORAS; METHOTREXATE; MUCINEX; ORENCIA; SUDAFED 12 HOUR; TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 2462797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 18.04.2022
Beginn: 05.09.2022
Tage bis Beginn: 140,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Mar2021 at 14:30 as dose 1, single (Lot number: EN6206), in left arm, on 19Mar2021 at 10:30 as dose 2, single (Lot number: EN6207), in left arm, on 26Oct2021 at 16:00 as dose 3 (booster), single (Lot number: FF8841), in left arm and on 18Apr2022 at 15:15 as dose 4 (booster), single (Lot number: FJ4991) at the age of 67 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 05Sep2022 at 10:00, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (05Sep2022) Positive, notes: Positive COVID infection 05Sep2022 and Rebound COVID infection 19Sep2022; (19Sep2022) Positive, notes: Positive COVID infection 05Sep2022 and Rebound COVID infection 19Sep2022. Therapeutic measures were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220905; Test Name: COVID infection; Test Result: Positive ; Comments: Positive COVID infection 05Sep2022 and Rebound COVID infection 19Sep2022.; Test Date: 20220919; Test Name: COVID infection; Test Result: Positive ; Comments: Positive COVID infection 05Sep2022 and Rebound COVID infection 19Sep2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Known allergies: None Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 23.06.2022
Beginn: 01.06.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Deafness Tinnitus

Symptomtext

Tinnitus in left ear

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deafness
Hospital-Tage: -
Labordaten: Primary care doctor visit, then ENT doctor visit. Hearing loss. Waiting for further testing.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lisinopril, Symvastatin
Allergien: None known
Vorherige Impfungen: -

VAERS 2456120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: 55,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 04.05.2022
Beginn: 22.09.2022
Tage bis Beginn: 141,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

COVID vaccine breakthrough case. Pfizer 5/5/21 EW 0165, 5/26/21 EW0191, 12/8/21 330308D and 5/4/22 FJ4991

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive COVID test on 9/22/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2453843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MA
Alter: 68,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 01.05.2022
Beginn: 01.08.2022
Tage bis Beginn: 92,0
Dosis: 4
Route/Site: IM / LA

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

Alopecia

Symptomtext

PATIENT STARTED LOSSING HAIR EXCESSIVELY 3 MONTHS AFTER THE SHOT ON 5/1/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: DEPRESSION, DESPEPSIA, GERD, PAIN/MIGRAINE
Vorgeschichte: SAME AS ABOVE
Andere Medikamente: UNKNOWN
Allergien: NSAIDS, SSRI, CORTICOSTEROIDS, SALICYLATES
Vorherige Impfungen: -

VAERS 2439897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 08.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 70-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Apr2022 as dose 4, (booster), single (Lot number: FJ4991) at the age of 70 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "asthma" (unspecified if ongoing); "psoriatic arthritis" (unspecified if ongoing); "known allergies: melons" (unspecified if ongoing), notes: known allergies: melons; "known allergies: airborne" (unspecified if ongoing), notes: known allergy: airborne; "Known Allergies: chemical sensitivity" (unspecified if ongoing), notes: Known Allergies: chemical sensitivity. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Negative, notes: I tested negative for 3 days; (unspecified date) Negative, notes: I tested negative for 3 days; (unspecified date) Negative, notes: I tested negative for 3 days; (unspecified date) Positive, notes: then have tested positive for 8 consecutive days including today; (unspecified date) Positive, notes: then have tested positive for 8 consecutive days including today; (unspecified date) Positive, notes: then have tested positive for 8 consecutive days including today; (unspecified date) Positive, notes: then have tested positive for 8 consecutive days including today; (unspecified date) Positive, notes: then have tested positive for 8 consecutive days including today; (unspecified date) Positive, notes: then have tested positive for 8 consecutive days including today; (unspecified date) Positive, notes: then have tested positive for 8 consecutive days including today; (unspecified date) Positive, notes: then have tested positive for 8 consecutive days including today; (06Sep2022) Positive, notes: then have tested positive for 8 consecutive days including today. Therapeutic measures were taken as a result of drug ineffective, covid-19. Patient received treatment for COVID 19 as Paxlovid on 21Aug2022 and stopped on 26Aug2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19 Treatment; Test Result: Negative ; Comments: I tested negative for 3 days; Test Name: COVID 19 Treatment; Test Result: Negative ; Comments: I tested negative for 3 days; Test Name: COVID 19 Treatment; Test Result: Negative ; Comments: I tested negative for 3 days; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today; Test Date: 20220906; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: then have tested positive for 8 consecutive days including today
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Air-borne transmission (known allergy: airborne); Asthma; Chemical sensitivity (Known Allergies: chemical sensitivity); Food allergy (known allergies: melons); Psoriatic arthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2439860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: OH
Alter: 74,0
Geschlecht: M
Eingang: 10.09.2022
Impfdatum: 08.04.2022
Beginn: 01.08.2022
Tage bis Beginn: 115,0
Dosis: 4
Route/Site: - / RA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 74-year-old male patient received BNT162b2 (BNT162B2), on 30Jan2021 at 14:00 as dose 1, single (Lot number: EL2965), in right arm, on 17Feb2021 at 14:00 as dose 2, single (Lot number: EM9809), in right arm, on 29Oct2021 at 10:00 as dose 3 (booster), single (Lot number: FH8020), in right arm and on 08Apr2022 at 11:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 74 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ATORVASTATIN, start date: Feb1995, stop date: 21Aug2022; PAROXETINE, start date: Jan1998; LISINOPRIL AND HYDROCHLOROTHIAZIDE, start date: Apr2008; MULTIVITAMIN [VITAMINS NOS], start date: Feb1998. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (31Aug2022) Negative, notes: Tested negative on day 10; (04Sep2022) Positive, notes: Retested for COVID on day 15 and tested positive (also on day 16, today.); (05Sep2022) Positive, notes: Retested for COVID on day 15 and tested positive (also on day 16, today.). Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Paxlovid start date=22Aug2022, stop date=26Aug2022, route: oral. The patient took the 5-day Paxlovid regimen during days 2-6 of covid. Tested negative on day 10.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Test Date: 20220831; Test Name: Covid-19 test; Test Result: Negative ; Comments: Tested negative on day 10; Test Date: 20220904; Test Name: Covid-19 test; Test Result: Positive ; Comments: Retested for COVID on day 15 and tested positive (also on day 16, today.); Test Date: 20220905; Test Name: Covid-19 test; Test Result: Positive ; Comments: Retested for COVID on day 15 and tested positive (also on day 16, today.)
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
Andere Medikamente: ATORVASTATIN; PAROXETINE; LISINOPRIL AND HYDROCHLOROTHIAZIDE; MULTIVITAMIN [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2439812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MD
Alter: 51,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 15.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Mar2021 as dose 1, single (Lot number: ER8734), in left arm, on 19Apr2021 as dose 2, single (Lot number: ER8734), in left arm, on 01Nov2021 as dose 3 (booster), single (Lot number: FH8028), in left arm and on 15Jul2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 51 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Graves disease" (unspecified if ongoing). Concomitant medication(s) included: LEVOXYL, start date: Jun1988. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19; Negative, notes: having a negative test. Therapeutic measures were taken as a result of vaccination failure, covid-19 included Paxlovid from 24Aug2022 to 29Aug2022. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Name: Covid-19 test; Test Result: Negative ; Comments: having a negative test
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Graves' disease
Andere Medikamente: LEVOXYL
Allergien: -
Vorherige Impfungen: -

VAERS 2433720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: OH
Alter: 70,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 09.06.2022
Beginn: 25.08.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

Near people who had COVID-19. Had sore throat then took a home COVID-19 test - positive. Had a telehealth appointment and decided not to take any prescriptions. Retested Home COVID-19 test - negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home COVID-19 test - positive. 3 weeks later, home COVID-19 test - negative.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroid; Hashimoto's; Barrett's Esophageal
Andere Medikamente: UNITHROID; vitamin D; magnesium; liothyronine; calcium; vitamin B12
Allergien: Tetanus
Vorherige Impfungen: -

VAERS 2430090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond date of product use. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 06.07.2022
Beginn: 01.07.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient beyond the use date of the product. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2428612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: WA
Alter: 37,0
Geschlecht: M
Eingang: 03.09.2022
Impfdatum: 01.09.2022
Beginn: 01.09.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient administered an expired Pfizer vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2426272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CO
Alter: -
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 05.05.2022
Beginn: 09.08.2022
Tage bis Beginn: 96,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Disease recurrence Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; COVID Rebound; This is a spontaneous report received from contactable reporter(s) (Physician) from product quality group. A female patient received BNT162b2 (BNT162B2), on 05May2022 at 15:00 as dose 4 (booster), single (Lot number: FJ4991), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DISEASE RECURRENCE (medically significant) with onset 09Aug2022, outcome "not recovered", described as "COVID Rebound"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Patient had all the same symptoms 4 days prior reporter with the same vacation history, Paxlovid & rebound. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Rebound with nasal congestion, cough, sneezing. Patient had all the same symptoms 4 days prior to reporter with the same vacation history, Paxlovid & rebound.; Sender's Comments: Based on temporal association, there is reasonable possibility of causal association between the Reported events and the suspect drug.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: Patient had all the same symptoms 4 days prior reporter with the same vacation history, Paxlovid & rebound
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2423947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: WI
Alter: 57,0
Geschlecht: M
Eingang: 30.08.2022
Impfdatum: 13.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Disease recurrence Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; Tested COVID positive on 10Aug. Started Paxlovid on 11Aug. Tested negative on 20Aug. Now tested COVID positive again on 25Aug; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old male patient received BNT162b2 (BNT162B2), on 13Apr2022 at 18:30 as dose 4 (booster), single (Lot number: FJ4991) at the age of 57 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "Latex allergy" (unspecified if ongoing); "penicillin allergy" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL; LUPIN, start date: 01Jan2020. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19"; DISEASE RECURRENCE (medically significant), outcome "not recovered", described as "Tested COVID positive on 10Aug. Started Paxlovid on 11Aug. Tested negative on 20Aug. Now tested COVID positive again on 25Aug". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (10Aug2022) Positive, notes: Tested COVID positive on 10Aug; (20Aug2022) Negative, notes: Started Paxlovid on 11Aug. Tested negative on 20Aug; (25Aug2022) Positive, notes: Now tested COVID positive again on 25Aug. Therapeutic measures were taken as a result of drug ineffective, covid-19, disease recurrence. The patient was treated with Paxlovid from 11Aug2022 to 15Aug2022 for the events. Clinical course: The patient has been isolating during this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220810; Test Name: COVID-19 test; Test Result: Positive ; Comments: Tested COVID positive on 10Aug.; Test Date: 20220820; Test Name: COVID-19 test; Test Result: Negative ; Comments: Started Paxlovid on 11Aug. Tested negative on 20Aug.; Test Date: 20220825; Test Name: COVID-19 test; Test Result: Positive ; Comments: Now tested COVID positive again on 25Aug.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Hypertension; Latex allergy; Penicillin allergy
Andere Medikamente: LISINOPRIL; LUPIN
Allergien: -
Vorherige Impfungen: -

VAERS 2423912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CO
Alter: 73,0
Geschlecht: M
Eingang: 30.08.2022
Impfdatum: 05.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Physician) from product quality group. The reporter is the patient. A 73-year-old male patient received BNT162b2 (BNT162B2), on 05May2022 at 15:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 73 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "hyperlipidemia" (unspecified if ongoing); "BPH" (unspecified if ongoing); "PVCs" (unspecified if ongoing). Concomitant medication(s) included: BYSTOLIC; ATORVASTATIN; FLOMAX [MORNIFLUMATE]; MULTAQ. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Product: COVID 19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient had no known allergies. Anti-viral COVID 19 treatment with Paxlovid.; Sender's Comments: Based on the available information and possible temporal association the causal relationship between the reported events and suspect BNT162B2 cannot be excluded .The case will be reviewed further with FU information. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: Product: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: BPH; Hyperlipidemia; Hypertension; Premature ventricular contractions
Andere Medikamente: BYSTOLIC; ATORVASTATIN; FLOMAX [MORNIFLUMATE]; MULTAQ
Allergien: -
Vorherige Impfungen: -

VAERS 2422440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: KY
Alter: 82,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 12.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID; COVID; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 82-year-old female patient received BNT162b2 (BNT162B2), on 21Jan2021 as dose 1, single (Lot number: 663249), in arm, on 11Feb2021 as dose 2, single (Lot number: EL9262), in arm, on 27Sep2021 as dose 3 (booster), single (Lot number: FC3184), in arm and on 12Apr2022 at 13:00 as dose 4 (booster), single (Lot number: FJ4991) at the age of 82 years, in right arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Macrobid for UTI infection, reaction(s): "Chills", notes: symptoms went away when stopped; Antibiotics, reaction(s): "Fainted", notes: When on the antibiotic, fainted both times. Vaccination history included: Shingles (Dose: 1 at arm, need another one but century), for Immunization; Polio (when a child), for Immunization. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive; Negative; Negative; Negative. Therapeutic measures were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Test Name: Home test; Test Result: Negative ; Test Name: Home test; Test Result: Negative ; Test Name: Home test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2422373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 27.08.2022
Impfdatum: 22.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: - / -

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

Skin hyperpigmentation

Symptomtext

This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 22Jun2022 as dose 4 (booster), single (Lot number: FJ4991) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6203; Expiration date: 30Jun2021), administration date: 20Feb2021, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: EP6955; Expiration date: 30Jun2021), administration date: 13Mar2021, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: FC3183), administration date: 25Sep2021, for COVID-19 Immunization. The following information was reported: SKIN HYPERPIGMENTATION (non-serious) with onset 25Jun2022, outcome "not recovered", described as "my upper lip got dark and still was hyperpigmentation". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2422270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 05.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / -

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

Lymphadenopathy SARS-CoV-2 test

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66-year-old female patient received BNT162b2 (BNT162B2), on 05Jul2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 66 years intramuscular for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose: 1st, Date: 26Apr2021, Anatomical site of injection: (withheld), Route of administration: Intramuscular, Batch/Lot number: Pfizer EN5318), administration date: 26Apr2021, when the patient was 64-year-old, for COVID-19 Immunization, reaction(s): "COVID-19"; BNT162b2 (Dose: 2nd, Date/ Time: 12May2021, Anatomical site of injection: (withheld), Route of administration: Intramuscular, Batch/Lot number: ER8735), administration date: 12May2021, when the patient was 64-year-old, for COVID-19 Immunization, reaction(s): "COVID-19", "Dose 1: 26Apr2021/Dose 2: 12May2021"; BNT162b2 (Dose: 3rd (Booster), Date/ Time: 13Dec2021, Anatomical site of injection: (withheld), Route of administration: Intramuscular, Batch/Lot number: FJ8762), administration date: 13Dec2021, when the patient was 65-year-old, for COVID-19 Immunization, reaction(s): "COVID-19". The following information was reported: LYMPHADENOPATHY (non-serious) with onset 2022, outcome "unknown", described as "lymph node swelling". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Additional information: Patient age at time of vaccination: 65, then 66 years. Patient had no prior reaction. Patient was later told this was reductant due to actual immunity. Develops Safeway should tall. This staff who was informed of my prior covid reaction to this booster. Lymph node swilling. Specific relevant test for thromboembolic events with thrombocytopenia is None. Comments/ Narrative: Following (positive) covid test, was given Paxlovid. No positive effect- I worsened later that it is for serious case, but mine was not: no fever, no breathing difficulty. No patient dude with doctor with list in hand-told to take the sheets of paper and go home and read them. (After administration of Paxlovid). Probably not Paxlovid had no positive effect. I found the drug to be hassle on my body. (I normally was natural healing and health maintain products). At the end of Paxlovid I returned to the same urgent call and pay temp. and respiration were tested both not serious (Although I felt worse than before when diagnosed) and was told to go to home and rest, was given nothing. I self-started zinc for immune with occasional supplement of olive leave immune. I was unsure about zinc and olive leaf did not wish further complications. To date (11Aug2022). I continue the zinc to finish the bottle and will return to my natural method afterwards. My covid brain frog coded fully 01Aug2022 (7Weeks) and fall energy returned 11Aug2022 for normal activity. Please excuse the dirty condition of this envelope and interior sheets, it came to me this way. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymphadenopathy
Hospital-Tage: -
Labordaten: Test Date: 20220612; Test Name: Covid test; Test Result: Positive; Test Date: 20220612; Test Name: Flu test; Test Result: Negative; Comments: Just in case of negative covid; Test Date: 20220407; Test Name: Home kit; Test Result: Negative; Test Date: 20220408; Test Name: Home kit; Test Result: Negative; Test Date: 20220409; Test Name: Home kit; Test Result: Negative; Test Date: 20220410; Test Name: Home kit; Test Result: Negative ; Test Date: 20220411; Test Name: Home kit; Test Result: Negative.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2422178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: GA
Alter: 57,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 12.04.2022
Beginn: 31.07.2022
Tage bis Beginn: 110,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Mar2021 at 12:00 as dose 1, single (Lot number: EN6205), in right arm, on 03Apr2021 at 14:00 as dose 2, single (Lot number: ER8733), in left arm, on 28Oct2021 at 16:30 as dose 3 (booster), single (Lot number: FF2593), in left arm and on 12Apr2022 at 12:45 as dose 4 (booster), single (Lot number: FJ4991) at the age of 57 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Cerebral aneurysm" (unspecified if ongoing); "Pituitary gland microadenoma" (unspecified if ongoing), notes: Pituitary gland microadenoma. Concomitant medication(s) included: VITAMIN D [COLECALCIFEROL], start date: Jan2011. Past drug history included: Morphine, reaction(s): "known_allergies Morphine", notes: known_allergies Morphine. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 31Jul2022, outcome "recovered" (18Aug2022) and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (12Aug2022) Positive; (18Aug2022) Negative; (31Jul2022) Positive; (07Aug2022) Negative. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: COVID 19 Treatment included the patient COVID-19 PCR test was positive on 31Jul2022. The nurse practitioner at # prescribed me Paxlovid for 5 days which she completed the regime on 05Aug2022. On 07Aug2022, She took another COVID-19 PCR test, the result was negative. On 12Aug2022 she took another covid (antigen) and tested positive, so she had a rebound event. She primary care doctor prescribed me a 2nd round of Paxlovid for 5 more days. On 18Aug2022 I took another COVID (antigen) test and tested negative. 2nd round of Paxlovid treatment was received for the adverse event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220812; Test Name: COVID-19 Antigen test; Test Result: Positive ; Test Date: 20220818; Test Name: COVID-19 Antigen test; Test Result: Negative ; Test Date: 20220731; Test Name: PCR test; Test Result: Positive ; Test Date: 20220807; Test Name: PCR test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cerebral aneurysm (unruptured); Pituitary microadenoma (Pituitary gland microadenoma)
Andere Medikamente: VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2420824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 22.05.2022
Beginn: 20.08.2022
Tage bis Beginn: 90,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Extra dose administered SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 4 vaccines Pfizer 2/10/21 Lot# El9267; Pfizer 3/5/21 Lot# EN6202; Pfizer 10/17/21 Lot# FH8020; Pfizer 5/22/22 Lot# FJ4991

Weitere VAERSDATA-Felder

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

VAERS 2418152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj4991

gering

Staat: NY
Alter: -
Geschlecht: F
Eingang: 23.08.2022
Impfdatum: 05.05.2022
Beginn: 01.08.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 19Mar2021 at 09:00 as dose 1, single (Lot number: En6207), in left arm, on 09Apr2021 at 09:00 as dose 2, single (Lot number: Ew0158), in left arm, on 03Dec2021 at 09:00 as dose 3 (booster), single (Lot number: Fj8762), in left arm and on 05May2022 at 09:00 as dose 4 (booster), single (Lot number: Fj4991), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Penicillin allergy" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "COVID-19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: The patient was treated with Anti viral Paxlovid from 08Aug2022 to 12Aug2022 for the treatment of COVID-19. The patient did not received any other medication in 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2416737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: FL
Alter: -
Geschlecht: F
Eingang: 20.08.2022
Impfdatum: 12.07.2022
Beginn: 18.08.2022
Tage bis Beginn: 37,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Caller is now testing positive for Covid illness 18Aug2022; Caller is now testing positive for Covid illness 18Aug2022; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A female patient received BNT162b2 (BNT162B2), on 12Jul2022 as dose number unknown (booster), single (Lot number: FJ4991) for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose number unknown (booster), single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 18Aug2022, outcome "unknown" and all described as "Caller is now testing positive for Covid illness 18Aug2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18Aug2022) positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220818; Test Name: COVID-19 Test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2416150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MD
Alter: 73,0
Geschlecht: M
Eingang: 19.08.2022
Impfdatum: 31.03.2022
Beginn: 01.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Audiogram Tinnitus

Symptomtext

Several days following my forth vaccination I noticed that I was experiencing Tinnitus, I saw the ENT and he stated that the Tinnitus was By Lateral and there were no other issues going on so it was determined to be Enidiopathic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Audiogram
Hospital-Tage: -
Labordaten: Auditory Test April 22,2022
Aktuelle Erkrankungen: None
Vorgeschichte: Cornary Artery Disease
Andere Medikamente: Metropolol; Rofuvostatin; Ezetimide; Aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2415694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 09.04.2022
Beginn: 17.08.2022
Tage bis Beginn: 130,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Disease recurrence SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Tested positive today on Day 12 (17Aug2022); This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Mar2021 as dose 1, single (Lot number: ER8734), on 16Apr2021 as dose 2, single (Batch/Lot number: unknown), on 16Oct2021 as dose 3 (booster ), single (Lot number: 3590) and on 09Apr2022 as dose 4 (booster), single (Lot number: FJ4991) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DISEASE RECURRENCE (medically significant) with onset 17Aug2022, outcome "not recovered", described as "Tested positive today on Day 12 (17Aug2022)"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (15Aug2022) Negative, notes: on Day 10; (17Aug2022) Positive, notes: on Day 12. Therapeutic measures were taken as a result of vaccination failure, covid-19 and treatment included Paxlovid from 07Aug2022 to 12Aug2022. Therapeutic measures were not taken as a result of disease recurrence. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20220815; Test Name: COVID-19 test; Test Result: Negative ; Comments: on Day 10; Test Date: 20220817; Test Name: COVID-19 test; Test Result: Positive ; Comments: on Day 12
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2415693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: SC
Alter: 79,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 05.04.2022
Beginn: 25.07.2022
Tage bis Beginn: 111,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 79-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Jan2021 as dose 1, single (Lot number: EL0140), in left arm, on 03Feb2021 as dose 2, single (Lot number: EN5318), in left arm, on 25Sep2021 as dose 3 (booster), single (Lot number: FF2566), in left arm and on 05Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 79 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications in 2weeks. Past drug history included: Tetracycline, reaction(s): "Allergy", notes: known allergies: Allergic to tetracycline. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 25Jul2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (26Jul2022) Positive, notes: Tested positive on July 26 with severe sore throat and fatigue; (04Aug2022) Negative, notes: tested negative on August 4; (07Aug2022) Positive, notes: August 7, I felt very congested and fatigued. Tested positive that evening. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: She felt ill 25July. Tested positive on 26July with severe sore throat and fatigue. Was prescribed Paxlovid which she started on 26July and finished on 31July. Recovered and tested negative on 04August. 07August, she felt very congested and fatigued. Tested positive that evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220726; Test Name: Covid-19 Test; Test Result: Positive ; Comments: Tested positive on July 26 with severe sore throat and fatigue; Test Date: 20220804; Test Name: Covid-19 Test; Test Result: Negative ; Comments: tested negative on August 4; Test Date: 20220807; Test Name: Covid-19 Test; Test Result: Positive ; Comments: August 7, I felt very congested and fatigued. Tested positive that evening.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2415639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 19.08.2022
Impfdatum: 01.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old male patient received BNT162b2 (BNT162B2), in Feb2022 as dose 4 (booster), single (Lot number: FJ4991), in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Migraine" (unspecified if ongoing). Concomitant medication(s) included: LOPRESSOR; LIPITOR, stop date: 06Aug2022; EFFEXOR; PREVACID. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: strong positive; Negative, notes: almost negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Other medication in 2weeks reported as Lopressor, Lipitor, Effexor XR and Prevacid. It was reported that Covid-19 treatment from 06Aug2022 to 11Aug2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19; Test Result: Positive ; Comments: strong positive; Test Name: COVID 19; Test Result: Negative ; Comments: almost negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine
Andere Medikamente: LOPRESSOR; LIPITOR; EFFEXOR; PREVACID
Allergien: -
Vorherige Impfungen: -

VAERS 2414480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 18.08.2022
Impfdatum: 22.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old male patient received BNT162b2 (BNT162B2), on 22Apr2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 64 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 22Apr2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative, notes: I've tested negative using the nasal swab Antigen test; Positive, notes: I've been concerned about my positive PCR covid test for over a month after my initial positive test; Positive, notes: my PCR test is still positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient stated, I have been concerned about my positive PCR covid test for over a month after my initial positive test. I have tested negative using the nasal swab Antigen test but still after a month, my PCR test is still positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 nasal swab Antigen test; Test Result: Negative ; Comments: I've tested negative using the nasal swab Antigen test; Test Name: Covid-19 PCR test; Test Result: Positive ; Comments: I've been concerned about my positive PCR covid test for over a month after my initial positive test.; Test Name: Covid-19 PCR test; Test Result: Positive ; Comments: my PCR test is still positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Verbatim: Other medical history- None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2414123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 17.08.2022
Impfdatum: 17.05.2022
Beginn: 01.07.2022
Tage bis Beginn: 45,0
Dosis: 4
Route/Site: UN / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Contracted a mild case of Covid 19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Rapid Test at home Test at county Covid treatment clinic
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Multiple vitamin, fish oil, calcium, magnesium, Zyrtec, vitamin D3, turmeric, CoQ10
Allergien: mango
Vorherige Impfungen: -

VAERS 2413214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: KS
Alter: 70,0
Geschlecht: F
Eingang: 17.08.2022
Impfdatum: 02.05.2022
Beginn: 01.08.2022
Tage bis Beginn: 91,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Sep2021 as dose 3 (booster), single (Lot number: PF8839), in left arm and on 02May2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 70 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. No known allergies. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 including received Paxlovid from 03Aug2022 to 07Aug2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
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 2413205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 17.08.2022
Impfdatum: 01.02.2022
Beginn: 01.08.2022
Tage bis Beginn: 181,0
Dosis: 4
Route/Site: - / RA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). A 64-year-old male patient received BNT162b2 (BNT162B2), in Feb2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 63 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing). No allergy. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2412690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 16.08.2022
Impfdatum: 08.04.2022
Beginn: 12.08.2022
Tage bis Beginn: 126,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Vaccine breakthrough infection

Symptomtext

Fully vaccinated with 2 boosters. COVID breakthrough infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2412283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: AZ
Alter: 65,0
Geschlecht: M
Eingang: 16.08.2022
Impfdatum: 16.07.2022
Beginn: 18.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Anxiety Supraventricular extrasystoles

Symptomtext

Within 2 days of vaccination, he started to have bigeminal PACs. HR in 60's. HR normally 50's-60's. This made him feel "anxious". Saw his cardiologist who said this was not dangerous. It continues off and on. In thinking back, he stated that he thinks this occurred after his first booster as well and took about 5 months to completely resolve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anxiety
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: Low testosterone, hypertension, low back pain
Andere Medikamente: testosterone cream, losartan
Allergien: None
Vorherige Impfungen: COVID Pfizer booster #1 30155BA, 10/1/2021.

VAERS 2303930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ 4991

gering

Staat: PA
Alter: 20,0
Geschlecht: M
Eingang: 15.08.2022
Impfdatum: 12.05.2022
Beginn: 13.05.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Anti-neutrophil cytoplasmic antibody positive vasculitis Antineutrophil cytoplasmic antibody Antinuclear antibody Biopsy kidney Biopsy kidney abnormal Blood creatinine increased Glomerulonephritis rapidly progressive Complement factor C3 Complement factor C4 Double stranded DNA antibody Full blood count Haematuria IgA nephropathy Metabolic function test Ultrasound kidney Urine abnormality Urine analysis

Symptomtext

Rapidly Progressive Concentric Glomerulonephritis (symptoms appearing 2 days after 2nd dose)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute kidney injury
Hospital-Tage: 8,0
Labordaten: ER visit May 15 and subsequent 8 day hospitalization for Accute Kidney Injury Kidney Biopsy confirmed Rapidly progressive Crescentic Glomerulonephritis IV Steroid infusion Rituximab infusion Creatinine rose to 4.2 in days
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Clonidine
Allergien: None
Vorherige Impfungen: -

VAERS 2410763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: MA
Alter: 74,0
Geschlecht: M
Eingang: 13.08.2022
Impfdatum: 22.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 75-year-old male patient received BNT162b2 (BNT162B2), on 22Feb2021 as dose 1, single (Lot number: FV6202), in left arm, on 16Mar2021 as dose 2, single (Lot number: EP7534), in left arm, on 09Nov2021 at 12:00 as dose 3 (booster), single (Lot number: WG3912), in left arm and on 22May2022 as dose 4 (booster), single (Lot number: FJ4991) at the age of 74 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06Aug2022) Negative; (10Aug2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: No other medication in 2 weeks. Patient received Anti-viral treatment for COVID-19 with Paxlovid from 28Jul2022 to 06Aug2022. Original Covid 19 Symptoms 28Jul2022, Aching muscles on 29Jul2022, Took Paxlovid on 30Jul2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220806; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20220810; Test Name: COVID-19 Test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2408548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: OH
Alter: 70,0
Geschlecht: M
Eingang: 11.08.2022
Impfdatum: 11.05.2022
Beginn: 22.06.2022
Tage bis Beginn: 42,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Influenza like illness SARS-CoV-2 test positive

Symptomtext

Flu-like symptoms 6/22/2022. Tested positive for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home rapid antigen test 6/22/2022, positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Glaucoma, high cholesterol
Andere Medikamente: Singulair, Minocycline, Zioptan, Pravastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2407450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj4991

gering

Staat: AK
Alter: 10,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 27.07.2022
Beginn: 27.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

underage adult booster administered to 10 year old

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2405838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 18.07.2022
Beginn: 02.08.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: - / RA

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

Influenza like illness

Symptomtext

Flu like illness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Influenza like illness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Long Covid, NAFLD, asthma, immuno compromised
Vorgeschichte: Asthma Long Covid Immunocompromised
Andere Medikamente: Trazodone, advair, ventolin, gabapentin, monteleukast, cyclosporine
Allergien: Dairy, pork, gluten, cats, dogs
Vorherige Impfungen: -

VAERS 2404126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 07.08.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine was administered beyond use date of the product by a handful of days. No adverse effects were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 07.08.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered beyond use date of the product by a handful of days. No adverse effects reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 94,0
Geschlecht: F
Eingang: 07.08.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered a handful of days beyond use date of the product. No adverse effects reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 07.08.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered beyond-use-date. No adverse effects reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 07.08.2022
Impfdatum: 05.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered beyond-use-date. No adverse effects reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 07.08.2022
Impfdatum: 05.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered to patient a handful of days beyond the use date of the product. No adverse reactions reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ4991

gering

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 07.08.2022
Impfdatum: 05.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered beyond-use-date. No adverse affects reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -