VAERS Reports 33130 BA

VAERS 2724789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: AZ
Alter: 79,0
Geschlecht: M
Eingang: 15.12.2023
Impfdatum: -
Beginn: 04.04.2023
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Cardiac telemetry Hypotension Hypoxia Pneumonia Respiratory symptom

Symptomtext

Reported Symptoms: 10021143:HYPOXIA; 10035664:PNEUMONIA; Narrative: The patient was admitted to the medical floor, maintained on supplemental oxygen, and monitored on telemetry. He was started on remdesivir for symptomatic COVID-19 infection. He was initially hypotensive; with concerns for acute adrenal insufficiency due to abrupt discontinuation of steroids at nursing facility, he was started on stress dose hydrocortisone with rapid improvement in hemodynamic stability. Once blood pressures were stabilized, patient was transitioned to previous home dose of dexamethasone. He completed a 5-day course of remdesivir with resolution of hypoxia and respiratory symptoms. Other Relevant HX: The patient was admitted to the medical floor, maintained on supplemental oxygen, and monitored on telemetry. He was stated on remdesivir for symptomatic COVID-19 infection. He was initially hypotensive; with concerns for acute adrenal insufficiency due to abrupt discontinuation of steroids at nursing facility, he was started on stress dose hydrocortisone with rapid improvement in hemodynamic stability. Once blood pressures were stabilized, patient was transitioned to previous home dose of dexamethasone. He completed a 5-day course of remdesivir with resolution of hypoxia and respiratory symptoms. Other: PNA, Acute hypoxic respiratory failure

Weitere VAERSDATA-Felder

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

VAERS 2623184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 28.04.2023
Impfdatum: 08.12.2021
Beginn: 23.07.2022
Tage bis Beginn: 227,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI 11/5/2022, 12/13/2022, 2/20/2023, 1/6/2023 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2618958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 14.12.2021
Beginn: 14.03.2022
Tage bis Beginn: 90,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Chronic respiratory failure Hypoxia

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 2595690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: MI
Alter: 45,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 07.02.2022
Beginn: 10.02.2023
Tage bis Beginn: 368,0
Dosis: 3
Route/Site: - / -

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

Acute myeloid leukaemia Acute respiratory failure Adrenal adenoma Biopsy bone marrow abnormal Blood aldosterone Blood catecholamines Blood culture negative Blood smear test abnormal COVID-19 Central venous catheterisation Chemotherapy Computerised tomogram abdomen abnormal Computerised tomogram abnormal Computerised tomogram neck Computerised tomogram thorax abnormal Cortisol free urine normal Dehydroepiandrosterone test Diuretic therapy

Symptomtext

Primary Care Physician at Discharge: DO Hematologist/Oncologist: Dr. Admission Date: 2/10/2023 Discharge Date: 03/11/2023 Patient's Discharge Disposition: Home in stable condition. This is a a 46 yo female with a history of ADHD who presented to the ED on 2/10/23 with findings of elevated WBC and concerns for acute leukemia. Peripheral smear on 2/10 was consistent with acute leukemia. On presentation she had anterior cervical lymphadenopathy and concerns for sinusitis and tonsillitis. CT neck 2/10 showed several mildly enlarged level 1 and 2 lymph nodes as well as mildly prominent retropharyngeal lymph nodes findings concerning for possible tonsillitis/sinusitis. The patient was found to be positive for Covid-19 on admisison. She was treated with dex 2/10-2/15 and Remdesivir and remained stable. Bone marrow biopsy done 2/13 (in IR) was positive for AML, normal kayotype, FLT3-TKD mutated and NPM! Mutated. Panorex with no acute findings. ECHO with LVEF 64%. Hepatitis and HIV were negative. HLA typing was sent. PICC line was placed 2/15. She started induction chemo on 2/15/23 with 7+3 and then started Rydapt/Midostaurin D8-21. Day 21 IR bone marrow done 3/7 showed approximately 80% cellular bone marrow, no evidence of leukemia. She did have recurrent sinus pain and neck swelling. CT sinus/neck on 3/5 showed pansinusitis, possible otomastoiditis. ENT did see her and did not have concern for acute mastoididits. Blood cultures were negative. ID was consulted. She was on broad spectrum antibiotics. . During her nadir she also had neutropenic fevers and recurrent acute hypoxemic respiratory failure. CT thorax 3/5 showed diffuse bilateral interstitial ground glass opacities. ECHO 3/5/23 showed an EF of 55%, previously was 64%. Pulmonary was consulted and felt respiratory failure related to fluid overload vs TRALI/TACO with frequent transfusions. She was started on IV lasix BID and had good results and improvement with diuresis. She developed a rash thought to be related to cefepime and ultimately improved once antibiotics were changed. She was treated with with merrem, vancomycin, micafungin, and nystatin through 3/10 when her counts recovered. ID recommended observing off antibiotics. At discharge they recommended ppx acyclovir but with negative bone marrow biopsy from Day 21 antifungal medications. She was also on IV steroids which will be quickly tapered down at discharge. She has been weaned off O2 inpatient. The patient's counts recovered with no evidence of leukemia on D21 Bone marrow biopsy the patient is stable for discharge home today. PICC line was removed. She lives in the area and would like to get labs on Tuesdays/Thursdays in the office but will follow-up with Dr. at clinic. Per weekend attending she will need another IR bone marrow biopsy next week now that her counts have recovered. We will arrange outpatient IR bone marrow biopsy and f/u with Dr. after that is done. She is discharging home in stable condition. Incidental findings this admission: -CT sinuses 3/5 showed prominence of the sella- probably related to empty sella-- patient was asymptomatic with these findings. -CT AP 2/10 showed splenomegaly, multiple vascular lesions throughout liver-likely hemangiomas and MRI abdomen 2/14 showed focal nodular hyperplasia in the right lobe of liver. Has had Mild LFT elevation, but stable. -CT AP 2/14 showed complex partially exophytic cyst at the upper pole of right kidney, ? Bosniak III cyst. Urology plans f/u in 4 months to discuss further treatment plan. -MRI 2/14 right adrenal adenoma- urology evaluated-- 24h urine cortisol (<3.4), plasma fractionated metanephrines (<0.20), DHEA sulfate (low at 12.4) and aldosterone (10.7) level

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 29,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Leukocytosis Acute myeloid leukemia not having achieved remission Neutropenic fever Morbid obesity with body mass index (BMI) of 50.0 to 59.9 in adult Tobacco use Adult ADHD Mucositis due to chemotherapy Alternating constipation and diarrhea Counseling regarding advanced care planning and goals of care Dysphagia with left side facial/neck swelling. Acute respiratory failure with hypoxia hx of COVID-19 Bilateral pulmonary infiltrates on Imaging
Andere Medikamente: acyclovir (ZOVIRAX) 200 MG capsule amLODIPine (NORVASC) 2.5 MG tablet benzonatate (TESSALON) 100 MG capsule furosemide (LASIX) 20 MG tablet guaiFENesin (MUCINEX) 600 MG 12 hr tablet lidocaine viscous (XYLOCAINE) 2 % solution loperamide (IMO
Allergien: None
Vorherige Impfungen: -

VAERS 2547066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 28.01.2022
Beginn: 29.11.2022
Tage bis Beginn: 305,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Adrenal disorder Angiogram pulmonary abnormal COVID-19 Central nervous system lesion Computerised tomogram head abnormal Cough Exposure to SARS-CoV-2 Glycosylated haemoglobin increased Haemoglobin decreased Hyperglycaemia Hypothyroidism Influenza Influenza A virus test positive Intracranial mass Lung consolidation Magnetic resonance imaging head abnormal Metastatic neoplasm

Symptomtext

Patient is a 65 y.o. female with a history of Stage 4 Squamous NSCLC of RLL with Peripheral Neuropathy, Chronic Hypoxic Respiratory Failure (1L oxygen), NIDDM2, Depression who presented to Hospital 11/29/2022 with several days of cough and sore throat, myalgias after recent COVID exposure. She was found to have acute on chronic hypoxemic respiratory failure and positive for SARS-CoV-2 and influenza A. Hospital course was complicated by finding of new brain mass and suspected progression of metastatic disease. No plan for surgical intervention. RadOnc plans for outpatient stereotactic radiation starting 12/9/22. Hospital course prolonged due to need for continued treatment of COVID/influenza and glycemic control. Patient was placed on insulin gtt on 12/5 with Endocrinology consult placed. Insulin gtt was then discontinued on 12/7/22 and transitioned to subcutaneous insulin regimen. 1. Acute on Chronic Hypoxemic Respiratory Failure, resolved Chronically on 1-2L via NC but required 5L NC in ED. Secondary to COVID and influenza A infection. CTPA 11/30/22: consolidation in right perihilar region consistent with post treatment changes and underlying pneumonia, no PE, progression of mediastinal adenopathy. Patient has returned to 2. Steroid-Induced Hyperglycemia, NIDDM2: A1c 12.8% on 10/14/2021, A1c 10.7% on admit. Home oral medications held. DM Educator consulted, met with patient and family on 12/5, will meet with them again prior to discharge. Patient required insulin gtt on 12/5, transitioned off on 12/7. Transitioned to Lantus 55 units nightly, lispro 55 units TID before meals. Resume metformin on discharge and discontinue all other home diabetes medications. Will need close follow up with PCP as outpatient. 3. New Brain Lesion: CT Head 11/30/22: new 1.8cm hypodense right frontal lobe lesion with vasogenic edema. MRI confirmed. Neurosurgery following with no plan for intervention. RadOnc mapping on 12/2 with outpatient follow up for radiation. Dexamethasone 4mg QID then 4mg TID (12/3-12/6) then 4mg BID until RadOnc follow up on 12/9 who will manage the remaining taper. 4. Adrenal Lesion: Incidentally seen on CT. Oncology follow up outpatient. Oncology Navigator consulted. 5. Stage IV Lung Cancer: Follows with Dr (Rad Onc), Dr. and Dr. (Onc). Diagnosed in 07/2020 on Taxol/Carboplatin prior to admission (missed dose due 11/23/22). Oncology followed, f/u per above. 6. Normocytic Anemia: Likely secondary to chemo medications. Hbg 9.5 on admit, baseline ~10. 9.5 on admit. Carboplatin nadir 28 days. Taxol nadir 15-21 days. Last chemo infusion 11/03. 7. Thrombocytopenia: Likely secondary to chemo medications. Continue to monitor clinically. 8. Hypothyroidism: Secondary to Keytruda use in past. Decreased levothyroxine to 150 mcg daily per Endocrinology recommendations, recommend repeat TSH and free T4 in 4 weeks. 9. Chronic Right-sided Vision Changes: Ongoing for months, possibly related to brain lesion. Encouraged outpatient Ophtho follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2543771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: OH
Alter: 56,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 21.12.2021
Beginn: 23.04.2022
Tage bis Beginn: 123,0
Dosis: 3
Route/Site: IM / AR

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

Glaucoma Retinal vein occlusion Vision blurred Visual impairment

Symptomtext

I was out working in my garage, and I was going into my basement and lighting in there is dark and my left eye responded normally but my right eye did not adjust correctly to the change in lighting, and I could not see as I should, this was the first thing I noticed. Then I thought that my contact was blurry and to try and fix that I cleaned them and that did not help, I changed it and that did not help either. This caused me to reach out to my eye doctor. The issue makes it seem like I am looking through a smoky room or that things are blurry, and I cannot see normally. I was able to get into my doctor on April 26th and he did some tests both on my eye and on what I am seeing. I was diagnosed as having a central venous occlusion in the right eye and then glaucoma in both eyes. They have given me a treatment that includes shots of bevacizumab 0.2mg and I have six shots of that thus far and my seventh shot which was aflibercept 1 mg. They also gave me eye drops which do help as well. Now when I have flare up and that retina in the right eye is swelling up, I can work to adjust my vision and see through the blurriness, but it takes concentration and work on my end. I am answering that I am recovered because I do go in to get the shots which help for seven weeks but by the end of the seven weeks my eye does get cloudy and blurry, but the shots do work and help with the blood clot that is in my eye. I was also told that this should heal, and I will not need these shots forever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Glaucoma
Hospital-Tage: -
Labordaten: Vision tests; tests on my eyes as well but I am unsure of the name
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart Burn; Chronic Stuffy Nose; High Cholesterol; Glaucoma
Andere Medikamente: Fluticasone propionate; omeprazole; atorvastatin; losartan
Allergien: N/A
Vorherige Impfungen: Pfizer COVID-19 first dose, I felt a sharp excruciating pain as if a spider or bug was biting me near the back of my heel this l

VAERS 2347569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: TN
Alter: 85,0
Geschlecht: M
Eingang: 01.07.2022
Impfdatum: 06.12.2021
Beginn: 16.01.2022
Tage bis Beginn: 41,0
Dosis: 2
Route/Site: SYR / -

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

Asthenia COVID-19 COVID-19 pneumonia Death Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient tested positive for Covid-19 on 01/16/2022 and was treated for Covid-19 at Medical Center. He was admitted for weakness, respiratory failure d/t Covid PNA. He was treated with remdesivir and steroids and improved and then was placed Health Center for Rehab and Healing for PT and OT. Patient expired on 02/09/2022.

Weitere VAERSDATA-Felder

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

VAERS 2196525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: SD
Alter: 58,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 02.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Autopsy Death Feeling abnormal Malaise Pain in extremity Headache Hip arthroplasty SARS-CoV-2 test Pulmonary embolism

Symptomtext

patient had total hip replacement on 15Oct2021; mild headache; Second dose: Had a sore arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 59-year-old female patient received BNT162b2 (BNT162B2), on 02Apr2021 as dose 2, single (Lot number: ER8733) at the age of 58 years intramuscular, in arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1; Anatomical location: Upper arm; Route: Intramuscular; Batch/Lot number: EN6206), administration date: 11Mar2021, when the patient was 58-year-old, for Covid-19 immunization, reaction(s): "Mild headache", "Sore arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Apr2021, outcome "unknown", described as "Second dose: Had a sore arm"; HIP ARTHROPLASTY (medically significant), outcome "unknown", described as "patient had total hip replacement on 15Oct2021"; HEADACHE (non-serious), outcome "unknown", described as "mild headache". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (15Oct2021) Negative, notes: Tested Negative cleared for surgery. Therapeutic measures were taken as a result of hip arthroplasty. Clinical course: Had a sore arm: The patient had a sore arm after receiving the first and second dose Adult Pfizer Covid Vaccine. Caller states the patients sore arm believes began shortly thereafter receiving the first and second dose Adult Pfizer Covid Vaccine. Patient received her 1st dose and 2nd dose of covid vaccine as the dates reflect. Side effects were not serious expect for a sore arm and a mild headache for a day. She then received the booster (3rd dose) on 28Dec2021. Her son reported she just felt "out of it" and just generally did not felt well. She had a post-Christmas gathering planned for family on the 30Dec but cancelled it because she wasn't feeling up to it. On the morning of new year's Day, she complained of her left leg hurting as if someone "hit her with a bat". Hours later, she was found, face down, in her home, deceased. The caller does not know exactly what it meant that the patient did not feel well, except that the patient postponed a Christmas gathering with family and friends. The patient passed away on 01Jan2022. The caller states the cause of death was Pulmonary Embolism. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Date: 20211015; Test Name: Covid Test; Result Unstructured Data: Test Result:Negative; Comments: Tested Negative cleared for surgery
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's Medical History (including any illness at time of vaccination)? none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2228399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 20.12.2021
Beginn: 26.01.2022
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction Angioplasty Aortic aneurysm Aortic disorder Arteriosclerosis coronary artery Catheterisation cardiac abnormal Chest pain Coronary arterial stent insertion Coronary artery occlusion Coronary artery thrombosis Electrocardiogram ST segment elevation Electrocardiogram abnormal Iliac artery dissection Iliac artery stenosis International normalised ratio increased

Symptomtext

Patient history of mechanical aortic valve and mitral valve and is on chronic anticoagulation with Coumadin with therapeutic INR of 2.6 today on arrival, presented with chest pain and EKG showed ST elevation she went for emergent cath coronary cardiac catheterization that showed bowel significant lesion in the LAD status post stenting now. Anterolateral ST elevation myocardial infarction, attempted access via right groin, 99% right common iliac stenosis seen with iatrogenic wire induced dissection up to the distal aorta involving the right common iliac. At the conclusion of the case a limited distal aortic runoff was performed with a pigtail catheter via the right radial artery which revealed distal abdominal aortic aneurysm which is mild with severe left common iliac stenosis, severe right common iliac stenosis with what appears to be collateral beds in the distal aorta that go to the lower extremities. Successful angioplasty and stenting of mid left anterior descending coronary atherosclerosis with thrombus see report for details. Patient recovered in hospital and discharged home. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2222911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 07.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / RA

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

Death Fistula Haemodialysis Peritoneal dialysis Peritoneal dialysis complication

Symptomtext

ESRD (end stage renal disease) on dialysis - Patient failed PD, had 1 CCPD on admission - Dialyzed through the HD tunneled catheter - MWF - Arrangement for Monday/Wednesday/Friday hemodialysis at DL. - Has LUE fistula - not ready for use yet - Continue calcitriol and Renvela - Patient was also updated of dialysis after rehab; discharged from Health clinic to Skilled nursing facility. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine. Patient passed away on 3/16/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2168212

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: CA
Alter: 45,0
Geschlecht: M
Eingang: 09.03.2022
Impfdatum: 07.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: - / -

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

Chest discomfort Death Malaise

Symptomtext

Few days after the vaccine, the decedent complained of chest heaviness and not feeling well. Found dead 10 days after the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Decedent received three COVID vaccines - Vero vaccines on dates: 2/2/21, 3/2/21 and 10/29/21.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Antihypertensive medication - name unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2134588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: FL
Alter: 58,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 21.08.2021
Beginn: 20.02.2022
Tage bis Beginn: 183,0
Dosis: UNK
Route/Site: - / -

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

Aphasia Asymptomatic COVID-19 Cerebrovascular accident Computerised tomogram head abnormal Dysarthria Hemiparesis Muscular weakness SARS-CoV-2 test positive Speech disorder Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine recieved on 07/31/2021. 59 y/o with no PMHx presents to ED with 3 day history of Right arm weakness that progressed to Difficulty getting words out, expressive aphasia, dysarthria. CT revealed Left PCA stroke. Pre procedure Covid test +. Pt asymptomatic, room air sats 96%, afebrile. No covid treatment ordered, monitoring.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected on 02/20/2022
Aktuelle Erkrankungen: -
Vorgeschichte: No past medical history
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2047665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: MN
Alter: 64,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 15.12.2021
Beginn: 17.01.2022
Tage bis Beginn: 33,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Cerebrovascular accident SARS-CoV-2 test positive Therapeutic procedure Thrombectomy

Symptomtext

Received Pfizer vaccines on 3/23, 4/13, 12/15/21 COVID-19 positive by PCR on 1/17/22 admitted to hospital on 1/17/22 after being found down after large MCA stroke underlying morbid obesity, HTN, DM2 expired 1/29/22 d/t complications of stroke

Weitere VAERSDATA-Felder

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

VAERS 2069199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: MA
Alter: 86,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Caller stated her mom was in the hospital for COVID. After taking the booster she started going downhill and was discharged and about 5 days later she passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 20,0
Labordaten: unknown
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: no
Allergien: unknown
Vorherige Impfungen: -

VAERS 2054159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: WI
Alter: 63,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 10.12.2021
Beginn: 19.01.2022
Tage bis Beginn: 40,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Death

Symptomtext

Death related to Complications of COVID-19

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Other significant conditions: CAD, DM1, ESRD with kidney transplant (2009), HTN, Obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: OH
Alter: 40,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / UN

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

Coma Dyspnoea

Symptomtext

Dyspnea, coma 01/17/2022 2:40 am.

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Praegender Schweregrund: Coma
Hospital-Tage: -
Labordaten: To be released
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: Fatigue and pain, 39, 04/29/2021,mRNA, Pfizer.

VAERS 2013956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

kritisch

Staat: VA
Alter: 39,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain Disturbance in attention Fear of death Feeling cold Headache Hot flush Injection site pain Insomnia Restlessness

Symptomtext

Excruciating back pain, headaches, insomnia, restlessness, hot/cold flashes, injection site pain, can't think/concentrate, sense of impending doom.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fear of death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: back pain, ptsd, asthma, sleep apnea, migraines, dry eye, ADHD,
Andere Medikamente: zyrtec, concerta, singulair, flonase
Allergien: sulfa drug
Vorherige Impfungen: flu shot

VAERS 2723432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: MN
Alter: 40,0
Geschlecht: F
Eingang: 19.12.2023
Impfdatum: 14.01.2022
Beginn: 01.03.2022
Tage bis Beginn: 46,0
Dosis: 1
Route/Site: SYR / LA

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

Alanine aminotransferase Anti-cyclic citrullinated peptide antibody Antinuclear antibody Aspartate aminotransferase Back pain Bacterial test Blood alkaline phosphatase Blood bilirubin Blood creatine phosphokinase Blood creatinine Blood electrolytes Blood gases Blood iron Blood lactic acid Blood magnesium C-reactive protein increased Candida test Chest X-ray

Symptomtext

Jun2022 pain in my neck again, radiating down my right arm, across my chest & right torso; neck pain, seemed muscular; During my 26Nov admission 200cc of fluid was drained around my heart; Pericarditis; This is a spontaneous report received from a Consumer or other non HCP. A 41-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Jan2022 as dose 3 (booster), single (Lot number: 33130BA) at the age of 40 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: IBUPROFEN. The patient also took other concomitant therapy. Past drug history included: Bacitracin, reaction(s): "Allergy". Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Batch/Lot number: ER7835), administration date: 16Apr2021, when the patient was 39-year-old, for COVID-19 immunisation; BNT162b2 (DOSE 2, SINGLE, Batch/Lot number: EW0167), administration date: 07May2021, when the patient was 40-year-old, for COVID-19 immunisation. The following information was reported: MYALGIA (hospitalization) with onset Mar2022, outcome "unknown", described as "neck pain, seemed muscular"; NECK PAIN (hospitalization) with onset Jun2022, outcome "unknown", described as "Jun2022 pain in my neck again, radiating down my right arm, across my chest & right torso"; PERICARDITIS (hospitalization) with onset 21Nov2022, outcome "recovered with sequelae"; PERICARDIAL EFFUSION (hospitalization) with onset 26Nov2022, outcome "recovered with sequelae", described as "During my 26Nov admission 200cc of fluid was drained around my heart". The patient was hospitalized for pericarditis, pericardial effusion (hospitalization duration: 24 day(s)). The events "neck pain, seemed muscular" and "jun2022 pain in my neck again, radiating down my right arm, across my chest & right torso" required physician office visit. The events "pericarditis" and "during my 26nov admission 200cc of fluid was drained around my heart" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: C-reactive protein: (unspecified date) Unknown results; Multiple test: (unspecified date) no diagnosis was determined; Polymerase chain reaction: (17Nov2022) Negative, notes: Nasal Swab; SARS-CoV-2 test: (17Nov2022) Negative, notes: Nasal Swab. Therapeutic measures were taken as a result of pericarditis, pericardial effusion. Clinical course: Mar2022 neck pain, seemed muscular. Better in 3-4 days. Jun2022 pain in neck again, radiating down right arm, across my chest & right torso. Multiple tests were completed, no diagnosis was determined. 17Nov2022 the pain returned more severe. After 4 days patient went to Emergency room, was diagnosed with Pericarditis. Treated with pain relievers & sent home with a prescription of Colchicine. Patient returned to the hospital twice more in the next 13 days, spending 8 days in the hospital. During my 26Nov admission 200cc of fluid was drained around heart. Patient was released. Severe pain returned 38 days later. Back to ER 07Jan, Released the same day. 09Jan pain returned, back to the ER. Admitted for 8 days. Pain was under control, patient was released. Back to ER 15 days later (31Jan), & admitted again. Patient stayed in for 7 days. Patient met Doctor he was starting a drug study. Patient participated, & completed the study 23Aug. Patient still had pains in chest. DR was still monitoring CRP levels due to continued pains. Adverse events resulted in: [Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization]. No covid prior vaccination. 24 days hospitalization. Patient Recovered with lasting effects. Adverse events treatment: Pericardiocentesis, Multiple prescriptions. Patient received within 2 weeks of vaccination: Tri Low, Ibuprofen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Name: CRP; Result Unstructured Data: Test Result:Unknown results; Test Name: Multiple test; Result Unstructured Data: Test Result:no diagnosis was determined; Test Date: 20221117; Test Name: Covid Test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20221117; Test Name: Covid test/ SARS-CoV-2 test, Rapid, V; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: IBUPROFEN
Allergien: -
Vorherige Impfungen: -

VAERS 2723432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: MN
Alter: 40,0
Geschlecht: F
Eingang: 19.12.2023
Impfdatum: 14.01.2022
Beginn: 01.03.2022
Tage bis Beginn: 46,0
Dosis: 3
Route/Site: - / LA

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

Alanine aminotransferase Anti-cyclic citrullinated peptide antibody Antinuclear antibody Aspartate aminotransferase Back pain Bacterial test Blood alkaline phosphatase Blood bilirubin Blood creatine phosphokinase Blood creatinine Blood electrolytes Blood gases Blood iron Blood lactic acid Blood magnesium C-reactive protein increased Candida test Chest X-ray

Symptomtext

Jun2022 pain in my neck again, radiating down my right arm, across my chest & right torso; neck pain, seemed muscular; During my 26Nov admission 200cc of fluid was drained around my heart; Pericarditis; This is a spontaneous report received from a Consumer or other non HCP. A 41-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Jan2022 as dose 3 (booster), single (Lot number: 33130BA) at the age of 40 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: IBUPROFEN. The patient also took other concomitant therapy. Past drug history included: Bacitracin, reaction(s): "Allergy". Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Batch/Lot number: ER7835), administration date: 16Apr2021, when the patient was 39-year-old, for COVID-19 immunisation; BNT162b2 (DOSE 2, SINGLE, Batch/Lot number: EW0167), administration date: 07May2021, when the patient was 40-year-old, for COVID-19 immunisation. The following information was reported: MYALGIA (hospitalization) with onset Mar2022, outcome "unknown", described as "neck pain, seemed muscular"; NECK PAIN (hospitalization) with onset Jun2022, outcome "unknown", described as "Jun2022 pain in my neck again, radiating down my right arm, across my chest & right torso"; PERICARDITIS (hospitalization) with onset 21Nov2022, outcome "recovered with sequelae"; PERICARDIAL EFFUSION (hospitalization) with onset 26Nov2022, outcome "recovered with sequelae", described as "During my 26Nov admission 200cc of fluid was drained around my heart". The patient was hospitalized for pericarditis, pericardial effusion (hospitalization duration: 24 day(s)). The events "neck pain, seemed muscular" and "jun2022 pain in my neck again, radiating down my right arm, across my chest & right torso" required physician office visit. The events "pericarditis" and "during my 26nov admission 200cc of fluid was drained around my heart" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: C-reactive protein: (unspecified date) Unknown results; Multiple test: (unspecified date) no diagnosis was determined; Polymerase chain reaction: (17Nov2022) Negative, notes: Nasal Swab; SARS-CoV-2 test: (17Nov2022) Negative, notes: Nasal Swab. Therapeutic measures were taken as a result of pericarditis, pericardial effusion. Clinical course: Mar2022 neck pain, seemed muscular. Better in 3-4 days. Jun2022 pain in neck again, radiating down right arm, across my chest & right torso. Multiple tests were completed, no diagnosis was determined. 17Nov2022 the pain returned more severe. After 4 days patient went to Emergency room, was diagnosed with Pericarditis. Treated with pain relievers & sent home with a prescription of Colchicine. Patient returned to the hospital twice more in the next 13 days, spending 8 days in the hospital. During my 26Nov admission 200cc of fluid was drained around heart. Patient was released. Severe pain returned 38 days later. Back to ER 07Jan, Released the same day. 09Jan pain returned, back to the ER. Admitted for 8 days. Pain was under control, patient was released. Back to ER 15 days later (31Jan), & admitted again. Patient stayed in for 7 days. Patient met Doctor he was starting a drug study. Patient participated, & completed the study 23Aug. Patient still had pains in chest. DR was still monitoring CRP levels due to continued pains. Adverse events resulted in: [Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization]. No covid prior vaccination. 24 days hospitalization. Patient Recovered with lasting effects. Adverse events treatment: Pericardiocentesis, Multiple prescriptions. Patient received within 2 weeks of vaccination: Tri Low, Ibuprofen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Name: CRP; Result Unstructured Data: Test Result:Unknown results; Test Name: Multiple test; Result Unstructured Data: Test Result:no diagnosis was determined; Test Date: 20221117; Test Name: Covid Test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20221117; Test Name: Covid test/ SARS-CoV-2 test, Rapid, V; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: IBUPROFEN
Allergien: -
Vorherige Impfungen: -

VAERS 2670104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 11.08.2023
Impfdatum: 28.12.2021
Beginn: 09.02.2023
Tage bis Beginn: 408,0
Dosis: 3
Route/Site: IM / LA

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

Partial seizures

Symptomtext

FOCAL MOTOR SEIZURE

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

VAERS 2628517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 08.05.2023
Impfdatum: 21.12.2021
Beginn: 19.02.2022
Tage bis Beginn: 60,0
Dosis: 3
Route/Site: IM / LA

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

Embolic stroke Intracardiac thrombus Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE MURAL THROMBUS OF HEART POST ACUTE MI ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY 7/22/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2565755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: IN
Alter: 46,0
Geschlecht: F
Eingang: 03.03.2023
Impfdatum: 18.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / RA

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

Abdominal pain upper Blood test normal Breast pain Burning sensation Eye pain Back pain Blindness Blood test Facial pain Fatigue Feeling cold Full blood count Gait inability Headache Formication Lymph node pain Lymphadenopathy Magnetic resonance imaging normal

Symptomtext

Raynaud's syndrome; hands turn blue, pale, purple and the doctor said it was Raynauds syndrome; sees lights and kind of zig zag and it obstructs half of her vision in right eye; doctor said her eye was fine and probably neurological; vision trouble/ She sees lights and kind of zig zag; she got flu and tested positive for the flu; She was so cold/ freezing cold; Caller could not stand up or move and her whole body was shaking; It was every night. In March it was the face and eye and then in April it was her whole body. The paralysis gradually started in Mar2022 and then progressively got worse; pain around eye; sinus infection; Paralysis/ paralysis gradually started in Mar2022 and then progressively got worse; terrible headache; Nausea; skin rash on both legs; twitches in her muscles/ twitches in her legs, arms, and in shoulders; Back pain; Weakness/ felt so weak/ body was so weak; Fatigue; She couldn't sleep at all; sometimes she couldn't move to walk; It was every night. In March it was the face and eye and then in April it was her whole body. The paralysis gradually started in Mar2022 and then progressively got worse; lymph nodes in armpit the size of plum and was so painful caller could not move her arm; lymph nodes in armpit the size of plum and was so painful caller could not move her arm; lymph nodes in armpit the size of plum; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID: (Unknown). The reporter is the patient. A 46-year-old female patient received BNT162b2 (BNT162B2), on 18Jan2022 as dose 3 (booster), single (Lot number: 33130BA, Expiration Date: Feb2022) at the age of 46 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (First Dose Covid19 Vaccine:, Date: 21Apr2021, NDC: unknown, LOT: EW0153, EXP: reading from vaccine card and the expiration is partially covered by another sticker. Thinks the expiration is 31Jul2021., Anatomical Location: right arm, dose: unknown), administration date: 21Apr2021, when the patient was 45-year-old, for COVID-19 immunization; BNT162b2 (Second Dose Covid19 Vaccine:, Date: 22May2021, NDC: unknown, LOT: EW0186, EXP: 31Aug2021, Anatomical Location: right arm. She always gets in right arm because she moves it so much and thinks it is a better idea since she is right handed. , dose: unknown), administration date: 22May2021, when the patient was 45-year-old, for COVID-19 immunization; Tetanus shot (Vaccine Name: unknown, Manufacturer: unknown, Lot Number/ Expiry Date: unknown, Route, Anatomical Location: unknown/right arm, Date: Oct2021), administration date: Oct2021, when the patient was 46 years old. The following information was reported: LYMPHADENOPATHY (non-serious) with onset 21Jan2022, outcome "recovered" (2022), described as "lymph nodes in armpit the size of plum"; PAIN IN EXTREMITY (non-serious), JOINT RANGE OF MOTION DECREASED (non-serious) all with onset 21Jan2022, outcome "recovered" (2022) and all described as "lymph nodes in armpit the size of plum and was so painful caller could not move her arm"; EYE PAIN (non-serious) with onset 12Mar2022, outcome "recovering", described as "pain around eye"; SINUSITIS (non-serious) with onset 12Mar2022, outcome "recovering", described as "sinus infection"; BACK PAIN (non-serious) with onset Mar2022, outcome "recovering"; FATIGUE (non-serious) with onset Mar2022, outcome "recovering"; FACIAL PAIN (non-serious) with onset Mar2022, outcome "not recovered", PAIN (non-serious) with onset Apr2022, outcome "not recovered" and all described as "It was every night. In March it was the face and eye and then in April it was her whole body. The paralysis gradually started in Mar2022 and then progressively got worse"; NAUSEA (non-serious) with onset Mar2022, outcome "recovering"; PARALYSIS (medically significant) with onset Mar2022, outcome "unknown", described as "Paralysis/ paralysis gradually started in Mar2022 and then progressively got worse"; INSOMNIA (non-serious) with onset Mar2022, outcome "recovering", described as "She couldn't sleep at all"; ASTHENIA (non-serious) with onset Mar2022, outcome "recovering", described as "Weakness/ felt so weak/ body was so weak"; RASH (non-serious) with onset Mar2022, outcome "recovering", described as "skin rash on both legs"; GAIT INABILITY (non-serious) with onset Mar2022, outcome "unknown", described as "sometimes she couldn't move to walk"; HEADACHE (non-serious) with onset Mar2022, outcome "recovering", described as "terrible headache"; MUSCLE TWITCHING (non-serious) with onset Mar2022, outcome "recovering", described as "twitches in her muscles/ twitches in her legs, arms, and in shoulders"; TREMOR (non-serious) with onset Jul2022, outcome "unknown", described as "Caller could not stand up or move and her whole body was shaking"; FEELING COLD (non-serious) with onset Jul2022, outcome "unknown", described as "She was so cold/ freezing cold"; INFLUENZA (non-serious) with onset Dec2022, outcome "unknown", described as "she got flu and tested positive for the flu"; NERVOUS SYSTEM DISORDER (non-serious) with onset 24Dec2022, outcome "not recovered", described as "doctor said her eye was fine and probably neurological"; BLINDNESS (non-serious) with onset 24Dec2022, outcome "not recovered", described as "sees lights and kind of zig zag and it obstructs half of her vision in right eye"; VISUAL IMPAIRMENT (non-serious) with onset 24Dec2022, outcome "not recovered", described as "vision trouble/ She sees lights and kind of zig zag"; RAYNAUD'S PHENOMENON (non-serious), outcome "unknown", described as "Raynaud's syndrome"; SKIN DISCOLOURATION (non-serious), outcome "unknown", described as "hands turn blue, pale, purple and the doctor said it was Raynauds syndrome". The events "paralysis/ paralysis gradually started in mar2022 and then progressively got worse", "pain around eye", "terrible headache", "nausea", "skin rash on both legs", "twitches in her muscles/ twitches in her legs, arms, and in shoulders", "back pain", "weakness/ felt so weak/ body was so weak", "fatigue", "sinus infection", "she got flu and tested positive for the flu", "vision trouble/ she sees lights and kind of zig zag", "she couldn't sleep at all", "sometimes she couldn't move to walk", "it was every night. in march it was the face and eye and then in april it was her whole body. the paralysis gradually started in mar2022 and then progressively got worse", "raynaud's syndrome", "sees lights and kind of zig zag and it obstructs half of her vision in right eye", "doctor said her eye was fine and probably neurological", "hands turn blue, pale, purple and the doctor said it was raynauds syndrome", "she was so cold/ freezing cold" and "caller could not stand up or move and her whole body was shaking" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: (2022) Negative, notes: Did blood test for Lupus and Fibromyalgia and all immune system disorders and they came back ok, negative; Full blood count: (2022) negative, notes: They tested a lot of things like infection and blood count; Influenza virus test: (unspecified date) Positive, notes: tested positive for the flu; Infection: (2022) negative, notes: They tested a lot of things like infection and blood count; Magnetic resonance imaging head: (14Jun2022) It didn't show anything. Clinical course: Clarified the symptoms she experienced on 12Mar2022 as starting with pain around eye. Eye doctor said it was fine and there was nothing wrong with her eye. Eye doctor thought caller had sinus infection. Referred caller to ENT who checked her out and ordered MRI. The symptoms she experienced was pain around the eye. It started getting stronger and more intense and spreading all over her forehead, cheeks, head on top and back, and all over her head. Then a little bit after that, caller does not know the exact date, she started getting paralysis especially at night. She could not sleep at all. She would put her head down for 30 minutes and then wake up with feeling like she could not move, it was her hands and legs. Could not move for 15-20 minutes. then started moving them a little and went downstairs to walk around to move her body a little bit. Three days after the booster vaccine she had lymph nodes in armpit the size of plum. That lasted about a week and was so painful caller could not move her arm. That went away so caller is not concerned about it. The symptoms that started in March lasted for a long time. She had paralysis especially at night. She had terrible headache. She had nausea and a skin rash on both legs. She feels twitches in her muscles. She has that on camera. She feels twitches in her legs, arms, and in shoulders. When having the paralysis, it felt like someone is squeezing her so tight that her blood flow stopped. She felt so squeezed she could not move. She had back pain, nausea, weakness, sometimes she could not move to walk, and she felt so weak. She had fatigue as well. The first thing she felt was pain around eye and it got worse and worse. That was from Mar2022 through Jul2022 and Aug2022. She started feeling a little better in Sep2022. It was every night. In March it was the face and eye and then in April it was her whole body. The paralysis gradually started in Mar2022 and then progressively got worse. Her body was so weak. if she put her finger on her ribs she could not touch anything. She could not stand a bra or t-shirt because it was so painful. She started feeling better in Sep2022. The symptoms faded away and she started feeling better. Then last December she got flu and tested positive for the flu. All of her symptoms came back. All of them plus a new one which is vision trouble. The vision trouble started 24Dec2022 and is still ongoing. She sees lights and kind of zig zag and it obstructs half of her vision in right eye. It lasts for 15 minutes and then goes away. She had it again on 04Jan2023. Went to see eye doctor again and doctor said her eye was fine and probably neurological. Occurred again on 24Jan2023 and it lasted 10-15 minutes and then went away. It gets worse and worse. She has had episodes at night of paralysis and seeing what looks like a volcano is bursting, the red flames. Everything is dark in her room and her eyes are closed and she stills sees those lights. She went to the doctor again last Thursday who checked her again. He said she her eyes are fine and what she is dealing with is neurological. That is why she is calling. She just needs help. Caller does not know if anyone can help her. Caller clarified that she is looking for any recommendation for vision disturbances and paralysis after the vaccination booster. Is there any medicine? She is willing to try anything. She thought Pfizer would have information about medications to take since Pfizer manufactured the vaccines. One more thing she forgot to tell. She believes it is important. Her hands turn blue, pale, purple and the doctor said it was Raynauds syndrome. She has never had this before. It started when all these symptoms started. Her hands and feet turn blue and sometimes purple, sometimes pale, sometimes red. They think it is Raynauds syndrome. It came with all the other symptoms. Regarding emergency room: At some point she was going to go to ER (emergency room), but did not go because she could not. That would have been around 11Jul2022. She could not move at all and could not hold her head up. Her husband got so concerned and wanted to take her ER. Caller could not stand up or move and her whole body was shaking. She was so cold and it was July. She had to be covered with 3 blankets. They had to turn the heat on because she was freezing cold. Caller told her husband to let her rest a little and see.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: Test Date: 2022; Test Name: blood test; Test Result: Negative; Comments: Did blood test for Lupus and Fibromyalgia and all immune system disorders and they came back ok, negative.; Test Date: 2022; Test Name: blood count; Test Result: Negative; Comments: They tested a lot of things like infection and blood count; Test Name: Flu test; Test Result: Positive; Comments: tested positive for the flu; Test Date: 2022; Test Name: Infection; Test Result: Negative; Comments: They tested a lot of things like infection and blood count; Test Date: 20220614; Test Name: MRI of brain; Result Unstructured Data: Test Result:It didn't show anything
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 2547016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: TN
Alter: 65,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 21.12.2021
Beginn: 14.02.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: IM / RA

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

Acoustic stimulation tests abnormal Balance disorder Balance test Cranial nerve disorder Eyelid disorder Facial paralysis Magnetic resonance imaging head abnormal Nystagmus Tinnitus Vertigo Viral infection

Symptomtext

Awoke 2/14/22 with vertigo that mostly resolved within 48 hours. 2/16/22 awoke with tinnitus. 2/17/22 awoke with right sided eye brow paralysis and lid drooping. Seen by ENT and sent for MRI. 3/08/2022 experienced nystagmus bilaterally with 3-4 recurrent episodes. Seen by neuro and multiple follow-ups with ENT. Diagnosed with involvement of Cranial nerves 6 and 7. Suspected reactivation of existing virus. Has been nearly one year and the tinnitus persists. Balance issues mostly resolved. Rare instances of nystagmus with repetitive change of positions (bending and raising back up.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: MRI, vision testing, hearing testing, balance testing
Aktuelle Erkrankungen: none
Vorgeschichte: Type II diabetes, depression
Andere Medikamente: bupropion, venlafaxine, rosuvastatin, aspirin, vitamin D, ozempic
Allergien: nka
Vorherige Impfungen: -

VAERS 2433658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 05.04.2021
Beginn: 29.08.2022
Tage bis Beginn: 511,0
Dosis: 2
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Syncope

Symptomtext

08/28/22 presents to EC ED for "Synocope". PMHx of "falls with intracranial hemorrhage, CVA, CAD, and orthostatic hypotension"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 08/28/22 SARS-CoV-2 (COVID-19) detected.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: FL
Alter: 53,0
Geschlecht: F
Eingang: 30.07.2022
Impfdatum: 24.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Amnesia Asthenia Autonomic nervous system imbalance Bartonella test Blood immunoglobulin G Blood immunoglobulin M Blood pressure abnormal Blood pressure measurement Body temperature Borrelia test Brain injury Cardiac disorder Cerebral atrophy Ear pain Gait disturbance Gastric disorder Immunology test Infection

Symptomtext

syncope; blood pressure; Can't regulate her body temperature; Chronic pain; long term chronic lyme disease came back; Heart issues; Fractured lower back; Dysautonomia; Ear ache; 3 active infections; POTS; Parkinson's like symptoms; Migraines; Chronic stomach problems; Major memory loss; Neurological issues; Can hardly walk; Slight brain damage; Major brain loss; Debilitated; 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 received BNT162b2 (BNT162B2), on 24Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 53 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Bipolar disorder", start date: 1999 (unspecified if ongoing), notes: Illness/AE: Bipolar disorder, Onset Date: Diagnosed in 1999, Stop Date: Unknown, Pertinent Details: she found out that the tick bite she had that went untreated in 1998 turns out it's not bipolar she has; this is stemming from the dysautonomia and lyme disease.; "Fibromyalgia" (ongoing), notes: Illness/AE: Fibromyalgia, Onset Date: Few years ago, Stop Date: Ongoing; "Degenerative disc disease", start date: 2007 (ongoing), notes: Illness/AE: Degenerative disc disease, Onset Date: 2007, Stop Date: Ongoing, Pertinent Details: Occurred after she fell in 2007.; "Neuropathy", start date: 2007 (ongoing), notes: Illness/AE: Neuropathy , Onset Date: 2007, Stop Date: Ongoing, Pertinent Details: From a slip and fall she had on her graduation day in 2007; "Asthma" (ongoing), notes: Illness/AE: Asthma, Onset Date: All her life, Stop Date: Ongoing; "Neck surgery", start date: 2007, stop date: 2007, notes: Illness/AE: Neck surgery, Onset Date: 2007, Stop Date: 2007, Pertinent Details: She needs neck surgery again; "Fractured lower back that went undiagnosed", start date: 2007 (ongoing), notes: Illness/AE: Fractured lower back that went undiagnosed, Onset Date: 2007, Stop Date: Ongoing, Pertinent Details: Occurred when she fell in 2007.; "Long term chronic Lyme disease", start date: 1998 (ongoing), notes: Start Date: 1998, Continuing: True, Comments: Long term chronic Lyme disease. The patient's family history included: "Dementia" (unspecified if ongoing), notes: Grandmother on the (ethnicity withheld) side of the family had dementia; "Parkinson's" (unspecified if ongoing), notes: She believes her great grandfather had Parkinson's. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Second dose: Date administered: 22Apr2021, Lot: 6W0170 or could be an EW0170, it is not clear on the CDC vaccine record card.), administration date: 22Apr2021, when the patient was 53-year-old, for COVID-19 immunization, reaction(s): "her long term chronic lyme disease came back", "Dysautonomia", "Slight brain damage", "Heart issues", "Can't regulate her body temperature", "Syncope", "Chronic pain", "Debilitated", "Ear ache", "Infection", "POTS", "Parkinson's like symptoms", "Migraines", "Chronic stomach problems", "Major memory loss", "Can hardly walk", "blood pressure"; Bnt162b2 (First dose: Date administered: Either 22Mar2021 or 23Mar2021, she can't read the CDC vaccine record card clearly because of their bad handwriting.), administration date: Mar2021, when the patient was 52 years old, for COVID-19 immunization. The following information was reported: INFECTION (non-serious) with onset 2021, outcome "unknown", described as "3 active infections"; GAIT DISTURBANCE (non-serious) with onset 2021, outcome "unknown", described as "Can hardly walk"; TEMPERATURE REGULATION DISORDER (hospitalization) with onset 2021, outcome "unknown", described as "Can't regulate her body temperature"; PAIN (hospitalization) with onset 2021, outcome "unknown", described as "Chronic pain"; GASTRIC DISORDER (non-serious) with onset 2021, outcome "unknown", described as "Chronic stomach problems"; ASTHENIA (disability) with onset 2021, outcome "unknown", described as "Debilitated"; AUTONOMIC NERVOUS SYSTEM IMBALANCE (non-serious) with onset 2021, outcome "unknown", described as "Dysautonomia"; EAR PAIN (non-serious) with onset 2021, outcome "unknown", described as "Ear ache"; CARDIAC DISORDER (hospitalization) with onset 2021, outcome "unknown", described as "Heart issues"; CEREBRAL ATROPHY (medically significant) with onset 2021, outcome "unknown", described as "Major brain loss"; AMNESIA (non-serious) with onset 2021, outcome "unknown", described as "Major memory loss"; MIGRAINE (non-serious) with onset 2021, outcome "unknown", described as "Migraines"; NERVOUS SYSTEM DISORDER (non-serious) with onset 2021, outcome "unknown", described as "Neurological issues"; POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME (non-serious) with onset 2021, outcome "unknown", described as "POTS"; PARKINSONISM (non-serious) with onset 2021, outcome "unknown", described as "Parkinson's like symptoms"; BRAIN INJURY (medically significant) with onset 2021, outcome "unknown", described as "Slight brain damage"; LYME DISEASE (hospitalization, medically significant, life threatening) with onset 2021, outcome "unknown", described as "long term chronic lyme disease came back"; SYNCOPE (hospitalization, medically significant), outcome "unknown"; BLOOD PRESSURE ABNORMAL (hospitalization), outcome "unknown", described as "blood pressure"; SPINAL FRACTURE (medically significant), outcome "unknown", described as "Fractured lower back". The patient was hospitalized for cardiac disorder, syncope, blood pressure abnormal (start date: May2022, discharge date: 2022); for temperature regulation disorder, pain (start date: 2022, discharge date: 2022). The events "long term chronic lyme disease came back", "slight brain damage", "major brain loss", "debilitated", "fractured lower back", "dysautonomia", "ear ache", "3 active infections", "pots", "parkinson's like symptoms", "migraines", "chronic stomach problems", "major memory loss", "neurological issues" and "can hardly walk" required physician office visit. The events "heart issues", "syncope", "blood pressure", "can't regulate her body temperature" and "chronic pain" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Bartonella test: (30Jun2022) Positive, notes: Result: Positive detected 2 or more; Unit: Not Provided; Blood immunoglobulin G: (30Jun2022) Positive, notes: Result: 320 positive active; Unit: Not Provided; Blood immunoglobulin M: (30Jun2022) Positive, notes: Result: Positive detected 2 or more TBRF borrelia species; Unit: Not Provided; (30Jun2022) Positive, notes: Result: Positive for lyme; Unit: Not Provided; (30Jun2022) or more of the starred bands are present, notes: Result: 2 or more of the starred bands are present; Unit: Not Provided; (30Jun2022) Positive, notes: Result: US generous burgdorferi positive; Unit: Not Provided; Blood pressure measurement: (unspecified date) Unknown results; Body temperature: (unspecified date) Unknown results, notes: can't regulate her body temperature; Borrelia test: (30Jun2022) Positive, notes: Result: Positive; Unit: Not Provided; (30Jun2022) indecisive she guessed, they were unsure, notes: Result: Inc-for indecisive she guessed, they were unsure; Unit: Not Provided; (30Jun2022) Positive, notes: Result: Positive; Unit: Not Provided; Immunology test: (30Jun2022) Positive, notes: Result: positive for ELISA lyme disease; Unit: Not Provided; Magnetic resonance imaging: (2022) brain is damaged, notes: Result: Part of her brain is damaged; Unit: Not Provided. Clinical course included: Vaccination facility type was noted as pharmacy. Vaccine administered at military facility was noted as no. Time the vaccination was given: was unknown. Additional vaccines administered on same date of the Pfizer suspect-If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect was noted as none. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) was noted as none. The Pfizer Covid-19 Vaccine was mandated; she did not want it. She has been to many different specialists and these events are all pointing back to the vaccine that she was told she had to take in order to fly. The patient was very upset and angry. She said that she received Pfizer Covid-19 Vaccine as well the booster shot, and this was the reason why she was experiencing everything. She did not mention specific situation or what happened to her. She had done every test and it was pointing to the Pfizer Covid-19 Vaccine. She clarified that she has had 3 doses of Pfizer Covid-19 Vaccine including 1 booster shot. She reported after being administered the products all of her symptoms started including: her long term chronic lyme disease came back; Dysautonomia; Neurological issues; Heart issues; Ear ache; Debilitated; slight brain damage; 3 active infections; POTS; Parkinson's like symptoms; migraines; chronic stomach problems; chronic pain; major brain loss; major memory loss; can hardly walk; can't regulate her body temperature. The patient was hospitalized for syncope, when she passed out in her dad's arms. It was unknown that how many days was the hospital stay. The provider was the one who diagnosed her and did all the bloodwork and everything. Dysautonomia noted as It affected her whole autonomic system. When you look up dysautonomia with long term symptoms of COVID she had all of those symptoms. It was very hard for her to do anything she is so debilitated. 3 active infections noted as she did not know how long she has had them. She clarified that they started in 2021 after her Apr2021 dose of Pfizer Covid-19 Vaccine. She reported there are no treatment or medical interventions to report. All events for physician's office; for emergency room events were chronic pain; heart issues including syncope and blood pressure; can not regulate her body temperature.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201009808 Same patient and drug, different event separated in time;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20220630; Test Name: Bartonella elizabethae; Test Result: Positive ; Comments: Result: Positive detected 2 or more; Unit: Not Provided; Test Date: 20220630; Test Name: Babesiosis IFA-IgG Duncani ISA-IgG; Test Result: Positive ; Comments: Result: 320 positive active; Unit: Not Provided; Test Date: 20220630; Test Name: ImmunoBlot IgM TBRF borrelia genus ImmunoBlot IgM; Test Result: Positive ; Comments: Result: Positive detected 2 or more TBRF borrelia species; Unit: Not Provided; Test Date: 20220630; Test Name: Lyme ImmunoBlot IgM IGeneX criteria and CDC NYS criteria; Test Result: Positive ; Comments: Result: Positive for lyme; Unit: Not Provided; Test Date: 20220630; Test Name: Lyme ImmunoBlot IgM which detects antibodies to Burgdorferi strains and species; Result Unstructured Data: Test Result:2 or more of the starred bands are present; Comments: Result: 2 or more of the starred bands are present; Unit: Not Provided; Test Date: 20220630; Test Name: Lyme ImmunoBlot IgM which detects antibodies to Burgdorferi strains and species; Test Result: Positive ; Comments: Result: US generous burgdorferi positive; Unit: Not Provided; Test Name: Blood Pressure; Result Unstructured Data: Test Result:Unknown results; Test Name: body temperature; Result Unstructured Data: Test Result:Unknown results; Comments: can't regulate her body temperature.; Test Date: 20220630; Test Name: Burgdorferi European Genus; Test Result: Positive ; Comments: Result: Positive; Unit: Not Provided; Test Date: 20220630; Test Name: Hermsii; Result Unstructured Data: Test Result:indecisive she guessed,they were unsure; Comments: Result: Inc-for indecisive she guessed,they were unsure; Unit: Not Provided; Test Date: 20220630; Test Name: Relapsing fever SPP borreliosis TBRF for borrelia; Test Result: Positive ; Comments: Result: Positive; Unit: Not Provided; Test Date: 20220630; Test Name: Burgdorferi IS-GMA; Test Result: Positive ; Comments: Result: positive for ELISA lyme disease; Unit: Not Provided; Test Date: 2022; Test Name: MRI; Result Unstructured Data: Test Result:brain is damaged; Comments: Result: Part of her brain is damaged; Unit: Not Provided
Aktuelle Erkrankungen: Asthma (Illness/AE: Asthma; Onset Date: All her life; Stop Date: Ongoing); Degenerative disc disease (Illness/AE: Degenerative disc disease; Onset Date: 2007; Stop Date: Ongoing;); Fibromyalgia (Illness/AE: Fibromyalgia; Onset Date: Few years ago; Stop Date: Ongoing); Lyme disease (Start Date: 1998; Continuing: True;); Neuropathy (Illness/AE: Neuropathy; Onset Date: 2007; Stop Date: Ongoing); Vertebral fracture (Illness/AE: Fractured lower back that went undiagnosed; Onset Date: 2007; Stop Date: Ongoing;)
Vorgeschichte: Medical History/Concurrent Conditions: Bipolar disorder (Illness/AE: Bipolar disorder; Onset Date: Diagnosed in 1999; Stop Date: Unknown); Dementia (Grandmother on the (ethnicity withheld) side of the family had dementia); Neck surgery (Illness/AE: Neck surgery; Onset Date: 2007; Stop Date: 2007; Note: She needs neck surgery again); Parkinson's disease (She believes her great grandfather had Parkinson's.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: MO
Alter: 30,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 20.12.2021
Beginn: 15.03.2022
Tage bis Beginn: 85,0
Dosis: 3
Route/Site: SYR / AR

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

Arthralgia Electric shock sensation Hypoaesthesia Laboratory test Paraesthesia

Symptomtext

roughly the middle of March started experiencing occasional numbness and tingling in hands and forearms. then in beginning of June started experiencing more frequent numbness and tingling, that turned into shock-type pains in my elbows, and pin-prick type feelings in my fingers. my hands and arms began feeling like they were asleep a good portion of the day as well. in the last week or so I have also started getting numbness in my feet as well, and that "fallen asleep" feeling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: preliminary test through office visit with my Internal Medicine PA (at Dr.'s office, listed in previous question). referred for EMG and nerve conduction study, which is to happen on June 30.
Aktuelle Erkrankungen: none recalled
Vorgeschichte: Anxiety, depression, gluten intolerance, asthma, carpal tunnel
Andere Medikamente: Gabapentin, Xanax, Promethazine, Dicyclomine, Hydroxychloroquine, Depakote, Montelukast, Allegra, Buspar, Wellbutrin, Zoloft, Probiotic
Allergien: Medications: Ceclor & Zolair Insect Stings
Vorherige Impfungen: Sept. 2019, at age 28, had anaphylactic shock and paralysis lasting several weeks following injection in back of both upper arms

VAERS 2320438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: PA
Alter: 35,0
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 14.12.2021
Beginn: 02.05.2022
Tage bis Beginn: 139,0
Dosis: 3
Route/Site: SYR / -

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

Anaphylactic reaction Bronchitis COVID-19 Laboratory test Upper respiratory tract infection Urticaria

Symptomtext

Beginning 12/26/2021 and continuing through 01/31/2022, three events of minor anaphylaxis. Beginning 12/26/2021 and continuing through April 2022, continuous evens of urticaria caused by unknown/indeterminable trigger. Treatment included over the counter allergy medicine. Urticaria cause is unknown. Beginning 02/01/2022 and continuing through 04/30/2022, a few instances of upper respiratory infections. On 05/02/2022, diagnosed with COVID-19. Upon recovery from COVID-19, diagnosed with a bronchial infection 05/23/2022 that continued through 06/10/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Medical tests and laboratory results related to the anaphylaxis and urticaria were inconclusive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2238691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: MI
Alter: 56,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 14.12.2021
Beginn: 30.03.2022
Tage bis Beginn: 106,0
Dosis: 2
Route/Site: UN / UN

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

Arthralgia COVID-19 Dental discomfort Dialysis Fall Head injury Headache Hypertension Influenza A virus test negative Influenza B virus test Loss of consciousness Nausea Pain in extremity Respiratory syncytial virus test negative SARS-CoV-2 test positive Vomiting

Symptomtext

Attending Physician: DO Specialty:Internal Medicine Date of H&P: 3/30/2022 HPI: This is a 56y.o. male evaluated on general medical floor. Patient reports that he was smoking a joint when he lost consciousness and fell down a few stairs. He reports he hit his head on the concrete landing. He denies feeling lightheaded or dizzy or experiencing any chest pain or difficulty in breathing prior to the fall. He does report some nausea and vomiting earlier in the day. He was unable to hold down his blood pressure medications and immediately vomited them up after taking them. He reports a headache as well as pain in the left arm as well as the left hip and knee. Denies any current chest pain or difficulty breathing. Denies abdominal pain, nausea, vomiting. Denies any blood thinner use. He states he was recently admitted to other hospital for elevated blood pressure. He signed out AMA (against medical advice) on Monday. He has dialysis MWF and did go to dialysis on Monday after signing out AMA. He reports marijuana use. He denies any cocaine abuse since August. This morning, good spirits, awake alert oriented times 3. He tells me he tested positive for Covid in January. He is in need of dental care. Horrific dental caries. Asking for pain therapy. No chest pain, shortness of breath, fever, chills. Most of his discomfort is dental

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 3,0
Labordaten: PT CLASS: Inpatient PATIENT STATUS: Discharged GENDER: male Results Covid-19, Flu, RSV by NAA Contains abnormal data Covid-19, Flu, RSV by NAA Status: Final result Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 03/29/22 9:49 PM Last Resulted: 03/29/22 10:39 PM
Aktuelle Erkrankungen: ? AIDS ? Chronic kidney disease ? Diabetes mellitus ? Diabetes mellitus, type II ? ETOH abuse 3/30/2022 ? Hep C w/o coma, chronic ? HIV disease ? Hypertension ? Marijuana use 3/30/2022 ? Sarcoidosis
Vorgeschichte: ? AIDS ? Chronic kidney disease ? Diabetes mellitus ? Diabetes mellitus, type II ? ETOH abuse 3/30/2022 ? Hep C w/o coma, chronic ? HIV disease ? Hypertension ? Marijuana use 3/30/2022 ? Sarcoidosis
Andere Medikamente: Abacavir-Dolutegravir-Lamivud 600-50-300 MG PO Tab 1 Tablet, Oral, DAILY ? acetaminophen (TYLENOL) 650 mg, Oral, EVERY 6 HOURS AS NEEDED ? albuterol (PROVENTIL, VENTOLIN) 2.5 mg, Nebulization, EVERY 6 HOURS AS NEEDED ? albuterol (PROVENTIL
Allergien: ? Sustiva [Efavirenz] Unable to specify Pt altered
Vorherige Impfungen: -

VAERS 2151903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 16.12.2021
Beginn: 10.02.2022
Tage bis Beginn: 56,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory distress syndrome Cough Dyspnoea Fatigue Myalgia Pneumonia

Symptomtext

Patient's medical records from system indicate patient had muscle aches, cough, shortness of breath, fatigue, difficulty breathing. Patient is reported to have acute respiratory distress and had developed pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cancer, Chronic Lung Disease, Hypertension, Psychological condition
Vorgeschichte: Chronic Lung Disease, Hypertension, Psychological condition
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: GA
Alter: 48,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Asthenia Blood test normal Cardiac discomfort Cardiac flutter Chest X-ray normal Chest discomfort Chest pain Dyspepsia Echocardiogram Electrocardiogram Eructation Fatigue Gastrooesophageal reflux disease Headache Injection site pain Lymphadenopathy Mitral valve incompetence

Symptomtext

Heart/chest pressure, tightness Heart palpitations, fluttering, racing Heart/chest pain GERD, burping, heart burn Vertigo Nausea Tired, weak Anxiety Cramps (back, knees, shoulders, neck, jaw) Headache On and off tinnitus Lymph node under arm sore Injection site sore Runny nose Sore throat Sneezing Wheezing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG 1-6-22, normal Blood draw for thyroid 1-6-22, normal Chest X-ray 1-6-22, normal Echo Cardiogram Ultrasound 1-13-22, mitral valve prolapse/mitral valve regurgitation Blood draw, urine sample 2-8-22, suspected myocarditis Heart monitor 1 week, scheduled 2-14-22 until 2-20-22 Stress test scheduled 2-18-22 MRI scheduled 3-16-22
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: B12 500 mcg Calcium 500 mg w/D3 Magnesium Glycinate 200 mg Potassium 99 mg Vitamin C 125 mg Iron 65 mg 2 x a week Sprintec birth control
Allergien: None
Vorherige Impfungen: -

VAERS 2065282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: OR
Alter: 14,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 10.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

C-reactive protein increased Chest pain Echocardiogram Electrocardiogram abnormal Headache Pericarditis Pyrexia Red blood cell sedimentation rate increased Tachycardia Troponin increased Vomiting

Symptomtext

Fever HA Tachycardia vomiting's chest pain + 12 EKG- Pericarditis +Tropin Pt referred to Pedi Cardiology

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: + 12 lead EKG Pericarditis +echo + Tropin high CRP HIGH sed rate
Aktuelle Erkrankungen: + Positive Covid 19 10/25/2021
Vorgeschichte: NO
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2062513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: AZ
Alter: 53,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 14.12.2021
Beginn: 21.01.2022
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: IM / RA

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

Blood culture Chest X-ray Chest discomfort Computerised tomogram Echocardiogram Electrocardiogram Full blood count Metabolic function test Presyncope Ultrasound scan

Symptomtext

Near faint, Chest tightness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 3,0
Labordaten: 1/22/2022: BMP, CBC, blood cultures, CT scan, Ultrasound, CXR, EKG, ECHO
Aktuelle Erkrankungen: Hypotension
Vorgeschichte: Allergies-Hayfever
Andere Medikamente: Xyzal, Nexium, Otezla, Paxil, Vit D, Vit C
Allergien: Keflex, Meclomen, Tessalon Pearls
Vorherige Impfungen: -

VAERS 2057045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: MA
Alter: 53,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Back pain Feeling abnormal Immunisation Loss of consciousness Mass Neck pain SARS-CoV-2 test

Symptomtext

Passed out; Felt terrible; Lump on the head; Sore back and neck; Sore back and neck; Dose number: 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 14:00 (Lot number: 33130BA) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "covid prior vaccination" (unspecified if ongoing). If other vaccine in four weeks was reported as unknown. No known allergies. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EWO170, Location of injection: Arm Right, Vaccine Administration Time: 09:00 AM), administration date: 31Aug2021, when the patient was 53 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Arm Right, Vaccine Administration Time: 09:00 AM), administration date: 31Jul2021, when the patient was 53 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 16Dec2021 14:00, outcome "unknown", described as "Dose number: 3"; LOSS OF CONSCIOUSNESS (medically significant) with onset 17Dec2021 09:00, outcome "recovering", described as "Passed out"; FEELING ABNORMAL (non-serious) with onset 17Dec2021 09:00, outcome "recovering", described as "Felt terrible"; MASS (non-serious) with onset 17Dec2021 09:00, outcome "recovering", described as "Lump on the head"; NECK PAIN (non-serious), BACK PAIN (non-serious) all with onset 17Dec2021 09:00, outcome "recovering" and all described as "Sore back and neck". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (04Jan2022) negative. Therapeutic measures were taken as a result of loss of consciousness, feeling abnormal, mass, neck pain, back pain. Patient said that like his first 2 doses, he felt fine for about 12 hours and then really bad for another 10 hours or so. He woke up and felt terrible, so he stayed in bed until 9 am. Finally, he decided to get up and take a shower. He passed out in the shower and woke up with a lump on the head, a sore back and neck. Treatment medication included chiropractor. The patient was tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20220104; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2055696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: WA
Alter: 18,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

The patient passed out shortly after receiving the vaccine. The patient was talking and looking around shortly after passing out and the paramedics were called as a precautionary measure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Infection
Vorgeschichte: Insomnia
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2053984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: OK
Alter: 19,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Seizure

Symptomtext

CLIENTS MOTHER STATES 5 MINUTES AFTER ADMINISTRATION OF PFIZER VACCINE CLIENT HAD A 4 MINUTE LONG SEIZURE - SEIZURE WAS NOT OBSERVED BY NURSES - MONITOR NOTIFIED NURSE ONCE THE 15 MINUTE OBSERVATION TIME WAS UP AND MOTHER HAD ASKED TO SPEAK WITH A NURSE BEFORE LEAVING - MOTHER STATES THIS IS NORMAL FOR HIM - HE HAS DAILY SEIZURES - BUT SHE DID NOT KNOW IF IT WAS DUE TO THE VACCINE OR NOT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: HAS A SEIZURE DISORDER WITH DAILY SEIZURES
Vorgeschichte: HAS A SEIZURE DISORDER WITH DAILY SEIZURES
Andere Medikamente: MOTHER DID NOT DISCLOSE DAILY MEDICATIONS - HAS A SEIZURE DISORDER
Allergien: NKA
Vorherige Impfungen: -

VAERS 2039811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

schwer

Staat: IL
Alter: 41,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 28.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Hypoaesthesia Migraine Syncope

Symptomtext

migraine headache started at 2am after recieving vaccine, headache has persisted on an intermitent basis for 3 weeks since, experienced face numbness and an episode of syncope lasting 15 minutes with "light headedness" in the shower on 12/29/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: migraine headaches
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: flu shot allergy
Vorherige Impfungen: flu shot

VAERS 2037650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: WA
Alter: 59,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 30.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Diplopia VIth nerve paralysis

Symptomtext

sixth nerve palsy right eye; Horizontal double vision/diagnosed with diplopia; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 59 year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 30Dec2021 09:30 (Lot number: 33130BA) at the age of 59 years as dose 2, single for COVID-19 immunization. Relevant medical history included: "Hypertension" (unspecified if ongoing). Patient had no allergies. Concomitant medication included: LISINOPRIL. Vaccination history included: Bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) (DOSE 1, SINGLE, Lot number: FJ8762, Administration time: 01:00 PM, Vaccine location: Left arm), administration date: 09Dec2021, when the patient was 59 years old, for COVID-19 Immunization. The following information was reported: VITH NERVE PARALYSIS (medically significant) with onset 03Jan2022, outcome "not recovered", described as "sixth nerve palsy right eye"; DIPLOPIA (non-serious) with onset 03Jan2022, outcome "not recovered", described as "Horizontal double vision/diagnosed with diplopia". The events "sixth nerve palsy right eye" and "horizontal double vision/diagnosed with diplopia" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were not taken as a result of vith nerve paralysis, diplopia. Clinical course: After 72 hours patient began experiencing horizontal double vision. It has become more pronounced since injection. Patient went to emergency room and was seen by urgent care physician and an ophthalmologist. Patient was diagnosed with diplopia and sixth nerve palsy right eye. Later notified by ophthalmologist that vaccination could be the cause of diplopia. The patient again went to emergency room and was seen by the ophthalmologist for further medical help for the events. Since the vaccination, the patient has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension
Andere Medikamente: LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 2032345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Bell's palsy Blood test

Symptomtext

Bells palsy on left-side of face. 2nd dose batch/lot #ER8729 did the same thing. Did not report. Shot date 04/09/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Steroid shot to stop the palsy; bloodwork.
Aktuelle Erkrankungen: Tonsillitis
Vorgeschichte: High blood pressure; thyroid
Andere Medikamente: Bupropion XL 150mg; Nifedipine 60mg ER CC; Levothyroxine 0.137mcg Bisoprolol/HCTZ 5mg/6.2mg; Lansoprazole 30mg OTC; allergy pill; Atorvastatin 10mg
Allergien: N/A
Vorherige Impfungen: 2nd shot 04/09/2021 - palsy on left-side of face.

VAERS 2028086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: MT
Alter: 17,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Feeling hot Hyperhidrosis Pain in extremity Pallor Paraesthesia Seizure Syncope Tremor

Symptomtext

7:35 am c/o arm pain, no redness or heat. Went to bathroom, called out to parent c/o tingly and hot. Pale and sweaty when I got there. When she reached for glass of water, she fainted or had a seizure. 911 called. Paramedics arrived within 10 minutes. She was alert and shaky, but vitals were normal. Paramedics said it was syncopal episode and recommended f/u with primary care provider.

Weitere VAERSDATA-Felder

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

VAERS 2014054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: WA
Alter: 26,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood glucose normal Cold sweat Seizure Skin discolouration

Symptomtext

Pt came in for Pfizer Booster. After administration pt asked for a glass of water. When returning with glass of water, pt's girlfriend, was yelling for help. Upon entering room pt was in chair convulsing, clammy and noted color change. Pt was breathing and able to answer questions. Alerted MA to get provider. While in room convulsing lasted for 10-15 seconds. BP was 122/76, HR 84 and PO 99. Provider assessed pt and requested glucose reading. Glucose reading 106. Juice and snacks provided. Pt advised to wait in office for 30 minutes. Continued 5 minute checks on pt. Pt alert and oriented. After 30 minutes assessed by provider. Pt continued to be free of symptoms and feeling better, pt then left office.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Glucose reading: 106 BP: 122/76 HR: 84 PO: 99
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: Per pt has had reactions to vaccines in the past, unable to verify due to not administering vaccines to pt prior to this visit.

VAERS 2011208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: HI
Alter: 25,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Seizure

Symptomtext

PATIENT WAS SEIZING IN THE WAITING CHAIR FOR ABOUT 30 SECONDS. PATENT STATES THAT SHE LIKE SHE "WENT TO SLEEP"

Weitere VAERSDATA-Felder

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

VAERS 2010864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Cold sweat Feeling cold Loss of consciousness Nausea Palpitations Presyncope Visual impairment

Symptomtext

Approximately 1-2 minutes post vaccination, I started becoming extremely nauseous and while looking around for a trash can in case needed, I began blacking out. My vision got narrower and narrower and darker. I called a nurse over who brought me back to lie down. An EMT checked and my vitals were fine but my heart was racing and I was extremely cold and clammy. They had me lie down and gave me a bottle of water while I recovered from nearly passing out. Symptoms fully resolved within 20 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: rheumatoid arthritis, crohn?s, sj?gren?s syndrome, chronic migraine, tinnitus
Andere Medikamente: rinvoq (15mg daily), nurtec every other day, vitamin d 2,000 iu daily, vitamin c 1,000 mg 3x week
Allergien: allergic to hydroxychloroquine and penicillin
Vorherige Impfungen: -

VAERS 2005845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: CT
Alter: 38,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chest discomfort Condition aggravated Dyspepsia Fatigue Headache Hypertension Pain Syncope

Symptomtext

Headache/Body aches developed approx 8 hrs after vaccine injection. Conditions worsened and extreme fatigue developed approx 24 hrs from time of injection. Body aches and fatigue subsided approx 36 hrs from injection but headache remained. Syncope event approx 132 hrs from injection (no history of this condition). Headache worsened and heartburn/chest tightness developed approx 24-36hrs after Syncope and blood pressure reading taken at Pharmacy 256/174 following this patient went to ER and blood pressure reading was confirmed and patient taken to ER Trauma and then admitted to hospital and treated for hypertension and put on medications when discharge due to continued hypertension. Prior to vaccine no hypertension and had normal blood pressure readings at recent annual physicals. History approx 9 yrs ago of GERD and borderline hypertension both conditions treated with change in diet that has been consistent. No reaction to previous 2 doses of Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: Blood pressure when arrived at ER 12/27/21 256/174 Blood pressure annual physical 9/29/2021 110/70 Blood pressure annual physical 9/28/2020 130/70
Aktuelle Erkrankungen: None
Vorgeschichte: History of GERD/borderline hypertension approx 9 yrs ago both conditions were resolved by change in diet
Andere Medikamente: Zyrtec 10mg once per day, daily multi-vitamin
Allergien: Mellon food allergy
Vorherige Impfungen: -

VAERS 2000708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

schwer

Staat: NE
Alter: 83,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 22.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 pneumonia Chest X-ray Computerised tomogram Haemoglobin decreased Pulmonary haemorrhage Pulmonary thrombosis Syncope Transfusion Transient ischaemic attack

Symptomtext

4 days after the vaccines began having multiple transient ischemic attacks, and episodes of syncope. Admitted to the hospital 10 days after vaccine with internal bleeding in her lungs, lungs full of blood clots and covid pneumonia. She required 2 blood transfusions because her hemoglobin was so low. She has been placed on hospice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 4,0
Labordaten: Chest x-ray, CT Scan, 1/1/2022
Aktuelle Erkrankungen: Alzheimers
Vorgeschichte: Diabetes, alzheimers
Andere Medikamente: Ibuprofen, tramadol, citalopram, metformin
Allergien: None
Vorherige Impfungen: -

VAERS 1995521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Asthenia Blood test Cardiac disorder Cardiac monitoring Fibrin D dimer Fibrin D dimer increased Investigation Myocarditis Urine analysis

Symptomtext

Heart complications/have inflammation around my heart; Heart complications/have inflammation around my heart; D-dimer levels were high; I feel weak; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 19 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 15Dec2021 12:15 (Lot number: 33130BA) at the age of 19 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. Covid prior vaccination: no. There were no concomitant medications. Other medications in two weeks: no. Other vaccine in four weeks: no. Past drug history included: Ibuprofen, reaction(s): "Allergy". Other medical history: nothing. The following information was reported: MYOCARDITIS (medically significant), CARDIAC DISORDER (non-serious) all with onset 16Dec2021, outcome "not recovered" and all described as "Heart complications/have inflammation around my heart"; FIBRIN D DIMER INCREASED (non-serious) with onset 16Dec2021, outcome "not recovered", described as "D-dimer levels were high"; ASTHENIA (non-serious) with onset 16Dec2021, outcome "not recovered", described as "I feel weak". Ever since the shot she had experienced heart complications. The patient was taken to the hospital, completed blood work, urine specimen, iodine test because D-dimer levels were high, no blood clot but had inflammation around her heart and she felt weak and on a heart monitor now. The events "heart complications/have inflammation around my heart", "heart complications/have inflammation around my heart", "d-dimer levels were high" and "i feel weak" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: blood test: (16Dec2021) unknown results; cardiac monitoring: (16Dec2021) unknown results; fibrin d dimer: (16Dec2021) high, notes: No blood clot; investigation: (16Dec2021) unknown results; urine analysis: (16Dec2021) unknown results. Covid tested post vaccination: No. Therapeutic measures were not taken as a result of myocarditis, cardiac disorder, fibrin d dimer increased, asthenia.; Sender's Comments: Based on the information available, the causal relationship between the reported events and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Date: 20211216; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211216; Test Name: heart monitor; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211216; Test Name: D-dimer; Result Unstructured Data: Test Result:High; Comments: No blood clot; Test Date: 20211216; Test Name: iodine test; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211216; Test Name: urine specimen; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: MI
Alter: 20,0
Geschlecht: M
Eingang: 26.12.2021
Impfdatum: 22.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / AR

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

Anticoagulant therapy Chest pain Echocardiogram abnormal Feeling abnormal Heart rate increased Hyponatraemia Hypotension Malaise Pericarditis Pyrexia Troponin increased

Symptomtext

Shot #3 at pharmacy 12/22/2021- Patient reported feeling very unwell 12/25/2021 around 8 am complaining of " feels like I'm having a heart attack". Fever of 101.1 around 4 pm same day. Requested to go to ER 12/26/21 around 12 am due to terrible chest pain. He is still in ER at Medical Clinic. DX is pericarditis. No prior history of cardiac events. Moderate malaise during 12/21 to 12/24. Being treated currently with heparin, toradol, nitroglycerin, K+.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: Pericarditis via echocardiogram 12/26 as per nurse via phone. Abnormal elevated troponin levels on admittance. Hyponatrimia. Low blood pressure 88/60?. Heart rate (resting) as high as 94 bpm.
Aktuelle Erkrankungen: Scalp dermatitis
Vorgeschichte: Possible past Lyme Disease, dysthymia
Andere Medikamente: None known
Allergien: Possible banana, wheat, dairy, rice allergies (Doctor has specific info)
Vorherige Impfungen: Dose #2 pfizer

VAERS 1978972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

schwer

Staat: CA
Alter: 34,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 1975245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: PA
Alter: 28,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Head injury Loss of consciousness Skin laceration

Symptomtext

Customer passed out around 09:13 am and hit his head off of a shelf resulting in a cut to the forehead and a large laceration to the middle of his head. Paramedics were called and began transport to the hospital. Customer recieved 4 staples to close the laceration on the top of his head.

Weitere VAERSDATA-Felder

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

VAERS 1970954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: IN
Alter: 33,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Injection site bruising Injection site haemorrhage Presyncope Tachycardia

Symptomtext

Site: Bruising at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Tachycardia-Mild, Additional Details: Patient received COVID vaccine in left deltoid at 1320pm 12/21/21 administered by RN BSN signee. Slight bruising and scant amount of blood noted to injection site. After injection stated, "I feel light headed and think I'm going to faint." Stated "I just finished working out and have not had anything to eat or drink today." Patient moved to floor on her back. BP taken 120/80 HR 66 O2 sat 99 on room air. Provided with gator aide and breakfast bar. Rested for 15 minutes.

Weitere VAERSDATA-Felder

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

VAERS 1970950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

schwer

Staat: FL
Alter: 20,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Chest discomfort Chest pain Hyperventilation Hypotension Pallor Paraesthesia Syncope Unresponsive to stimuli

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: Hyperventilation-Severe, Systemic: Hypotension-Severe, Additional Details: 5 min after giving the shot patient faints . low blood pressure and pale skin. some tingling on fingertips and pain below chest

Weitere VAERSDATA-Felder

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

VAERS 1964875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Vaccine positive rechallenge

Symptomtext

Patient left the pharmacy after waiting period subsequent to the vaccine. Pt had passed out when checking groceries at the front check stand. Pharmacy was notified by a clerk from the front of store check stand. I rushed to the front to check the patient, she was sitting on a chair. Asked the patient if she was okay?, patient replied "yes". Patient also stated she had passed out after flu shot before. Pt was offered water and some orange juice. Pt was feeling better and wanted to go home with her husband accompanying her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Followed up with patient on 12/20/2021 at 8:50 pm. Patient states she is fine and she has not had any reaction from vaccine.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: PT STATES SHE HAS PASSED OUT BEFORE FROM FLU SHOT.
Vorherige Impfungen: From Flu vaccine per patient

VAERS 1964859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: NV
Alter: 29,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Vomiting

Symptomtext

Patient received pfizer covid-19 vaccine ~4:00pm, patient advised to have a seat for 15 minutes, but patient tried to leave without waiting, and ended up fainting within 2 minutes of leaving, I advised him to have a seat and provided him a cold water bottle, within another 2 to 3 minutes, patient vomitted. After using the restroom, patient reported to feel better but I still advised him to sit for 15 more minutes where I continued to monitor him while firefighters also came to do quick tests and reporting as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None that the patient has reported of
Aktuelle Erkrankungen: Patient reported no illness any time recently
Vorgeschichte: Patient reported no health conditions
Andere Medikamente: Patient reported no prescription or over the counter medications or supplements
Allergien: Patient reported to drug, food, or other type of allergy
Vorherige Impfungen: -

VAERS 1963344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: CO
Alter: 32,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Muscle tightness Presyncope Seizure

Symptomtext

RN Called to the Waiting room by another member- reporting Pt was having a "seizure" Upon arrival to the waiting room patient was awake and able to speak verbally. Assisted patient to recliner in the vaccine room. Two Members in the lobby described the event stating patient was on his phone, dropped his phone, muscles tensed up, head fell back and was groaning. Estimated the event lasted 10-15 seconds total. Pt taken to clinic for observation. Md suspects vasovagal rx and and not seizure activity necessarily. Pt d'cd home to family after returning to baseline and requesting to go home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Umbilical hernia
Andere Medikamente: Diltiazem ointment
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 1963259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: SC
Alter: 21,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Syncope

Symptomtext

PATIENT FAINTED AFTER THE VACCINE AND WHILE FAINTED TONGUE BLOCKED AIRWAY AND PATIENT STOPPED BREATHING. PT WAS MOVED FROM SITTING POSITION TO THE FLOOR AND TONGUE WAS DISLODGE SO PT ABLE TO BREATHE AGAIN AND REGAINED CONSCIOUSNESS. 911 WAS CALLED AND EMS ARRIVED. PARENTS ELECTED FOR PT TO BE TAKEN TO HOSPITAL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: DOWN SYNDROME
Andere Medikamente: LEVOTHYROXINE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1962940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

schwer

Staat: FL
Alter: 30,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy Hypoaesthesia Paraesthesia

Symptomtext

Systemic: Bell's Palsy-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild

Weitere VAERSDATA-Felder

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

VAERS 1959125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: NV
Alter: 39,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Hypotension Seizure like phenomena Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Hypotension-Mild, Systemic: Weakness-Mild, Additional Details: Within 15 minutes of receiving the 2nd dose of Pfizer, the patient fainted. One of our pharmacy technicians described it as looking like a seizure episode. Pt was seen right away by the pharmacist and nurse practitioner. Patient came to and became alert and oriented. BP was measured to be 82/55. Pt was monitored and after resting, BP came back up to around 130/90. Pt was monitored until they felt normal and were comfortable to leave.

Weitere VAERSDATA-Felder

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

VAERS 1955973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: IN
Alter: 27,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chills Hyperhidrosis Loss of consciousness Muscular weakness Paraesthesia

Symptomtext

Patient experienced brief loss of consciousness (about 30 seconds) along with cold chills, sweating, tingling of hands and feet, and muscle weakness. Patient was taken via ambulance to hospital per patients request.

Weitere VAERSDATA-Felder

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

VAERS 1955249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: PA
Alter: 15,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: Shakiness-Medium, Additional Details: Fainted within 15 minutes of vaccination in Aisle 9

Weitere VAERSDATA-Felder

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

VAERS 1954481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: NE
Alter: 29,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Confusional state Dizziness Hypotension Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Severe, Systemic: Dizziness/Lightheadedness-Severe, Systemic: Fainting/Unresponsive-Severe, Systemic: Hypotension-Severe, Systemic: Seizure-Medium, Systemic: Weakness-Severe.

Weitere VAERSDATA-Felder

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

VAERS 1951857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Respiratory distress

Symptomtext

9mins post vaccination pt reported respiratory distress, flushing/sweating dizziness and lightheadedness. Pt layed on the floor. Pt was taken to a cot w/ feet elevated. Pt given water and orange juice. Vitals: 98/62, 71, 16 Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: Medications: Junel 1/20 PO Daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 1951828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: -
Alter: 24,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Dizziness Flushing Hyperhidrosis Paraesthesia Syncope

Symptomtext

7 mins post vaccination patient had a syncopal event with associated flushing/sweating, dizziness, and tingling sensation of fingers and toes. Vitals: 103/63, 58, 18 Pt has a hx of fainting at vaccination sites. Pt recieved vaccine, was taken to cot VS WNL. Pt rested and stated that she was feeling better. Pt given orange juice. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Bulimia nervosa
Andere Medikamente: Medications: Iron supplement
Allergien: Allergies: Mild Seasonal allergies
Vorherige Impfungen: -

VAERS 1950937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

schwer

Staat: TX
Alter: 24,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Flushing Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: pt recieved pfizer and flu vaccines in the right arm. pt then experienced flushing and sweating and then fainting. Rph on duty had pt lie down on her back with her feet elavated. tech then called emergency. paramedics checked her vitals which was normal. A medic checked her heart beat, which was also normal. after 30 minutes, pt was ok and able to leave the pharmacy by herself.

Weitere VAERSDATA-Felder

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

VAERS 1929027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: TX
Alter: 63,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Electrocardiogram Electrocardiogram normal Loss of consciousness Vision blurred

Symptomtext

Patient recieved Pfizer booster shot vaccination with her husband in the passenger seat, who did not receive a vaccination. After the shot they drove to observation, parked the car and shortly after patient passed out for "no more than 30 seconds" husband reported. Paramedics on site were called to assist. At that time she was responsive, pupils equal and reactive and talking to paramedics. Blood pressure reading initially read 53/36 with a heart rate of 44 with blurry vision. at 1442 blood pressure 111/75, HR 84, SPO2 97% respirations 13. At 1455 BP 103/56, HR 79, SPO2 95% and respirations 12. Patient refused a blood glucose check.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Electrocardiogram on site after vaccination 12/4/2021
Aktuelle Erkrankungen: Patient stated "high heart rate" but undiagnosed by a doctor
Vorgeschichte: Patient stated she was immunocompromised, but did not elaborate when asked
Andere Medikamente: Patient did not state
Allergien: None
Vorherige Impfungen: -

VAERS 1923455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Fall Loss of consciousness Walking distance test

Symptomtext

Patient passed out after receiving her 1st Pfizer vaccination. Patient mother was present with the patient and the fall was witnessed by nurse. The patient did not impact her head and patient fell onto her bottom after standing up. Patient was taken via wheelchair for observation. Patient had no obvious signs of injury, patient had full movement of her extremities, with no weakness in her arms or legs. Patient passed a walk test after her observation and her mother was advised to call 911 if she experienced weakness, chest pain, shortness of breath, dizziness, or fast heart rate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: BMI 85-94.9 percentile
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2712037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: OR
Alter: 67,0
Geschlecht: F
Eingang: 09.11.2023
Impfdatum: 07.12.2021
Beginn: 01.06.2023
Tage bis Beginn: 541,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Brain fog Epistaxis Hypoaesthesia Influenza Laboratory test normal Malaise Muscular weakness Myalgia Pain in extremity Paraesthesia

Symptomtext

Muscle pain in the left upper arm after the 2nd dose even though my shot was in the right arm. Adverse effects that started this past summer were nose bleeds which I have never had before, tingling in my arms and numbness in my hands. I have brain fog , weakness and reoccurring pain in my left arm. Some days I do not feel well and have no energy. I also got sick with the flu 2 months after the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Labs taken 2023 were normal.
Aktuelle Erkrankungen: none
Vorgeschichte: osteoporosis -mild
Andere Medikamente: multivitamin,vitD
Allergien: none
Vorherige Impfungen: -

VAERS 2628995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 09.05.2023
Impfdatum: 28.12.2021
Beginn: 25.03.2023
Tage bis Beginn: 452,0
Dosis: 3
Route/Site: - / -

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

Atrial fibrillation COVID-19 Condition aggravated Pyrexia SARS-CoV-2 test positive

Symptomtext

03/25/23 presents to ED for "fever and Afib w/RVR". PMHx of "atrial fibrillation on coumadin, cardiomyopathy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 03/25/23 SARS-CoV-2 (COVID-19) by detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2599854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: IL
Alter: -
Geschlecht: M
Eingang: 21.03.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chest discomfort Dyspnoea Photophobia Tinnitus

Symptomtext

Tightening of the Chest; Harder to breath; sensitive to lights and sounds; for 2 years Iv'e been hearing voices; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 31-year-old male patient received BNT162b2 (BNT162B2), as dose 3 (booster), single (Lot number: 33130BA), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Erb's Palsy" (unspecified if ongoing), notes: Erb's Palsy due to Birth Trauma. There were no concomitant medications. Past drug history included: Bnt162b2, start date: 02Apr2021, stop date: 02Apr2021, for COVID-19 immunization, notes: DOSE 1, SINGLE, Batch/Lot No: Pfizer ER8730, Location of injection: Arm Left; Bnt162b2, start date: 29Apr2021, stop date: 29Apr2021, for COVID-19 immunization, notes: DOSE 2, SINGLE, Batch/Lot No: Pfizer ER8735, Location of injection: Arm Left. The following information was reported: CHEST DISCOMFORT (disability, medically significant, life threatening), outcome "not recovered", described as "Tightening of the Chest"; DYSPNOEA (disability, medically significant, life threatening), outcome "not recovered", described as "Harder to breath"; PHOTOPHOBIA (disability, medically significant, life threatening), outcome "not recovered", described as "sensitive to lights and sounds"; TINNITUS (disability, medically significant, life threatening), outcome "not recovered", described as "for 2 years Iv'e been hearing voices". Therapeutic measures were taken as a result of chest discomfort, dyspnoea, photophobia, tinnitus. Clinical Course: No Other medication in 2weeks. Today was 16Mar2023 and I am still having really bad symptoms. Tightening of the Chest, Harder to breath, Became more sensitive to lights and sounds and now for 2 years Iv'e been hearing voices and want to kill myself so Screw Pfizer for what they did to me. I'm serious these symptoms are not going away and now I just got prescribe Quetiapine ER (150 MG Tablets) to get ride of the voices. I mean it that lost shot messed my life up but this better not last even though it's 2 years in. Adverse event start date was 19Jan2021.; Sender's Comments: Based on the information provided, and a temporal association, a causal association between reported events chest discomfort, dyspnoea, photophobia, tinnitus and suspect BNT162B2 cannot be excluded.The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-202300118031 same patient, different dose/AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Erb's palsy (Erb's Palsy due to Birth Trauma)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2563367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 01.12.2021
Beginn: 01.10.2022
Tage bis Beginn: 304,0
Dosis: 3
Route/Site: SYR / LA

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

Blood pressure fluctuation Dyspnoea Headache Palpitations SARS-CoV-2 test negative Vision blurred

Symptomtext

My blood pressure is higher than normal and also lower than normal. Heart palpitation Shortness of breathe Blur Vision Headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: no I take the tests on 1/21/23
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2562412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MO
Alter: 63,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 02.12.2021
Beginn: 16.01.2022
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: SYR / AR

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

Blood test Computerised tomogram Dizziness Foot deformity Jaw disorder Paraesthesia Paraesthesia oral Sciatica Transient ischaemic attack Visual impairment

Symptomtext

On January 16, 2022 I experienced what turned out to be a transient ischemic attack (TIA) of 4-5 minutes duration, went to the ER at a local Hospital. CT scan and exam performed, referred to Dr. for follow up care & testing. Symptoms presented with vision anomalies, left side tingling, and dizziness while speech remained normal. On February 11, 2022 I experienced another TIA of 20-25 minutes duration that resulted in the left foot pronation and left leg sciatic pain along with jaw misalignment, all of which resolved to normal over several months. It originally presented with left side tingling and dizziness. On November 30, 2022 I experienced a very minor TIA of approximately 30 seconds duration with lip tingles and dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CT scan and blood tests on January 16, 2021 at ER with follow up testing with Dr. in JAN or FEB 2022.
Aktuelle Erkrankungen: NA
Vorgeschichte: CABGx2 with mitral valve repair (2004). AFIB (2014)
Andere Medikamente: Eliquis, Simvastatin, Metoprolol, Aspirin, Omega 3, CoQ10, B-Complex, D-3
Allergien: NA
Vorherige Impfungen: -

VAERS 2552506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: PA
Alter: 51,0
Geschlecht: M
Eingang: 06.01.2023
Impfdatum: 05.01.2022
Beginn: 02.01.2023
Tage bis Beginn: 362,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Chills Cough Dyspnoea Fatigue Pain SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 1/2/23. I had chills, fatigue, shortness of breath, body aches, and a slight cough. I contacted my doctor and was prescribed 5 days worth of PAXLOVID and a cough medication, but I did not take the cough medicine. I started to feel better after taking PAXLOVID, but I still get fatigued easily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02JAN2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol
Andere Medikamente: Atorvastatin
Allergien: Sulfa; aspirin
Vorherige Impfungen: -

VAERS 2547011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: WA
Alter: 23,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 29.12.2021
Beginn: 26.12.2022
Tage bis Beginn: 362,0
Dosis: 3
Route/Site: SYR / AR

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

COVID-19 Chest pain Cough Exposure to SARS-CoV-2 Feeling abnormal Headache Insomnia Mental impairment Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

12/26/2022 I started with a headache and stuffiness. I figured it was the animals in the house with allergies. It would not go away. By 12/28/22, I was feeling dazed. I began having chest pains. I had been exposed to COVID. I took a home COVID test and it was positive. Coughing started later that day. I called my physician's office and spoke to the assistant. She had me call the urgent care telehealth. I was prescribed PAXLOVID, and was given a new albuterol inhaler, a FLOVENT inhaler and benzonatate. I began taking PAXLOVID that day. I have been taking those per the instructions. I am still having these symptoms, but they are all better. I can sleep better now. I feel sharper and feel better now. I have not recovered. My main concern has been my chest pain. I am still having the chest pains, but they are better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Home COVID test, positive
Aktuelle Erkrankungen: Just gotten over COVID right before the vaccine
Vorgeschichte: Brain Trauma after 8 concussions; Tourette's; Depression/Anxiety; ADHD; IBS; Hyperflexible tissues
Andere Medikamente: WELLBUTRIN; VYVANSE; clonidine; dicyclomine; rizatriptan; albuterol; cyclobenzaprine; ibuprofen
Allergien: Amoxicillin; clindamycin; VRAYLAR
Vorherige Impfungen: -

VAERS 2539102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 22.09.2021
Beginn: 04.10.2022
Tage bis Beginn: 377,0
Dosis: 2
Route/Site: - / -

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

Angiogram pulmonary abnormal COVID-19 Chest pain Coronary artery stenosis Electrocardiogram normal Refusal of treatment by patient SARS-CoV-2 test positive Troponin normal

Symptomtext

Patient is 58y.o. male who was admitted to the hospital with chest pain at home while wathcing TV --ECG non ischemic , Trop x 3 negative --CTA w > 70 % focal stenosis of LAD --seen by cards --FFR added per cards --patient does not want for echo and was cleared by cardiology for dc home Seen by ID as he tested covid +--had no symptoms but ID recommended paxlovid due to commorbidities --patient refused

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10/4 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2531062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: AZ
Alter: 46,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 10.12.2021
Beginn: 15.11.2022
Tage bis Beginn: 340,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Dyspnoea Feeling abnormal Headache Influenza Influenza virus test positive Mobility decreased Pain SARS-CoV-2 test negative

Symptomtext

I woke up with shortness of breath, aches, and an upset stomach. I just didn't feel like myself. I felt really weird. I also had a headache. The doctor confirmed I had the flu. I was in bed for four days. Urgent care gave me albuterol, ondansetron, and oseltamivir. The oseltamivir made me dizzy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/18/2022 at home COVID-19 test negative; 11/18/2022 flu test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes
Andere Medikamente: Pravastatin; metformin; OZEMPIC; biotin; vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2529920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 24.03.2021
Beginn: 01.11.2022
Tage bis Beginn: 587,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

11/01/22 presents to EC ED for "shortness of breath". PMHx of "A. fib, mitral valve replacement on anticoagulation, CHF, CKD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/01/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2504346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 21.12.2021
Beginn: 07.10.2022
Tage bis Beginn: 290,0
Dosis: 3
Route/Site: UN / UN

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

Cough Dyspnoea Myalgia Respiratory tract congestion Rhinorrhoea

Symptomtext

congestion, rhinorrhea, cough, SOB, myalgias

Weitere VAERSDATA-Felder

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

VAERS 2491225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 25.01.2022
Beginn: 16.10.2022
Tage bis Beginn: 264,0
Dosis: 3
Route/Site: - / -

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

Anticoagulant therapy Asthenia Atrial fibrillation Bone lesion Breast cancer metastatic COVID-19 Chronic left ventricular failure Computerised tomogram abdomen abnormal Computerised tomogram head normal Computerised tomogram thorax abnormal Depression Fall Hallucination Hypotension Hypothyroidism Hypoxia Pancytopenia SARS-CoV-2 test positive

Symptomtext

Discharge Provider: PA-C Attending Physician: MD Primary Care Provider at Discharge: MD Admission Date: 10/16/2022 Discharge Date: 10/24/2022 PRESENTING PROBLEM: Generalized weakness [R53.1] HOSPITAL COURSE: Patient is a 80 y.o. female metastatic breast cancer, chronic diastolic heart failure, permanent atrial fibrillation on Coumadin, hypothyroidism, depression who presented with worsening weakness and multiple falls. She had been seen in ED on 10/13 w/ hallucinations and found to be COVID positive, she was discharged to follow up outpatient. She presented back to ED on 10/16 and was found to be tachcardic and mildly hypotensive. She did have brief episode of severe hypotension and hypoxia which resolved after fluids. CT head was negative. CT thorax/abd/pelvis showed concern for metastatic disease. Care was discussed with oncology who recommended admission to medicine. Following admission pt completed 5 day course of remdesivir for COVID. She had no further episodes of hypoxia. She was seen by PT/OT with recommendations for SAR. Regarding her ill defined sclerotic and lytic bone lesions, oncology was consulted. Recommended continue letrozole and holding palbociclib and follow up outpatient. It was recommended she have outpatient MRI brain to evaluate for metastatic disease given hallucinations. She was note to have new pancytopenia, which stabilized. Peripheral smear without clear etiology for pancytopenia. Possibly related to acute illness. Recommend follow up CBC within 1 week and heme-onc follow up if persistent. She does have a follow up oncology visit scheduled on 10/26. She was incidentally found to have a thyroid nodule on CT. Ultrasound revealing two thyroid nodules of concern, for which FNA biopsy recommended. Information forwarded to PCP via Epic and discussed with patient/placed on follow up information on discharge paperwork. Coumadin was also held on admission with concern for recurrent falls. This was discussed with the patient and her son, ultimately felt benefit higher than risk (chadsvsac 4, hasbled 1) especially as plan for rehab and hopeful for LTC following. Alternative agents were discussed with the patient and her son, and she was started on eliquis. Once cleared from respiratory isolation, she was felt stable to transfer to subacute rehab on 10/24. All follow up recommendations discussed in detail prior to discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: EMERGENCY 1/4/2022 ATTENDING PHYSICIAN: CHIEF COMPLAINT: Weakness - Generalized; Covid-19
Vorgeschichte: Hypothyroidism Permanent atrial fibrillation (HCC) Essential hypertension Pulmonary hypertension (HCC) Chronic anticoagulation Chronic bilateral low back pain without sciatica Stage 3b chronic kidney disease (HCC) PUD (peptic ulcer disease) Depression Chronic diastolic heart failure (HCC) History of diverticulitis of colon Anemia Anxiety Arthritis Deep venous thrombosis (HCC) Vitamin D deficiency Osteopenia of spine History of DVT (deep vein thrombosis) Generalized weakness Lab test positive for detection of COVID-19 virus Thyroid nodule Metastatic breast cancer (HCC) Pancytopenia (HCC)
Andere Medikamente: apixaban (ELIQUIS) 5 MG tablet bumetanide (BUMEX) 0.5 MG tablet buPROPion (WELLBUTRIN XL) 150 MG 24 hr tablet Cholecalciferol (VITAMIN D3) 1.25 MG (50000 UT) CAPS digoxin (LANOXIN) 125 MCG tablet DULoxetine (CYMBALTA) 60 MG delayed release
Allergien: Metolazone Amoxicillin Keflex Sulfa Drugs
Vorherige Impfungen: -

VAERS 2493809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge 33130BA

moderat

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 22.03.2021
Beginn: 01.06.2022
Tage bis Beginn: 436,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Nasal congestion Pyrexia Tachycardia

Symptomtext

Narrative: This patient has received three doses of Pfizer COVID 19 vaccine in Mar/Apr/Dec 2021. The patient presented to the ED with cough, fever, and nasal congestion on 1 June 2022. The patient was admitted to the hospital with covid 19 and tachycardia. Patient was treated for symptoms and was discharged in stable condition on 4 June 2022. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2442879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 12.01.2022
Beginn: 05.09.2022
Tage bis Beginn: 236,0
Dosis: 3
Route/Site: UN / UN

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

Back pain Dyspnoea Hypoaesthesia Myalgia Oropharyngeal pain Respiratory tract congestion

Symptomtext

congestion, sore throat, SOB, back pain, myalgias, numbness

Weitere VAERSDATA-Felder

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

VAERS 2431013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 26.02.2021
Beginn: 05.08.2022
Tage bis Beginn: 525,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Arthritis Asthenia Blood creatinine increased Blood sodium decreased Blood test COVID-19 Cellulitis Confusional state Culture negative Delirium Fluid intake restriction Haemoglobin decreased Hypotension Mental status changes Mobility decreased SARS-CoV-2 test positive Urine analysis

Symptomtext

Patient is an 84-year-old female with recent cellulitis, who presented from home with reports of low blood pressure and mental status changes. Initially, there was concern over persistent infection, but her urinalysis and other blood work were not consistent with persistent infection. She remained afebrile and cultures were negative through her course. We kept off antibiotics. She did have followup with Dr.s team. She did have acute kidney injury with creatinine up to 1.8, likely due to the hypotension. Her ACE inhibitor was discontinued and we will keep her off this indefinitely now. She received some hypotonic saline for hydration, actually had D5 half-normal. Sodium fell down to 126. Did resume her Lasix thereafter and sodium was trending up to 128. This along with fluid restriction. She had some persistent delirium at night, sometimes calling her family and being more confused, but was oriented during the day and not combative. She has severe debility and degenerative arthritis, is able to stand, but her transfers are extremely slow and difficult. She was felt to be a better candidate for extended care facility placement in the short-term. Her creatinine was 0.9 at the time of discharge and sodium 128. Hemoglobin was 11.2 and white count was 9.3. Plan to discharge to nursing care facility hopefully later today. Follow up in the office 1 week after discharge from there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 6,0
Labordaten: 8/6 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2411681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

moderat

Staat: PA
Alter: 37,0
Geschlecht: F
Eingang: 16.08.2022
Impfdatum: 12.08.2022
Beginn: 12.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Cold sweat Diarrhoea Dizziness Dyspnoea Fatigue Hyperhidrosis Nausea Pain in extremity Peripheral swelling Rhinorrhoea Sneezing Somnolence

Symptomtext

Dizziness 4:08 pm On8/12/22 Running nose on and off plus Sleepiness 5:30. On 8/12/22. Arm soreness and sneezing around 6pm. On 8/12/22 Fatigue and clammy sweat around 7pm. 10 am on 8/13/22 diarrhea with nausea. Arm pain and swelling increased even though otc Tylenol. On and off from 8/14/22 diarrhea on and off. Clammy and occasional shortness of breath on and off 8/15/22 plus continued fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None; home resting then to do video call later
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, mild asthma, GERD.; hypoxia post Covid 2020. Sleep apnea; depression; anxiety. PTSD. Vitamin D deficiency. Anemia.
Andere Medikamente: Pneumonia vaccination
Allergien: Penicillin, amoxicillin, bactrim, Prilosec. Bee stings, seasonal allergies
Vorherige Impfungen: Covid Pfizer

VAERS 2401358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 22.12.2021
Beginn: 03.08.2022
Tage bis Beginn: 224,0
Dosis: 3
Route/Site: UN / UN

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

Chest discomfort Dyspnoea

Symptomtext

chest tightness, SOB

Weitere VAERSDATA-Felder

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

VAERS 2432361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 21.07.2022
Impfdatum: 23.12.2021
Beginn: 17.07.2022
Tage bis Beginn: 206,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 pneumonia

Symptomtext

Narrative: Fully vaccinated, admitted with COVID PNA

Weitere VAERSDATA-Felder

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

VAERS 2370522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 51,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 07.12.2021
Beginn: 07.07.2022
Tage bis Beginn: 212,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

07/07/22 presents to ED for "shortness of breath". PMHx of "asthma, pulmonary hypertension, obesity"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 07/07/22 SARS-CoV-2 (COVID-19) by detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2370474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: CO
Alter: 56,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 06.01.2022
Beginn: 29.05.2022
Tage bis Beginn: 143,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Cough Dyspnoea Fatigue Lacrimation increased Pain Rhinorrhoea SARS-CoV-2 test positive Sneezing Upper-airway cough syndrome

Symptomtext

05/29/2022 I had fatigue, sneezed a lot and watery eyes. It felt like allergies, and I do not have allergies. I was super tired. The next day I began coughing, had body aches, fatigue, runny nose, had shortness of breath and postnasal drip. I was no longer sneezing. I took an at home COVID test on 5/30/2022 around 1:30PM ET and it was positive. I had a tele health with my doctor and he prescribed me an inhaler which I never used. I did take Pepcid which I had seen would help with COVID. It took about a week to feel better but am still a little fatigued and a mild cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: At home COVID test, positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi Vitamin
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 2364464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 26.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / -

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

Asthenia COVID-19 Chest X-ray abnormal Cough Diarrhoea Dyspnoea Dyspnoea exertional Pneumonia Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Pfizer Dose 1 3/1/21 (EL9266) Pfizer Dose 2 3/24/21 (EN6204) Pfizer Dose 3 12/26/21 (33130BA) COVID Positive 1/1/22 1/1/22: Patient is 74 year old female with known history of hypertension, hypothyroidism, chronic pain, history of stroke, and other medical problems. She presents with generalized weakness, SOB, subjective fever, cough, vomiting, and diarrhea since 12/27/2021. Pt denies any chest pain or abdominal pain. Pt states she received her COVID-19 booster shot on 12/26/21 and her symptoms started to next day. She reported worsening dyspnea on exertion. Chest x-ray showed pneumonia on right side. She tested positive for SARS-CoV-2. 1/5/22: discharge home with Home Health

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN Hypothyroidism chornic pain h/o stroke CVA migraine osteoarthritis smoker
Andere Medikamente: APAP-hydrocodone 5-325 mg PO BID PRN aspirin 81 mg PO QD carvedilol 12.5 mg PO BID clopidogrel 75 mg PO QD cyanocobalamin 500 mcg PO QD dicyclomine 1 tab PO PRN loperamide 2 mg PO Q4h PRN rosuvastatin 10 mg PO HS
Allergien: NKA
Vorherige Impfungen: -

VAERS 2325505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MN
Alter: 73,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 15.12.2021
Beginn: 01.05.2022
Tage bis Beginn: 137,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Cardiac stress test Electrocardiogram abnormal Heart rate irregular Mobility decreased Muscular weakness

Symptomtext

My doctor gave me a machine to monitor my heart rate. I noticed that my heart rate was irregular after the booster. I also started to get weak in my arms, I used to be very active but now I can barely move my arm. My doctor said that if I keep exercising that it should help. However when I would take the lightest weight possible I could barely move it around. After about 30 mins I would gain some strength back. My doctor put me through stress testing at at that point my EKG was settling down. Right now everything is fine and I haven't had to self monitor my EKG in a while.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Stress test, EKG - cardiac, blood test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Kidney problems
Andere Medikamente: Aspirin; metoprolol; atorvastatin; ezetimibe; TRADJENTA; losartan
Allergien: Lisinopril; penicillin
Vorherige Impfungen: -

VAERS 2271073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 19.02.2021
Beginn: 30.01.2022
Tage bis Beginn: 345,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/30/22 presents to EC ED for "Breathing Problem". PMHx of "acid reflux, prediabetes, gout, hypertension"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/30/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: PA
Alter: 63,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 07.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arrhythmia Axillary pain Breast pain Burning sensation Condition aggravated Echocardiogram Electrocardiogram ambulatory Erythema Itching scar Lymph node pain Lymphadenopathy Pain Pulse abnormal Scar pain Supraventricular extrasystoles Swelling Ventricular extrasystoles

Symptomtext

Body aches and pain; swollen, painful lymph nodes. Left breast and left arm pit severe. Cardiac dysrhythmia, bounding pulse. (Dx: frequent PAC's and PVC's. Now taking Metoprolol succ ER 12.5 mg daily). Scar from surgery 3-8-2021 swollen, reddened, painful, burning, itching.(ongoing). Healing of surgery site WNL prior to COVID-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: 7 day Holter monitor-start 6-4-2021 removed 6-11-2021. Echocardiogram 8-12-2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Seizures, osteoporosis
Andere Medikamente: Oxcarbazepine, Plant based calcium, vitamin D, vitamin K, vitamin C, magnesium, omega 3 fish oil, egg protein.
Allergien: Topamax, dilantin, bactrim, sulfa, thimerosol, lamictol, latex, ASA, NSAIDS, gluten, lactose, bee stings-anaphylactic, dogs.
Vorherige Impfungen: -

VAERS 2250143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: TX
Alter: 25,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 08.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / LA

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

Alopecia Anaemia Condition aggravated Stress

Symptomtext

Mid December I started noticing major hair loss, big clumps by New Years. Continued through January. Went to PCP in January, who thought combo of stress, anemia. Saw Dermatologist in Feb. who said hair was growing back. Hair loss has stopped. By April hair was growing back, but still not as full as it was before vaccination. Did not have Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Anemia; depression
Andere Medikamente: Trazadone 50mg, Iron 65 mg, Vitamin C 500mg
Allergien: None
Vorherige Impfungen: -

VAERS 2247804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Mobility decreased

Symptomtext

Approximately a few minutes after my booster shot I experienced the following symptoms: Left shoulder pain, Unable to move. The doctor said it might have been an injury with how the vaccine was administered to me. I took ibuprofen for treatment and physical therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism; GERD
Andere Medikamente: Levothyroxine; Multivitamins; Vitamin B6 complex; Vitamin E; Vitamin D
Allergien: Codeine; Penicillin
Vorherige Impfungen: -

VAERS 2243604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chest X-ray Chest discomfort Chest pain Dizziness Dyspnoea Echocardiogram normal Electrocardiogram normal Electromyogram abnormal Fear Hypoaesthesia Magnetic resonance imaging Nerve conduction studies abnormal Paraesthesia Pharyngeal hypoaesthesia Pulmonary function test Throat tightness Visual impairment

Symptomtext

Facial tingling lasted one day; then sudden numbness/weakness from waist down which spread up to chest/arms and continued in waves for over 3 months, numbness waves changed to one sided (right side) numbness episodes with lightheadedness and spread to throat/larynx numbness and weakness. Vision weakness in right eye. During these symptoms, more symptoms came on including sudden chest tightness/pain, difficulty breathing (dyspnea.) If it was not during a surge of Covid in our community and understaffing at local hospitals, these symptoms felt so severe and frightening that I would have gone to the Emergency Room. Self treated with divided dose methylprednisolone (16mg total), then treated by physician with methylprednisolone pack which improved symptoms but not completely. Chest/throat tightness, breathing issues continue, as well as numbness on one side of body. After 4 months, still being evaluated. Unknown if there will be permanent numbness or damage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG/Echocardio normal (ruled out myocarditis.). Nerve Conduction Study/EMG (mostly unchanged since last testing prior to vaccine; one nerve decreased). Other tests that are scheduled include MRI, pulmonary function testing, and chest Xray.
Aktuelle Erkrankungen: Peripheral Neuropathy; Thyroid Nodule; Situational Anxiety
Vorgeschichte: Guillain Barre Syndrome; Peripheral Neuropathy
Andere Medikamente: -
Allergien: Reglan, Zofran, Phenergan, Ibuprofan, Aspirin
Vorherige Impfungen: -

VAERS 2237818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 44,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure Lymphadenopathy Mammogram Musculoskeletal stiffness Myalgia Pain in extremity Paraesthesia Peripheral swelling Ultrasound scan

Symptomtext

SARS-COV-2, qPCR: Positive; SARS-COV-2, qPCR: Positive; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44-year-old female patient received BNT162b2 (BNT162B2), on 11Mar2021 as dose 1, single (Lot number: EN6205), in left arm, on 01Apr2021 as dose 2, single (Lot number: EN6205), in left arm and on 10Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 44 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Allergy: Latex" (unspecified if ongoing), notes: Reaction. Concomitant medication(s) included: MULTIVITAMINS [VITAMINS NOS]. Past drug history included: Aspirin for known allergies: aspirin, notes: Reaction. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 10Dec2021, outcome "unknown" and all described as "SARS-COV-2, qPCR: Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (29Dec2021) Positive, notes: Other. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20211229; Test Name: SARS-COV-2, qPCR; Test Result: Positive ; Comments: Other
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Latex allergy (Reaction)
Andere Medikamente: MULTIVITAMINS [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2222633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: FL
Alter: -
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 10.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Dyspnoea Hypertrophic cardiomyopathy Left ventricular hypertrophy

Symptomtext

Hypertrophic cardiomyopathy; Left Ventricular Hypertrophy with Dyspnea; Left Ventricular Hypertrophy with Dyspnea; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program (005570). The reporter is the patient. A male patient received bnt162b2 (BNT162B2), administration date 10Dec2021 (Lot number: 33130BA) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1, Lot Number: EP7534), administration date: 22Mar2021, for COVID-19 Immunization; Bnt162b2 (Dose: 2, Lot Number: ER8737), administration date: 12Apr2021, for COVID-19 Immunization. The following information was reported: HYPERTROPHIC CARDIOMYOPATHY (medically significant), outcome "unknown", described as "Hypertrophic cardiomyopathy"; LEFT VENTRICULAR HYPERTROPHY (non-serious), DYSPNOEA (non-serious), outcome "unknown" and all described as "Left Ventricular Hypertrophy with Dyspnea". The events "hypertrophic cardiomyopathy", "left ventricular hypertrophy with dyspnea" and "left ventricular hypertrophy with dyspnea" were evaluated at the physician office visit. The patient reported that he has been diagnosed with Left Ventricular Hypertrophy with Dyspnea and Hypertrophic cardiomyopathy. His cardiologist cannot find the origin of heart condition. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2218639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: AL
Alter: 63,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Cough Dyspnoea Influenza like illness Pain Peripheral swelling Pyrexia

Symptomtext

I experienced a fever, cough, shortness of breathe, body aches, chills, arm swollen, general flu like symptoms that began the night of injection and lasted for 48 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Cancer including thyroid cancer, Diabetes, heart disease
Andere Medikamente: Amlodipine, Atenolol, Guanidine, Flaxseed oil, Jardiance, Lantus, Magnesium, Melatonin, Methphorn ER, Singulair, Oxybutynin ER, Pepcid, Potassium, Probiotics, Crestor, Savella, Carafate, Maxide, Phenylene, Vitamin d3, Zyrtec
Allergien: Benazepril, Toradol
Vorherige Impfungen: -

VAERS 2218323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MN
Alter: 53,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 13.12.2021
Beginn: 22.01.2022
Tage bis Beginn: 40,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 pneumonia

Symptomtext

Patient hospitalized for Pneumonia due to COVID-19 virus within 6 weeks of receiving covid vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: OH
Alter: 57,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Bedridden Blood pressure increased Blood pressure measurement Burning sensation Chills Cough Dizziness Dry mouth Dry throat Dysphagia Dyspnoea Feeling abnormal Feeling cold Gait disturbance Headache Fatigue Heart rate increased Hypoaesthesia

Symptomtext

Trouble eating and swallowing; States he was in bed for several days; Left arm numb and tingling; Throat scratchy and dry; Wasn't breathing normally; Racing heart; Headache; Left arm numb and tingling; Couldn't raise left arm; Throat scratchy and dry; Sore throat; Nauseous; Eyes felt heavy, irritated, and kind of foggy; Body aches; Slight cough; Feeling weird; Right hip and right leg felt weird; Chills; Goose bumps; Lightheadedness; Dry mouth; Couldn't move legs; Couldn't get warm; Blood pressure was up; Couldn't walk; Dizzy; Left calf had burning sensation; Slow and foggy; Throat feels like it's swollen; 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 57 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 29Dec2021 10:00 (Lot number: 33130BA) at the age of 57 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "C2, C3, C5, C6 narrowing" (unspecified if ongoing), notes: Verbatim: C2, C3, C5, C6 narrowing; "COVID-19" (unspecified if ongoing), notes: States he had COVID-19 the end of Apr2021 or beginning of May2021. There were no concomitant medications. The following information was reported: DYSPNOEA (non-serious) with onset 29Dec2021, outcome "unknown", described as "Wasn't breathing normally"; PALPITATIONS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Racing heart"; HEADACHE (non-serious) with onset 29Dec2021, outcome "unknown", described as "Headache"; PARAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 29Dec2021, outcome "unknown" and all described as "Left arm numb and tingling"; LIMB DISCOMFORT (non-serious) with onset 29Dec2021, outcome "unknown", described as "Couldn't raise left arm"; THROAT IRRITATION (non-serious), DRY THROAT (non-serious) all with onset 29Dec2021, outcome "unknown" and all described as "Throat scratchy and dry"; OROPHARYNGEAL PAIN (non-serious) with onset 29Dec2021, outcome "unknown", described as "Sore throat"; NAUSEA (non-serious) with onset 29Dec2021, outcome "unknown", described as "Nauseous"; DIZZINESS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Eyes felt heavy, irritated, and kind of foggy"; PAIN (non-serious) with onset 29Dec2021, outcome "unknown", described as "Body aches"; COUGH (non-serious) with onset 29Dec2021, outcome "unknown", described as "Slight cough"; FEELING ABNORMAL (non-serious) with onset 29Dec2021, outcome "unknown", described as "Feeling weird"; LIMB DISCOMFORT (non-serious) with onset 29Dec2021, outcome "unknown", described as "Right hip and right leg felt weird"; CHILLS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Chills"; PILOERECTION (non-serious) with onset 29Dec2021, outcome "unknown", described as "Goose bumps"; DIZZINESS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Lightheadedness"; DRY MOUTH (non-serious) with onset 29Dec2021, outcome "unknown", described as "Dry mouth"; MOVEMENT DISORDER (non-serious) with onset 29Dec2021, outcome "unknown", described as "Couldn't move legs"; FEELING COLD (non-serious) with onset 29Dec2021, outcome "unknown", described as "Couldn't get warm"; BLOOD PRESSURE INCREASED (non-serious) with onset 29Dec2021, outcome "unknown", described as "Blood pressure was up"; GAIT DISTURBANCE (non-serious) with onset 29Dec2021, outcome "unknown", described as "Couldn't walk"; DIZZINESS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Dizzy"; BURNING SENSATION (non-serious) with onset 29Dec2021, outcome "unknown", described as "Left calf had burning sensation"; FEELING ABNORMAL (non-serious) with onset 29Dec2021, outcome "unknown", described as "Slow and foggy"; PHARYNGEAL SWELLING (non-serious) with onset 29Dec2021, outcome "unknown", described as "Throat feels like it's swollen"; DYSPHAGIA (non-serious), outcome "unknown", described as "Trouble eating and swallowing"; BEDRIDDEN (non-serious), outcome "unknown", described as "States he was in bed for several days". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller states he had called and reported an adverse reaction to the vaccine and he didn't know, he thought they would send him something so he could send it to his work and he never received anything. Caller states he was told they would recommend he doesn't get the 2nd dose. Caller states he had a reaction and called his work to let them know the next day. States he was in bed for several days and they told him he should have gone to the hospital and he didn't and when they were getting ready to call a squad because he couldn't walk his daughter did some breathing relaxation things and he dozed off and woke up and felt a little better. States his heart was still racing. Caller states he didn't go in but when he called his work they told him to call the place that administered it to report it and so he did and they said they would have someone contact him and they didn't. States a about a week later he called them and said he never heard anything and they said ok they would check into it and call him back and he didn't hear anything back. States the following day he went to the place and they gave him this number and he called and he spoke to someone that took all the information and said they recommend he not get the 2nd dose and would send him something and his work is asking. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Blood pressure up; Result Unstructured Data: Test Result:High; Comments: Blood pressure was up; Test Name: Heart rate; Result Unstructured Data: Test Result:Unknown result; Comments: His heart was pounding.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cervical disc disease (Verbatim: C2, C3, C5, C6 narrowing); COVID-19 (States he had COVID-19 the end of Apr2021 or beginning of May2021.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: OH
Alter: 57,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Bedridden Blood pressure increased Blood pressure measurement Burning sensation Chills Cough Dizziness Dry mouth Dry throat Dysphagia Dyspnoea Feeling abnormal Feeling cold Gait disturbance Headache Fatigue Heart rate increased Hypoaesthesia

Symptomtext

Trouble eating and swallowing; States he was in bed for several days; Left arm numb and tingling; Throat scratchy and dry; Wasn't breathing normally; Racing heart; Headache; Left arm numb and tingling; Couldn't raise left arm; Throat scratchy and dry; Sore throat; Nauseous; Eyes felt heavy, irritated, and kind of foggy; Body aches; Slight cough; Feeling weird; Right hip and right leg felt weird; Chills; Goose bumps; Lightheadedness; Dry mouth; Couldn't move legs; Couldn't get warm; Blood pressure was up; Couldn't walk; Dizzy; Left calf had burning sensation; Slow and foggy; Throat feels like it's swollen; 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 57 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 29Dec2021 10:00 (Lot number: 33130BA) at the age of 57 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "C2, C3, C5, C6 narrowing" (unspecified if ongoing), notes: Verbatim: C2, C3, C5, C6 narrowing; "COVID-19" (unspecified if ongoing), notes: States he had COVID-19 the end of Apr2021 or beginning of May2021. There were no concomitant medications. The following information was reported: DYSPNOEA (non-serious) with onset 29Dec2021, outcome "unknown", described as "Wasn't breathing normally"; PALPITATIONS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Racing heart"; HEADACHE (non-serious) with onset 29Dec2021, outcome "unknown", described as "Headache"; PARAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 29Dec2021, outcome "unknown" and all described as "Left arm numb and tingling"; LIMB DISCOMFORT (non-serious) with onset 29Dec2021, outcome "unknown", described as "Couldn't raise left arm"; THROAT IRRITATION (non-serious), DRY THROAT (non-serious) all with onset 29Dec2021, outcome "unknown" and all described as "Throat scratchy and dry"; OROPHARYNGEAL PAIN (non-serious) with onset 29Dec2021, outcome "unknown", described as "Sore throat"; NAUSEA (non-serious) with onset 29Dec2021, outcome "unknown", described as "Nauseous"; DIZZINESS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Eyes felt heavy, irritated, and kind of foggy"; PAIN (non-serious) with onset 29Dec2021, outcome "unknown", described as "Body aches"; COUGH (non-serious) with onset 29Dec2021, outcome "unknown", described as "Slight cough"; FEELING ABNORMAL (non-serious) with onset 29Dec2021, outcome "unknown", described as "Feeling weird"; LIMB DISCOMFORT (non-serious) with onset 29Dec2021, outcome "unknown", described as "Right hip and right leg felt weird"; CHILLS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Chills"; PILOERECTION (non-serious) with onset 29Dec2021, outcome "unknown", described as "Goose bumps"; DIZZINESS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Lightheadedness"; DRY MOUTH (non-serious) with onset 29Dec2021, outcome "unknown", described as "Dry mouth"; MOVEMENT DISORDER (non-serious) with onset 29Dec2021, outcome "unknown", described as "Couldn't move legs"; FEELING COLD (non-serious) with onset 29Dec2021, outcome "unknown", described as "Couldn't get warm"; BLOOD PRESSURE INCREASED (non-serious) with onset 29Dec2021, outcome "unknown", described as "Blood pressure was up"; GAIT DISTURBANCE (non-serious) with onset 29Dec2021, outcome "unknown", described as "Couldn't walk"; DIZZINESS (non-serious) with onset 29Dec2021, outcome "unknown", described as "Dizzy"; BURNING SENSATION (non-serious) with onset 29Dec2021, outcome "unknown", described as "Left calf had burning sensation"; FEELING ABNORMAL (non-serious) with onset 29Dec2021, outcome "unknown", described as "Slow and foggy"; PHARYNGEAL SWELLING (non-serious) with onset 29Dec2021, outcome "unknown", described as "Throat feels like it's swollen"; DYSPHAGIA (non-serious), outcome "unknown", described as "Trouble eating and swallowing"; BEDRIDDEN (non-serious), outcome "unknown", described as "States he was in bed for several days". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller states he had called and reported an adverse reaction to the vaccine and he didn't know, he thought they would send him something so he could send it to his work and he never received anything. Caller states he was told they would recommend he doesn't get the 2nd dose. Caller states he had a reaction and called his work to let them know the next day. States he was in bed for several days and they told him he should have gone to the hospital and he didn't and when they were getting ready to call a squad because he couldn't walk his daughter did some breathing relaxation things and he dozed off and woke up and felt a little better. States his heart was still racing. Caller states he didn't go in but when he called his work they told him to call the place that administered it to report it and so he did and they said they would have someone contact him and they didn't. States a about a week later he called them and said he never heard anything and they said ok they would check into it and call him back and he didn't hear anything back. States the following day he went to the place and they gave him this number and he called and he spoke to someone that took all the information and said they recommend he not get the 2nd dose and would send him something and his work is asking. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Blood pressure up; Result Unstructured Data: Test Result:High; Comments: Blood pressure was up; Test Name: Heart rate; Result Unstructured Data: Test Result:Unknown result; Comments: His heart was pounding.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cervical disc disease (Verbatim: C2, C3, C5, C6 narrowing); COVID-19 (States he had COVID-19 the end of Apr2021 or beginning of May2021.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2177404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: PA
Alter: 51,0
Geschlecht: F
Eingang: 13.03.2022
Impfdatum: 10.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Acupuncture Arthralgia Bedridden C-reactive protein normal Central nervous system lesion Computerised tomogram abnormal Condition aggravated Full blood count normal Headache Laboratory test normal Magnetic resonance imaging head Magnetic resonance imaging head abnormal Migraine Nausea Paranasal cyst Pyrexia Red blood cell sedimentation rate normal Sinus disorder

Symptomtext

On 12/19/2021 in the evening, I started to have headaches that subsequently worsened over the next days. From 12/23 on, they were around the clock for several days, unresponsive to acute medications (triptans, tylenol) and I was bedbound. At the end of december 2021, there were a few headache free days. In January 2022, headahces became daily and severe 10/10 again, I increased Depakote to 500 mg daily without any relief. Ubrelvy for acute migraines without any relief. Started accupuncture with some relief. MRI and blood work as below. Started prednisone taper on 1/21 60-60-40-40-20-20, which decreased headches a lot, but after taper was over, headaches bounced back to 10/10 within 2 days; I went to ER and I was hospitalized for one day and given Decadron and longer steroid taper started from 60 mg x 3 days, 10 mg decrease every 3 days. Also started Nurtec 75 mg very other day for migraines. Botox prior authorization was started in January and approved in February and injected 2/23. After steroid taper was over, headahces were better and within 10 days after Botox injections, additional improvement was seen. As no other trigger was seen, this exacerbation of well controlled daily headaches 9 days after Covid booster shot seems mist likely association. Note that I had Moderna inital primary series in January and February 2021; however I had quite severe Grade 3 reactogenicity event after 2nd dose wih nausea, vomiting, fever, arthralgia, headaches; so decided to have Pfizer booster. Typically I have some degree of reactogenicity events after certain vaccines, including Shingrix and influenza. Headaches have been ongoing since July 2019, but well controlled on 125 mg of Depakote. I had concussion in 2018 with 4 months of pot concussive headaches that resolved after 4 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: MRI Brain Blood work: CBC, ESR, CRP, Chemistry: Within normal limits 1/19/2022 CT Sinus: mild sinus disease; mucocele right sphenoid sinus Feb 2022 MRI brain: stable T2 hyperinten MRI brain January 2022: stable T2 hyperintense lesion right parietal loce, stable since 2019.
Aktuelle Erkrankungen: -
Vorgeschichte: GERD, daily headaches (well controlled on Depakote)
Andere Medikamente: Depakote 120 mg, Dexilant 60 mg
Allergien: Cephalosporins
Vorherige Impfungen: typically I have mild to moderate reactogenicity events after influenza vaccines, Shingrix

VAERS 2148206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 28.02.2022
Impfdatum: 07.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Feeling abnormal Injection site pain Injection site swelling Mobility decreased Pain Sleep disorder

Symptomtext

He got his vaccine, they had him to wait as a precaution, about 20-30 minutes before he went to work. He did feel a little strange but did not affect his work ability. He understood the soreness for a couple of days. Then about after a week he noticed that the top corner and side of the left arm to the top of his left shoulder is very tender, feels like it is swollen, it hurts. He woke up this morning miserable. It bothers him at work and hurts a lot at night. It does not feel strained or sprained but has a difficult time putting on shirts and coats, etc.. Corner of the shoulder feels as if she gave him the shot too high on the left arm and the pain is right above it. He waited it about and now it's a nuisance. He does have an appointment tomorrow at 10:00 AM to have his shoulder looked at. He noticed that he can barely lift his arm to put on his deodorant when he gets out of a shower and does not remember lifting anything heavy and does lift anything heavy at work. The pain level is a 4-7 when it gives him a lot of problems. Throughout his work night it is a 3-4, but it does wake him up at night. He has taken some muscle relaxants and it helps it for a couple of hours. Says that the nurse said she may have hit a nerve and the needle was a little longer than the first one, which he did not even feel that one.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Triamterene, Men's 50+ vitamin.
Allergien: None.
Vorherige Impfungen: -

VAERS 2137145

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 33130BA

moderat

Staat: NC
Alter: 15,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 09.06.2021
Beginn: 26.09.2021
Tage bis Beginn: 109,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness Dyspnoea Heart rate increased

Symptomtext

Patient began to notice rapid HR alerts on her smart watch HR >200 Felt SOB, dizzy sometimes with rapid HR- Events usually happen with dancing- hip hop contemporary- on a dance team per smart watch, first event HR was elevated Sept 26- 193 , Nov 28th was 200 increasing events the last few weeks, but preparing for a dance competition has not counted peripheral or central pulse

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG today 2/24/2022 normal in office setting up Holter and referring to peds cardiology
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2104924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: AL
Alter: 63,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 20.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Headache Illness Migraine Mobility decreased Nausea

Symptomtext

Migraines are worse. Have to seek bedrest. Becomes very I?ll. Onset nausea and headaches. I had migraines previously but these are more severe . I have not seek treatment yet. Taking Motrin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: None
Allergien: Penicillin , some forms of iodines
Vorherige Impfungen: -

VAERS 2093149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Anxiety Hypersensitivity Palpitations Pharyngeal swelling

Symptomtext

Per provider onsite that documented progress note: 'Pt had feeling of heart racing at ~10min after booster dose. Pulse found to be 130, otherwise normal. Sensation of mild throat swelling; pt has eosinophilic esophagitis- thinks this may be related. No oral edema, sitting up, speaking in full sentences. Lungs clear. Heart rapid (100) but regular. Possible mild immediate allergic reaction vs anxiety. Medications give- Benadryl 25mg oral extended release. Follow up recommendation: follow for another 20 min , EMS if worsens. Pt has ride home.'

Weitere VAERSDATA-Felder

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

VAERS 2091254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

moderat

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 03.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Axillary pain Body temperature Chills Intermenstrual bleeding Lip swelling Lymphadenopathy Miliaria Paraesthesia Pyrexia SARS-CoV-2 test Urticaria

Symptomtext

Fever; chills; enlarged lymph nodes in armpit; extreme soreness/pain in armpit; full body heat rash; hives; swelling of lips; tingly fingers; period/spotting; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Jan2022 17:00 (Lot number: 33130ba) at the age of 33 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "hypothyroidism" (unspecified if ongoing); "skin cancer" (unspecified if ongoing); "Tree nuts" (unspecified if ongoing), notes: known allergies: Tree nuts. Concomitant medication(s) included: SERTRALINE; GIANVI; LYSINE; BUSPIRONE; SYNTHROID. Vaccination history included: Bnt162b2 (Dose 2, Product: COVID 19, Brand: Pfizer, Lot number: ew0158, Vaccine location: Left arm), administration date: 12Apr2021, when the patient was 33 years old, for Covid-19 immunization; Bnt162b2 (Dose: 1, Product: COVID 19 , Brand: Pfizer, Lot number: en6205, Dose administration time: 03:00 PM , Vaccine location: Left arm), administration date: 22Mar2021, when the patient was 33 years old, for Covid-19 immunization. The following information was reported: PYREXIA (non-serious), outcome "recovered", described as "Fever"; CHILLS (non-serious), outcome "recovered", described as "chills"; LYMPHADENOPATHY (non-serious), outcome "recovered", described as "enlarged lymph nodes in armpit"; AXILLARY PAIN (non-serious), outcome "recovered", described as "extreme soreness/pain in armpit"; MILIARIA (non-serious), outcome "recovered", described as "full body heat rash"; URTICARIA (non-serious), outcome "recovered", described as "hives"; LIP SWELLING (non-serious), outcome "recovered", described as "swelling of lips"; PARAESTHESIA (non-serious), outcome "recovered", described as "tingly fingers"; INTERMENSTRUAL BLEEDING (non-serious), outcome "recovered", described as "period/spotting". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, chills, lymphadenopathy, axillary pain, miliaria, urticaria, lip swelling, paraesthesia, intermenstrual bleeding. Additional Information: The patient had not received other vaccine in 4 weeks and covid prior vaccination. The patient had covid tested post vaccination. Covid test result was negative. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result:Unknown results; Test Name: Pool test; Test Result: Negative ; Comments: Other
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts (known allergies: Tree nuts); Hypothyroidism; Skin cancer
Andere Medikamente: SERTRALINE; GIANVI; LYSINE; BUSPIRONE; SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 2079851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: RI
Alter: 43,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 08.12.2021
Beginn: 07.01.2022
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Condition aggravated Herpes zoster Interchange of vaccine products Menstruation irregular Neck pain Pain Pain of skin Pruritus Rash Scab

Symptomtext

felt pain on the back of my lower neck/upper back. I thought I had a spider bite or some kind of bite. It was painful and then became itchy. After a few more days I started to feel pain on my skin. it started from the spot on the back of my neck and worked it's way toward my right shoulder and eventually across to the middle of my chest. in a gradual pattern over a few weeks the pain turned to burning and then itching and then looked like a rash. The pain and burning was so bad it was hard to wear a shirt and hard to shower. I went to the doctor to see if I was having an allergic reaction to something. They said it was a mild case of shingles and would go away in a few more weeks. The bumps eventually turned to little scabs. I no longer have pain but still have a bunch of the scabs. They are now only slightly bothersome and seem to be clearing up. Also, my periods are always regular but after my second shot(moderna) and again after my booster(pfizer) I had an extra period between my cycles. Also, my 11 year old daughter who has not yet begun menstruating got a period few weeks after her second shot. She has not had another period since.

Weitere VAERSDATA-Felder

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

VAERS 2075812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MD
Alter: 19,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Joint stiffness Loss of personal independence in daily activities Mobility decreased

Symptomtext

About two hours after receiving the injection, my joints began to ache. While the pain was mild for this first day, the next day I found that I had difficulty moving my body due to joint stiffness and pain.The third day after receiving the vaccine, I was able to walk around close to normally (although all of my joints still ached relatively severely), but I was not able to type or use my hands to complete activities requiring fine motor skills. I did not regain full use of my hands for around a week, and the joint pain and stiffness (though steadily decreasing) lasted for at least a second week after the injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Amoxicillin.
Vorherige Impfungen: Extreme joint pain leading to a loss of consciousness after the second dose of the Pfizer COVID-19 vaccine, Lot EW0167, age 19,

VAERS 2073322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MN
Alter: 47,0
Geschlecht: M
Eingang: 29.01.2022
Impfdatum: 15.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 10,0
Dosis: UNK
Route/Site: SYR / LA

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

Hypoaesthesia Impaired work ability Lymphadenopathy Malaise Pain Paraesthesia Vaccination site swelling

Symptomtext

I received my booster shot on December 15. 2021. That same night, the site of the vaccine which was my left arm got swollen like a lymphatic node. Body aches and just some unwell feelings. That kept me off work for about 4 days, and 6 days later, I started to feel numbness and tingling feeling beneath my left breast coming down to my left side stomach and back. It feels like you had placed ice on my skin for a while and took it off. All just on my left side.

Weitere VAERSDATA-Felder

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

VAERS 2058252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: UT
Alter: 27,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Angina pectoris Arthralgia Blood test normal Chest discomfort Chest pain Electrocardiogram normal Hypoaesthesia Muscle spasms X-ray normal

Symptomtext

After 3rd dose, later in the day started feeling aching on left side of chest/shoulder. This quickly moved directly around heart area and included sharp pain around heart. Heart felt very tight and was aching. Kept getting worse throughout week. Left arm went numb 6 days after vaccine. Went to ER on day 6 once arm numbness started. They took EKG, blood work and xray. Found nothing immediately wrong. Gave anti-inflammatory shot and 5 day anti-inflammatory prescription. A few days after prescription ended chest pain kicked up again, being very tight and painful at times. Would take ibuprofen to help pain. Started taking quercetin, vitamin c and zinc daily which seems to b helping. A month later has gotten better but still aches and feels like a cramp around heart from time to time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, blood work, x ray
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2057884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: PA
Alter: 57,0
Geschlecht: M
Eingang: 23.01.2022
Impfdatum: 02.01.2022
Beginn: 02.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypertension

Symptomtext

Patient stated he developed hypertension following Pfizer vaccination. He never had elevated blood pressure in the past.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Sumatriptan 100mg tablets PRN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2057740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: GA
Alter: 51,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 26.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Asthenia Injection site bruising Injection site pain Loss of personal independence in daily activities Mobility decreased Pain Pain in extremity Product administered at inappropriate site Sleep disorder

Symptomtext

Initially I had a sore arm at injection site, which I didn?t have with previous Covid shots. Within a few days my arm became more sore, internally. It didn?t hurt as much to touch as it did to move my arm or to lie on my arm, there was a slight bruise near the injection site and the injection site was lower than typical for shots. I assumed it would just go away. My arm continued to feel worse over the following two weeks. It was sore along the upper arm and into my shoulder area. It hurt to lift items, movement to the side and upward, painful to take my shirt off/on and to sleep at night. I took ibuprofen for the pain. It?s been four weeks and I still have soreness and pain internally and in my shoulder. The movement in my arm is somewhat limited and there is still some weakness. My arm has limited flexibility to move back and is still sore when lifting and moving in certain directions. Hurts to lift above my head when sleeping.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None so far.
Aktuelle Erkrankungen: None
Vorgeschichte: Monitor for high blood pressure. Follow up appointments for prior STUMP tumor.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2045432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 09.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chest pain Dizziness Dyspnoea

Symptomtext

Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Dizziness / Lightheadness-Medium, Additional Details: A few minutes after the patient's second dose of Pfizer was administered, the patient stated that she feels winded, like she just ran a few miles. She described chest discomfort and feeling lightheaded. We offered to call 911 but she refused. We monitored the patient and took her blood pressure (within normal limits, not hypotensive). We helped her get some fresh air outside the pharmacy after she was agreeable to it and soon she felt better and comfortable enough to depart the pharmacy.

Weitere VAERSDATA-Felder

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

VAERS 2042405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Cough Headache Immunisation Mobility decreased Pyrexia

Symptomtext

Headache; I can't get up; Coughing; booster; Giving the fever like for 3 holidays, after I got the booster I can''t get up; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date Dec2021 (Lot number: 33130BA) at the age of 29 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine ("The first one is on the 22Apr (Clarified as 22Apr2021) this year., dose 1 , MANUFACTURER UNKNOWN), administration date: 22Apr2021, when the patient was 28 years old, for COVID-19 Immunization; Covid-19 vaccine (Second one is on the May 17May (Clarified as 17May2021) this year.", dose 2 , MANUFACTURER UNKNOWN), administration date: 17May2021, when the patient was 28 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset Dec2021, outcome "unknown", described as "booster"; PYREXIA (non-serious) with onset Dec2021, outcome "not recovered", described as "Giving the fever like for 3 holidays, after I got the booster I can't get up"; HEADACHE (non-serious), outcome "unknown", described as "Headache"; DYSKINESIA (non-serious), outcome "unknown", described as "I can't get up"; COUGH (non-serious), outcome "unknown", described as "Coughing". Therapeutic measures were taken as a result of pyrexia. Therapeutic measures were not taken as a result of headache, dyskinesia, cough. Additional information Consumer stated, "I have some question, I on the Sunday of this Dec I got the booster Pfizer and after got that being, giving the fever like for 3 holidays, I don't know what to do with that, like before I get the booster I was everything was fine but after I got the booster I can't get up and I have a headache, I have fever, I have coughing and I don't know what is going on here, I don't know." Start of adverse event: Consumer stated, "Like after I take the booster on that night I was on the 'service' like at around 6 O'clock that was on 'light' I started to get fever, my fever continues on today I still having fever and it was such dull and 'light'." Treatment: Consumer stated, "I don't took any medications, in general it doesn't seems right." When again probed for the treatment, Consumer stated, "I take Advil to lower my fever because I have been keeping having fever for three days and it still continues on, I don't know what to do with that, I feel so helpless. That's why I call you." When probed if the, Consumer stated, "The Advil helps me just temporarily like I take it I feel little better and few hours later and then it comes back."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2040229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

moderat

Staat: PR
Alter: 38,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 01.07.2021
Beginn: 01.07.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Erythema Fatigue Mass Neck pain Nodule Pruritus Swelling

Symptomtext

Within 15 minutes of taking my 1st dose my neck felt weird like cramping. I had to visit the Doctor because my neck swelled up and the pain is quite strong. It was stated to me that it was a Lymph node. With the 2nd dose it got worse and with the 3rd dose I have itching on my arm, a red lump that doesn't go down and a fairly large nodule on my neck. It huts a lot and to tell you the truth since the 1rst dose the inflammation has not gone down and it comes and goes only that in this 3rd dose the neck area hurts a lot more with today I have been vaccinated with my 3rd dose for 5 days, and I feel very tired and that is not normal. I am worried about my salt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Visit to the doctor. This indicates this effect sounds a lot in the wake of the COVID vaccine in women. I don't dare visit the hospital in fear of being infected by COVID since the wards are full of patients.
Aktuelle Erkrankungen: None
Vorgeschichte: Cervical problems since 2021 but I have not been receiving medication for this pain for several months since no medication eliminates my pain. At the time of vaccination I was not taking any medication.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Swollen neck, nodule

VAERS 2035414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: CO
Alter: 41,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 06.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Back pain Crying Diarrhoea Fear Feeling abnormal Formication Hypersensitivity Hypoaesthesia Injection site pain Injection site reaction Mobility decreased Muscular weakness Pain Paraesthesia

Symptomtext

Jan 6,22 shot was given arm sore couldn?t move for 2 days on Sunday Jan 9,22 symptoms started diarrhea , Tingling in my arm , getting numb in areas elbow was hurting and throbbing also throbbing where the shot was administered and hurting sharp pains like real fast my arm gets weak my body is aching all over my who body has been tingling for three days my arm feels weird . Now my upper back is having shooting pains from where the shot was then goes to my upper back by my left shoulder . my arm has paint in different spots out of nowhere . My arm feels like ants are crawling all over my arm I?m getting sharp needle pains in the spot where the shot given . And the sharp pains keep coming like shooting needles . Wednesday Jan 12 ,22 I couldn?t get out of bed also Thursday I had to force myself and those two days my whole body felt so weird that I?ve never experienced before. I?m scared for my life and this is only my first dose of the vaccine . What will happen on the 2nd and the booster it will be worse and I don?t want to see what happens I have children I have to take care of I cannot be like this I feel like I?m dying I?m crying I cannot take this anymore . I?m against all vaccines but the only reason I got this was because I?m going to work in healthcare as a CNA and I feel like I shouldn?t be forced to take this if I?m having a allergic reaction to this and I know I am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: None at all haven?t been sick in about 2 years until I had the Pfizer vaccine
Vorgeschichte: Right shoulder injury
Andere Medikamente: None
Allergien: Corticosteroid injection and Steroid injection
Vorherige Impfungen: -

VAERS 2027988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: IN
Alter: 82,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 10.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / -

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

Arthralgia Chills Malaise Tremor

Symptomtext

Bad chills, could not stop shaking, joint pain, feeling unwell. 4 hrs. Second day course. After this time felt better, third day back to normal. Stayed in bed during the bad reaction . Should recommend people be off day after getting shot??

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: 02/12/ 2021 Pfizer 82 yrs

VAERS 2025555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 20,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 18.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Dyspnoea Pleuritic pain Respiratory symptom SARS-CoV-2 test negative Troponin increased

Symptomtext

20 Y male presented to the ed 12/24/21 with substernal, pleuritic cp and sob which started last pm. Patient returned from college a week ago and 6 days ago got a Phizer COVID booster immunization. Three days ago developed URI sxs and since has had 2 neg outpatient COVID tests(home test and PCR). Spoke to his pcp yeterday and requested a strep-test(not yet done). Chest pain and SOB started last pm before he went to bed and went away at one point but came back at 4 am which prompted him to come to the ed. Patient was discharged to home on 12/25/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: Troponin 12/24 - 7.8, 12/25-9.22, 12/25-8.22.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MN
Alter: 70,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 11.06.2021
Beginn: 04.01.2022
Tage bis Beginn: 207,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia COVID-19 Dyspnoea Pulmonary hypertension SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 5/21, 6/11, 12/23 COVID-19 positive on 1/4/22 admitted to hospital on 1/4/22 d/t SOB, weakness; underlying pulmonary HTN

Weitere VAERSDATA-Felder

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

VAERS 2024612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: PR
Alter: 31,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Malaise Tachycardia

Symptomtext

When the patient is called from his 15 minutes monitoring, the patient reports feeling unwell. Provider was notified and the patient was taken to the Treatment area. Patient Evaluated and Consulted by Doctor who indicates 30 minutes monitoring with ice on the neck to be revaluated. Patient states at 11:10 feeling better. Patient C/C Tachycardia, Color in the face. After 30 minutes of observation, the patient was consulted by Doctor who discharged him. Patient reports feeling well. Last evaluation 110/70 BP, 16 R, 86 P, 99% Saturation.

Weitere VAERSDATA-Felder

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

VAERS 2021789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain Headache Migraine Nausea Pain in extremity Palpitations Restlessness Sleep disorder

Symptomtext

It felt like my heart was in a vice grip, chest pain starting middle of the night day I received the vaccine. Restless, unable to sleep. Sat upright in a recliner most of the night. It felt like my heart was racing, chest pain, headache and arm ached. I continued to experience migraines and nausea for almost a week post vaccination. Peaking the Sunday following.

Weitere VAERSDATA-Felder

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

VAERS 2020964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Axillary pain Back pain Condition aggravated Dysstasia Fatigue Fibromyalgia Lymphadenopathy Migraine Mobility decreased Musculoskeletal chest pain Neck pain Pain Pain in extremity Sitting disability

Symptomtext

Started as a Fibromyalgia event with feeling aggravating pain throughout body, unable to sit or stand. Which then sends me to bed. But the pain increased to more intense than I would normally feel. I felt this pain from head to toes. Especially, upper back and neck with migraine-type headache, my lower back and hips, my knees radiated to ankles, felt the pain on top of my feet, also my rib cage, arms, hands and fingers. Needed to take a full Hydrochodone 7.5-325 but pain persisted on and off throughout night and next day. Still feeling increased amount of fatigue. Also experienced pain in left arm pit and found several enlarged lymphnodes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None. No tests for fibromyalgia problems.
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia, Cervical Stenosis, Lumbar/Sciatica, Hypertension, Hypothyroid, Type 2 Diabetes (controlled by diet).
Andere Medikamente: Ropinerole, Lisinopril -HCT, Duloxetine HCL, Levothyroxine, Rosuvastatin, Calcium, Magnesium, D3, Zinc, CoQ10, Curcumin.
Allergien: None
Vorherige Impfungen: -

VAERS 2019973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: OR
Alter: 35,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 08.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Angina pectoris Chest pain

Symptomtext

chest pain; left side; heart pain after 24 hours. contacted the doctor for more information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: asthma/bronchitis
Andere Medikamente: finasteride; escitalopram; albuterol; advair
Allergien: pineapple
Vorherige Impfungen: -

VAERS 2019907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: IL
Alter: 26,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 30.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain Hypoaesthesia

Symptomtext

Chest pain for 1 week, chest pressure, chest numbness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Allergic to cats
Vorherige Impfungen: -

VAERS 2018689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MS
Alter: 76,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 17.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chest pain Limb discomfort Lymphadenopathy Pain Pain in extremity Swelling

Symptomtext

pain in her arm and chest and all over; pain in her arm and chest and all over/felt like her pacemaker was coming out of her chest, it was hurting so bad; pain in her arm and chest and all over; swelling around her pacemaker; can't lift her arm; feels like drawing on her sides and het lymph nodes; 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 76 year-old female patient received bnt162b2 (BNT162B2), administered in arm, administration date 17Dec2021 (Lot number: 33130BA) at the age of 76 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "back pain" (unspecified if ongoing), notes: where she hurt her back; "stroke" (unspecified if ongoing), notes: 7 years ago; "pacemaker" (unspecified if ongoing); "uses oxygen" (unspecified if ongoing), notes: uses oxygen sometimes at night when she has a hard time breathing; "Problem with leg veins" (unspecified if ongoing); "heart" (unspecified if ongoing), notes: Verbatim: heart. Concomitant medication(s) included: XARELTO taken for cardiac assistance device user; MIRAPEX; LYRICA; NORCO taken for back pain. The following information was reported: LYMPHADENOPATHY (non-serious) with onset Dec2021, outcome "unknown", described as "feels like drawing on her sides and het lymph nodes"; PAIN IN EXTREMITY (non-serious), PAIN (non-serious) all with onset 17Dec2021, outcome "not recovered" and all described as "pain in her arm and chest and all over"; CHEST PAIN (non-serious) with onset 17Dec2021, outcome "not recovered", described as "pain in her arm and chest and all over/felt like her pacemaker was coming out of her chest, it was hurting so bad"; SWELLING (non-serious) with onset Dec2021, outcome "recovering", described as "swelling around her pacemaker"; LIMB DISCOMFORT (non-serious) with onset Dec2021, outcome "unknown", described as "can't lift her arm". Additional information: The patient asked on call: First dose 17Dec2021. Ever since then pain in her arm and chest and all over. Mentioned swelling around her pacemaker. What feels like drawing on her sides and het lymph nodes. Asks how long it will last. Keep thinking it maybe it's gonna go away. I tried to call. I read up on it. Been a pain to deal. I had no idea I would have such a bad reaction to it. Everyone I been around says fine. She has been attempting to contact HCP. Concerned about having additional dose. On follow up (27Dec2021) The caller clarifies and confirms that she got the Pfizer Covid vaccine on 17Dec2021, Patient: The caller was the same age she was now when that event happened. The caller can't get comfortable and feels like she has drawing on her sides in her lymph nodes and feels like she's drawing on both sides. The caller felt like her pacemaker was coming out of her chest, it was hurting so bad. The caller was worried about it. After the pacemaker swelling went down, its still bothering her but it went down. The caller's pain started that night of the vaccine and it went into the next day. The caller can't lift her arm its hurting so bad. The caller hasn't heard of anyone having the reaction she had. The caller's son kept fussing at her about getting it. It just seems like its not wanting to go away. History: The caller took her regular medication. The caller has back pain where she hurt her back. The caller is scared to take the other one. The caller clarifies that she got put on the Xarelto when she had her pacemaker put in. The caller cannot remember if she had the stroke before or after taking the Xarelto. No follow-up attempts are possible. No further information is expected. Follow-up (27Dec2021): New information received from same contactable consumer included updated information: Patient details, relevant medical history, Concomitant drugs, suspect drug details, event added and additional information: No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Artificial cardiac pacemaker user; Back pain (where she hurt her back); Heart disorder (Verbatim: heart); Oxygen supplementation (uses oxygen sometimes at night when she has a hard time breathing); Stroke (7 years ago); Vein disorder
Andere Medikamente: XARELTO; MIRAPEX; LYRICA; NORCO
Allergien: -
Vorherige Impfungen: -

VAERS 2018264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 52,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chills Fatigue Headache Immunisation Pain Tremor

Symptomtext

chills; my entire body was shaking; my body ached; headache; worn out; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 52-year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Dec2021 10:00 (Lot number: 33130BA) at the age of 52 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EK9231, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM), administration date: 09Jan2021, when the patient was 51 years old, for COVID-19 Immunisation, reaction(s): "No side effects"; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 05:00 PM), administration date: 30Jan2021, when the patient was 51 years old, for Covid-19 Immunisation, reaction(s): "minor chills"; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 05:00 PM), administration date: 30Jan2021, when the patient was 51 years old, for COVID-19 Immunization, reaction(s): "body ache", "headache". The following information was reported: IMMUNISATION (non-serious) with onset 07Dec2021 10:00, outcome "unknown", described as "Booster"; CHILLS (non-serious) with onset 07Dec2021 20:00, outcome "recovered" (2021), described as "chills"; TREMOR (non-serious) with onset 07Dec2021 20:00, outcome "recovered" (2021), described as "my entire body was shaking"; PAIN (non-serious) with onset 07Dec2021 20:00, outcome "recovered" (2021), described as "my body ached"; HEADACHE (non-serious) with onset 07Dec2021 20:00, outcome "recovered" (2021), described as "headache"; FATIGUE (non-serious) with onset 07Dec2021 20:00, outcome "recovered" (2021), described as "worn out". Therapeutic measures were not taken as a result of chills, tremor, pain, headache, fatigue. Additional Information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other vaccines within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. It was reported that 10-hours after the 3rd vaccination patient began to get the chills. He had the chills so bad entire body was shaking and body ached. Had a headache. This lasted for another 6 hours, and then just had minor chills. Patient was slept for 10 hours and woke up feeling better, but patient did not have minor chills and patient was just worn out. After another 8 hours he finally lost the chills and was pretty much back to normal but was just worn out. That was the sick-est patient have ever been in his life. Patient had minor chills and body ache that lasted about 12 hours and a headache that lasted for 4 days after the 2nd dose. No side effects from the first vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2014089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 02.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain upper Chills Condition aggravated Diarrhoea Fatigue Interchange of vaccine products Lymph node pain Nausea

Symptomtext

Started with tender lymph nodes in axilla in injection side, that progressed up the neck throughout the day. After 24hrs since Pfizer booster started with fatigue and chills, after 32 hours developed severe stomach pains with nausea and subsequent diarrhea that are improving but not resolved on pat vaccine day 5.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Afebrile per thermometer and palpationnif lymph nodes.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension.
Andere Medikamente: Lisinopril 5mg tablet (1/2 10mg tab)
Allergien: Codeine, hydrocodone, tramadol
Vorherige Impfungen: Moderna COVID Vaccine dose 1, given 01/08/2021, lot 039K20A, initial injection site reaction followed by delayed sensitivity rea

VAERS 2006516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: WA
Alter: 71,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 22.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Chest pain Dysgeusia Headache Paraesthesia Paraesthesia oral

Symptomtext

I received my 1st Pfizer vaccine on 4/7/21 and my 2nd on 4/27/21. I had mild headache and slight aches for a couple of days and a slight metallic taste for about a week after each shot. I received my Pfizer Booster on 12/22/21. As of today 1/5/22 I still have the headache (fuzzy behind the eyes). I also had shooting pains starting in my left shoulder blades reaching to my left neck, these only lasted a couple of days and were sporadic. I have had some chest pain as well. For the last 2 weeks I have been experiencing tingling in my legs/ feet progressed to my arms and now have constant tingling in my lips. I've taken tylenol and naproxen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: No medical tests done but I have been in contact with my HCP
Aktuelle Erkrankungen: No illnesses
Vorgeschichte: High blood pressure and cholesterol
Andere Medikamente: Apirin 81mg,---Atacand HCT 16mg-12.5mg---Calicium---Carvedilol 3.125mg 2x---Lovastatin 40mg---Multivitamin---Vitamin B12---Vitamin C---Vitamin D3
Allergien: No allergies
Vorherige Impfungen: -

VAERS 2006506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MN
Alter: 53,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 09.04.2021
Beginn: 01.01.2022
Tage bis Beginn: 267,0
Dosis: 3
Route/Site: - / -

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

Ageusia Anosmia Cough Diarrhoea Dyspnoea Ear pain Nasal congestion Oropharyngeal pain

Symptomtext

Nonproductive cough, nasal congestion, ear pain, diarrhea, sore throat, shortness of breath, loss of taste, and loss of smell. All starting 1/1/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: G2P2. Diverticulitis. Seasonal allergies. Gestational Diabetes. panic attacks seeing psychiatrist. Normal colonoscopy 9/2017 repeat 5 year.
Andere Medikamente: metFORMIN HCl 500 MG Tablet 1 tablet with a meal Orally Once a day, Multivitamins Capsule Orally, Citracal + D, Levothyroxine Sodium 88 MCG Tablet 1 tablet in the morning on an empty stomach Orally Once a day, Eliquis 5 MG Tablet 1 tablet O
Allergien: PENICILLIN DRUGS: rash - Allergy, Spironolactone: muscle pain
Vorherige Impfungen: -

VAERS 2005172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: OH
Alter: 39,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 09.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: IM / -

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

Blood magnesium Chest X-ray Chest discomfort Chest pain Differential white blood cell count Dyspnoea Electrocardiogram abnormal Fibrin D dimer Full blood count Human chorionic gonadotropin Inflammation Metabolic function test Pain Troponin I

Symptomtext

Starting on Monday morning December 13th woke up to pains and discomfort in chest on left side. If rolled over would be shooting pains across chest from left to right. Had fullness, tightness and discomfort in left chest. Did it again Tuesday morning and Wednesday morning when it happened again went to the ER. Have been having fullness, discomfort, tightness on and off since along with shortness of breath. Has gotten increasingly better a little each day. Discomfort is always in the same spot on left chest. I will list tests in the section below that have been done. ER doctor and my follow up physician both concluded heart wall inflammation is most likely from covid booster shot on 12/9/21. As of today, 1/5/2022 still experiencing mild discomfort & mild tightness, worse when initially woke and some shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: On 12/16/21 at MetroHealth Brecksville Emergency Department: Basic Metabolic Panel, CBC with Differential, D-Dimer, HCG Urine, Magnesium, Troponin I Lab Tests Completed. Additionally a EKG 12 Lead - Performed 2 times - both came back abnormal and a XR Chest 2 View PA & LAT was done On 12/22/2021 Health Center I followed up with, APRN, CNP who is in the office of my primary care doctor. She repeated the EKG and it was normal. I am scheduled for a Stress Echo on 1/5/2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: daily probiotic, women's daily vitamin with collagen, Elderberry
Allergien: contrast die/iodine
Vorherige Impfungen: -

VAERS 1997229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MN
Alter: 22,0
Geschlecht: M
Eingang: 01.01.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / AR

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

Angina pectoris Chest X-ray Chest discomfort Chills Computerised tomogram Dyspnoea Echocardiogram Full blood count Lipase Magnetic resonance imaging Metabolic function test Pain Troponin increased

Symptomtext

12/27 - chills and body aches. Light pain in heart region. 12/28 - chills and body aches. Same light pain in heart region. 12/29 - chills and body aches, tightness in chest increased throughout day. Sharp pains in heart, difficulty breathing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Troponin levels drawn upon admission to hospital. Baseline 268. 2 hr 628, 6 hr 882. Midnight draw 1221. 12/31 draw 531 and 1/1 draw increased to 681. CBC done. CT, MRI, ECHO, 2 chest XRAYS. Lipase and metabolic panels done.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ibuprofen following vaccine.
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1968202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: TN
Alter: 38,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Arthralgia Chills Condition aggravated Diarrhoea Erythema Body temperature Dizziness Fatigue Feeling hot Headache Muscle spasms Nausea Food aversion Immunisation Insomnia Maternal exposure during pregnancy Morning sickness Pain

Symptomtext

morning sickness; dizziness; headaches; food aversions; exhaustion; liquid water diarrhea; worse nausea; low grader fevers; chills; body aches; All became worse; I couldn't sleep; Sore arm / Became severe; I was almost 13 weeks when given dose 3; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 39-year-old female patient (pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 12Dec2021 14:30 (Lot number: 33130BA) at the age of 38 years as dose 3 (booster), single for covid-19 immunisation. The patient was pregnant at time of vaccination. Relevant medical history included: "partial autonomic seizures" (unspecified if ongoing); "hypothyroidism" (unspecified if ongoing). Date of last menstrual period: 15Sep2021. The patient was 12 weeks pregnant at the time of exposure to bnt162b2; 10 weeks pregnant to influenza vaccine. The patient was 12 weeks pregnant at the event onset. The patient is expected to deliver a baby(s) on 22Jun2022. Concomitant medication(s) included: FLU taken for immunisation, administration date 24Nov2021; KEPPRA [LEVETIRACETAM]; LAMICTAL; LEVOTHYROXINE; UNISOM [DOXYLAMINE SUCCINATE]; B6. Past drug history included: Tramadol, reaction(s): "Known allergies: Tramadol"; Ibuprofen, reaction(s): "Known allergies: Ibuprofen"; Naproxen, reaction(s): "Known allergies: naproxen"; Prozac, reaction(s): "Known allergies: prozac". Vaccination history included: Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: EW0169,, Previous dose lot unknown: False,, Previous dose administration date: 22Apr2021, Previous dose Administration time: 12:30 PM, Previous dose number: 2, Previous dose Vaccine location: Right arm), administration date: 22Apr2021, when the patient was 39 years old, for Covid-19 immunization; Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: ER8734,, Previous dose lot unknown: False,, Previous dose administration date: 30Mar2021 , Previous dose Administration time: 12:30 PM, Previous dose number: 1, Previous dose Vaccine location: Right arm), administration date: 30Mar2021, when the patient was 38 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 12Dec2021 14:30, outcome "unknown", described as "Booster"; PAIN IN EXTREMITY (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "Sore arm / Became severe"; MATERNAL EXPOSURE DURING PREGNANCY (non-serious) with onset 12Dec2021 14:30, outcome "unknown", described as "I was almost 13 weeks when given dose 3"; MORNING SICKNESS (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "morning sickness"; DIZZINESS (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "dizziness"; HEADACHE (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "headaches"; FOOD AVERSION (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "food aversions"; FATIGUE (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "exhaustion"; DIARRHOEA (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "liquid water diarrhea"; NAUSEA (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "worse nausea"; PYREXIA (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "low grader fevers"; CHILLS (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "chills"; PAIN (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "body aches"; CONDITION AGGRAVATED (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "All became worse"; INSOMNIA (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "I couldn't sleep". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, morning sickness, dizziness, headache, food aversion, fatigue, diarrhoea, nausea, pyrexia, chills, pain, condition aggravated, insomnia. Additional Information: It was reported that, Sore arm started 7.5 hours after shot 3 on Sunday. Became severe 12 hours after administration. No other side effects hit until 24 hours after shot. Same for my husband. I had not fun side effects after second shot. I was almost 13 weeks when given dose 3. Already had morning sickness that is off and on all day without puking, dizziness, headaches, food aversions and exhaustion. Headaches, liquid water diarrhea, even worse nausea, low grader fevers off and on, chills, body aches started, and dizziness became exacerbated 24 hours after shot. All became worse yesterday and especially last night. All I could eat yesterday before schedule nuchal ultrasound and doctors appt yesterday was one cracker. Could only eat a small amount of chicken afterwards and that was it. Side effects just worsened and I almost went into the obstetrics ER wing early this morning bc I could not sleep due to low grade fever and severe nausea and dizziness, especially. My pregnancy symptoms were not this bad before. The patient was taken other vaccines in within 4 weeks. The facility type vaccine was pharmacy or drug store. The patient was received any other vaccines within 4 weeks. Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not diagnosed. The patient did not received treatment for adverse events. The patient recovery for adverse events was unknown. The known allergies tramadol, naproxen, ibuprofen, prozac. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20211213; Test Name: Fever; Result Unstructured Data: Test Result:low grade fever
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autonomic seizure; Hypothyroidism
Andere Medikamente: KEPPRA [LEVETIRACETAM]; LAMICTAL; LEVOTHYROXINE; UNISOM [DOXYLAMINE SUCCINATE]; B6
Allergien: -
Vorherige Impfungen: -

VAERS 1968202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: TN
Alter: 38,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Chills Condition aggravated Diarrhoea Erythema Body temperature Dizziness Fatigue Feeling hot Headache Muscle spasms Nausea Food aversion Immunisation Insomnia Maternal exposure during pregnancy Morning sickness Pain

Symptomtext

morning sickness; dizziness; headaches; food aversions; exhaustion; liquid water diarrhea; worse nausea; low grader fevers; chills; body aches; All became worse; I couldn't sleep; Sore arm / Became severe; I was almost 13 weeks when given dose 3; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 39-year-old female patient (pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 12Dec2021 14:30 (Lot number: 33130BA) at the age of 38 years as dose 3 (booster), single for covid-19 immunisation. The patient was pregnant at time of vaccination. Relevant medical history included: "partial autonomic seizures" (unspecified if ongoing); "hypothyroidism" (unspecified if ongoing). Date of last menstrual period: 15Sep2021. The patient was 12 weeks pregnant at the time of exposure to bnt162b2; 10 weeks pregnant to influenza vaccine. The patient was 12 weeks pregnant at the event onset. The patient is expected to deliver a baby(s) on 22Jun2022. Concomitant medication(s) included: FLU taken for immunisation, administration date 24Nov2021; KEPPRA [LEVETIRACETAM]; LAMICTAL; LEVOTHYROXINE; UNISOM [DOXYLAMINE SUCCINATE]; B6. Past drug history included: Tramadol, reaction(s): "Known allergies: Tramadol"; Ibuprofen, reaction(s): "Known allergies: Ibuprofen"; Naproxen, reaction(s): "Known allergies: naproxen"; Prozac, reaction(s): "Known allergies: prozac". Vaccination history included: Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: EW0169,, Previous dose lot unknown: False,, Previous dose administration date: 22Apr2021, Previous dose Administration time: 12:30 PM, Previous dose number: 2, Previous dose Vaccine location: Right arm), administration date: 22Apr2021, when the patient was 39 years old, for Covid-19 immunization; Bnt162b2 (Previous dose details:, Previous dose Product: COVID 19,, Previous dose brand=Pfizer,, Previous dose brand unknown: False,, Previous dose lot number: ER8734,, Previous dose lot unknown: False,, Previous dose administration date: 30Mar2021 , Previous dose Administration time: 12:30 PM, Previous dose number: 1, Previous dose Vaccine location: Right arm), administration date: 30Mar2021, when the patient was 38 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 12Dec2021 14:30, outcome "unknown", described as "Booster"; PAIN IN EXTREMITY (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "Sore arm / Became severe"; MATERNAL EXPOSURE DURING PREGNANCY (non-serious) with onset 12Dec2021 14:30, outcome "unknown", described as "I was almost 13 weeks when given dose 3"; MORNING SICKNESS (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "morning sickness"; DIZZINESS (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "dizziness"; HEADACHE (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "headaches"; FOOD AVERSION (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "food aversions"; FATIGUE (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "exhaustion"; DIARRHOEA (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "liquid water diarrhea"; NAUSEA (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "worse nausea"; PYREXIA (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "low grader fevers"; CHILLS (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "chills"; PAIN (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "body aches"; CONDITION AGGRAVATED (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "All became worse"; INSOMNIA (non-serious) with onset 13Dec2021 15:30, outcome "unknown", described as "I couldn't sleep". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, morning sickness, dizziness, headache, food aversion, fatigue, diarrhoea, nausea, pyrexia, chills, pain, condition aggravated, insomnia. Additional Information: It was reported that, Sore arm started 7.5 hours after shot 3 on Sunday. Became severe 12 hours after administration. No other side effects hit until 24 hours after shot. Same for my husband. I had not fun side effects after second shot. I was almost 13 weeks when given dose 3. Already had morning sickness that is off and on all day without puking, dizziness, headaches, food aversions and exhaustion. Headaches, liquid water diarrhea, even worse nausea, low grader fevers off and on, chills, body aches started, and dizziness became exacerbated 24 hours after shot. All became worse yesterday and especially last night. All I could eat yesterday before schedule nuchal ultrasound and doctors appt yesterday was one cracker. Could only eat a small amount of chicken afterwards and that was it. Side effects just worsened and I almost went into the obstetrics ER wing early this morning bc I could not sleep due to low grade fever and severe nausea and dizziness, especially. My pregnancy symptoms were not this bad before. The patient was taken other vaccines in within 4 weeks. The facility type vaccine was pharmacy or drug store. The patient was received any other vaccines within 4 weeks. Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not diagnosed. The patient did not received treatment for adverse events. The patient recovery for adverse events was unknown. The known allergies tramadol, naproxen, ibuprofen, prozac. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20211213; Test Name: Fever; Result Unstructured Data: Test Result:low grade fever
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autonomic seizure; Hypothyroidism
Andere Medikamente: KEPPRA [LEVETIRACETAM]; LAMICTAL; LEVOTHYROXINE; UNISOM [DOXYLAMINE SUCCINATE]; B6
Allergien: -
Vorherige Impfungen: -

VAERS 1988981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Blood glucose increased Blood pressure increased Condition aggravated Headache Heart rate increased Incorrect dose administered Product preparation issue

Symptomtext

Patient came in for covid booster. She was accidently given the whole vial of pfizer 6 doses by the medical assistant who did not dilute before administering. The patient had no reaction and left after 15 minutes. Then it was discovered by the MA that she had made a mistake and given entire vial. Clinic Director, office manager, and chief of Infectious Disease were all notified. Dr. was patient. Vital signs were taken and blood pressure was initially 183/96 with pulse of 98 but came down to 163/83 with pulse of 88. Blood sugar was 226. Patient called daughters. Was given tylenol for slight headache and then eventually left office at about noon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Diabetes hypertension hyperlipidemia panic attack lymphedema
Vorgeschichte: see above
Andere Medikamente: e ALPRAZolam 1 mg tablet TAKE 1 TABLET(S) TWICE A DAY BY ORAL ROUTE AS NEEDED aspirin 81 mg chewable tablet Chew 1 tablet every day by oral route. atorvastatin 20 mg tablet TAKE 1 TABLET BY MOUTH EVERYDAY AT BEDTIME BenadryL 25 mg
Allergien: Codeine sulfa sulfadiazine
Vorherige Impfungen: -

VAERS 1985038

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 33130BA

moderat

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Dyspnoea Heart rate increased Wheezing

Symptomtext

Rapid heart rate of over 122, Blood pressure from baseline significantly increased, difficulty breathing, wheezing, and dizziness. I was examined by 2 EMT's that were on site already scheduled to work during clinic operating hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: none known allergies
Vorherige Impfungen: -

VAERS 1979209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Headache Injection site erythema Injection site pain Lymphadenopathy Myalgia Tinnitus

Symptomtext

In addition to pain and redness and soreness at the injection site, there has been mild headaches and muscle aches with large and painfully swollen lymph nodes in the neck, armpit and groin on the left/injection side of the body. Also a worsening of already existing tinnitus in one ear .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Did not seek treatment.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Took ibuprofen after vaccination
Allergien: -
Vorherige Impfungen: Same as this but with 2 shots of Moderna vaccine

VAERS 1978975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

moderat

Staat: FL
Alter: 21,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Headache Hypotension Injection site pain Tremor

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Headache-Medium, Systemic: Hypotension-Medium, Systemic: Shakiness-Medium

Weitere VAERSDATA-Felder

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

VAERS 1967162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: NJ
Alter: 16,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Aphthous ulcer Arthralgia Chest pain Deafness unilateral Fungal infection Headache Mouth ulceration Nausea Oropharyngeal pain Throat irritation Tongue ulceration Vaginal infection

Symptomtext

Severe chest pain in the left side of chest, stretching to the left shoulder (December 19th) Throat felt full, pain stretching from chest to throat (December 19th) Loss of hearing in right ear for approximately 2 hours (December 18th) Heightened anxiety (December 18th) Nausea and headache (December 18th) Canker sores, mouth ulcers, on the roof of the mouth, side of tongue, and under the tongue (December 19th-present) Suspected yeast infection/ vaginitis (December 19th-present)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Shellfish
Vorherige Impfungen: Pfizer 2nd Dose

VAERS 1967144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

moderat

Staat: NY
Alter: 86,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain Pain in extremity Paraesthesia

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: tingling/ pain down arm-Medium

Weitere VAERSDATA-Felder

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

VAERS 1962952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: CT
Alter: 39,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chills Dizziness Tremor

Symptomtext

Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Mild, Systemic: Shakiness-Medium, Systemic: Weakness-Medium

Weitere VAERSDATA-Felder

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

VAERS 1962190

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MA
Alter: 54,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Malaise Paraesthesia

Symptomtext

Within about 30 min. upon attempting to stand, realized left lower leg and foot and left lower arm and hand were tingling. Hand and foot were also numb. Also felt very unwell. Advised to go to ER, but did not feel emergent and did not want to incur ER costs. Monitored closely over next several hours. Within about 1-2 hours, numbness in hand and foot started to dissipate. Within 4 hours was completely fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Rheumatoid arthritis, Hashimoto's, sjogren's, endometriosis, migraines, various dermatologic issues, allergies.
Andere Medikamente: Orencia, synthroid, allegra, gabapentin, montelukast.
Allergien: Sulfonamides. Cefpodoxime. Pyrethrins. Lupron. Progestins. CoQ10. Odors in cleaning products, perfumes, other products. Perfumes, dyes in laundry detergent.
Vorherige Impfungen: -

VAERS 1962121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: VA
Alter: 51,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Limb injury Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 1961697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

moderat

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Blood pressure increased Chills Dizziness Hypertension Nausea

Symptomtext

Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Hypertension-Medium, Systemic: Nausea-Medium, Additional Details: patient reported dizziness, chills, nausea post vaccination. had patient lie down for 30 minutes, monitored blood pressure: readings 140/90, 168/110 and 170/111 every 10 minutes. we were going to call 911 due to elevated blood pressure but patient refused and stated she felt a lot better and wanted to go home and rest.

Weitere VAERSDATA-Felder

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

VAERS 1959296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: WA
Alter: 36,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 12.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: UN / LA

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

Breast pain Chest discomfort Chest pain Lymphadenopathy Pain Rash pruritic

Symptomtext

Started with lymph node swelling starting the 2nd day on 12/13. Continued to have shooting pain in the left breast/chest. General discomfort in the chest. Bad rash with itchness developed all over the back starting around 12/15.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: 2nd dose of Pfizer COVID19 vaccine, chill, fatigue.

VAERS 1959072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: CA
Alter: 49,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Chills Dizziness Fatigue Headache Lethargy Tremor Visual impairment

Symptomtext

Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Headache-Mild, Systemic: Shakiness-Medium, Systemic: Visual Changes/Disturbances-Medium, Systemic: Weakness-Mild, Additional Details: took blood pressure lying down 130/80 and again sitting up 130/90 within normal limits. patient also reported having history of anxiety. pt counseled to monitor symptoms while at home (has driver) and to go to urgent care or ER if symptoms worsen. offered to call 911 but pt said he is okay for now.

Weitere VAERSDATA-Felder

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

VAERS 1958924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 32,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Chest pain Fatigue Pyrexia

Symptomtext

10 mins post vaccination pt c/o anxiety. Vitals: 138/79, 126, 20 -- > 10:16 131/79, 111, 18, 100% Pt stable and released from the vaccination site @10:18 w/ girlfriend via wheelchair. Recommended that pt f/u w/ their healthcare provider, f/u instructions provided. 12/15/21 - Pt contacted Hospital from Hospital Notes: had Pfizer booster 3 days ago, devloped fever and fatigue the following 2 days, temp today 99, tried Tylenol with some relief, had mild chest pain yesterday lasting few seconds at at time every few hours throughout day, no chest pain today. No further information available as of 12/17/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: upper airway resistance syndrome
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1955301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

moderat

Staat: NJ
Alter: 44,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Hypotension Paraesthesia

Symptomtext

Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: ems called out of caution patient exhibited low blood pressure as well ems took vitals and patient was fine after about 30min patient declined further care

Weitere VAERSDATA-Felder

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

VAERS 1955117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MO
Alter: 66,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Extra dose administered

Symptomtext

Patient husband advised patient has been experiencing chest pain on her right side beginning the day after receiving booster vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1954909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: SC
Alter: 23,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Feeling hot Hypotension Nausea Vomiting

Symptomtext

After the administration of the Pfizer vaccine, the patient stated they felt warm and nauseous. The patient laid their head on the table and stated they were going to vomit. The patients blood pressure was taken and it was determined they were hypotensive so they were placed on the floor, where they then vomited. 911 was contacted and the patient was evaluated. After vomiting, the patients vitals stabilized and transport was refused to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: NKA
Vorherige Impfungen: -

VAERS 1944587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: MD
Alter: 54,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 07.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Chest pain

Symptomtext

sharp pain in middle upper chest area

Weitere VAERSDATA-Felder

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

VAERS 1942016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: IL
Alter: 32,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Arthralgia Bursitis Extra dose administered Injection site pain Injection site swelling Mobility decreased Pain in extremity

Symptomtext

Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Joint Pain-Severe, Additional Details: Patient received Pfizer Booster shot on Wednesday 12/8, complained of severe arm pain and lack of mobility following day. Patient saw urgent care physician who diagnosed bursitis, prescribed Medrol for inflammation and suggested an MRI if no improvement. MD suggested that the shot may have been placed too high, but reviewed technique with intern who administered and it was appropriate. The administrator has had alot of experience giving vaccines here at the store and at her place of work.

Weitere VAERSDATA-Felder

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

VAERS 2549848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: -
Alter: 28,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 07.12.2021
Beginn: 06.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Chest pain Chills Headache Migraine Myalgia Pyrexia

Symptomtext

Headache, Myalgia, Fever, chest pain, chills, migraine Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1931909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: CA
Alter: 24,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Hypotension

Symptomtext

Systemic: Dizziness/Lightheadedness-Mild, Systemic: Hypotension-Mild.

Weitere VAERSDATA-Felder

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

VAERS 1921675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia Paraesthesia oral Pruritus

Symptomtext

Patient brought into Covid Observation Area after reporting itchiness to her left forearm and tingling to mouth, lips and nose shortly after receiving Booster dose of Pfizer vaccination. Patient alert and oriented x 4, denies shortness of breath, itching or swelling to throat. No rash or hives noted to left forearm. No noted swelling to face, lips or tongue. Patient states she did not experience any similar symptoms after 1st two doses of Pfizer. 4:13 pm- VS: Temp 97.4, BP 150/84, HR 71, RR 18, 02 SATs 98%. RA. 4:16 pm- Call placed to on call ED physician, Dr. informed of patient symptoms above. Verbal order given per Dr. for Benadryl 25 mg capsule x 1 now. Per Dr., patient to come to ED via ambulance, for further observation due to tingling of mouth, lips and nose. Patient agreed to go to ED. Verbal order for Benadryl 25 mg capsule x 1 now, read back and confirmed. 4:20 pm- Benadryl 25 mg capsule x 1 given now as ordered. 4:23 pm- VS: BP 145/71. HR 75, RR 18, 02 SATs 98% RA. Will continue to monitor. 4:26- Called 911 for ambulance transport to Emergency Department. 911 Dispatcher recommended Epinephrine be administered to patient x 1 now. Patient and Nurse in agreement to administer Epinephrine. 4:30 pm- Epinephrine 0.3 mg auto-injector administered by nurse to patient left lateral thigh. 4:32 pm- Patient reports tingling in nose has resolved and the tingling to her mouth and lips improving. VS: BP 143/73, HR 71, RR 20, 02 SATs 98% RA 4:38 pm- EMT arrived, report of patient symptoms and interventions given to Paramedics. Patient reported tingling in mouth and lips improving and agreed to go to ED for further observation. VS: BP 141/78, HR 78, RR 20, 02 SATs 98% RA. 4:48pm- Paramedics received notification that ED now at new location and provided ED options to patient. Patient agreed to be taken to another ED. 4:50: Patient transported to ED via EMT in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: ADHD, Depression, Hypertension, Hyperlipidemia
Vorgeschichte: ADHD, Depression, Hypertension, Hyperlipidemia
Andere Medikamente: Celexa, Ritalin, Zanaflex, Pravachol, Hyzaar, Motrin, Voltaren
Allergien: Bee Venom, Penicillin, Latex, Aspirin, Vicodin, Cymbalta, Gabapentin
Vorherige Impfungen: -

VAERS 2676367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NJ
Alter: 58,0
Geschlecht: M
Eingang: 24.08.2023
Impfdatum: 13.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / -

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

Back pain Biopsy spinal cord abnormal Computerised tomogram abnormal Diffuse large B-cell lymphoma Hepatic mass Positron emission tomogram abnormal Spinal cord injury Spinal operation Splenic neoplasm malignancy unspecified

Symptomtext

Three weeks after having gotten the Pfizer Covid-19 booster I started experience severe back pain - which wound-up being three lesions pressing against my spinal cord; biopsy showed DLBCL (Diffuse Large B-Cell Lymphoma).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: 35,0
Labordaten: Back surgery March 2023 to relief pressure on spinal cord, biopsy indicated DLBCL. Subsequent PET and CT-Scans showed three lesion on spinal cord, 2 inch mass in spleen and multiple nodes in the liver.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: n/a
Allergien: Levaquin
Vorherige Impfungen: -

VAERS 2649033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MA
Alter: 65,0
Geschlecht: F
Eingang: 24.06.2023
Impfdatum: 14.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: - / LA

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

Blood test Dysphagia Ear pain Eating disorder Glossodynia Magnetic resonance imaging Pain in jaw Speech disorder

Symptomtext

the pain I was experiencing with my tongue/ had extreme pain around the right side of my tongue; it went in to my jaw and in to my ear.; it went in to my jaw and in to my ear.; had a hard time talking, swallowing and eating; had a hard time talking, swallowing and eating; had a hard time talking, swallowing and eating; The initial case was missing the following minimum criteria: No adverse event. Upon receipt of follow-up information on 20Jun2023, this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID: (159558). The reporter is the patient. A 65-year-old female patient received BNT162b2 (BNT162B2), on 14Dec2021 as dose 3 (booster), single (Lot number: 33130BA, Expiration Date: 28Feb2022) at the age of 65 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose 1, single, Lot# (First Dose): EW0164, Expiration Date (First Dose): Consumer stated, "I don't have it."), administration date: 19Apr2021, when the patient was 64-year-old, for COVID-19 Immunization; BNT162b2 (Lot# (Dose 2, single): Consumer stated, "I believe its EW0183."), administration date: 10May2021, when the patient was 65-year-old, for COVID-19 Immunization. The following information was reported: GLOSSODYNIA (non-serious) with onset Jan2022, outcome "recovered", described as "the pain I was experiencing with my tongue/ had extreme pain around the right side of my tongue"; SPEECH DISORDER (non-serious), DYSPHAGIA (non-serious), EATING DISORDER (non-serious) all with onset 2022, outcome "unknown" and all described as "had a hard time talking, swallowing and eating"; PAIN IN JAW (non-serious), EAR PAIN (non-serious) all with onset 2022, outcome "unknown" and all described as "it went in to my jaw and in to my ear.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of glossodynia. Additional information: Reported as, Patient told her that we are not able to link some and our next step would be to file a report with you and that you guys are not able to determine if the link correlates with what she received, patient did make her aware of that and then patient did confirm with our customer service department that she received the Pfizer COVID Monovalent, purple cap and she states that she 67 now, however during her reaction she was 65 at the time as the reaction happened in Jan2022. Other Medical Conditions or Other Medications: Consumer stated, "I take Vitamins, that's what I take". Consumer stated, "No, but I did undergo a series of lab tests after the two weeks time period because patient was going to different doctors and patient finally ended up at a Neurologist who ordered a number of blood tests to be done as well as a MRI. Treatment: Consumer stated, "They gave me at a clinic that was surely after it was Magic mouthwash that have Lidocaine in it to get in some of the pain patient was experiencing with her tongue, one of them was Magic mouthwash and patient was not able to see a infectious disease Doctor until May and at that time she put her on a antiviral medication, patient was not able to see a Doctor, an antiviral medication doctor until May and she put me on Valtrex 1 gm, it's an antiviral medication. When probed what reactions patient experienced, Consumer stated, "I had extreme pain around the right side of my tongue and that was the only reaction at that time, I had a hard time talking, swallowing and eating, after I had the antiviral medications in May2022, I then felt, it relieved the pain that I was experiencing but then I was exposed to COVID in Sep2022 and it started all over again except this time it went in to my jaw and in to my ear." Reassurance: Consumer stated, "No, except that I would like somebody to follow-up on this and patient was trying to determine if anyone else has experienced anything like patient have". Consumer was informed that the previous department, Pfizer Medical Information was the concerned department for the query. There was a product complaint to report. She was calling in regards to the Pfizer COVID vaccine. She states she received a booster dose on 14Dec2021 (14Dec2021) in (withheld) and two weeks later she had a a severe reaction, she provided that she has been through N number of tests and doctors and she was trying to find out if the vaccine was linked to her reaction. She wanted to determine if there has been some side effects from the vaccine. Caller mentioned that she had a possible side effect from the booster shot after 2 weeks she had the vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Test Name: Blood test; Result Unstructured Data: Test Result:Unknown; Test Name: MRI; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2610897

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 33130BA

mild

Staat: MN
Alter: 71,0
Geschlecht: M
Eingang: 06.04.2023
Impfdatum: 16.12.2021
Beginn: 23.03.2023
Tage bis Beginn: 462,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chest X-ray Dizziness Pyrexia SARS-CoV-2 test

Symptomtext

Weakness for 2 weeks. Presented to ER on 4/5/23, with continued weakness, dizziness, and fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: COVID PCR, Chest Xray
Aktuelle Erkrankungen: -
Vorgeschichte: CHF, HTN, CKD
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1929607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IL
Alter: -
Geschlecht: F
Eingang: 02.03.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Fatigue Hemianaesthesia Hypoaesthesia Hypoaesthesia oral Product after taste Heavy menstrual bleeding Menstrual disorder

Symptomtext

I have the heavy three menstrual cycle in a month; every single month for the last year and now I am not even having weekend between them I am on my 4th menstrual cycle for the month; Two months after consistent bleeding; this is not normal; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 23-year-old female patient received BNT162b2 (BNT162B2), as dose 1, single (Lot number: 33130BA), in arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: HEAVY MENSTRUAL BLEEDING (non-serious), outcome "unknown", described as "I have the heavy three menstrual cycle in a month; every single month for the last year and now I am not even having weekend between them I am on my 4th menstrual cycle for the month"; MENSTRUAL DISORDER (non-serious), outcome "unknown", described as "Two months after consistent bleeding; this is not normal". The events required physician office visit. Additional information: The patient wanted to report another side effects right after she got the vaccine (clarified as Pfizer COVID-19 Vaccine) last year, she called the same day. "I have the heavy three menstrual cycle in a month, every single month for the last year and now I am not even having weekend between them I am on my 4th menstrual cycle for the month and this all this Feb. I just got off my period 5 days ago and now I have it again and I don't take medicine and I don't take get vaccines the only vaccine I have had within the last 10 years of Pfizer. I don't need to take it." Consumer stated, "I went to try to get help and I have verified it's not just an symptoms of ovarian cancer. I went to an gynecologists like about two months after consistent bleeding and they are the ones that told me like that no, this is not normal. I have some documents back, because I ended up getting on birth control (Name could not be clarified hence, captured as unspecified medication) thinking it will stop the bleeding and they gave me signs of 'closure' before they gave me birth control things and I was bleeding three times a month before I even get birth control." Consumer stated, "I am not taking any other medications or I wasn't at that time either, I was perfectly healthy normal I won't even take aspirin, I don't do medicine." Consumer stated, "Yes, it is the first shot. I got was from withheld and the second vaccine was from withheld pharmacy. Sender's Comments: Linked Report(s) : US-PFIZER INC-202300083604 same patient/drug, different dose/event;

Weitere VAERSDATA-Felder

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

VAERS 2583911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 18.02.2023
Impfdatum: 14.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Vaccination site inflammation Vaccination site pruritus

Symptomtext

inflamed arm at the injection site; inflamed arm at the injection site; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). An adult female patient received BNT162b2 (COMIRNATY), on 14Dec2021 as dose 3 (booster), single (Lot number: 33130BA) 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. The following information was reported: VACCINATION SITE INFLAMMATION (non-serious), VACCINATION SITE PRURITUS (non-serious), outcome "recovering" and all described as "inflamed arm at the injection site". Therapeutic measures were not taken as a result of vaccination site inflammation, vaccination site pruritus. Additional information: Patient reports itchy and inflamed arm at the injection site of last vaccine administration months after receiving dose. The patient did not have COVID prior vaccination and it was unknown if the patient was tested for COVID post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2605749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 10.01.2023
Impfdatum: 22.12.2021
Beginn: 05.10.2022
Tage bis Beginn: 287,0
Dosis: 1
Route/Site: IM / RA

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

Rash

Symptomtext

Narrative: Patient received third dose of Pfizer vaccine in December 2021. In October 2022, patient declined COVID-19 vaccine due to reported rash with third dose.

Weitere VAERSDATA-Felder

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

VAERS 2550967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MA
Alter: 59,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 18.12.2021
Beginn: 27.07.2022
Tage bis Beginn: 221,0
Dosis: 3
Route/Site: - / LA

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

Arthritis Bursitis Polymyalgia rheumatica Rheumatoid arthritis Tendonitis COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Since the vaccination, has the patient been tested for COVID-19?:Yes; Since the vaccination, has the patient been tested for COVID-19?:Yes; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Apr2021 as dose 1, single (Lot number: en6198), in right arm, on 03May2021 as dose 2, single (Lot number: ew0170), in right arm and on 18Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: SYNTHROID. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 27Jul2022, outcome "unknown" and all described as "Since the vaccination, has the patient been tested for COVID-19?:Yes". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (27Jul2022) Positive, notes: Nasal Swab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Polymyalgia rheumatica
Hospital-Tage: -
Labordaten: Test Date: 20220727; Test Name: Abbott test; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 2549344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 05.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / RA

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

Basedow's disease Dizziness Laboratory test

Symptomtext

dizziness, graves disease

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: labwork
Aktuelle Erkrankungen: -
Vorgeschichte: seasonal asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2543525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 25.12.2021
Beginn: 27.12.2022
Tage bis Beginn: 367,0
Dosis: 2
Route/Site: - / -

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

Chills Pyrexia Respiratory tract congestion

Symptomtext

CONGESTION, FEVER, CHILLS

Weitere VAERSDATA-Felder

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

VAERS 2536726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 11.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Hypersensitivity Pruritus Rash Rash papular

Symptomtext

I started having like allergic reaction on my injection arm and that leg. It started general then it was very red and started itching. It looked like a skin rash very red a raised in the surface. I have to take allergy medication like CLARITIN/losartan/ZYRTEC. This kept going for about 4 weeks and then I saw a doctor and he told me to continue taking this medication. I then went for a physical and he told me to just keep taking the medication and to contact the CDC.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Thyroid Underactive
Andere Medikamente: SYNTHROID
Allergien: N/A
Vorherige Impfungen: -

VAERS 2529439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IL
Alter: 48,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chills Fatigue Pain Pyrexia

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 3 (booster), single (Lot number: 33130BA) at the age of 48 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: PREMPRO LOW DOSE oral. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Lot number: EN6207, Vaccine location: left Arm), for COVID-19 immunization, reaction(s): "Fatigue", "Body Aches", "Fever", "Chills"; Bnt162b2 (DOSE 1, SINGLE, Lot number: EN6205, Vaccine location: left Arm), for COVID-19 immunization, reaction(s): "Chills", "Fatigue", "Body Aches", "Fever". The following information was reported: PYREXIA (non-serious), outcome "unknown", described as "Fever"; CHILLS (non-serious), outcome "unknown"; PAIN (non-serious), outcome "unknown", described as "Body Aches"; FATIGUE (non-serious), outcome "unknown". Therapeutic measures were not taken as a result of pyrexia, chills, pain, fatigue. Additional information: patient experienced the events fever, chills, body aches, fatigue began Approximately 12 hrs post dose and continued for 12-16 hrs. This has happened after each of the vaccination doses. No COVID prior vaccination. Patient was not tested for COVID post vaccination. No known allergies. Patient received the other vaccine in four weeks included Influenza Vac Quadrivalent Prsv Free 3 Yrs + IM) on 16Nov2022, as dose 1, single in the left arm for immunisation. Sender's Comments: Linked Report(s) :PFIZER INC-202201358718 same patient/AE, different vaccine dose; PFIZER INC-202201359445 same patient/AE, different vaccine dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None known allergies: No
Andere Medikamente: PREMPRO LOW DOSE
Allergien: -
Vorherige Impfungen: -

VAERS 2510340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NV
Alter: 66,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 21.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Biopsy bone Blood test Body height Pain in extremity Platelet count Scan Weight

Symptomtext

sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID. A 67-year-old male patient received BNT162b2 (BNT162B2), on 21Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 66 years for covid-19 immunisation. The patient's relevant medical history included: "medical condition with the lungs", start date: 2017 (ongoing), notes: has oxygen for that and that was stable; "paralyzed lung" (unspecified if ongoing), notes: stable; "Wheelchair" (ongoing); "has oxygen" (unspecified if ongoing), notes: the lungs that he had already in 2017 and has oxygen for that and that was stable. There were no concomitant medications. Past drug history included: Sertraline, start date: Jun2021, for depression; Hydroxizine, notes: low dose. Vaccination history included: BNT162b2 (Dose: 2, Lot number: lot EW01), administration date: 14Jun2021, when the patient was 66-year-old, for Covid-19 immunization, reaction(s): "sore arm"; BNT162b2 (Dose: 1, Lot number: ER8737), administration date: 24May2021, when the patient was 66-year-old, for Covid-19 immunization, reaction(s): "sore arm". The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "sore arm". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The previous other three covid vaccine didn't do anything to him. He always gets his blood drawn and they check everything especially with him going to the (name withheld) and he was fine with the other vaccines and had three other covid vaccines that were Pfizer as caller states later in the call and he had no symptoms with those and only had a sore arm for all four doses of the vaccine but the sore arm only lasted for the first 24 hours with the first three vaccines and then he was good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: bone biopsy; Result Unstructured Data: Test Result:Unknown results; Test Name: Blood work; Result Unstructured Data: Test Result:he is great and is fine; Comments: they do blood tests for everything to see if he is great and is fine; Test Name: Blood work; Result Unstructured Data: Test Result:it does not show he has cancer; Comments: they have done blood work and it does not show he has cancer; Test Name: height; Result Unstructured Data: Test Result:5 feet 10 inches; Comments: height is supposed to be 5 feet 10 inches; Test Date: 20220928; Test Name: Platelet count; Result Unstructured Data: Test Result:10; Comments: his blood platelets in September 28th it was down to 10 which was low and critical; Test Date: 20221110; Test Name: Scan; Test Result: Negative ; Comments: she is not sure if it is MRI or cat scan but it was for his brain and it was yesterday and they were wanting to see if it was hemorrhaging; Test Name: weight; Result Unstructured Data: Test Result:maybe 250 lbs
Aktuelle Erkrankungen: Lung disorder (has oxygen for that and that was stable); Wheelchair user
Vorgeschichte: Medical History/Concurrent Conditions: Oxygen therapy (the lungs that he had already in 2017 and has oxygen for that and that was stable); Respiratory paralysis (stable)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2499117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 20.12.2021
Beginn: 25.10.2022
Tage bis Beginn: 309,0
Dosis: 3
Route/Site: IM / -

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

Asthenia Atrial fibrillation Bundle branch block left COVID-19 Cardiac failure chronic Chest X-ray abnormal Chronic kidney disease Computerised tomogram head normal Computerised tomogram spine Congestive cardiomyopathy Diabetic neuropathy Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Fall Fibula fracture Hydronephrosis Left ventricular failure

Symptomtext

COVID+ 10/27/2022 BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider: DO Admission Date: 10/25/2022 Discharge Date: Nov 2, 2022 Active Hospital Problems Diagnosis Date Noted POA ? Dilated cardiomyopathy 05/02/2022 Yes ? Chronic combined systolic and diastolic heart failure 04/08/2022 Yes ? Nephrostomy status 03/22/2022 Yes ? Lymphoma 03/22/2022 Yes ? Hydronephrosis 03/17/2022 Yes ? Type 2 diabetes mellitus with diabetic neuropathy 03/14/2022 Yes ? Retroperitoneal mass 03/14/2022 Yes ? Chronic kidney disease (CKD), stage IV (severe) 03/14/2022 Yes ? Paroxysmal atrial fibrillation 03/14/2022 Yes ? Subclinical hypothyroidism 03/12/2021 Yes ? Thoracic aortic aneurysm without rupture 05/22/2020 Yes ? Lymphadenopathy, retroperitoneal 04/21/2020 Yes ? At risk for falls 06/13/2017 Yes ? Persistent proteinuria associated with type 2 diabetes mellitus 03/22/2016 Yes ? History of prostate cancer 02/22/2012 Yes ? Hypertension 07/06/2010 Yes ? Type 2 diabetes 07/06/2010 Yes DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 88 y.o. male with past medical history significant for CHFrEF (now 20%), PAF on Eliquis, HTN, CKD4, DM2, hydronephrosis status post right nephrostomy, who present to emergency department with a complaint of weakness and fall. Patient developed generalized weakness, cold symptoms, and malaise and had a ground level fall after receiving his COVID-19 and flu vaccine. Upon arrival at emergency department patient's vitals blood pressure 123/60, pulse 114, temperature 97.7?, O2 sat 98% on room air, respiration 18. Imaging CT of the head and cervical spine showed no acute intracranial process or fracture. Chest x-ray showed mild left pleural effusion without evidence of infiltrate or opacity. EKG showed atrial fibrillation with heart rate at 117, as well as left anterior fascicular block. Given patient's frequent fall and generalized weakness as well as COVID-19 infection that patient tested positive for, patient was admitted to general medicine for further management and PT OT and case manager will be consulted for placement. Due to frequent falls patients eliquis was discontinued. Patient and son both agreed on this. Repeat ECHO did note decrease in EF from 40 to 21%. Patient was continued on his goal directed medical therapy of Toprol XL and lisinopril. No evidence of acute CHF. Recommend to follow up with Cardiology outpatient for repeat ECHO and optimization of medical therapy. This was communicated to his son who voiced understanding. Orthopedics was consulted for mildly displaced R fibular fracture during his stay for which orthopedic surgery recommended conservative management with weight-bearing as tolerated. Outpatient ortho follow up in 1 week. Patient discharged back to assisted living in stable condition. Discharge instructions reviewed with son over the phone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Type 2 diabetes Allergic rhinitis Impotence of organic origin History of prostate cancer Persistent proteinuria associated with type 2 diabetes mellitus At risk for falls Lymphadenopathy, retroperitoneal Thoracic aortic aneurysm without rupture Subclinical hypothyroidism Type 2 diabetes mellitus with diabetic neuropathy Retroperitoneal mass Chronic kidney disease (CKD), stage IV (severe) Paroxysmal atrial fibrillation Dyspnea on exertion Hydronephrosis Nephrostomy status Lymphoma Septic shock Urinary tract infection Chronic combined systolic and diastolic heart failure Bacteremia due to Gram-negative bacteria Hyperkalemia Dilated cardiomyopathy Sepsis secondary to polymicrobial pyelonephritis in the setting of percutaneous nephrostomy tube use secondary to hydronephrosis Moderate protein-calorie malnutrition Gross hematuria
Andere Medikamente: Ascorbic Acid 500 mg Daily Aspirin 81 mg Daily Atorvastatin Calcium 20 MG TAKE 1 TABLET BY MOUTH EVERY DAY Calcium Carbonate 1 tablet Oral Daily Cholecalciferol 125 MCG (5000 UT) Tabs, 1 tablet Oral Daily 125 MCG (5000 UT) Tabs, 1 tablet Fl
Allergien: seasonal allergies unspecified
Vorherige Impfungen: -

VAERS 2485514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 03.04.2021
Beginn: 30.08.2022
Tage bis Beginn: 514,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

08/30/22 presents to ED for "fevers, generalized weakness". PMHx of "HFpEF, CAD, HTN, HLD, GERD, hypothyroidism, MDD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 08/30/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2476253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TN
Alter: 23,0
Geschlecht: M
Eingang: 12.10.2022
Impfdatum: 20.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Back pain

Symptomtext

Lower back pain lasting ~2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Nkda, nkfa
Vorherige Impfungen: -

VAERS 2411265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 04.01.2022
Beginn: 13.09.2022
Tage bis Beginn: 252,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cough Fatigue Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

+ covid test in fully vaccinated pt.

Weitere VAERSDATA-Felder

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

VAERS 2411265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 04.01.2022
Beginn: 13.09.2022
Tage bis Beginn: 252,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Cough Fatigue Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

+ covid test in fully vaccinated pt.

Weitere VAERSDATA-Felder

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

VAERS 2402986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 30.12.2021
Beginn: 04.08.2022
Tage bis Beginn: 217,0
Dosis: 3
Route/Site: UN / UN

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

Cough Fatigue Oropharyngeal pain

Symptomtext

fatigue, sore throat, cough

Weitere VAERSDATA-Felder

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

VAERS 2364519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 08.04.2022
Beginn: 07.06.2022
Tage bis Beginn: 60,0
Dosis: 4
Route/Site: SYR / LA

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

Urticaria

Symptomtext

Please note: this event has occurred three months after the vaccination. Developed spontaneous hives (urticaria). appearing and disappearing within a matter of hours. Have not been able to discover cause, whether external allergen or internal idiopathic immune response.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma on exertion.
Andere Medikamente: Atorvastatin; Oxybutynin; Atrovent inhaler; Tretinoin Cream; OTC Calcium Supplement; OTC Vitamin E supplement; OTC fiber drink (Citrucel).
Allergien: Iodine and Iodinated Contrast Media.
Vorherige Impfungen: swollen red arm, age 64, given 1/22/2020, Zoster HZ/su (Shingrix)

VAERS 2362408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: SD
Alter: -
Geschlecht: U
Eingang: 08.07.2022
Impfdatum: 15.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / RA

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

Blood electrolytes abnormal Blood lactic acid Blood magnesium Blood phosphorus Blood thyroid stimulating hormone Body fluid analysis C-reactive protein Computerised tomogram Cranial nerve disorder Ear pain Eye pain Facial pain Full blood count Human chorionic gonadotropin Immunology test Liver function test Loss of personal independence in daily activities Lyme disease

Symptomtext

greater articular neuritis; Nerve pain; Possible trigeminal neuralgia / lighting bolt sensations; Lightning bolts would occur multiple times an hours making it hard to focus on any task; The pain began to shoot into my left cheek and ear / Severe pain daily on the left side of my face/ The pain was now in my eye, cheek, and behind my left ear; The pain began to shoot into my left cheek and ear / Severe pain daily on the left side of my face/ The pain was now in my eye, cheek, and behind my left ear; The pain began to shoot into my left cheek and ear / Severe pain daily on the left side of my face/ The pain was now in my eye, cheek, and behind my left ear; Unable to turn my neck at times due to the pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP), Program ID: (005570). A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 15Dec2021 at 13:00 as dose 3 (booster), single (Lot number: 33130BA) intramuscular, in right arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose number: 1, Time: 07:30, Anatomical site of injection: Right arm, Route of administration: Intramuscular, Batch/Lot number: EK5730), administration date: 17Dec2020, for COVID-19 Immunization; BNT162b2 (Dose number: 2, Time: 08:00, Anatomical site of injection: Left arm, Route of administration: Intramuscular, Batch/Lot number: EL8982), administration date: 21Jan2021, for COVID-19 Immunization, reaction(s): "Eye pain", "Ciliary muscle spasm", "dull ache/pressure only behind my left eye". The following information was reported: LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset Dec2021, outcome "unknown", described as "Lightning bolts would occur multiple times an hours making it hard to focus on any task"; FACIAL PAIN (non-serious), EAR PAIN (non-serious) all with onset Dec2021, outcome "unknown" and all described as "The pain began to shoot into my left cheek and ear / Severe pain daily on the left side of my face/ The pain was now in my eye, cheek, and behind my left ear"; EYE PAIN (non-serious) with onset Dec2021, outcome "not recovered", described as "The pain began to shoot into my left cheek and ear / Severe pain daily on the left side of my face/ The pain was now in my eye, cheek, and behind my left ear"; NECK PAIN (non-serious) with onset Dec2021, outcome "unknown", described as "Unable to turn my neck at times due to the pain"; TRIGEMINAL NEURALGIA (non-serious) with onset 18Jan2022, outcome "unknown", described as "Possible trigeminal neuralgia / lighting bolt sensations"; CRANIAL NERVE DISORDER (non-serious) with onset 11Apr2022, outcome "unknown", described as "greater articular neuritis"; NEURALGIA (non-serious) with onset Apr2022, outcome "unknown", described as "Nerve pain". The events "the pain began to shoot into my left cheek and ear / severe pain daily on the left side of my face/ the pain was now in my eye, cheek, and behind my left ear", "unable to turn my neck at times due to the pain", "possible trigeminal neuralgia / lighting bolt sensations", "greater articular neuritis" and "nerve pain" required physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of facial pain, ear pain, eye pain, neck pain, trigeminal neuralgia, cranial nerve disorder, neuralgia. Additional Information: Prior vaccinations was reported as none. Family medical history to AE(s) was reported as none. Specific relevant test was reported as none. Specific relevant test for thromboembolic events with thrombocytopenia was reported as none. 22Sep2021: First eye appointment left eye pain started about 2 weeks prior. I would describe the pain as a dull ache/pressure only behind my left eye. Tylenol or Motrin never relieved the pain. 04Nov2021: He was unsure of what was causing the eye pain. We re-checked my vision twice and no changes to my vision had beer. noted. He thought it could be a virus, so we tried OTC Zyrtec for two weeks with no symptom relief. 02Dec2021: Today I went to a new eye doctor for a second option. He initially diagnosed me with ciliary muscle spasms. He thought they possibly over corrected my vision, so we tried a new contact in the left eye only. Eye pain the next couple of weeks did not Change. 15Dec2021: Received my third dose (booster dose) of the Pfizer vaccine. The weeks following the booster dose were tough. The pain began to shoot into my left cheek and ear. Severe pain daily on the left side of my face. "Lightning bolts" would occur multiple times an hour making hard to focus on any task. The pain was never relieved by any OTC medications. was unable to turn my neck at times due to the pain. Pain worsened with any eye movement. The pain was now in my eye, cheek, and behind my left ear, Any touch of a mask, wind, or fabric would make the pain worse. 18Jan2022: Another appointment with second eye doctor. He diagnosed me with possible trigeminal neuralgia. He ordered 51000 neuro glasses for me to try, he said pain would be relieved 3-4 days after starting to wear the glasses. 26Jan2022: Received glasses. Three weeks of wearing the glasses when awake with no relief. 22Feb2022: Went to (Clinic name) ER due to pain and no relief from previous options. Was seen In the ER and had labs and an MRI done. All came back normal. Sent home with a prescription of Tegretol, began taking the Tegretol and could not tolerate the side effects. Also had follow-up appointments with neurology. 21Mar2022: Third eye appointment, options discussed with no new resolution for the pain Unable to wear glasses due to the pain when touching my race.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Test Date: 20220222; Test Name: Electrolytes; Result Unstructured Data: Test Result:within defined limits; Test Date: 20220222; Test Name: Lactate level; Result Unstructured Data: Test Result:1.1; Test Date: 20220222; Test Name: Magnesium; Result Unstructured Data: Test Result:2.1; Test Date: 20220222; Test Name: Phosphorus; Result Unstructured Data: Test Result:3.2; Test Date: 20220222; Test Name: TSH; Result Unstructured Data: Test Result:1.3; Test Date: 20220222; Test Name: Body fluid PH; Result Unstructured Data: Test Result:7.6; Test Date: 20220222; Test Name: CT contrast; Result Unstructured Data: Test Result:within defined limits; Test Date: 20220222; Test Name: C-Reactive protein; Result Unstructured Data: Test Result:within defined limits; Test Date: 20220222; Test Name: CBC; Result Unstructured Data: Test Result:within defined limits; Test Date: 20220222; Test Name: HCG; Test Result: Negative ; Test Date: 20220222; Test Name: CIA; Result Unstructured Data: Test Result:within defined limits; Test Date: 20220222; Test Name: Liver function; Result Unstructured Data: Test Result:within defined limits; Test Date: 20220222; Test Name: Lyme AB; Test Result: Negative ; Test Date: 20220222; Test Name: MRI with + without; Result Unstructured Data: Test Result:Normal; Comments: Brain, Face, Cervical, spine; Test Date: 20220222; Test Name: MRI with + without; Result Unstructured Data: Test Result:Normal; Comments: Cervical spine; Test Date: 20220222; Test Name: Microscopic automated; Result Unstructured Data: Test Result:within defined limits; Test Date: 20220222; Test Name: Sed Rate; Result Unstructured Data: Test Result:2; Test Date: 20220222; Test Name: Urine osmolality; Result Unstructured Data: Test Result:258
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2359620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NC
Alter: 14,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 31.12.2021
Beginn: 19.06.2022
Tage bis Beginn: 170,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Oropharyngeal pain Pyrexia Respiratory symptom Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

She started getting symptoms of cough, congestion, sore throat, tiredness, and mild feverish. Most of the symptoms were upper respiratory. We done an at home COVID-19 test that was positive. I called her doctor and due to dwarfism, they did suggest to go to the urgent care. The doctor at the urgent care prescribed PAXLOVID. The PAXLOVID did help her symptoms and within 24 hours she felt better.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Dwarfism
Andere Medikamente: None
Allergien: KEFLEX
Vorherige Impfungen: Pfizer 1, 2, and 3rd dose, pain at injection site.

VAERS 2342242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IL
Alter: 60,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Back pain Haemorrhage Nasopharyngitis Rhinorrhoea

Symptomtext

resident had cold, back sore and runny nose with blood clothes . she got better after three weeks .

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Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Hight blood pressure , high cholesterol and thyroid
Vorgeschichte: none
Andere Medikamente: resident was not taking any medication
Allergien: no allergies
Vorherige Impfungen: -

VAERS 2341853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 28.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 161,0
Dosis: 3
Route/Site: IM / LA

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

Anosmia COVID-19 Chills Cough Fatigue Headache Malaise Myalgia Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive Vomiting

Symptomtext

I contracted COVID-19 on 06/07/2022 with symptoms of congestion, sore throat, cough, loss of smell, vomiting, headache, fatigue, myalgia, and chills. I was not prescribed any medications or offered monoclonal antibodies. I was ill for 9 days before my symptoms began to resolve. I have fully recovered with no lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 PCR test taken on 06/09/2022 was positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: WELLBUTRIN; LATUDA
Allergien: N/A
Vorherige Impfungen: -

VAERS 2338878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MA
Alter: 61,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 06.12.2021
Beginn: 09.04.2022
Tage bis Beginn: 124,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Headache Laboratory test abnormal Oropharyngeal pain Paranasal sinus discomfort Sinusitis Throat irritation Upper-airway cough syndrome

Symptomtext

Starting 04/10/2022, I developed sinus infection symptoms: headache, sore throat, fatigue and sinus pressure. I tested positive on 04/11/2022 and I called my doctor on that monday 04/12/2022. She prescribed me Paxlovid. After taking the Paxlovid, my symptoms got a little milder but it took about a week for the major symptoms to resolve and only minor symptoms remained for another week or so (scratchy throat and post nasal drip). It basically felt like a sinus infection to me.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home test (04/11/2022): Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Wellbutrin XR, Multivitamin, Calcium, Vitamin B12 and Fiber
Allergien: Bactrim, Percocet and some shellfish
Vorherige Impfungen: After the second Shingles shot, I felt extremely worn down and exhausted for the first 24 hours and then it resolved

VAERS 2322101

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 33130BA

mild

Staat: PA
Alter: 26,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 01.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / RA

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

Antinuclear antibody positive Blood test abnormal Chronic cutaneous lupus erythematosus Fatigue Influenza like illness Laboratory test abnormal Pain Rash Scab Sjogren's syndrome Systemic lupus erythematosus

Symptomtext

A month after I received my first vaccine I started getting sores on my face that would break open and scab. I also started to feel tired all the time and my body hurt like I had the flu.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: My family doctor sent me to a dermatologist after failed attempts at treating the spots. The dermatologist said that is was discoid lupus and sent me for an ANA test. October 15th 2021 I got my results back that my ANA was positive and my dilution rate was consistent with systemic lupus. He set me up with rheumatology and on December 16th I received my blood work results and I was positive for sjorgens syndrome as well.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Junel Citalopram
Allergien: -
Vorherige Impfungen: -

VAERS 2317241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 29.01.2021
Beginn: 09.06.2022
Tage bis Beginn: 496,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Cardiac failure acute Cardiac failure congestive Cough Electrocardiogram abnormal Hypoxia Left ventricular failure Pyrexia SARS-CoV-2 test positive

Symptomtext

Pt was admitted on 6/1 for abnormal EKG and acute on chronic combined systolic and grade 2 diastolic CHF. On 6/9 he developed a cough, low grade fever, and hypoxia that required oxygen. He was found to be COVID positive.

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

VAERS 2303585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: FL
Alter: 96,0
Geschlecht: M
Eingang: 31.05.2022
Impfdatum: 18.12.2021
Beginn: 25.05.2022
Tage bis Beginn: 158,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Cough Fall Pyrexia SARS-CoV-2 test positive

Symptomtext

He received 3 doses of Pfizer vaccines on 3/13/21, 04/03/21, and 12/18/21. On 5/25/22, he presented at ER for one week of generalized weakness, cough, and falls. He was tested for covid, positive prior to ER arrival. He was admitted to the hospital same day for further treatments. He received Remdesivir and Steroids. He was originally febrile and given supplemental oxygen. He was discharged home on 5/29/22 without home oxygen therapy.

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Praegender Schweregrund: Pyrexia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: GERD, Prostatitis, HTN
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2284786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: FL
Alter: 48,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Dysgeusia Exercise tolerance decreased Injection site pain Injection site swelling Pain Parosmia

Symptomtext

Short Term Adverse Effect was that I got a strange chemical taste/smell in my mouth and nose on the second day . Became very weak and ached all over for a few short days. Injection site was very sore and swollen. Long Term Effect so far has been continued swelling and pain at the injection site. Find that exercise makes the area swell up. Loss of energy continues to occur.

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Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None at this time. Going to be setting up a Doctors Appointment to try to figure out what is going on. Has been enough time that it should have gone away.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin
Vorherige Impfungen: 03/23/2021 -COVID 19 First Shot - Pfizer - Strange taste - Injection Site Pain - Numbness in Right Hand - Shot was given in Rig

VAERS 2280637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MD
Alter: 52,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 04.04.2022
Beginn: 14.05.2022
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Headache Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

It started with a headache and scratchy throat one morning. The next days following, I had a runny nose and cough. I completed an at-home COVID-19 antigen test because of my symptoms on 05/15/2022, and it came back positive. I called my doctor's office, and she informed me for my symptoms to take Mucinex and take my Albuterol nebulizer treatments. Currently, I'm still exhibiting a deep cough and runny nose still of my COVID-19 symptoms.

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test: 05/15/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Mycobacterium Avium Complex (MAC)
Andere Medikamente: Protonic, Pepcid, Synthroid, Arthrotomies, Levocetirizine, Calcium D Glucoronate, Probiotics
Allergien: N/A
Vorherige Impfungen: -

VAERS 2278456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: WA
Alter: 57,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 24.12.2021
Beginn: 01.03.2022
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: SYR / AR

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

Erythema Hyperaesthesia Pain in extremity Raynaud's phenomenon Sensory disturbance Skin discolouration

Symptomtext

It started around March. I felt like my toes were sore. They were sensitive, if I wore shoes for a long length of time they felt weird. I thought they were blisters but I didn't see anything. It was the very tips of my toes. A few weeks went by and the tops were now red and sometimes purple. At night they would bother me and they were painful. I felt is anything touched them they were very painful. I went to an urgent care and the person diagnosed me with Athlete's foot without much information. She gave me an over the counter medication for 21 days and my feet got worse. I went back to the same urgent care and saw a different doctor and I was referred to a podiatrist and she didn't think it was athletes. It took a while to see the podiatrist and he diagnosed me with Raynaud's disease. He has given two other medications and I am to return in two weeks to see if his diagnosis is correct.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2277873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: WA
Alter: 52,0
Geschlecht: F
Eingang: 15.05.2022
Impfdatum: 11.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: SYR / RA

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

Alopecia Dry skin Erythema Pruritus Psoriasis Rash papular Skin discolouration Skin exfoliation

Symptomtext

1. No previous history with any skin condition 2. Onsite of Psorarias secondary to Booster Shot of Pfizer mRNA 3. Started experiencing redness under breasts, circle dry patches on neck and forehead. Attempted to treat with OTC Hydrocortisone, .1% 2x/day, which seemed to provide some relief - but not for long. 4. More dark circles, with raised bumps, scalp itching, and scaling continued to the point where I had over 30 patches of dry spots on my torso, back, neck, ears, buttocks, and right arm. 5. As things continued to get progressively worse, I went to see my PCP and he diagnosed me with the onset of psoriasis resulting from mRNA Pfizer booster. 6. by 5/14/22 - 75% of my hair has now fallen out due to dry patches, scalp flaking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Environmentally triggered Asthma Allergic rhinitis
Andere Medikamente: OTC Zyrtec
Allergien: Vicodin High Doses of Aspirin Bee Stings Dust Mosquito Bites Dogs Cats Smoke Insect Venon
Vorherige Impfungen: -

VAERS 2273264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 10.12.2021
Beginn: 15.01.2022
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Decreased appetite Malaise SARS-CoV-2 test positive

Symptomtext

Narrative: Fully vaccinated COVID positive upon hospital admission. Presented to hospital with malaise and decreased appetite found to be COVID positive. Patient with hx of prior COVID infection.

Weitere VAERSDATA-Felder

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

VAERS 2267650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: WA
Alter: 30,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 28.02.2022
Beginn: 01.03.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Exercise tolerance decreased Headache Loss of personal independence in daily activities Nausea Restlessness SARS-CoV-2 test positive

Symptomtext

After receiving my second dose (1st dose of Pfizer), I have been having 1-2 severe headaches per week. I become nauseated and I'm unable to even function. I also experience restlessness. I'm unable to go running like I used to before. I did test positive for COVID-19 in June of 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: I have not been in to see my doctor yet.
Aktuelle Erkrankungen: I was not experiencing any illness.
Vorgeschichte: I have major depressive disorder with panic attacks.
Andere Medikamente: I believe I started taking Lexapro around the time I received my vaccine.
Allergien: I had a bad reaction to Cephalexin.
Vorherige Impfungen: -

VAERS 2263126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MD
Alter: 15,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 26.01.2022
Beginn: 08.02.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

Computerised tomogram normal Epstein-Barr virus test negative Full blood count normal Headache Influenza virus test negative Laboratory test normal New daily persistent headache Streptococcus test negative

Symptomtext

Developed a headache evening 2/8/2022 and not subsided since as of today 5/4/2022, neurologist diagnosed patient with NDPH 3/24/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: All bloodwork negative (CBC, flu, strep, Cocos, EBV), CT scan WNL
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multivitamins
Allergien: No
Vorherige Impfungen: -

VAERS 2260489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MO
Alter: 54,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 12.12.2021
Beginn: 19.01.2022
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Bursitis Erythema Inflammation Injection site swelling Pain Peripheral swelling

Symptomtext

About a month post vaccine - noticed left upper arm was still a little larger (swollen) than right arm. By 01/19/22, had elbow bursitis in Left elbow - swelling continued down forearm and whole area became very red/inflamed, swollen, painful. Left hip area was very painful about 1-2 weeks prior to this. Sought help at Urgent Care on 01/20/22 - started Prednisone and Cephalexin which helped tremendously. Still have a minor swelling and tenderness of Left elbow to this date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: No testing done - just started on medicine.
Aktuelle Erkrankungen: none
Vorgeschichte: seasonal allergies
Andere Medikamente: Singulair, Calcium Tabs, Fish Oil capsules, Daily Multi Vitamin, Alieve
Allergien: none
Vorherige Impfungen: -

VAERS 2251891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IL
Alter: 67,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 13.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 49,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Back pain Bone marrow oedema Chondromalacia Inflammation Kyphosis Ligament calcification Lordosis Magnetic resonance imaging abnormal Multiple sclerosis Spinal X-ray abnormal Spinal pain

Symptomtext

Inflammation/pain in lower back/spine area. Prescribed orphenadrine citrate for treatment. Severe pain gone after treatment. Slight pain still remains. Inflammation/pain in left knee cap. Prescribed cortisone injection/physical therapy/tramadol. Severe pain was gone after treatment. Slight pain remains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 07/27/2021 - x-ray spine cervical: Upper cervical lordosis and lower cervical kyphosis is seen. Prominent ventral and posterior spur formation is seen at C6-C7. 07/27/2021 x-ray spine lumbar: Facet sclerosis is most conspicuous at L5-S1. Ventral spur formation and calcification of anterior longitudinal ligament. 12/03/2021- MRI left knee: Chondromalacia most pronounced at the patellofemoral articulation with mild moderate subchondral edema.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, high cholesterol
Andere Medikamente: Atorvastatin 20mg, Losartan 50mg
Allergien: None
Vorherige Impfungen: -

VAERS 2249962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: OK
Alter: 49,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 03.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LL

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

Axillary pain Lymphadenopathy Oedema peripheral

Symptomtext

Day 3 after the vaccine in the morning my left armpit was extremely swollen and sore. A gland around my clavicle was also swollen, it stayed this way for a week so I called the clinic who explained VAERS to me which I could not access.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Bayer Lisinopril Estradiol Pantoprazole
Allergien: Poison ivy or oak
Vorherige Impfungen: -

VAERS 2245899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: VA
Alter: 33,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 28.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: SYR / AR

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

Abdominal pain upper Clostridium difficile infection Computerised tomogram abdomen abnormal Fatigue Gastrointestinal disorder Hepatitis Hepatomegaly Laboratory test Nasopharyngitis Sinusitis

Symptomtext

I got a very bad cold at the end of February and I treated the cold over the counter for two weeks. I went to the Doctor on 03/01/22 and was diagnosed with a sinus infection and was prescribed amoxicillin for 10 days which I took. The following day the amoxicillin started giving me stomach issues and I went to a different doctor on 03/15/22 and was told to take over the counter medications and probiotics. Between 03/15/22 and 03/20/22 the stomach pain became worse. I went to the ER twice and was diagnosed with C-diff. I was then prescribed antibiotics for 7 days and I finished that antibiotic and have been finished for a month and I'm still having gastrointestinal issues and fatigue. I went to the ER and had both labs and CT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Labs and CT scan (enlargement and inflammation of liver) 03/2022
Aktuelle Erkrankungen: None
Vorgeschichte: History of Ovarian Cysts
Andere Medikamente: One daily birth control.
Allergien: None
Vorherige Impfungen: -

VAERS 2243546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 35,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Erythema Hypoaesthesia Impaired work ability Loss of personal independence in daily activities Pain in extremity Skin warm Sleep disorder Swelling

Symptomtext

Starting the evening I received my vaccine, my R arm was extremely painful and hot. Over the next 2 days it got worse, severe swelling, redness, hot to touch, pain in arm and numbness. This disrupted my sleep, daily activities and work (unable to type with R hand/arm). This started to subside on day 3-4 but lasted almost 2 weeks until the pain/swelling was completely gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: none - self treated at home with cold compress and reset
Aktuelle Erkrankungen: no known illnesses
Vorgeschichte: fibromyalgia, anxiety, depression, scoliosis, neuropathy
Andere Medikamente: sertraline, pantoprazole, Zofran, Ativan, Zanaflex, THC, CBD.
Allergien: NKA
Vorherige Impfungen: -

VAERS 2223111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: PR
Alter: 72,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 30.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

Biopsy skin Biopsy skin abnormal Bloch-Sulzberger syndrome Eczema Eosinophil count Eosinophil count normal Erythema Erythema multiforme Excessive granulation tissue Lichenoid keratosis Lymphocytic infiltration Pruritus Red blood cell vacuolisation Skin swelling Target skin lesion

Symptomtext

Generalized erythema multiforme and generalized "targetoid plaques" in both lower and upper extremities. They start as small red lesions that progress to larger dark scaly lesions. These lesions are very itchy, red and swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Superficial and lichenoid perivascular lymphocytic infiltrate with scattered eosinophils, vacuolar degeneration, "civatte" bodies, spongiosis, Hyper-granulation, orthokeratosis, and melanin incontinence. 03/11/2022- EOS count: 6.60 (normal range: 0.00-5.00) Skin biopsy and right knee: lichen planus, sclerosing dermatitis, consider
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: BREO ELLIPTA
Allergien: PNC, ASA, Sulfas, Quinolones
Vorherige Impfungen: -

VAERS 2213643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 03.04.2022
Impfdatum: 23.02.2021
Beginn: 11.01.2022
Tage bis Beginn: 322,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

Narrative: This patient received two doses of Pfizer vaccine and the booster on Feb/Mar/Dec 2021. The patient tested positive for COVID19 on 11 Jan 2022 and was admitted to the hospital with dry cough, fever, and malaise. The patient was treated with remdesivir, dexamethasone, and azithromycin. The patient was discharged on 16 Jan 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2195890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: AZ
Alter: 15,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 28.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Pruritus

Symptomtext

Caller states the mom mentioned that the patient experienced body itching after the first dose of the Covid-19 vaccine.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. A 15 year-old male patient received bnt162b2 (BNT162B2), administration date 28Jan2022 (Lot number: 33130BA, Expiration Date: 31May2022) at the age of 15 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PRURITUS (non-serious) with onset Jan2022, outcome "unknown", described as "Caller states the mom mentioned that the patient experienced body itching after the first dose of the Covid-19 vaccine.". Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2189656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MO
Alter: 38,0
Geschlecht: M
Eingang: 21.03.2022
Impfdatum: 04.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / LA

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

Heart rate increased Pruritus Swelling Tinnitus Urticaria

Symptomtext

Full Body Hives, swelling, itching, ears ringing, heart beat a lot stronger, swelling inside.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Been to Urgent Care, PCP, and Allergist and have just been prescribed pills and they said the tests they would do would come back normal.
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: Emeprozol
Allergien: Penecilin
Vorherige Impfungen: -

VAERS 2189032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: CA
Alter: 52,0
Geschlecht: M
Eingang: 19.03.2022
Impfdatum: 21.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Blister Injection site reaction Myalgia Neuralgia Pain

Symptomtext

Systemic: patient has experienced nerve pain around injection site-Medium, Additional Details: Nerve pain was radiating to right lower shoulder muscle also pt said there was a blister there

Weitere VAERSDATA-Felder

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

VAERS 2183879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NH
Alter: 61,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 08.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Chills Headache Pain Pyrexia

Symptomtext

Fever; Chills; Body aches; Joint pain; Headache very severe; 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), administered in arm left, administration date 08Feb2022 15:45 (Lot number: 33130BA) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "COPD" (unspecified if ongoing); "Chronic pain" (unspecified if ongoing); "depression" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose number=2, product=COVID 19, brand=Pfizer, lot number=EW0180, administration date=23Jun2021, vaccine location=Left arm), administration date: 23Jun2021, when the patient was 61 years old, for COVID-19 immunization; Bnt162b2 (Dose number=1, product=COVID 19, brand=Pfizer, lot number=EW0167, administration date=09May2021, vaccine location=Left arm), administration date: 09May2021, when the patient was 61 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 09Feb2022, outcome "recovering", described as "Fever"; CHILLS (non-serious) with onset 09Feb2022, outcome "recovering", described as "Chills"; PAIN (non-serious) with onset 09Feb2022, outcome "recovering", described as "Body aches"; ARTHRALGIA (non-serious) with onset 09Feb2022, outcome "recovering", described as "Joint pain"; HEADACHE (non-serious) with onset 09Feb2022, outcome "recovering", described as "Headache very severe". Therapeutic measures were not taken as a result of pyrexia, chills, pain, arthralgia, headache. Additional information: No other vaccine in four weeks, Patient took other medications in two weeks, Patient was not diagnosed with COVID prior vaccination, Patient was not tested for COVID post vaccination and No Known allergies. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic pain; COPD; Depression.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2183808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 35,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 24.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Lymphadenopathy Renal function test Swelling

Symptomtext

marble sized swelling in his armpit; swollen lymph nodes under the armpit/swollen lymph nodes under the armpit/swollen lymph nodes under the arm pit was worsened; marble sized swelling in his armpit that was painful; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. A 35 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 24Jan2022 14:00 (Lot number: 33130BA) at the age of 35 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1 , Lot: EW0186, Expiration: unknown), administration date: 23Jun2021, when the patient was 34 years old, for Covid-19 Immunization, reaction(s): "he had stage one kidney disease."; Bnt162b2 (Dose 2, Lot: EW0186 (confirms both doses are the same lot number. , Expiration: unknown), administration date: 14Jul2021, when the patient was 34 years old, for Covid-19 Immunization, reaction(s): "he had stage two kidney disease". The following information was reported: SWELLING (non-serious) with onset 24Jan2022 19:00, outcome "not recovered", described as "marble sized swelling in his armpit"; LYMPHADENOPATHY (non-serious) with onset 24Jan2022 19:00, outcome "not recovered", described as "swollen lymph nodes under the armpit/swollen lymph nodes under the armpit/swollen lymph nodes under the arm pit was worsened"; AXILLARY PAIN (non-serious) with onset 24Jan2022 19:00, outcome "unknown", described as "marble sized swelling in his armpit that was painful". The events "marble sized swelling in his armpit", "swollen lymph nodes under the armpit/swollen lymph nodes under the armpit/swollen lymph nodes under the arm pit was worsened" and "marble sized swelling in his armpit that was painful" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of swelling, lymphadenopathy. Additional information: As of 27Jan2022, it was "3/4 the size of a baseball" and the patient had to keep his arm raised/can't lower his arm all the way because of it. She wants to know if have information on swollen lymph nodes after the vaccine. The patient not received any other product. It was stated that Her partner also had swollen lymph nodes under the arm pit. She just does not know if it supposed to get that large under his armpit. The swelling underneath his arm pit was larger than her fist. No any additional vaccines administered on same date of the Pfizer suspect. The events did not cause Emergency Room visit. No any prior vaccination within 4 weeks. No any family medical history relevant to events. The patient was Advised to consult with HCP. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Test Date: 20210623; Test Name: kidney value; Result Unstructured Data: Test Result:normally to decreased; Comments: After the first dose, his kidney valued changed from being totally; Test Date: 20210714; Test Name: kidney value; Result Unstructured Data: Test Result:dipped down; Comments: After the second dose, his kidney value also
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2181723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NE
Alter: 35,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Fatigue Headache Pain

Symptomtext

Slight headache; Body aches; Weakness; Fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Dec2021 16:30 (Lot number: 33130BA) at the age of 35 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Pre-diabetes" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: HEADACHE (non-serious) with onset 08Dec2021 14:00, outcome "not recovered", described as "Slight headache"; PAIN (non-serious) with onset 08Dec2021 14:00, outcome "not recovered", described as "Body aches"; ASTHENIA (non-serious) with onset 08Dec2021 14:00, outcome "not recovered", described as "Weakness"; FATIGUE (non-serious) with onset 08Dec2021 14:00, outcome "not recovered", described as "Fatigue". Therapeutic measures were not taken as a result of headache, pain, asthenia, fatigue. Additional information: No vaccine in four weeks. Mens one-a-day multivitamin in two weeks. No covid prior vaccination and not tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pre-diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Adverse event Cough Headache Interchange of vaccine products Nausea Off label use Overdose Product preparation error SARS-CoV-2 test

Symptomtext

the patient had the Johnson and Johnson covid vaccine prior to this dose; the patient had the Johnson and Johnson covid vaccine prior to this dose; dministrating a full undiluted vial (purple cap) of the Pfizer-BioNTech COVID-19 vaccine as a single dose; dministrating a full undiluted vial (purple cap) of the Pfizer-BioNTech COVID-19 vaccine as a single dose; Headache; Nausea; vaccine overdose of chronic cough; various unspecified problems; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team. A 61 year-old female patient received bnt162b2 (COMIRNATY), intramuscular, administered in arm left, administration date 13Jan2022 (Lot number: 33130BA, Expiration Date: Feb2022) at the age of 61 years as dose 2 (booster), 1.8 ml, single for covid-19 immunisation. Relevant medical history included: "Blood pressure high" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Johnson and johnson covid vaccine (1st dose), administration date: Mar2021, for COVID-19 immunization. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 13Jan2022, outcome "unknown" and all described as "the patient had the Johnson and Johnson covid vaccine prior to this dose"; OVERDOSE (non-serious), PRODUCT PREPARATION ERROR (non-serious) all with onset 13Jan2022, outcome "unknown" and all described as "dministrating a full undiluted vial (purple cap) of the Pfizer-BioNTech COVID-19 vaccine as a single dose"; HEADACHE (non-serious) with onset 2022, outcome "not recovered", described as "Headache"; NAUSEA (non-serious) with onset 2022, outcome "not recovered", described as "Nausea"; COUGH (non-serious) with onset 2022, outcome "unknown", described as "vaccine overdose of chronic cough"; ADVERSE EVENT (non-serious) with onset 2022, outcome "not recovered", described as "various unspecified problems". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of overdose, headache, nausea, cough, adverse event. Additional Information: The caller had a pharmacist administer 1 vial of the medication to three patients, so each patient received a full vial of the vaccine that was undiluted. Per the previous agent this was the patient's booster dose, but the patient had the Johnson and Johnson COVID vaccine prior to this dose so she was unsure how many COVID vaccines the patient has received. Patient was not received other products. Investigation Assessment: Unknown. The pharmacist reported that the patient was still complaining of headache and nausea and various unspecified problems that are not resolved and keeps coming back to report the issues. Phone out 4:20pm: call answered by pharmacist who provided an update. The Patient came to pharmacy for prescriptions of the antibiotic Doxycycline hyclate 100mg, Spiriva inhaler, and Promethazine w/ codeine to treat adverse events attributed to the vaccine overdose of chronic cough. The patient also took a rapid covid test at the pharmacy on 21Feb2022 and was negative. Narrative: Phone-out 11:44 am to reporter for week 7 of 5xOD phone call follow-up. Phone answered by the reporter who stated that patient has not contacted them and so no new information to report. No follow-up attempts are possible. No further information is expected. Follow-up (16Feb2022): This is a spontaneous follow-up report from a contactable consumer. This consumer (pharmacy clerk) reported in response to via telephonic follow-up activity that included: New reporter, vaccination facility information, new events (Headache, nausea and various unspecified problems) and patient age at time of vaccination (61-year-old) were added. Follow-up attempts are completed. No further information is expected. Follow-up (24Feb2022): This is a follow up spontaneous report from a contactable pharmacist. This pharmacist reported in response to HCP telephonic follow up activity which included that: Updated information included the following: Treatment received, event and lab data was added. Follow-up attempts are completed. No further information is expected. Follow-up (02Mar2022): This is a spontaneous follow-up report from a contactable Pharmacist. This Pharmacist reported in response to HCP letter sent which included that: Updated information included the following: Institution name updated. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200064592 same reporter/drug, different patient/ event.;US-PFIZER INC-202200065430 same reporter/drug, different patient/ event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20220221; Test Name: rapid covid test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2168250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: AZ
Alter: 45,0
Geschlecht: M
Eingang: 09.03.2022
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Cold sweat Hyperhidrosis Nausea

Symptomtext

I felt nauseous and had the chills with hot and clods sweats. Ever since I received the second Pfizer shot on 12/13/2021, I have experienced profuse sweating underneath my arms on a daily basis. The sweating continues to this day.

Weitere VAERSDATA-Felder

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

VAERS 2161666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pain Swelling Urticaria

Symptomtext

Patient immediately developed a hive around the size of a half-dollar after receiving the third dose of her covid vaccination. She also experienced a lot of pain after the vaccination. A couple of days later while showering she noticed that an avocado sized lump appeared under her armpit. This lump has remained for the last couple of months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Over the last three months the patient has had many OBGYN visits to take a look at the lump in the arm and is having another upcoming visit to take a look at the lump and determine next steps which may include surgery.
Aktuelle Erkrankungen: unknown
Vorgeschichte: Renal (kidney disease) Dermatologic disorders
Andere Medikamente: Estradiol 0.01% vaginal cream meloxicam 7.5mg
Allergien: Medications that patient is allergic to: Cephalosporins, macrolides and ketolides Bactrim DS (800mg/160mg) Biaxin 500mg Ceclor 250mg capsules Cefazolin 10 gram Ceftin 500 Latex gloves Vancocin 250mg capsules
Vorherige Impfungen: -

VAERS 2158342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NY
Alter: 32,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 20.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / -

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

Abdominal pain Cyst Hydrocele Testicular pain Testicular swelling Ultrasound testes Varicocele Weight decreased

Symptomtext

Scrotal swelling and pain, leading to abdominal pain and a forty pound weight loss. He saw a urologist who ordered an ultrasound and treated him with antibiotics and ibuprofen. He is not any better as of today. His scrotum swells if he exercises, has intercourse, moves the wrong way, wears clothing that is too tight, or sometimes for no apparent reason.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Scrotal US 1/26/22. Right side: Testis normal. 9 mm epididymis cyst. Small hydrocele. Varicocele. Left side: Testis normal. Epididymis enlarged 10 mm. Varicocele.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Albuterol HFA, Metrogel, lorazepam, omeprazole, ranitidine.
Allergien: None
Vorherige Impfungen: -

VAERS 2151320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: FL
Alter: 26,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Overdose Pain in extremity Product preparation error

Symptomtext

administrating a full undiluted vial (purple cap) of the Pfizer-BioNTech COVID-19 vaccine as a single dose; administrating a full undiluted vial (purple cap) of the Pfizer-BioNTech COVID-19 vaccine as a single dose; sore arm; This is a spontaneous report received from contactable reporter(s) (Pharmacist and Consumer or other non HCP) from medical information team. A 26 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 13Jan2022 (Lot number: 33130BA, Expiration Date: Feb2022) at the age of 26 years as dose 2, 1.8 ml single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1), for Covid-19 Immunization. The following information was reported: OVERDOSE (non-serious), PRODUCT PREPARATION ERROR (non-serious) all with onset 13Jan2022, outcome "unknown" and all described as "administrating a full undiluted vial (purple cap) of the Pfizer-BioNTech COVID-19 vaccine as a single dose"; PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "unknown", described as "sore arm". Additional information: The patient received a full vial of the vaccine that was undiluted. It was reported that the patient came in for 2nd dose and only reported have a sore arm after the overdose. The pharmacist provided an alternate contact for the weekly check in phone call in case she is not in the store. Follow-up (16Feb2022): This is a follow up spontaneous report from a contactable consumer. This consumer reported in response to HCP letter sent via telephonic follow-up activity which included that: Updated field: New reporter added, historical vaccine added, dose number and dosage updated, event sore arm added, and additional information updated.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200065429 same reporter, same drug, similar event, different patients.;US-PFIZER INC-202200064592 same reporter, same drug, similar event, different patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2147305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: PA
Alter: 51,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 10.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: - / LA

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

Headache

Symptomtext

9 days after Covid booster with Pfizer mRNA vaccine I started to have severe exacerbation of typically well controlled chronic headaches; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 51 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Dec2021 17:15 (Lot number: 33130BA) at the age of 51 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "GERD" (unspecified if ongoing); "s/p mastectomies" (unspecified if ongoing), notes: s/p mastectomies; "known allergies: Cephalosporin" (unspecified if ongoing), notes: known allergies: Cephalosporin. Concomitant medication(s) included: INFLUENZA taken for immunisation, administration date 13Nov2021; DEXILANT; DEPAKOTE. Vaccination history included: Covid-19 vaccine (MANUFACTURER UNKNOWN, Dose number unknown), for COVID-19 immunization. The following information was reported: HEADACHE (hospitalization) with onset 19Dec2021 21:00, outcome "recovering", described as "9 days after Covid booster with Pfizer mRNA vaccine I started to have severe exacerbation of typically well controlled chronic headaches". The patient was hospitalized for headache (hospitalization duration: 1 day(s)). The event "9 days after covid booster with pfizer mrna vaccine i started to have severe exacerbation of typically well controlled chronic headaches" was evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of headache. Depakote and required steroid course in January to February, as well as multiple other medications. Now, two months later, headaches are slowly getting better. No other trigger identified. No laboratory or brain imaging changes. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.Device Date : 14Feb2022; Sender's Comments: Based on the available information in the case, the causal association between the event Headache and the suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy (known allergies: Cephalosporin); GERD; Mastectomy NOS (s/p mastectomies)
Andere Medikamente: DEXILANT; DEPAKOTE
Allergien: -
Vorherige Impfungen: -

VAERS 2131199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 17.12.2021
Beginn: 24.01.2022
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Ear discomfort Eustachian tube dysfunction Gastrooesophageal reflux disease Neck pain Pain in jaw Tinnitus

Symptomtext

Tinnitus, anxiety, eustachian tube dysfunction, ear fullness, jaw and neck pain, and acid reflux all on-going since booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: Scheduled appointments, waiting to see PCP and ENT.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: CBD and Advil dual action
Allergien: lactose intolerance
Vorherige Impfungen: -

VAERS 2113175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: FL
Alter: 60,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 03.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / RA

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

Hypoaesthesia Malaise Unevaluable event

Symptomtext

Was sick and numb for a few days and now metallic items are sticking to the site of the injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Lisinopril, amlodipineand atorvastatine
Allergien: n/a
Vorherige Impfungen: very sick with pior shots

VAERS 2110377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MN
Alter: 61,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 27.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Chest discomfort Fatigue Hyperhidrosis Macrocephaly Pain Pain in extremity

Symptomtext

I have a lot of muscle aches and fatigue since receiving my vaccine. I have joint pain and sometimes I get sharp pain in my left arm where I got the vaccine. I also got some tightening of my chest and will have it checked since I did have a heart attack in 2019. I also had body aches and also have sweats. I'm having complete physical in couple of weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None reported.
Aktuelle Erkrankungen: None reported
Vorgeschichte: Massive heart attack 01/05/2019
Andere Medikamente: Vitamin C, Vitamin D, Duloxetine
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2105696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: ID
Alter: 12,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 10.02.2022
Beginn: 11.02.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Headache Nausea Pain Vision blurred

Symptomtext

Mother called and stated child was nauseated, had a headache, feeling achy. However, the daughter also reveled she had some blurred vision an at one point it "went black" - Encouraged mother to take her to a ER for consult.

Weitere VAERSDATA-Felder

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

VAERS 2101794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: KY
Alter: 16,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 09.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac flutter Fatigue Muscle spasms Pain in extremity

Symptomtext

The patient presented to the clinic the day after vaccination with mom with c/o sore arm, hand/leg cramps/ fatigue, and states that she feels like her "heart may be fluttering" some.

Weitere VAERSDATA-Felder

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

VAERS 2087696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 7,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 04.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

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

Adverse reaction Chest discomfort Electrocardiogram normal Headache Incorrect dose administered Incorrect product formulation administered Nausea Pyrexia SARS-CoV-2 test negative

Symptomtext

2.4.22 - Patient received wrong dose of Pfizer vaccine at an outside facility (unknown) - was administered the Pfizer adult product and adult COVID vaccine dose. 2.5.22 - Patient's mother called nurse triage line to report adverse effects / side effect (possibly related to dosing error): Symptoms started last night. Symptoms include: Constant Moderate Chest Pressure. Received 2nd dose of pfizer vaccine yesterday and developed fever last night 103.9 and chest pressure this morning with headache. Mom received call yesterday that he received the adult dose of pfizer in error. Patient Has tried Motrin with mild improvement. 2.5.22 - Patient seen in ED: MEDICAL DECISION MAKING: Supervising Physician: MD 7-year-old male with cough variant asthma but of otherwise good health presenting to the emergency department for evaluation of chest tightness 1st noted this morning. Symptoms began following a 2nd dose of COVID-19 vaccination occurring yesterday. Yesterday he received the adult dose of the Pfizer 19 vaccine and this is also noted in his chart. Yesterday, patient had a fever of 103.9? F that resolved after doses of home ibuprofen and Tylenol. Patient noted a chest tightness, worse with exertion today, but otherwise without pleuritic pain, sharp pain, radiating pain, back pain, nausea vomiting, return if fever, or other new symptoms. No wheezing or dyspnea was noted with these symptoms. Patient has been nauseous since yesterday this is not acutely worsening. Patient is not vomiting, notes no abdominal pain, stool changes, or other symptoms. Patient is seen and evaluated. Vital signs are reassuring. Examination is unrevealing. Patient is a well-appearing child in no acute distress, but otherwise no findings indicative of process that is causing symptoms. Patient has no significant family medical history. EKG is obtained that is reassuring and otherwise demonstrates no evidence of myocardial injury. Given presenting symptoms, COVID-19 testing is obtained. Review of Pfizer FDA EUA shows that the administering provider is responsible for reporting of administration errors, and VAERS reporting if an adverse event occurs is required. Casse resulting in multisystem inflammatory syndrome and COVID-19 infections resulting in hospitalization and death are to be reported. Patient is demonstrating no symptoms of MIS, and symptoms and presentation are mild at this time. COVID-19 testing is normal. On re-evaluation, patient is now stating that his symptoms are consistent with his previously experience symptoms with asthma. Given proximity of fever to his vaccination, post vaccination fever suspected. Supportive care is recommended for home therapies. As he is not presenting with symptoms and findings consistent with acute asthma exacerbation requiring systemic steroids or further treatments, continued prescribed medications are recommended along with follow-up with PCP to optimize treatment. Patient is discharged home in stable condition. 2.7.22: Patient seen in another ED - for post-vaccination fevers. Pt comes in after calling the Drs office today stating child has had fevers form the Covid vaccine on Friday. Mom states the last does of tylenol given to child was this early am. No motrin given since the weekend. Child denies nausea or vomiting. Tolerating fluids, mouth is moist. Well appearing child playing games on phone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Narrative Ventricular Rate 117 BPM Atrial Rate 117 BPM P-R Interval 136 ms QRS Duration 80 ms Q-T Interval 312 ms QTC Calculation(Bazett) 435 ms Calculated P Axis 40 degrees Calculated R Axis 42 degrees Calculated T Axis 13 degrees Diagnosis ** * Pediatric ECG analysis * ** Normal sinus rhythm Normal ECG No previous ECGs available Confirmed by M.D., on 2/6/2022 7:08:12 PM COVID-19 PCR Rapid; results Ref Range & Units COVID-19 PCR Not Detected Not Detected
Aktuelle Erkrankungen: NA
Vorgeschichte: Cough variant asthma
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) 108 (90 BASE) MCG/ACT inhaler beclomethasone (QVAR) 80 MCG/ACT inhaler prednisoLONE (ORAPRED) 15 MG/5ML solution
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2203705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 28.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Pruritus Rash Urticaria

Symptomtext

Rash & Urticaria Pruritus Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2092633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: WA
Alter: 43,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 19.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Vertigo Vertigo positional

Symptomtext

Dizziness and vertigo still ongoing since the 2nd vaccine. Occurs with positional changes and also after looking up

Weitere VAERSDATA-Felder

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

VAERS 2088260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 04.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dysphagia Pruritus

Symptomtext

Patient reported generalized itching and difficulty swallowing spit. No rash noted. No difficulty breathing. Patient observed by emergency team.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Honey
Vorherige Impfungen: Itching with first dose of Pfizer vaccine.

VAERS 2085545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: GA
Alter: 11,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Pain in extremity

Symptomtext

Patient and her father both say that only complaint was a sore arm. They deny any further signs or symptoms after vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2082566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 27,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 22.12.2021
Beginn: 08.01.2022
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest X-ray Chills Fatigue Nausea Oropharyngeal pain Pain Pyrexia Respiratory tract congestion

Symptomtext

Patient is fully vaccinated. COVID + at ED visit on 1/8/2022. Patient states that he began experiencing diffuse, generalized body aches, intermittent subjective fevers and chills, sore throat, and congestion yesterday. He denies any significant shortness of breath or chest pain. Positive for fatigue, nausea. BP 132/84 | Pulse 65 | Temp 98.2 ?F (36.8 ?C) (Oral) | Resp 18 | Ht 185.4 cm (6' 1") | Wt 104 kg (230 lb) | SpO2 99% | BMI 30.34 kg/m? CXR: Patchy airspace opacities at the bilateral lung bases may reflect atelectasis or developing pneumonia. Medications; zofran, toradol. Stable for discharge. Referred for monoclonal antiboldy influsion.

Weitere VAERSDATA-Felder

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

VAERS 2082386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IL
Alter: 53,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Eye pain HLA-B*27 positive Photophobia Uveitis

Symptomtext

The night of the night and my left eye was in pain, my left eye. I thought I had an infection so I made an appointment because I though it was a pink eye. They called in some eye drops. 12/31/2021 I had intense pain, even if I closed my left eye or see the light. My dad ended up taking me to the ER and I was referred with an eye doctor and so I went and saw a doctor and he diagnosed me with uveitis and so they put me on new eye drops and steroids because my eye was attached to my lance or that's what they said. They do believe it was due to the booster. I see my eye doctor again in June/July. I was told that my white blood cells has a marker HLA-B27.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: Blood test Positive for HLA-B27
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Zyrtec and multivitamin, daily
Allergien: Ibuprofen
Vorherige Impfungen: -

VAERS 2079380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 16.12.2021
Beginn: 26.01.2022
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Herpes zoster Pain Rash erythematous Swelling

Symptomtext

Started with severe pain lower back radiating along sciatic nerve across buttocks over to bursa. Bright red swollen rash began after a few days. I went to ER on the day it appeared and was diagnosed with shingles.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Doctor observation and questions on Monday 01/31,2022.
Aktuelle Erkrankungen: Sjogren?s
Vorgeschichte: Sjogren?s
Andere Medikamente: Plaquenil, elavil, singulair, Zyrtec-d, Restasis, trazodone
Allergien: Augmentin, keflex, Levaquin, sulfa-based antibiotics, flagyl, zofran, Celebrex, zanaflex
Vorherige Impfungen: Pfizer 2nd dose shortness of breath 1.5 days relieved with Benadryl. Pfizer Covid vaccine #2 on March 31, 2021

VAERS 2075175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MD
Alter: 65,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 22.12.2021
Beginn: 15.01.2022
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: IM / RA

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

Headache Parosmia Taste disorder Visual impairment

Symptomtext

I have experienced several odd olfactory odors or aromas from foods like peanut butter, cheddar cheese, bacon, tuna fish all seem to have the same rancid taste, smell or phantom aroma. I have the same slight head ache repeatedly. also my vision seems to have deteriorated somewhat. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: arteriolosclerosis
Andere Medikamente: Metoprolol 50mg; Lisinopril 10mg; Clopidogrel 75mg; atorvastatin80mg; aspirin81mg
Allergien: none
Vorherige Impfungen: -

VAERS 2074412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 21.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Lymph node pain Lymphadenopathy Vaccination site pain

Symptomtext

Left arm at injection site was sore; Lymph node under left arm is swollen; lymph node under left arm is swollen and tender to touch.; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 52 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Jan2022 at 12:45 (Lot number: 33130BA) at the age of 52 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Penicillin allergy" (unspecified if ongoing), notes: Known allergies: Penicillin and "Egg allergy" (unspecified if ongoing), notes: Known allergies: eggs. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EW0153; Anatomical location: Left arm; Administration time: 11:00;Route of administration: Unspecified), administration date: 17Apr2021, when the patient was 51 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EW0172; Anatomical location: Left arm; Administration time: 09:30; Route of administration: Unspecified), administration date: 12May2021, when the patient was 51 years old, for COVID-19 immunisation. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 22Jan2022 at 12:00, outcome "not recovered", described as "Left arm at injection site was sore"; LYMPHADENOPATHY (non-serious) with onset 22Jan2022 at 12:00, outcome "not recovered", described as "Lymph node under left arm is swollen"; LYMPH NODE PAIN (non-serious) with onset 22Jan2022 at 12:00, outcome "not recovered", described as "lymph node under left arm is swollen and tender to touch". Therapeutic measures were not taken as a result of vaccination site pain, lymphadenopathy and lymph node pain. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room or urgent care. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Egg allergy (Known allergies: eggs); Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2074353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MS
Alter: 58,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 08.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Chills Fatigue Vaccination site erythema Vaccination site pruritus

Symptomtext

Over 24 hours the site became very red and itched very badly; Over 24 hours the site became very red and itched very badly; tiredness; chills; 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), administered in arm right, administration date 08Jan2022 13:15 (Lot number: 33130BA) at the age of 58 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing). Concomitant medication(s) included: LEXAPRO; LISINOPRIL. Vaccination history included: Bnt162b2 (Dose 2, Lot No: ER6727, Location of injection: Arm Right, Vaccine Administration Time: 14:00), administration date: 03Apr2021, when the patient was 57 years old, for Covid-19 immunization; Bnt162b2 (Dose 1, Lot No: EP7534, Location of injection: Arm Right, Vaccine Administration Time: 14:30), administration date: 13Mar2021, when the patient was 57 years old, for Covid-19 immunization. The following information was reported: FATIGUE (non-serious) with onset 08Jan2022 13:30, outcome "recovering", described as "tiredness"; CHILLS (non-serious) with onset 08Jan2022 13:30, outcome "recovering", described as "chills"; VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 09Jan2022, outcome "recovering" and all described as "Over 24 hours the site became very red and itched very badly". Therapeutic measures were taken as a result of vaccination site erythema, vaccination site pruritus. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no fever. I also didn't really have site pain at first. Over 24 hours the site became very red and itched very badly. I called the pharmacy and was told to just take a Benadryl. I did and as soon as it wears off it's back to the itching. I feel ok otherwise. Not sure how long this will last. The patient received treatment with Benadryl. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. No known allergies were reported. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: LEXAPRO; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 2074345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 29.01.2022
Impfdatum: 13.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Axillary mass Pain

Symptomtext

developing a small lump under my left arm that hurts, in the armpit, If I lay on it with my arm up high, it hurts; developing a small lump under my left arm that hurts, in the armpit, If I lay on it with my arm up high, it hurts; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 13Dec2021 (Lot number: 33130BA) as dose 3(booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose:1, Primary Immunization series complete but unknown manufacturer), for COVID-19 Immunization; Covid-19 vaccine (Dose: 2, Primary Immunization series complete but unknown manufacturer), for COVID-19 Immunization. The following information was reported: AXILLARY MASS (non-serious), PAIN (non-serious), outcome "unknown" and all described as "developing a small lump under my left arm that hurts, in the armpit, If I lay on it with my arm up high, it hurts". No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2074341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NC
Alter: 47,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Dizziness Headache Vomiting

Symptomtext

vomiting; Headache; dizziness; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 47 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 12:30 (Lot number: 33130BA) at the age of 47 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Migraines" (unspecified if ongoing); "Dysphonia" (unspecified if ongoing); "Vertigo (vestibular disorder)" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Known allergies: dilantin, reaction(s): "Known allergies: Dilantin"; Known allergies: venlafaxine, reaction(s): "Known allergies: Venlafaxine". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8730, Location of injection: Arm Left, Vaccine Administration Time: 02:15 PM), administration date: 30Mar2021, when the patient was 46 years old, for COVID-19 immunization. The following information was reported: VOMITING (non-serious) with onset 17Dec2021 02:30, outcome "unknown", described as "vomiting"; HEADACHE (non-serious) with onset 17Dec2021 02:30, outcome "unknown", described as "Headache"; DIZZINESS (non-serious) with onset 17Dec2021 02:30, outcome "unknown", described as "dizziness". Therapeutic measures were not taken as a result of vomiting, headache, dizziness. Additional information: Patient was not received other vaccine in four-weeks. The patient did not receive any other medications in two-weeks. Patient was not diagnosed with covid-19 prior to vaccination. The patient not tested COVID post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Dysphonia; Migraine; Vertigo
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2072290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blister Erythema Herpes zoster Neuralgia Pruritus Rash Skin swelling

Symptomtext

About 15 hours after receiving the vaccine I woke up with nerve pain under my left arm. It went under my arm into the back of my shoulder blade. I felt itchy under my arm. When I looked in the mirror I had red blisters that traveled up my back and towards my neck. They were red, raised, and circular. Then they became blisters during that daytime. I called the doctor and they had me come in. On 12/6/2021 the doctor confirmed that I had shingles. I was prescribed acyclovir pills, acyclovir ointment, and gabapentin. The nerve pain lasted for about 3 weeks, and the rash crusted and dried up within 2 weeks, but I still have the red marks.

Weitere VAERSDATA-Felder

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

VAERS 2069145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 56,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / -

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

Arthralgia Asthenia Fatigue Musculoskeletal pain Pain in extremity Somnolence

Symptomtext

Constant pain in hips, thighs and buttocks, extreme fatigue sleeping 12 hours at a time, no energy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: Chrons, ulcerative colitis
Andere Medikamente: Paxil 10 mg once daily
Allergien: No
Vorherige Impfungen: -

VAERS 2066042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: OK
Alter: 58,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 11.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

COUGH, FEELING TIRED/SICK

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: POSITIVE SARS-COV-2 RNA
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 2063061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Vomiting

Symptomtext

Patient felt faint right after receiving the COVID-19 Pfizer vaccine. He laid down with legs elevated. He did not loose consciousness and talked to us the whole time. After 15 minutes or so, he felt it was okay to sit up, so he did. He drank some water but then immediately vomited. Paramedics were called after this occurred. They came, assessed the patient and declared him healthy/well. Patient walked out of the pharmacy with no help. He went home with his family who was there with him.

Weitere VAERSDATA-Felder

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

VAERS 2062671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 18,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Feeling hot Nausea

Symptomtext

Patient stated to feel hot and nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid/ Covid Toes
Vorgeschichte: Adhd
Andere Medikamente: Adderall 30Mg Kenolog Cream
Allergien: None
Vorherige Impfungen: -

VAERS 2059058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: ND
Alter: 21,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 17.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / -

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

Headache Skin warm

Symptomtext

Severe headache, skin warm to touch.

Weitere VAERSDATA-Felder

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

VAERS 2058995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 0,8
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 01.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Asthenia Bone pain Chills Fatigue Headache

Symptomtext

Onset of S&S 3-4 hrs post jab. Develop profound fatigue, severe chills, joint and bone pain, profound weakness, headache. Considered going to ER, thought I might die. Took Motrin (I believe) with some relief. S&S gradually subsided over next 24-36 hrs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Cucumin bid
Allergien: Sulfa drugs
Vorherige Impfungen: Same reaction to Pfizer dose 1 &2. On 1/3/21 and 1/24/22

VAERS 2054230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Disturbance in attention Fatigue Inflammation Memory impairment Musculoskeletal stiffness Pain in extremity Photophobia Tenderness Visual impairment

Symptomtext

Developing within 3 hours of booster: Significant soreness in left arm. Inflammation of left hand. Inflammation and tenderness in left underarm. Stiffness in left side of neck. Significant eye sensitivity to light. Black spots in vision. Increased fatigue. Inability to focus. Short term memory retention issues.

Weitere VAERSDATA-Felder

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

VAERS 2053950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: GA
Alter: 21,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Vision blurred Vomiting

Symptomtext

Client states approximately 20 mins after receiving vaccine she became dizzy and vision was blurry. She states she vomited 7 times throughout the day. She states she was going to the DR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Not known
Vorgeschichte: Not known
Andere Medikamente: Not known
Allergien: Nkda
Vorherige Impfungen: -

VAERS 2053925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site bruising Injection site pruritus Injection site swelling

Symptomtext

MA administered vaccine. About 5 mins after administration, patient complained of itching so I was asked to evaluate the patient. No band-aid was applied to the site. The itching was just at the administration site. The area was swollen and bruising was noted. Patient denied any changes in shortness of breath (has COPD), denied throat tightness, itching only at injection site. Ice pack was applied and provider notified. Patient was observed for an additional 15 mins (30 mins total). At that time patient continued to deny symptoms other than itching at injection site. Swelling did go down slightly with application of ice pack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: COPD
Vorgeschichte: pulmonary HTN, osteoarthritis, hypothyroidism, iron deficiency anemia
Andere Medikamente: Albuterol 0.083% nebulizer solution formoterol 20 mcg/2ml ibuprofen 200mg levothyroxine 112 mcg prednisone 10 mg revefenacin 175 mcg/3 ml trazodone 50 mg Ventolin HFA
Allergien: Augmentin (Flushing), Hydrocodone (Hallucinations)
Vorherige Impfungen: -

VAERS 2052215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130bA

mild

Staat: WI
Alter: 51,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Hypersomnia Myalgia Somnolence

Symptomtext

drowsiness, slept for2 days,,muscles ache, chills

Weitere VAERSDATA-Felder

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

VAERS 2050304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MA
Alter: 36,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Blister Burning sensation Immunisation Myalgia Pain in extremity Tenderness

Symptomtext

blisters and pain on left deltoid; arm pain; blisters and pain on left deltoid; area started to feel tender; later to "burn" with blisters; booster dose; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 36 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 15Dec2021 14:15 (Lot number: 33130BA) at the age of 36 years as dose 3 (booster), single for covid-19 immunisation; hepatitis b vaccine (HEPATITIS B VACCINE), administered in arm left, administration date 15Dec2021 (Lot number: 9AX5P) as dose 1, single for immunisation. Relevant medical history included: "Seasonal allergies" (unspecified if ongoing), notes: Note: Seasonal allergies.; "Diabetes type II" (unspecified if ongoing), notes: Note: Diabetes type II; "chronic R knee pain" (unspecified if ongoing), notes: Note: Chronic R knee pain; "anxiety" (unspecified if ongoing), notes: Note: Anxiety. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: FB-EW0183), administration date: 11May2021, when the patient was 35 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: FB-ER8735), administration date: 20Apr2021, when the patient was 35 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021, outcome "unknown", described as "booster dose"; MYALGIA (non-serious), BLISTER (non-serious) all with onset 16Dec2021, outcome "recovering" and all described as "blisters and pain on left deltoid"; PAIN IN EXTREMITY (non-serious) with onset 16Dec2021, outcome "recovering", described as "arm pain"; TENDERNESS (non-serious) with onset 16Dec2021, outcome "recovering", described as "area started to feel tender"; BURNING SENSATION (non-serious) with onset 16Dec2021, outcome "recovering", described as "later to "burn" with blisters". The events "blisters and pain on left deltoid", "arm pain", "blisters and pain on left deltoid", "area started to feel tender" and "later to "burn" with blisters" were evaluated at the physician office visit. Therapeutic measures were taken as a result of myalgia, pain in extremity, blister, tenderness, burning sensation. No follow-up attempts are possible. No further information is expected. Additional information: The patient had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Adverse event treatment silvadene 1 % Cr and Motrin 400 mg QID (four times a day).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety (Note: Anxiety.); Diabetes mellitus non-insulin-dependent (Note: Diabetes type II); Knee pain (Note: Chronic R knee pain); Seasonal allergy (Note: Seasonal allergies.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2047750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: AZ
Alter: 60,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient received the vaccine and later that evening at approximately 8:00pm he stated that he began to feel feverish. The fever worsened throughout the night and led to the patient reaching out to his primary care doctor. The patient received a COVID-19 test and was confirmed positive the day following.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: Lisinopril, eye drops
Allergien: loperamide
Vorherige Impfungen: Patient stated he had a fever after his second Pfizer vaccination on 4/7/21 (ER8729)

VAERS 2046395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 23,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 17.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Limb discomfort Tenderness

Symptomtext

Left armpit pain, tightness, and tenderness under same arm where shot was received.

Weitere VAERSDATA-Felder

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

VAERS 2042868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: TX
Alter: 15,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 10.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Pain Pain in extremity Pyrexia

Symptomtext

fever, chills, body aches, sore arm for 9 hours. treatment was rest and liquids, after 10 hours 2 pills of 500mg acetaminophen were given. all symptoms subsided.

Weitere VAERSDATA-Felder

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

VAERS 2042591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Back pain Immunisation Lymph node pain Lymphadenopathy Pain

Symptomtext

On day two, I woke up and saw that my lymph node under my left armpit swelled up to the size of a grapefruit and it was quite painful; On day two, I woke up and saw that my lymph node under my left armpit swelled up to the size of a grapefruit and it was quite painful/ but exercise still caused pain in the armpit for an additonal 3-4 days.; It hurt to even put my arm down; In addition, I had bad mid-back pain.; Dose number: 3; This is a spontaneous report from a contactable reporter (consumer or other non HCP). The reporter is the patient. A 45-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 27Dec2021 at 17:15 (Lot number: 33130BA) at the age of 45 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. Concomitant medication included: MIRENA IUD. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number:ER8737; Anatomical location: Left Arm; Administration time: 17:30), administration date: 01Apr2021, when the patient was 44 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number:ER8731; Anatomical location: Left Arm; Administration time: 17:15), administration date: 22Apr2021, when the patient was 44 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 27Dec2021 at 17:15, outcome "unknown", described as "Dose number: 3"; LYMPHADENOPATHY (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (an unknown date in Jan2022), described as "On day two, I woke up and saw that my lymph node under my left armpit swelled up to the size of a grapefruit and it was quite painful"; LYMPH NODE PAIN (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (an unknown date in Jan2022), described as "On day two, I woke up and saw that my lymph node under my left armpit swelled up to the size of a grapefruit and it was quite painful/ but exercise still caused pain in the armpit for an additonal 3-4 days"; PAIN (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (an unknown date in Jan2022), described as "It hurt to even put my arm down"; BACK PAIN (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (an unknown date in Jan2022), described as "In addition, I had bad mid-back pain". Therapeutic measures were taken as a result of lymphadenopathy, lymph node pain, pain and back pain. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient reported that it lasted about 5 days for the back pain and 6-7 days for the swelling and armpit pain. After a week, the swelling and pain went down enough to wear a bra again but exercise still caused pain in the armpit for an additional 3-4 days. At the time of report, it was back to normal. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Treatment taken as a result of lymphadenopathy, lymph node pain, pain and back pain included hot compresses and massaging the area.

Weitere VAERSDATA-Felder

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

VAERS 2042587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TX
Alter: 47,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Chills Fatigue Feeling hot Headache Hyperhidrosis Immunisation Nausea Pain Pain in extremity Pyrexia

Symptomtext

Nausea; dull headache behind both eyes and top of head; warm and dull headache behind both eyes and top of head; Day 1 and 2 post booster: 101 Fever; fatigue; chills; sore arm; aches; sweating down front of torso; Dose received: 3; This is a spontaneous report from a contactable reporter (consumer or other non hcp). The reporter is the patient. A 47-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm , administration date 06Jan2022 at 14:30 (Lot number: 33130BA) at the age of 47 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing) and "Sulfonamide allergy" (unspecified if ongoing), notes: Known allergy: Sulfa. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Lot number: EN6203, Anatomical location: Arm Left, Administration Time: 14:30, Route of administration: Unspecified), administration date: 12Mar2021, when the patient was 46 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 1, SINGLE Lot number: EL9267, Administration Time: 14:30, Route of administration: Unspecified), administration date: 19Feb2021, when the patient was 46 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 06Jan2022 at 14:30, outcome "unknown", described as "Dose received: 3"; PYREXIA (non-serious) with onset 07Jan2022, outcome "recovered" (09Jan2022), described as "Day 1 and 2 post booster: 101 Fever"; FATIGUE (non-serious) with onset 07Jan2022, outcome "recovering", described as "fatigue"; CHILLS (non-serious) with onset 07Jan2022, outcome "recovering", described as "chills"; PAIN IN EXTREMITY (non-serious) with onset 07Jan2022, outcome "recovering", described as "sore arm"; PAIN (non-serious) with onset 07Jan2022, outcome "recovering", described as "aches"; HYPERHIDROSIS (non-serious) with onset 07Jan2022, outcome "recovering", described as "sweating down front of torso"; NAUSEA (non-serious) with onset 10Jan2022, outcome "recovering", described as "Nausea"; HEADACHE (non-serious) with onset 10Jan2022, outcome "recovering", described as "dull headache behind both eyes and top of head"; FEELING HOT (non-serious) with onset 10Jan2022, outcome "recovering", described as "warm and dull headache behind both eyes and top of head". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, fatigue, chills, pain in extremity, pain, hyperhidrosis, nausea, headache and feeling hot. Additional information: The patient did not receive other vaccines within four weeks prior to COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The patient reported the events as she was very concerned of timing of boosters and dosage. Her body cannot handle these two shots 10 months apart and she was concerned for any child, adult, senior, herself in future. The patient received round the clock Tylenol and cold, wash cloths as treatment for the reported events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220107; Test Name: Body temperature; Result Unstructured Data: Test Result:101 Centigrade; Comments: 101 Fever
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Sulfonamide allergy (Known allergies: Sulfa)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2042403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 28,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 31.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Chills Fatigue Headache Immunisation Myalgia Pyrexia Vaccination site pain

Symptomtext

Low grade fever; chills; muscle aches; soreness in arm of injection site; fatigue; headache; Dose number: 3; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 28 year-old male patient received bnt162b2 (BNT162B2), administered in arm, administration date 31Dec2021 09:00 (Lot number: 33130BA) at the age of 28 years as dose 3 (booster) , single for covid-19 immunisation. Relevant medical history included: "if covid prior vaccination: Yes" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0170, Location of injection: Arm Right, Vaccine Administration Time: 03:00 PM), administration date: 01May2021, when the patient was 27 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0151, Location of injection: Arm Right), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 31Dec2021 09:00, outcome "unknown", described as "Dose number: 3"; PYREXIA (non-serious) with onset 31Dec2021 22:30, outcome "recovered", described as "Low grade fever"; CHILLS (non-serious) with onset 31Dec2021 22:30, outcome "recovered", described as "chills"; MYALGIA (non-serious) with onset 31Dec2021 22:30, outcome "recovered", described as "muscle aches"; VACCINATION SITE PAIN (non-serious) with onset 31Dec2021 22:30, outcome "recovered", described as "soreness in arm of injection site"; FATIGUE (non-serious) with onset 31Dec2021 22:30, outcome "recovered", described as "fatigue"; HEADACHE (non-serious) with onset 31Dec2021 22:30, outcome "recovered", described as "headache". Therapeutic measures were not taken as a result of pyrexia, chills, myalgia, vaccination site pain, fatigue, headache. Additional information The patient was diagnosed with COVID-19 prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2038264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 14.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Chills Lymphadenopathy Pain Pyrexia Vomiting

Symptomtext

Fever, aches, vomiting, chills, swollen lymph nodes in left arm where injection was given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hiatal hernia
Andere Medikamente: 81mg aspirin, biotin, calcium, one a day vitamin
Allergien: Erythimiacin
Vorherige Impfungen: Pfizer COVID 19

VAERS 2032261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 64,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

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

Fatigue Insomnia Nausea Pain Pain in extremity Pyrexia

Symptomtext

fever/aches/tired/nausea /sore arm/insomnia/

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: multiple vitamin and vitamin d and aleeve
Allergien: hay fever / latex / bee stings / corn / oranges / mites / dust
Vorherige Impfungen: same as 1st 2 doses of pfizer - 03/23/21 and 04/22/21

VAERS 2028809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NE
Alter: 38,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Hangover Headache Pyrexia

Symptomtext

Prolonged "hang-over" headaches, fever

Weitere VAERSDATA-Felder

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

VAERS 2028770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MA
Alter: 48,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 10.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Injection site erythema Injection site pain Injection site swelling Injection site warmth

Symptomtext

Swollen raised red bump below the injection site. About 2 inches in diameter an d slightly warm and sore to the touch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: valacyclovir Levonorgestrel
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2028623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: OH
Alter: 28,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 14.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 19,0
Dosis: 2
Route/Site: SYR / RA

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

Ageusia Anosmia Chest discomfort Chills Cough Fatigue Headache Nasal congestion Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I had my first dose on 11/23/21. No adverse effects. I had my second dose on 12/14/21. No adverse effects. Just minor fatigued and body aches. On 12/29/21, I visited the ICU ward of the hospital to visit my unvaccinated father-in-law who had contracted covid earlier in the month. This was my first contact with him since Thanksgiving week. We were crying, so I was wiping my eyes, but wearing a mask and likely contracted covid at the hospital. On 1/2/22, I began coughing and on 1/3/22, I began self-isolating. I had a PCR test on 1/6/22 and it came back positive for covid on 1/8/22. I have been in quarantine since testing positive with plans to take another test on 1/13/22. My symptoms have been fairly mild; the first 2-3 days included fatigue, body aches, chills, a low grade fever, headache, and nasal and chest congestion. Within 4 days, I had lost my senses of taste and smell almost entirely. Over the past few days, my fever broke and my senses are slowly returning. I continue to have a cough and tickle in my upper airways. Because of my history of asthma, I sought care from an urgent care doctor on 1/10/22. He prescribed an oral steroid for 5 days and albuterol (nebulizer) as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: PCR test was taken on 1/6/22. Results came back positive on 1/8/22.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Symbicort
Allergien: Ceclor
Vorherige Impfungen: -

VAERS 2554196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 35,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Headache Myalgia

Symptomtext

Headache & Myalgia Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2515112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Headache Myalgia

Symptomtext

Headache, Myalgia, & Arthralgia

Weitere VAERSDATA-Felder

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

VAERS 2025345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Rash

Symptomtext

Patient reported breakout on her face around her mouth and nose area within about 6 hours after vaccination. Patient came in for second dose and the rash was still visible on her face.

Weitere VAERSDATA-Felder

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

VAERS 2024756

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 33130BA

mild

Staat: UT
Alter: 14,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 08.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Axillary pain Injection site erythema Injection site swelling Joint range of motion decreased Pain in extremity Peripheral swelling

Symptomtext

Saturday and Sunday- Pain in arm. Monday- Red, swollen at injection site, unable to move arm in full range of motion, pain under arm and halfway down side (She said, "My armpit feels swollen.")

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: 01/10/2022- Visit to urgent care, doctor examination, prescribed an antibiotic and encouraged to use warm compresses and take ibuprofen/Tylenol
Aktuelle Erkrankungen: None at time of vaccine; Runny nose/Cold symptoms December 23-26
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin, Penicillin, Clyndamicin
Vorherige Impfungen: -

VAERS 2024664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 84,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 08.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Injection site bruising Injection site erythema Injection site pruritus Injection site swelling Muscle spasms Peripheral coldness

Symptomtext

Vaccine Administered into left arm. Bruise at injection site. Below injection site skin is itchy, red, swollen. Left hand finger tips cold and exhibit cramping.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HBP, Osteoporosis, Glaucoma
Andere Medikamente: Losartan 50mg; Calcium & Vitamins, Metoprolol 50mg, Alendronate 70mg, Latanoprost .005, Restasis .05
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 2020514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: PA
Alter: 43,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain Blood pressure increased Chills Cold sweat Concussion Dizziness Erythema Headache Micturition urgency Nausea Feeling abnormal Pain Pyrexia Renal pain Sleep disorder Tinnitus Peripheral coldness

Symptomtext

10 minutes after receiving the vaccine, my blood pressure increased to 164/94. felt like i was going to pass out. face turned red, heart rate was in the 120s. They had me lie in the recliner for an hour while monitoring my BP. after an hour it was within normal range, so i came back to work. 15 minutes after getting back to work i felt off again, my coworker said my face turned bright red, so i rechecked my BP. It was back up to 160/90s. I left to go home and after another 10 minutes i felt like id pass out again. my right arm/hand felt clammy, while my left arm felt like i had an ice pack laying on top of my arm. I then had extreme pain in my kidney area that shot around to my abdomen, i then felt extreme urgency to urinate. after about 5 minutes those symptoms faded. i made it home at 3:45pm, still feeling like I could pass out. i woke in the night around 1:15am. felt chills, severe body ache, severe headache, nausea, and fever of 102. this lasted for 3 days. my head has felt like i had a concussion since getting the shot. I am having severe headaches ever since and ringing in my ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: previous reaction to covid vaccine
Vorgeschichte: -
Andere Medikamente: Flonase
Allergien: flu shot , omniceff, adverse reaction to the 1st covid shot, and now the 2nd as well
Vorherige Impfungen: -

VAERS 2555463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Rash

Symptomtext

SkinRash Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2018861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 29.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Axillary pain Immunisation Lymphadenopathy

Symptomtext

dose number=3; Swollen lymph nodes and pain under arm; Swollen lymph nodes and pain under arm; This is a spontaneous report from a non-contactable reporter (consumer or other non-HCP). The reporter is the patient. A 35 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 29Dec2021 at 08:45 (Lot number: 33130BA) at the age of 35 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication included: CABERGOLINE. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: ER8729, Route of Administration: Unspecified, Anatomical Location: Left arm), administration date: 07Apr2021, when the patient was 35 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EW0164, Route of Administration: Unspecified, Anatomical Location: Left arm.), administration date: 05May2021, when the patient was 35 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 29Dec2021 at 08:45, outcome "unknown", described as "dose number=3"; LYMPHADENOPATHY (non-serious), AXILLARY PAIN (non-serious) all with onset an unknown date in Dec2021, outcome "not recovered", and all described as "Swollen lymph nodes and pain under arm". Therapeutic measures were not taken as a result of lymphadenopathy and axillary pain. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2018831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Chills Headache Immunisation Lymph node pain Myalgia Nausea Pain in extremity Pyrexia

Symptomtext

Fever; Nausea; Slight headache; Chills; Sore arm; Extremely painful lymph node under left arm; Muscle ache/muscle pain; Joint ache/joint pain; dose number=3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 64-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 28Dec2021 at 15:00 (Batch/Lot number: 33130BA) at the age of 64 Year(s) as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Drug intolerance" (unspecified if ongoing), notes: known allergies: Intolerant of opioids. The patient did not receive concomitant medications. Past drug history included: Aspirin, reaction(s): "Drug intolerance", notes: known allergies: Intolerant of aspirin. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EN6206; Administration time: 10:00 Administration Location: Left Arm), administration date: 18Mar2021, when the patient was 63 year(s) old, for COVID-19 immunisation, reaction(s): "No adverse event" and Bnt162b2 (DOSE 2, SINGLE; Lot Number: ER8734; Administration time: 10:00 Administration Location: Left Arm), administration date: 08Apr2021, when the patient was 63 year(s) old, for COVID-19 immunisation, reaction(s): "No adverse event". The following information was reported: IMMUNISATION (non-serious) with onset 28Dec2021 at 15:00, outcome "unknown", described as "dose number=3"; PYREXIA (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (29Dec2021), described as "Fever"; NAUSEA (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (29Dec2021), described as "Nausea"; HEADACHE (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (29Dec2021), described as "Slight headache"; CHILLS (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (29Dec2021), described as "Chills"; PAIN IN EXTREMITY (non-serious) with onset 29Dec2021 at 06:00, outcome "recovered" (29Dec2021), described as "Sore arm"; LYMPH NODE PAIN (non-serious) with onset 29Dec2021 at 06:00, outcome "recovering", described as "Extremely painful lymph node under left arm"; MYALGIA (non-serious) with onset 29Dec2021 at 06:00, outcome "recovering", described as "Muscle ache/muscle pain"; ARTHRALGIA (non-serious) with onset 29Dec2021 at 06:00, outcome "recovering", described as "Joint ache/joint pain". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, nausea, headache, chills, pain in extremity, lymph node pain, myalgia and arthralgia. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug intolerance (known allergies: Intolerant of opioids.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TN
Alter: 78,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Dysstasia Immunisation Muscle disorder Muscle spasms Muscular weakness Pain

Symptomtext

severe cramping in his legs, from the knees down; woke up for about 50 minutes in the worst pain of his entire life; When he looked at the muscles, they were rock solid, hard; weakness in legs; excruciating pain in both extremities below the knees; I noticed weakness in both lower extremities; I was unable to rise from a sitting position in a chair; I recieved a booster shot; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 78 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 06Dec2021 (Lot number: 33130BA, Expiration Date: 31May2022) at the age of 78 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "impairment of recent memory and mild impairment/memory loss" (unspecified if ongoing), notes: treating for some impairment of recent memory and mild impairment.; "Restless leg" (unspecified if ongoing); "Bipolar" (unspecified if ongoing); "severe spinal stenosis" (unspecified if ongoing); "Prostate cancer" (unspecified if ongoing); "known allergies: penicillin" (unspecified if ongoing); "known allergies: sulfa" (unspecified if ongoing). Concomitant medication(s) included: ASPIRINE (ongoing); MEMANTINE taken for memory impairment (ongoing); LITHIUM; PRAMIPEXOLE. Vaccination history included: Bnt162b2 (dose 1, Lot number: EN5318, Expiration date: 31May2021, Prev dose vaccine location: Left leg), administration date: 26Jan2021, when the patient was 78 years old, for COVID-19 Immunization; Bnt162b2 (Dose 2, Lot number: EN6201, Expiration date: 31May2021, Prev dose vaccine location: Left arm), administration date: 19Feb2021, when the patient was 78 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 06Dec2021, outcome "unknown", described as "I recieved a booster shot"; MUSCLE SPASMS (non-serious) with onset 07Dec2021 08:00, outcome "recovered" (07Dec2021 08:00), described as "severe cramping in his legs, from the knees down"; PAIN (non-serious) with onset 07Dec2021 08:00, outcome "recovered" (07Dec2021 08:00), described as "woke up for about 50 minutes in the worst pain of his entire life"; MUSCLE DISORDER (non-serious) with onset 07Dec2021 08:00, outcome "recovered" (07Dec2021 08:00), described as "When he looked at the muscles, they were rock solid, hard"; MUSCULAR WEAKNESS (non-serious) with onset 07Dec2021 08:00, outcome "recovered" (07Dec2021 08:00), described as "weakness in legs"; ARTHRALGIA (non-serious) with onset 07Dec2021 08:00, outcome "recovered" (Dec2021), described as "excruciating pain in both extremities below the knees"; MUSCULAR WEAKNESS (non-serious) with onset 07Dec2021 08:00, outcome "recovered" (Dec2021), described as "I noticed weakness in both lower extremities"; DYSSTASIA (non-serious) with onset 07Dec2021 08:00, outcome "recovered" (Dec2021), described as "I was unable to rise from a sitting position in a chair". The events "severe cramping in his legs, from the knees down", "woke up for about 50 minutes in the worst pain of his entire life", "when he looked at the muscles, they were rock solid, hard", "weakness in legs" were evaluated at the emergency room visit. The events "excruciating pain in both extremities below the knees", "i noticed weakness in both lower extremities" and "i was unable to rise from a sitting position in a chair" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of muscle spasms, pain, muscle disorder, muscular weakness. Therapeutic measures were not taken as a result of arthralgia, muscular weakness, dysstasia. Additional information: The patient had been taking Aspirin at least 4 or 5 years. The patient had no cerebrovascular disease, even though he never had a disease. The patient had no definite diagnosis of Alzheimer's. The patient did not receive other vaccine in four weeks. The patient did not have covid prior vaccination and had not been tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bipolar disorder; Memory impairment (treating for some impairment of recent memory and mild impairment.); Penicillin allergy; Prostate cancer; Restless legs; Spinal stenosis; Sulfonamide allergy
Andere Medikamente: ASPIRINE; MEMANTINE; LITHIUM; PRAMIPEXOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1982213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: AR
Alter: 37,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 09.10.2021
Beginn: 10.12.2021
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Arthritis Asthenia Tendonitis Heart rate increased Joint stiffness Musculoskeletal stiffness Myalgia Pain Sleep disorder

Symptomtext

Arthralgias, weakness, Achilles tendinitis. Acute L knee arthritis Symptoms lasted 72 hrs. then improved but returned 12/25/21 and continued

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Anxiety
Andere Medikamente: Enskye
Allergien: Sulfa, neomycin
Vorherige Impfungen: -

VAERS 1982213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: AR
Alter: 37,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 09.10.2021
Beginn: 10.12.2021
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Arthritis Asthenia Tendonitis Heart rate increased Joint stiffness Musculoskeletal stiffness Myalgia Pain Sleep disorder

Symptomtext

Arthralgias, weakness, Achilles tendinitis. Acute L knee arthritis Symptoms lasted 72 hrs. then improved but returned 12/25/21 and continued

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Anxiety
Andere Medikamente: Enskye
Allergien: Sulfa, neomycin
Vorherige Impfungen: -

VAERS 2013960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NC
Alter: 18,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 03.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Heart rate increased Nausea Pyrexia Vomiting

Symptomtext

nausea, vomiting, chills, rapid heartbeat, fever- 18 hour to current (4 days out)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: nausea
Vorgeschichte: low iron
Andere Medikamente: Tylenol, Cryselle, Sertraline
Allergien: -
Vorherige Impfungen: COVID Vaccine shot 2 Pfizer

VAERS 2010080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Cough Fatigue Pain Pain in extremity SARS-CoV-2 test negative Throat irritation

Symptomtext

I had a sore arm, extreme fatigue, body aches. All lasted until Dec 19. On Dec 22 woke up with scratchy throat. That progressed into dry cough, body aches, extreme fatigue on 12/23. Lasted until Jan 2 when I noticed some improvements. Saw MD on 12/29. Scheduled PCR Covid test, results were negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Losartan 50mg, Vitamins A-E, Turmeric, Cinnamon, NAC
Allergien: None
Vorherige Impfungen: second Pfizer vaccs similar symptoms

VAERS 2005480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IL
Alter: 72,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 09.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Cough Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

Bad Cough, Fever

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: After this booster, he wasn't feeling well and tested positive for COVID
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes II Hyperlipidemia Hypothyroidism Osa Sleep Apnea
Andere Medikamente: Rosuvastatin 10mg Levothyroxine .088mg Metformin 1500mg Multi-vitamin Vitamin D3 Aspirin 81mg
Allergien: None
Vorherige Impfungen: -

VAERS 2001631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Asthenia Fatigue Inflammation Musculoskeletal stiffness Myalgia Pain Pyrexia

Symptomtext

So the first day or two I felt like I had been hit by a bus. Everything hurt, all my joints, extreme fatigue and pain in my muscles. I felt somewhat feverish and it hurt to move. I stayed in bed and took some pain medication the nurse recommended and just hydrated as much as possible, 2 liters of Pedialyte. After the 2nd day the symptoms receded a bit, the thing that didn't was this pain and weakness almost inflammation and stiffness in my hands. I couldn't easily grip things in my hands without being in extreme pain. I couldn't hold a mug, a pen, barely tie my shoelaces. This lasted for well over a week, in extreme pain. It has gone down, my fingers don't hurt anymore but I still feel stiffness and fatigue in my pointer and thumbs going down to my wrist in both hands. Opening jars, writing, scrolling through phone is very difficult. I called my doctor several times to get advice after this was continuing and they recommended ice or heat and take ibuprofen this was leading up to the holidays. They said get in touch post holidays if still an issues and I will since it's still an issue. it's primarily running along the side of my hands where my point finger and going down my wrist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Migraines; Fatigue issues
Andere Medikamente: Fexofenadine; Duloxetine; Nortriptyline
Allergien: I have allergies to Iodine; Morphine; Cats
Vorherige Impfungen: -

VAERS 2000270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 14,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Fatigue Pain in extremity Pyrexia

Symptomtext

Patient experienced fatigue, sore arm, and a slight fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: No KNown Drug Allergies
Vorherige Impfungen: -

VAERS 2000265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Pain in extremity Pyrexia

Symptomtext

Patient had sore arm, fever, fatigue, etc

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: No Known Drug Allergy
Vorherige Impfungen: -

VAERS 1999138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: OH
Alter: 63,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cold sweat Dizziness Nausea Vomiting

Symptomtext

Light Headed, Dizzy. Nausea, Vomiting. Cold Sweats.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia Diabetes
Andere Medikamente: Synthroid Liothyronine Rosuvastatin Metformin Claritin
Allergien: None Known
Vorherige Impfungen: -

VAERS 1997990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: MI
Alter: 45,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Angioedema Chills Diarrhoea Headache Nausea Pyrexia Urticaria

Symptomtext

Hives, angioedema, fever, nausea, diarrhea, chills, headaches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's thyroiditis
Andere Medikamente: Synthroid
Allergien: None
Vorherige Impfungen: -

VAERS 1996967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: FL
Alter: 25,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 24.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Immunisation SARS-CoV-2 test Swelling of eyelid Urticaria

Symptomtext

Dose received: 3; I had one hive on my butt cheek. Then woke up 2 mornings after shot with small hives under my eyes. On 3rd morning there were more hives under my eyes. The hive on my butt cheek is a little lower but still there.; Woke up 2 mornings after shot, my eye lids were slightly swollen. On 3rd morning, my eyelids were also still a little swollen.; This is a spontaneous report from a contactable reporter (Other healthcare professional). The reporter is the patient. A 25-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 24Dec2021 at 15:15 (Lot number: 33130BA) at the age of 25 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication included: LARIN 24 FE taken for Birth control. Past drug history included: Bactrim, reaction: "Drug allergy", notes: Known allergies: Bactrim and Zithromax, reaction: "Drug allergy", notes: Known allergies: Zithromax. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EW0170, Anatomical Location: Left arm, Administration Time: 14:00, Route of Administration: Unknown), administration date: 21Apr2021, when the patient was 24 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EW0185, Anatomical Location: Left arm, Administration Time: 14:00, Route of Administration: Unknown), administration date: 12May2021, when the patient was 24 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 24Dec2021 at 15:15, outcome "unknown", described as "Dose received: 3"; URTICARIA (non-serious) with onset an unknown date in Dec2021, outcome "not recovered", described as "I had one hive on my butt cheek. Then woke up 2 mornings after shot with small hives under my eyes. On 3rd morning there were more hives under my eyes. The hive on my butt cheek is a little lower but still there"; SWELLING OF EYELID (non-serious) with onset an unknown date in Dec2021, outcome "not recovered", described as "Woke up 2 mornings after shot, my eye lids were slightly swollen. On 3rd morning, my eyelids were also still a little swollen". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of urticaria and swelling of eyelid. Additional information: The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19 and the result was negative. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Test Date: 20211227; Test Name: On/go at home test; Test Result: Negative ; Comments: Nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LARIN 24 FE
Allergien: -
Vorherige Impfungen: -

VAERS 1996029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IL
Alter: 57,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Diarrhoea Vomiting

Symptomtext

Severe vomiting and severe diarrhea. Every 45 minutes for at least 7 hours. No treatment. Just waited to get better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperthyroidism, had a blood clot but was cleared by physician the a few days after the shot, had cancer but have been clear for a few years
Andere Medikamente: Anastrozole, Eliquis, Levothyroxine, Calcium Citrate + D3
Allergien: None
Vorherige Impfungen: -

VAERS 1995862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: UT
Alter: 53,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Pruritus

Symptomtext

Pruritus on soles of feet and palms of hands.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension
Andere Medikamente: Losartan 50 mg 1 tablet PO QD, Omeprazole 20mg 1 capsule PO BID, amitripyline 50mg 1 tablet PO QD
Allergien: Augmentin, clindamycin
Vorherige Impfungen: Influenza vaccine in 2008 and 2009

VAERS 1995592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NJ
Alter: 18,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Fatigue Immunisation Nausea Pain in extremity Pyrexia

Symptomtext

Fever of 101 F; Arm pain; Fatigue; Nausea; Dose received: 3/ Dose number =3; This is a spontaneous report from a contactable reporter (consumer or other non hcp). The reporter is the patient. A 18-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 20Dec2021 at 14:30 (Lot number: 33130BA) at the age of 18 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Constipation chronic" (unspecified if ongoing), notes: Chronic Constipation and "Penicillin allergy" (unspecified if ongoing), notes: Known allergies: Penicillin. Concomitant medication(s) included: TRULANCE. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: EP6955, Anatomical site: Left arm), administration date: 18Mar2021, when the patient was 17 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot number: EP6955, Anatomical site: Left arm), administration date: 08Apr2021, when the patient was 18 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 at 14:30, outcome "unknown", described as "Dose received: 3/ Dose number =3"; PYREXIA (non-serious) with onset 21Dec2021 at 06:30, outcome "recovered" (an unknown date in Dec2021), described as "Fever of 101 F"; PAIN IN EXTREMITY (non-serious) with onset 21Dec2021 at 06:30, outcome "recovered" (an unknown date in Dec2021), described as "Arm pain"; FATIGUE (non-serious) with onset 21Dec2021 at 06:30, outcome "recovered" (an unknown date in Dec2021), described as "Fatigue"; NAUSEA (non-serious) with onset 21Dec2021 at 06:30, outcome "recovered" (an unknown date in Dec2021), described as "Nausea". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, pain in extremity, fatigue and nausea. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20211221; Test Name: Body temperature; Result Unstructured Data: Test Result:101 F; Comments: Fever of 101 F
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Constipation chronic (Chronic Constipation); Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: TRULANCE
Allergien: -
Vorherige Impfungen: -

VAERS 1992982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: VT
Alter: 29,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Rash Rash pruritic

Symptomtext

Pt reports itchy rash on back of neck that began shortly after she got her first pfizer vaccine (approx 30 min after) and lasted for about a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: latex, ceclor
Vorherige Impfungen: -

VAERS 1992362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Blood thyroid stimulating hormone Dizziness Electrocardiogram Full blood count Metabolic function test Platelet count Thyroxine free Urine analysis

Symptomtext

Dizziness began the day after receiving third dose of Pfizer Covid-19 vaccine; patient has sought care or treatment from a doctor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: CMP14+CBC/D/PLT+TSH W/RFLX, Urinalysis/Complete, and ECG - adult, performed December 28, 2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zyrtec Allergy, Centrum multi-vitamin, Calcium, Vitamin D, Elderberry
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1992326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 43,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 28.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Axillary pain Fatigue Injection site pain Injection site swelling Pyrexia

Symptomtext

Sore arm with injection, raised bump 2 inches across, very sore spot in underarm, tired, fever for 12 hours. Took 2 Tylenol extra strength at 2pm and again at 10:30pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: None
Allergien: Antibiotics
Vorherige Impfungen: Sore arm sometimes with flu shot over the years. Sore arm not as bad with 1st does of covid

VAERS 1989470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: AZ
Alter: 56,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort Nausea Vomiting

Symptomtext

When patients 15 minute wait was done, she was advised she was ready to go as her recommended time was finished. Pt felt nauseous as she stood up and Vomited. Pt stated she developed a sudden stomach discomfort when she stood up. Pt Vomited twice within 15 minutes. Provider was immediately called and examined Pt. Vitals were taken and provider prescribed Pt Ondansetron 8 mg and recommended she is examined by ER if not feeling any better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Per Patient none that she is aware of.
Vorgeschichte: Type 2 diabetes Mellitus Hypertension
Andere Medikamente: Gabapentin 600 MG Invokana 300 MG Januvia 100 MG Lisinopril 10 MG Metformin 1,000 MG Zyrtec 10 MG
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 1988702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: PA
Alter: 28,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Erythema Fatigue Injection site swelling Nausea Pain Skin warm

Symptomtext

Redness, warmth, swelling at injection site. Body aches, fatigue, chills, nausea

Weitere VAERSDATA-Felder

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

VAERS 2523995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Axillary pain Headache Injection site pain Neck pain Pain Pain in extremity

Symptomtext

Headache left arm pain radiated to neck and shoulder, left armpit radiated to inner arm to elbow Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1985196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130 BA

mild

Staat: ND
Alter: 37,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Injection site mass Maternal exposure during breast feeding Suppressed lactation

Symptomtext

I experienced a loss of breast milk production. Before the vaccine my production was 16 oz a day, after the vaccine my production wasn't over 7 oz. When I went back for the booster on 12/23/2021 I lost the remainder of my breast milk production. Was not able to express any breast milk after the booster. I also have a hard lump at the injection site that has not gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site mass
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetic
Andere Medikamente: Metformin Milk Thistle Prenatal vitamins
Allergien: Allergic to metal and surgical steel
Vorherige Impfungen: -

VAERS 1985036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: HI
Alter: 35,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Feeling cold Heart rate increased Malaise Musculoskeletal stiffness Myalgia Nasopharyngitis Pain Pain in extremity Peripheral coldness

Symptomtext

Starting from 10:30pm the same day of my booster Pfizer appt, I started feeling very tired then my whole body started to ache really bad. My hands and feet were really cold and I felt like I was freezing. I put on more clothes and went under my comforter and was still freezing cold. No fever but my whole body's muscles ached really bad and I felt like my left arm was going to fall off. The muscles on the left side of my neck started to become stiff and my heart started beating extremely fast. I took a Tylenol and some of the symptoms went away but today (12/28) I still feel like I am sick maybe with a terrible cold and my whole body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None to report
Vorgeschichte: None
Andere Medikamente: Multi vitamins, and various other vitamins for health i.e. Vitamin C
Allergien: N/A
Vorherige Impfungen: -

VAERS 1984693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IL
Alter: 18,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Abscess drainage Abscess limb Gait disturbance Groin abscess Pain Pain in extremity

Symptomtext

After the booster shot, I had lots of soreness in my arms and legs. The next day I was having trouble walking due to intense leg pain on the left side. I went to the doctor who said that an abscess had formed on my leg after receiving the booster. It was extremely painful and I had to have emergency surgery to remove this groin abscess.

Weitere VAERSDATA-Felder

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

VAERS 1984274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TX
Alter: 16,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Pain in extremity

Symptomtext

Chills Left arm pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: COVID 19 Pfizer Vaccine

VAERS 1982172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: GA
Alter: 16,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Pallor Skin discolouration

Symptomtext

father of patient came to me shortly after giving him the vaccine and said is it normal to feel dizzy afterwards. I told him it could happen and checked on patient and told him to remain seated for a little bit. I then checked on him about 5 minutes later he had turned green and said he felt like he was going to throw up but did not feel like he could stand and make it to the restroom. I gave him a bag but he never vomited . in a few more minutes all color had drained from him and I offered him a bottle of water to sip on and after about 15 minutes he said he felt better and they left. I called in an hour or so and his parent said he was feeling much better

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: not known
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1982160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: WA
Alter: 64,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 14.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 10,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia

Symptomtext

Prolonged joint pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Gout, bladder ca, oa
Andere Medikamente: Allopurinol
Allergien: None
Vorherige Impfungen: Pfizer cocid

VAERS 1981201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 37,0
Geschlecht: F
Eingang: 26.12.2021
Impfdatum: 22.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Disorientation Fatigue Lymph node pain Lymph node palpable Lymphadenopathy

Symptomtext

This was the booster I received. Symptoms: Extreme fatigue and disorientation 20 hours after I received the injection. It resolved in 12 hours. I noticed some tenderness in my collarbone area about 48 hours after the injection. The supraclavicular lymph nodes are swollen on the left-side. The lump(s) are palpable on the surface and move around when pressure is exerted (pretty gross). It has been four days, and the area is still the same.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None at the moment. I will be seeking a medical professional's opinion if the situation does not resolve itself in a couple of weeks or if symptoms worsen. I just wanted to report the side effects since I did not have an issue with the first two doses.
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-diabetic
Andere Medikamente: Daily Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1980853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 48,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Cough Diarrhoea Headache Immunisation Oropharyngeal pain Pain Vaccination site erythema Vaccination site mass Vaccination site pruritus

Symptomtext

Headache; Body ache; Cough; Diarrhea; Sore throat; Hard lump and redness at injection site, itchy injection site; Hard lump and redness at injection site, itchy injection site; Hard lump and redness at injection site, itchy injection site; Dose number: 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 48-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 19Dec2021 at 11:15 (Lot number: 33130BA) at the age of 48 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Chronic pain" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Depression" (unspecified if ongoing); "ADD" (unspecified if ongoing), notes: ADD/ADHD; "ADHD" (unspecified if ongoing), notes: ADD/ADHD; "Egg allergy" (unspecified if ongoing), notes: Known allergies: Eggs and "Fruit allergy" (unspecified if ongoing), notes: banana. Concomitant medication(s) included: ADDERALL XR; CYMBALTA; WELLBUTRIN; TYLENOL and CODEINE. Past drug history included: Levaquin, reaction(s): "Drug allergy", notes: Known allergies: Levaquin and Cymbalta, reaction(s): "Drug allergy", notes: Known allergies: Cymbalta (must be watched). Vaccination history included: Bnt162b2 (DOSE 2, SINGLE; Lot number: Unknown; Route of administration: unspecified; Anatomical site: left arm), administration date: 28Apr2021, when the patient was 47 years old, for COVID-19 immunisation, reactions: "No adverse reaction" and Bnt162b2 (DOSE 1, SINGLE; Lot number: ER8734; Route of administration: unspecified; Anatomical site: left arm), administration date: 07Apr2021, when the patient was 47 years old, for COVID-19 immunisation, reactions: "No adverse reaction". The following information was reported: IMMUNISATION (non-serious) with onset 19Dec2021 at 11:15, outcome "unknown", described as "Dose number: 3"; HEADACHE (non-serious) with onset 20Dec2021, outcome "unknown", described as "Headache"; PAIN (non-serious) with onset 20Dec2021, outcome "unknown", described as "Body ache"; COUGH (non-serious) with onset 20Dec2021, outcome "unknown", described as "Cough"; DIARRHOEA (non-serious) with onset 20Dec2021, outcome "unknown", described as "Diarrhea"; OROPHARYNGEAL PAIN (non-serious) with onset 20Dec2021, outcome "unknown", described as "Sore throat"; VACCINATION SITE MASS (non-serious), VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 20Dec2021, outcome "unknown", and all described as "Hard lump and redness at injection site, itchy injection site". Therapeutic measures were not taken as a result of headache, pain, cough, diarrhoea, oropharyngeal pain, vaccination site mass, vaccination site erythema and vaccination site pruritus. Additional information: The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADD (ADD/ADHD); ADHD (ADD/ADHD); Anxiety; Chronic pain; Depression; Egg allergy (Known allergies: Eggs); Fruit allergy (banana)
Andere Medikamente: ADDERALL; CYMBALTA; WELLBUTRIN; TYLENOL; CODEINE
Allergien: -
Vorherige Impfungen: -

VAERS 1980852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Blepharospasm Headache Immunisation Pyrexia

Symptomtext

Joint pain; Eyelid twitching; Fever; Headache; Dose number 3; This is a spontaneous report from a contactable reporter (consumer or other non-hcp). The reporter is the patient. A 29-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Dec2021 (Lot number: 33130BA) at the age of 29 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None", notes: Other medical history: none; Known allergies: none. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: ER8732; Anatomical location: left arm), administration date: 27Mar2021, when the patient was 29 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EU0161; Anatomical location: left arm), administration date: 17Apr2021, when the patient was 29 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 14Dec2021, outcome "unknown", described as "Dose number 3"; ARTHRALGIA (non-serious) with onset 15Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Joint pain"; BLEPHAROSPASM (non-serious) with onset 15Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Eyelid twitching"; PYREXIA (non-serious) with onset 15Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Fever"; HEADACHE (non-serious) with onset 15Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Headache". Therapeutic measures were not taken as a result of arthralgia, blepharospasm, pyrexia and headache. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: no
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1979431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pain in extremity Product administered to patient of inappropriate age

Symptomtext

A 15-year-old received a Pfizer booster shot. We followed-up the day after patient received the injection. Patient's guardian claims she is only experiencing a sore arm and no other symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: No known drug allergy
Vorherige Impfungen: -

VAERS 1979358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: OH
Alter: 62,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Immediate post-injection reaction Injection site swelling

Symptomtext

pt had immediate swelling at injection site. rph stayed in room with pt for 5min to observe and then administered one dose of diphenhydramine 25mg. pt then stayed in the pharmacy area for 30 min while rph observed. no further reaction was reported.

Weitere VAERSDATA-Felder

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

VAERS 1979342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NC
Alter: 34,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 22.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Injection site reaction Rash Rash erythematous

Symptomtext

Painful red rash on arm near and around the injection site.

Weitere VAERSDATA-Felder

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

VAERS 1979290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 54,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 21.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Feeling abnormal Lymph node pain Lymphadenopathy

Symptomtext

Brain fog, fatigue, swollen and sore lymph node in armpit of arm where shot was given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Olmesartan medicinal, flax seed oil, garlic, vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1979205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: WI
Alter: 39,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Arthralgia Fatigue Tinnitus

Symptomtext

About 24 hours after my third booster, I felt very tired, had achy joints and ringing in my ears. The tinnitus has persisted and I still have high and medium pitched ringing in my ears pretty constantly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none yet
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: flonase
Allergien: allergic to penicillin
Vorherige Impfungen: -

VAERS 1976734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cough Oropharyngeal discomfort Pyrexia Rhinorrhoea

Symptomtext

coughing, throat issues, runny nose, fever

Weitere VAERSDATA-Felder

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

VAERS 1974464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: FL
Alter: 46,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain Injection site swelling Lymphadenopathy Oedema peripheral

Symptomtext

Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Lymph Node Swelling-Severe, Additional Details: swallowing golf ball size under arm

Weitere VAERSDATA-Felder

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

VAERS 1971530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: UT
Alter: 42,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 19.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymph node pain Lymphadenitis

Symptomtext

Left supraclavicular lymph node tenderness and inflammation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: None, palpated by myself (patient) I am a registered nurse.
Aktuelle Erkrankungen: Mild cold, no lymph nodes effected.
Vorgeschichte: -
Andere Medikamente: Levothyroxine, spironolactone, probiotics, vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 1971125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: NY
Alter: 61,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Nausea Pain Pain in extremity

Symptomtext

Pain in arm Body aches Nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Blood pressure Cholesterol Acid Pain medication
Allergien: No
Vorherige Impfungen: -

VAERS 1968043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: NY
Alter: 35,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Euphoric mood Feeling abnormal

Symptomtext

Brain fog, feeling of marijuana like high, dizziness since date of vaccine administration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: fever, chills for about 3 days following, COVID 19 pfizer biontech both dose 1 and 2

VAERS 1967460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130 BA

mild

Staat: OR
Alter: 44,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 14.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Ear discomfort Ear pain Herpes zoster Lymphadenopathy Otitis externa Pain Pain in jaw Rash

Symptomtext

Symptoms started about 1.5 days after injection. Presented as pressure in left ear that became more painful over the next 24 hours. Pain became constant and after four days the pain extended along the lower left jaw. Swollen nodes and the jaw was painful to the touch. Was initially diagnosed with an outer ear infection. Was given antibiotic ear drops. No relief was found using the drops. Sunday evening a pain rash appeared on my left temple. Pain was extreme. During follow up visit on 12/20/2021 and consultation with the Advising Physician, diagnosis was updated to shingles outbreak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Minor cold 2 weeks prior to vaccine
Vorgeschichte: -
Andere Medikamente: buPROPion Sertraline Methylphenidate
Allergien: None that I?m aware of
Vorherige Impfungen: -

VAERS 1966915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NY
Alter: 52,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Drug eruption Feeling hot Immunisation Pain Pain in extremity Rash erythematous

Symptomtext

developed what almost looks like a Niacin rash; rash on her chest and upper neck - the area is red and warm; rash on her chest and upper neck - the area is red and warm; body aches; body aches are mostly upper body, in the upper arms; Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Dec2021 (Lot number: 33130BA) at the age of 52 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Inflammatory arthritis" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "mild crohn''s colitis" (unspecified if ongoing); "Neuralgia" (unspecified if ongoing); "autoimmune disorder" (unspecified if ongoing); "Overweight" (unspecified if ongoing). Concomitant medication(s) included: INFLUENZA VACCINE taken for immunisation, administration date 27Nov2021; ENBREL taken for autoimmune disorder, overweight. Past drug history included: Niacin, reaction(s): "rash". Vaccination history included: Bnt162b2 (Dose:1, lot EP6955), administration date: 21Mar2021, when the patient was 52 years old, for COVID-19 immunization; Bnt162b2 (Dose:2, lot ER8737), administration date: 11Apr2021, when the patient was 52 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 03Dec2021, outcome "unknown", described as "Booster"; DRUG ERUPTION (non-serious) with onset 05Dec2021, outcome "not recovered", described as "developed what almost looks like a Niacin rash"; RASH ERYTHEMATOUS (non-serious), FEELING HOT (non-serious) all with onset 05Dec2021, outcome "not recovered" and all described as "rash on her chest and upper neck - the area is red and warm"; PAIN (non-serious) with onset 04Dec2021, outcome "recovering", described as "body aches"; PAIN IN EXTREMITY (non-serious) with onset 04Dec2021, outcome "recovering", described as "body aches are mostly upper body, in the upper arms". Therapeutic measures were taken as a result of drug eruption, rash erythematous, feeling hot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder; Crohn's colitis; Fibromyalgia; Inflammatory arthritis; Neuralgia; Overweight
Andere Medikamente: ENBREL
Allergien: -
Vorherige Impfungen: -

VAERS 1963878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NC
Alter: 24,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Fatigue Headache Nausea Pain Pyrexia Rash erythematous Vaccination site erythema Vaccination site pain Vaccination site pruritus Vaccination site rash Vaccination site swelling Vomiting

Symptomtext

I was just really tired on Saturday morning. I was nauseas and threw up a couple of times. I had really bad body aches that started around 3 PM on Saturday. In the afternoon I got a really high fever that was 104 degrees. My arm where I got the vaccine has been really itchy, painful, and swollen. There is a red rash around the area as the size of my palm. I have been putting Benadryl cream on it. I had a bad headache with the fever. I just did a call, and my doctor prescribed Ondansetron 4mg for the nausea which has helped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Adderall 40mg; Trintellix 10mg; Junel 21 day pack 1/20
Allergien: None
Vorherige Impfungen: Covid 1st Dose Vaccine- rash on my back and local reaction on arm. (April 23, 2021) Gardasil Vaccine- (10 years ago) It made me

VAERS 1963516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: VT
Alter: 10,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chills Headache Incorrect dose administered Loss of personal independence in daily activities

Symptomtext

Patient is a 10 year old female who came in for her dose. Client received a Pfizer, 12 year old and older, vaccination. Mother was informed of the error before they left the clinic. Nurse spoke with the client?s father 12/20/21. Father reports the client has a ?bad? headache and chills. Client missed a day of school as a result of symptoms which have since resolved. Client?s father denied having any questions or concerns regarding vaccination at this time.

Weitere VAERSDATA-Felder

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

VAERS 1963417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NC
Alter: 14,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Dysstasia Gait disturbance Hypotonia Pallor

Symptomtext

About 2 minutes after the patient received the first dose of the vaccine, she said she felt faint and her face turned pale. Her father and I helped her get to a safe area where she could lie down. Her body went limp and she could not stand or walk. I had her elevate her feet and placed cool ice packs around her neck and face. She did not fully lose consciousness and still had her eyes open and was talking. She did not have any symptoms of anaphylaxis. I had her lie there and sip on water for 30 m,inutes and the patient was able to walk away. I checked in on her in an hour and she was still fine.

Weitere VAERSDATA-Felder

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

VAERS 1962417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130 BA

mild

Staat: IN
Alter: 62,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Malaise

Symptomtext

General malaise lasted for about 7 days rather than the day of the vaccination and one or two days afterwards. It was the length of the after-effects (~8 days) that were concerning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Irritable bowel disorder Obesity
Andere Medikamente: Xanax
Allergien: -
Vorherige Impfungen: -

VAERS 1962159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 32,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Chills Headache Pain

Symptomtext

Chills, body aches and headache 24-36 hours after the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1962133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: WA
Alter: 45,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Injection site swelling Lethargy Lymphadenopathy Pain Pyrexia

Symptomtext

Site: Swelling at Injection Site-Medium, Systemic: Body Aches Generalized-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Fever-Mild, Systemic: Lymph Node Swelling-Medium, Additional Details: Patient's husband called to report baseball size swelling in axillary region of arm where COVID vaccine was given. Assessed via phone and recommended to monitor since swelling had decreased slightly in last 12-18 hours. Recommended they monitor and check for any increasing size, redness, and warmth and refer to urgent care for evaluation if occurring. Husband verbalized understanding and agreed to plan.

Weitere VAERSDATA-Felder

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

VAERS 1962056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: RI
Alter: 74,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Back pain Chills Fatigue Flushing Headache Injection site pain Injection site pruritus Lymph node pain Lymphadenopathy Nausea Pain Pain in extremity Pyrexia Respiratory tract congestion

Symptomtext

Almost immediate itching and aching at injection site. Extreme arm pain for approximately 20 hours, then moderate pain to present time (12/18/21 @ 9 pm). Extreme fatigue, chills within 12 hours. Pain in abdomen, aching and shooting pain, nausea. Headache and backache. Slight congestion, sore/swollen lymph nodes in axilla and neck. Fever and flushing (unknown temperature, no thermometer).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: microscopic colitis; breast cancer (treated)
Andere Medikamente: Calcium citrate, vitamin D, multivitamin, budesonide oral, ana anastrazole
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 1961871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: WA
Alter: 53,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 08.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Deafness bilateral Diplacusis Ear inflammation Ear pain Ear, nose and throat examination abnormal Hyperacusis Middle ear effusion Nasopharyngitis Sudden hearing loss Tinnitus

Symptomtext

I experienced a sudden hearing loss on 12/10, which developed into diplacusis dysharmonia. I had a head cold at the time, although not severe. By 12/11 I had very limited upper=frequency hearing in my left ear, and suppressed hearing in both ears. I experienced continuing ear pain and hearing problems, and saw my doctor on 12/14. I was prescribed Sudafed and amoxicillin. Later that day I began to hear sounds differently in each ear, with pure tones perceived about 1/2 tone different in pitch between my right and left ears. I called back to the doctor, and was prescribed Prednisone to take every day for six days. I had another doctor visit on 12/16. As of today, I?m still experiencing some hearing loss and tinnitus in my left ear, along with the feeling of having an ear full of fluid. My balance is not affected. The diplacusis persists, but has possibly become less intrusive. I still have decreased upper-frequency sensitivity in my left ear, compared to my right ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: The doctors at the HCF examined my ears and noted some inflammation and fluid during the first visit. On the second visit I believe they only noted mild fluid buildup in one ear. I haven?t had any audiological tests.
Aktuelle Erkrankungen: Viral head cold and congestion, starting 12/6/21 and resolving about 12/15/21.
Vorgeschichte: Retinitis pigmentosa
Andere Medikamente: Dorzolomide eye drops, guaifenesin expectorant, dextromethorphan decongestant
Allergien: None
Vorherige Impfungen: -

VAERS 2545461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 55,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 14.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Headache Myalgia Nausea Pyrexia Vomiting

Symptomtext

Headache, Myalgia, Fever, NauseaVomiting, chills, Narrative: N/A

Weitere VAERSDATA-Felder

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

VAERS 2545413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Headache Myalgia Nausea Vomiting

Symptomtext

Headache, Myalgia, NauseaVomiting, fatigue Narrative: N/A

Weitere VAERSDATA-Felder

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

VAERS 2545380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 14.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Headache Myalgia Pain in extremity

Symptomtext

Headache, Myalgia, right arm pain, fatigue Narrative: NA

Weitere VAERSDATA-Felder

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

VAERS 2541595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Injection site pain Myalgia Photosensitivity reaction

Symptomtext

Headache, Myalgia, photo sensitivity, arm tenderness at injection site Narrative: N/A

Weitere VAERSDATA-Felder

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

VAERS 1958867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TN
Alter: 27,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 14.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

Hives on both arms and legs, face, and buttocks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Prenatal vitamin
Allergien: None.
Vorherige Impfungen: -

VAERS 1956182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NY
Alter: 36,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 06.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Erythema Pain in extremity Pruritus Scar Skin discolouration Skin exfoliation Somnolence Urticaria

Symptomtext

I took the vaccine that morning by the night my arm was sore. I felt drowsy so I went to bed around 9-10pm I woke up to go to the bathroom but my body felt itchy from the inside out. I lightly rub my belly and went back to bed. When I woke up early that morning my stomach was broke out in hives. It stayed that way for a few hrs along with redness. It look like it went down but as the days went by my red marks turned into scar like marks. My belly started to turn real black and peel like as if I was burned from the inside out. I went to a city MD near my home and they couldn?t tell me anything but they gave me a steroid cream called Triamcinolone Acetonide cream 0.1% it didn?t work. I have a bad ugly black scar now on my upper torso.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Asthma pump Abuterol Sulfate 90mcg
Allergien: No
Vorherige Impfungen: -

VAERS 1954701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 14.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Pain Pain in extremity Vertigo Vertigo positional

Symptomtext

After normally expected side effects subsided (sore arm, body aches) I experienced 3 episodes of extreme vertigo between 2 AM - 6 AM. This included when rolling over in bed and when standing up and sitting down. At this point (8:16 AM) the vertigo seems to be gone although I remain light headed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none at this time
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vit D, Vit B12, Occuvite eye vitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1952685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Rash Rash pruritic

Symptomtext

Patient's mother states that 1 hour after the vaccine, child had itchy rash on face that self-resolved quickly. No medications were given. Parent informed me during a telephone call with me the day following the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Overweight, asthma, food allergy, medication allergy.
Andere Medikamente: -
Allergien: Miralax, amoxicillin, cefdinir, history of reaction to nuts (hazelnut, peanut, almond, walnut), vanilla extract.
Vorherige Impfungen: -

VAERS 1952255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: IN
Alter: 37,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Cough Fatigue Feeling of body temperature change Headache Hypersomnia Pain Pulmonary congestion

Symptomtext

Initially just started feeling tired. That night, started going back and forth between feeling very hot to feeling cold. Body aches, followed by a headache that got worse when coughing. Still had cough, but not frequent. Exhaustion continued. Next day, took over the counter cold/flu medication and slept for about 12 hours that night. Body aches subsided but headache and tiredness have continued. Today, (second day after dose) cough has stayed minimal but lungs feel congested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None, treating symptoms at home unless they persist.
Aktuelle Erkrankungen: Occasional cough
Vorgeschichte: Asthma
Andere Medikamente: Ambien, prebiotic
Allergien: Sulfa medication
Vorherige Impfungen: -

VAERS 1951551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 11.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Injection site erythema Injection site inflammation Injection site nodule Injection site pain Injection site warmth

Symptomtext

Patient has come in with a red, inflamed knot on her right arm. She stated that it is hot to the touch and sensitive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Na.
Vorgeschichte: Na.
Andere Medikamente: Na.
Allergien: Na.
Vorherige Impfungen: -

VAERS 2545470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 13.12.2021
Beginn: 11.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Fatigue Myalgia Pain in extremity

Symptomtext

Myalgia fatigue, arm soreness Narrative: N/A

Weitere VAERSDATA-Felder

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

VAERS 1948425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 10.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Chills Diarrhoea Fatigue Headache Vomiting

Symptomtext

tiredness, headache, chills, vomiting, diarhea

Weitere VAERSDATA-Felder

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

VAERS 1947838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TX
Alter: 28,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Exposure during pregnancy

Symptomtext

Patient is due on 4/28/2022. No said pregnancy complications stated. Patient indicated she she was lightheaded after vaccinated due to not eating in the morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Prenatal Vitamins
Allergien: NKA
Vorherige Impfungen: -

VAERS 1947770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TX
Alter: 57,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Dizziness Heart rate increased

Symptomtext

Patient received Pfizer Booster shot at vaccination shot on day above. In observation line, she reported feeling anxious, high heart rate and lightheaded. Vital signs at 12:45 pm were as followed, 144/82 blood pressure, 76 heart rate, 18 respirations and 96% SPO2. Patient was independently talking, no chest pain or shortness of breath reported. Monitored by paramedics. At 12:50 pm vital signs were: 151/80 blood pressure, heart rate 74, respirations 18 and 100% SPO2. At this time, patient reported feeling much better and stated she had gone for a walk that morning but had not eaten anything. Advised patient to get some lunch, drink water and rest for afternoon. Left site with no further symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Patient did not report any health conditions
Andere Medikamente: Patient did not report any medications
Allergien: None
Vorherige Impfungen: -

VAERS 1944889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chills Feeling hot Headache Induration Joint range of motion decreased Limb discomfort Myalgia Peripheral swelling Pyrexia Swelling

Symptomtext

Fever for two days following booster, with headache, chills, and muscle pain from shot location. Swollen shoulder, hot and hard to touch contiuing on day three, discomfort from shoulder to fingertips of right arm, slightly swollen hand compared to left hand, unable lift arm higher than parallel with shoulder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A. Messaged doctor's office requesting feedback about arm.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Gastroparesis, depression, GAD, panic disorder.
Andere Medikamente: Seroquel 25 MG as needed for panic disorder. One dose taken 12/11/21
Allergien: Gluten/dairy intolerances.
Vorherige Impfungen: COVID-19 Moderna Shot 2: fever, headache, chills, loss of appetite for 2 days, resolved on third. Minimal arm pain/swelling.

VAERS 1944236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: TN
Alter: 36,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pain Pain Sleep disorder

Symptomtext

right arm at site of injection sore/ache, underarm and side of torso on right side aching/sore (like a sore muscle), right shoulder, right side of chest at collar bone, right side of neck -- all sore/aching. Difficult to move and hurt enough to interrupt sleep. Started less than 24 hours after the dose, and persisted for approximately 80 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Kyleena, Escitalopram 10mg, CBD 30mg
Allergien: No
Vorherige Impfungen: -

VAERS 1943815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Diarrhoea Nausea Vomiting

Symptomtext

On the morning following my injection, I experienced mild diarrhea and nausea. I was unable to hold down my normal morning medication without vomiting until after I took some bismuth subsalicylate pills (generic for Pepto-Bismol). I also took some lopermaide pills to calm my digestion. I was able to perform most of my daily functions after that, but felt like I had been punched in the stomach for about 24 hours. I was completely recovered by Sunday morning, 12/12.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, Metabolic Syndrome X, mild arthritis
Andere Medikamente: Amlodipine, Atorvastatin, Losartan, COQ-10, Vitamin D3, Calcium, Vitamin C
Allergien: No known allergies
Vorherige Impfungen: Pfizer COVID-19 vaccine taken 3/30/2011, see VAERS ID 474241

VAERS 1943779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 11.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Axillary pain Injection site pain Pain in extremity

Symptomtext

Non localized pain and soreness of injection site. Patient had pain and soreness in his armpit and across his entire upper arm beyond injection site.

Weitere VAERSDATA-Felder

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

VAERS 1941630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: IL
Alter: 47,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Chills Feeling cold Pyrexia

Symptomtext

Reported chills around 7:30 pm on December 10, 2021. Fever of 102.7 degrees fahrenheit taken with the Braun No Touch + Forehead Thermometer on the same day around 10:00 pm. Gave two ibuprofen 200 mg gel caps at 10:30 pm. reported he still had cold chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Stroke 2015 Heart attack November 2011 and March 2012 (total of 5 stents) Defibrillator placement 2018 High Blood Pressure CHF Pre-Diabetic
Andere Medikamente: ? Aspirin 81 mg ? morning 1 tab once daily ? Atorvastatin 80 mg ? night 1 tab once daily ? Carvedilol 25 mg tab ? morning and night 1 tab BID ? Escitalopram 20 mg tab ? morning 1 tab once daily ? Ezetimibe 10 mg tab ? mornin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2549819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Diarrhoea Fatigue Headache Myalgia Nausea Pyrexia Vomiting

Symptomtext

Headache, Myalgia, Fever, Diarrhea, NauseaVomiting, fatigue Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1936286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: AZ
Alter: 29,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Back pain Fatigue Impaired work ability Injection site pain Insomnia Lymphadenopathy Pain Pain in extremity Somnolence

Symptomtext

I didn't have any symptoms that night but when I woke up I had all over body aches especially on my left side, back, and arm where shot was and then I was tired throughout the day and I took 1/2 day off work to get some sleep later on in the afternoon and the other symptoms went away but my arm pain got worse and then I had a lot of pain in armpit area and lymph nodes were swollen so I called my Dr and I was having trouble sleeping because of the pain and the Dr responded in the middle of the night and they said it was normal to have the immune response to swollen lymph nodes and to use a warm compress and Tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: PCOS
Andere Medikamente: Birth Control
Allergien: None
Vorherige Impfungen: HPV- Vomiting

VAERS 1933279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

mild

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Pruritus Rash Rash erythematous

Symptomtext

patient reports feeling itchy on the left arm, red rashes noted at 6:24pm on bilateral upper extremities, Benadryl 25mg administered symptoms resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: vs 5:47pm hr 90, r 18, bp 180/110/ sat 97% 6:02pm vs hr:76, r 18, bp 130/90, sat 98%
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: n/a
Allergien: latex, papaya, other fruits
Vorherige Impfungen: -

VAERS 1932568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: PR
Alter: 11,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Incorrect dose administered

Symptomtext

Incorrect vaccine administered to a pediatric patient of 11 y/o. Patient received a Pfizer vaccine for adult and an adult dose of 0.3 ml. Patient developed headache which resolved spontaneously. Mother was notified of mistake and upon follow up by phone was oriented to receive the proper pediatric vaccine dose in 21 days.

Weitere VAERSDATA-Felder

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

VAERS 1929502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: CO
Alter: 36,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Breast discomfort Breast swelling Erythema Hypoaesthesia Limb discomfort Oedema peripheral Peripheral swelling Pruritus

Symptomtext

Swelling and discomfort inner aspect left arm, and present in left axilla and breast tissue. Slightly red, intermittent itching. Feels some numbness in left arm.

Weitere VAERSDATA-Felder

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

VAERS 1929423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: PA
Alter: 33,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Fatigue Headache Injection site erythema Injection site pain Injection site swelling Myalgia Pyrexia

Symptomtext

Injection site pain/swelling/redness, fever, headache, fatigue, muscle pain, joint pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Velivet (oral contraceptive) Restasis (dry eye)
Allergien: None
Vorherige Impfungen: 1st dose of Pfizer COVID-19 vaccine

VAERS 1924993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: PR
Alter: 38,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Rash Rash maculo-papular Rash pruritic

Symptomtext

10 minutes after receiving immunization delivered pruritic maculo-papular rash on arms that spread to face back and chest, no other symptoms. No respiratory compromise, stable vital signs. 61 pulse, 129/80 BP, 36.5 C Temp. After 30 minutes patient received benadryl im. for pruritus and was transfered to Emergency room for further observation and evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Decadron, Tramadol
Vorherige Impfungen: -

VAERS 1923766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: IN
Alter: 30,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Axillary pain Injection site swelling Lip swelling Lymphadenopathy Pyrexia Swelling face

Symptomtext

Approximately 60-90 minutes post injection noted swelling in the face and lips as well as the injection site. Antihistamine taken with little relief. As time progressed, low grade fever around 100 degrees Fahrenheit. Intense pain approximately 8 hours post injection in the left axillary area in conjunction with increasing swelling. Facial swelling resolved within 12 hours, but swelling of the lymph nodes and fever still present 48 hours post injection at time of report submitted. Will seek medication attention with PCP when in office tomorrow.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bipolar 1, PTSD, ADHD
Andere Medikamente: Lithium, Adderall XR, Prazosin, Lorazepam
Allergien: Penicillin, ceclor, latex
Vorherige Impfungen: 2nd dose Pfizer covid 3/3/21 - anaphylactic type reaction age 29

VAERS 1917176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

mild

Staat: AR
Alter: 39,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pharyngeal swelling Urticaria

Symptomtext

PT CALLED AFTER GETTING THE VACCINE THAT MORNING. SHE HAD HIVES AND THROAT STARTED TO SWELL

Weitere VAERSDATA-Felder

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

VAERS 2718822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: KY
Alter: 16,0
Geschlecht: M
Eingang: 29.11.2023
Impfdatum: 10.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Illness

Symptomtext

He got sick with the first shot; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). An 18-year-old male patient received bnt162b2 (BNT162B2), on 10Feb2022 as dose 1, single (Lot number: 33130BA) at the age of 16 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: ILLNESS (non-serious), outcome "unknown", described as "He got sick with the first shot". Additional information: Patient did not receive any other vaccines within 4 weeks prior vaccination.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300392914 same reporter/patient/drug, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Illness
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 2699868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: FL
Alter: 84,0
Geschlecht: F
Eingang: 22.10.2023
Impfdatum: 13.01.2022
Beginn: 01.01.2023
Tage bis Beginn: 353,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Muscular weakness

Symptomtext

Since patient received the 1st booster (3rd shot) of Pfizer she cannot make a fist with her hands and she lost feeling in her feet - Her doctor told her that this is not the first time he has witnessed this happening with his patients after receiving the vaccine and that he has seen this happen to many of his patients

Weitere VAERSDATA-Felder

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

VAERS 2694514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 61,0
Geschlecht: M
Eingang: 11.10.2023
Impfdatum: 31.03.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Magnetic resonance imaging SARS-CoV-2 test Tinnitus

Symptomtext

Experienced bilateral, persistent tinnitus soon after receiving first dose, and worsens with each subsequent dose; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old male patient received bnt162b2 (BNT162B2), on 31Mar2022 as dose 4 (booster), single (Lot number: 33130BA) at the age of 61 years for covid-19 immunisation. The patient's relevant medical history included: "CTCL" (unspecified if ongoing); "Known allergies: PCN" (unspecified if ongoing); "Known allergies: bee venom" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: bnt162b2 (DOSE 3 (BOOSTER), SINGLE, Batch/Lot No: FF2590), administration date: 13Oct2021, when the patient was 61-year-old, for COVID-19 immunization, reaction(s): "Experienced bilateral, persistent tinnitus soon after receiving first dose, and worsens with each subsequent dose"; bnt162b2 (DOSE 2, SINGLE, Batch/Lot No: EP6955), administration date: 25Mar2021, when the patient was 60-year-old, for COVID-19 immunization, reaction(s): "Experienced bilateral, persistent tinnitus soon after receiving first dose, and worsens with each subsequent dose"; bnt162b2 (DOSE 1, SINGLE, Batch/Lot No: EN6198), administration date: 04Mar2021, when the patient was 60-year-old, for COVID-19 immunization, reaction(s): "Experienced bilateral, persistent tinnitus soon after receiving first dose". The following information was reported: TINNITUS (non-serious), outcome "not recovered", described as "Experienced bilateral, persistent tinnitus soon after receiving first dose, and worsens with each subsequent dose". The events "experienced bilateral, persistent tinnitus soon after receiving first dose, and worsens with each subsequent dose" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of tinnitus. Clinical course: Evaluated by ENT and audiologist. Event treated with diagnostic MRI, no treatment available (as reported). The patient had no covid prior vaccination.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300321222 same patient/AE, different drug dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Magnetic resonance imaging
Hospital-Tage: -
Labordaten: Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Comments: Diagnostic MRI; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab Self test
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to bee sting; Cutaneous T-cell lymphoma; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2690046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 03.10.2023
Impfdatum: 03.12.2021
Beginn: 01.09.2023
Tage bis Beginn: 637,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 03Dec2021 as dose 3 (booster), single (Lot number: 33130ba) at the age of 48 years, in left arm for covid-19 immunisation; covid-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2023, outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 (PAXLOVID Treatment).

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: antigen test & symptoms; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2681677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 13.09.2023
Impfdatum: 10.03.2021
Beginn: 30.06.2022
Tage bis Beginn: 477,0
Dosis: 2
Route/Site: - / -

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

COVID-19 COVID-19 immunisation SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a consumer via other manufacturer concerned a patient of unspecified age, sex, race and ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included: overweight, and allergy. The patient received first dose with covid-19 vaccine ad26.cov2.s (Dose number in series 1), (suspension for injection, route of admin not reported, batch number: 1805029, expiry: UNKNOWN) dose was not reported, 1 total administered on 10-MAR-2021 to right arm for covid-19 prophylaxis. Concomitant medications included ascorbic acid/calcium pantothenate/ergocalciferol/nicotinamide/pyridoxine hydrochloride/retinol/riboflavin/thiamine hydrochloride, bifidobacterium bifidum/bifidobacterium longum/lactobacillus gasseri, ergocalciferol, allergy pill and tirzepatide. The patient also received second dose with non-company suspect Pfizer Biontech Covid-19 Vaccine, (tozinameran), (Dose number in series 2), (batch number: 33130BA, expiry: UNKNOWN, form of admin, route of admin were not reported) dose was not reported, administered on 14-DEC-2021 to right arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination (Dose number in series 2). The patient also received third dose with non-company suspect Pfizer Biontech Covid-19 Vaccine, (tozinameran), (Dose number in series 3), (batch number: FK9893, expiry: UNKNOWN, form of admin, route of admin were not reported) dose was not reported, administered on 30-JUN-2022 to right arm for covid-19 prophylaxis which was a revaccination with different covid-19 vaccine (Dose number in series 3). On 17-AUG-2023, the patient tested positive for covid-19 and experienced confirmed covid-19 infection (Dose number in series 3) and confirmed clinical vaccination failure (Dose number in series 1). The patient was treated with paxlovid for 5 days from 19-AUG-2023 to 24-AUG-2023 for treatment of covid-19. 10 days after initial positive test patient tested negative for covid-19 on 27-AUG-2023. On 29-AUG-2023, 2 days after negative test patient experienced symptoms again, and 4 days after negative test, patient was tested positive for covid-19 on 31-AUG-2023. The patient reported to had cough, congestion, and fatigue which was almost worse than initial symptoms of covid-19. The action taken with covid-19 vaccine ad26.cov2.s, tozinameran (Dose number in series 2), and tozinameran (Dose number in series 3) was not applicable. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure and revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20230917219-confirmed clinical vaccination failure. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered inconsistent with vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230817; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Date: 20230827; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20230831; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
Aktuelle Erkrankungen: Allergy; Overweight
Vorgeschichte: -
Andere Medikamente: MOUNJARO; VITAMIN D [ERGOCALCIFEROL]; MULTIVITAMIN [ASCORBIC ACID;CALCIUM PANTOTHENATE;ERGOCALCIFEROL;NICOTINAMIDE;PYRIDOXINE HYDROCHLORID; COLON HEALTH
Allergien: -
Vorherige Impfungen: -

VAERS 2660681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 25.07.2023
Impfdatum: 14.12.2021
Beginn: 05.04.2023
Tage bis Beginn: 477,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 3/11/21 lot# En6207; Pfizer 4/1/21 lot# ER8732; 12/14/21 Pfizer lot#33130BA

Weitere VAERSDATA-Felder

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

VAERS 2649437

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 26.06.2023
Impfdatum: 02.02.2022
Beginn: 26.04.2023
Tage bis Beginn: 448,0
Dosis: 3
Route/Site: IM / -

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

CSF oligoclonal band present CSF test abnormal Cerebral disorder Demyelination Diplopia Flow cytometry Hemiparesis Pleocytosis Spinal cord disorder

Symptomtext

Acute CNS demyelinating disease affecting brain and spinal cord with diplopia and left hemiparesis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: CSF oligoclonal band present
Hospital-Tage: -
Labordaten: CSF pleocytosis with oligoclonal bands and abnormal B-cells on flow cytometry.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Methylphenidate
Allergien: -
Vorherige Impfungen: -

VAERS 2648331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 15.12.2021
Beginn: 13.08.2022
Tage bis Beginn: 241,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 2/28/21 lot# En6201; Pfizer 3/21/21 lot# EN6207; Pfizer 12/15/21 lot# 33130BA;

Weitere VAERSDATA-Felder

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

VAERS 2645285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 14.06.2023
Impfdatum: 16.12.2021
Beginn: 30.08.2022
Tage bis Beginn: 257,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 2/27/21 lot# EL3248; Pfizer 3/20/21 lot# EL9265; Pfizer 12/16/21 lot# 33130BA

Weitere VAERSDATA-Felder

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

VAERS 2640296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 02.06.2023
Impfdatum: 20.12.2021
Beginn: 22.11.2022
Tage bis Beginn: 337,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 2/24/21 lot# EL9267; Pfizer 3/17/21 lot# EN6205; Pfizer 12/20/21 lot# 33130BA

Weitere VAERSDATA-Felder

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

VAERS 2629705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 10.05.2023
Impfdatum: 14.12.2021
Beginn: 08.04.2023
Tage bis Beginn: 480,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 6/28/21 Lot# EN6207; Pfizer 7/23/21 Lot# Ew0173; Pfizer 12/14/21 Lot# 33130BA

Weitere VAERSDATA-Felder

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

VAERS 2629024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 09.05.2023
Impfdatum: 16.12.2021
Beginn: 12.04.2022
Tage bis Beginn: 117,0
Dosis: 3
Route/Site: IM / LA

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

Neuropathy peripheral

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE NEUROPATHY

Weitere VAERSDATA-Felder

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

VAERS 2626709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 15.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 28,0
Dosis: UNK
Route/Site: - / -

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

Angiogram cerebral normal Computerised tomogram Computerised tomogram head normal Computerised tomogram neck Magnetic resonance imaging normal Tinnitus

Symptomtext

Covid Vax 1 - 3/26/2021. Lot ER8732 Covid Vax 2 - 4/16/2021. Lot EW0169 Booster - 12/15/2021. Lot 33130BA 1 month after my booster, I started hearing my pulse in my right ear. This began on January 12, 2022 and HAS NOT STOPPED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Angiogram cerebral normal
Hospital-Tage: -
Labordaten: I have seen my primary care doctor, ENT, audiologist, neurosurgeon/ neurologist. I have had a CT of my head, neck, ear area, and MRI, and an unpleasant angiogram of my brain. Nothing is showing up as the cause. I had NO history of tinnitus.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure - genetic
Andere Medikamente: Citalopram , amlodipine, Carvedolol, Losartin
Allergien: Penicillins, Cipro, erithromycin, Liscinopril
Vorherige Impfungen: -

VAERS 2613850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 01.12.2021
Beginn: 29.12.2022
Tage bis Beginn: 393,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines THIS IS THE INFORMATION AS LISTED IN THE STATE DATABASE Pfizer 3/10/21 NO LOT # recorded; Pfizer 3/31/21 NO LOT # RECORDED; Pfizer 12/11/21 Lot# 33130BA

Weitere VAERSDATA-Felder

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

VAERS 2598158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: IL
Alter: 39,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-1 test

Symptomtext

COVID-19; COVID-19; vaccine brand other=Moderna,vaccine dose number=1/vaccine brand other=Moderna,vaccine dose number=2; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from product quality group. The reporter is the patient. A 40-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 39 years for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 21Apr2021 as dose 1, single (Lot number: 048B21A) and on 19May2021 as dose 2, single (Lot number: 038C21A) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin. The patient's concomitant medications were not reported. Past drug history included: Albuterol, reaction(s): "Cough"; Albuterol, reaction(s): "Wheezing". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 08Dec2021, outcome "unknown", described as "vaccine brand other=Moderna,vaccine dose number=1/vaccine brand other=Moderna,vaccine dose number=2"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-1 test: Positive, notes: positive home antigen test after 2 negative tests; Negative, notes: positive home antigen test after 2 negative tests; Negative, notes: positive home antigen test after 2 negative tests. Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid from 01Mar2023 to 06Mar2023.; Sender's Comments: The efficacy of a vaccine varies from one patient to another and can be affected by different factors; however, a contributory role of the suspect vaccine product BNT162B2 to the reported events drug ineffective and COVID-19 cannot be ruled out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Home antigen test; Test Result: Positive ; Comments: positive home antigen test after 2 negative tests; Test Name: Home antigen test; Test Result: Negative ; Comments: positive home antigen test after 2 negative tests; Test Name: Home antigen test; Test Result: Negative ; Comments: positive home antigen test after 2 negative tests
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2581169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 14.02.2023
Impfdatum: 29.12.2021
Beginn: 01.12.2022
Tage bis Beginn: 337,0
Dosis: 3
Route/Site: - / -

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

Deafness Tinnitus

Symptomtext

much worse tinnitus and hearing loss; much worse tinnitus; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient received BNT162b2 (BNT162B2), on 29Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 64 years for covid-19 immunisation. The patient's relevant medical history included: "hearing aids", start date: Oct2022 (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose: 1, Time: 10:00 AM, Anatomical site of injection: Left arm, Route of administration: Intramuscular, Batch/Lot number: ER8729), administration date: 14Apr2020, when the patient was 62-year-old, for COVID-19 Immunization, reaction(s): "COVID test result Positive", "after covid in Dec2022"; BNT162b2 (Dose: 2, Time: 10:00 AM, Anatomical site of injection: Left arm, Route of administration: Intramuscular, Batch/Lot number: EW0182), administration date: 19May2020, when the patient was 62-year-old, for COVID-19 Immunization, reaction(s): "Have lost half of my hearing ability", "Noticed ringing in my ears", "headache". The following information was reported: TINNITUS (disability) with onset Dec2022, outcome "not recovered", described as "much worse tinnitus"; DEAFNESS (disability, medically significant) with onset Dec2022, outcome "not recovered", described as "much worse tinnitus and hearing loss". The events "much worse tinnitus and hearing loss" and "much worse tinnitus" required physician office visit. Therapeutic measures were taken as a result of deafness, tinnitus. Clinical course: Aug2020: Tinnitus, gradual and continued hearing loss. Got hearing aids Oct2022. After COVID in Dec2022- much worse tinnitus and hearing loss under ENT Care- steroids, meds. Seriousness criteria was reported as being persistent/significant disability/incapacity.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201390482 same patient, different vaccine dose/event;US-PFIZER INC-202201390515 same patient, different vaccine dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deafness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hearing aid user
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1944480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: WI
Alter: 11,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 06.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

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

Extra dose administered Wrong product administered Incorrect dose administered No adverse event

Symptomtext

On 12/06/the 2021-Patient received Covid Pfizer vaccine. The dose was for 12+. She should have received the 5-11 dose as she was 11. No adverse effects

Weitere VAERSDATA-Felder

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

VAERS 2569340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: KS
Alter: 29,0
Geschlecht: F
Eingang: 27.01.2023
Impfdatum: 27.10.2021
Beginn: 23.09.2022
Tage bis Beginn: 331,0
Dosis: 3
Route/Site: IM / LA

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

Autoimmune disorder Benign hydatidiform mole

Symptomtext

Worsened autoimmunity precipitating molar pregnancy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Autoimmune disorder
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: levothyroxine
Allergien: -
Vorherige Impfungen: -

VAERS 2560118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 09.12.2021
Beginn: 07.12.2022
Tage bis Beginn: 363,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after three vaccines Pfizer 3/9/21 Lot# EN6206; Pfizer 3/30/21 Lot# ER8730; Pfizer 12/9/21 Lot# 33130BA

Weitere VAERSDATA-Felder

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

VAERS 2561207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 06.01.2022
Beginn: 19.08.2022
Tage bis Beginn: 225,0
Dosis: 1
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2545847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 20.12.2021
Beginn: 26.12.2022
Tage bis Beginn: 371,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID vaccine breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID positive test 12/26/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2545069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: TN
Alter: 40,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 22.12.2021
Beginn: 01.03.2022
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Fungal infection Herpes zoster Immune system disorder Influenza virus test negative SARS-CoV-2 test positive Tooth abscess Upper respiratory tract infection Urinary tract infection X-ray normal

Symptomtext

I've had immunity issues ever since receiving my third dose. I contracted COVID-19 in March of 2022. I then had a really bad upper respiratory infection. I've had a few other things but also contracted Shingles in July of 2022. After recovering from Shingles, I had a tooth abscess and since then I've had yeast infections and urinary tract infections. My immunity just hasn't been the same.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: MAR2022 at home COVID-19 positive; MAY2022 X-Ray, nothing found; Flu test negative
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril; FLEXERIL; BUSPAR; TYLENOL; ibuprofen
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2543742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 20.12.2022
Beginn: 26.12.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: - / -

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

Unevaluable event

Symptomtext

HOPITALIZATION

Weitere VAERSDATA-Felder

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

VAERS 2537705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 17.12.2021
Beginn: 07.09.2022
Tage bis Beginn: 264,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

9/7/2022 Asymptomatic until testing. A PCR COVID-19 test through a local hospital. Doctor prescribed treating symptomatically and to rest. After the recommended period of isolation, cleared by doctor to return to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 9/7/2022 A PCR COVID-19 positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Desmopressin; SYNTHROID
Allergien: No
Vorherige Impfungen: -

VAERS 2536770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MD
Alter: 45,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 18.12.2021
Beginn: 01.07.2022
Tage bis Beginn: 195,0
Dosis: 3
Route/Site: IM / LA

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

Sensory loss

Symptomtext

In July of 2022, I noticed loss of sensitivity of left index finger and right middle finger. I am seeing a doctor on Thursday regarding this. I saw my PCP and they referred me to Neurology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sensory loss
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Sleep Apnea
Andere Medikamente: Lisinopril; FLONASE; loratadine; multivitamin; albuterol
Allergien: N/A
Vorherige Impfungen: Dose 2 Pfizer, 11/24/2021, bilateral twitching of my cheeks

VAERS 2530977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: NJ
Alter: 57,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 29.12.2020
Beginn: 03.06.2022
Tage bis Beginn: 521,0
Dosis: UNK
Route/Site: - / -

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

Antiphospholipid syndrome Blood test Platelet count decreased

Symptomtext

On 06/03/2022 I had blood work done for upcoming surgery, it was noted that my platelet count was in the 80's. I had repeat blood work done on 06/08/2022 and my platelet count dropped into the 70's. I was scheduled to see a hemotologist and he scheduled a series of tests. My platelet count remained low dropping into the 60's. During the tests it was determined I had developed Antiphospholipid Antibody Syndrome. Since this diagnosis on 06/28/2022 I was placed on 81mg Aspirin daily. On 10/21/2022, I was put on hydroxychoroquine 200 mg twice a day in hopes to raise my platelet count. To date my count is 69. My surgery has been cancelled and I was advised not to have my surgery until platelets increase.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Antiphospholipid syndrome
Hospital-Tage: -
Labordaten: Platelet count 06/03/2022, 06/08/22, 06/21/22, 06/28/22, 09/15/22/, 10/17/22, 11/17/22, 12/12/22
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamin C and Elderberry
Allergien: sulfa, shellfish
Vorherige Impfungen: -

VAERS 2504563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 18,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 08.04.2021
Beginn: 13.09.2022
Tage bis Beginn: 523,0
Dosis: 3
Route/Site: - / -

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

Bone debridement COVID-19 Medical procedure SARS-CoV-2 test positive

Symptomtext

09/13/22 presents to Orthopedic Surgery for "Incision and debridement of right femur". PMHx of "no past medical history on file"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone debridement
Hospital-Tage: -
Labordaten: 09/12/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 08.05.2021
Beginn: 06.09.2022
Tage bis Beginn: 486,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Maternal exposure before pregnancy SARS-CoV-2 test positive Spontaneous rupture of membranes

Symptomtext

09/06/22 presents to Triage Center for "SROM" "40w1d" PMHx of "Hypothyroidism"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 09/06/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2485117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 16,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 13.01.2022
Beginn: 20.10.2022
Tage bis Beginn: 280,0
Dosis: 2
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

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID+ 10/20/22
Aktuelle Erkrankungen: -
Vorgeschichte: ADHD, bipolar, type 1 diabetes with frequent PICU admissions for DKA,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2482554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MA
Alter: 56,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 16.12.2021
Beginn: 01.10.2022
Tage bis Beginn: 289,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

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 male patient received BNT162b2 (BNT162B2), on 05Apr2021 as dose 1, single (Lot number: EB8737), in left arm, on 26Apr2021 as dose 2, single (Lot number: EW0172), in left arm and on 16Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 56 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Congenital Adrenal Hyperplasia" (unspecified if ongoing). Concomitant medication(s) included: FLUDROCORTISONE, start date: 01Sep2021; HYDROCORTISONE, start date: 01Feb2021. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Oct2022, outcome "unknown" and all described as "COVID 19 treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Oct2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221014; Test Name: Rapid test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Congenital adrenal hyperplasia
Andere Medikamente: FLUDROCORTISONE; HYDROCORTISONE
Allergien: -
Vorherige Impfungen: -

VAERS 2476525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 12.10.2022
Impfdatum: 03.01.2022
Beginn: 11.10.2022
Tage bis Beginn: 281,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

Asymptomatic

Weitere VAERSDATA-Felder

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

VAERS 2450317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MD
Alter: 42,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 29.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

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 43-year-old male patient received BNT162b2 (BNT162B2), on 31Mar2021 at 18:15 as dose 1, single (Lot number: EN6206), in left arm, on 28Apr2021 at 18:00 as dose 2, single (Lot number: EW0171), in left arm and on 29Dec2021 at 10:30 as dose 3 (booster), single (Lot number: 33130BA) at the age of 42 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "anxiety" (unspecified if ongoing); "depression" (unspecified if ongoing); "ADHD" (unspecified if ongoing). Concomitant medication(s) included: BUSPIRONE HCL, start date: 12Jan2022; SERTRALINE HCL, start date: 11Dec2021. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment; Negative, notes: Tested negative at 7th day after initial symptoms; Positive, notes: Tested positive again 2 days later. Therapeutic measures were taken as a result of vaccination failure, covid-19 with Anti-viral Paxlovid for started with 05Sep2022 and stopped on 09Sep2022. No known allergies. Other medication in 2weeks included Hydroxyzine HCL LLC started on 17Jan2022 and Bromphen-PSE-DM 2-30-10 mg/5 ml syrup started on 05Sep2022, Adderall XR started on 25Mar2022, Dextroamp-Amphetamine started on 25Mar2022. Tested negative at 7th day after initial symptoms and positive test. Tested positive again 2 days later. No worsening or recurrence of symptoms yet.

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 test; Test Result: Negative ; Comments: Tested negative at 7th day after initial symptoms; Test Name: Covid test; Test Result: Positive ; Comments: Tested positive again 2 days later
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD; Anxiety; Depression
Andere Medikamente: BUSPIRONE HCL; SERTRALINE HCL
Allergien: -
Vorherige Impfungen: -

VAERS 2440821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 11.01.2022
Beginn: 12.09.2022
Tage bis Beginn: 244,0
Dosis: 3
Route/Site: - / -

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

No adverse event

Symptomtext

NO SYMPTOMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: OH
Alter: 68,0
Geschlecht: M
Eingang: 09.09.2022
Impfdatum: 16.02.2022
Beginn: 21.08.2022
Tage bis Beginn: 186,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

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

VAERS 2433408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 47,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 05.05.2021
Beginn: 12.08.2022
Tage bis Beginn: 464,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Skin irritation Stoma site irritation

Symptomtext

48 y.o. female who presented with peristomal skin irritation. Ostomy nursing evaluated the patient and taught her how to use a new appliance. Diet was advanced to regular diet and patient was taking sufficient PO intake to maintain hydration.Patient was ambulating. The patient was deemed stable for discharge on 8/14/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 4,0
Labordaten: 8/12 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2426692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: TN
Alter: 16,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 01.09.2022
Beginn: 01.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine expired on 8/31/22 and unknowingly gave vaccine 9/1/22. No adverse reaction noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2426679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: TN
Alter: 14,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 01.09.2022
Beginn: 01.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine expired 8/31/2022. Unknowingly gave vaccine 9/1/2022. No reaction reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2426675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: TN
Alter: 47,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 01.09.2022
Beginn: 01.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine expired 8/31/22 and given, unknowingly on 9/1/22. No reaction noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2422185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: WA
Alter: 42,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 27.12.2021
Beginn: 19.08.2022
Tage bis Beginn: 235,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

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 43-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Apr2021 as dose 1, single (Lot number: er8737), in left arm, on 23Apr2021 as dose 2, single (Lot number: ew0161), in right arm and on 27Dec2021 as dose 3 (booster), single (Lot number: 33130ba) at the age of 42 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Overweight" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Demerol, reaction(s): "Known allergies: Demerol"; Topamax, reaction(s): "Known allergies: Topamax". The following information was reported: VACCINATION FAILURE (medically significant) with onset 19Aug2022, outcome "unknown", COVID-19 (medically significant) with onset 19Aug2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Aug2022) Negative, notes: I started feeling unwell the last couple of days after testing negative on 14Aug22 and 15Aug22; (15Aug2022) Negative, notes: I started feeling unwell the last couple of days after testing negative on 14Aug22 and 15Aug22; (19Aug2022) Positive, notes: I just took another home test today 19Aug22 and it is positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Additional information: Patient did not receive any other medications in 2 weeks. Patient had COVID rebound. She started feeling unwell the last couple of days after testing negative on 14Aug22 and 15Aug22. She just took another home test today 19Aug22 and it was positive. No follow-up attempts are possible. No further information is expected. Follow-up (23Aug2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220814; Test Name: Covid-19 test; Test Result: Negative ; Comments: I started feeling unwell the last couple of days after testing negative on 14Aug22 and 15Aug22.; Test Date: 20220815; Test Name: Covid-19 test; Test Result: Negative ; Comments: I started feeling unwell the last couple of days after testing negative on 14Aug22 and 15Aug22.; Test Date: 20220819; Test Name: Covid-19 test; Test Result: Positive ; Comments: I just took another home test today 19Aug22 and it is positive.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Overweight
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2420898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 08.12.2021
Beginn: 26.08.2022
Tage bis Beginn: 261,0
Dosis: 3
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 1/22/21 EL9261, 2/12/21 EL9267, and boosted 12/8/21 33130BA

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive COVID test 08/26/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2417277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: TX
Alter: 64,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 30.12.2021
Beginn: 22.08.2022
Tage bis Beginn: 235,0
Dosis: 2
Route/Site: IM / -

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

Wrong product administered

Symptomtext

Dose 1: Moderna; dose 2: Pfizer in primary series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2415878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 19.08.2022
Impfdatum: 08.12.2021
Beginn: 07.08.2022
Tage bis Beginn: 242,0
Dosis: 2
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Pt tested positive for COVID on 08/07/2022.

Weitere VAERSDATA-Felder

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

VAERS 2415662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 28.01.2022
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 non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 15Jan2021 at 15:00 as dose 1, single (Lot number: EL1042), in left arm, on 05Feb2021 at 14:00 as dose 2, single (Lot number: EL3302), in left arm, on 17Aug2021 at 13:00 as dose 3 (booster), single (Lot number: FC3180), in left leg and on 28Jan2022 at 13:00 as dose 4 (booster), single (Lot number: 33130BA) at the age of 47 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Multiple Sclerosis" (unspecified if ongoing), notes: (taking immunosuppressant); "Beta Thalassemia Minor" (unspecified if ongoing). Concomitant medication(s) included: GILENYA, start date: 22Nov2020. 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 vaccination failure, 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: Beta thalassemia minor; Multiple sclerosis ((taking immunosuppressant))
Andere Medikamente: GILENYA
Allergien: -
Vorherige Impfungen: -

VAERS 2412024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: AZ
Alter: 40,0
Geschlecht: M
Eingang: 16.08.2022
Impfdatum: 28.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19; COVID 19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40-year-old male patient received BNT162b2 (BNT162B2), on 28Feb2022 as dose 3 (booster), single (Lot number: 33130BA) at the age of 40 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Epilepsy" (unspecified if ongoing); "gout" (unspecified if ongoing); "skin cancer" (unspecified if ongoing). Concomitant medication(s) included: LACOSAMIDE; ZONISAMIDE; ALLOPURINOL. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06Aug2022) Negative, notes: Tested negative on 6Aug2022; (11Aug2022) Positive, notes: on 11Aug2022 and tested positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: Rebound. Patient took paxlovid on 1Aug2022-5Aug2022. Tested negative on 6Aug2022, no symptoms 6Aug2022-10Aug2022, then started having symptoms again (runny nose & congestion) on 11Aug2022 and tested positive. Had bad diarrhea while on paxlovid from 1Aug2022-5Aug2022.The patient had no known allergies. No follow-up attempts are possible. No further information is expected

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220806; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Tested negative on 6Aug2022; Test Date: 20220811; Test Name: Covid-19 Test; Test Result: Positive ; Comments: on 11Aug2022 and tested positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Epilepsy; Gout; Skin cancer
Andere Medikamente: LACOSAMIDE; ZONISAMIDE; ALLOPURINOL
Allergien: -
Vorherige Impfungen: -

VAERS 2407303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: KY
Alter: 54,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 26.08.2021
Beginn: 08.05.2022
Tage bis Beginn: 255,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Nephrolithiasis

Symptomtext

Patient was admitted to the hospital with COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Autoimmune disease, Depression, Glaucoma, Kidney stone (10/2021), MS (multiple sclerosis), and Staghorn calculus
Andere Medikamente: restasis, aspirin, fosamax, zoloft, cialis, psilosec, singulair, vitamin C, vitamin d3
Allergien: None known
Vorherige Impfungen: -

VAERS 2395984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: MO
Alter: 37,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 22.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective

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 37-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 22Dec2021 at 15:00 as dose 3 (booster), single (Lot number: 33130ba) at the age of 37 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 was not reported. Concomitant medication(s) included: MUCINEX, start date: 12Jul2022, stop date: 21Jul2022; IBUPROFEN, start date: 12Jul2022, stop date: 21Jul2022. Past drug history included: Septra, reaction(s): "Known allergies: Septra". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Paxlovid treatment given from 14Jul2022 to 18Jul2022 for covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: MUCINEX; IBUPROFEN
Allergien: -
Vorherige Impfungen: -

VAERS 2395881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: AZ
Alter: 47,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 09.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

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 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 22Mar2021 at 20:00 as dose 1, single (Lot number: ER2613), in left arm, on 12Apr2021 at 01:00 as dose 2, single (Lot number: ER8729), in left arm and on 09Dec2021 at 19:00 as dose 3 (booster), single (Lot number: 33130BA) at the age of 47 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Obesity" (unspecified if ongoing), notes: Other medical history: Obesity; "Known allergies: Mango" (unspecified if ongoing), notes: Known allergies: Mango. Concomitant medication(s) included: TYLENOL, start date: 10Jul2022, stop date: 12Jul2022. The following information was reported: 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 information:-Patient received paxlovid from 11jul2022 to 15jul2022 for COVID 19 treatment. Completed Paxlovid prescription as directed. No symptoms as of Saturday 16Jul2022. Started having symptoms again Tuesday 19Jul2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fruit allergy (Known allergies: Mango); Obesity (Other medical history: Obesity)
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 2388074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 06.01.2022
Beginn: 21.07.2022
Tage bis Beginn: 196,0
Dosis: 2
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 two vaccines Pfizer 12/16/21 Lot# 33130BA; Pfizer 1/6/22 Lot# 33130BA

Weitere VAERSDATA-Felder

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

VAERS 2432367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 32,0
Geschlecht: M
Eingang: 22.07.2022
Impfdatum: 04.01.2022
Beginn: 13.07.2022
Tage bis Beginn: 190,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Narrative: Fully vaccinated, admitted for SI and found to be COVID positive

Weitere VAERSDATA-Felder

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

VAERS 2371656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: AZ
Alter: 44,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 12.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 45-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Dec2021 at 10:00 as dose 3 (booster), single (Lot number: 33130BA) at the age of 44 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Penicillin" (unspecified if ongoing). 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) Positive, notes: Treatment of COVID-19; (unspecified date) Negative, notes: after days of testing negative; (11Jul2022) Positive, notes: tested positive again. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Information: Anti-viral details included: Product: COVID 19 Treatment, Brand was Paxlovid. Treatment start date was on 02Jul2022, Treatment stop date was on 06Jul2022, Indication was for Treatment of COVID-19. 6 days after completing course of Paxlovid, patient feel sick and tested positive again, after days of testing negative. No follow-up attempts possible. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19; Test Result: Positive ; Comments: Treatment of COVID-19; Test Name: Covid-19; Test Result: Negative ; Comments: after days of testing negative; Test Date: 20220711; Test Name: Covid-19; Test Result: Positive ; Comments: tested positive again
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2367722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 88,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 12.01.2022
Beginn: 22.06.2022
Tage bis Beginn: 161,0
Dosis: 2
Route/Site: - / -

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

COVID-19

Symptomtext

covid

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 19,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2366471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: OK
Alter: 51,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Flushing Head discomfort Hyperhidrosis Lip swelling

Symptomtext

1447 NURSES CALLED TO OBSERVATION ROOM IN REGARDS TO A CLIENT WHO SAYS HER UPPER LIP IS SWELLING AND HER HEAD IS FEELING HEAVY. CLIENTS DAUGHTER PRESENT BESIDE HER. UPON ARRIVAL TO ROOM, CLIENT PRESENTS WITH REDNESS/FLUSHING TO FACE, SWEATING, AND UPPER LIP SWELLING. BP 119/73. O2 ADMINISTERED @ 8L VIA NON-REBEATHER MASK. BENADRYL 1 ML GIVEN TO LEFT DELTOID @ 1453. BP RECHECK 166/115. 1456 EMS CALLED BY AA. 1458 0.3 MG OF EPI ADMINISTERED TO LVL. 1500 BP RECHECK 153/98. 1502 EMS ARRIVED AND TOOK OVER CARE. REPORT GIVEN AT ER. EMS TRANSFERRED CLIENT WITH NO FURTHER INTERVENTIONS AT THAT TIME @ 1521.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Erythema
Hospital-Tage: -
Labordaten: TRANSPORTED TO HOSPITAL BY EMS
Aktuelle Erkrankungen: RAPID HEART PALPATATIONS, RHEUMATIOD ARTHRITIS, AND THYRIOD PROBLEMS
Vorgeschichte: SEE ABOVE
Andere Medikamente: CLIENTS DAUGHTER STATES SHE TAKES MULTIPLE DIFFERENT DAILY MEDICATIONS
Allergien: SEAFOOD
Vorherige Impfungen: -

VAERS 2359272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 20.12.2021
Beginn: 01.06.2022
Tage bis Beginn: 163,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Investigation SARS-CoV-2 test Vaccination failure

Symptomtext

testing positive for COVID; testing positive for COVID; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 48-year-old male patient received BNT162b2 (BNT162B2), on 30Mar2021 as dose 1, single (Lot number: EM9809), on 20Apr2021 as dose 2, single (Lot number: EW0164) and on 20Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 48 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "type 2 diabetes" (unspecified if ongoing); "primary HTN" (unspecified if ongoing); "kidney transplant" (unspecified if ongoing); "GERD" (unspecified if ongoing). Concomitant medication(s) included: CARVEDILOL; GABAPENTIN; INSULIN ASPART; INSULIN DEGLUDEC; MYCOPHENOLATE SODIUM; PANTOPRAZOLE; PREDNISONE; ENVARSUS XR. Past drug history included: Lisinopril, reaction(s): "Known allergies: Lisinopril", notes: Known allergies: Lisinopril. The following information was reported: VACCINATION FAILURE (hospitalization, medically significant), COVID-19 (hospitalization, medically significant) all with onset Jun2022, outcome "unknown" and all described as "testing positive for COVID". The patient was hospitalized for vaccination failure, covid-19 (hospitalization duration: 4 day(s)). The event "testing positive for covid" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: tacrolimus level: (13Jun2022) 80.8 ng/ml, notes: Level was drawn on 13Jun at 04:43 and resulted at 80.8 ng/mL; (14Jun2022) 102.9 ng/ml, notes: An additional level on 14Jun am which was 102.9 ng/mL; (15Jun2022) 70.8 ng/ml, notes: Level down to 70.8 on 15Jun and patient discharged; SARS-CoV-2 test: (09Jun2022) positive, notes: Patient reported testing positive for COVID on a home test on 9Jun. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient reported testing positive for COVID on a home test on 09Jun. contacted his PCP and was prescribed paxlovid (Nirmatrelvir/Ritonavir) for 5 days beginning 09Jun. The patient has taken Paxlovid orally for the treatment of COVID-19 Treatment start date was 08Jun2022 and stop date was 11Jun2022. Patient presented to the ED (emergency department) on the afternoon of 12Jun with main c/o (complaint of) worsening severe headache as well dry cough and sore throat. Patient had taken 7 of 10 prescribed doses of Paxlovid prior to admission. Patient was on immunosuppression with Envarsus XR 4 mg daily so tacrolimus level was ordered for 13Jun due to interaction. Level was drawn on 13Jun at 04:43 and resulted at 80.8 ng/mL (therapeutic range for this patient is 4-8 ng/mL). An additional level on 14Jun am which was 102.9 ng/mL. Ordered phenytoin 300mg po daily in an attempt to increase the rate of metabolism of the tacrolimus. Level down to 70.8 on 15Jun and patient discharged. AKI (Acute kidney injury) and supra therapeutic levels resolved within days of discharge. The patient was hospitalized for 4days. Phenytoin was received as the treatment for the adverse event.; Sender's Comments: Based on plausible dose -event relationship post vaccination and no other alternate explanation the causal role of BNT162B2 cannot be excluded for the reported LOE events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 4,0
Labordaten: Test Date: 20220613; Test Name: tacrolimus level; Result Unstructured Data: Test Result:80.8 ng/ml; Comments: Level was drawn on 13Jun at 04:43 and resulted at 80.8 ng/mL; Test Date: 20220614; Test Name: tacrolimus level; Result Unstructured Data: Test Result:102.9 ng/ml; Comments: An additional level on 14Jun am which was 102.9 ng/mL; Test Date: 20220615; Test Name: tacrolimus level; Result Unstructured Data: Test Result:70.8 ng/ml; Comments: Level down to 70.8 on 15Jun and patient discharged.; Test Date: 20220609; Test Name: home test; Test Result: Positive ; Comments: Patient reported testing positive for COVID on a home test on 9Jun
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD; Kidney transplant; Primary hypertension; Type 2 diabetes mellitus
Andere Medikamente: CARVEDILOL; GABAPENTIN; INSULIN ASPART; INSULIN DEGLUDEC; MYCOPHENOLATE SODIUM; PANTOPRAZOLE; PREDNISONE; ENVARSUS XR
Allergien: -
Vorherige Impfungen: -

VAERS 2357246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 04.07.2022
Impfdatum: 04.01.2022
Beginn: 01.07.2022
Tage bis Beginn: 178,0
Dosis: 3
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

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID+ 7/1/22
Aktuelle Erkrankungen: -
Vorgeschichte: obesity, afib,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2344904

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 33130BA

gering

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 04.07.2022
Impfdatum: 02.01.2022
Beginn: 23.06.2022
Tage bis Beginn: 172,0
Dosis: 3
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

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID+6/23/22
Aktuelle Erkrankungen: -
Vorgeschichte: atrial fibrillation on Eliquis, and chronic kidney disease, Acute kidney insufficiency, Frontal mass of brain, Hypercalcemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2342979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CO
Alter: 72,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 01.12.2021
Beginn: 10.01.2022
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: IM / AR

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

Biopsy Neuropathy peripheral

Symptomtext

Peripheral neuropathy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy
Hospital-Tage: -
Labordaten: Leg biopsy
Aktuelle Erkrankungen: -
Vorgeschichte: PBC., Hashimoto?s
Andere Medikamente: Synthoid, ursodiol, valsartan, Vit D
Allergien: None
Vorherige Impfungen: -

VAERS 2325287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 15.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / RA

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

Papilloma viral infection SARS-CoV-2 test

Symptomtext

Recurrence of HPV; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 15Jan2022 as dose 3 (booster), single (Lot number: 33130BA) at the age of 31 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Allergies" (unspecified if ongoing), notes: Allergies; "Asthma" (unspecified if ongoing); "Soy allergy" (unspecified if ongoing); "Egg allergy" (unspecified if ongoing); "HPV" (unspecified if ongoing), notes: Had a recurrence of HPV which had been dormant for over 10 years prior to booster. Concomitant medication(s) included: ALLEGRA D; SINGULAIR; NUVARING; OMEPRAZOLE. Vaccination history included: pfizer (DOSE NUMBER; 2, Batch/Lot No: FC3180, Location of injection: Arm Left), administration date: 22Aug2021, for COVID-19 immunization; pfizer (DOSE NUMBER: 1, Batch/Lot No: EW0181, Location of injection: Arm Right), administration date: 31Jul2021, for COVID-19 immunization. The following information was reported: PAPILLOMA VIRAL INFECTION (non-serious) with onset 25Jan2022, outcome "recovering", described as "Recurrence of HPV". The event "recurrence of hpv" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of papilloma viral infection. Additional information: No any other vaccine in four weeks. Patient did not experience COVID prior vaccination. If COVID tested post vaccination: Yes. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination,patient been tested for COVID-19. Device date: 16Jun2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Papilloma viral infection
Hospital-Tage: -
Labordaten: Test Date: 20220131; Test Name: COVID test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Allergies); Asthma; Egg allergy; HPV infection (Had a recurrence of HPV which had been dormant for over 10 years prior to booster); Soy allergy
Andere Medikamente: ALLEGRA D; SINGULAIR; NUVARING; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2325202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: MN
Alter: 72,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 08.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Nurse) from product quality group. A 72-year-old male patient received BNT162b2 (BNT162B2), on 08Dec2021 as dose 3 (booster), single (Lot number: 33130ba) at the age of 72 years, in left arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 05Feb2021 as dose 1, single (Batch/Lot number: unknown), in left arm and on 05Mar2021 as dose 2, single (Lot number: 022m20A), 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: COVID-19 (medically significant), DRUG INEFFECTIVE (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; Unknown results. Therapeutic measures were taken as a result of covid-19, drug ineffective. Conclusion of Previously Completed Investigation : The complaint for a lack of effect in a vial of PFIZER-BIONTECH COVID-19 VACCINE was investigated. The investigation included reviewing incoming quality and manufacturing batch records, deviation investigations, an analysis of the complaint history for the reported lot and product type and final release assay testing. This product is received as preformulated bulk, and is manufactured, labeled, and packaged by Pfizer. The final scope was determined to be lot 33130BA. No quality issues were identified during the investigation. There is no impact on product quality. An NTM was not issued for the complaint. No regulatory notification or SQRTs/AQRTs were held because of this complaint. The complaint condition of lack of effect was not confirmed, therefore the root cause cannot be attributed to the manufacture or vendor processes as incoming quality component testing and all analytical tests performed at the time of lot release confirmed that the batch met all release specifications. No corrective or preventative actions are required as the complaint condition was not determined to be manufacture or vendor related and there are quality systems in place to detect defects prior to any lot being released to the market. Follow-up (16Jun2022): This is a spontaneous follow-up report from product quality group providing investigation results. This report included that: Updated Information included: Batch and lot tested and found within specifications in Product tab per verbatim (The complaint condition of lack of effect was not confirmed, therefore the root cause cannot be attributed to the manufacture or vendor processes as incoming quality component testing and all analytical tests performed at the time of lot release confirmed that the batch met all release specifications); Sender's Comments: The reported COVID-19 positive after COVID-19 immunization is considered ineffective of BNT162B2, and the Company cannot completely exclude the possible causality between the reported events and BNT162B2 administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Sars-CoV-2 test; Test Result: Positive ; Test Name: Sars-CoV-2 test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 17.12.2021
Beginn: 15.06.2022
Tage bis Beginn: 180,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Inappropriate schedule of product administration SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

covid vaccine breakthrough case dose 1 Pfizer 6/22/21 EW0191 dose 2 Pfizer 7/22/21 FA7485

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid + test on 6/15/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2320177

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 09.12.2021
Beginn: 08.06.2022
Tage bis Beginn: 181,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Rectal haemorrhage SARS-CoV-2 test positive

Symptomtext

Narrative: COVID fully vaccinated, incidentally COVID positive on admit for BRBPR

Weitere VAERSDATA-Felder

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

VAERS 2314036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 09.06.2022
Impfdatum: 08.06.2022
Beginn: 09.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient was given 2nd booster (4th dose), thinking it was the first booster, and after vaccine was administered, it was realized that patient already received the first booster and was not eligible for the 2nd booster yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19 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 43-year-old male patient received BNT162b2 (BNT162B2), as dose 3 (booster), single (Lot number: 33130BA) 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 was not reported. The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), outcome "unknown", 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: Unknown results. Therapeutic measures were taken as a result of drug ineffective, covid-19. This report was about COVID-19 treatment. Patient did receive the vaccine. Patient received other medication in 2 weeks. Patient received paxlovid as a treatment for COVID-19. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200781668 Same patient, different product and event

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2306905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 27.03.2021
Beginn: 14.02.2022
Tage bis Beginn: 324,0
Dosis: 3
Route/Site: IM / UN

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

COVID-19 Mental status changes SARS-CoV-2 test positive

Symptomtext

This is a 74-year-old female brought from home for altered mental status per EMS on 2/14. Found to be COVID positive 2/14. Pt in no apparent distress, respirations even & non labored. Pt. awake, alert and oriented x2, external cath placed, gown/linens are clean & dry. IV site without redness or swelling, pt denies pain/discomfort at insertion site and denied any needs. States able to breathe easy. Tolerating very well. RA O2. No anti-COVID rx needed 2/15. Found to be drastically improved the morning after admission without any complaints and discharged to home 2/15.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 2,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic hepatitis C Endocrine Diabetic polyneuropathy Chronic hepatitis C Dysphagia GERD (gastroesophageal reflux disease) Diabetic polyneuropathy associated with type 2 diabetes mellitus Type 2 diabetes mellitus with stage 4 chronic kidney disease Chest pain Hypertension Paresis Weakness of left side of body Accelerated hypertension Fall Hypertensive urgency Dizziness Acute renal failure superimposed on stage 3 chronic kidney disease Intracranial bleed Hypertensive emergency Left spastic hemiparesis & left basal ganglia and frontal lobe ICH Macular degeneration of right eye Anemia Left facial hypoesthesia Mild cognitive impairment, so stated Hemorrhagic cerebrovascular accident (CVA) Sepsis AKI on CKD stage 4, GFR 15-29 ml/min QTc prolongation Left knee pain Situational stress Diarrhea COVID-19 virus infection Stage 3b chronic kidney disease
Andere Medikamente: acetaminophen (TYLENOL) 325 MG PO Tab, acetaminophen (TYLENOL) 325 MG PO Tab amLODIPine (NORVASC) 10 MG PO Tab atorvastatin (LIPITOR) 20 MG PO Tab calcium carbonate antacid (TUMS) 500 MG PO Chew Tab cloNIDine (CATAPRES) 0.2 MG/24HR TRANSD
Allergien: Compazine, shellfish-derived products, almonds
Vorherige Impfungen: -

VAERS 2306343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: FL
Alter: 37,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 14.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 38-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Apr2021 at 15:00 as dose 1, single (Batch/Lot number: unknown), in left arm, on 03Jun2021 at 12:00 as dose 2, single (Batch/Lot number: unknown), in left arm and on 14Dec2021 at 10:00 as dose 3(booster), single (Lot number: 33130BA) at the age of 37 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Sulfa drugs 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), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Treatment of COVID-19; (07May2022) Negative, notes: Tested negative 8 days after I began my Paxlovid treatment; (09May2022) Positive, notes: 2 days later I tested positive again. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical closure: The patient was taking other medications/products within 2 weeks of starting COVID-19 treatment (Ibuprofen from 28Apr2022 to 02may2022 and Prednisone from 29-Apr2022 to 05May2022). The patient previously received a COVID-19 Vaccine. Tested negative 8 days after she began her Paxlovid treatment. From 29Apr2022 to 03May2022 2 days later she tested positive again and had completely different symptoms and felt worse than she did the first time around. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: Based on reported information, causal association of event vaccination failure, covid-19 with BNT162b2 cannot be excluded. However, response to vaccine can vary in individuals.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20220507; Test Name: COVID-19 test; Test Result: Negative ; Comments: Tested negative 8 days after I began my Paxlovid treatment.; Test Date: 20220509; Test Name: COVID-19 test; Test Result: Positive ; Comments: 2 days later I tested positive again.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2306324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MA
Alter: 54,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 06.12.2021
Beginn: 01.05.2022
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: - / LA

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). The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Apr2021 at 10:00 as dose 1, single (Lot number: ER8737), in left arm, on 19Apr2021 at 14:00 as dose 2, single (Lot number: EW0164), in left arm and on 06Dec2021 at 10:00 as dose 3 (booster), single (Lot number: 33130BA) at the age of 54 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: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset May2022, outcome "unknown" and all described as "COVID-19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course information: It was reported that the patient had no known allergies and the patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment. No follow-up attempts are possible and no further information is expected.

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, Comment: No other medical history, No known allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2294470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 09.12.2021
Beginn: 25.05.2022
Tage bis Beginn: 167,0
Dosis: 3
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Patient received Moderna as D1 and D2 and then received Pfizer as AD in error, as indicated on this report. AD dose was given 12/09/2021 and error discovered today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2294371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 08.12.2021
Beginn: 23.05.2022
Tage bis Beginn: 166,0
Dosis: 2
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

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID+ test on 5/23/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2294110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 09.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

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 52-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Mar2021 at 13:30 as dose 1, single (Lot number: EN6205), in left arm, on 30Mar2021 as dose 2, single (Lot number: EP7533), in left arm and on 09Dec2021 as dose 3 (booster), single (Lot number: 33130BA) at the age of 51 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: soy allergy" (unspecified if ongoing), notes: Known allergies: soy allergy. Concomitant medication(s) included: QVAR REDIHALER, start date: 06May2022, stop date: 15May2022. Past drug history included: Allergic to cipro antibiotic, reaction(s): "Allergy: Cipro", notes: Known allergies: Allergic to Cipro antibiotic. The following information was reported: COVID-19 (medically significant), VACCINATION FAILURE (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: (13May2022) Positive, notes: I tested still positive with Covid. Therapeutic measures were taken as a result of covid-19, vaccination failure. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220513; Test Name: Covid; Test Result: Positive ; Comments: I tested still positive with Covid
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Soy allergy (Known allergies: soy allergy)
Andere Medikamente: QVAR REDIHALER
Allergien: -
Vorherige Impfungen: -

VAERS 2289330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: NE
Alter: 19,0
Geschlecht: M
Eingang: 21.05.2022
Impfdatum: 10.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / UN

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

Blood test normal Breast tenderness Mammogram normal Ultrasound breast normal

Symptomtext

NOTICED BREAST TENDERNESS AND DEVELOPMENT OUT OF NOWHERE. WENT TO PRIMARY PHYSICIAN AND HAD BLOOD TESTS, MAMMOGRAM AND ULTRASOUND PERFORMED. FOUND NO CONCLUSIVE PATHOPHYSIOLOGY FROM ALL THE TESTS CONCLUSION IS IDIOPATHIC. NEVER BEEN OVERWEIGHT AND BMI IS NORMAL SO THIS WAS ALSO RULED OUT AS A CAUSE

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Praegender Schweregrund: Blood test normal
Hospital-Tage: -
Labordaten: ALL BLOOD WORK, MAMMOGRAM, ULTRASOUND ON 05/11/2022 AND 05/16/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: SEASONAL
Vorherige Impfungen: -

VAERS 2287211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 28.12.2021
Beginn: 19.05.2022
Tage bis Beginn: 142,0
Dosis: UNK
Route/Site: - / -

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

Asymptomatic COVID-19 SARS-CoV-2 test positive

Symptomtext

positive covid test in vaccinated and boostered asymptomatic pt

Weitere VAERSDATA-Felder

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

VAERS 2286629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 14.01.2022
Beginn: 24.04.2022
Tage bis Beginn: 100,0
Dosis: 4
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

tested positive for Covid on 24Apr2022; tested positive for Covid on 24Apr2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team and product quality group. The reporter is the patient. A 70-year-old male patient received BNT162b2 (BNT162B2), on 08Feb2021 as dose 1, single (Lot number: FN6201), on 01Mar2021 as dose 2, single (Lot number: EN6201), on 14Aug2021 as dose 3 (booster), single (Lot number: FC3180) and on 14Jan2022 as dose 4 (booster), single (Lot number: 33130BA) at the age of 69 years for covid-19 immunisation. The patient's relevant medical history included: "AIDS" (unspecified if ongoing), notes: AIDS had Aids for 30 years or more, viral load is at 150 last time; "Blood pressure high" (ongoing), notes: Blood pressure high controlled, diagnosed 6 or 7 years ago, not completely sure; "mild kidney issue" (unspecified if ongoing), notes: been on for 5 or 6 years splits up the doses because of a mild kidney issue. The patient's family history included: "Prediabetes" (ongoing), notes: Prediabetes Has always been pre diabetic, his father was also diabetic. Concomitant medication(s) included: LOSARTAN taken for hypertension. The following information was reported: VACCINATION FAILURE (medically significant) with onset 24Apr2022 at 08:00, outcome "unknown", COVID-19 (medically significant) with onset 24Apr2022 at 08:00, outcome "not recovered" and all described as "tested positive for Covid on 24Apr2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (24Apr2022) Positive, notes: States he first tested positive for Covid on 24Apr2022 at 8am; (02May2022) Negative, notes: States he did test negative, first on 02May2022, and then again on 03May2022 and 06May2022; (03May2022) Negative, notes: States he did test negative, first on 02May2022, and then again on 03May2022 and 06May2022; (06May2022) Negative, notes: States he did test negative, first on 02May2022, and then again on 03May2022 and 06May2022; (12May2022) Positive, notes: and tested again on 12May2022 and it was positive; (13May2022) Positive, notes: states he tested again today to make sure and he was even more positive today than he was yesterday. Therapeutic measures were taken as a result of covid-19. Clinical course: Additional information: Caller states he is calling about Paxlovid, caller began a treatment of Paxlovid in the evening of 24Apr2022 and went through the course for 5 days and states yesterday he retested positive for Covid again, wanting to know if he can do Paxlovid a second time, doctor advised not to, but he wanted to know if we had any information about a second treatment of Paxlovid Caller states he does have health is. ues that we should know about. Caller states he goes to (Name withheld) and it is a little convoluted. Called a number and someone (Name withheld) prescribed the medication, caller states he has a primary care doctor as well but there is an HIV Pharmacist he sees, states that is who he would like to be contacted if necessary, goes by "(Name withheld)" but her name is listed as (Name withheld), Pharmacist Doctor, HIV Coordinator, the chief pharmacist, states she has been his primary contact been with her for 30 years. States he first tested positive for Covid on 24Apr2022 at 8am, that is the day he started the medication. Continued the medication for 5 days and ended the doses on 29Apr2022, caller states he never felt completely better, states he even wrote a letter to primary care and Phooey that he thought maybe he had long Covid since he did not get to feeling better with the Paxlovid treatment. States he did test negative, first on 02May2022, and then again on 03May2022 and 06May2022. States he started feeling a little bit worse and tested again on 12May2022 and it was positive, states he tested again today to make sure and he was even more positive today than he was yesterday. States he uses the Health tests. States they have a control line and test line and test line changed faster than the control line, states it was darker today than yesterday, which is interesting because he states he feels better today than yesterday. Caller states he does have AIDS, has had it for 30 years or so. Caller also wants to know if Paxlovid can make HIV drugs less effective, caller states he is just wondering because he heard that somewhere and does not believe it. Caller during transfer to agent mentioned he also had 4 doses of the Pfizer Covid vaccine prior to the Paxlovid treatment. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220424; Test Name: tested positive for Covid; Test Result: Positive ; Comments: States he first tested positive for Covid on 24Apr2022 at 8am; Test Date: 20220502; Test Name: tested positive for Covid; Test Result: Negative ; Comments: States he did test negative, first on 02May2022, and then again on 03May2022 and 06May2022; Test Date: 20220503; Test Name: tested positive for Covid; Test Result: Negative ; Comments: States he did test negative, first on 02May2022, and then again on 03May2022 and 06May2022; Test Date: 20220506; Test Name: tested positive for Covid; Test Result: Negative ; Comments: States he did test negative, first on 02May2022, and then again on 03May2022 and 06May2022; Test Date: 20220512; Test Name: tested positive for Covid; Test Result: Positive ; Comments: and tested again on 12May2022 and it was positive; Test Date: 20220513; Test Name: tested positive for Covid; Test Result: Positive ; Comments: states he tested again today to make sure and he was even more positive today than he was yesterday.
Aktuelle Erkrankungen: Blood pressure high (Blood pressure high controlled, diagnosed 6 or 7 years ago, not completely sure); Prediabetes (Prediabetes Has always been pre diabetic, his father was also diabetic.)
Vorgeschichte: Medical History/Concurrent Conditions: AIDS (AIDS had Aids for 30 years or more, viral load is at 150 last time); Kidney disorder (been on for 5 or 6 years splits up the doses because of a mild kidney issue.)
Andere Medikamente: LOSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2286609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: PA
Alter: 50,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 28.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

Did you/the patient previously receive a COVID-19 Vaccine?: Yes; COVID-19; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 19Mar2021 as dose 1, single (Lot number: EP7534), in left arm, on 08Apr2021 as dose 2, single (Lot number: EW015B), in left arm and on 28Jan2022 as dose 3 (booster), single (Lot number: 33130BA) at the age of 50 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "HTN" (unspecified if ongoing); "hysterectomy" (unspecified if ongoing); "depression" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "cholecystectomy" (unspecified if ongoing); "appendectomy" (unspecified if ongoing); "tubal ligation" (unspecified if ongoing). Concomitant medication(s) included: DULOXETINE; PREVACID; RESTASIS; METOPROLOL; VITAMIN D NOS; CLARITINE; VITAMIN B COMPLEX. Past drug history included: Taviste-d, reaction(s): "known allergies Taviste-D", notes: known allergies Taviste-D. The following information was reported: VACCINATION FAILURE (medically significant), outcome "unknown", described as "Did you/the patient previously receive a COVID-19 Vaccine?: Yes"; COVID-19 (medically significant), outcome "unknown". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course included Known allergies of Taviste-D. Treatment for COVID-19 included paxlovid. No follow-up attempts possible. No further information expected.; Sender's Comments: Based on the information currently available, a possible contributory role of the suspect drug to the reported events Vaccination failure , COVID-19 cannot be completely excluded based on temporal association.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Appendectomy; Cholecystectomy; Depression; Hypertension; Hysterectomy; Tubal ligation
Andere Medikamente: DULOXETINE; PREVACID; RESTASIS; METOPROLOL; VITAMIN D NOS; CLARITINE; VITAMIN B COMPLEX
Allergien: -
Vorherige Impfungen: -

VAERS 2283063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 27,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 13.12.2021
Beginn: 26.04.2022
Tage bis Beginn: 134,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Inguinal hernia Inguinal hernia repair SARS-CoV-2 test positive

Symptomtext

4/26 The patient was admitted to the hospital after presenting to the emergency department with the left inguinal hernia. Underwent hernia repair.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 5,0
Labordaten: 4/27 SARS-CoV-2 (COVID-19), Micro Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2275354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: SC
Alter: 69,0
Geschlecht: M
Eingang: 13.05.2022
Impfdatum: 17.12.2021
Beginn: 26.04.2022
Tage bis Beginn: 130,0
Dosis: 3
Route/Site: - / RA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment/Tested positive on 26Apr2022; COVID 19 Treatment/Tested positive on 26Apr2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received BNT162b2 (BNT162B2), on 13Jan2021 at 09:00 as dose 1, single (Lot number: EL0142), in left arm, on 03Feb2021 at 12:00 as dose 2, single (Lot number: EL9265), in right arm and on 17Dec2021 at 10:00 as dose 3 (booster), single (Lot number: 33130BA) at the age of 69 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "High BP" (unspecified if ongoing); "arterial plaque" (unspecified if ongoing). Concomitant medication(s) included: IRON. The following information was reported: VACCINATION FAILURE (medically significant) with onset 26Apr2022, outcome "unknown", COVID-19 (medically significant) with onset 26Apr2022, outcome "recovered" (04May2022) and all described as "COVID 19 Treatment/Tested positive on 26Apr2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (17Apr2022) Negative; (20Apr2022) Negative; (26Apr2022) Positive; (04May2022) Negative. Therapeutic measures were taken as a result of covid-19. Clinical Course: Second vaccine dose caused gastric bloating and ultimately anemia. After seeing a half-dozen mds, convinced my GP to prescribe a steroid dose. Have been taking iron pills for a year. Blood levels after the steroid dose began climbing and are back to normal. Had Covid rebound. After negative tests on 17Apr2022 and 20Apr2022 felt a bad cold hit me on 25Apr2022. Tested positive on 26Apr2022. Began a steriod and antibiotic dose with minerals and vitamins. Tested negative 4May2022. Patient had no other medication in 2 weeks. AE treatment with Methypredisone, azithromyican, vc, vd3, Turmeric. No Known allergies. Other medical history includes High BP, arterial plaque. Anti viral details: Product=COVID 19 Treatment; Treatment start date=13Apr2022; Treatment stop date=17Apr2022; Lot number=Didn't keep this information; Indication=Treatment of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220417; Test Name: Covid Test; Test Result: Negative ; Test Date: 20220420; Test Name: Covid Test; Test Result: Negative ; Test Date: 20220426; Test Name: Covid Test; Test Result: Positive ; Test Date: 20220504; Test Name: Covid Test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atherosclerosis; Blood pressure high
Andere Medikamente: IRON
Allergien: -
Vorherige Impfungen: -

VAERS 2274610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

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Staat: OR
Alter: 52,0
Geschlecht: M
Eingang: 12.05.2022
Impfdatum: 16.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / LA

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

Tinnitus

Symptomtext

I received my first Covid Booster on December 16, 2021. Within the first two days I began to experience extreme ringing in both ears. This has been constant and not subsided since that time (now 5/12/22).

Weitere VAERSDATA-Felder

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

VAERS 2267321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: FL
Alter: 77,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 05.03.2021
Beginn: 08.05.2022
Tage bis Beginn: 429,0
Dosis: 4
Route/Site: - / -

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

Unevaluable event

Symptomtext

patient hospitalized

Weitere VAERSDATA-Felder

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

VAERS 2261941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 27.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Swelling face

Symptomtext

Swelling of the left jaw and left neck for 7 days, pain for 4 wks on the left neck

Weitere VAERSDATA-Felder

Praegender Schweregrund: Swelling face
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: Had COVID 19 Dec 5, 2021 diagnosis
Vorgeschichte: NONE
Andere Medikamente: No other medictaions
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2252806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: NE
Alter: 63,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 22.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Menstruation irregular Postmenopausal haemorrhage

Symptomtext

When I went to the doctor because I started having periods on 12/31/2021. My doctor told me it was due to the vaccine. My periods were be a week long and I would have them on and off every two weeks. I have been menopausal since the early 2000s. It wasn't spotting but it was like a regular menstrual cycle that would taper off towards the end of the week.

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Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Blood work
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid arthritis; Chronic back pain; High cholesterol; Depression; Anxiety
Andere Medikamente: Pristiq; Citalopram; Progesterone; Testosterone; Estradiol; Levomefolate/Algal; Mirtazapine; Lorazepam; Vitamin D3; Curcumin; Probiotic; Tramadol; Ibuprofen; Levothyroxine
Allergien: Compazine; Zofran
Vorherige Impfungen: -

VAERS 2244056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 18,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 03.01.2022
Beginn: 12.03.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / AR

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

Appendicectomy Appendicitis Computerised tomogram abdomen abnormal Laboratory test White blood cell count increased

Symptomtext

Acute appendicitis requiring emergency appendectomy

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Praegender Schweregrund: Appendicectomy
Hospital-Tage: 2,0
Labordaten: 3/13/22: ER visit / labs / CT revealed high white count and CT showed dilated inflamed appendix
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2241015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: AK
Alter: 46,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 18.04.2022
Beginn: 18.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered Product administered to patient of inappropriate age

Symptomtext

Pt was given a second booster, but she does not meet the current CDC guideline requirements (younger than 50 y/o.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: n/a.
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, pre-diabetes.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: IL
Alter: 82,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 19.12.2021
Beginn: 16.04.2022
Tage bis Beginn: 118,0
Dosis: 3
Route/Site: - / -

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

Craniocerebral injury Fall

Symptomtext

s/p mechanical fall, closed head trauma

Weitere VAERSDATA-Felder

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

VAERS 2238607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MN
Alter: 87,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 06.01.2022
Beginn: 17.04.2022
Tage bis Beginn: 101,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Vaccine breakthrough infection

Symptomtext

admitted/hospitalized with breakthrough COVID infection

Weitere VAERSDATA-Felder

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

VAERS 2226094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 21.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / UN

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

Aortic valve incompetence Rhinovirus infection Troponin increased

Symptomtext

Patient presented to the ED and was subsequently hospitalized for rhinovirus infection, severe aortic insufficiency, elevated troponin within 6 weeks of receiving covid vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Aortic valve incompetence
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2216043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 12,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 09.01.2022
Beginn: 15.02.2022
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: IM / UN

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

Chemotherapy Ovarian cancer

Symptomtext

Patient hospitalized for Malignant neoplasm of left ovary, Admission for chemotherapy within 6 weeks of receiving covid vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2214181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 21,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 30.11.2021
Beginn: 24.01.2022
Tage bis Beginn: 55,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Road traffic accident SARS-CoV-2 test positive

Symptomtext

01/24/22 presents to ED for "Motor Vehicle Crash". PMHx of "asthma, GERD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 01/24/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2210897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: RI
Alter: 39,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 28.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Amenorrhoea Dysmenorrhoea Heavy menstrual bleeding SARS-CoV-2 test

Symptomtext

Bleeding for 20 days. Once her period started again, it did not stop; Sometimes heavy flow with several medium sized clots a day; Some slight soreness/cramping; Some slight soreness/cramping; She did not have a period for 65 days; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 28Dec2021 (Lot number: 33130BA) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. The patient had not received any other vaccines within 4 weeks prior to the BNT162B2 vaccine. Relevant medical history included: "Sulfonamide allergy" (unspecified if ongoing); "Shrimp allergy" (unspecified if ongoing). The patient had not experienced Covid-19 prior vaccination. Concomitant medication(s) included: SERTRALINE. Vaccination history included: Bnt162b2 (First dose, Lot. EW0170. Location of injection: arm left), administration date: 22Apr2021, when the patient was 38 years old, for COVID-19 immunization; Bnt162b2 (Second dose, Lot. EW0187), administration date: 27May2021, when the patient was 38 years old, for COVID-19 immunization. The following information was reported: HEAVY MENSTRUAL BLEEDING (medically significant), outcome "unknown", described as "Bleeding for 20 days. Once her period started again, it did not stop"; HEAVY MENSTRUAL BLEEDING (non-serious), outcome "unknown", described as "Sometimes heavy flow with several medium sized clots a day"; DYSMENORRHOEA (non-serious), DYSMENORRHOEA (non-serious), outcome "unknown" and all described as "Some slight soreness/cramping"; AMENORRHOEA (non-serious), outcome "unknown", described as "She did not have a period for 65 days". The events "bleeding for 20 days. once her period started again, it did not stop", "sometimes heavy flow with several medium sized clots a day", "some slight soreness/cramping" and "she did not have a period for 65 days" were evaluated at the physician office visit. Clinical course was the following: patient's period completely changed after receiving her booster shot. Her last cycle ended on the 28Dec2021, the day she got her booster, and then she did not have a period for 65 days. Once her period started again, it did not stop. She had been bleeding for 20 days. Sometimes heavy flow with several medium sized clots a day and some slight soreness/cramping. There were no signs of her cycle changing before the booster. She contacted her doctor to check in and to schedule an appointment at the beginning of the week. Post the vaccination, the patient has been tested for COVID-19. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (19Mar2022) negative, notes: Abbot BinaxNOW Antigen Self Test, Nasal Swab; (08Feb2022) negative, notes: iHealth Antigen Rapid Test, Nasal Swab; (04Jan2022) negative, notes: SARS-CoV-2 RNA (NAA/RT-PCR)(NAA), Nasal Swab. It was unknown if therapeutic measures were taken as a result of heavy menstrual bleeding, heavy menstrual bleeding, dysmenorrhoea, dysmenorrhoea, amenorrhoea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Amenorrhoea
Hospital-Tage: -
Labordaten: Test Date: 20220319; Test Name: Abbot BinaxNOW Antigen Self Test; Test Result: Negative ; Comments: Abbot BinaxNOW Antigen Self Test, Nasal Swab; Test Date: 20220208; Test Name: iHealth Antigen Rapid Test; Test Result: Negative ; Comments: iHealth Antigen Rapid Test, Nasal Swab; Test Date: 20220104; Test Name: SARS-CoV-2 RNA (NAA/RT-PCR)(NAA); Test Result: Negative ; Comments: SARS-CoV-2 RNA (NAA/RT-PCR)(NAA), Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shellfish allergy; Sulfonamide allergy
Andere Medikamente: SERTRALINE
Allergien: -
Vorherige Impfungen: -

VAERS 2054339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

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Staat: HI
Alter: 69,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 23.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: - / LA

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

Loss of personal independence in daily activities Tinnitus

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 23Dec2021 (Lot number: 33130BA) at the age of 69 years as dose 3 (booster), single for Covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6208, Location of injection: Arm Right), administration date: 15Mar2021, when the patient was 68 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6200, Location of injection: Arm Left), administration date: 22Feb2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: TINNITUS (medically significant) with onset 29Dec2021, outcome "not recovered", described as "Tinnitus left ear 6 days after 3rd vaccine (the booster) which has persisted since then"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (medically significant) with onset 29Dec2021, outcome "not recovered", described as "Having follow up referrals to specialists as had impacted well being and work". The events "tinnitus left ear 6 days after 3rd vaccine (the booster) which has persisted since then" and "having follow up referrals to specialists as had impacted well being and work" were evaluated at the physician office visit. Therapeutic measures were taken as a result of tinnitus, loss of personal independence in daily activities. The patient received steroid as treatment. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, has the patient been not tested for COVID-19.; Sender's Comments: Based on the information provide and plausible temporal association, the causality between BNT162B2 and events cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
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 2054339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: HI
Alter: 69,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 23.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Loss of personal independence in daily activities Tinnitus

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 23Dec2021 (Lot number: 33130BA) at the age of 69 years as dose 3 (booster), single for Covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6208, Location of injection: Arm Right), administration date: 15Mar2021, when the patient was 68 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6200, Location of injection: Arm Left), administration date: 22Feb2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: TINNITUS (medically significant) with onset 29Dec2021, outcome "not recovered", described as "Tinnitus left ear 6 days after 3rd vaccine (the booster) which has persisted since then"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (medically significant) with onset 29Dec2021, outcome "not recovered", described as "Having follow up referrals to specialists as had impacted well being and work". The events "tinnitus left ear 6 days after 3rd vaccine (the booster) which has persisted since then" and "having follow up referrals to specialists as had impacted well being and work" were evaluated at the physician office visit. Therapeutic measures were taken as a result of tinnitus, loss of personal independence in daily activities. The patient received steroid as treatment. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, has the patient been not tested for COVID-19.; Sender's Comments: Based on the information provide and plausible temporal association, the causality between BNT162B2 and events cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
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 2192668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 16.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered No adverse event

Symptomtext

Patient is not immunocompromise and was given a 4th Pfizer dose. Patient is fine no adverse reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2185925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: NH
Alter: 31,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 25.02.2022
Beginn: 25.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Underdose

Symptomtext

Purple cap given rather than grey cap.

Weitere VAERSDATA-Felder

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

VAERS 2185923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: NH
Alter: 20,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 27.02.2022
Beginn: 27.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Purple cap given rather than grey cap.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2185914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: NH
Alter: 62,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 25.02.2022
Beginn: 25.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

gave vaccine outside of the vaccine viability

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: chronic pain
Andere Medikamente: morphine sulfate IR 15mg tablet
Allergien: n/a
Vorherige Impfungen: -

VAERS 2185908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: NH
Alter: 12,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 27.02.2022
Beginn: 27.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

vaccine was given outside of the vaccine viability window

Weitere VAERSDATA-Felder

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

VAERS 2185902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: NH
Alter: 12,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 26.02.2022
Beginn: 26.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

the vaccine was given outside of the vaccine viability window

Weitere VAERSDATA-Felder

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

VAERS 2185897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: NH
Alter: 36,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 28.02.2022
Beginn: 28.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

the vaccine was given outside of the vaccine viability

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: sulfa antibiotics
Vorherige Impfungen: -

VAERS 2184739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: NH
Alter: 16,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 26.02.2022
Beginn: 26.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

patient received vaccine outside of the vaccine viability window

Weitere VAERSDATA-Felder

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

VAERS 2184734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: NH
Alter: 25,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 27.02.2022
Beginn: 27.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

n/a

Weitere VAERSDATA-Felder

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

VAERS 2184730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: NH
Alter: 20,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 25.02.2022
Beginn: 25.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

patient received the vaccine outside of the vaccine viability window

Weitere VAERSDATA-Felder

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

VAERS 2184723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: NH
Alter: 36,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 28.02.2022
Beginn: 28.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received Pfizer vaccine outside of the viability window.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2184421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: WA
Alter: 32,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 26.02.2022
Beginn: 15.03.2022
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine may have been stored under conditions that departed from the manufacturer's recommended specifications. The manufacturer deemed the vaccine not to be viable. No harm was caused; however, patient may not receive the optimum benefit of the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2180633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: ID
Alter: 17,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 02.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

No adverse event Product storage error

Symptomtext

Pt was given vaccine that had exceeded the 45 days in the refrigerator. Pt did not report any symptoms and was notified of the vaccine error

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Menorrhagia
Andere Medikamente: tretinoin topical cream, Proair inhaler, Minocycline
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2180629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: ID
Alter: 62,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 02.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

No adverse event Product storage error

Symptomtext

Pt was given vaccine that had exceeded the 45 days allowed in the refrigerator. Pt did not report any symptoms and was notified of the vaccine error

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2180627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: ID
Alter: 63,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 02.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Patient was given vaccine that exceeded the 45 days allowed in the refrigerator. No symptoms were reported and patient was notified of the error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertensive disorder
Andere Medikamente: clonidine, olmesartan, tadalafil, tamsulosin, tramadol, solifenacin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2180617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: ID
Alter: 19,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 02.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Product storage error

Symptomtext

Pt was given vaccine that exceeded the 45 days allowed in the refrigerator. No symptoms were reported, patient has been notified of the error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ADHD
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2180614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: ID
Alter: 15,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 02.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Patient was given vaccine that had exceeded 45 days allowed in the refrigerator

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: triamcinolone topical cream
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2180066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 03.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: - / -

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

Infusion Injection Prostate cancer

Symptomtext

Injection therapy for prostate cancer. This infusion was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2179756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 27.12.2021
Beginn: 13.02.2022
Tage bis Beginn: 48,0
Dosis: 3
Route/Site: UN / UN

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

Amnesia COVID-19 Foaming at mouth Influenza A virus test negative Influenza B virus test Mental status changes Respiratory syncytial virus test negative SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

Date of Admission: 2/13/2022 Chief Complaint: AMS Source of Information: Patient and Available medical record History of Present Illness: This is a 61y.o. male with past medical history of ischemic stroke of right corona radiata, Bell's palsy, and hypertension who presented to ED for concern of altered mental status. Per patient's wife she last saw the patient at his normal at around 1330, spoke to him on the phone at 1430 without issues, and returned home around 1515 to find the patient lying on the floor in the bedroom, alert, with foam coming from his mouth. Patient's wife denies seeing any convulsions and denies patient has history of seizures. She proceeded to call EMS. Per EMS record, patient found AO x1, with no obvious trauma or incontinence, no foam noted in your mouth. Patient was unable to follow commands and was transferred to ED. At bedside, patient is alert and oriented to himself, place and surrounding individuals-he is unable to recall events leading up to admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Amnesia
Hospital-Tage: 2,0
Labordaten: <NOCOVER> 1 HEALTH SYSTEM LABORATORY Chart Review Copy Patient PT CLASS: Inpatient DEPT: EMERGENCY DEPARTMENT PATIENT STATUS: Discharged GENDER: male ORD DR: AUTH DR: Results Covid-19, Flu, RSV by NAA (Order) Contains abnormal data Covid-19, Flu, RSV by NAA Order Status: Final result Visible to patient: Yes (not seen) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 02/13/22 4:44 PM Last Resulted: 02/13/22 5:34 PM Order Details View Encounter Lab and Collection Details Routing Result History Result Care Coordination Patient Communication Released Not seen Back to Top System Result Comments Released Not seen View System Info Covid-19, Flu, RSV by NAA (Order #) on 2/13/22 Order Covid-19, Flu, RSV by NAA (Order) Reports Transmitted at Order Entry Transmitted to: Device ID: Order Details Open Order Details Specimen Collection Record Collection: Date/Time: By: Spec ID: Feb 13, 2022 4:44 PM Specimen Received Record Received: Date/Time: By: Spec ID: Feb 13, 2022 4:52 PM Order Requisition Covid-19, Flu, RSV by NAA (Order #) on 2/13/22
Aktuelle Erkrankungen: ? Hypertension ? Stroke
Vorgeschichte: ? Hypertension ? Stroke
Andere Medikamente: acetaminophen (TYLENOL) tablet 650 mg 650 mg Oral Q 6 H PRN ? amLODIPine (NORVASC) tablet 10 mg 10 mg Oral DAILY ? atorvastatin (LIPITOR) tablet 80 mg 80 mg Oral Q HS ? enoxaparin (LOVENOX) injection 40 mg 40 mg Subcut
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2170858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MS
Alter: 15,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 10.03.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

No adverse event

Symptomtext

NO ADVERSE EFFECTS NO TREATMENT REQUIRED NO SYMPTOMS OR SIGNS

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2170850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: MS
Alter: 13,0
Geschlecht: M
Eingang: 10.03.2022
Impfdatum: 10.03.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

expired vaccine 2/28/22 given misread extended exp dates ---no symptoms no ill effects--no treatment required

Weitere VAERSDATA-Felder

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

VAERS 2162736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: TN
Alter: 16,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 01.03.2022
Beginn: 01.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Underdose

Symptomtext

A 16 year old male patient inadvertently received a pediatric Pfizer dose, lot number Fk5618, dosage amount 0.2 ml instead of the adult dose of Pfizer vaccine. Once it was realized that the pediatric dose 0.2 ml was given, the patient was then given 0.1 ml of the adult Pfizer vaccine with lot number 33130BA. Patient remained in clinic for observation for 15-20 minutes and displayed no adverse symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 2191851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 29.12.2021
Beginn: 27.01.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / LA

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

Asymptomatic COVID-19 SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection with hospitalization after COVID vaccine series 02/17/21 COVID vaccine dose #1 03/15/21 COVID dose #2 12/29/21 COVID dose #3 01/27/22 COVID positive 01/28/22 Admitted to hospital d/t COVID + for quarantine and observation 02/03/22 Discharge from hospital remained asymptomatic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: Date Test Name Result 02/24/2022@11 COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected 02/10/2022@14: 10 COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected 01/27/2022@11 COVID-19 PCR (FLUVID) DETECTED cov1D-19 ANTIGEN (BINAX) Not Detected 01/02/2022@15: 18 COVID-19 PCR (FLUVID) Not Detected COVID- 19 PCR (FLUVID) Not Detected 06/06/2021@08: 15 COVID-19 DIAG (ORL) Not Detected COVID-19 PCR (FLUVID) Not Detected 02/14/2021@ 21:14:03 COVID-19 PCR (FLUVID) Not Detected COVID-19 (ORL) Not Detected 06/03/2020 @ 11:15 COMD-19 (ORL) Not Detected Date Test Name Result 02/24/2022 @ 11 COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected 02/10/2022 @ 14:10 COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected COVID-19 ANTIGEN (BINAX) Not Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2161787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: IL
Alter: 64,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 19.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: - / LA

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

Biopsy Blood test Computerised tomogram Optic neuritis Urine analysis

Symptomtext

Optic neuritis/one eye was blurry. Then one day she happen to close one eye and the other way blurry; 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 64 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Dec2021 (Lot number: 33130BA, Expiration Date: Feb2022) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "chronic hives" (unspecified if ongoing), notes: Verbatim:chronic hives; "lot of allergies so the only vaccine they let her get or advised was to get the covid vaccine" (unspecified if ongoing), notes: lot of the allergies so the only vaccine they let her get or advised was to get the covid vaccine. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number:01, LOT Number: EW0177, Expiration Date: Aug2021, Anatomical Location of Administration of Pfizer vaccine considered as suspect: caller states left arm every time.), administration date: 26May2021, when the patient was 64 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number:02, LOT Number: EW0191, Expiration Date: Sep2021, Anatomical Location of Administration of Pfizer vaccine considered as suspect: caller states left arm every time.), administration date: 18Jun2021, when the patient was 64 years old, for Covid-19 Immunization. The following information was reported: OPTIC NEURITIS (caused and prolonged hospitalization, medically significant) with onset Jan2022, outcome "not recovered", described as "Optic neuritis/one eye was blurry. Then one day she happen to close one eye and the other way blurry". The patient was hospitalized and prolonged hospitalization for optic neuritis (start date: 01Feb2022, discharge date: 05Feb2022, hospitalization duration: 5 day(s)). The event "optic neuritis/one eye was blurry. then one day she happen to close one eye and the other way blurry" was evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: biopsy: unknown result, notes: They did a temple biopsy, they wanted to make sure her veins in her head weren't closing up or getting too thin; blood test: unknown result; computerised tomogram: unknown result; urine analysis: unknown result. Therapeutic measures were taken as a result of optic neuritis. Clinical Information: Reporter mentioned that, No other Products administered. Patient had both the Pfizer shots and the booster on 23Dec2021, she did well, thought she did, three weeks later, in Jan2022, she developed optic neuritis. She went to the hospital and all kinds of stuff. Caller clarifies optic neuritis as swelling of the optic nerve behind the eye. Caller explains that she had blurry vision in the middle of Jan2022, about 3 weeks after the shot. Somebody told her it was conjunctivitis, and she was misdiagnosed, then it progressively got worse, and they sent her to the hospital. After discharged from hospital, Doctor was concerned saying that she needed more testing like an MRI and she ended up going to the hospital.Caller states she is on prednisone and is foggy. She said everything isnt clear like it normally is.Regarding concomitant medications and medical history, caller states she gets shots for chronic hives and she has been on those for like 7 years. Reporter states while in the hospital she had blood work, a lot of stuff, a lot of black and blue marks. Thats why she is going to the neurologist, some of the numbers were out of whack. Vaccination Facility Type reported as Pharmacy. No additional Vaccines Administered on Same Date of the Pfizer Suspect. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): Caller states she has a lot of the allergies so the only vaccine they let her get or advised was to get the covid vaccine, she doesnt get the flu shot, shingles or anything else. Caller states that she receive allergy shots, No additional lot numbers, caller states she gets them at the doctors office every two weeks. No AE(s) following prior vaccinations. Patient had no Medical History (including any illness at time of vaccination), Caller state she felt pretty good after. No Family Medical History Relevant to AE(s). None or Unknown Relevant Tests. In the hospital they did CT scans, urine ones a couple of times, she doesnt remember the number times, treated with prednisone. Caller clarifies when in the hospital she received Prednisone 60mg intravenously for 5 days. She came home with the pills to take at home. The Prednisone is down to 40mg, she is doing a taper, she was doing 50mg now down to 40 mg once day, by mouth. Caller states they gave her two different prescriptions. She has 20mg pills and 10mg in pharmacy bottles. No NDC/Lot/Expiration to provide. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy
Hospital-Tage: 5,0
Labordaten: Test Name: temple biopsy; Result Unstructured Data: Test Result:Unknown Result; Comments: They did a temple biopsy, they wanted to make sure her veins in her head weren't closing up or getting too thin.; Test Name: Bloodwork; Result Unstructured Data: Test Result:Unknown Result; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown Result; Test Name: Urine Test; Result Unstructured Data: Test Result:Unknown Result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (lot of the allergies so the only vaccine they let her get or advised was to get the covid vaccine); Hives (Verbatim:chronic hives)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2151809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 71,0
Geschlecht: U
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 77,0
Geschlecht: U
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 14,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 50,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 47,0
Geschlecht: U
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 51,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 16,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 19,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 14,0
Geschlecht: U
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 33,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 62,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 35,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 72,0
Geschlecht: U
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 50,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 71,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 52,0
Geschlecht: U
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 54,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2151658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 14,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Unevaluable event

Symptomtext

Unknown

Weitere VAERSDATA-Felder

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

VAERS 2151643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 39,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Unevaluable event

Symptomtext

Unknown

Weitere VAERSDATA-Felder

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

VAERS 2140522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: IL
Alter: 21,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 14.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Since having Covid, I have this Raspatory infection, chest pain and sore lymph nodes. I do have a little bit of side pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Peanuts
Vorherige Impfungen: -

VAERS 2130055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: IL
Alter: 11,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 19.02.2022
Beginn: 19.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

11-year-old female patient given the Pfizer vaccine indicated for those 12 years and older.

Weitere VAERSDATA-Felder

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

VAERS 2128264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130ba

gering

Staat: MA
Alter: 20,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 20,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error related to temperature excursion from recommended storage temperature, not known to this writer to be associated with an adverse event. The clinic has relayed to this writer that prior to the vaccine's thawing and administration to the vaccine recipient, the administered vaccine was stored in frozen temperatures for longer than recommended by the manufacturer. (This VAERS writer assigned to form completion was not the administrator of this vaccine.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 13,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error related to temperature excursion from recommended storage temperature, not known to this writer to be associated with an adverse event The has relayed to this writer that prior to the vaccine's thawing and administration to the vaccine recipient, the administered vaccine was stored in frozen temperatures for longer than recommended by the manufacturer. (This VAERS writer assigned to form completion was not the administrator of this vaccine.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 54,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder

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

VAERS 2123896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 40,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error related to temperature excursion from recommended storage temperature, not known to this writer to be associated with an adverse event. The clinic has relayed to this writer that prior to the vaccine's thawing and administration to the vaccine recipient, the administered vaccine was stored in frozen temperatures for longer than recommended by the manufacturer. (This VAERS writer assigned to form completion was not the administrator of this vaccine.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 60,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder

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

VAERS 2123890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 71,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error, related to temperature excursion, associated with an adverse event. The clinic explained prior to thawing and administration of the vaccine, it was stored in frozen temperatures for longer than recommended by the manufacturer. Outcome: Vaccine recipient contacted by staff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 17,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder

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

VAERS 2123887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 82,0
Geschlecht: U
Eingang: 18.02.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

No adverse event Product storage error

Symptomtext

?Pfizer-BioNTech COVID-19 Vaccine? Vaccine administration error related to temperature excursion from recommended storage temperature, not known to this writer to be associated with an adverse event. The clinic has relayed to this writer that prior to the vaccine's thawing and administration to the vaccine recipient, the administered vaccine was stored in frozen temperatures for longer than recommended by the manufacturer. (This VAERS writer assigned to form completion was not the administrator of this vaccine). Outcome: Vaccine recipient was contacted by staff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 15,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error related to temperature excursion from recommended storage temperature, not known to this writer to be associated with an adverse event. The clinic has relayed to this writer that prior to the vaccine's thawing and administration to the vaccine recipient, the administered vaccine was stored in frozen temperatures for longer than recommended by the manufacturer. (This VAERS writer assigned to form completion was not the administrator of this vaccine.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 59,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error, related to temperature excursion, associated with an adverse event. The clinic explained prior to thawing and administration of the vaccine, it was stored in frozen temperatures for longer than recommended by the manufacturer. Outcome: Vaccine recipient contacted by staff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 17,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder

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

VAERS 2123876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 51,0
Geschlecht: U
Eingang: 18.02.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine improperly stored.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 75,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error, related to temperature excursion, associated with an adverse event. The clinic explained prior to thawing and administration of the vaccine, it was stored in frozen temperatures for longer than recommended by the manufacturer. Outcome: Vaccine recipient contacted by staff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 54,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder

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

VAERS 2123872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 15,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error related to temperature excursion from recommended storage temperature, not known to this writer to be associated with an adverse event. The clinic has relayed to this writer that prior to the vaccine's thawing and administration to the vaccine recipient, the administered vaccine was stored in frozen temperatures for longer than recommended by the manufacturer. (This VAERS writer assigned to form completion was not the administrator of this vaccine.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 17,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error, related to temperature excursion, associated with an adverse event. The clinic explained prior to thawing and administration of the vaccine, it was stored in frozen temperatures for longer than recommended by the manufacturer. Outcome: Vaccine recipient contacted by staff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 54,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder

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

VAERS 2123865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine stored improperly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 30,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error, related to temperature excursion, associated with an adverse event. The clinic explained prior to thawing and administration of the vaccine, it was stored in frozen temperatures for longer than recommended by the manufacturer. Outcome: Staff attempted contact x 3 and mailed letter to vaccine recipient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 74,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error related to temperature excursion from recommended storage temperature, not known to this writer to be associated with an adverse event. The clinic has relayed to this writer that prior to the vaccine's thawing and administration to the vaccine recipient, the administered vaccine was stored in frozen temperatures for longer than recommended by the manufacturer. (This VAERS writer assigned to form completion was not the administrator of this vaccine.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 18,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine stored improperly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 57,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder

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

VAERS 2123860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine stored improperly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 23,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine stored improperly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 33,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder

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

VAERS 2123855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 17,0
Geschlecht: U
Eingang: 18.02.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error, related to temperature excursion, associated with an adverse event. The clinic explained prior to thawing and administration of the vaccine, it was stored in frozen temperatures for longer than recommended by the manufacturer. Outcome: Vaccine recipient contacted by staff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine stored improperly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine stored improperly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 17,0
Geschlecht: U
Eingang: 18.02.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error, related to temperature excursion, associated with an adverse event. The clinic explained prior to thawing and administration of the vaccine, it was stored in frozen temperatures for longer than recommended by the manufacturer. Outcome: Vaccine recipient contacted by staff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: CT
Alter: 69,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

No adverse event Product storage error

Symptomtext

Vaccine administration error related to temperature excursion from recommended storage temperature, not known to this writer to be associated with an adverse event. The clinic has relayed to this writer that prior to the vaccine's thawing and administration to the vaccine recipient, the administered vaccine was stored in frozen temperatures for longer than recommended by the manufacturer. (This VAERS writer assigned to form completion was not the administrator of this vaccine.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine stored improperly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 17,0
Geschlecht: U
Eingang: 18.02.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

contacted patient

Weitere VAERSDATA-Felder

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

VAERS 2123845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33130BA

gering

Staat: -
Alter: 45,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Product storage error

Symptomtext

Vaccine stored improperly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -