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Page 222 of 126801 Results 2211 - 2220 of 1268006

Deceased
Recovered
VAERS ID: 2272639
AGE: UNK SEX: F

Vaccination failure; COVID-19; Aggravation of the urticaria; Dose 1: unbearable urticaria - Booster Dose 1: generalised urticaria: neck, thighs, entire thorax, arms; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from a Regulatory Authority. The reporter is the patient. Regulatory number: FR-AFSSAPS-ST20221143. A 54-year-old female patient received BNT162b2 (COMIRNATY), on 24May2021 as dose 1, 0.3 ml single (Batch/Lot number: unknown), on 23Jun2021 …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Biopsy, Vaccination failure, COVID-19, SARS-CoV-2 test, Specialist consultation, Urticaria

VAERS ID: 2272638
ONSET: 309 days AGE: 73 SEX: F

COVID-19 respiratory infection; Vaccination failure; This case was received via regulatory authority on 06-May-2022 and was forwarded to Moderna on 06-May-2022. This regulatory authority case was reported by a pharmacist and describes the occurrence of COVID-19 (COVID-19 respiratory infection) and VACCINATION FAILURE (Vaccination failure) in a 73-year-old female patient who received mRNA-1273 (Spikevax) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (COMIRNATY) …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (MODERNA)), COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): COVID-19, Vaccination failure

VAERS ID: 2272637
AGE: UNK SEX: F

Myocardial infarction acute; chest pain with elevated troponins; elevated troponins; This is a spontaneous report received from a contactable reporter(s) (Physician) from the regulatory authority. Regulatory number: FR-AFSSAPS-ST20221103. A 40-year-old female patient received BNT162b2 (COMIRNATY), on 14Jan2022 as dose 1, 0.3 ml, single (Lot number: PCA0007) intramuscular for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Acute myocardial infarction, Troponin increased, Angiocardiogram, Chest pain, Magnetic resonance imaging, Troponin

VAERS ID: 2272636
ONSET: 5 days AGE: UNK SEX: F

left bundle branch block; she was stressed; sore spot in the left breast; occasional pain at night; Chest discomfort / Chest pain; Tachycardia; Vaccination site pain; Feeling sick; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from the regulatory authority. The reporter is the patient. Regulatory number: FR-AFSSAPS-ST20221101. A 71-year-old female patient received BNT162b2 (COMIRNATY), on 17Nov2021 as dose 3 (booster), 0.3ml single (Lot number: 1F1019A) …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Breast pain, Malaise, Vaccination site pain, Bundle branch block left, Pain, Chest discomfort, Radioisotope scan, Heart rate, Stress, Investigation, Tachycardia

VAERS ID: 2272635
AGE: 47 SEX: M

Myocarditis; Embolism pulmonary; Fever; Dyspnea; This case was received via regulatory authority on 09-May-2022 and was forwarded to Moderna on 09-May-2022. This regulatory authority case was reported by a physician and describes the occurrence of MYOCARDITIS (Myocarditis), PULMONARY EMBOLISM (Embolism pulmonary), PYREXIA (Fever) and DYSPNOEA (Dyspnea) in a 47-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 000010A) for COVID-19 vaccination. The patient's past medical history …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (MODERNA))


SYMPTOM(S): Dyspnoea, Myocarditis, Pulmonary embolism, Pyrexia, SARS-CoV-2 test

VAERS ID: 2272633
ONSET: 1 days AGE: UNK SEX: M

Loss of balance; decreased hearing, strong in the left ear and weak in the right ear; tinnitus; Blood pressure measurement: (25Oct2021) 156/90 mmHg; (29Nov2021) 130/75 mmHg; (31Jan2022) 125/75 mmHg;; Meniere's syndrome; Shoulder pain; This is a spontaneous report received from a contactable reporter(s) (Physician) from the Regulatory authority-WEB. Regulatory number: FR-AFSSAPS-RE20220629. A 63-year-old male patient received BNT162b2 (COMIRNATY), on 01Sep2021 as dose 3 (booster), single (Lot number: …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Arthralgia, Brain scan normal, Audiogram, Hypoacusis, Balance disorder, Magnetic resonance imaging, Blood pressure increased, Meniere's disease, Blood pressure measurement, Tinnitus

VAERS ID: 2272632
ONSET: 4 days AGE: UNK SEX: M

Arterial hypotension; Chest tightness; Pain chest; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from the Agency Agency-WEB. Regulatory number: FR-AFSSAPS-RE20220617. A 56-year-old male patient received BNT162b2 (COMIRNATY), on 07Apr2022 as dose 2 (booster), single (Lot number: PCB0016) intramuscular for covid-19 immunisation. The patient's relevant medical history included: "COVID-19" (unspecified if ongoing). The patient's concomitant medications were not reported. …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Chest discomfort, Chest pain, Hypotension

VAERS ID: 2272631
AGE: UNK SEX: F

Photophobia; Phonophobia; Rotatory vertigo, need to hold onto the wall.; Rotatory vertigo with nausea; Dizziness; Headache; First and second injection with MODERNA COVID-19/ booster injection of COMIRNATY; First and second injection with MODERNA COVID-19/ booster injection of COMIRNATY; This is a spontaneous report received from a contactable reporter(s) (Physician) from the regulatory authority. Regulatory number: FR-AFSSAPS-RE20220604. A 70-year-old female patient received BNT162b2 (COMIRNATY), …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Dizziness, Off label use, Vertigo, Headache, Phonophobia, Visual analogue scale, Interchange of vaccine products, Photophobia, Magnetic resonance imaging head, SARS-CoV-2 test, Nausea, Specialist consultation

VAERS ID: 2272630
AGE: 55 SEX: F

Tinnitus; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from the regulatory authority. Regulatory number: FR-AFSSAPS-PS20220770. A 55-year-old female patient received BNT162b2 (COMIRNATY), on 22Dec2021 as dose 1, single (Lot number: FL7645) at the age of 55 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "COVID-19", start date: 31Mar2021 (unspecified if ongoing), notes: Test performed …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): SARS-CoV-2 test, Specialist consultation, Tinnitus, Ultrasound Doppler

VAERS ID: 2272629
ONSET: 894 days AGE: UNK SEX: F

Alopecia areata; This is a spontaneous report received from a contactable reporter(s) (Physician) from the regulatory authority. Regulatory number: FR-AFSSAPS-PS20220756. A 66-year-old female patient received BNT162b2 (COMIRNATY), on 19Apr2021 as dose 2, 30 ug, single (Lot number: EW2246) intramuscular, in left arm for covid-19 immunisation; enalapril (ENALAPRIL), (ongoing) at 20 mg 1x/day, oral for hypertension; amlodipine (AMLODIPINE), at 10 mg 1x/day, oral for hypertension; rituximab (RITUXIMAB), …
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VACCINE TYPE(S): COVID19, UNK
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH)), VACCINE NOT SPECIFIED (NO BRAND NAME)


SYMPTOM(S): Alopecia areata, Magnetic resonance imaging

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