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1,929,324 reports(784 ms)
She developed progressive weakness starting on 2/26/2026 and was admitted to the hospital on 3/11/2026 and ultimately diagnosed with Guillan Barre Syndrome. She was treated with IVIG x 4 days. She was discharged from inpatient rehab on 3/18/2026 with improvem…
Atrial fibrillation onset after first two doses and one booster.
My daughter was forced to get the shot when she was 4 months pregnant. My granddaughter was born June xx, 2021. She was diagnosed with Leukemia [holiday name withheld] day 2021. She was treated at [facility name withheld] Affiliate clinic in [city name withhe…
Patient was seen in the clinic 3/19/26 for a Hepatitis B vaccine booster due to being non-immune from a titer done 3/13/26. Patient presented with swelling and bruising at the injection site (left deltoid) from the Meningococcal B Bexsero vaccine given on 3/13…
No additional AE; Nurse called reporting an AE for VARIVAX. Caller reported that on 2/13/2026, a patient was inadvertently administered VARIVAX that was reconstituted with GSK SHINGRIX DILUENT.; This spontaneous report was received from a nurse and refers to…
my daughter died after receiving your vaccine; behavior change; This is a spontaneous report received from a Consumer or other non HCP. An adult female patient received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), as dose 1, single (Batch/Lot nu…
INJECTION SITE WARMTH/feels warm to the touch; INJECTION SITE PAIN/some pain at the site of injection; Injection site erythema/The entire upper arm is red; INJECTION SITE SWELLING/The entire upper arm is swollen; This spontaneous case was reported by a consume…
No adverse effects reported; received VARIVAX on 1/28/2026 and MMR II on 2/16/2026 which was 2 weeks early; This spontaneous report was received from a Nurse and referred to a 13-month-old patient of unknown gender. The patient's medical history, concurrent c…
The patient is not experiencing any symptoms; Patient is 13 months old and was inadvertently given GARDASIL 9. Patient was there to get a different vaccine.; This spontaneous report was received from a pharmacist and refers to his daughter a(n) 13-month-old…
No additional AE; expired dose of GARDASIL 9 was administered to a patient; product experienced a temperature excursion on 1/26/2026; This spontaneous report was received from a medical assistant and refers to a(n) patient of unknown age and gender. The pati…
Pharmacist reported that a patient had MMR vaccine in childhood and has a low titer; Pharmacist reported that a patient had MMR vaccine in childhood and has a low titer; Pharmacist reported that a patient had MMR vaccine in childhood and has a low titer; the p…
Autistic; This spontaneous report was received from a Physician via vendor and refers to a Child patient of unknown gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not…
The patient received only three doses of Vivotif capsule; The patient developed a worsening rash on the face after first dose of Vivotif; Case reference number US-BN-2025-000007 is a spontaneous case initially received from *pharmacist* via Communication (refe…
Patient left Vivotif outside of the fridge for approximately one week, reaching a maximum temperature of 67 degrees Fahrenheit, and patient took one dose today while it was not refrigerated; Patient left Vivotif outside of the fridge for approximately one week…
The patient took two consecutive doses of Vivotif; Case reference number US-BN-2025-000287 is a spontaneous case initially received from nurse via Communications (reference number: USBAV25-0440) on 26-Feb-2025 and concerns patient of unknown age and gender. T…
The patient did not refrigerate Vivotif vaccine and took four doses; The patient did not refrigerate Vivotif vaccine and took four doses; The patient did not refrigerate Vivotif vaccine and took four doses; Case reference number US-BN-2025-000317 is a spontane…
Patient stated that he can feel a difference when he took Vivotif and obviously he had some reaction.; The patient took Vivotif that stayed out of the fridge for a few days, at temperature 65 Fahrenheits; The patient took Vivotif that stayed out of the fridge…
The patient took dose two and dose three of Vivotif vaccine 24 hours apart instead of 48 hours; Case reference number US-BN-2025-000388 is a spontaneous case report initially received from a pharmacist via Communication (reference number: USBAV25-0618) on 19-M…
On 29-May-2025, the patient took first capsule, on 31-may-2025, the patient took second and then forgot the remaining two capsules; Case reference number US-BN-2025-001021 is a spontaneous case report initially received from a pharmacist via Communication (ref…
Facial drooping; Ear pain; dizziness; nausea; This serious case was reported by a consumer and described the occurrence of facial droop in a 64-year-old female patient who received Herpes zoster (Shingles vaccine) for prophylaxis. Concurrent medical conditio…