Search and filter adverse-event reports.
1,929,324 reports(815 ms)
After receiving the Fluarix, patient was fainted and fell. Patient said that she was very nervous also. Her head and elbow hit the counter.
Patient came in for his Typhim vaccine prescribed from doctor. Pharmacist injected the typhim vaccine using a 5/8 inch needle instead of 1 inch. Pharmacist called Dr. on 9/30/25 and notified the doctor of the error. Doctor recommended the patient receive anot…
Severe diarrhea, loss of appetite, ear infection. All resulting in ER visit for IV fluids. Diarrhea began before any antibiotics were prescribed. 1 pee diaper in a 24 hour period resulting in ER visit where they tested her blood and found she was moderately de…
The first vaccination had a mechanical failure in which the vaccine expelled out of the needle junction as the needle may have come loose during administration. This resulted in a subtherapeutic dose. As a result, a second dose was given to the patient to give…
Patient has filed a complaint with the agency after being given Spikevax in lieu of mNexSpike.
Pregnant patient received an expired dose of fluzone np with no adverse event; Pregnant patient received an expired dose of fluzone np with no adverse event; Initial information received on 23-Sep-2025 regarding an unsolicited valid non-serious case received f…
Suspected vaccination failure/Lack of drug effect; Neuropathy; possible Shingles; Fibromyalgia aggravated; Shivering; Shaking; This serious case was reported by a consumer via call center representative and described the occurrence of vaccination failure in a…
Body rash began 36 hours after vaccine; This is a spontaneous report received from a Consumer or other non HCP. A 64-year-old female patient (not pregnant) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 23Sep2025 at 12:00 as dose 1, si…
Vertigo and vomiting for 4-5 days and had to be admitted to hospital
No additional AE reported; t PROQUAD was administered during a T/E to 1 patient on 8/13/2025.; This spontaneous report was received from a Physician and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and c…
vaccine was administered after temperature excursion; This spontaneous report was received from a physician assistant and refers to a patient of unknown age and gender. The patient's medical history, drug history, concurrent conditions and concomitant therap…
no symptoms; an adult patient received a pediatric dose of VAQTA that was administered on 9/11/2025; This spontaneous report was received from a nurse and refers to an adult patient of unknown age and gender. The patient's medical history, concurrent conditi…
The patient recently had a miscarriage (before PROQUAD administration); HCP reports that the patient has received her MMR and varicella vaccines in the past (unknown brand name) but recently undergone titer testing that did not show immunity.; the patient has…
A fib with no history on same day of vaccine; This serious case was reported by a physician via sales rep and described the occurrence of atrial fibrillation in a 52-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknow…
Bell's palsy; This serious case was reported by a consumer via interactive digital media and described the occurrence of bell's palsy in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingle…
After the vaccine patient got the dreaded Guillain Barre; paralyzed; This serious case was reported by a consumer via interactive digital media and described the occurrence of guillain barre syndrome in a patient who received RSVPreF3 adjuvanted (RSV vaccine)…
Kinrix was administered instead of Pedirix to a four-month-old patient; Underage administration of Kinrix instead of Pediarix; This non-serious case was reported by a nurse via call center representative and described the occurrence of wrong vaccine administer…
patient was administered only the diluent for the dose of Shingrix and it was not reconstituted with the powder; patient was administered only the diluent for the dose of Shingrix and it was not reconstituted with the powder; This non-serious case was reported…
arm got swollen after receiving Shingrix.; This non-serious case was reported by a consumer via patient support programs and described the occurrence of swelling arm in a female patient who received Herpes zoster (Shingrix) for prophylaxis. Concomitant prod…
Hives; This non-serious case was reported by a consumer and described the occurrence of hives in a 24-year-old female patient who received HBV (Engerix B) (batch number C3207) for prophylaxis. On an unknown date, the patient received Engerix B. On an unknown…