Search and filter adverse-event reports.
1,929,324 reports(805 ms)
PATIENT STATED THAT ARM BECAME VERY RED AND SORE OVER THE NEXT COUPLE OF DAYS, HAD A TELEMED DR VISIT AND WAS INSTRUCTED TO GO TO THE ER. AT THE ER SHE WAS DIAGNOSED AS HAVING CELLULITIS
Patient presented to the emergency department with red, flaking, rash to back that he noticed approximately 2 days after getting COVID booster.
Patient experienced systemic symptoms beginning 1.5 days after receiving high-dose influenza vaccine on October 6th at pharmacy, including gastrointestinal upset, headache, pruritus, congestion, rhinorrhea, and lacrimation lasting approximately one week.
Patient was being seen for his 4 month wellness exam and vaccines. When it was time to to receive vaccines medical assistant got confused and got the MCV instead of PCV vaccine by mistake. Medical assistant did no realize mistake until it was time to add into…
Two weeks following injection, patient developed muscle aches, weakness, and fatigue. Went to PCP 2/18/25 with initial labs showing elevated inflammatory markers. Additional labs order and showed severely elevated liver enzymes. Sent for Stat Liver ultrasound…
BULLSEYE-LIKE WOUND WITH LARGE, RED AND PURPLE KNOT IN THE CENTER OF INJECTION SITE
PEDIATRIC COVID-19 0.25ML GIVEN TO 34 YEAR OLD IN ERROR
a change in the patient's walk; The vaccines were mixed with flu vaccine instead of the dilution solvent; This spontaneous report was received from an employee and refers to a 13-month-old female patient. The patient's medical history, concurrent conditions…
No additional AE/no PQC.; inadvertent administration of VARIVAX after a temperature excursion; This spontaneous report was received from a registered nurse and refers to a patient of unknown age and gender. The patient's medical history was not reported. The p…
The patient accidentally received second dose of Jynneos vaccine intramuscularly instead of subcutaneously; The patient received second dose of Jynneos vaccine 32 days after first dose; Nausea; Case reference number US-BN-2025-000221 is a spontaneous case init…
The patients received Jynneos vaccine which was stored at five degrees Celsius more than eight weeks; The patients received Jynnoes vaccine intramuscularly; The female patient received one dose of Jynneos vaccine; Case reference number US-BN-2025-000426 is a s…
now cannot use hand; This non-serious case was reported by a consumer and described the occurrence of injected limb mobility decreased in a 74-year-old female patient who received Flu unspecified (Flu vaccine) for prophylaxis. Co-suspect products included CO…
the powder was expired; This non-serious case was reported by a pharmacist via sales rep and described the occurrence of expired vaccine used in a 62-year-old female patient who received RSVPreF3 adjuvanted (Arexvy) (batch number 5K4X4, expiry date 03-OCT-2025…
Skin sensitization; This non-serious case was reported by a consumer via call center representative and described the occurrence of skin sensitization in a 59-year-old male patient who received Herpes zoster (Shingrix) for prophylaxis. Co-suspect products in…
Menveo 1 vial expired dose administration (less than 30 days since expiration); This non-serious case was reported by a pharmacist via call center representative and described the occurrence of expired vaccine used in a 12-year-old female patient who received…
The adult dose was given to a 19 year-old; Overdose; This non-serious case was reported by a other health professional via sales rep and described the occurrence of adult product administered to child in a 19-year-old male patient who received HBV (Engerix B a…
septic arthritis due to kingella (left knee swelling, pain and joint effusion); This 12-month-old male subject was enrolled in a blinded study titled A Phase 3a, observer-blind, randomized, controlled study to evaluate the safety of an investigational varicell…
Itchy at injection site to the point of going to the ER; possible infection at injection site; This non-serious case was reported by a nurse via other manufacturer and described the occurrence of injection site itching in a 20-year-old patient who received DTP…
Sick; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of sickness in a patient who received RSVPreF3 adjuvanted (RSV vaccine) for prophylaxis. On an unknown date, the patient received RSV vaccine. O…
The other one was awful; Not going to get the last one; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of feels awful in a patient who received Herpes zoster (Shingrix) for prophylaxis. Co-suspect…