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1,929,324 reports(785 ms)
Site: Shoulder Joint Injury (prolonged pain, tingling, etc.)-Medium, Other Vaccines: VaccineTypeBrand: Tdap Boostrix; Manufacturer: GlaxoSmithKline; LotNumber: PF44A; Route: IM; BodySite: right deltoid; Dose: ; VaxDate: 11/23/2025
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: neck pain started two days after which brought the patient back…
Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Shakiness-Mild, Other Vaccines: VaccineTypeBrand: Gardasil 9; Manufacturer: Merck; LotNumber: z011258; Rou…
Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Additional Details: patient fainted after getting the shot for a several minutes (2 to 4 min) , then slowly regain conciousness, gave her water and chocolate to eat since she ask for…
Site: Bruising at Injection Site-Mild, Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Site: Bruising at Injection Site-Severe, Additional Details: patient presented to the pharmacy on jan 9.2026 with severe bruising of the left arm radiating to her elbow. she was advised to go to the doctor as soon as possible
no adverse event; Medical Assistant calling with a report of an adverse event regarding VAQTA. Medical Assistant stated that they administered a dose of VAQTA to a 4 month old patient during a routine vaccination appointment out of error. Medical Assist stat…
Systemic: Fainting / Unresponsive-Mild
Patient has significant pain at site of injection in the deltoid
POTENTIAL ERROR COULD HAVE BEEN MADE WHERE PATIENT DID NOT RECEIVE THE COMBINATION OF THE ADJUVANT AND ANTIGEN. AFTER ANALYIS MADE BY RISK MANAGEMENT AND PER RECOMMENDATIONS OF INFECTIOUS DISEASE MEDICAL DOCTOR, PATIENT WILL BE OFFERED REPEAT DOSE.
Partial vaccination may have been administered. Potential error where patient did not receive adjuvant along with antigen. Risk management analysis conducted. Per recommendations of MD with Infectious Disease, patient offered repeat dose.
We received a call from Rehab facility that the patient had passed away.
Patient was transferred to the ER with trouble breathing and ended up going through a full code and passing away
Patient may have received partial dose. Error could have been made where patient did not receive adjuvant with antigen. Risk Management completed analysis and consulted with Dr. with Infectious Disease. Patient will be offered repeat vaccination.
Patient may have received partial dose. Error may have occurred where patient did not receive adjuvant with antigen. Risk management performed analysis and collaborated with Dr. with Infectious Disease. Patient will be offered repeat vaccination.
Patient may have received partial dose. Error may have occurred where patient did not receive adjuvant with antigen. Risk management performed analysis and collaborated with MD with Infectious Disease. Patient will be offered repeat vaccination.
Patient wanted the flu vaccine, but received the Covid vaccine. There was no known adverse reaction from the Covid vaccine; rather, it was the wrong vaccine given.
Patient received an extra dose, she received 3 doses instead of the recommended 2 doses.
The vaccine was given after the beyond use date. Vaccine was given on 1-19-2026. Beyond use date was 1-6-2026.
Nodule at Inj Site - W/o redness, irritation, swelling, or pain. Discomfort on palpation