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1,929,324 reports(791 ms)
Hardness around the side of injection. Redness that started at 3 cm and by day two was 3 inches in diameter increase in redness and harden around the side. Child reported pain immediately upon receiving and persisted throughout the leg the following days
TE for ROTATEQ and Pentacel; No adverse effects reported; This spontaneous report was received from a pharmacy technician and refers to a patient of unknown gender and age. The patient's concurrent conditions, medical history and concomitant therapies were not…
the patient started gaging and vomiting a little after the administration of the ROTATEQ vaccine; the taste of the ROTATEQ vaccine could have contributed to the vomiting / HCP stated that she could not confirm the taste of the ROTATEQ vaccine; the patient did…
5/8- Patient reported that they had chest immediately after the vaccine was administered.
warm, erythematous, pruritic injection site s/p day 1 after receiving vaccines.
unknown
Redness/ warmth at vaccination site, malaise, elevated temperature
no adverse reactions per parents/guardians. we did call to let them know what happened and 3/4 decided to revaccinate.
MODERNA #1 8/7/21 MODERNA #2 9/7/21 COVID ILLNESS AFTER VACCINE FAILURE DEVELOPED VACCINE AND SARS-COV-2 PULMONARY HYPERTENSION WITHOUT EVIDENCE OF THROMBOSIS IN 2024. ALSO HAD VACCINE INDUCED MYOPERICARDITIS. TREATED WITH PROTOCOL BASE SPIKE DETOXIFICATION…
Resident passed away
The patient was administered the one vial prep of Menveo instead of the intended two vial prep. No adverse events were observed or reported following administration upon identification of the variance, the event was documented and the care team was notified.
no adverse events. sw guardian and no concerns with symptoms or side effects. aware of situation. decided not to revaccinate
Patient received only the sterile water (diluent) of the Arexvy vaccine/Maladministration of diluent only (Inappropriate reconstitution technique); Patient received only the sterile water (diluent) of the Arexvy vaccine/Maladministration of diluent only (Inapp…
The patient was administered the one vial prep of Menveo instead of the intended two vial prep. No adverse events were observed or reported following administration upon identification of the variance, the event was documented and the care team was notified.
Administered expired vaccine.Vaccine expired in 4/2026 No adverse impact witnessed or identified.
Bilateral bicept, forarm, shoulder and neck pain.
no adverse events. mom aware and decided to revaccinate
Allergic reaction- face, throat, and body started swelling.
Red, tender, swollen arm at injection site
The patient was administered the one vial prep of Menveo instead of the intended two vial prep. No adverse events were observed or reported following administration upon identification of the variance, the event was documented and the care team was notified.