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1,929,324 reports(864 ms)
Patient developed diarrhea the day after his vaccines, which persisted until he developed a fever, conjunctivitis, lethargy, and diffuse macular rash on 3/4/25. He was admitted to the hospital, and after CBC showed elevated platelets and UA showed pyuria, he w…
Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per manufacturer, patient needing to be revaccinated. No adverse symptoms or outcome related to the event.
7 am patient woke up as normal ate breakfast, by 7:22 she was crying, her nose turned red, she was pale and warm, threw up mucous, no fever, but not acting right. I changed her diaper, she was lethargic on the changing table. 7:39 i put her on the living room…
Patient developed cellulitis at the site of injection following administration. Evaluated at the clinic and received antibiotics.
Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per manufacturer, patient needing to be revaccinated. No adverse symptoms or outcome related to the event.
Patient reported he experienced hot flashes the evening he received his first dose of Shingrix. He felt anxious about the sudden hot flashes that lasted about 24 hours; as a result, his blood pressure increased (he currently takes nifedipine and olmesartan fo…
Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per manufacturer, patient needing to be revaccinated. No adverse symptoms or outcome related to the event.
Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per manufacturer, patient needing to be revaccinated. No adverse symptoms or outcome related to the event.
AT APPROX 1500, HEARD MOTHER SCREAMING PT'S NAME IN HALLWAY, RN X2 IMMEDIATELY ASSESSED. CHILD FOUND IN FLOOR OUTSIDE WIC LAB. UNWITNESSED FALL. CHILD AWAKE, ALERT, AND ORIENTED. STATED HE HIT HIS HEAD. SMALL RED AREA NOTED TO L FOREHEAD. CHILD ASSISTED TO…
No adverse events - this report is being submitted because the Pfizer-BioNTech vaccine (2024 - 2025 formula, NDC: 59267-4438-02) was inadvertently administered past the product's 10 week Beyond Use Date (BUD). The products BUD as marked on the box by facility…
No adverse events - this report is being submitted because the Pfizer-BioNTech vaccine (2024 - 2025 formula, NDC: 59267-4438-02) was inadvertently administered past the product's 10 week Beyond Use Date (BUD). The products BUD as marked on the box by facility…
MMRV given instead of MMR to an adult. No adverse reactions noted.
Office Visit Note 3/18/25 - Pain began after vaccine administration. Pain is throbbing and affects sleep. She has been sleeping in recliner to try and reduce pain. She has used heat and ice. Patiently, she has significantly reduced range of motion of the l…
No adverse events - This report is being submitted due to the Pfizer-BioNTech COVID-19 vaccine (2024 - 2025 formula, NDC 59267-4438-02) being inadvertently administered past its 10 week Beyond Use Date (BUD). It's BUD as marked by facility was 12/24/2024.
Patient reports 2 weeks hospitalization after receiving Pfizer COVID-19 vaccine. No other information provided.
STUDENT BROUGHT TO NURSE AT 2;28PM 03/24/25BY TEACHER STATING SHE COULD NOT WALK ON HER LEG AND CHILLING THROUGHOUT THE DAY AFTER ARRIVING TO SCHOOL FROM HE DOCOTOR'S APPOINTMENT. INITIALLY TEMPERATURE WAS WNL AT 98.6 TAKEN BY INFRA-RED FOREHEAD THERMOMETER.…
Duplicate vaccine - Prevnar20 was previously administered 4/2024 - patient reports no adverse reactions.
Patient has had pain in left arm since day after receiving vaccine. After 2 weeks went to a physician that recommended treatment with ibuprofen. Patient is still having pain in arm after 42 days. Reseen by physician who is referring him to orthopedic doct…
Patient became dizzy and felt faint 3 minutes after her vaccine. She remained seated and was given an ice pack to put behind her neck. She then stated that her legs and arms felt stiff and numb. I asked if patient has eaten and she only had a protein bar all d…
Patient received an extra Arexvy dose outside of recommendation guidlines. Received first dose on Jan 28, 2024 and received a second dose by error on May 24, 2024