Received Oct 21, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | OT |
rash; itchy; This is a spontaneous report received from a Consumer or other non HCP. Other Case identifier(s): MOD-2025-790242 (Moderna). A patient (age and gender not provided) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), in 2025 as dose 1, single (Batch/Lot number: unknown) intramuscular for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PRURITUS (non-serious) with onset 2025, outcome "unknown", described as "itchy"; RASH (non-serious) with onset 2025, outcome "unknown". Additional information: Reporter stated, "I was looking for the mNEXSPIKE myself and I was having trouble finding it. I went to something our town had and they did not have it. They didn't have Moderna. They only had Pfizer and I couldn't do Pfizer. I mean, I just have a bad reaction. My arm didn't like it. Alright, so I was actually. And so I've only gotten Moderna of late." Reporter added, "No, it's not with Moderna though it's a Pfizer. I just didn't take Pfizer anymore." Reporter provided "just a rash" and "itchy." Caller did not want to provide additional information and stated, "it's my private medical information and it had to do with Pfizer. It had nothing to do with Moderna, so it's really not any of Moderna's business. "When further asked about rash, Reporter stated, "Right, it just was really itchy. That's all. It's not anything life threatening or dangerous. It's just uncomfortable. It was unknown if the patient experienced any additional symptoms/events. Relatedness: Non-Health care professional did not provide any causality assessment. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.