Received Oct 21, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| UNK | VACCINE NOT SPECIFIED (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
it triggered an immune response to my Dysport (neurotoxin quit working overnight).; it triggered an immune response to my Dysport (neurotoxin quit working overnight).; This is a spontaneous report received from a Consumer or other non HCP, Program ID. 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) for covid-19 immunisation; botulinum toxin type a HAemagglutinin complex (DYSPORT [BOTULINUM TOXIN TYPE A HAEMAGGLUTININ COMPLEX]). The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization. The following information was reported: DRUG INTERACTION (non-serious), IMMUNE SYSTEM DISORDER (non-serious) all with onset 2025, outcome "unknown" and all described as "it triggered an immune response to my Dysport (neurotoxin quit working overnight).". The action taken for botulinum toxin type a HAemagglutinin complex was unknown. Additional information: Patient got COVID booster but it triggered an immune response to Dysport (neurotoxin quit working overnight). This effect's been reported (n45). The information on the batch/lot number for BNT162b2 omicron (lp.8.1) will be requested and submitted if and when received.
Comirnaty (2025-2026 Formula); DYSPORT [BOTULINUM TOXIN TYPE A HAEMAGGLUTININ COMPLEX]