Received Jan 14, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | — |
The vaccine causes blood clot and killed people, it does to his father (patient); SUPPORT This is a solicited report received from a Consumer or other non HCP, Program ID. A male patient received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: THROMBOSIS (death, medically significant), outcome "fatal", described as "The vaccine causes blood clot and killed people, it does to his father (patient)". The patient date of death was unknown. Reported cause of death: "The vaccine causes blood clot and killed people, it does to his father (patient)". It was not reported if an autopsy was performed. Clinical information: The reporter wanted to know why the vaccine causes blood cloth and killed people, it does to his father (patient). The reporter said he will get a lawyer. He stated his father died because of the vaccine. The reporter's assessment of the causal relationship of "the vaccine causes blood clot and killed people, it does to his father (patient)" with the suspect product(s) BNT162b2 omicron (lp.8.1) was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.; Sender's Comments: As there is limited information in the case provided, the causal association between the event thrombosis and the suspect drug BNT162B2 OMICRON (LP.8.1) cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit-risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, ethics committees and investigators, as appropriate. Linked Report(s) : US-PFIZER INC-202600007230 Same reporter/product/AE, different patient; Reported Cause(s) of Death: The vaccine causes blood clot and killed people, it does to his father (patient)