Received May 28, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | — |
When she was sick she got better after she was sick for 3 days and said that it was covid and as far as she was concerned she was vaccinated.; Fever; This is a spontaneous report received from a Consumer or other non HCP. A female patient received BNT162b2 omicron (lp.8.1) (BNT162B2 OMICRON (LP.8.1)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "pneumonia" (unspecified if ongoing); "emergency hernia surgery" (unspecified if ongoing); "COVID" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: ILLNESS (non-serious), outcome "unknown", described as "When she was sick she got better after she was sick for 3 days and said that it was covid and as far as she was concerned she was vaccinated."; PYREXIA (non-serious), outcome "unknown", described as "Fever". Additional Information: Caller said that she took the Pfizer Covid-19 vaccine and said that she got sick for 3 days and had a fever. She called the CDC and they took the report at the time. The first time she had pneumonia she had a tetanus shot in 1987 and 3 days later she had pneumonia and stayed in the hospital. The next time she had pneumonia was in and the next time she got sick was when she was in the hospital and had emergency hernia surgery and ended up with Covid. Caller said that she had Covid after being vaccinated. Caller said that her doctor told her to only take the Pfizer Covid -19 Vaccine and said that it has gotten better each time she has gotten the Covid-19 vaccine. When she was sick she got better after she was sick for 3 days and said that it was covid and as far as she was concerned she was vaccinated. She wants to find out and is supposed to go ahead and get the pneumovax 23 or 21 and the Mediclinic does not have the Pneumovax 23 or Pneumovax 21 and she needs to find out if Pfizer was going to stop making the Pneumovax 21. Caller was notified that Pneumovax 21 is not a Pfizer product and was referred to the manufacturer for more information. The reason the immunologist wants her to take the same vaccination was because they did a baseline for her 6-8 weeks after her immunization with Pneumovax 23 because she has common variable immune disorder and wanted her to have blood work in 4-6 weeks to see if they are producing for the antigens. Caller declined to complete a report for the Pfizer Covid-19 vaccine and requested to be transferred to the USMI department to have her questions addressed about the Prevnar 20. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.
Medical History/Concurrent Conditions: COVID-19; Hernia repair; Pneumonia