Received Aug 4, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| PNC20 | PNEUMO (PREVNAR20) | PFIZER\WYETH | UNK | — | — |
Patient experienced local site reaction of erythema, extended warmth and redness; Patient experienced local site reaction of erythema, extended warmth and redness; This is a spontaneous report received from a Nurse from a sales representative. A 58-year-old female patient (not pregnant) received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history included: "Allergy" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION SITE WARMTH (non-serious), VACCINATION SITE ERYTHEMA (non-serious), outcome "recovered" and all described as "Patient experienced local site reaction of erythema, extended warmth and redness". Therapeutic measures were taken as a result of vaccination site warmth, vaccination site erythema. Additional information: Patient did not receive any other vaccines on the same date as the vaccine(s) for which you are reporting., the patient did not received any other vaccines within 4 weeks PRIOR to the vaccine(s) for which you are reporting, the patient not taking any other medications within 2 weeks of the event starting. Treatment received for the adverse event with Ice and Recommended Ibuprofen and Zyrtec. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.
Medical History/Concurrent Conditions: Allergy