Received Jul 28, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| PNC20 | PNEUMO (PREVNAR20) | PFIZER\WYETH | UNK | — | — |
Patient reported that when administered it felt like a bee sting that persisted for 2/3 days.; Area where it was administered was red and had some swelling; Area where it was administered was red and had some swelling; This is a spontaneous report received from a Consumer or other non HCP from a sales representative. A female patient (not pregnant) received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), on 21Jul2025 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION SITE SWELLING (non-serious), VACCINATION SITE ERYTHEMA (non-serious) all with onset 21Jul2025, outcome "recovering" and all described as "Area where it was administered was red and had some swelling"; VACCINATION SITE PAIN (non-serious) with onset 21Jul2025, outcome "recovering", described as "Patient reported that when administered it felt like a bee sting that persisted for 2/3 days.". It was unknown if therapeutic measures were taken as a result of vaccination site pain, vaccination site swelling, vaccination site erythema. Additional information: The patient didn't receive any other vaccines on the same date as the vaccine(s) for which you are reporting. It was unknown if the patient received any other vaccines within 4 weeks PRIOR to the vaccine(s) for which you are reporting. It was unknown if the patient was taking any other medications within 2 weeks of the event starting. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.