Received Apr 26, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| PNC20 | PNEUMO (PREVNAR20) | PFIZER\WYETH | UNK | LK6650 | OT / LA |
Pain at the injection site; Pain at the injection site, edema, erythema; This is a spontaneous report received from a Nurse. A 57-year-old female patient (not pregnant) received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), on 24Feb2025 as dose number unknown, 0.5ml single (Lot number: LK6650, Expiration Date: 31May2026) at the age of 57 years intramuscular, in left deltoid for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 25Feb2025, outcome "recovered" (2025), described as "Pain at the injection site"; VACCINATION SITE ERYTHEMA (non-serious) with onset 25Feb2025, outcome "recovered" (2025), described as "Pain at the injection site, edema, erythema". Therapeutic measures were taken as a result of vaccination site pain, vaccination site erythema. Additional information: Patient did not receive any other vaccines on the same date as the vaccine. Patient did not receive any other vaccines within 4 weeks prior to the vaccine. Patient was taking any other medications within 2 weeks of the event starting. Reporter seriousness for pain and erythema at the injection site was not serious. Patient had an adverse event with Prevnar 20 back in February with a different lot. They thought it was a one off thing. She had reported that today also online but that was a different lot. It was reported pain and erythema at the injection site was non serious. States this was not reported to her on time. She was going to say patient noted pain and erythema at the injection site the next day, 25Feb2025.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202500086589 same reporter/product/event, different patient;