Received Jun 17, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| PNC21 | PNEUMO (CAPVAXIVE) | MERCK & CO. INC. | UNK | — | — |
a nurse had administered CAPVAXIVE to a pediatric patient; no adverse event; This Spontaneous report was received from Nurse and referred to a/an ( Race Unknown ) ( Ethnicity Unknown) Child patient of unknown age and gender. The patient's medical history was not reported. The patient's past medications were not reported. The patient's concomitant medications were not reported. On an unknown date, patient started therapy with Pneumococcal 21-valent Conjugate Vaccine Solution for injection 114412038:4347Unknown Batch/Lot Number dose form was Solution for injection. The patient started therapy with Pneumococcal 21-valent Conjugate Vaccine Solution for injection 114412038:4347 for the treatment of prophylaxis, On an unknown date, the patient experienced a nurse had administered CAPVAXIVE to a pediatric patient (Product administered to patient of inappropriate age). On an unknown date, the patient experienced no adverse event (No adverse event). The Outcome of Product administered to patient of inappropriate age was not provided. The Outcome of No adverse event was not provided. The action taken with Pneumococcal 21-valent Conjugate Vaccine Solution for injection 114412038:4347 regarding Product administered to patient of inappropriate age was Not applicable with Not Applicable dechallenge and rechallenge results. Case Assessments: Pneumococcal 21-valent Conjugate Vaccine Solution for injection 114412038:4347 regarding No adverse event with Not Applicable dechallenge and rechallenge results. The Nurse considered the event Product administered to patient of inappropriate age (,) to be not assessed to Pneumococcal 21-valent Conjugate Vaccine Solution for injection 114412038:4347 and the event No adverse event (,) to be not assessed to Pneumococcal 21-valent Conjugate Vaccine Solution for injection 114412038:4347 The Nurse considered the event Product administered to patient of inappropriate age to be non-serious and the event No adverse event to be non-serious. Additional information is not expected.