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Report #2833361

Received Mar 27, 2025

A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

Overview

Sex
Unknown
Age
Age unknown
State
TN
Recovered
Unknown
Vaccinated
Mar 14, 2024
Onset
Mar 14, 2025
Days to onset
365
Hospital days
—

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
PNC21PNEUMO (CAPVAXIVE)MERCK & CO. INC.UNKY011819—
PNC21PNEUMO (CAPVAXIVE)MERCK & CO. INC.UNKY011819—

Symptoms (2)

Inappropriate schedule of product administrationNo adverse event

Symptom narrative

Caller confirmed no side effects/symptoms reported at this time; Caller is a nurse who reports they had a patient that received a dose of CAPVAXIVE on 2/13/2025 and an additional dose on 3/14/2025.; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 13-FEB-2025 and on 14-MAR-2024, the patient was vaccinated with the first and second dose respectively of pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE), lot #Y011819, which has been verified to be valid lot number for pneumococcal 21-valent Conjugate Vaccine, expiration date reported and upon internal validation establish as 01-OCT-2025 (strength, exact quantity volume, route and anatomical site of administration were not reported), administered for prophylaxis (Inappropriate schedule of product administration). The reported confirmed no side effects or symptoms at this time (No adverse event).