Received Mar 27, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| HEP | HEP B (RECOMBIVAX HB) | MERCK & CO. INC. | 3 | z004729 | IM / RA |
| IPV | POLIO VIRUS, INACT. (IPOL) | SANOFI PASTEUR | 4 | y1d49p1 | SC / RA |
| TDAP | TDAP (ADACEL) | SANOFI PASTEUR | 3 | 3ca30c1 | IM / LA |
| VARCEL | VARICELLA (VARIVAX) | MERCK & CO. INC. | 3 | y014868 | IM / LA |
An additional dose of Varicella (VARIVAX) was administered at 4:20 PM on March 25, 2026. . This resulted in the administration of a third dose of the vaccine. Involved Product: VARIVAX (Varicella Virus Vaccine Live), 0.5 mL vial, manufactured by Merck and Co. Dose/Strength: 0.5 mL (standard dose). Error Type: Administration of an extra dose (overdose/excess dose). The patient was still in the examination room, allowing for immediate notification of the parent. The patient's health care provider, MD, has been notified. Patient was observed for 30 minutes in the office. No adverse reaction was noted.
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