Received Mar 5, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| MMR | MEASLES + MUMPS + RUBELLA (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
| PPV | PNEUMO (PNEUMOVAX) | MERCK & CO. INC. | UNK | — | RA |
| UNK | VACCINE NOT SPECIFIED (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
| UNK | VACCINE NOT SPECIFIED (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
reaction at injection site of swelling the size of the palm of her hand in her right arm; painful; swelling the size of the lymph nodes under right arm; This spontaneous report was received from a consumer referring to herself, a 67-year-old female patient. The patient's medical history was not reported. The patient's concurrent conditions included guaifenesin (DIMETAPP) reaction and latex allergy. Concomitant therapies were not reported. On an unknown date in 2020 (reported as 5 years ago), the patient was vaccinated with Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX 23) solution for injection, administered as vaccine in right arm (strength, dose, route, lot #, and expiration date were not reported). On the same date, the patient was also vaccinated with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (manufacturer unknown) lyophilisate and solvent for solution for injection and unspecified hepatitis vaccine (Hepatitis A Vaccine, Inactivated (manufacturer unknown) suspension for injection or Hepatitis B Vaccine (Recombinant) (manufacturer unknown) suspension for injection), administered for prophylaxis (formulation, strength, dose, route, lot#, and expiration date were not reported). On an unknown date in 2020 (reported as about five years ago), the patient experienced reaction at injection site of swelling the size of the palm of her hand in her right arm (Vaccination site swelling) and the lymph nodes under right arm (injected on right side) (Lymphadenopathy). The events did not happen immediately, but they ended up swollen the whole upper portion of her arm. Painful was for 3-5 days then subsided. The patient had sought medical attention. No treatment was given. Outcome of the events was recovered 3-5 days later. Causality between the events and all the suspect vaccines was not reported. Lot# is being requested and will be submitted if received.
Drug hypersensitivity; Latex allergy
Sterile diluent