Symptomtext
side effect in her throat; swelling under her arm; swelling next to her shoulder blade; She had received the first two doses of Pfizer. The boosted with moderna vaccine; A lot of aches and pains; This spontaneous case was reported by a consumer and describes the occurrence of SWELLING (swelling next to her shoulder blade), SWELLING (swelling under her arm), OROPHARYNGEAL DISCOMFORT (side effect in her throat), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (She had received the first two doses of Pfizer. The boosted with moderna vaccine) and MYALGIA (A lot of aches and pains) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 034FUA) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for COVID-19 vaccination. No Medical History information was reported. On 13-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient started TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On an unknown date, TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On 13-Nov-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (She had received the first two doses of Pfizer. The boosted with moderna vaccine) and MYALGIA (A lot of aches and pains). On 14-Nov-2021, the patient experienced SWELLING (swelling next to her shoulder blade). On 15-Nov-2021, the patient experienced SWELLING (swelling under her arm). On an unknown date, the patient experienced OROPHARYNGEAL DISCOMFORT (side effect in her throat). On 13-Nov-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (She had received the first two doses of Pfizer. The boosted with moderna vaccine) had resolved. On 14-Nov-2021, MYALGIA (A lot of aches and pains) had resolved. At the time of the report, SWELLING (swelling next to her shoulder blade), SWELLING (swelling under her arm) and OROPHARYNGEAL DISCOMFORT (side effect in her throat) outcome was unknown. Concomitant products were not provided. Treatment medication were not reported.