Symptomtext
COVID 19 Treatment; COVID 19 Treatment; vaccine brand other= Moderna/vaccine administration date=02Nov2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 78-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Oct2022 as dose 4 (booster), single (Lot number: Gn9703) at the age of 78 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 27Jan2021 as dose 1, single (Batch/Lot number: unknown), in right arm, on 25Feb2021 as dose 2, single (Lot number: 013a21a), in right arm and on 02Nov2021 as dose 3 (booster), single (Lot number: 014f21a), in right arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: AVASTATIN; LISINOPRIL. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown", described as "vaccine brand other= Moderna/vaccine administration date=02Nov2021". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Negative, notes: negative rapid test; (01Jan2023) Positive, notes: Symptoms resumed and rapid test positive about 10 days after finishing Paxlovid. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received other medication in 2 weeks. Patient received Paxlovid for COVID 19 treatment from 18Dec2022 to 22Dec2022. No known allergies reported.