VAERS 2722913
MODERNA · COVID19 (COVID19 (MODERNA)) · Charge NDC 80777-0102-
- Staat
- CT
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.12.2023
- Impfdatum
- 13.10.2023
- Beginn
- 14.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Symptomtext
Fainting; muscle ache; Fatigue; Nausea; This spontaneous case was reported by a consumer and describes the occurrence of SYNCOPE (Fainting) in a 69-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024) (batch no. NDC 80777-0102-96) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 13-Oct-2023, the patient received dose of mRNA-1273.815 (SPIKEVAX 2023-2024) (Intramuscular use) .5 microgram. On 14-Oct-2023, the patient experienced SYNCOPE (Fainting) (seriousness criterion medically significant), MYALGIA (muscle ache), FATIGUE (Fatigue) and NAUSEA (Nausea). At the time of the report, SYNCOPE (Fainting), MYALGIA (muscle ache), FATIGUE (Fatigue) and NAUSEA (Nausea) had resolved. The action taken with mRNA-1273.815 (SPIKEVAX 2023-2024) (Intramuscular use) was unknown. For mRNA-1273.815 (SPIKEVAX 2023-2024) (Intramuscular use), the reporter did not provide any causality assessments. No concomitant medication was not reported. It was unknown if the patient experienced any additional symptoms/events. No treatment information was reported. Company comment: This spontaneous case concerns a 69 ? year ? old female patient, with no medical history reported, who experienced the unexpected (according to CCDS data sheet), serious (medically significant) event of syncope. The event occurred the day after a dose of Spikevax 2023 - 2024 vaccine (Andusomeran); no information about previous immunisation schedule was provided. The report stated that the patient experienced muscle ache, fatigue, nausea, and fainting. The outcome was recovered. No further clinical details were provided for medical reviewing. The benefit-risk relationship of Spikevax 2023 - 2024 vaccine (Andusomeran) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -