🇺🇸 Measles Mumps and Rubella Vaccine in United States
25 US adverse-event reports
Safety signals — FAERS
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
- Window: 22 April 2025 – 22 April 2026
- Total reports: 25
Most-reported reactions
- Upper Respiratory Tract Infection — 5 reports (20%)
- Pyrexia — 3 reports (12%)
- Vaccination Complication — 3 reports (12%)
- Abnormal Behaviour — 2 reports (8%)
- Arthralgia — 2 reports (8%)
- Condition Aggravated — 2 reports (8%)
- Contraindication To Vaccination — 2 reports (8%)
- Convulsion — 2 reports (8%)
- Drug Exposure During Pregnancy — 2 reports (8%)
- Drug Ineffective — 2 reports (8%)
Other Immunology approved in United States
Frequently asked questions
Is Measles Mumps and Rubella Vaccine approved in United States?
Measles Mumps and Rubella Vaccine does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Measles Mumps and Rubella Vaccine in United States?
Sanofi is the originator. The local marketing authorisation holder may differ — check the official source linked above.