🇺🇸 Prosicca sine in United States
4 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: 4
Most-reported reactions
- Cerebral Haemorrhage — 1 report (25%)
- Drug Interaction — 1 report (25%)
- Dysphagia — 1 report (25%)
- Pneumonia — 1 report (25%)
Other Ophthalmology approved in United States
Frequently asked questions
Is Prosicca sine approved in United States?
Prosicca sine does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Prosicca sine in United States?
Medical University of Vienna is the originator. The local marketing authorisation holder may differ — check the official source linked above.