🇺🇸 Preservative-free artificial tears in United States
35 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: 35
Most-reported reactions
- Eye Pain — 10 reports (28.57%)
- Eye Irritation — 5 reports (14.29%)
- Impaired Healing — 4 reports (11.43%)
- Ocular Hyperaemia — 3 reports (8.57%)
- Product Administration Error — 3 reports (8.57%)
- Drug Ineffective — 2 reports (5.71%)
- Dry Eye — 2 reports (5.71%)
- Eyelid Oedema — 2 reports (5.71%)
- Intraocular Pressure Increased — 2 reports (5.71%)
- No Adverse Event — 2 reports (5.71%)
Other Ophthalmology approved in United States
Frequently asked questions
Is Preservative-free artificial tears approved in United States?
Preservative-free artificial tears does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Preservative-free artificial tears in United States?
University Hospital, Ghent is the originator. The local marketing authorisation holder may differ — check the official source linked above.