🇺🇸 Advanced Eye Relief in United States

113 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.

Most-reported reactions

  1. Eye Irritation — 30 reports (26.55%)
  2. Eye Pain — 17 reports (15.04%)
  3. Ocular Hyperaemia — 14 reports (12.39%)
  4. Drug Ineffective — 10 reports (8.85%)
  5. Vision Blurred — 9 reports (7.96%)
  6. Eye Pruritus — 8 reports (7.08%)
  7. Condition Aggravated — 7 reports (6.19%)
  8. Erythema — 7 reports (6.19%)
  9. Lacrimation Increased — 6 reports (5.31%)
  10. Expired Product Administered — 5 reports (4.42%)

Source database →

Other Ophthalmology approved in United States

Frequently asked questions

Is Advanced Eye Relief approved in United States?

Advanced Eye Relief does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Advanced Eye Relief in United States?

Galderma R&D is the originator. The local marketing authorisation holder may differ — check the official source linked above.