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: 20 April 2025 – 20 April 2026
Total reports: 279
Most-reported reactions
Inappropriate Schedule Of Product Administration — 35 reports (12.54%)
Metrorrhagia — 35 reports (12.54%)
No Adverse Event — 30 reports (10.75%)
Nausea — 29 reports (10.39%)
Drug Ineffective — 27 reports (9.68%)
Product Substitution Issue — 27 reports (9.68%)
Product Use In Unapproved Indication — 27 reports (9.68%)
Who is the marketing authorisation holder for Estradiol Tablets in United States?
Copenhagen University Hospital at Herlev is the originator. The local marketing authorisation holder may differ — check the official source linked above.