← FDATracker
HomeAdverse Events

PROPECIA Adverse Event: Cognitive disorder

PROPECIA Adverse Event: Cognitive disorder is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: PROPECIA; Product category: Drug; Primary reaction: Cognitive disorder.

Primary drugPROPECIA
Product categoryDrug
Primary reactionCognitive disorder
All reactionsCognitive disorder; Anxiety; Depression; Sexual dysfunction; Blood testosterone free decreased
SeriousnessSerious
Patient outcomeNot Recovered/Not Resolved
Patient sexMale
All drugs reportedPROPECIA; PROPECIA
Reporter countryUS
Reporter type1
Report date20140312
Report ID10004188

🔍 Search all adverse events →