The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
109716773 10971677 3 F 2007 20160718 20150331 20160722 PER US-009507513-1503USA014218 MERCK 0.00 M Y 0.00000 20160722 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
109716773 10971677 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNKNOWN U 20788 1 MG FILM-COATED TABLET
109716773 10971677 2 SS PROPECIA FINASTERIDE 1 U 20788 FILM-COATED TABLET
109716773 10971677 3 SS FINASTERIDE. FINASTERIDE 1 Oral 1 MG, UNKNOWN U 20788 1 MG FILM-COATED TABLET
109716773 10971677 4 SS FINASTERIDE. FINASTERIDE 1 U 20788 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109716773 10971677 1 Androgenetic alopecia
109716773 10971677 2 Alopecia
109716773 10971677 3 Androgenetic alopecia
109716773 10971677 4 Alopecia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
109716773 10971677 Cognitive disorder
109716773 10971677 Erectile dysfunction
109716773 10971677 Hypertonic bladder
109716773 10971677 Loss of libido
109716773 10971677 Sexual dysfunction

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
109716773 10971677 1 2003 200909 0
109716773 10971677 3 200909 2012 0