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
98069535 9806953 5 F 199809 20160808 20140109 20160812 PER US-009507513-1202USA00565 MERCK 0.00 M Y 0.00000 20160812 LW 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
98069535 9806953 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK N 20788 1 MG FILM-COATED TABLET
98069535 9806953 2 SS PROSCAR FINASTERIDE 1 Oral UNK N U 0 FILM-COATED TABLET
98069535 9806953 3 SS FINASTERIDE. FINASTERIDE 1 Oral N U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98069535 9806953 1 Androgenetic alopecia
98069535 9806953 2 Androgenetic alopecia
98069535 9806953 3 Androgenetic alopecia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
98069535 9806953 Acne
98069535 9806953 Anxiety
98069535 9806953 Cognitive disorder
98069535 9806953 Depression
98069535 9806953 Erectile dysfunction
98069535 9806953 Fibrous histiocytoma
98069535 9806953 Flat affect
98069535 9806953 Hyperhidrosis
98069535 9806953 Loss of libido
98069535 9806953 Miliaria
98069535 9806953 Off label use
98069535 9806953 Rash vesicular
98069535 9806953 Semen volume decreased

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
98069535 9806953 1 199710 2000 0