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
92484144 9248414 4 F 2010 20160928 20130423 20160930 EXP US-009507513-1304USA008280 MERCK 0.00 M Y 0.00000 20160930 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
92484144 9248414 1 PS PROPECIA FINASTERIDE 1 Unknown 1 MG, UNKNOWN U 20788 1 MG FILM-COATED TABLET
92484144 9248414 2 SS FINASTERIDE. FINASTERIDE 1 Unknown 5 MG, UNKNOWN 0 5 MG
92484144 9248414 3 SS FINASTERIDE. FINASTERIDE 1 Unknown 5 MG, UNK 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92484144 9248414 1 Androgenetic alopecia
92484144 9248414 2 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
92484144 9248414 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
92484144 9248414 Anxiety
92484144 9248414 Cognitive disorder
92484144 9248414 Depression
92484144 9248414 Drug administration error
92484144 9248414 Ejaculation disorder
92484144 9248414 Erectile dysfunction
92484144 9248414 Libido decreased
92484144 9248414 Memory impairment
92484144 9248414 Orgasm abnormal
92484144 9248414 Semen volume decreased
92484144 9248414 Sexual dysfunction
92484144 9248414 Tonsillectomy
92484144 9248414 Wrong technique in product usage process

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
92484144 9248414 1 200610 201001 0
92484144 9248414 2 20100831 20101026 0
92484144 9248414 3 20110421 20120430 0