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
92143564 9214356 4 F 200708 20160711 20130405 20160713 PER US-009507513-1304USA002494 MERCK 0.00 M Y 0.00000 20160713 CN 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
92143564 9214356 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK 20788 1 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92143564 9214356 1 Androgenetic alopecia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
92143564 9214356 Circumcision
92143564 9214356 Cognitive disorder
92143564 9214356 Disturbance in sexual arousal
92143564 9214356 Dysuria
92143564 9214356 Libido decreased
92143564 9214356 Organic erectile dysfunction
92143564 9214356 Painful ejaculation
92143564 9214356 Performance fear
92143564 9214356 Prostatitis
92143564 9214356 Semen volume decreased
92143564 9214356 Sexual dysfunction
92143564 9214356 Testicular pain

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
92143564 9214356 1 20070314 2009 0