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
110260643 11026064 3 F 2001 20160706 20150414 20160713 EXP US-009507513-1504USA010708 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
110260643 11026064 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110260643 11026064 1 Alopecia

Outcome of event

Event ID CASEID OUTC COD
110260643 11026064 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110260643 11026064 Anxiety
110260643 11026064 Brain injury
110260643 11026064 Depression
110260643 11026064 Ejaculation disorder
110260643 11026064 Endocrine disorder
110260643 11026064 Erectile dysfunction
110260643 11026064 Hormone level abnormal
110260643 11026064 Loss of libido
110260643 11026064 Male sexual dysfunction
110260643 11026064 Nephrolithiasis
110260643 11026064 Painful ejaculation
110260643 11026064 Penile size reduced
110260643 11026064 Penis injury
110260643 11026064 Testicular atrophy

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
110260643 11026064 1 2001 2002 0