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
110260623 11026062 3 F 200602 20160914 20150414 20160921 PER US-009507513-1504USA005255 MERCK 0.00 M Y 0.00000 20160921 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
110260623 11026062 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNKNOWN D 20788 1 MG FILM-COATED TABLET
110260623 11026062 2 SS FINASTERIDE. FINASTERIDE 1 Oral 1 MG, UNKNOWN 20788 1 MG FILM-COATED TABLET
110260623 11026062 3 SS FINASTERIDE. FINASTERIDE 1 Oral 1 MG, QD D 20788 1 MG FILM-COATED TABLET QD
110260623 11026062 4 SS BIOTIN BIOTIN 1 Oral 5 MG, QD D 0 5 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110260623 11026062 1 Androgenetic alopecia
110260623 11026062 2 Androgenetic alopecia
110260623 11026062 3 Androgenetic alopecia
110260623 11026062 4 Androgenetic alopecia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
110260623 11026062 Erectile dysfunction
110260623 11026062 Loss of libido
110260623 11026062 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
110260623 11026062 1 1999 2002 0
110260623 11026062 2 2002 2007 0
110260623 11026062 3 200707 201011 0
110260623 11026062 4 200707 201011 0