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
110473113 11047311 3 F 2004 20160628 20150420 20160701 PER US-009507513-1504USA017805 MERCK 0.00 M Y 0.00000 20160701 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
110473113 11047311 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNKNOWN 20788 1 MG FILM-COATED TABLET
110473113 11047311 2 SS FINASTERIDE. FINASTERIDE 1 Oral 1 MG, UNKNOWN 20788 1 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110473113 11047311 1 Alopecia
110473113 11047311 2 Alopecia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
110473113 11047311 Erectile dysfunction
110473113 11047311 Hypercholesterolaemia
110473113 11047311 Hyperglycaemia
110473113 11047311 Loss of libido
110473113 11047311 Myalgia
110473113 11047311 Overweight
110473113 11047311 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
110473113 11047311 1 20030312 0
110473113 11047311 2 2009 0